超临界流体技术在非均相催化反应中的应用研究

利用超临界流体良好的溶解性能和扩散性能可以很好地解决非均相催化剂的失活问题。介绍了超临界流体的特性及其化学反应的基础理论,进一步探讨了超临界流体技术在非均相催化反应和酶催化反应方面的应用研究,并指出其存在的问题和发展方向。     

废钻井液复合固化处理技术及应用研究

为了达到“以废治废、变废为宝”的目的,胜利油田对废钻井液固化处理技术进行了研究。详细分析了钻井液的有害成分及固化处理的作用机理,在确定了固化物设计指标的前提下,进行了大量实验室分析、检测及试样配比研究,得到了适合不同钻井液体系的固化处理配方,并对复合固结材料进行了击实、抗干湿、抗冻融等耐久性试验。结果表明,28d后,复合固结材料的抗压强度一般为0.5～1.5 MPa,可用于铺设简易道路或修建井场用。另外,在废钻井液中添加固结材料、稳定剂及骨料,并利用废钻井液的潜在活性,使其成为具有硅酸盐凝胶结构或水泥石结构的建筑材料,可以进行砌体施工。该项技术具有显著的经济效益和社会效益。     

常用钻井液填加剂对钻井污水化学需氧量的影响

针对石油工业钻井污水化学需氧量（ＣＯＤ）严重超标的状况,从分析测定目前油田常用的８种钻井液添加剂的ＣＯＤ入手,探讨了钻井液添加剂对钻井污水的影响。实验结果表明：８种钻井液添加剂按油田现场配比复配后,对钻井污水ＣＯＤ的影响程度各不相同,其大小依次为：柴油、ＨＰＡＮ、磺化沥青、ＰＡＮ、ＰＡＭ－１、ＦＡ－３６７、ＸＹ－２７、ＣＭＣ;钻井污水中ＣＯＤ值严重超标的主要因素是钻井液添加剂;并且钻井液添加剂浓度与其对应的ＣＯＤ之间存在良好的一元线性关系。根据一元线性回归方程可较好地预测油田现场各钻井液添加剂对ＣＯＤ的影响,为解决钻井污水处理这一难题提供科学依据。     

废弃泥浆无害化处理方法研究

由于钻井废弃泥浆丢弃会对环境造成严重污染,所以对废弃泥浆的无害化处理尤为重要.针对国内现有几种主要的无害化处理方法(固化处理、废弃泥浆的二次利用)进行了系统的分析研究,指出了固化处理在环境上存在的隐患,废弃泥浆的二次利用在推广上的缺陷,并在此基础上提出了土地处理法来处理废气泥浆,且简要的分析了在土地处理法的可行性以及其处理泥浆时在技术上需要注意的问题,最后得出该方法能较好的满足废弃泥浆的无害化处理;实现环境的可持续发展的要求.     

江西红山隐爆角砾岩-斑岩型铜矿床气液包体特征及成矿物理化学条件

红山铜矿为隐爆角陈岩一斑岩型铜矿床．通过对矿床包理体地球化学和成矿实验地球化学的讨地阐明矿床成矿物理化学条件。     

Enhancement of amniocyte growth on a precoated surface

This study investigates whether cell-free amniotic fluid facilitates cell attachment to the surface of culture plates and thereby promotes rapid amniocyte growth. Isolated or pooled cell-free amniotic fluid samples at different volumes were added to culture plates. Trypsinized subcultures, grown in Eagle's minimum essential alpha medium supplemented with fetal bovine serum (4–20 per cent), were monitored by cell counts. The results demonstrated growth stimulation on culture plates precoated with amniotic fluid. The minimal time for coating the culture plates was 6h. Maximal coating was observed after an overnight incubation with 2–3 ml of the fluid per culture vessel. No synergistic effect from addition of fetal bovine serum to amniotic fluid was observed. A freshly coated surface provided the best amniocyte growth. When primary cultures are grown on a precoated surface, there is an increase in colony counts in 80 per cent of the samples tested. This method may be used to improve amniocyte growth, especially in samples with relatively small numbers of cells.     

