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Yanfeng Wang Wei Chen Xiao Chen Huajun Feng Dongsheng Shen Bin Huang Yufeng Ji Yuyang Zhou Yuxiang Liang 《环境科学学报(英文版)》2018,30(3):347-355
Cd S/Mo S_2,an extremely efficient photocatalyst,has been extensively used in hydrogen photoproduction and pollutant degradation.Cd S/Mo S_2can be synthesized by a facile one-step hydrothermal process.However,the effect of the sulfur source on the synthesis of Cd S/Mo S_2via one-step hydrothermal methods has seldom been investigated.We report herein a series of one-step hydrothermal preparations of Cd S/Mo S_2using three different sulfur sources:thioacetamide,L-cysteine,and thiourea.The results revealed that the sulfur source strongly affected the crystallization,morphology,elemental composition and ultraviolet(UV)–visible-light-absorption ability of the Cd S/Mo S_2.Among the investigated sulfur sources,thioacetamide provided the highest visible-light absorption ability for Cd S/Mo S_2,with the smallest average particle size and largest surface area,resulting in the highest efficiency in Methylene Blue(MB)degradation.The photocatalytic activity of Cd S/Mo S_2synthesized from the three sulfur sources can be arranged in the following order:thioacetamideL-cysteinethiourea.The reaction rate constants(k)for thioacetamide,L-cysteine,and thiourea were estimated to be 0.0197,0.0140,and 0.0084 min~(-1),respectively.However,thioacetamide may be limited in practical application in terms of its price and toxicity,while L-cysteine is relatively economical,less toxic and exhibited good photocatalytic degradation performance toward MB. 相似文献
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Persulfate activation has been applied as one of the efficient advanced oxidation processes(AOPs) to remediate polluted environments. In this study, a novel α-FeOOH anchored by graphene oxide(GO)-carbon nanotubes(CNTs) aerogel(α-FeOOH@GCA) nanocomposite activated persulfate system(α-FeOOH@GCA + K_2S_2O_8) was applied for decolorization of Orange Ⅱ(OⅡ). The decolorization of OⅡ was remarkably enhanced to a level of ~ 99% in this system compared with that of pristine α-FeOOH(~ 44%) or GO-CNTs(~18%). The enhanced catalytic activity of α-FeOOH@GCA was due to the formation of a heterojunction byα-FeOOH and GO-CNTs as confirmed by the presence of Fe–O–C chemical bonds. The degradation intermediates of OⅡ were comprehensively identified. The proposed degradation pathway of OⅡ begins with the destruction of the conjugated structures of OⅡ by the dominant reactive oxygen species, surface-bound SO_4~(·-). The decolorization efficiency of OⅡ by the α-FeOOH@GCA activated persulfate system decreased from the first to third cycle of recycling. Ultraviolet(UV) irradiation or introduction of a small amount of Fe~(2+) could restore the activation of this system. The results show that the α-FeOOH@GCA persulfate activation system promises to be a highly efficient environmental remediation method for organic pollutants. 相似文献
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Lili Yang Yuyang Zhao Miwei Shi Minghui Zheng Yang Xu Cui Li Yuanping Yang Linjun Qin Guorui Liu 《环境科学学报(英文版)》2019,31(5):339-345
