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		<title>2,4,6-tri-tert-butylphenol - Bewerkingsoverzicht</title>
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			<title>Daphnisd op 19 mrt 2013 om 15:25</title>
			<link>http://www.vliz.be/v/index.php?title=2,4,6-tri-tert-butylphenol&amp;diff=57471&amp;oldid=prev</link>
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			&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;← Oudere versie&lt;/td&gt;
			&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;Versie van 19 mrt 2013 om 15:25&lt;/td&gt;
			&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Regel 1:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Regel 1:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;background: #ffa; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;__TOC__&lt;/del&gt;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;{{Tocright&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;background: #ffa; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;}}&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;{{Definition|title=2,4,6-tri-''tert''-butylphenol&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;{{Definition|title=2,4,6-tri-''tert''-butylphenol&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;/tr&gt;
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			<pubDate>Tue, 19 Mar 2013 15:25:49 GMT</pubDate>			<dc:creator>Daphnisd</dc:creator>			<comments>http://www.vliz.be/wiki/Overleg:2,4,6-tri-tert-butylphenol</comments>		</item>
		<item>
			<title>Daphnisd: /* See also */</title>
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			<description>&lt;p&gt;‎&lt;span dir=&quot;auto&quot;&gt;&lt;span class=&quot;autocomment&quot;&gt;See also&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;
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			&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;Versie van 19 mrt 2013 om 15:21&lt;/td&gt;
			&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Regel 42:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Regel 42:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&amp;lt;BR&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&amp;lt;BR&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&amp;lt;P&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&amp;lt;P&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot;&gt;&amp;#160;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;color: red; font-weight: bold; text-decoration: none;&quot;&gt;{{author&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot;&gt;&amp;#160;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;color: red; font-weight: bold; text-decoration: none;&quot;&gt;|AuthorID=19826&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot;&gt;&amp;#160;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;color: red; font-weight: bold; text-decoration: none;&quot;&gt;|AuthorFullName=Daphnis De Pooter&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot;&gt;&amp;#160;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;color: red; font-weight: bold; text-decoration: none;&quot;&gt;|AuthorName=Daphnisd}}&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;==References==&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;==References==&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</description>
			<pubDate>Tue, 19 Mar 2013 15:21:46 GMT</pubDate>			<dc:creator>Daphnisd</dc:creator>			<comments>http://www.vliz.be/wiki/Overleg:2,4,6-tri-tert-butylphenol</comments>		</item>
		<item>
			<title>Daphnisd op 19 mrt 2013 om 15:21</title>
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			<description>&lt;p&gt;&lt;/p&gt;
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			&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;← Oudere versie&lt;/td&gt;
			&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;Versie van 19 mrt 2013 om 15:21&lt;/td&gt;
			&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Regel 1:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Regel 1:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;background: #ffa; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;===&amp;#160;  ===&lt;/del&gt;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;__TOC__&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot;&gt;&amp;#160;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;{{Definition|title=2,4,6-tri-''tert''-butylphenol&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;{{Definition|title=2,4,6-tri-''tert''-butylphenol&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</description>
			<pubDate>Tue, 19 Mar 2013 15:21:27 GMT</pubDate>			<dc:creator>Daphnisd</dc:creator>			<comments>http://www.vliz.be/wiki/Overleg:2,4,6-tri-tert-butylphenol</comments>		</item>
		<item>
			<title>Daphnisd op 2 okt 2009 om 10:51</title>
			<link>http://www.vliz.be/v/index.php?title=2,4,6-tri-tert-butylphenol&amp;diff=34765&amp;oldid=prev</link>
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			<description>&lt;p&gt;&lt;/p&gt;
&lt;table class='diff diff-contentalign-left'&gt;
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			&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;Versie van 2 okt 2009 om 10:51&lt;/td&gt;
