全文获取类型
收费全文 | 1850篇 |
免费 | 34篇 |
国内免费 | 5篇 |
专业分类
电工技术 | 72篇 |
综合类 | 5篇 |
化学工业 | 359篇 |
金属工艺 | 66篇 |
机械仪表 | 22篇 |
建筑科学 | 38篇 |
能源动力 | 88篇 |
轻工业 | 124篇 |
水利工程 | 3篇 |
石油天然气 | 3篇 |
无线电 | 196篇 |
一般工业技术 | 380篇 |
冶金工业 | 341篇 |
原子能技术 | 47篇 |
自动化技术 | 145篇 |
出版年
2023年 | 4篇 |
2022年 | 20篇 |
2021年 | 25篇 |
2020年 | 17篇 |
2019年 | 24篇 |
2018年 | 28篇 |
2017年 | 21篇 |
2016年 | 27篇 |
2015年 | 17篇 |
2014年 | 61篇 |
2013年 | 67篇 |
2012年 | 64篇 |
2011年 | 74篇 |
2010年 | 73篇 |
2009年 | 87篇 |
2008年 | 85篇 |
2007年 | 80篇 |
2006年 | 81篇 |
2005年 | 53篇 |
2004年 | 53篇 |
2003年 | 47篇 |
2002年 | 50篇 |
2001年 | 48篇 |
2000年 | 23篇 |
1999年 | 28篇 |
1998年 | 127篇 |
1997年 | 82篇 |
1996年 | 90篇 |
1995年 | 47篇 |
1994年 | 42篇 |
1993年 | 34篇 |
1992年 | 23篇 |
1991年 | 27篇 |
1990年 | 28篇 |
1989年 | 22篇 |
1988年 | 26篇 |
1987年 | 21篇 |
1986年 | 18篇 |
1985年 | 18篇 |
1984年 | 8篇 |
1983年 | 10篇 |
1982年 | 14篇 |
1981年 | 7篇 |
1980年 | 19篇 |
1979年 | 12篇 |
1978年 | 10篇 |
1977年 | 10篇 |
1976年 | 11篇 |
1973年 | 5篇 |
1965年 | 3篇 |
排序方式: 共有1889条查询结果,搜索用时 15 毫秒
61.
Sequential anodic and cathodic pulse voltages were applied on anodised Al micro-electrodes in alkaline silicate electrolyte to explore the role of cathodic pulse in AC or bipolar plasma electrolytic oxidation (PEO) process. SEM observation was carried out to observe the sites of anodic and cathodic breakdown and their morphologies. The prior anodic breakdown accelerated the cathodic breakdown at ?50 V, and the acceleration was associated with the preferential cathodic breakdown at the anodic breakdown sites. However, the succeeding anodic breakdown during applying anodic pulse of 420 V for 2 ms was highly suppressed at the cathodic breakdown sites. This would randomise the anodic breakdown sites. Such role may contribute to the formation of rather uniform coatings on aluminium in this electrolyte without large discharge channels when larger cathodic current is applied with respect to the anodic current in AC PEO. 相似文献
62.
Susumu Fujii Masato Yoshiya Akuto Yumura Yohei Miyauchi Masahiro Tada Hideyuki Yasuda 《Journal of Electronic Materials》2014,43(6):1905-1915
The phonon thermal conductivity of misfit-layered Ca3Co4O9 has been calculated by perturbed molecular dynamics using a classical force field. Detailed numerical analyses reveal that, in spite of its smaller cross-sectional area, the CoO2 layer transports more heat than the thicker rock salt (RS) layer, although its local thermal conduction is more suppressed than in another layered cobaltite, Na x CoO2. The origins of these differences have been elucidated through careful examination of the atomic arrangements in each layer. Since thermal conduction in the RS layer can be reduced without deteriorating electronic properties for which the CoO2 layer is responsible, it is suggested that the RS layer should be modified to further suppress the overall in-plane thermal conductivity. Computational experiments with increasing number of Ca–O planes in the RS layer showed the opposite trend to what can be predicted based on the misfit between two dissimilar layers. Further analyses to reveal the origin of these unexpected results provide yet another strategy to further decrease the thermal conductivity, namely to control the dynamic interference between atoms across the interface between two layers. 相似文献
63.
