Mechanical and thermal properties of materials prepared by curing epoxidized soybean oil with various cyclic acid anhydrides in the presence of tertiary amines were investigated by dynamic mechanical thermal analysis and thermogravimetry. All samples presented thermoset material characteristics that were dependent upon the type of anhydride, the anhydride/epoxy molar ratio, and epoxy group content. The thermosets obtained from anhydrides with rigid structures as such phthalic, maleic, and hexahydrophthalic showed higher glass transition temperatures (Tg) and cross-linking densities. As expected, the Tg decreased as the anhydride/epoxy ratio decreased. The influence of the degree of epoxidation of soybean oil on the mechanical properties and Tg was also investigated. It was found that the higher the epoxy group amount, the higher the Tg and hardness. Cured resins exhibited thermal stability up to 300°C, except for those prepared with dodecenylsuccinic anhydride, which began to decompose at lower temperature. They presented excellent chemical resistance when immersed in 1% wt/vol NaOH and 3% wt/vol H 2 SO 4 solutions but poor chemical resistance in the presence of organic solvents.Vegetable oils represent an interesting renewable source for the production of useful chemicals and new materials (1). Soybean oil is readily available in bulk and is mainly composed of TG molecules derived from unsaturated acids, such as oleic acid (22%), linoleic acid (55%), and linolenic acid (7%). Although unsaturated acids possess double bonds, which are the reactive sites for coatings and paints, they need to be functionalized by the introduction of epoxy, hydroxyl, or carboxyl groups in order to be used for preparation of polymeric materials.Soybean oil can be epoxidized by different methods (2-4) yielding conversions and selectivities higher than 90%. Industrially, it is used mainly as a polyvinyl chloride additive to improve stability and flexibility. New applications have been made possible by the use of photochemically initiated cationic curing (5) and by the preparation of thermosetting materials such as epoxy resins.Epoxy resins are widely used as adhesives and as matrices in composite materials because of their good physical and chemical properties. Toughness and other properties of epoxy resins can be significantly improved by the modification of classical epoxy resins, such as those based on diglycidylether of bisphenol A (DGEBA). Epoxidized vegetable oils prepared from the most unsaturated oils, e.g., soybean oil or linseed oil, can be used for such purpose.In this work we report dynamic mechanical properties of different materials prepared by curing fully and partially epoxidized soybean oil (ESO) with various cyclic acid anhydrides in the presence of tertiary amines. Thermal and chemical resistance were also investigated. MATERIALS AND METHODSPhthalic anhydride (PA), hexahydrophthalic anhydride (CH), maleic anhydride (MAL), and N,N′-dimethylaniline (ARO) were purchased from Aldrich Chemical Co. (Milwaukee, WI) and purif...

