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221.
羟乙基瓜尔胶中羟乙基摩尔取代度以及取代位置的表征   总被引:2,自引:1,他引:1  
本文探索了表征羟乙基瓜尔胶(HEG)中羟乙基摩尔取代度(MS)以及取代位置的化学方法。当反应温度为110℃,时间为14hr,HEG中羟基与混酐比例为1:2.5时,用混酐化学法可准确测定HEG的羟乙基MS,测定结果与计算值的相对误差小于10%。在pH=10.30和0℃的条件下,瓜尔胶的伯羟基被2,2,6,6-四甲基哌啶氮氧化物(TEMPO)-NaClO-NaBr体系选择性氧化成羧基,由此可表征羟乙基链段的取代位置。在瓜尔胶醚化生成羟乙基瓜尔胶的过程中,醚化反应并不是完全发生在伯羟基上。伯羟基的反应活性是仲羟基的6-10倍。随着MS的增大,连接在仲羟基上羟乙基链段占所有羟乙基链段的比例逐渐增大,当MS=0.4时该比例基本不再变化,为40%左右。  相似文献   
222.
Eucommia ulmoides gum (EUG) was applied in blend rubber with a heavily limited amount because of its duality of rubber and plastic, and an efficient way of triazolinedione (TAD)‐based Alder‐ene reaction was used to improve the elastic properties of EUG. Binary modification of EUG with two TADs containing hexyl and polyhedral oligomeric silsesquioxane (POSS) groups were conducted to generate the modified EUG elastomers with tunable mechanical properties and good compatibility by varying TAD contents. When the low hexyl (1%) and POSS (0.2%) TADs incorporated, the modified EUGs displayed high tensile strength of 36.57 MPa with the elongation at break of 876%, and thus high toughness of 152.14 MJ m?3. If high contents of hexyl (20%) and POSS (0.2%) TADs employed, the modified EUGs exhibited excellent elongation at break of 1165% and recovery rate of 60%, and especially its loss factor reached up to 0.83?0.65 at 20?70°C. Therefore, the modified EUGs containing the polar urazole and POSS groups should be a novel elastomer with good compatibility, wear resistance, and damping properties. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019  相似文献   
223.
Dispersion of carbon nanotubes in a polymer matrix is one of the most critical issues in carbon nanotube/polymer composites. In this paper we discuss the considerable improvement in the dispersion of multiwalled carbon nanotubes (MWNTs) in poly(vinyl alcohol) (PVA) matrix that was attained through gum arabic treatment. The mechanical properties of these MWNT/PVA composites show that only 2 wt% nanotube loading increases the tensile modulus by more than 130%.  相似文献   
224.
The relation between the molecular relaxation processes and the results of tensile experiments has been studied for hard and toughened polyvinyl chloride (PVC). The relaxation spectra have been determined between 10?4 and 10+4 sec by means of stress relaxation, flexural vibration experiments, and tensile tests. Yield stress, yield strain, rupture stress, rupture strain, and rupture energy have been determined at 23° and 50° C as functions of yield time or rupture time, respectively, over a time-range from 10?2 to 10+4 sec approximately. It is shown that the molecular relaxation processes observed in the range of small deformations also influence the behavior in the nonlinear range, especially the elongation at rupture in tensile experiments. In addition, effects of the molecular processes on the yield stress, the rupture stress, and, consequently, the rupture energy have been observed. These effects are due to the time- and temperature-dependent decrease of the macroscopic stress and of the microscopic notch stresses by certain relaxation mechanisms. The most suitable characteristic parameters in tensile experiments are the yield stress and the rupture strain. It is pointed out that the usefulness of a single value of a mechanical property as determined in a standard “one-point” test is very restricted.  相似文献   
225.
The characterization of a polyelectrolyte complex material comprised of two biopolymers, a chitosan upper layer and a gellan gum under layer, is reported. It is shown that the upper layer of chitosan with incorporated levofloxacin displays an antibacterial activity, while the under layer of a gellan gum/TiO(2) composite supports the growth of fibroblastic cells.  相似文献   
226.
