美国地表水水源的流域管理

对地表水水源有效的流域管理,是保持水源良好水质的关键最近美国自来水协会(AWWA)发表了地表水水源流域管理的研究报告,强调重视和统一规划,控制流域内土地及水源利用的重要性,并列举了流域管理中各种措施的实施及其效果.     

平原河网地区地表水环境保护功能区划分的研究

从地表水环境保护功能区划分工作的实践出发 ,针对复杂的水文、水质条件 ,探讨平原河网地区地表水环境保护功能区划分的工作方法和实现区划目标的对策措施。     

Surface characterization of metal oxides-supported activated carbon fiber catalysts for simultaneous catalytic hydrolysis of carbonyl sulfide and carbon disulfide

The sol–gel method was used to synthesize a series of metal oxides-supported activated carbon fiber (ACF) and the simultaneous catalytic hydrolysis activity of carbonyl sulfide (COS) and carbon disulfide (CS₂) at relatively low temperatures of 60°C was tested. The effects of preparation conditions on the catalyst properties were investigated, including the kinds and amount of metal oxides and calcination temperatures. The activity tests indicated that catalysts with 5 wt.% Ni after calcining at 400°C (Ni(5)/ACF(400)) had the best performance for the simultaneous catalytic hydrolysis of COS and CS₂. The surface and structure properties of prepared ACF were characterized by scanning electron microscope-energy disperse spectroscopy (SEM-EDS), Brunauer–Emmett–Teller (BET), X-ray diffraction (XRD), carbon dioxide-temperature programmed desorption (CO₂-TPD) and diffuse reflectance Fourier transform infrared reflection (DRFTIR). And the metal cation defects were researched by electron paramagnetic resonance (EPR) method. The characterization results showed that the supporting of Ni on the ACF made the ACF catalyst show alkaline and increased the specific surface area and the number of micropores, then improved catalytic hydrolysis activity. The DRFTIR results revealed that -OH species could facilitate the hydrolysis of COS and CS₂; -COO and -C–O species could facilitate the oxidation of catalytic hydrolysate H₂S. And the EPR results showed that high calcination temperature conditions provide more active reaction center for the COS and CS₂ adsorption.     

石家庄城市地表灰尘中多环芳烃的污染特征及来源

采用高效液相色谱法,对2017年2月12~19日所采集的石家庄市64个地表灰尘样品中16种优先控制的多环芳烃(PAHs)的含量和组分特征进行分析,并运用比值法和主成分因子载荷法揭示其污染来源。结果表明,16种PAHs的总量(Σ16PAHs)范围为0.897~81.458 mg/kg,平均值为8.138 mg/kg,其中Fla的含量最高为1.136 mg/kg,Flu最低为0.129 mg/kg,强致癌物质Bap为0.567 mg/kg。7种致癌多环芳烃(Σ7CPAHs)的含量范围为0.213~43.690 mg/kg,平均值为3.402 mg/kg,占Σ16PAHs的41.80%。与国内外其他城市相比,石家庄城市地表灰尘中PAHs含量处于较高水平,且以4环为主。来源分析结果表明,石家庄市地表灰尘中PAHs主要来源于化石燃料的燃烧,以石油燃烧为主,其方差贡献率为69.30%,柴油燃烧和石油泄漏的方差贡献率分别为8.67%和7.43%。由石家庄灰尘中PAHs的空间分布分析得出交通源对石家庄二环内冬季灰尘中PAHs贡献显著。     

隧道施工通风壁面粗糙度评定方法及其工程应用

隧道通风数值计算中定义壁面粗糙程度的参数由粗糙高度和粗糙常数构成,参数的选取很难利用数学推导的方式进行研究。依托衢宁铁路鹫峰山隧道的施工通风项目,采用数值模拟并结合现场实测数据研究了隧道内壁面粗糙度的评定方法、取值和工程应用。结果表明:隧道壁面平均粗糙高度由隧道内实际开挖轮廓线和设计开挖轮廓线之间包络的面积与取样长度的比值确定,计算得到了隧道横断面平均粗糙高度为0. 191 m,纵向平均粗糙高度为0. 231 m;建立了粗糙常数Rc与粗糙单元间距、形状的关系,同时得到基本模型对应的Rc计算公式;基于典型理想壁面模型,以原模型面积减去理想模型的面积(绝对值)除以原模型面积所得值最小定义了最优简化模型,提出了关于壁面粗糙常数取值的计算方法,并以此计算出鹫峰山隧道壁面粗糙常数Rc为0.46。最终根据Rh和Rc的取值,采用三维数值模拟,分析了隧道内CO质量浓度不同时间段的分布规律。由于压入式通风自身的缺陷(无法突破长度瓶颈),且受现场布置及施工方式所限,通风距离超过3 000 m很难满足施工条件的需要,无法达到规定的洞内作业环境条件。因此,急需对现有的通风方式进行优化和调整。     

Comparison of surface water chemistry and weathering effects of two lake basins in the Changtang Nature Reserve, China

The geochemistry of natural waters in the Changtang Nature Reserve,northern Tibet,can help us understand the geology of catchments,and provide additional insight in surface processes that influence water chemistry such as rock weathering on the Qinghai–Tibet Plateau.However,severe natural conditions are responsible for a lack of scientific data for this area.This study represents the first investigation of the chemical composition of surface waters and weathering effects in two lake basins in the reserve(Lake Dogaicoring Qiangco and Lake Longwei Co).The results indicate that total dissolved solids(TDS)in the two lakes are significantly higher than in other gauged lakes on the Qinghai–Tibet Plateau,reaching 20–40 g/L,and that TDS of the tectonic lake(Lake Dogaicoring Qiangco)is significantly higher than that of the barrier lake(Lake Longwei Co).Na+and Cl-are the dominant ions in the lake waters as well as in the glacier-fed lake inflows,with chemical compositions mainly affected by halite weathering.In contrast,ion contents of inflowing rivers fed by nearby runoff are lower and concentrations of dominant ions are not significant.Evaporite,silicate,and carbonate weathering has relatively equal effects on these rivers.Due to their limited scope,small streams near the lakes are less affected by carbonate than by silicate weathering.     

