脉冲放电等离子体烟气脱硫脱硝工业试验

40000—50000Nm^3／h工业试验结果表明：烟气温度75℃-80℃，脱硫效率大于90％，脱硝效率大于40％，烟气温度90℃-95℃，脱硫效率大于80％，脱硝效率大于50％；能耗小于3.0Wh／Nm^2；随着温度升高，SO2热化学反应效率逐渐降低；随着氨硫化学计量比增大，氨泄漏逐渐增加，烟气温度90℃。95％，氨泄漏增加更为迅速。并分析了副产物的成分，阐述了脱硫脱硝的机理，探讨了烟气排放的温度。     

车库内氢气扩散和分布状态的数值模拟

为研究车库内氢气连续性泄漏的浓度分布和聚集状态,采用ICEM-CFD软件建模,利用Fluent软件对氢气连续性泄漏过程进行了模拟。通过分析监测点氢气物质的量分数、氢气分布和可燃性区域体积分数,研究了横梁及其间距(L)、自然通风、通风口面积(A)对车库内氢气的扩散和分布状态的影响。结果表明:在密闭状态下,无横梁时可燃性区域最小,L=3 m时可燃性区域最大;当A=0.5 m2时,在自然通风的作用下,车库底部氢气物质的量分数明显下降,但车库中部和上部氢气物质的量分数与密闭时相近;当A=1 m2时,虽然初始阶段氢气物质的量分数上升很快,但很快就趋于稳定,监测点氢气物质的量分数均在爆炸下限以下,此时自然通风能够消除氢气爆炸的风险。     

A nanocomposite of CoFe2O4-carbon microspheres for electrochemical energy storage applications

A carbon/CoFe₂O₄ composite was synthesized by precipitation method. The morphology of the composite was analyzed using scanning electron microscopy, X-ray diffraction, transmission electron microscopy, Fourier Transform Infrared Spectra, and vibrating sample magnetometry. The electrocapacitive behaviors of the composite has been studies by cycle voltammogram and galvanic charge/discharge. The size of the nanoparticles carbon composite of CoFe₂O₄ was uniform and 209 nm. Due to a high percent of carbon, electrochemical measurements showed electrical double layer mechanism. Specifically, the carbon/cobalt ferrite electrode exhibited high specific capacitance of 102.5 F g^?1 at a current density of 0.16 A g^?1, and high rate capability with 30% retention of capacitance even up to 20 A g^?1, and excellent cycling stability with 81.5% retention of the initial capacitance after 6000 charge/discharge cycles, supporting that the carbon cobalt ferrite composite electrode could be a potential candidate for supercapacitor application.     

Carbon reduction potential and cost evaluation of different mitigation approaches in China's coal to olefin Industry

Coal-based olefin (CTO) industry as a complement of traditional petrochemical industry plays vital role in China's national economic development. However, high CO₂ emission in CTO industry is one of the fatal problems to hinder its development. In this work, the carbon emission and mitigation potentials by different reduction pathways are evaluated. The economic cost is analyzed and compared as well. According to the industry development plan, the carbon emissions from China's CTO industry will attain 189.43 million ton CO₂ (MtCO₂) and 314.11 MtCO₂ in 2020 and 2030, respectively. With the advanced technology level, the maximal carbon mitigation potential could be attained to 15.3% and 21.9% in 2020 and 2030. If the other optional mitigation ways are combined together, the carbon emission could further reduce to some extent. In general, the order of mitigation potential is followed as: feedstock alteration by natural gas > CO₂ hydrogenation with renewable electricity applied > CCS technology. The mitigation cost analysis indicates that on the basis of 2015 situation, the economic penalty for feedstock alteration is the lowest, ranged between 186 and 451 CNY/tCO₂, and the cost from CCS technology is ranged between 404 and 562 CNY/tCO₂, which is acceptable if the CO₂ enhanced oil recovery and carbon tax are considered. However, for the CO₂ hydrogenation technology, the cost is extremely high and there is almost no application possibility at present.     

