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81.
介绍了一种操作简单且广泛适应于多种材料的涂层制备工艺,在制备过程中,以粒度精细,分散度好的铁电,铁磁微粉和挥发平缓,且在450℃前挥发完全的聚丙烯酸酯不干胶为原料,经过简单的涂抹工艺后得到涂层。在退火过程中控制升温速率,可得到平整的高质量涂层表面。通过控制涂层退火温度可以得到浸润性由超疏水到超亲水变化的涂层表面,扫描电镜图像显示涂层表面呈现阶层结构,表面晶粒和孔洞尺寸随退火温度升高而增大。 相似文献
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A novel method to produce fluorine‐containing polyacrylate emulsion is presented. It is prepared by the copolymerization of n‐methyl methacrylate, n‐styrene, n‐butyl acrylate, and α‐methacrylic acid in the presence of swollen particles of PTFE. The structure and properties of the polymers are characterized by GPC, PSD, SEM, and XPS. The number‐average molar mass (Mn) 51,332, and the polydispersity 5.8688 are obtained. The mean diameter of latex particles is 300nm. Scanning electron microscopy reveals that particles of the emulsion are well dispersed. Meanwhile, the F1S content of the surface on the latex membrane is 8.99%. It is shown that the method of mixing micron and nanometer‐sized particles should be made the next step of research. It is also proved that inertia polymers can be used in emulsion property modification. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 99: 558–562, 2006 相似文献
84.
核壳型聚丙烯酸酯复合乳液的性能研究 总被引:1,自引:0,他引:1
采用半连续种子乳液聚合法合成了"硬核软壳"核壳型复合乳液,研究了聚合工艺、乳化剂复配类型对乳液性能、乳胶粒粒径及粒径分布的影响。结果表明:种子聚合采用间歇法、核层及壳层聚合都采用预乳化工艺,乳液聚合稳定且乳胶粒粒径分布窄;乳化剂壬基酚聚氧乙烯醚-2-磺酸基琥珀酸单酯二钠盐(MS-1)分别与十二烷基硫酸钠(SDS)、十二烷基苯磺酸钠(SDBS)以及脂肪醇聚氧乙烯醚(OS)复配用于乳液聚合,当m(MS-1):m(SDS)为6:4时所合成乳液的乳胶粒粒径小且分布窄、聚合稳定性好。最后采用红外和透射电镜分别对聚合物分子链结构和乳胶粒形貌进行了表征。 相似文献
85.
丙烯酸酯类黏合剂无皂乳液聚合 总被引:6,自引:1,他引:5
以甲基丙烯酸甲酯(MMA)为硬单体,丙烯酸丁酯(BA)为软单体,甲基丙烯酸(MAA)为功能单体,聚乙烯醇(PVA)为胶体保护剂,丙烯酸羟乙酯(HEA)为交联单体,采用无皂乳液聚合法合成了聚丙烯酸酯类黏合剂。优化的聚合工艺为:75~78℃聚合3 h,80℃保温1 h,胶体保护剂PVA 1%,交联单体HEA 3.0%,功能单体MAA 10%。合成的丙烯酸酯黏合剂含固量20%~22%,pH值稳定范围为6~14,应用性能较好。 相似文献
86.
探讨了砂土和溶液中水量、时间、pH值、温度、肥料对聚丙烯酸钠吸液倍率的影响以及聚丙烯酸钠对肥料的缓释作用。实验表明,在砂土中,聚丙烯酸钠的吸液倍率比溶液中降低105g;吸液饱和时间比溶液中延长60min;pH值(4~10),温度(20℃~80℃)对聚丙烯酸钠吸液倍率影响不大;非电解质肥料对吸液倍率影响很小,电解质肥料对吸液倍率影响较大。经过96小时,吸收1.0%KCl和1.0%尿素溶液的聚丙烯酸钠对钾和氮素累积释放率分别不到25.0%和80.0%,说明聚丙烯酸钠对尿素和KCl均有一定的缓释作用。 相似文献
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88.
Bulk photopolymerization was used to synthesize a series of semi‐interpenetrating polymer network (s‐IPN) based on linear poly(vinyl acetate) and crosslinked N‐butyl acrylate/1,6‐hexandiol diacrylate (HDDA) copolymer. Different formulations were used by varying the monoacrylate/diacrylate molar ratio and the linear polymer concentration. The polymerization kinetics was studied as a function of the s‐IPN composition by FTIR spectroscopy. It was observed that the reaction rate increases by increasing the linear polymer amount. This effect is much more pronounced in the reaction mixtures with a higher diacrylate concentration, playing a key role the restricted mobility of the macroradicals involved in the bimolecular termination. The maximum conversion increases regularly with linear polymer concentration in the blend and resulted to be very high, ranging from 95 to 98%. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 相似文献
89.
Jung-Hsin Yang 《Powder Technology》2009,193(2):170-2559
High surface area CaCO3 was produced through the reaction between CO2 and an aqueous suspension of Ca(OH)2 with the addition of an additive, sodium polyacrylate. The surface area of CaCO3 prepared was affected markedly by the amount of additive and the solution pH when adding the additive. The CaCO3 with the highest surface area (87.7 ± 1.3 m2/g) was obtained under the conditions that the initial Ca(OH)2 concentration was 2.4 wt.%, the amount of sodium polyacrylate added was 0.2 wt.%, and the solution pH at which the additive was added was in the range of 11.4-11.1. The high surface area CaCO3 also had a high pore volume. The CaCO3 was highly reactive toward SO2, and a conversion of 0.95 was achieved when it was sulfated at 950 °C and 4000 ppm SO2 in air for 1 min. Prior calcination reduced the reactivity of this high surface area CaCO3. 相似文献
90.