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441.
臭氧/沸石工艺处理水中硝基苯的效能研究 总被引:7,自引:2,他引:5
在连续反应器中,考察了臭氧/沸石工艺在不同条件下去除硝基苯的效果.结果表明,臭氧/沸石工艺对硝基苯的去除效率明显高于单纯臭氧氧化,反应7 min后,硝基苯去除率达到100%,并且该反应符合假一级反应动力学.叔丁醇能抑制臭氧/沸石工艺对硝基苯的去除效率,表明在氧化去除硝基苯过程中羟基自由基起主导作用.增加沸石投量和臭氧浓度均能有效地提高臭氧/沸石工艺对硝基苯的去除效率,并且臭氧/沸石工艺对硝基苯的去除速率与沸石投量之间存在1个最优值,与臭氧浓度呈线性关系.臭氧/沸石工艺对硝基苯的去除速率与初始硝基苯浓度无关.离子强度对臭氧/沸石工艺降解硝基苯的效率影响较大,当离子强度从0增加到1×10-3 mol/L时,臭氧/沸石工艺对硝基苯的去除率从81.2%降低至31.6%.pH值主要影响臭氧的分解能力,随着溶液pH降低,臭氧/沸石工艺对硝基苯的去除效率逐渐下降.沸石具有较长的使用寿命. 相似文献
442.
臭氧降解高浓度腐殖酸动力学 总被引:4,自引:1,他引:3
采用臭氧氧化法降解高浓度腐殖酸废水,并研究了臭氧对腐殖酸的降解动力学,考察了臭氧投量、初始腐殖酸浓度、初始pH和反应温度对臭氧降解高浓度腐殖酸废水的影响.结果表明,在臭氧投量为3.46 g.h-1,初始腐殖酸浓度为1 000mg.L-1,初始pH=8.0,反应温度为303 K,反应30 min的条件下,腐殖酸的去除率达到89.04%.在臭氧投量为1.52~6.01g.h-1,初始腐殖酸浓度为250~1 000 mg.L-1,初始pH为2.0~10.0,反应温度在283~323 K的范围内,臭氧降解腐殖酸符合拟一级动力学模型,通过对实验数据拟合,得到反应动力学方程,反应活化能较低(Ea=1.30×104J.mol-1),并且模型计算数值与实际数据吻合良好(平均相对误差为7.62%). 相似文献
443.
赤铁矿光助类Fenton降解有毒有机污染物 总被引:3,自引:2,他引:1
可见光照射下(λ>420 nm)采用天然赤铁矿为催化剂降解罗丹明B(rhodamine B,RhB)和无色小分子2,4-二氯苯酚(2,4-dichlorophenol,DCP),探讨了溶液pH、催化剂用量、溶液中溶铁量对降解反应的影响,通过紫外-可见分光光度计、红外光谱仪、苯甲酸荧光光度法以及COD等跟踪降解过程,并对反应机制做了初步探讨.结果表明,Cata/RhB/H2O2/vis体系能有效地降解RhB,降解最佳条件为:催化剂用量0.6 g.L-1、pH为3.0、H2O2浓度1.5×10-3mol.L-1,反应180 min可完全脱色,且溶铁对催化体系的贡献较小;对2,4-DCP的降解,24 h后,降解率达56%.且该催化剂具有良好的稳定性,循环使用6次,催化剂活性无明显变化.苯甲酸荧光光度法检测到反应体系中产生了高活性氧化物种.OH,反应机制主要是.OH的异相类Fenton过程. 相似文献
444.
Arsenic has a suppressive influence on spermatogenesis and induces impairment in male reproductive system due to oxidative stress. The present study was aimed to test the arsenic induced toxicity and protection by Chlorophytum borivilianum. The effect of sodium arsenite (4 mg/(kg body weight (bw). day)) via double distilled water without or with C. borivilianum (800 mg/(kg bw. day)) was evaluated in Swiss albino mice for 30 days. The radical scavenging activity of the aqueous C. borivilianum root extract was measured using DPPH (1,1-diphenyl-2-picryl hydrayzyl) radical. Qualitative assessment of various cell types in the testis, sperm count and motility, testicular activity of lipid peroxidation (LPO), reduced glutathione (GSH), acid and alkaline phosphatase, cholesterol and serum testosterone were monitored. Arsenic treatment showed a significant increase in LPO, acid and alkaline phosphatase, cholesterol and decrease in sperm count, sperm motility, GSH and serum testosterone. Combined treatment showed significant decrease in LPO, acid and alkaline phosphatase, cholesterol and elevation in sperm count, sperm motility, GSH and serum testosterone. Testicular histopathology showed that C. borivilianum had reduced degeneration of germ cell in the seminiferous tubules and loss of sperms induced by arsenic intoxication. The results thus led us to conclude that administration of C. borivilianum root extract is found to be protective against arsenic induced toxicity. 相似文献
445.
