全文获取类型
收费全文 | 1524篇 |
免费 | 49篇 |
学科分类
工业技术 | 1573篇 |
出版年
2023年 | 8篇 |
2022年 | 10篇 |
2021年 | 27篇 |
2020年 | 14篇 |
2019年 | 14篇 |
2018年 | 24篇 |
2017年 | 18篇 |
2016年 | 48篇 |
2015年 | 21篇 |
2014年 | 38篇 |
2013年 | 103篇 |
2012年 | 85篇 |
2011年 | 89篇 |
2010年 | 85篇 |
2009年 | 79篇 |
2008年 | 80篇 |
2007年 | 76篇 |
2006年 | 68篇 |
2005年 | 58篇 |
2004年 | 45篇 |
2003年 | 45篇 |
2002年 | 46篇 |
2001年 | 32篇 |
2000年 | 21篇 |
1999年 | 23篇 |
1998年 | 54篇 |
1997年 | 38篇 |
1996年 | 31篇 |
1995年 | 27篇 |
1994年 | 22篇 |
1993年 | 23篇 |
1992年 | 14篇 |
1991年 | 16篇 |
1990年 | 17篇 |
1989年 | 16篇 |
1988年 | 7篇 |
1987年 | 19篇 |
1986年 | 14篇 |
1985年 | 12篇 |
1984年 | 16篇 |
1983年 | 15篇 |
1982年 | 16篇 |
1981年 | 14篇 |
1980年 | 8篇 |
1979年 | 11篇 |
1978年 | 8篇 |
1977年 | 4篇 |
1976年 | 7篇 |
1975年 | 2篇 |
1971年 | 2篇 |
排序方式: 共有1573条查询结果,搜索用时 15 毫秒
21.
Masayuki Nogami Yoshihiro Abe Ayako Kato 《Journal of the American Ceramic Society》1995,78(4):1066-1070
Silica glasses doped with small-sized CdSx -Se1-x crystals were prepared by the sol-gel method. Gels synthesized by the hydrolysis of Si(OC2 H5 )4 , in the presence of CdSeO4 with NH4 SCN dissolved in HNO3 or NH4 OH, were heated in H2 -N2 atmosphere. The pH value of solutions for CdSeO4 and NH4 SCN primarily determined the fraction of anions in CdSx Se1-x crystals. The anion content in crystals was dependent on the pH value of the solvent and/or heat-treatment temperature, and the sulfur fraction changed from 0.1 to 0.6. The optical absorption spectra were red-shifted as the selenium content and the crystal size increased, and the emission spectra showed a sharp band near the absorption edge position and a broad tail extending into the long wavelength. The optical band gap energies increased reciprocally proportional to the square of the crystal size. 相似文献
22.
Yoshihiro Kubota Yusuke Nishizaki Hisanori Ikeya Masami Saeki Tetsunari Hida Sachiko Kawazu Michitaka Yoshida Hidekazu Fujii Yoshihiro Sugi 《Microporous and mesoporous materials》2004,70(1-3):135-149
Two types of organic–inorganic hybrid base catalysts are prepared. Organic-functionalized molecular sieves (OFMSs), particularly “amine-immobilized porous silicates”, are designed based on common idea to immobilize catalytic active sites on silicate surface. Silicate–organic composite materials (SOCMs), such as “ordered porous silicate–quaternary ammonium composite materials”, are the precursors of ordered porous silicates obtained during the synthesis. Both the OFMS and the SOCM are used as the catalysts for Knoevenagel condensation. Among the OFMSs, there is clear tendency that the use of molecular sieve with larger pore volume and/or surface area gives the product in higher yield. Aminopropylsilyl (AP)-functionalized mesoporous silicates such as AP-MCM-41 gives the product in high yield under mild conditions. No loss of activity is observed after repeated use for three times. The SOCMs are also active for the same reaction. The precursors of the mesoporous silicates are more active than those of microporous silicates. This material can be repeatedly used without significant loss of activity. High activity is not due to the leached species. The active sites of the SOCM catalysts are considered to be SiO− moieties located on the pore-mouth. Activity of the SOCM increases when the reaction is carried out without solvent, whereas decrease in activity of the OFMS is observed in the solvent-free system. 相似文献
23.
