用植物清除土壤中的重金属

介绍了生物修复技术去除土壤中的重金属及对植物的要求.植物能去除土壤中的有毒金属,将金属富集在生物体内,或将金属变成挥发性气体.     

Results of a questionnaire investigation on the management of environmental issues during conceptual design. A case study of two large made-to-order companies

This paper investigates the current treatment of environmental issues by two companies within the large made-to-order sector. Fifty questionnaires were issued to the design team of each company to assess current practice in the integration of environmental issues with design activities, awareness of environmental issues, awareness of existing environmental design tools and the preferred format for a potential clean design tool.     

脉冲等离子法烟气脱硫的放大实验

锅炉烟气进行脉冲等离子法脱硫的扩大实验，得到与模拟烟气实验相近的结果。研究表明，脉冲等离子法对锅炉烟气中的ＳＯ２去除率可达９５％以上，烟气在反应器内的停留时间（ｔｓ）、脉冲电源的放电功率（Ｐ）和添加ＮＨ３等条件，对脱硫效率９η）有较大影响。ｔｓ、Ｐ越大、η越高。处理烟气量（Ｑ）、能耗（Ｐ）与η存在函数关系：η＝１１８．０（Ｐ／Ｑ）＾０．１１１１。烟气中加入适量ＮＨ３，对脱硫效率有显著提高，以ＮＨ３     

长江,嘉陵江重庆城区段二维水质对流扩散数学模型

对二水质对流扩散数学模型的有限差分解作了较详细的叙述，同时对距离步长，时间步长计算，网络内水深，流速，横向扩散系数的求取也作了简要介绍。     

Use of the chemical cleavage of mismatch method for prenatal deficiency diagnosis of alpha-1-antitrypsin

The most common mutation in alpha-1-antitrypsin deficiency, conversion of a G to an A at base 9989 (PI-Z), was detected with the chemical cleavage of mismatch method, demonstrating the power of the method for prenatal diagnosis. Exon V of the gene was amplified using the polymerase chain reaction and heteroduplexes were formed to test for the presence of the mutation. The predicted C mismatch was readily detectable with hydroxylamine, and by making the probe from the chorionic villus sample it was possible to determine that the fetus was heterozygous, not homozygous, for the mutation.     

Prenatal diagnosis of a partial 8p

The index patient is a female fetus in which prenatal diagnosis of 8p trisomy was established after amniocentesis at 16 weeks of gestation. This fetus was the unbalanced product of a maternal translocation of 5q/8p (karyotype: 46,XX,t(5;8)(q35;pl 1). Internal malformations include an anomalous lobature of the right lung, a little and high atrio-ventricular communication, and an anomaly in the number and shape of the aortic semilunar valves. The possible relationship between the phenotype and the chromosomal abnormality is briefly discussed.