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Abbreviations
WEEE Waste of electrical and electronic equipment
E-waste Electronic waste
DNA Deoxyribose nucleic acid
CRT Cathode ray tube
PCBs Polychlorinated biphenyls
NADH Nicotinamide adenine dinucleotide
HXRF Handheld X-ray fluorescence analysis
IC Ion Chromatography
ICP Inductively coupled plasma mass spectrometry
OES Optical Emission Spectroscopy, Mt: Million Ton
1 Introduction
There are several disadvantages of various chemical and biological techniques for
e-waste management (Table 2). Future perspective of sustainable development
depends upon the use of new techniques which must be suitable from economic as
well as environmental point of view. The field of metal extraction involves the
using of various processes that have been continuously expanding its applications
for the discovery of new eco-friendly, economic, and efficient technique for metal
recovery.
2 Mechanisms of Bioleaching
A:ferrooxidansis
Fe2 þ þ O2 þ H þ ! Fe3 þ þ H2 O ð1Þ
(ii) Fe3+ formed by A. ferrooxidans in reaction (1) oxidizes the elemental copper
to Cu2+ through following chemical reaction (2), (Bard et al. 1985).
þ 2þ 2þ
Cu0 þ Fe3ðAq Þ ! FeðAqÞ þ CuðAqÞ ð2Þ
Microorganism can also oxidize metal sulfide by direct and indirect mechanism.
In direct mechanism, the source of electron is direct minerals, and in the indirect
mechanism, oxidation of reduced metals occurs through ferric iron (Fe3+) (Brandl
2008). Following equation explains both direct and indirect mechanism of
bioleaching of pyrite.
Thiobacilli
2FeS2 þ 7O2 þ 2H2 O þ 2H2 SO4 ! 2FeSO4 þ 2H2 SO4 ð3Þ
T:Ferrooxidans; L:Ferrooxidans
4FeS2 þ O2 þ 2H2 SO4 ! 2Fe2 ðSO4 Þ3 þ 2H2 O ð4Þ
Fig. 2 Fe(II) oxidation in M. sedula (ferrous iron oxidation gene C is primary electron acceptor
from metal ions and transfers the electron to a rusticyanin, copper protein). The dotted line shows
the direction of electron flow; a represents heme a center in ferrous iron oxidation gene A;
(CuBa3) is binuclear center in ferrous iron oxidation gene A (site for reduction of O2 to H2O);
b represents heme b center in ferrous iron oxidation gene C; and sulphur iron oxidation gene N
(soxN), (CuA) is copper center in FoxB, (Fe–S) represents iron sulfur clusters in ferrous iron
oxidation gene G and sulphur iron oxidation gene (SoxL); (Q) and (QH2) represents ubiquinone
and hydroquinone) (Auernik et al. 2008; Kozubal et al. 2011; Wheaton et al. 2015).
5 Bioremediation Techniques for E-waste Management 111
A. Ferrooxidens cell
O2 CO 2 N2 H2 Extracellular matrix
pH= 1-3.5
H 20 3PG NH 4 H 2O
pH =6.5
So4 2-
Mineral Surface
SO4 2- S0
S2 O 3 2- FeIII FeIII Cu
Cu III
Cu I CuII
Fe2S + 6(Fe(H 2oO6)3+ + 9H20 S2032+ + 6(Fe(H2O)6)3++6H+
2Fe+2 2Fe+3
Rus
Cyc- 1 Cyc- 2
QH 2 Cytoplasmic membrane
sdrA-1
bc1 Aa3
NADH
Cyt Ox
2 e-
2 e-
Fig. 4 Enzymes and electron transfer proteins involved in the oxidation of ferrous iron (Levican
et al. 2002)
(a)
Fe 3+
O2
(Af, Lf)
MS
Fe 3+
M2++ S2O32-
SnO62- ,S8
SO42+ + H+
(b)
Fe 3+
H+
O2
(Af, Lf)
MS
Fe 3+
H2Sn , S8
SO42+ + H+
Fig. 5 Comparison of the thiosulfate (a) and polysulfide (b) mechanisms (from Schippers and
Sand 1999, modified)
4 Organic Part
Table 3 (continued)
Species involved Leaching Condition/ References
agent pH range
Archaea Sulfobacillus thermosulfidooxidans Ferric iron Extremely Barrett (1993)
species acidophilic
Sulfobacillus thermosulfidooxidans
Sulfobacillus
thermosulfidooxidans sub. asporogenes
Sulfolobus acidocaldarius 0.9–5.8 Olson (1994),
Sulfolobus ambivalens – Rossi (1990)
Sulfolobus solfataricus –
Sulfolobus thermosulfidooxidans –
Sulfolobus brierleyi – Brierley (1982)
Sulfolobus yellowstonii – Olson (1994)
Fungal Actinomucor sp. Oxalate, –
species Alternaria sp. malate,
pyruvate,
Aspergillus amstelodami
oxalacetate
Aspergillus clavatus Aspartate
Aspergillus ficuum Oxalate Strasser et al.
(1994)
Aspergillus fumigatus –
Aspergillus niger Oxalate, Bosshard et al.
citrate, (1996), Sayer
gluconate, et al. (1995)
lactate
Aspergillus ochraceus Citrate,
glutamate
Candida sp. –
Cerostamella sp. –
Cladosporium resinae –
Coriolus versicolor –
Cunninghamiella sp. –
Fusarium sp. –
Gleophyllum trabeum Oxalate Strasser et al.
(1994)
Mucor sp. Fumarate,
gluconate
Paecilomyces variotii Malate
Penicillium cyclopium
Penicillium funiculosum Citrate,
glutamate
Penicillium notatum –
Penicillium ochrochloron Oxalate
Penicillium oxalicum Strasser et al.
