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11.
Norio Maruyama Sachiko Hiromoto Eiji Akiyama Morihiko Nakamura 《Science and Technology of Advanced Materials》2013,14(2)
AbstractFretting fatigue behaviour of Ni-free high-nitrogen steel (HNS) with a yield strength of about 800 MPa, which was prepared by nitrogen gas pressurized electroslag remelting, was studied in air and in phosphate-buffered saline (PBS(-)). For comparison, fretting fatigue behaviour of cold-rolled SUS316L steel (SUS316L(CR)) with similar yield strength was examined. The plain fatigue limit of HNS was slightly lower than that of SUS316L(CR) although the former had a higher tensile strength than the latter. The fretting fatigue limit of HNS was higher than that of SUS316L(CR) both in air and in PBS(-). A decrease in fatigue limit of HNS by fretting was significantly smaller than that of SUS316L(CR) in both environments, indicating that HNS has better fretting fatigue resistance than SUS316L(CR). The decrease in fatigue limit by fretting is discussed taking into account the effect of friction stress due to fretting and the additional influences of wear, tribocorrosion and plastic deformation in the fretted area. 相似文献
12.
Photoluminescence properties from water soluble CdSe/ZnS QDs encapsulated with hybrid trioctylphosphine-poly(acrylamide-co-acrylic acid)-ethanolamine (TOPO-PSMA-EA) shell have been investigated. It was found that PL efficiency of CdSe/ZnS QDs in water was increased 5–30% after introducing PSMA-EA polymers to encapsulate CdSe/ZnS-TOPO QDs. Higher PSMA concentrations were found to enhance the PL efficiency of QDs up to 1.8 folds, which is ascribed to a better packing and passivation of the TOPO-PSMA-EA shell over the QDs. Time-resolved photoluminescence suggested that the mean lifetime of photoexcited carriers in the water-soluble CdSe/ZnS-TOPO-PSMA-EA QDs elongated 2–17 ns compared with that of uncoated samples, indicating that PL quenching defects were effectively removed for CdSe/ZnS QDs with hybrid TOPO-PSMA-EA shell. 相似文献
13.
Hiromi Nabeshi Tomoaki Yoshikawa Akihiro Arimori Tokuyuki Yoshida Saeko Tochigi Toshiro Hirai Takanori Akase Kazuya Nagano Yasuhiro Abe Haruhiko Kamada Shin-ichi Tsunoda Norio Itoh Yasuo Yoshioka Yasuo Tsutsumi 《Nanoscale research letters》2011,6(1):1-6
In this study, complexes composed of poly-l-tyrosine (pLT) and single-walled carbon nanotubes (SWCNTs) were produced and the dispersibility of the pLT/SWCNT complexes in water by measuring the ζ potential of the complexes and the turbidity of the solution were investigated. It is found that the absolute value of the ζ potential of the pLT/SWCNT complexes is as high as that of SWCNTs modified with double-stranded DNA (dsDNA) and that the complexes remain stably dispersed in the water at least for two weeks. Thermogravimetry analysis (TGA) and visualization of the surface structures of pLT/SWCNT complexes using an atomic force microscope (AFM) were also carried out. 相似文献
14.
Koji Fushimi Takatoshi Shimada Hiroki Habazaki Hidetaka Konno Masahiro Seo 《Electrochimica acta》2011,(4):1773
Depassivation–repassivation of iron surfaces in boric–borate solutions were investigated by using the micro-indentation test. A pair of current peaks due to repair of the passive film following rupture of the film were observed during a series of indenter drives, i.e., loading and unloading of the indenter. The shape of the current peak depended on environmental conditions (conductivity and pH of the solution) and substrate conditions (mechanical processing history, alloyed element) as well as indentation conditions (repetition, maximum depth, and maximum load). Plastic deformation of the surface was accompanied by surface depassivation, while no depassivation occurred during the elastic deformation, indicating that the passive film on iron has a ductile property. The solution conditions did not affect the scale of depassivation but affected the rate of repassivation. Dislocations in the substrate made surface depassivation difficult but enhanced reactivity during the repassivation. The test also revealed that type-312L stainless steel has high corrosion resistance in a concentrated NaCl solution. 相似文献
15.
16.
