固相萃取气相色谱法测定地表水中有机磷农药

建立了固相萃取(SPE)气相色谱火焰光度(GC-FPD)检测方法,并且检测了地表水中8种有机磷农药,检测限在0.09～0.26μg/L之间,相对标准偏差为3.1%～9.7%(n=8),加标回收率达到61.3%～103.2%,与传统的气相色谱法相比,该方法具有比较高的重现性和选择性,在地表水有机磷农药的测定中具有很好的应用前景.     

Electroosmotic dewatering of dredged sediments: bench-scale investigation

The Indiana Harbor (Indiana, USA) has not been dredged since 1972 due to lack of a suitable disposal site for dredged sediment. As a result of this, over a million cubic yards of highly contaminated sediment has accumulated in the harbor. Recently, the United States Army Corps of Engineers (USACE) has selected a site for the confined disposal facility (CDF) and is in the process of designing it. Although dredging can be accomplished rapidly, the disposal in the CDF has to be done slowly to allow adequate time for consolidation to occur. The sediment possesses very high moisture content and very low hydraulic conductivity, which cause consolidation to occur slowly. Consolidation of the sediment is essential in order to achieve adequate shear strength of sediments and also to provide enough air space to accommodate the large amount of sediment that requires disposal. Currently, it has been estimated that if a one 3-foot (0.9-m) thick layer of sediment was disposed of at the CDF annually, it would take approximately 10 years to dispose of all the sediment that is to be dredged from the Indiana Harbor. This study investigated the feasibility of using an electroosmotic dewatering technology to accelerate dewatering and consolidation of sediment, thereby allowing more rapid disposal of sediment into the CDF. Electroosmotic dewatering essentially involves applying a small electric potential across the sediment layer, thereby inducing rapid flow as a result of physico-chemical and electrochemical processes. A series of bench-scale electrokinetic experiments were conducted on actual dredged sediment samples from the Indiana Harbor to investigate dewatering rates caused by gravity alone, dewatering rates caused by gravity and electric potential, and the effects of the addition of polymer flocculants on dewatering of the sediments. The results showed that electroosmotic dewatering under an applied electric potential of 1.0VDC/cm could increase the rate of dewatering and consolidation by an order of magnitude as compared to gravity drainage alone. Amending the sediment with polymers at low concentrations (0.5-1% by dry weight) will enhance this dewatering process; however, the optimal polymer concentration and the cost-effectiveness of using polymers should be investigated further.     

Effects of calcination temperature on physicochemical property and activity of CuSO4/TiO2 ammonia-selective catalytic reduction catalysts

CuSO_4/TiO_2 catalysts with high catalytic activity and excellent resistant to SO_2 and H_2 O,were thought to be promising catalysts used in Selective catalytic reduction of nitrogen oxides by NH_3.The performance of catalysts is largely affected by calcination temperature.Here,effects of calcination temperature on physicochemical property and catalytic activity of CuSO_4/TiO_2 catalysts were investigated in depth.Catalyst samples calcined at different temperatures were prepared first and then physicochemical properties of the catalyst were characterized by N2 adsorption-desorption,X-ray diffraction,thermogravimetric analysis,Raman spectra,Fourier-transform infrared spectroscopy,X-ray photoelectron spectroscopy,temperature-pro grammed desorption of NH_3,temperature-programmed reduction of H_2 and in situ diffuse reflectance infrared Fourier transform spectroscopy.Results revealed that high calcination temperature had three main effects on the catalyst.First,sintering and anatase transform into rutile with increase of calcination temperature,causing a decrement of specific surface area.Second,decomposition of CuSO_4 under higher calcination temperature,resulting in disappears of Br(?)nsted acid sites(S-OH),which had an adverse effect on surface acidity.Third,CuO from the decomposition of CuSO_4 changed surface reducibility of the catalyst and favored the process of NH_3 oxidation to nitrogen oxides(NO_x).Thus,catalytic activity of the catalyst calcined under high temperatures(≥600℃) decreased largely.     

红壤丘陵区典型流域地表水水环境特征研究——以浏阳河流域为例

选取浏阳河流域为例,根据近十年河流断面监测数据,采用改进的综合污染指数法来评价水质污染程度,研究了该红壤丘陵区典型河流水质的时空变化特征,并结合土地利用和土壤特征等分析地表水质变化原因。结果表明,改进的综合污染指数法有较好的适用性;从时间特征上看,由于面源污染加剧,使得浏阳河近十年的水质污染呈增长趋势;从空间特征上看,浏阳河从上游到下游,河流污染呈增长趋势,上游水质较好,中游表现为重金属铅和汞的污染较大,而下游则是氨氮污染加剧。     

悬浮物对三峡水库水质测定结果的影响

以长江寸滩断面和嘉陵江大溪沟断面水样为测定样品,探讨了悬浮物对三峡水库水质测定结果的影响,提出在三峡水库水质监测中,应对经0.45μm滤膜过滤的滤液进行指标测定,同时测定悬浮物含量,并对悬浮物进行组分分析;建议在地表水环境质量标准中,纳入悬浮物项目。     

北京市地表水环境面临的主要问题及防治对策

针对北京市地表水水质污染现状、污染特点及其变化趋势,深入剖析了目前地表水环境及其治理过程中存在的主要问题,提出进一步改善北京市地表水环境的措施与建议。     

浑河沈阳段地表水有机污染物对水环境影响的安全性评估

用GB 3838-2002《地表水质量标准》和美国EPA推荐的“地面水质量标准”对浑河沈阳段地表水中的有机污染状况进行了安全性评估。用两种不同的方法评估,结果虽然有所差别,但结论是一致的,即浑河沈阳段地表水有机污染物十分严重,已经对人体健康和生态环境安全构成危害。     

楔横轧轴肩的成形曲面的设计

此文分析在二辊楔横轧中轧制各类轴肩的过程。在假想工件轴端固定的图上确定楔侧面截面轮廓形状,再通过叠加轴向刚性移动量确定各截面实际位置,比较直观简便地设计出轧制轴肩的辊面上的成形曲面。最后归纳了设计步骤。     

无顺市水污染物总量分配探讨

根据抚顺市地表水系和水域功能区划的分布情况，采用了定额达标分配、治理费用最小，及按现有排污总量进行达标分配的方法对水污染物进行总量分配，从而对减少污染物排放，控制水体污染提供了技术支持。     

久效磷在黄河水体沉积物中的吸附特征及机理

研究了黄河水体沉积物对有机磷农药久效磷的吸附特性及机理 ,结果表明 ,沉积物对黄河水中久效磷的吸附符合 L angmuir和 Freundlich等温式 ,是分配作用和表面吸附共同作用的结果。对分配作用和表面吸附在沉积物吸附久效磷中的相对贡献率进行了定量描述 :它们均为浓度的函数 ,吸附作用以分配作用为主。