施用石灰对酸性土壤中氧化亚氮形成的影响

对酸性红壤施用石灰和N2O生成之间的关系进行了探讨。结果表明,在好气条件下,石灰的施用与NH4＋氧化过程中N2O的产生量之间的关系不明显。但随着石灰施用量的增加,厌气条件下NO3－还原过程中N2O的积累量明显增加了,这与施用石灰后土壤pH升高而提高了硝酸还原酶活性有关。试验还表明,尽管在厌气条件下土壤pH较高有利于NO3－还原成NO2－,但当缺乏有效碳源时,NO2－向N2O的进一步还原受到限制,易发生NO2－的积累。     

对燃气轮机发电厂NOx排放执行标准问题的探讨

针对实际工作中,燃气轮机发电厂ＮＯｘ排放情况,就燃气轮机发电厂执行大气污染物排放标准问题进行了讨论。     

纳米银在水环境中的环境行为和毒性效应研究进展

纳米材料的环境行为和生态效应是目前国内外研究的热点,其中纳米银颗粒(Ag NPs)是使用量最高的纳米材料。本文主要总结了Ag NPs在水环境中的赋存、Ag NPs的环境行为、Ag NPs对不同种类微生物的毒性效应以及影响Ag NPs毒性效应的因素,最后对Ag NPs在河口区的研究进行了展望。     

Electroconductive RGO-MXene membranes with wettability-regulated channels: improved water permeability and electro-enhanced rejection performance

● Electroconductive RGO-MXene membranes were fabricated. ● Wettable membrane channels were established between RGO and MXene nanosheets. ● Hydrophilic MXene reduces the resistance of water entering the membrane channels. ● Water permeance of RGO-MXene membrane is 16.8 times higher than that of RGO membrane. ● Electro-assistance can enhance the dye rejection performance of RGO-MXene membrane. Reduced graphene oxide (RGO) membranes are theoretically more conducive to the rapid transport of water molecules in their channels compared with graphene oxide (GO) membranes, as they have fewer oxygen-containing functional groups and more non-oxidized regions. However, the weak hydrophilicity of RGO membranes inhibits water entry into their channels, resulting in their low water permeability. In this work, we constructed wettable RGO-MXene channels by intercalating hydrophilic MXene nanosheets into the RGO membrane for improving the water permeance. The RGO-MXene composite membrane exhibits high pure water permeance of 62.1 L/(m²·h·bar), approximately 16.8 times that of the RGO membrane (3.7 L/(m²·h·bar)). Wettability test results and molecular dynamics simulations suggest that the improved water permeance results from the enhanced wettability of RGO-MXene membrane and increased rate of water molecules entering the RGO-MXene channels. Benefiting from good conductivity, the RGO-MXene membrane with electro-assistance exhibits significantly increased rejection rates for negatively charged dyes (from 56.0% at 0 V to 91.4% at 2.0 V for Orange G) without decreasing the permeate flux, which could be attributed to enhanced electrostatic repulsion under electro-assistance.     

氧化锌脱硫技术研究进展

在分析了无机硫化物、有机硫化物脱硫机理的基础上,着重探讨了氧化锌脱硫技术存在的问题及国内外的研究现状。针对氧化锌脱硫剂在中温、高温脱硫时稳定性较差、低温硫容低、再生温度高导致脱硫活性下降、脱硫过程未实现无害化等问题,提出了研制纳米氧化锌脱硫剂是提高氧化锌脱硫技术水平的研究方向。     

微波辐射在二氧化锰诱导下对六氯苯污染土壤的修复研究

以二氧化锰为微波吸附剂,在密封体系中研究了微波辐射技术对六氯苯污染土壤的修复效果。分别以不同浓度的酸碱水溶液添加到土壤中,在模拟含水率为20%情况下,硫酸(50%)介质下六氯苯处理效果最好,10min的微波辐射即可使50mg/kg的六氯苯达到完全去除;但是在纯水和10mol/L氢氧化钠介质下,六氯苯基本上没有去除;随着硫酸浓度的降低,六氯苯的去除率显著降低。气相色谱/质谱联用(GC/MS)分析没有检测到新物质。六氯苯去除机理推测为,直接矿化或者HCB及其分解的中间产物同土壤发生化学结合而被固定起来,以致难以萃取出来。     

