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61.
Summary A melt-grafting approach was employed to prepare a novel functional polypropylene(FPP)—amino-terminated polyurethane grafted
polypropylene (PP-g-ATPU). The crystallization behaviors of PP and PP/FPP blends were characterized using differential scanning
calorimetry (DSC), wide angle X-ray scattering (WAXS) and polarized optical microscopy (POM). The effects of FPP composition
on crystallization behavior, crystal transformation, and morphology of PP/FPP crystalline were investigated. The results showed
that at a low dosage (<2.0 wt%) ATPU acted as a heterogeneous nucleation agent during the crystallization of PP/FPP blends.
However, when the content of ATPU reached 2.0 wt% or higher, ATPU deteriorated the crystallization of PP or PP/FPP blends.
The crystallite size decreased and the number of crystallites increased as the ATPU content increased. The Avrami analysis
was adopted to describe the isothermal crystallization process. The difference in the exponent n between PP and PP/FPP suggested that the isothermal crystallization kinetics of PP/FPP blends followed a three-dimensional
growth via heterogeneous nucleation. In terms of the half-time of the crystallization, t1/2, the crystallization rate of functional PP blends was faster than that of PP homopolymer at a given crystallization temperature. 相似文献
62.
An aromatic liquid crystalline epoxy monomer based on biphenyl mesogen was synthesized and cured with three different aromatic diamines. The curing reaction characteristics were analyzed by DSC, and the data were introduced to the Kissinger equation to attain the kinetic parameters. Diglycidyl ether of 4,4′‐biphenyl (DGEBP)/4,4′‐diaminobiphenyl (DABP), and DGEBP/4,4′‐methylenediamine (MDA) systems showed an exotherm curing reaction after comelting of the monomers; the DGEBP/p‐phenylenediamine (PDA) system's curing reaction took place in the solid state without melting of monomers. The activation energy and preexponential factor for the DGEBP/DABP system were 55.6 kJ/mol and 4.0 × 106 min?1, respectively. Those values for DGEBP/MDA and DGEBP/PDA systems were 55.1 kJ/mol and 1.0 × 106 min?1 and 148.8 kJ/mol and 7.7 × 1019 min?1, respectively. The rate constant at 100°C for DGEBP/PDA is 2 times higher than those for DGEBP/DABP and DGEBP/MDA, which have almost the same values. Strictly speaking, the rate constant of DGEBP/DABP is a little higher than that of DGEBP/MDA, and these results are in good agreement with the DSC curves. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 2419–2425, 2002 相似文献
63.
Abdellatif Mohamed Mila P. Hojilla-Evangelista Steve C. Peterson Girma Biresaw 《Journal of the American Oil Chemists' Society》2007,84(3):281-288
Barley protein isolate (BPI) was extracted in 0.015 N NaOH in a 10:1 ratio solvent:flour and was precipitated by adjusting
the pH to 4.5 and freeze-dried. The thermal properties of BPI were determined using modulated differential scanning calorimetry
(MDSC). BPI with 4% moisture content exhibited a glass transition (T
g) with 140 °C onset, 153 °C middle, and 165 °C end temperatures and a ΔC
p of 0.454 J/g per °C. The high moisture content sample (50%) showed a T
g at 89, 91, or 94 °C and 0.067 ΔC
p. Acetylation had no apparent effect on the foaming and emulsifying properties of protein from barley flour but exhibited
the least-stable foam among BPI samples. Foaming capacities of both barley protein isolates were ∼12% less than that of acid-precipitated
soy protein isolate reported in the literature. Acetylated BPI showed the highest surface hydrophobicity compared to the other
samples. The surface-tension test confirmed that unmodified and modified BPI possessed surface activity. BPI phosphorous oxycloride-crosslinked
was the most effective in lowering the surface tension of aqueous NaCl, while the crosslinked BPI was the least effective.
The G′ value of BPI suspension was greater than G″ at all frequencies from 0.1 to 100 rad/s. The strain value at which linear behavior ceased and nonlinear behavior began
ranged from 3 to 10%.
Names are necessary to report factually on available data; however, the United States Department of Agriculture (USDA) neither
guarantees nor warrants the standard of the product, and the use of the name by the USDA implies no approval of the product
to the exclusion of others that may also be suitable. 相似文献
64.
