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21.
Kunio Saegusa 《Journal of the American Ceramic Society》1997,80(10):2510-2516
PbTiO3 (PT)-PbO-SiO2 glass-ceramic thin films were pro-duced by a sol-gel process. The crystallization of PT oc-curred at ∼700°C and was higher than that in PT-PbO-B2 O3 sol-gel glass-ceramics. A pinhole-free thin film was obtained by a rapid thermal annealing process when the designed glass-forming phase content in the thin film was >24 vol%. The measured dielectric constants of the films fairly agreed with the predicted values, based on a parallel mixing model. The dielectric constant was 219 and the di-electric loss was 0.04 in the 0.6PT-0.4(PbO-SiO2 ) film that was fired at 700°C. 相似文献
22.
Kazuyuki Tsubone Noriko Uchida Kunio Mimura 《Journal of the American Oil Chemists' Society》1990,67(7):451-454
A series of new amphoteric surfactants having a phosphoric acid group, a tertiary amino group and a 2-hydroxyalkyl group, sodium 2-(N-2-hydroxyalkyl-N-methyl-amino)ethyl hydrogen phosphates (alkyl: n-tetradecyl, n-hexadecyl, n-octadecyl), were prepared by an addition reaction of 1,2-epoxyalkanes to N-methylaminoethanol, followed by the introduction of a phosphoric acid group and neutralization with sodium hydroxide. The structures of these compounds were confirmed by spectroscopy and elemental analysis. The solubility in solvents, Krafft point, surface tension, critical micelle concentration (CMC), occupation area of the molecule at the surface of aqueous solutions and foaming power were measured. It was shown that a 2-hydroxyethyl group in a long alkyl chain seemed to behave as a hydrophobic part. 相似文献
23.
Y. Sugi T. Sugimura S. Tawada Y. Kubota T. Hanaoka T. Matsuzaki 《Catalysis Letters》2001,77(1-3):159-163
The isopropylation of mixtures of 3- and 4-isopropylbiphenyls (3- and 4-IPBPs) was examined over a dealuminated H-mordenite (HM) to elucidate the role of 3- and 4-IPBPs in the isopropylation of biphenyl (BP). 4-IPBP was consumed much faster than 3-IPBP in all cases. 4-IPBP was an exclusive precursor to diisopropylbiphenyls (DIPBs), particularly 4,4-DIPB, and 4,4-DIPB was found in encapsulated products during the reaction. These results show that 4-IPBP can allow establishment of an active complex with propylene and acid site in HM pores, whereas 3-IPBP cannot. It is concluded that the isopropylation of BP over HM occurs through a reactant selectivity mechanism, and through a restricted transition state mechanism, but not through a product selectivity mechanism. 相似文献
24.
An investigation was made of the magnitude and mechanism of shear degradation of a narrow distribution, high molecular weight (Mw = 670,000) polystyrene. An Instron rheometer was used to perform the extrusion at temperatures from 164° to 250°C. The change in molecular weight distribution was studied by gel permeation chromatography. The maximum shear stress employed was 5.83 kg/cm2. It was found that degradation could be induced at high stress at temperatures of 50°C lower than degradation of polystyrene would occur exclusively due to thermal forces. An activation energy for the degradation, calculated at constant shear rate, was +20.2 kcal/mole. The direction and magnitude of this value are consistent with degradation induced through a mechanical reduced activation for thermal degradation. 相似文献
25.
Hitoshi Masuda Chiyoshi Kamizawa Kunio Hata Kingo Yokota Tomoo Sakai Mitsuhiro Sato 《Desalination》1978,25(1):89-97
The evaporation drain of sulfite pulp spent liquor contains few volatile fatty acids, most of which is acetic acid. The main objective of this study is to recover acetic acid as the concentrated solution (about 4%), which could be used as a culture medium of the yeast. As acetic acid can easily pass through the cellulose acetate membrane, SP drains neutralized by NaOH, NH4OH and Ca(OH)2 were used as the feed solutions. In all cases, concentration by reverse osmosis was successfully carried out provided the appropriate pretreatment was employed. The recovery of acetic acid was 95.6, 90.5 and 98.2% for Na-, NH4-, and Ca-drain, respectively. In addition, the recovered (permeated) water may be used as an industrial one. 相似文献
26.
