You are on page 1of 18

Journal of Environmental Management 345 (2023) 118917

Contents lists available at ScienceDirect

Journal of Environmental Management


journal homepage: www.elsevier.com/locate/jenvman

Review

Nutrient treatment of greywater in green wall systems: A critical review of


removal mechanisms, performance efficiencies and system
design parameters
Moeen Gholami a, Aisling D. O’Sullivan a, b, **, Hamish R. Mackey a, *
a
Department of Civil and Natural Resources Engineering, University of Canterbury, Private Bag 4800, Christchurch, 8140, New Zealand
b
Centre for Ecological Technical Solutions (CELTS.org.nz), University of Canterbury, Private Bag 4800, Christchurch, 8140, New Zealand

A R T I C L E I N F O A B S T R A C T

Handling Editor: Dr. Lixiao Zhang Greywater has lower pathogen and nutrient levels than other mixed wastewaters, making it easier to treat and to
reuse in nature-based wastewater treatment systems. Green walls (GWs) are one type of nature-based solutions
Keywords: (NBS) that are evolving in design to support on-site and low-cost greywater treatment. Greywater treatment in
Decentralized treatment GWs involves interacting and complex physical, chemical, and biological processes. Design and operational
Nature-based technologies
considerations of such green technologies must facilitate these pivotal processes to achieve effective greywater
Nitrogen removal
treatment. This critical review comprehensively analyses the scientific literature on nutrient removal from
Phosphorus removal
greywater in GWs. It discusses nutrient removal efficiency in different GW types. Total nitrogen removal ranges
from 7 to 91% in indirect green facades (IGF), 48–93% for modular living walls (MLW), and 8–26% for
continuous living walls (CLW). Total phosphorus removal ranges from 7 to 67% for IGF and 2–53% for MLW. The
review also discusses the specific nutrient removal mechanisms orchestrated by vegetation, substrates, and
biofilms to understand their role in nitrogen and phosphorus removal within GWs. The effects of key GW design
parameters on nutrient removal, including substrate characteristics, vegetation species, biodegradation, tem­
perature, and operating parameters such as irrigation cycle and hydraulic loading rate, are assessed. Results show
that greater substrate depth enhances nutrient removal efficiency in GWs by facilitating efficient filtration,
straining, adsorption, and various biological processes at varying depths. Particle size and pore size are critical
substrate characteristics in GWs. They can significantly impact the effectiveness of physicochemical and bio­
logical removal processes by providing sufficient pollutant contact time, active surface area, and by influencing
saturation and redox conditions. Hydraulic loading rate (HLR) also impacts the contact time and redox condi­
tions. An HLR between 50 and 60 mm/d during the vegetation growing season provides optimal nutrient
removal. Furthermore, nutrient removal was higher when watering cycles were customized to specific vegetation
types and their drought tolerances.

wastewater treatment plants (WWTPs) are generally effective to meet


1. Introduction local standards, they are expensive capital and operational assets and
incur high carbon footprints. For example, in the United States, WWTPs
Rapid urbanization results from economic and social growth and is and drinking water treatment accounts for up to 3–4% of the country’s
accelerating the key global environmental issues including air, water electricity consumption (Glover et al., 2021). Furthermore, aging
and waste pollution, decreased vegetative land cover, and urban heat wastewater infrastructure is propelling the need to consider alternative
island effects (Liang et al., 2019). One of the most challenging impacts of options including nature-based solutions that are decentralized.
urbanization is voluminous wastewater generation (Zheng and Kamal, Nature-based wastewater treatment systems, such as treatment wetlands
2020), which is anticipated to rise by 51% by 2050 (Qadir et al., 2020). (TWs), green walls (GWs), and green roofs (GRs), offer many advantages
Treatment of this wastewater in centralized treatment plants in towns over centralized WWTPs.
and cities requires substantial infrastructure, land, and energy. Although Municipal wastewater is mainly produced by households (and other

* Corresponding author.
** Corresponding author. Department of Civil and Natural Resources Engineering, University of Canterbury, Private Bag 4800, Christchurch, 8140, New Zealand.
E-mail addresses: aisling.osullivan@canterbury.ac.nz (A.D. O’Sullivan), hamish.mackey@canterbury.ac.nz (H.R. Mackey).

https://doi.org/10.1016/j.jenvman.2023.118917
Received 8 June 2023; Received in revised form 28 August 2023; Accepted 29 August 2023
Available online 7 September 2023
0301-4797/© 2023 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-
nc-nd/4.0/).
M. Gholami et al. Journal of Environmental Management 345 (2023) 118917

Abbreviation list/nomenclature N Nitrogen


NBS Nature-based solutions
AFP Air-filled porosity NH3 Ammonia
BOD Biochemical oxygen demand NH+4 Ammonium
CEC Cation exchange capacity NLR Nitrogen loading rate
CLR Contaminant loading rate NO−2 Nitrite
CLW Continuous living wall NO−3 Nitrate
COD Chemical oxygen demand OrgN Organic nitrogen
DO Dissolved oxygen P Phosphorus
DON Dissolved organic nitrogen PAOs Polyphosphate-accumulating organisms
EC Electrical conductivity PLR Phosphorus loading rate
GRs Green roofs PO34 Phosphate
GWs Green walls WSI Water Stress Index
HDI Human Development Index TDN Total dissolved nitrogen
HLR Hydraulic loading rate TKN Total Kjeldahl nitrogen
HRT Hydraulic retention time TN Total nitrogen
IGF Indirect green façade TP Total phosphorus
LECA Light expanded clay aggregate TWs Treatment wetlands
MLW Modular living wall WWTPs Wastewater treatment plants

tenanted buildings) and can be split into two key forms: blackwater and TWs that typically command substantial land footprints not readily
greywater. Blackwater comes from toilets and contains urine, toilet available, or affordable, in urban environments, and which require
paper, and faecal matter; while greywater comes from baths, showers, vegetation to be hydrophytic (water-loving) to withstand their water­
hand basins, washing machines and dishwashers. Kitchen sinks may be logged conditions, GW have minimal land requirements and can support
directed to greywater or blackwater due to their high organic, nutrient non-hydrophytic vegetation that can align to the native ecosystem and
and microbial load. Greywater has a relatively lower pathogenic risk and be more aesthetic.
lower nutrient concentration (median TN: 11.0 and TP: 7.5 mg/L) Most studies of greywater treatment by GWs have focused on the
compared to blackwater or to mixed domestic sewage, making it easier pollutant removal performance by different vegetation species and/or
to treat and reuse in a decentralized manner (Patil et al., 2022; Paulo substrate composition, along with some design aspects (e.g. planter di­
et al., 2013). Up to 70% of total household water use ends up as grey­ mensions, biofilter units, or irrigation method). Specifically, only four
water (Shaikh and Ahammed, 2020). While usually mixed with black­ review papers related to greywater treatment by GWs, GRs, and/or TWs
water, separating greywater from it offers a number of reuse are published (Arden and Ma, 2018; Boano et al., 2020b; Mahmoudi
opportunities including irrigation, toilet flushing, and laundry that can et al., 2021; Pradhan et al., 2019a). Boano et al. (2020b) reviewed
also help reduce household water use by up to 50% in arid regions greywater treatment performance in TWs, GWs, and GRs (until August
(Radingoana et al., 2020). On-site greywater treatment could also lower 2019) as a function of their hydraulics, as well as assessing some envi­
the risk of relying on centralized WWTPs and/or on centralized water ronmental impact considerations using life cycle assessments. Pradhan
supply systems. Areas of most relevance are those that experience water et al. (2019a) assessed the social, cultural, health, and cost consider­
shortages (Paulo et al., 2013) or in regions at risk of natural disasters ations of GWs and GRs (until August 2018) for greywater treatment,
such as earthquakes, flooding and tsunamis, which can lead to infra­ providing a brief description of the roles of substrate and vegetation in
structure failures, including pipe damage, treatment plant disruptions, nutrient removal. Arden and Ma (2018) focused only on greywater
and contamination of water sources. Furthermore, a decentralized treatment in TWs while Mahmoudi et al. (2021) reviewed GRs only.
wastewater treatment-reuse approach can negate high energy and other While these studies summarised the performance of different substrate
costs associated with conveyance and treatment at centralized systems and vegetation types, they lacked detailed explanation of how specific
(Li et al., 2022). The NBS approach can also sequester carbon through nutrient removal processes, such as vegetative uptake and biofilm
vegetation, offer biodiversity enhancements and reduce heat island ef­ degradation, contribute to nutrient removal. Moreover, these studies did
fects (Castellar et al., 2022). not specifically assess nutrient removal from greywater in GWs with
Successful removal of nutrients in NBS for low-cost greywater reuse regards to green wall type and configurations. Furthermore, specific
has been demonstrated primarily in TWs (Lakho et al., 2020), although operational criteria, such as pollutant and hydraulic loading rates, sea­
there has been growing interest in the use of GWs for greywater treat­ sonality, and irrigation cycle have not been investigated in relation to
ment (Gattringer et al., 2016; Masi et al., 2016). GWs are constructed nutrient treatment. Removal of nutrients becomes crucial in internal
with vegetation grown in substrate-filled containers suspended on the greywater reuse scenarios (e.g. toilet flushing) to prevent the growth of
side of buildings with a vertical support frame. They require little hor­ biofilms within pipes. Additionally, when utilizing greywater for out­
izontal footprint, can improve the aesthetics of residential and office door irrigation purposes, effective nutrient removal is essential to
buildings, and provide thermal regulation through shading and insu­ minimize the risks of nutrient leaching into surface and groundwater
lation (Bakhshoodeh et al., 2022). Additionally, GWs can mitigate sources. Green walls treating greywater can therefore help mitigate the
external noise, improve local air quality and are reportedly relatively potential for nutrient-related water quality pollution, ensuring envi­
easily maintained (Perini and Rosasco, 2013). Compared to TWs, GWs ronmentally responsible and sustainable water management practices.
require lightweight substrates, they convey (waste)water through With the growing number of published studies trialling GWs to treat
shorter vertical (as opposed to horizontal) unsaturated flow paths, and greywater, it’s apt timing to critically assess the nutrient removal effi­
vegetation is typically ornamental species. It has recently been demon­ ciencies and treatment mechanisms at play with respect to different
strated that greywater can be safely applied as ‘fertigation’ (fertilizer substrate properties, vegetation species and operational conditions of
and irrigation) to green wall vegetation without negative effects on the various studies.
vegetation growth (Chung et al., 2021). Compared to horizontal-flow The main objectives of this critical review are to (i) assess the

2
M. Gholami et al. Journal of Environmental Management 345 (2023) 118917

variations in greywater source characteristics suitable for treatment in one of the three predefined inclusion-exclusion criteria established
GWs; (ii) synthesize the literature on nutrient removal efficiencies from during the screening process; otherwise, it was excluded (Step 2). The
greywater by different types of GWs; (iii) summarize the nutrient criteria were: (2.1) Does the study provide information on nutrient
removal mechanisms and fate of the nutrients in GWs; (iv) assess the removal from greywater by green walls? (2.2) Does the complementary
effects of key operating parameters (hydraulic loading rates, nutrient (i.e. if not specifically GW) study discuss nutrient removal mechanisms
loads, temperature, seasonal changes, irrigation cycle, and biofilter and operating parameter effects in vertical-flow TWs and GRs treating
design) on nutrient removal; (v) explain the critical physicochemical greywater? (2.3) Does the study investigate the role of substrate, mi­
characteristics of the GW substrates and; (vi) highlight research gaps/ croorganisms, or vegetation in nutrient removal from greywater? The
limitations related to the success of GW greywater treatment systems to most relevant studies meeting the criteria were further examined in Step
remove nutrients. 3, from which key data relevant to the research objectives (Step 4) were
retrieved, organized into summary figures and tables, and then assessed
2. Methodology and discussed (Step 5).

This study searched Scopus and Google Scholar databases for sci­ 3. Results and discussion
entific literature on greywater treatment in green walls, green roofs, and
treatment wetlands. The TW and GR considered in this search included 3.1. Discipline and region-specific studies on green walls to treat
only vertical-flow systems, which share common nutrient removal greywater
mechanisms with GWs. By including all three NBS in the literature
search, a richer data-set was obtained to understand the effects of The total number (n) of scientific reports published on different as­
common operating parameters on nutrient removal. Furthermore, pub­ pects of green walls are mainly in the engineering (225), environmental
lications on substrate properties, vegetation species, biofilm character­ science (190), social science (101), and energy disciplines (89) as pre­
istics, and their role in nutrient removal from greywater or wastewater, sented in Fig. 2(a). Since 2016 (Gattringer et al., 2016; Masi et al.,
were captured. 2016), there have been an increasing number of studies on using GWs to
A detailed methodology was developed for the literature review treat greywater (Fig. 2(b)). This trend is expected to continue because
process as illustrated in Fig. 1, which outlines the search criteria and the more recent studies have focused on the development and optimi­
publication selection process. Eligible research papers were initially zation of GWs by examining their substrates, vegetation, system design,
screened based on a high-level review of their title, keywords, and ab­ operational parameters, and removal of emerging pollutants (Abd-ur-­
stract (Step 1). To be accepted, a study was required to satisfy at least Rehman et al., 2022). Moreover, GWs are becoming more prominent as

Fig. 1. Summary of data gathering and analysis methodology.

