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排序方式: 共有245条查询结果,搜索用时 15 毫秒
1.
Phase separation which occurs in parallel to the hydrolysis and gelation of alkoxysilane solution containing poly(sodium styrenesulfonate) (NaPSS) has been investigated. Depending on the reaction conditions, gel morphologies such as isolated pores, particle aggregates, and interconnected continuous pores from 0.1 to 100 μm long have been observed. Time-resolved light scattering of gelling solution suggested the occurrence of spinodal phase separation through the polymerization of silica and the subsequent freezing of the developing structure by sol-gel transition. The effects of reaction parameters on the periodic size are explained mainly in terms of their influence on the "chemical cooling" rate which is determined by the polymerizatica rate of silica and the solubility of NaPSS in the reacting solution. 相似文献
2.
Lingyun Lyu Takeshi Hanada Naohiro Yamahira Jun Morita Ryota Yamamoto Ken Itomi Takumi Adachi Sho Kubouchi Shin Horiuchi 《应用聚合物科学杂志》2021,138(45):51443
The distribution of nano-sized silica in binary rubber blends is characterized by scanning transmission electron microscopy (STEM) tomography combined with energy dispersive X-ray spectrometry (EDX). 3D distribution of silica is visualized by STEM-EDX tomography with the tilt-series of silicon elemental maps, while the phase-separated morphologies of polyisoprene rubber (IR) and styrene-butadiene rubber (SBR) are visualized by STEM-tomography in high-angle-annular-dark field (HAADF) mode. The combination of STEM-EDX and STEM-HAADF tomography enables us to determine the distribution of silica between the two rubber phases quantitatively even with high contents of silica up to 70 phr (weight parts per hundred rubber). It is found that silica is preferentially distributed in the SBR phase, but it is also distributed in the IR phase when the IR fraction in the total rubber components is higher than 40 wt%. The preferential distribution of silica in the SBR phase improves the dispersion of the IR domains. This is the first use of this technique for a multicomponent polymer system, showing the advantage to characterize the complicated multicomponent polymer composite morphologies. 相似文献
3.
Molecular monolayer nanotubes produced by self‐assembly of an amphiphile modified with a 2‐nitrobenzyl group as a photoresponsive unit are able to encapsulate dinucleotides via electrostatic attraction. Upon photoirradiation, the 18 nm inner diameter of the nanotubes shrinks to less than 2 nm as a result of photochemical cleavage of the 2‐nitrobenzyl group in the amphiphile. This shrinking of the nanotube channels leads to a propulsive release of the dinucleotides into the bulk solution and simultaneously accelerates formation of the dinucleotide duplexes. The larger nanotube channels without photoirradiation merely release each dinucleotide into the bulk solution, indicating that the squeezing via transportation in the narrow nanotube channels is necessary for duplex formation. In addition to the size effect, water with a lower polarity confined within the narrow nanotube channels helps to stabilize the energetically unfavorable hydrogen‐bonded base pair between the dinucleotides. This system should enable researchers to perform biological reactions that occur only in specific environments and conditions in living organisms. 相似文献
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5.
Islam Z Capatina D Ruff JP Das RK Trakhtenberg E Nojiri H Narumi Y Welp U Canfield PC 《The Review of scientific instruments》2012,83(3):035101
We present a pulsed-magnet system that enables x-ray single-crystal diffraction in addition to powder and spectroscopic studies with the magnetic field applied on or close to the scattering plane. The apparatus consists of a single large-bore solenoid, cooled by liquid nitrogen. A second independent closed-cycle cryostat is used for cooling samples near liquid helium temperatures. Pulsed magnetic fields close to ~30 T with a zero-to-peak-field rise time of ~2.9 ms are generated by discharging a 40 kJ capacitor bank into the magnet coil. The unique characteristic of this instrument is the preservation of maximum scattering angle (~23.6°) on the entrance and exit sides of the magnet bore by virtue of a novel double-funnel insert. This instrument will facilitate x-ray diffraction and spectroscopic studies that are impractical, if not impossible, to perform using split-pair and narrow-opening solenoid magnets. Furthermore, it offers a practical solution for preserving optical access in future higher-field pulsed magnets. 相似文献
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7.
