有机酸与表面活性剂联合作用对土壤重金属的浸提效果研究

重金属污染土壤的原位淋洗修复既要实现对重金属的高效去除,还要尽量减少对土壤性质的破坏,这一点在农业污染土壤修复中尤为重要。以张士污灌区农田土壤为研究对象,利用振荡浸提技术筛选有机酸和表面活性剂组合,并确定了两者联合淋洗修复污染土壤的最佳配比。结果表明:有机酸(酒石酸、乙酸、柠檬酸和苹果酸)中的酒石酸浓度为0.5 mol.L-1和表面活性剂(SDBS、鼠李糖和皂素)中的皂素质量分数为0.7%时对土壤Cd、Pb、Zn的浸提效果较好;在酒石酸与皂素体积配比为1∶1时,对重金属Cd、Pb、Zn浸提效果最好,浸提率分别为87.62%、36.30%、20.67%;单一有机酸、表面活性剂或者有机酸与表面活性剂的混合溶液,对土壤重金属的浸提效果均为Cd>Pb>Zn。虽然有机酸与表面活性剂联合浸提效果略低于酒石酸浸提,但其弱酸性对土壤性质影响较小,在原位淋洗修复工程中有较好的应用前景。     

The energy-environment nexus: aerosol science and technology enabling solutions

Energy issues are important and consumption is slated to increase across the globe in the future. The energy-environment nexus is very important as strategies to meet future energy demand are developed. To ensure sustainable growth and development, it is essential that energy production is environmentally benign. There are two temporal issues??one that is immediate, and needs to address the environmental compliance of energy generation from fossil fuel sources; and second that is the need to develop newer alternate and more sustainable approaches in the future. Aerosol science and technology is an enabling discipline that addresses the energy issue over both these time scales. The paper is a review of aspects of aerosol science and engineering that helps address carbon neutrality of fossil fuels. Advanced materials to meet these challenges are discussed. Future approaches to effective harvesting of sunlight that are enabled by aerosol studies are discussed.     

Distribution and ecotoxicological significance of trace element contamination in a ~150 yr record of sediments in Lake Chaohu, Eastern China

This paper presents the concentrations, vertical profiles and possible sources of selected major and trace elements in a sediment core covering ～150 years of sedimentation in Lake Chaohu, eastern China. Element concentrations were measured by portable X-ray Fluorescence Spectroscopy (XRF) and were used to evaluate possible environmental consequences of the recent industrialization in China. Statistical analyses identify four groups: (1) organic carbon (OC), total nitrogen (TN), Pb, Zn, and As associated with the use of chemical fertilizers and pesticides; (2) Mn, Cr, Ni and Cu from industrial and mining activities; (3) Fe, Rb, K, Co, Ti and Ca influenced by post-depositional processes and land exploitation; and (4) Zr and Sr from the soil. The vertical profiles of elements placed in the first two groups show distinct increases in concentrations above depths of 20 cm (~1978), coincident with the timing of industrialization in China, and the anthropogenic-derived fluxes are higher than the lithogenic-derived fluxes over the last three decades. With the exception of Zr and Sr, association of the measured metals with organic carbon and nitrogen suggests that organic matter may act as a carrier phase. The geoaccumulation index (I(geo)) reveals increased contamination from elements in the first two groups in recent years. Element concentrations, compared with the Effects Range-Low (ERL) and Effects Range-Median (ERM) levels set by NOAA, suggest that adverse biological effects from Ni contamination are very likely.     

Efficient visible light photo-Fenton-like degradation of organic pollutants using in situ surface-modified BiFeO3 as a catalyst

The visible light photo-Fenton-like catalytic performance of BiFeO₃ nanoparticles was investigated using Methyl Violet (MV), Rhodamine B (RhB) and phenol as probes. Under optimum conditions, the pseudo first-order rate constant (k) was determined to be 2.21×10^-2, 5.56×10^-2 and 2.01×10^-2 min^-1 for the degradation of MV (30 μmol/L), RhB (10 μmol/L) and phenol (3 mmol/L), respectively, in the BiFeO₃-H₂O₂-visible light (Vis) system. The introduction of visible light irradiation increased the k values of MV, RhB and phenol degradation 3.47, 1.95 and 2.07 times in comparison with those in dark. Generally, the k values in the BiFeO₃-H₂O₂-Vis system were accelerated by increasing BiFeO₃ load and H₂O₂ concentration, but decreased with increasing initial pollutant concentration. To further enhance the degradation of pollutants at high concentrations, BiFeO₃ was modified with the addition of surface modifiers. The addition of ethylenediamineteraacetic acid (EDTA, 0.4 mmol/L) increased the k value of MV degradation (60 μmol/L) from 1.01×10^-2 min^-1 in the BiFeO₃-H₂O₂-Vis system to 1.30 min^-1 in the EDTA-BiFeO₃-H₂O₂-Vis system by a factor of 128. This suggests that in situ surface modification can enable BiFeO₃ nano-particles to be a promising visible light photo-Fenton-like catalyst for the degradation of organic pollutants.     

