全文获取类型
收费全文 | 18264篇 |
免费 | 2878篇 |
国内免费 | 2376篇 |
专业分类
化学 | 14400篇 |
晶体学 | 149篇 |
力学 | 1479篇 |
综合类 | 101篇 |
数学 | 641篇 |
物理学 | 6748篇 |
出版年
2024年 | 15篇 |
2023年 | 180篇 |
2022年 | 310篇 |
2021年 | 552篇 |
2020年 | 690篇 |
2019年 | 561篇 |
2018年 | 465篇 |
2017年 | 565篇 |
2016年 | 742篇 |
2015年 | 800篇 |
2014年 | 995篇 |
2013年 | 1485篇 |
2012年 | 1152篇 |
2011年 | 1395篇 |
2010年 | 1127篇 |
2009年 | 1208篇 |
2008年 | 1311篇 |
2007年 | 1259篇 |
2006年 | 1220篇 |
2005年 | 1037篇 |
2004年 | 963篇 |
2003年 | 767篇 |
2002年 | 748篇 |
2001年 | 503篇 |
2000年 | 465篇 |
1999年 | 411篇 |
1998年 | 360篇 |
1997年 | 329篇 |
1996年 | 266篇 |
1995年 | 264篇 |
1994年 | 216篇 |
1993年 | 185篇 |
1992年 | 175篇 |
1991年 | 138篇 |
1990年 | 114篇 |
1989年 | 80篇 |
1988年 | 89篇 |
1987年 | 49篇 |
1986年 | 55篇 |
1985年 | 42篇 |
1984年 | 45篇 |
1983年 | 15篇 |
1982年 | 41篇 |
1981年 | 21篇 |
1980年 | 25篇 |
1979年 | 24篇 |
1978年 | 11篇 |
1977年 | 10篇 |
1976年 | 15篇 |
1973年 | 7篇 |
排序方式: 共有10000条查询结果,搜索用时 31 毫秒
61.
Xiaojuan Hao Camilla Nilsson Martin Jesberger Martina H. Stenzel Eva Malmstrm Thomas P. Davis Emma
stmark Christopher Barner‐Kowollik 《Journal of polymer science. Part A, Polymer chemistry》2004,42(23):5877-5890
The synthesis and characterization of novel first‐ and second‐generation true dendritic reversible addition–fragmentation chain transfer (RAFT) agents carrying 6 or 12 pendant 3‐benzylsulfanylthiocarbonylsulfanylpropionic acid RAFT end groups with Z‐group architecture based on 1,1,1‐hydroxyphenyl ethane and trimethylolpropane cores are described in detail. The multifunctional dendritic RAFT agents have been used to prepare star polymers of poly(butyl acrylate) (PBA) and polystyrene (PS) of narrow polydispersities (1.4 < polydispersity index < 1.1 for PBA and 1.5 < polydispersity index < 1.3 for PS) via bulk free‐radical polymerization at 60 °C. The novel dendrimer‐based multifunctional RAFT agents effect an efficient living polymerization process, as evidenced by the linear evolution of the number‐average molecular weight (Mn) with the monomer–polymer conversion, yielding star polymers with molecular weights of up to Mn = 160,000 g mol?1 for PBA (based on a linear PBA calibration) and up to Mn = 70,000 g mol?1 for PS (based on a linear PS calibration). A structural change in the chemical nature of the dendritic core (i.e., 1,1,1‐hydroxyphenyl ethane vs trimethylolpropane) has no influence on the observed molecular weight distributions. The star‐shaped structure of the generated polymers has been confirmed through the cleavage of the pendant arms off the core of the star‐shaped polymeric materials. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 5877–5890, 2004 相似文献
62.
