污泥基活性炭去除水中重金属离子效能与动力学研究

以城市污泥为主要原料制备了污泥基活性炭(SAC),考察了其对重金属离子的吸附去除效能和吸附动力学规律.并选择了2种商品活性炭(煤质炭,MAC和椰壳炭,YAC)作为对比,以初始浓度为50mg/L的Cu(II),Pb(II),Cd(II),Cr(VI)4种重金属离子为去除对象,分别进行了3种活性炭的表面理化性质分析及其对4种重金属离子的吸附试验.结果表明,SAC的比表面积和微孔容积仅为YAC和MAC的1/3~1/2,吸附速率也相对较慢,但其对Cu(II),Pb(II),Cr(VI),Cd(II)的平衡吸附量却远大于2种商品活性炭,分别为9.9,8.9,8.2,5.4mg/g,说明SAC表面的高酸性基团含量对重金属离子的吸附起到了关键作用;Langmuir与Freundlich吸附等温模型均能较好地拟合SAC对Cu(II)和Pb(II)的吸附,SAC对Cr(VI)的吸附过程更符合Langmuir模型,而SAC对于Cd(II)的吸附过程用Langmuir与Freundlich两个模型均不能较好地拟合,说明SAC表面缺少能够与Cd(II)发生反应的结合位点.     

介质阻挡放电反应器中的二硫化碳降解特性

为了解CS₂(二硫化碳)在介质阻挡放电反应器中的降解特性,提高其去除率,设计并制作了同轴圆柱介质阻挡放电反应器,研究了介质层数、外施电压、中心电极材料及直径、背景气氛种类和RH(相对湿度)对CS₂去除率的影响. 结果表明:在外施电压(4.0～6.5kV)较低时,单介质反应器的CS₂去除率高于双介质反应器;而在外施电压(6.5～9.0kV)较高时,双介质反应器对CS₂的去除效果更好,增大外施电压有利于CS₂的降解. 铜丝比不锈钢丝更适合用作反应器的中心电极,此外,增加中心电极的直径也可提高CS₂去除率. 当中心电极直径从 3.2mm增至4.8mm时,CS₂平均去除率由63%增至75%,但平均质量能耗由510kJ/mg增至611kJ/mg. 同等条件下,CS₂在氧气中的平均去除率(74%)最大,空气(59%)中次之,氮气(48%)中最小;背景气氛中适量的RH(26%)有助于提高CS₂去除率,但RH太大(大于50%)反而会降低CS₂去除率.      

太原市工、商业区PM10中PAHs碳同位素组成及来源

利用中流量大气综合采样仪采集太原市工业区和商业区PM₁₀样品,使用GC/IRMS技术分析了PAHs的δ13C值(碳同位素组成),并根据碳同位素质量平衡计算了煤烟尘和机动车尾气对2类功能区的贡献率. 结果表明:工业区PM₁₀中PAHs的δ13C值在-26.0‰~-24.5‰之间,随环数增加呈贫13C趋势,与煤烟尘δ13C值的变化趋势一致,表明煤烟尘是工业区的一个主要污染源;商业区PAHs的δ13C值在-26.6‰~-26.2‰之间,较工业区显著贫13C,商业区与工业区的污染源有明显差异;除机动车尾气和煤烟尘外,工业区和商业区还有其他污染源输入,其中工业区有生物质燃烧排放输入,商业区有机动车曲轴箱润滑油残渣输入;煤烟尘和生物质燃烧对工业区的贡献率分别为59.3%~70.8%和29.2%~40.7%,表明工业区煤烟污染严重;机动车对商业区PAHs的贡献率在86.1%~95.8%之间,是商业区PM₁₀中PAHs的主要排放源,其中润滑油残渣的贡献率(在40.9%~85.3%之间)最大,机动车尾气的贡献率在8.3%~54.9%范围内,而煤烟尘的贡献率(在4.2%~13.9%之间)最小.      

