多场耦合作用下瓦斯与煤自燃协同预防数值模拟

为解决某综放面采用顶板巷与上隅角联合抽采方式可能引起的煤自燃及瓦斯爆炸等重大安全隐患问题,采用数值模拟从瓦斯、氧气体积分数分布特点和温度场角度综合分析合理顶板巷位置与抽采流量,为协同预防瓦斯和煤自燃复合灾害提供指导。结果表明:抽采口、上隅角瓦斯体积分数随抽采流量增加而降低;抽采流量100m3/min是影响氧化带宽度变化幅度的拐点;抽采流量对采空区最高温度的影响较大,对高温范围宽度影响较小;综合确定合理顶板巷位置为内错回风巷15 m,合理抽采流量为100~150 m~3/min;现场应用表明该方案既能解决瓦斯超限问题,又能有效控制煤自燃威胁,表明数值模拟具有较好的可靠性。     

Biofiltration and disinfection codetermine the bacterial antibiotic resistome in drinking water: A review and meta-analysis

• Published data was used to analyze the fate of ARGs in water treatment. • Biomass removal leads to the reduction in absolute abundance of ARGs. • Mechanism that filter biofilm maintain ARB/ARGs was summarized. • Potential BAR risks caused by biofiltration and chlorination were proposed. The bacterial antibiotic resistome (BAR) is one of the most serious contemporary medical challenges. The BAR problem in drinking water is receiving growing attention. In this study, we focused on the distribution, changes, and health risks of the BAR throughout the drinking water treatment system. We extracted the antibiotic resistance gene (ARG) data from recent publications and analyzed ARG profiles based on diversity, absolute abundance, and relative abundance. The absolute abundance of ARG was found to decrease with water treatment processes and was positively correlated with the abundance of 16S rRNA (r² = 0.963, p<0.001), indicating that the reduction of ARG concentration was accompanied by decreasing biomass. Among treatment processes, biofiltration and chlorination were discovered to play important roles in shaping the bacterial antibiotic resistome. Chlorination exhibited positive effects in controlling the diversity of ARG, while biofiltration, especially granular activated carbon filtration, increased the diversity of ARG. Both biofiltration and chlorination altered the structure of the resistome by affecting relative ARG abundance. In addition, we analyzed the mechanism behind the impact of biofiltration and chlorination on the bacterial antibiotic resistome. By intercepting influent ARG-carrying bacteria, biofilters can enrich various ARGs and maintain ARGs in biofilm. Chlorination further selects bacteria co-resistant to chlorine and antibiotics. Finally, we proposed the BAR health risks caused by biofiltration and chlorination in water treatment. To reduce potential BAR risk in drinking water, membrane filtration technology and water boiling are recommended at the point of use.     

全国大气背景地区黑碳浓度特征

分析了2015年14个背景站黑碳浓度水平及分布规律,结果表明:我国背景地区黑碳小时浓度均值呈现明显的对数正态分布特征,14个背景站880 nm波长时年均质量浓度为88.7~1 487.6 ng/m~3,小时最大峰值为685.0~13 731.0 ng/m~3,长岛和衡山相对较高;24 h日浓度变化基本呈现"单峰"状,但峰值出现时刻有所不同;工作日和周末的浓度变化趋势基本相似,但浓度高低与所在区域生产生活方式不同而有所差异。初步探讨了风速和风向与浓度污染水平的关系,相对风速而言,风向对黑碳的浓度影响较大,后向轨迹结果也印证了风向的影响。     

室内空气和灰尘中全(多)氟烷基化合物的研究进展

全(多)氟烷基化合物(per(poly)fluoroalkyl substances,PFASs)在环境各个介质及人体样品中广泛被检出,近年,在室内空气和灰尘中也普遍发现PFASs.研究表明,室内空气中PFASs的含量普遍高于室外空气,室内空气和灰尘中的PFASs可能是室外空气的污染来源及人体暴露源,因此室内环境中PFASs成为环境领域的又一个研究热点.但目前为止,我国还没有开展室内空气中PFASs的相关研究,室内灰尘中PFASs的研究也相对较少.本文就室内空气和灰尘中PFASs的采样与分析方法、污染现状、来源分析及人体暴露等4个方面进行了综合阐述,以期为我国室内环境中PFASs的研究提供参考.     

关于我国环境空气质量监测点位设置的思考

设置各种空气质量监测点位时,应以监测网络的监测目的为根本出发点,并同时考虑点位功能和空间代表尺度、点位环境条件以及实际经济技术条件等因素。一个完整的环境空气质量监测网络应涵盖各类功能的监测点位,从而达到监测网络建设的多目标要求,然而空气质量监测点位的建设是一个不断发展和完善的过程。目前我国城市空气质量监测点以空气质量评价点为主,其目的是掌握城市整体空气质量状况和长期变化趋势,为环境管理和污染防治提供决策依据,但这类监测点位的功能相对单一,难以满足公众了解详尽的空气质量状况信息的需求。未来,随着监测投入的增加,我国应进一步完善地方监测网络建设,使之涵盖不同功能的监测点位,从而更好地为公众提供空气质量预警信息和健康指引。     

