Performance of amine-multilayered solid sorbents for CO2 removal: Effect of fabrication variables

The emission of fossil fuel carbon dioxide (CO₂) to the atmosphere is implicated as the predominant cause of global climate change; therefore, advanced CO₂ capture technologies are of the utmost importance. In this study, innovative amine-multilayered sorbents were fabricated using layer-by-layer (LbL) nanoassembly technology via alternate deposition of a CO₂-adsorbing amine polymer (e.g. polyethylenimine or PEI) and an oppositely-charged polymer (e.g. polystyrene sulfonate or PSS). We found that the developed sorbents could be used for CO₂ capture and that LbL nanoassembly allows us to engineer their CO₂ capture performance through the fabrication variables (e.g. deposition polymers, deposition media, and number of bilayers). PEI/PSS was found to be the best polymer combination for developing sorbents with relatively high CO₂ capture capacity. The amine-multilayered solid sorbents possessed fine microstructures and may have similar polymer deposition within and on the surface of solid sorbents. These amine-multilayered sorbents had much faster CO₂ desorption rates compared to sorbents prepared using the current PEI-impregnation approach. Such fast CO₂ desorption could make sorbents a good option for CO₂ removal from power plants and even the atmosphere.     

重大工业危险源(罐区)监控预警系统

系统建立了管理软件和硬件监控相结合的安全生产监控预警系统，在安全管理的基 础上，把罐区诸多的危险参数给予实时监测、报警和控制。本系统实现了生产过程控制与安全监控 相结合，安全监测报警与事故预案相结合，既满足了生产控制又实现了动态的安全管理，对安全生产 具有较大意义。     

基于FDS的车厢火灾烟气流动的数值模拟分析

使用FDS火灾模拟软件对列车车厢进行火灾模拟,得到车厢内温度与烟气浓度随时间变化的规律,计算出临界温度与临界可视距离出现的时间,发现在车厢火灾中,总是烟气浓度先达到临界点。车厢火灾的疏散防控措施中,控制烟气浓度应是重点工作。     

基于多Agent的危险化学品安全生产信息采集系统设计

安全生产监管是政府的重要职责,直接关系到国家财产和人民生命安全.安全生产监管中,以危险化学品的监管为重中之重.提高安全生产监管的信息化程度是降低监管强度、提高监管效率行之有效的方法.构建了由管理Agent、采集Agent、故障诊断Agent、通信Agent组成的分布式信息采集多Agent系统,将安监局监管中心对危险化学品生产过程监管的信息采集任务下移到企业端,利用多Agent系统实现危险源生产状态参数的采集、监控及分析;设计了该信息采集系统各类Agent的结构和功能.利用多Agent系统实现分散于各企业的危险源生产状态参数的信息采集、监控及分析,预测和诊断生产过程中的异常状况.通过Agent之间的合作、并行求解使危险化学品安全生产信息采集的问题得到较好地解决.     

Seasonal trend of ambient PCDD/Fs in Tianjin City, northern China using active sampling strategy

The spatial concentrations, seasonal trends, profiles and congener pairs of ambient polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs) were investigated within a seasonally active sampling scheme during Jun 2008 and Jan 2009 in Tianjin City, northern China. The PCDD/F concentrations ranged 14.2-172 fg I-TEQ/m³ (average 69.3 fg I-TEQ/m³) in summer and (89.8-1.01) × 10³ fg I-TEQ/m³ (average 509 fg I-TEQ/m³) in winter, respectively, except for the E-waste dismantling site where much higher values were observed (1.04 × 10³ fg I-TEQ/m³ in summer and 7.123 × 10³ fg I-TEQ/m³ in winter). The results indicated a significantly seasonal trend with higher TEQ values in winter as compared with summer, which could be related to increased emission sources and seasonal variations of the atmospheric boundary layer height. 2,3,4,7,8-PeCDF was the dominant contributor to the total PCDD/F toxic equivalents, and 2,3,7,8-TCDD was detected at almost all the sampling sites in winter. Most of the similarly substituted PCDD/F congener pairs exhibited high correlations, suggesting that they might have similar environmental fate or sources. But different seasonal and spatial distributions of PCDD/F concentrations indicated that the emission sources might be intermittent.     

Control concept and countermeasures for shallow lakes’ eutrophication in China

Research on lake eutrophication in China began in the early 1970s, and many lakes in China are now known to be in meso-eutrophic status. Lake eutrophication has been showing a rapidly increasing trend since 2000. Investigations show that the main reasons for lake eutrophication include a fragile lake background environment, excessive nutrient loading into lakes, excessive human activities, ecological degeneration, weak environmental protection awareness, and lax lake management. Major mechanisms resulting from lake eutrophication include nutrient recycling imbalance, major changes in water chemistry (pH, oxygen, and carbon), lake ecosystem imbalance, and algal prevalence in lakes. Some concepts for controlling eutrophication should be persistently proposed, including lake catchment control, combination of pollutant source control with ecological restoration, protection of three important aspects (terrestrial ecology, lake coast zone, and submerged plant), and combination of lake management with regulation. Measures to control lake eutrophication should include pollution source control (i.e., optimize industrial structural adjustments in the lake catchment, reduce nitrogen and phosphorus emission amounts, and control endogenous pollution) and lake ecological restoration (i.e. establish a zone-lake buffer region and lakeside zone, protect regional vegetation, utilize hydrophytes in renovation technology); countermeasures for lake management should include implementing water quality management, identifying environmental and lake water goals, legislating and formulating laws and regulations to protect lakes, strengthening publicity and the education of people, increasing public awareness through participation in systems and mechanic innovations, establishing lake region management institutions, and ensuring implementation of governance and management measures.     

