Simultaneous quantification of fifty-one odor-causing compounds in drinking water using gas chromatography-triple quadrupole tandem mass spectrometry

A wide range of compounds with various structural features can cause taste and odor(TO)problems in drinking water. It would be desirable to determine all of these compounds using a simple analytical method. In this paper, a sensitive method combining liquid–liquid extraction(LLE) with gas chromatography-triple quadrupole tandem mass spectrometry(GC–MS/MS)was established to simultaneously analyze 51 odor-causing compounds in drinking water,including organic sulfides, aldehydes, benzenes, phenols, ethers, esters, ketones, nitrogenous heterocyclic compounds, 2-methylisoborneol and geosmin. Three deuterated analogs of target analytes, dimethyl disulfide-d6, benzaldehyde-d6 and o-cresol-3,4,5,6-d4,were used to correct the variations in recovery, and five isotope-labeled internal standards(4-chlorotoluene-d4, 1, 4-dichlorobenzene-d4, naphthalene-d8, acenaphthene-d10, phenanthrene-d10 respectively) were used prior to analysis to correct the variations arising from instrument fluctuations and injection errors. The calibration curves of the target compounds showed good linearity(R2 0.99, level = 7),and method detection limits(MDLs) below 1/10 of the odor threshold concentrations were achieved for most of the odorants(0.10–20.55 ng/L). The average recoveries of most of the analytes in tap water samples were between 70% and 120%, and the method was reproducible(RSD 20%, n = 7). Additionally, concentrations of odor-causing compounds in water samples collected from three drinking water treatment plants(DWTPs) were analyzed by this method.According to the results, dimethyl trisulfide, dimethyl disulfide and indole were considered to be the key odorants responsible for the swampy/septic odor. 2-Methylisoborneol and geosmin were detected as the main odor-causing compounds for musty/earthy odor in DWTP B.     

One-step synthesis of Cu(II) metal–organic gel as recyclable material for rapid, efficient and size selective cationic dyes adsorption

Efficient removal of non-biodegradable and hazardous dyes from wastewater remains a hot research topic. Herein, a rationally designed a Cu(Ⅱ)-based metal–organic gel(Cu-MOG) with a nanoporous 3 D network structure prepared via a simple one-step mixing method was successfully employed for the removal of cationic dyes. The Cu-MOG exhibited high efficiency, with an adsorption capacity of up to 650.32 mg/g, and rapid adsorption efficiency, with the ability to adsorb 80% of Neutral Red within 1 min. The high adsorption efficiency was attributed to its large specific surface area, which enabled it to massively bind cationic dyes through electrostatic interaction, and a nanoporous structure that promoted intra-pore diffusion. Remarkably, the Cu-MOG displayed size-selective adsorption, based on adsorption studies concerning dyes of different sizes as calculated by density functional theory. Additionally, the adsorption performance of the Cu-MOG still maintained removal efficiency of 100% after three regeneration cycles. These results suggested that the Cu-MOG could be expected to be a promising and competitive candidate to conveniently process wastewater.     

Enzyme-electrolytic degradation of dichloromethane: Efficiency, kinetics and mechanism

Enzymatic electrolysis cell(EEC) has advantages over microbial electrolysis cell(MEC) due to the needless of microbe inoculation and high-efficiency of enzymatic reaction. In this study, an EEC was first applied to achieve the effective degradation of halogenated organic pollutants and dichloromethane(CH_2Cl_2) was utilized as a model pollutant. The results indicate that the degradation efficiency of CH_2Cl_2 after 2 hr reaction in the EEC was almost100%, which was significantly higher than that with enzyme(51.1%) or current(19.0%). The current induced the continuous regeneration of reduced glutathione(GSH), thus CH_2Cl_2 was degraded under the catalysis of GSH-dependent dehalogenase through stepwise dechlorination, and successively formed monochloromethane(CH_3Cl) and methane(CH_4). The kinetic result shows that with a current of 15 mA, the maximum specific degradation rate of CH_2Cl_2(3.77 × 10~(-3) hr~(-1)) was increased by 5.7 times. The optimum condition for CH_2Cl_2 dechlorination was also obtained with pH, current and temperature of 7.0, 15 mA and 35°C,respectively. Importantly, this study helps to understand the behavior of enzymes and the fate of halogenated organic pollutants with EEC, providing a possible treatment technology for halogenated organic pollutants.     