Kazuyuki Ishikawa Naohiro Kameta Masaru Aoyagi Masumi Asakawa Toshimi Shimizu 《Advanced functional materials》2013,23(13):1606-1606
8.
Cooperative Control by System Voltage Control Equipments in Consideration of Reducing Capacity of STATCOM 下载免费PDF全文
Shoji Kawasaki Naohiro Kurokawa Hisao Taoka Yuya Nakashima 《Electrical Engineering in Japan》2016,194(1):1-9
In recent years, the number of renewable energy sources (RESs) such as photovoltaic generation systems and wind power generation systems connected to the grid has been increasing as a way of reducing negative effects on the environment. The outputs of these RESs vary rapidly because of the influence of the weather and the conditions of the location. Therefore, there are concerns that the point voltages in a distribution system may vary drastically and that the voltages may deviate from the appropriate voltage range as a result of the influence of the RES connected to the distribution system or to the diversification of loads. Furthermore, there are concerns about adverse effects on electric power quality, such as voltage imbalances and harmonics. In this paper, we propose a cooperative voltage control method for a distribution system using system voltage control equipment in order to reduce the capacity of the static synchronous compensator. Numerical calculations were performed in order to verify the validity of the proposed method. 相似文献
9.
Kazuyuki Ishikawa Naohiro Kameta Mitsutoshi Masuda Masumi Asakawa Toshimi Shimizu 《Advanced functional materials》2014,24(5):603-609
Boroxines, (R‐BO)3, which can be easily synthesized via a dehydration reaction of boronic acids, R–B(OH)2, selectively self‐assemble in toluene into nanofibers, nanorods, nanotapes, and nanotubes, depending on the aromatic substituent (R). Spectroscopic measurements show that the nanotube consists of a J‐aggregate of the boroxine. Humidification converts the morphology from the nanotube to a sheet as a result of the hydrolysis of the boroxine components and subsequent molecular‐packing rearrangement from the J‐aggregate to an H‐aggregate. Such a transformation leads to the compulsive release of guest molecules encapsulated in the hollow cylinder of the nanotube. The hydrolysis and the molecular‐packing rearrangement described above are suppressed by coordination of pyridine to the boron atom, with the resulting moiety acting as a Lewis acid of the boroxine component. The pyridine‐coordinated nanotube is transformed into a helical coil by humidification. Guest release during the nanotube‐to‐helical‐coil transformation is much slower than during the nanotube‐to‐sheet transformation, but faster than from a nanotube that did not undergo morphological transformation. The storage and release of guest molecules from the boroxine nanotubes can be precisely controlled by adjusting the moisture level and the concentration of Lewis bases, such as amines. 相似文献
10.
Naohiro Gotoh Shino Miyake Hiroko Takei Kumi Sasaki Saori Okuda Michitaka Ishinaga Shun Wada 《Food Analytical Methods》2011,4(4):525-530
We developed a simple method for quantification of the peroxide value (PV) in colored lipids on the basis of the reaction
between triphenylphosphine (TPP) and oxidized oil to afford triphenylphosphineoxide (TPPO). Diphenylphosphineoxide (DPPO)
was employed as internal standard. The formed TPPO was analyzed by high-pressure liquid chromatography–UV spectroscopy with
absorption at 260 nm. The conditions that gave the highest correlative calibration curve between the peak area on the chromatogram
and peroxide value were identified: the optimum TPP–oxidized oil mix ratio, reaction temperature, and reaction time were found
to be 2:1, 40 °C, and 30 min, respectively. Linear calibration curves, passing through the origin, were obtained for PV versus
TPPO and TPPO versus DPPO. The quantification limit for this method was 2.01 pmol hydroperoxyl group, which corresponds to
a PV value of 0.2 meq/kg in a 10-mg oil sample. This method was used to measure the PV in colored fats and oils or lipids
extracted from dark meat and processed food containing a coloring agent. Though the official method could not measure the
PVs in the colored lipids, the method proposed here, which uses an inexpensive chemical reagent and machine, could. The developed
method could play an important role for food quality control. 相似文献