Adsorption removal of thiocyanate from aqueous solution by calcined hydrotalcite

A hydrotalcite with Mg/AI molar ratio 2 was prepared by co-precipitation method and was characterized by XRD, TG/DTA, Zeta potential and BET surface area. The hydrotalcite was calcined at 500℃, with the dehydration from interlayer, the dehydroxilation from the brucite-like layer and the decomposition of carbonate successively, transformed into the mixed oxide type. The removal of thiocyanate from aqueous solution by using the original hydrotalcite and calcined hydrotalcite （HTC-500） was investigated. The results showed that the thiocyanate adsorption capacity of calcined hydrotalcite was much higher than that of the original form. Calcined hydrotalcite was particularly effective at removing thiocyanate, and that the effective range of pH for the thiocyanate removal are between 5.5-10.0. The experimental data of thiocyanate removal fit nicely with Langmuir isotherm, and the saturated adsorption uptake was 96.2 mg SCN-/g HTC-500. The adsorption of thiocyanate by calcined hydrotalcite follows first-order kinetics. And the intercalation to the structure recovery for calcined hydrotalcite. But the presence of additional anions could affect the adsorption behavior of thiocyanate.     

Enhanced photocatalytic activities of silicon nanowires/graphene oxide nanocomposite: Effect of etching parameters

Homogeneous and vertically aligned silicon nanowires (SiNWs) were successfully fabricated using silver assisted chemical etching technique. The prepared samples were characterized using scanning electron microscopy, transmission electron microscopy and atomic force microscopy. Photocatalytic degradation properties of graphene oxide (GO) modified SiNWs have been investigated. We found that the SiNWs morphology depends on etching time and etchant composition. The SiNWs length could be tuned from 1 to 42 µm, respectively when varying the etching time from 5 to 30 min. The etchant concentration was found to accelerate the etching process; doubling the concentrations increases the length of the SiNWs by a factor of two for fixed etching time. Changes in bundle morphology were also studied as function of etching parameters. The SiNWs diameter was found to be independent of etching time or etchant composition while the size of the SiNWs bundle increases with increasing etching time and etchant concentration. The addition of GO was found to improve significantly the photocatalytic activity of SiNWs. A strong correlation between etching parameters and photocatalysis efficiency has been observed, mainly for SiNWs prepared at optimum etching time and etchant concentrations of 10 min and 4:1:8. A degradation of 92% was obtained which further improved to 96% by addition of hydrogen peroxide. Only degradation efficiency of 16% and 31% has been observed for bare Si and GO/bare Si samples respectively. The obtained results demonstrate that the developed SiNWs/GO composite exhibits excellent photocatalytic performance and could be used as potential platform for the degradation of organic pollutants.     

太湖水-气界面温室气体N2O日通量变化特征

阐述了最重要的温室效应气体N2O的来源,湖泊中N2O产生机理,监测了太湖水-气界面四季N2O日通量,并分析了N2O日通量变化特征,发现太湖大部分时间是N2O的源,少部分时间是N2O的汇.春、夏、秋、冬四季的平均N2O日通量分别是0.018 mg/(m2·h)、0.065 mg/(m2·h)、0.003 mg/(m2·h)和-0.002 mg/(m2·h).夏季较高,而春、秋、冬季较低.     

SIMP钢在高温液态铅铋合金中的腐蚀行为

目的 研究SIMP钢在不同溶解氧浓度的高温液态铅铋合金中长期浸泡后腐蚀产物的变化规律。方法 在550 ℃静态液态铅铋合金(饱和氧状态和贫氧状态)中对SIMP钢进行500、1 000、2 000、3 500、5 000 h的腐蚀试验。通过观察腐蚀后试样的表面和截面形貌,进行物化分析,对比不同时间下腐蚀层厚度以及腐蚀产物结构的变化,得出溶解氧浓度和浸泡时间的变化对腐蚀产物的影响规律。结果 在贫氧环境中,SIMP钢的腐蚀类型主要为氧化腐蚀,氧化腐蚀产物具有双层结构,外层为Fe-Cr尖晶石氧化层,内层为富铬氧化物与基体的混合物层;在饱和氧环境,SIMP钢腐蚀产物则具有3层结构,外层为Fe3O4磁铁矿层,中层为Fe-Cr尖晶石氧化层,最内层为富铬氧化物与基体的混合物层。结论 溶解氧浓度和浸泡时间的变化对腐蚀产物的结构和厚度产生了显著影响,SIMP钢在贫氧环境中呈现出优异的耐腐蚀性能。