Rajib Bandyopadhyay Mahuya Bandyopadhyay Yoshihiro Kubota Yoshihiro Sugi 《Journal of Porous Materials》2002,9(2):83-95
AlPO4-5 and AlPO4-11 were synthesized by dry-gel conversion (DGC) method. Steam-assisted conversion (SAC) and vapor-phase transport (VPT) techniques were applied for this purpose. The synthesis was successful in presence of a certain minimum amount of external bulk water, without which the crystallization failed. Crystallization by VPT method was slower than corresponding SAC and HTS method. SAPO analogs of the samples, SAPO-5 and SAPO-11 were also synthesized by DGC method. Samples made by DGC methods had higher yield than the conventional hydrothermal synthesis (HTS); otherwise the samples showed similar characteristics as that made by HTS. XRD, SEM and N2-adsorption results showed high crystallinity and purity of the samples made by DGC, and 27Al MAS NMR spectra indicated the tetrahedral framework nature of Al. SAPO-5 and SAPO-11 were tested for their catalytic activity in isopropylation of biphenyl, and in terms of conversion and selectivity, SAPO-5 was found to be suitable for this application. 相似文献
24.
ihiro Kasuga † ‡ Tatsuya Inoue† Kenji Tsuji† Yoshio Ota† § Yoshihiro Abe † 《Journal of the American Ceramic Society》1995,78(1):245-247
High-strength calcium metaphosphate fibers for biomedical applications are extracted from crystallized products of calcium ultraphosphate glasses by aqueous leaching. In the present work, new types of porous ceramics with a skeleton composed of the crystalline fibers are prepared by heating the fibrous products extracted. The fibers in the ceramic are interlinked to each other by glassy phases formed during the heating. This porous material has a large porosity of >60%. The surface of the skeleton can be successfully converted into new calcium phosphate phases such as apatite by heating the porous material treated with a molten salt mixture of CaCl2 -Ca(NO3 )2 . 相似文献
25.
Taeko Izumi Yoshihiro Yagimuma Masanori Haga 《Journal of the American Oil Chemists' Society》1997,74(7):875-878
Enyzmatic amidation of the primary amines β-alanine ethyl ester and 3-aminopropionitrile with methyl laurate by means of immobilized
lipase (Candida antarctica lipase, CAL) resulted in the formation in good yield of N-lauroyl-β-alanine ethyl ester and 3-(N-lauroylamino)-propionitrile, respectively. When 3-amino-propionitrile was used as substrate, diisopropyl ether was a suitable
solvent. Changing the reaction temperature (12–80°C) did not affect the yields, and room temperature was a suitable temperature
for this reaction. In the investigation of reaction conditions, the use of equimolar amounts (5 mmol) of substrate and ester,
along with 0.5 g of CAL, in diisopropyl ether gave the best yield (99.3%) after 24 h of incubation at 24°C. The enzyme activity
in the amidation reaction did not decrease even after six uses. With β-alanine ethyl ester hydrochloride as substrate, diisopropyl
ether was unsuited as a solvent owing to the low solubility of the substrate in this solvent.
In this reaction, the best yield (82.0%) was attained by using dioxane as solvent. CAL achieved higher extents of amide synthesis
with long-chain than with short-chain ester substrates. The enzyme accepted only nonbulky primary amines as substrates. 相似文献
26.
Yoshihiro Hirata Kazuyoshi Sakeda Yumi Matsushita Kinji Shimada Yoshimi Ishihara 《Journal of the American Ceramic Society》1989,72(6):995-1002
Submicrometer SiO2 -Al2 O3 powders with compositions of 46.5 to 76.6 wt% Al2 O3 were prepared by hydrolysis of mixed alkoxides. Phase change, mullite composition, and particle size of powders with heating were analyzed by DTA, XRD, IR, BET, and TEM. As-produced amorphous powders partially transformed to mullite and Al-Si spinel at around 980°C. The compositions of mullite produced at 1400° and 1550°C were richer in Al2 O3 than the compositions of stable mullite solid solutions predicted from the phase diagram of the SiO2 -Al2 O3 system. Particle size decreased with increasing Al2 O3 content. The sintered densities depended upon the amount of SiO2 -rich glassy phase formed during sintering and the green density expressed as a function of particle size. 相似文献
27.
