生物阴极式碳纸隔膜微生物燃料电池的反硝化和产电性能

为了探讨生物阴极式廉价隔膜微生物燃料电池(microbial fuel cell,MFC)的基本性能,首先以生物反硝化作用为基础构建了生物阴极MFC,并进一步以涂布聚四氟乙烯(PTFE)的廉价碳纸代替昂贵的质子交换膜(PEM)构建碳纸隔膜生物阴极式MFC。研究结果显示,对于生物阴极式MFC,阴极室中最适宜反硝化细菌生长的NO-3-N浓度为99.2 mg/L,此时输出电压最高可达0.11 V,1 h内NO-3-N的去除率达到80.0%,COD去除率为62.8%;以涂PTFE的碳纸代替PEM的生物阴极式MFC与有PEM的MFC最高输出电压基本一致(均达到0.22 V,外阻500Ω),但碳纸隔膜MFC的产电更稳定。结果验证了廉价隔膜生物阴极式MFC的可行性,并为其应用于污水脱氮奠定基础。     

基于CA-MAS的水域总有机碳扩散模拟研究

当前水环境污染扩散研究一般基于普通数值模型模拟,忽略了水污染扩散微观驱动力的影响。为能更真实地反映其动态扩散过程,针对水域总有机碳(TOC)扩散机理,基于CA和MAS技术,将影响TOC扩散的自然和社会经济因素抽象为微观的水流Agent、风速Agent、径流量Agent、污水排放口Agent、人工管理Agent以及农业生产地Agent,将研究水域抽象为CA元胞空间,建立了CA-MAS水域总有机碳扩散模型,对水域总有机碳的动态演化过程进行模拟,并以武汉理工大学鉴湖水域作为实验区域,借助NetLogo仿真平台完成了模型的实现与验证。模拟结果表明,该模型基本能够反映水体总有机碳的扩散规律,可以为水环境污染控制提供参考。     

A full-scale sequencing batch reactor system for swine wastewater treatment

A full-scale sequencing batch reactor (SBR) system was evaluated for its ability to remove carbon and nitrogen from swine wastewater. The SBR was operated on four, six-hour cycles each day, with each cycle consisting of 4.5 hours of “React,” 0.75 hours of “Settling”, 0.75 hours for “Draw” and “Fill.” Within each cycle, an amount of wastewater equivalent to about 5% of the reactor volume (5,500 litres) was removed and added. The SBR system was able to remove 82% of biochemical oxygen demand (BOD) and more than 75% of nitrogen. Even though the SBR effluent, with an average effluent BOD₅ of about 588 mg L^{? 1}, did not meet the discharge criteria, it enabled a reduction of the land base required for land application of swine wastewater by about 75%. Results indicated that the SBR system was a viable method for the treatment of swine wastewater.     

黑龙江省森林碳汇市场构建的可行性设计

随着全球森林碳汇市场市场份额扩大,黑龙江省凭借资源和区位等内在优势,森林碳汇市场发展前景可观。基于市场原则和组织框架的构建设想,依据市场定位和产品开发,对黑龙江省森林碳汇市场发展的可行性分阶段设计,提出适合的保障机制,为黑龙江省森林碳汇市场运行提供理论参考和现实依据。     

煤炭企业发展低碳经济的动力机制

将影响煤炭企业发展低碳经济的动力因素分为四大类,包括4个拉力因素、1个支撑因素、2个压力因素和4个推动力因素。设计了煤炭企业发展低碳经济的动力机制模型,在分析各个动力因素的基础上,构建了煤炭企业发展低碳经济的拉力机制模型、支撑机制模型、压力机制模型和推动力机制模型。     

森林碳汇资源开发潜力定量评价与研究——以黑龙江省为例

森林碳汇资源是开展森林碳汇贸易的基础。森林碳汇潜力的定量评价,将为森林碳汇贸易提供可靠的依据。在对森林碳汇资源开发潜力的定量方法进行深入研究的基础上,以黑龙江省为案例进行潜力评价,明确了黑龙江省具有巨大的森林碳汇增量潜力,提出了进一步发展森林碳汇贸易及构建森林碳汇交易市场的可行性。     

