蚯蚓细胞色素P450酶系对土壤中芘或苯并[a]芘的响应

以赤子爱胜蚓(Eisenia fetida)为受试生物,通过人工污染草甸棕壤微宇宙试验方法,研究了暴露于不同环境浓度芘或苯并[a]芘(添加量分别为0.12、0.24、0.48、0.96 mg·kg~(-1))污染的土壤中14 d后,蚯蚓体内细胞色素P450(CYPs)酶系,如CYPs总量、CYP1A1及CYP2C9活性的变化.结果显示,芘或苯并[a]芘暴露导致蚯蚓CYPs总量、CYP1A1及CYP2C9活性的变化不同.其中,CYPs总量与CYP1A1活性对芘的响应趋势相似:试验3 d后,0.96 mg·kg~(-1)芘导致二者都显著高于对照水平;14 d后,都显著低于对照水平;CYP1A1活性对芘的响应更为敏感.CYPs总量与CYP2C9活性对苯并[a]芘的响应趋势相似:暴露初期,苯并[a]芘最高暴露剂量(0.96 mg·kg~(-1))导致二者都显著低于对照水平;试验结束后,苯并[a]芘最低暴露剂量(0.12 mg·kg~(-1))导致二者都显著高于对照水平,最高剂量暴露导致二者都显著低于对照水平,CYP2C9活性对苯并[a]芘的响应更为敏感.因此,推断CYPs亚酶对污染物的响应具有选择性且亚酶的响应敏感度高于CYPs总量.将CYPs总量与CYP1A1活性结合,或与CYP2C9活性结合分别诊断土壤芘污染或并[a]芘污染,较为准确有效.     

Process of rice straw degradation and dynamic trend of pH by the microbial community MC1

The process of the rice straw degradation in the fermentor with aeration at 290 ml/h was studied. The results of dissolved oxygen （DO） indicated that the optimum DO during cellulose degradation by microbial community MC1 ranged from 0.01 to 0.12 mg/L. The change model ofpH values was as follows： irrespective of the initial pH of the medium, pH values decreased rapidly to approximate 6.0 after being inoculated within 48 h when cellulose was strongly degraded, and then increased slowly to 8.0--9.0 until cellulose was degraded completely. During the degradation process, 15 kinds of organic compounds were checked out by GC-MS. Most of them were organic acids. Quantity analysis was carried out, and the maximum content compound was ethyl acetate which reached 13.56 g/L on the day 4. The cellulose degradation quantity and ratio analyses showed that less quantity （under batch fermentation conditions） and longer interval （under semi-fermentation conditions） of rice straw added to fermentation system were contributed to matching the change model of pH, and increasing the quantity and ratio of rice straw degradation during cellulose degrading process. The highest degradation ratio was observed under the condition office straw added one time every five days （under semi-fermentation conditions）.     

铁磁流体对煤粒瓦斯解吸性能影响实验研究*

为探究铁磁流体对煤体瓦斯解吸性能的影响,采用水浴恒温吸附解吸系统,开展0.44,0.65,1.14 MPa 3组不同平衡压力下加铁磁流体前后的瓦斯解吸对比实验,根据Langmuir方程经验公式计算瓦斯极限解吸量和初始扩散系数,分析铁磁流体对煤体瓦斯解吸影响的机理。结果表明:在3组不同平衡压力下加入铁磁流体后瓦斯极限解吸量由2.5,10,20 mL/g降低为2.22,3.33,10 mL/g,降低11.2%,66.7%,50%;初始扩散系数由0.997 1,1.629 9,3.888 3 μm2·s降低为0.685 5,0.997 1,2.933 5 μm2·s,降低31.25%,38.82%,24.56%。在铁磁流体的作用下,煤体瓦斯解吸性能得到大幅降低。     

时间因素对钻屑瓦斯解吸指标K1值测定的影响分析

针对时间因素对钻屑瓦斯解吸指标K1测定结果的影响,采用恒温瓦斯放散试验深入分析钻屑瓦斯解吸指标K1测定理论的准确性,总结因时间因素导致K1值测定误差所带来的现场问题。研究结果表明:K1值的测定误差与时间关系密切,测定启动时间越晚,误差越大;测定启动时间由第1 min延后至第2 min,绝对误差和相对误差最大值分别增加0.081 cm3/(g·min1/2)和2.20%;高瓦斯压力条件矿井或煤层的局部高瓦斯压力区域、构造煤发育区的钻屑瓦斯解吸指标K1值测定结果偏低,测定误差偏大。研究结果可为煤与瓦斯突出预测水平的提升提供技术支撑。     

Determination of Steroid Estrogens in Wastewater Treatment Plant of A Controceptives Producing Factory

