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51.
To investigate the effects of multiple weak interactions on the binding of phenolic compounds by polymeric adsorbents, macroporous polystyrene (PS) resin and PS‐based adsorbents with different hydrogen‐bond acceptor atoms (PS CH2( OCH2CH2)n OCH3, n = 0, 1, 2, and 3, denoted as PS‐EG0, PS‐EG1, PS‐EG2, and PS‐EG3) were prepared. The phenol adsorption strength order on these adsorbents was PS/PS‐EG0 < PS‐EG1 < PS‐EG2 < PS‐EG3, indicating that the adsorption on PS and PS‐EG0 was driven by hydrophobic and π–π interactions, and the adsorption on PS‐EG1, PS‐EG2, and PS‐EG3 was driven by a hydrogen bond in addition to hydrophobic and π–π interactions. PS‐EG2 may adsorb a second phenol molecule on each binding site and PS‐EG3 may adsorb second and third ones. The adsorption strength of resorcinol increased in the order of PS, PS‐EG1, and PS‐EG2, indicating that the adsorption was driven by 0, 1, and 2 hydrogen bonds in addition to hydrophobic and π–π interactions. Similarly, the adsorption of phloroglucinol on PS, PS‐EG1, PS‐EG2, and PS‐EG3 was driven by 0, 1, 2, and 3 hydrogen bonds in addition to hydrophobic and π–π interactions because the adsorption strength increased in this order. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 4652–4658, 2006 相似文献
52.
Plastisols, which are a blend of poly(vinyl chloride) resin and a plasticizer (DEHP), were used as a toughening agent of a resol resin in order to improve the mechanical properties. It was not possible to formulate resol blends by adding more than 10 % of plastisol owing to a lack of apparent homogeneity in the systems, which also showed many air bubbles. The relationship between dynamic mechanical, mechanical and thermal properties and the amount of plastisol added was studied. It was determined from the infrared spectroscopy and dynamic mechanical results that the resol–plastisol blends seem to be formed by a reaction between the phenol and PVC giving a higher crosslinked structure. An improvement in the thermal resistance of the blends at lower temperatures was observed with an increase in the percentage of plastisol. Flexural analysis showed the elastic behaviour of the systems. However, it was not possible to observe the effect of the plasticizer (DEHP) owing to the low quantity of plastisol that was added to the resol. Copyright © 2004 Society of Chemical Industry 相似文献
53.
双组分树脂冷压法制备摩擦材料 总被引:8,自引:0,他引:8
研究甲、乙双组分液体树脂作为粘结剂制备制动摩擦材料的冷压工艺方法,甲组分树脂为硼改性腰果壳油树脂,乙组分树脂为三聚氰胺改性酚醛树脂。该工艺可使模压料在室温下具有良好的成型效果,在固化处理中不使用夹具,可以使成型料具有良好的保型效果。冷压制备的制动摩擦材料具有硬度低、摩擦系数稳定和恢复性好等特点。 相似文献
54.
中原高温高盐油藏疏水缔合聚合物凝胶调剖剂研究 总被引:3,自引:1,他引:2
针对中原油田高温(>80℃)、高盐度(>50 g/L)、高硬度(>1 g/L)砂岩油藏,研制了地下成胶的高热稳定性聚合物凝胶调剖剂。所用聚合物为疏水缔合聚合物AP-P4,M=9.0×106,HD=27%,疏水基摩尔分数0.2%;交联剂为可生成酚醛树脂的3种化合物;调剖剂胶液用矿化度160 g/L的马寨油田污水配制;实验温度95℃。根据形成的凝胶黏度(95℃,1.1 s-1)确定交联剂各组分用量为:MZ-YL 0.429%,MZ-BE 0.060%,MZ-XS 0.012%;酸度调整剂用量0.12%;成胶时间10~15小时。2.5、3.0、3.5 g/L AP-P4的凝胶在95℃老化100天后黏度保持在~40 Pa.s及以上。初配制胶液在3000 r/min下剪切15分钟后黏度降低87.5%~89.0%,但成胶后和老化过程中凝胶黏度只比未剪切样降低17.1%~6.6%。3.5 g/L AP-P4的调剖剂对~1μm2的6支储层岩心的堵塞率在88.1%~95.8%范围,平均93.3%,造成的残余阻力系数在15.2~28.6范围,平均19.8,使渗透率级差2.3~8.0的4组双人造岩心的注水流量比发生不同程度的反转。认为该凝胶调剖剂高温下稳定性好的原因,是强化学交联密度低,因而凝胶脱水收缩作用弱。图2表5参5。 相似文献
55.
