First trimester maternal serum placenta growth factor (PIGF)concentrations in pregnancies with fetal trisomy 21 or trisomy 18

Placenta growth factor (PIGF), an angiogenic factor belonging to the vascular endothelial growth factor family, pregnancy-associated plasma protein A (PAPP-A) and free β-human chorionic gonadotrophin (β-hCG) were measured in maternal serum from 45 pregnancies with trisomy 21, 45 with trisomy 18 and 493 normal controls at 10–13 completed weeks of gestation. In the normal pregnancies maternal serum PIGF levels increased exponentially with gestation. The median multiple of the median (MoM) PIGF concentration in the trisomy 21 group (1.26 MoM) was significantly higher (p<0.0001) than in the control group (1.00 MoM). In the trisomy 18 group the median PIGF was lower (0.889 MoM) but this did not quite reach significance (p=0.064). The corresponding median MoM values for PAPP-A were 1.00 MoM for the controls, 0.49 MoM for trisomy 21 and 0.16 MoM for trisomy 18. The median MoM values for free β-hCG were 1.00 MoM for the controls, 2.05 MoM for trisomy 21 and 0.38 MoM for trisomy 18. In the control group there was a small but significant correlation of PIGF with free β-hCG (r=+0.1024) and PAPP-A (r=+0.2288). In the trisomy 18 group there was a significant association between PIGF and free β-hCG (r=+0.2629) but not with PAPP-A (r=+0.0038). In the trisomy 21 group there was a small but significant association with PAPP-A (r=+0.1028) but not with free β-hCG (r=+0.0339). The separation of affected and unaffected pregnancies in maternal serum PIGF is small, and therefore it is unlikely that measurement of PIGF would improve screening for these abnormalities provided by the combination of fetal nuchal translucency and maternal serum PAPP-A and free β-hCG. Copyright © 2001 John Wiley & Sons, Ltd.     

氧化沟在炼油污水中的运行

通过对氧化沟工艺处理在炼油污水中的运行分析，提出影响氧化沟运行的几个问题，并进行分析和探讨。     

温差拉深法在制造大型杯形件中的应用

用温差拉深法制造大型杯形件毛坯,可避免毛坯拉断和起皱,最大限度地降低拉深系数、减少拉深次数、降低加工成本。     

光电化学法处理水体中腐殖酸的初步研究

结合９０年代欧美学者提出了高级化学氧化过程（Ａｄｖａｎｃｅｄｃｈｅｍｉｃａｌｏｘｉｄａｔｉｏｎｐｒｏｃｅｓｓ，ＡＯＰ）原理，提出了并建立了一套光电化学联用的新用于处理难以生物降解的腐殖酸废水，实验表明，在通电１ｈ加光条件下（Ｉ＝０．２Ａ）总有碳（ＴＯＣ）去除率达到９０％，色度去除率达到９５％。     

香料生产废水的生化处理研究

某合成洋茉莉醛香料厂的生产废水中含有香料、香料副产品、降解物以及原辅材料,具有CODcr浓度高、水质波动大以及水中污染物成分复杂等特点,属于典型的高浓度难降解有机废水,而该厂现有的废水处理工艺不仅流程长、费用高且出水难以达到GB8978—1996一级排放标准。本文采用活性污泥法及MBR工艺研究了洋茉莉醛香料废水的处理效果及其影响因素,并结合GC—MS对降解产物进行了分析。试验结果表明：采用本文方法对洋茉莉醛香料废水有较好的降解作用,可经较少的步骤处理实现达标排放。     

Removal of polycyclic aromatic hydrocarbons from different soil fractions by persulfate oxidation

