土壤有机质矿化与温室气体释放初探

通过土壤有机质的矿化作用，模拟估算温室气体在中国土壤中的释放量，结果表明，ＣＯ_２从土壤中的释放量为３７．５亿ｔ／ａ，ＣＨ_４从稻田中的释放量为０．２０亿ｔ／ａ，Ｎ_２Ｏ从稻田中的释放量为３．４５万ｔ／ａ。对土壤中温室气体释放估算提供了一种简便方法。由于掌握资料不足，准确估算需进一步研究。     

全球能源消费与CO2排放量

在收集全球能源储量和流通状况的基础上，综述了世界各地区能源消费量和各国人均能源水平，汇总了全球ＣＯ２排放总量及各大洲对全球ＣＯ２排放量的贡献率，到２１００年，全球Ｃ矿量预计将从目前６０亿ｔ／ａ增加到３６０亿ｔ／ａ，同时，旨出１９９６年中世界人口１８．８％的北美、欧洲、日本、ＣＯ２排放３１．６亿ｔ（碳），占全球当年ＣＯ２排放总量的５２．４％。     

水稻土中胱氨酸分解产生含硫气体的研究

测定在室内培养情况下南京水稻土中挥发性含硫气体的释放．结果表明,该土壤中产生Ｈ２Ｓ、羰基硫（ＣＯＳ）和二甲基硫（ＭＤＳ）气体．当土壤中加入胱氨酸后,检测到甲硫醇（ＣＨ３ＳＨ）、二硫化碳（ＣＳ２）、ＣＯＳ、Ｈ２Ｓ和ＤＭＳ气体．除ＤＭＳ之外,这些气体的释放量随胱氨酸添加量增加而增加．据此推测,水稻土中胱氨酸的分解可能是ＣＨ３ＳＨ、ＣＳ２、ＣＯＳ、Ｈ２Ｓ等４种气体产生释放的来源之一．在厌氧条件（充氮淹水）下检测到的含硫气体低于好氧条件（普通大气淹水）．光照、ｐＨ值、土壤含水量等对含硫气体的释放量均有影响     

水稻土中胱氨酸分解产生含硫氧气体的研究

测定在室内培养情况下南京水稻土中挥发性含硫气体的释放。结果表明，该土壤中产生Ｈ２Ｓ、羟基硫（ＣＯＳ）和二甲基硫（ＭＤＳ）气体，当土壤中加入胱氨酸后，检测到甲硫醇（ＣＨ３ＳＨ）、二硫化碳（ＣＳ２）、ＣＯＳ、Ｈ２Ｓ和ＭＤＳ气体，除ＤＭＳ之外，这些气体的释放量随胱氨酸添加量而增加。据此推测，水稻土中胱氨酸的分解可能是ＣＨ３ＳＨ、ＣＳ２、ＣＯＳ、Ｈ２Ｓ等４种气体产生释放的来源之一，在厌氧条件（充氮淹水）下     

微生物絮凝剂的絮凝实验研究

用ＧＣＩ培养基从曲阳污水厂污泥和俞泾浦底泥中分离出３株产生高絮凝活性的微生物，所研制出的微生物絮凝剂，对主同岭土悬浊液，土壤悬浊液和碱性染料废水均有良好的净化效果，在助凝作用上，ＣａＯ的效果明显优于ＣａＣｌ２，微生物絮凝剂（液体）适宜的投加量为１．０％，助凝剂ＣａＯ（１．０％浓度）投加量为２．０％，在研制微生物絮凝剂的过程中，适宜的摇瓶培养时间为７２ｈ离心条件为中高速（５０００，１００００ｒ／ｍｉ     

城市生活垃圾填埋产气规模研究

通过理论计算及实验室和现场的试验，研究了生活垃圾填埋产气规律。结果表明，理想条件下上海市生活垃圾填坦产气量最大不超过９６．３１Ｌ／ｋｇ，填埋后１－５ａ内，产气速率为１．７－２４７．２ｍＬ／ｋｇ．ｄ填蛙后２ａ的产气速率为４．６ｍＬ／ｋｇ．ｄ填埋气体中ＣＨ４和ＣＯ２的体系分数范围分别为５５＝－５６０＾     

