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71.
Fumiaki Kobayashi Toru Ogawa Mitsuo Akabori Yoshio Kato 《Journal of the American Ceramic Society》1995,78(8):2279-2281
Uranium-plutonium nitride is a candidate fuel for fast reactors, but its major drawback is 14 C formation from natural nitrogen. One would probably have to use highly 15 N-enriched nitrogen. A pyrochemical process with molten-salt electroreflning has been proposed as a means to increase the nuclear proliferation resistance of the fuel cycle. Molten-salt electroreflning could also be applied to nitride fuels to make possible the recycling of 15 N. The anodic dissolution behavior of UN in LiCI-KCI melt was studied to provide the basis for a feasibility study of electroreflning of irradiated nitride fuels. 相似文献
72.
Influence of tetrabutyl-, tetrapentyl- and tetraisopentylammonium ions on the reduction of nickel(II) in thiocyanate solutions at the dropping mercury electrode has been investigated. These tetraalkylammonium ions, at their low concentrations, inhibit the reduction of nickel(II). However, at their high concentrations, the strong inhibiting effect disappers with the formation of a new wave corresponding to the reduction of a negatively charged nickel(II) thiocyanate complex, which is stabilized by the formation of ion pair with tetraalkylammonium cation. The variation of the reduction current with tetraalkalylammonium concentration was explained by taking into consideration both the change of the total charge of nickel(II) thocyanate complex involved in the reduction process and the simultaneous adsorption of tetraalkylammonium and thiocyanate ions on the mercury electrode. 相似文献
73.
Koichiro Kato 《应用聚合物科学杂志》1975,19(6):1593-1599
Polypropylene films were treated with chromic acid mixture. The change in the treated films was investigated by comparing change in amount of 2,4-dinitrophenylhydrazones formed in the treated films with their change in wettability with water. Oxidation of the film surface zone, partial breakdown of polymer in the film surface zone, and oxidation of surface zone bared from the film inner zone seemed to occur with increase in treatment time or with increase in treatment temperature. 相似文献
74.
Yoshiyuki Sugahara Ken-Ichi Sugimoto Kazuyuki Kuroda Chuzo Kato 《Journal of the American Ceramic Society》1988,71(7):325-C
Both silicon carbide and aluminum silicon carbide have simultaneously been obtained directly from naturally occurring aluminosilicate by carbothermal reduction for the first time. A precursor of a montmorillonite–polyacrylonitrile (PAN) intercalation compound was heated at 1700°C in Ar. For comparison, montmorillonite–carbon mixtures were similarly heated. α-SiC, β-SiC, and Al4 Si2 C5 formed from the montmorillonite–PAN intercalation compound. Mainly α-Al4 SiC4 was obtained with ternary carbides from the montmorillonite–carbon mixtures in addition to a large amount of β-SiC. Hence, aluminum silicon carbide formation was affected by the mixing condition of the starting materials. 相似文献
75.
Uphill transport of ammonium ions through a membrane with sulfonic acid groups were investigated with pH-controllers which keep the solution at a constant pH. A membrane with sulfonic acid groups was prepared by casting an aqueous solution containing poly(styrenesulfonic acid) and poly(vinyl alcohol) on a glass plate. When a membrane with one side alkaline and the other acidic was fixed as a diaphragm in a cell, ammonium ions were transported from the alkaline side to the acidic side through the membrane against the concentration gradient of the adjacent solutions. Uphill transport of ammonium ions with pH-controllers was more efficient than without, thus keeping the pH difference between both sides of the membrane constant, which is a driving force for the uphill transport. Furthermore, the effect of pH of the acidic side on the uphill transport was investigated and the mechanism of the pH-controlled uphill transport is discussed. 相似文献
76.
Ichiro Kudo Toshiyuki Kato Hidetoshi Hayashi Ryohei Yanoshita Koichi Ikizawa Hiroko Uda Keizo Inoue 《Lipids》1991,26(12):1065-1070
We have previously reported that platelet-activating factor (PAF) induces proliferation and microbicidal activity of guinea
pig bone marrow cells. In the present study, we have found that the conditioned medium of PAF- or nonmetabolizable PAF agonist-treated
guinea pig bone marrow cells augmented DNA synthesis and induced microbicial activity of bone marrow cells. A PAF specific
antagonist, CV-6209, inhibited generation of the active conditioned medium by PAF. Addition of the PAF antagonist only partially
suppressed the augmentative effect of the active conditioned medium on DNA synthesis; this is consistent with the fact that,
because of the rapid breakdown, no appreciable amount of PAF remained in the conditioned medium of PAF-treated cells. Although
mouse bone marrow cells did not respond to PAF unlike guinea pig cells, their DNA synthesis was significantly enhanced by
the conditioned medium of PAF-treated guinea pig bone marrow cells. Thus, some newly generated factor(s) distinct from the
originally inoculated PAF seemed to modulate the bioactions of PAF on bone marrow cells. An appreciable amount of PAF was
produced by calcium ionophore-treated guinea pig bone marrow cells. These findings indicate that PAF synthesized in guinea
pig bone marrow cells induces generation in the cells of some factor(s) which affects proliferation or microbicidal activity.
