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951.
María González González Juan Carlos Cabanelas Javier Pozuelo Juan Baselga 《Journal of Thermal Analysis and Calorimetry》2011,103(2):717-723
Cycloaliphatic epoxy resin has been successfully thermally cured using a polyamino siloxane oligomer as hardener. The curing reaction was followed by infrared spectroscopy in the near range, and thermal transitions were measured by dynamic mechanical thermal analysis. The use of accelerants and a plasticizer (dodecylphenol), and different curing schedules were explored. Cured materials showed high Tg values (around 125–164 °C), and the analysis of laser scanning confocal microscopy images showed that they are homogeneous in the microscale. 相似文献
952.
Brum Junior L Pugens AM Pritsch MC Mantovani PB dos Santos MB Manfio JL 《Journal of AOAC International》2008,91(4):731-738
A fast, sensitive, and specific liquid chromatographic/tandem mass spectrometric method was developed and validated for determination of tetracycline in human plasma. Tetracycline and oxytetracycline [internal standard (IS)] were extracted from the plasma by protein precipitation. The mobile phase consisted of acetonitrile-formic acid 0.1% (48 + 52, v/v), run at a flow rate of 1 ml/min (split 1:5). Detection was performed by positive electrospray ionization in multiple reaction monitoring mode, monitoring the transitions 444.8 > 410.0 and 461.0 > 426.0 for tetracycline and IS, respectively. The analysis was performed in 3.5 min and the method was linear in the plasma concentration range of 50-6000 ng/mL. The mean extraction recoveries for tetracycline and IS from plasma were 92.14 and 94.04%, respectively. Method validation investigated parameters such as the linearity, precision, accuracy, specificity, and stability, giving results within the acceptable range. The proposed method was successfully applied for determination of tetracycline in human plasma samples to support bioequivalence studies. 相似文献
953.
Iglesias-García I Barriada-Pereira M González-Castro MJ Muniategui-Lorenzo S López-Mahía P Prada-Rodríguez D 《Analytical and bioanalytical chemistry》2008,391(3):745-752
A method to determine 21 organochlorine pesticides in animal feed samples using microwave assisted extraction and solid phase extraction cleanup was optimised regarding its main parameters. After extraction with hexane-acetone (50:50), three different sorbents (alumina/ENVI-Florisil, ENVI-Carb and ENVI-Carb II/PSA) were assayed for the cleanup step. Analytes were eluted with hexane-ethyl acetate (80:20) and determined by gas chromatography and electron capture detection followed by gas chromatography-mass spectrometry. ENVI-Carb and ENVI-Carb II/PSA provided colourless eluates but fewer interferent compounds were found in ENVI-Carb II/PSA chromatograms, so this system was selected to carry out the purification of the extracts. The analytical recoveries obtained with this method were close to 100% in most cases with relative standard deviations lower than 10%. These percentages were similar to those obtained with the Soxhlet extraction procedure, which shows the method suitable for the determination of organochlorine pesticides in animal feed material. The method was also validated with the analysis of a certified reference material (CRM-115 BCR), and the results obtained were in good accordance with the certified values. 相似文献
954.
Garcia CC Angeli JP Freitas FP Gomes OF de Oliveira TF Loureiro AP Di Mascio P Medeiros MH 《Journal of the American Chemical Society》2011,133(24):9140-9143
Acetaldehyde is an environmentally widespread genotoxic aldehyde present in tobacco smoke, vehicle exhaust and several food products. Endogenously, acetaldehyde is produced by the metabolic oxidation of ethanol by hepatic NAD-dependent alcohol dehydrogenase and during threonine catabolism. The formation of DNA adducts has been regarded as a critical factor in the mechanisms of acetaldehyde mutagenicity and carcinogenesis. Acetaldehyde reacts with 2'-deoxyguanosine in DNA to form primarily N(2)-ethylidene-2'-deoxyguanosine. The subsequent reaction of N(2)-ethylidenedGuo with another molecule of acetaldehyde gives rise to 1,N(2)-propano-2'-deoxyguanosine (1,N(2)-propanodGuo), an adduct also found as a product of the crotonaldehyde reaction with dGuo. However, adducts resulting from the reaction of more than one molecule of acetaldehyde in vivo are still controversial. In this study, the unequivocal formation of 1,N(2)-propanodGuo by acetaldehyde was assessed in human cells via treatment with [(13)C(2)]-acetaldehyde. Detection of labeled 1,N(2)-propanodGuo was performed by HPLC/MS/MS. Upon acetaldehyde exposure (703 μM), increased levels of both 1,N(2)-etheno-2'-deoxyguanosine (1,N(2)-εdGuo), which is produced from α,β-unsaturated aldehydes formed during the lipid peroxidation process, and 1,N(2)-propanodGuo were observed. The unequivocal formation of 1,N(2)-propanodGuo in cells exposed to this aldehyde can be used to elucidate the mechanisms associated with acetaldehyde exposure and cancer risk. 相似文献
955.
