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281.
冶金高炉高温熔融处理垃圾飞灰 总被引:1,自引:0,他引:1
为了探讨冶金高炉处理垃圾飞灰的可能性,将一定量的垃圾飞灰作为造球原料通过快凝水泥固化制备冷固飞灰球团,模拟高炉温度、气氛条件对飞灰球团进行高温冶金性能实验研究,并采用X射线衍射仪对飞灰球团中物相变化进行了研究。结果表明:在造球原料里配入5%左右的飞灰通过水泥固化造出的球团能达到入炉要求;配入10%飞灰球团的高炉炉料的高温冶金性能变化不大,且能够保持高炉内的工作环境相对稳定,符合当前冶炼要求的炉内工程条件;在高温下飞灰中的重金属能有效还原固封,二恶英能有效分解,为垃圾飞灰的资源化处理开辟了新的途径。 相似文献
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284.
Naile JE Khim JS Wang T Wan Y Luo W Hu W Jiao W Park J Ryu J Hong S Jones PD Lu Y Giesy JP 《Environmental pollution (Barking, Essex : 1987)》2011,159(4):907-917
Polychlorinated-dibenzo-p-dioxins and -dibenzofurans (PCDD/Fs) were measured in soils and sediments from the Yellow Sea region. Korean soils and sediments mostly contained detectable PCDD/Fs and showed a widespread distribution among locations. Soil and sedimentary PCDD/Fs from China were comparable to or less than those in Korea. The patterns of relative concentrations of individual congeners in soils were different between the two countries, but similar in sediments. Sources of PCDD/Fs in China and Korea were found to be independent of each other and their distributions reflected matrix-dependent accumulation. Spatial distribution indicated some point sources in Korea while Chinese sources were more widespread and diffuse. PCDD/Fs measured in the coastal areas of the Yellow Sea were comparable to or less than those previously reported in for eastern Asia. However, ∑TEQs in soils and sediments were near to or, in some cases exceeded environmental quality guidelines. 相似文献
285.
A rapid and high-throughput quantum dots bioassay for monitoring of perfluorooctane sulfonate in environmental water samples 总被引:1,自引:0,他引:1
Zhang J Wan Y Li Y Zhang Q Xu S Zhu H Shu B 《Environmental pollution (Barking, Essex : 1987)》2011,159(5):1348-1353
Currently HPLC/MS is the state of the art tool for environmental/drinking water perfluorooctane sulfonate (PFOS) monitoring. PFOS can bind to peroxisomal proliferator-activated receptor-alpha (PPARα), which forms heterodimers with retinoid X receptors (RXRs) and binds to PPAR response elements. In this bioassay free PFOS in water samples competes with immobilized PFOS in ELISA plates for a given amount of PPARα-RXRα. It can be determined indirectly by immobilizing PPARα-RXRα-PFOS complex to another plate coated with PPARα antibody and subsequent measuring the level of PPARα-RXRα by using biotin-modified PPARα-RXRα probes-quantum dots-streptavidin detection system. The rapid and high-throughput bioassay demonstrated a detection limit of 2.5 ng L−1 with linear range between 2.5 ng L−1 and 75 ng L−1. Detection results of environmental water samples were highly consistent between the bioassay and HPLC/MS. 相似文献
286.
Yoon Yee Then Nor Azowa Ibrahim Wan Md Zin Wan Yunus 《Journal of Polymers and the Environment》2011,19(2):535-539
Polycaprolactone/tapioca starch/octadecylamine modified clay (OMMT) nanocomposites were successfully prepared by melt blending.
X-ray diffraction and transmission electron microscopy (TEM) of the products showed that they are nanocomposites of a mixture
intercalated and exfoliated types. In addition, the TEM also revealed that the OMMT layers are homogeneously distributed in
the polymer matrix. The presence of 1 php of OMMT improved the compatibility of the polymers in the blends which consequently
increased the tensile strength of the blend of more than 60% and elongation at break of more than 1,000%. 相似文献
287.
The incomplete understanding of the processes which control aquatic nitrous oxide (N2O) production is partially due to a lack of onsite data with which to describe the temporal resolution of N2O production. To help resolve this, we directly measured the N2O saturation (relative to atmospheric partial pressure) on an hourly basis over two survey periods (July and September 2003) in Lake Taihu, a large eutrophic lake in eastern China. July N2O saturations displayed a distinct diurnal pattern, opposite to those observed by others in subtropical streams, but similar to N2O emissions observed from incubated estuarine sediments. Correlative analyses indicate that biogeochemical processes operate as important controls on N2O production over very short time scales. Nitrous oxide production processes are not only regulated by O2 dynamics related to microalgal photosynthesis, but also closely related to organic matter decay at the sediment-water interface. While large-scale changes (approximately 25-fold) in N2O fluxes in Lake Taihu are a function of variable N loading, biogeochemical processes concerning O2 and N transformation at the sediment-water interface have significant (-twofold) impacts on the regulation of N2O production over very short time scales. Further, high temporal resolution research focused on developing a comprehensive understanding of lacustrine N2O production, including natural and anthropogenic loading and biogeochemical transformation processes, is clearly needed. 相似文献
288.
289.
Leakage of saline-alkaline tank waste solutions often creates a serious environmental contamination problem. To better understand the mechanisms controlling the fate of such waste solutions in the Hanford vadose zone, we simulated reactive transport in columns designed to represent local site conditions. The Pitzer ion interaction module was used, with principal geochemical processes considered in the simulation including quartz dissolution, precipitation of brucite, calcite, and portlandite, multi-component cation exchange, and aqueous complexation reactions. Good matches were observed between the simulated and measured column data at ambient temperature ( approximately 21 degrees C). Relatively good agreement was also obtained at high temperature ( approximately 70 degrees C). The decrease of pH at the plume front is examined through formation of secondary mineral phases and/or quartz dissolution. Substantial formation of secondary mineral phases resulting from multi-component cation exchange suggests that these phases are responsible for a decrease in pH within the plume front. In addition, a sensitivity analysis was conducted with respect to cation exchange capacity, selectivity coefficient, mineral assemblage, temperature, and ionic strength. This study could serve as a useful guide to subsequent experimental work, to thermodynamic models developed for the concentrated solutions at high ionic strength and to other types of waste plume studies. 相似文献
290.
在氰基硼氢化钠存在的弱酸性条件下将6-去氧-6-甲酰基-α-环糊精接枝到壳聚糖纤维上,制备了α-环糊精接枝壳聚糖纤维.测定了不同温度和时间下,α-环糊精接枝壳聚糖纤维对对硝基酚(PNP)的包合吸附与释放性能,及其包合稳定性常数和热力学参数.结果表明,α-环糊精接枝壳聚糖纤维是一种高效的PNP分离剂,对PNP具有良好的分子识别、包合吸附和释放性能,其PNP包合吸附容量可达到2.93 mg/g,318 K时PNP释放度可达到70%左右,并可反复包合吸附与释放;该包合反应为放热反应,分子间的范德华力起主导作用;包合物的稳定性受温度影响较大,低于298 K时较稳定,318 K时PNP释放达到平衡;在同一温度下,PNP释放度随时间的增加而提高. 相似文献