A field study and theoretical calculations were performed to clarify the levels, profiles, and distributions of polybrominated dibenzo-p-dioxins and dibenzofurans(PBDD/Fs) in a cement kiln co-processing solid waste, with a focus on the PBDF formation mechanism.The raw materials contributed greatly to input of PBDD/Fs into the cement kiln. The PBDD/F concentrations in the raw materials were much higher than those in particle samples from different process stages in the cement kiln. The PBDD/F concentrations in the clinkers were1.40% of the concentrations in the raw materials, which indicated that the high destruction efficiencies for PBDD/Fs by cement kiln. PBDD/F distribution patterns in particle samples collected from different process stages indicated the cement kiln backend was a major site for PBDD/F formation. PBDFs with high levels of halogenation, such as heptabrominated furans(Hp BDF), were the dominant contributors to the total PBDD/F concentrations and accounted for 42%–73% of the total PBDD/F concentrations in the particle samples. Our results showed that co-processing of municipal solid waste in a cement kiln may influence the congener profile of PBDD/Fs, especially for the higher halogenated PBDD fraction. In addition, there were significant correlations between the decabromodiphenyl ether and heptabrominated furan concentrations, which is an indicator of transformation from polybrominated diphenyl ethers to PBDD/Fs. Theoretical calculations were performed and demonstrated that elimination of HBr and Br_2 from polybrominated diphenyl ethers were the dominant formation pathways for PBDD/Fs. These pathways differed from that for polychlorinated dibenzo-p-dioxins and dibenzofurans(PCDD/Fs). 相似文献
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同步脱氮除磷复配菌剂对河流水质净化效果研究 总被引:1,自引:0,他引:1
通过选择培养基、溴麝香草酚蓝(Bromothymol Blue,BTB)培养基筛选及脱氮除磷性能检测,从城市河道中成功筛选出6株异养硝化-好氧反硝化菌株,分别属于假单胞菌属(Pseudomonas)、产碱杆菌属(Alcaligenes)、无色杆菌属(Achromobacter)和陶厄氏菌属(Thauera),其中3株菌株兼具硝化、反硝化和聚磷能力,菌株MC-5除磷能力最优.在此基础上,将筛选出的6株单菌株进行复配,考察了复配菌剂在不同COD/TN下的脱氮除磷性能.根据群落结构变化分析,发现复配菌剂中的产碱杆菌属在脱氮除磷中发挥了更为关键的作用.水中碳源耗尽时补加碳源能显著提升复配菌剂的脱氮除磷性能,氨氮和总磷去除率分别由55.87%和50.48%提高到100%和98.89%,而水中COD/TN高于20会对微生物产生抑制作用.探究复配菌剂处理受污染河水最佳投加量的试验结果表明,投加量为1.69 g·m-3时,总磷指标能够从地表水劣Ⅴ类提高至Ⅲ类水质标准,氮类指标能够提升至接近地表水Ⅴ类水质标准.适当提高菌剂投加量能提高氮、磷元素降解速率,缩短河道水质修复时间.这说明本研究中的同步脱氮除磷... 相似文献
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Haoduo Zhao Min Liu Junjie Yang Yuyang Chen Mingliang Fang 《Frontiers of Environmental Science & Engineering》2023,17(1):4
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为研究泄爆夹层内障碍物位置对燃气泄爆效果的影响,以某大型商业综合体暗厨房为研究对象,考虑泄爆夹层中结构梁不同位置的泄爆效果,对暗厨房燃气爆炸的泄爆过程开展数值模拟研究。研究结果表明:在火焰没有到达泄爆窗前的爆炸初始阶段,障碍物对火焰结构和传播速度基本没有影响,当火焰进入泄爆夹层后,障碍物的存在可引发火焰加速现象;当障碍物距离泄爆窗1.7 m时,火焰加速现象较为明显,火焰最大传播速度可达591.5 m/s,此时厨房内压力峰值约2.9 MPa,约为没有结构梁情况下1.42倍;障碍物距离泄爆窗较近时,二者将协同影响火焰传播;厨房内压力峰值随着障碍物与泄爆窗距离的增大遵循增大-突降-增大的规律。研究结果可为商业综合体暗厨房泄爆设计提供一定理论依据。 相似文献
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生物可降解络合剂聚天冬氨酸治理土壤重金属污染 总被引:5,自引:0,他引:5
土壤重金属污染会产生严重的生态环境问题,土壤淋洗技术可达到土壤修复的目的,其中络合剂的选择是达到安全、有效修复效果的关键.聚天冬氨酸(PASP)可生物降解,对环境安全.文章选择PASP作为重金属的络合剂,研究其修复土壤重金属污染的效果.结果表明,PASP对金属离子Cd、Zn和Ca均有较好的提取率,均超过50%,并且络合剂/重金属的摩尔比越高,提取效果越好,受pH的影响就越少,提取速率开始比较快,而后趋于平缓.在PASP络合物的形态分布中,在pH较低阶段,PASP-Cd络合物所占的比例较大,随着pH的升高,PASP-Zn和PASP-Ca的比例增加,同时微生物对聚天冬氨酸的降解作用对治理效果产生负面影响.PASP可作为环保型的络合剂,达到修复土壤重金属污染的目的. 相似文献