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Sorbent-modified biodegradation studies of the biocidal cationic surfactant cetylpyridinium chloride
被引:9
|作者:
Timmer, Niels
[1
]
Gore, David
[2
]
Sanders, David
[2
]
Gouin, Todd
[2
]
Droge, Steven T. J.
[1
,3
]
机构:
[1] Univ Utrecht, Inst Risk Assessment Sci, NL-3508 TD Utrecht, Netherlands
[2] Unilever, Safety & Environm Assurance Ctr, Colworth Sci Pk, Sharnbrook MK44 1LQ, Beds, England
[3] Univ Amsterdam, Inst Biodivers & Ecosyst Dynam, Dept Freshwater & Marine Ecol, POB 94248, NL-1090 GE Amsterdam, Netherlands
关键词:
Cationic surfactant;
Environmental risk assessment;
Toxicity mitigation;
Ready biodegradability testing;
Cetylpyridinium chloride;
Bioaccessibility;
POLYCYCLIC AROMATIC-HYDROCARBONS;
AMMONIUM-COMPOUNDS;
ORGANIC CATIONS;
GEMINI SURFACTANTS;
SORPTION;
DEGRADATION;
TOXICITY;
CLAY;
DIFFUSION;
BIOAVAILABILITY;
D O I:
10.1016/j.ecoenv.2019.109417
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
Biodegradability studies for the cationic surfactant cetylpyridinium chloride (CPC) are hampered by inhibitory effects on inoculum at prescribed test concentrations (10-20 mg organic carbon/L). In this study, we used C-14 labeled CPC in the 28 d Headspace Test (OECD 310) and demonstrated that CPC was readily biodegradable (10- > 60% mineralization within a 10 day window) at test concentrations 0.006-0.3 mg/L with CPC as single substrate. Biodegradation efficiency was comparable over this concentration range. CPC inhibited degradation at 1 mg/L and completely suppressed inoculum activity at 3 mg/L. In an extensive sorbent modified biodegradation study we evaluated the balance between CPC bioaccessibility and toxicity. A non-inhibitory concentration of 0.1 mg/L CPC was readily biodegradable with 83% sorbed to SiO2, while biodegradation was slower when 96% was sorbed. SiO2 mitigated inhibitory effects of 1 mg/L CPC, reaching > 60% biodegradation within 28 d; inhibitory effects were also mitigated by addition of commercial clay powder (illite) but this was primarily reflected by a reduced lag phase. At 10 mg/L CPC SiO2 was still able to mitigate inhibitory effects, but bioaccessibility seemed limited as only 20% biodegradation was reached. Elite limited bioaccessibility more strongly and was not able to sustain biodegradation at 10 mg/L CPC.
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