Hernández-Chávez JF González-Córdova AF Rodríguez-Ramírez R Vallejo-Cordoba B 《Analytica chimica acta》2011,708(1-2):149-154
A polymerase chain reaction and capillary gel electrophoresis (PCR-CGE) method with ultraviolet (UV) or laser induced fluorescence detection (LIF) was established for the detection of chicken or turkey in heat-treated pork meat mixtures. Mitochondrial DNA samples extracted from heat treated meat were amplified with their corresponding specific primers yielding PCR products between 200 and 300 bp. LIF detection was superior than UV detection in terms of precision and sensitivity for the study of DNA fragments. The CGE-LIF method was highly reproducible and accurate for determining DNA fragment size. The PCR-CGE-LIF was sensitive since a significant fluorescent signal was obtained at the minimum admixture level employed of 1% in meat mixtures. Thus, the PCR-CGE-LIF method established was useful for the detection of chicken or turkey in heat treated meat mixtures and may prove to be useful for the detection of poultry meat in pork processed products. 相似文献
956.
Hernández-Hierro JM García-Villanova RJ González-Martín I 《Analytica chimica acta》2008,622(1-2):189-194
The potential of the near infrared spectroscopy (NIRS) technique for the analysis of red paprika for aflatoxin B(1), ochratoxin A and total aflatoxins is explored. As a reference, the results from a chromatographic method with fluorescence detection (HPLC-FD) following an immunoaffinity cleanup (IAC) were employed. For the NIRS measurement, a remote reflectance fibre-optic probe was applied directly onto the samples of paprika. There was no need for pre-treatment or manipulation of the sample. The modified partial least squares (MPLS) algorithm was employed as a regression method. The multiple correlation coefficients (RSQ) and the prediction corrected standard errors (SEP(C)) were respectively 0.955 and 0.2 microg kg(-1), 0.853 and 2.3 microg kg(-1), 0.938 and 0.3 microg kg(-1) for aflatoxin B(1), ochratoxin A and total aflatoxins, respectively. The capacity for prediction of the developed model measured as ratio performance deviation (RPD) for aflatoxin B(1) (5.2), ochratoxin A (2.8) and total aflatoxins (4.4) indicate that NIRS technique using a fibre-optic probe offers an alternative for the determination of these three parameters in paprika, with an advantageously lower cost and higher speed as compared with the chemical method. Content of aflatoxin B(1) and total aflatoxins are the parameters currently employed by the food regulations to limit the levels of the four aflatoxins in many foodstuffs. In addition, aflatoxin B(1) itself is an excellent indicator for aflatoxins' contamination since it is always the most abundant and toxic. 相似文献
957.
Rubén Sanabria Rafael Herrera Raúl Aguilar Carlos González‐Romero Hugo A. Jiménez‐Vázquez Francisco Delgado Björn C. G. Söderberg Joaquín Tamariz 《Helvetica chimica acta》2008,91(10):1807-1827
The reactivity and selectivity of the the captodative olefins 1‐acylvinyl benzoates 1a – 1f and 3a as heterodienes in hetero‐Diels–Alder reactions in the presence of electron‐rich dienophiles is described. Heterodienes 1 undergo regioselective cycloaddition with the alkyl vinyl etherdienophiles 6a , b and 9 to give the corresponding dihydro‐2H‐pyrans 7, 8 , and 10 under thermal conditions. The reactivity of these cycloadditions depends, to a large extent, on the electronic demand of the substituent in the aroyloxy group of the heterodiene. Frontier‐molecular‐orbital (FMO; ab initio) and density‐functional‐theory (DFT) calculations of the ground and transition states account for the reactivity and regioselectivity observed in these processes. 相似文献
958.
