高等职业教育中提高教师教学质量的思考

主要从4个方面对提高高等职业教育教师教学质量的途径和方法进行探讨:一是认真学习高等职业教育的文件政策,熟悉高等职业教育的教学规律;二是与时俱进,树立先进的高职教育理念;三是实事求是,忠于职守,坚持认真负责的教学态度;四是勇于创新,钻研教学艺术,形成高职教育的教学风格。     

Current Status and Problems in Certification of Sustainable Forest Management in China

Forest certification is a mechanism involving the regulation of trade of forest products in order to protect forest resources and improve forest management. Although China had a late start in adopting this process, the country has made good progress in recent years. As of July 31, 2009, 17 forest management enterprises and more than one million hectares of forests in China have been certified by the Forest Stewardship Council (FSC). Several major factors affect forest certification in China. The first set is institutional in nature. Forest management in China is based on centralized national plans and therefore lacks flexibility. A second factor is public awareness. The importance and value of forest certification are not widely understood and thus consumers do not make informed choices regarding certified forest products. The third major factor is the cost of certification. Together these factors have constrained the development of China’s forest certification efforts. However, the process does have great potential. According to preliminary calculations, if 50% of China’s commercial forests were certified, the economic cost of forest certification would range from US$0.66–86.63 million while the economic benefits for the forestry business sector could exceed US$0.66–86.63 million while the economic benefits for the forestry business sector could exceed US150 million. With continuing progress in forest management practices and the development of international trade in forest products, it becomes important to improve the forest certification process in China. This can be achieved by improving the forest management system, constructing and perfecting market access mechanisms for certificated forest products, and increasing public awareness of environmental protection, forest certification, and their interrelationship.     

炼化浓盐水处理与资源化工艺探讨＊

炼化污水深度处理回用是各炼化企业节水减排的主要措施之一。炼化企业反渗透(简称RO)污水脱盐回用装置在运行中暴露出末端高含盐污水的处置难题,影响了污水回用生产的连续运行。文章阐述近年来炼化企业高含盐污水处置现状、存在问题、国内外处理技术及发展趋势,在此基础上针对炼化企业特点,提出以热法、膜法为核心技术的浓盐水处理工艺耦合方案,为炼化企业解决污水回用瓶颈技术难题、实施污水"零排放"与发展循环经济提供借鉴与参考。     

生物技术在环境监测中的应用

文章介绍了实验室常用的生物监测方法,从生物学角度来判断环境污染的程度,为环境质量的监测和评价提供依据。着重对细菌学监测、隐孢子虫和贾第鞭毛虫的监测、浮游动植物监测、生物综合毒性监测等进行了专门论述。     

上覆水营养盐浓度对底泥氮磷释放的影响

采用校园水体底泥进行上覆水营养盐浓度对底泥释放量之间的关系研究。结果表明,在本实验条件下,上覆水水质影响底泥氮、磷的释放,尤其显著影响氮、磷的初期释放;上覆水氮、磷的浓度越小,底泥氮、磷的释放量越大;上覆水氮、磷的浓度超过一定值,会抑制底泥氮、磷的释放。     

Low-temperature CO oxidation over Au-doped 13X-type zeolite catalysts: preparation and catalytic activity

Au-supported 13X-type zeolite (Au/13X) was synthesized using a common deposition–precipitation (DP) method with a solution of sodium carbonate as a precipitate agent. Further testing was conducted to test for catalytic oxidation of CO. A study was conducted on the effects of different preparation conditions (i.e., chloroauric acid concentration, solution temperature, pH of solution, and calcinations temperature) on Au/13X for CO oxidation. In respect to the catalytic activity, the relationship between different the preparation conditions and gold particles in 13X zeolite was analyzed using X-ray diffraction, TEM and XPS. The activity of Au/13X catalysts in CO oxidation was dependent on the chloroauric acid concentration. From XRD results, a higher chloroauric acid concentration induced larger gold nanoparticles, which resulted in lower catalytic activity. Results revealed that higher temperatures induced higher Au loading, homogeneous deposit, and smaller gold clusters on the support of 13X, resulting in higher CO activity. Furthermore, a pH of 5 or 6 generated greater amounts of Au loading and smaller Au particles on 13X than at a pH of 8 or 9. This may be a result of an effective exchange between Au(OH)2Cl2- and Au(OH)₃Cl^- on specific surface sites of zeolite under the pH’s 5 and 6. The sample calcined at 300°C showed the highest activity, which may be due to the sample’s calcined at 200°C inability to decompose completely to metallic gold while the sample calcined at 400°C had larger particles of gold deposited on the support. It can be concluded from this study that Au/13X prepared from a gold solution with an initial chloroauric acid solution concentration of 1.5 × 10^-3 mol·L^-1 gold solution pH of 6, solution temperature of around 90°C, and a calcination temperature of 300°C provides optimum catalytic activity for CO oxidation.     

