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.     

O池溶解氧水平对石化废水A/O工艺污染物去除效果和污泥微生物群落的影响

以实际石化废水为处理对象,研究溶解氧浓度对A/O反应器生物降解特性的影响.A、B两组反应器平行运行以进行对比,O段的溶解氧浓度分别控制在2~3 mg·L-1和5~6 mg·L-1.反应器稳定运行近半年的结果表明:在HRT为20 h时,A组反应器出水的COD(72.5 mg·L-1±14.8 mg·L-1)略高于B组(68.7 mg·L-1±14.6 mg·L-1),COD平均去除率分别为67.0%和68.8%;出水氨氮的平均浓度和去除率为0.8 mg·L-1和95%左右.出水的BOD5均低于5 mg·L-1.表明A/O反应器对有机物的生物降解比较彻底,溶解氧浓度对其没有显著影响.对O段污泥进行454高通量测序结果表明:变形菌门、浮霉菌门和拟杆菌门细菌所占比例较高,在A、B组反应器中的比例分别为58.7%和59.2%、14.7%和12.7%以及10.8%和12.4%.高溶解氧运行的反应器B具有较高的菌群丰度和多样性,氨氧化菌Nitrosomonas、亚硝酸氧化菌Nitrospira和专性好氧菌如Planctomyces的比例较高.厌氧反硝化菌如Azospira和Acidovora在反应器A中的含量较高.在属的水平,鉴定出的Novosphingobium、Comamonas、Sphingobium和Altererythrobacter属细菌具有降解多环芳烃、氯代硝基苯、农药和石油化合物的功能,有利于石化废水的降解.     

铜、毒死蜱单一与复合暴露对蚯蚓的毒性作用

土壤环境中重金属-农药复合污染已经对土壤生态和人类生存环境构成严重威胁.其中重金属铜和有机磷农药毒死蜱作为土壤环境中两类常见的污染物,其复合污染的环境效应值得关注.本文采用OECD标准滤纸接触法、人工土壤法研究了铜-毒死蜱单一及复合暴露对蚯蚓急性致死作用及回避行为的影响.结果表明,滤纸法和人工土壤法Cu对蚯蚓急性毒性的48h-LC50和14 d-LC50分别为2.23μg·cm-2和496.05 mg·kg-1;而毒死蜱对蚯蚓急性毒性的48 h-LC50和14 d-LC50分别为5.94μg·cm-2和186.07 mg·kg-1.滤纸法和人工土壤法铜、毒死蜱浓度单位配比1∶1时,铜、毒死蜱对蚯蚓急性毒性联合作用类型均近似表现为相加作用,而毒性单位配比1∶1的滤纸法和人工土壤法试验结果分别为协同作用和拮抗作用.回避行为试验结果表明,铜、毒死蜱对蚯蚓回避行为的联合作用类型为拮抗作用.     

微塑料诱导下污泥造粒潜能变化及微生物富集特征

微塑料(MPs)是污水处理厂中普遍检出的新兴污染物之一,目前研究主要集中于传统污水处理系统的污染水平及分布特征,但有关微塑料暴露对污泥颗粒化过程的研究鲜见报道.为探究微塑料对污泥颗粒化的诱导影响,选用环境中广泛检出的聚对苯二甲酸乙二醇酯微塑料(PET-MPs)作为研究对象,通过微塑料暴露试验研究PET-MPs对污泥造粒过程中系统潜能、胞外聚合物(EPS)组成和菌群富集特征的影响.结果表明,PET-MPs暴露显著加快污泥颗粒化进程,同时以蛋白质(PN)为主导的EPS含量上升会增强污泥表面疏水性,造粒速度和EPS分泌量与暴露粒径成正比,微塑料和EPS协同促进颗粒污泥的形成.然而微塑料持续暴露会导致系统除污性能恶化,250μm PET-MPs暴露下亚硝酸盐氮积累的负面影响最严重,浓度高达(5.08±0.24)mg·L^-1.高通量测序结果进一步表明,变形菌门(Proteobacteria)和拟杆菌门(Bacteroidota)是促进颗粒污泥形成的主要优势门;红环菌科(Rhodocyclaceae)、鞘氨醇杆菌科(Sphingomonadaceae)、黄杆菌科(Flavob...     