3
M. Gholami et al. Journal of Environmental Management 345 (2023) 118917

<0.6), to 30 L/(p.d) in Mali with a HDI of 0.42 and low WSI (<0.3). The
variation is attributed to the different living standards and relatedly,
water availability (Khanam and Patidar, 2022). In the more ‘developed’
nations, greywater volumes and average daily per person water con­
sumption were reported at median per capita rates of between 62 and
223 L/(p.d) and 78–343 L/(p.d) by Shaikh and Ahammed (2020). The
figures for low income countries were 14–140 L/(p.d) and 35–234 L/(p.
d). Not surprisingly, Yemen, one of the least developed countries with
low water availability (WSI>1), produces an average of only 35 L/(p.d)
greywater (Ghaitidak and Yadav, 2013).
The greywater pollution signature is very dependent on the use of
chemical products such as soaps, shampoos and body wash, toothpaste,
cosmetics, detergent, shaving cream, and other personal care and
cleaning products that contain a wide range of resulting pollutants
(Shaikh and Ahammed, 2020). Overall, greywater contains up to 30% of
the organic carbon load and 9–20% of nutrients in domestic wastewater
(Fountoulakis et al., 2016). Table 1 shows two categories of greywater
based on its pollution strength and associated source. Light greywater
includes wastewater from the bathroom washbasin, shower and floor
cleaning, while dark greywater is typically only wastewater from the
kitchen and laundry. The presence of oil and food waste from kitchen
greywater, as well as detergent from laundry greywater, leads to high
levels of organic pollution and phosphorus in dark greywater compared
to light greywater. Moreover, dark greywater has elevated suspended
solids (SS) at 35–2945 mg/L and turbidity at 50–332 NTU (Table 1),
arising from food particles from kitchen greywater, as well as hair and
fibres from laundry greywater.
Table 2 summarizes water quality across the different greywater
streams and studies. The main water quality variables measured in
greywater include BOD5, COD, pH, and nutrients in the form of various
N and P forms. The data reveal that overall concentrations of these
pollutants vary greatly from one country to another, as well between
sources within the same study (Table 2). Even within the same neigh­
bourhood, it has been found that greywater characteristics vary
depending on inhabitant water usage, lifestyle and household/personal
care product usage (Boyjoo et al., 2013).
Oxygen demands are a measure of the oxygen required by respiring

Table 1
Dark and light greywater constituents and quality characteristics (Antonopoulou
Fig. 2. (a) The total number of scientific reports published on different aspects et al., 2013; Boyjoo et al., 2013; Dal Ferro et al., 2021; do Couto et al., 2013;
of green walls; (b) Number of studies on treatment wetlands, green walls, and Eriksson et al., 2002; Khajvand et al., 2022; Khanam and Patidar, 2022; Shaikh
green roofs treating greywater between 2010 and 2023; (c) Number of studies and Ahammed, 2020; Verma et al., 2021; Vuppaladadiyam et al., 2019). Values
on greywater treatment by green walls by country. represent min-max ranges and (median) ± standard deviation.
Source/water Types
part of sustainable building design; thus the integration with greywater quality Dark greywater Light greywater
characteristics Kitchen: Dish washing Bathroom: Shampoo, soap,
treatment becomes increasingly attractive (Pradhan et al., 2019a).
detergents, oil and fats, food toothpaste, lint, traces of
Globally, Australia (n = 10 studies) and Italy (n = 7 studies) have residue, hot water, raw meat urine, body care products,
dominated the literature on greywater treatment by GWs (Fig. 2(c)), washing, fruit and vegetable hairs, skin, hair oil, body
possibly because of the significant droughts and arid conditions those peels, tea or coffee, traces of fats, hot water and sand/
regions encountered in the past decade. food preservatives, sand and clay particles a.
clay particles a.
Laundry: Chemicals from Hand basin: Toothpaste,
3.2. Greywater quantity and quality detergents, oils, solvents, soaps, body care products,
bleaches, paints, hot water, shaving waste, hairs, and
The quantity and water quality of greywater varies according to its nonbiodegradable fibres from skin cells a.
clothing a.
origin. The average daily volume of greywater generated per person
pH 6.8–10.0 (8.4) ±1.6 6.5–8.1 (7.3) ±0.8
significantly differs across countries, depending on their Human EC (μS/cm) 190-5700 (2945) ±2755 80.-250 (165) ±85
Development Index (HDI) and Water Stress Index (WSI). HDI is a Turbidity (NTU) 50–332 (191) ±141 28–240 (134) ±106
normalized indicator that measures a country’s level of development, TSS (mg/L) 35-2945 (1490) ±1455 28-120 (74) ±46
while WSI defines the availability of water resources in a particular re­ COD (mg/L) 88-5150 (2619) ±2531 72-380 (226) ±154
BOD5 (mg/L) 70-998 (534) ±464 20-200 (110) ±90
gion. Water consumption in countries, such as USA, with HDI >0.8 is TN (mg/L) 2.7–21.0 (12.0) ±9.1 5.0–17.0 (11.0) ±6.0
high, exemplifying that higher quantities of greywater are generated in Ammonium (mg/ <0.1–11.0 (5.6) ±5.5 <0.1–15.0 (7.5) ±7.4
developed countries compared to countries with a low HDI of <0.5, such L)
as Yemen, Ghana, and Mali (Khanam and Patidar, 2022; Shaikh and Nitrate (mg/L) <0.005–2.0 (1) ±0.9 <0.05–6.0 (3.1) ±2.9
TP (mg/L) 0.062–57.0 (28.5) ±28.4 0.1–15.1 (7.5) ±7.4
Ahammed, 2020). Consumption volumes ranged from 208 L/(p.d) in the
USA with a corresponding HDI of 0.92 and moderate WSI (0.3 ≤ WSI a
(Shaikh and Ahammed, 2020).

4
M. Gholami et al.
Table 2
Kitchen, laundry, shower, bath, and mixed greywater quality characteristics from different greywater streams.
Greywater pH EC (μS/cm) Turbidity TSS (mg/L) COD (mg/L) BOD5 (mg/ N (mg/L) P (mg/L) BOD5/ Surfactants Country/Ref.
source (NTU) L) COD (mg/L)

Kitchen 7.8–9.5 (8.7) 880–1065 (992) 88–333 (139) – 455–1102 (855) 70–255 TKN: 16–45 (28) TP: (0.2) 8.9–19 (12.6) Italy (Dal Ferro et al.,
(200) NH+4 : 2.5–11 (6.9) 13.9–17.7 (15.7) 2021)
NO−3 : <0.005–0.02 P-PO3-4 : 5–7.5
(0.01) (6.5)
Laundry Household: Household: 82- Household: Laundry facility: Hospital: (280) – Hospital: TN: (2.8) Hospital: TP: – – South Korea (Kim and
8.1–9.4 250 60-240 56-230 Laundry facility: Laundry facility: TN: (9.9) Park, 2022)
Hospital: (9.6) Laundry facility: Dormitory: 20- 727-1434 6.7–12.7 Laundry facility:
Laundry facility: 2009-5747 2946 Dormitory: 792- TP: 1.8–22
7.9–9.0 Dormitory: 284- 5150
Dormitory: 740
6.1–8.5
Laundry 7-9 (8) – 40–150 90–200 400–1000 – – – – 1–15 Italy (Ciabattia et al.,
industrial 2009)
Shower (7.6) ± 0.4 (645) ± 67 (29) ± 11 – (109) ± 33 (59) ± 13 TKN: (15.2) ± 4.5 TP: (1.6) ± 0.5 (0.5) (0.3) Morocco (Merz et al.,
5

NH+
4 : (11.8) ±4.2 P-PO3-
4 : (1.0) ± 2007)
0.4
Public bath (8) ± 0.1 (811) ± 185 (68) ± 28 (40) ± 30 (72.) ±51 – TN: (7.0) ± 3.5 TP: (0.4) ± 0.2 – – Denmark (Prajapati
et al., 2019)
Bathroom 7.3–7.(7.6) 358-627 (468) 35-462 (150) 37-360 (125) 112-1001 (399) 78-670 TN: 4–16 (9.5) TP: 0.2–1.1 (0.4) (0.6) 0.3–11 (6.8) France (Chaillou et al.,
(240) 2011)
Mixed 6.9–7.4 (7.1) – 39-254 (103) 28-146 (79) 179-525 (347) 72-182 TKN: 2–13 (8.0) TP: 4–15 (9.5) (0.3) – Turkey (Baban et al.,
(119) NH+4 : 0.6–5.5 (2.2) 2010)
Mixed 5-8 (7) 1208-2530 (2044) – 333-744 (537) 270-1595 (758) 270-1595 NH+4 : 7–2 (14.8) TP: 1–3 (2) (0.3) – Ghana (Oteng-Peprah
(253) NO−3 : 0.1–5 (2.5) et al., 2018b)
Mixed (8.3) ± 0.3 – (185) ± 6 – (350) ± 23 (280) ± 16 – – (0.8) – Iran (Bahrami et al.,
2020)

Journal of Environmental Management 345 (2023) 118917


Laundry (8.6) – (247) (266) (1590) (260) – – (0.2) India (Patil et al.,
Kitchen (7.1) (298) (717) (1083) (998) (0.9) 2022)
Wash basin (8.1) (102) (181) (424) (252) (0.6)
Bathing (7.4) (209) (256) (366) (215) (0.6)
Mixed (7.4) (133) (216) (831) (245) (0.3)

N: Nitrogen, P: Phosphorus.
M. Gholami et al. Journal of Environmental Management 345 (2023) 118917

microorganisms (BOD5) or strong chemical oxidants (COD) to oxidize water hardness to improve cleaning performance (Turner et al., 2013).
carbon in the water. Laundry wastewater accounts for the highest con­ Concentrations of TKN and TP in kitchen greywater are between 16-45
centration of COD (Tables 1 and 2), which is mainly generated from and 14–18 mg/L, respectively (Dal Ferro et al., 2021), while Kim and
surfactants and other disinfectants in cleaning or washing activities Park (2022) reported that TN and TP concentrations for laundry facil­
(Verma et al., 2021). This source of greywater is not so easily treated in ities varied between 7-13 and 2–22 mg/L, respectively (Table 2).
biofilters because the carbon is less bioavailable to microorganisms.
When the BOD5/COD ratio is ≥ 0.5, the greywater is readily degradable 3.3. Green wall types
by microbial assimilation – meaning there is sufficient carbon to support
biological growth and hence wastewater treatment. Low biodegrad­ GWs are categorized into two major groups (Fig. 3) – green façades
ability (when BOD5/COD is < 0.5) can sometimes be attributed to the and living walls. These are further subcategorized depending on how the
presence of surfactants and other more recalcitrant chemicals, which substrate and vegetation are supported (Cuce, 2017). Green facades
impede biodegrading microorganisms (Khajvand et al., 2022). Where include direct green façade systems (DGF) in which climbing or
data was reported, the BOD5/COD ratio for all types of greywater ranged cascading vegetation grow directly on the wall (Fig. 3(a)) and indirect
between 0.16 and 0.92 (Table 2), with a mean > 0.54 (Patil et al., 2022), green facades (IGF) which use detached vertical supporters (e.g. trellis,
indicating there is generally sufficient biodegradable carbon to support steel cables and wires, rope, and mesh systems) (Fig. 3(b)) to support the
microbial growth during greywater treatment. substrate and vegetation (El Menshawy et al., 2022). Living wall systems
High pH values in greywater are primarily caused by alkaline sub­ (LWS) are categorized into modular and continuous forms, as shown in
stances in detergents, particularly from laundry sources (Oteng-Peprah Fig. 3(c) and (d). Modular living walls (MLW) consist of several modular
et al., 2018a). Strongly acidic or alkaline pH (pH < 6.0 and pH > 8.0, containers containing substrate and vegetation (Manso and
respectively) can hinder the treatment processes in vegetated biofilters Castro-Gomes, 2015). These modules may take different forms such as
(Saeed and Sun, 2012), so it is critical to achieve a balanced pH. The pH panels, wire cages, trays, vessels, planter tiles, flexible bags, etc,
is also important for healthy growth of vegetation in GWs, as the sub­ although container pots are most common. They are attached to a spe­
strate acidity/alkalinity affects the solubility and availability of mac­ cific supporting structure, one above the other, thus if the vegetation
ronutrients (Gentili et al., 2018). From Table 2, the pH values in dies in one module, the affected module can be easily replaced
different greywater sources varied widely between 5.0 and 9.6, with (Addo-Bankas et al., 2021). In contrast, continuous living walls (CLW)
laundry greywater having the highest pH levels because of alkaline are a single sheet of mat-like material or permeable frames containing a
materials in detergents (Khajvand et al., 2022). Therefore, day equal­ small amount of substrate (Al-Kayiem et al., 2020; Prodanovic et al.,
ization tanks or pH-buffering may be required before conveying grey­ 2019a). CLWs are lighter but more challenging to maintain because they
water directly to GWs. Of all the studies that tested greywater treatment comprise one unit and therefore are less easy to replace if needed. In
in GWs, only Lakho et al. (2022) used real (as opposed to synthetic) comparison to green façades, LWS require more complicated planter
greywater, which they stored without any pre-treatment before modules, irrigation systems, structural support, specific growing sub­
conveying it to the green walls. strate, and installation needs, leading to higher total construction and
Electrical conductivity (EC), total suspended solids (TSS), and maintenance costs (Vox et al., 2022). However, they do provide a rapid
turbidity levels are also higher in kitchen and laundry greywater, in coverage of large surfaces and a more uniform growth along the wall (El
comparison to bathroom and handbasin greywater, due to solid re­ Menshawy et al., 2022).
siduals from food particles, oil and grease (O&G), soil, sand and dis­ The design and operation of different green wall types differ pri­
solved solids (Boyjoo et al., 2013). Values for EC, TSS and turbidity in marily according to their substrate characteristics and substrate depth.
dark greywater ranged from 190 to 5700 μS/cm, 35 to 2945 mg/L, and These substrate attributes affect the specific surface area available for
50 to 332 NTU, respectively (Table 1). Specifically, EC values are higher pollutant exchange and transformation, effective root depth and aera­
in mixed (1208–2530 μS/cm), laundry (2009–5747 μS/cm), and kitchen tion capacity that influences substrate redox conditions. The number
(880–1065 μS/cm) greywater compared to other sources (Table 2). EC is and type of vegetation that can be supported in different GWs therefore
a measure of the total ionic strength (from dissolved elements or com­ varies and, in turn, also influences nutrient removal from the greywater.
pounds) of wastewater, which tends to be higher in laundry wastewater Green facades typically use climbing plants, while living walls pre­
due to the alkali salts in laundry detergents. It has been suggested that dominantly use non-climbing ornamental species that require additional
higher EC values, representing high concentrations of dissolved ions, supporting structures to accommodate multiple units and provide
may compete for substrate adsorption sites affecting nutrient removal adequate surface area for pollutant removal (El Menshawy et al., 2022).
(Nikpay, 2022) and can hinder nutrient uptake by vegetation (at EC > However, weight restrictions on supporting structures may limit the
3000 μS/cm or TDS >2000 mg/L) due to an increase in the osmotic design of biofilters in MLW, particularly when implementing saturated
pressure of the solution (Yuvaraj et al., 2021). Therefore, lower EC zone designs. Green facades can accommodate vegetation with exten­
values in greywater could help nutrient removal and vegetation survival sive roots and heavier substrate loads compared to living walls. The
in GWs, though more research effort is required, particularly in the case number of plants and biofilter units, along with their shape, structure,
of long-term studies that include assessment of changes in both the and substrate volume, play a crucial role in sustaining nutrient removal
planting media and plant metabolism. However, nitrification and under various operating conditions. For instance, living wall formats
denitrification process are generally not so affected by EC, while phos­ with greater surface openings (e.g. CLW) can enhance substrate aeration
phate is typically removed by co-precipitation with solids and (Lakho et al., 2021b) compared to individual deeper modules, but may
adsorption. also face increased evapotranspiration losses. For instance a study
Nutrients in greywater mainly originate in the kitchen and laundry comparing pot-based and closed-block (column) designs found no sig­
with TN and TP ranging from 2.75 to 21 and 0.062–57 mg/L, respec­ nificant difference in nutrient removal, while the block design had
tively, so greywater with high proportions of kitchen and laundry higher resistance to dry periods due to its more enclosed structure
sources have higher nutrient concentrations (Oteng-Peprah et al., (Prodanovic et al., 2020). The optimal number of vertical treatment
2018a). Kitchen wastewater is rich in nitrogen because of biogenic units (or levels) in GWs is a crucial design consideration, as the addition
amines present in food (Eriksson et al., 2002) while bathroom greywater of extra units may result in higher construction costs and higher organic
has the lowest nitrogen concentrations (Eriksson et al., 2002). The main leaching from the longer passage through the organic media (Proda­
source of phosphorus in greywater is from frequent use of detergents novic et al., 2019a). The number of treatment units employed in GWs
used in the kitchen and/or laundry because they typically contain so­ should therefore consider factors such as vegetation type, removal ef­
dium tripolyphosphates or potassium phosphates; agents that decrease ficiency goals, and cost-effectiveness.