基于密度泛函理论模拟单壁碳纳米管对五种核酸碱基的吸附

基于密度泛函理论,模拟了单壁碳纳米管(SWNTs)对5种碱基的吸附作用.考察了SWNTs直径、电荷转移量、碱基最高占据分子轨道能(EHOMO)和最低未占据分子轨道能(ELUMO)与SWNTs吸附碱基的吸附能之间的关系.结果表明,随着SWNTs直径的增大,SWNTs吸附碱基的吸附能降低.SWNT(6,6)吸附5种碱基的最低吸附能Emin与由碱基转移到SWNTs的电荷转移量(Q)及碱基的EHOMO线性负相关,相关系数分别为-0.966和-0.804(P<0.05).吸附后SWNTs与碱基的前线轨道无重叠,且SWNTs电子结构未受影响,表明吸附行为属于物理吸附.     

Removal of Remazol Brilliant Violet-5R dye using periwinkle shells

The purpose of this research is to obtain optimal processing conditions for the adsorption of Remazol Brilliant Violet-5R (RBV-5R) dye onto activated carbon prepared from periwinkle shells (PSAC) by chemical activation with KOH using response surface methodology. Central composite design (CCD) was used to determine the effects of three preparation variables; CO₂ activation temperature, CO₂ activation time and KOH:char impregnation ratio (IR) on two responses; percentage RBV-5R dye removal and PSAC yield. Based on the CCD, two quadratic models were developed for percentage RBV-5R dye removal and PSAC yield, respectively. The most influential factor on each experimental design response was identified from the analysis of variance (ANOVA). The optimum conditions for the adsorption of RBV-5R dye onto PSAC were CO₂ activation temperature of 811 °C, CO₂ activation time of 1.70 h and IR of 3.0, resulting in 81.28% RBV-5R dye removal and 28.18% PSAC yield. PSAC prepared under optimum conditions was mesoporous with a Brunauer–Emmett–Teller surface area of 1894 m²·g^?1, total pore volume of 1.107 cm³·g^?1 and average pore diameter of 2.32 nm. The surface morphology and functional groups of the activated carbon were respectively determined from the scanning electron microscopy and Fourier transform infrared analysis.     

Trophic transfer of polybrominated diphenyl ethers and polychlorinated biphenyls in a tidal freshwater marsh

The John Heinz National Wildlife Refuge (NWR) at Tinicum Marsh contains one of the last remaining tidal freshwater marsh communities along the Pennsylvania side of the Delaware River Estuary. The marsh receives a significant load of nutrients and sediment-associated contaminants and is hypothesised to act as an effective trap for these chemicals. The goal of this study was to quantify the levels of polybrominated diphenyl ethers (PBDEs) and polychlorinated biphenyls (PCBs) at various trophic levels at two sites within Tinicum Marsh and assess the factors important in determining their bioaccumulation and trophic transfer. For both PCBs and PBDEs, lipid variation for all species was a large factor in determining contaminant body burden. Also, concentrations in biota increased with increasing trophic level as determined by nitrogen isotope analysis (δ¹⁵N values) at the downstream site within Tinicum Marsh. This trend was less apparent at the upstream site and may be due to differences in feeding behaviours among species between the two sites and/or differences in carbon and nitrogen sources and recycling. These data are valuable in assisting bioaccumulation/trophic transfer studies and serve as benchmarks to which future PCB and PBDE concentrations will be compared.     

A comprehensive model to estimate the simultaneous release of acidic and basic gaseous pollutants from swine slurry under different scenarios

Swine slurry is a source of atmospheric pollutants. Emissions of basic and acidic compounds from slurry are largely dependent on the surface pH. In a storage system, the pH at the surface layers changes over time due to the volatilisation of ammonia (NH₃), carbon dioxide (CO₂) and acetic acid (HAc). In this article, a comprehensive gas emission–pH (GE–pH) coupled model is proposed to describe the simultaneous release of acidic and basic gaseous pollutants from swine slurry. The model was applied to describe the release of NH₃, CO₂, HAc and hydrogen sulphide (H₂S) from standard slurries stored in animal houses, outside storage tanks and lagoons. The modelled results agreed well with values reported in the literature and could be reasonably interpreted. The key parameters affecting the release of gases were: initial pH, initial concentration of total ammonium nitrogen and inorganic carbon, slurry temperature and air velocity. This study suggests that future modelling studies on gas emissions from animal slurry should consider the concentration of inorganic carbon and the frequency in which the slurry surface is mixed or altered, because they affect the surface pH and the release of gaseous pollutants from slurry.     

