微波改性锆-铝柱撑膨润土对水中Cr(Ⅵ)的吸附

以膨润土为原料,通过微波辐射加热法制备锆-铝柱撑膨润土(MZAPB)吸附剂,研究了 MZAPB 加入量、溶液 pH、吸附时间、温度等因素对 Cr(Ⅵ)吸附效果的影响.研究结果表明:当溶液初始 Cr(Ⅵ)质量浓度为 25mg/L、MZAPB 加入量为 10 g/L、溶液 pH 为 5.6、吸附温度 25℃、吸附时间为 6...     

Global Research Trends Related to CO2 Emissions and Their Enlightenment to China

Given the growing awareness of the likely catastrophic impacts of climate change and close association of climate change with global emissions of greenhouse gases (of which carbon dioxide is more prominent) , considerable research efforts have been devoted to the analysis of carbon dioxide (CO2) emissions and its relationship to sustainable development. Now GHG reduction programs have been coming into effect in many developed countries that have more responsibility for historical CO2 emissions, and the studies have become mature. First, the GHG emissions accounting system is more all-inclusive and the methods are more rational with the effort of IPCC from 1995 and all other researchers related. Second, the responsibility allocation is more rational and fair. Along with the clarity of "carbon transfer" and "carbon leakage", the perspective and methodology for allocating regional CO2 emissions responsibility is turning from production base to consumption base. Third, the decomposition method has become more mature and more complex. For example, the decomposition formulas are including KAYA expression and input-output expression and the decomposition techniques are developed from index analysis to simple average divisia and then adaptive-weighting divisia. Fourth, projection models have become more integrated and long-term. The top-down model and bottom-up model are both inter-embedded and synergetic. Trends above give some advice for the research on CO2 in China, such as emissions factors database construction, deeper-going research on emissions responsibility and structure analysis, promotion of modeling technology and technology-environment database.     

The oxidation mechanism of polychlorinated dibenzo-p-dioxins under the atmospheric conditions - A theoretical study

The atmospheric polychlorinated dibenzo-p-dioxins (PCDDs) partition appreciably in the gas phase, where they undergo rapid oxidation. The atmospheric oxidation mechanisms of a few PCDDs, initiated by OH radical, are studied using density functional theory calculations. The oxidations start with OH-addition to the aromatic rings, dominantly at γ-sites, followed by the non-chlorinated β-sites; while additions to the α-sites or chlorinated sites are negligible. For PCDDs with all β-sites being chlorinated, formation of PCDD-γ-OH adducts become virtually the only reaction path. Under the atmospheric conditions, the PCDD-β/γ-OH adducts combine with O₂ slowly at rates <1 s⁻¹. Instead, the PCDD-β-OH adducts will react with O₂ through hydrogen abstraction at rates <50 s⁻¹, forming PCDD-β-ol, and the PCDD-γ-OH adducts will decompose to the substituted phenoxy radicals by fused-ring C-O bond cleavage at rates of 10³ ∼ 10⁵ s⁻¹. The reaction mechanisms of PCDDs are drastically different from the peroxy mechanism for the atmospheric oxidations of benzene and dibenzofuran.     

亚甲基蓝在污泥活性炭上的吸附

以剩余污泥为原料,氯化锌为活化剂制备污泥活性炭。研究了初始pH值、吸附温度及离子强度对污泥活性炭吸附亚甲基蓝效果的影响。采用高分辨电子扫描电镜(SEM)和氮吸脱附曲线对污泥活性炭进行了表征。结果表明,随着pH值的升高,吸附量增大,碱性条件下最好。在15～55℃的范围内,亚甲基蓝的吸附量先增加后降低,温度为35℃时吸附量达到最大值。加入氯化钠后的污泥活性炭的吸附能力变弱,但随着离子强度的增大,变弱的强度减少。污泥活性炭以中孔为主和污泥活性炭具有不规则结构,预示着污泥活性炭较高的吸附能力。污泥活性炭对亚甲基蓝的吸附符合Lang-muir等温吸附方程。污泥壳活性炭对亚甲基蓝的吸附符合二级反应动力学方程反应特征。     

利用滩涂污灌土壤制备吸附剂

研究了滩涂污灌土壤吸附剂的制备方法。通过正交实验,比较了氯化锌、磷酸、氢氧化钾、盐酸几种活化剂在不同秸秆加入量、活化剂浓度、活化时间、活化温度的情况下制备的吸附剂,对水中邻硝基甲苯的吸附效果影响。实验结果表明,选择盐酸活化法制备吸附剂,在秸秆加入量为15%,经2 mol/L的盐酸按液固比为1∶1浸泡处理滩涂污灌土壤后,用氮气做保护气在400℃的条件下碳化1 h,制备的土壤吸附剂对水中邻硝基甲苯的吸附效率可以达到90%以上。     