Drought can offset potential water use efficiency of forest ecosystems from rising atmospheric CO2

Increasing atmospheric CO₂ is both leading to climate change and providing a potential fertilisation effect on plant growth. However, southern Australia has also experienced a significant decline in rainfall over the last 30 years, resulting in increased vegetative water stress. To better understand the dynamics and responses of Australian forest ecosystems to drought and elevated CO₂, the magnitude and trend in water use efficiency (WUE) of forests, and their response to drought and elevated CO₂ from 1982 to 2014 were analysed, using the best available model estimates constrained by observed fluxes from simulations with fixed and time-varying CO₂. The ratio of gross primary productivity (GPP) to evapotranspiration (ET) (WUEe) was used to identify the ecosystem scale WUE, while the ratio of GPP to transpiration (Tr) (WUEc) was used as a measure of canopy scale WUE. WUE increased significantly in northern Australia (p < 0.001) for woody savannas (WSA), whereas there was a slight decline in the WUE of evergreen broadleaf forests (EBF) in the southeast and southwest of Australia. The lag of WUEc to drought was consistent and relatively short and stable between biomes (≤3 months), but notably varied for WUEe, with a long time-lag (mean of 10 months). The dissimilar responses of WUEe and WUEc to climate change for different geographical areas result from the different proportion of Tr in ET. CO₂ fertilization and a wetter climate enhanced WUE in northern Australia, whereas drought offset the CO₂ fertilization effect in southern Australia.     

Surface characterization of metal oxides-supported activated carbon fiber catalysts for simultaneous catalytic hydrolysis of carbonyl sulfide and carbon disulfide

The sol–gel method was used to synthesize a series of metal oxides-supported activated carbon fiber (ACF) and the simultaneous catalytic hydrolysis activity of carbonyl sulfide (COS) and carbon disulfide (CS₂) at relatively low temperatures of 60°C was tested. The effects of preparation conditions on the catalyst properties were investigated, including the kinds and amount of metal oxides and calcination temperatures. The activity tests indicated that catalysts with 5 wt.% Ni after calcining at 400°C (Ni(5)/ACF(400)) had the best performance for the simultaneous catalytic hydrolysis of COS and CS₂. The surface and structure properties of prepared ACF were characterized by scanning electron microscope-energy disperse spectroscopy (SEM-EDS), Brunauer–Emmett–Teller (BET), X-ray diffraction (XRD), carbon dioxide-temperature programmed desorption (CO₂-TPD) and diffuse reflectance Fourier transform infrared reflection (DRFTIR). And the metal cation defects were researched by electron paramagnetic resonance (EPR) method. The characterization results showed that the supporting of Ni on the ACF made the ACF catalyst show alkaline and increased the specific surface area and the number of micropores, then improved catalytic hydrolysis activity. The DRFTIR results revealed that -OH species could facilitate the hydrolysis of COS and CS₂; -COO and -C–O species could facilitate the oxidation of catalytic hydrolysate H₂S. And the EPR results showed that high calcination temperature conditions provide more active reaction center for the COS and CS₂ adsorption.     

Adsorption mechanisms of PFOA onto activated carbon anchored with quaternary ammonium/epoxide-forming compounds: A combination of experiment and model studies

When wood-based activated carbon was tailored with quaternary ammonium/epoxide (QAE) forming compounds (QAE-AC), this tailoring dramatically improved the carbon's effectiveness for removing perfluorooctanoic acid (PFOA) from groundwater. With favorable tailoring, QAE-AC removed PFOA from groundwater for 118,000 bed volumes before half-breakthrough in rapid small scale column tests, while the influent PFOA concentration was 200 ng/L. The tailoring involved pre-dosing QAE at an array of proportions onto this carbon, and then monitoring bed life for PFOA removal. When pre-dosing with 1 mL QAE, this PFOA bed life reached an interim peak, whereas bed life was less following 3 mL QAE pre-dosing, then PFOA bed life exhibited a steady rise for yet subsequently higher QAE pre-dosing levels. Large-scale atomistic modelling was used herein to provide new insight into the mechanism of PFOA removal by QAE-AC. Based on experimental results and modelling, the authors perceived that the QAE's epoxide functionalities cross-linked with phenolics that were present along the activated carbon's graphene edge sites, in a manner that created mesopores within macroporous regions or created micropores within mesopores regions. Also, the QAE could react with hydroxyls outside of these pore, including the hydroxyls of both graphene edge sites and other QAE molecules. This latter reaction formed new pore-like structures that were external to the activated carbon grains. Adsorption of PFOA could occur via either charge balance between negatively charged PFOA with positively charged QAE, or by van der Waals forces between PFOA's fluoro-carbon tail and the graphene or QAE carbon surfaces.     

