河流型油污染应急监测案例分析研究

以在湘江中下游发生的跨多市的油污染事故为例,详细阐述了对该污染事故开展应急监测的全过程,包括基本情况介绍、应急响应、应急监测方案编制、应急监测结果综合分析等内容;并针对该类型污染事故应急监测进行了管理和技术经验总结,包括强调多部门联合处置的必要性,摆正应急监测在应急中的正确位置,应急监测时信息流转通畅的关键作用,妥善开展应急处置的重要性以及明确应急处置责任主体等内容.     

基于种群、功能群对比分析洞庭湖浮游植物群落驱动因素及水质评价

浮游植物是水生态系统中最重要的组成部分,因其对水环境变化敏感而常被用于指示水环境状态,但其对环境的响应受分类方法的影响.为了解洞庭湖浮游植物种群(门、属)和功能群(FG)两种分类法对环境的驱动响应特征和适用性,于2019年3～12月分水期对该湖共进行了4次采样,比较分析了浮游植物种群和功能群的分布特征及其与环境因子的响应关系,并对比了TLI指数、 Shannon-Wiener指数、Q指数等评价方法在洞庭湖的适用性.结果表明,洞庭湖共检出浮游植物6门61属,可划分为23个功能群和9个优势功能群,功能群演替趋势为P/MP/D(3月)■月)■月)■(12月).层次分割结果表明,洞庭湖浮游植物的种群分布与变化受环境因子的驱动大于空间驱动;影响浮游植物种群和功能群的主要环境因子为水温(WT)、高锰酸盐指数、溶解氧(DO)、电导率(Cond)、水位(WL)和总磷(TP),环境因子对两者的独立解释性排序相差不大.RDA分析表明,浮游植物功能群对环境因子的响应要优于浮游植物种群.综合对比分析发现,利用Q指数进行水质评价在洞庭湖水体有较好的适用性.     

车人碰撞事故再现技术研究进展

车人碰撞事故再现已成为国内外研究热点,提高结果可信性为事故再现的核心。根据事故再现所需痕迹将再现方法分为6类,即"行人抛距"、"车辆制动距离"、"行人损伤"、"车辆变形"、"其他"以及"仿真"。通过分析各类方法的优缺点,提出可综合利用这些方法获得客观、可信的事故再现结果。然后探讨提高车人碰撞事故再现结果可信性的新发展方向:开发国产、高精度的事故再现软件,研究事故再现结果的不确定性问题,以及研究痕迹间关系在事故再现中的应用。而其中仿真所得事故再现结果的不确定性问题、车人碰撞事故再现区间不确定优化方法以及事故现场痕迹间关系为值得期待的新研究内容。     

施用农药人员的安全与防护——ASTMF2669《旋用农药人员用防护服性能标准》介绍

本文主要介绍了ASTMF2669-2009《施用农药人员用防护服性能标准》的分级和检测要求、防护服材料性能要求、材料的抗渗透性指标等,并就施药人员的安全与防护以及完善防护服标准体系提出建议．以为我国广大相关领域人员了解标准和应用标准提供帮助．     

Ag/TiO2光电催化降解染料及出水有机质影响机制

本研究以阳极氧化法结合电化学沉积法成功制备的具有高度整齐有序纳米管结构的Ag/TiO₂纳米管阵列（Ag/TNTAs）为阳极,碳/聚四氟乙烯为阴极构建光电催化（PEC）体系.并探究其光电催化降解甲基橙（MO）效能,结果表明,Ag/TNTAs光电催化降解能力（68.2%）远高于光催化（18.9%）、电化学氧化（38.2%）和直接光解;另外在水质净化厂出水有机质（EfOM）参与的光电体系中,当EfOM的初始浓度小于或等于1.0mgC/L时,其对光电催化降解MO起到促进作用,其中当其浓度为0.4mgC/L时促进作用最为明显.而高浓度的EfOM则抑制光电催化活性.此研究表明光电催化体系能高效催化染料降解,且EfOM能在一定阈值范围内促进光电催化降解污染物.     

分子模拟方法在爆炸反应机理方面的应用进展

针对爆炸过程反应机理异常复杂,实验检测手段对其认识匮乏的现状,综述了量子化学、反应分子动力学等分子模拟方法的特点及研究进展,分析了分子模拟技术在燃爆机理研究中的应用进展,包括量子化学方法对于燃料热解/燃烧、瓦斯等可燃体系爆炸过程的微观基元反应步骤、反应能垒及热力学参数的计算,以及反应分子动力学(ReaxFF MD)在含能材料、可燃混合气等复杂爆炸体系获取可能的反应路径及中间自由基变化的应用。对分子模拟方法在爆炸领域研究的应用提出了建议及展望,指出ReaxFF MD和密度泛函理论(DFT)相结合是一种研究复杂爆炸体系微观反应机理极具潜力的方法,借助先进的分析检测手段对模拟方法的验证及修正,能获取更准确、全面的微观反应动力学模型。     

