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891.
赵锦 《中国个体防护装备》2011,(4):9-12
现代运动服装越来越重视功能性及舒适性。运动服装功能性具体体现在服装款式结构设计的功能性和功能性面料的选择两个方面。结构设计应考虑运动项目的特点、人体工学以及运动所处环境等因素:运动服装的面料应选择具有耐牢性、舒适性能较好的材料。 相似文献
892.
Jong Ho Kim Byoung Kyu Kwak Chee Burm Shin Won Jin Jeon Hyeon-Soo Park Sun Woo Lee Kyunghee Choi Woon Gi Lee Jun Hee Lee Sun Ho Baek Jongheop Yi 《Environmental Modeling and Assessment》2011,16(3):265-281
A local-scale spatially refined multimedia fate model (LSRMFM) was developed to evaluate in detail the multimedia transport of organic compounds at a spatial level. The model was derived using a combination of an advection?Cdispersion?Creaction partial differential equation, a steady-state multimedia fugacity model, and a geographical information system. The model was applied to predicting four major volatile organic compounds that are produced as emissions (benzene, toluene, xylene, and styrene) in an urban and industrial area (the 50?×?50-km area was divided into 0.5?×?0.5-km segments) in Korea. To test the accuracy of the model, the LSRMFM was used to predict the extent of dispersion and the data compared with actual measured concentrations and the results of a generic multimedia fate model (GMFM). The results indicated that the method developed herein is appropriate for predicting long-term multimedia pollution. However, the comparison study also illustrated that the developed model has some limitations (e.g., steady-state assumption) in terms of explaining all the observed concentrations, and additional verification and study (e.g., validation using a large observed data set, integration with a more accurate runoff model) would be desirable. In comparing LSRMFM and GMFM, discrepancies between the LSRMFM and GMFM outputs were found, as the result of geographical effects, even though the environmental parameters were identical. The geographical variation for LSRMFM output indicated the existence of considerable local human and ecological risks, whereas the GMFM output indicated less average risk. These results demonstrate that the model has the potential for improving the management of pollutant levels under these refined spatial conditions. 相似文献
893.
Moon HB Kim SJ Park H Jung YS Lee S Kim YH Choi M 《Journal of environmental monitoring : JEM》2011,13(9):2400-2405
Reports on the occurrence and intake assessment of mercury for Korean seafood are currently not available. This is the first report to estimate the intake of methyl (Me-Hg) and total mercury (T-Hg) from seafood consumption in Korea. The concentrations of Me-Hg and T-Hg in seafood ranged from 1.02 to 780 (mean: 55.6) ng g(-1) wet weight and 4.89 to 1008 (mean: 100) ng g(-1) wet weight, respectively. The residue levels of Me-Hg and T-Hg in Korean seafood were moderate compared with those found in other countries. The methylation ratios of fish, cephalopods and crustaceans were similar, but shellfish had lower values compared with other species. The intakes of Me-Hg and T-Hg from seafood consumption for the general population were estimated to be 38.8 and 73.8 ng kg(-1) body weight per day, respectively. Mackerel, tuna and squid made the highest contributions to the total intake of these contaminants. Among eight age groups, 30-49 year and 3-6 year age groups had the highest exposure to Me-Hg and T-Hg. The concentrations and intakes of Me-Hg and T-Hg from Korean seafood were less than the allowable residue levels and threshold intake levels suggested by Korean and international authorities. The present study may be useful for risk management of mercury in Korean seafood. 相似文献
894.
随着国际原油价格持续高位运行,实施能源的多元化战略已是当前世界各国政府做出的重要抉择.我国是一个缺油少气、相对富煤的国家,合理、高效、节能、安全的发展煤基替代燃料是我国能源发展的惟一出路,甲醇汽油是车用燃料替代,是新能源的重要组成部分.本文对此进行了论述. 相似文献
895.
