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81.
壳聚糖/羧甲基壳聚糖止血膜的制备与表征 总被引:1,自引:0,他引:1
针对壳聚糖止血膜柔韧性差的问题,以丙三醇和酚磺乙胺作为改性剂,采用溶液浇膜的方法制备了不同组成配比的壳聚糖(CS)/羧甲基壳聚糖(CMCS)止血膜,并评价了CS/CMCS止血膜拉伸性能和止血效果.丙三醇的引入可使CS/CMCS止血膜的断裂伸长率提高4~7倍,尽管其拉伸强度也降低了70%.丙三醇改性的CS/CMCS=8/2载药止血膜具有较好的拉伸强度(10.4±0.9 MPa)和断裂伸长率(50.4±4.5%);与未加入酚磺乙胺的CS/CMCS止血膜相比,酚磺乙胺的离子交联作用使CS/CMCS载药止血膜的拉伸强度提高55%,而断裂伸长率仅降低24%.止血评价结果表明经丙三醇改性的CS/CMCS=8/2止血膜均能使血液发生分离的时间明显缩短,并具有促使血液凝结形成黑色血块的能力. 相似文献
82.
为了研制符合食品包装要求的彩色防水纸浆模塑制品,选用食用色素对壳聚糖处理后的纸浆纤维进行染色,并在染色纸浆中加入防水剂H,讨论了防水剂质量分数对纸浆纤维防水效果和染色效果的影响。结果表明,染色温度为60℃,染料用量为0.6%(对绝干浆质量),染浴pH=3.5的条件下染色效果较好。结合生产实际,可进行常温染色,上染率达71.43%,褪色率为7.12%。防水剂的加入除能明显提高纸模制品的湿环压强度外还能改善其染色效果,添加量为5%(对绝干浆质量)时,纸模可达到较好的湿环压强度,上染率可提高到79.30%,褪色率降低为0.31%。 相似文献
83.
A novel technique of immobilizing indicator dyes by electrostatic adsorption and covalent bonding to fabricate optical sensors
was developed. 3-Amino-9-ethylcarbazole (AEC) was attached to the outmost surface of quartz glass slide via aminosilanizing
the slide, crosslinking chitosan, adsorbing Au nanoparticle, self-assembling HS(CH2)11OH, and coupling AEC. Thus, an AEC-immobilized optical sensor was obtained. The sensor exhibits a wide linear response range
from 7.0×10−7 to 1.0×10−4 mol/L and a correlation coefficient of 0.995 9 for the detection of 2-nitrophenol. The detection limit and response time
of the sensor are 1.0×10−7 mol/L and less than 10 s, respectively. The fluorescence intensity of the used sensor can be restored to the blank value
by simply rinsing with blank buffer. A very effective matrix for immobilizing indicator dye is provided by the proposed technique,
which is adaptable to other indicator dyes with amino groups besides AEC.
Foundation item: Project(20775010) supported by the National Natural Science Foundation of China; Project(208095) supported by the Key Project
of Ministry of Education, China; Project(07A006) supported by the Scientific Research Fund of Hunan Provincial Education Department,
China; Project(07JJ3020) supported by Hunan Provincial Natural Science Foundation of China 相似文献
84.
合成了对壳聚糖溶解效果好、可重复使用的离子液体氯化2-氨基乙酸[Gly]Cl,用1H NMR和FT-IR对其结构进行了确定。在制得的离子液体水溶液中,制备了水溶性N-乙酰化壳聚糖。用XRD和FT-IR对产物进行了结构表征。通过单因素实验得到了较佳反应条件:n(乙酸酐)∶n(壳聚糖)=2.75∶1,反应温度60℃,反应时间5 h。并对产物的吸湿保湿性能进行初步研究,结果表明,产物具有良好的吸湿保温性能。还考察了离子液体的重复使用性能,重复使用3次后,N-乙酰化壳聚糖的取代度仍大于89%。 相似文献
85.
采用超声波辐射,以壳聚糖为原料、乙醇为分散介质、一氯乙酸为羧甲基化试剂合成了羧甲基壳聚糖,通过四因素三水平正交实验得出最优合成条件为:mNaOH/m壳聚糖为1.5;mclCH2COOH/m壳聚糖为1.5;反应时间2h;反应温度60℃;采用红外光谱仪、紫外-可见分光光度计、热重/差热分析仪、X射线衍射仪、扫描电镜对产物结构进行了表征. 相似文献
86.
