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101.
Summary Degradation products of chlorsulfuron, chlortoluron, diuron, fluometuron, isoproturon, linuron, metabenzthiazuron, metobromuron,
and monuron formed in the gas chromatographic injector have been used for identification of the respective herbicides. Mass
spectra of the derived compounds were obtained with a quadrupole mass spectrometric detector working in scan mode (20–450
amu). The compounds generated often depended on the solvent used for phenylurea herbicide injection (ethanol, methanol, dichloromethane,
and acetonitrile). When methanol and ethanol were used as solvents the major products formed from phenylureas were carbamic
acid esters. When acetonitrile or dichloromethane were used the main derivatives were phenylisocyanates. Chlorsulfuron and
metabenzthiazuron, however, generated a triazine plus a phenylsulfonamide and a benzothiazolamine, respectively, irrespective
of the solvent used. Linuron and diuron behaved similarly and gave degradation products with the same mass spectra. The thermal
reactions occurred instantaneously in the injector block and were promoted by the high temperature selected (300°C).
Detemination of the compounds derived from urea herbicides, by use of a 30 m BP10 column and a selected ion registering (SIR)
program based on two or three ions, can be used for sensitive detection of the presence of urea herbicides in environmental
extracts. With standards in methanol instrument detection limits ranged from 0.1 pg for chlorsulfuron (detected as 2-chlorobenzensulfonamide)
to 1 pg for monuron and metobromuron (both detected as their carbamic acid methyl esters).RSD were below 9% at the 5 ng L−1 level. The response was linearly dependent on quantily (r>0.9986) in the 5 ng L−1 to 25 μg L−1 range. Unequivocal identification of some phenylurea herbicides was not always possible because some herbicides with similar
structures, for example diuron and linuron, gave the same derivative. 相似文献
102.
Ashok Kumar Malik Jatinder Singh Aulakh Agnes Fekete Philippe Schmitt‐Kopplin 《中国化学会会志》2009,56(6):1163-1167
The study of the chiral compounds and their fate in the environment is receiving an increasing attention — enantiomeric ratios are being measured and enantioselective degradation processes are being reported. It is particularly important with the toxic compounds like the pesticides, which are being freely used in the environment to control the harmful pests. Capillary zone electrophoresis was used for the chiral and mutual separation of four phenoxy acid herbicides using highly sulphated cyclodextrins (HSCD) in the buffer. The CE runs were performed with reverse polarity (anode in the outlet vial) using the acidic ammonium formate buffer (20 mmol, pH 3). Under these conditions of suppressed the electroendoosmotic flow (EOF), the analytes are mobilized to the anode by entering into host guest relation with the migrating negatively charged sulphated cyclodextrin. The phenoxy acid herbicides selected for the purpose were fenoprop, dicloprop, mecoprop and 2,4‐DB. The α‐HSCD and β‐HSCD have been tested as resolving agents in the CE for the separation of the enantiomers of the herbicides. Though the chiral separation of the dicloprop and mecoprop were achieved with α‐HSCD but it was not able to resolve fenoprop. With β‐HSCD the required base line separation was achieved. Potential difference selected was 10 kV. The limit of detection (S/N= 3) achieved in present case is 0.15 ppm for fenoprop, 0.14 ppm for dicloprop and mecoprop and 0.11 ppm for 2,4‐DB. 相似文献
103.
Pereira Félix M. Gonçalves Adilson R. Ferraz André Silva Flávio T. Oliveira Samuel C. 《Applied biochemistry and biotechnology》2001,91(1-9):563-574
Applied Biochemistry and Biotechnology - Release of herbicides from lignin-based formulations follows a diffusion-controlled mechanism. For mathematical modeling of diffusive transport, the... 相似文献
104.
Monosulfuron-ester is a novel sulfonylurea herbicide with ultra-low dosage. Herein sodium monosulfuron-ester was synthesized and its crystal structure was determined by X-ray diffraction method. The title compound belongs to monoclinic, space group P21/c with a = 9.335(5), b = 20.632(12), c = 13.853(8) (A), β = 107.193(9)°, Mr = 487.46, Z = 4, Dc = 1.270 g/cm3, μ = 0.293 mm-1, F(000) = 1015, R = 0.0859 and wR = 0.2633. In the title compound, Na coordinates with N(1), O(1) and O(3) from one monosulfuron-ester molecule, N(4A) and O(5A) from the other monosulfuron-ester molecule and one oxygen atom from DMSO to give six coordination bonds. 相似文献
105.
