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991.
992.
The Sterol and Erythrodiol + Uvaol Content of Virgin Olive Oils Produced in Five Olive-Growing Zones of Extremadura (Spain) 下载免费PDF全文
Manuel Martínez Cano Concepción de Miguel Gordillo Manuel Fuentes Mendoza Daniel Martín Vertedor Jacinto Sánchez Casas 《Journal of the American Oil Chemists' Society》2016,93(2):227-235
The content of sterols and erythrodiol + uvaol was studied in 273 virgin olive oil samples from 40 mills in five olive‐growing zones of Extremadura (Spain). An analysis of variance showed significant differences at a confidence level of 95 % between the different zones in each of the main sterols and in the sum of erythrodiol + uvaol. The results of a linear discriminant analysis, considering the different olive‐growing areas as categorical dependent variables and the different sterols as independent variables, explained 78.2 % of the variance with the first two discriminant functions. The resulting model correctly classified 86.9 % of the samples analysed. A validation study was conducted to verify the goodness of the discriminant analysis, resulting in 79.3 % of the new samples used for validation being correctly classified. In the graphical representation of the different groups studied considering the proposed model's first two discriminant functions, the centroids of the Sierra Norte de Cáceres, Vegas del Guadiana and Tierra de Barros olive‐growing zones were clearly separated, but this was not the case for the other two zones—La Serena and La Siberia. 相似文献
993.
994.
Acid catalyst influence on the polymerization time of polyfurfuryl alcohol and on the porosity of monolithic vitreous carbon 下载免费PDF全文
Fábio Dondeo Origo Júlia Cassiano Arisseto Fernanda Lini Seixas Walter Miyakawa Alvaro José Damião Sílvia Sizuka Oishi Edson Cocchieri Botelho 《应用聚合物科学杂志》2016,133(20)
This study compares the influence of different acid catalysts on the polymerization rate of polyfurfuryl alcohol (PFA) precursor and especially on the respective porosity of Monolithic Vitreous Carbon (MVC) produced from that. Five acid catalysts commonly used were compared: p‐toluenesulfonic (PTLS), hydrochloric, sulfuric, nitric, and phosphoric. A fixed molar concentration of catalyst was diluted in PFA resin under room pressure and temperature. The time dependence of PFA resin polymerization was investigated by optical transmittance of PFA films, and the polymerization degree, characterized by ATR spectroscopy and thermogravimetry. MVC samples prepared with the same PFA resin and each catalyst were carbonized up to 1200 °C, under inert atmosphere. MVC porosity was studied by nitrogen adsorption/desorption, and by SEM and optical microscopy. Higher polymerization degree and higher residual mass were obtained with faster catalysts. No direct relation between the polymerization rate and the acid force was observed. PTLS promoted the fastest PFA polymerization process and the sulfuric acid, the slowest one. MVC samples were obtained by slow carbonization. MVC presented low specific surface SBET from 1.4 to 7.4 m2/g. Nitric acid catalyst contributed the most to micropores formation. Micrometric apparent porosity was smaller for the catalysts having longer polymerizations times, such as phosphoric and sulfuric acid. Phosphoric catalyst corresponded to the lowest porosity in MVC. As the polymerization time increased, the average size of the micrometric surface pores tended to augment. The MVC macroscopic porosity increased with the SBET increment. Acid catalysts choice exerted a fundamental role on the porosity of MVC. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43272. 相似文献
995.