446.
It remains unclear whether dicofol should be defined as a persistent organic pollutant. Its environmental persistence has gained attention. This study focused on its degradation by cellulase. Cellulase was separated using a gel chromatogram, and its degradation activity towards dicofol involved its endoglucanase activity. By analyzing the kinetic parameters of cellulase reacting with mixed substrates, it was shown that cellulase reacted on dicofol and carboxyl methyl cellulose through two different active centers. Thus, the degradation of dicofol was shown to be an oxidative process by cellulase. Next, by comparing the impacts of tert-butyl alcohol (a typical OH free-radical inhibitor) on the removal efficiencies of dicofol under both cellulase and Fenton reagent systems, it was shown that the removal of dicofol was initiated by OH free radicals produced by cellulase. Finally, 4,4′-dichloro-dibenzophenone and chloride were detected using gas chromatography mass spectrometry and ion chromatography analysis, which supported our hypothesis. The reaction mechanism was analyzed and involved an attack by OH free radicals at the orthocarbon of dicofol, resulting in the degradation product 4,4′-dichloro-dibenzophenone. 相似文献
447.
448.
Edward W. Kern Rollin H. Hotchkiss Daniel P. Ames 《Journal of the American Water Resources Association》2015,51(5):1453-1459
Low‐head dams can cause dangerous currents near the downstream face of the structure. Fatalities at low‐head dams with such currents, often referred to as “drowning machines,” are poorly documented. This technical note presents a new database of fatalities at low‐head dams in the United States together with an interactive map and web‐based user interface. The primary purpose of the system is to raise awareness, generate interest, and educate the general public and decision makers regarding these dangerous structures and the need for remediation. The database was designed as a normalized relational database of event dates, severity, location, reporter, and other circumstances. The open‐access user interface allows the general public to browse fatal incidents by geographic location and to read incident circumstances. The system allows submission of new contributions from users including all metadata needed to characterize the incident. The database is structured to include documentation verifying each entry. The site can be viewed at http://dams.byu.edu/ . 相似文献
449.
M. Srensen M. D. Hurley T. J. Wallington T. S. Dibble O. J. Nielsen 《Atmospheric environment (Oxford, England : 1994)》2002,36(39-40)
Smog chamber/FTIR techniques were used to study the relative reactivity of OH radicals with methanol, ethanol, phenol, C2H4, C2H2, and p-xylene in 750 Torr of air diluent at 296±2 K. Experiments were performed with, and without, 500–8000 μg m−3 (4000–50 000 μm2 cm−3 surface area per volume) of NaCl, (NH4)2SO4 or NH4NO3 aerosol. In contrast to the recent findings of Oh and Andino (Atmospheric Environment 34 (2000) 2901, 36 (2002) 149; International Journal of Chemical Kinetics 33 (2001) 422) there was no discernable effect of aerosol on the rate of loss of the organic compounds via reaction with OH radicals. Gas kinetic theory arguments cast doubt upon the findings of Oh and Andino. The available data suggest that the answer to the title question is “No”. As part of this work the rate constants for reactions of OH radicals with methanol, ethanol, and phenol in 750 Torr of air at 296 K were determined to be: kOH+CH3OH=(8.12±0.54)×10−13, kOH+C2H5OH=(3.47±0.32)×10−12 and kOH+phenol=(3.27±0.31)×10−11 cm3 molecule−1 s−1. 相似文献
450.
采用共沉淀法制备了铁锰双金属复合催化剂(MnFe2O4),用于活化过一硫酸盐(PMS)产生强氧化性的硫酸根自由基(SO4-·)氧化降解水中阴离子表面活性剂(LAS).采用傅立叶变换红外光谱仪(FTIR)、X射线粉末衍射仪(XRD)、扫描电子显微镜(SEM)对催化剂进行表征,表明成功合成了具有尖晶石结构的MnFe2O4催化剂.考察了催化剂投加量、PMS投加量以及初始pH值等各种因素条件对LAS的降解效率以及反应动力学的影响.实验结果表明,MnFe2O4活化PMS降解LAS的过程符合准一级动力学(R2>0.9).在LAS初始浓度为80mg/L,催化剂投加量为2.0g/L,PMS的浓度为2.5mmol/L,初始pH值为7.0,反应时间为30min的情况下,LAS降解效率达到94.1%,此时LAS的降解速率常数达到0.192min-1.通过自由基猝灭实验证明了MnFe2O4/PMS体系中起主要氧化降解作用的活性自由基为SO4-·.通过反应前后催化剂的X射线光电子能谱(XPS),证实Fe和Mn之间存在协同作用,提高了MnFe2O4对PMS的活化效率. 相似文献