离子型金属有机骨架材料(iMOFs)对离子型化合物具有良好的选择吸附性,利用水热法合成了一种金属有机骨架材料MIL-101-NH2,以聚偏二氟乙烯(PVDF)为交联剂将其制备成混合基质膜(MMM),然后用三氟甲烷磺酸甲酯进行季胺基功能化改性,最终得到阳离子型金属有机骨架膜材料MIL-101-$NMe_{3}^{+}$-PVDF MMM,采用分散固相萃取方式富集水中的苯氧羧酸类除草剂,建立了一种基于阳离子型MOF混合基质膜的分散固相萃取-超高效液相色谱-串联质谱(UPLC-MS/MS)测定水体中7种苯氧羧酸类除草剂的分析方法。通过傅里叶变换红外光谱和扫描电子显微镜对制备的混合基质膜进行表征,结果表明季胺基功能化改性是成功的,得到了阳离子型MOF膜。对影响萃取效果的主要因素(吸附剂用量、水样pH值、萃取时间、洗脱剂种类、洗脱剂体积及洗脱时间)进行了优化,确定了最佳萃取条件。以0.01%(v/v)甲酸水溶液和乙腈作为流动相进行梯度洗脱,目标化合物在ACQUITY UPLC BEH C18色谱柱(100 mm×2.1 mm, 1.7 μm)上分离,在电喷雾电离源、负离子模式下进行多反应监测(MRM),外标法定量。结果表明,7种苯氧羧酸类除草剂在各自范围内线性关系良好,线性相关系数均大于0.997,方法的检出限(LOD)和定量限(LOQ)分别为0.00010~0.00090 μg/L和0.00033~0.00300 μg/L。在0.005、0.05和0.2 μg/L 3个加标水平下进行加标回收率试验,7种待测物的平均回收率为80%~102%,日内、日间相对标准偏差分别为1.4%~9.4%和4.2%~12.6%。该方法操作简单、快速,灵敏度高,适用于环境水体中7种苯氧羧酸类除草剂的检测。 相似文献
106.
Michel Maguet Yves Poirier Francis Garnier Robert Guglielmetti 《Phosphorus, sulfur, and silicon and the related elements》2013,188(1-2):193-194
Abstract The acid catalyzed rate for hydrolysis of methylphosponfluoridic acid has been determined at several hydrogen ion concentrations and temperatures. The acid hydrolysis is second order (in acid and substrate). Assumed rate expressions, observed rate constants, and hydrogen ion concentrations were used to calculate the thermodynamic equilibrium constant (K a=0.56) and rate constants for acid catalysis. The activation energy E a has been determined as 18.3 Kcal/mole. Finally, the acid catalyzed deuterolysis was determined to be about 1.47 times the rate of hydrolysis. The data suggest a two-step mechanism consisting of a rapid proton transfer, followed by slow hydration of the protonated complex. 相似文献
107.
108.
A simple and efficient procedure was developed to determine eight herbicides in corn flour by gas chromatography–mass spectrometry in selected ion-monitoring mode. Samples were prepared with a modified, quick, easy, rapid, effective, rugged, and safe procedure. The type and volume of extraction solvent, type and amount of adsorbent, and time of sonication were optimized. The protocol method was rigorously verified. The mean recoveries were from 85 to 108% at various fortification levels with relative standard deviations below 15% and limits of quantification from 4 to 48?ng g?1. The method was used to determine herbicides in corn flour. 相似文献
109.
《Journal of separation science》2017,40(14):2992-2998
Zinc oxide nanoparticles have recently been used as effective adsorbent materials for sample pretreatment in analytical chemistry because of their excellent properties, such as high specific surface area, high effective porosity, non‐toxicity, and ease of fabrication. In this study, the zinc oxide nanoparticles functionalized by an ionic liquid, 1‐carboxyethyl‐3‐methylimidazolium chloride, were fabricated and used as the adsorbent for the solid phase extraction of five triazine herbicides in corn for the first time. High‐performance liquid chromatography was employed for the determination of these triazine herbicides. Several experimental parameters affecting the extraction efficiency were investigated, including the volume of extraction solvent, the extraction time, the type of extraction solvent and elution solvent, the amount of absorbent, and the volume of elution solvent. By using the proposed method, low limits of detection and quantification for all the five triazine herbicides were obtained between 0.71–1.08 and 2.67–3.64 ng/g, respectively. Recoveries of the proposed method range from 89.05 to 100.33% with intra‐ and inter‐day relative standard deviations lower than 8.45%. The calibration curves are linear in the concentration range of 0.005–1.00 μg/g with the correlation coefficient higher than 0.9954. 相似文献
110.