大孔强碱阴树脂去除饮用水中微量有机物

比较了大孔强碱阴树脂和颗粒活性炭在饮用水的深度处理中对有机物的去除效果。结果表明：(1)大孔强碱阴树脂的吸附容量比颗粒活性炭的大。在pH为8时,大孔强碱阴树脂对TOC的去除率最高。pH6～8时,对TOC的去除率没有明显的区别,而颗粒活性炭在pH为2时。对TOC的去除率最高;水温低能提高2种吸附材料的吸附容量。(2)在动态实验条件下。当流速相同,大孔强碱阴树脂的穿透时间明显比颗粒活性炭的长,大孔强碱阴树脂的制水量约是吸附床的10000倍。而颗粒活性炭却只有吸附床的4000倍。在饮用水的深度处理中,大孔强碱阴树脂可作为活性炭的最佳替代品。     

氧化铝厂1100m2自然循环蒸发器制造技术

蒸发是氧化铝生产一道非常重要的工序，蒸发器为其主要设备，中国铝业集团河南分公司共有1100m^2自然循环蒸发器21台，均已进入大修更换周期，为了保证制造质量及投产后的安全运行，对蒸发器制造工艺相关技术进行探讨。     

Development of Layered Sediment Structure and its Effects on Pore Water Transport and Hyporheic Exchange

Hyporheic exchange is known to provide an important control on nutrient and contaminant fluxes across the stream-subsurface interface. Similar processes also mediate interfacial transport in other permeable sediments. Recent research has focused on understanding the mechanics of these exchange processes and improving estimation of exchange rates in natural systems. While the structure of sediment beds obviously influences pore water flow rates and patterns, little is known about the interplay of typical sedimentary structures, hyporheic exchange, and other transport processes in fluvial/alluvial sediments. Here we discuss several processes that contribute to local-scale sediment heterogeneity and present results that illustrate the interaction of overlying flow conditions, the development of sediment structure, pore water transport, and stream-subsurface exchange. Layered structures are shown to develop at several scales within sediment beds. Surface sampling is used to analyze the development of an armor layer in a sand-and-gravel bed, while innovative synchrotron-based X-ray microtomography is used to observe patterns of grain sorting within sand bedforms. We show that layered bed structures involving coarsening of the bed surface increase interfacial solute flux but produce an effective anisotropy that favors horizontal pore water transport while limiting vertical penetration.     

淮河流域旱涝易发区农田的陆气相互作用——CO2通量、能量交换和水汽输送的季节变化特征

利用淮河流域旱涝易发区的安徽省寿县农田下垫面陆气相互作用观测试验资料,重点分析观测期内CO2通量、能量交换和水汽输送的季节变化,并讨论了与此有关的辐射分量通量、下垫面反射率、波恩比、能量闭合守恒、土壤温度和土壤湿度的季节变化.结果表明CO2通量、能量分配受地表农作物长势影响明显,其中,水稻灌浆、成熟期,被稻田吸收的CO2通量最大可超过2 mg·m-2·s-1,潜热通量达到正的极大值.稻田光合作用最旺盛时期吸收的CO2通量和释放的潜热通量均大于小麦田光合作用最旺盛时期的对应量.较大土壤热通量对应于较低的土壤水含量.试验观测期的下垫面平均反射率为0.14.作物生长期,稻田表面潜热是下垫面吸收能量的主要消费者,小麦田表面潜热和感热相当.能量闭合率ε的变化范围为0.4～1.     

涉外企业的货币经营风险管理

结合涉外企业投入与产出所处市场的分割程度或一体化程度,分析了当地企业、进口企业、出口企业或全球经营企业所面临的货币经营风险;对计量涉外企业货币经营风险的方法进行比较,认为管理层估计法对于计量货币经营风险以及制定相应的竞争对策有着重要作用;分别从金融性套期保值、经营性套期保值和营销策略等视角讨论货币经营风险的管理。笔者认为:金融性套期保值通过锁定涉外企业的外币现金流出或流入,可部分抵消涉外企业的货币经营风险暴露;经营性套期保值通过调整企业的经营业务并尽可能多地增加经营现金流,可从根本上提高涉外企业适应汇率变化的能力;通过影响涉外企业及其竞争对手所处的经营环境,营销策略有助于降低涉外企业的货币经营风险暴露。     

新疆草地资源特征与生态治理

从新疆草地资源发生条件分析其多样性,对草地退化进行了生态分析,提出了草地生态恢复的生态置换理论与实施方案。     

论对社会弱势群体的职业卫生与安全的法律保护

结合对“社会弱势群体”含义、产生原因的分析以及对我国社会弱势群职业卫生与安全法律保护现状的总结，本文指出了法律对社会弱势群体职业卫生与安全给予倾斜性保护的重要意义，并进一步提出了加强对社会弱势群体职业卫生与安全法律保护具体措施的设想。     