Complex coacervation of whey protein(WP) with acacia gum(AG) was carried out in water with the presence of dodecyl acetate (DA),a component of insect sex pheromones,in order to obtain microcapsules with DA as the core material and WP-AG coacervate as the wall materials.Through variations in wall/core ratios,concentrations of the wall materials in capsule preparations,DA encapsulation was optimized,which showed a high DA encapsulation was achieved when coacervation was conducted at pH 3.5 with wall/core mass ratio at 3 combined with concentration of wall materials at 1.0 wt%.Morphology and the structure of DA loaded microcapsules were examined by scanning electron microscope,which showed the microcapsules were of core/shell structure with DA encapsulated in the inner of the microcapsules.DA release was examined and the behavior of the release was discussed.  相似文献   
227.
在碱催化条件下,利用N,N-二乙基氯乙胺盐酸盐与瓜尔胶和羟丙基瓜尔胶一步法合成得到N,N-二乙基胺乙基瓜尔胶和N,N-二乙基胺乙基羟丙基瓜尔胶。结果显示合成过程中温度、反应时间、羟丙基取代度及溶剂等因素对产品分子量和N,N-二乙基胺乙基取代度有影响。通过红外光谱和核磁法对N,N-二乙基胺乙基瓜尔胶和羟丙基N,N-二乙基胺乙基瓜尔胶的分子结构进行了分析,并通过碳谱对N,N-二乙基胺乙基在瓜尔胶分子链中糖环上的取代分布进行了分析。  相似文献   
228.
This study focused on the preparation and characterization of water-in-oil-in-water (W1/O/W2)-type double emulsions designed by food-grade emulsifiers and stabilizers. The primary objective of this study was to compare different emulsion formulations in terms of droplet size, rheology, and stability and to reduce the amount of polyglycerol poliricinoleate (PGPR). To achieve these goals, PGPR and a PGPR–lecithin blend were utilized in the formation of the primary phase (W1/O), while varying concentrations of guar gum (GG) and gum tragacanth (GT) incorporated in the secondary water phase (W2). Shear thinning behavior was observed for all emulsion formulations. Sauter mean diameters of the emulsions prepared with PGPR as a hydrophobic emulsifier ranged between 30?µm and 75?µm, while those prepared with the PGPR–lecithin blend varied between 25?µm and 85?µm based on the first day’s measurements. In emulsions with the PGPR–lecithin blend, the smallest droplet size was obtained when the GG–GT blend was incorporated in the external aqueous phase. Moreover, GG–GT blends had high consistency coefficients and high apparent viscosity values. It was also observed that PGPR–lecithin containing emulsions were more stable.  相似文献   
229.
A facile and green route for the synthesis of palladium nanoparticles (Pd‐NPs) was developed utilizing non‐toxic and renewable natural green tea extract as the reducing, stabilizing and capping agent. The as‐prepared Pd‐NPs@Oak Gum catalyst was characterized using UV–visible spectroscopy, X‐ray diffraction, Fourier transform infrared spectroscopy, field emission scanning electron microscopy, transmission electron microscopy and energy dispersive X‐ray spectroscopy. The Pd‐NPs@Oak Gum catalyst could be used as an efficient and heterogeneous catalyst for Suzuki coupling reactions between phenylboronic acid and a range of aryl halides containing iodo, bromo and chloro moieties and also for the reduction of nitroarenes using sodium borohydride in an environmental friendly medium. Excellent yields of products were obtained with a wide range of substrates and the catalyst was recycled multiple times without any significant loss of its catalytic activity. Copyright © 2016 John Wiley & Sons, Ltd.  相似文献   
230.
Polysaccharide based semi interpenetrating hydrogel (SIH) networks of cross-linked poly(acrylamide) was synthesised through an redox initiating free radical polymerization utilizing almond gum as a grafting backbone, N,N′– methylenebisacrylamide (MBA) as the cross-linker and ammonium persulphate (APS) – N,N,N′,N′-tetramethyl ethylenediamine (TEMED) as the redox initiator pair. Silver ions were introduced into the hydrogel matrix and silver nanoparticles of invariable size were developed insitu of the swollen hydrogel by the reduction of silver ions (Ag+) using azadirachta indica (neem) leaf extract. The prepared hydrogel - silver nanocomposite (HSN) was characterized by UV–visible diffused reflectance spectroscopy (DRS), fourier transform infrared spectroscopy (FT-IR), high resolution scanning electron microscopy (HR-SEM), energy dispersive X-ray analysis (EDX) and thermogravimetric analysis (TGA). The influence of pH on the swelling behavior of HSN was studied and the antibacterial activity of the developed nanocomposite was evaluated.  相似文献   
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