NaOH改性鱼骨粉材料对Cd(II)的吸附

以鱼骨粉（FBM）为原料,利用NaOH处理制备高性能改性鱼骨粉材料（FBM_T）,通过比表面积仪（BET）、X射线衍射仪（XRD）、傅里叶红外光谱（FTIR）、扫描电镜-光电子能谱（SEM-EDS）、透射电镜（TEM）等手段对吸附前后材料形貌、孔结构、功能基团进行表征分析.结果表明,与FBM相比,FBM_T出现一定数目中孔和大孔,具备了高孔容和平均孔径,分别增加68.57%和24.69%.FBM_T材料表面-OH、C=O和PO₄^3-等官能团含量增加,显示出一定的缓冲性能.FBM和FBM_T对Cd（Ⅱ）的吸附经历快速的分配和慢速的吸附两个阶段,符合准二级动力学模型,相关系数R²分别达到0.8635及0.9480.Langmuir模型较好地拟合FBM和FBM_T对Cd（Ⅱ）的等温吸附过程,对Cd（Ⅱ）饱和吸附量由改性前的9.28mg/g增至改性后的22.47mg/g,对应的吸附强度K_F值也随之增加.分离因子0 < R_L < 1表明Cd（Ⅱ）的去除过程为有利吸附.功能材料与Cd（Ⅱ）的作用机理主要包括阳离子专性吸附、静电吸附、离子交换、表面络合及沉淀作用.以上研究为鱼骨粉修复Cd污染提供一种经济有效的方法.     

白鲢罗非鱼对微囊藻毒素急性、亚急性毒性响应

为了探究不同控藻鱼类对产毒微囊藻的适应机制,为生物操纵的鱼种选择提供依据,研究了白鲢和罗非鱼对微囊藻毒素（MC）的生物富集、降解,及两种鱼对毒素的抗性、解毒机制的差异性.结果发现：在喂食微囊藻实验中,白鲢、罗非鱼对MC日摄入量达到10mg/kg,2种鱼均对MC有较强抗性.微囊藻经鱼摄入后,MC总含量在白鲢、罗非鱼粪便中分别下降到71.5%、6.0%,罗非鱼对MC降解能力远高于白鲢.白鲢和罗非鱼的肝系数分别从（1.19±0.21）%、（2.24±0.19）%下降到（0.79±0.06）%、（1.72±0.07）%,均表现出显著差异性下降（P<0.05）.微囊藻毒素在白鲢、罗非鱼肌肉中积累量分别为（1.57±0.31）μg/kg、（10.81±6.52）μg/kg （鲜重）、肝脏中积累量分别为（4.28±1.64）mg/kg、（2.48±0.15）mg/kg （鲜重）.MC在白鲢、罗非鱼肌肉、肝脏中的积累量均存在显著差异性（P<0.05）.罗非鱼肌肉中毒素含量是白鲢的6.9倍.在微囊藻毒素LR （MC-LR）对白鲢和罗非鱼的急性毒性效应实验中,MC-LR对白鲢、罗非鱼的LD₅₀为270和790μg/kg,罗非鱼对毒素有更强耐受性.喂食毒藻和i.p.注射MC均导致白鲢和罗非鱼肝细胞内脂滴大量出现.2种鱼在MC-LR注射后,谷胱甘肽（GSH）含量均表现出6h内明显下降.6h后两种鱼GSH含量均逐步回升,二者差异显著（p<0.05）.实验结果表明,罗非鱼对MC降解能力远高于白鲢.白鲢主要摄食群体微囊藻的群体胶鞘和附着细菌,胞内微囊藻毒素释放量小,白鲢这种摄食机制导致它能以产毒微囊藻为食而受到较轻危害.罗非鱼体内消化酶对微囊藻和MC具较强的消化降解能力;GSH含量及相关酶活性水平高,对体内毒素清除效率高.从食用安全性角度出发,与罗非鱼相比,白鲢是更适合用于控制蓝藻水华的鱼种,可广泛应用于蓝藻水华控制中.     

