In certain applications copolymer P123 (E21P67E21) is dissolved in water-ethanol mixtures, initially to form micellar solutions and eventually to gel. For P123 in 10, 20, and 30 wt % aqueous ethanol we used dynamic light scattering from dilute solutions to confirm micellization, oscillatory rheometry, and visual observation of mobility (tube inversion) to determine gel formation in concentrated solutions and small-angle X-ray scattering (SAXS) to determine gel structure. Except for solutions in 30 wt % aqueous ethanol, a clear-turbid transition was encountered on heating dilute and concentrated micellar solutions alike, and as for solutions in water alone (Chaibundit et al. Langmuir 2007, 23, 9229) this could be ascribed to formation of wormlike micelles. Dense clouding, typical of phase separation, was observed at higher temperatures. Regions of isotropic and birefringent gel were defined for concentrated solutions and shown (by SAXS) to have cubic (fcc and hcp) and hexagonal structures, consistent with packed spherical and elongated micelles, respectively. The cubic gels (0, 10, and 20 wt % ethanol) were clear, while the hex gels were either turbid (0 and 10 wt % ethanol), turbid enclosing a clear region (20 wt % ethanol), or entirely clear (30 wt % ethanol). The SAXS profile was unchanged between turbid and clear regions of the 20 wt % ethanol gel. Temperature scans of dynamic moduli showed (as expected) a clear distinction between high-modulus cubic gels (G'max approximately 20-30 kPa) and lower modulus hex gels (G'max<10 kPa).
LCC (Líquido da Castanha de Caju), ou CNSL (Cashew Nut Shell Liquid), é uma mistura de meta-alquilfenóis, que variam no grau de insaturação do grupo ligado ao núcleo benzênico. A degradação térmica do poli(1,4-cis-isopreno) sintético a 140 °C foi estudada na presença do LCC técnico e de alguns derivados (cardanol, cardanol hidrogenado e cardanol hidrogenado e alquilado), através de FTIR. A quantidade de grupamentos OH/OOH e C=O formados e de C=C consumidos foi determinada durante a degradação. Todos os materiais aumentaram o tempo de indução e diminuíram as constantes aparentes de velocidade. Com base nos parâmetros cinéticos, a ordem de atividade antioxidante é: LCC >> cardanol ≅ cardanol hidrogenado e alquilado > cardanol hidrogenado. O efeito do LCC pode ser atribuído à contribuição extra de seus outros componentes, além do cardanol, e à insaturação na longa cadeia lateral. Essa maior atividade é importante, considerando que o LCC tem mais baixo custo do que seus derivados.CNSL is a mixture of meta-alkylphenols with variable degree of unsaturation attached to the benzene ring. The kinetic study of the thermal degradation at 140 °C of synthetic cis-1,4-polyisoprene film, in the presence of technical CNSL and some derivatives (cardanol, hydrogenated cardanol and alkylated hydrogenated cardanol) was carried out by FTIR. The amount of OH/OOH and C=O formed and also of C=C consumed during the degradation was determined. All materials increase the induction period and decrease the apparent rate constants of thermal-oxidation. Based on kinetic parameters, the order of antioxidant activity was: CNSL >> cardanol ≅ hydrogenated and alkylated cardanol > hydrogenated cardanol. The effect of CNSL could be attributed to the extra contribution of the other components besides cardanol and to the unsaturation on the long side chain. This greater activity is important because CNSL is much more cost effective than its derivatives.
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