化工园区空气中非甲烷总烃与挥发性有机物的定量关系

采用美国环保署(EPA)推荐的TO14/15方法和自动监测测定了某化工园区空气中挥发性有机物(VOC)以及非甲烷总烃,测定结果显示化工园区空气中非甲烷总烃与VOC的定量关系可以通过有效碳质量浓度建立,即非甲烷总烃有效碳质量浓度和VOC有效碳质量浓度之和相等。并藉此定义总有效碳解析度(R)以表征空气自动监测选定项目对空气有机污染的覆盖率指标,计算结果表明该空气自动监测选定的11项指标平均可表征该区域空气有机污染的71%。     

固定化白腐真菌反应器与接触氧化反应器联用处理癸二酸生产废水

采用固定化白腐真菌(WRF)反应器与接触氧化反应器联用处理癸二酸废水。在WRF反应器中,以汽曝玉米秸秆为载体,并添加铜、铁促进白腐真菌生长和产酶作用,载体的使用寿命约为45 d。在进水苯酚平均质量浓度为69.36 mg/L、平均进水COD为1 648.81 mg/L的条件下,经WRF反应器处理后,苯酚平均质量浓度降至7.59 mg/L,平均出水COD降至478.03 mg/L;再经接触氧化反应器处理后,苯酚平均质量浓度降至1.65 mg/L,平均出水COD降至297.31 mg/L。     

采用Zn-Se/不锈钢阴极的超声-电解法处理罗丹明B废水

采用超声-电解法考察了Zn-Se/不锈钢阴极处理罗丹明B废水的效果及影响因素。正交实验优化结果表明:在电流密度为2.4A/dm2、废水初始pH为6、超声功率为160W、通气量为10L/h、m(Zn)∶m(Se)为1∶1.5的Zn-Se/不锈钢作阴极、Ti/TiO2和铁网为双阳极的条件下,超声-电解法处理罗丹明B废水120min,废水脱色率为98.97%,COD去除率为88.11%。     

TiO2/SiO2@γ-Fe2O3光催化剂的制备及其光催化性能

以共沉淀法制备的纳米Fe3O4为核,以正硅酸乙酯为硅源,通过溶胶-凝胶法制备了SiO2@Fe3O4壳-核结构纳米颗粒,再以钛酸四丁酯为钛源,通过溶胶-凝胶法、经焙烧制得TiO2/SiO2@γ-Fe2O3磁性纳米光催化剂。采用X射线衍射仪、透射电子显微镜、比表面分析仪、振动磁强计对光催化剂的结构进行了表征,以苯酚溶液为模拟废水对光催化剂的光催化性能进行了评价。实验结果表明:经500℃焙烧的光催化剂活性相为锐钛矿型TiO2;在苯酚溶液初始浓度为0.2mmol/L、苯酚溶液pH为7的条件下,COD去除率为70.9%。     

Diurnal and spatial variations of soil NOx fluxes in the northern steppe of China

NO_x emissions from biogenic sources in soils play a significant role in the gaseous loss of soil nitrogen and consequent changes in tropospheric chemistry. In order to investigate the characteristics of NO_x fluxes and factors influencing these fluxes in degraded sandy grasslands in northern China, diurnal and spatial variations of NO_x fluxes were measured in situ. A dynamic flux chamber method was used at eight sites with various vegetation coverages and soil types in the northern steppe of China in the summer season of 2010. Fluxes of NO_x from soils with plant covers were generally higher than those in the corresponding bare vegetation-free soils, indicating that the canopy plays an important role in the exchange of NO_x between soil and air. The fluxes of NO_x increased in the daytime, and decreased during the nighttime, with peak emissions occurring between 12:00 and 14:00. The results of multiple linear regression analysis indicated that the diurnal variation of NO_x fluxes was positively correlated with soil temperature (P < 0.05) and negatively with soil moisture content (P < 0.05). Based on measurement over a season, the overall variation in NO_x flux was lower than that of soil nitrogen contents, suggesting that the gaseous loss of N fromthe grasslands of northern China was not a significant contributor to the high C/N in the northern steppe of China. The concentration of NO_x emitted from soils in the region did not exceed the 1-hr National Ambient Air Quality Standard (0.25 mg/m³).     

基于在线观测的太原市冬季PM2.5中金属元素污染水平及来源解析

为更好地识别太原市PM_2.5的来源,于2022年1月采用在线多金属监测仪对太原市区PM_2.5中13种金属元素(K、Ca、Ba、Cr、Mn、Fe、Cu、Ni、Zn、As、Se、Pb和Sr)小时浓度进行了监测,分析了其污染特征,采用正定矩阵因子分解(PMF)模型解析了其来源.结果表明,13种金属元素浓度之和均值为(3 901.6±2 611.2)ng·m^-3,在PM_2.5中平均占比为(7.1±7.7)%.Fe、Ca和K是3种主要的金属元素,浓度平均值分别为(1 319.5±1 003.5)、(1 181.0±1 241.6)和(883.3±357.3)ng·m^-3.ρ[Cr(Ⅵ)](4.6ng·m^-3)和ρ(As)(11.2 ng·m^-3)平均值高于国家环境空气质量(GB 3095-2012)和世界卫生组织的标准值.PMF源解析结果显示：扬尘、机动车排放、不锈钢制造、生物质燃烧与垃圾焚烧、散煤燃烧和工业燃煤是PM_2.5     

