LINEAR ALKYLBENZENE SULFONATE (LAS) - UNEP Chemicals
LINEAR ALKYLBENZENE SULFONATE (LAS) - UNEP Chemicals
LINEAR ALKYLBENZENE SULFONATE (LAS) - UNEP Chemicals
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OECD SIDS <strong>LINEAR</strong> <strong>ALKYLBENZENE</strong> <strong>SULFONATE</strong> (<strong>LAS</strong>)<br />
Test Substance: C10-14 <strong>LAS</strong>, activity 66.62%; average alkyl chain length = C11.7<br />
Remarks: In most cases, sea water samples showed a similar evolution of<br />
bacterioplankton over time, characterized by three phases: (a) a progressive<br />
increase in bacterial density; (b) a later decrease; and (c) a fluctuating<br />
stationary phase. Bacterioplankton degraded the <strong>LAS</strong> by growing to<br />
populations with a high percentage of viable bacteria. The bacteria were<br />
readily grazed by protozoa, preventing anomalous high bacterial growth and<br />
ensuring the later channeling of <strong>LAS</strong> carbon to upper trophic levels.<br />
Reference: Vives-Rego, J., Lopez-Amoros, R., Guindulain, T., Garcia, M.T., Comas, J.,<br />
and Sanchez-Leal, J. 2000. Microbial aspects of linear alkylbenzene<br />
sulfonate degradation in coastal water. Journal of Surfactants and<br />
Detergents. 3:303-308.<br />
Reliability: 2 Valid with restrictions<br />
(v)<br />
Type: Respirometer<br />
Method: Degradation of <strong>LAS</strong> in Ohio River water collected below the discharge of a<br />
municipal wastewater treatment plant (Muddy Creek, OH) was measured in<br />
an electrolytic respirometer. Background <strong>LAS</strong> concentrations were less than<br />
0.5 mg/L. Oxygen consumption over time was determined at five <strong>LAS</strong><br />
concentrations (5, 10, 20, 40, and 80 mg/L) plus a control until plateau values<br />
were reached. The maximum initial rates of oxygen uptake were calculated<br />
based on methods described in Larson and Perry (1981).<br />
Results: <strong>LAS</strong> degradation was not affected in river water until the <strong>LAS</strong> concentration<br />
exceeded 10 mg/L. The degradation was partially affected at 20 mg/L but<br />
was not completely inhibited until 40 mg/L.<br />
Substance: <strong>LAS</strong>; average chain length C11.6.<br />
Remarks: The level at which inhibition of degradation was complete (40 mg/L) is<br />
significantly higher than the levels observed in model ecosystem studies<br />
conducted by these researchers [see 4.7 (h) and (i)].<br />
Reference: 1) Larson, R.J. and Maki, A.W. 1982. Effect of <strong>LAS</strong> on the structure and<br />
function of microbial communities in model ecosystems. Aquatic<br />
Toxicology and Hazard Assessment: Fifth Conference, ASTM STP 766,<br />
Pearson, J.G., Foster, R.B., and Bishop, W.E., Eds., American Society for<br />
Testing and Materials, pp. 120-136.<br />
2) Maki, A.W. 1981. A laboratory model ecosystem approach to<br />
environmental fate and effects studies. Unpublished Internal Report,<br />
Environmental Safety Department Procter & Gamble Company, Cincinnati,<br />
Ohio.<br />
3) Larson, R.J. and Perry, R.L. 1981. Water Research 15:697-702.<br />
Reliability: 2 Valid with restrictions<br />
(w)<br />
Type: aerobic [X]; anaerobic [ ]<br />
Substance: <strong>LAS</strong><br />
Remarks: The biodegradation of <strong>LAS</strong> has been thoroughly studied for its primary and<br />
total degradation and catabolism. It is mineralized biologically to form<br />
carbon dioxide, water and sulphate. Using UV spectroscopic analysis,<br />
Swisher (1987) and others showed the aromatic ring to be degradable up to<br />
80%. Using the more reliable tracer technique with 14 C-ring labelled <strong>LAS</strong>, it<br />
was determined that degradation of the ring is predominantly between 50 and<br />
80%. Further studies have shown that <strong>LAS</strong> degradation proceeds through<br />
oxidative conversion of the methyl groups of the alkyl chain into a carboxyl<br />
group (ω-oxidation), oxidative shortening of the alkyl chain by 2-carbon<br />
units (β-oxidation), oxidative ring splitting, then cleavage of the carbonsulfur<br />
bond. This process forms sulfophenyl carboxylates (SPCs) as<br />
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