Publications by authors named "Luis F Barral-Losada"

Active biobased packaging materials based on poly(lactic acid)-poly(hydroxybutyrate) (PLA-PHB) blends were prepared by melt blending and fully characterized. Catechin incorporation, as antioxidant compound, enhanced the thermal stability, whereas its release was improved by the addition of acetyl(tributyl citrate) (ATBC) as plasticizer. Whereas the incorporation of ATBC resulted in a reduction of elastic modulus and hardness, catechin addition produced more rigid materials due to hydrogen-bonding interactions between catechin hydroxyl groups and carbonyl groups of PLA and PHB.

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Molecularly imprinted polymer (MIP) for solid extraction and preconcentration of catechins have been successfully prepared by a thermal polymerization method using quercetin as template, 4-vinylpyridine as functional monomer and ethylene glycol dimethacrylate as crosslinker. A solution mixture of acetone and acetonitrile was used as porogen. Systematic investigations of the influence of monomer, cross-linker, porogen, as well as polymerization conditions on the properties of the MIPs were carried out.

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A chromatographic method using ultra performance LC with ultraviolet spectrophotometry detection system (UPLC-UV-visible (UV/Vis)) (UPLC, ultra performance LC) was developed to determine Chimassorb 944 and Tinuvin 770, high- and low-molecular mass hindered amine light stabilizers, respectively. The use of a bridge ethylene hybrid-based particles C(18) UPLC column, being compatible with a buffered mobile phase adjusted to pH 11.5, was used to achieve a satisfactory elution of possible non-ionizated units of polymeric Chimassorb 944.

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An analytical method for the simultaneous separation and quantitation of ten colorants and six antioxidants used as polymer additives has been developed by transferring chromatographic conditions from two independent HPLC methods to a single ultraperformance liquid chromatography system. An experimental design was carried out to achieve the best elution gradient for separation of all the studied compounds with the best possible peak resolution and in the shortest possible analysis time. The new method gives good values for the analytical quality parameters evaluated.

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