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Compatibility Assessment of Elastomer Materials to Test Fuels Representing Gasoline Blends Containing Ethanol and Isobutanol

机译:弹性体材料相容性评估,以测试代表含乙醇和异丁醇的汽油混合物的燃料

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The compatibility of elastomeric materials used in fuel storage and dispensing applications was determined for test fuels representing neat gasoline and gasoline blends containing 10 and 17 vol.% ethanol, and 16 and 24 vol.% isobutanol. The actual test fuel chemistries were based on the aggressive formulations described in SAE J1681 for oxygenated gasoline. Elastomer specimens of fluorocarbon, fluorosilicone, acrylonitrile rubber (NBR), polyurethane, neoprene, styrene butadiene rubber (SBR) and silicone were exposed to the test fuels for 4 weeks at 60℃. After measuring the wetted volume and hardness, the specimens were dried for 20 hours at 60℃ and then remeasured for volume and hardness. Dynamic mechanical analysis (DMA) was also performed to determine the glass transition temperature (T_g). Comparison to the original values showed that all elastomer materials experienced volume expansion and softening when wetted by the test fuels. The fluorocarbons underwent the least amount of swelling (<25%) while the SBR and silicone samples exhibited the highest level of expansion (>100%). The level of swelling for each elastomer was higher for the test fuels containing the alcohol additions. In general, ethanol produced slightly higher swell than the oxygen equivalent level of isobutanol. When dried, the fluorocarbon specimens were slightly swollen (relative to the baseline values) due to fuel retention. The NBRs and neoprene exhibited shrinkage and embrittlement associated with the extraction of plasticizers. SBR also experienced shrinkage (after drying) but its hardness returned to the baseline value. The dried volumes (and hardness values) of the silicone, SBR and fluorosilicone rubbers closely matched their original values, but the polyurethane specimen showed degradation with exposure to the test fuels containing ethanol or isobutanol. The DMA results showed that the test fuels effectively decreased T_g for the fluorocarbons, but increased T_g for the NBR materials. The T_g values other elastomers were not affected by the test fuels.
机译:确定了用于燃料存储和分配应用的弹性体材料的相容性,适用于代表纯汽油的汽油和包含10%和17%(体积)乙醇,16%和24%(体积)异丁醇的汽油混合物。实际的测试燃料化学是基于SAE J1681中描述的用于氧化汽油的腐蚀性配方。碳氟化合物,氟硅橡胶,丙烯腈橡胶(NBR),聚氨酯,氯丁橡胶,丁苯橡胶(SBR)和硅橡胶的弹性体样品在60℃下暴露于测试燃料中4周。在测量润湿体积和硬度之后,将样品在60℃下干燥20小时,然后重新测量体积和硬度。还进行了动态机械分析(DMA),以确定玻璃化转变温度(T_g)。与原始值的比较表明,所有弹性体材料在被测试燃料润湿时都会经历体积膨胀和软化。碳氟化合物的溶胀最少(<25%),而SBR和有机硅样品的膨胀程度最高(> 100%)。对于含有醇添加剂的测试燃料,每种弹性体的溶胀水平较高。通常,乙醇产生的溶胀度高于异丁醇的氧当量水平。干燥后,由于燃料滞留,碳氟化合物样品略有肿胀(相对于基线值)。 NBR和氯丁橡胶显示出与增塑剂提取有关的收缩和脆化。 SBR也经历了收缩(干燥后),但其硬度恢复到基线值。硅橡胶,丁苯橡胶和氟硅橡胶的干燥体积(和硬度值)与它们的原始值非常匹配,但聚氨酯样品在暴露于含乙醇或异丁醇的测试燃料时显示出降解。 DMA结果表明,测试燃料有效降低了碳氟化合物的T_g,但提高了NBR材料的T_g。其他弹性体的T_g值不受测试燃料的影响。

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