Biodegradation of tribenuron methyl that is mediated by microbial acidohydrolysis at cell-soil interface

Tribenuron methyl (TBM) is a member of the sulfonylurea herbicide family and is widely used in weed control. Due to its phytotoxicity to rotating-crops, concerns on TBM-pollution to soil have been raised. In this study, experimental results indicated that microbial activity played a key role in TBM removal from polluted soil. Twenty-six bacterial strains were isolated and their degradation of TBM was evaluated. Serratia sp. strain BW30 was selected and subjected to further investigation on its degradative mechanism. TBM degradation by strain BW30 was dependent on glucose that was converted into lactic or oxalic acids. HPLC-MS analysis revealed two end-products from TBM degradation, and they were identical to the products from TBM acidohydrolysis. Based on this observation, it is proposed that microbe-mediated acidohydrolysis of TBM was involved in TBM degradation in soil, and possible application of this observation in bioremediation of TBM-polluted soil is discussed.     

Estrogenic effects of dissolved organic matter and its impact on the activity of 17β-estradiol

Background and purpose  

The ubiquitous dissolved organic matter (DOM) is actually not inert as we always think, and the hormone-like effects of DOM have been reported. The objective of this study was to investigate the estrogenic effects of DOM and its impact on the activity of the natural estrogen 17β-estradiol (E2).     

The emission patterns of volatile organic compounds during aerobic biotreatment of municipal solid waste using continuous and intermittent aeration

Because volatile organic compounds (VOCs) are one of the main concerns during municipal solid waste (MSW) treatment, the release patterns and the environmental effects of VOCs were investigated during laboratory-scale aerobic biotreatments of MSW with continuous and intermittent negative ventilation. When the same airflow amounts were used, intermittent ventilation was found to reduce the total VOC emissions from continuous ventilation process by 28%. In this study, 23 types of volatile organic compounds were analyzed, of which butyraldehyde, ethanol, and butanone were emitted in the highest concentrations of 748, 372, and 260 mg/m3, respectively. During the aerobic biotreatment process, ketones, aldehydes, and alcohols were primarily released during the first 4 days, accounting for 86-98% of the total VOC emissions during this period. The emission concentrations of malodorous sulfide compounds displayed two peaks on day 4 and day 9, with the contribution to the total VOC emissions being enhanced from less than 10% to 76-83%. The release of terpenes and aromatics lasted for more than 10 days with no significant emission peaks and the proportions of those compounds in the total VOCs increased gradually, but no more than 50% even at the end of the process. Considering the strength of the odors, aldehydes were the predominant contributors at the beginning of the experiment, whereas malodorous sulfide compounds became the most odorous compound as the biological process continued. Most of the VOCs emitted at the concentrations beneath the level causing health threat to the workers.     

利用盐泥制取轻质氧化镁

采用二氧化碳法提取盐泥中的镁,研究了使之转化为轻质氧化镁的影响因素以及主要反应的动力学性质。实验确定的最佳条件为固液比1∶15、二氧化碳通入时间90min、水解温度90℃、水解时间25min,在此条件下,盐泥中镁的总提取率为75%;采用微分法求得氢氧化镁与二氧化碳反应的反应级数和活化能分别为1.7和68.1kJ/mol。     

炭化柚子皮对废水中双酚A的吸附

采用磷酸二氢钾活化原材料柚子皮,分别在300℃和600℃对活化后柚子皮进行炭化,制得吸附剂（CC300和CC600）,通过静态吸附实验研究了炭化柚子皮对双酚A的吸附性能。采用比表面积分析仪对炭化柚子皮进行表征,实验考察了pH值、吸附时间和温度对双酚A吸附的影响,并详细研究了炭化柚子皮对双酚A的吸附行为和机理。结果表明,高温炭化柚子皮（CC600）吸附双酚A能力比低温炭化（CC300）的强,其吸附较好地满足Langmuir和Freundlich等温方程;动力学研究表明,其吸附速率快,在150min内能达到吸附平衡,准二级动力学模型较好地描述该吸附行为,相关系数高达0．99：计算了热力学参数△G、△H和△S的值,△G为负值,说明该吸附过程为自发过程。