			&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Regel 17:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Regel 17:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;|}&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;|}&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;background: #ffa; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;Less than 50 tonnes of 2,4,6-tri-''tert''-butylphenol are used in the EU each year. It can be used as an intermediate in the production of antioxidants, in rubber or plastic and as an lubricating agent in the transport sector. As an intermediate it shouldn't enter the environment unless by discharges&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;. &lt;/del&gt;&amp;lt;ref name = OECD&amp;gt;[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00274_BD%202_4_6_tri_tert-butylphenol%20_2006%20version_.pdf&amp;#160; OSPAR Commission, 2006: OSPAR background document on 2,4,6-tri-''tert''-butylphenol]&amp;lt;/ref&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;Less than 50 tonnes of 2,4,6-tri-''tert''-butylphenol are used in the EU each year. It can be used as an intermediate in the production of antioxidants, in rubber or plastic and as an lubricating agent in the transport sector. As an intermediate it shouldn't enter the environment unless by discharges&amp;lt;ref name = OECD&amp;gt;[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00274_BD%202_4_6_tri_tert-butylphenol%20_2006%20version_.pdf&amp;#160; OSPAR Commission, 2006: OSPAR background document on 2,4,6-tri-''tert''-butylphenol]&amp;lt;/ref&amp;gt;&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;. &lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;It is a chemical with a low [[volatile|volatility]], making it unlikely that it enters the atmosphere, where it would be degraded rapidly. It has a low water solubility (0,521 mg/l) and a strong tendency to [[adsorption|adsorb]] to soils and sediments. Both in water and sediments, it isn't readily (bio)degraded and considered [[persistent]].&amp;#160; &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;It is a chemical with a low [[volatile|volatility]], making it unlikely that it enters the atmosphere, where it would be degraded rapidly. It has a low water solubility (0,521 mg/l) and a strong tendency to [[adsorption|adsorb]] to soils and sediments. Both in water and sediments, it isn't readily (bio)degraded and considered [[persistent]].&amp;#160; &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Regel 23:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Regel 23:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;In fresh water is has been shown to be acutely [[toxic]] for fish and for algae at concentrations above 0,061 mg/l and 0,033 mg/l respectively. &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;In fresh water is has been shown to be acutely [[toxic]] for fish and for algae at concentrations above 0,061 mg/l and 0,033 mg/l respectively. &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;background: #ffa; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;There is currently little information available on the levels of 2,4,6-tri-''tert''-butylphenol in the marine environment. It has been estimated (by modelling the emissions) that concentrations might reach 0,32 µg/l&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;.&lt;/del&gt;&amp;lt;ref name = OECD&amp;gt;[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00274_BD%202_4_6_tri_tert-butylphenol%20_2006%20version_.pdf&amp;#160; OSPAR Commission, 2006: OSPAR background document on 2,4,6-tri-''tert''-butylphenol]&amp;lt;/ref&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;There is currently little information available on the levels of 2,4,6-tri-''tert''-butylphenol in the marine environment. It has been estimated (by modelling the emissions) that concentrations might reach 0,32 µg/l&amp;lt;ref name = OECD&amp;gt;[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00274_BD%202_4_6_tri_tert-butylphenol%20_2006%20version_.pdf&amp;#160; OSPAR Commission, 2006: OSPAR background document on 2,4,6-tri-''tert''-butylphenol]&amp;lt;/ref&amp;gt;&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;.&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&amp;lt;P&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&amp;lt;P&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&amp;lt;BR&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&amp;lt;BR&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</description>
			<pubDate>Fri, 02 Oct 2009 10:51:54 GMT</pubDate>			<dc:creator>Daphnisd</dc:creator>			<comments>http://www.vliz.be/wiki/Overleg:2,4,6-tri-tert-butylphenol</comments>		</item>
		<item>
			<title>Daphnisd op 2 okt 2009 om 10:51</title>
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			<description>&lt;p&gt;&lt;/p&gt;
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			&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;← Oudere versie&lt;/td&gt;
			&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;Versie van 2 okt 2009 om 10:51&lt;/td&gt;
