介质材料在可渗透反应墙中的应用进展

可渗透反应墙正发展成为修复污染地下水技术的新方向,其中介质材料是可渗透反应墙成功修复污染地下水的关键。可渗透反应墙介质材料可以细分为还原型、吸附型、沉淀型和降解型介质材料等四类,并分别从不同类型的介质材料的反应机理、应用情况以及存在的问题等方面加以阐述。可渗透反应墙介质材料的选择应在其反应机理的基础上,结合实际的地下水环境条件、污染源、人类活动和经济费用等加以综合考虑,以保证可渗透反应墙长期有效经济安全地运行。     

Adsorption of humic acid from aqueous solution on bilayer hexadecyltrimethyl ammonium bromide-modified zeolite

Surfactant-modified natural zeolites (SMNZ) with different coverage types were prepared by loading hexadecyltrimethyl ammonium bromide (HTAB) onto the surface of a natural zeolite. The adsorption behavior of humic acid (HA) on SMNZ was investigated. Results indicate that the adsorbent SMNZ exhibited a higher affinity toward HA than the natural zeolite. HA removal efficiency by SMNZ increased with HTAB loading. Coexisting Ca²⁺ in solution favored HA adsorption onto SMNZ. Adsorption capacity decreased with an increasing solution pH. For typical SMNZ with bilayer HTAB coverage, HA adsorption process is well described by a pseudo-second-order kinetic model. The experimental isotherm data fitted well with the Langmuir model. Calculated maximum HA adsorption capacities for SMNZ with bilayer HTAB coverage at pH 5.5 and 7.5 were 63 and 41 mg·g⁻¹, respectively. E2/E3 (absorbance at 250 nm to that at 365 nm) and E4/E6 (absorbance at 465 nm to that at 665 nm) ratios of the residual HA in solution were lower than that of the original HA solution. This indicates that the HA fractions with high polar functional groups, low molecular weight (MW), and aromaticity had a stronger tendency for adsorption onto SMNZ with bilayer HTAB coverage. Results show that HTAB-modified natural zeolite is a promising adsorbent for removal of HA from aqueous solution.     

高灵敏度光度法测定地表水中硝酸盐和亚硝酸盐氮

本文详细研究了在硫酸介质中,邻苯氨基苯甲酸与NO_3~-和NO_2~-离子显色体系的光度性质与形成条件。结果表明,显色产物的最大吸收λ_(?)位于560—565nm。在此波长下,表观摩尔吸光系数分别为:ε′NO_3~-=1.07×10~5和ε′NO_2~-=1.77×10~5。符合Beer定律的浓度范围为:0.03—0.15 μg/ml(NO_2~--N)和0.05—0.20 μg/ml(NO_3~--N)。据此,拟定了分光光度联合训定NO_3~--N和NO_2~--N的新方法,应用于地表水的测定,得到了满意的结果。     

环境污染对生态危害经济损失风险评估模式的综述

从风险评价和环境经济学角度,综述了环境污染对生态环境危害经济报失的评估模式。     

废水监测分析的系统化问题

详细、全面地阐述了废水监测工作系统应具备的基本条件和设施及各个环节之间的协调配合关系,指出了该系统管理中应注意的主要问题。     

Improved product selectivity of electrochemical reduction of carbon dioxide by tuning local carbon dioxide concentration with multiphysics models

Environmental Chemistry Letters - Electrochemical reduction of carbon dioxide (CO2) is promising to alleviate carbon emissions and produce fuels and materials in a circular way, yet effective...     

A pyrazine based metal-organic framework for selective removal of copper from strongly acidic solutions

● pz-UiO-66 was synthesized facilely by a solvothermal method. ● Efficient capture of copper from highly acidic solution was achieved by pz-UiO-66. ● pz-UiO-66 exhibited excellent selectivity and capacity for copper capture. ● Pyrazine-N in pz-UiO-66 was shown to be the dominant adsorption site. The selective capture of copper from strongly acidic solutions is of vital importance from the perspective of sustainable development and environmental protection. Metal organic frameworks (MOFs) have attracted the interest of many scholars for adsorption due to their fascinating physicochemical characteristics, including adjustable structure, strong stability and porosity. Herein, pz-UiO-66 containing a pyrazine structure is successfully synthesized for the efficient separation of copper from strongly acidic conditions. Selective copper removal at low pH values is accomplished by using this material that is not available in previously reported metal–organic frameworks. Furthermore, the material exhibits excellent adsorption capacity, with a theoretical maximum copper uptake of 247 mg/g. As proven by XPS and FT-IR analysis, the coordination of pyrazine nitrogen atoms with copper ions is the dominant adsorption mechanism of copper by pz-UiO-66. This work provides an opportunity for efficient and selective copper removal under strongly acidic conditions, and promises extensive application prospects for the removal of copper in the treatment for acid metallurgical wastewater.     

Experimental study on pollutant movement in surf zone

The experiments on pollutant movement in surf zone were conducted on the two gentle beaches(with slope of 1:100 and 1:40, respectively), for diverse wave cases. The movement contours and direction of pollutants, under the action of regular and random waves with diverse wave amplitudes, were provided and studied in this paper. It was shown that, due to complicated hydrodynamics in surf zone, the pollutant movement state is quite complicated and different from that in pure current zone.     

H2O2处理酸性大红GR染料废水的研究

通过对废水pH值、H2O2用量、催化剂用量、反应时间、反应温度等工艺条件的考察,确定了H2O2催化氧化处理酸性大红染料废水的最佳工艺条件pH 4、H2O2用量6 mL/L、催化剂用量3 g/L、反应时间100 min、反应温度70℃.在该条件下,COD和色度的去除率分别为76.7%和99.4%;通过反应前后的紫外-可见光光谱分析表明,H2O2催化氧化处理酸性大红GR染料废水有比较好的效果,为该工艺处理酸性大红GR染料废水提供了科学依据.     

7种拟除虫菊酯农药对卤虫的急性毒性研究

为了研究7种拟除虫菊酯农药对美国大盐湖卤虫(GSL Artemia)的急性毒性效应,挑选18~24 h内孵出的卤虫,继续培养24 h后得到Ⅱ~Ⅲ龄卤虫无节幼体,将其暴露于所设浓度梯度的拟除虫菊酯溶液中进行24 h急性毒性实验,记录卤虫无节幼体在各浓度溶液中的死亡情况,并将所得数据进行Probit分析。结果表明,卤虫对不同拟除虫菊酯的敏感性相差较大。氯菊酯、氯烯炔菊酯、炔咪菊酯、胺菊酯、联苯菊酯、高效氯氟氰菊酯和溴氰菊酯对卤虫的24 h半致死浓度(24 h-LC50)分别为4.68、14.82、18.12、38.21、>100、>100和>100 mg.L-1。因此,在含有卤虫的盐水环境中,应尽量避免使用毒性较高的氯菊酯,而选择使用联苯菊酯、高效氯氟氰菊酯和溴氰菊酯等毒性较低的农药。