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231.
232.
由于Z箍缩动态黑腔负载中的低密度聚合物泡沫柱具有多孔结构和极低的力学强度,在装配过程中对胶粘剂有一定的特殊要求。实验以聚氨酯丙烯酸酯为主体树脂,丙烯酸异冰片酯为活性单体,配以光引发剂和偶联剂制得了适用于低密度泡沫粘接用的紫外光固化胶粘剂。测试表明,所研制的胶粘剂的体积收缩率仅为2.25%,且具有较高的固化速率和适当的粘接强度,能够满足稳固、快速装配的要求。通过对粘接界面的观测发现,胶粘剂在诊断孔内没有明显的扩散,且在低密度致密结构泡沫中的扩散厚度较小,均匀性好。 相似文献
233.
为建立混合物中羟基封端聚丁二烯(HTPB)的临界点色谱定量方法,以C18为固定相,考察了HTPB在四氢呋喃-乙腈和四氢呋喃-水两种流动相体系下的临界点色谱条件。结果表明,四氢呋喃-乙腈体积比为70.7:29.3以及四氢呋喃-水体积比为92:8时,HTPB的保留值与其相对分子质量无关。将该临界点色谱方法用于胶黏剂混合组分中HTPB的测定,结果表明,HTPB在46.7~216.4 mg/L范围内呈良好线性关系,相关系数(r)>0.99,检出限为4.2 mg/L。自配HTPB和矿物油双组分样品的加标回收率为89.2%~101.1%,相对标准偏差小于0.66%(n=6)。应用该方法对市售聚氨酯胶黏剂进行检测,测定结果为HTPB成分占26.6%。该方法快速、准确,能满足聚合物混合产品的生产质量控制和失效分析的要求。 相似文献
234.
Substrate plays an essential role in the construction of flexible electrode and related wearable sensors. Compared with conventional flexible substrates such as Polyethylene terephthalate (PET), the common transparent adhesive tape exhibits the unique advantages in the non-adhesive surface with good printability, allowing the conductive layer to be deposited directly on its surface, and in another adhesive surface with good fastening, thus facilitating the fabrication of as-prepared electrode in subsequent wearable sensors. Herein, we constructed a new type of flexible sensor to detect ascorbic acid which is closely related to human health in sweat by integrating flexible electrode based on transparent adhesive tape with potentiostat that incorporate the critical signal conditioning, processing, and transmission functions. Experiment results show that resulting electrode still has the good electrochemistry performance even after 1000 bending cycles (20 % bending degrees). By connecting as-prepared flexible electrode to the potentiostat to carry out real time analysis, the resulting sensor exhibits excellent sensitivity, detection limit and repeatability (0.15 V detection potential vs printed Ag/AgCl reference electrode, 3.8 μM detection limit, 25 μM-1 mM linearity, and good selectivity). 相似文献
235.
This study used controlled microwaves to elucidate the response of adhesive components to microwaves and examined the advantages of microwave radiation in curing epoxy adhesives. Curing of adhesives with microwaves proceeded very rapidly, even though each component of the adhesive was not efficiently heated by the microwaves. The reason the adhesive cured rapidly is that microwave heating was enhanced by the electrically charged (ionic) intermediates produced by the curing reaction. In contrast, the cured adhesive displayed lower microwave absorption and lower heating efficiency, suggesting that the cured adhesive stopped heating even if it continued to be exposed to microwaves. This is a definite advantage in the curing of adhesives with microwaves, as, for example, adhesives dropped onto polystyrene could be cured using microwave heating without degrading the polystyrene base substrate. 相似文献
236.
化学接枝改进ZnO-有机硅纳米复合材料的光学性能 总被引:1,自引:0,他引:1
采用N-(三甲氧基硅丙基)-4-叠氮-2,3,5,6-四氟苯甲酰胺(PFPA-silane)改性纳米氧化锌,并将PFPA-silane接枝在有机硅聚合物链上.接枝反应改变了纳米复合物的折光指数,并使ZnO纳米粒子与有机硅基体的折光指数更加匹配.这减少了纳米氧化锌粒子对光的散射作用,增加了纳米ZnO-有机硅纳米复合物的透明性.所制备的复合物通过接枝改性后透光率最多可提高50%.研究结果表明无机物和聚合物的折光指数的匹配程度可以通过偶联剂与聚合物基体的反应来进行调控. 相似文献
237.
238.
以2-苯基咪唑(2PZ)为芯材,聚甲基丙烯酸缩水甘油酯(PGMA)为壁材,采用溶剂挥发技术,成功地制备了一种新型潜伏性热释放型微胶囊固化剂2PZ-PGMA。通过FT-IR、TGA、SEM、粒度分析和DSC对微胶囊固化剂的化学结构、芯材含量、表面形貌、粒径分布及固化性能等进行了表征。所制备的微胶囊固化剂表面光滑,粒径分布较窄,平均粒径为约17.6μm,壁材厚度为约1.1μm,芯材2PZ含量为20.1(wt)%。由微胶囊固化剂与环氧树脂E-51制备的单组分胶粘剂,具有优良的固化特性、潜伏性能和粘接性能,可在100℃下30min内实现固化,室温储存期达33d以上,拉伸剪切强度达15.36MPa。 相似文献
239.
A new kind of 1,2,3‐triazole‐containing aromatic diamines were synthesized by the Cu(I)‐catalyzed 1,3‐dipolar cycloaddition reaction. These diamines were employed to synthesize a series of novel polytriazoleimides (PTAIs) by polycondensation with various aromatic dianhydrides in N,N‐dimethylacetamide (DMAc) via the conventional two‐step method. The obtained polyimides were characterized by Fourier transform infrared, hydrogen‐1 nuclear magnetic resonance, X‐ray diffraction, differential scanning calorimetry, and thermogravimetric analysis techniques. The results show that the PTAIs are soluble in most of strong polar solvents and have inherent viscosity values of 0.47–0.68 dl/g (DMAc). PTAI films have tensile strengths of 60.6–102.6 MPa and elongations at breakage of 3.0–4.1%, glass transition temperatures (Tg) of 208–262°C, and decomposition temperatures (at 5% weight loss) of 368–401°C in N2 atmosphere, which depend on the structure of the polymers. The PTAIs also exhibit good adhesion to copper and gas separation properties. Copyright © 2011 John Wiley & Sons, Ltd. 相似文献
240.
Lili Qie 《European Polymer Journal》2010,46(6):1225-1236
N-Dodecyl mercaptan (NDM) chain transfer agent and allyl methacrylate (AMA) cross-linker were used to manipulate latex properties in a starved seeded semi-batch emulsion polymerization of butyl acrylate (BA) and methyl methacrylate (MMA) or with a third monomer, acrylic acid (AA). Latexes with higher gel content and lower sol polymer molecular weight (Mw) were produced by adding only AMA. On the other hand, latexes with lower gel content and Mw were produced by adding only NDM. In addition, at a constant AMA concentration (0.2 phm), the addition of NDM (0.2 phm) decreased gel content, increased molecular weight between cross-linking points (Mc), and decreased Mw. Adding more NDM (to a total of 0.4 phm) further decreased the gel content, while decreasing the tested Mc and increasing Mw. It was also found that using higher concentrations of both AMA and NDM could produce latex with similar gel content, but smaller Mc and Mw, compared to the latex produced at lower concentrations of both NDM and AMA. Regarding the influence of AA, gel content was increased and Mw was significantly decreased with an increase in AA concentration and a decrease in MMA concentration. The performance of the latexes was evaluated for application as a pressure-sensitive adhesive (PSA). 相似文献