镀液循环流量对封闭循环电沉积Ni-SiC复合镀层的影响

目的 研究封闭式镀液循环装置中不同镀液循环流量对Ni-SiC复合镀层的影响规律,优化镀液循环流量参数.方法 以Q235管状工件为待镀基体,以添加SiC颗粒的改良瓦特镀液为母液,在自主研发的封闭式镀液循环电镀装置中以0.3、0.5、0.7 m3/h的镀液循环流量于管件内壁制备Ni-SiC复合镀层,通过SEM检测、XRD测试、硬度测试和摩擦磨损性能测试等手段,对各Ni-SiC复合镀层宏微观形貌、厚度、成分、结构、硬度和耐磨性进行分析研究.结果 在0.5 m3/h流量条件下,镀层厚度为32.98μm,SiC颗粒含量为15.37％,镀层晶粒尺寸和硬度分别为10.84 nm和704HK0.245,该条件下制备的Ni-SiC复合镀层具有最佳耐磨性,摩擦系数为0.41,体积磨损率仅2.83×10–5 mm3/Nm.结论 在不同镀液循环流量参数下,采用该封闭式循环电镀装置,均可制得均匀完整的Ni-SiC复合镀层.随镀液循环流量的升高,镀层厚度和SiC颗粒体积含量均降低,镀层颜色金属光泽增强,镀层晶粒尺寸先减小、后增大,镀层硬度则先升高、后降低.     

Association of generalized dystrophic epidermolysis bullosa with positive acetylcholinesterase and markedly elevated maternal serum and amniotic fluid alpha-fetoprotein

A case of fatal generalized dystrophic epidermolysis bullosa is described in a prematurely born female whose mother had strikingly elevated mid-trimester serum and amniotic fluid alpha-fetoprotein concentrations, a positive amniotic fluid acetylcholinesterase band, and negative serial ultrasound studies. This case lends further support to an association between autosomal recessive generalized dystrophic epidermolysis bullosa and increased levels of alpha-fetoprotein, positive amniotic fluid acetylcholines'terase, and normal ultrasound findings.     

铜山口铜(钼)矿床成矿流体水-岩反应数值模拟

铜山口铜(钼)矿床位于湖北省大冶市境内,是一典型的矽卡岩-斑岩复合型矿床。通过对其流体包裹体的系统研究,确定了成矿阶段成矿流体的成分及温压条件,并结合矿床学研究,将成矿过程分解为两个平行的成矿阶段,即矽卡岩型矿化阶段和斑岩型矿化阶段。根据Johson和Reed等人建立的水 岩反应模型,对本矿床成矿流体与围岩反应并析出金属沉淀的过程进行了数值模拟计算,其结果与实际地质情况吻合较好。     

降低气流粉碎过程中噪声强度的研究

主要报导了超音速气流超细粉碎过程中噪声产生的原因、影响因素及降低噪声强度所采取的技术原理途径与措施。研究结果表明 :采用CSQ消声装置完全可以将超音速气流粉碎过程中产生的噪声 130dB(A)降低到国家规定的标准 85dB(A)之下。该装置结构简单 ,既能消除噪声 ,又便于产品卸料 ,拆卸清理方便 ,综合性能良好。     

旋进型颗粒层除尘器的研究与试验

本文阐述了一种新型二级立式族进型颗粒层除尘器，它的关键技术采用独创的床外清灰及气流输送、滤料循环系统。该除尘器适用范围广、除尘效率高、成为新一代的除尘器专利产品。     

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.     

Rapid prenatal diagnosis of aneuploidy from uncultured amniotic fluid cells using five-colour fluorescence in situ hybridization

In this paper we describe the use of five-colour fluorescence in situ hybridization for prenatal diagnosis of aneuploidy using uncultured amniotic fluid cells. The analysis is based on ratio mixing of dual-labelled probes and digital imaging for the detection and visualization of five different probes specific for the five target chromosomes, 13, 18, 21, X, and Y. A retrospective blind analysis of 30 coded uncultured amniotic fluid samples correctly detected fetal sex and five trisomy 21 cases. Multicolour fluorescence in situ hybridization used in this way allows rapid and simultaneous detection of the most frequent aneuploidies.     

Kinetic-spectrophotometric determination of free cyanide by stopped-flow reversed flow injection analysis

A stopped-flow reversed flow injection method for the determination of free cyanide is proposed. Pyridine-barbituric acid mixture is injected in the flow system as reagent to form the colour species with cyanide. The flow is stopped when the reagent zone comes in the flow cell, where absorbance-time data are collected at 580nm wavelength. The linear range of the determination is 0.1 -10μg/ml CN-. The sampling rate is 60h-1 and the relative standard deviation is 1.6% (n=16) at 5.0 μg/ml CN-1 level. With satisfactory results, the proposed method was applied to the determination of free cyanide in wastewater without sample pretreatment.     

Prenatal confirmation of trisomy 12 mosaicism by fetal skin biopsy

Trisomy 12 mosaicism diagnosed at 16 weeks' amniocentesis in a 42-year-old woman was not confirmed at 18 weeks' gestational age in amniotic fluid or fetal blood. Fetal skin biopsy performed at the same time did, however, allow the detection of trisomy 12 in 1 of 14 fibroblasts analysed. Fetal skin biopsy can be included within the diagnostic procedures to be performed when a level III mosaicism is found in the amniotic fluid.