15 research outputs found

    New Trends in Beverage Packaging Systems: A Review

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    New trends in beverage packaging are focusing on the structure modification of packaging materials and the development of new active and/or intelligent systems, which can interact with the product or its environment, improving the conservation of beverages, such as wine, juice or beer, customer acceptability, and food security. In this paper, the main nutritional and organoleptic degradation processes of beverages, such as oxidative degradation or changes in the aromatic profiles, which influence their color and volatile composition are summarized. Finally, the description of the current situation of beverage packaging materials and new possible, emerging strategies to overcome some of the pending issues are discussed

    Covalent Immobilization of Redox-Active Fe(κ 2 ‑dppe)(η 5 ‑C 5 Me 5 )‑Based π‑Conjugated Wires on Oxide-Free Hydrogen-Terminated Silicon Surfaces

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    International audienceSeveral redox-active Fe(κ 2 -dppe)(η 5 -C 5 Me 5) arylacetylide complexes (dppe = 1,2-bis(diphenylphosphino)ethane) featuring a pendant ethynyl (1b−d and 2) or ethenyl (3) group have been grafted on oxide-free hydrogen-terminated silicon (Si−H) surfaces through a covalent interfacial Si−C bond. They form densely packed redox-active monolayers. The charge-transfer process between the terminal redox center and the underlying silicon interface was subsequently studied by cyclic voltammetry. The latter turned out to be strongly dependent on the nature of the spacer linking the organometallic end groups to the silicon surface, the highest charge-transfer rates being obtained for monolayers anchored through conjugated and unsaturated spacers. Although the rates measured were among the highest values obtained for redox-active systems grafted to Si− H surfaces, this study nevertheless suggests that the electron tunnelling is not entirely controlling the interfacial charge-transfer process for the shorter linkers tested. In this respect, strategies to improve further the charge-transfer kinetics of the produced redox-active films are briefly discussed
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