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Polyurethanes can be prepared using polyols obtained from vegetable oils in natura, such as castor oil, or from functionalized vegetable oils, such as hydroxylated soybean oil. These polyurethanes have different valuable properties, determined by their chemical composition and cross-linking density. In this study, soy epoxy polyols with different OH contents were prepared through a one-step reaction using the method of in situ performic acid generation. Polyols with OH functionalities from 1.9 to 3.2 were reacted in bulk with different diisocyanates at a NCO/OH molar ratio of 0.8 and 60°C for 24 h. Mechanical properties of the polyurethanes were determined by dynamic mechanical thermal analysis, hardness (Shore A), and swelling measurements. Polymer networks with glass-transition temperatures (T g ) from -13 to 48°C were obtained. We observed that the higher the OH functionality of the polyols, the higher the T g and cross-linking density of the polyurethane network. The influence of diisocyanate structure (rigid or flexible chain), curing temperature, and curing reaction time on mechanical properties was also investigated.Paper no. J10956 in JAOCS 82, 365-371 (May 2005). KEY WORDS:Hydroxylated soybean oil, mechanical properties, polyurethane, soy epoxy polyol.The use of renewable resources has attracted the attention of many researchers because of their potential to replace petrochemical derivatives (1-3). Soybean oil is an inexpensive, readily available, renewable resource and provides an excellent platform for polymeric materials. Soybean oil is mainly composed of TG molecules derived from unsaturated FA such as oleic acid (22%), linoleic acid (55%), and linolenic acid (7%). Although they possess double bonds, which are the reactive sites for coatings and paints, they need to be functionalized to prepare polymers (4). Polyurethanes (PU) have been prepared from vegetable oils in natura, such as castor oil, or from polyols obtained from vegetable oils, such as corn, sunflower, and soybean oils, and show a number of excellent properties because of the hydrophobic nature of TG (5,6). To use natural oils as raw materials for PU production, multiple hydroxyl functionalities are required. Usually these are obtained by reacting epoxidized oils with low-M.W. mono-or polyfunctional alcohols or acids.Recently, Petrovic et al. (7) reported the effect of the NCO/OH molar ratio on soy-based PU network properties using a methoxylated soy polyol (OH functionality = 3.7) and 4,4′-methylenebis(phenyl isocyanate) (MDI). Glassy polymers were produced when the NCO/OH ratio was between 0.8 and 1.05. Higher cross-linking densities, glass-transition temperatures (T g ), and tensile strengths were observed as the NCO/OH ratio increased. The influence of the diisocyanate structure on the properties of these soy-based PU was also investigated (8).Guo et al. (9) reported the physical and mechanical properties of soy polyol-derived PU prepared by the hydrogenation of hydroformylated soybean oil. When the hydroformylation reaction was rhod...

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We studied the methyltrioxorhenium (MTO)-CH 2 Cl 2 /H 2 O 2 biphasic system for epoxidizing soybean oil. The reactions were optimized (reactant ratio, time, and temperature), which resulted in a better performance (higher conversion and selectivity) than those described in the literature. Total doublebond conversion and 95% selectivity were obtained in 2 h at room temperature. Furthermore, it was possible to reach desired epoxidation degrees by changing the oxidant and MTO amounts. The rhenium-epoxidized soybean oil remained stable in the absence of stabilizers for up to 30 d when stored at mild conditions.

de todas as unidades que utilizam produtos químicos em suas rotinas de trabalho, têm sido confrontados, ao longo de muitos anos, com o problema relacionado ao tratamento e à disposição final dos resíduos gerados em seus laboratórios de ensino e pesquisa. Esses resíduos diferenciam-se daqueles gerados em unidades industriais por apresentarem baixo volume, mas grande diversidade de composições, o que dificulta a tarefa de estabelecer um tratamento químico e/ou uma disposição final padrão para todos. De maneira geral, esse problema atinge graves proporções e tem sido relegado a um plano secundário. Na maioria dos casos os resíduos são estocados de forma inadequada e ficam aguardando um destino final, isso quando são estocados. Infelizmente, a cultura ainda dominante é de descartá-los na pia do laboratório, já que a maioria das instituições públicas brasileiras de ensino e pesquisa não tem uma política institucional clara que permita um tratamento global do problema. A Química é uma das ciências básicas que mais benefícios trouxe à humanidade ao longo dos últimos tempos. Com os seus vários segmentos, ela permeia a vida de todas as pessoas que vivem em uma sociedade moderna e de alto grau tecnológico (p. ex., fármacos, materiais especiais, defensivos agrícolas, insumos para vários segmentos industriais, materiais de limpeza, higiene pessoal, beleza, etc.). Infelizmente, esse quadro, como uma moeda, não tem um lado só. O mau uso dessa Ciência tem causado graves problemas à humanidade e vem sendo responsável pela percepção negativa da Química. Dentro desse quadro, pode-se dizer que um dos problemas mais graves relacionado ao mau uso da Química refere-se aos danos ambientais. Para contornar essa situação, as legislações ambientais de todos os países do mundo, inclusive a do Brasil, vêm evoluindo e se adaptando às novas realidades, visando coibir severamente os abusos. Essas legislações vêm também incorporando novas exigências no monitoramento das emissões de voláteis no ar e no lançamento de resíduos industriais nos corpos aqüíferos.

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