Publications by authors named "Dominik Wolosz"

This study reveals insights into the transurethanization reactions leading to the aliphatic-aromatic non-isocyanate poly(carbonate-urethane)s (NIPCUs) and their structure-property relationships. The crucial impact of the alkyl chain length in 4,4'-diphenylmethylene bis(hydroxyalkyl carbamate) (BHAC) on the process of transurethanization reactions was proved. The strong susceptibility of hydroxyethyl- and hydroxybutyl carbamate moieties to the back-biting side reactions was observed due to the formation of thermodynamically stable cyclic products and urea bonds in the BHACs and NIPCUs.

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Article Synopsis
  • The development of hydrophobically modified ethoxylated urethane (HEUR) rheology modifiers has shifted waterborne paints and coatings away from harmful solvent-based alternatives, but conventional HEUR synthesis uses toxic diisocyanates, harming eco-sustainability.
  • This research introduces an innovative method to create isocyanate-free hydrophobically modified ethoxylated poly(hydroxy-urethane)s (IFHEURs), using CO-based cyclic carbonate and biobased hydrophobic diamine in a reactive extrusion process.
  • The resulting IFHEURs exhibit flexible structures and tunable thickening performance in aqueous solutions, confirmed through various analytical techniques, paving the way for safer and more sustainable rheology modifiers
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The presented research focuses on the synthesis and structure-properties relationship of poly(carbonate-urea-urethane) (PCUU) systems including investigations on shape-memory effect capability. Furthermore, we approached the topic from a broader perspective by conducting extensive analysis of the relationship between the synthesized compounds and the results of computer simulations by means of the Monte Carlo method. For the first time, by using a unique simulation tool, the dynamic lattice liquid model (DLL), all steps of multi-step synthesis of these materials were covered by the simulations.

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In this article we report an easy synthetic route towards hyperbranched polyglycerols (Amm-HBPGs) containing trimethylammonium groups and siloxane or hydroxyl end-groups. Siloxane derivatives of Amm-HBPGs were synthesized in an efficient five-step procedure including an anionic ring opening copolymerization of the phthalimide-epoxy monomer with glycidol, followed by reactions with allyl bromide, hydrosililation with hydrogenheptamethyltrisiloxane, hydrazinolysis of phthalimide groups and quaternization of resulting amine groups with methyl iodide. Hydroxyl derivatives were obtained by quaternization of previously reported aminated HBPG's with methyl iodide.

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