6
M. Gholami et al. Journal of Environmental Management 345 (2023) 118917

Fig. 3. Schematic diagrams of different green wall types: (a) Direct green façade (DGF); (b) Indirect green façade (IGF); (c) Modular living wall (MLW); (d)
Continuous living wall (CLW).

3.4. Greywater treatment in green walls areas of 14.4 m2 and 5.4 m2 were assessed for treating 100 L per day of
the same greywater. Their results showed low TN removal of 8% for the
A number of studies have examined the treatment of greywater in low (7 L m− 2 d− 1) loading rate and 26% for the higher rate (11.7 L m− 2
LWS using a variety of vegetation species (e.g. climbing, ornamental, d− 1) (Lakho et al., 2021b, 2022). The authors attributed poor nitrate
ferns, etc.) and growing substrates (e.g. perlite, sand, coir, and LECA) removal to aerobic conditions that inhibited denitrification at both the
(Table S1). From a total of 17 studies reporting GWs treating greywater, front and back side of CLW. However, more than 85% TN removal by
13 studies (76%) examined MLW designs in bench-scale and pilot-scale MLWs has been frequently reported in other studies (Fowdar et al.,
applications to evaluate the water quality treatment and suitability of 2017; Prodanovic et al., 2019a, 2020), highlighting the importance of
various substrates and vegetation. From Table S1, these studies reveal system sizing, substrate redox conditions, choice of vegetation and
that LWS are typically able to remove nitrogen (up to 93%), but not as suitable hydraulic loading rates for effective greywater treatment in
much phosphorus (67%). Only one study focused on the IGF system, GWs.
which was based on a single planter box at the base of the wall (Fowdar
et al., 2017). The MLW design was found to be more suitable for grey­
3.5. Nutrient removal mechanisms from greywater in green walls
water treatment due to its flexible design and adequate substrate volume
supporting a high root density and mixed vegetation and substrates
The different nitrogen and phosphorous removal mechanisms likely
(Prodanovic et al., 2019).
occurring in GWs involving vegetation uptake, bacterial metabolism,
The TN removal efficiency for the different types of green walls
filtration, and adsorption, are illustrated in Fig. 4(a). These mechanisms
varies between 7 and 91% for IGF, 48–93% for MLW, and 8–26% for
are summarised from the literature on greywater treatment using green
CLW, respectively, while the TP removal ranges are 7–67% for IGF and
walls and vertical-flow treatment systems and the occurrence of each
2–53% for MLW systems (Table S1). These different removal efficiencies
process is strongly dependent on specific experimental conditions and
can be attributed to the use of different substrates, vegetation species,
the design type of the system. Nitrogen removal mechanisms involve
pollutant concentrations and hydraulic loading rates across the studies
numerous N-species, ranging from inorganic (NO−3 , NO−2 , NH+ 4 , N2O, and
(Table S1). The sorption capacity of different substrates and nutrient
N2) to particulate and dissolved organic nitrogen. Vegetation uptake,
uptake of different vegetation species can vary over time due to several
biofilm encapsulation, substrate adsorption, and filtration processes of
factors, including biological activity, substrate saturation, and accu­
particulate organic nutrients, followed by hydrolysis and dissolved
mulation of phosphorus in the system. Over the operating period of
nutrient removal mechanisms, are regarded as the dominant pathways
GWs, these factors can adversely influence the effectiveness of P
in removing nitrogen in GWs (Pradhan et al., 2019a). However, their
removal. Gattringer et al. (2016) implemented a MLW design (in Spain)
individual roles in GWs are still a matter of discussion due to the com­
using mixed vegetation and expanded clay that removed 96% COD,
plex inter-dependency between these mechanisms.
>97% BOD5, 99% TSS and 97% ammonium from greywater. However,
Processes responsible for greywater treatment can also vary within
nitrate leaching was observed in their GW effluent due to intensive
the different layers of GWs. There are four main depth zones in a GW
aeration of the substrate by perforated hoses at the bottom of the con­
treatment system, namely upper, rhizosphere, middle, and bottom
tainers, thereby impeding denitrification (Table S1). In two more recent
(Fig. 4(b)). While the relationships between removal mechanisms and
studies by Lakho et al., in 2021 and in 2022, a CLW was established
specific pollutants in GWs are inconclusive, several key studies have
using individual GW panels consisting of an iron-mesh frame with a bag
hypothesized the presence of particular removal mechanisms in
of substrate enclosed within a geotextile filter. Two different GW surface
different layers of GWs (Fowdar et al., 2017; Pradhan et al., 2019b,

7
M. Gholami et al. Journal of Environmental Management 345 (2023) 118917

Fig. 4. (a) Potential nutrient removal mechanisms by vegetation, substrate, and biofilm interactions within GWs; (b) Targeted pollutants and potential associated
removal mechanisms listed underneath (Fowdar et al., 2017; Pradhan et al., 2019b, 2020; Prodanovic et al., 2017, 2019a, 2020).

2020; Prodanovic et al., 2017, 2019a, 2020). These are summarised in (Pradhan et al., 2019b). In vertical-flow TW treating greywater, nitrogen
Fig. 4 to serve as a point for readers to consider in the design and is typically removed via ammonification, nitrification, denitrification
optimization of GW systems, and as a starting point for further research (especially in lower layers) and, biomass assimilation (e.g. dissimilatory
to better understand the specific contribution of each mechanism. The nitrate reduction) (Ramprasad and Philip, 2018). Conversely, in a GW
intent is not to indicate dominant mechanisms or their relative system, most organic nitrogen is removed from greywater in the upper
contributions. layers (Fig. 4(b)), where aerobic conditions support autotrophic nitri­
The occurrence and effectiveness of greywater treatment processes fying bacteria to nitrify organic nitrogen and ammonia into nitrogen
depend heavily on the design of the system, such as whether it is satu­ oxides (NOx) (Fowdar et al., 2017). The uppermost layer is constantly
rated or unsaturated, the depth, porosity and particle size of the sub­ reoxygenated because of its exposure to air (Fowdar et al., 2018) which
strate, and operational factors (e.g. temperature, pollutant loading rate, rarely occurs in waterlogged treatment wetland systems. Various forms
etc.). For instance, nitrogen is mainly transformed by the action of of particulates, including particulate nitrogen, can also be removed by
suspended microorganisms from the greywater accumulated on the filtration in the upper substrate layers while suspended solids can adsorb
substrate upper surface or within its pores through biological processes both organic and inorganic nutrients via exchangeable adsorption (Li

8
M. Gholami et al. Journal of Environmental Management 345 (2023) 118917

and Zuo, 2020). Ammonification may also rapidly occur in the upper and phosphate removal significantly increased from 37 to 45% and
zones under aerobic conditions, converting amino acids to ammonia 25–35%, respectively. Similarly, Thomaidi et al. (2022) observed that
(Saeed and Sun, 2012). better COD, TP, and TN were removed from greywater by increasing the
Under saturated (i.e. waterlogged) conditions, dissolved oxygen substrate depth from 10 to 20 cm. Prodanovic et al. (2023) revealed that
(DO) concentrations in the middle and bottom zones may decrease from the 700 mm depth exhibited almost complete nitrification with 93%
microbial aerobic respiration, leading to anaerobic and eventually ammonia removal, likely attributed to favourable contact time and
anoxic conditions in some parts of the media where denitrifying bacteria efficient activity of nitrite oxidizing bacteria, whereas the 300 mm and
may be active (Fowdar et al., 2017). This could be ascertained by 150 mm depths achieved average removal rates of 43% and 19%
measuring dissolved oxygen (DO) levels in different layers of the GW respectively. The enhanced removal efficiency could be ascribed to the
biofilter or by identifying and studying the microbial communities improved specific conditions for oxic, anoxic, and anaerobic processes,
present. These approaches would offer valuable information to elucidate but may also be attributed to superior physicochemical capture of pol­
the impacts of each removal mechanism. For a typical MLW-style GW, a lutants, possibly due to the linear increase in TN and TP removal with
study by Pradhan et al. (2019b) showed that even after vegetation was substrate depth. To enhance understanding of the effects of substrate
removed, nitrogen continued to be removed in the lower layers, indi­ depth, nutrient removal could be measured along the entire length of the
cating the occurrence of denitrification. Sami et al. (2023) observed GW biofilter. This approach allows for the assessment of nutrient con­
significant ammonium reductions and transformations, with volatiliza­ centrations at different wastewater treatment stages and provides
tion and/or nitrification (aided by pumice and biochar), and possible valuable information regarding the effectiveness of the biofilter in
denitrification occuring in a green wall, resulting in lower total nitrogen removing nutrients throughout its depth.
levels primarily in the form of nitrite and nitrate in the effluent. How­
ever, microbial identification using PCR techniques (DNA extraction) 3.6. Effect of substrate properties on nutrient removal in green walls
would be necessary to confirm the specific activity of nitrifying and
denitrifying bacteria in nitrification and denitrification zones. GW substrates play an essential role in nutrient removal from grey­
Phosphorus is mainly removed from greywater by substrate water, facilitating filtration and adsorption processes and supporting
adsorption and filtration in the upper layers (Fig. 4) (Shen et al., 2020). vegetation and microbial development. The physical and chemical
Prodanovic et al. (2019a) showed that 88% particulate phosphorous and characteristics of GW substrates affect the hydraulic, chemical and
90% TSS removal was achieved by substrates alone in GWs. For particles physical interactions of the water, roots and biofilm with some sub­
with a size larger than the substrate pore size, straining filtration is strates better suited and more cost-effective than others (Shen et al.,
dominant, and for smaller particles, other mechanisms such as inter­ 2020). The removal of nitrogen and phosphorus can exhibit consider­
ception and diffusion are involved (Cescon and Jiang, 2020). Major able variation depending on the types of substrates used. Sami et al.
fractions of phosphorus such as inorganic (metal-bound forms), organic, (2023) observed that biochar exhibited a 75% average removal rate for
and solid-adsorbed inorganic forms, can be separated by physical TN through significant nitrification, while hemp and pumice achieved
entrapment. Other adsorption mechanisms based on substrate compo­ an average TN removal of 58%; however, in terms of TP removal, hemp
sition such as electrostatic interactions, Lewis acid–base interaction, ion outperformed pumice and biochar by creating anaerobic zones and
exchange, ligand exchange, inner sphere complexation, outer sphere utilizing the contribution of PAOs, resulting in removal rates of 66%,
complexation, and hydrogen bonding may also occur (Almanassra et al., 61%, and 57%, respectively (Table 3). Specific substrate properties to
2021). Soluble phosphate can be precipitated as insoluble metal com­ consider include particle size, pore size, porosity, air-filled porosity
plexes by reacting with metal ions within the substrate, and insoluble (AFP), specific surface area, cation exchange capacity (CEC),
phosphorus can be trapped by straining or by other physical filtration water-holding capacity (WHC), pH, and EC, and there are complex in­
mechanisms, which depends on the pH, particle and pore size (Shen terrelationships between them. To gain a better understanding of the
et al., 2020). To gain a comprehensive understanding of these mecha­ specific role of each removal mechanism and their interactions, it would
nisms, several techniques can be employed, such as Fourier-transform be beneficial to conduct experiments under different conditions while
infrared spectroscopy (FTIR), X-ray diffraction (XRD), keeping other parameters constant. Table 3 summarizes nutrient
energy-dispersive X-ray spectroscopy (EDX), scanning electron micro­ removal by various commercial and waste substrates with different
scopy (SEM), zeta potential analysis, and other physicochemical ana­ physicochemical characteristics for greywater treatment by GWs. The
lyses. These techniques can help elucidate the role of adsorption removal of TN varied between 10% with a removal rate of 0.68 (g/m3/d)
mechanisms in pollutant removal. However, some phosphorus may also using light-weight expanded clay aggregate (LECA), and 45% with a
be removed through biological activities in GWs. When anaerobic con­ removal rate of 4.72 (g/m3/d) using grow stone. For TP removal, the
ditions exist, such as in saturated pores of the lower GW layers, poly­ range was from 10% with a removal rate of 0.57 (g/m3/d) using
phosphate accumulating organisms (PAOs) are able to establish fyto-foam, to 20% with a removal rate of 1.14 (g/m3/d) using perlite.
(Prodanovic et al., 2017). Given polyphosphate storage is generally While some studies investigated the removal efficiency of a single sub­
associated with alternating redox, nutrient or substrate availability, such strate, others revealed the importance of using a mixture of substrates
a mechanism may be strongly linked to irrigation frequency and the for numerous reasons. To simultaneously target a wide range of pol­
changing saturation of pore volumes. lutants in a green wall, a mixture of substrates with different physico­
Various substrate depths from 15 cm to 94 cm are reported for GWs chemical characteristics is needed. Masi et al. (2016) found that the
treating greywater (Fowdar et al., 2017; Prodanovic et al., 2019a) and mixture of LECA plus coconut fibres performed better than only sand or
nutrient removal occurs at different depth zones (Fig. 4(b)). While it LECA in removing organic matter and nutrients in GWs (Table 3). The
may appear improbable to encounter anaerobic conditions at shallower authors attributed this predominantly to the longer hydraulic retention
depths with traditional MLW, it is conceivable that specific areas of time of 40 min with mixed substrates compared to only 12 min using
agglomerated particles or biofilm situated at the bottom of the material LECA plus sand. Moreover, the mixture of LECA-coconut showed better
could generate anaerobic conditions. However, knowledge in this area TKN removal performance (23%) than LECA-sand with only 15%
of GWs is constrained, and current literature merely speculates the removal efficiency (Table 3). Galvão et al. (2022) similarly reported that
possibility based on theoretical assumptions derived from packed bed textile fibres in a GW were more prone to clogging and decreased
trickling filters and similar systems (Fowdar et al., 2017; Pradhan et al., vegetation health due to their high water-retention capacity compared
2019b). Microbial identification may help determine the specific groups to a more porous mixture of ceramic tiles and coconut fibres. However,
of aerobic or anaerobic microorganisms involved. Pradhan et al. (2020) using a mixture of substrates makes it difficult to optimize the charac­
found that with increasing substrate depth from 15 cm to 40–60 cm, TN teristics for efficient nutrient removal and concurrently the treatment of

