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钾碱和钠碱对超临界水中邻氯苯酚脱氯的影响。

Effects of potassium alkalis and sodium alkalis on the dechlorination of o-chlorophenol in supercritical water.

作者信息

Sun Zhirong, Takahashi Fumitake, Odaka Yu, Fukushi Kensuke, Oshima Yoshito, Yamamoto Kazuo

机构信息

School of Environmental and Energy Engineering, Beijing University of Technology, Beijing 100022, PR China.

出版信息

Chemosphere. 2007 Jan;66(1):151-7. doi: 10.1016/j.chemosphere.2006.04.038. Epub 2006 Sep 26.

Abstract

Effects of potassium alkalis and sodium alkalis on the dechlorination of o-chlorophenol (o-CP) in supercritical water (SCW) were studied in this paper under the conditions of 450 degrees C and 25 MPa. Experimental results indicated that the dechlorination of o-CP can be accelerated significantly by all alkalis investigated. The dechlorination of o-CP proceeded mainly via two pathways: hydrodechlorination and hydrolysis. Both of the two pathways can be promoted by alkalis, and the dechlorination of o-CP can be accelerated by both the cations and hydroxide ion dissociated from alkalis. The overall dechlorination of o-CP can be accelerated by cations via promoting the hydrodechlorination pathway, while, hydroxide ion via promoting the hydrolysis pathway. In addition, the hydrodechlorination can be accelerated faster by sodium alkalis than that by potassium ones, while, the hydrolysis can be promoted faster by potassium alkalis. This difference may be caused by the different charge density between potassium ion and sodium ion, and the different solubility and dissociation constant between potassium alkalis and sodium alkalis in SCW. Dechlorination of o-CP with addition of alkalis prior to supercritical water oxidation (SCWO) process not only can avoid the reactor corrosion caused by the generated hydrochloric acid in direct SCWO of o-CP, but also can reduce the formation of toxic chlorinated byproducts compared with direct SCWO process or SCWO of o-CP with addition of alkali.

摘要

本文研究了在450℃和25MPa条件下,钾碱和钠碱对超临界水(SCW)中邻氯苯酚(o-CP)脱氯的影响。实验结果表明,所研究的所有碱均可显著加速o-CP的脱氯。o-CP的脱氯主要通过两条途径进行:加氢脱氯和水解。这两条途径均可被碱促进,o-CP的脱氯可被碱离解出的阳离子和氢氧根离子加速。o-CP的整体脱氯可通过阳离子促进加氢脱氯途径来加速,而氢氧根离子则通过促进水解途径来加速。此外,钠碱对加氢脱氯的加速作用比钾碱更快,而钾碱对水解的促进作用更快。这种差异可能是由钾离子和钠离子之间不同的电荷密度,以及钾碱和钠碱在超临界水中不同的溶解度和解离常数造成的。在超临界水氧化(SCWO)过程之前添加碱对o-CP进行脱氯,不仅可以避免o-CP直接进行SCWO时生成的盐酸对反应器造成腐蚀,而且与直接SCWO过程或添加碱对o-CP进行SCWO相比,还可以减少有毒氯代副产物的形成。

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