全文获取类型
收费全文 | 30612篇 |
免费 | 4567篇 |
国内免费 | 3520篇 |
专业分类
化学 | 18422篇 |
晶体学 | 653篇 |
力学 | 1539篇 |
综合类 | 214篇 |
数学 | 1933篇 |
物理学 | 15938篇 |
出版年
2024年 | 82篇 |
2023年 | 291篇 |
2022年 | 735篇 |
2021年 | 736篇 |
2020年 | 955篇 |
2019年 | 835篇 |
2018年 | 841篇 |
2017年 | 1055篇 |
2016年 | 1345篇 |
2015年 | 1284篇 |
2014年 | 1652篇 |
2013年 | 2782篇 |
2012年 | 1984篇 |
2011年 | 2373篇 |
2010年 | 1867篇 |
2009年 | 2168篇 |
2008年 | 2109篇 |
2007年 | 2197篇 |
2006年 | 1873篇 |
2005年 | 1585篇 |
2004年 | 1348篇 |
2003年 | 1283篇 |
2002年 | 1300篇 |
2001年 | 885篇 |
2000年 | 794篇 |
1999年 | 729篇 |
1998年 | 594篇 |
1997年 | 454篇 |
1996年 | 405篇 |
1995年 | 320篇 |
1994年 | 321篇 |
1993年 | 219篇 |
1992年 | 238篇 |
1991年 | 159篇 |
1990年 | 99篇 |
1989年 | 113篇 |
1988年 | 100篇 |
1987年 | 86篇 |
1986年 | 58篇 |
1985年 | 81篇 |
1984年 | 64篇 |
1983年 | 33篇 |
1982年 | 63篇 |
1981年 | 40篇 |
1980年 | 22篇 |
1979年 | 36篇 |
1978年 | 16篇 |
1977年 | 17篇 |
1976年 | 15篇 |
1973年 | 24篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
991.
Study on microstructure and mechanical properties relationship of short fibers/rubber foam composites 总被引:1,自引:0,他引:1
Research on short fibers/rubber foam composites is rarely found in the literature. In this paper, microcellular rubber foams unfilled (MF), strengthened by pretreated short fibers (MFPS) and untreated short fibers (MFUS) are prepared, respectively. The microstructure and mechanical properties of the three composites have been studied via scanning electron microscope (SEM) and mechanical testing, respectively. The SEM results show that both pretreated and untreated short fibers disperse uniformly in the composites and in bidimensional orientation. Moreover, the pretreated short fibers have much better adhesion with the rubber matrix than untreated ones. The experimental results also indicate that the introduction of short fibers is mainly responsible for the great enhancement of most mechanical properties of the microcellular rubber foams, and the good interfacial adhesion of the short fibers with the matrix contributes to the more extensive improvement in the mechanical properties. It is also found that the reinforcement effect of short fibers to compressive modulus strongly depends on the density of microcellular rubber foams, the orientation of short fiber and the deformation ratio. The compressive modulus of microcellular rubber foams at the normalized density less than 0.70 and beyond 0.70 is predicted by the modified Simple Blending Model and the Halpin-Kerner Model, respectively. The theoretically predicted values are in good accordance with the experimental results. 相似文献
992.
993.
Solid solutions NaCl—CdCl2 were studied in an interval of CdCl2 concentrations of 0.05—3 mol.% by Raman spectroscopy. The molecular form Na2CdCl4 decomposes: Na2CdCl4 2Na+ + Cd2+ + 2Cl2
– + 2e–; 2Na + 2e– 2Na0. Free sodium atoms form color centers of crystal (F centers) in the region of jumpwise changing the partition coefficient of CdCl2 in NaCl (K jump). 相似文献
994.
