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51.
A. Fendler M. P. Villanueva E. Gimenez J. M. Lagarón 《Cellulose (London, England)》2007,14(5):427-438
The present work presents and discusses the interrelation between composition, morphology, thermal history, mechanical and
barrier properties to oxygen and limonene of composites of HDPE/MA-PE/cellulose fibers of significant interest in, among others,
food packaging applications. From the overall results, it was observed that increasing the loading of purified alpha-cellulose
fibers in the polyethylene matrix beyond 10 wt.% led to a decrease in the permeability coefficient of d-limonene, effect which was found to be primarily related to a decrease in the overall solubility of this strongly plasticizing
aroma component. On the other hand, the oxygen permeability was found to decrease to a significant extend with increasing
fiber content beyond 5 wt.%, but this effect was more strongly ascribed to a significant decrease in the diffusion coefficient.
Therefore, the fibers are thought to generate a more tortuous path for the non-interacting gas molecules to travel across
the composites thickness, even when tested at high relative humidity conditions. Optimum fiber loading levels in terms of
overall property balance were found to be around 20 wt.%. 相似文献
52.
Thirteen phosphorus-containing flame retardants were synthesized in this work. The solubilities of flame retardant [(6-oxide-6H-dibenz[c,e][1,2]oxaphosphorin-6-yl)-methyl]-butanedioic acid (DDP) in selected solvents are measured. TGA measurements of the 13 phosphorus-containing flame retardants were carried out and thermal stabilities of three flame-resistant PET (FRPET) resins were investigated. A FRPET incorporated by DDP with terephthalic acid and ethylene glycol reported in literature was also discussed and compared. The thermal stability of the FRPET is improved by the incorporation of phosphorus-containing flame retardants. The LOI values of all phosphorus-containing polyesters are higher than 27%. The improvement of the flame-resistant ability is due to the formation of the char that is not only caused by the existence of phosphorus elements in the resin but also by the relative large number of carbon atoms of the phenyl group in the flame retardants. 相似文献
53.
Mechanical properties of BPDA-ODA polyimide fibers 总被引:1,自引:0,他引:1
An aromatic polyimide was synthesized via a one-step polycondensation reaction between biphenyltetracarboxylic dianhydride (BPDA) and 4,4′-oxydianiline (ODA) in p-chlorophenol. The polyimide (BPDA-ODA) solution dopes were spun into fibers by means of dry-jet wet spinning. The as-spun fibers were drawn and treated in heating tubes for improving the mechanical properties. The thermal treatment on the fibers resulted in a relatively high tensile strength and modulus. Thermal mechanical analysis (TMA) was employed to study the linear coefficient of thermal expansion (CTE). Thermal gravimetry analysis (TGA) spectra showed that the BPDA-ODA fibers possessed an excellent property of thermo-oxidative degradation resistance. The sonic modulus Es of the polyimide fibers was measured. 相似文献
54.
Der-Jang Liaw 《Journal of polymer science. Part A, Polymer chemistry》1995,33(4):605-613
Several sulfone-containing polyesters having inherent viscosities 0.43-0.19 dL g?1 were prepared by direct polycondensation of 4,4′-dicarboxydiphenyl sulfone (DCDPS) with various aromatic and aliphatic diols, by p-toluenesulfonyl chloride and N,N′-dimethylformamide in pyridine solution. The polyesters were examined by elementary analysis, IR spectra, inherent viscosity, x-ray diffraction, solubility, DSC, and TGA. The diffraction diagram showed that all polyesters were crystalline except that obtained from bisphenol-A. All polymers were soluble in sulfonic acid (18M), phenol and p-chlorophenol, but not in acetone and toluene. These polymers obtained from aromatic bisphenols lost no mass below 325°C, but 10% loss of mass was recorded above 396°C in nitrogen. DCDPS copolymerized with isophthalic acid (IPA) and bisphenol-A had inherent viscosity up to 0.49 dL g?1, with relatively narrow distribution of molar mass . © 1995 John Wiley & Sons, Inc. 相似文献
55.