Presented at The Third International Conference on Platelet-Activating Factor and Structurally Related Ether Lipids, Tokyo,
Japan, May 1989. 相似文献
77.
The agronomic effectiveness of two natural phosphate rocks (PRs) from North Carolina (USA) and Togo and their 50% partially acidulated products (PAPRs) was evaluated in two greenhouse experiments using32P isotopic dilution techniques, namely L and AL values.In the first experiment rye grass was grown in a soil from Ghana. While the proportion of P in the plant derived from the P fertilizer (Pdff) ranged on. the average from about 10% for the PRs up to 80% for the PAPRs, the P fertilizer recovery was less than 1% for a 60-day growth period. In the second experiment, average values of P in the maize plants derived from the PAPRs ranged from 35% to 75% in 3 different soils. Both PRs were ineffective with the exception of North Carolina PR in the Seibersdorf soil. The P fertilizer recovery was 0.25% for the North Carolina PR in this soil whereas the recovery values ranged from 1.2% to 1.6% for the PAPRs.Mean values of the relative fertilizer efficiency estimated from the L values of each soil were less than 1% for the PRs whereas the values for the PAPRs which were dependent on soil type ranged from 20% up to 45%. The coefficient of relative effect of partial acidulation, that was calculated from the ratio of AL values for PR and PAPR in each soil indicated that partial acidulation increased the effectiveness of the natural PRs in all soils under study.This study showed that the use of32P isotope dilution techniques allows an accurate measurement of the P availability from natural and modified PR products to crops. Another advantage is that quantitative comparison of the P sources under study, PRs and PAPRs in this case, can be made even in soils where there is no response to the applied P sources. 相似文献
78.
H. Kominami J. Kato Y. Takada Y. Doushi B. Ohtani S. Nishimoto M. Inoue T. Inui Y. Kera 《Catalysis Letters》1997,46(3-4):235-240
Thermal decomposition of titanium(IV) tetra-tert-butoxide (TTB) in inert organic solvents at 573 K yielded microcrystalline
anatase (titanium(IV) oxide, TiO2) powders with a crystallite size of ca. 9 nm and a surface area of <100 m2 g-1. Primary and secondary alkoxides of titanium(IV), however, were not decomposed under similar conditions, indicating that
the thermal stability of C-O bonds in the alkoxides was a decisive factor for their decomposition. The TiO2 prepared from TTB by this manner was thermally stable upon calcination in air and retained high surface area of ca. 100 m2 g-1 even after calcination at 823 K. The as-prepared TiO2 powders, without calcination, exhibited much higher rate of carbon dioxide formation than any other active photocatalysts
such as Degussa P-25 and Ishihara ST-01 in the photocatalytic mineralization of acetic acid in aerated aqueous solutions.
The higher activity of the present TiO2 photocatalysts is attributed to both high crystallinity and large surface of the present product. The calcination of the
as-prepared TiO2 in air reduced the photocatalytic activity, but it was still higher than the other commercially available TiO2's.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
79.
α-Tocopherol was reacted with methyl linoleateperoxyl radicals at 37°C. The peroxyl radicals were generated by the reaction
of methyl linoleate with a free radical initiator, 2,2′-azobis(2,4-dimethylvaleronitrile). The primary products of α-tocopherol with methyl linoleate-peroxyl radicals were isolated by
reversephase and normal-phase high performance liquid chromatography (HPLC), and their structures were characterized by ultraviolet
(UV), infrared (IR),1H and13C nuclear magnetic resonance (NMR) and mass spectrometry (MS). There were four stereoisomers of methyl 13-(8a-peroxy-α-tocopherone)-9(Z),11(E)-octadecadienoate and four stereoisomers of methyl9-(8a-peroxy-α-tocopherone)-10(E),12(Z)-octadecadienoate. 相似文献
80.
Mean gas holdup, lateral distribution of gas holdup and axial mixing of gas and liquid were measured in bubble columns of 12 and 19cm i.d. The lateral distribution of gas holdup was strongly dependent on the flow regimes in the column. The axial mixing of liquid in the homogeneous bubble flow regime was much smaller than that in the heterogeneous bubble flow regime, and was not expressed by existing correlations. The axial mixing of liquid in the homogeneous bubble flow and the intermediate flow regime was simulated with a flow model based on the lateral distribution of buoyancy force and the effective viscosity. The axial mixing of gas was larger than that of liquid. 相似文献