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91.
《Surface and interface analysis : SIA》2004,36(11):1449-1468
The adsorption of a commercial adhesive and two of its major components—an amine curing agent [2,4‐toluene diisocyanate urone (TDI urone)] and an adhesive prepolymer resin [diglycidyl ether of bisphenol A (DGEBA)]—on a hydrated aluminium surface and the hydrated surface coated with γ‐glycidoxypropyltrimethoxysilane (GPS) has been investigated by x‐ray photoelectron spectroscopy (XPS) and time‐of‐flight secondary ion mass spectrometry (ToF‐SIMS). The study of TDI urone adsorption indicated that adsorption was of the chemisorption type, and a specific interaction involving this molecule and the GPS immobilized on the hydrated aluminium surface was identified. From XPS and ToF‐SIMS data it was found that the types of interaction of the curing agent with the bare substrate were of the donor–acceptor type. Study of the DGEBA adsorption showed different‐shaped isotherms for the bare and the GPS‐coated substrates. It was found that the typical Langmuir isotherm type was obtained for the GPS‐coated substrate whereas no adsorption plateau was observed for the bare substrate within the concentration range studied. This resulted from a change in the conformation of the DGEBA molecule on the substrate when the concentration of DGEBA solution was increased. The bonding of DGEBA with both types of substrates was assumed to be via acid–base interactions (i.e. donor–acceptor interactions). Adsorption of the commercial adhesive on the hydrated surfaces was of BET Type IV form, rather than the simple monolayer adsorption isotherm (Langmuir type). This indicates multilayer adsorption, presumably in the pores of the hydrated substrate, as a result of a process analogous to adsorption condensation. Copyright © 2004 John Wiley & Sons, Ltd. 相似文献
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Jingzhou Liu Chung‐Yuen Hui Anand Jagota 《Journal of Polymer Science.Polymer Physics》2009,47(23):2368-2384
We present a three‐dimensional (3D) model for adhesion enhancement due to crack trapping in a film‐terminated fibrillar structure. Adhesion enhancement occurs due to trapping of the interfacial crack in the region between fibrils. Energy release to the crack tip is attenuated because, between fibrils, it has to pass through the compliant terminal film. Using perturbation theory and a finite element method, we solve for the shape of crack front, which is unknown. Our model thus also allows us to study how adhesion enhancement depends on the arrangement of fibrils. For example, our model explains why, for a fixed area density of fibrils and for similar crack orientations, hexagonal arrays have higher adhesion than square arrays. © 2009 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 47: 2368–2384, 2009 相似文献
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Takahiro Gunji Yasuhito Iizuka Koji Arimitsu Yoshimoto Abe 《Journal of polymer science. Part A, Polymer chemistry》2004,42(15):3676-3684
Polysilsesquioxanes were prepared through the acid‐catalyzed hydrolytic polycondensation of triethoxy(methyl)silane, triisopropoxy(methyl)silane, or triisobutoxy(methyl)silane and subjected to dip coating to form coating films. The film formation depended on the polarity and crystallinity of the substrate, and a correlation was found between the substrate and polysilsesquioxane solubility parameters. When the coating film was heated, thermal condensation occurred at about 500 °C between hydroxy groups or between hydroxy and alkoxy groups. The methyl group attached to silicon decomposed, and siloxane bonding formed at about 800 °C. The adhesion and hardness of the coating films were evaluated with the Japanese Industrial Standard K5400 protocol, and they increased with increases in the heating time and heat‐treatment temperature. The refractive index of the coating films decreased when the heat‐treatment temperature was increased to 500 °C because of the combustion of organic groups. In contrast, the surface electric resistance increased with the heat‐treatment temperature up to 500 °C. The dielectric constant was 2.6–2.8 and decreased with an increases in the molecular weight and the degree of crosslinking of the polysilsesquioxanes. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 3676–3684, 2004 相似文献
95.
B. Bernu 《Journal of statistical physics》1979,21(4):447-464
We present molecular dynamics computations of the time-dependent auto-correlation function of the single-particle density in a classical one-component plasma for three thermodynamic states in the range of intermediate and strong coupling. The deviations from the Gaussian approximation are calculated and the data are analyzed by the standard memory function formalism. 相似文献
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不凝血性 (Nonthrombogenicity)又称抗凝血性 (Antithrombogenicity) ,是指材料不会触发血液凝固的能力 .如何提高不凝血性一直是高分子生物材料研究的主要任务和中心内容 [1~ 3 ] .但目前抗凝血性最好的三类抗凝血材料 ,即聚乙二醇衍生物 (PEO)、聚磷酰胆碱及肝素化材料等 [4~ 10 ] 仍不能满足心血管医用装置的需要 .材料界面血小板的粘附和活化是导致凝血的重要因素 .活化的血小板不仅可激活多种凝血因子 ,也是材料表面血栓的重要组成部分 .因此 ,对材料界面血小板粘附行为的研究可初步评价材料的血液相容性 [11,12 ] .根据“维持正常… 相似文献
99.
成核剂对共聚酯热熔胶结晶动力学的影响 总被引:1,自引:0,他引:1
热熔胶因具有粘接迅速、强度高、无毒害、无污染等优良性能而被誉为“绿色胶粘剂”.近十多年来 ,热熔胶在纺织品工业 (如服装工业、粘合衬工业 )领域中已得到了广泛的应用 ,而高质量粘合衬的制造 ,关键在于要有高性能的热熔胶[1] .共聚酰胺和共聚酯热熔胶是两大类性能优良的粘合衬用热熔胶 ,由于共聚酯类热熔胶在手感、价格以及耐水洗、砂洗和蒸汽压烫等方面优于共聚酰胺热熔胶 ,而有着更为广阔的发展前景 .但结晶速率缓慢一直是共聚酯尚未解决的一个技术难题 .本文主要研究了成核剂对共聚酯热熔胶结晶速率的促进作用 ,并取得了较为理想的结… 相似文献
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