光催化剂AgBr/Ag2MoO4@AgVO3的结构表征及其抗菌防污性能

目的制备新型的光催化复合材料,提高其光催化性能。方法通过水热法和原位生长法制备不同摩尔比的AgBr/Ag_2MoO_4@AgVO_3光催化剂。采用X射线衍射(XRD)、扫描电镜(SEM)和高分辨透射电子显微镜(HRTEM)等一系列手段对所制备的光催化剂进行表征,并以可见光为光源,有机污染物罗丹明B(RhB)为降解对象,进行光催化活性测试,考察不同复合量的光催化剂对反应活性的影响。同时,以铜绿假单胞菌细胞、金黄色葡萄球菌和大肠杆菌为模式菌,进行抗菌试验考察光催化剂的杀菌性能。结果该复合材料通过AgVO_3的(501)晶面、Ag_2MoO_4的(311)面和AgBr的(200)晶面紧密连接。在罗丹明B(RhB)溶液中加入该复合材料,120 min内降解率达到了94.9%,而纯AgVO_3的降解率为7.8%,说明复合后的材料光催化性能明显提高。此外,在光催化杀菌实验中,超过99.99%的大肠杆菌、金黄色葡萄球菌和铜绿假单胞菌细胞均在90 min内被杀死。结论复合后的AgBr/Ag_2MoO_4@AgVO_3异质结光催化剂具有优异的光催化降解性能、杀菌性能和稳定性,该催化剂对于环境污染的治理以及海洋杀菌防污处理都起到一定的作用。     

油田用钨合金镀层腐蚀性能评价研究

目的评价钨合金镀层油管的腐蚀性能。方法利用高压釜模拟高压气井和高含硫气井的腐蚀环境,进行高压高温腐蚀试验,以及标准的氢致开裂(HIC)和硫化氢应力腐蚀试验。采用电子扫描显微镜(SEM)及其能谱仪(EDS)和X射线衍射分析仪(XRD),分析或检测钨合金镀层和基管的腐蚀形貌、腐蚀产物的组成。结果油管表面的钨合金镀层平整而致密,其主要组成元素为W和Ni。高温高压腐蚀试验后,镀层仍然致密平整,腐蚀程度轻微。在60、90、120、140℃试验7天时,镀层和基材的H_2S/CO_2腐蚀速率分别为0.0179、0.0093、0.0102、0.0369 mm/a和1.030、1.272、1.183、0.991 mm/a。试验30天,在120℃时,其H_2S/CO_2腐蚀速率分别为-0.0085、0.1789 mm/a;在160℃时,其CO_2腐蚀速率分别为0.0091、0.8976 mm/a。该钨合金镀层均通过了标准的氢致开裂和硫化氢应力腐蚀试验。结论该钨合金镀层具有很好的耐腐蚀性能。     

自然生境中厌氧氨氧化功能微生物生态学研究进展

自然生境中发生的厌氧氨氧化过程是继反硝化和好氧氨氧化后的又一条氮损失途径,对全球生态系统氮循环具有重要意义,但不同自然生态系统中存在不同种类的厌氧氨氧化微生物.通过阐述厌氧氨氧化反应发生的生理机制,并对不同自然环境中发现的厌氧氨氧化功能微生物进行梳理,分析了厌氧氨氧化菌分布的空间异质性成因.结果表明,适量的无机氮可以促进厌氧氨氧化的发生,有机碳含量低和低氧条件更有利于厌氧氨氧化菌的生存且厌氧氨氧化的活性较高,这与厌氧氨氧化菌的化能自养代谢途径有着紧密的联系,低养分条件下反硝化菌的活性受到短暂抑制,促进了厌氧氨氧化的发生.同时,适当的高盐环境会提高厌氧氨氧化活性并促进厌氧氨氧化菌群落结构转变,高盐度环境下Scalindua属占优势,低盐度环境下Brocadia属更占优势.厌氧氨氧化菌对温度变化有很好的适应性,大部分厌氧氨氧化菌（如Scalindua属、Kuenenia属和Brocadia属）对于极端环境均有较强的环境适应性;此外,悬浮颗粒物浓度、含水量等因素也会影响厌氧氨氧化菌的分布及其代谢活性.建议今后从基因组学、蛋白组学和转录组学相结合的角度对自然环境中的厌氧氨氧化菌开展生理生态机理的研究,并探明厌氧条件下Fe3+、Mn4+、SO₄2-等电子受体与厌氧氨氧化过程的生物化学联系,以更好地应用于工程技术研究,并为生态环境修复提供理论依据.      

