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981.
982.
Dana G. Miloaga Hazel‐Ann A. Hosein Manjusri Misra Lawrence T. Drzal 《应用聚合物科学杂志》2007,106(4):2548-2558
Poly(3‐hydroxybutyrate) (PHB) has been shown to be efficiently nucleated by exfoliated graphite nanoplatelets (xGnP). The nucleating effect of xGnP was investigated using differential scanning calorimetry, optical microscopy and atomic force microscopy. Nonisothermal crystallization of PHB from the melt required lower activation energies for PHB containing 1 wt % and 3 wt % xGnP (?214 and ?102 kJ/mol respectively) than for pure PHB (?60 kJ/mol). A kinetic study of the PHB/xGnP crystallization employing a modified form of the Avrami equation revealed that the presence of xGnP increased the PHB crystallization temperature, as well as the crystallization rates, and generated smaller and more numerous spherulites. Optical microscopy and atomic force microscopy confirmed the incorporation of xGnP into the lamellar structure of the PHB spherulites and provided insight into the influence of xGnP on spherulite size and lamellae thickness. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007 相似文献
983.
The thermal degradation of poly(vinyl butyral) (PVB)/glass ceramic, PVB/Ag, and PVB/glass ceramic/Ag composites was investigated with thermogravimetric analysis in nitrogen and air. Thermogravimetric data revealed that the compositions of both inorganic materials in air could greatly influence the thermal degradation of PVB. The degradation reactions of PVB/ceramic and PVB/Ag composites began earlier and accelerated rapidly at lower temperatures. The overall degradation period was obviously shortened for the thermal degradation of PVB/Ag in air, whereas a longer time was required for the PVB/ceramic composite than for PVB. Moreover, dual effects of ceramic and Ag on the thermal degradation of PVB were observed for PVB/ceramic/Ag composites. In addition, the catalytic effects of ceramic and Ag on the degradation reaction of PVB in air were verified with a kinetic analysis. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 93: 2142–2149, 2004 相似文献
984.
985.
To impart easy‐care properties to cellulose‐containing fabrics along with avoiding any harmful effects of formaldehyde on both the health and the environment, attempts have been made to use citric acid (CA) as an ester crosslinking agent along with different catalytic systems in the absence and presence of certain additives. Further, fixation conditions, type of crosslinking agent, as well as type of substrate have been studied. Results revealed that the enhancement in carboxyl content, performance properties, and the decrease in tear strength (TS) as well as in whiteness indices (WI) of the finished fabric samples were increased by increasing CA concentration up to 80 g/L and by raising thermofixation temperature from 140 up to 180°C for 90 s. Inclusion of triethanolamine hydrochloride (TEA. HCl), decreased the carboxyl content, TS, color strength K/S, as well as oily stain release rating (SRR) of the finished fabric samples along with an increase in bound nitrogen (%N), wrinkle recovery angle WRA, and an improvement in WI without affecting the durable press rating (DP). Within the range examined (0–30 g/L), increasing PEG‐600 concentration improved the wet resiliency, TS, as well as WI properties of the finished samples. Increasing DMDHEU ratio in the CA/DMDHEU crosslinking system gave rise to an increase in %N, WRA (dry and wet), DP, as well as in free CH2O of finished fabrics, along with a slight improvement in WI values. On the other hand, the TS, carboxyl content, K/S, SRR values of the finished fabric samples were lower at a higher DMDHEU ratio. Increase in carboxyl content, %N, WRA (dry and wet), DP and SRR, as well as extent of post dyeing (K/S) of the treated fabric samples upon using different ester crosslinking agents followed the descending order: citric acid > pyromellitic dianhydride. The opposite holds true for the TS, and WI values. Among the esterifying catalysts used, and for a given set of finishing conditions, NaH2PO2 · H2O proved to be the most effective one, and the following order of effectiveness may be drawn: NaH2PO2 · H2O > K2HPO4 > Na3–citrate > Na2–tartrate. Inclusion of silicone softener in the finishing formulation brought about an improvement in softeness degree, WRA, %N, DP, TS as well as K/S values along with a decrease in carboxyl content, SRR, and WI values of the treated fabric samples, regardless of the used silicone softener.The performance properties of the finished fabric samples were determined by the type and nature of the substrate. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 2243–2253, 2002 相似文献
986.