酸性条件下红壤表面Pb反应动力学的能量特征

用自行设计的动力学装置研究了酸性条件下Pb在红壤表面的反应动力学能量特征.结果表明,酸性条件下,Pb吸附分为快反应和慢反应.用一级动力学方程拟合的Pb最大吸附量,随酸度增加显著下降,随温度升高提前达到平衡.用扩散速率常数计算的活化能(△E*)随酸度的增加而增加,Pb扩散需克服的能障加大;△H值为正,温度升高可促进Pb的扩散;AS值均为负,说明吸附反应使体系有序度增加.原液pH为4.5和5.6时,流出液的pH急剧下降;pH3.8和3.3时流入液比流出液的pH高,是由于土壤的缓冲作用和土壤表面质子化;当溶液中H+超过一定数量后,反应初期的H+消耗是快反应过程.H+对矿物的溶蚀成为速率控制步骤.     

污泥处置方式对污水处理系统可持续性的影响

脱水污泥的污染问题影响了城市污水处理厂的生存和发展,不同的中水处置方式对经济和环境的影响也不一样.将污水处理、脱水污泥和中水处置结合起来构建污水处理生态系统有利于研究污水处理的综合效益、探索促进污水处理事业可持续发展的途径.在考虑废物处理处置和排放的影响基础上,提出了针对污水处理生态系统的改进的能值分析方法和指标体系,即能值产出率(WEYR)、环境负载率(WELR) 和可持续发展指标(WESI), 指标反映了资源消耗和废物排放对系统可持续性的影响.以明镜滩污水处理生态系统作为案例,评价了"污水处理系统 污泥填埋系统 中水排放"(方案1)、"污水处理系统 陶粒生产系统 中水排放"(方案2)、"污水处理系统 聚合材料生产系统 中水排放"(方案3)和"污水处理系统 好氧堆肥生产系统 中水排放"(方案4)等4种方案的可持续性.方案1、2、3和4的WEYR分别为1.65、3.84、3.95和3.63, WELR分别为5.19、5.41、7.69和4.24,WESI分别为0.32、0.71、0.51和0.86.方案1由于未对污泥进行资源化利用,其能值产出率远远低于其他3个方案,故可持续性最低;其他三个方案的能值产出率比较接近,但方案4的环境负载率远远低于其他2个方案,故方案4的可持续性最高.结果表明,污泥利用可提高污水处理生态系统的可持续性,而不同废物利用方式由于对不可更新资源的消耗不同对污水处理生态系统的可持续性影响不一样;改进的能值分析方法适合于评价污水处理生态系统的可持续性.     

聚丙烯酰胺对紫色土中磷素吸附特征的影响

通过等温吸附实验分别研究了特定磷质量浓度下系列PAM用量和系列磷质量浓度下特定PAM用量对磷素在土壤中吸附特征的影响.试验表明,土壤经过PAM处理后其对磷素的吸附性能发生了明显改变.施用PAM使紫色土磷的吸附量降低,PAM用量较低时,吸附量随PAM用量的增加而减少,并且在0.1%～0.5%PAM内两者之间达到极显著负相关.紫色土磷最大吸附量为277.8 靏穏-1 ,0.1%、0.2%、0.4%PAM处理后紫色土对磷的最大吸附量均降低,分别为263.28 靏穏-1、227.38 靏穏-1、212.88 靏穏-1,但吸附强度却没减弱,甚至得到加强.PAM通过改变土壤集结状态和表面性质对土壤磷慢速吸附阶段产生了显著影响,但对快吸附阶段无明显影响.     

Enhanced debromination of 2,2′,4,4′-tetrabromodiphenyl ether (BDE-47) by zero-valent zinc with ascorbic acid

• Highly efficient debromination of BDE-47 was achieved in the ZVZ/AA system. • BDE-47 debromination by the ZVZ/AA can be applied to a wide range of pH. • AA inhibits the formation of (hydr)oxide and accelerates the corrosion of ZVZ. • Reduction mechanism of BDE-47 debromination by the ZVZ/AA system was proposed. A new technique of zero-valent zinc coupled with ascorbic acid (ZVZ/AA) was developed and applied to debrominate the 2,2′,4,4′-Tetrabromodiphenyl ether (BDE-47), which achieved high conversion and rapid debromination of BDE-47 to less- or non-toxic forms. The reaction conditions were optimized by the addition of 100 mg/L ZVZ particles and 3 mmol/L AA at original solution pH= 4.00 using the solvent of methanol/H₂O (v:v= 4:6), which could convert approximately 94% of 5 mg/L BDE-47 into lower-brominated diphenyl ethers within a 90 min at the ZVZ/AA system. The high debromination of BDE-47 was mainly attributed to the effect of AA that inhibits the formation of Zn(II)(hydr)oxide passivation layers and promotes the corrosion of ZVZ, which leads to increase the reactivity of ZVZ. Additionally, ion chromatography and gas chromatography mass spectrometry analyses revealed that bromine ion and lower-debromination diphenyl ethers formed during the reduction of BDE-47. Furthermore, based on the generation of the intermediates products, and its concentration changes over time, it was proposed that the dominant pathway for conversion of BDE-47 was sequential debromination and the final products were diphenyl ethers. These results suggested that the ZVZ/AA system has the potential for highly efficient debromination of BDE-47 from wastewater.