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1978 1
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Page 1
Why Does 2,3,5,6-Tetrachlorophenol Generate the Strongest Intrinsic Chemiluminescence among All Nineteen Chlorophenolic Persistent Organic Pollutants during Environmentally-friendly Advanced Oxidation Process?
Gao HY, Mao L, Shao B, Huang CH, Zhu BZ. Gao HY, et al. Sci Rep. 2016 Oct 17;6:33159. doi: 10.1038/srep33159. Sci Rep. 2016. PMID: 27748358 Free PMC article.
Interestingly and unexpectedly, the strongest CL was produced not by the most-highly chlorinated pentachlorophenol (PCP), but rather by the less chlorinated 2,3,5,6-tetrachlorophenol (2,3,5,6-TeCP), one of the three t …
Interestingly and unexpectedly, the strongest CL was produced not by the most-highly chlorinated pentachlorophenol (PCP), but rather by the …
Degradation of 2,4,5-trichlorophenol and 2,3,5,6-tetrachlorophenol by combining pulse electric discharge with bioremediation.
Chauhan S, Yankelevich E, Bystritskii VM, Wood TK. Chauhan S, et al. Appl Microbiol Biotechnol. 1999 Aug;52(2):261-6. doi: 10.1007/s002530051519. Appl Microbiol Biotechnol. 1999. PMID: 10499266
Degradation of 2,4,5-trichlorophenol (2,4,5-TCP) and 2,3,5,6-tetrachlorophenol (TeCP) was studied using a two-stage approach that utilized efficient pulse electric discharge (PED) followed by biological degradation with a consortium from acclima …
Degradation of 2,4,5-trichlorophenol (2,4,5-TCP) and 2,3,5,6-tetrachlorophenol (TeCP) was studied using a …
Metabolism of 1,2,3,4-, 1,2,3,5-, and 1,2,4,5-tetrachlorobenzene in the rat.
Chu I, Villeneuve DC, Viau A, Barnes CR, Benoit FM, Qin YH. Chu I, et al. J Toxicol Environ Health. 1984;13(4-6):777-86. doi: 10.1080/15287398409530539. J Toxicol Environ Health. 1984. PMID: 6492199
The metabolites for each of the three TCBs in decreasing order of quantities were as follows: 1,2,3,4-TCB, to 2,3,4,5- and 2,3,4,6-tetrachlorophenol and a trace of tetrachlorothiophenol and 2,3,4-trichlorophenol; 1,2,3,5-TCB, to 2,3,4,6-tetrachlorophenol, isomeric hydroxythrichlo …
The metabolites for each of the three TCBs in decreasing order of quantities were as follows: 1,2,3,4-TCB, to 2,3,4,5- and 2,3,4,6-tetrachlo …
Reductive dechlorination of chlorophenols by a pentachlorophenol- acclimated methanogenic consortium.
Nicholson DK, Woods SL, Istok JD, Peek DC. Nicholson DK, et al. Appl Environ Microbiol. 1992 Jul;58(7):2280-6. doi: 10.1128/aem.58.7.2280-2286.1992. Appl Environ Microbiol. 1992. PMID: 1637165 Free PMC article.
Pentachlorophenol was degraded to produce 2,3,4,5-tetrachlorophenol, 2,3,4,6-tetrachlorophenol, and 2,3,5,6-tetrachlorophenol. Dechlorination of 2,3,4,5-tetrachlorophenol produced 3,4,5-trichlorophenol, which was subsequently degraded to produce …
Pentachlorophenol was degraded to produce 2,3,4,5-tetrachlorophenol, 2,3,4,6-tetrachlorophenol, and 2,3,5,6-t
Metabolism of tetrachlorophenols in the rat.
Ahlborg UG, Larsson K. Ahlborg UG, et al. Arch Toxicol. 1978 Feb 21;40(1):63-74. doi: 10.1007/BF00353280. Arch Toxicol. 1978. PMID: 580377
Tetrachloro-p-hydroquinone was identified as a major metabolite of 2,3,5,6-tetrachlorophenol, constituting about 35% of the dose given. Trichloro-p-hydroquinone was identified as a minor metabolite of both 2,3,4,5- and 2,3,4,6-tetrachl
Tetrachloro-p-hydroquinone was identified as a major metabolite of 2,3,5,6-tetrachlorophenol, constitutin …
In vitro cytotoxicity of organic pollutants to bluegill sunfish (BF-2) cells.
Babich H, Borenfreund E. Babich H, et al. Environ Res. 1987 Feb;42(1):229-37. doi: 10.1016/s0013-9351(87)80024-5. Environ Res. 1987. PMID: 3803339
Based on the concentration of toxicant that reduced lysosomal uptake of neutral red by 50% (NR50), the rank order of cytotoxicity was methyl mercury greater than pentachlorophenol greater than 2,3,5,6-tetrachlorophenol greater than 2,3,5-trichlo …
Based on the concentration of toxicant that reduced lysosomal uptake of neutral red by 50% (NR50), the rank order of cytotoxicity was methyl …
Effects of pentachlorophenol and some of its known and possible metabolites on different species of bacteria.
Ruckdeschel G, Renner G, Schwarz K. Ruckdeschel G, et al. Appl Environ Microbiol. 1987 Nov;53(11):2689-92. doi: 10.1128/aem.53.11.2689-2692.1987. Appl Environ Microbiol. 1987. PMID: 3426227 Free PMC article.
In comparison with pentachlorophenol, no increase of inhibitory activity was found for any of the chlorinated anisoles tested (except for pentachloroanisole against Streptomyces spp.), 2-chlorophenol, 2,6-dichlorophenol, 2,3,6- and 2,4,6-trichlorophenol, 2,3,5
In comparison with pentachlorophenol, no increase of inhibitory activity was found for any of the chlorinated anisoles tested (except for pe …
Hydroxyl free radical reactivity toward aqueous chlorinated phenols.
Zimbron JA, Reardon KF. Zimbron JA, et al. Water Res. 2005 Mar;39(5):865-9. doi: 10.1016/j.watres.2004.11.026. Epub 2005 Jan 28. Water Res. 2005. PMID: 15743632
Second-order kinetic constants (k(OH,S)) for the hydroxyl free radical attack on a series of nine chlorophenols (2-chlorophenol, 2,4-dichlorophenol, 2,5-dichlorophenol, 2,4,5-trichlorophenol, 2,4,6-trichlorophenol, 2,3,5,6-tetrachlorophenol, …
Second-order kinetic constants (k(OH,S)) for the hydroxyl free radical attack on a series of nine chlorophenols (2-chlorophenol, 2,4-dichlor …
Regiospecific dechlorination of pentachlorophenol by dichlorophenol-adapted microorganisms in freshwater, anaerobic sediment slurries.
Bryant FO, Hale DD, Rogers JE. Bryant FO, et al. Appl Environ Microbiol. 1991 Aug;57(8):2293-301. doi: 10.1128/aem.57.8.2293-2301.1991. Appl Environ Microbiol. 1991. PMID: 1768102 Free PMC article.
Dechlorination by the mixture was regiospecific, following a para greater than ortho greater than meta order of chlorine removal. Intermediate products of degradation, 2,3,5,6-tetrachlorophenol, 2,3,5-trichlorophenol, 3,5-DC …
Dechlorination by the mixture was regiospecific, following a para greater than ortho greater than meta order of chlorine removal. Intermedia …
28 results