Anilkumar Appajaiah Volker Wachtendorf Werner Daum 《Polymer Degradation and Stability》2006,91(11):2605-2613
The thermo-oxidative stability of commercially available polymer optical fibers (POFs) and their components (cores and claddings) was investigated. All the bare POFs (core and cladding only) studied here were based on poly(methyl methacrylate) (PMMA) core. The fibers were exposed to 100 °C/low humidity for about 4200 h. Chemiluminescence (CL) technique was applied to investigate the thermo-oxidative stability and for measuring the transmission loss during exposure a prototype device called multiplexer was used. POFs exhibited variation in thermo-oxidative stability although they possessed identical core material PMMA. This was due to difference in the chemical compositions of claddings. Claddings were more susceptible to the thermo-oxidative degradation compared to cores. The thermo-oxidative degradation of both the cladding and the core was found in POFs as a result of climatic exposure. POFs showed an early drop-off followed by a slow decline of transmission. The early drop-off of transmission was attributed to physical changes like thermal expansion and the slow decline of transmission to chemical changes like oxidative degradation of POFs. A good linear relationship between optical transmission stability and thermo-oxidative stability of POFs was established from these studies. 相似文献
56.
液晶聚酯与环氧嵌段共聚物的合成及表征 总被引:5,自引:0,他引:5
近年来 ,人们利用高分子液晶作为热固性环氧树脂的改性剂 ,不仅可以提高环氧树脂的韧性和强度 ,而且可以改善其热性能 ,为制备高性能的环氧树脂提供了一条新的途径[1,2 ] .目前报道所使用的液晶聚合物大多为液晶聚酯[3 ] 或液晶性聚氨酯[4] ,这些液晶聚合物与环氧树脂由于存在相容性不好的问题 ,给其实际应用带来了困难 .为了改善二者的相容性 ,本文采用溶液法合成了末端带有反应活性基团的聚酯型液晶聚合物 ,将它再与双酚A环氧预聚物反应 ,制得了高分子液晶环氧嵌段共聚物 ,其合成路线如下 :2HOCOOCH3+ HO(CH2 ) 6 OH H… 相似文献
57.
Two types of commercial glass fibers were subjected to attack in strongly basic KOH solutions. The resulting leach solutions were analysed for Na, Ca, and Si. This showed that the corrosion process attacks the fibers incongruently. Although there are some distinct differences in the performance of these fibers, to a first approximation both types behave similarly. Further, the fibers were depth profiled using a recently developed SNMS technique for fiber in-depth analysis. This showed that both types of fibers behave in a quite dissimilar manner. The fibers were weathered already without any treatment. Although both fibers show alkali ion exchange and network splitting processes, on one of the fiber layers enriched in SiO2, Fe2O3, and CaO are formed by a redeposition process from the leach solution.Dedicated to Professor Dr. rer. nat. Dr. h.c. Hubertus Nickel on the occasion of his 65th birthday 相似文献
58.
M. Mucha 《Colloid and polymer science》1994,272(9):1090-1097
The miscibility of polyethylene oxide (PEO) with oligoester and polyester resin, the morphology of the blends and the kinetics of PEO crystallization in the blends were studied by optical microscopy and differential scanning calorimetry. The blends were found to be miscible with uncured resin at 60°C. After isothermal crystallization of PEO from liquid oligoester or UV cured polyester about 20% of the PEO material is still dissolved in the resin and it is incorporated between lamellae or in the interspherulitic regions. It was observed that the growth rate of PEO spherulites and the degree of crystallinity of PEO in the blends decreases very fast together with a decrease of the PEO content and the progress of the resin crosslinking. 相似文献
59.
通过原位直接缩聚反应,制备了刚性棒状聚对羟基苯甲酸酯(PHB)和聚对苯二甲酸丁二醇酯-聚四亚甲基醚多嵌段共聚物(PBT-PTMG)的微相复合物.复合物可溶于氯仿等溶剂,可以浇铸成膜.本文研究了PHB含量和聚合过程中,基体聚合物溶液浓度对微相复合物形态以及力学性能影响.同共混法相比,原位缩聚法可得到分散更均匀,力学性能更优良的微相复合物. 相似文献
60.
Effect of Hydration–Dehydration Processes on the Structure and Porosity of Detemplated Silica Fibers
Kovalenko V. V. Tel'biz G. M. Bobonich F. M. 《Theoretical and Experimental Chemistry》2004,40(1):64-68
A study was carried out on the conditions of template removal (calcination or extraction by solvents) and hydration–dehydration processes on the hexagonal structure and porosity of detemplated fibers. The hydration–dehydration cycle leads to a decrease in fiber porosity, especially in fiber detemplation by extraction with surfactant solvents such as ethanol and acetic acid. 相似文献