污染减排预警系统设计

随着经济的发展和人民生活水平的提高,污染物的排放量也越来越大,节能减排已经成为中国最重要的环保政策。要想实现节能减排,关键是实现从末端治理到污染预防的转变。本设计从源头控制的角度出发,结合中国社会经济的发展情况,运用预警理论和多种数学分析工具,研究建立了基于中国两大约束性指标SO2和COD的污染减排预警系统。该系统旨在对中国各省份的污染减排状况趋势进行预测和评估预警,最终通过一组类似于交通信号灯的标志发布预警信号,从而更加直观地反映出全国各省市的减排形势,为决策者提供形象、直观的理论依据。     

锆基柱撑粘土材料对铅离子的吸附作用

以沉降法提纯的蒙脱石和累托石为基质粘土,以ZrOCl2·8H2O为锆源,用稀溶液法制备锫基柱撑蒙脱石和累托石材料。用该类材料作为吸附剂,对人工配制的含铅废水进行静态吸附处理试验,得出错基柱撑粘土材料对铅离子有较好的吸附作用,而且锆基柱撑蒙脱石比锆基柱撑累托石的吸附效果好。当废水pH为6.5、锆基柱撑蒙脱石材料的用量为12g/L时,Pb2+的吸附率达99.8％,吸附量达10 mg/g。     

现行的UASB反应器的设计问题及改良的可行性

探讨了UASB反应器的设计问题和改良的可行性。重点介绍并评价了UASB反应器的器内流速关系以及对应的问题。对比第 3代厌氧反应器的特点 ,提出了UASB反应器可行的改良方法。作为改良可行性证据 ,提供了改良后的实验数据     

矿产资源综合开发利用的评价方法

矿产资源的综合利用,一直没有科学的评价标准。本文提出一套综合利用的评价方法体系,包括参考标准的建立,评价对比方案设计,综合开发利用程度评价,方案排序选优等。本方法体系可用于考核矿山开发阶段的综合利用水平     

饮用水中硝酸根的催化还原研究进展

由于化肥的过度使用 ,造成地下水中硝酸盐的污染日益严重。饮用水中高浓度的硝酸盐对人类健康会产生极大的威胁。本文综述了催化还原脱除水中硝酸根的研究进展和现状 ,并对其发展趋势进行了简单的论述。     

Catalytic fast pyrolysis of walnut shell for alkylphenols production with nitrogen-doped activated carbon catalyst

• N-doped activated carbon was prepared for catalytic pyrolysis of walnut shell. • Alkylphenols were selectively produced from catalytic pyrolysis process. • The alkylphenols yield increased by 8.5 times under the optimal conditions. • Formation mechanism of alkylphenols was proposed. Alkylphenols are a group of valuable phenolic compounds that can be derived from lignocellulosic biomass. In this study, three activated carbons (ACs) were prepared for catalytic fast pyrolysis (CFP) of walnut shell to produce alkylphenols, including nitrogen-doped walnut shell-derived activated carbon (N/WSAC), nitrogen-doped rice husk-derived activated carbon (N/RHAC) and walnut shell-derived activated carbon (WSAC). Pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) experiments were carried out to reveal the influences of AC type, pyrolytic temperature, and AC-to-walnut shell (AC-to-WS) ratio on the product distributions. Results showed that with nitrogen doping, the N/WSAC possessed stronger capability than WSAC toward the alkylphenols production, and moreover, the N/WSAC also exhibited better effects than N/RHAC to prepare alkylphenols. Under the catalysis of N/WSAC, yields of alkylphenols were significantly increased, especially phenol, cresol and 4-ethylphenol. As the increase of pyrolytic temperature, the alkylphenols yield first increased and then decreased, while high selectivity could be obtained at low pyrolytic temperatures. Such a trend was also observed as the AC-to-WS ratio continuously increased. The alkylphenols production achieved a maximal yield of 44.19 mg/g with the corresponding selectivity of 34.7% at the pyrolytic temperature of 400°C and AC-to-WS ratio of 3, compared with those of only 4.67 mg/g and 6.1% without catalyst. In addition, the possible formation mechanism of alkylphenols was also proposed with the catalysis of N/WSAC.     

