云南高原典型林分林下枯落物持水特征研究

森林枯落物具有重要生态水文功能,通过实地调查与实验分析,对云南高原湖泊纳帕海流域3种典型林分枯落物储量、持水量和持水过程进行了研究。结果表明：高山松（pinus densata）林下枯落物储量最大,白桦林（Betula platyphylla Suk.）次之,川滇高山栎（Quercus aquifolioides）灌丛最小,林下枯落物储量最大持水量和有效拦蓄量大小排序表现出和枯落物储量相同的顺序;不论是储量、最大持水量还是有效拦蓄量,各林分枯落物都表现出半分层大于未分解层。3种林下枯落物在0～2 h内吸水较快,在10 h后吸水速明显减缓,用对数方程对3种林下枯落物未分解层和半分解层持水量与浸水时间进行拟合,用幂函数方程对吸水速率与浸水时间进行拟合,结果显示相关系数都较高。     

Ag3PO4掺杂g-C3N4催化剂的制备及其可见光催化降解含碘类造影剂性能

以沉淀-回流方法于磷酸银(Ag₃PO₄)中掺杂氮化碳(g-C₃N₄)制备新型复合光催化剂,同时采用扫描电子显微镜(SEM)、透射电子显微镜(TEM)、X射线衍射图(XRD)等手段对合成催化剂的形态特征、晶型结构以及物理化学性质进行表征.以碘帕醇(IPM)作为目标污染物,通过改变催化剂的使用条件考察了氙灯光照下催化剂对水溶液中含碘类造影剂(ICMs)的光催化降解性能,并且分析了催化氧化过程中可能的污染物降解途径以及转化产物.结果表明,合成后的催化剂结构稳定,相对于使用单一催化剂(Ag₃PO₄或g-C₃N₄)条件下,复合催化剂对ICMs的光降解性能都得到大幅度提升,经条件优化后,确定Ag₃PO₄与g-C₃N₄的质量比例为0.15∶0.1时降解效果最佳,但不可超过0.2∶0.1,且降解性能与催化剂的投加浓度呈正相关,浓度在0.75 ...     

Promotional catalytic activity and reaction mechanism of Ag-modified Ce0.6Zr0.4O2 catalyst for catalytic oxidation of ammonia

Ce_1-xZr_xO₂ composite oxides (molar, x = 0-1.0, interval of 0.2) were prepared by a cetyltrimethylammonium bromide-assisted precipitation method. The enhancement of silver-species modification and catalytic mechanism of adsorption-transformation-desorption process were investigated over the Ag-impregnated catalysts for low-temperature selective catalytic oxidation of ammonia (NH₃-SCO). The optimal 5 wt.% Ag/Ce_0.6Zr_0.4O₂ catalyst presented good NH₃-SCO performance with >90% NH₃ conversion at temperature (T) ≥ 250°C and 89% N₂ selectivity. Despite the irregular block shape and underdeveloped specific surface area (∼60 m²/g), the naked and Ag-modified Ce_0.6Zr_0.4O₂ solid solution still obtained highly dispersed distribution of surface elements analyzed by scanning electron microscope-energy dispersive spectrometer (SEM-EDS) (mapping), N₂ adsorption-desorption test and X-ray diffraction (XRD). H₂ temperature programmed reduction (H₂-TPR) and X-ray photoelectron spectroscopy (XPS) results indicated that Ag-modification enhanced the mobility and activation of oxygen-species leading to a promotion on CeO₂ reducibility and synergistic Ag⁰/Ag⁺ and Ce⁴⁺/Ce³⁺ redox cycles. Besides, Ag⁺/Ag₂O clusters could facilitate the formation of surface oxygen vacancies that was beneficial to the adsorption and activation of ammonia. NH₃-temperature programmed desorption (NH₃-TPD) showed more adsorption-desorption capacity to ammonia were provided by physical, weak- and medium-strong acid sites. Diffused reflectance infrared Fourier transform spectroscopy (DRIFTS) experiments revealed the activation of ammonia might be the control step of NH₃-SCO procedure, during which NH₃ dehydrogenation derived from NH_x-species and also internal selective catalytic reduction (i-SCR) reactions were proposed.     

Progress in quantitative research on the relationship between atmospheric oxidation and air quality

