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21.
Attempts were carried out to enhance the surface hydrophilicity of poly(L ‐lactide), that is, poly(L ‐lactic acid) (PLLA) film, utilizing enzymatic, alkaline, and autocatalytic hydrolyses in a proteinase K/Tris–HCL buffered solution system (37°C), in a 0.01N NaOH solution (37°C), and in a phosphate‐buffered solution (100°C), respectively. Moreover, its chain‐scission mechanisms in these different media were studied. The advancing contact‐angle (θa) value of the amorphous‐made PLLA film decreased monotonically with the hydrolysis time from 100° to 75° and 80° without a significant molecular weight decrease, when enzymatic and alkaline hydrolyses were continued for 60 min and 8 h, respectively. In contrast, a negligible change in the θa value was observed for the PLLA films even after the autocatalytic hydrolysis was continured for 16 h, when their bulk Mn decreased from 1.2 × 105 to 2.2 × 104 g mol?1 or the number of hydrophilic terminal groups per unit weight increased from 1.7 × 10?5 to 9.1 × 10?5 mol g?1. These findings, together with the result of gravimetry, revealed that the enzymatic and alkaline hydrolyses are powerful enough to enhance the practical surface hydrophilicity of the PLLA films because of their surface‐erosion mechanisms and that its practical surface hydrophilicity is controllable by varying the hydrolysis time. Moreover, autocatalytic hydrolysis is inappropriate to enhance the surface hydrophilicity, because of its bulk‐erosion mechanism. Alkaline hydrolysis is the best to enhance the hydrophilicity of the PLLA films without hydrolysis of the film cores, while the enzymatic hydrolysis is appropriate and inappropriate to enhance the surface hydrophilicity of bulky and thin PLLA materials, respectively, because a significant weight loss occurs before saturation of θa value. The changes in the weight loss and θa values during hydrolysis showed that exo chain scission as well as endo chain scission occurs in the presence of proteinase K, while in the alkaline and phosphate‐buffered solutions, hydrolysis proceeds via endo chain scission. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 87: 1628–1633, 2003 相似文献
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Radial distribution of particle velocities, solids circulation rate and radial variation in bed voidage in a jet-spouted bed were investigated in a 0.2 m diameter conical-cylindrical column. The upward particle velocity is strongly dependent on gas velocity and its radial profile is the Gaussian. The solids circulation rates are of the same order of magnitude as those in a conventional spouted bed and are proportional to the gas velocity. Estimation of the variation in bed voidage in the radial direction revealed that the annulus voidage of about 0.90 was greater than the spout voidage of around 0.70. This tendency is contrary to that in a conventional spouted bed. 相似文献
24.
Uniaxially oriented thin films of poly(ethylene terephthalate) (PET), poly(ethylene 2,6-naphthalene dicarboxylate) (PEN) and their blends were prepared by applying shear strain to their respective melts, and the resulting morphologies were studied by transmission electron microscopy. Selected-area electron diffraction of each film revealed well-defined uniaxial orientation of polymer chains in the shearing direction. In the uniaxially oriented thin film of PEN, stacked-lamellar structure with the average long period of 27 nm consisting of a crystalline region about 15 nm thick and an amorphous one about 12 nm thick was found here and there in the dark-field image: PEN-type. On the other hand, stacked-lamellar structure was rarely observed in the case of PET: PET-type. In PET/PEN blends, the morphologies changed from the PET-type to the PEN-type with increasing content of PEN. 相似文献
25.