Behaviour of pendimethalin and oxyfluorfen in peanut field soil: effects on soil biological and biochemical activities

A field experiment was conducted to study the dissipation kinetics of herbicides pendimethalin and oxyfluorfen in black soil of peanut field at half recommended rate (HRE), recommended rate and double recommended rate as well as to assess their effects on soil microbial parameters and enzymatic activities. In addition, their role in the transformations and availability of some plant nutrients like nitrogen transformation (through ammonification and nitrification processes) and availability of phosphorous were also studied. Incorporation of these herbicides was found to stimulate the activity of soil microbial biomass carbon, fluorescein diacetate hydrolysing activity, alkaline phosphatase and ammonification rates, while dehydrogenase activity, acid phosphatase, nitrification rate and available phosphorous was adversely affected. However, urease remains almost unchanged except for little stimulation at later stages. Dissipation of pendimethalin and oxy?uorfen followed first-order reaction kinetics with half-life (T_1/2) of 13.7–20.1 and 21.5–27.4 days, respectively. Residues of both herbicides persisted up to 60 days in the soil at all the doses except 45 days for pendimethalin at HRE.     

Changes in nutrient content and stable isotope ratios of C and N during decomposition of seagrasses and mangrove leaves along a nutrient availability gradient in Florida Bay,USA

The decomposition of the mangrove Rhizophora mangle and the seagrass Thalassia testudinum was examined using litterbags along a natural gradient in nutrient availability. Seagrass leaves had a higher fraction of their biomass in the labile pool (57%), compared to mangrove leaves (36%) and seagrass rhizomes (29%); the overall decomposition rates of the starting material reflected the fractionation into labile and refractory components. There was no relationship between the N or P content of the starting material and the decomposition rate.

Nutrient availability had no influence on decomposition rate, and mass was lost at the same rate from litterbags that were buried in the sediment and litterbags that were left on the sediment surface. The dynamics of N and P content during decomposition varied as a function of starting material and burial state. N content of decomposing mangrove leaves increased, but seagrass rhizomes decreased in N content during decomposition while there was no change in seagrass leaf N content. These same general patterns held for P content, but buried seagrass leaves increased in P content while surficial leaves decreased. δ¹³C and δ¹⁵N changed by as much as 2‰ during decomposition.     

影响中国碳排放绩效的区域特征研究——基于熵值法的聚类分析

论文选择影响碳排放绩效的主要指标,基于熵值法确定各指标权重,采用系统聚类分析的方法,以中国省域为研究对象,将全国分为7类区域。分析结果显示:区域分工特征是造成目前中国省级碳排放绩效区域差异的主要影响因素,其次是高碳产业工艺特征和能源结构特征,而经济结构对解释省级碳排放绩效区域差异的贡献有限。北方地区高碳产品生产份额高且工艺水平相对低,能源消费中极高的煤炭比例加重了负面影响,造成其二氧化碳排放绩效水平低,特别是华北地区;近年来东南沿海地区高碳产业也逐步增加,但由于其工艺先进,在一定程度上抵消了高碳产品份额高的负面影响;中西部地区目前高碳产品份额虽然低于东部地区,但工艺水平也低,造成了其低水平的二氧化碳排放绩效。由于各省历史发展、自然资源禀赋、区域分工角色等因素不同,且遵从经济宏观发展客观规律和经济区位理论,除了少数发达地区之外,中国其他区域短时间内很难改变其经济和能源结构,低碳政策制定的重点应放在提高高碳产业工艺水平方面。