Atmospheric oxidizing capacity (AOC) is an essential driving force of troposphere chemistry and self-cleaning, but the definition of AOC and its quantitative representation remain uncertain. Driven by national demand for air pollution control in recent years, Chinese scholars have carried out studies on theories of atmospheric chemistry and have made considerable progress in AOC research. This paper will give a brief review of these developments. First, AOC indexes were established that represent apparent atmospheric oxidizing ability (AOIe) and potential atmospheric oxidizing ability (AOIp) based on aspects of macrothermodynamics and microdynamics, respectively. A closed study refined the quantitative contributions of heterogeneous chemistry to AOC in Beijing, and these AOC methods were further applied in Beijing-Tianjin-Hebei and key areas across the country. In addition, the detection of ground or vertical profiles for atmospheric OH·, HO₂·, NO₃· radicals and reservoir molecules can now be obtained with domestic instruments in diverse environments. Moreover, laboratory smoke chamber simulations revealed heterogeneous processes involving reactions of O₃ and NO₂, which are typical oxidants in the surface/interface atmosphere, and the evolutionary and budgetary implications of atmospheric oxidants reacting under multispecies, multiphase and multi-interface conditions were obtained. Finally, based on the GRAPES-CUACE adjoint model improved by Chinese scholars, simulations of key substances affecting atmospheric oxidation and secondary organic and inorganic aerosol formation have been optimized. Normalized numerical simulations of AOIe and AOIp were performed, and regional coordination of AOC was adjusted. An optimized plan for controlling O₃ and PM_2.5 was analyzed by scenario simulation.     

Al2O3/Ni-P-SiC复合涂层组织与性能的研究

目的 采用化学复合镀技术对微弧氧化进行封孔,进而得到抗烧蚀性能优良的Al2O3/Ni-P-SiC复合涂层。方法 通过采用扫描电镜(SEM)、光学金相显微镜(OM)、显微硬度仪(Microhardness Tester)、X射线衍射仪(XRD)、氧–乙炔烧蚀试验(Oxy-Acetylene Ablation Test)等方法,对复合涂层的表面形貌、截面形貌、厚度、显微硬度、物相和抗烧蚀性能等进行分析。结果 陶瓷层原始表面完全被化学镀层覆盖,所制得的复合涂层厚度均匀,化学镀层与陶瓷层紧密嵌合。镀液中的SiC浓度对镀覆的速度、镀层中SiC粒子的共沉积量有着较大的影响。当粒子质量浓度为16~20 g/L时,颗粒的共沉积量较大。化学复合镀60 min可以得到厚度20 μm左右的Ni-P-SiC镀层,SiC颗粒分布均匀。当镀液中SiC质量浓度为16 g/L时,镀层具有最高的硬度。对比未处理、仅微弧氧化和Al2O3/Ni-P-SiC复合涂层试样,Al2O3/Ni-P-SiC复合涂层试样具有最佳的抗烧蚀性能。结论 Al2O3/Ni-P-SiC复合涂层均匀、致密,具有良好的抗烧蚀。     

含缺陷圆轴结构极限承载规律研究

目的 研究车辆传动轴在受损情况下极限承载能力的变化规律。方法 在圆轴上预制缺陷,并对含缺陷圆轴结构承受扭转载荷的能力进行试验和数值模拟研究。结果 当圆孔缺陷深径比保持不变时,圆轴极限扭矩下降比随圆孔缺陷孔径比的增加而减小;当圆孔缺陷孔径比保持不变时,圆轴极限扭矩下降比随圆孔缺陷深径比的增加而减小。当深径比大于0.4时,圆轴极限扭矩下降比与圆孔缺陷孔径比近似呈负线性相关。当缺陷孔径比大于0.4、深径比大于0.2时,圆轴最大扭角减小为15°~35°,各存在缺陷的圆轴的最大扭角差距不大。结论 圆轴扭转失效时,其最大扭角、极限扭矩与圆孔缺陷孔径比、深径比整体均呈负相关趋势。在孔径比和深径比逐渐增大的过程中,极限扭矩呈近似线性关系逐渐降低,而最大扭角先急剧减小,后逐渐趋于平稳。     

2017年春季常州HONO观测及对大气氧化能力影响的评估

本研究于2017年4月在江苏省常州市环境监测中心使用一套基于湿化学法的仪器对大气中的HONO进行了实时在线观测,HONO浓度范围在0.2～13.9μg·m~(-3)之间,平均值为(2.9±2.3)μg·m~(-3);同时,对O_3、 HCHO、 VOCs、光解频率以及气象参数进行了同步监测.利用MCM箱体模式模拟得到白天·OH浓度最大值范围在1.0×10~6～1.4×10~7个·cm~(-3)之间.同时结合观测结果与模式模拟结果计算了HONO、 O_3、 HCHO和H_2O_2的光解以及烯烃臭氧化反应对·OH的生成速率,定量表征大气氧化性,揭示了这5种来源对大气氧化能力的影响:整体上O_3光解(46.4%)HONO光解(41.1%)烯烃臭氧化反应(10.9%)HCHO光解(1.5%)H_2O_2光解(0.1%);清晨时HONO光解对·OH生成起主要作用,之后随着O_3浓度的增加,O_3光解对·OH的贡献占主导地位;在17:00之后,由于太阳光解频率显著降低,烯烃臭氧化反应对·OH生成有主要贡献;甲醛与过氧化氢的光解对·OH的贡献可忽略.     

