CHAPTER SIX

WORKING PRINCIPLE OF VRLA BATTERY

MAINTENANCE FREE SECONDARY CELLS (VRLA)
General
Maintenance free, valve-regulated lead-acid (VRLA) batteries ensure a reliable,
effective and user friendly source of power. It is spill proof, leak proof and explosion resistant
and there is no need to add water or to clean terminals. It has low self-discharge rate which
eliminates the need for equalizing charges. The container is made of polypropylene. Each
plate is individually wrapped by a highly absorbent, micro porous glass separate developed
specially for VRLA batteries. The chemically inert glass ensures life long service. The
absorbed electrolyte ensures that there is no spillage even in the unlikely event of puncture of
the cell. Gas evolution under float conditions is negligible. The water loss throughout life due
to gassing is roughly 0.1% of the total electrolyte present in the cell. This will in no way
affect performance and also eliminate the need for specially ventilated battery room and acid
resisting flooring. As the batteries can be installed in stacks, there will be considerable space
saving also.
Various capacities of Batteries are 120 AH, 200 AH, 400 AH, 600 AH, 1000 AH, 1500
AH, 2000 AH, 2500 AH, 3000 AH, 4000 AH and 5000 AH.
VRLA Technology A brief review of Chemical Reaction
The electrode reactions in all lead acid batteries including VRLA battery is basically
identical. As the battery is discharged, the lead dioxide positive active material and the
spongy lead negative active material react with the sulphuric acid electrolyte to form lead
sulphate and water. During charge, this process is reversed. The Columbic efficiency of the
charging process is less than 100% on reaching final stage of charging or under over charge
conditions, the charging energy is consumed for electrolytic decomposition of water and the
positive plates generate oxygen gas and the negative plates generate hydrogen gas.
Under typical charging conditions, oxygen at the positive plate occurs before
hydrogen evolution at the negative. This feature is utilized in the design of VRLA batteries.
In flooded cells, the oxygen gas evolved at the positive plate bubbles upwards through the
electrolyte and is released through the vents. In MF-VRLA batteries the oxygen gas evolved,
at the positive plate, instead of bubbling upwards is transported in the gas phase through the
separator medium to the negative plate. The separator is a highly absorbent glass matrix type
with very high porosity, designed to have pore volume in excess of the electrolyte volume
(starved electrolyte design), due to which the oxygen gas finds an unimpeded path to the
negative plate. The oxygen gas gets reduced by reaction with the spongy lead at the negative
plate, turning a part of it into a partially discharged condition, there by effectively
suppressing the hydrogen gas evolution at the negative plate. This is what is known as the
oxygen recombination principle. The part of negative plate which was partially discharged is
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then reverted to the original spongy lead by subsequent charging. Thus, a negative plate
keeps equilibrium between the amount which turns into spongy lead by charging and the
amount of spongy lead which turns into lead sulphate by absorbing the oxygen gas generated
at the positive plate. The oxygen recombination principle can be shown by the following
reaction :
1.

Reaction at positive plate :

H2O =

2.

O2 + 2e

(1)

Reaction at negative plate :

Pb + 1/2O2

PbO+H2SO4

PbO

(2)

PbSO4 + H2O

(3)
To reaction (1)

PbSO4 + 2H + 2e

Pb + H2SO4

(4)
To reaction (3)
To reaction (2)

3.

The total reaction at negative plate

O2 +2H+

H2O

Thus, the oxygen recombination technology makes the battery virtually maintenance Free.

Section 3 :
Technical Specification of 1000 AH Battery
1.
2.
3.
4.

5.
6.
7.
8.