A preliminary analysis of the surface chemistry of atmospheric aerosol particles in a typical urban area of Beijing

Atmospheric aerosol particle samples were collected using an Ambient Eight Stage(Non-Viable) Cascade Impactor Sampler in a typical urban area of Beijing from 27 th Sep.to 5th Oct.,2009.The surface chemistry of these aerosol particles was analyzed using Static Time of Flight-Secondary Ion Mass Spectrometry(Static TOF-SIMS).The factors influencing surface compositions were evaluated in conjunction with the air pollution levels,meteorological factors,and air mass transport for the sampling period.The results show that a variety of organic ion groups and inorganic ions/ion groups were accumulated on the surfaces of aerosol particles in urban areas of Beijing;and hydrophobic organic compounds with short-or middle-chain alkyl as well as hydrophilic secondary inorganic compounds were observed.All these compounds have the potential to affect the atmospheric behavior of urban aerosol particles.PM1.1–2.1and PM3.3–4.7had similar elements on their surfaces,but some molecules and ionic groups demonstrated differences in Time of Flight-Secondary Ion Mass Spectrometry spectra.This suggests that the quantities of elements varied between PM1.1–2.1and PM3.3–4.7.In particular,more intense research efforts into fluoride pollution are required,because the fluorides on aerosol surfaces have the potential to harm human health.The levels of air pollution had the most significant influence on the surface compositions of aerosol particles in our study.Hence,heavier air pollution was associated with more complex surface compositions on aerosol particles.In addition,wind,rainfall,and air masses from the south also greatly influenced the surface compositions of these urban aerosol particles.     

基体表面状态对硅烷环氧杂化树脂涂层/2024铝合金间附着力影响

目的研究不同表面状态对硅烷环氧杂化树脂涂层/2024铝合金间附着力影响规律。方法结合硅烷环氧杂化树脂涂层的综合性能与实际应用情况,选取4种常见的预处理方式来改变基体表面状态,采用拉拔测试仪测试不同基体表面状态(基体表面p H值、基体表面粗糙度、基体表面能),涂层/基体间的附着力值,研究基体表面状态对该涂层/基体间附着力的影响关系。结果基体表面状体影响涂层附着力的根本原因是基体表面能、基体表面p H值和基体表面粗糙度。结论对于硅烷环氧杂化树脂涂层,其表面处理方式可用热碱清洗方法代替传统铬酸盐钝化;当硅烷环氧杂化树脂涂层喷涂厚度为30μm时,将铝合金基体表面粗糙度控制在Ra=4.75μm左右,可保证涂层有好的附着性,附着力值为8.84 MPa。     

Application of Automated Mass Spectrometry Deconvolution and Identification Software for Pesticide Analysis in Surface Waters

A new approach to surface water analysis has been investigated in order to enhance the detection of different organic contaminants in Nathan Creek, British Columbia. Water samples from Nathan Creek were prepared by liquid/liquid extraction using dichloromethane (DCM) as an extraction solvent and analyzed by gas chromatography mass spectrometry method in scan mode (GC-MS scan). To increase sensitivity for pesticides detection, acquired scan data were further analyzed by Automated Mass Spectrometry Deconvolution and Identification Software (AMDIS) incorporated into the Agilent Deconvolution Reporting Software (DRS), which also includes mass spectral libraries for 567 pesticides. Extracts were reanalyzed by gas chromatography mass spectrometry single ion monitoring (GC-MS-SIM) to confirm and quantitate detected pesticides. Pesticides: atrazine, dimethoate, diazinone, metalaxyl, myclobutanil, napropamide, oxadiazon, propazine and simazine were detected at three sampling sites on the mainstream of the Nathan Creek. Results of the study are further discussed in terms of detectivity and identification level for each pesticide found. The proposed approach of monitoring pesticides in surface waters enables their detection and identification at trace levels.     

The legacy of surface mining: Remediation,restoration, reclamation and rehabilitation

Surface mining is a global phenomenon. When dealing with the land disturbances caused by surface mining operations, the terms remediation, reclamation, restoration and rehabilitation (R4) are commonly used interchangeably or otherwise vaguely defined. Expectations associated with these terms may differ significantly from one stakeholder to another, however. Regulators, industry, environmental practitioners, local communities and the general public therefore stand to benefit from a precise terminology based on agreed-upon end-goals. The latter range from the avoidance of exposure to pollutants (remediation) to the full recovery of the original ecosystem (restoration). Although frequently claimed as the end-goal, restoration may often not be unachievable, because of altered hydrology, habitat fragmentation, contamination, climate change, prohibitive costs and other environmental and socio-economic boundary conditions. Mostly, the definitions of reclamation and rehabilitation may overlap in their definitions and approaches. Here we attempt the creation of a road-map that can clearly translate end-goals for each of the R4 terms. According to the definitions encountered and exposed here, reclamation, which aims to recover key ecosystem services and biogeochemical functions within a replacement ecosystem or rehabilitation, which implies a repurposing of the landscape, may be the best approaches to deal with surface mining legacies.