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介绍了大孔径网状聚氨酯泡沫塑料的制备工艺,着重讨论了催化剂、表面活性剂对泡沫孔径、经络的影响,分析了影响发泡反应的多种因素。实验结果表明:聚醚组份混合料预混时间应控制在2min以上为宜,物料温度控制在25±1℃为宜。调整L-580与T-7用量可制备不同孔径、不同密度、不同经络粗细的网状聚氨酯泡沫塑料;采用A-33与A-22或A-33与有机锡类催化剂配合体系,易于控制反应的平稳进行;在污水处理中,网状聚氨酯泡沫塑料附着的菌体最多,填料的形状和填充方式对污水处理效果影响较大。 相似文献
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IMO-SBR处理高浓度氨氮废水的实验研究 总被引:1,自引:0,他引:1
IMO-SBR工艺是结合了固定化微生物技术与SBR工艺的一种全新污水处理工艺。该工艺充分利用了固定化微生物和SBR的优点,既保留了固定化微生物,又较好地利用了成熟的SBR工艺。在实验反应器内装填由聚氨酯泡沫制成的生物膜载体,并以实际高浓度氨氮废水为研究对象,通过考察温度、进水m(C)∶m(N)、pH对IMO-SBR工艺脱氮效果的影响,确定最佳的运行条件为:温度在30℃、m(C)∶m(N)=3∶1、pH=8,该工艺条件下,氨氮去除率稳定在55%以上。 相似文献
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聚氨酯泡沫对微生物、水环境友好,且成本相对低廉,来源广泛,适用于大规模的应用,是一种国内外普遍应用的微生物固定化载体材料.将优势菌株使用聚乙烯醇(PVA)固定化处理后,模拟大庆地区浅层地下水环境,耦合聚氨酯泡沫分析BTEX降解反应的量效关系,得到最佳工艺参数.初始苯系物质量浓度为400 mg·L-1,pH值为6.5,最适温度为10℃,Fe离子质量浓度为16 mg·L-1、Mn离子质量浓度为12 mg·L-1,最适接种量为3块,所占体积比为40.5%,该固定化体系培养48 h后,对苯系物的降解率达91.86%.模拟低温地下水苯系物的去除实验表明,在苯系物初始质量浓度为400 mg·L-1的模拟水样中,48 h苯系物的去除率最高,达98.92%,苯系物最终质量浓度为4.19 mg·L-1.固定化体系前期聚氨酯泡沫的吸附作用对苯系物的去除贡献较大,吸附达到饱和时,生物降解才是更为重要的去除机理.通过扫描电镜观察载体内部的微生物,聚氨酯泡沫上纵横交错分布的孔隙为菌胶团的生长提供了支撑骨架;并利用分光光度计测定不同苯系物初始质量浓度的载体内的生物量的变化,苯系物质量浓度为400 mg·L-1时,聚氨酯泡沫载体附着生物量可达6734.41μg·g-1.在不固定条件下的菌液中蛋白质质量浓度为71.48μg·mL-1,固定化菌能够较好适应低温条件下地下水中苯系物的污染环境,生物载体填料为工业化应用提供了基础. 相似文献
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低密度及难燃低密度高回弹聚氨酯泡沫的研制 总被引:1,自引:0,他引:1
分别采用高活性聚醚多元醇和阻燃聚合物多元醇(TM-300)为主要原料,制备了低密度及难燃低密度高回弹泡沫.介绍了低密度高回弹泡沫的性能,讨论了TM-300的用量对难燃低密度高回弹泡沫性能的影响.结果表明,低密度高回弹泡沫密度可低至35 kg/m3,性能与一般密度高回弹聚氨酯泡沫相当;随着TM-300用量的增加,难燃低密度高回弹聚氨酯泡沫的硬度和拉伸强度增加,撕裂强度和伸长率下降;当TM-300用量为50份时,难燃低密度高回弹聚氨酯泡沫密度为40 kg/m3,氧指数达32,各项性能优于使用添加阻燃剂型泡沫. 相似文献
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A composite foam, polyurethane–melamine formaldehyde (PU/MF) foam, was prepared through foaming PU resins in the three‐dimensional netlike skeleton of MF foam. The chemical structure, morphology, cell size and distribution, flame retardancy, thermal properties and mechanical properties of such composite foam were systematically investigated. It was found that the PU/MF foam possessed better fire retardancy than pristine PU foam and achieved self‐extinguishment. Moreover, no melt dripping occurred due to the contribution of the carbonized MF skeleton network. In order to further improve the flame retardancy of the composite foam, a small amount of a phosphorus flame retardant (ammonium polyphosphate) and a char‐forming agent (pentaerythritol) were incorporated into the foam, together with the nitrogen‐rich MF, thus constituting an intumescent flame‐retardant (IFR) system. Owing to the IFR system, the flame‐retardant PU/MF foam can generate a large bulk of expanded char acting as an efficient shielding layer to hold back the diffusion of heat and oxygen. As a result, the flame‐retardant PU/MF foam achieved a higher limiting oxygen index of 31.2% and exhibited immediate self‐extinguishment. It exhibited significantly reduced peak heat release rate and total heat release, as well as higher char residual ratio compared to PU foam. Furthermore, the composite foam also showed obviously improved mechanical performance in comparison with PU foam. Overall, the present investigation provided a new approach for fabricating a polymer composite foam with satisfactory flame retardancy and good comprehensive properties. © 2018 Society of Chemical Industry 相似文献
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The objective of this study was to investigate the effects of isocyanate/hydroxyl ratio and ammonium polyphosphate (APP) content on the properties of polyurethane foam. Polyurethane (PU) foam was prepared from polymeric diphenylmethane diisocyanate and polyethylene glycol with molecular weight of 200, reinforced with oil palm empty fruit bunch (EFB) using one shot process. The effect of EFB content on the properties of PU foam was also studied. It was noticed that EFB enhanced the properties of the PU foam. This was due to EFB acting as hard segment in PU foam system. The NCO/OH ratio played an important role in determining the properties of the PU foam produced. However, since EFB is a highly flammable material, APP was introduced to the PU foam system. From the results, APP improved the fire retardant behavior of the PU foam. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012 相似文献
