The pollution halo effect of technology spillover and pollution haven effect of economic growth in agricultural foreign trade: two sides of the same coin?

Environmental Science and Pollution Research - The existing literature on the environmental Kuznets curve (EKC) fails to investigate the spatial attribute of the “pollution halo” effect...     

Ultrasound-assisted electrodeposition synthesis of nZVI-Pd/AC toward reductive degradation of methylene blue

Environmental Science and Pollution Research - A novel composite (nZVI/Pd-AC) was prepared by loading nanoscale zero-valent iron (nZVI) and Pd on activated carbon (AC) electrode under...     

Determination of the residue dynamics and dietary risk of thiamethoxam and its metabolite clothianidin in citrus and soil by LC-MS/MS

A modified quick, easy, cheap, effective, rugged and safe (QuEChERS) method was developed for the determination of thiamethoxam and its metabolite clothianidin in citrus (including the whole citrus, peel and pulp) and soil samples by liquid chromatography-tandem mass spectrometry. The sample was extracted with acetonitrile and purified with octadecylsilane. The detection limits of both compounds were 0.0001–0.0002?mg kg^–1, while the limit of quantification of thiamethoxam was 0.002?mg kg^–1 and the limit of quantitation of metabolites was 0.001?mg kg^–1. The recovery was 70.37%–109.76%, with inter-day relative standard deviations (RSD) (n?=?15) values ≤9.46% for the two compounds in the four matrices. The degradation curve of thiamethoxam in whole citrus and soil was plotted using the first-order kinetic model. The half-life of the whole citrus was 1.9–6.2?days, and the half-life of the soil was 3.9–4.2?days. The terminal residue of thiamethoxam (the sum of thiamethoxam and clothianidin, expressed as thiamethoxam) was found to be concentrated on the peel. The final residual amount of thiamethoxam in the edible portion (pulp) was less than 0.061?mg kg^–1. The risk quotient values were all below 1, indicating that thiamethoxam as a citrus insecticide does not pose a health risk to humans at the recommended dosage.     

Studies on polycyclic aromatic hydrocarbons in two sediment cores from the huaxi reservoir,china: Assessment of levels,sources, and ecological risk

This study investigated the levels, sources and ecological risks of 16 polycyclic aromatic hydrocarbons (PAHs) in two sediment cores that were collected along the Huaxi Reservoir. The spatial distributions and residue levels of the 16 priority PAHs in the sediments from the Huaxi Reservoir were analyzed for their potential ecological risk, source apportionment and contribution to the total PAH residue. The concentration level of the total PAHs (TPAHs) was in the range 1805 ng·g^?1 to 20023 ng·g^?1 based on dry weight, and the content of PAHs in the Huaxi Reservoir exhibited a gradual upward trend. The PAH congener ratios fluoranthene/(fluoranthene + pyrene) and indeno[1, 2, 3-cd]pyrene/(indeno[1, 2, 3-cd]pyrene + benzo[g, h, i]perylene) were used to identify the source. The main source of the low molecular weight PAHs was wood and coal combustion, whereas the high molecular weight PAHs were primarily from petroleum combustion sources. The results of an ecological risk assessment demonstrated that ACE poses a potential ecological risk, while FLU, NAP, ANT, BaP, DBA, PHEN and PYR can have serious ecological risks.     

湘江干流水环境质量演变特征及其关键因素定量识别

为科学有效地保护湘江流域水环境，定量识别湘江干流主要水质指标的驱动因素，该研究基于1990~2016年水质监测数据及沿岸永州 长沙五市社会经济发展指标，采用Mann-Kendall检验法分析湘江干流水环境演变趋势，通过逐步回归分析确定各地区各水质指标主要驱动因素。结果表明：湘江干流COD_Mn、Cd、As整体呈下降趋势，上游BOD₅呈下降趋势，上中游NH₃-N呈上升趋势，中游衡阳、株洲市重金属Cr⁶⁺呈上升趋势，衡阳市TP呈上升趋势，中下游BOD₅呈上升趋势；定量追溯各水质指标影响因素得出工业污染是湘江干流重金属As、Cr⁶⁺、Cd主要驱动因素，永衡株潭地区NH₃-N，衡阳市BOD₅、COD_Mn、TP及衡株潭地区BOD₅均以农业污染影响为主；发现产业结构调整对干流水环境有显著影响，建议在流域产业结构调整过程中加强转型升级。     

