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1.
通通过卡拉胶(KC)对三聚磷酸铝(ATP)进行接枝改性获得KC-ATP改性填料,再将其添加到水性环氧树脂(WEP)中制备复合防腐涂层。采用FTIR、XPS、TG、SEM对ATP改性前后的形貌、结构进行表征。结果表明,KC成功地接枝到ATP表面,改善了ATP的水溶性。采用电化学阻抗谱(EIS)和盐雾实验考察了复合涂层的防腐性能。结果表明,复合涂层的防腐性能明显优于纯水性环氧涂层,且当KC-ATP功能填料含量为1.0%时(以水性环氧树脂的质量为基准,下同),涂层的耐腐蚀性能达到最佳,浸泡48 h后涂层的极化电阻Rp为8.183×107 Ω∙cm2,远高于ATP改性复合涂层和纯环氧涂层。  相似文献   
2.
In this study, a novel micro porous honeycomb structured Crg-GG-IPN material was incepted to be applicable as scaffold and accomplished. The hydrophilicity was confirmed by FT-IR and OCA. Amorphous nature and micro-rough surface were confirmed by XRD and AFM. Void fraction was 0.61?±?0.04. Void space, hemocompatibility and platelet adhesion were captured by SEM. Degradability of the material was confirmed by in-vitro degradation study. Incision method using mice model was a clear evidence for cell attachment and non-toxicity and was confirmed from hematology and histopathology. Thus, it appears that Crg-GG scaffolds can be useful as wound healing material for clinical applications.  相似文献   
3.
In this study, the gel strength and visible microstructure of fat containing β-lactoglobulin-κ-carrageenan gels were investigated using puncture testing and confocal scanning laser microscopy, respectively. The gel strength was closely linked to the visible microstructure of the whey protein network as stained with Rhodamine B. Covalent labelling of κ-carrageenan with FITC prior to gel formation enabled localisation of the hydrocolloid phase, but caused a significant drop in the gel strength. This effect coincided with the observed reduction of the κ-carrageenan intrinsic viscosity, which was found to be a result of the labelling process. The use of a novel dye, V03-01136, for the staining of fat allowed for the specific and concurrent visualisation of the protein, hydrocolloid and fat phases under the conditions applied in the study.  相似文献   
4.
魔芋葡甘聚糖-卡拉胶共混膜制备及其性能研究初探   总被引:3,自引:0,他引:3       下载免费PDF全文
本文以魔芋葡甘聚糖(KGM)和卡拉胶制作魔芋葡甘聚糖-卡拉胶共混制成复合膜,研究了不同比例对膜的透明度、厚度、洗刷性能等性能的影响。结果表明,魔芋葡甘聚糖与卡拉胶用量比为6:4时,共混膜的能达到较好的效果。  相似文献   
5.
6.
The objective of this research was to find an optimum Carrageenan matrix formulation with the desired drug release and physical properties prepared by direct compression. In order to achieve this, matrices containing 10% theophylline, different Carrageenan level, and different excipient were prepared and evaluated. A selected matrix containing 40% Carrageenan and lactose fast flo was tested for dissolution in three different dissolution media (distilled water, 0.1 N HCl, and phosphate buffer pH 7.4). The same formulation was also tested for dissolution at 50 rpm, 100 rpm, and 150 rpm, and using different dissolution apparatus (Apparatus 1 and 2).

All matrices showed a decrease in drug release as the polymer level was increased. Only Avicel PH-101 did not show any significant difference between matrices prepared with 30% and 40% polymer. At 10% polymer level, it appears that the type of diluent used controls the drug release. However, at high polymer level, 30% and 40%, it appears that the polymer level controls the drug release. Phosphate buffer pH 7.4 and 0.1 N HCl increase drug release and appear to increase Carrageenan solubility and decrease gel formation. Also, as the rotational speed of the apparatus was increased, the integrity of the gel layer was decreased, and the release of drug was increased. The drug release from Carrageenan matrices appears to follow the diffusion model for inert matrix up to 90 min. After 90 min, the drug release follows a zero-order model.

This study demonstrated that matrices using Carrageenan can be successfully prepared by direct compression.  相似文献   
7.
The influence of carrageenan on the properties of low-fat frankfurters   总被引:2,自引:0,他引:2  
Research was undertaken to study the technological properties of six carrageenan fractions and their usefulness as fat substitutes in frankfurter type sausages. In the first stage of the experiment hardness of gels made of 3% solutions of carrageenan preparations with different pH (5.5, 6.0 and 6.5) was evaluated. The highest Fmax. values were noted in gels obtained from G-WG carrageenan (kappa I fraction). In the second stage of the study frankfurter type sausages were produced, containing 20% and 10% of fat in meat batter with or without (control) kappa I carrageenan (G-WG). Carrageenan as a fat substitute caused a reduction in cooking and storage weight losses, increased hardness, gumminess and chewiness. All frankfurters produced with carrageenan, irrespective of fat content, were characterized by significantly higher sensory evaluation scores for texture, color and taste in comparison to control sausages.  相似文献   
8.
A new method was developed to produce uniform spherical magnetic carrageenan-gel particles suitable for the affinity chromatography purification of large molecules. A sol-phase of k-carrageenan is pumped into an air jet to produce an aerosol of gel particles. The particle size can be varied by adjusting the air jet velocity. The gel particles are stable in 0-5 mol dm?3 KCI to 190 psi. The gel particles were used to immobilize soy trypsin inhibitor for the affinity purification of trypsin. The affinity matrix was tested in a packed-bed separator, fluidized-bed separator and a magnetically-stabilized fluidized-bed separator with similar column capacity for each separator.  相似文献   
9.
A series of microwave irradiated IPN of Crg and GG have been synthesized and cross linking through hydrogen bonding was confirmed by FTIR spectroscopy. Thermal sensitivity at 48°C, degradation above 200°C is an emblem of uniqueness. We obtained micro rough surface morphology, hydrophilicity and muco-adhesion supporting S6 for targeted drug delivery. Honey comb like internal architecture will provide high mechanical strength. The sample S6 showed 72% drug release in 12 hours. Based on the results, it was concluded that the S6 can be used as target oriented controlled drug delivery devices enabling control over swelling and drug release.  相似文献   
10.
Carrageenan was used to prepare carrageenan films reinforced with chitin nanowhiskers. Atomic force microscopy was used to characterize the morphology and roughness of the films. Structural characterization was performed using X-ray diffraction and Fourier transform infrared spectroscopy. The mechanical properties were assessed by tensile tests. The prepared nanocomposites were used as cell substrate in order to explore their potential biological applications. HeLa cells were seeded on the samples in order to assess their biocompatibility. The preliminary results show good cell proliferation but low cell adhesion, demonstrating a potential application of this novel material as substrate for tumor cell culture.  相似文献   
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