张仲明 《石油化工腐蚀与防护》2003,20(6):46-47,62
中国石化股份有限公司洛阳分公司炼油厂污水汽提装置的原料水罐(V303)由于接触的污水中含有H2S,NH3,CO2,CN-,酚等多种腐蚀介质因此经常发生腐蚀泄漏事故。经涂刷WF40玻璃鳞片防腐蚀涂料后,已平稳运行两年。2002年检修检查,涂层完好,仍在继续使用。WF40涂料为环氧型玻璃鳞片涂料,其热膨胀系数与钢质基体接近,因此具有耐热冲击性强等优点。待涂罐体经喷砂除锈到Sa2.5级后,涂底漆2道,中间涂层2道、面漆2道,使干膜厚度达到350μm,可有效防止腐蚀性介质的渗透。 相似文献
56.
If a low weight percentage of crude fine fillers can improve properties of polymer materials directly without complicated chemical treatment process involved, it will be significant for many industrial applications. Our previous study indicated that a kind of Cancun natural sand could be an effective filler material for polymer composites. In this current work, the epoxy composites reinforced by this kind of natural sand particles were prepared and thermal and mechanical properties of the composites containing up to 5 wt % of the sand particles were characterized. Results showed that the highest flexural strength appears in the epoxy composite containing 1 wt % sand particles. A damage model was used to interpret the flexural properties, which showed an acceptable agreement with the experimental results. The glass transition temperature, high temperature storage modulus, and dimensional stability of the sand/epoxy composites monotonically increased with the addition of the sand particles. The sand particle/epoxy composites also displayed a noticeable enhancement in thermal conductivity. Theoretical analysis showed that in addition to conduction, other heat transport mechanisms played roles in the improved heat transmission through the composites. As a natural porous micron-scale material, Cancun sand has the potential for applications in cost-effective composites with enhanced mechanical and thermal properties. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 相似文献
57.
Polymeric oxidants in the bead form that were macroporous styrene/divinylbenzene copolymers containing N‐chlorosulfonamide functional groups (in sodium or hydrogen form) or N‐bromosulfonamide groups (in sodium form) were synthesized and investigated to determine their oxidizing powers. The redox potentials of the N‐chlorosulfonamide/sulfonamide and N‐bromosulfonamide/sulfonamide systems were determined by potentiometric studies at different pH values with aqueous solutions of Na2SO3, KCN, and KSCN as reducers. The formal redox potentials of the N‐chlorosulfonamide copolymers were 0.79, 0.44, and ?0.12 V at pH's of 1.8, 8.45, and 13.6, respectively. The formal redox potential of the N‐bromosulfonamide copolymer was about 100 mV higher in comparable conditions and in solutions over pH = 5 (e.g., 0.56 V at pH = 8.56). The comparatively higher oxidizing power of the N‐bromosulfonamide copolymer was particularly evident in a strong alkaline medium (in which the N‐chlorosulfonamide copolymer was not reactive). In contrast, the N‐chlorosulfonamide copolymer showed strong oxidative properties in acidic media (in which the N‐bromosulfonamide copolymer decomposed itself). © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2008 相似文献
58.
In the present study, the transition of a polymeric material from the linear to the nonlinear viscoelastic behavior and the determination of the nonlinearity stress threshold variation with time and temperature are investigated. For this purpose a systematic experimental program consisted of thermal and mechanical characterization of certain polymeric material followed by isothermal creep tests at different stress levels and temperatures was conducted. Through isochronal curves that occurred from creep tests, the nonlinearity threshold dependence on both time and temperature is presented. The reported results provide information that is critical for the design and development of polymer structures and components. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 相似文献
59.
介绍了用常温法生产微粒状 PVB 树脂的新工艺,从而简化了传统法低温生产 PVB 树脂的工艺和设备,减少了设备投资,节省了动力和能源消耗,降低了生产成本。 相似文献
60.
通过对中温固化环氧树脂DSC、扭辫分析、凝胶时间、粘度、力学性能的测定,固化反应活化能的计算,研究了在贮存树脂的过程中环境湿度对树脂的固化反应和性能的影响。 相似文献