乌鲁木齐河地表水化学组成及时空分布特征

乌鲁木齐河作为乌鲁木齐市的主要水源地,在生态保护和城市供水中均具有重要的战略意义。为了研究乌鲁木齐河水化学特征及水环境质量,于2016年4—10月逐月对乌鲁木齐河6个采样断面进行地表水样采集,获取水样41个,对主要离子(K~+、Na~+、Ca~(2+)、Mg~(2+)、Cl~-、HCO_3~-、SO_4~(2-))浓度及pH、DO、TDS、CODMn、TN、TP、NH3-N进行监测分析,探讨了水化学组成的时空差异及影响因素,研究了乌鲁木齐河的水环境质量状况。结果显示,乌鲁木齐河水域年离子总量平均值为213.27 mg/L,属弱矿化度水,年离子总量在空间上表现出沿主河道由南向北逐步增加的趋势。主要阴离子为HCO_3~-和SO_4~(2-),主要阳离子为Ca~(2+),水质类型为Ca~(2+)-HCO_3~--SO_4~(2-)型。2016年河水年内不同时期TDS平均浓度排序为:9月10月4月5月6月8月7月。对水化学离子含量基于时间序列分析,结果显示除Ca~(2+)、HCO_3~-外,其他离子含量在各月份间均存在显著差异。SO_4~(2-)浓度在年内变化最为明显,呈现先减少后增加的趋势。对主要离子含量基于空间序列进行分析,结果显示,仅Na+含量存在显著差异。现阶段乌鲁木齐河的水环境质量为轻度污染。     

Seasonal variations of monocarbonyl and dicarbonyl in urban and sub-urban sites of Xi’an,China

Seventeen airborne carbonyls including monocarbonyls and dicarbonyls were determined in urban and sub-urban sites of Xi’an, China in three seasons in 2010. In winter, acetone was the most abundant carbonyl in the urban site due to usage of organic solvents in constructions and laboratories and its slower atmospheric removal mechanisms by photolysis and reaction with hydroxyl radical than those of formaldehyde and acetaldehyde. In the sub-urban site, acetaldehyde was the most abundant carbonyl, followed by formaldehyde and acetone. During summer, however, formaldehyde was the most dominant carbonyl in both sites. The photooxidations of a wide range of volatile organic compounds (VOCs) yielded much more formaldehyde than other carbonyls under high solar radiation and temperature. In the urban site, the average concentrations of dicarbonyls (i.e., glyoxal and methyglyoxal) in spring and summer were higher than that in winter. Transformation of aromatic VOCs emitted from fuel evaporation leads to the formation of 1,2-dicarbonyls. A reverse trend was observed in sub-urban sites, as explained by the relatively low abundances and accumulations of VOC precursors in the rural atmosphere during warm seasons. Moreover, cumulative cancer risk based on measured outdoor carbonyls (formaldehyde and acetaldehyde) in Xi’an Jiaotong University and Heihe was estimated (8.82?×?10^?5 and 4.96?×?10^?5, respectively). This study provides a clear map on the abundances of carbonyls and their source interpretation in the largest and the most economic city in Northwestern China.     

磷石膏水热法合成硫酸钙晶须

以磷石膏为原料，二水合硫酸钙、硫酸镁、甘油为添加剂，采用水热法合成硫酸钙晶须，考察了料浆含量、反应温度、反应时间、体系pH等因素对晶须的直径和长径比的影响；并采用SEM技术观察硫酸钙晶须的形貌。实验结果表明，当磷石膏含量2.5%（w）、反应温度130 ℃、反应时间4 h、体系pH 4时，制备得到的硫酸钙晶须长径比为56.24，平均直径为0.17 μm。SEM表征结果显示，硫酸钙晶须形貌规整、分散均匀、直径较小，达百纳米级。     