			&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Regel 2:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Regel 2:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;{{Definition|title=2,4,6-tri-''tert''-butylphenol&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;{{Definition|title=2,4,6-tri-''tert''-butylphenol&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;background: #ffa; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;|definition=2,4,6-tri-''tert''-butylphenol is a chemical which has been confused with an other chemical called dodecylphenol which has the same molecular formula but a different structure&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;.&lt;/del&gt;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;|definition=2,4,6-tri-''tert''-butylphenol is a chemical which has been confused with an other chemical called dodecylphenol which has the same molecular formula but a different structure&amp;lt;ref name = OECD&amp;gt;[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00274_BD%202_4_6_tri_tert-butylphenol%20_2006%20version_.pdf&amp;#160; OSPAR Commission, 2006: OSPAR background document on 2,4,6-tri-''tert''-butylphenol]&amp;lt;/ref&amp;gt;&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;. &lt;/ins&gt;}}&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;background: #ffa; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&amp;lt;ref name = OECD&amp;gt;[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00274_BD%202_4_6_tri_tert-butylphenol%20_2006%20version_.pdf&amp;#160; OSPAR Commission, 2006: OSPAR background document on 2,4,6-tri-''tert''-butylphenol]&amp;lt;/ref&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;background: #ffa; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&lt;del class=&quot;diffchange diffchange-inline&quot;&gt; &lt;/del&gt;}}&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;== Notes ==&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;== Notes ==&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Regel 19:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Regel 17:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;|}&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;|}&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;background: #ffa; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;Less than 50 tonnes of 2,4,6-tri-''tert''-butylphenol &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;is &lt;/del&gt;used in the EU each year. It can be used as an intermediate in the production of antioxidants, &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;which are used &lt;/del&gt;in rubber or plastic and as an lubricating agent in the transport sector. As an intermediate it shouldn't enter the environment unless by discharges. &amp;lt;ref name = OECD&amp;gt;[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00274_BD%202_4_6_tri_tert-butylphenol%20_2006%20version_.pdf&amp;#160; OSPAR Commission, 2006: OSPAR background document on 2,4,6-tri-''tert''-butylphenol]&amp;lt;/ref&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;Less than 50 tonnes of 2,4,6-tri-''tert''-butylphenol &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;are &lt;/ins&gt;used in the EU each year. It can be used as an intermediate in the production of antioxidants, in rubber or plastic and as an lubricating agent in the transport sector. As an intermediate it shouldn't enter the environment unless by discharges. &amp;lt;ref name = OECD&amp;gt;[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00274_BD%202_4_6_tri_tert-butylphenol%20_2006%20version_.pdf&amp;#160; OSPAR Commission, 2006: OSPAR background document on 2,4,6-tri-''tert''-butylphenol]&amp;lt;/ref&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;background: #ffa; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;It is a chemical with a low volatility, making it unlikely &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;to enter &lt;/del&gt;the atmosphere, where it would be &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;rapidly &lt;/del&gt;degraded. It has a low water solubility (0,521 mg/l) and a strong tendency to [[adsorption|adsorb]] to soils and sediments&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;, &lt;/del&gt;in &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;both mediums &lt;/del&gt;it isn't readily (bio)degraded and considered [[persistent]].&amp;#160; &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;It is a chemical with a low &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;[[volatile|&lt;/ins&gt;volatility&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;]]&lt;/ins&gt;, making it unlikely &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;that it enters &lt;/ins&gt;the atmosphere, where it would be degraded &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;rapidly&lt;/ins&gt;. It has a low water solubility (0,521 mg/l) and a strong tendency to [[adsorption|adsorb]] to soils and sediments&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;. Both &lt;/ins&gt;in &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;water and sediments, &lt;/ins&gt;it isn't readily (bio)degraded and considered [[persistent]].&amp;#160; &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;It has a high tendency to [[bioaccumulation|bioaccumulate]] and is likely to [[biomagnification|biomagnify]] through [[food chain|food chains]].