溴素的有机化学──I．2，4，6－三溴苯甲酸溴代和非溴代芳酯的合成

用ｍ－氨基苯甲酸作原料，经溴代、重氮化、还原脱氨、酰氯化和酯化反应等步骤，合成了六种新型的三溴苯甲酸的溴代和非溴代芳酯，即；双（２，４，６－三溴苯甲酸）－２＇，３＇，５＇，６＇－四溴－１＇，４＇－苯二酯，２，４，６－三溴苯甲酸－２＇，３＇，４＇，５＇，６＇－五溴苯酯，２，４，６－三溴苯甲酸－２＇，４＇，６＇－三溴苯酯，２，４，６－三溴苯甲酸－４＇－溴苯酯，２，４，６－三溴苯甲酸－４＇－甲基苯酯和２，４，６－三溴苯甲酸苯酯．通过对产物中碳、氢、溴元素的定量分析以及红外吸收光谱和氢核磁共振谱的研究，验证了合成产物的结构。     

Catalytic ozonation of phenol in water with natural brucite and magnesia

Catalytic ozonation has attracted much attention in treatment of wastewater for its mild conditions. Phenol and its ramifications are common components in a wide variety of wastewaters including those from coal conversion processes, coking plants, petroleum refineries and several chemical industries. In this paper, natural brucite and magnesia have been successfully used in catalytic ozonation of phenol. And the mechanisms of catalysis were also investigated. From Figs. 1 and 2, it can be found that both brucite and magnesia have remarkable catalysis on degradation of phenol and removal of Chemical Oxygen Demand （COD）. The pH of solutions on the process of ozonation alone, catalytic ozonation with brucites and with magnesia were 6.35-2.76, 10.18-8.52 and 10.58-10.83, respectively. It can be concluded that alkali environment plays a critical role for catalytic ozonation of phenol. We also found that the alkaline minerals reacted on the surface with oxalic acid and other low molecular-weight acids which are intermediate products in ozonation, but those intermediate products could be mineralized into carbon dioxide completely with enough ozonation time.     

GDX-502树脂富集高效液相色谱法测定地表水中酚类化合物

采用自制GDX-502固相萃取小柱萃取水中苯酚、对硝基酚、间甲酚、2，4-二氯酚、2，4，6-三氯酚、五氯酚等6种酚类化合物，以乙腈作为洗脱剂，选择280nm和290nm双波长紫外高效液相色谱进行检测。结果表明，方法检出限为0．01-0．05mg／L，IL水的平均加标回收率为82．5％-95．0％，精密度（RSD，n=7）为3．6％-9．2％。方法用于实际地表水中痕量酚类化合物的检测，操作简单，有机溶剂用量少，分析效率高；萃取小柱可多次重复使用，分析成本低。     

锰钾矿光催化降解苯酚及其影响因素研究

利用回流法合成隧道结构的锰钾矿,并研究其光化学降解苯酚的效果及影响因素。分别采用X射线衍射、原子吸收光谱、扫描电镜、透射电镜和BET氮气吸附法对锰钾矿的晶体结构(包括晶型、晶胞参数和结晶度)、化学组成、微观形貌和比表面积进行了表征。研究表明,非光照时锰钾矿对苯酚的降解效果较差,光照能显著促进锰钾矿对苯酚的降解;光照条件下,p H值减小能显著促进锰钾矿对苯酚的降解;锰钾矿用量增加至1.00 g/L时能显著促进锰钾矿降解苯酚,但继续增加矿物用量却显著降低苯酚降解率;非光照条件下,p H值减小和矿物用量增加不能显著促进锰钾矿降解苯酚。     

酚羟基从乙酰基保护到苄基保护的一锅法转换

在Lemieux方法的基础上,将应用于糖类化合物的方法首次应用到酚类化合物上,报道了乙酰基保护的酚类化合物,在苄溴、氢氧化钾作用下于四氢呋喃中回流通过一锅转化法转换得到苄基保护化合物;在有多个乙酰基同时存在条件下,通过调节氢氧化钾的用量来控制苄基取代的程度。该方法操作简便,收率较高。     

