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71.
Scanning calorimetric methods permit determination of heat capacities at high temperatures up to 1600°C. For disk systems
with power compensation application limits are in order of 700°C, and for cylindrical systems with electrical calibration
up to 1000°C. For the high temperature range above 1000°C DSC plates and a cylindrical calorimetric systems based on the CALVET
principle ('MULTI HTC’) are known. For cylindrical calorimetric systems the precision of the Cp data is between 2 and 5% even
at high temperatures without any requirements on the kind and shape of samples. These results are better than data provided
by DSC plate systems.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
72.
Moriya K. Yamada T. Sakai K. Yano S. Baluja S. Matsuo T. Pritz I. Vysochanskii Y. M. 《Journal of Thermal Analysis and Calorimetry》2002,70(2):321-328
Heat capacities of the Pb2xSn2(1-x)P2Se6 crystals (x=0, 0.098, 0.251, 0.402 and 1.0) were measured using an adiabatic calorimeter at temperatures between 10 and 350 K. In the
crystal of x=0, two heat capacity anomalies corresponding to the ferroelectric commensurate - intermediate incommensurate(C-IC) phase
transition temperature T
i, and the incommensurate - paraelectric (IC-N) phase transition temperature T
c, were observed at 193.24±0.10 and 220.07±0.15 K, respectively. The phase transition temperatures decreased with an increase
in Pb2+ concentration. The anomaly at Ti disappeared at x=0.251 in the mixed systems of the Pb2xSn2(1-x)P2Se6. In the crystal of Pb2P2Se6 (x=1.0), no phase transition was observed. The normal heat capacities for the mixed crystals were determined by least squares
fitting of the Debye and Einstein functions to the experimental data. The anomalous heat capacities gave the phase transition
entropies of 8.5 and 1.5 J mol-1 K-1 for x=0. The large transition entropies are consistent with an order-disorder mechanism in the ferroelectric-paraelectric phase
transitions in x=0.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
73.
Cyclical bifurcated hydrogen bonded structures are proposed for aqueous solutions of hydrofluoric acid and for the bifluoride ion which are consistent with the spectral data. The structure proposed for HF is also applicable to solutions in organic solvents. Raman spectra of tetramethylguanidinium perchlorate suggest that the corresponding Raman spectra of perchloric acid solutions may not be interpreted in terms of a completely dissociated acid. Other evidence including activity coefficient, heat capacity and partial molal volume data suggest that there is some association in relatively dilute perchloric acid solutions between the perchlorate ion and the hydrated proton. This association decreases in concentrated aqueous solutions. 相似文献
74.
Apparent molar heat capacities and volumes of amylamine (PentNH2) 0.02m, capronitrile (PentCN) 0.02m and nitropentane (PentNO2) 0.009m in decyltrimethylammonium bromide (DeTAB) micellar solutions, in water and in octane were measured at 25°C. By assuming that their concentration approaches the standard infinite dilution state, heat capacities and volumes were rationalized by means of previously reported equations following which the distribution constant between the aqueous and the micellar phase and heat capacity and volume of the additives in both phases are simultaneously derived. The present results are compared to those we have previously obtained for pentanol (PentOH). The thermodynamic properties of PentNH2 in water and in micellar phase are substantially identical to those of PentOH but different from those of PentCN and PentNO2 whereas the opposite behavior was observed in their pure liquid state and in octane. The nature of the solvent medium seems to affect the thermodynamic behavior of PentNH2. Also, the study of the apparent molar heat capacities of the amyl compounds investigated here in micellar solutions as a function of surfactant concentration shows evidence of a maximum at about 0.4m DeTAB, which can be attributed to a micellar structural transition. Accordingly, the solubilities of PentCN and PentNO2 as a function of the DeTAB concentration drop in the neighborhood of the concentration where heat capacities display the maximum. 相似文献
75.
Gérald Perron Jean-François Côté Daniel Lambert Johanne Pageau Jacques E. Desnoyers 《Journal of solution chemistry》1994,23(2):121-133
Blends of immiscible polymers are often stabilized by block copolymers which can form non-aqueous micelles and microemulsions in the liquid polymers. The phase diagrans, apparent volumes and apparent heat capacities of model non-aqueous binary and ternary systems were studied in order to investigate the conditions under which such self-assembly systems could form. 1,2-Hexanediol, which can cosolubilize hexane and ethyleneglycol, forms inverse micelles in hexane and weak microaggregates in ethyleneglycol. Genapol X-060, a commercial alcoholic surfactant containing on the average an aliphatic chain of 13 carbons and 6 oxyethylenes (C13E6), forms microaggregates in poly(ethyleneglycol) 400. These self-assembly systems are strengthen in the presence of a third component which has an affinity for the inner phase.Presented at the Symposium, 76th CSC Congress, Sherbrooke, Quebec, May 30–June 3, 1993, honoring Professor Donald Patterson on the occasion of his 65th birthday. 相似文献
76.
J.?MajumdarEmail author F.?Cser M.?C.?Jollands R.?A.?Shanks 《Journal of Thermal Analysis and Calorimetry》2004,78(3):849-863
Differential scanning calorimetry has been used to study the heat flow during melting and crystallisation of a range of polypropylene post-consumer waste (PP PCW) grades and blends. The heat flow curves and the heat capacity curves indicated that the PP PCW grades and blends contained contaminants even after manual sorting and a cleaning process. The enthalpies of the PP PCW grades were lower than that for the virgin grades, as a result of degradation. Small amounts of polymeric contaminants (up to 10%) did not affect the enthalpies of PP PCW although other contaminants may have had some effect. The enthalpies of the PCW blends could in general be predicted by a linear additive rule, which is of importance for recycling a variety of PP PCW products.The authors would like to thank Dr. M. Killen (Basell Australia Pty. Ltd.), Mr. P. Slaven (Citiwide MRF), Dasma Valley Waste Prop. Ltd. and Mr. I. Janetzki (Huhtamaki Australia Ltd.) for supplying materials for this project. Financial support for the project was provided by Basell Australia and Ecorecycle Victoria, Australia. 相似文献
77.
The heat of formation (H
f) of unsymmetrical ketone phenylhydrazones and their enehydrazine tautomers was calculated by the semi-empirical quantum-chemical AM1 method. It is concluded that from H
f values it is possible to judge the regioselectivity of indolization of unsymmetrical ketone phenylhydrazones.Translated fromIzvestiya Akademii Nauk, Seriya Khimicheskaya, No. 1, pp. 220–221, January, 1993. 相似文献
78.
Y. Marcus 《Journal of solution chemistry》1994,23(7):831-848
The water-structural contributions to the entropies and heat capacities of hydration of over 120 ions and the viscosity B-coefficients of nearly 80 aqueous ions are tabulated and correlated. B-coefficients for many more ions are predicted from this relationship and from their dependence on ionic size and charge. The structural entropies determine a unique scale of water structure making and breaking by the ions. 相似文献
79.
顺—反异构体的研究,在配合物化学中占有重要的地位。二水二草酸合铬酸钾这一配合物顺、反异构体的制备和异构化现象的研究已有报导,但多限于水溶液体系。也有关于该配合物热稳定性和热分解动力学研究的报导但对固相中该配合物异构体转变的研究尚未见报导。本文利用DTA方法,对二水二草酸合铬酸钾顺、反异构体的制备以及固相中异 相似文献
80.