ClO2消毒工艺对污水处理厂出水超级耐药基因的影响

为了研究二氧化氯（chlorine dioxide,ClO₂）消毒工艺对污水处理厂出水中超级耐药基因（super antibiotic resistance genes,SARGs）的去除效果,对污水处理厂出水消毒前后的水样进行了全年采集,并采用微孔滤膜正压过滤法及核酸吸附柱-洗脱法分别富集水中细菌和胞外核酸后,利用荧光定量PCR技术对其中的9种SARGs进行定量检测.结果表明,无论是胞内还是胞外核酸,均有NDM-1、MCR-1 和MEC-A被检测出;同时,ClO₂消毒后上述3种SARGs的胞内相对总浓度明显上升（P<0.05）,且ClO₂消毒对胞内SARGs相对浓度的影响与季节有关,其中春季、夏季和秋季均发生上升,且春季升高最为明显,达2倍,而冬季出水在消毒前后均未测出胞内SARGs;胞外SARGs则在ClO₂消毒前后没有明显浓度变化.因此,ClO₂消毒不能有效去除污水处理厂出水中胞内和胞外SARGs污染.     

燃煤电厂排放细颗粒物的水溶性无机离子特征综述

当前我国面临严重的大气细颗粒物(PM2.5)污染,燃煤电厂是大气中PM2.5的重要来源之一.为了实现国家"十一五"和"十二五"规划对二氧化硫(SO2)和氮氧化物(NOx)的总量减排目标,燃煤电厂大规模安装烟气脱硫和脱硝设施,这虽然减少了气态污染物转化生成的二次PM2.5,但另一方面也会对烟气中PM2.5的物理化学特征产生影响,有可能增加一次PM2.5的排放.本文综述了燃煤电厂排放PM2.5及其水溶性离子的粒径分布特征,重点介绍了脱硫和脱硝这两种烟气处理设施对燃煤电厂排放PM2.5的影响原理及相关研究结果,特别是对细颗粒物中水溶性离子(如SO2-4、Ca2+和NH+4)的影响.在目前我国PM2.5污染十分严重和燃煤电厂大量安装脱硫和脱硝装置的背景下,定量研究脱硫和脱硝对PM2.5排放特征的影响具有十分重要的意义.     

Photodegradation mechanism of two dyes: the influence of adsorption behavior on the novel TiO2 particles

The relationship between adsorption behavior and photocatalytic mechanism of the two dyes was investigated. Adsorption isotherms showed that the adsorption of cationic pink FG was Langmuir type behavior, while the reactive brilliant red k-2G was Freundlich type behavior. The increasing pH favored the adsorption of FG but have little effect on the photodegradation. The increasing pH favored the adsorption and the photodegradation of k-2G. The presence of scavenger of hvb^ and OH. radical potassium iodide inhibited the degradation of k-2G, free radicals scavenger tetranitromethane inhibited the photodegradation of FG. These results indicated that the photodegradation of FG mainly via free radicals in solution, and the photodegradation of k-2G was mainly on the catalysts surface or near the interface of solid and solution by react with hvb^ and surface-bound OH.. The different effect of SO4^2- , HCO3^- on the adsorption and photodegradation of two dyes confirmed these results.     

T-2毒素的毒性效应及致毒机制研究进展

T-2毒素是由多种镰刀菌产生的单端孢霉烯族化合物中毒性较强的一种毒素,广泛存在于谷物和谷类食品中.经食物连续摄入T-2毒素会对人类和动物的健康造成潜在危害.目前,T-2毒素对人和动物健康的影响受到了社会的广泛关注,已成为毒理学领域研究的热点课题之一.在综述了T-2毒素的生物转化、代谢途径及其毒理学效应与机制基础上,对现...     

Synthesis, crystal structure, photodegradation kinetics and photocatalytic activity of novel photocatalyst ZnBiYO4

ZnBiYO₄ was synthesized by a solid-state reaction method for the first time. The structural and photocatalytic properties of ZnBiYO₄ were characterized by X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy and UV-Vis diffuse reflectance. ZnBiYO₄ crystallized with a tetragonal spinel structure with space group I41/A. The lattice parameters for ZnBiYO₄ were a = b = 11.176479 Å and c= 10.014323 Å. The band gap of ZnBiYO₄ was estimated to be 1.58 eV. The photocatalytic activity of ZnBiYO₄ was assessed by photodegradation of methyl orange under visible light irradiation. The results showed that ZnBiYO₄ had higher catalytic activity compared with N-doped TiO₂ under the same experimental conditions using visible light irradiation. The photocatalytic degradation of methyl orange with ZnBiYO₄ or N-doped TiO₂ as catalyst followed first-order reaction kinetics, and the first-order rate constant was 0.01575 and 0.00416 min^-1 for ZnBiYO₄ and N-doped TiO₂, respectively. After visible light irradiation for 220 min with ZnBiYO₄ as catalyst, complete removal and mineralization of methyl orange were observed. The reduction of total organic carbon, formation of inorganic products, SO₄^2- and NO₃^-, and evolution of CO₂ revealed the continuous mineralization of methyl orange during the photocatalytic process. The intermediate products were identified using liquid chromatography- mass spectrometry. The ZnBiYO₄/(visible light) photocatalysis system was found to be suitable for textile industry wastewater treatment and could be used to solve other environmental chemical pollution problems.     