过硫酸钾去除水中的TCE

以地水中的氯代烃污染物三氯乙烯(TCE)为目标污染物,以过硫酸钾溶液为氧化剂,探讨了不同条件下过硫酸钾对TCE的去除效果。实验结果表明,在40℃,过硫酸钾初始浓度为2.43 g/L条件下,反应2 h后,TCE的去除率就可达到96.8%;过硫酸钾对TCE的去除符合一级反应动力学方程,速率常数(K)为1.3364 h-1,半衰期(t1/2)为0.51 h;过硫酸钾对TCE的去除速率在pH为中性附近时最大,其后无论pH升高或降低去除速率均减小;受温度和pH影响较明显,并且反应温度越高,受pH的影响越明显;随离子强度的增加而减小;反应活化能为119.6 kJ/mol;过硫酸钾溶于水生成过硫酸根离子(S2O28-),S2O28-会进一步生成硫酸根自由基(SO4-.),在碱性条件下,SO4-.与OH-反应会进一步生成羟基自由基(.OH)。过硫酸钾对于TCE的去除主要源自SO4-.和.OH的强氧化性。     

好氧颗粒污泥自生动态膜生物反应器处理碱减量印染废水

自生动态膜生物反应器(SFDMBR)接种颗粒污泥启动,研究溶解氧浓度和水力停留时间对该反应器处理碱减量印染废水的影响。自生动态膜生物反应器形成稳定的动态膜后,出水浊度小于10 NTU,系统对浊度的去除率在90%以上,溶解氧和水力停留时间对反应器出水浊度基本无影响。系统对废水色度的去除率随着溶解氧浓度的提高和水力停留时间的延长而增加,但是系统对色度的去除效率一般不超过40%。溶解氧浓度由0.3 mg/L逐渐增大至2.4 mg/L,COD的去除率由40%提升至80%,而当溶解氧浓度大于1.0 mg/L后,UV254的去除率达到95%。水力停留时间在8~48 h时,COD去除效率由65%逐渐上升至85%左右;水力停留时间在8~32 h,UV254去除效率为68%~93%,超过32 h后水力停留时间对UV254去除效率的影响已不明显。     

酵母菌对厨余垃圾厌氧发酵产乙酸的影响

研究了酵母菌对厌氧发酵过程中垃圾水解速率、挥发性有机酸(VFA)产量、乙酸产量的影响。结果表明：控制反应器中pH值为7时，接种酵母菌后，垃圾的水解速率明显提高，产酸速率和产酸量都明显高于不接种酵母菌的反应器，乙酸浓度能够达到9 458 mg/L，占挥发性有机酸总量的58.2%。垃圾本身含有的微生物对产酸也有促进作用，酵母菌和垃圾本身含有的微生物共同作用才能使得乙酸的产生最大化。     

A modeling assessment of association between East Asian summer monsoon and fate/outflow of α-HCH in Northeast Asia

Using a dynamic numerical atmospheric transport model for organochlorine pesticides (OCPs), the relationship between the East Asian summer monsoon and the fate of α-hexachlorocyclohexane (α-HCH), a banned OCP, in the atmosphere over Northeast Asia was investigated and assessed. The modeled temporal and spatial patterns and variability of α-HCH air concentrations during the summer months of 2005 revealed a strong link between this chemical in the atmosphere over Northeast Asia and the East Asian summer monsoon. At lower atmospheric levels, easterly and southeasterly winds blowing from relatively cold ocean surface convey α-HCH air concentration from southeast China to northeast China. A monsoon front extending from southeast China to Japan, characterized by a strong wind convergence, carried the air concentration to a high elevation of the atmosphere where it was delivered by southerly monsoon flow to northern China and North Pacific Ocean. This summer monsoon associated northward atmospheric transport caused a reversal of the soil/air exchange from outgassing to net deposition during spring–summer period. The modeled wet deposition fluxes of α-HCH agreed well with the changes in the typical summer monsoon rain bands, designated as Meiyu in China, Changma in Korea, and Baiu in Japan. The major wet deposition flux paralleled with the monsoon front as well as the monsoon rain bands. The temporal change in the fluxes exhibits abrupt northward advances, which is associated with a stepwise northward and northeastward advance of the East Asian summer monsoon. The modeled α-HCH outflow in the atmosphere from China occurs mostly in the summer months and through northeast China, featured strongly by the evolution of the summer month. This study suggests that the East Asian summer monsoon provides a major atmospheric pathway and summer outflows to α-HCH over East Asia.     