Effects of salinity and organic matter on the partitioning of perfluoroalkyl acid (PFAs) to clay particles 总被引:1,自引:0,他引:1
The influence of salinity and organic matter on the distribution coefficient (K(d)) for perfluorooctane sulfonic acid (PFOS) and perfluorooctanoic acid (PFOA) in a brackish water-clay system was studied. The distribution coefficients (K(d)) for PFAs onto inorganic clay surfaces increased with salinity, providing evidence for electrostatic interaction for the sorption of PFAs, whereas the relationship between K(d) and organic carbon content (f(oc)) suggested that hydrophobic interaction is the primary driving force for the sorption of PFAs onto organic matter. The organic carbon normalized adsorption coefficient (K(oc)) of PFAs can be slightly overestimated due to the electrostatic interaction within uncoated inorganic surfaces. In addition, the dissolved organic matter released from coated clay particles seemed to solvate PFA molecules in solution, which contributed to a decrease in K(d). A positive relationship between K(d) and salinity was apparent, but an empirical relationship for the 'salting-out' effect was not evident. The K(d) values of PFAs are relatively small compared with those reported for persistent organic pollutants. Thus, sorption may not be a significant route of mass transfer of PFAs from water columns in estuarine environments. However, enhancement of sorption of PFAs to particulate matter at high salinity values could evoke potential risks to benthic organisms in estuarine areas. 相似文献
896.
Yuanhang Zhang Yuesi Wang Xin Jin Zirui Liu Gehui Wang Guiqian Tang Keding Lu Bo Hu Shanshan Wang Guohui Li Xinqin An Chao Wang Qihou Hu Lingyan He Fenfen Zhang 《环境科学学报(英文版)》2023,123(1):350-366
Atmospheric oxidizing capacity (AOC) is an essential driving force of troposphere chemistry and self-cleaning, but the definition of AOC and its quantitative representation remain uncertain. Driven by national demand for air pollution control in recent years, Chinese scholars have carried out studies on theories of atmospheric chemistry and have made considerable progress in AOC research. This paper will give a brief review of these developments. First, AOC indexes were established that represent apparent atmospheric oxidizing ability (AOIe) and potential atmospheric oxidizing ability (AOIp) based on aspects of macrothermodynamics and microdynamics, respectively. A closed study refined the quantitative contributions of heterogeneous chemistry to AOC in Beijing, and these AOC methods were further applied in Beijing-Tianjin-Hebei and key areas across the country. In addition, the detection of ground or vertical profiles for atmospheric OH·, HO2·, NO3· radicals and reservoir molecules can now be obtained with domestic instruments in diverse environments. Moreover, laboratory smoke chamber simulations revealed heterogeneous processes involving reactions of O3 and NO2, which are typical oxidants in the surface/interface atmosphere, and the evolutionary and budgetary implications of atmospheric oxidants reacting under multispecies, multiphase and multi-interface conditions were obtained. Finally, based on the GRAPES-CUACE adjoint model improved by Chinese scholars, simulations of key substances affecting atmospheric oxidation and secondary organic and inorganic aerosol formation have been optimized. Normalized numerical simulations of AOIe and AOIp were performed, and regional coordination of AOC was adjusted. An optimized plan for controlling O3 and PM2.5 was analyzed by scenario simulation. 相似文献
897.
Wang Zhaoqi Jung Soontag Yeo Daseul Park Sunho Woo Seoyoung Seo Yeeun Hossain Md. Iqbal Kim Minji Choi Changsun 《Food and environmental virology》2023,15(1):61-70
Food and Environmental Virology - The performance of dishwashers in removing live viruses is an important informative value in practical applications. Since foodborne viruses are present in... 相似文献
898.
