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国家自然科学基金(51378368)

作品数:10 被引量:35H指数:5
相关作者:夏四清徐晓茵王晨辉林华李海翔更多>>
相关机构:同济大学桂林理工大学学研究院更多>>
发文基金:国家自然科学基金广西壮族自治区自然科学基金更多>>
相关领域:环境科学与工程建筑科学更多>>

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Bioreduction of vanadium(V) in groundwater by autohydrogentrophic bacteria:Mechanisms and microorganisms被引量:4
2015年
As one of the transition metals, vanadium(V)(V(V)) in trace amounts represents an essential element for normal cell growth, but becomes toxic when its concentration is above 1 mg/L. V(V) can alter cellular differentiation, gene expression, and other biochemical and metabolic phenomena. A feasible method to detoxify V(V) is to reduce it to V(IV), which precipitates and can be readily removed from the water. The bioreduction of V(V) in a contaminated groundwater was investigated using autohydrogentrophic bacteria and hydrogen gas as the electron donor. Compared with the previous organic donors,H2 shows the advantages as an ideal electron donor, including nontoxicity and less production of excess biomass. V(V) was 95.5% removed by biochemical reduction when autohydrogentrophic bacteria and hydrogen were both present, and the reduced V(IV)precipitated, leading to total-V removal. Reduction kinetics could be described by a first-order model and were sensitive to p H and temperature, with the optimum ranges of p H 7.5–8.0 and 35–40°C, respectively. Phylogenetic analysis by clone library showed that the dominant species in the experiments with V(V) bioreduction belonged to theβ-Proteobacteria. Previously known V(V)-reducing species were absent, suggesting that V(V)reduction was carried out by novel species. Their selective enrichment during V(V)bioreduction suggests that Rhodocyclus, a denitrifying bacterium, and Clostridium, a fermenter known to carry out metal reduction, were responsible for V(V) bioreduction.
Xiaoyin XuSiqing XiaLijie ZhouZhiqiang ZhangBruce E.Rittmann
C8-oxo-HSl对P.aeruginosa在污水处理中生长特性影响被引量:1
2017年
通过24孔板序批实验对群体效应(QS)信号分子C_8-oxo-HSL对铜绿假单胞菌(P.aeruginosa)在污水处理过程中生长特性影响作用进行分析探讨.研究发现C_8-oxo-HSL有效刺激P.aeruginosa大量生长,其对应的阙值浓度为10^(-10)g/L C_8-oxo-HSL.同时推知具有Lux I/R群体效应系统的革兰氏阴性菌可在较低的信号分子浓度作用下大量增殖.C_8-oxo-HSL还可有效刺激P.aeruginosa分泌大量蛋白质至紧密型胞外聚合物(TB-EPS)中,其对应的阙值浓度为10^(-7)g/LC_8-oxo-HSL.但C_8-oxo-HSL对P.aeruginosa的TB-EPS中多糖没有明显影响作用.C_8-oxo-HSL通过促使P.aeruginosa的增殖和团聚从而增强菌胶团稳定性.此外C_8-oxo-HSL可促进P.aeruginosa生物膜形成.但由于P.aeruginosa生物膜的形成同时和细菌菌量与胞外聚合物浓度直接相关.所以P.aeruginosa生物膜快速生长的C_8-oxo-HSL阙值浓度相对较高(约10^(-8)g/L).
周礼杰王鑫韩倩朱婷婷成功夏四清
关键词:铜绿假单胞菌菌胶团生物膜
氢基质生物膜反应器去除水中硒酸盐研究被引量:6
2014年
利用连续搅拌氢基质生物膜反应器研究氢气(H2)分压,NO3^--N,SO4^2-,SeO4^2-进水浓度对水中硒酸盐去除效果的影响.结果表明,H2分压是水中氧化态污染物NO3^-,SO4^2-,SeO4^2-去除效果的重要影响因素,随着H2分压从0.02MPa上升到0.08MPa,SO4^2-的去除率从3.5%上升到46.3%,总Se的去除率从60.7%上升到82.1%,NO3^-全过程都完全被还原为N2;随着NO3^--N进水浓度从5mg/L增加到50mg/L,SO4^2-,SeO4^2-的去除率逐渐下降至0,并出现NO2-的积累;SO4^2-进水浓度的增加对NO3^-,SeO4^2-去除效果影响不大,去除率分别保持在99.5%和65%以上,三种氧化态污染物得电子的优先级为NO3^-〉SeO4^2-〉SO4^2-.在NO3^--N浓度为10mg/L,SO4^2-浓度为25mg/L的水质条件下,反应器设置H2分压为0.04MPa,进水Se(VI)浓度在0.25~2mg/L的范围内总Se可以取得80%以上的去除效果.