大气中有机硫酸酯研究进展

介绍了国内外大气环境中有机硫酸酯（OSs）的研究现状,分别简述了OSs的理化特征及影响因素、不同分析方法及对应特征、OSs的分类、来源及形成机制、OSs在大气中的转化及归趋等内容,并对目前常见的OSs分子式和结构式以及三种典型的形成机制进行了归纳总结.聚焦目前OSs研究的前沿领域,探讨了目前OSs研究中有待解决的热点问题,并对未来的研究工作提出建议与展望.     

Monitoring biofouling based on aerobic respiration in reverse osmosis system

A monitoring method of biofouling in reverse osmosis (RO) system was proposed based on the fluorescent signal of resorufin, which is reduced by nicotinamide adenine dinucleotide released from viable cells during aerobic respiration. The fluorescent signal of resorufin reduced by planktonic cells and microorganisms of biofilm showed linearity, indicating its feasibility to monitor biofouling in a RO system. For the application of the method to the lab-scale RO system, the injection concentration of resazurin and the injection flow rate were optimized. Biofilm on RO membranes continuously operated in a lab-scale RO system was estimated by resorufin fluorescence under optimized detection condition. As a result, resorufin fluorescence on RO membrane showed a significant increase in which the permeability of RO system decreased by 30.48%. Moreover, it represented the development of biofilm as much as conventional biofilm parameters such as adenosine triphosphate, extracellular polymeric substances, and biofilm thickness. The proposed method could be used as a sensitive and low-cost technology to monitor biofouling without autopsy of membranes.     

紫外活化过硫酸盐降解二苯甲酮-4的动力学影响及降解机理与风险评价

活化PS（过硫酸盐）氧化工艺对于降解水中新兴微污染物具有潜在应用价值.为研究活化PS体系对BPs（二苯甲酮类）有机防晒剂的降解性能,以BP4（二苯甲酮-4）为研究对象,采用UV/PS（紫外活化过硫酸盐）工艺降解BP4,比较单一UV、单一PS和UV/PS 3种工艺对BP4的去除效果,考察各因素对UV/PS工艺去除BP4动力学的影响,同时探究BP4降解机理并进行风险评价.结果表明:BP4降解过程符合准一级反应动力学模型;最佳PS投加量为1.0 mmol/L,反应30 min后BP4去除率可达94%,增加PS投加量或降低初始c（BP4）均可促进BP4降解,无机阴离子（HCO₃-和Cl-）对BP4降解均有抑制作用,酸性条件有利于BP4降解;基于HPLC-MS/MS鉴定出8种中间产物,并提出降解路径,费氏弧菌毒性试验和ECOSAR v1.10软件预测表明,UV/PS工艺降解BP4过程中生成的中间产物比母物质毒性更高.研究显示,UV/PS工艺可有效去除BP4,但其中间产物可能会造成潜在的生态风险,后续需进一步深入研究.      

Novel chitosan–ethylene glycol hydrogel for the removal of aqueous perfluorooctanoic acid

It is urgent to explore an effective removal method for perfluorooctanoic acid (PFOA) due to its recalcitrant nature. In this study, a novel chitosan-based hydrogel (CEGH) was prepared with a simple method using chitosan and ethylene glycol through a repeated freezing–thawing procedure. The adsorption of PFOA anions to CEGH agreed well to the Freundlich–Langmuir model with a maximum adsorption capacity as high as 1275.9?mg/g, which is higher than reported values of most adsorbents for PFOA. The adsorption was influenced by experimental conditions. Experimental results showed that the main removal mechanism was the ionic hydrogen bond interaction between carbonyl groups (COO^?) of PFOA and protonated amine (NH⁺) of the CEGH adsorbent. Therefore, CEGH is a very attractive adsorbent that can be used to remove PFOA from water in the future.     

