首页> 外文期刊>Environmental Science & Technology >Effect of Hydroxypropyl-β-cyclo-dextrin on the Degradation of Pentachlorophenol by Potassium Monopersulfate Catalyzed with Iron(Ⅲ)—Porphyrin Complex
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Effect of Hydroxypropyl-β-cyclo-dextrin on the Degradation of Pentachlorophenol by Potassium Monopersulfate Catalyzed with Iron(Ⅲ)—Porphyrin Complex

机译:铁(Ⅲ)-卟啉配合物催化羟丙基-β-环糊精对单过硫酸钾降解五氯酚的影响

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摘要

A novel biomimetic catalytic system containing a supramolecular complex between iron(Ⅲ)—tetrakis(p-sulfonatophenyl)porphyrin [Fe(Ⅲ)-TPPS] and hydroxypropyl-β-cyclodextrin (HP-β-CD) was examined for the potassium monopersulfate catalyzed oxidation of pentachlorophenol (PCP). In the absence of HP-β-CD, the percentage of PCP disappearance and the numbers of chlorine atoms released from PCP increased to 50% and 1.5 for a 1-day reaction period, respectively. However, in the presence of HP-β-CD, the PCP completely disappeared and the number of chlorine atoms from PCP was increased to 3.1. o-Tetrachloroquinone, 2- and 4-hydroxyl-nonachlorodiphenyl ethers, and octachlorodibenzo-p-dioxin were detected among the oxidation products. In the absence of HP-β-CD,the percentage of PCP conversion to oxidation products increased and then reached plateau. In the presence of HP-β-CD, the amount of oxidation products produced initially increased for the first 10 min and thereafter decreased gradually. These results suggest that the addition of HP-β-CD results in the further degradation of oxidation products. In addition, the mineralization of PCP to CO_2 was investigated using ~(14)C_6-labeled PCP. After a 1-day reaction period, 24% of the ~(14)C_6-labeled PCP was converted to ~(14)CO_2 in the presence of HP-β-CD, although significant ~(14)CO_2 generation was not observed in its absence. The effect of HP-β-CD on the facilitation of PCP degradation can be attributed to the fact that the self-oxidation of Fe(Ⅲ)—TPPS is prevented by the formstion of a stable supramolecular complex between HP-β-CD and Fe(Ⅲ)-TPPS.
机译:研究了一种新型的仿生催化体系,该体系包含铁(Ⅲ)-四(对-磺基苯基)卟啉[Fe(Ⅲ)-TPPS]和羟丙基-β-环糊精(HP-β-CD)之间的超分子络合物催化的单过硫酸钾催化五氯苯酚(PCP)的氧化。在没有HP-β-CD的情况下,在1天的反应期间,PCP消失的百分比和从PCP释放的氯原子数分别增加到50%和1.5。但是,在存在HP-β-CD的情况下,PCP完全消失,来自PCP的氯原子数增加到3.1。在氧化产物中检测到邻四氯醌,2-和4-羟基九氯二苯醚和八氯二苯并-对二恶英。在没有HP-β-CD的情况下,PCP转化为氧化产物的百分比增加,然后达到平稳。在HP-β-CD的存在下,最初10分钟内产生的氧化产物数量先增加,然后逐渐减少。这些结果表明,HP-β-CD的加入导致氧化产物的进一步降解。此外,使用〜(14)C_6标记的PCP研究了PCP矿化为CO_2。在1天的反应时间后,在HP-β-CD存在下,〜(14)C_6标记的PCP中有24%转化为〜(14)CO_2,尽管在此期间未观察到明显的〜(14)CO_2生成。它的缺席。 HP-β-CD促进PCP降解的作用可归因于以下事实:HP-β-CD和Fe之间形成稳定的超分子复合物可防止Fe(Ⅲ)-TPPS的自氧化(Ⅲ)-TPPS。

著录项

  • 来源
    《Environmental Science & Technology》 |2005年第23期|p.9337-9342|共6页
  • 作者单位

    National Institute of Advanced Industrial Science and Technology (AIST), 16-1 Onogawa, Tsukuba-West, Tsukuba 305-8569, Japan;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 环境化学;
  • 关键词

  • 入库时间 2022-08-17 14:08:09

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