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1.
Effect of low-molecular weight organic acids on phosphorus release and phytoavailabilty of phosphorus in phosphate rocks added to soils 总被引:2,自引:0,他引:2
Phosphorus (P) is critically needed to improve soil fertility in many parts of the world. The use of water-soluble P fertilizers, e.g., single super-phosphate and triple super-phosphate in developing countries to improve crop production has been limited primarily by their high cost. The presence of indigenous phosphate deposits in some countries provides an incentive for direct application or local chemical treatment at low cost to improve the solubility of low reactive phosphate rocks (PRs). The use of naturally occurring low-molecular weight organic acids (LMWOAs) that are produced in soil as microbial metabolites or plant exudates from dead or living cells represents a new perspective in PR research. The LMWOAs contain various functional groups that may play a significant role in PR dissolution. Little information is available, however, about the potential of LMWOAs in releasing P from PRs. This study reports P release from 12 PRs, four each of low, medium, and high reactivity, obtained from various deposits (Kodjari, Tahoua, North Carolina, Gafsa, Khouribga, Tilemsi Valley, Central Florida, Sechura, Minjingu, North Florida, Hahotoe, and Parc W) using nine LMWOAs containing mono-, di-, and tri-carboxylic groups and a mineral acid (H2SO4). Laboratory studies showed that the organic acids are effective in releasing P from low and medium reactive PRs, but very ineffective in releasing P from high reactive PRs. The average amounts of P released by all the organic acids from the three types of PRs were 65.5 mmol kg−1 PR from the low reactive PRs, 55.1 mmol kg−1 from the medium, and 11.1 mmol kg−1 from the high; those released from across all the PRs were 21.9 by the mono-carboxylic acid group, 54.2 by the di-carboxylic acid group, and 57.0 mmol P kg−1 by the tri-carboxylic acid group. The P released was negatively correlated with the equilibrium pH, but positively correlated with Ca released from the PRs. Laboratory incubation studies on the release of P from PRs added to soils with or without organic acids and incubated at 25 °C for 15, 30, and 45 days showed that the percentage of plant-available P released varied considerably from 0.95 in the Kodjari PR to 40.1% in the North Carolina PR and was related to PR reactivity. A greenhouse study with corn (Zea mays L.) grown for 60 days on soils treated with PRs or with PRs mixed with organic acids showed that corn response to addition of oxalic or citric acid varied with P rates and PR sources, suggesting that organic acids have potential as amendments for increasing plant-available P in PR-treated soils. 相似文献
2.
臭氧(O3)污染日趋严重,控制光化学反应前体物之一的挥发性有机污染物(volatile organic compounds,VOCs)对减少臭氧生成有重要意义.为研究天津某工业园区VOCs臭氧生成潜势,采集了园区6个代表企业厂界气体样品,使用质子转移反应飞行时间质谱仪(PTR-TOF-MS)对VOCs进行了定量分析,估算了各企业臭氧生成潜势,运用VOCs/NO_x研究了臭氧生成控制敏感性因素,并在熵值法基础上筛选出了减少臭氧生成优先控制VOCs物种.结果表明,通过PEC法估算臭氧生成F企业最高为0.423 3 mg·m~(-3),MIR法估算结果 C企业最高为1.573 3 mg·m~(-3);PEC法估算结果与臭氧浓度更接近,适用于园区对臭氧生成的估算;VOCs和NOx均为工业园区臭氧生成敏感性因素,需同时控制;园区内VOCs物种臭氧生成贡献大小为烷烃烯炔烃醇类芳香烃,优先控制物种为正庚烷及其同分异构体、正壬烷、正辛烷及其同分异构体、正十一烷、戊烷、正癸烷、甲醇. 相似文献
3.
大气环境质量的物元分析评价法 总被引:10,自引:0,他引:10
为了探索物元分析评价法用大气象环境质量评价的可行性和合理性,应用物元分析方法构建大气环境质量的综合评价模型,并将该方法用于实例分析。结果表明,物元分析方法用于大气环境质量评价是可行的。 相似文献
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本文介绍采用航空遥感技术和实地调查研究相结合的方法,分析了沈阳市烟囱数量、高度、密度以及高、中、低架烟囱的分布状况和特点,同时与大气污染监测结果对照分析了沈阳市煤烟型大气污染的规律及特点,研究了沈阳市烟囱分布对大气污染的影响。最后,提出了沈阳市燃煤污染的防治途径。 相似文献
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7.
Dragana??or?evi?Email author Drubavka?Radmanovi? Aleksandra?Mihajlidi-Zeli? Mila?Ili? Petar?Pfendt Zorka?Vukmirovi? Pedrag?Poli? 《Environmental Chemistry Letters》2004,2(3):147-150
We applied statistical methods to the data of a 5-year sampling period to characterize the features of trace elements in airborne particulate matter at the South Adriatic Coast. The analysis of surface soil samples was also performed. The data were processed by cluster analysis, enrichment factor determination and receptor rose statistics. It is shown that the principal element association consists of Fe, Mn and Ti originating from surface material resuspension. Hg and Se were shown to originate from more complex natural and anthropogenic processes. A strong emission source of Cd and Se was identified in the SSE direction.Selected article from the Regional Symposium on Chemistry and Environment Krusevac, Serbia, June 2003, organized by Dr. Branimir Jovancicevic. 相似文献
8.
大气中的碘直接影响对流层中多种光化学反应并间接影响全球气候变化,因而碘的大气化学机制研究受到越来越多关注.气溶胶中的碘是其大气化学反应的最终产物,通过其赋存形态可以推测和了解碘的大气化学过程.大气碘化学理论一直认为IO3-是大气碘沉降中最主要的碘形态,但近年来的各地实测数据发现大气气溶胶中的碘形态大多以可溶性有机碘或I-为主.这种分歧说明目前的大气碘化学理论尚有待完善.本文详细介绍了近年来碘的大气化学以及气溶胶颗粒物中碘形态的研究进展. 相似文献
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10.
《环境科学学报(英文版)》2024,36(3):732-740
Amino acids(AAs)including D-and L-enantiomers are a group of organic nitrogen species in ambient aerosol.Due to the low abundances of AAs(level of ng/m3)and the matrix effects by coexistent components,it is challenging to quantify AA enantiomers in ambient aerosols especially under pollution conditions.In this study,we present an optimized method for an-alyzing AA enantiomers in atmospheric aerosol samples including a pretreatment process and the detection by high performance liquid chromatography coupled to a fluorescence de-tector(HPLC-FLD).Matrix effects caused by coexistent chemicals on AA enantiomers analy-sis in ambient aerosol samples were investigated especially for those collected in pollution episodes.The results revealed that the determination of AA enantiomers is significantly affected by the coexistent organic carbon(as a proxy of organic matter)and water-soluble ion of NH4+.To remove the matrix effects,we applied a pretreatment using the solid phase extraction column coupled with alkaline adjustment to sample extract.After pretreatment,18 AAs including 6 pairs of D-and L-enantiomers(i.e.,leucine,isoleucine,valine,alanine,serine,and aspartic acid)can be successfully separated and quantified in aerosol samples by HPLC-FLD.The recoveries are in the range of 67%-106%.This method was successfully applied to the urban aerosol samples from pollution and non-pollution periods for AA enan-tiomers determination.We suggest that the concentrations of D-AAs and the ratio of D-AA/L-AA are indicative of the contribution of bacterial sources and the influence of biomass burning. 相似文献