Prenatal diagnosis of smith–lemli–opitz syndrome is possible by measurement of 7-dehydrocholesterol in amniotic fluid

Amniocentesis was performed at 17.3 weeks in a pregnancy with severe intrauterine growth retardation. Cytogenetic studies on amniocytes were normal, 46,XX, and the pregnancy was continued. The diagnosis of Smith–Lemli–Opitz syndrome was suspected in the neonatal period and confirmed by the presence of 7-dehydrocholesterol (7-DHC) in the plasma (0.4 mmol/l, normal = not detectable) associated with a low total cholesterol concentration (0.4 mmol/l, normal = 2.56 ± 0.23). Retrospective analysis of the amniotic fluid sample revealed an elevated level of 7-DHC (0.022 mmol/l; normal = undetectable). Therefore measurement of 7-DHC levels in amniotic fluid during the second trimester of pregnancy is useful for the prenatal diagnosis of Smith–Lemli–Opitz syndrome in families at risk and should be considered in cases of severe growth retardation of unknown aetiology for which amniotic fluid is available and in which a normal chromosomal pattern in amniocytes is present.     

HUMAN CHORIONIC GONADOTROPHIN AND ALPHA-FETOPROTEIN LEVELS IN MATCHED SAMPLES OF AMNIOTIC FLUID,EXTRAEMBRYONIC COELOMIC FLUID,AND MATERNAL SERUM IN THE FIRST TRIMESTER OF PREGNANCY

Separately identified samples of amniotic fluid and extraembryonic coelomic fluid obtained by high resolution transvaginal ultrasound-guided amniocentesis from 32 women between 7 and 12 weeks of pregnancy were analysed for human chorionic gonadotrophin (hCG) and alpha-fetoprotein (AFP). There was a highly significant difference between the hCG levels in amniotic fluid (median level 6.3 U/ml; range 1.6–310.0 U/ml) and those in extraembryonic coelomic fluid (median level 400.0U/ml; range 135.0–2250.0U/ml) (p<0.001; Mann-Whitney U/–test). The levels of AFP were very similar in amniotic fluid (median 26.0 kU/ml; range 10.0–116.5 kU/ml) and extraembryonic coelomic fluid (median level 24.1 kU/ml; range 12.4–94.4 kU/ml).     

Isoelectric focusing pattern of human amniotic fluid α-fetoprotein

Isoelectric focusing (IEF) of amniotic fluid α-fetoprotein (AFP) in thin-layer polyacrylamide gels containing 8 M urea followed by immunoblotting reveals at least nine bands, band I lying next to the cathode. Compared with 298 amniotic fluid samples from normal pregnancies, we found that the density of band V was increased in seven cases of fetal death. In 16 amniotic fluid samples from pregnancies with open neural tube defects (ONTO), band V disappeared or was markedly decreased. In seven cases with elevated AFP and positive acetylcholines-terase (AChE) due to contamination with fetal blood, no difference in pattern was observed compared with samples from normal pregnancies. It is suggested that IEF of AFP and subsequent immunoblotting are an apparently diagnostic test for ONTD and intrauterine fetal death (IUFD).     

Amniotic fluid microvillar enzyme activities in the early detection of fetal abnormalities

Measurement of the microvillar enzymes, γ-glutamyltranspeptidase (GGTP), aminopeptidase M (APM) and alkaline phosphatase (ALP), in amniotic fluid supernatant has been proposed as a method for the early prenatal diagnosis of cystic fibrosis. The activities of these enzymes in a series of other fetal abnormalities have now been examined. GGTP activities were below the 5th percentile in 28 out of 54 cases of trisomy 21 and 9 of 14 cases of trisomy 18, while APM values were below this cut-off in 26 of 54 cases of trisomy 21 and 8 of 14 cases of trisomy 18. Abnormal ALP isoenzyme ratios were found in 6 of 54 cases of trisomy 21 and 4 of 14 cases of trisomy 18. If prenatal cytogenetic studies are routinely carried out on amniotic fluid cells, the occasional confounding effect of abnormal microvillar enzymes associated with fetal trisomies rather than with cystic fibrosis should be avoided.