9
M. Gholami et al.
Table 3
N and P removal efficiencies from greywater treated in different green wall experimental substrates of varying physiochemical characteristics.
Substrate pH EC Air filled Porosity Water-holding CEC Bulk Particle BET surface N removal P removal Volumetric N Volumetric P
(μs/ porosity (AFP) (%) capacity (WHC) (mmol/ Density (g/ size (mm) area (m2/g) (%) (%) removal (g/m3/d) removal (g/m3/d)
cm) (%) (%) kg) cm3)

Spent coffee grounds (SCG) – 3.5 – 55 40 4.8 0.34 0.1(d10)- 0.82 TN: 37 a P-PO3-
4 : 24 TN: 2.52 a P-PO3-
4 : 1.05
a
a a a
0.24(d60) NH+
4 : 40 NH+4 : 1.2
Date seeds – 2.4 – 68 28 2.4 0.84 0.42(d10)- 0.52 TN: 37 a P-PO3-
4 : 13 TN: 2.52 a P-PO3-
4 : 0.57
a
a a a
1.98(d60) NH+
4 : 38 NH+4 : 1.14
Coco coir 6.0 1.8 13 80 32 4.1 0.08 0.15(d10)- 1.098 TN: 35 a TP: 12 b TN: 2.38 a TP: 0.68 b
a
1.00(d60) NH+
4 : 38 P-PO3-
4 : 24 NH+4 : 1.14
a
P-PO3-
4 : 1.05
a
a

Rockwool 8.0 – 13 96 – – 0.85 – 0.17 TN: 35 b TP: 20 b TN: 3.67 b TP: 1.14 b
Fyto-foam – – – 99 – – 0.017 – 2.842 TN: 20 b TP: 10 b TN: 2.10 b TP: 0.57 b
Grow stone 7.0 – – 88 – – 0.202 – 0.132 TN: 45 b TP: 19 b TN: 4.72 b TP: 1.08 b
Light expanded clay 7.0 0.05 – 80 20 0.4 0.429 1.15(d10)- 0.587 TN: 10 a P-PO3-
4: 6
a
TN: 0.68 a P-PO3-
4 : 0.26
a
a a
aggregate (LECA) 2.00(d60) NH+
4 : 15 NH+4 : 0.45
Perlite 7.0 0.1 30 75 22 0.1 0.1 0.35(d10)- 1.345 TN: 12 a TP: 20 b TN: 0.81 a TP: 1.14 b
a
1.60(d60) NH+
4 : 30 P-PO3-
4: 8
a
NH+4 : 0.90
a
P-PO3-
4 : 0.35
a

Sand – 3.8 – 35 45 0.4 1.6 0.16(d10)- 0.076 TN: 20 a TP: 3 b TN: 1.36 a TP: 0.17 b
a
1.75(d60) NH+
4 : 58 P-PO3-
4 : 32 NH+4 : 1.74
a
P-PO3-
4 : 1.40
a
a
c
Coir:perlite (3:1) – – – 93 – – 0.091 – – TN: 50 TP: 40 TN: 5.25 (3:1) TP: 2.29 (3:1) c
(3:1) c (3:1) c
NH+4 : 35 P-PO3-
4 : 15 NH+
4 : 1.05 (2:1)
a
P-PO3-
4 : 0.65 (2:1)
10

(2:1) a (2:1) a a

Date seeds:SCG (1:2) – – – – – – – – – TN: 30 a P-PO3-


4 : 17 TN: 2.04 a P-PO3-
4 : 0.74
a
a a a
NH+4 : 36 NH+4 : 1.08
Base medium (BM: 80% – – – 65 – – 0.337 – – TKN: 34 d TP: 21 d – –
coconut fiber + 20% NO−3 : 25 d
perlite)
90% BM+10% granular – – – 10 – 0.373 – – TKN: 43 d TP: 21 d – –
activated carbon (GAC) NO−3 : 37 d
80% BM+20% compost – – – 5 – 0.215 – – TKN: 41 d TP: 16.4 d
– –
NO−3 : 35 d
80% BM+20% biochar – – – 14 – – 0.284 – – TKN: 46 d TP: 16 d
– –
NO−3 : 46 d

Journal of Environmental Management 345 (2023) 118917


80% BM+20% polyacrylate – – – 20 – – 0.663 – – TKN: 31 d TP: 31 d – –
NO−3 : 22 d
60% BM+20% – – – – – – – – – TKN: 40 d TP: 29 d – –
polyacrylate+20% biochar NO−3 : 38 d
Biochar – – – – – – – – – TN: 75 e TP: 57 e
TN: 3.89–10.37 e
TP: 0.48–2.23 e

Pumice – – – – – – – – – TN: 58 e TP: 61 e


Hemp – – – – – – – – – TN: 58 e TP: 66 e
a
(Pradhan et al., 2020) (without vegetation).
b
(Prodanovic et al., 2017) (without vegetation).
c
(Prodanovic et al., 2018) (without vegetation).
d
(Boano et al., 2021) (with vegetation).
e
(Sami et al., 2023) (with vegetation).
M. Gholami et al. Journal of Environmental Management 345 (2023) 118917

other pollutants in greywater due to their competing interactions and/or specific surfaces areas of fyto-foam (2.842 m2/g) and perlite (1.345
different characteristics, while also meeting their hydraulic re­ m2/g) provided TN and TP removal efficiencies of only 20 and 10%, and
quirements. For example, Abd-ur-Rehman et al. (2022) demonstrated 12 and 20%, respectively (Table 3). Apart from surface area, other
that carbonaceous waste materials (date seeds, coffee grinds, and coco surface characteristics of substrates, such as roughness, play a crucial
coir) all had higher removal performance for hydrophobic XOCs from role in enhancing pollutant adsorption ability. Pradhan et al. (2020)
greywater compared to zeolite and perlite, showing the importance of found that substrates with a smooth surface structure may have limited
hydrophobicity of these target pollutants and their interaction with ability to filter and adsorb pollutants, despite having a high surface area.
substrates, whereas ionic nutrients are better removed by hydrophilic LECA (0.429 m2/g) and sand (1.6 m2/g), both with moderate surface
substrates. areas and roughness, and SCG (0.82 m2/g) and date seeds (0.52 m2/g)
having high degree of small roughness and pores but lower BET surface
3.6.1. Substrate particle size, pore size, and porosity area, outperformed other substrates in terms of nutrient removal from
Substrate particle size, pore size and porosity affect water and greywater in GW systems (Pradhan et al., 2020). In gravity-driven sys­
nutrient movement and hence pollutant contact time in the system as tems, such as GWs, very high surface areas may not be critical as flow
well as biofilm growth and aerobicity within different GW layers (Liu travels primarily around the outer surfaces of the substrate rather than
et al., 2021). In turn, these parameters influence vegetation growth, within particles. This is in comparison to fixed bed up-flow (adsorption)
substrate clogging, infiltration rate and the presence and efficacy of columns where saturated flow under pressure drives liquid into and
processes that cause pollutant transformations (i.e. water quality treat­ through pores providing better flow and hence pollutant dispersion.
ment). While porous substrates can offer plenty of adsorption sites and
internal surface area available for pollutant transformations, porosity 3.6.4. Water holding capacity (WHC)
alone does not guarantee high pollutant removal efficiency because The WHC of a substrate influences the contact time between water,
particle size and pore sizes are also important. For instance, low porosity pollutants in solution and the substrate surfaces. Substrates with higher
substrates (e.g. SCG) with smaller particle sizes tend to have a higher WHC retain more water, which promotes microbial activity and en­
WHC, or time the water is detained within the substrate, leading to hances nutrient uptake by plants. This increased moisture content fa­
higher nutrient removal (Pradhan et al., 2020), when compared to cilitates the biological processes involved in nutrient cycling and
higher porosity substrates (e.g. LECA). Similarly, 99% porous fyto-foam removal, leading to improved nutrient retention and reduced leaching
showed low nutrient removal efficiency because of its low contact time (Young et al., 2014). This is especially important to consider in NBS that
and limited adsorption capacity with the polluted water (Table 3). are vegetated because there may be periods when wastewater is not
Pradhan et al. (2020) found that substrates consisting of smaller produced if the building is periodically uninhabited and so vegetation
particles (less than 0.5 mm) were more effective at removing phosphate, will rely on residual water held in substrate pores. For instance, the FLL
with removal rates of 24% (1.05 g/m3/d) for SCG and 13% (0.57 recommends a WHC range of 35–65% for extensive living roofs to
g/m3/d) for date seeds, in comparison to substrates with larger particles support both succulent and non-succulent plants during droughts (Cas­
exceeding 1 mm diameter such as LECA, which only removed 6%. The cone, 2019; FLL, 2018; Koviessen et al., 2023). Spent substrates derived
longer contact time between pollutants and the treating agents resulted from manufacturing/agriculture/forestry used in green roofs are typi­
in improved treatment because of the smaller particle sizes. Prodanovic cally within this range (12.9–51%, 23.7–54%), while construction waste
et al. (2017) also observed that slow filtering substrates, including coir, materials typically have lower WHC values (2–44%), often below the
rockwool, and fyto-foam, demonstrated better TN removal rates recommended range for GRs (Koviessen et al., 2023). Particle size and
(ranging from 35 to 75%, with an average of 50%) compared to fast porosity are the most significant factors affecting WHC in GWs (Pradhan
filtering ones such as perlite, vermiculite, growstone, expanded clay, et al., 2020). Generally, the WHC decreases with an increase in porosity
and river sand. However, the small pore size of these slow filtering and AFP (Farrell et al., 2012), but adding more organic matter can in­
substrates often resulted in clogging issues (Prodanovic et al., 2017). crease the WHC (Xue and Farrell, 2020). Furthermore, lower WHC
substrates can be mitigated by increasing the substrate depth and hence
3.6.2. Air-filled porosity (AFP) volume providing adequate water and nutrients to vegetation, especially
AFP is the relative volume of substrate pore space filled by air. Air during long dry periods (Farrell et al., 2012). In GWs, higher WHC
within the substrate pores is necessary for biological aerobic respiration substrates like coco coir (30%), sand (40%), and SCG (45%) showed
and reducing compaction risks (Graceson et al., 2014). Generally, sub­ higher nutrient removal compared to LECA with a WHC <15%
strates with larger particles can improve AFP, bulk density, and hy­ (Table 3), probably because of the longer nutrient contact time within
draulic conductivity, but may decrease water retention and pollutant substrates.
contact time (Vijayaraghavan and Raja, 2014). Perlite was found to
exhibit a significantly higher AFP of 30%, compared to coir and rock­ 3.6.5. pH
wool at 13%. High AFP promotes oxygen transfer to all layers in GWs, The pH influences the speciation of nutrients and the treatment
which may prevent anoxic conditions necessary for denitrification and processes within a GW treating greywater (outlined in Fig. 4(a) and
PAOs processes (Pradhan et al., 2020). However, high AFP values can discussed earlier), including the electrostatic attraction forces between
cause lower water retention and for vegetation, water stress and rapid negatively charged ions and the substrate surface (Almanassra et al.,
moisture fluctuations (Farrell et al., 2013). These factors also lead to 2021). Chowdhury and Abaya (2018) showed that pH levels in the
lower contact time between nutrients and substrates, thus compromising discharge from a green roof treating greywater ranged from 7.24 to 8.95,
treatment performance. The TN removal from greywater in GWs that and in some cases even exceeded 10. The pH levels of GW substrates in
used coir and rockwool and had an AFP of 13% was 35% while it was the reviewed studies range between 6 and 8 (Table 3), the variation
only 12% using perlite with APF of 30% (Table 3). For context, a min­ attributed to the differing amounts of carbonyl, nitrile, and phosphoryl
imum AFP of 10% v/v is recommended by the green roof FLL guidelines groups present in the substrate compositions. These chemical groups
(FLL, 2018) necessary to support vegetation with no current guidelines promote the formation of free hydrogen (protons causing pH change)
provided for GWs. through intermolecular reactions (Kader et al., 2022). The GR FLL
guidelines recommend a pH range of 6.0–8.5 for substrates used in
3.6.3. Surface area extensive living roof systems to minimize potential effluent eco-toxicity
Substrates with larger specific surface areas (e.g. BET) are expected (Chowdhury and Abaya, 2018; FLL, 2018). Substrates within this pH
to adsorb substances more effectively (Liu et al., 2021), although this range also foster semi-alkaline growth conditions that facilitate the
positive relationship has not always held. For example, the largest BET thriving of a wide variety of plant species (Koviessen et al., 2023;

