全文获取类型
收费全文 | 17230篇 |
免费 | 2660篇 |
国内免费 | 1407篇 |
专业分类
电工技术 | 2659篇 |
综合类 | 2663篇 |
化学工业 | 2028篇 |
金属工艺 | 283篇 |
机械仪表 | 971篇 |
建筑科学 | 543篇 |
矿业工程 | 256篇 |
能源动力 | 347篇 |
轻工业 | 671篇 |
水利工程 | 301篇 |
石油天然气 | 560篇 |
武器工业 | 168篇 |
无线电 | 2327篇 |
一般工业技术 | 1324篇 |
冶金工业 | 401篇 |
原子能技术 | 130篇 |
自动化技术 | 5665篇 |
出版年
2024年 | 37篇 |
2023年 | 200篇 |
2022年 | 349篇 |
2021年 | 519篇 |
2020年 | 569篇 |
2019年 | 562篇 |
2018年 | 582篇 |
2017年 | 604篇 |
2016年 | 724篇 |
2015年 | 782篇 |
2014年 | 1071篇 |
2013年 | 1156篇 |
2012年 | 1480篇 |
2011年 | 1445篇 |
2010年 | 1094篇 |
2009年 | 1121篇 |
2008年 | 1083篇 |
2007年 | 1203篇 |
2006年 | 1091篇 |
2005年 | 859篇 |
2004年 | 701篇 |
2003年 | 714篇 |
2002年 | 555篇 |
2001年 | 404篇 |
2000年 | 358篇 |
1999年 | 299篇 |
1998年 | 257篇 |
1997年 | 187篇 |
1996年 | 196篇 |
1995年 | 171篇 |
1994年 | 152篇 |
1993年 | 123篇 |
1992年 | 108篇 |
1991年 | 92篇 |
1990年 | 74篇 |
1989年 | 69篇 |
1988年 | 49篇 |
1987年 | 34篇 |
1986年 | 18篇 |
1985年 | 30篇 |
1984年 | 21篇 |
1983年 | 24篇 |
1982年 | 28篇 |
1981年 | 16篇 |
1979年 | 5篇 |
1978年 | 6篇 |
1977年 | 9篇 |
1964年 | 10篇 |
1963年 | 6篇 |
1961年 | 5篇 |
排序方式: 共有10000条查询结果,搜索用时 19 毫秒
81.
Rheological and thermal properties of saponified cassava starch‐g‐poly(acrylamide) superabsorbent polymers varying in grafting parameters and absorbency 下载免费PDF全文
Cassava starch‐graft‐poly(acrylamide) superabsorbent polymers (SAPs) with varying absorbencies were synthesized. Weight average molecular weight (Mw) of the hydrolyzed starch‐graft‐copolymers ranged from 1.6 × 106 to 2.8 × 106 g/mol, the largest being shown by the sample with highest percentage grafting. The storage (G′) and loss modulus (G″) of hydrogels were determined as a function of frequency. G″ was larger than G′ for the hydrogels with higher absorbencies and exhibited a liquid‐like behavior. However, hydrogels with lower absorbencies showed a reverse viscoelastic behavior. The viscosity of hydrogels determined using a Brookfield viscometer at different shear rates was found to be larger for the hydrogels with higher absorbencies. The melting temperature (Tm) and enthalpy change of fusion (ΔHf) of the SAPs ranged from 149.7 to 177.7°C and 65 to 494.9 J/g, respectively and showed a positive correlation with grafting parameters and Mw. Heavy metal ion removal capacity of hydrogel followed the order Cu2+ > Pb2+ > Zn2+. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40368. 相似文献
82.
Isothermal and non‐isothermal crystallization of poly(L‐lactic acid)/poly(butylene terephthalate) blends 下载免费PDF全文
Isothermal and non‐isothermal crystallization kinetics of poly(l ‐lactic acid)/poly(butylene terephthalate) (PLLA/PBT) blends containing PLLA as major component is detailed in this contribution. PLLA and PBT are not miscible, but compatibility of the polymer pair is ensured by interactions between the functional groups of the two polyesters, established upon melt mixing. Crystal polymorphism of the two polyesters is not influenced by blending, as probed by wide‐angle X‐ray analysis. The addition of PLLA does not affect the temperature range of crystallization kinetics of PBT, nor the crystallinity level attained when the blends are cooled from the melt at constant rate. Conversely, PBT favors crystallization of the biodegradable polyester. The addition of PBT results in an anticipated onset of crystallization of PLLA during cooling at a fixed rate, with a sizeable enhancement of the crystal fraction. Isothermal crystallization analysis confirmed the faster crystallization rate of PLLA in the presence of PBT. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40372. 相似文献
83.