Nitrifying population dynamics in a redox stratified membrane biofilm reactor (RSMBR) for treating ammonium-rich wastewater

Nitrogen removal performance and nitrifying population dynamics were investigated in a redox stratified membrane biofilm reactor (RSMBR) under oxygen limited condition to treat ammonium-rich wastewater. When the NH4+-N loading rate increased from 11.1±1.0 to 37.2±3.2 gNH4+-N·m-2·d-1, the nitrogen removal in the RSMBR system increased from 18.0±9.6 mgN·d^-1 to 128.9±61.7 mgN·d^-1. Shortcut nitrogen removal was achieved with nitrite accumulation of about 22.3±5.3 mgNO2--N·L-1. Confocal micrographs showed the stratified distributions of nitrifiers and denitrifiers in the membrane aerated biofilms (MABs) at day 120, i.e., ammonia and nitrite oxidizing bacteria (AOB and NOB) were dominant in the region adjacent to the membrane, while heterotrophic bacteria propagated at the top of the biofilm. Real-time qPCR results showed that the abundance of amoA gene was two orders of magnitude higher than the abundance of nxrA gene in the MABs. However, the nxrA gene was always detected during the operation time, which indicates the difficulty of complete washout of NOB in MABs. The growth of heterotrophic bacteria compromised the dominance of nitrifiers in biofilm communities, but it enhanced the denitrification performance of the RSMBR system. Applying a high ammonia loading together with oxygen limitation was found to be an effective way to start nitrite accumulation in MABs, but other approaches were needed to sustain or improve the extent of nitritation in nitrogen conversion in MABs.     

二氯喹啉酸在水稻、土壤和田水中消解动态及残留

为评价二氯喹啉酸在水稻及其土壤中的安全性,建立其在水稻上的使用规范,于2008、2009年在杭州、济南和铁力三地进行田间试验,研究了二氯喹啉酸在水稻、土壤和田水中消解动态及最终残留量。建立了二氯喹啉酸在水稻、土壤和田水中残留量的超高效液相色谱串联质谱测定方法。在添加水平5～100μg.kg-1范围内,二氯喹啉酸的平均回收率在81.6%～105.7%之间,相对标准偏差均低于17.9%。残留试验结果表明,二氯喹啉酸在植株、土壤和田水中消解均符合一级动力学方程,消解半衰期分别为16.4～18.6、16.6～21.9和15.4～16.9 d;二氯喹啉酸在植株、土壤、糙米和稻壳中最终残留量均未检出（〈5μg.kg-1）。若二氯喹啉酸在水稻中的最高残留限量推荐值为0.5 mg.kg-1,建议每年以有效成分25 g.mu-1的剂量,于水稻移栽后10 d喷施1次,用于防治水稻田中稗草。     

Contaminant mass flux and forensic assessment of polycyclic aromatic hydrocarbons: Tools to inform remediation decision making at a contaminated site in Canada

Polycyclic aromatic hydrocarbons (PAHs) and metal(loid) mass flux estimates and forensic assessment using PAH diagnostic ratios were used to inform remediation decision making at the Sydney Tar Ponds (STPs) and Coke Ovens cleanup project in eastern Canada. Environmental effects monitoring of surface marine sediments in Sydney Harbor indicated significantly higher PAH concentrations during the first year of remediation monitoring compared to baseline. This was equivalent to PAH loadings of ～2,000 kg over a 15‐month period. Increases in sediment PAH concentrations raised serious concerns for regulators, who requested cessation of remediation activities early in the $400 M (CAD) project. Historically, the STPs were reported as the primary source of PAH contamination in Sydney Harbor with estimated discharges of 300 to 800 kg/year between 1989 and 2001. Mass flux estimates of PAHs and metal(loid)s and PAH diagnostic ratios were used to evaluate if increases in PAH concentrations in marine sediments were the result of the STPs remediation activities. PAH mass flux estimates approximated that 17 to 97 kg/year were discharged from the STPs during three years of remediation and were corroborated by an independent PAH flux estimate of 119 kg in year 1. PAH fluxes to the Sydney Harbor were mostly surface water derived, with groundwater contributing negligible quantities (0.002–0.005 kg/year). Fluxes of metal(loid)s to harbor sediments were stable or declining across all years and were mirrored in sediment metal(loid) concentrations, which lacked temporal variation, unlike total PAH concentrations. Flux results were also corroborated using PAH diagnostic ratios, which found a common source of PAHs. Coal combustion was likely the principal source of PAHs and not migration from the STPs during remediation. Although short‐term residual sediment PAH increases during onset of remediation raised concerns for regulators, calls for premature cessation of remediation early in the project were unwarranted based on only one year of monitoring data. Mass flux estimates and forensic assessments using PAH diagnostic ratios proved useful tools to inform remediation decision making that helped environmental protection and reduced costs associated with lost cleanup time.