Tribological Characteristics of SiC Ceramics in High-Temperature and High-Pressure Water 总被引:2,自引:0,他引:2
Satoshi Kitaoka Toshihide Tsuji Toshio Katoh Yoshimi Yamaguchi† Kazumi Kashiwagi 《Journal of the American Ceramic Society》1994,77(7):1851-1856
The effects of temperature and sliding speed on the tribological behavior of a SiC ceramic by sliding on the same material in deoxygenated water were investigated from room temperature to 300°C under the corresponding saturated vapor pressures. The friction coefficient and specific wear rates of both plates and disks increased at elevated temperatures at all sliding speeds, but decreased with increasing sliding speed at 120° and 300°C. Fine mirrorlike worn surfaces were observed without wear debris under all sliding conditions. The wear mechanism appears to consist of hydrothermal oxidation of SiC and dissolution of reaction products such as silica. 相似文献
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Development of flexible displays using back‐channel‐etched In–Sn–Zn–O thin‐film transistors and air‐stable inverted organic light‐emitting diodes 下载免费PDF全文
Mitsuru Nakata Genichi Motomura Yoshiki Nakajima Tatsuya Takei Hiroshi Tsuji Hirohiko Fukagawa Takahisa Shimizu Toshimitsu Tsuzuki Yoshihide Fujisaki Toshihiro Yamamoto 《Journal of the Society for Information Display》2016,24(1):3-11
We developed flexible displays using back‐channel‐etched In–Sn–Zn–O (ITZO) thin‐film transistors (TFTs) and air‐stable inverted organic light‐emitting diodes (iOLEDs). The TFTs fabricated on a polyimide film exhibited high mobility (32.9 cm2/Vs) and stability by utilization of a solution‐processed organic passivation layer. ITZO was also used as an electron injection layer (EIL) in the iOLEDs instead of conventional air‐sensitive materials. The iOLED with ITZO as an EIL exhibited higher efficiency and a lower driving voltage than that of conventional iOLEDs. Our approach of the simultaneous formation of ITZO film as both of a channel layer in TFTs and of an EIL in iOLEDs offers simple fabrication process. 相似文献
28.
Naoki Sakamoto Mitsuru Higashimori Toshio Tsuji Makoto Kaneko 《Intelligent Service Robotics》2009,2(1):53-60
This paper discusses an optimum design approach on robotic food handling by considering the characteristics of viscoelasticity
of object. We pick up a traditional Japanese food, “Norimaki” as a typical example with the viscoelastic characteristics.
We first show that the dynamic characteristics of Norimaki can be expressed by utilizing the Burger model. After testing the
parameter sensitivity, we show an example of the optimum design for determining the combination of the hand stiffness and
the operating velocity. We further show that the resultant plastic deformation can be formulated with the exact solution. 相似文献
29.
H. Watanabe K. Hirota O. Yamaguchi S. Inamura H. Miyamoto N. Shiokawa K. Tsuji 《Journal of Materials Science》1994,29(14):3719-3723
In compositions having ZrO2/Y2O3=(74.25–71.25)/(0.75–3.75) (mol% ratio) with 25 mol% Al2O3, metastable t-ZrO2 solid solutions crystallize at 780° to 860°C from amorphous materials prepared by the simultaneous hydrolysis of zirconium, yttrium and aluminium acetylacetonates. Hot isostatic pressing has been performed for 1 h at 1130 and 1230°C under 196 MPa using their powders. Two kinds of material are fabricated: (i) perfect ZrO2 solid-solution ceramics and (ii) composites of ZrO2 solid solution and -Al2O3. Their mechanical properties are examined, in connection with microstructures and t/m ZrO2 ratios. Composites with a homogeneous dispersed -Al2O3 derived from solid-solution ceramics result in a remarkable increase of strength. 相似文献
30.
K. Nishizawa H. Kato K. Mimori T. Yoshida N. Hasegawa M. Tsuji Y. Tamaura 《Journal of Materials Science》1994,29(3):768-772
Methanation reactivity was studied for the surface carbon deposited from CO2 on the surface of Rh-bearing activated magnetite. The most active material (Rh=0.83 wt %) for methanation was prepared by the impregnation method at 60°C and showed 98% conversion at 300°C. The surface carbon was composed of elemental carbon (-carbon) and polymerized carbon (-carbon), the proportion being dependent on the density of carbon deposited. In temperature-programmed surface reaction, the extent of conversion of the - and -carbon to CH4 was 0.34 (-carbon) and 0.53 (-carbon), respectively, and the total conversion was 0.87. This result indicates that not only elemental carbon but polymerized carbon (-carbon) could be converted to CH4 on the Rh-bearing activated (-carbon) magnetite, whereas -carbon is not hydrogenated on activated magnetite. 相似文献