Thermotropic systems with fixed domains exhibiting enhanced overheating protection performance 下载免费PDF全文
Within this study, a time saving photo‐initiated miniemulsion polymerization process (duration of polymerization was 15 min) was established in order to encapsulate a paraffin wax with an acrylate polymer shell. The obtained freeze‐dried latex was an off‐white powder exhibiting spherical particles with mean diameters around 400 nm and a concentration of paraffin wax around 56%. Mixing the reaction product with a UV‐curable resin matrix resulted in thermotropic overheating protection glazings with high light‐shielding efficiency. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40417. 相似文献
84.
Study of polyarylene ether nitrile terminated with phthalonitrile/hybrid Fe3O4 nanospheres composites by orthogonal experiments 下载免费PDF全文
A novel series of composites of polyarylene ether nitrile terminated with phthalonitrile (PEN‐t‐Ph) filled with hybrid Fe3O4 nanospheres (h‐Fe3O4) was prepared via in situ composition. Based on the cross‐linking interactions between the phthalonitrile at the end of PEN‐t‐Ph molecular chains and the phthalonitrile on the surface of h‐Fe3O4 particles to form phthalocyanine ring, it was shown that the PEN‐t‐Ph/h‐Fe3O4 system had superior interfacial compatibility and the h‐Fe3O4 particles were locked in the matrix resin. These results had been confirmed by scanning electron microscope analysis. By orthogonal experiments and statistic analysis, the optimal conditions of cure temperature, type of h‐Fe3O4 and content of h‐Fe3O4 had been determined. Meanwhile, the results of range analysis and variance analysis indicated that the cure temperature had great effects on the thermal properties. Thermal studies revealed that the glass transition temperature of PEN‐t‐Ph/h‐Fe3O4 cured at 320°C was 214.7°C, increased by about 40°C compared to the PEN‐t‐Ph/h‐Fe3O4 without heat treatment, and the temperature corresponding to the weight loss of 5 wt % was increased by about 20°C. Mechanical measurements indicated that PEN‐t‐Ph/h‐Fe3O4 cured at 320°C possesses excellent mechanical properties with tensile strength of 93.33 MPa and tensile modulus of 2414.05 MPa, 9.91 MPa, 355.76 MPa higher than pure PEN‐t‐Ph film cured at 320°C, and 13.26 MPa, 397.90 MPa higher than PEN‐t‐Ph/h‐Fe3O4 without heat treatment. Most importantly, the presence of h‐Fe3O4 particles endows PEN‐t‐Ph/h‐Fe3O4 system with good magnetic property. Thus, PEN‐t‐Ph/h‐Fe3O4 cured at 320°C may have potential applications in field of magnetic materials. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40418. 相似文献
85.
The aim of research was to elaborate the non‐biodegradable (made of polypropylene (PP)) and resorbable (made of polylactide (PLA)) tubular fibrous structures for the reconstruction of the vascular vessels. For the mentioned structures design, nonconventional manufacturing techniques such as melt blown, melt electrospinning, and melt electroblowing were used. Three techniques were chosen as methods allowing on the fibrous structures manufacture containing fibers in nano‐ or submicro‐size diameter. Other advantages of free‐solvent technique use is the reduction in the clinical adverse events associated with solvent resided in the fibrous structure during the fabrication. The tubular fibrous structures of PP and PLA using above‐mentioned techniques were designed. In first stage, the analysis of the processing parameters influence on the nonbiodegradable and biodegradable tubular structures fiber diameter was performed. Subsequently, the validation step was the analysis of the influence of processing parameters on PP and PLA structural properties for each manufacturing techniques was investigated. The research results confirmed the ability of the tubular structures manufacture with various fiber diameter depending on the applied technique and processing parameters. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40147. 相似文献
86.
Nonisothermal crystallization kinetics of highly‐filled polyolefin composites was studied by means of differential scanning calorimetry (DSC). Two types of commercial calcium carbonate based fillers (modified with stearic acid and nonmodified one) were used for our investigations. In order to evaluate the crystallization kinetics changes of composites, the Avrami theory modified by Jeziorny was used. Validity of mineral fillers modification with stearic acid has been proved by thermal analysis. Because of the suppression of the heterogeneous nucleation effect resulting from calcium carbonate with stearic acid modification, an increase in the processability of highly‐filled polyolefin cast films might occur. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 41201. 相似文献
87.