Remediation of arsenic contaminated soil by sulfidated zero-valent iron

• Sulfidation significantly enhanced As(V) immobilization in soil by zerovalent iron. • S-ZVI promoted the conversion of exchangeable As to less mobile Fe-Mn bound As. • Column test further confirmed the feasibility of sulfidated ZVI on As retention. • S-ZVI amendment and magnetic separation markedly reduced TCLP leachability of As. In this study, the influences of sulfidation on zero-valent iron (ZVI) performance toward As(V) immobilization in soil were systemically investigated. It was found that, compared to unamended ZVI, sulfidated ZVI (S-ZVI) is more favorable to immobilize As(V) in soil and promote the conversion of water soluble As to less mobile Fe-Mn bound As. Specifically, under the optimal S/Fe molar ratio of 0.05, almost all of the leached As could be sequestrated by>0.5 wt.% S-ZVI within 3 h. Although the presence of HA could decrease the desorption of As from soil, HA inhibited the reactivity of S-ZVI to a greater extent. Column experiments further proved the feasibility of applying S-ZVI on soil As(V) immobilization. More importantly, to achieve a good As retention performance, S-ZVI should be fully mixed with soil or located on the downstream side of As migration. The test simulating the flooding conditions in rice culture revealed there was also a good long-term stability of soil As(V) after S-ZVI remediation, where only 0.7% of As was desorbed after 30 days of incubation. Magnetic separation was employed to separate the immobilized As(V) from soil after S-ZVI amendment, where the separation efficiency was found to be dependent of the iron dosage, liquid to soil ratio, and reaction time. Toxicity characteristic leaching procedure (TCLP) tests revealed that the leachability of As from soil was significantly reduced after the S-ZVI amendment and magnetic separation treatment. All these findings provided some insights into the remediation of As(V)-polluted soil by ZVI.     

Recent advances in the photocatalytic reduction of carbon dioxide

Fossil fuels are currently the major energy source and are rapidly consumed to supply the increasing energy demands of mankind. CO₂, a product of fossil fuel combustion, leads to climate change and will have a serious impact on our environment. There is an increasing need to mitigate CO₂ emissions using carbon–neutral energy sources. Therefore, research activities are devoted to CO₂ capture, storage and utilization. For instance, photocatalytic reduction of CO₂ into hydrocarbon fuels is a promising avenue to recycle carbon dioxide. Here we review the present status of the emission and utilization of CO₂. Then we review the photocatalytic conversion of CO₂ by TiO₂, modified TiO₂ and non-titanium metal oxides. Finally, the challenges and prospects for further development of CO₂ photocatalytic reduction are presented.     

压力容器设计中的环境温度与最低设计金属温度

环境温度在容器设计中不仅影响设计压力的合理确定,而且更影响最低设计金属温度的确定直至影响材料的正确选择。通过对规程标准的解读,结合液化石油气储罐设计对此进行了讨论,认为环境温度应视为容器的特例工况条件,容器设计应将与其对应的设计压力一起作为设计载荷条件,不仅要对容器的壁厚进行校核,而且尚需根据容器的一次应力判断并确认是否需要修订完善容器设计的选材、制造及检验等技术要求,使容器设计文件正确完整,保证容器制造的安全可靠性。     

N2O emission from a sequencing batch reactor for biological N and P removal from wastewater

Nitrous oxide （N2O） is a greenhouse gas that can be released during biological nitrogen removal from wastewater. N2O emission from a sequencing batch reactor （SBR） for biological nitrogen and phosphorus removal from wastewater was investigated, and the aims were to examine which process, nitrification or denitrification, would contribute more to N2Oemission and to study the effects of heterotrophic activities on N2O emission during nitrification. The results showed that N2O emission was mainly attributed to nitrification rather than to denitrification. N2O emission during denitrification mainly occurred with stored organic carbon as the electron donor. During nitrification, NaO emission was increased with increasing initial ammonium or nitrite concentrations. The ratio of N2O emission to the removed ammonium nitrogen （N2O- N/NH4-N） was 2.5% in the SBR system with high heterotrophic activities, while this ratio was in the range from 0.14% to 1.06% in batch nitrification experiments with limited heterotrophic activities.