微域培养试验中影响石油降解的几个因素

试验研究微域培养中土壤深度，油水添加次序以及搅拌等因素对石油降解速率的影响，结果表明：微域中随着土壤深度由４ｍｍ增加到３２ｍｍ，ＣＯ２累积释放量下降１６．７Ｔ％，石油碳氢化合物降解量减少１８．２％；先加水后加油可增加ＣＯ２累积释放量达３６．５％，ＴＰＨ降解量提高２１．５％；搅拌可以增加ＣＯ２释放与ＴＰＨ的降解。     

我国SO_2和NO_X排放强度地理分布和历史趋势

根据我国燃料消费、燃料的含硫量和硫与氮氧化物排放因子，计算我国各地区ＳＯ_２和ＮＯ_Ｘ排放强度地理分布。结果指出，我国原煤含硫量为１．１２％。１９９０年全国ＳＯ_２和ＮＯ_Ｘ的排放量分别为１７５１．８万ｔ和８４２．２万ｔ，排放强度最大的地区是中东部地区，即辽宁、河北、山东、山西和浙江。这些地区平均排放强度大于７ｔ／ｋｍ￣２·ａ。还估算了全国１９５０～１９９０年ＳＯ_２和ＮＯ_Ｘ历年的排放量。     

华北地区旱田土壤氧化亚氮的排放

在１９９１－１９９３年间用封闭罩测定了对照田、施肥田Ｎ２Ｏ的排放量。结果表明，Ｎ２Ｏ通量显示出、空变化规律。对照田，施尿素田和施混合肥田（尿素加有机肥）Ｎ２Ｏ排放量分别是１．０３±０．４ｋｇＮ／ｈｍ＾２ａ；１．９１±０．６ｋｇＮ／ｈｍ＾２ａ和２．１１±１．０ｋｇＮ／ｈｍ＾２ａ，尿素和混合肥释放Ｎ２Ｏ系数分别为０．２９％和０．３５％。由土壤含水量，土壤温度和速效氮浓度等土壤变量建立了Ｎ２Ｏ排放的统计     

黔中岩溶地区草地下土壤CO2含量的变化特征

全球碳循环中，ＣＯ２的未知汇可能是陆地生态系统中某一部分，如土壤。土壤中ＣＯ２的含量是大气的几倍至近百倍。它的吸收与释放将影响大气中的ＣＯ２浓度，岩溶地区占全球陆地面积的１／１５，对典型的岩溶地区－黔中某地土壤的ＣＯ２进行了四季及昼夜的采样测定，结果表明，该地地表大气的ＣＯ２含量具有季节变化的特征，土壤气中的ＣＯ２浓度为大气ＯＣ２浓度的几倍至一百多倍；自地表向下，随着土壤浓度的增大，ＣＯ２浓度升高     

CH4 emission and conversion from A2O and SBR processes in full-scale wastewater treatment plants

Wastewater treatment systems are important anthropogenic sources of CH4emission. A full-scale experiment was carried out to monitor the CH4 emission from anoxic/anaerobic/oxic process(A2O) and sequencing batch reactor(SBR) wastewater treatment plants(WWTPs) for one year from May 2011 to April 2012. The main emission unit of the A2O process was an oxic tank, accounting for 76.2% of CH4emissions; the main emission unit of the SBR process was the feeding and aeration phase, accounting for 99.5% of CH4emissions. CH4can be produced in the anaerobic condition, such as in the primary settling tank and anaerobic tank of the A2O process. While CH4can be consumed in anoxic denitrification or the aeration condition, such as in the anoxic tank and oxic tank of the A2O process and the feeding and aeration phase of the SBR process. The CH4emission flux and the dissolved CH4concentration rapidly decreased in the oxic tank of the A2O process. These metrics increased during the first half of the phase and then decreased during the latter half of the phase in the feeding and aeration phase of the SBR process. The CH4oxidation rate ranged from 32.47% to 89.52%(mean: 67.96%) in the A2O process and from 12.65% to 88.31%(mean: 47.62%) in the SBR process. The mean CH4 emission factors were 0.182 g/ton of wastewater and 24.75 g CH4 /(person·year) for the A2O process, and 0.457 g/ton of wastewater and 36.55 g CH4 /(person·year) for the SBR process.     