&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;It has a high tendency to [[bioaccumulation|bioaccumulate]] and is likely to [[biomagnification|biomagnify]] through [[food chain|food chains]].&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;In fresh water is has been shown to be acutely [[toxic]] for fish and for algae at concentrations above 0,061 mg/l and 0,033 mg/l respectively. &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;In fresh water is has been shown to be acutely [[toxic]] for fish and for algae at concentrations above 0,061 mg/l and 0,033 mg/l respectively. &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;background: #ffa; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;There is currently &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;no &lt;/del&gt;information available the levels of 2,4,6-tri-''tert''-butylphenol in the marine environment. It &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;is however &lt;/del&gt;estimated (by modelling the emissions) that concentrations might &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;be as high as &lt;/del&gt;0,32 µg/l.&amp;lt;ref name = OECD&amp;gt;[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00274_BD%202_4_6_tri_tert-butylphenol%20_2006%20version_.pdf&amp;#160; OSPAR Commission, 2006: OSPAR background document on 2,4,6-tri-''tert''-butylphenol]&amp;lt;/ref&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;There is currently &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;little &lt;/ins&gt;information available &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;on &lt;/ins&gt;the levels of 2,4,6-tri-''tert''-butylphenol in the marine environment. It &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;has been &lt;/ins&gt;estimated (by modelling the emissions) that concentrations might &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;reach &lt;/ins&gt;0,32 µg/l.&amp;lt;ref name = OECD&amp;gt;[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00274_BD%202_4_6_tri_tert-butylphenol%20_2006%20version_.pdf&amp;#160; OSPAR Commission, 2006: OSPAR background document on 2,4,6-tri-''tert''-butylphenol]&amp;lt;/ref&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&amp;lt;P&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&amp;lt;P&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&amp;lt;BR&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&amp;lt;BR&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</description>
			<pubDate>Fri, 02 Oct 2009 10:51:30 GMT</pubDate>			<dc:creator>Daphnisd</dc:creator>			<comments>http://www.vliz.be/wiki/Overleg:2,4,6-tri-tert-butylphenol</comments>		</item>
		<item>
			<title>Daphnisd: /* Notes */</title>
			<link>http://www.vliz.be/v/index.php?title=2,4,6-tri-tert-butylphenol&amp;diff=34747&amp;oldid=prev</link>
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			<description>&lt;p&gt;‎&lt;span dir=&quot;auto&quot;&gt;&lt;span class=&quot;autocomment&quot;&gt;Notes&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;
&lt;table class='diff diff-contentalign-left'&gt;
				&lt;col class='diff-marker' /&gt;
				&lt;col class='diff-content' /&gt;
				&lt;col class='diff-marker' /&gt;
				&lt;col class='diff-content' /&gt;
			&lt;tr valign='top'&gt;
			&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;← Oudere versie&lt;/td&gt;
			&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;Versie van 1 okt 2009 om 14:22&lt;/td&gt;
			&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Regel 21:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Regel 21:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;Less than 50 tonnes of 2,4,6-tri-''tert''-butylphenol is used in the EU each year. It can be used as an intermediate in the production of antioxidants, which are used in rubber or plastic and as an lubricating agent in the transport sector. As an intermediate it shouldn't enter the environment unless by discharges. &amp;lt;ref name = OECD&amp;gt;[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00274_BD%202_4_6_tri_tert-butylphenol%20_2006%20version_.pdf&amp;#160; OSPAR Commission, 2006: OSPAR background document on 2,4,6-tri-''tert''-butylphenol]&amp;lt;/ref&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;Less than 50 tonnes of 2,4,6-tri-''tert''-butylphenol is used in the EU each year. It can be used as an intermediate in the production of antioxidants, which are used in rubber or plastic and as an lubricating agent in the transport sector. As an intermediate it shouldn't enter the environment unless by discharges. &amp;lt;ref name = OECD&amp;gt;[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00274_BD%202_4_6_tri_tert-butylphenol%20_2006%20version_.pdf&amp;#160; OSPAR Commission, 2006: OSPAR background document on 2,4,6-tri-''tert''-butylphenol]&amp;lt;/ref&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;background: #ffa; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;It is a chemical with a low volatility, making it &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;unlike &lt;/del&gt;to enter the atmosphere, where it would be rapidly degraded. &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;It is a chemical with a low volatility, making it &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;unlikely &lt;/ins&gt;to enter the atmosphere, where it would be rapidly degraded. It has a low water solubility (0,521 mg/l) and a strong tendency to [[adsorption|adsorb]] to soils and sediments, in both mediums it isn't readily (bio)degraded and considered &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;[[&lt;/ins&gt;persistent&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;]]&lt;/ins&gt;.