11
M. Gholami et al. Journal of Environmental Management 345 (2023) 118917

Molineux et al., 2009). However, slightly acidic substrates are thought and biochar, to an inorganic substrate containing perlite and coir, in
to make nutrients more accessible for plant uptake (Xu et al., 2020). GWs increased the removal of TKN and NO−3 by up to 46%. However,
Also, a slightly acidic substrate can buffer pH increases (alkalinity) selecting the appropriate organic matter is important, as adding poly­
resulting from water from laundry detergents in greywater (Boano et al., acrylate actually decreased TKN and NO−3 removal efficiency to 31 and
2020a; Galvão et al., 2022). However, extreme acidity or alkalinity 22%, respectively, due to its physico-chemical properties (Table 3). It
conditions can affect macronutrient availability and solubility (Gentili should be noted that some guidelines for GRs (FLL, 2018) suggest
et al., 2018). In strongly alkaline conditions, NH3 predominates, while in limiting organic content in substrates to <10% due to effects of
neutral and acidic conditions, NH+ 4 dominates. Ammonium is a posi­ compaction, associated hydraulic constraints and, fire risks.
tively charged ion that can be directly assimilated by plant roots and
used as a source of nitrogen for growth and development, while NH3 can 3.6.8. Bulk density
be toxic to plants at high concentrations. Moreover, different forms of In GRs, a minimum bulk density of 600 kg/m3 is recommended to
phosphate such as H2PO−4 , HPO2− 3−
4 , and PO4 are available at a pH lower stabilize the substrates from wind-blown or wash-out processes (FLL,
than 8, 8–12, and above 12, respectively (Chen et al., 2021), affecting 2018). Substrates with lower bulk density allow for better root pene­
vegetation uptake and adsorption. For instance, phosphorus adsorption tration and aeration, promoting root growth and nutrient uptake (Cor­
by roots is hindered at low pH, because the orthophosphates react with rea et al., 2019). This improved root development facilitates the uptake
iron and aluminium to form ferric phosphate and aluminium phosphate and assimilation of nutrients by plants, enhancing nutrient removal from
precipitates (Kader et al., 2022). the system. It is suggested that lower bulk densities can cause challenges
with vegetation anchorage, create wider pathways in the biofilter bed,
3.6.6. Electric conductivity (EC) and result in substrate flotation on the surface of the biofilter (Vijayar­
The effect of substrate EC is similar to the effect of the EC of grey­ aghavan, 2016). However, in green wall substrates, a lower bulk density
water (discussed in section 3.2). Higher EC values in substrates can lead may be possible due to the smaller exposed soil surface area. The bulk
to an increased concentration of dissolved salts, which can affect density of applied substrates in GWs treating greywater ranges from
nutrient availability and uptake by plants (Gondek et al., 2020). High EC 17.6 kg/m3 for fyto-foam to 1600 kg/m3 for sand (Table 3). One way to
levels can inhibit the growth of certain plant species and disrupt nutrient reduce the substrate weight is to use/include low-density inorganic
cycling processes (Yuvaraj et al., 2021). Sand and SCG with the highest materials like perlite (100 kg/m3) and fyto-foam. Low-density substrates
EC values of 3.5–3.8 μs/cm achieved the greatest ammonium (40–58%) enable greater substrate depths in GW, which offers numerous advan­
and phosphate (24–32%) removal compared to other substrates tages. Firstly, the nutrient contact time in GWs treating greywater is
(Table 3). These substrates have more divalent metal cations (e.g. Ca2+) extended and hence nutrient removal improves. Also, vegetation species
providing a larger binding capacity to remove nutrient anions, while with extended and hairy root systems can thrive thus greater nutrient
LECA with a much lower EC (0.05 μs/cm) was the least effective sub­ assimilation by vegetation is supported. Further, anaerobic conditions
strate for removing nutrients (Pradhan et al., 2020). However, high EC are promoted at the deeper layers that promote denitrification and also
could potentially lower the photosynthesis rate due to poor water uptake phosphate removal by PAO processes (e.g. Fig. 4(b)).
in xylem tissues. Therefore, it is essential to check whether the salinity
level of the substrate is below the maximum threshold. Nevertheless, the 3.7. The role of vegetation in nutrient removal
impact of substrate EC on greywater effluent EC between 600 and 850
μS/cm was found to be insignificant in GW treating greywater (Boano Most vegetated GWs can achieve higher nutrient removal efficiencies
et al., 2020a; Galvão et al., 2022). Small variations in EC values between (TN> 90% and TP> 65%) than non-vegetated biofilters (TN~ 40% and
the influent and effluent in such systems mostly occurred during warmer TP~ 10%) (Fowdar et al., 2017) and there is generally greater TN
months due to evapotranspiration effects. The EC variations can also be removal than TP removal. This is attributed to vegetation influencing
strongly dependant on the design of NBS using the same substrates and nitrogen transformations and also because, on a stoichiometric basis,
vegetation species. Chowdhury and Abaya (2018) showed that the mean more nitrogen than phosphorus is needed by plant biomass (Prodanovic
EC values in GRs treating greywater were 1990 and 2520 μS/cm for the et al., 2019a). Pradhan et al. (2019b) conducted lab-studies in single GW
intensive and extensive green roof systems, respectively. The differences biofilters treating greywater and removed the vegetation. They found
were attributed to the reduced water retention and evapotranspiration that TN and phosphate removal dropped by 25% and 31–36%, respec­
in extensive roofs, leading to elevated EC levels in the effluent. tively, indicating the importance of nutrient uptake by vegetation and
removal by plant-associated biofilms. While it may be hypothesized that
3.6.7. Cation exchange capacity (CEC) more vegetation and substrate would provide concomitant nutrient
Substrate cation exchange capacity plays a crucial role in providing removal, a three-tiered modular system study found no significant in­
essential nutrients for vegetation uptake by replenishing adsorbed cat­ crease in removal efficiency beyond two in-series units (Prodanovic
ions as vegetation roots deplete ion concentrations in water (Solano et al., 2020). In that study, nutrient removal was highest in the upper
et al., 2012). The presence of different functional groups such as amine module and lowest in the lower levels. It was concluded that for systems
groups, quaternary ammonium functional groups, and chloride ions can implemented in practice, adding another module would incur additional
make the substrate a cation or anion exchanger by which a nitrate or costs and increase coloration in the discharge, so would not provide
phosphate ion can be exchanged with another ion from the substrate additional gains (Prodanovic et al., 2020). Multi-stage treatment can
(Gizaw et al., 2021). Substrates with higher CEC have a greater ability to also result in lower vegetation growth due to partial shading effects and
retain and exchange positively charged nutrients. This enhanced CEC limited nutrient supply for the lower plants, but it is suggested that these
promotes nutrient retention in the substrate, reducing the likelihood of effects may be resolved after approximately two years of system oper­
nutrient leaching and improving nutrient availability for plant uptake ation (Costamagna et al., 2022). To better understand the effects of
(Chowdhury et al., 2021). Cation exchange capacity can be increased in vegetation on longer-term nutrient removal, multi-seasonal experiments
substrates through the addition of organic matter, which can also result should be undertaken.
in improved water retention (Pradhan et al., 2020). Table 3 shows that
highly organic substrates had the greatest CEC, such as SCG with 4.8 3.7.1. Mechanisms of nutrient removal in green wall vegetation
mmol/kg, followed by coco coir at 4.1 mmol/kg and date seeds at 2.4 Vegetation can directly adsorb, assimilate, and uptake macronutri­
mmol/kg, while more inorganic substrates (such as perlite) had lower ents on their root tissues by plasma transporters, which act as selective
CEC values ranging from 0.1 to 0.4 mmol/kg. Boano et al. (2021) found passage of most mineral nutrients and metabolites through cellular and
that adding organic matter, such as granular activated carbon, compost, intracellular membranes (Kiba and Krapp, 2016). Concurrently,

12
M. Gholami et al. Journal of Environmental Management 345 (2023) 118917

vegetation can release considerable amounts of oxygen from their roots vegetated biofilter, but the denitrifying bacteria populations were low­
through radial oxygen loss, creating aerobic conditions believed to help ered due to substrate biofilm loss, which was the main habitat for de­
detoxify potentially toxic compounds. Root structures can also release nitrifiers. However, the relative dominance of various removal
exudates as a source of carbon for denitrifying microorganisms when mechanisms in green walls is still a topic of debate and warrants further
there is insufficient carbon available in the wastewater feed (Zhai et al., investigation.
2013). Isotropic tracer experiments showed that vegetation assimilation
and substrate adsorption had significant roles in nitrogen removal 3.7.2. Effects of different vegetation species in nutrient removal in green
(Fowdar et al., 2018). However, other studies identified nitrification and walls
denitrification as the major nitrogen removal processes, possibly Vegetation species have varying capacities to take up phosphorus
explained by the different vegetation species, substrate, and/or oper­ and nitrogen, which depends on their root systems, growth cycles, and
ating conditions (e.g. temperature, light exposure, organic and hy­ temperature (Bonvin et al., 2015). Almost all species can absorb and
draulic loading rates) (Pradhan et al., 2019a) between studies. utilize orthophosphate, ammonia, and nitrate. However, some species
In the rhizosphere, microorganisms also colonize vegetation roots, such as Phragmites australis, Strelitzia reginae, Phormium tenax, Ophiopo­
leading to the formation and development of biofilms (Rudrappa et al., gon japonicus, and Phormium spp. offer little or no benefits in terms of
2008). Biofilms in GW systems, consisting of microorganisms and nutrient removal over non-vegetated biofilters (Fowdar et al., 2017;
extracellular polymetric substances, can enhance nutrient mineraliza­ Prodanovic et al., 2019a), highlighting the importance of vegetation
tion and transformation, but excessive thickness can reduce nutrient selection in GWs for the intended goal. Ornamental species are
removal efficiency, limit oxygen diffusion, impede nutrient uptake, frequently used in GWs to meet aesthetic requirements (Pradhan et al.,
obstruct substrate gas exchange, and clog the GW filter bed (Badhe et al., 2019a) yet vegetable crops have been considered, especially for coun­
2014). Limited information on GW biofilms exists compared to con­ tries threatened by immediate water stress and a related food crisis. For
structed wetlands. This highlights the need for determining biofilm instance, Eregno et al. (2017) evaluated the performance of an inte­
characteristics and development with different substrates and greywater grated GW system for growing different lettuce species planted in
loading and irrigation patterns, as well as identifying microbial species perlite. The TP (87%) and TN (60%) removal efficiencies were good,
to understand the role of nitrification-denitrification and PAOs in though it should be noted that influent wastewater N and P concentra­
nutrient removal. Pradhan et al. (2019b) replaced biologically-active tions were relatively low at 4.36 mg/L and 0.53 mg/L, respectively.
substrates in GW treating greywater with fresh uncolonized ones, Despite potential microbial and chemical health risks associated with
while keeping the same vegetation, and found that NOx increased in the growing food using wastewater nutrients, the study demonstrated that
effluent due to reduced TN removal. They suggested that nitrifying the lettuces grown met World Health Organisation (WHO) health-based
microorganisms, attached on roots, were still predominant in the targets (Eregno et al., 2017).

Fig. 5. Different N (a) and P (b) forms removed by various vegetation species in GWs. C and NC represent climbing and non-climbing species, respectively. Plants
bordered in red are the best performing from that study.