CO2泄漏对稻田水基础水质指标的影响研究

碳捕集与封存（CCS）技术是当前抑制大气中CO₂过快增长的有效方法,但在CCS项目实施过程中仍存在CO₂泄漏而影响地表环境及生态的风险.本研究以龙粳31号和龙稻18号为实验对象,模拟研究地质封存CO₂以不同速率泄漏对稻田水环境基础水质指标D_CO2、pH、DO和ORP的影响,探讨稻田水对地质封存CO₂泄漏的响应规律.结果表明：CO₂泄漏对稻田水的D_CO2、pH、DO和ORP长期影响显著,不同CO₂泄漏速率对稻田水质指标的影响差异显著.在各指标平衡后,稻田水各水质指标均呈现明显的日变化规律,其中D_CO2呈早晚高、午间低的先减后增规律,而pH、DO和ORP均呈早晚低、午间高的先增后减规律.根据各指标差异性分析,建议将稻田水D_CO2作为稻田系统CO₂泄漏监测的主要指标,将pH、DO、ORP作为CO₂泄漏监测的辅助指标.     

Comparative study of carbonic anhydrase activity in waters among different geological eco-environments of Yangtze River basin and its ecological significance

This study provides the presence of carbonic anhydrase(CA) activity in waters of the Yangtze River basin, China, as well as the correlation of CA activity with HCO-3 concentration and CO_2 sink flux. Different degrees of CA activity could be detected in almost all of the water samples from different geological eco-environments in all four seasons. The CA activity of water samples from karst areas was significantly higher than from non-karst areas(PP3-concentration(r = 0.672, P2 sink flux(r = 0.602, P = 0.076) in karst areas. This suggests that CA in waters might have a promoting effect on carbon sinks for atmospheric CO_2 in karst river basins. In conditions of similar geological type, higher CA activity was generally detected in water samples taken from areas that exhibited better eco-environments, implying that the CA activity index of waters could be used as an indicator for monitoring ecological environments and protection of river basins. These findings suggest that the role of CA in waters in the karst carbon sink potential of river basins is worthy of further in-depth studies.     

Effects of turbulence on carbon emission in shallow lakes

Turbulent mixing is enhanced in shallow lakes. As a result, exchanges across the air–water and sediment–water interfaces are increased, causing these systems to be large sources of greenhouse gases. This study investigated the effects of turbulence on carbon dioxide(CO_2)and methane(CH_4) emissions in shallow lakes using simulated mesocosm experiments.Results demonstrated that turbulence increased CO_2 emissions, while simultaneously decreasing CH_4 emissions by altering microbial processes. Under turbulent conditions, a greater fraction of organic carbon was recycled as CO_2 instead of CH_4, potentially reducing the net global warming effect because of the lower global warming potential of CO_2 relative to CH_4. The CH_4/CO_2 flux ratio was approximately 0.006 under turbulent conditions, but reached 0.078 in the control. The real-time quantitative PCR analysis indicated that methanogen abundance decreased and methanotroph abundance increased under turbulent conditions, inhibiting CH_4 production and favoring the oxidation of CH_4 to CO2.These findings suggest that turbulence may play an important role in the global carbon cycle by limiting CH4 emissions, thereby reducing the net global warming effect of shallow lakes.