&amp;#160; &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;background: #ffa; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;It has a low water solubility (0,521 mg/l) and a strong tendency to [[adsorption|adsorb]] to soils and sediments, in both mediums it isn't readily (bio)degraded and considered persistent.&amp;#160; &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;It has a high tendency to [[bioaccumulation|bioaccumulate]] and is likely to [[biomagnification|biomagnify]] through [[food chain|food chains]].&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;It has a high tendency to [[bioaccumulation|bioaccumulate]] and is likely to [[biomagnification|biomagnify]] through [[food chain|food chains]].&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;background: #ffa; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;In fresh water is has been shown to be acutely toxic for fish and for algae at concentrations above 0,061 mg/l and 0,033 mg/l respectively. &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;In fresh water is has been shown to be acutely &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;[[&lt;/ins&gt;toxic&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;]] &lt;/ins&gt;for fish and for algae at concentrations above 0,061 mg/l and 0,033 mg/l respectively. &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;There is currently no information available the levels of 2,4,6-tri-''tert''-butylphenol in the marine environment. It is however estimated (by modelling the emissions) that concentrations might be as high as 0,32 µg/l.&amp;lt;ref name = OECD&amp;gt;[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00274_BD%202_4_6_tri_tert-butylphenol%20_2006%20version_.pdf&amp;#160; OSPAR Commission, 2006: OSPAR background document on 2,4,6-tri-''tert''-butylphenol]&amp;lt;/ref&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;There is currently no information available the levels of 2,4,6-tri-''tert''-butylphenol in the marine environment. It is however estimated (by modelling the emissions) that concentrations might be as high as 0,32 µg/l.&amp;lt;ref name = OECD&amp;gt;[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00274_BD%202_4_6_tri_tert-butylphenol%20_2006%20version_.pdf&amp;#160; OSPAR Commission, 2006: OSPAR background document on 2,4,6-tri-''tert''-butylphenol]&amp;lt;/ref&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&amp;lt;P&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&amp;lt;P&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</description>
			<pubDate>Thu, 01 Oct 2009 14:22:25 GMT</pubDate>			<dc:creator>Daphnisd</dc:creator>			<comments>http://www.vliz.be/wiki/Overleg:2,4,6-tri-tert-butylphenol</comments>		</item>
		<item>
			<title>Daphnisd op 27 aug 2009 om 07:47</title>
			<link>http://www.vliz.be/v/index.php?title=2,4,6-tri-tert-butylphenol&amp;diff=33339&amp;oldid=prev</link>
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			<description>&lt;p&gt;&lt;/p&gt;
&lt;table class='diff diff-contentalign-left'&gt;
				&lt;col class='diff-marker' /&gt;
				&lt;col class='diff-content' /&gt;
				&lt;col class='diff-marker' /&gt;
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			&lt;tr valign='top'&gt;
			&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;← Oudere versie&lt;/td&gt;
			&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;Versie van 27 aug 2009 om 07:47&lt;/td&gt;
			&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Regel 24:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Regel 24:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;It has a low water solubility (0,521 mg/l) and a strong tendency to [[adsorption|adsorb]] to soils and sediments, in both mediums it isn't readily (bio)degraded and considered persistent.&amp;#160; &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;It has a low water solubility (0,521 mg/l) and a strong tendency to [[adsorption|adsorb]] to soils and sediments, in both mediums it isn't readily (bio)degraded and considered persistent.&amp;#160; &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;It has a high tendency to [[bioaccumulation|bioaccumulate]] and is likely to [[biomagnification|biomagnify]] through [[food chain|food chains]].&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;It has a high tendency to [[bioaccumulation|bioaccumulate]] and is likely to [[biomagnification|biomagnify]] through [[food chain|food chains]].&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot;&gt;&amp;#160;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;color: red; font-weight: bold; text-decoration: none;&quot;&gt;&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;In fresh water is has been shown to be acutely toxic for fish and for algae at concentrations above 0,061 mg/l and 0,033 mg/l respectively. &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;In fresh water is has been shown to be acutely toxic for fish and for algae at concentrations above 0,061 mg/l and 0,033 mg/l respectively. &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;There is currently no information available the levels of 2,4,6-tri-''tert''-butylphenol in the marine environment. It is however estimated (by modelling the emissions) that concentrations might be as high as 0,32 µg/l.