王晨辉徐晓茵夏四清
关键词:硒酸盐硝酸盐硫酸盐
利用CO_2为碳源的新型氢基质生物膜技术去除水中硝酸盐被引量:5
2016年
本文研发了利用二氧化碳(CO_2)为碳源的双膜曝气式氢基质生物膜反应器(MBfR),并系统研究了CO_2分压对出水硝酸盐、pH和朗格利尔系数(LSI)的影响,建立了数学模型预测系统最适CO_2分压从而对实际工况运行具有指导意义.对双膜曝气MBfR长期运行的稳定性进行了考察,反应器CO_2分压设置为0.05 MPa时,反应器内的pH值控制良好,出水效果稳定,硝酸盐去除率达99%以上.
夏四清徐晓茵王晨辉
关键词:硝酸盐
Potential acute effects of suspended aluminum nitride (AlN) nanoparticles on soluble microbial products (SMP) of activated sludge
2017年
The study aims to identify the potential acute effects of suspended aluminum nitride(Al N)nanoparticles(NPs) on soluble microbial products(SMP) of activated sludge.Cultured activated sludge loaded with 1,10,50,100,150 and 200 mg/L of Al N NPs were carried out in this study.As results showed,Al N NPs had a highly inverse proportionality to bacterial dehydrogenase and OUR,indicating its direct toxicity to the activated sludge viability.The toxicity of Al N NPs was mainly due to the nano-scale of Al N NPs.In SMP,Al N NPs led to the decrease of polysaccharide and humic compounds,but had slight effects on protein.The decrease of tryptophan-like substances in SMP indicated the inhibition of Al N NPs on the bacterial metabolism.Additionally,Al N NPs reduced obviously the molecular weight of SMP,which might be due to the nano-scale of Al N.
Lijie ZhouWeiqin ZhuangXin WangKe YuShufang YangSiqing Xia
氢基质生物膜反应器去除对氯硝基苯的影响因素分析被引量:2
2015年
基于MBfR(氢基质生物膜反应器)研究进水中ρ(p-CNB)(p-CNB为对氯硝基苯)和氢气压力对氢基质自养微生物还原降解p-CNB的影响,同时分析在ρ(p-CNB)和氢气压力影响下生物膜内电子受体生物还原的当量电子通量和还原动力学.结果表明:提高进水中的ρ(p-CNB),p-CNB、p-CAN(对氯苯胺)的去除通量分别由0.014、0.011 g/(m2·d)升至0.099、0.060 g/(m2·d),但p-CNB的去除率由95.9%降至68.4%;提高氢气压力,p-CNB、p-CAN的去除通量分别由0.027、0.019 g/(m2·d)升至0.028、0.022g/(m2·d),p-CNB去除率由93.1%升至95.1%,升幅均不大,说明进水ρ(p-CNB)比氢气压力更能直接影响p-CNB和p-CAN的去除通量及p-CNB去除率.当量电子通量分配和还原动力学结果表明,p-CNB和p-CAN的还原对氢气压力升高的敏感性不强烈,进一步揭示降低进水中ρ(p-CNB)比提高氢气压力更能明显地促进微生物对p-CNB和p-CAN的去除效果.氢气压力变化对硫酸盐还原和反硝化的影响程度高于p-CNB或p-CAN的还原,当氢气可利用率受限时,p-CNB或p-CAN的还原会由于电子供体的竞争而受到抑制.
李海翔林华游少鸿徐晓茵夏四清
关键词:生物还原
Arsenic removal from groundwater by acclimated sludge under autohydrogenotrophic conditions被引量:5
2014年
Arsenic in the environment is attracting increasing attention due to its chronic health effects. Although arsenite (As(III)) is generally more mobile and more toxic than arsenate (As(V)), reducing As(V) to As(III) may still be a means for decontamination, because As(III) can be removed from solution by precipitation with sulfide or by adsorption or complexation with other metal sulfides. The performance of As(V) bio-reduction under autohydrogenotrophic conditions was investigated with batch experiments. The results showed that As(V) reduction was a biochemical process while both acclimated sludge and hydrogen were essential. Most of the reduced arsenic remained in a soluble form, although 20% was removed with no addition of sulfate, while 82% was removed when sulfate was reduced to sulfide. The results demonstrated that the reduced arsenic was re-sequestered in the precipitates, probably as arsenic sulfides. Kinetic analysis showed that pseudo first-order kinetics described the bio-reduction process better than pseudo second-order. In particular, the influences of pH and temperature on As(V) reduction by acclimated sludge under autohydrogenotrophic conditions and total soluble As removal were examined. The reduction process was highly sensitive to both pH and temperature, with the optimum ranges of pH 6.5-7.0 and 30-40℃ respectively. Furthermore, Arrhenius modeling results for the temperature effect indicated that the As(V) reduction trend was systematic. Total soluble As removal was consistent with the trend of As(V) reduction.