13
M. Gholami et al. Journal of Environmental Management 345 (2023) 118917

Fig. 5(a) displays N removal by different vegetation species in GWs in those studies (Costamagna et al., 2022; Lakho et al., 2021a, 2022).
from five studies. Fowdar et al. (2017) investigated climbing (C) and
non-climbing (NC) species’ performance at removing N from greywater. 3.8. Effects of operating parameters on nutrient removal in GWs treating
The non-climbing species C. appressa, C. lilies, L. japonica, V. vinifera, and greywater
P. jasminoides demonstrated excellent mean TN removal of 94%, 90%,
89%, and 88%, respectively (Fig. 5(a)), slightly outperforming climbing 3.8.1. Hydraulic loading
species. Species with strong TN removal also showed strong removal of Hydraulic parameters are important in the optimization of GWs
ammonia and NOx (Fig. 5(a)). However, in slow growing species such as treating greywater because pollutant removal efficiency, clogging po­
S. reginae, NOx leaching was observed in the effluent (represented as tential, wastewater application rate and the size of GWs are ultimately
negative removal in Fig. 5(a)) under aerobic conditions (Fowdar et al., dependent on hydraulic loading rate (HLR; mm/d) and the related pa­
2017). C. appressa, V. vinifera, and C. lilies achieved the highest TDN rameters, contaminant loading rate (CLR; mg/d) and hydraulic retention
removal of >90%, likely due to the high NOx uptake rate compared with time (HRT; d). Higher HLRs may hinder anaerobic and anoxic conditions
the (control) non-vegetated biofilter of 20% TDN removal. necessary for some pollutant removal processes (e.g. denitrification) by
Prodanovic et al. (2019a) demonstrated that TN removal in vege­ creating macro channels in the substrate, a conduit for oxygen to reach
tated columns was 7–10% higher than in unvegetated ones, with all 13 the deeper layers (Panuvatvanich et al., 2009). High HLRs can also
vegetation species exhibiting high TN (82–93%) and DON removal overload a treatment system if pollutant concentrations are high leading
(89–94%) (Fig. 5(a)). C. appressa showed the highest TN removal at to compromised treatment.
93%. However, DON removal was mainly attributed to microorganisms Most studies on GWs treating greywater have focused on optimizing
in the soil under aerobic conditions (Prodanovic et al., 2019a). Pradhan the substrate and vegetation, with little investigation about the effects of
et al. (2019b) investigated the removal of greywater nutrients and hydraulic parameters on nutrient removal. One study by Boano et al.
organic compounds in a GW using ornamental species, with Ruellia (2020b) reviewed the general effects of system hydraulics and nutrient
brittoniana removing the most (> 90%) of all nitrogen species (TDN, treatment in TWs, GRs, and GWs. Results indicated that while there was
nitrate, nitrite, organic nitrogen, and dissolved Kjeldahl nitrogen). The no clear trend between HLR and TP removal, increasing HLR led to
best performance by R. brittoniana was attributed to its hairy-root system lower TN removal (Boano et al., 2020b). The TN and TP removal re­
which creates an extended and microporous root zone, facilitating high lationships with HLR in the studies treating greywater in GWs is shown
contact with pollutants in the greywater. C. appressa and Cana lilies were in Fig. 6(a) and (b), albeit the studies had different operating conditions.
especially successful at removing TN from greywater in GWs, ranging It is important to note that all studies except Pradhan et al. (2020)
from 89 to 93%, likely due to their higher growth rates, longer root assessed substrates that were vegetated under various HLRs. HLRs
lengths (up to 1.21 m), and extensive root growth (Schwammberger ranged between 15 and 237 mm/d and each study used different sub­
et al., 2020). Vegetation with shallower roots and shorter life cycles (e.g. strates, vegetation, temperature conditions, and wastewater character­
N. officinale, O. japonicus) did not provide sufficient oxygenation to the istics (Fig. 6) so the ability to ascertain nutrient removal with HLR alone
rhizosphere zone (Prodanovic et al., 2019a), resulting in less pollutant from the published studies is complex.
removal, including NOx leaching, because of fewer hydraulic channels Despite the variability of experimental conditions in the studies,
within the substrate. higher HLRs (>100 mm/d) generally resulted in lower TN (Fig. 6(a))
In all five studies, TP was removed less than TN, ranging from 7% and TP (Fig. 6(b)) removal efficiencies. Fowdar et al. (2017) compared
(Phormium spp.) to 67% (C. appressa) (Fig. 5(b)). This was attributed to TN and TP removal at an HLR of 110 mm/d (HRT 48 h) and at a lower
the fact that there is a significant correlation between vegetation HLR of 55 mm/d (HRT 92 h), finding that TN and TP removal efficiency
biomass and nitrogen concentration but not so with phosphorus (Fowdar of C. appressa (as the best-performing species) significantly increased to
et al., 2017). Rather, phosphorus is removed primarily by precipitation over 90% at the lower HLR. Another study based on multi-stage GWs
and filtration mechanisms (e.g. Fig. 4). using C. appressa reported that TN removal slightly fell at higher HLRs
The lower TP uptake in O. japonicus and Nasturtium officinale was (60 mm/d) by about 3%. This was associated with lower ammonifica­
explained by their slower growth rates and less efficient root systems tion and nitrification of DON transformed into NOx, probably from
(Prodanovic et al., 2019a; Read et al., 2008). As for TN removal, insufficient contact time of roots and biofilm with pollutants at higher
C. appressa provided high TP and also filterable reactive phosphorus inflow rates (Prodanovic et al., 2019a). Decreasing TP removal also
(FRP) removal up to 67% and 87%, respectively (Fig. 5(b)). FRP (over occurred at higher HLRs (110 mm/d), suggesting that TP removal is
85% of TP) containing soluble and inorganic phosphorus (e.g. phos­ sufficiently removed by substrate adsorption, straining, and filtration
phate) is directly taken up by vegetation, and its negative removal by during low and standard HLRs due to sufficient contact time and flow
some species, such as Phormium (Fig. 5(b)), might be due to the release rate (Fowdar et al., 2017). It should be noted that the contact time is also
of previously adsorbed inorganic phosphorus (Fowdar et al., 2017). influenced by air filled porosity, particle diameter, porosity, and water
Fig. 5(b) shows that over 95% of phosphate was removed by holding capacity as interconnected factors that influence the behaviour
R. brittoniana which also had slightly higher N species removal than of fluid flow. When the contact between the fluid and the media is
other species. However, this does not necessarily mean that a vegetation increased at slower flow rates, it results in more effective treatment even
with high nitrogen removal has simultaneously high phosphorus under the same HLRs. Sotiropoulou et al. (2022) examined the effect of
removal. For instance, V. vinifera and P. jasminoides showed high TN HLR on nutrient removal in a vertical flow TW treating laundry grey­
removal of 82% and 87% (Fig. 5(a)), while only 19% and 14% TP water and found that low HLRs (between 31.8 mm/d to 15.9 mm/d) had
removal (Fig. 5(b)) were observed for these species, respectively. no significant effect on removing insoluble particulate pollutants such as
A diversity of vegetation species with high N and P uptake rates in microfibres, mainly removed by filtration and straining. Similarly,
GWs treating greywater can overcome the deficiency of relying on a Kotsia et al. (2020) found that higher HLRs (110 mm/d) in vertical TWs
single species to remove TP and/or TN. This also provides other benefits treating greywater did not compromise nutrient removal, although they
such as ecological diversity and associated risk mitigation from plant used coarser substrates. Ramprasad et al. (2017) found sustained
diseases. Ramprasad et al. (2017) found that using a range of vegetation pollutant removal in a GW treating greywater by incorporating a
led to higher removal rates of TN (99%) and TP (92%) from greywater mixture of vegetation that provided buffering from high HLRs (120
than using only one vegetation type (Canna sp.). However, some studies mm/d) over time. Interestingly, Sami et al. (2023) observed an increase
using mixed vegetation species in GWs reported low TN and TP removal in nutrient removal with high loading rates (from 54 to 216 mm/d). The
ranging from 8 to 26% and 2–57% (Table S1), respectively, which may highest TN removal (>85%) using biochar occurred at an HLR of 216
be related to the cold temperature, GW design, and substrate type tested mm/d, while reducing the HLRs to 108 and 54 mm/d resulted in

14
M. Gholami et al. Journal of Environmental Management 345 (2023) 118917

Fig. 6. TN and TP relative removal efficiency as a function of hydraulic (HLR) (a and b), (c) N (NLR), and (d) P (PLR) loading rates. Note: Different scales for nutrient
(NLR, PLR) loading rates. Pradhan et al. (2020) data in Fig. 6 (b) report phosphate (not TP) removal.

decreased TN removal rates of 78% and 75% respectively (Sami et al., vegetative water and nutrient uptake and thus, plant and microbial
2023). Similarly, TP removal by biochar improved from 31% to 75%, growth. Lower temperatures slow photosynthesis, respiration, and
and hemp and pumice exhibited similar effects. The researchers pro­ transpiration rates (Wang et al., 2022) that can impede nutrient uptake
posed that the improved greywater distribution during high loading rates (Fowdar et al., 2017). Low temperature (<15 ◦ C) can also inhibit
rates likely enhanced particle surface area and pore availability for microorganisms responsible for nitrogen and organic matter removal
adsorption and microbial growth (Sami et al., 2023), but the conflicting (Akratos and Tsihrintzis, 2007). A study of five vegetation species
negative impact on BOD removal suggests that further investigation is (O. japonicus, C. appressa, N. obliterate, L. muscari, M. parvifolium) used in
needed to understand the underlying reasons and competing pollutant a green wall for greywater treatment found that water uptake and
transformations. transpiration in summer was three to four times higher than in winter
conditions (Prodanovic et al., 2019b). The species which showed best N
3.8.2. Pollutant loading and P removal, C. appressa and N. obliterate, also had higher annual
Fig. 6(c) and (d) show greywater treatment in GWs as a function of maximum water uptakes of 912–913 L/m2, while O. japonicus with
nitrogen (NLR) and phosphorus (PLR) loading rates ranging from 75 to lower nutrient removal had only 377 L/m2 water uptake (Prodanovic
1166 N mg/m2/d and from 45 to 660 P mg/m2/d, respectively. Since et al., 2019b). The performance of GWs treating greywater at different
NLR and PLR values were not previously reported in the literature, this temperatures indicates that a temperature range of 10–30 ◦ C only
study calculated these parameters to specifically demonstrate the resulted in about 3% difference in TN removal efficiency (at a low HLR
threshold of GWs for nutrient removal. The TP and TN removal effi­ of 30 mm/d, shown in Fig. 6(a)), but a more noticeable effect occurred
ciencies show an increase with higher N and P loading rates, more on TP removal reducing by up to 20% at the same HLR (Fig. 6(b)).
apparently so at the lower pollutant loads and for TP more than TN Generally, temperatures in the higher range (>25 ◦ C, darker colours in
(Fig. 6). These data may suggest that, at the pollutant loading rates Fig. 6) coincided with better nutrient removal rates, although there are
tested in these studies, GW systems are able to increase nutrient removal some fluctuations in the trends, due to the different hydraulic and
accordingly so have not reached their capacities. It is probable that pollutant loading rates used across studies, as well as effects of drying
higher wastewater (nutrient) loading rates also provide enhanced car­ periods between experimental runs.
bon (i.e. BOD) amounts which enhance microbial activity, driving The selection of vegetation which can adapt to seasonal temperature
nutrient transformation (removal) processes, especially in lower sub­ changes should be considered in GWs designs. Temperature-resistant
strate depths. However, some species such as C. lilies have shown an vegetation can decrease the unsaturation degree of membrane lipids
opposite behaviour during higher inflow TP concentrations, as TP under high temperature and enhance it under low temperature, enabling
removal decreased by 10% (Fowdar et al., 2017), indicating that vege­ them to survive in either extreme temperature conditions (Zheng et al.,
tation species have different tolerance thresholds to higher nutrient 2011). In a study by Boano et al. (2020a), an outdoor GW was operated
loading rates. for three winter months in which pollutant removal of TKN (61%), ni­
trate (56%), and TP (57%) was observed with temperature-resistant
3.8.3. Temperature and seasonal changes vegetation (Lonicera, Carex and Hedera). It may be that vegetation
Seasonal changes, primarily due to temperature differences, affect roots and insulating substrate effects can maintain the inner biofilter

15
M. Gholami et al. Journal of Environmental Management 345 (2023) 118917

temperature up to 3 ◦ C higher than the colder ambient air, allowing the through their complementary properties designed to withstand fluctu­
microbial activity to continue effectively in winter (Akratos and Tsih­ ating pollutant loads, temperature variations and drought effects.
rintzis, 2007). Overlying insulating materials (e.g. gravel, sawdust, etc.) However, studies to-date have been conducted under varying experi­
is also reported to facilitate temperature buffering in cold seasons in TW mental conditions and it is not yet conclusive which specific substrate
systems (Saeed and Sun, 2012; Wu et al., 2011). properties can support and sustain nutrient removal whilst maintaining
hydraulic efficiency. Based on the identified research gaps in this paper,
3.8.4. Irrigation cycle several potential research questions arise that can be explored in future
Scheduled watering and drying cycles may establish beneficial con­ studies:
ditions for the nitrification, denitrification, and anaerobic processes in
GW substrates treating greywater (Pradhan et al., 2019b) although this 1. What is the composition, diversity and function of microbial com­
depends on the duration and frequency. Prolonged drying can inhibit munities in GWs?
biological and chemical processes, including decomposition and 2. Which specific and dominant nutrient transformations occur for each
mineralization, and limit bacterial and vegetation uptake, especially nutrient form at different depths of GWs and what are the in­
when the soil moisture is lowest (Prodanovic et al., 2019a). Prolonged terrelationships of these?
dry periods also create substrate surface cracking and macropores gen­ 3. How do environmental and operating factors, such as temperature,
eration, creating preferential water flow paths and hence higher infil­ irrigation scheduling, humidity, nutrient availability, PLR, and HLR
tration rates and reduced HRT leading to lower nutrient removal. influence the efficiency of physicochemical and biological treatment
However, Fowdar et al. (2017) and Prodanovic et al. (2017) found that processes within GWs?
filtration rates decrease again after reverting to using more frequent 4. How can the complex relationships between substrate characteristics
dosing cycles. and vegetation be optimized to enhance nutrient removal efficiency?
Researchers observed that the effect of a daily watering cycle was 5. What is the interaction and competition between nutrients and other
detrimental to stem quality of some ornamental vegetation, but this was pollutants in greywater treated in GWs, and how does this affect
rectified by implementing a regular two-day cycle with rest day in be­ nutrient removal in green walls?
tween (Pradhan et al., 2019b). In another study using longer watering
periods (e.g. 5-day wetting cycles, 2 days dry) the effects of wetting/­ Declaration of competing interest
drying cycle on nutrient removal efficiency varied according to how
each species responded to drought-induced stress conditions (Fowdar The authors declare that they have no known competing financial
et al., 2017). A two-week drying then wetting cycle was also undertaken interests or personal relationships that could have appeared to influence
to simulate when greywater is not generated if, for instance, a building is the work reported in this paper.
periodically uninhabited. Results showed TN leaching in some vegeta­
tion (up to 24% TN export) and 35% less TN removal for other species Data availability
such as C. appressa (Prodanovic et al., 2019a).
Like other NBS vegetated technologies, prolonged drying periods in No data was used for the research described in the article.
GWs can adversely affect the aesthetics and possibly wastewater treat­
ment efficiency, which may take time to become restored. To help Acknowledgments
mitigate this, drought-tolerant vegetation, deeper planter modules and,
substrates with high moisture retention (i.e., WHC) capacity can be The authors would like to thank the University of Canterbury, New
used. Moreover, recirculating greywater within a vegetated biofilter Zealand, for supporting Moeen Gholami on a Sustainable Development
could help during drought conditions. This can also improve pollutant Goals PhD Scholarship.
removal. For instance, when a GR system treating greywater was oper­
ated under a recirculation ratio of 40% flow, 87% of TN was removed Appendix A. Supplementary data
compared to an initial (non-recirculated) removal efficiency of 56%
(Thomaidi et al., 2022). The improved TN removal may have resulted Supplementary data to this article can be found online at https://doi.
from enhanced denitrification by mixing nitrified effluent with organics org/10.1016/j.jenvman.2023.118917.
in the fresh effluent. In comparison, no significant effect on TP removal
was found. References