Díaz V. González Armas A. González Martí C. Ossuna Pérez Pont M. L. 《Mikrochimica acta》1993,111(1-3):113-118
A sensitive, selective Spectrofluorimetric method has been developed for the determination of thiabendazole in a sodium dodecylsulphate micellar medium. The method features a linear determination range of 0.020-15 g and a detection limit of 0.2 ng/ml, with a relative standard deviation of less than 3%. By using a straightforward extraction procedure with ethyl acetate and hydrochloric acid, the method provided average thiabendazole recoveries above 96% from apple, pear and potato samples. 相似文献
959.
Juan M. Ramírez‐Anguita Àngels González‐Lafont José M. Lluch 《Journal of computational chemistry》2009,30(9):1477-1489
The production of dimethyl sulfoxide (DMSO) and dimethyl sulfone (DMSO2) in the dimethyl sulfide (DMS) degradation scheme initiated by the hydroxyl (OH) radical has been shown to be very sensitive to nitrogen oxides (NOx) levels. In the present work we have explored the potential energy surfaces corresponding to several reaction pathways which yield DMSO2 from the CH3S(O)(OH)CH3 adduct [including the formation of CH3S(O)(OH)CH3 from the reaction of DMSO with OH] and the reaction channels that yield DMSO or/and DMSO2 from the CH3S(O2)(OH)CH3 adduct are also studied. The formation of the CH3S(O2)(OH)CH3 adduct from CH3S(OH)CH3 (DMS‐OH) and O2 was analyzed in our previous work. All these pathways due to the presence of NOx (NO and NO2) and also due to the reactions with O2, OH and HO2 are compared with the objective of inferring their kinetic relevance in the laboratory experiments that measure DMSO2 (and DMSO) formation yields. In particular, our theoretical results clearly show the existence of NOx‐dependent pathways leading to the formation of DMSO2, which could explain some of these experimental results in comparison with experimental measurements carried out in NOx‐free conditions. Our results indicate that the relative importance of the addition channel in the DMS oxidation process can be dependent on the NOx content of chamber experiments and of atmospheric conditions. © 2008 Wiley Periodicals, Inc. J Comput Chem, 2009 相似文献
960.
J. A. González I. G. de la Fuente J. C. Cobos C. Casanova 《Journal of solution chemistry》1994,23(3):399-420
Literature data for phase equilibria: vapor-liquid VLE, liquid-liquid LLE, and solid-liquid SLE; molar excess Gibbs energies G
E
, molar excess enthalpies H
E
; activity coefficients
i
and partial molar excess enthalpies H
i
E,o
at infinite dilution for 1-alkanol (1)+cyclohexane (2) mixtures are examined by the DISQUAC group contribution model. For a more sensitive test of DISQUAC, the azeotropes, obtained from the reduction of the original isothermal VLE data, are also examined for systems characterized by hydroxyl, alkane and cyclohexane groups. The alkane/cyclohexane and alkane/hydroxyl interaction parameters have been estimated previously. The cyclohexane/hydroxyl interaction parameters are reported in this work. The first dispersive parameters increase regularly with the size of the alkanol; from 1-octadecanol they are constant; an opposite behavior is encountered for the third dispersive parameters, which are constant from 1-dodecanol. The second dispersive parameters decrease as far as 1-propanol and then increase regularly; from 1-octadecanol they are constant. The quasichemical parameters are equal to those for the alkane/hydroxyl interactions. Phase equilibria, the molar excess functions, and activity coefficients at infinite dilution are reasonably well reproduced. Poor results are found for H
i
E,o
and DISQUAC predictions for H
i
E,o
are strongly dependent on temperature. 相似文献