Concentrations and distributions of 18 organochlorine pesticides listed in the Stockholm Convention in surface sediments from the Liaohe River basin,China

Organochlorine pesticides (OCPs) were analyzed in 26 surface sediment samples from the Liaohe River basin, and the distributions of and potential environmental risks posed by OCPs in the basin were evaluated. Eighteen OCPs listed in the Stockholm Convention were determined using isotope-dilution gas chromatography–high resolution mass spectrometry. This is the first study of hexachlorobenzene (HCB) in the Liaohe River basin sediments. The total OCP concentrations were 0.39–68.06 ng g^?1 dry weight. The total α-, β-, γ-, and δ-hexachlorocyclohexane (HCH), the total dichlorodiphenyltrichloroethane (DDT – p,p′-dichlorodiphenyldichloroethane (DDD), p,p′-dichlorodiphenyldichloroethylene (DDE), o,p^'-DDT, and p,p′-DDT), and the HCB concentrations in the sediment samples were 0.1–28.48 ng g^?1 (mean 4.01 ng g^?1), 0.08–6.52 ng g^?1 (mean 3.07 ng g^?1), and 0.18–24.8 ng g^?1 (mean 4.38 ng g^?1), respectively. The HCB concentrations were higher than the concentrations of the other OCPs, and the HCHs and HCB together were the dominant OCPs. β-HCH was the most abundant HCH isomer. The concentrations of DDTs and other OCPs were relatively low, and the (DDE+DDD)/DDT ratios (>0.5) and DDD/DDE ratios (<1) indicated that no recent DDT inputs had occurred in the Liaohe River system. The main sources of HCHs were probably the historical production and agricultural use of HCH in the study area. The DDT and HCH concentrations were generally below or similar to the concentrations that have been found in other parts of the world. An ecotoxicological evaluation indicated that HCHs in surface sediments pose slight risks to human and ecological health in the Liaohe River basin.     

Iodine enrichment and the underlying mechanism in deep groundwater in the Cangzhou Region,North China

Environmental Science and Pollution Research - The lack of information on the origin and behavior of iodine in deep groundwater restricts the development and use of groundwater resources. To...     

高地下水位地区透水停车场的水文控制效果

为确定高地下水位地区透水铺装对路面径流的水文控制效果,在上海市区建造了4个实验性透水铺装单元与1个不透水铺装对照,其中3个为设有防水衬底的不透型设施分别为透水混凝土铺装(设施Ⅰ)、水泥稳定碎石基层/缝隙透水砖面层(设施Ⅱ)、碎石基层/缝隙透水砖面层(设施Ⅲ),1个普通缝隙透水砖铺装(设施Ⅳ),以及1个不透水混凝土对照(设施0).历时1年监测了实际降雨条件下4种实验设施的表面径流、排水管出流流量及表面渗透速率,考察不同设施的径流总量削减率、峰值削减及峰现延迟能力.结果表明,缝隙透水砖面层的表面稳定渗透速率明显小于透水混凝土面层,使用1年后,2种面层表面稳定渗透速率均明显下降;4种设施的表面产流均无显著差异;3种不透型设施的就地消纳水量能力均较弱,年径流总量控制率分别为24.2%、28.5%、28.4%,排水管不发生出流的控制降雨量分别为5.2 mm、7.8 mm、7.8 mm;设施Ⅰ的峰值削减与峰现延迟效果弱于设施Ⅱ及设施Ⅲ,且3种设施的峰值削减率和峰现延迟时间与降雨强度呈现显著负相关性.