The aim of this study was to optimize the formula of free blended coating membrane of ethyl cellulose (EC) and chitosan (CS), including their suitable ratio range and the best plasticizer used. The dry films were produced by a casting/solvent evaporation method, with different volume ratio of EC and CS solution plasticized by various plasticizers, respectively. The wet films were prepared by immersing dry films in pH 6.8 phosphate buffer saline (PBS) for 24 h. The promising ratio range of EC/CS was below 20/5 or 20/6 with various plasticizer, which was determined by comparing the viscosity of the blended solutions and the morphology of the blended films. The efficiency of plasticization was evaluated by measuring glass transition temperature (Tg). All the testing plasticizers have good compatibility with EC or CS and dibutyl phthalate (DBP) have the strongest efficiency inducing the lowest Tg (39.9°C) of the film. Mechanical properties were evaluated by the ratio of tensile strength (T) to elastic modulus (E). In the wet state, the films with DBP had the highest T/E value (1.2). The results of leaching of plasticizers also verified that DBP was the most stable plasticizer in the films. The release rates of tetramethylpyrazine phosphate (TMPP) through the pellets coated with the blended films of EC/CS (20 : 6 v/v) plasticized by various plasticizers showed that the more water‐soluble the plasticizer was, the more quickly TMPP dissolved from the coated pellets, which further indicated that the water‐insoluble plasticizers (such as DBP) could be more applicable to keep the sustained or controlled release property of the blended films in wet state. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 1932–1939, 2006 相似文献
87.
阿司匹林壳聚糖纳米缓释微球的制备及体外释放性能的研究 总被引:5,自引:0,他引:5
以自制阿司匹林为药物,壳聚糖为载体,采用乳化-化学交联法制备了阿司匹林-壳聚糖载药微球,确定了阿司匹林-壳聚糖载药微球的制备工艺条件,探讨搅拌速度、阿司匹林/壳聚糖质量比、交联剂戊二醛、乳化剂Span-80用量对微球的药物包封率、载药量和释药性能的影响。研究结果表明,室温条件下,以液体石蜡为介质,选用3%的壳聚糖冰醋酸溶液、按阿司匹林∶壳聚糖=1.5∶1、4%的戊二醛为交联剂、Span-80用量为体积比6%、中等搅拌速度制备出的微球药物包封率可达79%,微球粒径最小可达20 nm,制得的载药微球在16 h内对药物有良好的缓释作用,在25 h之内仍存在缓药效果。 相似文献
88.
棉织物的抗菌免烫整理研究 总被引:3,自引:0,他引:3
通过正交试验探讨了用H2 O2 氧化降解法制备适用于与聚羧酸MAA - 1配合进行抗菌免烫整理的低聚水溶性壳聚糖的最佳工艺 ,研究了降解壳聚糖与聚羧酸MAA - 1配合对棉织物进行抗菌免烫整理的工艺以及降解壳聚糖的质量浓度和相对分子质量对整理效果的影响。结果表明 :用 80g/L的聚羧酸MAA - 1和 4 0 g/L相对分子质量为 90 0 0的降解壳聚糖分两浴整理的棉织物的褶皱回复角为 2 71°,DP等级为 4 .0 ,断裂强力保留率为 6 4 % ,对大肠杆菌和金黄色葡萄球菌的抗菌率分别为 94%和 83%。经过 2 0次洗涤 ,其WRA为 2 5 7° ,DP等级为 3.7,而抗菌率则均保持在洗涤前的 80 %以上。阴离子染料 (直接冻黄G)染色的K/S值较用聚羧酸MAA - 1整理的棉织物提高了 1 .85。 相似文献
89.
Sibel Akgün Gülsüm Ekici Nilüfer Mutlu Necati Beşirli Baki Hazer 《Journal of Polymer Research》2007,14(3):215-221
Modification of chitosan by grafting of vinyl butyrate was carried out in homogeneous phase using potassium persulfate as
redox initator and 1.5% acetic acid as solvent. The percent grafting and grafting efficiency were analysed and the high grafting
efficiency up to 94% was observed. The effects of reaction variables such as monomer concentration, initiator concentration,
temperature and reaction time were investigated. It was observed that the solubility of chitosan was markedly reduced after
grafting with vinyl butyrate. The grafted product is insoluble in common organic solvents as well in dilute organic and inorganic
acids. Characterization of the graft copolymers were carried out by using Fourier Transform Infrared Spectroscopy (FTIR),
Differential Scanning Calorimetry (DSC) and Scanning Electron Microscopy (SEM) technics. Characteristic signal of carbonyl
group was observed at 1,731 cm−1 which belongs to the poly vinyl butyrate segments in the graft copolymer. The melting transition of the chitosan main chain
in the copolymer shifted to 124°C from its original value 101°C. In addition to these, we have also studied topology of the
graft copolymer and the SEM micrograph showed continuous homogenous matrix which means there is no phase separation. 相似文献
90.