油田压裂返排液处理技术实验研究

油气井压裂作业过程中产生的压裂返排液已成为当前油田水体的主要污染源之一。文章对吉林油田公司压裂返排液处理工艺进行了实验研究。结果表明:在采用絮凝、微波强氧化、活性炭毡处理、纳滤/反渗透集成处理工艺后,压裂返排液CODCr可以达到GB 8978-1996《污水综合排放标准》一级标准要求。该研究为压裂返排液处理装置的设计和现场实施提供了实验基础。     

Sorption of PAHs and PCBs to activated carbon: coal versus biomass-based quality

The addition of activated carbon (AC) is an increasingly popular method for pollutant immobilization, and the AC material can be made of biomass or coal/fossil feedstock. The aim of the present study was to investigate whether there are differences between pollutant sorption to biomass and coal-based AC in the presence and absence of sediment. Through N₂ and CO₂ adsorption to probe surface area and pore size it was shown that the biomass-based AC had a stronger dominance of narrow pores in the size range 3.5-15 Å than the anthracite-based material. In the absence of sediment, sorption isotherms for the probe compounds pyrene and PCB-101 showed stronger sorption for the biomass-based AC (logarithmic Freundlich coefficients 8.15 for pyrene; 9.91 for PCB-101) than for the anthracite-based one (logarithmic Freundlich coefficients 7.20 and 9.70, respectively). In the presence of sediment, the opposite trend was observed, with the stronger sorption for anthracite-based AC. Thus, the presence of competing and/or pore-blocking sediment constituents reduces sorption to a larger extent for biomass-derived AC (factor of 5 for pyrene to almost 100 for PCB-101) than for anthracite-based AC (no reduction for pyrene to factor of 5 for PCB-101). This difference is tentatively attributed to the difference in pore size distribution, narrow pores being more prone to clogging, and could have implications for remediation feasibility with AC from different sources.     

Visualization and localization of bromotoluene distribution in Hedera helix using NanoSIMS

Some plants are known as indoor air purifiers. A large number of studies report kinetic purification results for an extensive panel of plants, i.e. the pollutant concentration (volatile organic compounds, as known as VOC, most of the time) is continuously monitored by gas chromatography. However, only a few papers describe the mechanisms involved in such processes. This study deals with the use of secondary ion mass spectrometry imaging as an efficient tool to locate atmospheric pollutant as bromotoluene within the Hedera helix plant (leaf, roots) and the substrate on which it was previously grown. Hedera helix plants have been placed in a pollution chamber with control of the exposure parameters. Plant and soil samples excised were transferred into a fixative solution of glutaraldehyde and paraformaldehyde for a few days, were dehydrated using ethanol and were embedded with resin. Cross sections were made from the pale brown solids obtained. Then, a device using a cathodic pulverization device capable of depositing a few nanometers of gold atoms over the sample was used to make the surface electronically conductive for the NanoSIMS. Hence, polluted and unpolluted samples of Hedera helix and substrates were obtained following a careful procedure that allowed for the discrimination between polluted and nonpolluted ones. Nanoscale spatial resolution was an invaluable tool (NanoSIMS) to achieve this, and proved that VOCs, such as bromotoluene, were actually trapped by plants such as Hedera helix.     

Nonideal transport of contaminants in heterogeneous porous media: 10. Impact of co-solutes on sorption by porous media with low organic-carbon contents

The impact of co-solutes on sorption of tetrachloroethene (PCE) by two porous media with low organic-carbon contents was examined by conducting batch experiments. The two media (Borden and Eustis) have similar physical properties, but significantly different organic-carbon (OC) contents. Sorption of PCE was nonlinear for both media, and well-described by the Freundlich equation. For the Borden aquifer material (OC = 0.03%), the isotherms measured with a suite of co-solutes present (1,2-dichlorobenzene, bromoform, carbon tetrachloride, and hexachloroethane) were identical to the isotherms measured for PCE alone. These results indicate that there was no measurable impact of the co-solutes on PCE sorption for this system. In contrast to the Borden results, there was a measurable reduction in sorption of PCE by the Eustis soil (OC = 0.38%) in the presence of the co-solutes. The organic-carbon fractions of both media contain hard-carbon components, which have been associated with the manifestation of nonideal sorption phenomena. The disparity in results observed for the two media may relate to relative differences in the magnitude and geochemical nature of these hard-carbon components.