Steroid estrogens such as estrone (E1), 17β-estradiol (E2), estriol (E3), and 17α-ethynylestradiol (EE2) have been suspected to be the main contaminants, which can affect the endocrine system of animals. Many authors have investigated these chemicals in the domestic wastewater treatment plants (WTP). However, wastewater from industries producing steroid contraceptives has not got ample attention. From the environmental point of view, the four steroids are very significant because even very low concentrations (ng/L) can cause reproductive disturbances in human, livestock and wildlife. The main purpose of the present investigation was to develop an analytical method for the determination of the four steroid estrogens present in WTP of a pharmacy factory, mainly producing contraceptive medicine in Beijing, China. Analysis was performed by solid-phase extraction (SPE) system and liquid chromatography combined with tandem mass spectrometry (LC/MS/MS). The average recoveries from effluent samples ranged from 88% to 103% and the precision of the method ranged from 9% to 4%. Based on 0.5-L wastewater samples, the limit of quantification (LOQ) was determined at 0.7 ng/L for E1, 0.8 for E2, 0.9 ng/L for E3, and 0.5 ng/L for EE2 in influent, and 1.0 ng/L for E2 and EE2, and 2.0 ng/L for E1 and E3 in effluent. In the influent samples, average concentrations of 80, 85, 73 and 155 ng/L were determined for E1, E2, E3 and EE2, respectively, showing that they were removed in this WTP to the extent of 79, 73, 85 and 67%, respectively.     

乌鲁木齐市大气中二氧化硫的灰色预测

根据灰色系统理论,联系乌鲁木齐市大气环境的实际状况,建立了精度检验为一级的灰色预测模型,经模型检验其精度完全满足要求。对乌鲁木齐大气中的SO2值进行预测分析的结果表明,乌鲁木齐市大气中SO2值呈上升的趋势,在未来几年中,乌鲁木齐市大气中SO2的预测值超过国家三级标准值(即大气中SO2的质量浓度年均值≤0.10mg/m3),这种发展趋势应引起有关部门的关注。     

催化超临界水氧化处理1,5-萘二磺酸

采用Mn2O3/γ-AL2O3和V2O5/γ-Al2O/为催化剂,在一连续流固定床反应器中进行了超临界水氧化1,5-萘二磺酸实验.实验结果表明,在380～440℃,24 MPa条件下,Mn2O3/γ-Al2O3和V2O5/y-Al2O3催化剂对1,5-萘二磺酸的氧化降解具有显著的促进作用,TOC去除率达到90%以上;催化剂的催化效果随反应温度的升高而增强,随pH值的降低而增强,随停留时间的延长先增强后趋于平缓.     

Growth factors, kinetics and biodegradation mechanism associated with Pseudomonas nitroreducens TX1 grown on octylphenol polyethoxylates

The growth properties and biodegradation mechanism of a Gram-negative bacterium, Pseudomonas nitroreducens TX1 that was able to grow on branched octylphenol polyethoxylates (OPEO(n), average n=9.5) as the sole carbon source over a wide concentration range (1-100,000 mgl(-1)) were studied. Analysis of growth factors indicated the highest specific growth rate (micro) of 0.53 h(-1) was obtained at an initial concentration of 5,000 mgl(-1) OPEO(n). An optimal C/N ratio of 12 was obtained for (NH(4))(2)SO(4) as the nitrogen source in a cultivated medium at pH 7. The kinetic analysis demonstrated that bacterial growth and OPEO(n) degradation followed the Monod equation and were based on a substrate concentration inhibition model and pseudo-first-order reaction, respectively. The substrate inhibition coefficient was over 18,000 mgl(-1) and this indicates that the strain has an ability to sustain growth at high concentrations of OPEO(n) and use it as the sole carbon source under such a stress condition. Furthermore, LC-MS analysis showed that the biodegradation mechanism of dodecyl octaethoxylate (AEO8) by P. nitroreducens TX1 was the sequential cleavage of the ethoxylate chain.     

苹果角质层的组分特征及其对甲萘酚的吸附作用

为能够准确预测有机污染物在植物角质层上的吸附行为,用化学方法(脱蜡、皂化、酸解)分离得到7种苹果角质层组分,探讨了角质组分对甲萘酚的吸附特征及其与结构组成之间的关系.结果表明.苹果角质层由44.7%蜡质、34.6%角质单体、13.6%糖类、7.5%生物高聚物(cutan)组成,脱蜡、皂化脱角质单体后角质组分的极性指数((O N)/C)增大,而酸解脱糖后(O N)/C则减小.角质层组分对甲萘酚的等温吸附曲线均呈非线性(N=0.551～0.918),而高浓度时的等温吸附曲线则呈线性,表明植物角质与有机物的相互作用除了分配作用之外,还存在其它的特殊作用.苹果角质层(ACI)对甲萘酚的吸附系数(Knc)为442,脱蜡、脱糖后角质组分的KDC.值增大,而脱角质单体后Kuc值则大大减小,表明角质单体是主要的吸附介质;蜡质、角质单体、糖类组分对角质层吸附行为的影响存在交互作用.角质组分的Koc值随其(O N)/C变化出现"峰值",意味着甲萘酚与角质组分之间的相互作用存在最佳的极性匹配.     

热解析-固相微萃取-气相色谱法测定空气样品中挥发性有机化合物

建立了热解析-固相微萃取-气相色谱法测定空气样品中挥发性有机化合物的分析方法,并对色谱分离条件、玻璃针筒保存样品的稳定性、固相微萃取萃取纤维、萃取时间、色谱进样时间等条件进行了优化,9种挥发性有机化合物的峰面积与其质量浓度在所测范围内有较好的线性关系,相对标准偏差＜8.8%,检出限为0.05～0.75 μg/100 mL,满足实际空气样品测定需要。