Removal of polycyclic aromatic hydrocarbons (PAHs) from different soil fractions of contaminated soil was investigated by using activated persulfate oxidation remediation in our research. The results showed that the light fraction, which accounted for only 10% of the soil, contained 30% of the PAHs at a concentration of 4352?mg/kg. The heavy fraction contained more high-molecular-weight PAHs, and the total PAH concentration was 625?mg/kg. After being oxidized, the removal rate of PAHs was 39% in the light fraction and nearly 90% in the heavy fraction. Among the different fractions of the heavy fraction, humic acid contained the highest concentration of PAHs, and consequently, the highest removal efficiency of PAHs was also in humic acid. Compared with the light fraction, the heavy fraction has more aromatic compounds and those compounds were broken down during the oxidation process, which may be the removal mechanism involved in the oxidation of high-ring PAHs. Similarly, the enhancement of C = C bonds after oxidation can also explain the poor removal of high-ring PAHs in the light fraction. These results imply that different fractions of soil vary in composition and structure, leading to differences in the distribution and oxidation efficiencies of PAHs.     

中国典型城市PM2.5浓度时空演绎规律及影响因素分析

为探讨空气中ρ（PM_2.5）的空间集聚特征和气候、大气成分变量对空气中ρ（PM_2.5）的影响,利用首批纳入PM_2.5监测的74个城市的ρ（PM_2.5）数据计算Moran's I指数,并选取其中38个典型城市进行计量分析.在基于引力模型的空间权重矩阵基础上,构建面板数据SDM（空间面板杜宾模型）.结果表明:ρ（PM₁₀）、ρ（SO₂）、ρ（CO）、ρ（O₃）、RH（relative humidity,相对湿度）与城市ρ（PM_2.5）呈正相关,而T（temperature,温度）和WS（wind speed,风速）与城市ρ（PM_2.5）呈负相关;ρ（PM₁₀）、ρ（CO）、RH是位于前3位影响城市ρ（PM_2.5）的关键性因素,其总效应分别为0.720 1、0.241 7、0.133 9.地理上邻近城市ρ（PM_2.5）具有明显的外部空间溢出效应,即邻近城市ρ（PM_2.5）每增加10百分点,将导致该地区ρ（PM_2.5）增长6.12百分点.300 km左右是保证PM_2.5区域"联防联控"最佳效果的最大门槛距离,超过该门槛距离,区域"联防联控"的力度和效果会随着距离的增加而逐渐减弱;当门槛距离大于500 km时,ρ（PM_2.5）的空间自相关性不显著.气候变量中,RH和ρ（PM_2.5）呈同方向变化,而T、WS与ρ（PM_2.5）呈反方向变化.研究显示,关注单一地区或单一因素（气候或大气成分）均不能有效控制PM_2.5污染,在保持经济稳定增长的前提下,各地治理PM_2.5应从调整产业结构、优化能源结构、完善防控机制等多个维度共同推进,促使经济增长方式早日从"粗放型"向"集约型"转变.      

异质结型SnO2-TiO2纳米纤维光催化降解柴油机多环芳烃

采用同轴静电纺丝法制备了SnO_2-TiO_2纳米纤维,用X射线衍射仪(XRD)、扫描电子显微镜(SEM)、红外光谱仪(FTIR)和紫外-可见光谱能谱仪(UV-Vis),表征了SnO_2-TiO_2纳米纤维相组成和微观形貌,评价了催化剂表面化学形态和吸光特性,研究了SnO_2含量、光源条件、温度和催化稳定性对降解萘污染物的影响规律.结果表明,催化剂Sn25对萘降解效率最高.在暗光、可见光和紫外光条件下,萘降解效率分别为13.8%、37%和98%.Sn25对萘降解稳定率(标准差率)为0.36%.利用催化剂Sn25对柴油机尾气中多环芳烃(PAHs)排放污染物光催化降解应用发现,Sn25对低苯环PAHs、中苯环PAHs和高苯环PAHs的平均催化降解效率分别为80.2%、75.4%和60.2%.表明SnO_2-TiO_2纳米纤维具有较强光催化降解多环芳烃污染物能力.     