铁锰氧化物对苯酚氧化降解的实验研究

为了考察铁锰氧化物对酚类污染物的氧化降解能力,采用天然以及合成的铁锰氧化物对苯酚的氧化降解进行对比实验研究。土壤中铁锰氧化物样品分别为天然针铁矿及氧化锰,合成铁锰氧化物样品分别为合成针铁矿及软锰矿。结果表明：苯酚与铁锰氧化物发生氧化还原作用时,还可能与土壤中杂质发生吸附等作用;铁锰氧化物还原反应强度随着反应介质pH值的升高而迅速下降;可用零级反应动力学方程拟合铁氧化物还原溶解反应,针铁矿溶解反应的强度与介质的pH值呈负相关关系;天然针铁矿对酚类污染物的氧化降解能力明显高于合成针铁矿,pH值对天然针铁矿溶解反应影响较大;可用一级指数衰减方程拟合锰氧化物还原溶解反应,锰氧化物溶解反应的强度与介质的pH值呈指数衰减关系;pH值对软锰矿还原溶解反应的影响大于对土壤中氧化锰的影响,pH值越小,影响越显著;对比pH值对铁和锰还原作用的影响发现,在pH=6.5时,锰氧化物仍有较强的氧化性能。     

铁锰氧化物对苯酚氧化降解的实验研究

为了考察铁锰氧化物对酚类污染物的氧化降解能力,采用天然以及合成的铁锰氧化物对苯酚的氧化降解进行对比实验研究.土壤中铁锰氧化物样品分别为天然针铁矿及氧化锰,合成铁锰氧化物样品分别为合成针铁矿及软锰矿.结果表明:苯酚与铁锰氧化物发生氧化还原作用时,还可能与土壤中杂质发生吸附等作用;铁锰氧化物还原反应强度随着反应介质pH值的...     

Dissolved Folin Phenol Active Substances (Tannin and Lignin) in the Seawater along the West Coast of India

Information on the distribution of dissolved Folin phenol active substances (FPAS) such as tannin and lignin in the seawater along the west coast of India is provided. Notable amounts of FPAS (surface concentrations: 80 g/l to 147 g/l and bottom concentrations: 80 g/l to 116 g/l) were detected in the seawater along the coast. The distribution pattern brings about a general depth-wise decrease. A seaward decrease was observed in the southern stations whereas reverse was the case in northern stations. A significant negative correlation was observed between FPAS concentration and dissolved oxygen in sub-surface samples. The appreciable amounts of FPAS detected in the coastal waters indicate the presence of organic matter principally originating from terrestrial (upland and coastal marsh) ecosystems in the marine environment. In this context, they may be used as tracers to determine the fate of coastalborn dissolved organic matter in the ocean and to determine directly the relationship between allochthonous and autochthonous organic matter.     

Organization of amphiphiles, Part VIII: Role of polyoxyethylated alkylphenols in optimizing the beneficiation of hydrophilic mineral

The floatability of silica has been determined by adsorbing various concentrations of a series of polyoxyethylated nonyl and octyl alkyl phenols of varying oxyethylene units (10–40 units) to investigate the role of adsorbed layer. It is seen that the floatability of silica increases with increase in concentration till a maximum of  90% in premicellar region and then decrease to minimum of 40–45% in all cases in spite of the significant differences in adsorption densities. Zeta potential measurement reveals that a thin oxyethylene layer is formed at silica–water interface masking silica surface (Pramila K. Misra, P. Somasundaran, J. Surf. Deterg., Vol. 7, 2004, 373). This layer with oxyethylene units lying on silica surface and alkyl chain dangling to the bulk solution provides the same extent of hydrophobicity. The decrease in flotation recovery has been attributed to increase in the solvent hydrophobicity due to formation of premicellar aggregates and micelles.     

TiO2-蒙脱石光催化降解苯酚的实验研究

本文采用TiCl4在HCl中水解制备二氧化钛柱撑蒙脱石(TiO2-PILM)纳米材料，通过X射线衍射和BET N2比表面积分析对其进行表征，并研究其对苯酚在紫外光下的催化降解曲线，考察了苯酚的初始浓度、TiO2-PILM投放量、苯酚溶液pH值对光催化降解效果的影响。结果表明，制备的结构稳定的TiO2-PILM具有2．26nm大晶面间距和285．7m^2／g大比表面积。TiO2-PILM对苯酚有一定的光催化降解性，其过程是先吸附后降解。随苯酚初始浓度、TiO2-PILM投入量和苯酚溶液pH值的升高，TiO2-PILM对苯酚降解速率增大。在苯酚初始浓度为5mg／L、投样量为1g／L、pH为10时，TiO2-PILM对苯酚有较好的降解效果。