Masayuki Ohta Keitaro Kondo Masayuki Matsunaka Hiroyuki Miyamaru Isao Murata Toshiyuki Iida Kentaro Ochiai Chikara Konno 《Fusion Engineering and Design》2009,84(7-11):1446-1449
Integral benchmark experiments with DT neutrons are not always sufficient for nuclear data benchmarking in the MeV region, below 10 MeV. A neutron spectrum shifter, which will be placed between a sample and a DT neutron source, is effective to moderate DT neutrons incident to the sample. In order to estimate effects of the spectrum shifter, the ratio of the contribution of 14 MeV neutrons in the leakage neutron and gamma-ray spectra was calculated with MCNP-4C for an experimental configuration at FNS of JAEA, Japan. The calculations were carried out for a Li2TiO3 sample with a Be, D2O, or 7LiD spectrum shifter. It was found out that the Be shifter was superior to others and the Be shifter was effective to decrease the contribution of 14 MeV neutrons especially for secondary gamma-ray spectrum measurements. 相似文献
17.
Chikara Konno Kentaro Ochiai Masayuki Wada Kosuke Takakura Satoshi Sato 《Fusion Engineering and Design》2009,84(7-11):1095-1098
In order to specify the best nuclear data on iron, the fusion neutronics benchmark experiment on iron at Japan Atomic Energy Agency (JAEA)/Fusion Neutronics Source (FNS) was analyzed in detail with MCNP-4C and the latest nuclear data libraries, JENDL-3.3, FENDL-2.1, JEFF-3.1 and ENDF/B-VII.0. As a result, totally the calculation result with ENDF/B-VII.0 agreed with the measurement best, except that it underestimated the measured neutron flux above 10 MeV with the depth. It was noted that the calculation result with JENDL-3.3 overestimated the measured neutrons below a few keV. Through the DORT calculations based on the iron data in ENDF/B-VII.0, it was found out that the first inelastic scattering cross-section data of 57Fe in JENDL-3.3 caused the overestimation. 相似文献
18.
Satoshi Akamaru Masanori Hara Norio Nunomura Masao Matsuyama 《International Journal of Hydrogen Energy》2013
The magnetic susceptibility and the pressure-composition isotherm were measured simultaneously for Pd–Rh–H and Pd–Ag–H systems in order to clarify the effect of Rh or Ag substitution on the hydrogen uptake from viewpoint of the electronic band structure. The magnetic susceptibility of all Pd binary alloys prepared decreased monotonically with increasing hydrogen content. At high hydrogen contents, the magnetic susceptibility became approximately zero for Pd–Rh–H and Pd–Ag–H system, and the hydrogen content at which the magnetic susceptibility gives zero corresponded with the terminal of the plateau region in the isotherm curve. The results indicated that the magnetic susceptibility of hydride phase was almost zero for all Pd binary alloys. On the basis of the band structure of Pd metal, we concluded that atom substitution only affected shift of the energy at Fermi level, and the amount of the hydrogen uptake was dominated by the number of unoccupied d-band in the alloys. 相似文献
19.
We studied the relationship between the structure of aromatic compounds and the overcharge protection effect, using cyclohexylbenzene, isopropylbenzene, and toluene as the overcharge protection agents. Cyclohexylbenzene proved to be the most effective overcharge protection agent among these aromatic compounds. The effect is enhanced using a higher concentration of cyclohexylbenzene and elevated temperatures. The reaction product of cyclohexylbenzene was analyzed using field desorption mass spectrometry to elucidate its reaction mechanism. The results suggested that some of the overcharge reaction products of CHB were more reactive than that of IPB, which is consistent with the better suppressing effect on overcharging of the active material in the positive electrode. 相似文献
20.
Synthesis and hydrophilic property of polypropylene-graft-poly(polyethylene glycol-methacrylate) (PP-g-P(PEGMA)) 总被引:1,自引:0,他引:1
Nobuo Kawahara Junji Saito Shingo Matsuo Hideyuki Kaneko Tomoaki Matsugi Norio Kashiwa 《Polymer Bulletin》2010,64(7):657-666
Polypropylene-graft-poly(polyethylene glycol-methacrylate) (PP-g-P(PEGMA)), which is a hydrophobic-hydrophilic graft copolymer, was synthesized by a combination of an atom transfer radical
polymerization (ATRP) of PEGMA with brominated polypropylene (PP-Br), which was synthesized from PP-OH prepared by metallocene-catalyzed
copolymerization. Its structure was confirmed by 1H NMR and GPC analyses. Transmission electron microscope (TEM) micrographs of PP-g-P(PEGMA) revealed the nanometer level microphase-separation morphology between the PP segment and the P(PEGMA) segment. The
obtained PP-g-P(PEGMA) showed water-absorbing property as well as thermostability. 相似文献