Advanced oxidation of bromide-containing drinking water：A balance between bromate and trihalomethane formation control

Addition of H2O2 has been employed to repress bromate formation during ozonation of bromide-containing source water. However, the addition of H2O2 will change the oxidation pathways of organic compounds due to the generation of abundant hydroxyl radicals, which could affect the removal efficacy of trihalomethane precursors via the combination of ozone and biological activated carbon （O3-BAC）. In this study, we evaluated the effects of H2O2 addition on bromate formation and trihalomethane formation potential （THMFP） reduction during treatment of bromide-containing （97.6-129.1 μg/L） source water by the O3-BAC process. At an ozone dose of 4.2 mg/L, an H2O2/O3 （g/g） ratio of over 1.0 was required to maintain the bromate concentration below 10.0 μg/L, while a much lower H2O2/O3 ratio was sufficient for a lower ozone dose. An H2O2/O3 （g/g） ratio below 0.3 should be avoided since the bromate concentration will increase with increasing H2O2 dose below this ratio. However, the addition of H2O2 at an ozone dose of 3.2 mg/L and an H2O2/O3 ratio of 1.0 resulted in a 43% decrease in THMFP removal when compared with the O3-BAC process. The optimum H2O2/O3 （g/g） ratio for balancing bromate and trihalomethane control was about 0.7-1.0. Fractionation of organic materials showed that the addition of H2O2 decreased the removal efficacy of the hydrophilic matter fraction of DOC by ozonation and increased the reactivity of the hydrophobic fractions during formation of trihalomethane, which may be the two main reasons responsible for the decrease in THMFP reduction efficacy. Overall, this study clearly demonstrated that it is necessary to balance bromate reduction and THMFP control when adopting an H2O2 addition strategy.     

Influence of reactivation on the electrochemical performances of activated carbon based on coconut shell

Coconut shell-based activated carbon (AC) were prepared by CO₂ activation, and then the ACs with higher mesopore ratio were obtained by steam activation and by impregnating iron catalyst followed by steam activation, respectively. The AC with the highest mesopore ratio (AC_hmr) shows superior capacitive behavior, power output and high-frequency performance in supercapacitors. The results should attribute to the connection of its wide micropores and mesopores larger than 3 nm, which is more favorable for fast ionic transportation. The pore size distribution exhibits that the mesopore ratios of the ACs are significantly increased by reactivation of steam or catalyst up to 75% and 78%, respectively. As evidenced by cyclic voltammetry, electrochemical impedance spectroscopy, and galvanostatic measurements, the AC_hmr shows superior capacitive behaviors, conductivity and performance of electrolytic ionic transportation. The response current densities are evidently enhanced through the cyclic voltammery test at 50 mV/sec scan rate. The electrochemical impedance spectroscopy demonstrates that the conductivity and ion transport performance of the ACs are improved. The specific capacitances of the ACs were increased from 140 to 240 F/g at 500 mA/g current density. The AC_hmr can provide much higher power density while still maintaining good energy density, and demonstrate excellent high-frequency performances. The pore structure and conductivity of the AC_hmr also improve the cycleability and self-discharge of supercapacitors. Such AC_hmr exhibits a great potential in supercapacitors, particularly for applications where high power output and good high-frequency capacitive performances are required.     

Influence of reactivation on the electrochemical performances of activated carbon based on coconut shell

Coconut shell-based activated carbon (AC) were prepared by CO₂ activation, and then the ACs with higher mesopore ratio were obtained by steam activation and by impregnating iron catalyst followed by steam activation, respectively. The AC with the highest mesopore ratio (AC_hmr) shows superior capacitive behavior, power output and high-frequency performance in supercapacitors. The results should attribute to the connection of its wide micropores and mesopores larger than 3 nm, which is more favorable for fast ionic transportation. The pore size distribution exhibits that the mesopore ratios of the ACs are significantly increased by reactivation of steam or catalyst up to 75% and 78%, respectively. As evidenced by cyclic voltammetry, electrochemical impedance spectroscopy, and galvanostatic measurements, the AC_hmr shows superior capacitive behaviors, conductivity and performance of electrolytic ionic transportation. The response current densities are evidently enhanced through the cyclic voltammery test at 50 mV/sec scan rate. The electrochemical impedance spectroscopy demonstrates that the conductivity and ion transport performance of the ACs are improved. The specific capacitances of the ACs were increased from 140 to 240 F/g at 500 mA/g current density. The AC_hmr can provide much higher power density while still maintaining good energy density, and demonstrate excellent high-frequency performances. The pore structure and conductivity of the AC_hmr also improve the cycleability and self-discharge of supercapacitors. Such AC_hmr exhibits a great potential in supercapacitors, particularly for applications where high power output and good high-frequency capacitive performances are required.     

Heavy metal contamination in surface sediments from lakes and their surrounding topsoils of China

Environmental Science and Pollution Research - Due to rapid urbanization, industrialization, agricultural development, and mining activities, soil heavy metal pollution has become a severe issue in...     

Nexus between green logistic operations and triple bottom line: evidence from infrastructure-led Chinese outward foreign direct investment in Belt and Road host countries

Environmental Science and Pollution Research - The Belt and Road initiative (BRI) mainly relies on the traditional and underdeveloped logistical trade routes including the terrestrial and oceanic...     

小城镇发展与耕地保护

在分析小城镇发展过程中耕地保护的重要性的基础上 ,从土地供给和需求两个方面对小城镇外延扩张的机制进行了探讨。从土地供给来看 ,城镇土地对其供给主体具有四重效用 ,土地供给主体有多供地的内在动机 ;从土地需求来看 ,小城镇土地对其需求主体具有双重效用 ,土地需求主体有多占地的内在动机。若对土地供、需主体的行为缺乏有效约束 ,就会导致小城镇盲目向外扩张而使耕地大量减少。因此 ,要在小城镇发展过程中保护好耕地 ,就应建立有效的管理机制 ,对土地供、需主体的行为进行约束。最后提出了在小城镇发展过程中保护耕地的对策和措施