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Thermosetting phenolic resins, bearing varying extents of propargyl ether groups (PN resins), have been synthesized by the Williamson reaction of a novolac with propargyl bromide and the products characterized. The resin precursors were cured through Claisen rearrangement of the propargyl ether groups and thermal polymerization. The activation energy for thermal cure is substantially lower than that of model bispropargyl ether compounds but is quite independent of the degree of functionalization. The isothermal cure profile, extrapolated from non‐isothermal DSC kinetics studies is consistent with the results from DMA studies. The mechanical properties of glass composites of the resins, of varying propargyl contents, reveal good consolidation of the interphases, evident from the initial gain in both interlaminar shear strength (ILSS) and flexural strength. The benefits of better resin–reinforcement interactions are not retained on crosslinking the resin further, wherein the composite fails by a combination of fibre debonding and brittle fracture of the matrix. Although the resins show better thermal stability than cured resoles, a higher extent of propargylation is detrimental for the thermal stability. Resins with moderate propargylation show good mechanical and thermal properties. © 2001 Society of Chemical Industry 相似文献
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Jesús M. Arsuaga 《Desalination》2010,250(2):829-832
Equilibrium adsorption experiments of phenol, 3-chlorophenol, 4-chlorophenol, and 3-nitrophenol aqueous solutions on NF90 membrane were conducted to obtain the corresponding adsorption isotherms at 25 ºC. Single-compound solutions with concentration ranging from 0.1 to 8 mmol L− 1 were used. Freundlich and Langmuir models were compared to the experimental isotherms and their characteristic parameters were obtained from linear fits. In addition, the adsorptive behaviour of twelve aqueous phenolic compounds on the NF90 membrane was studied in order to investigate the relationship between adsorption and retention of selected solutes. An inverse correlation between the adsorbed amount, at the same equilibrium concentration (1 mmol L− 1), and retention was found. The influence of the molecular hydrophobicity and dipole moment of phenolic compounds on membrane adsorption, solute retention and water flux decline was also investigated. 相似文献
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催化臭氧化技术具有操作简单、氧化效率高、二次污染小等特点,在水中酚类化合物的去除方面具有较大的技术优势。本文以酚类化合物的催化臭氧化处理为切入点,介绍了均相催化臭氧化(二价铁离子)和非均相催化臭氧化(金属型、硅基负载型、碳基负载型、铝基负载型)处理不同浓度梯度酚类化合物的研究进展。然后,基于上述研究进展,根据污染物氧化过程的探针实验结果、催化剂表征特性和有机物转化规律,阐述了苯酚等酚类化合物的催化臭氧化机理。最后,从新型催化剂的再开发、酚类化合物的广谱催化和催化氧化机理的进一步探讨方面对催化臭氧化处理酚类化合物进行了展望。 相似文献
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Three wastes originated from outer surface, shallow surface, and inner surface of bamboo during bamboo-mat preparation were liquefied using microwave energy in a binary solvent (glycerol/methanol). The properties (yield, molecular structure, and molecular weight distribution) of the lignin fractions in the obtained phenolic compounds were contrastively analyzed with proto-lignin in the materials. Results showed that >58% of the lignin in the bamboo cell walls could be degraded and moved to the phenolic compounds via the cleavage of β-O-4′ aryl ether bonds during the microwave liquefaction process. Some polysaccharides still connected with the lignin fraction in the phenolic compounds through covalent bonds. The phenolic compounds displayed well solubility in common organic solvents (ethanol/water cosolvent, acetone, tetrahydrofuran, 1,4-dioxane, and dimethyl sulfoxide). A fast-curing phenol-formaldehyde resin was successfully synthesized with the phenolic compounds under the presence of MgO, and a 23.23% curing time reduction was achieved. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 46952. 相似文献
