Reassessment of the Ocean-To-Atmosphere Flux of Carbon Monoxide

Carbon monoxide (CO) in the surface sea waters is produced predominantly by photochemical processes, oxidized by micro-organisms and outgassed to the atmosphere. to assess carbon monoxide flux from the oceans to the atmosphere, the photochemical production and microbial oxidation of carbon monoxide in the oceanic mixed-layer was investigated during several oeanographic cruises and in the laboratory. the photoproduction rate of carbon monoxide was found to be well correlated to the concentration of dissolved organic carbon (DOC) in coastal and open ocean surface waters. Taking a global average carbon monoxide production rate of 10 ± 2 nmole litre^-1 (mg DOC hr)^-1 in the surface open ocean water, and 25 ± 7 nmole litre^-1 (mg DOC hr)^-1 in coastal sea water, at cloud-free summer solar noon, the photochemical production of carbon monoxide in the global oceans is estimated to be at a rate of 1200 ± 200 Tg CO y^-1. the microbial carbon monoxide turnover time in the mixed-layer was observed to range from hours in a coastal estuary to 16 days in the Pacific along 1057deg; W in dark incubations. Natural sunlight can largely inhibit the microbial consumption of carbon monoxide in surface water. On a global scale, microbial consumption is responsible for the loss of less than 10% of photochemical produced carbon monoxide in the surface ocean. Field measurements have shown that the net transport of carbon monoxide from the euphotic zone to the underlying deeper ocean water is limited and that the overall life time in surface sea waters is less than 3-4 hours. When combined, these field measurements with the photoproduction and microbial consumption rates obtained, we estimate the oceanic flux to the atmosphere is about 1000 ± 200 Tg CO y^-1, which represents the largest single source of atmospheric carbon monoxide.     

Biodegradability of Quaternized, Crosslinked Sugarcane Bagasse

Quaternized, crosslinked sugarcane bagasse can adsorb anionic dyes from textile wastewater. Disposal of dye-saturated adsorbent by composting or land application would require that modifications made to the bagasse do not interfere with its decomposition. The impact of quaternization and crosslinking on bagasse biodegradability was examined. Bagasse in varying states of modification was mixed with soil and monitored for carbon dioxide evolution for four weeks at 27°C. After subtracting the amount of carbon evolved from control soil samples, the net carbon evolved from the bagasse samples was determined and used as a measure of their extent of biodegradation. Biodegradability decreased in the order: bagasse (approx. 60% degraded after four weeks) > quaternized bagasse > quaternized, epichlorohydrin-crosslinked bagasse > quaternized, methylene-bis-acrylamide-crosslinked bagasse > epichlorohydrin-crosslinked bagasse (less than 5% degraded). Crosslinking severely impacted biodegration, probably by preventing the penetration of (hemi)cellulytic and lignolytic enzymes into the interior of the modified bagasse particles. It is concluded that the biodegradability of quaternized, crosslinked bagasse is too low for composting or land application.     

BOD微生物膜的再利用研究初探

对失去大部分活性的微生物膜进行再培养，以研究膜再利用的可能性。试验结果初部表明：在1／2MS培养基中加入一定量的植物激素，不仅可以使膜的电位值（I0）显著升高，且活性强，稳定性好，可使膜重复利用。     

The dyadic level of conceptualization and analysis: A missing link in multilevel OB research?

Despite burgeoning multilevel research in organizational behavior over the past two decades, our understanding of dyadic relationships at work remains underdeveloped. Focusing on leader–member exchange, we discuss conceptual and methodological challenges that have hampered research at this level and illustrate how and why such analysis might provide new insights. Copyright © 2015 John Wiley & Sons, Ltd.     

离子液体对CO2吸收性能的研究进展

CO2引起的气候变暖已成为全球最关注的环境问题之一,利用离子液体固定CO2引起了众多学者的关注。介绍了近年来离子液体吸收CO2的研究进展,包括常规离子液体和含氨基离子液体、氨基酸离子液体、聚离子液体及其他离子液体等4种功能化离子液体,并简要分析了吸收机理。综合分析了每种离子液体的吸收性能,离子液体对CO2的吸收能力均随温度上升而减小,随压力升高而增加。烷基链的增长以及含氟基团的增加有利于对CO2的吸收。功能化离子液体由于引入了功能化基团,相同条件下,其对CO2的吸收力几乎是常规离子液体的两倍。此外,将离子液体与有机溶液(特别是醇胺溶液)混合能提高离子液体对CO2的吸收能力,且能降低生产费用。最后指出了高吸收性能、低黏度、低毒以及低成本是未来离子液体的研究方向。     

