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21.
William Doherty Peter Halley Les Edye David Rogers Francisco Cardona Yoosup Park Tim Woo 《先进技术聚合物》2007,18(8):673-678
Sugarcane fiber (i.e. bagasse) lignin has a larger fraction of aromatics unsubstitution in the ortho position than hardwood or softwood lignin and hence has the greater ability to be derivatized. Furthermore, organosolv lignin has a higher purity than sulfonated and kraft lignins. This work examines the purification of organosolv lignin derived from bagasse and the physico‐chemical properties of the lignin and lignin‐phenol formaldehyde (PF) resin coatings, and composites. The wetability tests have shown that lignin and lignin‐PF resin films are effective water barrier coatings, though the contact angles of lignin‐PF resin films were considerably less than the wax films. The overall mechanical properties (i.e. peak stress, peak strain and modulus) of the bagasse fiber composites were lower than the values obtained with the composites without the inclusion of bagasse fiber. Copyright © 2007 John Wiley & Sons, Ltd. 相似文献
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The first stereoselective syntheses of the naturally occurring, ,β-unsaturated lactone hyptolide 1 and of its nonnatural epimer at C-6 are described. Ethyl l-lactate was the chiral starting material. Key steps of these syntheses were a Brown's asymmetric allylation, a Carreira's asymmetric ethynylation and a ring closing metathesis. 相似文献
24.
飞秒激光高精细加工柴油机喷油嘴倒锥孔法 总被引:2,自引:0,他引:2
利用飞秒激光加工热效应小、高精细、对材料无选择性等特点,针对柴油发动机高压共轨系统中关键零件——喷油嘴偶件喷油孔的加工需求,设计了一种利用三光楔扫描的飞秒激光加工装置,并进行了喷油嘴倒锥孔加工工艺研究.采用微孔三座标测量机(测量准确度1.2μm)对倒锥孔尺寸准确度进行检测,通过喷油嘴高压液体流量试验台(测量准确度±0.1%)对批量制孔后的油嘴进行了流量测试,结果表明:所设计装置加工的油嘴性能可以满足欧V排放法规的应用要求,对提升汽车制造业水平及柴油车排放标准具有重要意义. 相似文献
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A highly rigid diamine monomer derived from naturally occurring myo‐inositol and its use for polyamide synthesis 下载免费PDF全文
Atsushi Sudo Shou Sugita 《Journal of polymer science. Part A, Polymer chemistry》2016,54(21):3436-3443
A rigid diamine was synthesized from myo‐inositol, a naturally occurring cyclic hexaol, and used as a monomer to synthesize polyamides. myo‐Inositol was treated with 1,1‐dimethoxycyclohexane to yield a bisketal bearing two hydroxyl groups, and from this bisketal, the target diamine was synthesized in three steps: (1) derivation of the diol into the corresponding bistriflate, (2) nucleophilic substitution of the bistriflate with sodium azide yielding a diazide, and (3) reduction of the diazide to the target diamine. The target diamine readily underwent polycondensation with dicarboxylic acid chloride in solution. The resulting polyamides, whose main chain inherited the rigid 5‐6‐5 system from the diamine monomers, have high glass transition temperatures. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 3436–3443 相似文献
27.
Chetan Tambe John Kaufmann Daniel Graiver Ramani Narayan 《Journal of polymer science. Part A, Polymer chemistry》2016,54(19):3086-3093
Reactive blends prepared from methoxysilane terminated silicone polymers and silylated soybean oil are described and characterized. Although simple mixing of soy and silicones results in gross phase separation, homogeneous polymeric products are obtained by introducing reactive sites. These products can be used as protective coatings, additives to adhesives and new sealants. Exposure of the mixtures to moisture leads to hydrolysis of the methoxysilanes and subsequent condensation of the resulting silanols that yields stable siloxane linkages between the two immiscible phases. FTIR, TGA, and swell‐gel analyses indicate effective formation of these siloxane crosslinks. Reactive blends containing less than 20% silylated oil appeared completely transparent but increasing the soy content decreased the optical transparency. SEM micrographs reveal the silicone polymer as the continuous phase with individual spherical silylated soy oil particles distributed in it. The properties of these reactive blends vary from high elongation elastomers to high modulus resins depending on the composition. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 3086–3093 相似文献
28.
Hailing Liu Hoyong Chung 《Journal of polymer science. Part A, Polymer chemistry》2017,55(21):3515-3528
Lignin is an important source of synthetic materials because of its abundance in nature, low cost, stable supply, and no competition to the human food supply. Lignin, a cross‐linked phenolic polymer, contains a large number of aromatic groups that can be used as a substitute for petroleum‐based aromatic fine chemicals. However, modification of lignin is necessary for its application in advanced materials due to its chemically inert nature and structural complexity. Polymeric modification of lignin via graft copolymerization represents an important avenue for modification because this method forms stable covalent bond linkages between lignin and synthetic functional polymers. In this review, we discuss recent synthetic strategies toward polymeric modification of lignin using graft copolymerization and the special properties and applications of the produced lignin copolymers. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55, 3515–3528 相似文献
29.
C. Lavilla A. Alla A. Martínez de Ilarduya E. Benito M.G. García‐Martín J.A. Galbis S. Muñoz‐Guerra 《Journal of polymer science. Part A, Polymer chemistry》2012,50(16):3393-3406
Random poly(hexamethylene terephthalate‐co‐galactarate)s and poly(dodecamethylene terephthalate‐co‐galactarate)s copolyesters covering the whole range of compositions were obtained with weight‐average molecular weights of ~30,000–50,000 g mol?1 by melt polycondensation. They were thermally stable above 300 °C, and displayed Tg in the +20 to ?20 °C range with values steadily decreasing with the content in galactarate units. All the copolyesters were semicrystalline with Tm between 50 and 150 °C and those made from dodecanediol were able to crystallize from the melt at a crystallization rate depending on composition. Copolyesters containing up to 50% of galactaric units retained the crystal structure of their respective polyterephthalate homopolyesters, whereas they adopted the structure of the respective polygalactarates when the content in Galx units reached 70%. Stress‐strain essays revealed decay in the mechanical parameters as the aromatic units were replaced by Galx. Incubation in aqueous buffer revealed that hydrolysis of the polyesters were largely enhanced by copolymerization and evidenced the capacity of the Galx unit for making aromatic polyesters susceptible to biodegradation. A detailed NMR analysis complemented by SEM observations indicated that hydrolysis took place by preferred splitting of galactarate ester bonds with releasing of alkanediol and Galx‐diacid. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 相似文献
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