Information Network Topologies for Enhanced Local Adaptive Management

We examined the principal effects of different information network topologies for local adaptive management of natural resources. We used computerized agents with adaptive decision algorithms with the following three fundamental constraints: (1) Complete understanding of the processes maintaining the natural resource can never be achieved, (2) agents can only learn by experimentation and information sharing, and (3) memory is limited. The agents were given the task to manage a system that had two states: one that provided high utility returns (desired) and one that provided low returns (undesired). In addition, the threshold between the states was close to the optimal return of the desired state. We found that networks of low to moderate link densities significantly increased the resilience of the utility returns. Networks of high link densities contributed to highly synchronized behavior among the agents, which caused occasional large-scale ecological crises between periods of stable and high utility returns. A constructed network involving a small set of experimenting agents was capable of combining high utility returns with high resilience, conforming to theories underlying the concept of adaptive comanagement. We conclude that (1) the ability to manage for resilience (i.e., to stay clear of the threshold leading to the undesired state as well as the ability to re-enter the desired state following a collapse) resides in the network structure and (2) in a coupled social–ecological system, the systemwide state transition occurs not because the ecological system flips into the undesired state, but because managers lose their capacity to reorganize back to the desired state. An erratum to this article can be found at .     

Removal of perfluorinated surfactants from wastewater by adsorption and ion exchange——Influence of material properties,sorption mechanism and modeling

Perfluorooctane sulfonate(PFOS) has attracted increasing concern in recent years due to its world-wide distribution, persistence, bioaccumulation and potential toxicity. The influence of sorbent properties on the adsorptive elimination of PFOS from wastewater by activated carbons, polymer adsorbents and anion exchange resins was investigated with regard to their isotherms and kinetics. The batch and column tests were combined with physicochemical characterization methods, e.g., N_2 physisorption, mercury porosimetry, infrared spectroscopy, differential scanning calorimetry, titrations, as well as modeling. Sorption kinetics was successfully modelled applying the linear driving force(LDF) approach for surface diffusion after introducing a load dependency of the mass transfer coefficient βs.The big difference in the initial mass transfer coefficient βs,0, when non-functionalized adsorbents and ion-exchange resins are compared, suggests that the presence of functional groups impedes the intraparticle mass transport. The more functional groups a resin possesses and the longer the alkyl moieties are the bigger is the decrease in sorption rate.But the selectivity for PFOS sorption is increasing when the character of the functional groups becomes more hydrophobic. Accordingly, ion exchange and hydrophobic interaction were found to be involved in the sorption processes on resins, while PFOS is only physisorptively bound to activated carbons and polymer adsorbents. In agreement with the different adsorption mechanisms, resins possess higher total sorption capacities than adsorbents. Hence, the latter ones are rendered more effective in PFOS elimination at concentrations in the low μg/L range, due to a less pronounced convex curvature of the sorption isotherm in this concentration range.     

Simultaneous removal of Cu(II) and Cr(VI) by Mg–Al–Cl layered double hydroxide and mechanism insight

Mg–Al–Cl layered double hydroxide (Cl-LDH) was prepared to simultaneously remove Cu(II) and Cr(VI) from aqueous solution. The coexisting Cu(II) (20 mg/L) and Cr(VI) (40 mg/L) were completely removed within 30 min by Cl-LDH in a dosage of 2.0 g/L; the removal rate of Cu(II) was accelerated in the presence of Cr(VI). Moreover, compared with the adsorption of single Cu(II) or Cr(VI), the adsorption capacities of Cl-LDH for Cu(II) and Cr(VI) can be improved by 81.05% and 49.56%, respectively, in the case of coexisting Cu(II) (200 mg/L) and Cr(VI) (400 mg/L). The affecting factors (such as solution initial pH, adsorbent dosage, and contact time) have been systematically investigated. Besides, the changes of pH values and the concentrations of Mg²⁺ and Al³⁺ in relevant solutions were monitored. To get the underlying mechanism, the Cl-LDH samples before and after adsorption were thoroughly characterized by X-ray powder diffraction, transmission electron microscopy, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy. On the basis of these analyses, a possible mechanism was proposed. The coadsorption process involves anion exchange of Cr(VI) with Cl⁻ in Cl-LDH interlayer, isomorphic substitution of Mg²⁺ with Cu²⁺, formation of Cu₂Cl(OH)₃ precipitation, and the adsorption of Cr(VI) by Cu₂Cl(OH)₃. This work provides a new insight into simultaneous removal of heavy metal cations and anions from wastewater by Cl-LDH.