全文获取类型
收费全文 | 2111篇 |
免费 | 66篇 |
国内免费 | 5篇 |
专业分类
化学 | 1596篇 |
晶体学 | 29篇 |
力学 | 23篇 |
数学 | 125篇 |
物理学 | 409篇 |
出版年
2021年 | 10篇 |
2020年 | 13篇 |
2019年 | 25篇 |
2018年 | 24篇 |
2017年 | 10篇 |
2016年 | 42篇 |
2015年 | 38篇 |
2014年 | 45篇 |
2013年 | 92篇 |
2012年 | 104篇 |
2011年 | 97篇 |
2010年 | 67篇 |
2009年 | 47篇 |
2008年 | 110篇 |
2007年 | 91篇 |
2006年 | 103篇 |
2005年 | 100篇 |
2004年 | 102篇 |
2003年 | 119篇 |
2002年 | 89篇 |
2001年 | 36篇 |
2000年 | 66篇 |
1999年 | 30篇 |
1998年 | 28篇 |
1997年 | 25篇 |
1996年 | 38篇 |
1995年 | 37篇 |
1994年 | 32篇 |
1993年 | 31篇 |
1992年 | 43篇 |
1991年 | 27篇 |
1990年 | 26篇 |
1989年 | 19篇 |
1988年 | 23篇 |
1987年 | 13篇 |
1986年 | 12篇 |
1985年 | 36篇 |
1984年 | 32篇 |
1983年 | 15篇 |
1982年 | 25篇 |
1981年 | 30篇 |
1980年 | 35篇 |
1979年 | 34篇 |
1978年 | 28篇 |
1977年 | 25篇 |
1976年 | 23篇 |
1975年 | 14篇 |
1974年 | 11篇 |
1973年 | 15篇 |
1968年 | 6篇 |
排序方式: 共有2182条查询结果,搜索用时 15 毫秒
11.
A micro-phase sorbent in situ formation from an aqueous solution was proposed for the sensitive spectrophotometric determination of nitrite in environmental waters. Nitrite in a 10 mL sample solution was converted into a cationic azo dye by the reaction with 4-trifluoromethylanilinium ion and N-1-naphthylethylenediammonium ion in an acidic medium. Addition of dodecylbenzenesulfonate ion caused the formation of a suspension of ion associate in the solution. Centrifugation of the solution led to the isolation of a liquid organic phase that extracted the azo dye at the bottom of the centrifuge tube. The volume of the new phase was ca. 5 microL. After the aqueous phase was discarded, the organic phase was dissolved with 1 mL of 2-methoxyethanol to measure the absorbance. Nitrogen as NO2- at concentrations from 1.5 to 30 microg L(-1) was determined with sufficient precision. When 0.2 mL of 2-methoxyethanol was applied to dissolve the organic phase, 0.3-4.8 microg NO2--N L(-1) was determined. The recovery tests for nitrite added to some river water and seawater were satisfactory. This method is very simple and rapid. It takes only 30 min from the dye formation to the measurement of the absorbance. 相似文献
12.
Shigeru Maeda 《Journal of Functional Analysis》2004,209(2):414-424
Hamiltonian formulation of various energy conservative evolution equations is given by means of wavelet expansion of solutions on the whole real axis R. The KdV equation, wave equations and Schrödinger equations are treated in a unified similar manner. A matrix representation of operators with respect to a nice wavelet base plays an important role in the formulation. Since the procedure is very concrete, our results can be used to efficiently compute numerical solutions of partial differential equations described in the text. In fact, we may also use symplectic schemes to solve derived Hamiltonian systems. 相似文献
13.