4. Conclusions and future research Abd-ur-Rehman, H., Deletic, A., Zhang, K., Prodanovic, V., 2022. The comparative
performance of lightweight green wall media for the removal of xenobiotic organic
compounds from domestic greywater. Water Res. 221, 118774.
Nutrient removal efficiency in different green wall types is influ­ Addo-Bankas, O., Zhao, Y., Vymazal, J., Yuan, Y., Fu, J., Wei, T., 2021. Green walls: a
enced by physical and chemical substrate characteristics, vegetation form of constructed wetland in green buildings. Ecol. Eng. 169, 106321.
Akratos, C.S., Tsihrintzis, V.A., 2007. Effect of temperature, HRT, vegetation and porous
species, pollutant concentration, temperature and hydraulic loading media on removal efficiency of pilot-scale horizontal subsurface flow constructed
rate. IGF and MLW GW designs are commonly employed and show wetlands. Ecol. Eng. 29, 173–191.
similar TN and TP removal of up to 93% TN and 67% TP. Regarding Al-Kayiem, H.H., Koh, K., Riyadi, T.W., Effendy, M., 2020. A comparative review on
greenery ecosystems and their impacts on sustainability of building environment.
various nutrient removal mechanisms, N is removed by vegetation Sustainability 12, 8529.
assimilation and soil and root microbial activity, while P is removed Almanassra, I.W., Mckay, G., Kochkodan, V., Atieh, M.A., Al-Ansari, T., 2021. A state of
mainly through adsorption and filtration. However, further data is the art review on phosphate removal from water by biochars. Chem. Eng. J. 409,
128211.
needed to better ascertain the microbial distribution and microbial in­ Antonopoulou, G., Kirkou, A., Stasinakis, A.S., 2013. Quantitative and qualitative
teractions between substrate, plant roots and greywater in GWs; in greywater characterization in Greek households and investigation of their treatment
particular to elucidate the role of nitrification-denitrification in TN using physicochemical methods. Sci. Total Environ. 454, 426–432.
Arden, S., Ma, X., 2018. Constructed wetlands for greywater recycle and reuse: a review.
removal and microbial storage by PAOs in P removal. Higher HLRs
Sci. Total Environ. 630, 587–599.
compromise the contact time needed for nutrients to be transformed Baban, A., Hocaoglu, S.M., Atasoy, E.A., Gunes, K., Ayaz, S., Regelsberger, M., 2010.
within the treatment system, and an optimal HLR range of 50–60 mm/ Grey water treatment and reuse by using RBC: a kinetic approach. Desalination
d has been suggested but based on some reports of nutrient removal Water Treat. 23, 89–94.
Badhe, N., Saha, S., Biswas, R., Nandy, T., 2014. Role of algal biofilm in improving the
improving at higher HLRs, further research is required. Incorporating a performance of free surface, up-flow constructed wetland. Bioresour. Technol. 169,
mixture of substrates and vegetation can enhance greywater treatment 596–604.

16
M. Gholami et al. Journal of Environmental Management 345 (2023) 118917

Bahrami, M., Amiri, M.J., Badkubi, M., 2020. Application of horizontal series filtration in Gattringer, H., Claret, A., Radtke, M., Kisser, J., Zraunig, A., Rodriguez-Roda, I.,
greywater treatment: a semi-industrial study. Aust. J. Water Resour. 24, 236–247. Buttiglieri, G., 2016. Novel vertical ecosystem for sustainable water treatment and
Bakhshoodeh, R., Ocampo, C., Oldham, C., 2022. Exploring the evapotranspirative reuse in tourist resorts. Int. J. Sustain. Dev. Plann. 11, 263–274.
cooling effect of a green façade. Sustain. Cities Soc. 81, 103822. Gentili, R., Ambrosini, R., Montagnani, C., Caronni, S., Citterio, S., 2018. Effect of soil pH
Boano, F., Caruso, A., Costamagna, E., Fiore, S., Demichelis, F., Galvao, A., Pisoeiro, J., on the growth, reproductive investment and pollen allergenicity of Ambrosia
Rizzo, A., Masi, F., 2020a. Assessment of the treatment performance of an open-air artemisiifolia L. Front. Plant Sci. 9, 1335.
green wall fed with graywater under winter conditions. ACS ES&T Water 1, Ghaitidak, D.M., Yadav, K.D., 2013. Characteristics and treatment of greywater—a
595–602. review. Environ. Sci. Pollut. Control Ser. 20, 2795–2809.
Boano, F., Caruso, A., Costamagna, E., Ridolfi, L., Fiore, S., Demichelis, F., Galvão, A., Gizaw, A., Zewge, F., Kumar, A., Mekonnen, A., Tesfaye, M., 2021. A comprehensive
Pisoeiro, J., Rizzo, A., Masi, F., 2020b. A review of nature-based solutions for review on nitrate and phosphate removal and recovery from aqueous solutions by
greywater treatment: applications, hydraulic design, and environmental benefits. adsorption. AQUA—Water Infrastruct. Ecosyst. Soc. 70, 921–947.
Sci. Total Environ. 711, 134731. Glover, C.M., Liu, Y., Liu, J., 2021. Assessing the risk from trace organic contaminants
Boano, F., Costamagna, E., Caruso, A., Fiore, S., Chiappero, M., Galvão, A., Pisoeiro, J., released via greywater irrigation to the aquatic environment. Water Res. 205,
Rizzo, A., Masi, F., 2021. Evaluation of the influence of filter medium composition 117664.
on treatment performances in an open-air green wall fed with greywater. J. Environ. Gondek, M., Weindorf, D.C., Thiel, C., Kleinheinz, G., 2020. Soluble salts in compost and
Manag. 300, 113646. their effects on soil and plants: a review. Compost Sci. Util. 28, 59–75.
Bonvin, C., Etter, B., Udert, K.M., Frossard, E., Nanzer, S., Tamburini, F., Oberson, A., Graceson, A., Hare, M., Hall, N., Monaghan, J., 2014. Use of inorganic substrates and
2015. Plant uptake of phosphorus and nitrogen recycled from synthetic source- composted green waste in growing media for green roofs. Biosyst. Eng. 124, 1–7.
separated urine. Ambio 44, 217–227. Kader, S.A., Spalevic, V., Dudic, B., 2022. Feasibility study for estimating optimal
Boyjoo, Y., Pareek, V.K., Ang, M., 2013. A review of greywater characteristics and substrate parameters for sustainable green roof in Sri Lanka. Environ. Dev. Sustain.
treatment processes. Water Sci. Technol. 67, 1403–1424. 1–27. https://doi.org/10.1007/s10668-022-02837-y.
Cascone, S., 2019. Green roof design: state of the art on technology and materials. Khajvand, M., Mostafazadeh, A.K., Drogui, P., Tyagi, R.D., Brien, E., 2022. Greywater
Sustainability 11, 3020. characteristics, impacts, treatment, and reclamation using adsorption processes
Castellar, J.A., Torrens, A., Buttiglieri, G., Monclús, H., Arias, C.A., Carvalho, P.N., towards the circular economy. Environ. Sci. Pollut. Control Ser. 29, 10966–11003.
Galvao, A., Comas, J., 2022. Nature-based solutions coupled with advanced Khanam, K., Patidar, S., 2022. Greywater characteristics in developed and developing
technologies: an opportunity for decentralized water reuse in cities. J. Clean. Prod. countries. Mater. Today: Proc. 57, 1494–1499.
340, 130660. Kiba, T., Krapp, A., 2016. Plant nitrogen acquisition under low availability: regulation of
Cescon, A., Jiang, J.-Q., 2020. Filtration process and alternative filter media material in uptake and root architecture. Plant Cell Physiol. 57, 707–714.
water treatment. Water 12, 3377. Kim, S., Park, C., 2022. Fouling behavior and cleaning strategies of ceramic
Chaillou, K., Gérente, C., Andrès, Y., Wolbert, D., 2011. Bathroom greywater ultrafiltration membranes for the treatment and reuse of laundry wastewater.
characterization and potential treatments for reuse. Water, Air, Soil Pollut. 215, J. Water Process Eng. 48, 102840.
31–42. Kotsia, D., Deligianni, A., Fyllas, N., Stasinakis, A., Fountoulakis, M., 2020. Converting
Chen, R.-F., Liu, T., Rong, H.-W., Zhong, H.-T., Wei, C.-H., 2021. Effect of organic treatment wetlands into “treatment gardens”: use of ornamental plants for greywater
substances on nutrients recovery by struvite electrochemical precipitation from treatment. Sci. Total Environ. 744, 140889.
synthetic anaerobically treated swine wastewater. Membranes 11, 594. Koviessen, S., O’Sullivan, A., Gholami, M., Vining, M., de Vries, T., 2023. Physical and
Chowdhury, R.K., Abaya, J.S., 2018. An experimental study of greywater irrigated green chemical parameters of various waste materials for living roof systems: a critical
roof systems in an arid climate. J. Water Manag. Model. 26, 1–10. review. Ecol. Eng. 194, 107013.
Chowdhury, S., Bolan, N., Farrell, M., Sarkar, B., Sarker, J.R., Kirkham, M.B., Hossain, M. Lakho, F.H., Le, H.Q., Mattheeuws, F., Igodt, W., Depuydt, V., Desloover, J., Rousseau, D.
Z., Kim, G.-H., 2021. Chapter Two - role of cultural and nutrient management P., Van Hulle, S.W., 2021a. Decentralized grey and black water reuse by combining a
practices in carbon sequestration in agricultural soil. In: Sparks, D.L. (Ed.), Advances vertical flow constructed wetland and membrane based potable water system: full
in Agronomy. Academic Press, pp. 131–196. scale demonstration. J. Environ. Chem. Eng. 9, 104688.
Chung, P.-W., Livesley, S.J., Rayner, J.P., Farrell, C., 2021. Greywater irrigation can Lakho, F.H., Le, H.Q., Van Kerkhove, F., Igodt, W., Depuydt, V., Desloover, J.,
support climbing plant growth on building green façades. Urban For. Urban Green. Rousseau, D.P., Van Hulle, S.W., 2020. Water treatment and re-use at temporary
62, 127119. events using a mobile constructed wetland and drinking water production system.
Ciabattia, I., Cesaro, F., Faralli, L., Fatarella, E., Tognotti, F., 2009. Demonstration of a Sci. Total Environ. 737, 139630.
treatment system for purification and reuse of laundry wastewater. Desalination 245, Lakho, F.H., Qureshi, A., Novelli, L.D.D., Depuydt, V., Depreeuw, T., Van Hulle, S.W.,
451–459. Rousseau, D.P., 2022. Performance of a green wall (total value Wall™) at high
Correa, J., Postma, J.A., Watt, M., Wojciechowski, T., 2019. Soil compaction and the greywater loading rates and life cycle impact assessment. Sci. Total Environ. 821,
architectural plasticity of root systems. J. Exp. Bot. 70, 6019–6034. 153470.
Costamagna, E., Fiore, S., Boano, F., 2022. Influence of the number of levels and system Lakho, F.H., Vergote, J., Khan, H.I.-U.-H., Depuydt, V., Depreeuw, T., Van Hulle, S.W.,
age on greywater treatment in a green wall. Ecol. Eng. 183, 106755. Rousseau, D.P., 2021b. Total value wall: full scale demonstration of a green wall for
Cuce, E., 2017. Thermal regulation impact of green walls: an experimental and numerical grey water treatment and recycling. J. Environ. Manag. 298, 113489.
investigation. Appl. Energy 194, 247–254. Li, J., Zuo, Q., 2020. Forms of nitrogen and phosphorus in suspended solids: a case study
Dal Ferro, N., De Mattia, C., Gandini, M.A., Maucieri, C., Stevanato, P., Squartini, A., of Lihu lake, China. Sustainability 12, 5026.
Borin, M., 2021. Green walls to treat kitchen greywater in urban areas: performance Li, X., Zhou, J., Tang, Y., Li, Y., Jin, Z., Kong, H., Zhao, M., Zheng, X., Bei, K., 2022.
from a pilot-scale experiment. Sci. Total Environ. 757, 144189. A hydroponic vertical greening system for disposal and utilization of pre-treated
do Couto, E.d.A., Calijuri, M.L., Assemany, P.P., da Fonseca Santiago, A., de Castro Blackwater: optimization of the operating conditions. Ecol. Eng. 183, 106739.
Carvalho, I., 2013. Greywater production in airports: Qualitative and quantitative Liang, L., Wang, Z., Li, J., 2019. The effect of urbanization on environmental pollution in
assessment. Resourc. Conserv. Recycl. vol. 77, 44–51. rapidly developing urban agglomerations. J. Clean. Prod. 237, 117649.
El Menshawy, A.S., Mohamed, A.F., Fathy, N.M., 2022. A comparative study on green Liu, W., Zhang, Y., Wang, S., Bai, L., Deng, Y., Tao, J., 2021. Effect of pore size
wall construction systems, case study: south valley campus of AASTMT. Case Stud. distribution and amination on adsorption capacities of polymeric adsorbents.
Constr. Mater. 16, e00808. Molecules 26, 5267.
Eregno, F.E., Moges, M.E., Heistad, A., 2017. Treated greywater reuse for hydroponic Mahmoudi, A., Mousavi, S.A., Darvishi, P., 2021. Greywater as a sustainable source for
lettuce production in a green wall system: quantitative health risk assessment. Water development of green roofs: characteristics, treatment technologies, reuse, case
9, 454. studies and future developments. J. Environ. Manag. 295, 112991.
Eriksson, E., Auffarth, K., Henze, M., Ledin, A., 2002. Characteristics of grey wastewater. Manso, M., Castro-Gomes, J., 2015. Green wall systems: a review of their characteristics.
Urban Water 4, 85–104. Renew. Sustain. Energy Rev. 41, 863–871.
Farrell, C., Ang, X.Q., Rayner, J.P., 2013. Water-retention additives increase plant Masi, F., Bresciani, R., Rizzo, A., Edathoot, A., Patwardhan, N., Panse, D.,
available water in green roof substrates. Ecol. Eng. 52, 112–118. Langergraber, G., 2016. Green walls for greywater treatment and recycling in dense
Farrell, C., Mitchell, R., Szota, C., Rayner, J., Williams, N., 2012. Green roofs for hot and urban areas: a case-study in Pune. J. Water, Sanit. Hyg. Dev. 6, 342–347.
dry climates: interacting effects of plant water use, succulence and substrate. Ecol. Merz, C., Scheumann, R., El Hamouri, B., Kraume, M., 2007. Membrane bioreactor
Eng. 49, 270–276. technology for the treatment of greywater from a sports and leisure club.
FLL, F.L.L.e.V., 2018. Green Roof Guidelines–Guidelines for the Planning, Construction Desalination 215, 37–43.
and Maintenance of Green Roofs. Forschungsgesellschaft Landschaftsentwicklung Molineux, C.J., Fentiman, C.H., Gange, A.C., 2009. Characterising alternative recycled
Landschaftsbau eV (FLL), Bonn. waste materials for use as green roof growing media in the UK. Ecol. Eng. 35,
Fountoulakis, M., Markakis, N., Petousi, I., Manios, T., 2016. Single house on-site grey 1507–1513.
water treatment using a submerged membrane bioreactor for toilet flushing. Sci. Nikpay, M., 2022. Wastewater fines influence the adsorption behavior of pollutants onto
Total Environ. 551, 706–711. microplastics. J. Polym. Environ. 30, 776–783.
Fowdar, H.S., Deletic, A., Hatt, B.E., Cook, P.L., 2018. Nitrogen removal in greywater Oteng-Peprah, M., Acheampong, M.A., DeVries, N.K., 2018a. Greywater characteristics,
living walls: insights into the governing mechanisms. Water 10, 527. treatment systems, reuse strategies and user perception—a review. Water, Air, Soil
Fowdar, H.S., Hatt, B.E., Breen, P., Cook, P.L., Deletic, A., 2017. Designing living walls Pollut. 229, 1–16.
for greywater treatment. Water Res. 110, 218–232. Oteng-Peprah, M., De Vries, N., Acheampong, M., 2018b. Greywater characterization
Galvão, A., Martins, D., Rodrigues, A., Manso, M., Ferreira, J., Silva, C.M., 2022. Green and generation rates in a peri urban municipality of a developing country.
walls with recycled filling media to treat greywater. Sci. Total Environ. 842, 156748. J. Environ. Manag. 206, 498–506.

