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21.
    
Poly (glycerol sebacate) (PGS) is a thermoset biodegradable elastomer considered as a promising candidate material for nerve applications. However, PGS synthesis is very time and energy consuming. In this study, the PGS pre‐polymer (pPGS) was synthesized using three synthesis times of 3, 5, and 7 hours at 170°C. Fourier transform infrared (FTIR), nuclear magnetic resonance spectroscopy, X‐ray diffraction analysis, and differential scanning calorimetry thermogram were utilized to study the pPGS behavior. Poly (vinyl alcohol) was used as a carrier to fabricate aligned poly (vinyl alcohol)‐poly (glycerol sebacate) (PVA‐PGS) fibers with various ratios (60:40, 50:50, and 40:60) using electrospinning and crosslinked through the thermal crosslinking method. Morphology of the fibers was studied before and after crosslinking using scanning electron microscopy (SEM). FTIR, mechanical properties in the dry and wet state, water contact angle, in vitro degradation, and water uptake behavior of crosslinked scaffolds were also investigated. 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide (MTT) assay, SEM analysis, and 4′, 6‐diamidino‐2‐phenylindole (DAPI) staining were utilized to determine the biocompatibility of scaffolds. The results show the synthesized pPGS in 3 hours at 170°C is the optimized sample in the terms of chemical reaction. All scaffolds have bead‐free and a uniform fiber diameter. The Young's modulus of crosslinked PVA‐PGS (50:50 and 40:60) fibers is shown to be in the expected range for nerve applications. The cell culture studies reveal PVA‐PGS (50:50 and 40:60) fibers could lead to better cell adhesion and proliferation. The results suggest that PVA‐PGS (50:50 and 40:60) is a suitable and promising biodegradable material in the fabrication of scaffolds for nerve regeneration.  相似文献   
22.
In this paper we establish a sharp result concerning integral mean estimates for self-reciprocal polynomials.  相似文献   
23.
The interaction between Cd2+ and Pb2+ ions and 18-crown-6 (18C6), 1,10-diaza-18-crown-6 (C22) and 1,7-diaza-15-crown-5 (C21) were studied in water solvent at 25, 35, 45 and 55° using square wave voltammetric technique. The stoichiometry and stability of the complexes were determined by monitoring the shift in half-wave or peak potential of the polarographic waves of metal against the ligand concentration. Thermodynamic parameters such as G, H and S were obtained by using a polarographic double wall cell in which the temperature could be fixed to ±0.1°C. The results of all experiments show 1 : 1 complexes, but in addition to 1 : 1 ratio, a 2 : 1 ratio of ligand to cation is also obtained for C22–Pb2+ complex. The selectivity order for 18C6 and C22 is Pb2+ > Cd2+. The thermodynamic data G, H and S values show that the complexes are stabilized by both the enthalpy and entropy terms, but C22–Pb2+ complex is stabilized by only enthalpy term.  相似文献   
24.
In this paper we extend a classical result due to Cauchy and its improvement due to Datt and Govil to a class of lacunary type polynomials.  相似文献   
25.
26.
Rate of polymer degradation is very important for implantable biomaterials since controlling the degradation rate may complement the biological response and affected mechanical property requirements. In spite of numerous publications on the potential use of combinations of poly lactic acid/bioactive glass fillers for degradable bone plate, little information exists on the controlling degradation rate and its effects on the other aspects such as biomechanical compatibility, bioactivity, etc. Our previous study revealed that a composite bone plate consist of poly l-lactic acid/braided bioactive glass fibers has the initial mechanical properties near to cortical bone. In this study, degradation rate and mechanical behavior of the composite bone plate were assessed, and also degradation rate was controlled by using proper manufacturing process and improving bonding between matrix and reinforcement. Moreover, bioactivity of the composite was considered before and after controlling degradation rate, because of the important role of bioactivity and ion release in healing acceleration. Results showed that degradation process of the composite could be controlled properly. Strength of the treated composite decreased only about 5% through 2 weeks and about 35% after 8 weeks while, the strength loss for the untreated composites was about 50 and 70 percent after 2 weeks and 8 weeks of degradation respectively. Although calcium-phosphate formation on the surface of the composite was postponed in the treated samples, the bioactivity of the composite remained unchanged and bone-like apatite was formed on the composite surface which is important for the application of the composite in bone tissue environment.  相似文献   
27.