Capacity of the Battery @ 10 Hr. rate : 1000 AH

discharge to 1.75 ECV
Nominal Voltage per cell of fully charged : 2.0 V
battery at 27oC
Open Circuit Voltage (OCV) of fully : 2.15 V
charged battery at 27oC
Recommended Float Voltage Condition
(i) Terminal Voltage of Charger
2.25 V/Cell
(ii) Float charging current at 2.25 V/cell : Maximum current to be limited to 20% of the
rated AH
Recommended Boost charging condition : 2.30 V/Cell
for quick charging at 27oC
Internal resistance of the cell
: 0.257 milli ohms
Life Expectancy of the Battery
: 4000 Cycles at 20% Depth of Discharge or 20
years under Float condition
Containers :
(i) Material
: Polypropylene (Spl. Grade)
(ii) Thickness of wall
: 2.3 mm (Approx.)
Container and cover
- Polypropylene Co-polymer housed in a steel tray

Separator
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- Spun glass micro porous matrix

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 Safety valve

- Explosion proof, pressure-regulating and selfresealing type

Positive plate

- Patented MFX alloy

Negative plate

- Lead Calcium alloy

Terminal

- Integral lead terminal with solid copper core

Self discharge

- Less than 0.5% per week

Charging

- Current limited, constant potential

Float charge

- 2.25 VPC at 27oC with a max. current limit of

20% of rated capacity in amperes

Boost charge

- 2.30 VPC at 27oC with a max. current limit of

20% of rated capacity in amperes

Connectors

- Heavy-duty, lead plated copper connectors

Life expectancy

- Float service at 27oC upto 20 years

- Cycle duty at 27oC 80% DOD 1200 Cycles
- Cycle duty at 27oC 20% DOD 4000 Cycles

Fig. Power Stack Cell Cut Section

Section 4 Freshening Charge

General
Batteries lose some charge during transportation as well as during the period prior to
installation. A battery should be installed and given a freshening charge after receipt as soon
as possible. Battery positive (+) terminal should be connected to charge positive (+) terminal
and battery negative (-) terminal to charger negative (-) terminal.
The charge intervals for storage is given in the table below.
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Temp in 0 c

Charging interval in months

32

6.0

37

4.5

42

3.0

47

2.25

52

1.5

Storage beyond this period without freshening charge can result in excessive
sulphation of the plates.
Requirement of Charger
It is preferable to have the following characteristics in the battery charger being used
with these batteries

High voltage cut-off at 2.37 VPC

Low voltage trip at 1.60 VPC

Voltage ripple to be limited to 2 % of rms.

Voltage regulation to be limited to 1 %

Constant Voltage Method
Constant voltage is the only charging method recommended. Most modern chargers
are of the constant voltage type.
Determine the maximum voltage that may be applied to the system equipment. This
voltage, divided by the number of cells connected in series, will establish the maximum volts
per cell (VPC) that may be used.
Table B lists recommended voltages and charge times for the freshening charge.
Select the highest voltage the system allows but not exceeding 2.37 volts per cell to perform
the freshening charge in the shortest time period. The charging current should be limited to a
maximum of 20% of the rated capacity in Amps.
Table B

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Cell Volts

Time

2.25

30 hrs

2.30

12 hrs

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Note : Time periods listed in Table B are for temperatures from 15 oC to 40oC. For
temperatures below 15oC double the number of hours.
Charging
The charging current should be limited to a maximum of 0.2 times of AH Capacity.
Widely accepted charging methods use a current of 0.1xC10 (C10 = AH Capacity when
discharged at 10 hr rate) Example:
A 2000 AH VRLA battery is to be charged as under
0.2 x 2000
0.2 x 2000 = 400 Amps or
0.1 x 2000 = 200 Amps ( as per TEC recommendation)
Raise the voltage to the maximum value not exceeding 2.37 volts per cell permitted
by the system equipment. When charging current has tapered and stabilized (no further
reduction for three hours), charge for the hours shown in the above table or until the lowest
cell voltage ceases to rise. Correct charge time for the temperature at the time of stabilization.
To determine lowest cell, monitoring should be performed during the final 10% of the charge
time.

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