厌氧时聚-β-羟基丁酸酯(PHB)最大化积累的影响因子

为实现有限碳源的最大化利用,在厌氧/限氧曝气序批式生物系统的基础上,以碳源偏低的模拟城市污水为对象,分析比较厌氧阶段典型周期内不同碳源浓度,总磷浓度对聚-β-羟基丁酸酯(PHB)积累的影响,并考察了运用新的前曝气模式对PHB积累的影响。结果表明,当碳源浓度为140、280和400 mg/L时,PHB积累的最大值分别为10.53、22.75和32.61 mg/g;当总磷浓度为6、12和18 mg/L时,PHB最大积累值分别为25.75、32.54和38.27 mg/g。说明进水碳源浓度和总磷浓度与PHB的最大积累量呈正相关,且碳源浓度对PHB积累量的影响比总磷浓度的影响大。比较无前曝气时厌氧PHB最大积累量,前曝气时间为10、20和30 min的最大积累量分别增长了25.1%、57.1%和69.5%,说明增设前曝气运行方式有利于PHB的积累。     

Theoretical analysis and experimental study on critical conditions of backdraft

Backdraft is one of the most special behaviors of enclosure fires which has strong characteristics of concealment and suddenness. Once backdraft occurs in an enclosure, the fire will quickly engulf the entire enclosure and create a huge extrusive fireball out of the openings. In such circumstance, it is very difficult for people inside to evacuate and firefighters to enter to perform rescue. That’s why backdraft usually leads to serious consequences in both industrial and civil building fires. Experimental investigations on backdraft in enclosure fires caused by solid fuels have been carried out in the study, and the backdraft phenomenon has been reproduced in the small-scale enclosure fire tests. Based on the theories of heat transfer and fire dynamics, the theoretical model of conditions that backdraft occurs in enclosure fires has been established and the critical condition expressions have been deduced. Combining the results of theoretical analyses with those of experimental studies, a new backdraft criterion expressed by β, which is the ration between the combustible gas volume fraction and the lower explosive limit of the mixture, has been put forward.     

Preparation and evaluation of Zr-β-FeOOH for efficient arsenic removal

A Zr-β-FeOOH adsorbent for both As(V) and As(III) removal was prepared by a chemical co-precipitation method.Compared with β-FeOOH,the addition of Zr enhanced the adsorption capacities for As(V) and As(III),especially As(III).The maximum adsorption capacities for As(III) and As(V) were 120 and 60mg/g respectively at pH 7.0,much higher than for many reported adsorbents.The adsorption data accorded with Freundlich isotherms.At neutral pH,for As(V),adsorption equilibrium was approached after 3 hr,while for As(III),adsorption equilibrium was approached after 5 hr.Kinetic data fitted well to the pseudo second-order reaction model.As(V) elimination was favored at acidic pH,whereas the adsorption of As(III) by Zr-β-FeOOH was found to be effective over a wide pH range of 4-10.Competitive anions hindered the adsorption according to the sequence:phosphate > silicate > bicarbonate > sulfate > nitrate,while Ca2+ and Mg2+ increased the removal of As(III) and As(V) slightly.The high adsorption capability and good performance in other aspects make Zr-β-FeOOH a potentially attractive adsorbent for the removal of both As(III) and As(V) from water.     

氯消毒对产ESBLs菌β-内酰胺酶类抗性基因接合转移的抑制作用

以产超广谱β-内酰胺酶（ESBLs）的大肠杆菌T413和NK5449分别作为供体菌和受体菌进行接合试验,研究氯消毒处理供体菌对β-内酰胺酶类抗性基因接合转移的抑制作用.结果表明,供体菌质粒上的bla_CTX-M和bla_TEM基因可接合转移至受体菌,接合转移频率为6.57×10^-2.当氯消毒接触时间为30min,有效氯浓度在0.25~1.5mg/L时,接合转移频率未出现数量级的降低,而有效氯浓度为2mg/L时,接合转移频率则骤降至2.02×10^-5.在CT值为60（mg·min）/L的各种组合中,4mg/L×15min对接合转移的抑制效果最佳.氯消毒后的供体菌数量与接合转移频率呈正相关.经高剂量氯消毒后的供体菌具有较高的再生长率,但接合转移频率却很低.高剂量氯消毒会损伤供体菌菌体结构和功能,使胞外分泌物减少,阻碍质粒传递.     

催化动力学光度法测定工业废水中的Cr（Ⅵ）

采用β-环糊精作为H₂O₂氧化茜素红褪色反应的增敏剂,建立了催化动力学光度法测定工业废水中Cr（Ⅵ）的新方法。该方法最佳反应条件为：反应体系总体积25 mL,0.1 mol/L的H₂SO₄溶液加入量2.0 mL,1.0×10^-3 mol/L茜素红溶液加入量1.5 mL,30%的H₂O₂溶液加入量4.0 mL,100 g/L的β-环糊精溶液加入量3.0 mL。在最大吸收波长554 nm处测定反应前后溶液的吸光度,Cr（Ⅵ）的质量浓度与吸光度差值（ΔA）在4.0×10^-4~5.4×10^-2 mg/L范围内符合比尔定律,线性回归方程为：ΔA=18.52ρ+ 0.018,相关系数为0.996 6,检出限为3.5×10^-4 mg/L,加标回收率为99.46%~101.3%,6次测定的相对标准偏差小于等于2.4%。该法的测定结果与GB/T 7467-1987中的二苯碳酰二肼分光光度法相近。     

Methyl-β-cyclodextrin enhanced biodegradation of polycyclic aromatic hydrocarbons and associated microbial activity in contaminated soil

The contamination of soils by polycyclic aromatic hydrocarbons (PAHs) is a widespread environmental problem and the remediation of PAHs from these areas has been a major concern.The effectiveness of ma...     

水环境中雌激素的酶联免疫快速生物筛选技术研究

采用酶联免疫(ELISA)检测技术,对来自长江口及污水处理厂的水样分析典型雌激素雌二醇(E2)的浓度,将检测结果与化学方法检测数据进行比较验证,以阐明ELISA应用于水环境雌激素快速筛选的可行性。结果表明:ELISA的检测限可低至0.5 ng/L,试验的变异系数<30%,具有较高的灵敏性和良好的重复性;ELISA检测长江口水样中E2浓度范围≤0.7 ng/L,污水处理厂水样为2.5～11.5 ng/L,与液相色谱串联质谱(LC-MS/MS)的检测数据进行比较分析,其相关系数R~2为0.9147,表明2种方法具有良好的相关性;ELISA检测所需的水样量比LC-MS/MS更少,使用96微孔板可同时对43个样品进行检测,缩短了多个样品的分析时间,具有快速简便、经济适用的特点。因此,ELISA作为1种快速、简便、灵敏的雌激素高通量筛选技术,可为环境保护部门开展水环境雌激素物质调查和水体雌激素快速诊断等工作提供技术支持。     

气相色谱/负离子化学电离质谱法测定地表水中硫丹及其代谢物

采用气相色谱/负离子化学电离质谱法测定地表水中的硫丹及其代谢物,用正己烷提取,外标法定量。α-硫丹、β-硫丹及硫丹硫酸酯在0.200μg/L～10.0μg/L范围内线性良好,方法检出限分别为0.010μg/L、0.008μg/L及0.010μg/L,空白加标平行测定的RSD为3.9%～4.8%,地表水样品加标回收率为85.5%～93.8%。