The crystal-growth process and growth conditions of β-alumina (Na2 O · Al2 O3 ) were investigated using the Na2 B4 O7 -Na3 AlF6 flux method. β-Alumina (electric fusion brick) was used as both nutrient and seed. Weight loss of the flux varied widely for various runs: ≅ 10 wt% of flux evaporated at 100 h, ≅ 17 wt% at 150 h, and 43 wt% at 600 h. When β-alumina crystal was grown, only 20 wt% Na2 B4 O7 was added to the Na3 AlF6 flux. The linear growth rates of the β-alumina single crystal grown by an Na3 AlF6 -20 wt% Na2 B4 O7 flux method at 1040°C and Δ t = 18°C were ≅ 1.0 × 10−3 mm/h ( a face) and ≅0.3 × 10−3 mm/h ( c face). The β-alumina single crystals grown were bounded by only c [001] and a [100] and were colorless and transparent. 相似文献
28.
Preparation of Aragonite Whiskers 总被引:10,自引:0,他引:10
Yoshio Ota Saburo Inui† Tetsushi Iwashita† Toshihiro Kasuga† Yoshihiro Abe† 《Journal of the American Ceramic Society》1995,78(7):1983-1984
A simple synthetic method for preparing aragonite whiskers has been developed. A suspension of CaCl2 -MgCl2 -Mg(OH)2 with pH ∼9 has been prepared by adding Ca(OH)2 to MgCl2 aqueous solution. CaCO3 whiskers (aragonite phase) have been prepared easily by blowing CO2 -containing gas into the suspension. The whiskers have high aspect ratios ranging from 20 to 80 with diameters of 0.5–1 μm . 相似文献
29.
New nanocomposites based on a vinylester resin (VER) and the organo‐montmorillonites (ODA‐M, BHL‐M, DEM‐M, BHLV‐M) modified with octadecylammonium, bis(2‐hydroxyethyl)lauryl ammonium, diethyl[2‐(methacryloyloxyl)ethyl]ammonium, and bis(2‐hydroxyethyl)lauryl(vinylbenzyl)‐ammonium chlorides, respectively, were prepared by dispersing the organoclays in VER, and subsequent crosslinking at finally 120°C. X‐ray diffraction studies and morphological studies using transmission electron microscopy revealed that exfoliation occurs for the VER/ODA‐M and BHL‐M composites, intercalation occurs for the VER/BHLV‐M composite, and neither intercalation nor exfoliation occur for the VER/DEM‐M and unmodified montmorillonite composites. On the whole, although the enhancement in flexural modulus was observed for the exfoliated ODA‐M and BHL‐M composites, the flexural strength was rather lowered. Dynamic viscoelastic measurement revealed that the ODA‐M, BHL‐M, and BHLV‐M nanocomposites have significantly higher storage modulus at the rubbery state than the other composites. Polym. Eng. Sci. 44:2041–2046, 2004. © 2004 Society of Plastics Engineers. 相似文献
30.
Poly(L ‐lactic acid) (PLLA: Mw = 19.4 × 104)/poly(ethylene glycol) (PEG: Mw = 400) blend films were formed by use of a solvent‐cast technique. The properties and structures of these blend films were investigated. The Young's modulus of the PLLA decreased from 1220 to 417 MPa with the addition of PEG 5 wt %, but the elongation at break increased from 19 to 126%. The melting point of PLLA linearly decreased with increases in the PEG content (i.e., pure PLLA: 172.5°C, PLLA/PEG = 60/40 wt %: 159.6°C). The PEG 20 wt % blend film had a porous structure. The pore diameter was 3–5 μm. The alkali hydrolysis rate of this blend film was accelerated due to its porous structure. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 965–970, 2004 相似文献