Dong‐Cheol Shin Yun‐Hi Kim Hong You Jae Gyu Jin Soon‐Ki Kwon 《Journal of polymer science. Part A, Polymer chemistry》2004,42(22):5636-5646
A poly(p‐phenylenevinylene) (PPV) derivative containing a bulky (2,2‐diphenylvinyl)phenyl group in the side chain, EHDVP‐PPV, was synthesized by Gilch route. The reduced tolane‐bisbenzyl (TBB) defects, as well as the structure of the polymer, was confirmed by various spectroscopic methods. The intramolecular energy transfer from the (2,2‐diphenylvinyl)phenyl side group to the PPV backbone was studied by UV‐vis and photoluminescence (PL) of the obtained polymer and model compound. The polymer film showed maximum absorption and emission peaks at 454 and 546 nm, respectively, and high PL efficiency of 57%. A yellow electroluminescence (λmax = 548 nm) was obtained with intensities of 6479 cd/m2 when the light‐emitting diodes of ITO/PEDOT/EHDVP‐PPV/LiF/Al were fabricated. The maximum power efficiency of the devices was 0.729 lm/W with a turn‐on voltage of 3.6 V. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 5636–5646, 2004 相似文献
63.
Small amounts of certain halogenated compounds are found to have, at most, only a slight enhancing effect on the radiolytic decay rates of added poly-unsaturated compounds in polyethylene, but significantly increase the elastic modulus at 433 K (melt modulus) obtained thereby. Experiments with model chlorine-containing additives suggest that this increase is due to a more random distribution of polymer and monomer mediated crosslinks in the polymer, that it does not result from a significant increase in crosslinking and that it is mediated by chlorine atoms, in a similar manner to radiolytic hydrogen atoms, through facilitation of long range free radical migration. Although low molecular weight chloro-paraffins inhibit radiolytically induced growth of melt modulus in monomer containing polyethylenes, even very small additions of chlorinated polyethylenes, which form a separate phase, increase the melt modulus. This again indicates that the active species is the chlorine radical. 相似文献
64.
Chun‐Yan Hong Ye‐Zi You Cai‐Yuan Pan 《Journal of polymer science. Part A, Polymer chemistry》2004,42(19):4873-4881
Well‐defined diblock and triblock copolymers composed of poly(N‐isopropylacrylamide) (PNIPAM) and poly(ethylene oxide) (PEO) were successfully synthesized through the reversible addition–fragmentation chain transfer polymerization of N‐isopropylacrylamide (NIPAM) with PEO capped with one or two dithiobenzoyl groups as a macrotransfer agent. 1H NMR, Fourier transform infrared, and gel permeation chromatography instruments were used to characterize the block copolymers obtained. The results showed that the diblock and triblock copolymers had well‐defined structures and narrow molecular weight distributions (weight‐average molecular weight/number‐average molecular weight < 1.2), and the molecular weight of the PNIPAM block in the diblock and triblock copolymers could be controlled by the initial molar ratio of NIPAM to dithiobenzoate‐terminated PEO and the NIPAM conversion. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 4873–4881, 2004 相似文献
65.
Tae Young Kim Dong Myung Kim Won Jung Kim Tae Hee Lee Kwang S. Suh 《Journal of Polymer Science.Polymer Physics》2004,42(15):2813-2820
The effect of the triblock copolymer poly[styrene‐b‐(ethylene‐co‐butylene)‐b‐styrene] (SEBS) on the formation of the space charge of immiscible low‐density polyethylene (LDPE)/polystyrene (PS) blends was investigated. Blends of 70/30 (wt %) LDPE/PS were prepared through melt blending in an internal mixer at a blend temperature of 220 °C. The amount of charge that accumulated in the 70% LDPE/30% PS blends decreased when the SEBS content increased up to 10 wt %. For compatibilized and uncompatibilized blends, no significant change in the degree of crystallinity of LDPE in the blends was observed, and so the effect of crystallization on the space charge distribution could be excluded. Morphological observations showed that the addition of SEBS resulted in a domain size reduction of the dispersed PS phase and better interfacial adhesion between the LDPE and PS phases. The location of SEBS at a domain interface enabled charges to migrate from one phase to the other via the domain interface and, therefore, resulted in a significant decrease in the amount of space charge for the LDPE/PS blends with SEBS. © 2004 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 42: 2813–2820, 2004 相似文献
66.
