Oxidative degradation of polyamide reverse osmosis membranes: Studies of molecular model compounds and selected membranes

Selected aromatic amides were used to model the chemical reactivity of aromatic polyamides found in thin‐film composite reverse osmosis (RO) membranes. Chlorination and possible amide bond cleavage of aromatic amides upon exposure to aqueous chlorine, which can lead to membrane failure, were investigated. Correlations are made of the available chlorine concentration, pH, and exposure time with chemical changes in the model compounds. From the observed reactivity trends, insights are obtained into the mechanism of RO membrane performance loss upon chlorine exposure. Two chemical pathways for degradation are shown, one at constant pH and another that is pH‐history dependent. An alternative strategy is presented for the design of chlorine‐resistant RO membranes, and an initial performance study of RO membranes incorporating this strategy is reported. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 1173–1184, 2003     

直接氯化法合成对硝基氯化苄

介绍了以对硝基甲苯和氯气为原料 ,在催化剂存在下合成对硝基氯化苄的方法 ,考察了催化剂种类、反应温度、溶剂配比等因素对反应的影响 ,优化的反应条件为 :对硝基甲苯用量 1 3 7g,对硝基甲苯 /邻二氯苯 (摩尔比 ) =1∶ 0 .6,w (偶氮二异丁腈 ) =0 .6% ,反应时间 3 h,反应温度 1 60℃ ,产物单程收率大于 65 % ;将反应混合物中未反应的原料分离后 ,以无水乙醇为溶剂结晶纯化 ,物料 /溶剂 (摩尔比 ) =1∶ 1 .5时晶体含量在 99.0 %以上 ,结晶收率达 67     

2,4-二氯氟苯的合成

论述了2，4－二氯氟苯合成的新方法。以对氯硝基苯为起站原料，经氟化反应、硝化反应及氯化反应制得2，4-二氯氟苯，总收率达59．0％。本合成路线工艺简单、操作安全、原料易得、成本低廉，适合于工业化生产。     

对氯甲苯氯化制2，4－二氯甲苯

用正交试验法研究了由对氯甲苯经催化氯化制取２，４－二氯甲苯的最佳反应条件。反应温度３３３Ｋ，催化剂《ＳｂＣｌ＿３）用量１．５％时，对氯甲苯转化率为５９．７％，２，４－二氯甲苯的收率为４５．１３％。     

五氯吡啶的合成研究

以吡啶为原料，氯气为氯化剂，通过固定床催化反应合成了五氯吡啶。为此，在分析反应机理的基础上，分别以第Ⅱ、Ⅷ和IB族的金属盐类或其混合物为活性成分制备了一系列催化剂，并在493-663K、空速200—1200hr^-1、吡啶/氯气摩尔比(R)1：6—1：12范围内，对上述各催化剂性能进行考察。结果表明，Ba、Ca、La、Rh等金属的盐类混合物对本反应有较高的活性，收率高达95％，纯度96％(GC)。同时还获得了针对该催化剂适宜的工艺参数：温度590-650K，空速600-800hr^-1，R为8．5。     

甲苯定向氯化合成对氯甲苯

采用天然沸石作为甲苯氯化催化剂再加入助催化剂,进行甲苯氯化反应研究,探讨氯化工艺及各因素的影响,结果表明,甲苯转化率达到99.7%,一氯甲苯产物中55%为对氯甲苯.     

The identification of highly chlorinated ethers and diethers in river sediment near an epichlorohydrin plant

In harbour sediment samples taken near an epichlorohydrin production plant, a series of highly chlorinated ethers and diethers were detected viz. three isomeric bis(dichloropropyl)ethers, several structurally closely related ethers with 9 carbon atoms (C₉ ethers), a number of C₁₂ ethers and diethers, and finally several C₁₅ ethers. The formation of this new class of ether compounds can be explained on the basis of the chemistry of the addition of HOCl to allylchloride. After initial addition of Cl⁻, a reactive intermediate is formed which may react with the product dichloropropanol, to give the C₆ ethers, or may polymerize with the starting compound allylchloride followed by reaction with the product, to give the C₉, C₁₂ and C₁₅ ethers.     

浅析铂钯精矿的提取技术

本文简述湿法工艺提取铂钯金属精矿的工艺技术及主要生产过程     

钛铁矿选择氯化法制取人造金红石的热力学与动力学

研究了钛铁矿选择氯化制取人造金红石反应的Fe-Ti-C-O2-Cl2系平衡图，计算了氧与某些氯化物相互作用的自由能变化，采用“通氧一步选择氯化法”，解决了选择氯化“自热”反应持续进行的技术关键，对反应参数进行了实验室，半工业和工业化生产试验研究，研究证明，选择氯化过程的动力学模型是“固体颗粒粒度保持不变的缩核反应模型”，动力学区的活性能为34．33kJ/mol；扩散区的活化能为0．80kJ/mol，研究开发的无筛板沸腾氯化炉可以长期稳定地连续运转，生产出的人造金红石品位为92．10％，经摇床和磁选，品位达到95％，床层单位炉产能达12．4t/(m2.d)，该工艺和设备已成功地应用于工业生产。     

饮用水氯化中氯仿形成的动力学模式

以黄腐酸（ＦＡ）为卤仿前驱物质，分别测定不同投氯量、ＴＯＣ水平、温度以及ｐＨ值对ＣＨＣｌ３形成速率的影响，确定出ＣＨＣｌ３形成的动力学模式。该模式可用于预测投氯后的管网水中ＣＨＣｌ３的形成量，以便采取必要措施保证饮用水符合国家规定ＣＨＣｌ３〈６０μｇ／Ｌ的标准。