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81.
Poly(ether ester) (PEE) copolymers were synthesized in a two‐stage process involving transesterification and polycondensation. The synthesized copolymer and the zinc oxide (ZnO) were used in composite preparation by melt compounding. The influence of ZnO type and concentration on the morphology, thermal and mechanical properties of the composites were studied. DSC and XRD analyses indicated that crystallinity of composites was slightly reduced with ZnO content. Homogeneous dispersion of fillers in the polymer matrix was observed through morphological analyses. While in general tensile strength and elongation at break values of the composites decreased with increasing ZnO content, elastic modulus values increased with the addition of ZnO. Moreover, ZnO particles were modified with poly(N‐vinyl pyrrolidone) and a slight improvement in mechanical properties was observed, respectively over the composites containing unmodified particles. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013 相似文献
82.
Demet Aydınoğlu Özkan Akgül Vildan Bayram 《Polymer-Plastics Technology and Engineering》2013,52(16):1706-1722
Polacrylamide nanocomposite hydrogels were prepared by in situ free radical polymerization reaction in presence of Spirulina microalgae, which is immobilized in montmorillonite clay (Sp-MMT). The nanocomposite hydrogel having 1 wt.% Sp-MMT clay was found to have desired exfoliated structure, maximum swelling and improved thermal stability. It also showed maximum metal adsorption capacity, which is about 312% higher than that of neat PAAm hydrogel at the highest metal concentration. The presence of Spirulina's porous network structure where all potential binding sites are under receptive position was found to be responsible for the dramatic increase in the metal adsorption and swelling behavior. 相似文献
83.
Structural, electrochemical and optical comparisons of tungsten oxide coatings derived from tungsten powder-based sols 总被引:2,自引:0,他引:2
Tungsten trioxide (WO3) electrochromic coatings have been formed on indium tin oxide-coated glass substrates by aqueous routes. Coating sols are obtained by dissolving tungsten powder in acetylated (APTA) or plain peroxotungstic acid (PTA) solutions. The structural evolution and electrochromic performance of the coatings as a function of calcination temperature (250 °C and 400 °C) have been reported. Differential scanning calorimetry and X-ray diffraction have shown that amorphous WO3 films are formed after calcination at 250 °C for both processing routes; however, the coatings that calcined at 400 °C were crystalline in both cases. The calcination temperature-dependent crystallinity of the coatings results in differences in optical properties of the coatings. Higher coloration efficiencies can be achieved with amorphous coatings than could be seen in the crystalline coatings. The transmittance values (at 800 nm) in the colored state are 35% and 56% for 250 °C and 400 °C-calcined coatings, respectively. The electrochemical properties are more significantly influenced by the method of sol preparation. The ion storage capacities designating the electrochemical properties are found in the range of 1.62–2.74 × 10− 3 (mC cm− 2) for APTA coatings; and 0.35–1.62 × 10− 3 (mC cm− 2) for PTA coatings. As a result, a correlation between the microstructure and the electrochromic performance has been established. 相似文献
84.
Glucose isomerase (GI) from Streptomycesrubiginosus was immobilized covalently onto Eupergit C 250 L made by copolymerization of N,N-methylene-bis-methacrylamide, glycidyl methacrylate, allyl glycidyl ether and methacrylamide. The catalytic efficiency of immobilized GI in isomerization of glucose to fructose was found as three fold higher than that of free GI. The residual activity of immobilized GI after 18 reuses in a batch type stirred reactor was about 85% of its initial activity. The thermal stability of immobilized GI was almost same with that of the free GI at 60 °C for 18 h preincubation time. The residual activities of immobilized GI when stored at 5 °C and 25 °C for four weeks were 72% and 69% of the initial activity, respectively. However, free GI retained 88% and 78% of its initial activity at 5 °C and 25 °C upon four weeks storage, respectively. Thus, the use of Eupergit C 250 L immobilized GI instead of free GI is suggested in enzymatic isomerization of glucose to fructose. 相似文献
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Poly(methyl phenyl silane) was used to photoinitiate the polymerization of methyl methacrylate. Poly(methyl methacrylate) (PMMA), obtained this way, contains remaining polysilane chains. Photolysis of this PMMA in the presence of vinyl monomers such as styrene makes it possible to prepare block copolymers. Such PMMA prepolymers were also used to induce the polymerization of cyclohexene oxide through formation of PMMA-attached silyl radicals and subsequent oxidation to the corresponding ions in the presence of N-ethoxy-2-methylpyridinium hexafluorophosphate resulting in the formation of a block copolymer. 相似文献
88.
BACKGROUND: Twin reversed arterial perfusion (TRAP) sequence and development of an acardiac monster is a rare event. Even more rare are conjoined acardiac, acephalic twins complicating a triplet pregnancy with TRAP sequence. The mortality for the acardius is 100%, and morbidity for the normal, pump fetus is 50%. The morbidity of the pump twin or triplet is attributed mostly to in utero congestive heart failure. CASE: A 24-year-old woman, gravida 1, para 0, at 35 weeks' intrauterine pregnancy, gave birth via low transverse cesarean section to a normal female and a pair of conjoined, acardiac, acephalic, pelvipagus twins. CONCLUSION: The diagnosis of acardius in multiple gestation pregnancy, with no fetal heart tone on ultrasound, must be ruled out in every case so that proper counseling, management and avoidance of complications in these patients can be achieved. 相似文献
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90.
Two different types of surface modifiers, 3‐aminopropyltriethoxysilane and formamide, were applied to carbon black (CB) particles to lower electrical resistivity of polymer composites prepared by treated CB. Two different matrices, low‐density polyethylene and nylon 6, were chosen to compound with surface modified CB. Surface energy of CB was increased by adding amine or amide functional groups during surface treatment of CB. According to electron spectroscopy for chemical analysis (ESCA), chemical modification in surface chemistry of CB was obtained with the chemicals used for the treatment due to the nitrogen atoms in their structures, which may act as dopant atom. As a result of this, electrical resistivity of composites prepared by treated CB decreased. In addition, there was not any significant change in tensile strength and tensile modulus of the composites with the surface treatment. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007 相似文献