Microbial reduction of uranium (VI) by Bacillus sp. dwc-2: A macroscopic and spectroscopic study

The microbial reduction of U(VI) by Bacillus sp. dwc-2, isolated from soil in Southwest China, was explored using transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and X-ray absorption near edge spectroscopy (XANES). Our studies indicated that approximately 16.0% of U(VI) at an initial concentration of 100 mg/L uranium nitrate could be reduced by Bacillus sp. dwc-2 at pH 8.2 under anaerobic conditions at room temperature. Additionally, natural organic matter (NOM) played an important role in enhancing the bioreduction of U(VI) by Bacillus sp. dwc-2. XPS results demonstrated that the uranium presented mixed valence states (U(VI) and U(IV)) after bioreduction, which was subsequently confirmed by XANES. Furthermore, the TEM and high resolution transmission electron microscopy (HRTEM) analysis suggested that the reduced uranium was bioaccumulated mainly within the cell and as a crystalline structure on the cell wall. These observations implied that the reduction of uranium may have a significant effect on its fate in the soil environment in which these bacterial strains occur.     

北江中上游地表水和沉积物中PAHs和PCBs污染特征和风险评估

采用气相色谱-质谱法（GC-MS）测定了北江中上游流域地表水和沉积物样品中多环芳烃（PAHs）和多氯联苯（PCBs）类污染物的含量,分析了PAHs和PCBs的污染水平和空间分布,并评估了污染物的健康风险和生态风险.结果表明,16种PAHs单体在所有水样和沉积物样品中均被检出,检出范围分别为41.82~443.04 ng·L^-1和59.58~635.73 ng·g^-1,北江中上游PAHs的污染水平为中、轻度.水中PAHs以二环芳烃和三环芳烃为主,沉积物中以三环芳烃和四环芳烃为主.在水样中检出了17种PCBs,浓度范围0.81~287.50 ng·L^-1,以六氯联苯和七氯联苯为主;沉积物中检出了8种PCBs,含量范围0.13~3.96 ng·g^-1,以五氯联苯和七氯联苯为主.整个调查区域内地表水中PAHs和PCBs的终生致癌风险指数小于10^-4,处于中、低水平;非致癌风险指数均小于1,不存在非致癌风险.采用风险商值（RQ）法对地表水中污染物进行生态风险评价,研究区域内地表水中PAHs和PCBs生态风险总体处于中低风险水平,个别点位存在重度风险的污染物单体,值得引起重视.采用沉积物质量基准法（SQGs）对沉积物中污染物进行生态风险评估,沉积物中PAHs和PCBs均处于较低的生态风险水平.     

Layered sphere-shaped TiO2 capped with gold nanoparticles on structural defects and their catalysis of formaldehyde oxidation

We describe here a one-step method for the synthesis of Au/TiO₂ nanosphere materials, which were formed by layered deposition of multiple anatase TiO₂ nanosheets. The Au nanoparticles were stabilized by structural defects in each TiO₂ nanosheet, including crystal steps and edges, thereby fixing the Au–TiO₂ perimeter interface. Reactant transfer occurred along the gaps between these TiO₂ nanosheet layers and in contact with catalytically active sites at the Au–TiO₂ interface. The doped Au induced the formation of oxygen vacancies in the Au–TiO₂ interface. Such vacancies are essential for generating active oxygen species (*O⁻) on the TiO₂ surface and Ti^3 + ions in bulk TiO₂. These ions can then form Ti^3 +–O⁻–Ti^4 + species, which are known to enhance the catalytic activity of formaldehyde (HCHO) oxidation. These studies on structural and oxygen vacancy defects in Au/TiO₂ samples provide a theoretical foundation for the catalytic mechanism of HCHO oxidation on oxide-supported Au materials.     

松花江流域冰封期水体中多环芳烃的污染特征研究

在松花江流域的3个主要江段：嫩江、第二松花江和松花江干流,于2010年冰封期采集了21个水体样品,分析了多环芳烃的污染特征.结果表明,15种PAHs的浓度范围为23.4～85.1 ng·L-1,平均浓度为（50.3±17）ng·L-1,与我国其它地区地表水中PAHs的污染程度相当.松花江流域水体中PAHs具有明显的空间分布特征,城市下游浓度高于上游,说明沿岸城市的污水排放可能是松花江水体中PAHs的主要污染源,主成分分析表明,PAHs的主要来源是化石燃料的燃烧源.商值法生态风险评价结果显示,相对分子质量高的PAHs造成的生态风险可以忽略,相对分子质量低的PAHs对松花江水体会造成一定的危害.