Chun Xia Tan Ruo Fei Feng Xiao Xia Peng 《中国化学快报》2007,18(5):505-508
By the condensation of 2,6-bis(4-amino-5-mercapto-[1,2,4]-triazoles-2)pyridine with aromatic acid in the presence of phosphorus oxychloride. Compounds of 2,6-bis(6-aryl-[1,2,4]-triazolo[3,4-b][1,3,4]-thiadiazole-3-yl)pyridines were synthesized. Their structures were confirmed by IR, ^1H NMR spectroscopies and elemental analysis. Their electrochemical behavior and cyclic voltammogram also were be studied. The results showed that they have high ionization potentials and good affinity. 相似文献
995.
Emerson Lourenço 《Polymer Degradation and Stability》2006,91(12):2968-2978
The influence of photochemical aging of in situ polymerized PS/AES blends on their mechanical properties has been studied. The PS/AES blends were subjected to photochemical aging for 168 h and 720 h. Tensile properties and Izod impact resistance of aged and non-aged samples were evaluated. The mechanical properties of the PS/AES blends are influenced by the polymerization temperature and blend composition and represent a balance between the toughness of EPDM and the stiffness of SAN in the PS matrix. Even though the impact resistance and strain at break of HIPS are higher than those of the PS/AES blends, after the aging period all PS/AES blends showed higher strain at break than HIPS. PS/AES blends present higher photochemical stability than HIPS. 相似文献
996.
State Miao Ming-Ming Liao Dai-Zheng Jiang Zong-Hui Cheng Peng Wang Geng-Lin 《中国化学》1996,14(4):326-330
Four new heterotrinuclear complexes have been synthesized and characterized, namely {[Ni(L)2]2[Cu(opba)]}(ClO4)2, where opba denotes o-phenylenebis(oxamato) and L stands for 1,10-phenanthroline(phen) (1), 5-nitro-l,10-phenanthroline(NO2-phen) (2), 2,2′-bipyridyl(bpy) (S) and 4,4′-dimethyl-2,2′-bipyridyl(Me2bpy) (4). The temperature dependence of the magnetic susceptibility of {[Ni(phen)2]2[Cu(opba)]}(ClO4)23H2O has been studied in the 4–300 K range, giving the exchange integral J—109 cm?1. The HMT vs. T plot exhibits a minimum at about 100 K, characteristic of this kind of coupled polymetallic complex with an irregular spin-state structure. 相似文献
997.
Mutual diffusion coefficients and densities were measured for aqueous ZnCl2–KCl mixtures at 25° by using free-diffusion Rayleigh interferometry and pycnometry, respectively. The ZnCl2 concentrations were fixed at 1.5 mol-dm–3, whereas those of KCl were 0.5, 1.25, 2.0, or 4.0 mol-dm–3. This corresponds to a half charged zinc-chlorine storage battery at various suporting electrolyte concentrations. The main-term coefficient of ZnCl2 only varies by 10% with KCl concentration, whereas that of KCl varies by about 22%. The ZnCl2 cross-term coefficient remains small and positive; in contrast the KCl cross-term coefficient goes through a maximum and is negative at high and low KCl concentrations. At KCl concentrations of 0.5 and 4.0 mol-dm–3, solutions with the KCl c0 are statically and dynamically (diffusively) unstable at the top and bottom of the boundary. Evaluation of the parameters of the non-linear least-squares solution to the diffusion equation is difficult for the 1.25 mol-dm–3 KCl case, since this system has nearly equal eigenvalues in its diffusion coefficient matrix. 相似文献
998.
Valérie Chevalier-Billosta Jean-Paul Joseleau Alain Cochaux Katia Ruel 《Cellulose (London, England)》2007,14(2):141-152
The composition and ultrastructural arrangement of cell wall polymers in wood fibres have determining influence on the properties
of wood derived materials. It is therefore important to improve our understanding of the relationship between fibres organisation,
the modifications induced by pulping treatments, and the resulting paper sheet mechanical properties. The different treatments
to which fibres are subjected during the manufacturing of pulps and papers induce morphological and micro-structural alterations
due to the removal of wall constituents and of microfibrillar elements. The impact of pulping processes on fibres was investigated
at the ultrastructural scale of transmission electron microscopy. Particular attention was given to the effects of beating
in refiners at various intensities on the ultrastructure of fibres. The most characteristic effects consisted of delaminations,
microfibril disorganisation, and even fractures, of varying importance depending on the intensity of the mechanical refining.
