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次氯酸盐对三级聚酰胺反渗透膜的降解机制。

Deterioration Mechanism of a Tertiary Polyamide Reverse Osmosis Membrane by Hypochlorite.

机构信息

Department of Chemical Engineering, Graduate school of Engineering , Hiroshima University , Hiroshima 739-8527 , Japan.

Department of Applied Life Science , Niigata University of Pharmacy and Applied Life Science , Niigata 956-8603 , Japan.

出版信息

Environ Sci Technol. 2019 Aug 6;53(15):9109-9117. doi: 10.1021/acs.est.9b00663. Epub 2019 Jul 18.

Abstract

A tertiary polyamide membrane was synthesized using ,'-dimethyl--phenylenediamine. The durability of this membrane to chlorination by hypochlorite treatment followed by sodium hydroxide treatment was examined, and then deterioration mechanisms were proposed. The tertiary polyamide membrane demonstrated better durability to free chlorine than a conventional secondary polyamide one; however, the former was deteriorated by hypochlorite for 24 h at 2000 ppm of free chlorine below pH 7.5. The salt rejection and permeation performance of the membrane were almost unchanged, and the least chlorination of the active layer occurred during hypochlorite treatment at pH 10. These results indicated that hypochlorous acid rather than hypochlorite ion was the free chlorine species that induced membrane deterioration. The deterioration became severe as chlorination progressed, resulting in collapse of the active layer below pH 7.5. Chlorination and hydrolysis of the model tertiary amide -methylbenzanilide and Fourier transfer infrared spectroscopy of a deteriorated membrane showed that chlorination of the tertiary polyamide occurred via direct chlorination of the benzene bound to the amidic nitrogen. Silver ion probing of the deteriorated membrane revealed that amide bond scission occurred in the active layer, which might be related to the electron deficiency of the amidic nitrogen caused by chlorination of its benzene ring.

摘要

采用,'-二甲基--对苯二胺合成了一种三级聚酰胺膜。考察了该膜在次氯酸钠处理后再用氢氧化钠处理时的耐氯化性,并提出了劣化机理。与传统的二级聚酰胺相比,三级聚酰胺膜对游离氯具有更好的耐久性;然而,在 pH 值低于 7.5 时,在 2000ppm 游离氯下,该膜在 24 小时内会被次氯酸盐破坏。膜的盐截留率和渗透性能几乎没有变化,在 pH 值为 10 时的次氯酸盐处理中,活性层的氯代作用最小。这些结果表明,次氯酸而不是次氯酸根离子是导致膜劣化的游离氯物种。随着氯化作用的进行,劣化变得更加严重,导致活性层在 pH 值低于 7.5 时崩溃。对模型叔酰胺 -甲基苯甲酰苯胺的氯化和傅里叶变换红外光谱分析以及劣化膜的研究表明,三级聚酰胺的氯化是通过与酰胺氮结合的苯的直接氯化发生的。对劣化膜的银离子探测表明,酰胺键在活性层中发生了断裂,这可能与苯环氯化导致的酰胺氮的电子缺失有关。

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