上海合流污水深海排放强化一级预处理的研究

复合式厌氧污泥床反应器是一种改进的厌氧处理工艺 ,可有效去除城市生活污水中的污染物 ,并提高了污水的可生化性 ,是一种较理想的城市污水强化一级处理工艺 ,为上海合流污水深海排放的实施提供了保障。本文对该工艺的装置特点和处理效果进行了分析研究 ,并对其应用前景进行了展望。     

厌氧水解改善富马酸废水的可生化性研究

炼油厂产生的难于生物降解的富马酸废水 ,其BOD5/CODcr均值 (比值平均值 )仅为 0 .2 83。采用厌氧水解对其进行处理 ,实验研究表明 :通过厌氧水解 ,其BOD5/CODcr可提高至 0 .433 ,废水的可生化性显著提高 ,为后续好氧处理创造了有利条件。     

乙醇废水的超临界水氧化反应路径及动力学研究

研究了超临界水氧化法 (SCWO)处理乙醇废水过程的反应路径和动力学 .乙醇SCWO反应的最终产物为CO2 ,CO是此过程的中间产物 .以幂指数方程描述乙醇SCWO反应动力学 ,得到对于乙醇的反应级数为 1,对氧气的反应级数为 0 .求出活化能和指前因子分别为 3 5 1× 10 5J·mol-1和 7 74× 10 2 1s-1.方程计算值和实验值吻合较好 ,误差基本在 10 %以内     

Mechanisms of granular activated carbon anaerobic fluidized-bed process for treating phenols wastewater

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Detection of fetal HLA-DQα sequences in maternal blood: A gender-independent technique of fetal cell identification

The objective of this study was to detect fetal HLA-DQα gene sequences in maternal blood. HLA-DQα genotypes of 70 pregnant women and their partners were determined for type A1. We specifically sought couples where the father, but not the mother, had genotype A1. In 12 women, maternal blood samples were flow-sorted. Candidate fetal cells were isolated and amplified by using PCR primers specific for a paternal HLA-DQα A1 allele. Fetal HLA-DQα A1 genotype was predicted from sorted cells; amniocytes or cheek swabs were used for confirmation. Six of twelve sorted samples had amplification products indicating the presence of the HLA-DQα A1 allele; 6/12 did not. Prediction of the fetal genotype was 100 per cent correct, as determined by subsequent amplification of amniocytes or cheek swabs. We conclude that paternally inherited uniquely fetal HLA-DQα gene sequences can be identified in maternal blood. This system permits the identification of fetal cells independent of fetal gender, and has the potential for non-invasive prenatal diagnosis of paternally inherited conditions.     

绿色高强混凝土——硅灰混凝土

硅灰是冶金厂生产硅铁和工业硅过程中产生的废灰，硅灰混凝土为绿色混凝土，它不仅节约了水泥熟料，而且改善了环境，大大促进了混凝土和建筑工程的健康发展，混凝土中掺入硅灰可得到高强和超高强混凝土，用此混凝土浇制的结构物其安全度大大提高，经济效益显著，硅灰混凝土还可以有效抑制碱骨料反应，提高结构物的安全度和耐久性，延长使用寿命。     

2-Chlorophenol oxidation kinetic by photo-assisted Fenton process

Experimental data are presented to test and validate a kinetic model for the oxidation of 2-chlorophenol wastewater by photo-assisted Fenton process. The data showed that this process had produced good effects under acidic conductions. Up to 90% 2-chlorophenol was removed after 90-minute reaction time with H2O2 of 25% CODCr. in, while in UV/H2O2 system ordy 16.8% 2-chlorophenol was removed after one hour treatment. The optimal pH in this reaction occurred between pH 3.0 and pH 4.0. The reaction kinetics for photo-assisted Fenton process experimented in this research was investigated. Kinetic models were proposed for the treatment of 2-chlorophenol wastewater. The reaction was found to follow the 2nd order. The equations of reaction kinetics are as follows:-d[RH]/dt=KRH[RH][H2O2]0exp(-KH2o2t);-d[CODCr]/dt=KCODCr[CODCr][H2O2]0exp(-K′t).The prediction of the models was found to be in a good agreement with experimental results, thus confimfing the proposed reaction mechanism.     

海水、大气化学演化对动物起源和进化方向的制约

动物的起源主要依赖于氨基酸等有机小分子在海水中能否进行脱水缩合反应而生成生物高分子，后者则依赖于海水pH值升高和大气CO2浓度降低的历史演化进程。有机小分子只有在海水pH值演化到近中性，即寒或纪时彼此才能发生脱水缩合反应而合成生物高分子。只有大气CO2分压降到1000Pa以下，即泥盆纪以后，陆地上才能出现稳定的土壤层和植物，动物也才能从海洋扩展到陆地。随后大气CO2浓度继续降低导致了气温下降和植物生长率的衰减，促使动物进一步演化。     

Prenatal diagnosis for dystrophia myotonica using the polymerase chain reaction

The polymerase chain reaction has been used to detect an abundant class of short repeat DNA families of the form (dC-dA)n.(dG-dT)n, known as microsatellites. These units are found throughout the human genome and have been characterized for several loci including APOC2 on chromosome 19ql2-ql3.2. The locus APOC2 is linked to the gene for dystrophia myotonica and a microsatellite within this locus was used to derive polymorphisms in a family to predict the inheritance of the disease. Chorionic villus sampling (CVS) was performed at 151/2 weeks' gestation. Following DNA extraction from the CVS material and parental blood samples, microsatellite analysis was carried out by the polymerase chain reaction.     

Prenatal diagnosis of β-thalassaemia in Mediterranean populations by dot blot analysis with DNA amplification and allele specific oligonucleotide probes

In this study, we describe a simple strategy to detect β-thalassaemia mutations in prospective parents and to make prenatal diagnosis in pregnancies at risk in the Mediterranean population. Screening of prospective parents is carried out by dot blot analysis on enzymatically amplified DNA with a set of oligonucleotide probes complementary to the most common mutations in this population. Prenatal diagnosis is accomplished by the same procedure on enzymatically amplified amniocyte or trophoblast DNA. The main advantages of this procedure are the simplicity, sensitivity (0.05 μg of DNA), and rapidity (12–24 h). Further simplification is obtained by amplification of the DNA from crude amniotic cell lysate. The very low amount of fetal material necessary for this analysis eliminates the need to culture amniotic fluid cells and may decrease the fetal loss rate associated with trophoblast sampling. The number of specific DNA sequences obtained by the amplification procedure allowed us to use non-radioactive labelled oligonucleotide probes, which have several advantages compared to radioactive probes.