Toshiki Ozaki Tatsuya KotoTam V. Nguyen Hideyuki NakanishiTomohisa Norisuye Qui Tran-Cong-Miyata 《Polymer》2014
Influence of the Trommsdorff–Norrish (T–N) effect on the phase separation of methyl methacrylate (MMA)/poly(ethyl acrylate) (PEA) mixtures undergoing photo-polymerization was examined by a combination of several experimental techniques. By FT-IR spectroscopy, it was found that the polymerization conversion explosively increases at the onset of this T–N effect. The characteristic irradiation time τ at which this effect occurs, strongly depends on the light intensity and gradually shifts to early time as the irradiation intensity increases. The shrinkage of the mixture observed in situ by laser-scanning confocal microscopy exhibits a transition at a particular irradiation time which is slightly longer than the characteristic time τ. By gel permeation chromatography (GPC), it was found that the molecular weight of the resulting PMMA was almost unchanged before τ and suddenly increases about an order of magnitude after the onset of the auto-acceleration effect. Finally, the characteristic length scales of the morphology also quickly increase with irradiation time and are eventually frozen by this T–N effect. These experimental results indicate that the Trommsdorff–Norrish effect plays an important role in the kinetic processes of polymerization-induced phase separation, suggesting an efficient tool to control the morphology of the polymerizing mixture. 相似文献
64.
Poly(3-hexylthiophene-2,5-diyl) is among the most widely used conjugated polymers for opto-electronic applications. To enhance its properties, researchers have attempted to nanostructure this polymer using various processes including breath figure arrays, nanolithography and elaborated organic synthesis. We here demonstrate a simple process to nanostructure the conjugated polymer using self-assembly with polystyrene and selective removal of one of the phases. The influence of the molecular weight of each polymer on the thin film morphology was systematically studied by atomic force microscopy. Using this approach, we observe two types of nanostructure, namely, nanoporous and nanoisland structures, of which the dimensions can be tuned by modifying the molecular weight of each polymer in the blend. This simple process introduces a cost-effective alternative to produce thin films of conjugated polymer with average nano-features from 100 nm up to 500 nm which could be used in a wide range of applications. 相似文献
65.
66.
Yoshinori Nishiki Koichi Aoki Koichi Tokuda Hiroaki Matsuda 《Journal of Applied Electrochemistry》1987,17(1):67-76
On the basis of the observation of gas bubbles evolved by electrolysis, a two-dimensional vertical model cell composed of electrodes with open parts for releasing gas bubbles to the back side is proposed. The model cell consists of two layers. One layer forms a bubble curtain with a maximum volume fraction of gas bubbles in the vicinity of the working electrode with open parts. The other. being located out of the bubble layer, is a convection layer with a small volume fraction distributed in the vertical direction under forced convection conditions. The cell resistance and the current distribution were computed by the finite element method when resistivity in the back side varied in the vertical direction along the cell. The following three cases for overpotential were considered: no overpotential, overpotential of the linear type and overpotential of the Butler-Volmer type. It was found that the cell resistance was determined not only by the interelectrode gap but also by the percentage of open area and in some cases by the superficial surface area. The cell resistance varied only slightly with the distribution of the bubble layer in the back side.Nomenclature
b
linear overpotential coefficient given byb=/i
-
C
proportionality constant given by Equation 15
-
d
1
distance between front side of working electrode and separator
-
d
2
thickness of separator
-
F
Faraday constant
-
I
total current per half pitch
-
i
current density at working electrode
-
i
0
exchange current density
-
L
length of a real electrolysis cell
-
n
number of electrons transferred in electrode reaction
-
O
p
percentage of open area given by Equation 1
-
p
pitch, i.e. twice the length of the unit cell, defined by 2(BC) in Fig. 4
-
q
thickness of bubble curtain, defined by (AM) in Fig. 4
-
R
gas constant
-
r
t
total cell resistance
-
r
unit-cell resistance defined by (V – V
eq)/I
-
r
rs
residue ofr from sum ofr
0 andr
-
r
0
ohmic resistance of solution when0
p=0
-
r
resistance due to overpotential when0
p=0
-
s
electrode surface ratio or superficial surface area given by Equation 2 for the present model
-
T
absolute temperature
-
t
thickness of working electrode defined by EF in Fig. 4
-
V
cell voltage
-
V
eq
open circuit potential difference between working and counter electrodes
-
solution velocity in cell
- 0
solution velocity at bottom of cell
-
w
width of working electrode, defined by 2(DE) in Fig. 4
-
x
abscissa located on cell model
-
y
ordinate located on cell model
-
anodic transfer coefficient
-
linear overpotential kinetic parameter defined byb/[bc(p/2)]
- d
infinitesimally small length on the boundary
-
volume fraction of gas bubbles in cell
-
dimensionless cell voltage defined bynF(V – V
eq)/RT
-
overpotential at working electrode
-
Butler-Volmer overpotential kinetic parameter defined by [nFi
0bc(p/2)]/RT
-
coordinate perpendicular to boundary of model cell
- 1
resistivity of bubble-free solution
- 2
resistivity of separator
- bc
resistivity of bubble curtain
-
potential in cell 相似文献
67.