Kazuhiro Kurata Masataka Shibata Shigeru Sakamoto 《Applied Mathematics and Optimization》2004,50(3):259-278
Let $\Omega$ be a bounded domain in ${\bf R^n}$ with Lipschitz
boundary,
$\lambda >0,$ and $1\le p \le (n+2)/(n-2)$ if $n\ge 3$ and $1\le p< +\infty$
if $n=1,2$. Let $D$ be a measurable subset of $\Omega$ which belongs
to the class
$
{\cal C}_{\beta}=\{D\subset \Omega \quad | \quad |D|=\beta\}
$
for the prescribed $\beta\in (0, |\Omega|).$
For any $D\in{\cal C}_{\beta}$, it is well known that
there exists a unique
global minimizer $u\in H^1_0(\Omega)$, which we denote by
$u_D$, of the functional
\[\quad
J_{\Omega,D}(v)=\frac12\int_{\Omega}|\nabla v|^2\,
dx+\frac{\lambda}{p+1}\int_{\Omega}|v|^{p+1}\, dx
-\int_{\Omega}\chi_Dv\,dx
\]
on $H^1_0(\Omega)$.
We consider the optimization problem
$
E_{\beta,\Omega}=\inf_{D\in {\cal C}_{\beta}} J_D(u_D)
$
and say that
a subset $D^*\in {\cal C}_{\beta}$ which attains
$E_{\beta,\Omega}$
is an optimal configuration to this problem.
In this paper we show the existence, uniqueness
and non-uniqueness, and
symmetry-preserving and symmetry-breaking phenomena of the
optimal configuration $D^*$ to this
optimization problem in various settings. 相似文献
14.
Akira Shimazu Tukasa Miyazaki Shigeru Katayama Yasuo Ito 《Journal of Polymer Science.Polymer Physics》2003,41(3):308-318
The ortho‐positronium (o‐Ps) lifetime τ3 and its intensity I3 in various fluorinated polyimides were determined by the positron annihilation technique and were studied with the spin–lattice relaxation time T1 and the propylene permeability, solubility, diffusivity, and permselectivity for propylene/propane in them. τ3, I3, and the distribution of τ3 changed when the bulky moieties in the polyimides were changed. The polyimides, having both large τ3 and I3 values, exhibited a short T1 and a high permeability with a low permselectivity. The propylene permeability and diffusivity were exponentially correlated with the product of I3 and the average free‐volume hole size estimated from τ3. In highly plasticized states induced by the sorption of propylene, the permeability increased with the propylene pressure in excellent agreement with the change in the free‐volume hole properties probed by o‐Ps. The large and broad distribution of the free‐volume holes and increased local chain mobility for the 2,2‐bis(3,4‐decarboxyphenyl) hexafluoropropane dianhydride‐based polyimides are thought to be important physical properties for promoting penetrant‐induced plasticization. These results suggest that o‐Ps is a powerful probe of not only the free‐volume holes but also the corresponding permeation mechanism and penetrant‐induced plasticization phenomenon. © 2003 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 41: 308–318, 2003 相似文献
15.
K. M. A. Salam Hidekazu Konishi Masahiro Mizuno Hisashi Fukuda Shigeru Nomura 《Applied Surface Science》2002,190(1-4):88-95
Polycrystalline (1−x)Ta2O5−xTiO2 thin films were formed on Si by metalorganic decomposition (MOD) and annealed at various temperatures. As-deposited films were in the amorphous state and were completely transformed to crystalline after annealing above 600 °C. During crystallization, a thin interfacial SiO2 layer was formed at the (1−x)Ta2O5−xTiO2/Si interface. Thin films with 0.92Ta2O5–0.08TiO2 composition exhibited superior insulating properties. The measured dielectric constant and dissipation factor at 1 MHz were 9 and 0.015, respectively, for films annealed at 900 °C. The interface trap density was 2.5×1011 cm−2 eV−1, and flatband voltage was −0.38 V. A charge storage density of 22.8 fC/μm2 was obtained at an applied electric field of 3 MV/cm. The leakage current density was lower than 4×10−9 A/cm2 up to an applied electric field of 6 MV/cm. 相似文献
16.
