为了揭示腾冲地区降水中氢氧稳定同位素特征,利用2009年1月~2011年12月腾冲地区339个降水样品资料,对降水中的氢、氧同位素组成及其影响因素进行了分析和研究。结果表明:腾冲地区大气降水中δ18O值变化范围为-2678‰~405‰,δD值变化范围为-20095‰~3689‰,均处于全球降水δ18O与δD值变化范围内。天气尺度下,腾冲地区降水中δ18O的变化具有显著的降水量效应以及反温度效应。但是,在季风降水期间,如果相邻两天都有降水发生时,腾冲地区降水中δ18O值变化并不一定遵循“降水量效应”。利用ECMWF(European Centre for Medium Range Weather Forecasts)提供的TCWV(Total Column Water Vapour)再分析资料,发现TCWV与δ18O的日变化存在明显的反位相对应关系。腾冲地区的大气降水线为:δD=818δ18O+1172,斜率与截距均比全球和全国的大气降水线偏大,说明该地区气候湿润多雨。d值分布具有季节差异,在雨季(4~9月),腾冲地区降水的水汽主要来源于低纬度海洋,空气湿度大,降水中d值较小;在干季(10~3月),由于受大陆性气团控制,腾冲地区降水的水汽主要来源于西风带的输送以及局地再蒸发水汽的补充,空气湿度小,降水中d值较大 相似文献
A new method for bisphenol A (BPA) degradation in aqueous solution was developed. The characteristics of BPA degradation in a heterogeneous ultraviolet (UV)/Fenton reaction catalyzed by FeCo2O4/TiO2/graphite oxide (GO) were studied. The properties of the synthesized catalysts were characterized using scanning electron microscopy, X-ray diffraction, and vibrating sample magnetometry. FeCo2O4 and TiO2 were grown as spherical shape, rough surface, and relatively uniform on the surface of GO (FeCo2O4/TiO2/GO). Batch tests were conducted to evaluate the effects of the initial pH, FeCo2O4/TiO2/GO dosage, and H2O2 concentration on BPA degradation. In a system with 0.5 g L−1 of FeCo2O4/TiO2/GO and 10 mmol L−1 of H2O2, approximately 90 % of BPA (20 mg L−1) was degraded within 240 min of UV irradiation at pH 6.0. The reused FeCo2O4/TiO2/GO catalyst retained its activity after three cycles, which indicates that it is stable and reusable. The heterogeneous UV/Fenton reaction catalyzed by FeCo2O4/TiO2/GO is a promising advanced oxidation technology for treating wastewater that contains BPA.
The effects of biofilm growth and methane gas generation on water flow in porous media were investigated in an anaerobic two-dimensional sand-filled cell. Inoculation of the lower portion of the cell with a methanogenic culture and addition of methanol to the bottom of the cell led to biomass growth and formation of a gas phase. Biomass distributions in the water and on the sand in the cell were measured by protein analysis. The biofilm distribution on sand was observed by confocal laser scanning microscopy. The formation, migration, distribution and saturation of gases in the cell were visualized by the charge-coupled device (CCD) camera. The effects of biofilm and gas generation on water flow were separated by performing one tracer test in the presence of both biofilm and a gas phase and a second tracer test after removal of the gas phase through water flushing. The results of tracer tests demonstrated that flow and transport in the two-dimensional cell were significantly affected by both gas generation and biofilm growth. Gas generated at the bottom of the cell in the biologically active zone moved upwards in discrete fingers, so that gas phase saturations (gas-filled fraction of void space) in the biologically active zone at the bottom of the cell did not exceed 40-50%, while gas accumulation at the top of the cell produced gas phase saturations as high as 80%. The greatest reductions in water phase permeability, based on measurements of reductions in water phase saturations, occurred near the top of the box as a result of the gas accumulation. In contrast the greatest reductions in permeability due to biofilm growth, based on measurements of biofilm thickness, occurred in the most biologically active zone at the bottom of the cell, where gas phase saturations were approximately 40-50%, but permeability reductions due to biofilm growth were estimated to be 80-95%. 相似文献