理论等温方程式在CS2—ACF静态吸附体系的应用

测定了CS_2蒸气在4种ACF(活性炭纤维)和GAC(粒状活性炭)上的若干吸附等温线。用BET方程、H-J方程和D-A方程对CS_2-ACF静态吸附体系进行了处理。结果表明,除H-J方程外,其它两个方程适用良好。通过理论等温方程式,求出了吸附剂的比表面积和微孔体积。     

Origins of black carbon from anthropogenic emissions and open biomass burning transported to Xishuangbanna, Southwest China

Black carbon (BC) has importance regarding aerosol composition, radiative balance, and human exposure. This study adopted a backward-trajectory approach to quantify the origins of BC from anthropogenic emissions ($\mathrm{B}{\mathrm{C}}_{\text{An}}$) and open biomass burning ($\mathrm{B}{\mathrm{C}}_{\text{BB}}$) transported to Xishuangbanna in 2017. Haze months, between haze and clean months, and clean months in Xishuangbanna were defined according to daily PM_2.5 concentrations of >75, 35–75, and <35 µg/m³, respectively. Results showed that the transport efficiency density (TED) of BC transported to Xishuangbanna was controlled by the prevailing winds in different seasons. The yearly contributions to the effective emission intensity of $\mathrm{B}{\mathrm{C}}_{\text{An}}$ and $\mathrm{B}{\mathrm{C}}_{\text{BB}}$ transported to Xishuangbanna were 52% and 48%, respectively. However, when haze occurred in Xishuangbanna, the average $\mathrm{B}{\mathrm{C}}_{\text{An}}$ and $\mathrm{B}{\mathrm{C}}_{\text{BB}}$ contributions were 23% and 77%, respectively. This suggests that open biomass burning (BB) becomes the dominant source in haze months. Myanmar, India, and Laos were the dominant source regions of BC transported to Xishuangbanna during haze months, accounting for 59%, 18%, and 13% of the total, respectively. Furthermore, India was identified as the most important source regions of $\mathrm{B}{\mathrm{C}}_{\text{An}}$ transported to Xishuangbanna in haze months, accounting for 14%. The two countries making the greatest contributions to $\mathrm{B}{\mathrm{C}}_{\text{BB}}$ transported to Xishuangbanna were Myanmar and Laos in haze months, accounting for 55% and 13%, respectively. BC emissions from Xishuangbanna had minimal effects on the results of the present study. It is suggested that open BB in Myanmar and Laos, and anthropogenic emissions in India were responsible for poor air quality in Xishuangbanna.     

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.     

黑水虻转化厨余垃圾过程中病原菌灭活规律的研究与综合评价

黑水虻能够有效取食厨余垃圾等有机固体废弃物,其自身转化为昆虫蛋白和脂肪等生物质,将厨余垃圾转化为虫沙有机肥,处理过程是一种有机固体废弃物的资源化新方法.为评估黑水虻处理厨余垃圾的效率与安全性,本课题研究黑水虻在厨余垃圾处理过程中,对大肠杆菌O157：H7（EC）、鼠伤寒沙门氏菌（ST）及金黄色葡萄球（SA）的灭活能力,评价黑水虻体内的抑菌因子,分析3种病原菌对黑水虻生长增重及厨余转化效率的影响.经过18 d的黑水虻处理,研究发现：①第0和第6 d两次以6.4~7.1 log₁₀ CFU·g^-1的浓度向厨余垃圾中分别接种EC、ST和SA以后,EC经4~6 d处理被全部灭活、ST经3~4 d处理被全部灭活,SA经6 d处理,浓度下降到1.9~2.6 log₁₀ CFU·g^-1,但不能被全部灭活,病原菌的灭活效率呈现EC=ST>SA的趋势（p < 0.001）,且黑水虻体内无EC、ST或SA残留;②厨余垃圾降解过程中,初期和中期pH值主要呈现酸性（4.0~5.3）,对抑制EC、ST和SA起到了促进作用,后期pH值呈中性至弱碱性;③黑水虻对于EC和ST能够产生自身免疫抑制因子,且抑制活性ST>EC,但对SA无明显的免疫抑制能力,SA的灭活主要依赖于黑水虻肠道菌群的竞争性抑制作用;④黑水虻的体长、体重、预蛹率、产率,以及厨余垃圾的生物转化率和减量化率未受病原菌存在的影响,18 d后EC组、ST组和SA组的预蛹率均达到在80%以上,厨余减量化率分别达到74.0%、79.1%和78.5%,生物转化率分别达到13.0%、13.2%、19.4%.综上,黑水虻能够在彻底灭活EC、ST,99%灭活SA的同时,高效降解厨余垃圾（减量化率>74%）,并转化为虫体有机质（虫产率>10%）,是一种高效卫生的厨余垃圾资源化方法.今后的研究中,还需要加强以金葡菌为代表的抗逆性病原菌的灭活机制的探讨.     

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.