营养条件对污水中小球藻生长及产能效应的影响

以过滤的富营养化的鱼塘废水为培养液,添加外源的碳、氮、磷元素,考察污水中不同的外源无机碳浓度、总氮浓度、总磷浓度对小球藻(Chlorella vulgaris)的生长、油脂含量和烃类含量的影响。在25℃、光照强度为4 500 Lux、光暗比为12L:12D的条件下培养10 d。单因子方差分析和多重比较结果表明:(1)以Na2CO3做碳源,小球藻生物量和烃类含量在外源无机碳浓度为6 mg/L时最高,油脂含量在外源无机碳浓度为12 mg/L最高。(2)以KNO3做氮源,小球藻生物量在总氮浓度为25 mg/L时最高,油脂含量在总氮浓度为15 mg/L时最高,烃含量在总氮浓度为20 mg/L时最高。(3)以KH2PO4做磷源,小球藻生物量和烃类含量在总磷浓度为2 mg/L时最高,油脂含量在总磷浓度为1.5 mg/L时最高。     

潮白河周丛生物群落元素组成与水质变化的生态计量学关系研究

研究了潮白河流域中污染水体对周丛生物群落的碳(C)、氮(N)、磷(P)元素含量以及生态计量组成的影响.结果表明,下游潮白河NH4+-N、NOx--N分别占TN的52%和28%;上游白河则分别占1.6%和38%.潮白河TP含量(0.104 mg.L-1)为白河TP含量(0.005 mg.L-1)的21倍.白河和潮白河周丛生物C、N、P元素的变异系数分别为0.55、0.41、0.62和0.24、0.13、0.18,表明生长于白河周丛生物的元素结构变化更大.无周丛生物的水体NH4+-N和TP的浓度分别为有周丛生物的21倍和11倍.通过对TOC、TN、NOx--N、NH4+-N、TP、pH、氧化还原电位(ORP)和电导率(conductivity)等水质指标进行二元Logistic回归分析得知,水体TP为影响潮白河周丛生物生存的主要因素,其预测正确率为87.3%.周丛生物C、N、P元素间有强相关性,其中N起了"桥梁"作用.生态计量学分析进一步显示周丛生物的N∶P的比值追随水体TN∶TP的变化;并且该比值主要受水体TP浓度影响.周丛生物N∶P可用于水体TN∶TP变化的生态计量学的指示因子.本研究为进一步探究周丛生物群落结构变化,以及对高一级营养级生物群落结构和元素循环的影响奠定了基础.     

太湖流域不同管理模式的社会经济环境系统演化模拟

基于复杂自适应系统理论构建了社会经济环境系统模型,采用计算实验方法模拟分析了太湖流域在经济优先和水环境保护优先2种管理模式下的动态演化过程,得到了农业与工业经济发展水平、就业状况和水环境改善情况的演化规律.结果表明,在综合考虑社会、经济、水环境的基础上,2种管理模式均能在一定程度上实现经济和就业的增长,同时改善水环境.环境保护优先模式虽能有效保护水环境,却会牺牲部分经济发展和就业保证.不同地区在演化过程中表现出差异性,常州和湖州经济获得较快增长;苏州、上海在就业方面做出较大贡献;无锡和苏州水环境改善效果最为明显.     

污泥中重金属处理技术的研究现状及发展趋势

随着世界各国经济迅速发展和人口的不断增长,污泥中重金属的污染已成为全球关注的热点问题之一,污泥中的重金属迫切需要综合整治。本文在对污泥中重金属处理技术概述的基础上,就近年来污泥中重金属的现状进行了分析,探讨出污泥中重金属处理技术的发展前景。     

Selective sorption of perfluorooctane sulfonate on molecularly imprinted polymer adsorbents

Perfluorooctane sulfonate (PFOS), as a potential persistent organic pollutant, has been widely detected in water environments, and has become a great concern in recent years. PFOS is very stable and difficult to decompose using conventional techniques. Sorption may be an attractive method to remove it from water. In this study, the molecularly imprinted polymer (MIP) adsorbents were prepared through the polymerization of 4-vinylpyridine under different preparation conditions in order to remove perfluorooctane sulfonate (PFOS) from water. The MIP adsorbents using perfluorooctanoic acid (PFOA) as the template had good imprinting effects and could selectively remove PFOS from aqueous solution. The sorption behaviors including sorption kinetics, isotherms, and effect of pH, salt, and competitive anions were investigated. Experimental results showed that the sorption of PFOS on the MIP adsorbents was very fast, pH-dependent, and highly selective. The achieved fast sorption equilibrium within 1 h was attributed to the surface sorption on the fine adsorbents. The sorption isotherms showed that the sorption selectivity of PFOS on the MIP adsorbents decreased at high PFOS concentrations, which may be due to the double-layer sorption and the formation of PFOS micelles on the sorbent surface. The sorption of PFOS on the MIP adsorbents was mainly dominated by the electrostatic interaction between the protonated vinylpyridine on the adsorbent surface and the anionic PFOS. The prepared MIP adsorbents can potentially be applied in water and wastewater treatment for selective removal of PFOS.