Jin Xie Xiao-Dong Niu Jiao-Jiao Xie Kai-Qiang He Meng-Dan Shi Su-Juan Yu Chun-Gang Yuan Jing-Fu Liu 《环境科学学报(英文版)》2021,33(10):1-7
The distribution and chemical speciation of arsenic (As) in different sized atmospheric particulate matters (PMs), including total suspended particles (TSP), PM10, and PM2.5, collected from Baoding, China were analyzed. The average total mass concentrations of As in TSP, PM10, and PM2.5 were 31.5, 35.3, and 54.1 µg/g, respectively, with an order of PM2.5 >PM 10 > TSP, revealing that As is prone to accumulate on fine particles. Due to the divergent toxicities of different As species, speciation analysis of As in PMs is further conducted. Most of previous studies mainly focused on inorganic arsenite (iAsIII), inorganic arsenate (iAsV), monomethylarsonate (MMA), and dimethylarsinate (DMA) in PMs, while the identification and sensitive quantification of trimethylarsine oxide (TMAO) were rarely reported. In this study, a high-performance liquid chromatography coupled to inductively coupled plasma mass spectrometry system was optimized for As speciation including TMAO in PMs. An anion exchange column was used to separate MMA, DMA and iAsV, while a cation exchange column to separate TMAO and iAsIII. Results showed that iAsV was the dominate component in all the samples, corresponding to a portion of 79.2% ± 9.3% of the total extractable species, while iAsIII, TMAO and DMA made up the remaining 21%. Our study demonstrated that iAsIII accounted for about 14.4% ± 11.4% of the total extracted species, with an average concentration of 1.7 ± 1.6 ng/m3. It is worth noting that TMAO was widely present in the samples (84 out of 97 samples), which supported the assumption that TMAO was ubiquitous in atmospheric particles. 相似文献
899.
Over the recent past, fluoroquinolone antibiotics (FQs) have raised extensive attention due to their potential to induce the formation of resistance genes and “superbugs”, thus various advanced oxidation techniques have been developed to eliminate their release into the environment. In the present study, the prototype tetraamido macrocyclic ligand (FeIII-TAML)/hydrogen peroxide (H2O2) system is employed to degrade FQs (i.e., norfloxacin and ciprofloxacin) over a wide pH range (i.e., pH 6-10), and the reaction rate increases with the increase in pH level. The effect of dosage of FeIII-TAML and H2O2 on the degradation of FQs is evaluated, and the reaction rate is linearly correlated with the added amount of chemicals. Moreover, the impact of natural organic matters (NOM) on the removal of FQs is investigated, and the degradation kinetics show that both NOM type and experimental concentration exhibit negligible influence on the oxidative degradation of selected antibiotics. Based on the results of liquid chromatography-high resolution mass spectrometry and theoretical calculations, the reaction sites and pathways of FQs by FeIII-TAML/H2O2 system are further predicted and elucidated. 相似文献
900.
Sang-Won Park Sung-Kuk Kim Jeong-Bae Kim Sung-Woo Choi Hilary I. Inyang Shuzo Tokunaga 《Water, Air, & Soil Pollution: Focus》2006,6(1-2):97-110
Halogenated aliphatic compounds (HACs) can be reduced by iron sulfides in aqueous systems. Generally, the thermodynamics and
kinetics of dehalogenation reactions are controlled by the mineralogical and particle surface characteristics of the iron
sulfide, the composition of the HAC and reaction conditions such as component concentrations, pH and Eh. In this theoretical
and experimental investigation of CCl4 and C2Cl6 reduction by FeS and FeS2, the roles of hydrophobic and hydrophilic sites on the iron sulfides were analyzed. Experimental data obtained through zeta
potential measurements, were used along with the Gouy-Chapman model and the simple two-layer surface complexation model to
relate iron sulfide surface hydroxyl densities to the degree of HAC dehalogenation. The surface hydroxyl site densities of
FeS and FeS2 were found to be 0.11 sites/nm2 and 0.21 sites/nm2, respectively. During the dehalogenation reaction process, CCl4 was found to decrease to its first intermediate product CHCl3 within the first 20 hours followed by a slower process of conversion to CH2Cl2. The results also show that FeS is less hydrated (more hydrophobic) than FeS2. For CCl4 and C2Cl6, FeS is a better dehalogenator than FeS2. These results imply that particle surface hydrophobicity is a critical factor in surface-mediated dehalogenation of chlorinated
compounds. 相似文献