Lianqi Zhang Hideyuki Noguchi Decheng Li Takahisa Muta Xiaoqing Wang Masaki Yoshio Izumi Taniguchi 《Journal of power sources》2008
On the basis of extreme similarity between the triangle phase diagrams of LiNiO2–LiTiO2–Li[Li1/3Ti2/3]O2 and LiNiO2–LiMnO2–Li[Li1/3Mn2/3]O2, new Li–Ni–Ti–O series with a nominal composition of Li1+z/3Ni1/2−z/2Ti1/2+z/6O2 (0 ≤ z ≤ 0.5) was designed and attempted to prepare via a spray-drying method. XRD identified that new Li–Ni–Ti–O compounds had cubic rocksalt structure, in which Li, Ni and Ti were evenly distributed on the octahedral sites in cubic closely packed lattice of oxygen ions. They can be considered as the solid solution between cubic LiNi1/2Ti1/2O2 and Li[Li1/3Ti2/3]O2 (high temperature form). Charge–discharge tests showed that Li–Ni–Ti–O compounds with appropriate compositions could display a considerable capacity (more than 80 mAh g−1 for 0.2 ≤ z ≤ 0.27) at room temperature in the voltage range of 4.5–2.5 V and good electrochemical properties within respect to capacity (more than 150 mAh g−1 for 0 ≤ z ≤ 0.27), cycleability and rate capability at an elevated temperature of 50 °C. These suggest that the disordered cubic structure in some cases may function as a good host structure for intercalation/deintercalation of Li+. A preliminary electrochemical comparison between Li1+z/3Ni1/2−z/2Ti1/2+z/6O2 (0 ≤ z ≤ 0.5) and Li6/5Ni2/5Ti2/5O2 indicated that charge–discharge mechanism based on Ni redox at the voltage of >3.0 V behaved somewhat differently, that is, Ni could be reduced to +2 in Li1+z/3Ni1/2−z/2Ti1/2+z/6O2 while +3 in Li6/5Ni2/5Ti2/5O2. Reduction of Ti4+ at a plateau of around 2.3 V could be clearly detected in Li1+z/3Ni1/2−z/2Ti1/2+z/6O2 with 0.27 ≤ z ≤ 0.5 at 50 °C after a deep charge associated with charge compensation from oxygen ion during initial cycle. 相似文献
68.
Yunosuke Abe Toshiki Aoki Hongge Jia Shingo Hadano Takeshi Namikoshi Yuriko Kakihana Lijia Liu Yu Zang Masahiro Teraguchi Takashi Kaneko 《Polymer》2012,53(11):2129-2133
A soluble and stable one-handed helical conjugated polymer without the coexistence of any other chiral moieties was successfully synthesized by asymmetric-induced polymerization of a chiral monomer having two hydroxyl groups followed by desubstitution of the chiral groups in a solid membrane state. The reason for the success was the polymer reaction was carried out in the membrane state. This is an alternative method to obtain such a unique chiral polymer which was obtained only by the helix-sense-selective polymerization (HSSP) we reported before. In addition the efficiency of the chiral induction was higher than that of the HSSP. It is interesting that the “Membrane state” acted like as if a protecting group. 相似文献
69.
Takaaki Aoki Toshio Seki Satoshi Ninomiya Kazuya Ichiki Jiro Matsuo 《Nuclear instruments & methods in physics research. Section B, Beam interactions with materials and atoms》2009,267(8-9):1424-1427
Molecular dynamics (MD) simulations of large argon clusters impacting on silicon solid targets were performed in order to study the transient process of crater formation and sputtering. The MD simulations demonstrate that the initial momentum of incident cluster is transferred to target surface atoms through multiple collision mechanism, where the initial momentum, which is along to the surface normal before impact, is deflected to lateral direction. This momentum transfer process was analyzed by the calculation of the velocity at the crater edge (the interface between cluster and target). In the case of Ar1000 cluster impact on Si(1 0 0) target at low energy per atom less than 40 eV/atom, the maximum value of lateral velocity of the crater edge increases in proportional to the velocity of incident cluster atoms. On the other hand, the crater edge velocity saturates over 40 eV/atom of incident energy per atom. In this case, the whole of constituent cluster atoms are implanted into the target and expand in both lateral and reflective directions at the subsurface region of the target. These MD simulations demonstrated that this collisional process result in the high yield sputtering of the target atoms. 相似文献
70.