膜电解法退镀废ABS电镀件及回收铜和镍

采用膜电解法对废丙烯腈-丁二烯-苯乙烯（ABS）电镀件进行退镀处理。以退镀废液作为阴极液和阳极液,在阳极室退镀ABS电镀件,在阴极室电解退镀废液,进行铜镍分离,回收铜粉和NiCl₂。实验结果表明：在阴极电流密度为500 A/m²、初始铜离子质量浓度为24.00 g/L的条件下电解160 min,阴极铜回收率可达97.65%,电流效率达86.60%,得到的铜粉纯度为97%~99%,处理1 L退镀废液可回收铜粉20.0 g,2 mol/L盐酸0.87 L,NiCl₂晶体43.8 g;在阳极电流密度为500 A/m²、液固比为6的条件下电解60 min, ABS电镀件的退镀率为77.22%。     

吹扫捕集气质联用测定水中嗅味物质的研究

文章建立了一种用吹扫捕集—气相色谱质谱联用技术测定饮用水中土臭素(GSM)和二甲基异冰片(2-MIB)等嗅味物质的分析方法,确定了最佳的色谱条件、质谱条件和水样处理方法。当取样量为25mL时,回收率分别为96%和89%,RSD<10%,检出限为0.002mg/L。     

Low-carbon transition of iron and steel industry in China: Carbon intensity, economic growth and policy intervention

As the biggest iron and steel producer in the world and one of the highest CO₂ emission sectors, China's iron and steel industry is undergoing a low-carbon transition accompanied by remarkable technological progress and investment adjustment, in response to the macroeconomic climate and policy intervention. Many drivers of the CO₂ emissions of the iron and steel industry have been explored, but the relationships between CO₂ abatement, investment and technological expenditure, and their connections with the economic growth and governmental policies in China, have not been conjointly and empirically examined. We proposed a concise conceptual model and an econometric model to investigate this crucial question. The results of regression, Granger causality test and impulse response analysis indicated that technological expenditure can significantly reduce CO₂ emissions, and that investment expansion showed a negative impact on CO₂ emission reduction. It was also argued with empirical evidence that a good economic situation favored CO₂ abatement in China's iron and steel industry, while achieving CO₂ emission reduction in this industrial sector did not necessarily threaten economic growth. This shed light on the dispute over balancing emission cutting and economic growth. Regarding the policy aspects, the year 2000 was found to be an important turning point for policy evolution and the development of the iron and steel industry in China. The subsequent command and control policies had a significant, positive effect on CO₂ abatement.     

电化学还原-氧化工艺降解4-氯酚的毒性研究

采用紫外光还原法制备了Pd-Fe/石墨烯催化阴极,并以Ti/IrO_2/RuO_2为阳极,构成三电极体系(双阴极)和两电极体系(单阴极)的电化学还原-氧化降解工艺,分别对4-氯酚进行降解.采用离子色谱、高效液相色谱、TOC仪对4-氯酚降解过程中中间产物及其浓度进行测定.根据公式计算降解过程中理论计算毒性值,应用发光细菌法测定降解过程中的实际毒性值,对理论计算毒性值与实际毒性值进行比较,分析不同体系下降解过程中毒性的变化规律.结果表明,两种工艺体系在最佳降解条件下,阴极室毒性均呈下降的趋势,由于降解过程中在阳极室生成高毒性的苯醌,阳极室毒性均先升高后降低.通过相关性分析得到,两种体系理论计算毒性与实际毒性在P=0.01水平下,相关性系数均为1,显著相关,表明降解过程中实际毒性的测定结果真实可靠.降解至120 min时,三电极体系毒性小于两电极体系,表明三电极体系优于两电极体系.据此提出实际毒性测定方法在电化学还原-氧化工艺降解氯酚类有机废水毒性测试的工业应用中有着广泛的前景.     

考虑公众选择偏好的应急避难安置双阶段选址-分配模型

为使开放避难场所符合公众自行避难的实际情况,借鉴Huff模型量化公众选择行为,构建双阶段选址-分配模型,第1阶段确定开放避难场所位置,第2阶段将溢出容量的灾民二次分配到有剩余容量的避难场所,并利用改进粒子群算法进行求解。研究结果表明：双阶段选址-分配模型能够实现同一需求点灾民前往不同避难场所的过程,管理者干预政策能够使服务人数大幅度增加,避免资源浪费、灾民流离失所且二次分配情况主要依赖于第1阶段的结果。研究结果可为管理部门规划应急避难场所提供参考。