Preconcentration and determination of trace copper(II) in natural water using silica gel modified with 1-(2-pyridylazo)-2-naphthol

Trace copper (II) in water can be preconcentrated using silica gel modified with 1-(2-pyridylazo)-2-naphthol (PAN) and be determined spectrophotometri-cally. The conditions for the preconcentration were studied. The method was applied to both artificial and natural water samples and the results suggest that copper (II) of ppb level in water can be measured accurately after the preconcentration.     

False-negative amniotic fluid acetylcholinesterase in a case of meningo-encephalocele

We describe a patient with a significantly elevated serum alphafetoprotein (AFP) concentration at 17 weeks of gestation, who showed only a marginally increased amniotic fluid AFP and lacked the second rapidly migrating band of acetylcholinesterase electrophoresis. Ultrasound examination revealed an encephalocele and ventriculomegaly. Autopsy showed that the encephalocele was not covered by skin.     

锅炉烟气脱硫技术发展综述

在调查研究的基础上，论述国内外烟道气脱硫技术的发展与前景，提出开发生产适合我国国情的烟气脱硫技术势在必行。还简要介绍了最为普遍的石灰／石灰石法脱硫基本原理。     

膜分离技术用于非电解质除杂

介绍电渗析装置工艺及基本原理，提出使用离子选择性透过膜的依据及极限电流的确定方法．论述了不同方法对冷冻液与ＮａＳＣＮ分离效果影响，指出采用电渗析法分离冷冻液中的ＮａＳＣＮ，使除杂率可达９５％以上。本工艺为腈纶冷冻液除杂及防治污染提供了新途径。     

环烷酸脱油工艺的实验研究

以锦州化工二厂生产的２＃环烷酸为原料，采用减压蒸馏──初馏分皂化萃取脱油工艺，可制得中性油含量分别低于１０％和５％的一级品环烷酸．该工艺具有流程简单、物料消耗少、产品收率高等优点．通过实验，初步探讨了蒸馏真空度、氢氧化钠浓度及用量、乙醇用量、萃取剂用量等工艺条件对脱油效果及产品质量的影响。     

大运河常州段水质变化及其影响因素

根据目前已建立的基本水质数据库，对大运河常州段的水质现状和趋势作了分析。利用质量平衡，建立了污染物量和水质之间的直观关系，发展了繁忙的机动船只动输运河产生油污染的同时，会对水体中溶解氧产生有的贡献。     

Verification of carrier status for Becker muscular dystrophy from analysis of a blighted ovum

The polymerase chain reaction (PCR) was used on material from a blighted ovum to confirm indirectly the carrier status of a woman with a family history of Becker muscular dystrophy. Conventional testing including creatine kinase levels, muscle biopsy, and EMG had been inconclusive, and on the basis of one elevated creatine kinase level, the woman had been designated a possible carrier. Ultrasound examination at 10 weeks of pregnancy indicated a blighted ovum, from which DNA was subsequently extracted and subjected to PCR testing for determination of sex and genotypic status with respect to the known familial deletion of the dystrophin gene. The blighted ovum was found to have a Y chromosome and also to be deleted for at least exon 6 of the dystrophin gene, indirectly indicating that the mother most likely carried the family mutation for Becker muscular dystrophy.