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931.
D. Miholová P. Mader J. Száková A. Slámová Z. Svato 《Fresenius' Journal of Analytical Chemistry》1993,345(2-4):256-260
Summary The Trace Element Laboratory of the University of Agriculture in Prague (CSFR) participated successfully in interlaboratory experiments on the determination of the contents of trace elements in seven Czechoslovakian reference materials. Czechoslovakian certified reference material CRM 12-02-01 (Bovine liver) was used for the development of a new analytical method using the Dry Mineralizer Apion as well as in analytical quality assessment of data in the determination of Cd, Pb, and Hg contents in routinely analyzed animal tissues. 相似文献
932.
Pulverized coal plasma gasification 总被引:11,自引:0,他引:11
R. A. Kalinenko A. P. Kuznetsov A. A. Levitsky V. E. Messerle Yu. A. Mirokhin L. S. Polak Z. B. Sakipov A. B. Ustimenko 《Plasma Chemistry and Plasma Processing》1993,13(1):141-167
A number of experiments on the plasma-vapor gasification of brown coals of three types have been carried out using an experimental plant with an electric-arc reactor of the combined type. On the basis of the material and heat balances, process parameters have been obtained: the degree of carbon gasification (c), the level of sulfur conversion into the gas phase (s), the synthesis gas concentration (CO+Hz) in the gaseous products, and the specific power consumption for the gasification process. The degree of gasification was 90.5-95.0%, the concentration of the synthesis gas amounted to 84.7–85.7%, and the level of sulfur conversion into the gas phase was 94.3–96.7%. Numerical study of the process of plasma gasification of coals was carried out using a mathematical model of motion, heating, and gasification of polydisperse coal particles in an electric-arc reactor of the combined type with an internal heat source (arc). The initial conditions for a conjugate system of nonlinear differential equations of the gas dynamics and kinetics of a pulverized coal stream interacting with the electric arc and oxidizer (water vapor) agree with the initial conditions of the experiments. The computation results satisfactorily correlate with the experimental data. The mathematical model can be used for the determination of reagent residence time and geometrical dimensions of the plasma reactor for the gasification of coals.Nomenclature
c
i
volume concentration of components (kmol m–3)
-
x
longitudinal coordinate (m)
-
f
i
source members, determined by variation of the ith component due to chemical reactions in unit volume in unit time (kmol m–3s–1)
-
velocity (m s–1)
-
M
s
ash mass in one particle (kg)
-
C
D
particle drag coefficient
-
3.14
-
r
s
particle radius (m)
-
d
particle diameter (m)
-
density (kg m–3)
-
C
p
heat capacity of components (J molt– K–1)
-
Q
j
thermal effect of reaction (J kmol–1)
- Ej
activation energy of reaction
-
N
l
volume concentration of particles of thelth fraction (m–3)
-
T
temperature (K)
-
emissivity factor of coal particles
-
5.67 × 10–8, blackbody emissivity coefficient (W m–2 K–4)
-
P
pressure (Pa)
-
S
reactor cross section (m2)
-
D
reactor diameter (m)
-
V
reactor volume (m3)
-
L
R
reactor length (m)
-
F
W
friction force on the wall (N)
-
f
g
friction coefficient
-
residence time (s)
- Nu
Nusselt number
- Re
Reynolds number
- Pr
Prandtl number
-
thermal conductivity of gas (J m– s–1 K–1)
-
R
8.3 × 103, universal gas constant (J kmol K–1)
- µ
i
molecular mass of component (kg kmol–1)
-
dynamic viscosity coefficient of gas (kg m–1 s–1)
-
thermal efficiency of plasma reactor
- qarc
specific heat flow from arc (W m–3)
-
P
1
heat supplied in vapor at T = 405 K (W)
-
P
2
heat loss to wall (W)
-
P
3
heat loss in the gas and slag separator chamber (W)
-
P
4
heat loss in the synthesis gas oxidation chamber (W)
-
P
5
heat loss in the slag catcher (W)
-
P
6
heat carried away in the off-gas (W)
- P
heat input of arc (W)
-
P
arc
electric power of arc (W)
- Qsp
specific power consumption (kw Hr kg–1)
-
d
w
specific heat flow to wall (W m–2)
-
c
degree of carbon gasification (%)
-
s
level of sulfur conversion into gas phase (%) 相似文献
933.
In this paper, Co-60γ ray was used to irradiate the ointment cold cream at room temperature (25°C). We also used FTIR, GC and thin film chromatogram to analyse various irradiated samples. It was found that the ointment cold cream can be irradiated at dose of 5–35 kGy and at dose rate from 0.2 to 0.6 kGy/h at room temperature (25°C) without evident decomposition. At dose of 5–15 kGy, the number of bacteria can be reduced to hygienic standard value. The radiation sterilization is a safe method for killing the bacteria in the ointment cold cream. 相似文献
934.