序批式动态膜生物反应器处理低碳氮比废水的试验研究

以序批式动态膜反应器为研究对象,对其处理低碳氮比废水的效果进行了试验研究.试验温度为19 ～ 21℃,MLSS为3～5g/L;好氧阶段溶解氧质量浓度为2 ～4 mg/L,厌氧阶段溶解氧质量浓度为0.2～0.5 mg/L;水力停留时间共12 h,其中好氧阶段8h,厌氧阶段4h.结果表明:当进水COD、TN和NH4+-N质量浓度分别为250～300mg/L、103 ～ 156 mg/L和92～140 mg/L时,反应器对上述污染物表现出较高且稳定的去除效率,COD、TN和NH4+-N平均去除率分别达到76.15％、82.16％和90.13％.同时,反应器系统中污泥的比硝化速率与常规处理装置中的活性污泥相比较高,以NH4+-N的降解量计为0.101 d-1,以NO3--N的积累量计为0.091 d-.     

Ion exchange membrane-assisted electro-activation of aqueous solutions: Effect of the operating parameters on solutions properties and system electric resistance

The properties of electro-activated (EA) aqueous solutions as well as the dynamics of their changes were considered in the current study using aqueous solutions of NaCl and NaHCO₃. The concentrations of the salt solutions were 0.5, 0.25, 0.125 and 0.05 M. The tests were performed at the DC current densities of 25, 37.5, and 50 Å/m². The electro-activation reactor consisted of three individual cells assembled together and separated by anion-exchange (AEM) and cation-exchange (CEM) membranes. During the experiments, four configurations of the membrane placements and solutions concentrations were studied. The obtained results showed the dynamics of the electro-activation process that allows obtaining electro-activated solutions with targeted properties such as pH and oxydo-reduction potential (ORP). It was possible to obtain electro-activated solutions at the anodic side (acid anolyte) with pH of 3.0, 3.5, and 4.0 and ORP of +1100 ± 15 mV when NaCl solution was used as electrolyte. Furthermore, several types of electro-activated solutions with high redox potential (ORP = +921 ± 12 mV) and neutral pH (6.48 ± 0.05) were obtained on the anode side when sodium carbonate was used. At the same time, two types of solutions, one with acid pH (2.14 ± 0.14) and the other one with alkaline pH (10.46 ± 0.03) with ORP = +689 ± 10 and 110 ± 21 mV, respectively, were obtained in the central compartment which considered as electro-activated solutions obtained by means of noncontact electro-activation.     

中和-络合萃取-双极膜电渗析处理金刚烷胺制药废水

采用中和沉淀-络合萃取-双极膜电渗析组合工艺协同处理金刚烷胺制药胺化废水与溴化废水.结果表明,通过胺化废水与溴化废水的中和反应,可以大幅消减废水中溶解性固体和有机污染物,避免后续萃取过程中的乳化现象.在pH值为8.0、油/水相比为1∶1的条件下,P204∶正辛醇=3∶2的复配萃取剂对废水中TOC和TN的萃取效率分别为56.9%和20.6%,金刚烷胺及其衍生物几乎被完全萃取.以2.0 mol·L-1的HCl溶液为反萃取剂,可以将47.5%的金刚烷胺从负载有机相中反萃分离,再生后的萃取剂可以多次重复使用.对萃余液采用双极膜电渗析进行处理,可以去除64.2%的无机盐和部分有机物,同时还能回收到较高浓度的酸,但由于氢离子的渗漏难以回收高浓度的碱.     

黄姜皂素废酸液在均相离子膜中渗析规律的研究

为了研究皂素水解废液在离子交换膜中的渗析规律,实验考察了废液中电导率、含盐量、氢离子浓度、硫酸盐浓度、Ca离子浓度、Mg离子浓度和有机物浓度随渗析时间的关系。研究结果表明:渗析时间进行100 h后,处理效果达到稳定状态;废液与渗析液的电导率几乎相等;含盐量、H+浓度、SO2-4浓度的分离效率分别为71%、62%、78%;Ca去除效果优于Mg去除效果;大部分有机物无法通过离子交换膜。