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121.
E. C. da Silva Filho Oberto G. da Silva Maria G. da Fonseca Luiza N. H. Arakaki C. Airoldi 《Journal of Thermal Analysis and Calorimetry》2007,87(3):775-778
A series of compounds with
composition of Ca1–xCuxHPO4,
where x varied from 0.05 to 0.5 were synthesized
by precipitation method. The compounds were characterized by elemental analysis,
X-ray diffraction, infrared spectroscopy, scanning electron microscopy, and
thermogravimetry. The chemical stabilities of solids were investigated at
several pH. Elemental analysis of copper, calcium and phosphorus are in agreement
with the proposed composition. The formation of lamellar phosphates was evidenced.
The stability of the set of compounds was better for samples with high copper
content. 相似文献
122.
The dependence of the frequency factor on the temperature (A=A
0
T
m) has been examined and the errors involved in the activation energy calculated from some integral methods without considering
such dependence have been estimated. Investigated integral methods are the Coats-Redfern method, the Gorbachev-Lee-Beck method,
the Wanjun-Yuwen method and the Junmeng-Fusheng method. The results have shown that the error in the determination of the
activation energy calculated ignoring the dependence of the frequency factor on the temperature can be rather large and it
is dependent on x=E/RT and the exponent m. 相似文献
123.
The mathematical evaluation of the activation
energy, E, of non-isothermal degradation
reactions is usually made using the Ozawa/Flynn–Wall isoconversion principle
and involves the numerical resolution of a set of integrals without closed
form solution, which are solved by polynomial approximation or by numeric
integration. In the present work, the isoconversion principle, originally
described and maintained until now as an algebraic problem, was written as
a set of ordinary differential equations (ODEs). The individual ODEs obtained
are integrated by numeric methods and are used to estimate the activation
energy of simulated examples. A least square error (LSE) objective function
using the introduced ODEs was written to deal with multiple heating rate CaCO3
thermal decomposition TG experiments. 相似文献
124.
The thermal decomposition of cobalt acetate tetrahydrate (Co(CH3COO)2 · 4H2O) has been studied via thermogravimetric (TG) analysis, in situ X-ray powder diffraction (XRD), and Fourier transform infrared spectroscopy (FTIR). The results of TG and XRD showed that
the parent salt melted and then the dissolved crystalline water was vaporized in two steps. The dehydration process was followed
by a major step concerning the decomposition of the acetate group, leading to basic acetate as an intermediate, which then
produced CoO and Co in N2 and H2 atmosphere, respectively. Three decomposition intermediates Co(CH3COO)2 · 0.5H2O, Co(CH3COO)2, and Co(OH)(CH3COO) were presumed. In situ XRD experiments revealed that the intermediate basic acetate was poorly crystallized or even amorphous. Evolved gases analysis
indicated that the volatile products of acetate decomposition were water vapor, acetic acid, ethylenone, acetone, and CO2. A detailed thermal decomposition mechanism of Co(CH3COO)2 · 4H2O was discussed. 相似文献
125.
Summary The thermal behavior of KH2PO4, NaH2PO4 and Na2HPO4 under non-isothermal conditions using TG method with different heating rates was studied. The values of the reaction rate were processed by means of Friedmans differential-isoconversional method. A dependence of the activation energy vs. conversion was observed. Therefore a procedure based on the compensation effect (suggested by Budrugeac and Segal) was applied. A less speculative data processing protocol was offered by the non-parametric kinetics method suggested by Serra, Nomen and Sempere. Three steps were observed by non-isothermal heating: a dehydration, a dimerization and a polycondensation. The differences in the intimate reaction mechanism are determined by the initial number of water molecules. 相似文献
126.
Summary Kinetics of dehydration of equilibrium swollen poly(acrylic acid) hydrogel was investigated using methods of non-isothermal
thermal analysis. Methods of Kissinger, Coats-Redfern, Van Krevelen and Horowitz-Metzger were applied for determination the
kinetics parameters: activation energy (E), pre-exponent (lnA) as well as the kinetics model ƒ(69) for the process of hydrogel dehydration under different heating rates. An existence
of good agreement between determined values of kinetic parameters (Eand A), which were obtained applying different methods under the same heating rate. Functional relationship between changes of
kinetic parameters of dehydration and changes of heating rate was established. An existence of compensation effect is accepted
and explanation of compensation effect appearance during the hydrogel dehydration is suggested. 相似文献
127.
V. A. Drebushchak L. N. Mylnikova T. N. Drebushchak V. V. Boldyrev 《Journal of Thermal Analysis and Calorimetry》2005,82(3):617-626
Summary Ancient ceramic samples (single fragments and different parts of pots, unbroken and repaired; total about 180 samples) dated
from the transitional period of late Bronze to early Iron Age (VIII-VI centuries BC) and early Iron Age (VII-IV centuries
BC) were investigated by thermal analysis, X-ray powder diffraction, petrography, and scanning electron microscopy equipped
with the energy-dispersive X-ray analyzer. In addition to that, to identify the clay sources for the ceramic manufacturing,
about 15 samples of clays and soils found near archeological digs and taken from the mineralogical museum were investigated.
We found out that the calcite content of ceramics is a very informative parameter for the identification of the clay source
for the pottery manufactured at low technological level (low-temperature firing). 相似文献
128.
129.
B. Zhou S. Jiang L. Zou X. Wang D. Wang J. Liu S. Shang D. Zhou 《Journal of Thermal Analysis and Calorimetry》1999,58(2):487-493
A new compound cyclohexyl-t-butyldimethylammonium tetraphenylborate, [C6H11N(CH3)2(C(CH3)3)]BPh4 has been prepared, and its decomposition mechanism was studied by TG. The IR spectra of the products of thermal decomposition were examined at every stage. Kinetic analysis for the first stage of thermal decomposition process was obtained by TG and DTG curves, and kinetic parameters were obtained from the analysis of the TG-DTG curves with integral and differential equations. The most probable kinetic function was suggested by comparison of kinetic parameters.This revised version was published online in November 2005 with corrections to the Cover Date. 相似文献
130.
El Watik L. Claire Y. Zineddine H. Rossi C. Kaloustian J. Sergent M. Périchaud A. 《Journal of Thermal Analysis and Calorimetry》1999,58(1):19-28
The study of the thermal degradation of the fireproof polystyrene—butadiene copolymer by an intumescent system: ammonium polyphosphate (APP)—pentaerythritol (PER)—talc (TAL), was done through an experimental process. Thermogravimetry under air sweeping was used. We observed for the degradation rate of the mixture with fireproofing agents, in the field of 20 to 50% mass loss, a better linear increasing when this mixture contains more TAL and the ratio APP/PER is smaller.
This revised version was published online in November 2005 with corrections to the Cover Date. 相似文献