Copolymers of N‐acryloylcarbazole (A) and vinyl acetate (V) were synthesized by bulk polymerization using benzoyl peroxide (BPO) as free‐radical initiator at 65°C in different in‐feed ratios. The composition of the copolymer was determined by 1H‐NMR spectrum. The comonomer reactivity ratios, determined by Kelen–Tudos (KT) and nonlinear error‐in‐variables (EVM) methods, were rA= 16.75 ± 1.38, rV = 0.015 ± 0.002, and rA = 16.36, rV = 0.015, respectively. Complete spectral assignments of the 1H and 13C{1H} NMR spectra of the copolymers were done by the help of distortionless enhancement by polarization transfer (DEPT) and two‐dimensional NMR techniques such as heteronuclear single quantum coherence (HSQC) and total correlation spectroscopy (TOCSY). The methine and methylene carbon resonances were found to be compositional as well as configurational sensitive. The signals obtained were broad pertaining to the restricted rotation of bulky carbazole group. The thermal stability and glass‐transition temperatures (Tg) of the copolymers were found to be dependant on polymer composition and characteristic of rotational rigidity of the polymer chain. Variation in the values of Tg with the copolymer composition was found to be in good agreement with theoretical values obtained from Johnston and Barton equations. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 2720–2733, 2007 相似文献
65.
Melting curves, obtained by differential scanning calorimetry, are used to estimate crystal size distributions. The proposed theoretical analysis is applied to different types of polyethylene, including high‐density polyethylene (HDPE), metallocene catalyzed linear low‐density polyethylenes (m‐LLDPE), blends of m‐LLDPEs, and Ziegler‐Natta catalyzed LLDPEs (ZN‐LLDPE). Theoretical predictions are in agreement with experimental results. A generalized melting temperature equation successfully predicts the melting temperatures of all the LLDPEs, although it was initially proposed for homogeneous copolymers with excluded comonomers. A new definition of the heat of fusion for pure crystals is proposed. This heat of fusion can be calculated from the average crystal size or the crystal size number distribution. 相似文献
66.
The influence of styrene-butadiene rubber (SBR) latex on cement hydrates Ca(OH)2, ettringite, C4AH13 and C-S-H gel and the degree of cement hydration is studied by means of several measure methods. The results of DSC and XRD show that the Ca(OH)2 content in wet-cured SBR-modified cement pastes increases with polymer-cement ratio (P/C) and reaches a maximum when P/C is 5%, 10% and 10% for the pastes hydrated for 3 d, 7 d and 28 d, respectively. With wet cure, appropriate addition of SBR promotes the hydration of cement, while the effect of SBR on the content of Ca(OH)2 and the degree of cement hydration is not remarkable in mixed-cured SBR-modified cement pastes. XRD results illustrate that SBR accelerates the reaction of calcium aluminate with gypsum, and thus enhances the formation and stability of the ettringite and inhibits the formation of C4AH13. The structure of aluminum-oxide and silicon-oxide polyhedron is characterized by 27Al and 29Si solid state NMR spectrum method, which shows that tetrahedron and octahedron are the main forms of aluminum-oxide polyhedrons in SBR-modified cement pastes. There are only [SiO4]4− tetrahedron monomer and dimer in the modified pastes hydrated for 3 d, but there appears three-tetrahedron polymer in the modified pastes hydrated for 28 d. The effect of low SBR dosage on the structure of aluminum-oxide and silicon-oxide polyhedron is slight. However, the combination of Al3+ with [SiO4]4− is restrained when P/C is above 15%, and the structure of Al3+ is changed obviously. Meantime, the polymerization of the [SiO4]4− tetrahedron in C-S-H gel is controlled. 相似文献
67.