Siqing XiaShuang ShenXiaoyin XuJun LiangLijie Zhou
关键词:GROUNDWATER
pH对氢基质自养微生物还原降解对氯硝基苯的影响被引量:6
2015年
在建立的一种MBfR(氢基质生物膜反应器)中系统考察pH对氢基质自养微生物还原降解p-CNB(对氯硝基苯)的影响,并重点分析pH影响下p-CNB、p-CAN(对氯苯胺)、NO-3-N(硝酸盐)和SO2-4(硫酸盐)的去除效率、通量及当量电子转移通量的变化趋势.结果表明,pH在5.7~8.7之间变化时对硝基还原、还原脱氯、反硝化和硫酸盐还原过程影响显著.氢基质自养微生物生长较适宜的pH范围为6.7~8.2,其中硝基还原、还原脱氯、反硝化和硫酸盐还原的最佳pH分别是7.7、8.2、7.2和7.2.当量电子转移通量分析表明,反硝化和硫酸盐还原对pH变化的敏感性均强于p-CNB还原.为了维持较高水平的p-CNB、NO-3-N和SO2-4同步去除效率,可将pH调控在7.2~8.2之间.适当地调节pH有利于微生物的生长以及控制中空纤维膜表面矿物质沉淀引起的膜污染.
李海翔林华游少鸿徐晓茵夏四清
关键词:PH还原降解
双膜曝气生物膜反应器除水中硝氮和高氯酸盐被引量:7
2016年
构建了一种以CO_2为唯一碳源的膜曝气氢基质生物膜反应器(H_2-MBf R)对模拟地下水中2种主要的氧化型无机无污染物(NO_3^--N和ClO_4^-)进行生物还原去除.通过膜曝气方式使CO_2起到提供碳源和调节反硝化过程中pH值跃升的双重作用,克服了传统方法所带来的二次污染和运行成本增加的问题.通过调整H_2和CO_2压力能够实现对反应器出水pH值的较为稳定的控制,当CO_2压力分别为0.05MPa和0.08MPa 2个阶段时,在平均NO_3^--N和ClO_4^-进水浓度分别为20.73mg/L和10.57mg/L条件下,两阶段出水平均pH值分别为8.45和8.06,NO_3^--N和ClO_4^-去除率均大于95%;当第3阶段CO_2压力提升至0.12MPa时,平均出水pH值下降至6.93,此时NO_3^--N和ClO_4^-去除通量明显降低.而提供过量的CO_2会导致在偏酸性条件下甲烷化过程的产生,从而会导致其对H_2的负面消耗进而使目标污染物的还原速率下降.因此,合理控制CO_2压力使反应体系pH值维持在中性偏碱性条件下有利于NO_3^--N和ClO_4^-还原过程的高效进行.
杨潇潇汪作炜夏四清
关键词:碳源硝酸盐高氯酸盐
利用氢基质生物膜反应器去除水中砷酸盐被引量:6
2015年
利用氢基质生物膜反应器(Hydrogen-based membrane biofilm reactor,MBfR)研究了NO_3^--N负荷、SO_4^(2-)负荷、As(Ⅴ)负荷、氢分压对水中砷去除效果的影响.结果表明,随着NO_3^--N进水负荷的增加,As(Ⅴ)和SO_4^(2-)还原受到明显抑制,系统产生As(Ⅲ)和NO_2^-的积累;随着SO_4^(2-)进水负荷的增加,反应器内总砷去除率由78.6%(25 mg·L-1SO_4^(2-))降低至1.1%(200 mg·L^(-1)SO_4^(2-)),而此时NO_3^--N的去除基本不受影响.同时,随着进水As(Ⅴ)负荷从0.25 mg·L^(-1)增至2 mg·L^(-1),出水SO_4^(2-)浓度明显升高,反应器内总砷去除率从70.0%降低至47.3%,而此时NO_3^--N的去除基本不受影响;当氢分压低于0.06 MPa时,提高氢分压可降低出水As(Ⅴ)浓度,当氢分压高于0.06 MPa后便不再是控制因素.由于体系中氢自养还原微生物会优先利用NO_3^--N和SO_4^(2-)作为电子受体,因此,为了保证As(Ⅴ)的高效还原去除,必须控制氢分压在0.05~0.07 MPa之间.
潘思宇夏四清王晨辉沈双
关键词:砷酸盐影响因素
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