Penicillium simplicissimum (1994)
(continued)
5 Bioremediation Techniques for E-waste Management 117
Table 3 (continued)
Species involved Leaching Condition/ References
agent pH range
Citrate,
oxalate,
gluconate
Penicillium spinulosum Oxalate
Penicillium variotii –
Phanerochaete chrysosporium –
Pichia sp. –
compounds (Hornung et al. 2006). Another two processes: (i) staged gasification
and (ii) co-combustion were compared by researchers in 2009 (Bientinesi and
Petarca 2009). After the experiment, they conclude that the co-combustion pro-
duces less emission of HCl, HBr, NOx than the staged gasification. But the later
process is more energy efficient method and saves resources and lowers carbon
dioxide emissions. Its environmental impact is less than the previous method.
Therefore, performance ability of staged gasification is much better as compared to
co-combustion and also results in high Br yield (Bientinesi and Petarca 2009).
Above study concludes that WEEE thermal high-temperature treatment for energy
and metal recovery is much efficient and effective process to deal with such type of
waste. Following conclusions are being made on the basis of studies carried on the
process of high-temperature thermal degradation process:
(1) The degradation product obtained is highly enriched with free halogens and
hydrogen halides when bench scale oxidation reactor is used (Yang et al. 2011).
(2) In the process of pyrolysis, alkali metals have effective role in decreasing Br
percentage and VOCs in the resultant product.
(3) Starting temperature is 400 °C, and for complete degradation, a temperature of
1000 °C is required.
118 D. Pant et al.
Apart from that, fungi (Pestalotiopsis microspora), a plastic eating fungi, has
been recently discovered, and the enzymes (serine hydrolase) can breakdown the
plastics (Mohammed et al. 2013). This may also help in remediating e-waste from
environment.
Factors
Biological leaching (Fig. 7) of metals from any electronic waste or metals ore is a
cost-effective technique, but it is time-consuming because microbial growth is a
complex process involving numerous anabolic and catabolic reactions within the
microbial cells (Maier 2000), and several environmental issues in chemical leaching
hybrid technique involving combination of chemical (eco-friendly chemicals) and
biological leaching may be the best and efficient techniques for metal extraction
(Table 5; Pant et al. 2012). In hybrid technique, various combinations of ligands
with associated microbes can be used for metal extraction. For the extraction of Zn,
Cd, Pb, and Cu from electronic waste or their ores, EDTA (Wasay et al. 1998) can
reasonably enhance the efficiency of metal extraction with either A. ferrooxidan
(Cheikh et al. 2010) or Shewanella putrefaciens (Dobbin et al. 1995). Various
organic acids like citric, tartaric, and oxalic acids secreted from fungi (A. niger,
Penicillium bilaiae, and other Penicillium sp.) act as a chelating agents for the
extraction of Cu, Cd, Zn, and Pb (Arwidsson and Allard 2010; Wasay et al. 1998;
Reuse
Ligand
Mixture
of metals
Metal- ligand-
microbes interaction Microbes + Ligand
Metal
Recovery
Mulligan and Kamali 2003; Elliott and Shastri 1999). The combination of oxalate
along with ammonium citrate and A. niger or Penicillium spp. (Arwidsson and
Allard 2010) can be used for the extraction of Cd, Pb, Cu, and Zn (Wasay et al.
1998) and can enhance the leaching efficiency (Pant et al. 2012). Some sulfide
ligands along with microbes like A. ferrooxidans, Sulfobolus spp., A. thiooxidans
(Bosecker 1997), and fungus Phanerochaete chrysosporium can enhance the rate
recovery rate. As per some environmental issue regarding use of chemical ligands,
some biodegradable ligands may also play some important role in eco-friendly
metal extraction. Biodegradable ligands like EDDS (ethylene diamine di-succinic
acid), DTPA (diethylene triamine penta-acetate), and NTA (nitrilotriacetic acid) are
well known for the extraction of Cd, Pb, Cu, Zn, and Fe from their ores (Hong et al.
2000).
Bioremediation techniques can be efficiently managed by the compatible
chemical, biological, or hybrid leaching techniques. Hybrid mechanism by the use
of certain metal-specific ligands and microbes can also achieve metal-specific
extraction from waste (Ilyas et al. 2010).
5 Bioremediation Techniques for E-waste Management 121
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Author Biographies
Dr. Deepak Pant is currently the Dean and Head of Environmental Science, Central University of
Himachal Pradesh, Dharamshala. He received the Silver Jubilee Research Fellowship Award in
2003 from Kumaun University, Nainital, India; the UCOST Young Scientist Award 2009, INSA
Fellow (2010), DST-SERC, Visiting Fellow (2010) and DST-SERC Young Scientist Award
(2011). He has 5 patents in the area of waste management using green techniques and published 10
5 Bioremediation Techniques for E-waste Management 125
books, 45 research papers in various national and international journals. He recently received
Visitor’s Award 2017 from the President of India for his innovations in the area of waste
management.
Mr. Anand Giri currently perusing his Ph.D under the supervision of Prof. Deepak Pant in the
subject of Environmental Science from Central University of Himachal Pradesh, Dharamshala,
Himachal Pradesh, India. He did his post graduation in Environmental Science from G.B. Pant
University of Agriculture and Technology Pantnagar, Uttarakhand in year of 2012.
Mr. Varun Dhiman currently perusing his Ph.D under the supervision of Prof. Deepak Pant in the
subject of Environmental Sciences from Central University of Himachal Pradesh, Dharamshala,
Himachal Pradesh, India. He did his post graduation in Environmental Science from Central
University of Himachal Pradesh (CUHP), Himachal Pradesh in year of 2014.