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Green epoxy synthesized from Perilla frutescens: A study on epoxidation and oxirane cleavage kinetics of high-linolenic oil

机译:从紫苏紫罗兰树合成的绿色环氧树脂:高亚麻油环氧化和氧化氧乙烷裂解动力学的研究

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Despite the growing interest in epoxidized vegetable oils (EVOs) as sustainable alternatives to petroleum-based epoxies, their high epoxy equivalent weight (EEW) (& 250 g/eq) hinders use in high-strength applications. This study reports the synthesis of a sustainable EVO that possesses EEW of similar to 164 g/eq - comparable to that of diglycidyl ether of bisphenol-A (DGEBA). Non-edible perilla oil, extracted from the non-edible seeds of Perilla frutescens, was used to synthesize sustainable green epoxy via Prilezhaev epoxidation reaction at 40, 50 and 60 degrees C for 8 h. Perilla oil was chosen due to its higher number of chemically modifiable groups (& 90%), i.e. similar to 62-65 wt. % linolenic acid (C18:3), similar to 13-15 wt. % linoleic acid (C18:2) and similar to 12-15 wt. % oleic acid (C18:1) moieties. Rates of epoxidation and side reactions were estimated by experimentally determining iodine, epoxy and alpha-glycol value of epoxidized perilla oil (EPeO) extracted at regular time intervals during synthesis. Kinetics of post-oxirane cleavage was studied at aforementioned reaction temperatures and times by reacting EPeO with formic acid in weight ratio of 1:3. Reaction kinetics studies for both epoxidation and ring opening reactions (pseudo) showed reaction rate constants in the order of 10(-6) L mol(-1) s(-1) (for both reactions) and activation energies of 20.10 kJ/mol (epoxidation) and 43.11 kJ/mol (ring opening) respectively. Thermodynamic parameters - such as activation enthalpy, activation entropy, and Gibbs' free energy of activation - were calculated for both epoxidation and oxirane ring cleavage reactions. All the thermodynamic parameters were observed to be lower for epoxidation reaction compared to post-oxirane cleavage reaction. Enthalpy of activation was found to be similar to 18 kJ/mol for epoxidation reaction while it was similar to 56 kJ/mol for post-oxirane cleavage reaction.
机译:尽管对石油基环氧树脂的可持续替代品越来越感兴趣,但它们的高环氧当量重量(EEW)(& 250 g / eq)阻碍在高强度应用中使用。本研究报告了具有与双酚-A(DGEBA)的二缩水甘油醚相当的EEW的可持续EVO的合成。从Perilla Frutescens的不可食用种子中提取的非食用紫苏纤维油通过PriTzhaev环氧化反应在40,50和60℃下合成可持续的绿色环氧树脂8小时。由于其较高数量的化学可改性基团(& 90%),即类似于62-65重量。 %亚麻酸(C18:3),类似于13-15重量%。 %亚油酸(C18:2)和类似于12-15重量的。 %油酸(C18:1)部分。通过在合成期间以规则的时间间隔提取的环氧化紫薇(EPEO)的碘,环氧树脂和α-二醇值估计环氧化和副反应的速率。在上述反应温度下研究了氧化乙烷裂解的动力学,并通过以1:3的重量比反应EPeo与甲酸反应。对环氧化和开环反应(假)的反应动力学研究显示了10(-6)L mol(-1)s(-1)(反应)的10(-6)摩尔(-1)(反应)的反应速率常数和20.10kJ / mol的活化能量(环氧化)和43.11kJ / mol(开环)。热力学参数 - 如活化焓,激活熵和吉布斯的活化 - 用于对环氧化和环氧烷环切割反应计算的。与后氧化乙烷裂解反应相比,观察到环氧化反应的所有热力学参数较低。发现活化的焓与环氧化反应相似的相对于18kJ / mol,同时氧化乙烷后裂解反应的56kJ / mol。

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