Effect of phosphogypsum and dicyandiamide as additives on NH3, N2O and CH4 emissions during composting

A laboratory scale experiment of composting in a forced aeration system using pig manure with cornstalks was carried out to investigate the effects of both phosphogypsum and dicyandiamide (DCD, C2H4N4) as additives on gaseous emissions and compost quality. Besides a control, there were three amended treatments with different amounts of additives. The results indicated that the phosphogypsum addition at the rate of 10% of mixture dry weight decreased NH₃ and CH₄ emissions significantly during composting. The addition of DCD at the rate of 0.2% of mixture dry weight together with 10% of phosphogypsum further reduced the N₂O emission by affecting the nitrification process. Reducing the phosphogypsum addition to 5% in the presence of 0.2% DCD moderately increased the NH₃ emissions but not N₂O emission. The additives increased the ammonium content and electrical conductivity significantly in the final compost. No adverse effect on organic matter degradation or the germination index of the compost was found in the amended treatments. It was recommended that phosphogypsum and DCD could be used in composting for the purpose of reducing NH₃, CH₄ and N₂O emissions. Optimal conditions and dose of DCD additive during composting should be determined with different materials and composting systems in further study.     

CO2 reaction with Ca(OH)2 during SO2 removal with convective pass sorbent injection and high temperature filtration

The Kyoto Protocol calls for greenhouse gas emission reductions which could affect the use of coal for producing electricity. Carbon credits are being explored as a method for countries to meet their reduction commitments. Carbon dioxide removal in flue gas desulfurization (FGD) systems should be considered if and when the concept of carbon credits are implemented. This paper addresses the factors affecting sulfur dioxide removal, including the reaction of carbon dioxide, occurring during convective pass sorbent injection with high temperature filtration for a typical coal-fired power plant. Significant carbonation is found to occur, and the levels are found to depend on injection/filtration temperatures and the residence time on the filter. Ca/S stoichiometry during sorbent injection is found to affect not only the sorbent conversions in the convective pass sorbent injection stage but also the final sorbent conversions in the filtration stage. Even though high sorbent carbonation hinders the sorbent utilization for SO₂ removal, slight alterations in CO₂ concentration are found to have no significant effects on the SO₂ removal of the process.     

放射示踪法研究O2存在时14CS2与OH的光化学反应

用放射示踪法研究~(14)CS_2和OH的光化学反应,指出氧对反应有促进作用,在反应体系中(~(14)CS_2-H_2O_2-C_3H_8-N_2-O_2)主要产物为O~(14)CS,~(14)CO及少量~(14)CO_2。O~(14)CS和~(14)CO有相似的动力学曲线,~(14)CO_2则是另一种情况。总反应速率常数随氧压增加而增大,在氧压为33330Pa时,~(14)CS_2消失的总速率常数可高达3.4×10~(-12)cm~3mol~(-1)S~(-1)。在实验中观察到~(14)CS_2能在室温下转变为~(14)CO_2的现象。讨论了光化学反应的历程。     

Simulated-sunlight-activated photocatalysis of Methylene Blue using cerium-doped SiO2/TiO2 nanostructured fibers

Cerium-doped SiO₂/TiO₂ nanostructured fibers were fabricated by electrospinning technology. The prepared fibers were characterized by thermogravimetric analysis (TGA), scanning electron microscopy (SEM), X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FT-IR). Using the fibers as catalysts, photocatalytic degradation of Methylene Blue (MB) aqueous solution was carried out under simulated sunlight. The 0.2% Ce doping proved to be the optimal concentration for the doping of TiO₂/SiO₂, compared to other Ce-doped molar concentrations. The 0.2% Ce-doped SiO₂/TiO₂ fibers exhibited higher photocatalytic activity than industrial Degussa P25 and the samples doped with only Ce or SiO₂. The reasons for improving the photocatalytic activity were also discussed. Several operational parameters were studied, which showed that the photocatalytic efficiency of MB was influenced by parameters such as the initial dye concentration, the initial pH, inorganic anions, and so on. In addition, the influences of an electron acceptor and a radical scavenger suggested that OH was the dominant photooxidant during the photocatalytic process. The reuse evaluation of the fibers indicated that their photocatalytic activity had good stability.     