Hirosuke Oku Jyutaro Shudo Kunio Mimura Akinori Haratake Junichi Nagata Isao Chinen 《Lipids》1995,30(2):169-172
A neutral lipid class was isolated by thin-layer chromatography from the skin surface lipids of the hairless mouse. The fraction
migrated faster than triglycerides and had a migration rate similar to that of diacyl alkanediols (diester wax). Upon deacylation,
however, the long-chain diols were identified as 1-alkylglycerol ethers based on their chromatographic properties and on the
mass spectra of their nicotinylidene derivatives. Thus, the skin lipid fraction was identified as 1-O-alkyl-diacylglycerol. The alkyl moieties were all saturated and even-numbered and ranged in chainlength from C16 to C22 with 1-O-hexadecylglycerol amounting to 34% of the total glycerol ether moieties. The fatty acids derived from this lipid fraction
were mostly monoenoic with chainlengths ranging from C16 to C24. The major acyl component was eicosenoic acid (20∶1) representing 61% of the total fatty acids. 相似文献
27.
Individual action and synergistic effect in the combination of 6-anilino-1,3,5-triazine-2,4-dithiol (AF), zinc stearate, and barium stearate on the color stabilization of PVC were investigated. In this system, AF selectively reacts with allylic chlorine atoms in PVC. Consequently, unstable allylic chlorine units were converted to thermally stable allylic structures, thus retarding the development of polyene sequences. Zinc stearate accelerated the reaction of AF with allylic chlorine atoms in PVC, forming the zinc salts of AF (AFZnSt, St?C1–H35COO? ) by reacting with AF. Barium stearate reacted with ZnCl2 which is formed in the above reaction to give St2Zn and BaCl2. Consequently, barium stearate led to the selective reaction of AF with allylic chlorine atoms in PVC and the remarkable retarding effect of discoloration of PVC. 相似文献
28.
Kunio Mori Wataru Ibashi Hidetoshi Hirahara Yoshiyuki Oishi Masanari Katayama 《应用聚合物科学杂志》1995,58(13):2451-2458
2-Dibutylamino-1,3,5-triazine-4,6-dithiol (DB) and a mixture of DB and triallylisocyanurate (TAIC) were used as a lubricant during steel wire drawing due to a dry process. DB gave a polymer film with 180 nm in thickness to wire surfaces during the wire drawing. The polymer film had a disulfide structure on the backbone and contained a small amount of DB monomer and olygomer. Molecular weight and polymer weight increased with the drawing rate. The mixture of DB and TAIC gave mainly a three-dimensional polymer film with 225 nm in thickness to wire surfaces during drawing. The polymer film insoluble in THF had mono and disulfide structures and contained a small amount of linear polymer, DB, and TAIC. Such tribological polymerizations are estimated as follows: DB produces dithiyl radicals on a nascent surface formed during drawing and in the presence of oxygen and heat. The dithiyl radicals were polymerized by coupling with each other to give disulfide bonds or added to allyl groups in TAIC to give monosulfide bonds. It is concluded that this technique should be possible to use for unifying metal processing and surface treatment. © 1995 John Wiley & Sons, Inc. 相似文献
29.
Styrene was grafted onto cellulose acetate p-nitrobenzoate (CANB) by chain transfer reaction of growing polymer radicals to the pendant nitro groups of CANB. A copolymer with a branch for every 17.2 nitro groups was obtained. This result indicates that the pendant aromatic nitro group is more effective in obtaining a graft copolymer by radical mechanism than pendant double bond on the trunk polymer previously reported, where graft copolymers with a branch for several hundred of double bonds are produced. 相似文献
30.
Mixtures of styrene and n-butyl acrylate of various compositions were grafted onto cellulose and cellulose triacetate fibers preirradiated with γ-rays at 0°C in air. Monomer reactivity ratios of the grafted copolymers were found to be different from those of the nongrafted copolymers or those of AIBN-initiated copolymers. The active species initiating the graft copolymerization were trapped radicals for cellulose and peroxides for cellulose triacetate. Kinetic investigations of the graft copolymerization of styrene onto preirradiated cellulose triacetate fibers were also carried out, and it was found that the kinetic scheme for radical polymerization is also applicable to graft copolymerization in a heterogeneous system. 相似文献