Shigeru Katayama Mika Horiike Kazuyuki Hirao Naoto Tsutsumi 《Journal of Polymer Science.Polymer Physics》2002,40(24):2800-2806
We investigated the structures induced by an irradiation of a near‐infrared (NIR) femtosecond laser pulse in dye‐doped polymeric materials {poly(methyl methacrylate) (PMMA), thermoplastic epoxy resin (Epoxy), and a block copolymer of methyl methacrylate and ethyl acrylate‐butyl acrylate [p(MMA/EA‐BA) block copolymer]}. Dyes used were classified into two types—type 1 with absorption at 400 nm and type 2 with no absorption at 400 nm. The 400‐nm wavelength corresponds to the two‐photon absorption region by the irradiated NIR laser pulse at 800 nm. Type 1 dye‐doped PMMA and p(MMA/EA‐BA) block copolymer showed a peculiar dye additive effect for the structures induced by the line irradiation of a NIR femtosecond laser pulse. On the contrary, dye‐doped Epoxy did not exhibit a dye additive effect. The different results among PMMA, p(MMA/EA‐BA) block copolymer, and Epoxy matrix polymers are supposed to be related to the difference of electron‐acceptor properties. The mechanism of this type 1 dye‐additive‐effect phenomenon for PMMA and p(MMA/EA‐BA) block copolymer is discussed on the basis of two‐photon absorption of type 1 dye at 400 nm by the irradiation of a femtosecond laser pulse with 800 nm wavelength and the dissipation of the absorbed energy to the polymer matrix among various transition processes. Dyes with a low‐fluorescence quantum yield favored the formation of thicker grating structures. © 2002 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 40: 2800–2806, 2002 相似文献
17.
A method to determine alpha-, beta- and gamma-hexabromocyclododecane (HBCD) and tetrabromobisphenol A (TBBPA) in water and sediments was presented using solid phase extraction (SPE) and/or solvent extraction. Recoveries from sediments were approximately 100% for all the chemicals, while recoveries of alpha-, beta- and gamma-HBCDs from water were dependent on the extraction method. In the case of dichloromethane (CH2Cl2) extraction, recoveries of alpha-, beta- and gamma-HBCD from landfill leachates were 77%, 88% and 92%, respectively. Technical difficulties in HBCD measurement are discussed in terms of the physico-chemical properties of HBCD isomers. The method was applied to landfill samples and marine sediment. 相似文献
18.
Alam MS Katayama N Kim IJ Li WC Lou XC Sun CR Bortoletto D Goldberg M Horwitz N Mestayer MD Moneti GC Sharma V Shipsey IP Skwarnicki T Csorna SE Letson T Brock IC Ferguson T Artuso M Bebek C Berkelman K Blucher E Byrd J Cassel DG Cheu E Coffman DM Crawford G DeSalvo R DeWire JW Drell PS Ehrlich R Galik RS Gittelman B Gray SW Halling AM Hartill DL Heltsley BK Kandaswamy J Kowalewski R Kreinick DL Kubota Y Lewis JD Mistry NB Mueller J Namjoshi R Nandi S Nordberg E O'Grady C Peterson D Pisharody M 《Physical review D: Particles and fields》1989,40(11):3790
19.
Yasufumi Otsubo Masahiro Sekine Shingo Katayama 《Journal of colloid and interface science》1992,150(2)
Monodisperse silica particles were formed by hydrolyzing tetraethylorthosilicate in an ethanol solution and the silica suspensions dispersed in a silicone oil were prepared by a different procedure. The effects of adsorbed water on the electrorheological (ER) behavior were studied under oscillatory shear. The amounts of adsorbed water and surface silanol groups were determined by thermogravimetric analysis. The magnitude of the complex viscosity, |η*|, increases with the application of electric fields. The physically adsorbed water is primarily responsible for the ER effect. However, the fluids containing large amounts of adsorbed water do not always show excellent ER performance. The surface silanol groups have an important role in promoting the ER effect. Not only the amount but also the situation of silanol groups determines the ER activity of adsorbed water. 相似文献
20.