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91.
Yimin Qin 《Polymer International》2008,57(2):171-180
Alginate fibers are made from sodium alginate, which is a natural polymer extracted from brown seaweeds. Over the last two decades, alginate fibers have become well established in the wound management industry where their ion‐exchange and gel‐forming abilities are particularly useful for the treatment of exuding wounds. In order to deliver functional performances for advanced wound management products, many improvements have been made in recent years to enhance the absorption and gel‐forming capabilities and the anti‐microbial properties of alginate fibers. In addition, attempts have been made to use alginate fibers as a carrier to deliver zinc, silver and other active ingredients that are beneficial to wound healing. This paper reviews the development in the production of various fibers from alginate, and summarizes the production processes for calcium alginate, calcium/sodium alginate, sodium alginate, zinc alginate, silver alginate and other types of alginate fibers containing novel functional ingredients. Copyright © 2007 Society of Chemical Industry 相似文献
92.
M. J. Ramazani‐Harandi M. J. Zohuriaan‐Mehr A. A. Yousefi A. Ershad‐Langroudi K. Kabiri 《应用聚合物科学杂志》2009,113(6):3676-3686
The swelling properties of superabsorbent polymers (SAPs) under real conditions are extremely important for selecting the material suitable for a given application, e.g. feminine napkin or agriculture. This new practical research represents deeper synthetic and physicochemical studies on the structure–property relation in acrylic SAP hydrogels and composites. Thus, the values of saline‐absorbency under load (AUL; a measurable simulation of the real circumstances of SAP applications, at pressures 0.3–0.9 psi) were measured for the SAP or SAP composite samples prepared under different conditions, i.e. type and content of crosslinker, type and concentration of initiator, percentage of inorganic filler (kaolin), and type and percentage of porosity generators. The samples were subsequently used to determine the rheological and morphological characteristics. Dynamic storage modulus (G′) measurements were carried out at constant strain in a wide range of frequency. Linear correlations were frequently found to be active between AUL and G′ data over the rubber‐elastic plateau. Thus, for a given SAP: AUL = ktotalG′ + C. The coefficient k total is a function of (nature and content of crosslinker, initiator, inorganic component, particle morphology, etc.). Therefore, the easily measured AUL values could be simply correlated to the main synthesis variables and molecular structure of SAP gels through a rheological material function (G′). © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 相似文献
93.
PEO/PVA水凝胶伤口敷料的毒性和疗效评价 总被引:4,自引:0,他引:4
为了证价经冻融循环处理和电子束辐射交联接技术术合成的聚氧化乙烯与聚乙烯醇(PEO/PVA)混合物水凝胶伤口敷料的性能,研究了该水凝胶膜对机体和细胞的毒性以及对皮肤伤口的愈合作用。毒性作用通过仇性全身毒性试验、细胞毒性试验和皮肤斑贴试验检测。细胞毒性试验应用高敏感性的成纤维细胞持续培养7d的RPMI-16402培养系统,检测细胞生长抑制和镜下细胞形态学变化。结果显示,PEO/PVA水凝胶敷料没有引起 相似文献
94.
Softwood kraft lignin (SKL) pH-responsive hydrogels were prepared through controlled aggregation using poly[2-(dimethylamino)ethyl methacrylate] (PDMAEMA) and poly(2-(dimethylamino)ethyl methacrylate)-block-poly(ethylene oxide)-block-poly(2-(dimethylamino) ethyl methacrylate) triblock copolymer (PDMAEMA-co-PEO-co-PDMAEMA). At low SKL concentrations, the SKL/polymer (PDMAEMA and PDMAEMA-co-PEO-co-PDMAEMA) aqueous solutions exhibited pH-dependent aggregation arising from the formation of strong intermolecular hydrogen bonds. Decreasing the SKL/polymer weight ratio resulted in the pH-reversible soluble-insoluble (S-I) transition to become a soluble-insoluble-soluble (S-I-S) transition, which upon increasing the SKL concentration resulted in hydrogel formation. Under neutral conditions relatively strong hydrogels were formed, which upon either increasing or decreasing solution pH resulted in the hydrogels collapsing to liquid solutions, but were readily reformed upon neutralization. The effects of polymer structure, concentration, and intermolecular interactions on solution behavior and gelation are thoroughly discussed. 相似文献
95.
以N-异丙基丙烯酰胺和海藻酸钠(SA)为主要原料,制备了具有pH敏感型的智能水凝胶。探究了不同海藻酸钠、引发剂、交联剂等配比的凝胶在不同pH值环境下的溶胀性能,并对制备的凝胶进行甲基紫的吸附性能测试。结果表明:碱性条件下,凝胶溶胀度随SA用量的增加而增大,酸性条件下则相反;凝胶的溶胀度随交联剂用量的增加而减小;引发剂用量为3%时凝胶的溶胀度较高;凝胶在适宜条件下对甲基紫溶液有良好的吸附性能。 相似文献
96.