&amp;lt;ref name = OECD&amp;gt;[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00274_BD%202_4_6_tri_tert-butylphenol%20_2006%20version_.pdf&amp;#160; OSPAR Commission, 2006: OSPAR background document on 2,4,6-tri-''tert''-butylphenol]&amp;lt;/ref&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;There is currently no information available the levels of 2,4,6-tri-''tert''-butylphenol in the marine environment. It is however estimated (by modelling the emissions) that concentrations might be as high as 0,32 µg/l.&amp;lt;ref name = OECD&amp;gt;[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00274_BD%202_4_6_tri_tert-butylphenol%20_2006%20version_.pdf&amp;#160; OSPAR Commission, 2006: OSPAR background document on 2,4,6-tri-''tert''-butylphenol]&amp;lt;/ref&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</description>
			<pubDate>Thu, 27 Aug 2009 07:47:02 GMT</pubDate>			<dc:creator>Daphnisd</dc:creator>			<comments>http://www.vliz.be/wiki/Overleg:2,4,6-tri-tert-butylphenol</comments>		</item>
		<item>
			<title>Daphnisd op 27 aug 2009 om 07:46</title>
			<link>http://www.vliz.be/v/index.php?title=2,4,6-tri-tert-butylphenol&amp;diff=33338&amp;oldid=prev</link>
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			<description>&lt;p&gt;&lt;/p&gt;
&lt;table class='diff diff-contentalign-left'&gt;
				&lt;col class='diff-marker' /&gt;
				&lt;col class='diff-content' /&gt;
				&lt;col class='diff-marker' /&gt;
				&lt;col class='diff-content' /&gt;
			&lt;tr valign='top'&gt;
			&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;← Oudere versie&lt;/td&gt;
			&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;Versie van 27 aug 2009 om 07:46&lt;/td&gt;
			&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Regel 23:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Regel 23:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;It is a chemical with a low volatility, making it unlike to enter the atmosphere, where it would be rapidly degraded. &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;It is a chemical with a low volatility, making it unlike to enter the atmosphere, where it would be rapidly degraded. &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;It has a low water solubility (0,521 mg/l) and a strong tendency to [[adsorption|adsorb]] to soils and sediments, in both mediums it isn't readily (bio)degraded and considered persistent.&amp;#160; &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;It has a low water solubility (0,521 mg/l) and a strong tendency to [[adsorption|adsorb]] to soils and sediments, in both mediums it isn't readily (bio)degraded and considered persistent.&amp;#160; &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;background: #ffa; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;It has a high tendency to [[bioaccumulation|bioaccumulate]] and is likely to [[biomagnification|biomagnify]] through [[food chains]].&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;It has a high tendency to [[bioaccumulation|bioaccumulate]] and is likely to [[biomagnification|biomagnify]] through [[&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;food chain|&lt;/ins&gt;food chains]].&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;In fresh water is has been shown to be acutely toxic for fish and for algae at concentrations above 0,061 mg/l and 0,033 mg/l respectively. &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;In fresh water is has been shown to be acutely toxic for fish and for algae at concentrations above 0,061 mg/l and 0,033 mg/l respectively. &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;There is currently no information available the levels of 2,4,6-tri-''tert''-butylphenol in the marine environment. It is however estimated (by modelling the emissions) that concentrations might be as high as 0,32 µg/l.&amp;lt;ref name = OECD&amp;gt;[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00274_BD%202_4_6_tri_tert-butylphenol%20_2006%20version_.pdf&amp;#160; OSPAR Commission, 2006: OSPAR background document on 2,4,6-tri-''tert''-butylphenol]&amp;lt;/ref&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;There is currently no information available the levels of 2,4,6-tri-''tert''-butylphenol in the marine environment. It is however estimated (by modelling the emissions) that concentrations might be as high as 0,32 µg/l.&amp;lt;ref name = OECD&amp;gt;[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00274_BD%202_4_6_tri_tert-butylphenol%20_2006%20version_.pdf&amp;#160; OSPAR Commission, 2006: OSPAR background document on 2,4,6-tri-''tert''-butylphenol]&amp;lt;/ref&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</description>
			<pubDate>Thu, 27 Aug 2009 07:46:43 GMT</pubDate>			<dc:creator>Daphnisd</dc:creator>			<comments>http://www.vliz.be/wiki/Overleg:2,4,6-tri-tert-butylphenol</comments>		</item>