我国PM2.5与臭氧污染协同控制策略研究

近年来,我国大气污染格局发生了深刻变化,PM_2.5与臭氧（O₃）成为影响我国城市和区域空气质量的主要空气污染物,二者协同控制已成为我国空气质量改善的焦点和打赢蓝天保卫战的关键.PM_2.5与臭氧之间具有复杂的关联性,使得二者的协同控制具有复杂性与艰巨性.分析了PM_2.5与臭氧成因的关联性及其相互影响,阐明了PM_2.5与臭氧污染协同控制所涉及的重要科学问题,并在此基础上研究了目前我国PM_2.5与臭氧的污染形势及二者的关联性,梳理了我国自2013年以来在PM_2.5与臭氧污染控制中已采取的重要举措,论述了目前我国PM_2.5与臭氧协同控制在科学与管理上所面临的挑战.结合对国外成功经验的分析,提出推进我国PM_2.5与臭氧污染协同控制工作的相关建议:①加快监测能力建设,完善管理体系;②强化科技支撑,提高PM_2.5与臭氧污染控制精准性;③加快构建VOCs与NO_x治理技术体系;④加大VOCs与NO_x的协同减排力度,保障减排方案落实到位.      

Characteristics of one-year observation of VOCs, NOx, and O3 at an urban site in Wuhan, China

A continuous online observation of ozone and its precursors(NOx, VOCs) was carried out in central urban Wuhan from September 2016 to August 2017. The concentration levels of ozone,NOx, VOCs and their variations in urban Wuhan were analyzed, as well as effects of VOCs on ozone photochemical generation and the main controlling factors for ozone production. During the observation period, the average concentrations of ozone and NOx in Wuhan was 22.63 and30.14 ppbv, respectively, and the average concentration of VOCs was 32.61 ppbv(42.3% alkanes,13.0% alkenes, 10.0% aromatics, 7.3% acetylene, 9.9% OVOCs, and 10.5% halohydrocarbons).Ozone concentration was higher in spring and summer as compared with autumn and winter,wheras VOCs and NOx concentratios were lower in spring and summer but higher in autumn and winter. Aromatics and alkenes, two of VOCs species, showed the highest contributions to ozone formation potential in Wuhan(35.7% alkenes, 35.4 aromatics, 17.5% alkanes, 8.6% OVOCs,1.6% halogenated hydrocarbons, and 1.4% acetylene). Among all VOCs species, those with the highest contribution were ethylene, m-xylene, toluene, propylene and o-xylene. The contribution of these five compounds to the total ozone formation potential concentration was 43.90%.Ozone-controlling factors in Wuhan changed within one day; during the early morning hours(6:00–9:00), VOCs/NOx was low, and ozone generation followed a VOCs-limited regime.However, during the peak time of ozone concentration(12:00–16:00), the ratio of VOCs/NOx was relatively high, suggesting that ozone generation followed a NOx-limited regime.     

Influence of metal ions on sulfonamide antibiotics biochemical behavior in fiber coexisting system

Metal ions and fiber are common compounds in the livestock and poultry manure,which will affect the fate of organic compounds in aqueous environment. However,limited research has addressed the effect of coexisting metal ions and fiber on the biodegradation of sulfonamide antibiotics. Accordingly, a compositing study was performed to assess the effect of metal ions(Fe3+and Cu2+) on the biodegradation of sulfadimethoxine sodium salt(SDM) in the presence of fiber. The enhanced adsorption of SDM onto fiber in the presence of metal ions can be attributed to the π+–π electron donor acceptor(EDA) interaction. The microbial(Phanerochaete chrysosprium) could easily attach onto fiber forming attached microbial, and the degradation rates of SDM of immobilized bacteria in the presence of Fe3 +were 100%, which were significantly higher than those of free bacteria(45%). This study indicates that Fe3 +and fiber could enhance the biodegradation of SDM. Fiber acts as adsorbent, carrier, and substrate which enhanced the removal of SDM.     

Brominated dioxins and furans in a cement kiln co-processing municipal solid waste

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).