Csilla Lakatos Katalin Czifrák József Karger‐Kocsis Lajos Daróczi Miklós Zsuga Sándor Kéki 《应用聚合物科学杂志》2016,133(43)
Crosslinked polyurethanes (PUs) containing irreversible (allophanate) and reversible Diels‐Alder chemical bonds were synthesized using various diisocyanates (methylene diphenyl diisocyanate MDI, 1,6‐hexamethylenediisocyanate HDI) and poly(?‐caprolactone) ((PCL) with different molecular weights (Mn = 10 kg/mol, 25 kg/mol, 50 kg/mol) as diol component. The melting/crystallization of PCL and the reversible DA bonds acted as temperature‐activated switches for shape memory performances, while allophanate network provided the permanent crosslinks for these PUs. The reversible DA bonds were obtained by the reaction of diisocyanate‐ended prepolymers with furfurylamine (FA) followed by the addition of bismaleimide (BMI). The permanent crosslinks between the linear chains containing DA bonds were achieved using additional amounts of diisocyanates (MDI or HDI). The above reaction path was supported by infrared spectroscopic results and swelling experiments. Tensile mechanical and shape memory properties in tension of the PUs were determined and discussed as a function of composition and crosslink densities deduced from swelling and dynamic mechanical analysis. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44145. 相似文献
996.
Biodegradable composites with improved barrier properties and transparency from the impregnation of PLA to bacterial cellulose membranes 下载免费PDF全文
Leire Urbina Itxaso Algar Clara García‐Astrain Nagore Gabilondo Alba González MaAngeles Corcuera Arantxa Eceiza Aloña Retegi 《应用聚合物科学杂志》2016,133(28)
Poly(lactic acid) (PLA) was impregnated in bacterial cellulose (BC) membranes. BC/PLA films were prepared by solvent casting and mechanical, optical and barrier properties, and biodegradation process were investigated. The transparency of processed films was higher than that of neat BC and increased with PLA content. Moreover, the incorporation of PLA to BC enhanced significantly the water vapor barrier properties of the BC membranes. The bionanocomposites contained a high percentage of cellulose due to the impregnation method that leads to the film with a BC content of 94%, which practically maintains the excellent mechanical properties of BC. However, when increasing the PLA content in the bionanocomposites the mechanical properties decreased slightly with respect to BC. Biodegradation under real soil conditions was determined indirectly through the study of the visual degradation and disintegration, demonstrating that the bionanocomposites were degraded faster than the neat PLA. The successful production of BC/PLA bionanocomposites suggested the possible application of them for active food packaging. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43669. 相似文献
997.
Helium permeability of polymer materials as liners for composite overwrapped pressure vessels 下载免费PDF全文
Brendan R. Murray Sean B. Leen Christopher O. A. Semprimoschnig Conchúr M. Ó Brádaigh 《应用聚合物科学杂志》2016,133(29)
Polymers have been identified as replacement materials for metallic liners in composite overwrapped pressure vessels (COPVs) for future space launchers. PEEK, Nylon, and PVDF plastics formed from base powder grades have been permeability tested to determine their susceptibility to the diffusion of helium through flatwise panel cross sections. Permeability, diffusion, and solubility coefficients have been obtained for each material with PVDF and PA11 grades showing the lowest permeability coefficients and hence the best barrier properties to permeation. Crystallinity percentages and internal air void contents in the polymer samples have also been used to assess the differences in permeability between materials with an analysis of void dispersion effects given through X‐ray CT scanning techniques. The measured permeability coefficients have been used to assess the ability of all materials tested to act as a functional polymer liner in a standard COPV with final leak rates predicted based on liner thicknesses and weights. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43675. 相似文献
998.