		<item>
			<title>Daphnisd op 27 aug 2009 om 07:46</title>
			<link>http://www.vliz.be/v/index.php?title=2,4,6-tri-tert-butylphenol&amp;diff=33337&amp;oldid=prev</link>
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			<description>&lt;p&gt;&lt;/p&gt;
&lt;table class='diff diff-contentalign-left'&gt;
				&lt;col class='diff-marker' /&gt;
				&lt;col class='diff-content' /&gt;
				&lt;col class='diff-marker' /&gt;
				&lt;col class='diff-content' /&gt;
			&lt;tr valign='top'&gt;
			&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;← Oudere versie&lt;/td&gt;
			&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;Versie van 27 aug 2009 om 07:46&lt;/td&gt;
			&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Regel 2:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Regel 2:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;{{Definition|title=2,4,6-tri-''tert''-butylphenol&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;{{Definition|title=2,4,6-tri-''tert''-butylphenol&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;background: #ffa; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;|definition=2,4,6-tri-''tert''-butylphenol has been confused with an other chemical called dodecylphenol which has the same molecular formula but a different structure.&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;|definition=2,4,6-tri-''tert''-butylphenol &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;is a chemical which &lt;/ins&gt;has been confused with an other chemical called dodecylphenol which has the same molecular formula but a different structure.&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&amp;lt;ref name = OECD&amp;gt;[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00274_BD%202_4_6_tri_tert-butylphenol%20_2006%20version_.pdf&amp;#160; OSPAR Commission, 2006: OSPAR background document on 2,4,6-tri-''tert''-butylphenol]&amp;lt;/ref&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&amp;lt;ref name = OECD&amp;gt;[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00274_BD%202_4_6_tri_tert-butylphenol%20_2006%20version_.pdf&amp;#160; OSPAR Commission, 2006: OSPAR background document on 2,4,6-tri-''tert''-butylphenol]&amp;lt;/ref&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&amp;#160; }}&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&amp;#160; }}&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Regel 19:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Regel 19:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;|}&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;|}&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;background: #ffa; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;Less than 50 tonnes of 2,4,6-tri-''tert''-butylphenol is used in the EU each year. It can be used as an intermediate in the production of antioxidants which are used in rubber or plastic and as an lubricating agent in the transport sector. As an intermediate it shouldn't enter the environment unless by &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;discharged&lt;/del&gt;. &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;Less than 50 tonnes of 2,4,6-tri-''tert''-butylphenol is used in the EU each year. It can be used as an intermediate in the production of antioxidants&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;, &lt;/ins&gt;which are used in rubber or plastic and as an lubricating agent in the transport sector. As an intermediate it shouldn't enter the environment unless by &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;discharges&lt;/ins&gt;. &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;&amp;lt;ref name = OECD&amp;gt;[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00274_BD%202_4_6_tri_tert-butylphenol%20_2006%20version_.pdf&amp;#160; OSPAR Commission, 2006: OSPAR background document on 2,4,6-tri-''tert''-butylphenol]&amp;lt;/ref&amp;gt;&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;It is a chemical with a low volatility, making it unlike to enter the atmosphere, where it would be rapidly degraded. &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;It is a chemical with a low volatility, making it unlike to enter the atmosphere, where it would be rapidly degraded. &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;background: #ffa; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;It has a low water solubility (0,521 mg/l) and a strong tendency to adsorb to soils and sediments, in both mediums it isn't readily (bio)degraded and considered persistent.&amp;#160; &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;It has a low water solubility (0,521 mg/l) and a strong tendency to &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;[[adsorption|&lt;/ins&gt;adsorb&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;]] &lt;/ins&gt;to soils and sediments, in both mediums it isn't readily (bio)degraded and considered persistent.&amp;#160; &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;background: #ffa; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;It has a high tendency to bioaccumulate and is likely to [[biomagnification|biomagnify]]&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;It has a high tendency to &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;[[bioaccumulation|&lt;/ins&gt;bioaccumulate&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;]] &lt;/ins&gt;and is likely to [[biomagnification|biomagnify]] &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;through [[food chains]].