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.     

Modeling the competitive effect of phosphate, sulfate, silicate, and tungstate anions on the adsorption of molybdate onto goethite

The mobility of Mo in soils and sediments depends on several factors including soil mineralogy and the presence of other oxyanions that compete with Mo for the adsorbent's retention sites. Batch experiments addressing Mo adsorption onto goethite were conducted with phosphate, sulfate, silicate, and tungstate as competing anions in order to produce competitive two anions adsorption envelopes, as well as competitive two anions adsorption isotherms. Tungstate and phosphate appear to be the strongest competitors of Mo for the adsorption sites of goethite, whereas little competitive effects were observed in the case of silicate and sulfate. Mo adsorption isotherm from a phosphate solution was similar to the one from a tungstate solution. The charge distribution multi-site complexation (CD-MUSIC) model was used to predict competitive adsorption between MoO(4)(2-) and other anions (i.e., phosphate, sulfate, silicate and tungstate) using model parameters obtained from the fitting of single ion adsorption envelopes. CD-MUSIC results strongly agree with the experimental adsorption envelopes of molybdate over the pH range from 3.5 to 10. Furthermore, CD-MUSIC prediction of the molybdate adsorption isotherm show a satisfactory fit of the experimental results. Modeling results suggest that the diprotonated monodentate complexes, FeOW(OH)(5)(-0.5) and FeOMo(OH)(5)(-0.5), were respectively the dominant complexes of adsorbed W and Mo on goethite 110 faces at low pH. The model suggests that Mo and W are retained mainly by the formation of monodentate complexes on the goethite surface. Our results indicate that surface complexation modeling may have applications in predicting competitive adsorption in more complex systems containing multiple competing ions.     

氢气添加对乙醇/空气预混火焰燃烧特性影响的数值模拟研究

通过对不同混合比率的乙醇/氢气/空气燃烧特性进行数值模拟,研究氢气添加量对点火延迟时间、层流燃烧速度、火焰厚度、化学反应滞留时间及组分分布情况的影响。研究发现一定程度上氢气添加量的增加能够缩短混合气体的点火延迟时间,并且氢气对点火延迟时间的影响随着温度的升高而逐渐减小。随着混合比率的增大,层流燃烧速度增大,并且在混合比率大于0.4时显著增大。火焰厚度及化学反应滞留时间随氢气增加而逐渐减小。此外,进一步分析组分分布情况得知氢气添加使火焰中H*、O*、OH*自由基摩尔分数峰值增大,并且H+O+OH摩尔分数峰值与层流燃烧速度存在线性关系。     

新型多功能森林消防人员睡袋的研究

针对目前我国在森林草原防火工作中,森林消防人员在森林火灾扑救中携行装备落后、繁重的状况,为保护扑火队员免受寒冻之苦,减轻单兵负荷,提高扑火效率,根据我国森林消防工作特点和实际需要,研制出了森林消防多功能睡袋,该实用新型睡袋具有多种功能、多种用途,可用作单人睡袋、背包、担架和吊床。设计合理,使用方便、快捷,质量轻,便于携带,可折叠成背包,是适合于森林消防人员使用的野外装备用具。     

Phosphorus adsorption by functionalized biochar: a review

Environmental Chemistry Letters - Phosphorus is essential element for agricultural production, yet phosphorus ore resources are non-renewable and become depleted. Moreover, phosphate release from...     

利用脂肪酶提高鱼油中多不饱和脂肪酸(PUFAs)甘油酯

利用脂肪酶选择性的水解作用研究提高鱼油中多不饱和脂肪酸(PUFAs)甘油酯的含量.通过对5种不同来源脂肪酶的筛选,以来源于米曲霉脂肪酶为最佳酶种;同时研究该酶水解鱼油的最佳工艺条件:反应温度、加酶量、反应转速、添加剂影响;最后确定最佳的富集PUFAs甘油酯时间.在此工艺条件下,鱼油中EPA由3.0%提高到9.0%,DHA由4.3%提高到16.5%,EPA DHA由7.3%提高到25.5%.图3表1参8