H. K. Barrenscheen Margarete Frey F. Feigl L. T. Fairhall M. Settimj D. Ganassini A. Necke H. Müller Ch. Badham H. B. Taylor G. Moillère F. Weyrauch St. Litzner F. Grendel N. Schoorl H. Begemann A. Berat G. Widmark B. Vahlquist E. M. P. Widmar S. L. Oerskov J. P. Gregersen P. Iversen H. W. Mook D. D. van Sluke W. M. Kirjan W. C. Stadie E. C. Ross K. Lang H. Waelsch Gertrud Klepetar I. St. Lorant L. Kopetz J. W. Heim W. W. Práwdicz-Neminski Z. Babitsch J. F. Reith Th. von Fellenberg R. G. Turner Mina Z. Weeks A. Castille V. Henri 《Analytical and bioanalytical chemistry》1934,98(3-4):147-160
935.
Samples of poly(12-dodecanelactam) (polylaurolactam, nylon 12) with n 1 × 103?33 × 103 were prepared. Polymerizations initiated with water or with lauric acid proceeded under conditions for minimum changes in end-group concentration. Values of n were calculated from the end-group content and n from light scattering in the mixture m-cresol/60 vol% of 2.2,3,3-tetrafluoropropanol. From measurements of intrinsic viscosity in m-cresol, the relationship [n] ? n was established in the given range of n. The relationship [n] ? w for w from 3.3 × 103 to 125 × 103 has been established. 相似文献
936.
The scope and limitations of the 7-hydroxy-2-ethylbenzisoxazolium salt method of forming amide bonds are outlined through the synthesis of a variety of simple peptide derivatives containing all of the common amino acids with the exceptions of arginine and histidine. The 3-acyloxy-2-hydroxy-N-ethylbenzamides derived from C-terminal serine or threonine containing peptides are found to react with amines at anomalously slow rates and with the formation of transesterified byproducts; a mechanistic explanation is offered. The utility of the method for the synthesis of medium sized peptides is examined by synthesis of oligomers of Gly-L-Leu-Gly. 相似文献
937.
From Melampyrum silvaticum L. (Scrophulariaceae) the new Iridoid melampyrosid (2) was isolated beside aucubin (1). The structure of 2 is determined by spectral data and chemical reactions. 相似文献
938.
S. A. Andronati A. V. Bogat-skii G. N. Gordiichuk Z. I. Zhilina L. M. Yagupol'skii 《Chemistry of Heterocyclic Compounds》1975,11(2):230-233
5-Difluoromethylsulfonyl-2-aminobenzophenone was synthesized by condensation of p-difluoromethylsulfonylaniline with benzoyl chloride. 5-Difluoromethoxy- and 5-difluoromethylthio-2-aminobenzophenones were obtained by condensation of phenylacetonitrile with the appropriate p-substituted nitrobenzenes and subsequent reduction of the resulting anthranils. 7-Difluoromethoxy-, 7-difluoromethylthio-, and 7-difluoromethylsulfonyl-5-phenyl-1,2-dihydro-3H-1,4-benzodiazepin-2-ones were obtained by the successive action of bromoacetyl bromide and ammonia on the 2-aminobenzophenone derivatives or by reaction of 2-aminobenzophenones with aminoacetyl chloride hydrochloride. The structure of the 1,4-benzodiazepines was confirmed by a study of the UV, IR, PMR, and mass spectra. 相似文献
939.
940.
B. A. Arbuzov O. A. Erastov A. B. Remizov L. Z. Nikonova 《Chemistry of Heterocyclic Compounds》1972,5(6):730-736
The tautomerism of N-butyl-2-methoxycarbonyl-4-methylpyrrolid-3-one (I), N-butyl-4-methoxycarbonylpyrrolid-3-one (II), N-butyl-4-methoxycarbonyl-2-methylpyrrolid-3-one (III), N-butyl-4-methoxycarbonylpyrrolid-3-one hydrochloride (IV), and N-butyl-4-methoxy-carbonyl-2-methylpyrrolid-3-one hydrochloride (V) has been studied by UV and IR spectroscopy. It has been found that the esters I–V are highly ionized in aqueous and ethanolic solutions at concentrations of 10–2–10–3 M. On passing from methyl cyclopentran-1-one-2-carboxylate to the esters II and III the position of the equilibrium in heptane and CCl4 shifts in the direction of the keto form. On passing from the esters II and III to the esters IV and V, the position of the equilibrium shifts in the direction of the enol. Meyer's relationship is not satisfied for the esters II and III, while it is satisfied for the esters IV and V. Hypotheses have been put forward on the causes of the phenomena mentioned. 相似文献