Isabel Patrícia Fernandes¹, Mariana Barbosa¹, Joana Soares Amaral², Vera Pinto³, José Luís Rodrigues³, Maria José Ferreira³, Maria Filomena Barreiro^1*

Journal of Renewable Materials, Vol.4, No.1, pp. 47-56, 2016, DOI:10.7569/JRM.2015.634126

Abstract Among the wide variety of materials employed in the manufacture of shoes, thermoplastic polyurethanes (TPUs) are one of the most widely used. Given its widespread use, and associated waste management problems, the development of more biodegradable and evironmentally compatible solutions is needed. In this work, a polyester-based TPU used in the footwear industry for outsoles production was modifi ed by compounding with lignin, starch and cellulose at content of 4% (w/w). The biodegradability was evaluated by using agar plate tests with the fungi Aspergillus niger ATCC16404, the Gram-negative bacteria Pseudomonas aeruginosa ATCC9027 and an association More >

Shunjie Liu^1,2, Yusheng Qin^1,*, Xianhong Wang^1,*, Fosong Wang¹

Journal of Renewable Materials, Vol.3, No.2, pp. 101-112, 2015, DOI:10.7569/JRM.2014.634140

Abstract Precursors with sharp crystalline transition temperature have attracted signifi cant attention in the fi eld of shape-memory materials; however, seldom have reports been related to amorphous ones with industrial application prospects. This study introduced a new family of amorphous CO₂ -based hydroxyl-telechelic three-armed oligo(carbonate-ether) triol (Triol) with controllable molecular weight (M_n) and carbonate unit content (CU), which was coupled with PEG and 1,6-hexamethylene diisocyanate (HDI) to afford crosslinked polyurethanes (PU) networks with well-defi ned architecture. A crosslinking point was provided by Triol and PEG was used to afford networks some crystallinity. The resulting networks were characterized… More >

L. Poussard^1,*, A. Mecheri¹, J. Mariage¹, I. Barakat¹, L. Bonnaud¹, J.-M. Raquez^1,2, P. Dubois^1,2

Journal of Renewable Materials, Vol.2, No.1, pp. 13-22, 2014, DOI:10.7569/JRM.2013.634132

Abstract Biobased oligo(butylene succinate)-based thermoplastic polyurethanes (TPUs) were prepared following a twostep polymerization process: condensation of succinic acid and butanediol and the chain extension of resulting hydroxyl-terminated butylene succinate oligomers (OBS) in the presence of butanediol as chain extender and isophorone diisocyanate (IPDI) as coupling agent. Mechanical and thermal properties of the elaborated TPUs were evaluated in terms of hard segment and compared with those of commercial polybutylene succinate (PBS), Bionolle 1001. Whatever the compositions, the ultimate tensile properties of OBS-based TPUs and Bionolle 1001 were found to exhibit similar values (ε_r ≈ 400%, σ_r ≈ 40 More >

Donglin Tang^1,2, Shanmugam Thiyagarajan^2,3, Bart A.J. Noordover^1,*, Cor E. Koning¹, Daan S. van Es³, Jacco van Haveren

Journal of Renewable Materials, Vol.1, No.3, pp. 222-230, 2013, DOI:10.7569/JRM.2013.634116

Abstract A series of fully renewable poly(ester urethane urea)s (PEUs) were synthesized from bio-based starting materials, e.g., the polyester diol, the diisocyanates including L-lysine diisocyanate (LDI) and isoidide diisocyanate (IIDI), the chain-extenders including 1,4-diaminobutane (bDA), diaminoisoidide (iDA) and di(aminobutyl) urea (b2 DA). It is found that the PEU based on the novel diisocyanate, IIDI, exhibits satisfactory thermal and mechanical properties. The LDI-based PEUs show less favorable thermal and mechanical properties than the IIDI-based counterpart, since the chemical structure of LDI is less regular than that of IIDI. However, by introducing a urea-containing dimeric diamine (b2 DA) More >

Rodolfo J. González-Paz, Gerard Lligadas^*, Juan C. Ronda, Marina Galià, Virginia Cádiz

Journal of Renewable Materials, Vol.1, No.3, pp. 187-194, 2013, DOI:10.7569/JRM.2013.634114

Abstract A thiol-reactive linear polyurethane was synthesized from a vinyl-sulphide-containing diol and a commercial diisocyanate. The diol was obtained from 10-undecynol, an alkyne-derivatized fatty compound, using hydrothiolation as a key reaction step. 10-Undecynol was prepared by reduction of 10-undecinoic acid methyl ester, which was prepared by successive bromation, dehydrobromination of the corresponding alkenic fatty acid. Solution and surface polymer modifi cation with a fl uorescent thiol was successful. More >