甲基橙褪色法测定生活饮用水中余氯的探讨

在酸性介质中,余氯使甲基橙褪色,最大吸收波长510 nm,摩尔吸光系数A510=5.41×10-3 l/mol·cm,余氯质量浓度在(0.05～1.00) mg/l范围内遵守朗伯--比耳定律.对甲基橙溶液的加入量、样品溶液褪色后其吸光值的稳定性等方面作了条件试验,同时与邻联甲苯胺(OT)比色法和N,N-二乙基对苯二胺(DPD)分光光度法进行比对测定,结果表明三种方法测定结果基本一致.     

Effects of acid,acid-ZVI/PMS,Fe(Ⅱ)/PMS and ZVI/PMS conditioning on the wastewater activated sludge(WAS)dewaterability and extracellular polymeric substances(EPS)

The effects of four conditioning approaches:Acid,Acid-zero-valent iron(ZVI)/peroxydisulfate(PMS),Fe(Ⅱ)/PMS and ZVI/PMS,on wastewater activated sludge(WAS) dewatering and organics distribution in supernatant and extracellular polymeric substances(EPS) layers were investigated.The highest reduction in bound water and the most WAS destruction was achieved by Acid-ZVI/PMS,and the optimum conditions were pH 3,ZVI dosage 0.15 g/g dry solid(DS),oxone dosage 0.07 g/g DS and reaction time 10.6 min with the reductions in capillary suction time(CST) and water content(Wc) as 19.67% and 8.49%,respectively.Four conditioning approaches could result in TOC increase in EPS layers and supernatant,and protein(PN) content in tightly bound EPS(TB-EPS).After conditioning,organics in EPS layers could migrate to supernatant.Polysaccharide(PS) was easier to migrate to supernatant than PN.In addition,Acid,Acid-ZVI/PMS or Fe(Ⅱ)/PMS conditioning promoted the release of some polysaccharides containing ring vibrations v P=O,v C-O-C,v C-O-P functional groups from TB-EPS.ESR spectra proved that both radicals of SO_4~-· and·OH contributed to dewatering and organics transformation and migration.CST value of WAS positively correlated with the ratios of PN/PS in LB-EPS and total EPS,while it negatively correlated with TOC,PN content and PS content in TB-EPS,as well as PS content in supernatant and LB-EPS.BWC negatively correlated to zeta potential and TOC value,PN content,and HA content in supernatant.     

关于建设(开发)项目环境影响评价报告书编制两个版本的思考

为充分发挥环境影响评价报告书的作用，提出应在环境影响报告书技术版的基础上编制一个面向领导决策者和公众的参考版。并就参考版的主要内容及编制应注意的问题进行了概述。     

焦化废水的危害度评价

炼焦废水以产生量大,毒性强而广泛引起中外读者的关注.本文通过具体实例对焦化废水的监测分析,明确了废水中可检出的有机污染物可达139种,其中有氰化物、挥发酚、苯并(a)芘等6项超标.为焦化厂环境影响评价及水污染提供依据.     

碳酸锶废水对生态环境的影响调查及治理方案

碳酸锶因电子工业飞速发展而身价百倍，但其生产废水的直接排放则造成了严重的环境污染，本文通过对水体、农业、渔业、人体健康和水生生物等多种因素调查，掌握了碳酸锶废水污染成因，同时提出了资源再利用方案。     

显像管玻壳铅尘污染特性的研究

以石家庄市显像管玻壳厂排放的铅尘为研究对象，通过在该玻壳厂周围土壤布点采样，较系统地研究了铅尘在大气和周围土壤中的迁移和转化规律，研究表明，用高斯模式能成功地预测铅尘在大气中的迁移扩散规律，玻壳厂周围土壤表层铅含量较大值出现在当地年主导风向（SSE，N）下风向，铅在土壤中的分布主要集中在0－20cm的耕作层，在20－40cm深度范围内，铅含量呈下降趋势，最大降幅达50％。     

高效菌活性污泥法处理分散染料废水实验研究

针对复合微生物的筛选和分离进行了研究 ,分离出处理分散染料废水起高效降解作用的 2株菌种。结果表明 ,2株高效菌对分散染料废水降解能力很强 ,与普通菌结果对比CODCr去除率提高 17% ,并且高效菌对废水浓度的耐受性也明显提高     

农药杀虫单的稻田流失规律研究

通过测坑、人工降雨等手段，对水溶性农药杀虫单的稻田消解动态、渗漏流失和径流流失等进行了研究。结果表明，(1)无水稻时，杀虫单在稻田水中消解的半衰期为0．76d；分蘖初期，杀虫单在稻田水中降解的半衰期为1．02d；平均为0．89d。(2)杀虫单的渗漏流失量在用药后8d内可达总用药量的7％—10％，平均为8．48％。(3)极端情况下，用药当天如果遇暴雨(50mm雨量)，杀虫单的径流流失量将达到用药量的30％左右。杀虫单的渗漏损失不可避免，故其流失控制应从径流损失着手，尽量避免在可能有暴雨的当天或雨前1—2d用药。     

有机锡化合物测定方法研究进展

总结了有机锡化合物常用的测定方法，包括气相色谱－火焰光度法，气相色谱与原子吸收联用，气相色谱－微波等离子体发射光谱法，气相色谱－质谱法以及液相色谱与名种检测方法联用等。对样品前处理、衍生化方法、色谱分离及测定等也进行了讨论     

A juvenile coelurosaurian theropod from China indicates arboreal habits

Here we report an unequivocal arboreal coelurosaur, Epidendrosaurus ningchengensis gen. et sp. nov. This juvenile coelurosaur's third manual digit is extremely elongated, distinctively different from that of other known dinosaurs and birds. It represents certainly a type of adaptation previously unreported from the Mesozoic although the exact function of the third manual digit is unclear. The relatively long forelimb, penultimate phalanx of manual digit II, and pedal penultimate phalanges, are interpreted as evidence for the arboreal habit of Epidendrosaurus. Because Epidendrosaurus is more similar to advanced birds in some arboreal features than to Archaeopteryx, we suggest that the initial appearance of tree-adaptation in theropods was probably not directly related to flight but to other functions, such as seeking food or escaping from predators. Electronic Supplementary Material is available if you access this article at http://dx.doi.org/10.1007/s00114-002-0353-8. On that page (frame on the left side), a link takes you directly to the supplementary material.