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121.
Mohamad Fared Murshe Zeeshan Aslam Rosmala Lewis Christopher Chow Dongsheng Wang Mary Drikas John van Leeuwen 《环境科学学报(英文版)》2014,26(10):1985-1993
The treatment of organics present in the lower reaches of a major river system(the Murray–Darling Basin, Australia) before(March–July 2010), during(December 2010–May 2011) and after(April–December 2012) a major flood period was investigated. The flood period(over 6 months)occurred during an intense La Nia cycle, leading to rapid and high increases in river flows and organic loads in the river water. Dissolved organic carbon(DOC) increased(2–3 times) to high concentrations(up to 16 mg/L) and was found to correlate with river flow rates. The treatability of organics was studied using conventional jar tests with alum and an enhanced coagulation model(mEnCo). Predicted mean alum dose rates(per mg DOC) were higher before(9.1 mg alum/mg DOC) and after(8.5 mg alum/mg DOC) than during the flood event(8.0 mg alum/mg DOC),indicating differences in the character of the organics in raw waters. To assess the character of natural organic matter present in raw and treated waters, high performance size exclusion chromatography with UV and fluorescence detectors were used. During the flood period, high molecular weight UV absorbing compounds(〉2 kDa) were mostly detected in waters collected,but were not evident in waters collected before and afterwards. The relative abundances of humic-like and protein-like compounds during and following the flood period were also investigated and found to be of a higher molecular weight during the flood period. The treatability of the organics was found to vary over the three climate conditions investigated. 相似文献
122.
采用混凝-SBR生化-砂滤工艺,以超滤处理后的冷轧废水进行了处理。结果表明,CODcr为590 ̄1000mg/L的冷轧超滤废水经该工艺处理后,CODcr和BOD5的平均去除率分别为82.5%和94.3%,出水达到国家排放标准。 相似文献
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124.
城市污水处理过程中有机物迁移转化的研究(甲苯) 总被引:1,自引:1,他引:1
讨论了城市污水分别经过混凝沉降和A/O工艺处理时,污水中有机物的迁移和转化。所采用的方法是将原水、处理后的出水及污泥用甲苯萃取,萃取相经过真空浓缩后,采用GC/MS测定了样品中的有机化合物,对两种处理过程中有机物的迁移转化后进行了对比。结果表明,在A/O工艺处理城市污水过程中,吸附作用是主要的,降解作用是次要的。 相似文献
125.
直接超滤和混凝-超滤组合工艺的膜污染比较 总被引:6,自引:0,他引:6
利用滤饼层过滤模型和膜孔窄化模型,结合国产中空纤维超滤膜对提取的天然腐植酸进行直接超滤和混凝-超滤2种工艺的试验结果分析,表明混凝预处理基本消除了膜孔污染,并且大大降低了膜表面滤饼层污染阻力,从而使超滤保持高渗透通量。另外,与原水直接超滤相比,混凝-超滤组合工艺对溶解性天然有机物的去除率较高,DOC去除率从28%提高到53%,UV254去除率从40%提高到78%。 相似文献
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127.
In coastal areas, estuaries, and inland waters, dispersant use after oil spills is not allowed due to sensitivity of the ecosystems. The purpose of this study was to investigate the removal of emulsified fuel oils from brackish and pond water by dissolved air flotation (DAF) with and without use of coagulants. Experiments were conducted with a 60 L DAF system. Fuel oil-water emulsions were prepared with regular unleaded gasoline, jet fuel, and diesel fuel mixed at 1:1:1 (v/v/v) ratio. Batch and continuous runs were conducted at air pressurization of 354.6 kPa. During both batch and continuous modes, significant petroleum hydrocarbon (PHC) removal was achieved within 10 min. Coagulant addition initially increased the PHC removal by about 5-15%. However, effectiveness of the coagulant was not significant after 20 min due to breakage of the aggregates. In general, the pond water had higher PHC removal than the brackish water. With longer run times, PHC removal improved slightly and the effluent contained increasing fractions of higher molecular weight compounds indicating that PHC removal was due to both DAF and stripping processes. Results indicate that DAF process can be effective both with and without the use of coagulants for removing PHCs from brackish and pond waters. 相似文献
128.
Batch experiments were carried out to investigate the influences of H2O2/Fe(II) molar ratio, pH, sequence of pH adjustment, initial As(V) concentration, and interfering ions on As(V) removal in H2O2-Fe(II) process from synthetic acid mine drainage (AMD). The optimum H2O2/Fe(II) molar ratio was one for arsenate removal over the pH range of 4-7. Arsenate removal at pH 3 was poor even at high Fe(II) dosage due to the high solubility of Fe(III) formed in situ. With the increase of Fe(II) dosage, arsenate removal increased progressively before a plateau was reached at pH 5 as arsenate concentration varied from 0.05 to 2.0 mg L−1. However, arsenate removal was negligible at Fe/As molar ratio <3 and then experienced a striking increase before a plateau was reached at pH 7 and arsenate concentration ≥1.0 mg L−1. The co-occurring ions exerted no significant effect on arsenate removal at pH 5. The experimental results with synthetic AMD revealed that this method is highly selective for arsenate removal and the co-occurring ions either improved arsenate removal or slightly depressed arsenate removal at pH 5-7. The extended X-ray absorption fine structure (EXAFS) derived As-Fe length, 3.27-3.30 Å, indicated that arsenate was removed by forming bidentate-binuclear complexes with FeO(OH) octahydra. The economic analysis revealed that the cost of the H2O2-Fe(II) process was only 17-32% of that of conventional Fe(III) coagulation process to achieve arsenate concentration below 10 μg L−1 in treated solution. The results suggested that the H2O2-Fe(II) process is an efficient, economical, selective and practical method for arsenate removal from AMD. 相似文献
129.
Yanxia Zhao Huiqing Lian Chang Tian Haibo Li Weiying Xu Sherub Phuntsho Kaimin Shih 《Frontiers of Environmental Science & Engineering》2021,15(4):58
130.