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

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Chapter 3<br />

<strong>of</strong> chlorine capacity. The first one is economic and <strong>the</strong> second technical. For economic reasons,<br />

a plant will always prefer to run all its cells because it is <strong>the</strong> cheapest way <strong>of</strong> operating and<br />

minimising costs. This is particularly true in countries like Spain or <strong>the</strong> United Kingdom where<br />

electricity tariffs can vary a lot during <strong>the</strong> year or even <strong>the</strong> day. Running at lower current<br />

densities is cheaper than switching <strong>of</strong>f <strong>the</strong> some cells. The second reason given is <strong>the</strong> design <strong>of</strong><br />

<strong>the</strong> electrical circuit. The rectifier is specified <strong>for</strong> a certain voltage and <strong>the</strong> electrical equipment<br />

may not support a voltage drop, especially <strong>for</strong> processes plants using a combination <strong>of</strong><br />

diaphragm and mercury cell techniques amalgam technologies or amalgam mercury and<br />

membrane cell techniques. In Europe, however, <strong>the</strong> figures reported refer to 90 % running<br />

capacity.<br />

The industry also reports that production figures on a plant by plant basis are confidential data<br />

<strong>for</strong> ‘competitivity competitive reasons’.<br />

Contrary to what is described above, a minor share <strong>of</strong> <strong>the</strong> mercury emission is indeed dependent<br />

on <strong>the</strong> production rate. For example, emissions via products or via <strong>the</strong> brine purge are directly<br />

linked to production [ 83, Euro <strong>Chlor</strong> 2010 ]. In addition, maintenance frequencies and related<br />

emissions also increase with current densities and thus production rates.<br />

The emissions <strong>of</strong> pollutants o<strong>the</strong>r than mercury depend mainly on <strong>the</strong> production rate and<br />

should thus preferably be expressed per actual production.<br />

3.5.4 Consumption <strong>of</strong> mercury<br />

Reported consumption <strong>of</strong> mercury ranges from 2.6 – 10.9 g/t annual chlorine capacity [ 75,<br />

COM 2001 ]. {These data are contained in Table 3.1 and stem from <strong>the</strong> original BREF. Please<br />

TWG provide updated data.}<br />

3.5.5 Overall mercury emissions and waste generation<br />

Mercury emissions and waste generation from individual chlor-<strong>alkali</strong> installations in EU-27 and<br />

EFTA countries in 2010 as reported by Euro <strong>Chlor</strong> are summarised in Table 3.23. These figures<br />

will be discussed in more detail in <strong>the</strong> subsequent sections.<br />

Figure 3.3 shows <strong>the</strong> weighted averages <strong>of</strong> <strong>the</strong> total emissions from all chlor-<strong>alkali</strong> installations<br />

in Western Europe (OSPAR countries) from 1977 – 1998 and Figure 3.4 <strong>for</strong> EU-27 and EFTA<br />

countries from 1995 – 2009. For <strong>the</strong> OSPAR countries, emissions decreased by approximately<br />

92 % from 1977 – 1995 while <strong>for</strong> EU-27 and EFTA countries, emissions decreased by<br />

approximately 66 % from 1995 – 2010. The observed decreases are due to reduced emissions<br />

from individual installations. However, <strong>the</strong> weighted average may also be influenced by <strong>the</strong><br />

shutdown or inclusion <strong>of</strong> installations with emissions higher or lower than <strong>the</strong> average. For<br />

example, <strong>the</strong> slight increase from 2008 to 2009 is caused by a plant with high mercury<br />

emissions to water which in 2009 was <strong>for</strong> <strong>the</strong> first time included in <strong>the</strong> calculations. O<strong>the</strong>rwise<br />

<strong>the</strong> weighted average <strong>of</strong> <strong>the</strong> total emissions would have decreased to 0.81 g Hg/t annual<br />

chlorine capacity.<br />

WORKING DRAFT IN PROGRESS<br />

The reported figures <strong>for</strong> mercury emissions and <strong>for</strong> mercury in waste disposed <strong>of</strong> are subject to<br />

some uncertainty which is due to several factors such as [ 97, Concorde 2006 ]:<br />

<strong>the</strong> diffuse nature <strong>of</strong> <strong>the</strong> majority <strong>of</strong> mercury emissions to air;<br />

<strong>the</strong> temporal variations <strong>of</strong> <strong>the</strong>se diffuse emissions;<br />

<strong>the</strong> inhomogeneous nature <strong>of</strong> mercury-contaminated waste;<br />

<strong>the</strong> measurement uncertainty related to <strong>the</strong> monitoring technique;<br />

<strong>the</strong> uncertainty related to <strong>the</strong> measurement <strong>of</strong> <strong>the</strong> airflow in <strong>the</strong> cell room;<br />

<strong>the</strong> differences in applied monitoring techniques.<br />

TB/EIPPCB/CAK_Draft_1 December 2011 105

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