A series of phosphorus‐containing, wholly aromatic thermotropic copolyesters from acetylated 2‐(6‐oxide‐6H‐dibenz〈c,e〉〈1,2〉oxa phosphorin‐6‐yl)‐1,4‐dihydroxy phenylene, p‐acetoxybenzoic acid, terephthalic acid, and isophthalic acid were prepared by melting polycondensation. The structure and basic properties of the polymers, such as the glass‐transition temperature (Tg), melting temperature (Tm), thermal stability, crystallinity, and liquid crystallinity, were investigated with Fourier transform infrared, elemental analysis, differential scanning calorimetry (DSC), thermogravimetric analysis, wide‐angle X‐ray diffraction, and hot‐stage polarizing optical microscopy. The copolyesters had relatively high Tg values ranging from 183 to 192°C. The Tm values obtained from DSC curves for samples P‐20 and P‐25 were 290 and 287°C, respectively (where the number in the sample name indicates the molar fraction of the phosphorus‐containing monomer in the reactants). The initial flow temperatures of other samples observed with hot‐stage polarizing microscopy were 271–290°C. The 5% degradation temperatures in nitrogen ranged from 431 to 462°C, and the char yields at 640°C were 41–52%. All the copolyesters, except P‐40, were thermotropic and nematic. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 1278–1284, 2002 相似文献
987.
A novel aromatic amine organo‐modifier synthesized in our previous work was used to treat montmorillonite (MMT) and the organo‐modified MMT was used to prepare poly(etherimide) (PEI)/MMT nanocomposites by a melt intercalation method. MMT treated by this amine exhibited large layer‐to‐layer spacing and a high ion‐exchange ratio (>95%). The nanocomposites were characterized with X‐ray diffraction (XRD), transmission electron microscopy (TEM), dynamic mechanical analysis, a universal tester, thermogravimetric analysis, and by differential scanning calorimetry. The results of XRD and TEM showed that the nanocomposites formed exfoliated structures even when the MMT content was 10 wt %. When the MMT content was below 3 wt %, the PEI/MMT nanocomposites were strengthened and toughened at the same time. The nanocomposites also showed marked decreases in coefficient of thermal expansion and solvent uptake. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 1857–1863, 2003 相似文献
988.
Corn starch was crosslinked with sodium trimetaphosphate (STMP) in solid state under microwave irradiation to improve the degree of substitution (DS) and decrease the reaction time. The effects of modification factors on the crosslinking of starch were systematically studied. It was found that the microwave irradiation provided a convenient and efficient method to prepare crosslinked starch with sufficient DS. The DS value of crosslinked starches obtained by microwave irradiation was significantly improved and the reaction time was also dramatically decreased to achieve an appropriate DS value by microwave irradiation, when compared with using traditional method. The high microwave power provided faster reaction kinetics to obtain the desired DS value at an identical reaction condition. If the reaction temperature is lower than the decomposition temperature of crosslinked starch, the higher DS value can be achieved at the higher microwave power. It was detected that the DS data obtained by reacting intermittently was higher than those by reacting continuously. It was also noticed that DS data varied drastically with the increasing of the amount of STMP and sodium carbonate. The swelling ratio of crosslinked starch in water was lower than that of native starch because of the nongelatinization of highly crosslinked starch. SEM analysis indicated that the crosslinking of corn starch by microwave irradiation caused no significant changes in the microstructure of starch granules. Light microscope analysis also showed the uniformity of so‐prepared crosslinked corn starch applying microwave irradiation. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 5854–5860, 2006 相似文献
989.
990.
Yudong Wang Minying Liu Zhimin Wang Xiaoguang Li Qingxiang Zhao Peng‐Fei Fu 《应用聚合物科学杂志》2007,104(3):1415-1422
The crystallization process of a new polyamide, nylon 1313, from the melt has been thoroughly investigated under isothermal and nonisothermal conditions. During isothermal crystallization, relative crystallinity develops in accordance with the Avrami equation with the exponent n ≈ 2 based on DSC analysis. Under nonisothermal conditions, several different analysis methods were used to elucidate the crystallization process. The Avrami exponent n is greater in the isothermal crystallization process, indicating that the mode of nucleation and the growth of the nonisothermal crystallization for nylon 1313 are more complicated, and that the nucleation mode might include both homogeneous and heterogeneous nucleation simultaneously. The calculated activation energy is 214.25 kJ/mol for isothermal crystallization by Arrhenius form and 135.1 kJ/mol for nonisothermal crystallization by Kissinger method, respectively. In addition, the crystallization ability of nylon 1313 was assessed by using the kinetic crystallizability parameters G. Based on this parameter, the crystallizability of many different polymers was compared theoretically. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 1415–1422, 2007 相似文献