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全面介绍了耐火材料用酚醛树脂的改性方法,包括无机物改性、有机物改性等,着重介绍了最有前景的钼酸、硼酸改性方法和邻苯基苯酚改性方法,说明了其反应原理、改性合成工艺、主要影响因素。对其他几种改性工艺也作了简要说明,并对耐火材料用酚醛树脂改性方法的发展前景作出了分析。 相似文献
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综述了近3年采酚醛树脂耐热和增韧改性的研究进展简要介绍了各种方法的改性机理及研究现状最后对酚醛树脂改性方法的发展前景作出了展望. 相似文献
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蒸馏妥尔油改性酚醛树脂的合成与应用 总被引:3,自引:0,他引:3
利用造纸厂纸浆废液中分离出的蒸馏妥尔油,合成了改性酚醛树脂,并对反应机理和树脂结构进行了分析。结果表明,当苯酚与甲醛的摩尔比控制为1∶0.6~0.9,蒸馏妥尔油加入量为苯酚的40%~60%时,改性的酚醛树脂性能最佳,与聚合物和溶剂的混溶性得到提高。 相似文献
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In this study, high-performance thermoset polymer composites are synthesized by using both long fibers and nanoclays. Epoxy and phenolic resins, the two most important thermoset polymers, are used as the polymer matrix. The hydrophobic epoxy resin is mixed with surface modified nanoclay, while the hydrophilic phenolic resin is mixed with unmodified raw nanoclay to form nanocomposites. Long carbon fibers are also added into the nanocomposites to produce hybrid composites. Mechanical and thermal properties of synthesized composites are compared with both long-fiber-reinforced composites and polymer- layered silicate composites. The optimal conditions of sample preparation and processing are also investigated to achieve the best properties of the hybrid composites. It is found that mechanical and thermal properties of epoxy and phenolic nanocomposites can be substantially improved. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 相似文献
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有机硼改性酚醛树脂的合成 总被引:9,自引:4,他引:9
以硼酸,苯酚,甲醛为原料,碳酸钠作催化剂合成具有耐高温性能的硼酚醛树脂。通过IR,对这种热固性有机硼改性酚醛树脂的结构进行了表征。树脂的热失重分析结果表明此树脂耐热性优于普通酚醛树脂,所得产物在900℃残留物为76.38%。确定了最佳反应条件为:苯酚:甲醛:硼酸=1:2:0.3(摩尔比),缩合反应温度70-75℃,硼酯化反应温度100-104℃,在控制反血时间下脱水一次。 相似文献
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2‐[4‐(2‐hydroxyphenyl)tricyclo[5.2.1.02,6]dec‐8‐yl]phenol (HPTCDP) were prepared from dicyclopentadiene (DCPD) and phenol via Friedel‐Crafts alkylation. DCPD‐containing phenolic resin (DPR) was also synthesized by incorporating the DCPD‐containing monomer HPTCDP with formaldehyde. DPR was further modified by grafting the phosphate group. The phosphorylation was confirmed by a Fourier transform infrared, 31P‐NMR spectroscopy, and an element analysis. The phosphorus content in the DPR could be successfully tailored to give values of 3.46 to 7.79 wt % by varying the feeding ratios of the phosphorus group. The thermal stabilities of the phosphorus‐containing polymers were identified by differential scanning calorimeter and thermogravimetric analysis. The glass transition temperature values were decreased as the content of phosphorus increased. High char yield 39–47 wt % in thermogravimetric analysis evaluation and limiting oxygen index values of 27 to 34 were found for all the phosphorylated phenolic resins. Such properties make these polymers highly promising for flame‐retardant applications. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 79: 342–349, 2001 相似文献
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A novel magnetic biochar was prepared via pyrolysis method and modification. The influence factors of contact time, initial concentration, temperature, and pH on the adsorption were investigated. The experimental results exhibited that the adsorption ability of methyl salicylate onto biochar was higher than that of phenol and para-chlorophenol under the same condition, which may be owing to the effect of hydrogen bonding, hydrophobicity, and π–π interaction. The maximum adsorption capacities of phenol, para-chlorophenol and methyl salicylate were 62.6, 131.6, and 169.7 mg/g at 298 K, respectively. This magnetic biochar exhibited high reusability (retained 82.1% after five cycles) and sharply magnetic performance (21.4emu/g). 相似文献