空调控温过程的系统动力学模拟分析

以房间、人员、设备和空调设备组成的空调控温系统为单元,以室温为目标,研究影响室温的各因素之间的关系,找出哪种因素是主要因素.运用Vensim软件建立空调控温系统的因果图和流图,并建立速率方程,进而进行模拟.根据模拟结果,对室温和温差进行分析,并探讨了空调调节系数、房子散热系数变动时对室温和波动时间的影响情况.验证了空调控温过程中室温的震荡过程和空调机发生作用的反应延迟时间.     

脆弱生态环境耦合下的贫困地区可持续发展研究

研究表明，中国贫困地区的分布与脆弱生态环境的分布存在一种地理空间意义上的耦合，这种耦合是一种非良性的耦合，存在着诸多问题并我着当地的社会经济发展，要改变这一现状，实现区域社会经济可持续发展，必须革新现有的贫困人口生存方式和社会经济发展模式，据此，本文提出了实现贫困地区社会经济可持续发展的战略措施应是依托现有的资源优势，推广生态农业技术，发展绿色食品和开展生态旅游。     

Destruction of Aspergillus versicolor,Penicillium chrysogenum,Stachybotrys chartarum,and Cladosporium cladosporioides spores using chemical oxidation treatment process

The survival of aqueous suspensions of Penicillium chrysogenum, Stachybotrys chartarum, Aspergillus versicolor, and Cladosporium cladosporioides spores was evaluated using various combinations of hydrogen peroxide and Fe²⁺ as catalyst. Spore concentrations of 10⁶–10⁷ colony forming units per milliliter (CFU/mL) were suspended in water and treated with initial hydrogen peroxide and iron concentrations ranging from 0.05 to 10 percent and 100 to 200 ppm, respectively. After four hours of reaction time, samples were plated on agar plates, and the viable fraction of spores was determined by the number of colonies formed. Hydrogen peroxide concentrations above 50,000 ppm resulted in greater than 6‐log₁₀ reduction of viable spores for both catalyzed and noncatalyzed reactions. Iron had a strong catalytic effect when added to solutions with hydrogen peroxide concentration above 5,000 ppm and resulted in two to three orders of magnitude greater reduction compared to hydrogen peroxide alone. Additional samples taken after 24 hours of reaction time showed that the effect of the addition of 100 and 200 ppm of Fe²⁺ catalyst was mostly kinetic, and noncatalyzed hydrogen peroxide had sporicidal effects similar to catalyzed hydrogen peroxide. This study identified initial reagent concentrations of hydrogen peroxide and Fe²⁺ that accomplish a 6‐log₁₀ reduction of viable mold spores within reaction times of 4 and 24 hours. © 2007 Wiley Periodicals, Inc.     

氯苯嘧啶醇在水体中的光解机制研究

以太阳光为实验光源研究了氯苯嘧啶醇在水溶液中的光解,考察了pH、水体类型、溶解氧及卤素离子等对其光解的影响.结果表明,氯苯嘧啶醇在水溶液中的光解符合一级动力学方程,在不同水体中氯苯嘧啶醇光解的速率大小顺序为:重蒸水>水库水>湖水>池塘水;氯苯嘧啶醇光解的半衰期随着溶液pH的增大而延长,当pH为5、7、9、11时光解半衰期分别为5.00、6.86、7.45、7.53 h;3种卤素离子对氯苯嘧啶醇光解有很大的影响,均表现出强的猝灭作用,3种离子的猝灭能力的大小顺序为Ⅰ->Br->Cl-;溶解氧和三重态光猝灭剂山梨酸均对氯苯嘧啶醇在水中的光解没有影响,而三重态光敏剂丙酮则对其光解有较强的猝灭作用,表明氯苯嘧啶醇在水中的光解主要以直接光解为主,光解过程不经历三重态.