The cure kinetics and mechanisms of an epoxy oligomer based on diglycidyl ether of bisphenol A (DGEBA), polymerized with a liquid aromatic diamine based on diethyl toluene diamine (DETDA 80), and its blends with poly(ether imide) (PEI) at concentrations of 0–15 wt % were studied with differential scanning calorimetry under dynamic and isothermal conditions. The kinetic analyses were performed with a phenomenological approach. The reaction mechanism of the blends remained the same as that of the neat epoxy. However, the addition of PEI had a marked effect on the cure kinetics in the DGEBA/DETDA 80 system. The rate of reaction decreased with an increase in the thermoplastic content. Diffusion control was incorporated to describe the cure behavior of the blends in the latter stages. Greater diffusion control was observed as the PEI concentration increased and the cure temperature decreased. Polymer blends based on this epoxy/liquid aromatic diamine had not been previously studied from a kinetic viewpoint. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 660–672, 2005 相似文献
68.
Guadalupe Del C. Pizarro Oscar G. Marambio Manuel Jeria O Margarita Huerta Bernab L. Rivas 《应用聚合物科学杂志》2006,100(1):178-185
The free‐radical copolymerization of water‐soluble poly(1‐vinyl‐2‐pyrrolidone‐co‐hydroxyethylmethacrylate) was carried out with a feed monomer ratio of 75:25 mol %, and the total monomer concentration was 2.67M. The synthesis of the copolymer was carried out in dioxane at 70°C with benzoyl peroxide as the initiator. The copolymer composition was obtained with elemental analysis and 1H‐NMR spectroscopy. The water‐soluble polymer was characterized with elemental analysis, Fourier transform infrared, 1H‐ and 13C‐NMR spectroscopy, and thermal analysis. Additionally, viscosimetric measurements of the copolymer were performed. The thermal behavior of the copolymer and its complexes were investigated with differential scanning calorimetry (DSC) and thermogravimetry techniques under a nitrogen atmosphere. The copolymer showed high thermal stability and a glass transition in the DSC curves. The separation of various metal ions by the water‐soluble poly(1‐vinyl‐2‐pyrrolidone‐co‐hydroxyethylmethacrylate) reagent in the aqueous phase with liquid‐phase polymer‐based retention was investigated. The method was based on the retention of inorganic ions by this polymer in a membrane filtration cell and subsequent separation of low‐molar‐mass species from the polymer/metal‐ion complex formed. Poly(1‐vinyl‐2‐pyrrolidone‐co‐hydroxyethylmethacrylate) could bind metal ions such as Cr(III), Co(II), Zn(II), Ni(II), Cu(II), Cd(II), and Fe(III) in aqueous solutions at pHs 3, 5, and 7. The retention percentage for all the metal ions in the polymer was increased at pH 7, at which the maximum retention capacity could be observed. The interaction of inorganic ions with the hydrophilic polymer was determined as a function of the pH and filtration factor. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 178–185, 2006 相似文献
69.
玻璃形成能力(GFA)是判断合金非晶态结构形成的重要指标。利用甩带快冷技术制备了Mg70(Ni3RE)30(RE=La、Ce、Pr、Nd、Y)非晶合金条带(宽5 mm,厚0.2 mm),通过差示扫描量热技术(DSC)表征了合金条带的非晶结构转变及其热稳定性。从原子尺度,对合金的原子尺寸参数(δ)、电负性差(Δx)以及原子结构参数(λ)进行了计算和分析。实验数据和理论分析结果表明:RE=Pr时,相应合金的玻璃形成能力最大,RE=Y的最小,其大小次序为:Mg70(Ni3Pr)30〉Mg70(Ni3la)30〉Mg70(Ni3Ce)30〉Mg70(Ni3Nd)30〉Mg70(Ni3Y)30,影响Mg70(Ni3RE)30非晶合金玻璃形成能力的主要因素是电负性差,原子尺寸参数和原子结构参数的作用次之。 相似文献
70.
张小宁 《上海电力学院学报》2010,(3)
为改善累积发光驱动方法显示静态图像时的灰度级轮廓,提出了一种基于有效灰度级均匀分割采样的动态子场编码(DSC)算法。首先对输入图像中的孤立灰度区间进行灰度采样,然后对剩余灰度级均匀分割,选择各灰度区间概率密度较大的灰度级作为采样灰度级,相邻采样灰度级之差即为子场编码权值,从而使采样灰度级均匀分布在输入图像的有效灰度区间,并使采样灰度级和子场编码权值随图像变化。仿真和实验结果表明,该算法不仅能真实再现大面积的背景,而且使图像细节信息尽可能保留,显著减小了静态图像的轮廓。 相似文献