株洲市工业区大气中SO2转化速率的研究

在湖南省株洲市工业区的下风向布点,同时测定大气中ＳＯ２的浓度、ＴＳＰ和＜０．２５μｍ细粒子中ＳＯ２－４的浓度．结果表明,大气中ＳＯ２浓度随着离污染源距离的增加迅速下降,和ＳＯ２相比,颗粒物中ＳＯ２－４浓度随距离的增加而降低的程度要慢得多．同步测定的ＳＯ２浓度和细粒子ＳＯ２－４浓度有显著的相关关系．根据风向、风速和新产生的细粒子中的ＳＯ２－４浓度及大气中ＳＯ２的浓度计算了株洲教育学院处ＳＯ２的转化速率,春季湿度大,ＳＯ２转化速率也大,为４．８％／ｈ,秋季湿度小,ＳＯ２的转化速率变低,为１．５％／ｈ．春季中路铺ＳＯ２转化速率为３．１％／ｈ．     

碳底物含量对厌氧条件下水稻土N2、N2O、NO、CO2和CH4排放的影响

理解底物碳氮对厌氧条件下水稻土排放氮素气体——氮气(N2)、氧化亚氮(N2O)和一氧化氮(NO)以及二氧化碳(CO2)和甲烷(CH4)的影响,有助于制定合理的温室气体减排措施,定量了解反硝化产物组成对碳底物水平的依赖性,也有助于氮转化过程模型研发中制定正确的关键过程参数选取方法或参数化方案.本研究采用粉砂壤质水稻土为研究对象,设置对照(CK)和加碳(C+)两个处理,前者的初始硝态氮和可溶性有机碳(DOC)含量分别为~50 mg·kg-1和~28 mg·kg-1,后者的分别为~50 mg·kg-1和~300 mg·kg-1.采用氦环境培养-气体及碳氮底物直接同步测定系统,研究了完全厌氧条件下碳底物水平对上述气体排放的影响.结果表明,CK处理无CH4排放,而C+处理可观测到CH4排放;C+处理的综合增温潜势显著高于CK处理(P<0.01);NO、N2O和N2排放量占这3种氮素气体排放总量的比重,在CK处理分别约为9%、35%和56%,在C+处理分别约为31%、50%和19%,处理间差异显著(P<0.01).由此表明,碳底物水平可显著改变所排放氮素气体的组成;对于旱地阶段硝态氮比较丰富的水稻土,避免在淹水前或淹水期间施用有机肥,有利于削减温室气体排放.     

地质时期的CO2及其温室效应

本文对当前流行的人类活动导致CO_2增加使未来气候变暖的温室效应的说法提出质疑,研究表明,自大气圈形成以来,CO_2已由原始大气主要成分(91％)波动下降到现在的微量组分(0.034％),其演化过程主要受自热因素控制,当前CO_2浓度增加是人为因素与自然作用叠加的结果,并不一定是人类活动或工业革命的产物,与此同时已经证实,冰期降温不是因为CO_2减少、温室效应减弱,而近年CO_2增加,温室效应加强又未得到确证,因此,以未来人为活动导致的CO_2变化趋势预测气候变化及可能的环境影响还为时尚早。     

甲基橙溶液多相光催化降解研究

利用中压汞灯作为光源,在ＴｉＯ２粉末悬浆体系内,以甲基橙溶液光降解脱色速率为例,探讨间歇式电光源圆柱形光化学反应器的运行情况及影响因素．分别考察了使用３００Ｗ和５００Ｗ中压汞灯、石英和玻璃冷阱、甲基橙溶液温度在２０℃或５０℃、不同ＴｉＯ２催化剂以及不同催化剂投加量对甲基橙溶液脱色速率的影响．从而得出在现有电光源圆柱形反应器的最佳运行条件下,２０ｍｇ／Ｌ的甲基橙溶液光照１０ｍｉｎ,脱色率达９７．４％．