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排序方式: 共有846条查询结果,搜索用时 234 毫秒
841.
赤泥在控制沉积物磷释放中的应用研究 总被引:3,自引:1,他引:3
利用烧结法赤泥中富含Ca、Fe等金属元素的氧化物而具有吸附性的特点,通过室内模拟研究赤泥投加对沉积物中各种磷形态含量及分布比例的影响,进而探讨利用赤泥控制沉积物中磷释放的可行性。对经过处理后的沉积物磷形态分析后表明,投加赤泥能促使沉积物中铁铝磷向钙磷转化(Pearson相关分析,r=-0.892,P<0.01,n=9),且赤泥的强碱性使沉积物pH值逐渐升高。确定了赤泥最佳投加比例为5%,此时沉积物的pH为9.03,铁铝磷含量由初始的148 mg/kg降至107 mg/kg,占总磷比例也由18.1%降至13.4%,钙磷含量由486 mg/kg升至546 mg/kg,其占总磷比例则由60%增至68.7%,铁铝磷和钙磷之间的转化已基本完成,继续增加赤泥投加量对沉积物中磷形态间的相互转化影响甚微。由于铁铝磷较钙磷活性高而易释放,可见投加赤泥能降低沉积物中磷的释放风险。赤泥可以作为吸附材料被应用于沉积物磷污染控制技术中,为有效控制水体内源磷负荷提供一种新思路和廉价材料。 相似文献
842.
采用锆对高岭土进行改性,通过批量吸附实验考察了锆改性高岭土对水中磷酸盐的吸附性能,并通过底泥培养实验考察了锆改性高岭土原位改良技术对底泥磷释放的控制效果.结果表明,锆改性高岭土对水中磷酸盐的吸附能力随改性所用锆投加量的增加而增加.在制备锆改性高岭土过程中,溶液沉淀p H值由8增加到10时,锆改性高岭土对水中磷酸盐的吸附能力增加;沉淀p H值由10增加到11时,锆改性高岭土对磷的吸附能力基本不变;沉淀p H值由11增加到12时,锆改性高岭土的吸磷能力则下降.沉淀p H值为10时制备得到的锆改性高岭土对水中磷酸盐的吸附平衡数据可以采用Langmuir模型加以描述.大部分被锆改性高岭土中锆所吸附的磷酸盐(84%左右)主要以Na OH提取态磷(Na OH-P)和残渣态磷(Res-P)形态存在,低溶解氧情况下不容易被重新释放出来,同时重污染河道底泥会释放出大量的溶解性磷酸盐进入上覆水体;向重污染河道底泥中添加锆改性高岭土可以极大地削减底泥中磷向上覆水体迁移的通量.采用锆改性高岭土对底泥进行改良不仅增强了底泥对水中磷的吸附能力,而且降低了底泥的磷吸附-解吸平衡浓度(EPC0).因此,应用锆改性高岭土作为底泥改良剂可以有效控制重污染河道底泥磷释放. 相似文献
843.
844.
845.
Accidental subsea gas releases can pose a threat to people, equipment, and facilities since gas can be toxic or flammable at the concentrations in which the leak occurs. The accurate prediction of the behavior of the gas plume formed in the leaks can be fundamental to the development of techniques of accident prevention or, in some cases, remediation measures, avoiding the emergence of more serious consequences. Among the different ways to analyze the behavior of gas plumes formed underwater, the Computational Fluid Dynamics (CFD) tool stands out for allowing the study of plume behavior to be done in a safer, simpler, and less expensive way, if compared to experimental studies. Inspired by the accidental release of the subsea gas scenario, this work validated a CFD setup of a 2D two-phase air–water flow using the VOF method in Ansys Fluent. The use of the VOF method differs this work from other works that use a hybrid Eulerian–Lagrangian methodology to model such types of flow. In this validation, simulations with a 9 m base tank, and 7 m water depth, and 0.050, 0.100, and 0.450 m/s gas flow were performed. The simulated data were compared to experimental results available in literature. After the validation of the setup, a study was carried out varying the size of the leak to 0.24 and 0.17 m, and the gas flow from 0.006 to 0.150 m/s aiming to verify how some plume characteristics are affected by the changes. Finally, following the directions from literature for analyzing the ascending gas behavior, and combining it with a dimensional analysis of the data, we proposed a mathematical model for calculating the gas ascending time using only properties of the gas leak. With future modifications of the proposed methodology, we hope that soon it will be possible to simulate gas releases under more realistic conditions. Even so, the findings of this work are already a significant step forward in the study of underwater gas releases. 相似文献
846.
Initial carbon release characteristics, mechanisms and denitrification performance of a novel slow release carbon source 下载免费PDF全文
Congyu Li Haiyan Wang Guokai Yan Weiyang Dong Zhaosheng Chu Huan Wang Yang Chang Yu Ling Yanjie Zhang 《环境科学学报(英文版)》2022,34(8):32-45
External carbon source addition is one of the effective methods for the treatment of wastewater with low carbon to nitrogen ratio (C/N). Compared with fast-release liquid carbon sources, slow-release solid carbon sources are more suitable for the denitrification process. A novel slow-release solid carbon source (corncob-polyvinyl alcohol sodium alginate- poly-caprolactone, i.e. CPSP) was prepared using corn cob (CC) and poly-caprolactone with polyvinyl alcohol sodium alginate as hybrid scaffold. The physical properties and carbon release characteristics of CPSP and three other carbon sources were compared. CPSP had stable framework and good carbon release performance, which followed the second order release equation. The formic acid, acetic acid, propionic acid and butyric acid released from CPSP accounted for 8.27% ± 1.66 %, 56.48% ± 3.71 %, 18.46% ± 2.69% and 16.79% ± 3.02% of the total released acids respectively. The start-up period of CPSP was shorter than that of the other carbon sources in denitrification experiment, and no COD pollution was observed in the start-up phase (25–72 h) and stable phase (73–240 hr). The composition and structure of the dissolved organic compounds released by CPSP and other carbon sources were analyzed by UV-Vis absorption spectroscopy and three-dimensional fluorescence spectroscopy, which indicated that CPSP was more suitable for denitrification than the other studied carbon sources. 相似文献