环境风险评价内涵与外延研究

在简要介绍环境风险评价(Environmental Risk Assessment,ERA)发展历程的基础上,总结现阶段国内外普遍采用的ERA定义,深入分析ERA的内涵和类型,在重新给出涵盖性更全面的ERA定义的同时,对3种评价内容的评价程序和评价方法进行了横向比较。收集整理了ERA的研究进展和应用现状,从时间、范畴和应用范围3个方面划定了ERA的外延。     

防护鞋靴有害物质限量值研究

本文对防护鞋靴有害物质限量值研究进行了阐述。参考国内外标准,设定防护鞋靴有害物质限制项目和限量值。在检测分析我国具有市场代表性的16个防护鞋靴产品中有害物质含量数据基础上,判断设定限制项目及限量值的可行性。检测结果表明我国防护鞋靴生产技术水平基本能够达到限量要求,设定的限量值可以作为制定国家标准的参考依据。     

微囊藻毒素-LR对鸡肝脏的氧化损伤影响

蓝藻虽然能产生有毒的生物毒素,但是也含有较高的蛋白质。为探索蓝藻饲料化利用的可能性,本文通过腹腔注射的方式研究了微囊藻毒素-LR(MC-LR)对崇仁麻鸡的半数致死剂量(LD_(50))及其对肝脏的氧化损伤。实验设计了4个剂量组(对照组、5、10和20μg·kg~(-1)MC-LR),并在1、3、12、24和48 h检测了谷胱甘肽(GSH)含量以及谷胱甘肽S-转移酶(GST)、谷胱甘肽过氧化物酶(GPX)、超氧化物歧化酶(SOD)和过氧化氢酶(CAT)活性变化。结果表明,MC-LR对崇仁麻鸡的LD_(50)值为34.67μg·kg~(-1)体重(bw),95%的置信限为33.51～35.83μg·kg~(-1)bw。在MC-LR的作用下,鸡肝出现了氧化应激现象。3个染毒组鸡肝中GSH含量呈现先下降而后上升恢复至正常水平的趋势,GST酶活力表现为先上升而后下降至正常值的趋势,这说明GSH和GST共同参与了鸡肝中MC-LR的解毒;鸡肝中GPX酶活性在前3小时先保持不变(除了1 h的高剂量组),随即显著上升,这说明GPX和GSH共同参与了鸡肝中过量活性氧自由基(ROS)的清除,GPX可以作为监测MC-LR引起鸡毒性作用的生物标志物。CAT酶活力表现为先显著下降(P<0.05)而后快速上升至正常值的趋势,SOD酶在整个实验期间几乎保持稳定,这可能与SOD酶活性较高所致。     

洪水泥石流等自然灾害对旅游景区的破坏作用研究

通过泥石流灾害模拟模型与灾害损失率计算方法了解旅游景区的损失状况,研究自然灾害对旅游景区的破坏作用。旅游景区洪灾模拟模型由分流模型与汇流模型构成,根据泥石流多相流成分中固液两相分离原则构建泥石流分流模型;引用DEM数据得到泥石流流域栅格的汇流方向,根据经验模型计算汇流用时,采用八方向方法获取河道信息,基于这些数据构建泥石流模拟的汇流模型,采用ArcGis软件实时呈现该模型的泥石流灾害模拟效果;结合ArcGis软件显示的灾情数据,采用洪灾损失率计算方法获取旅游景区自然灾害损失率。实验结果表明,该模型计算旅游景区建筑损失率误差均小于5%,在有效模拟泥石流灾害的同时,可准确描述自然灾害对旅游景区的破坏作用。     

Degradation of antipyrine in the Fenton-like process with a La-doped heterogeneous catalyst

A La-doped Co-Cu-Fe catalyst was synthesized for the antipyrine (ANT) removal. The La-doped catalyst had higher ANT removal than the control (95% vs. 54%). La reduced the particle size and increased the specific surface area of catalyst. The aim of this study was to synthesize a novel lanthanum (La) doped catalyst and to investigate antipyrine removal in wastewater using the Fenton-like process with the catalyst. The La-doped Co-Cu-Fe catalyst was synthesized using the modified hydrothermal method. Results showed that the La-doped catalyst had higher specific surface area and lower particle size than the catalyst without La doping (i.e., the control) (267 vs. 163 m²/g and 14 vs. 32 nm, respectively). Under the conditions of catalyst dosage 0.5 g/L, H₂O₂ concentration 1.70 g/L, and NaHCO₃ 0.1 g/L, the antipyrine removal within 60 min using the Fenton-like process with the La-doped catalyst was much higher than that with the control (95% vs. 54%). The hydroxyl radical concentration with the La-doped catalyst within 60 min was two times higher than that with the control (49.2 vs. 22.1 mg/L). The high catalytic activity of La-doped catalyst was mainly attributed to its high specific surface area based on the X-ray photoelectron spectroscopy result. Our La-doped catalyst should have great potential to remove antipyrine in wastewater using the heterogeneous Fenton-like process.     