The consequences of internal alterations and surface modifications of the fibres were examined in relation to the paper sheet
mechanical properties. Correlations between the type of alteration observed in the fibres and its possible impact on a given
paper mechanical property are suggested. With similar approaches, the effects of drying and recycling were studied. 相似文献
999.
James L. Hedrick W. Volksen Dillip K. Mohanty 《Journal of polymer science. Part A, Polymer chemistry》1992,30(10):2085-2097
Imide-aryl ether ketone block copolymers were prepared and their morphology and thermal and mechanical properties investigated. Two aryl ether ketone blocks were incorporated; the first was an amorphous block derived from bisphenol–A and the second block was a semi-crystalline poly(aryl ether ether ketone) prepared from a soluble and amorphous ketimine precursor. Bis(amino) aryl ether ketone and aryl ether ketimine oligomers were prepared via a nucleophilic aromaic substitution reaction with molecular weights ranging from 6,000 to 12,000 g/mol. The oligomers were co-reacted with 4,4′-oxydianiline (ODA) and pyromellitic dianhydride (PMDA) diethyl ester diacyl chloride in N-methyl–2-pyrrolidone (NMP) in the presence of N-methylmorpholine. The copolymer compositions, determined by H-NMR, of the resulting amic ester based copolymers ranged from 8 to 50 wt % aryl ether ketone or ketimine content. Prior to imide formation, the ketimine moiety of the aryl ether ketimine block was hydrolyzed (p-toluene sulfonic acid) to the ketone form producing the aryl ether ether ketone block. Compositions of this block were maintained low to retain solubility. Solutions of the copolymers were cast and cured to effect imidization, producing clear films with high moduli (ca. 2200 MPa) and elongations (33–100%). The copolymers displayed good thermal stability with decomposition temperatures in excess of 450°C. Multiphase morphologies were observed irrespective of the co-block type, block length or composition. © 1992 John Wiley & Sons, Inc. 相似文献
1000.
Mund G Vidovic D Batchelor RJ Britten JF Sharma RD Jones CH Leznoff DB 《Chemistry (Weinheim an der Bergstrasse, Germany)》2003,9(19):4757-4763
Several iron(III) complexes incorporating diamidoether ligands are described. The reaction between [Li(2)[RN(SiMe(2))](2)O] and FeX(3) (X=Cl or Br; R=2,4,6-Me(3)Ph or 2,6-iPr(2)Ph) form unusual ate complexes, [FeX(2)Li[RN(SiMe(2))](2)O](2) (2, X=Cl, R=2,4,6-Me(3)Ph; 3, X=Br, R=2,4,6-Me(3)Ph; 4, X=Cl, R=2,6-iPr(2)Ph) which are stabilized by Li-pi interactions. These dimeric iron(III)-diamido complexes exhibit magnetic behaviour characteristic of uncoupled high spin (S= 5/2 ) iron(III) centres. They also undergo halide metathesis resulting in reduced iron(II) species. Thus, reaction of 2 with alkyllithium reagents leads to the formation of iron(II) dimer [Fe[Me(3)PhN(SiMe(2))](2)O](2) (6). Similarly, the previously reported iron(III)-diamido complex [FeCl[tBuN(SiMe(2))](2)O](2) (1) reacts with LiPPh(2) to yield the iron(II) dimer [Fe[tBuN(SiMe(2))](2)O](2) but reaction with LiNPh(2) gives the iron(II) product [Fe(2)(NPh(2))(2)[tBuN(SiMe(2))](2)O] (5). Some redox chemistry is also observed as side reactions in the syntheses of 2-4, yielding THF adducts of FeX(2): the one-dimensional chain [FeBr(2)(THF)(2)](n) (7) and the cluster [Fe(4)Cl(8)(THF)(6)]. The X-ray crystal structures of 3, 5 and 7 are described. 相似文献