Chemically modified Jatropha curcas oil for biolubricant applications

Nurazira Nor Mohd, N. Salih, J. Salimon
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引用次数: 14

Abstract

Jatropha curcas oil is one of interesting renewable resources for preparation of biolubricants. However, direct application of this oil as a biolubricant is restricted due to its low oxidative stability. This drawback can be overcome by molecule structural redesign through a chemical modification process at its unsaturated functional groups. Jatropha curcas oil was modified via epoxidation, ring opening and esterification processes. Its conversion to the epoxidized oil was performed by using in situ performic acid as a catalyst, then reaction with oleic acid in the presence of p-toluenesulfonic acid as a catalyst in the ring opening process. The final esterification process with oleic acid was catalyzed by sulfuric acid. Molecular structures of the modified oil were determined by measurements of the oxirane oxygen content and by Fourier-transform infrared (FTIR), proton and carbon nuclear magnetic resonance (1H NMR and 13C NMR) spectroscopy analyses. The results showed that the oxidative stability, viscosity, flash point and pour point of the final product were significantly improved. In specific, the ring opening and esterification processes inducing branching and bending in the final oil molecular structure have resulted in the improved viscosity index of 135, the pour point of -29?C and the increased flash point of 250?C.
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化学改性麻疯树油的生物润滑剂应用
麻疯树油是一种很有前途的生物润滑剂再生资源。然而,由于其低氧化稳定性,这种油作为生物润滑剂的直接应用受到限制。这一缺陷可以通过对其不饱和官能团的化学修饰过程来重新设计分子结构来克服。对麻疯树油进行了环氧化、开环和酯化改性。以原位甲酸为催化剂,再以对甲苯磺酸为催化剂,与油酸进行开环反应,得到环氧化油。用硫酸催化与油酸的最终酯化反应。改性油的分子结构通过测量氧烷含量和傅里叶变换红外(FTIR)、质子和碳核磁共振(1H NMR和13C NMR)光谱分析来确定。结果表明,最终产品的氧化稳定性、粘度、闪点和倾点均有明显改善。具体来说,开环和酯化过程在最终油分子结构中引起分支和弯曲,导致粘度指数提高到135,倾点提高到-29?C,闪点增加250℃。
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