某型飞机4号油箱结构损伤分析及修复评估

目的 某型双座机使用中发现4号油箱存在不同程度结构损伤,分析其损伤原因和制定修理方案。方法 对4号油箱结构状态进行深入检查评估后,从结构损伤过程、载荷情况、设计制造和外场使用等方面综合分析损伤原因。对实际损伤结构进行强度计算和评估,制定结构损伤补强修理方案,并提出修理改进建议。结果 通过分析得出,损伤原因主要是4号油箱局部存在设计制造缺陷,且飞机在作大过载飞行时,4号油箱可能处于满油或大量余油的高负载状态。根据损伤原因制定的修理方案合理可行,通过了静强度校核和评估。结论 基于该损伤结构提出的修理方案通过实际修理验证,能够满足油箱结构强度设计要求,提出的改进建议能够改善飞机疲劳品质。     

湖南慈利马尾松树轮宽度对气候的响应及1854年以来冬季极端低温重建

利用采自湖南慈利的马尾松树轮样本,建立研究区的标准树轮宽度年表。树轮气候响应分析发现:马尾松径向生长与月最大日降水量在生长季之前部分月份显著负相关(p0.05),在生长季之内部分月份显著正相关(p0.05),与月平均温度、月平均最低温度、月极端最低温度在生长季之前和之内大多月份均显著正相关(p0.05),其中与上一年11月到当年2月(冬季)的平均极端最低温度相关最好(r=0.62,p0.01)。重建了湖南慈利地区1854年以来冬季极端最低温度,重建气温在十年尺度上表现出明显的反"S"型,1854—1916年和1981—2015年处于暖冬时期,1917—1980年处于寒冬时期。此外,共发现29个寒冬年,其中包括3个寒冬时段,分别为1922—1925年、1927—1930年和1953—1960年,其中1953—1960年是自1854年以来最冷的时段。空间相关性分析表明重建序列可以指示我国中东部的冬季低温变化,而冬季低温可能与热带印度洋、西太平洋海温变化异常有关。     

鄱阳湖典型河湖交汇区浮游植物现状分析

鄱阳湖典型河湖交汇区（尾闾区）易受人类频繁活动的影响,属于敏感区且是蓝藻水华易暴发区域.为探究鄱阳湖典型河湖交汇区浮游植物群落结构的差异性及相关驱动机制,于2019年至2020年1月（枯水期）、4月（涨水期）、7月（丰水期）和10月（退水期）对鄱阳湖典型河湖交汇区7个采样点位和鄱阳湖河流中段6个采样点位以及主湖区1个采样点位水质状况和浮游植物进行野外调查.结果表明,鄱阳湖典型河湖交汇区浮游植物共有7门64属,浮游植物生物量和相对丰度以硅藻和蓝藻为主.鄱阳湖典型河湖交汇区生物量和丰度东部总体上高于西部,河湖交汇区生物量和丰度高于河流中段.湖区和河湖交汇区蓝藻门优势度较大,河流中段硅藻门优势度较大.蒙特卡罗检验结果显示：总氮（TN）、总磷（TP）、正磷酸盐（PO₄^3--P）、水深（WD）、水温（WT）和透明度（SD）是影响浮游植物群落分布的显著相关环境因子.冗余分析（RDA）结果显示,鄱阳湖西部典型河湖交汇区受水化因子（TN、TP和PO₄^3--P）作用更明显,东部典型河湖交汇区水文因子（WT、WD和SD）影响更为显著.鄱阳湖典型河湖交汇区浮游植物影响因子具有季节性,冬季受水化因子影响较大,夏季受水文因子影响较大.