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采用聚醚多元醇和阻燃聚合物多元醇为主要原料,制备了低密度及阻燃低密度高回弹聚氨酯泡沫,讨论了低密度高回弹聚氨酯泡沫性能及阻燃聚合物多元醇TM-300用量对聚氨酯泡沫性能的影响。结果表明,低密度高回弹泡沫密度可低至35kg/m3,性能与一般密度聚氨酯泡沫相当。随着TM-300用量增加,阻燃低密度高回弹聚氨酯泡沫的硬度和拉伸强度增加,撕裂强度和伸长率下降;TM-300可有效提高聚氨酯泡沫的阻燃性能,氧指数可达到32,各项性能均较优异。 相似文献
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用含有小分子醇的交联剂和催化剂使废旧聚氨酯(PU)硬泡进行降解能够获得多元醇,将降解料与聚醚多元醇、催化剂和发泡剂共混以制备白料,然后与黑料异氰酸酯混合均匀,得到再生PU硬泡。通过对降解产物的黏度、羟值以及获得的再生PU硬泡材料的密度、强度、吸水率、热稳定性、扫描电子显微镜、红外光谱和热失重等进行测试分析,得出了催化剂添加量对废旧PU材料回收再利用的影响因素。结果表明,催化剂(KOH)用量为0.9 g时废旧PU的降解效果最好,获得的再生PU硬泡的密度为37.6 kg/cm3,压缩强度为164.2 kPa,热导率为0.015 24 W/(m·K),吸水率为0.429 5 %。 相似文献
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The effect of the trimerization catalyst on the thermal stability and the fire performance of the polyisocyanurate‐polyurethane foam 下载免费PDF全文
In this work, 3 currently used trimerization catalysts, TMR‐2 (quaternary ammonium), K‐15 (potassium octoate), and PU‐1792 (potassium acetate) were used to produce rigid polyisocyanurate (PIR) foams with certain amounts of isocyanurate contents. The results from Fourier transform infrared (FTIR) quantitative analysis showed that PU‐1792 had the highest catalytic efficiency in isocyanurate formation. Then, the effect of different amounts of PU‐1792 catalyst on isocyanurate ring output was further investigated, and the result showed that the highest amount of isocyanurate ring formation could be attained by the 5 pphp of PU‐1792 catalyst. It was also found that the increased amount of isocyanurate ring could result in reduced cell size, improved compressive strength, and lowered thermal conductivity of PIR foam. The results from thermogravimetric analysis (TGA) and cone calorimeter (CONE) test revealed that the thermal stability and fire performance of PIR foam could be improved with the increased amount of isocyanurate ring. Furthermore, the CONE test indicated that the smoke production of PIR foam decreased approximately 51.7% in comparison to the reference polyurethane (PU) foam, and the SEM image of char morphology showed that the char of PIR foam was more compact than PU foam. 相似文献
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The adhesion and interfacial properties of polyurethane (PU) foams with thermoplastic (TP) materials were investigated using different techniques. The adhesion performance of PU foam with TP materials was evaluated using the peel test method, and the adhesion durability was checked after different climate treatments. X‐ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM), and contact angle measurements were used to study the surface and interface morphology of PU foam and TP material system. Three types of PU foam samples which differ in their composition and also five commercially available TP blends systems, based on poly(carbonate), poly(styrene‐co‐maleic anhydride), poly(acrylonitrile‐butadiene‐styrene), and silicone acrylate rubber have been used. The slow reacting foam shows the best adhesion properties with all the TP materials. The climate treatments strongly effected the PU foam adhesion durability with poly(carbonate) containing TP materials (70–80% loss in adhesion), but nearly no effect with poly(styrene‐co‐maleic anhydride). The samples with lowered adhesion could be separated by peeling without visible foam residues on the TP surface. AFM, XPS, and surface tension studies have shown that the surface properties of the TP material are still governed by the PU foam. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 479–488, 2007 相似文献