17
M. Gholami et al. Journal of Environmental Management 345 (2023) 118917

Panuvatvanich, A., Koottatep, T., Koné, D., 2009. Hydraulic behaviour of vertical-flow Sami, M., Hedström, A., Kvarnström, E., McCarthy, D., Herrmann, I., 2023. Greywater
constructed wetland under different operating conditions. Environ. Technol. 30, treatment in a green wall using different filter materials and hydraulic loading rates.
1031–1040. J. Environ. Manag. 340, 117998.
Patil, P.D., Bhange, V.P., Shende, S.S., Ghorpade, P.S., 2022. Greywater characterization Schwammberger, P.F., Yule, C.M., Tindale, N.W., 2020. Rapid plant responses following
of an Indian household and potential treatment for reuse. Water-Energy Nexus 5, relocation of a constructed floating wetland from a construction site into an urban
1–7. stormwater retention pond. Sci. Total Environ. 699, 134372.
Paulo, P.L., Azevedo, C., Begosso, L., Galbiati, A.F., Boncz, M.A., 2013. Natural systems Shaikh, I.N., Ahammed, M.M., 2020. Quantity and quality characteristics of greywater: a
treating greywater and blackwater on-site: integrating treatment, reuse and review. J. Environ. Manag. 261, 110266.
landscaping. Ecol. Eng. 50, 95–100. Shen, S., Li, X., Cheng, F., Zha, X., Lu, X., 2020. Recent developments of substrates for
Perini, K., Rosasco, P., 2013. Cost–benefit analysis for green façades and living wall nitrogen and phosphorus removal in CWs treating municipal wastewater. Environ.
systems. Build. Environ. 70, 110–121. Sci. Pollut. Control Ser. 27, 29837–29855.
Pradhan, S., Al-Ghamdi, S.G., Mackey, H.R., 2019a. Greywater recycling in buildings Solano, L., Ristvey, A.G., Lea-Cox, J.D., Cohan, S.M., 2012. Sequestering zinc from
using living walls and green roofs: a review of the applicability and challenges. Sci. recycled crumb rubber in extensive green roof media. Ecol. Eng. 47, 284–290.
Total Environ. 652, 330–344. Sotiropoulou, M., Stefanatou, A., Schiza, S., Petousi, I., Stasinakis, A., Fountoulakis, M.,
Pradhan, S., Al-Ghamdi, S.G., Mackey, H.R., 2019b. Greywater treatment by ornamental 2022. Removal of microfiber in vertical flow constructed wetlands treating
plants and media for an integrated green wall system. Int. Biodeterior. Biodegrad. greywater. Sci. Total Environ., 159723
145, 104792. Thomaidi, V., Petousi, I., Kotsia, D., Kalogerakis, N., Fountoulakis, M., 2022. Use of green
Pradhan, S., Helal, M.I., Al-Ghamdi, S.G., Mackey, H.R., 2020. Performance evaluation of roofs for greywater treatment: role of substrate, depth, plants, and recirculation. Sci.
various individual and mixed media for greywater treatment in vertical nature-based Total Environ. 807, 151004.
systems. Chemosphere 245, 125564. Turner, R.D., Will, G.D., Dawes, L.A., Gardner, E.A., Lyons, D.J., 2013. Phosphorus as a
Prajapati, B., Jensen, M., Jørgensen, N., Petersen, N., 2019. Grey water treatment in limiting factor on sustainable greywater irrigation. Sci. Total Environ. 456, 287–298.
stacked multi-layer reactors with passive aeration and particle trapping. Water Res. Verma, A.K., Dash, A.K., Bhunia, P., Dash, R.R., 2021. Removal of surfactants in
161, 181–190. greywater using low-cost natural adsorbents: a review. Surface. Interfac. 27, 101532.
Prodanovic, V., Hatt, B., McCarthy, D., Deletic, A., 2020. Green wall height and design Vijayaraghavan, K., 2016. Green roofs: a critical review on the role of components,
optimisation for effective greywater pollution treatment and reuse. J. Environ. benefits, limitations and trends. Renew. Sustain. Energy Rev. 57, 740–752.
Manag. 261, 110173. Vijayaraghavan, K., Raja, F.D., 2014. Design and development of green roof substrate to
Prodanovic, V., Hatt, B., McCarthy, D., Zhang, K., Deletic, A., 2017. Green walls for improve runoff water quality: plant growth experiments and adsorption. Water Res.
greywater reuse: understanding the role of media on pollutant removal. Ecol. Eng. 63, 94–101.
102, 625–635. Vox, G., Blanco, I., Convertino, F., Schettini, E., 2022. Heat transfer reduction in building
Prodanovic, V., McCarthy, D., Hatt, B., Deletic, A., 2019a. Designing green walls for envelope with green façade system: a year-round balance in Mediterranean climate
greywater treatment: the role of plants and operational factors on nutrient removal. conditions. Energy Build. 274, 112439.
Ecol. Eng. 130, 184–195. Vuppaladadiyam, A.K., Merayo, N., Prinsen, P., Luque, R., Blanco, A., Zhao, M., 2019.
Prodanovic, V., Wang, A., Deletic, A., 2019b. Assessing water retention and correlation A review on greywater reuse: quality, risks, barriers and global scenarios. Rev.
to climate conditions of five plant species in greywater treating green walls. Water Environ. Sci. Biotechnol. 18, 77–99.
Res. 167, 115092. Wang, J., Li, Y., Wang, W., Wu, H., Kong, F., Wang, S., 2022. Enhancement of wastewater
Prodanovic, V., Zhang, K., Hatt, B., McCarthy, D., Deletic, A., 2018. Optimisation of treatment under low temperature using novel electrochemical active biofilms
lightweight green wall media for greywater treatment and reuse. Build. Environ. constructed wetland. J. Environ. Manag. 312, 114913.
131, 99–107. Wu, S., Austin, D., Liu, L., Dong, R., 2011. Performance of integrated household
Prodanovic, V., Zhang, K., Zheng, M., Hu, S., Hong, P.-Y., Yuan, Z., Deletic, A., 2023. constructed wetland for domestic wastewater treatment in rural areas. Ecol. Eng. 37,
Nitrification potential of daily-watered biofiltration designs for high ammonium 948–954.
wastewater treatment. Sci. Total Environ. 863, 160989. Xu, C., Yuan, Q., Zhao, S., He, T., Song, N., 2020. Effects of pretreatments on physical
Qadir, M., Drechsel, P., Jiménez Cisneros, B., Kim, Y., Pramanik, A., Mehta, P., and chemical characteristics of wheat straw used as a maintenance-free compressed
Olaniyan, O., 2020. Global and regional potential of wastewater as a water, nutrient green roof substrate material. J. Clean. Prod. 277, 123381.
and energy source. Nat. Resour. Forum 44 (1), 40–51. Xue, M., Farrell, C., 2020. Use of organic wastes to create lightweight green roof
Radingoana, M.P., Dube, T., Mazvimavi, D., 2020. Progress in greywater reuse for home substrates with increased plant-available water. Urban For. Urban Green. 48,
gardening: opportunities, perceptions and challenges. Phys. Chem. Earth, Parts A/B/ 126569.
C 116, 102853. Young, T., Cameron, D.D., Sorrill, J., Edwards, T., Phoenix, G.K., 2014. Importance of
Ramprasad, C., Philip, L., 2018. Greywater treatment using horizontal, vertical and different components of green roof substrate on plant growth and physiological
hybrid flow constructed wetlands. Curr. Sci. 114 (1), 155–165. performance. Urban For. Urban Green. 13, 507–516.
Ramprasad, C., Smith, C.S., Memon, F.A., Philip, L., 2017. Removal of chemical and Yuvaraj, M., Bose, K.S.C., Elavarasi, P., Tawfik, E., 2021. Soil salinity and its
microbial contaminants from greywater using a novel constructed wetland: grow. management. In: Meena, R.S., Datta, R. (Eds.), Soil Moisture Importance.
Ecol. Eng. 106, 55–65. IntechOpen, p. 109.
Read, J., Wevill, T., Fletcher, T., Deletic, A., 2008. Variation among plant species in Zhai, X., Piwpuan, N., Arias, C.A., Headley, T., Brix, H., 2013. Can root exudates from
pollutant removal from stormwater in biofiltration systems. Water Res. 42, 893–902. emergent wetland plants fuel denitrification in subsurface flow constructed wetland
Rudrappa, T., Biedrzycki, M.L., Bais, H.P., 2008. Causes and consequences of plant- systems? Ecol. Eng. 61, 555–563.
associated biofilms. FEMS (Fed. Eur. Microbiol. Soc.) Microbiol. Ecol. 64, 153–166. Zheng, G., Tian, B., Zhang, F., Tao, F., Li, W., 2011. Plant adaptation to frequent
Saeed, T., Sun, G., 2012. A review on nitrogen and organics removal mechanisms in alterations between high and low temperatures: remodelling of membrane lipids and
subsurface flow constructed wetlands: dependency on environmental parameters, maintenance of unsaturation levels. Plant Cell Environ. 34, 1431–1442.
operating conditions and supporting media. J. Environ. Manag. 112, 429–448. Zheng, J., Kamal, M.A., 2020. The effect of household income on residential wastewater
output: evidence from urban China. Util. Pol. 63, 101000.

18

You might also like