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101.
102.
Fenton试剂处理有机氯农药废水的研究 总被引:15,自引:0,他引:15
研究了Fenton氧化法预处理有机氯农药废水的反应特性.通过正交实验确定了氧化反应各种影响因子的最佳操作条件.在此条件下,废水1、2的COD去除率分别为47.8%和87.9%;色度去除率分别为84.4%和99.4%.Fenton试剂处理后,2种废水的可生化性也得到了提高.在各影响因子与COD去除率的关系曲线基础上,分析了废水中各影响因子的作用机理. 相似文献
103.
A. M. Cicero M. G. Finoia M. Gabellini E. Veschetti 《Environmental monitoring and assessment》2000,64(3):607-616
The Italian guidelines concerning the dumping of dredgingmaterials implies chemical, physical and microbiologicalcharacterisation of dumping sediments collected through aspecific sampling strategy.POP's such as PCB's and organochlorine pesticides, areconsidered as priority pollutants in all the InternationalConventions for the protection of the marine environment, inconsequence of their persistence, toxicity and bioaccumulation capacity.In the present article the concentrations and distribution ofPCB's and organochlorine pesticides in dredging sediments ofPiombino harbour (northern Thyrrenian sea) were investigates.The results showed high POP's concentrations in all the studiedareas. The maximum values were: 3.94 mg kg-1 dry weight for PCB's(IUPAC Nos. 28; 52; 101, 118; 137; 153; 180; 209); 2.04 mg kg-1 d.w.for HCH's (-, -, - and -hexachlorocyclohexane isomers); 0.28 mg kg-1 d.w. for DD's (DDT + DDE + DDD).Subsequently, the data related to each pollutant were treatedwith statistical tests, in order to verify how well the samplingstrategy is able to represent the distribution of contaminantsin the dredging area. Finally, management strategies werederived for the studied dredging sediments. 相似文献
104.
固相微萃取-毛细管气相色谱法快速同步分析水中有机氯及有机磷农药 总被引:9,自引:2,他引:9
固相微萃取是一种快速、简便,集萃取浓缩进样于一体的样品前处理技术,具有分析时间短、灵敏度高、无需有机溶剂的优点.用固相微萃取富集水中8种有机氯及7种有机磷农药,毛细管气相色谱ECD检测器分离分析,整个分析过程只需26min,检出限可达0.002~1μg/L,已用于地表水中有机氯及有机磷农药含量的测定. 相似文献
105.
106.
色谱、光谱及联用技术在多农药残留检测中的应用 总被引:5,自引:4,他引:5
介绍了国内外多农药残留检测的发展状况,综述了色谱法、光谱法、色谱-质谱联用技术、色谱-光谱联用法、多维气相色谱技术的特点及在多农药残留检测中的应用,指出多农药残留检测在今后的农药残留检测中将占据主导地位. 相似文献
107.
One hundred forty seven samples of bovine milk were collected from 14 districts of Haryana, India during December 1998–February
1999 and analysed for the presence of organochlorine pesticide (OCPs) residues. ∑HCH, ∑DDT, ∑endosulfan and aldrin were detected
in 100%, 97%, 43% and 12% samples and with mean values of 0.0292, 0.0367, 0.0022 and 0.0036 μg/ml, respectively. Eight percent
samples exceeded the maximum residue limit (MRL) of 0.10 mg/kg as recommended by WHO for ∑HCH, 4% samples of 0.05 mg/kg for
α-HCH, 5% samples of 0.01 mg/kg for γ-HCH, 26% samples of 0.02 mg/kg for β-HCH as recommended by PFAA and 24% samples of 0.05 mg/kg
as recommended by FAO for ∑DDT. Concentrations of β-HCH and p,p′-DDE were more as compared to other isomers and metabolites
of HCH and DDT. 相似文献
108.
Wang H He M Lin C Quan X Guo W Yang Z 《Environmental monitoring and assessment》2007,133(1-3):231-242
Surface sediment samples from 12 sites of the three selected rivers in Daliaohe River watershed (Hunhe River, Taizihe River
and Daliaohe River) were analyzed with the objective of establishing sources and hazard of the organochlorinae pesticides
(OCPs) and polychlorinated biphenyl (PCBs) in surface sediments. The total concentrations of OCPs varied from 3.06 to 23.24
ng g−1. ∑HCH (α-HCH, β-HCH, δ-HCH, γ-HCH), ∑DDT (p, p′-DDE, p, p′-DDD, o, p′-DDT, p, p′-DDT) and ∑Cyclodiene (Heptachlor, Aldrin,
Heptachlor epoxide, Dieldrin, Endrin) ranged from 1.86 to 21.48, 0.5 to 2.81 and 0.56 to 1.53 ng g−1, respectively. Results of OCPs also illustrate that the most dominant pollutants among the OCPs was ∑HCH, and γ-HCH was the
most dominant isomer in HCH, which was evidence of recent input of lindane. It possibly came from the runoff of polluted soils
and long-scale transportation. Total PCB concentrations ranged between 1.88 and 16.88 ng g−1. The peak concentrations of PCBs were found in sediments from station T5 and D3, which are in the vicinity of industrial
areas and ferry, respectively. These data show a moderate level of OCPs and PCBs contaminations compared to that in other
countries. 相似文献
109.
110.
Market samples (60) of six seasonal vegetables were monitoredduring 1996–1997 to determine the magnitude of pesticidalcontamination. The estimation of insecticide residuesrepresenting four major chemical groups i.e. organochlorine,organophosphorous, synthetic pyrethroid and carbamate, was doneby adopting a multiresidue analytical technique employingGC-ECD and GC-NPD systems with capillary columns. The testedsamples showed 100% contamination with low but measurableamounts of residues. Among the four chemical groups, theorganophosphates were dominant followed by organochlorines,synthetic pyrethroids and carbamates. About 23% of the samplesshowed contamination with organophosphorous compounds abovetheir respective MRL values. More extensive studies coveringdifferent regions of Haryana state are suggested to get a clearidea of the magnitude of vegetable contamination with pesticideresidues. 相似文献