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1	Selective ester cleavage in phospholipids Mohan, Vijitha 09 August 2008 (has links) Selective ester bond cleavage using lithium and zinc halides was attempted in a select group of phospholipids, namely phosphatidylcholine (PC), phosphatidylethanolamine (PE), and phosphatidylserine (PS). Several reaction parameters including catalyst (lithium chloride, lithium bromide, lithium iodide, zinc chloride, zinc bromide and zinc iodide), reaction temperature (21, 30, 50 and 60 oC), and reaction time (2 and 4 hours) were varied and the effects on cleavage studied. Reacted phospholipid samples were characterized by attenuated total reflectance (ATR) and transmission FTIR spectroscopy. The FTIR spectra of pure (unreacted) and reacted PC, PE and PE were analyzed qualitatively and quantitatively (Peak Height Ratio). The appearance of asymmetric carboxylate anion stretch (1577 cm-1) and symmetric phosphonyl dianion stretch (1006 cm-1) in the reacted phospholipid spectra reveals cleavage of ester bonds in carbonyl and phosphonyl. Reaction temperature and time did not significantly influence the cleavage results over the temperature and time range tested. cleavage of ester bonds
2	Sustainable Polymer Production: Investigating Synthesis and Copolymerization of Cyclic Ketene Acetals / Hållbar polymerproduktion: Undersökning och syntes samt sampolymerisation av cykliska ketenacetaler Bourraman, Soufian, Staffas, Stella, Brandt, Adam, Isaksson, Simon January 2023 (has links) The large amount of non-degradable plastic waste has become a significant environmental concern, leading to an increased need for degradable plastics. Here in, to create degradable polymers, polyesters were produced through radical ring opening polymerization using cyclic ketene acetals. The cyclic ketene acetal monomer 5,6-benzo-2-methylene-1,3-dioxepane has been prepared for the synthesis of homo- and copolymers with methyl methacrylate, α-methylene-γ-valerolactone, α-methylene-γ-butyrolactone, cholesterol methacrylate and limonene acrylate. The polymerization was conducted using radical ring opening polymerization both in bulk and solution polymerization. The structural characteristics of the polymer were determined by different characterization methodologies, including TGA, DSC, SEC, FTIR and 1D 1H-NMR. The results obtained from 1H-NMR analysis showed the composition of the copolymers. TGA analysis revealed the thermal stability of the polymers and their degradation patterns. DSC analysis provided information about the glass transition temperatures (Tg’s) of the polymers. Moreover, the Tg indicated the presence and amounts of comonomers in the copolymers. Overall, the results showed the influence of different comonomers on the properties of the polymers by successfully incorporating the comonomers in the polymer. The thermal properties for polymers containing methyl methacrylate became more thermally stable. The Tg, analyzed with DSC, shifted from the Tg of homopolymers indicating the incorporation of both monomers. The polymers were successfully degraded via hydrolysis in alkaline conditions breaking them down into smaller pieces making them easier to recycle. To conclude, the results all indicate that the incorporation of BMDO and thereby possibly other CKA-monomers into the polymer chains of commonly used plastics could provide valuable tools in the recycling of said plastics. Monomers polymers radical radical ring opening polymerization polymerization BMDO MMA MVL MBL comonomer copolymer rROP sustainable biobased degradable monomer synthesis plastic polyester bulk solution NMR FTIR TGA DSC SEC hydrolysis molecular weight diol ester bonds Polymer Chemistry Polymerkemi

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Selective ester cleavage in phospholipids

Sustainable Polymer Production: Investigating Synthesis and Copolymerization of Cyclic Ketene Acetals / Hållbar polymerproduktion: Undersökning och syntes samt sampolymerisation av cykliska ketenacetaler