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(BAT) Reference Document for the Production of Chlor-alkali ...

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Chapter 2<br />

Characteristics <strong>of</strong> <strong>the</strong> cathode: The cathode is made by a shallow layer <strong>of</strong> mercury which flows<br />

from one extremity <strong>of</strong> <strong>the</strong> cell to <strong>the</strong> o<strong>the</strong>r because <strong>of</strong> due to <strong>the</strong> slight inclination from <strong>the</strong><br />

horizontal <strong>of</strong> <strong>the</strong> cell base. The quantity <strong>of</strong> mercury per cell can be up to 6 t. A high level <strong>of</strong><br />

purity, [ 99.9 wt-% mercury, and very low concentrations <strong>of</strong> metals, in particular heavy metals,<br />

are required [ 3, Euro <strong>Chlor</strong> 2011 ].<br />

Characteristics <strong>of</strong> <strong>the</strong> anode: Graphite was exclusively used as <strong>the</strong> anode <strong>for</strong> chlorine production<br />

<strong>for</strong> more than 60 years, even though it exhibited high chlorine overpotential and dimensional<br />

instability caused by <strong>the</strong> electrochemical oxidation <strong>of</strong> carbon to carbon dioxide, and hence led to<br />

high energy consumption and <strong>the</strong> need <strong>for</strong> frequent maintenance operations. Electrolytic cell<br />

anodes were made <strong>of</strong> graphite until <strong>the</strong> late 1960s in Western Europe when In <strong>the</strong> late 1960s,<br />

anodes <strong>of</strong> titanium coated with ru<strong>the</strong>nium dioxide (RuO2) and titanium dioxide (TiO2) were<br />

developed, <strong>the</strong> so-called dimensionally stable anodes. The use <strong>of</strong> RuO2- and TiO2-coated metal<br />

anodes reduces energy consumption by approximately about 10 % compared to graphite and<br />

<strong>the</strong>ir life expectancy is higher (300 – 400 t Cl2/m 2 ; ranging from less than one to more than five<br />

years depending on current density and gap between anode and cathode). In recent years <strong>the</strong>re<br />

have been competitive developments in detailed The anode geometry <strong>for</strong> mercury cells has been<br />

optimised, all with <strong>the</strong> aim <strong>of</strong> improving gas release in order to reduce ohmic losses and<br />

increasing <strong>the</strong> homogeneity <strong>of</strong> <strong>the</strong> brine to improve anode coating life [ 1, Ullmann's 2006 ],<br />

[ 10, Kirk-Othmer 2002 ], [ 21, Kirk-Othmer 1995 ].<br />

An ‘end box’ is attached to each end <strong>of</strong> <strong>the</strong> cell electrolyser. The end box incorporates<br />

compartments <strong>for</strong> collecting <strong>the</strong> chlorine gas and weirs <strong>for</strong> separating <strong>the</strong> mercury and brine<br />

streams as well as washing <strong>the</strong> mercury and permitting <strong>the</strong> removal <strong>of</strong> thick mercury ‘butter’<br />

that is <strong>for</strong>med by impurities.<br />

The whole cell electrolyser is insulated from <strong>the</strong> floor to prevent stray ground currents. Usually,<br />

several cells electrolysers are placed in series by means <strong>of</strong> electrically connecting <strong>the</strong> cathode <strong>of</strong><br />

one cell electrolyser to <strong>the</strong> anodes <strong>of</strong> <strong>the</strong> next cell electrolyser. Individual cells can be bypassed<br />

<strong>for</strong> maintenance and replacement. The cells are usually situated in a building (Figure 2.4),<br />

although sometimes <strong>the</strong>y are erected in open air [ 1, Ullmann's 2006 ], [ 17, Dutch Ministry<br />

1998 ].<br />

WORKING DRAFT IN PROGRESS<br />

Source: [ 18, BASF 2010 ]<br />

Figure 2.4: View <strong>of</strong> a mercury cell room<br />

TB/EIPPCB/CAK_Draft_1 December 2011 25

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