Fabrication,characterization, and properties of poly(ethylene‐co‐vinyl acetate)/magnetite nanocomposites 下载免费PDF全文
M. T. Ramesan 《应用聚合物科学杂志》2014,131(7)
Poly(ethylene‐co‐vinyl acetate) (EVA)/magnetite (Fe3O4) nanocomposite was prepared with different loading of Fe3O4 nanoparticles. The mixing and compounding were carried out on a two‐roll mixing mill and the sheets were prepared in a compression‐molding machine. The effect of loading of nanoparticles in EVA was investigated thoroughly by different characterization technique such as transmission electron microscopy (TEM), X‐ray diffraction (XRD), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), limiting oxygen index (LOI), and technological properties. TEM analysis showed the uniform dispersion of filler in the polymer matrix and the dispersion of filler decreased with increase in filler content. XRD of the nanocomposite revealed the more ordered structure of the polymer chain. An appreciable increase in glass transition temperature was observed owing to the restricted mobility of Fe3O4‐filled EVA nanocomposite. TGA and flame resistance studies indicated that the composites attain better thermal and flame resistance than EVA owing to the interaction of filler and polymer segments. Mechanical properties such as tensile strength, tear resistance, and modulus were increased for composites up to 7 phr of filler, which is presumably owing to aggregation of Fe3O4 nanoparticle at higher loading. The presence of Fe3O4 nanoparticles in the polymer matrix reduced the elongation at break and impact strength while improved hardness of the composite than unfilled EVA. The change in technological properties had been correlated with the variation of polymer–filler interaction estimated from the swelling behavior. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40116. 相似文献
88.
Electroactive behavior assessment of poly(acrylic acid)‐graphene oxide composite hydrogel in the detection of cadmium 下载免费PDF全文
Areli Bejarano‐Jiménez Vladimir A. Escobar‐Barrios J. Mieke Kleijn Cesar A. Ortíz‐Ledón Luis F. Cházaro‐Ruiz 《应用聚合物科学杂志》2014,131(19)
Super absorbent polymers of acrylic acid‐graphene oxide (PAA‐GO) were synthesized with different percentage of chemical neutralization (0, 10, and 20%) of the acrylic acid monomer before its polymerization. The influence of their swelling and adsorption/desorption capacity of cadmium ions in aqueous solutions were studied and revealed that the GO enables greater mechanical stability in the materials. The PAA hydrogels, with the same degrees of neutralization, were also prepared without GO to compare with the composites. Additionally, carbon paste electrodes (CPE) modified with the composites PAA‐GO were used to asses and compare their adsorption properties with cadmium(II). The anodic stripping voltammetry (ASV) peak, in the differential pulse voltammetry mode, for cadmium oxidation was found to be influenced by the presence of GO into the polymer, and also by their percentage of neutralization. The accumulation of cadmium(II) on the surface of the modified CPEs was performed under open‐circuit conditions taking an account the preconcentration time of the metal cation. The presence of GO enhances the electrical signal of the electrodes in short times of immersion in cadmium(II) solutions. This property contributed to get linear responses of the CPEs modified with the composites, which were influenced by their degrees of neutralization. The PAA‐GO 10N electrode with 10% of neutralization combined the influence of GO and the degree of neutralization in the same matrix, and also showed good performance in terms of its mechanical stability, it was chosen for preliminary studies on the selectivity of the electrode toward Zn(II) and Cu(II). © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40846. 相似文献
89.
Nonisothermal crystallization kinetics of poly(butylene terephthalate)/multiwalled carbon nanotubes nanocomposites prepared by in situ polymerization 下载免费PDF全文
Poly(butylene terephthalate)/multiwalled carbon nanotubes (PBT/MWNT) nanocomposites were prepared by in situ ring‐opening polymerization of cyclic butylene terephthalate oligomers (CBT). The nonisothermal crystallization behavior of the neat PBT and the PBT/MWNT nanocomposites was analyzed quantitatively. The results reveal that the combined Avrami/Ozawa equation exhibits great advantages in describing the nonisothermal crystallization of PBT and its nanocomposites. The presence of MWNTs has the nucleation effect promoting crystallization rate for the nanocomposites, and the maximum one is observed in the nanocomposite having 0.75 wt % MWNT content. On the other hand, the addition of MWNTs has the impeding effect reducing the chain mobility and retarding crystallization, which is confirmed by the crystallization activation energies. However, the nucleation effect of MWNTs plays the dominant role in the crystallization of PBT/MWNT nanocomposites, in other words, the incorporation of MWNTs is increasing the crystallization rate of the nanocomposites. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40849. 相似文献
90.
Toughening‐modified epoxy‐amine system: Cure kinetics,mechanical behavior,and shape memory performances 下载免费PDF全文
Shape memory epoxy resins are derived on reacting E51 with triethylenetetramine in presence of the toughening agent polypropylene glycol diglycidyl ether (PPGDGE). The curing behaviors are studied with differential scanning calorimetry. The toughening system shows a decrease in activation energy. ?esták–Berggren model is utilized to establish the kinetic equations. The fitting results prove that the equations can well describe the reactions. Tensile tests and dynamic mechanical analysis are used to analyze mechanical performances and thermodynamics. Shape memory properties are characterized by fold‐deploy tests. The elongation at break increases as the concentration of PPGDGE increases. The toughening materials have lower glass transition temperature (Tg). The fixable ratios of all systems are greater than 99.5%. The shape recovery time decreases with increasing the PPGDGE concentration. The optimal system can fully recover its original shape in about 2 min at Tg + 30°C, and exhibit the maximum fold‐deploy cycles as 13 cycles. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40853. 相似文献