北京森林土壤富里酸亚组分的表征及荧光指标分析

为探究土壤FA（富里酸）的结构组成及其腐殖化和芳香性特征,采用SFS（同步荧光光谱）技术结合FRI（荧光区域积分）、DSFS（导数荧光光谱）及PCA（主成分分析）对土壤FA亚组分的荧光光谱特征及荧光指标间的相关性进行了分析.利用XAD-8吸附树脂结合初始pH为3、5、7、9和13的Na₄P₂O₇（焦磷酸钠）缓冲溶液逐步洗脱技术将土壤FA分别分级得5种亚组分（FA₃、FA₅、FA₇、FA₉和FA₁₃）.结果表明:①FA₃-FA₁₃的SFS体现3类荧光峰,分别代表类蛋白、类富里酸和类腐殖酸物质.FA₃和FA₅含有含量相近的类蛋白、类富里酸和类腐殖酸物质,而FA₇-FA₁₃含有的主要成分是类蛋白物质;同时,FA₇-FA₁₃的类富里酸和类腐殖酸较FA₃和FA₅更为复杂,且FA₇-FA₁₃含有更多易降解的单环芳香族化合物.②FA₃和FA₅的类酪氨酸和类色氨酸物质被识别,且FA₇-FA₁₃的类色氨酸含量明显大于类富里酸和类腐殖酸含量.③FA₃-FA₁₃光谱荧光强度指标（I₂₄₀/I₃₄₀、I₂₄₀/I₄₅₀、I₃₄₀/I₂₇₀、I₄₅₀/I₂₇₀和I₄₅₀/I₃₄₀）的对比分析表明,FA₃和FA₅的腐殖化程度和芳香性均大于FA₇-FA₁₃.④荧光指标A_FLR/A、A_HLR/A、S_270-340、S_270-450、A₂/A₁和A₃/A₁可作为指示亚组分芳香性的优化指标,且A_HLR/A、A₂/A₁和A₃/A₁可作为最佳指标反映亚组分的腐殖化程度.研究显示,土壤FA亚组分的结构表征及荧光指标分析为后续FA亚组分与环境污染物相互机理研究提供依据,为探究有机质的结构特性和环境行为提供理论支撑.      

黄河兰州段沉积物对水体中萘的吸附行为及影响

为研究典型有机污染物在黄河兰州段沉积物的吸附规律及影响,以黄河兰州段的沉积物为供试样品,选择萘（naphthalene）为代表性有机污染物,采用批量试验法研究了污染物萘在黄河沉积物上的吸附动力学、吸附热力学、初始质量浓度、pH、离子强度、粒径等影响因素以及解吸动力学.结果表明:黄河沉积物对萘的吸附动力学更符合准二级动力学模型,且吸附过程主要分为快吸附（0~4 h）和慢吸附（4~8 h）两个阶段,在8 h左右达到平衡;Freundlich模型能较好地拟合热力学吸附特征.在25~45℃的温度范围内,E（吸附平均自由能）为0.288~0.316 kJ/mol（< 8 kJ/mol）,吸附过程中,ΔGθ（吉布斯自由能）小于0,ΔSθ（熵变）与ΔHθ（焓变）均大于0,说明萘在黄河沉积物上的吸附是一个自发的混乱度增大的吸热过程,且以物理吸附为主.影响因素分析结果显示,随着沉积物粒径的增大,萘在其上的吸附量逐渐减小;增大吸附体系中的离子强度时,萘在沉积物上的吸附过程受到抑制;当萘初始浓度增大时,吸附量增加;酸性条件抑制吸附过程,碱性环境促进吸附过程;黄河沉积物对萘的解吸量远小于吸附量,存在解吸滞后现象.研究显示,萘在黄河沉积物中的吸附速率受内部扩散、表面吸附和液膜扩散的共同影响,并且吸附过程同时受到沉积物粒径和溶液的pH和离子强度的影响.