The pH‐sensitive poly(vinyl alcohol)/poly(acrylic acid) hydrogel microcapsules containing vitamin B12‐loaded Al2O3 core were prepared with a three‐step emulsion polymerization. Al2O3 was chemically treated with HCl or NaOH solutions at room temperature for 24 h to modify the binding properties with vitamin B12. The colon‐targeted release characteristics of vitamin B12 from the microcapsules were evaluated at different pHs. These microcapsules showed the faster and larger release of vitamin B12 due to the high swelling of microcapsule shell as the pH was changed into more basic condition. However, these microcapsules showed the slower and less release of vitamin B12 as the acid value of Al2O3 increased due to the strong binding interaction between Al2O3 core and vitamin B12 even though the initial loading of vitamin B12 was higher. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 相似文献
97.
Amany I. Raafat 《应用聚合物科学杂志》2010,118(5):2642-2649
Based on gelatin (Gltn) and acrylic acid (AAc), biodegradable pH‐sensitive hydrogel was prepared using gamma radiation as super clean source for polymerization and crosslinking. Incorporation of PAAc in the prepared hydrogel was confirmed by Fourier transform infrared spectroscopy (FTIR). The effect of PAAc content on the morphological structure of the prepared hydrogel swollen at pH 1, 5, and 7 was examined using scanning electron microscopy (SEM). The results showed the dependence of the porous structure of the prepared hydrogels on AAc content and the pH of the swelling medium. Swelling properties of gelatin/acrylic acid copolymer hydrogels with different AAc contents were investigated at different pH values. Swelling data showed that the prepared hydrogels possessed pronounced pH sensitivity. In vitro release studies were performed to evaluate the hydrogel potential as drug carrier using ketoprofen as a model drug. Experimental data showed that the release profile depends on both hydrogel composition and pH of the releasing medium. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 相似文献
98.
Debajyoti Ray P. Sunny Gils Guru P. Mohanta R. Manavalan Prafulla K. Sahoo 《应用聚合物科学杂志》2010,116(2):959-968
In this study, interpenetrating polymer network (IPN) hydrogel based on polyvinyl alcohol (PVA) networking with polyacrylic acid (PAA) were prepared by a non‐conventional emulsion method without any added crosslinker, using benzoyl peroxide as initiator and sodium chloride (NaCl) as additive. The IPN hydrogel was characterized by using Fourier transformed infrared (FTIR) spectrophotometry, Thermo gravimetric analysis (TGA), and Scanning electron microscopy (SEM). (PVA‐co‐PAA)/NaCl normal IPN hydrogel (H) were fabricated into hydrogel microspheres (HM) by modified emulsion crosslinking method using glutaraldehyde‐saturated toluene as crosslinker and were loaded with Diltiazem hydrochloride (DL). The IPN hydrogel showed more swelling in simulated intestinal fluid (SIF). (PVA‐co‐PAA)/NaCl HM formulation A1 showed comparatively higher DL entrapment (79%) and better control over DL release up to 24 h. By comparing antihypertensive activity of DL loaded two formulations in normotensive rats, HM formulation A1 found more effective in reducing blood pressure to 40.1%. The experimental results demonstrated that (PVA‐co‐PAA)/NaCl HM had the greater potential than normal hydrogel to be used as a drug carrier. A single use of the prepared hydrogel microsphere system of DL can effectively control hypertension in rats. The system holds promise for clinical studies. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 相似文献
99.
Zhongying Hui Xiaolan Zhang Jiahui Yu Jin Huang Zhongshi Liang Daxin Wang Haitao Huang Peihu Xu 《应用聚合物科学杂志》2010,116(4):1894-1901
In virtue of the potential biomedical application of carbon nanotube (CNT), the CNT was hybridized into a supramolecular hydrogel based on the selective inclusion of α‐cyclodextrin (α‐CD) onto poly(ethylene oxide) (PEO) segments of a triblock copolymer, i.e., PEO‐block‐poly(propylene oxide)‐block‐PEO. Different from the previous report, the content of α‐CD, in contrast to that of ethylene oxide unit, was decreased to decrease the network density in hydrogel and hence improve the diffusion of encapsulated substances. As a result, the modulus of the hydrogels climbed slightly after introducing CNT. Furthermore, as the essential properties for wound dressing, the antimicrobial activity, the skin‐adhesion, and water‐retention of such supramolecular hybrid hydrogels were also verified. On the other hand, the supramolecular hybrid hydrogels inherited the shear‐thinning property and are suitable as an injectable biomaterial. The cell viability assay confirmed the equivalent cytotoxicity of the supramolecular hybrid hydrogels to that of the native hydrogels without CNT. Consequently, such CNT‐hybridized supramolecular hydrogel shows a great potential in the biomedical application. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 相似文献
100.
ZnO nanoparticles have been prepared successfully by hydrogel decomposition method (HDM). Synthesized ZnO nanoparticles were characterized by X‐ray diffraction (XRD), fourier transforms infrared spectroscopy (FTIR), and transition electron microscopy (TEM) techniques. Narrow distribution of sizes with a 20–30 nm diameter and regular distribution of ZnO nanoparticles are attributed to the application of poly(acrylic acid‐co‐acrylamide) grafted chitosan hydrogel as coating agent. The results show that the polymer thermal decomposition technique is a perfect method for the synthesis of ZnO nanoparticles. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 相似文献