Acid Orange 7 degradation using methane as the sole carbon source and electron donor

• AO7 degradation was coupled with anaerobic methane oxidation. • Higher concentration of AO7 inhibited the degradation. • The maximum removal rate of AO7 reached 280 mg/(L·d) in HfMBR. • ANME-2d dominated the microbial community in both batch reactor and HfMBR. • ANME-2d alone or synergistic with the partner bacteria played a significant role. Azo dyes are widely applied in the textile industry but are not entirely consumed during the dyeing process and can thus be discharged to the environment in wastewater. However, azo dyes can be degraded using various electron donors, and in this paper, Acid Orange 7 (AO7) degradation performance is investigated using methane (CH₄) as the sole electron donor. Methane has multiple sources and is readily available and inexpensive. Experiments using ¹³C-labeled isotopes showed that AO7 degradation was coupled with anaerobic oxidation of methane (AOM) and, subsequently, affected by the initial concentrations of AO7. Higher concentrations of AO7 could inhibit the activity of microorganisms, which was confirmed by the long-term performance of AO7 degradation, with maximum removal rates of 8.94 mg/(L·d) in a batch reactor and 280 mg/(L·d) in a hollow fiber membrane bioreactor (HfMBR). High-throughput sequencing using 16S rRNA genes showed that Candidatus Methanoperedens, affiliated to ANME-2d, dominated the microbial community in the batch reactor and HfMBR. Additionally, the relative abundance of Proteobacteria bacteria (Phenylobacterium, Pseudomonas, and Geothermobacter) improved after AO7 degradation. This outcome suggested that ANME-2d alone, or acting synergistically with partner bacteria, played a key role in the process of AO7 degradation coupled with AOM.     

Mutual effects of cadmium and phosphate on their adsorption and desorption by goethite

Adsorption of cadmium (Cd) and phosphate by oxides or soils has been extensively studied, but the adsorption/desorption kinetics and mutual effects of these two species in co-existing systems has received little attention. In this study, a batch equilibration method was used to investigate the effect of phosphate and its application time on Cd adsorption and desorption on goethite. The influence of Cd and its application time on phosphate sorption and desorption kinetics was also determined. For Cd adsorption, phosphate was introduced into the system by two sequences: pre-treating goethite at 40 (degrees)C for 1 week, and applying with Cd simultaneously. Similarly, for phosphate sorption, Cd was applied by pre-treating goethite at 40 (degrees)C for 1 week or simultaneous addition with phosphate. Results demonstrated that phosphate added to goethite enhanced Cd adsorption, and facilitated Cd release as compared to untreated goethite. Cadmium had slightly higher adsorption, but a significantly faster desorption rate from the goethite simultaneously treated with phosphate and Cd, as compared to phosphate-pretreated goethite. Cadmium and its application time had little impact on phosphate sorption by goethite. However, phosphate desorption kinetics was affected by Cd application time. When the sorption time was short (15 min), phosphate desorption was faster from the goethite that was simultaneously treated with phosphate and Cd, as compared to Cd pretreated or untreated goethite. In contrast, a longer sorption time (4 weeks) resulted in a higher desorption rate of phosphate from Cd pretreated goethite than simultaneously phosphate-Cd treated goethite. This study provided useful information on adsorption/desorption kinetics in complicated Cd-phosphate-goethite systems.     

A Highly Efficient Adsorbent Based on Starch-Graphene Oxide Architecture for Scavenging Aqueous Pb(II): Isotherms,Kinetics, Thermodynamics and Interaction Mechanism

Journal of Polymers and the Environment - Heavy metal pollution stems from the modern industry is a severe environmental problem. In this work, a highly efficient adsorbent based on starch-graphene...     

Semi-closed synthesis of nitrogen and oxygen Co-doped mesoporous carbon for selective aqueous oxidation

Heteroatom-doped meso/micro-porous carbon materials are conventionally produced by harsh carbonization under an inert atmosphere involving specific precursors, hard/soft templates, and heteroatom-containing agents. Herein, we report a facile synthesis of N and O co-doped meso/micro-porous carbon (NOMC) by template-free carbonization of a small-molecule precursor in a semi-closed system. The semi-closed carbonizaiton process yields hydrophilic NOMCs with large surface area in a high yield. The porous structure as well as the elemental composition of NOMCs can be modulated by changing the holding time at a particular temperature. NOMCs as metal-free heterogeneous catalysts can selectively oxidize benzyl alcohol and its derivatives into aldehydes/ketones with>85％conversion in aqueous solution, which is much higher than that of the control sample obtained in tube furnace (21％conversion), mainly due to their high N content, high percentage of pyridinic N, and large surface area. The presence of O-containing moieties also helps to improve the hydrophilicity and dispersion ability of catalysts and thus facilitates the mass transfer process during aqueous oxidation. The NOMC catalysts also dispayed excellent activity for a wide range of substrates with a selectivity of>99％.