    
A novel synthetic method was developed to prepare a difunctional surfactant using sulfanilic acid and dodecyl bromide. In the first step, sulfanilic acid was protected by acetic anhydride. Then, Friedel–Crafts alkylation of the synthesized acetanilide with dodecyl bromide was performed in the presence of aluminum chloride. The protecting group (amide) was removed easily by acid hydrolysis. The formation of surfactant was confirmed with Fourier transform infrared and proton nuclear magnetic resonance spectroscopy. The demulsification property of this surfactant was studied using brine-fuel oil emulsion, and its result was compared with a commercially available demulsifier. The results showed that 52% of water was separated from emulsion at room temperature, but at elevated temperature 98% of water was separated from brine-fuel oil emulsion.  相似文献   
28.
Zargar  Behrooz  Khazaeifar  Ali 《Mikrochimica acta》2017,184(11):4521-4529
Microchimica Acta - The authors report on the preparation of sol-gel coated magnetized carbon nanotubes whose surface were imprinted with Cd2+ ions and the application of these materials on...  相似文献   
29.
Understanding the genetic diversity of a crop is useful for its effective utilization in breeding programmes. For better understanding of the genetic variability in common bean, the first and foremost step is to study its genetic diversity. In the present investigation, 138 genotypes of common bean collected from various regions of Jammu and Kashmir, India, representing major common bean growing areas of this region, were evaluated using 23 SSRs. These SSRs were found highly polymorphic and possess high values for various parameters indicating their high discriminatory power. The average PIC value observed was 0.692, with 0.730 as average gene diversity value, and 0.267 as heterozygosity. Twenty-three SSRs produced a total of 251 alleles. The dendrogram generated with un-weighted neighbour joining cluster analysis grouped genotypes into three main clusters with various degrees of sub-clustering within the clusters. The model-based STRUCTURE analysis using 23 SSR markers identified a population with 3 sub-populations which corresponds to distance-based groupings with average F ST value and expected heterozygosity of 0.1497 and 0.6696, respectively, within the sub-population, as such high level of genetic diversity was observed within the population. Further, Core Hunter II was used to identify a core set of 96 diverse genotypes. This core set of diverse 96 genotypes is a potential resource for association mapping studies and can be used by breeders as a material to make desirable genetic crosses to generate elite varieties for the fulfilling global market needs. These findings have further implications in common bean breeding as well as conservation programs.  相似文献   
30.
For the first time, ZrO?-HA-TiO? layers were synthesized through EPD-Enhanced MAO (EEMAO) technique in only one step where no supplementary treatment was required. SEM, XRD, EDX, and XPS techniques were employed to propose a correlation between the growth parameters and the physical and chemical properties of the layers. The layers revealed a porous structure where applying higher voltages and/or utilizing higher concentrated electrolytes resulted in formation of wider pores and increasing the zirconium concentration in the layers; meanwhile, prolonging the growth time had the same effects. The layers mainly consisted of anatase, hydroxyapatite, monoclinic ZrO?, and tetragonal ZrO? phases. Increasing the voltage, electrolyte concentration, and time, hydroxyapatite as well as tetragonal ZrO? was decomposed to α-TCP, monoclinic ZrO?, and ZrO. The nanosized zirconia particles (d = 20-60 nm) were further accumulated on the vicinity of the layers when thicker electrolytes were utilized or higher voltages were applied. Emphasizing on the chemical and electrochemical foundations, a probable formation mechanism was finally put forward.  相似文献   
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