Per B. Zetterlund Kazuki Miyake Kunihiro Goto Bunichiro Yamada 《Journal of polymer science. Part A, Polymer chemistry》2004,42(11):2640-2650
A detailed investigation of addition–fragmentation chain transfer (AFCT) in the free‐radical polymerization of methyl methacrylate (MMA) in the presence of methyl α‐(bromomethyl)acrylate (MBMA) was carried out to elucidate mechanistic details with efficient macromonomer synthesis as an underlying goal. Advanced modeling techniques were used in connection with the experimental work. Curve fitting of simulated and experimental molecular weight distributions with respect to the rate coefficient for addition of propagating radicals to MBMA (kadd) over 60–120 °C resulted in Eadd = 21.7 kJ mol?1 and Aadd = 2.18 × 106 M?1 s?1 and a very weak temperature dependence of the chain‐transfer constant (Eadd ≈ Ep). The rate coefficient for fragmentation of adduct radicals at 60 °C was estimated as kf ≈ 39 s?1 on the basis of experimental data of the MMA conversion and the concentration of 2‐carbomethoxy‐2‐propenyl end groups. The approach developed is generic and can be applied to any AFCT system in which copolymerization does not occur and in which the resulting unsaturated end groups do not undergo further reactions. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 2640–2650, 2004 相似文献
67.
以Du Pont公司的商用Teflon FEP A型薄膜为例,通过热脉冲技术、等温表面电位衰减测量和开路热刺激放电电流谱分析等实验结果,讨论了经常温和高温电晕充电后样品厚度对薄膜驻极体的沉积电荷密度、薄膜驻极体的内电场、体电导率以及电荷储存稳定性的影响.通过热脉冲技术组合电导率温度曲线的测量,研究了在不同温度条件下样品厚度对沉积电荷层的平均电荷重心移动的影响.结果表明:在充电参数一定的条件下,随着膜厚的降低,储存电荷密度上升,但电荷稳定性有所下降.因此,合理地调控薄膜厚度,可以有效地优化驻极体的电荷储存能
关键词:
厚度
驻极体
电荷储存能力
电荷稳定性 相似文献
68.
以三能级V型系统为例研究修饰态布居的选择性激发对无反转激光增益的作用. 当非 相干驱动场的频谱宽度远小于驱动场产生的修饰态能级的间距时,非相干驱动场只将一个修 饰态的布居抽运至激发态. 借助原子的衰减通道,系统中形成单向布居转移通道,从而建立 修饰态布居的选择性激发. 利用修饰态布居的选择性激发,可以摆脱裸态共振无反转激光的 三个限制: (1) 不再要求辅助的低频驱动跃迁比高频激光跃迁具有更高的衰减速率;(2) 显 著降低非相干激发速率的阈值;(3) 无反转激光的线性增益不再反比于相干驱动场的强
关键词:
修饰态布居的选择性激发
无反转激光增益
原子衰减速率
非相干激发阈值速率 相似文献
69.
利用常温下恒流和恒压电晕充电、充电后的等温表面电位衰减、热刺激放电和扫描电镜等实 验手段研究了恒流和恒压电晕充电技术对聚四氟乙烯多孔薄膜驻极体驻极态的影响.与恒压电晕充电相比较,恒流电晕充电时由于流过薄膜的电流恒定,增加了注入电荷在多孔结构厚度方向界面处的俘获概率,使沉积电荷密度上升,改善了驻极体的储电能力.然而,这些位于不同层深多孔界面处的俘获电荷在这类功能膜储存或使用过程中,经外激发从脱阱位置 以跳动(hopping)模式输运至背电极的路径相对缩短将导致脱阱电荷衰减较快.
关键词:
恒流电晕充电
聚四氟乙烯多孔膜
驻极体
电荷稳定性 相似文献
70.