&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;background: #ffa; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;In fresh water is has been shown to be toxic for fish and for algae at concentrations above 0,061 mg/l and 0,033 mg/l respectively. &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;In fresh water is has been shown to be &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;acutely &lt;/ins&gt;toxic for fish and for algae at concentrations above 0,061 mg/l and 0,033 mg/l respectively. &amp;#160;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;background: #ffa; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;There is currently no information available the levels of 2,4,6-tri-''tert''-butylphenol in the marine environment. It is however estimated (&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;based on modeling &lt;/del&gt;the emissions) that concentrations might be as high as 0,32 µg/l.&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;There is currently no information available the levels of 2,4,6-tri-''tert''-butylphenol in the marine environment. It is however estimated (&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;by modelling &lt;/ins&gt;the emissions) that concentrations might be as high as 0,32 µg/l.&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;&amp;lt;ref name = OECD&amp;gt;[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00274_BD%202_4_6_tri_tert-butylphenol%20_2006%20version_.pdf&amp;#160; OSPAR Commission, 2006: OSPAR background document on 2,4,6-tri-''tert''-butylphenol]&amp;lt;/ref&amp;gt;&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&amp;lt;P&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&amp;lt;P&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&amp;lt;BR&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&amp;lt;BR&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</description>
			<pubDate>Thu, 27 Aug 2009 07:46:13 GMT</pubDate>			<dc:creator>Daphnisd</dc:creator>			<comments>http://www.vliz.be/wiki/Overleg:2,4,6-tri-tert-butylphenol</comments>		</item>
		<item>
			<title>Daphnisd op 27 aug 2009 om 07:41</title>
			<link>http://www.vliz.be/v/index.php?title=2,4,6-tri-tert-butylphenol&amp;diff=33336&amp;oldid=prev</link>
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			<description>&lt;p&gt;&lt;/p&gt;
&lt;table class='diff diff-contentalign-left'&gt;
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				&lt;col class='diff-content' /&gt;
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			&lt;tr valign='top'&gt;
			&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;← Oudere versie&lt;/td&gt;
			&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;Versie van 27 aug 2009 om 07:41&lt;/td&gt;
			&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Regel 2:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Regel 2:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;{{Definition|title=2,4,6-tri-''tert''-butylphenol&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;{{Definition|title=2,4,6-tri-''tert''-butylphenol&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;−&lt;/td&gt;&lt;td style=&quot;background: #ffa; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;|definition=2,4,6-tri-''tert''-butylphenol &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;is a toxic, persistent and [[bioaccumulation|bioaccumulative]] chemical. It &lt;/del&gt;has been confused with an other chemical called dodecylphenol which &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;ahs &lt;/del&gt;the same molecular formula but a different structure.&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;|definition=2,4,6-tri-''tert''-butylphenol has been confused with an other chemical called dodecylphenol which &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;has &lt;/ins&gt;the same molecular formula but a different structure.&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&amp;lt;ref name = OECD&amp;gt;[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00274_BD%202_4_6_tri_tert-butylphenol%20_2006%20version_.pdf&amp;#160; OSPAR Commission, 2006: OSPAR background document on 2,4,6-tri-''tert''-butylphenol]&amp;lt;/ref&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&amp;lt;ref name = OECD&amp;gt;[http://www.ospar.org/documents%5Cdbase%5Cpublications%5Cp00274_BD%202_4_6_tri_tert-butylphenol%20_2006%20version_.pdf&amp;#160; OSPAR Commission, 2006: OSPAR background document on 2,4,6-tri-''tert''-butylphenol]&amp;lt;/ref&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&amp;#160; }}&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;&amp;#160;&lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&amp;#160; }}&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</description>
			<pubDate>Thu, 27 Aug 2009 07:41:29 GMT</pubDate>			<dc:creator>Daphnisd</dc:creator>			<comments>http://www.vliz.be/wiki/Overleg:2,4,6-tri-tert-butylphenol</comments>		</item>
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