脱硫灰-石灰石湿法脱硫石膏中杂质悬浮分离实验

根据脱硫灰及石膏的特性,在无挡板平底圆筒搅拌槽内,对脱硫石膏中的杂质进行完全离底悬浮分离实验,研究结果表明,完全离底悬浮搅拌时,悬浮高度比越低,越有利于杂质分离。对于直径D≥24cm的搅拌槽,当桨叶离底高度cb=4cm,桨径槽比d／D=0．65,杂质分离效率叼最高,约82％;当直径D=20cm时,杂质分离效率η随d／D的增大而增大,桨叶离底间距减小,杂质分离效率受d／D影响程度减小;当桨叶离底高度cb=4cm时,随着搅拌槽直径D的增大,杂质分离效率总体呈现增大趋势,降低桨叶离底高度cb杂质分离效率变化较大;进行完全离底悬浮分离后,石膏纯度提高。     

共价键型絮凝剂去除水中水杨酸的性能和机理

制备了带有季铵基团的共价键型硅铝复合絮凝剂(CBHy C)。通过透射电镜(TEM)表征,与聚合氯化铝絮凝剂(PAC)相比,CBHy C絮凝剂的分子粒径更大。以烧杯实验考察了CBHy C对水中低浓度污染物水杨酸的去除效果和对高岭土标准液的除浊效果。结果表明,CBHy C絮凝剂去除低浓度下SA的混凝效果明显优于PAC,并且絮凝效果随着絮凝剂的投加量、Si/Al摩尔比和碱化度(B值)的增大而提高;CBHy C絮凝剂的除浊效果与PAC相比差别并不明显,且受Si/Al摩尔比和B值的影响不大。通过辛醇-水分配比实验,与PAC和聚合硅酸铝(PASi C)做比较,探讨了CBHy C的作用机理,发现絮凝剂的辛醇-水分配比(Kow)与絮凝剂对SA的混凝效果存在正相关性。     

生物铁泥的Fe（Ⅲ）还原能力及影响因素

以生物铁泥和普通活性污泥为对象,在不同碳源及兼氧/厌氧条件下采用实验室恒温培养的方法考察了不同活性污泥的Fe（Ⅲ）还原性能。研究结果表明,不同活性污泥Fe（Ⅲ）还原能力相差较大,生物铁泥的Fe（Ⅲ）还原性能明显优于普通活性污泥,在兼性厌氧与严格厌氧条件下,分别是普通活性污泥的1.87倍和1.76倍;碳源对生物铁泥的Fe（Ⅲ）还原影响较小,而对普通活性污泥的Fe（Ⅲ）还原过程呈现出较明显的负影响;在实验控制的兼氧/厌氧条件下,2种活性污泥厌氧条件下Fe（Ⅲ）还原能力均大于兼氧条件。为活性污泥Fe（Ⅲ）还原过程的工程实际应用提供了理论依据。     

Cd、Pb复合污染下柠檬酸对龙葵修复效率及抗氧化酶的影响

植物修复土壤重金属被普遍认为是清洁、经济的生物修复方法。为了提高生物修复土壤重金属污染的效率,在室内盆栽实验中添加柠檬酸作为螯合剂促进龙葵对重金属的吸收,并研究其生理活性的变化。结果表明:当添加柠檬酸浓度为10 nmol/kg时,龙葵生物量显著提高(P<0.05),各部分生物量表现为:茎>叶>根;随着柠檬酸浓度的增加,龙葵对重金属Cd的吸收量显著(P<0.05)增加,在10 nmol时总吸收量最大,为229.85μg/g DW;龙葵对Cd、Pb的富集系数均在柠檬酸浓度为5 nmol/kg时达到最大;Pb吸收量随柠檬酸浓度增加表现出先增大后减小的趋势;添加柠檬酸促进了龙葵对Cd的吸收,增强了抗氧化酶活性,而对Pb的吸收效果不明显。     

重庆典型灰霾天气下大气气溶胶的激光雷达探测

简要介绍了法国Losphere公司ALS300型偏振Mie散射激光雷达的基本结构、探测原理及反演算法,并通过在重庆主城区2009年11月23～27日一次典型灰霾天气条件下连续的气溶胶激光雷达探测结果分析得出,重庆冬季典型灰霾天气下PBL平均高度约为600米,AOD值在4及以上。     

Photo-production of dissolved inorganic carbon from dissolved organic matter in contrasting coastal waters in the southwestern Taiwan Strait, China

Photo-production of dissolved inorganic carbon (DIC) from chromophoric dissolved organic matter (CDOM) is an important transformation process in marine carbon cycle, but little is known about this process in Chinese coastal systems. This study investigated an estuarine water sample and a coastal seawater sample from the subtropical waters in southeast of China. Water samples were exposed to natural sunlight and the absorption and fluorescence of CDOM as well as the DIC concentration were measured in the summer of 2009. The estuarine water had higher CDOM level, molecular weight and proportion of humic-like fluorescent components than the seawater that exhibited abundant tryptophan-like fluorescent component. After a 3-day irradiation, the CDOM level decreased by 45% in the estuarine water and 20% in the seawater, accompanied with a decrease in the molecular weight and aromaticity of DOM which was inferred from an increase in the absorption spectral slope parameter. The photo-degradation rates of all the five fluorescent components were also notable, in particular two humic-like components (C4 and C5) were removed by 78% and 69% in the estuarine water and by 69% and 56% in the seawater. The estuarine water had a higher photo-production rate of DIC than the seawater (4.4 vs. 2.5 μupmol/(L.day)), in part due to its higher CDOM abundance. The differences in CDOM compositions between the two types of waters might be responsible for the higher susceptibility of the estuarine water to photo-degradation and hence could also affect the photo-production process of DIC.     