Reaction mechanism of arsenic capture by a calcium-based sorbent during the combustion of arsenic-contaminated biomass: A pilot-scale experience

Pilot-scale combustion is required to treat arsenic-enriched biomass in China. CaO addition to arsenic-enriched biomass reduces arsenic emission. CaO captures arsenic via chemical adsorption to form Ca₃(AsO₄)₂. Large quantities of contaminated biomass due to phytoremediation were disposed through combustion in low-income rural regions of China. This process provided a solution to reduce waste volume and disposal cost. Pilot-scale combustion trials were conducted for in site disposal at phytoremediation sites. The reaction mechanism of arsenic capture during pilot-scale combustion should be determined to control the arsenic emission in flue gas. This study investigated three Pteris vittata L. biomass with a disposal capacity of 600 kg/d and different arsenic concentrations from three sites in China. The arsenic concentration in flue gas was greater than that of the national standard in the trial with no emission control, and the arsenic concentration in biomass was 486 mg/kg. CaO addition notably reduced arsenic emission in flue gas, and absorption was efficient when CaO was mixed with biomass at 10% of the total weight. For the trial with 10% CaO addition, arsenic recovery from ash reached 76%, which is an ~8-fold increase compared with the control. Synchrotron radiation analysis confirmed that calcium arsenate is the dominant reaction product.     

Phosphorus adsorption by functionalized biochar: a review

Environmental Chemistry Letters - Phosphorus is essential element for agricultural production, yet phosphorus ore resources are non-renewable and become depleted. Moreover, phosphate release from...     

Research status and future challenge for CO2 sequestration by mineral carbonation strategy using iron and steel slag

Environmental Science and Pollution Research - Mineral carbonation can simultaneously realize the effective treatment of CO2 and iron and steel slag; thus, it is of great significance for the low...     

Personal exposure to PM2.5-bound heavy metals associated with cardiopulmonary function in general population

Environmental Science and Pollution Research - To better understand the cardiopulmonary alterations associated with personal exposed PM2.5-bound heavy meals, we conducted a cross-sectional study in...     

In situ electron-induced reduction of NOx via CNTs activated by DBD at low temperature

• An in situ electron-induced deNO_x process with CNT activated by DBD was achieved. • Carbon atoms on CNT surface were verified to be excited by plasma in DBD-CNT system. • Reactions between NO_x and excited C result in synergistic effect of DBD-CNT system. In this study, a new in situ electron-induced process is presented with carbon nanotubes (CNTs) as a reduction agent activated by dielectric barrier discharge (DBD) for nitrogen oxide (NO_x) abatement at low temperature (<407 K). Compared with a single DBD system and a DBD system with activated carbon (DBD-AC), a DBD system with carbon nanotubes (DBD-CNT) showed a significant promotion of NO_x removal efficiency and N₂ selectivity. Although the O₂ content was 10%, the NO_x conversion and N₂ selectivity in the DBD-CNT system still reached 64.9% and 81.9% at a specific input energy (SIE) of 1424 J/L, and these values decreased to 16.8%, 31.9% and 43.2%, 62.3% in the single DBD system and the DBD-AC system, respectively. X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM) were utilized to investigate surface changes in the CNTs after activation by DBD to explore the NO_x reduction abatement mechanism of this new process. Furthermore, the outlet gas components were also observed via Fourier transform infrared spectroscopy (FTIR) to help reveal the NO_x reduction mechanism. Experimental results verified that carbon atoms excited by DBD and the structure of CNTs contributed to the synergistic activity of the DBD-CNT system. The new deNO_x process was accomplished through in situ heterogenetic reduction reactions between the NO_x and carbon atoms activated by the plasma on the CNTs. In addition, further results indicated that the new deNO_x process exhibited acceptable SO₂ tolerance and water resistance.