夏秋季宁波市气态元素汞(GEM)污染特征及潜在源区贡献分析

气态元素汞(gaseous elemental mercury,GEM)是普遍存在于大气中的对生物体有害的重金属元素其化学性质稳定,在大气中停留时间长,可随气团长距离输送属于全球性污染物.本研究于2017年夏秋季对宁波市大气GEM、常规污染物和气象参数进行综合观测,研究沿海地区GEM受人为源和自然源共同作用下的迁移转化规律及潜在源贡献来源.结果表明:①观测期间大气GEM的平均质量浓度为(2.32±0.90) ng·m~(-3),变化范围为0.97～10.95 ng·m~(-3),且夏季低于秋季.②GEM、O_3和GOM在夏季、秋季、晴天和阴雨天的日内浓度变化表明,高浓度的O_3和强烈的光照可加速GEM发生光化学反应,GEM在晴天的光化学氧化强度高于阴雨天.③相关性分析表明,GEM与PM_(2.5)(R=0.65,P0.01)、PM_(10)(R=0.47,P0.01)、NO_2(R=0.46,P0.01)和CO(R=0.57,P0.01)呈显著正相关关系,其来源与化石燃料等物质燃烧有关.④O_3等光化学氧化剂的浓度、GEM在颗粒物上的气粒分配及PM_(2.5)、水汽和NO_2的消光效应,可对GEM光化学氧化速率产生重要影响.⑤潜在源贡献分析(potential source contribution function analysis,PSCF)结果表明夏季浙江省北部(包含宁波市)、西北部,安徽省南部和江西省大部分地区构成一个三角形区域是NBUEORS大气GEM的潜在源贡献区域,且本地源、区域源和长距离源输送对GEM污染均具有重要影响.秋季的潜在源贡献区域主要为浙江省北部区域,范围小于夏季.GEM主要来自本地源和区域源输送影响.因此,针对大气GEM污染的控制,需要跨省的区域联防联控,综合治理,方可有效减轻大气汞的污染.     

不同沉水植物净水能力与植株体细菌群落组成相关性

选取苦草(Vallisneria natans)、密刺苦草(Vallisneria denseserrulata)、黑藻(Hydrilla verticillata)、伊乐藻(Elodea canadensis)、金鱼藻(Ceratophyllum demersum)、竹叶眼子菜(Potamogeton malaianus)、篦齿眼子菜(Potamogeton pectinatus)和微齿眼子菜(Potamogeton maackianus)这8种亚热带地区常见的沉水植物为研究对象,在室内静水条件下对其氮、磷吸收和水质净化能力进行对比试验,并结合16S rRNA基因测序对沉水植物关联细菌群落组成进行测定,研究沉水植物对水体的净化能力与植株体菌群之间的相关性.结果表明,8种沉水植物对水体中的氮磷的去除主要通过植物增效作用,植物吸收富集作用去除率较低.其中密刺苦草对水体中TN、TP的去除率最高,达到了91. 58%和96. 81%.伊乐藻、金鱼藻对水中氮磷自身吸收能力高于其他组,密刺苦草和苦草的植物增效的净化能力最强.经分析,8种沉水植物对水体中氮磷的净化能力较强可能是因为植物关联的细菌大多具有降解作用.根瘤菌目(Rhizobiales)、伯克霍尔德氏菌目(Burkholderiales)、黄杆菌目(Flavobacteriales)、产碱杆菌科(Alcaligenaceae)、贪铜菌属(Cupriavidus)和芽孢杆菌属(Bacillales)的细菌可能是引起密刺苦草增效的净化能力较强的优势菌群,异常球菌纲(Deinococci)、丛毛单胞菌科(Comamonadaceae)、腐螺旋菌科(Saprospiraceae)和生丝微菌属(Hyphomicrobium)的细菌可能是引起苦草增效的净化能力较强的优势菌群.     

环渤海芦苇湿地磷的吸附容量及释放风险评估

滨海湿地地处陆海交汇的关键带,是磷的"汇"、"源"和"转化器",在全球磷循环过程中扮演着十分重要的角色,其对水体磷素的截留能力日益受到关注.本文以环渤海地区芦苇湿地沉积物为研究对象,利用批处理实验研究了湿地磷的吸附容量和释放风险.结果表明,湿地沉积物磷的最大吸附容量（Q_max）为693.7~2117.2 mg·kg^-1,平均值为1468.6 mg·kg^-1,Q_max的大小顺序为七里海湿地 > 北大港湿地 > 南大港湿地 > 辽河三角洲湿地 > 寿光滨海湿地 > 黄河三角洲湿地.环渤海湿地沉积物磷吸附主要受Ca、Mg和TOC含量的影响.环渤海湿地磷吸附饱和度（DPS）和释放风险指数（ERI）分别为0.28%~4.50%和0.53%~10.10%,结果表明除寿光滨海湿地磷释放风险为中度风险外,其它湿地磷释放风险较低.总之,环渤海地区芦苇湿地沉积物具有较强磷吸附能力,沉积物为水体磷的"汇",沉积物释磷风险较低.建议在环渤海污染治理过程中充分发挥滨海湿地对磷的净化拦截作用,以降低陆源污染对近海水环境的影响.