Adsorption and redox reactions of heavy metals on synthesized Mn oxide minerals

Several Mn oxide minerals commonly occurring in soils were synthesized by modified or optimized methods. The morphologies, structures, compositions and surface properties of the synthesized Mn oxide minerals were characterized. Adsorption and redox reactions of heavy metals on these minerals in relation to the mineral structures and surface properties were also investigated. The synthesized birnessite, todorokite, cryptomelane, and hausmannite were single-phased minerals and had the typical morphologies from analyses of XRD and TEM/ED. The PZCs of the synthesized birnessite, todorokite and cryptomelane were 1.75, 3.50 and 2.10, respectively. The magnitude order of their surface variable negative charge was: birnessite> or =cryptomelane>todorokite. The hausmannite had a much higher PZC than others with the least surface variable negative charge. Birnessite exhibited the largest adsorption capacity on heavy metals Pb(2+), Cu(2+), Co(2+), Cd(2+) and Zn(2+), while hausmannite the smallest one. Birnessite, cryptomelane and todorokite showed the greatest adsorption capacity on Pb(2+) among the tested heavy metals. Hydration tendency (pK(1)) of the heavy metals and the surface variable charge of the Mn minerals had significant impacts on the adsorption. The ability in Cr(III) oxidation and concomitant release of Mn(2+) varied greatly depending on the structure, composition, surface properties and crystallinity of the minerals. The maximum amounts of Cr(III) oxidized by the Mn oxide minerals in order were (mmol/kg): birnessite (1330.0)>cryptomelane (422.6)>todorokite (59.7)>hausmannite (36.6).     

Black carbon (BC) in urban and surrounding rural soils of Beijing, China: spatial distribution and relationship with polycyclic aromatic hydrocarbons (PAHs)

The concentrations of black carbon (BC), total organic carbon (TOC) and polycyclic aromatic hydrocarbons (PAHs) have been determined in soils from urban and rural areas of Beijing. The rural area can be divided into plain and mountainous areas which are close to and relatively far from the urban area, respectively. Concentration of BC (5.83 ± 3.05 mg g⁻¹) and BC/TOC concentration ratio (0.37 ± 0.15) in Beijing’s urban soil are high compared with that in world background soils and rural soils of Beijing, suggesting the urban environment to be an essential source and sink of BC. Concentration of BC in the urban area decreases from the inner city to exterior areas, which correlates with the urbanization history of Beijing and infers accumulation of BC in old urban soils. Black carbon in Beijing soils mainly comes from fossil fuel combustion, especially traffic emission. Median PAH concentration in the urban area (502 ng g⁻¹) is one order of magnitude higher than that in the rural plain (148 ng g⁻¹) and mountainous area (146 ng g⁻¹) where PAHs are supposed to mainly come from atmospheric deposition from the urban area. Concentrations of BC correlate significantly with those of PAHs (p < 0.01, except naphthalene) in the urban area and with those of heavier 4-, 5- and 6- ring PAHs (p < 0.01) in the adjacent rural plain area, while there is no significant correlation with any PAH in the farther rural mountainous area.     

Ultraviolet degradation of methyltins: elucidating the mechanism by identification of a detected new intermediary product and investigating the kinetics at various environmental conditions

The photodegradation of methyltins, as environmental pollutants, has scarcely been studied so far because of the shortage of rapid and sensitive speciation methods, even though they have very simple structures. The photodegradation of monomethyltin trichloride (MMT), dimethyltin dichloride (DMT) and trimethyltin chloride (TMT) was studied with our new developed HPLC-FPD hyphenated system, which enables rapid and sensitive detection of methyltins. The half-life times and kinetic rate constants of their degradation at different pH were calculated. The results suggest that MMT, DMT and TMT can be degraded under the UV irradiation rapidly at different pH, with a degradation rate sequence of TMT相似文献   

全氟辛酸(PFOA)对菲律宾蛤仔体内酶活性的影响

采用半静态毒性实验方法,将菲律宾蛤仔(Ruditapes philippinarum)分别暴露于0.2、2、20μg·L-1的全氟辛酸(perfluorooctanoic acid,PFOA)中,在处理后第1、3、6、10、15、21天分别取样,测定整体组织中超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、过氧化物酶(POD)、谷胱甘肽-S-转移酶(GST)、7-乙氧基异吩噁唑酮脱乙基酶(EROD)活性和过氧化脂质(LPO)含量。酶活性分析结果显示:PFOA对菲律宾蛤仔组织SOD、CAT和POD活性均呈现先促进后抑制的作用;低浓度组SOD活性在暴露第1天达到最高,显著高于对照组(P<0.01);中高浓度组SOD活性在暴露第6天达到最低;暴露1~15 d,低浓度组CAT活性均显著高于对照组(P<0.05);高浓度组CAT活性在暴露第6天得到显著诱导,其余时间基本处于抑制状态;中浓度组POD活性在暴露第3天即达到最高,高浓度组POD活性基本一直处于抑制状态;随着PFOA暴露时间的延长,菲律宾蛤仔组织LPO含量呈现了先降低后升高的趋势;各浓度组中EROD的活力都显著被诱导(P<0.01),与处理浓度呈正相关;中高浓度组的GST活性在胁迫期间变化比较显著,呈现诱导-抑制的变化规律。研究表明,PFOA暴露能够引起菲律宾蛤仔组织抗氧化酶和生物转化酶的变化,可以与其他敏感性指标一起作为指示早期海洋PFOA污染的生物标志物。