Roseli de Souza Santos da Costa Flavia da Silva Santos Daniela de Barros Mucci Tânia Vignuda de Souza Fátima Lucia de Carvalho Sardinha Célia Regina Moutinho de Miranda Chaves Maria das Graças Tavares do Carmo 《Lipids》2016,51(12):1363-1373
The purpose of this study was to investigate the trans fatty acids (TFA) content and distribution in colostrum, mature milk, and diet of adolescent mothers, after TFA declaration in food labels became mandatory in Brazil. Participants were healthy adolescents (n 54, 15–19 years, 1–90 days postpartum) practicing exclusive breastfeeding. Milk samples were collected 3 days after delivery (colostrum) and in the third month postpartum (mature milk) by hand expression. The fatty acid composition of the milk samples was determined by gas chromatography. TFA intake corresponded to 1.23 % of total energy value. Total 18:2 TFA accounted for less than 0.5 % of the energy intake. The amount of total 18:1 TFA (mean ± SEM) was 1.9 % ± 0.14 in colostrum and 1.5 % ± 0.2 in mature milk. The total content of n‐3 PUFA was inversely correlated with the total content of 18:1 TFA in colostrum. Both in colostrum and in mature milk, vaccenic acid (11t‐18:1) was found to be the most abundant 18:1 trans isomer, followed by elaidic acid (9t‐18:1), whereas rumenic acid (9c,11t‐18:2 CLA) was the predominant 18:2 trans isomer. In conclusion, the levels of TFA of industrial sources found in the mother's diet and breast milk (colostrum and mature milk) showed a decrease in relation to those observed in studies conducted prior to the TFA labeling resolution in Brazil. However, the current low intake levels of n‐3 LCPUFA and DHA content in the milk of lactating adolescents may be insufficient for supporting adequate neurological development of the infants. 相似文献
999.
Nanocomposites of PBAT and cellulose nanocrystals modified by in situ polymerization and melt extrusion 总被引:1,自引:0,他引:1 下载免费PDF全文
Carolina L. Morelli Mohamed N. Belgacem Márcia C. Branciforti Marie C. B. Salon Julien Bras Rosario E. S. Bretas 《Polymer Engineering and Science》2016,56(12):1339-1348
Cellulose nanocrystals (CNC) were successfully grafted with a low molecular weight poly(butylene glutarate) through an in situ polymerization procedure. The grafting treatment decreased the CNC hydrophilic character and increased the onset of their thermal degradation by approximately 20°C, thus increasing the possibilities of CNC application. Composites of grafted and nongrafted CNC with a poly(butylene‐adipate‐co‐terephthalate) (PBAT) matrix were prepared by melt extrusion. The CNC addition led to an increase of 50% of the tensile elastic modulus of the PBAT. In addition, dynamic mechanical thermal analysis showed that the composite with CNC retained its high modulus even at temperatures far above the glass transition temperature of PBAT. At 60°C the storage modulus of the composite with CNC was approximately 200% higher than that of the pure PBAT. Thus, in this work, nanocomposites of improved properties were obtained through a combination of in situ polymerization and melt extrusion. POLYM. ENG. SCI., 56:1339–1348, 2016. © 2016 Society of Plastics Engineers 相似文献
1000.
Functionalized galactoglucomannan‐based hydrogels for the removal of metal cations from aqueous solutions 下载免费PDF全文
Elizabeth Elgueta Julio Sánchez Daniel Dax Chunlin Xu Stefan Willför Bernabé L Rivas Marianela González 《应用聚合物科学杂志》2016,133(41)
New types of hydrogels derived from O‐acetyl galactoglucomannan (AcGGM) hemicellulose have been synthesized and characterized. The objective of this work was to analyze the sorption capacity (S) of three types of hydrogels containing AcGGM derivatives incorporated into the carboxylic groups of the polymer chain in the AA hydrogel, sulfonic groups in the APA hydrogel, and amide groups in the acrylamide (Aam) hydrogel. These hydrogels are capable of interacting and removing ions such as cadmium [Cd(II)], copper [Cu(II)], lead [Pb(II)], nickel [Ni(II)], and zinc [Zn(II)]. The results show that AA and Aam hydrogels had a lower sorption capacity of ions compared to the APA hydrogel, which had a high sorption capacity. The maximal sorption capacity was determined by the successive enrichment method, obtaining Pb(II) amount of 48.3 mg/g of AA hydrogel, 65.8 mg/g of APA hydrogel, and 40.8 mg/g of Aam hydrogel. Hence, Pb(II) ions are greatly retained by the three hydrogels. These results are promising for the development of new materials with potential applications in metal ion removal. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44093. 相似文献