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http://dx.doi.org/10.1007/s00128-002-0195-2 | DOI Listing |
Polymers (Basel)
November 2024
INESCOP Footwear Technology Centre, Alemania 102, 03600 Elda, Alicante, Spain.
This study aimed to enhance the initial adhesion performance of reactive polyurethane hot-melt adhesives by using a bio-based polycarbonate polyol instead of traditional polyester or polyether polyols and by incorporating thermoplastic polyurethane (TPU) in varied proportions. Adhesives synthesized from bio-based polycarbonate polyols and polypropylene glycol with MDI as the isocyanate were characterized chemically, thermally, and mechanically (FTIR, DSC, plate-plate rheology, DMA, and T-peel strength test). Adding 10-15 wt.
View Article and Find Full Text PDFChemSusChem
December 2024
Department of Chemistry, NIS Interdepartmental Centre and INSTM Reference Centre, University of Turin, Via G. Quarello 15 A, 10135, Torino, Italy.
In this contribution, we tackle the replacement of the Hg-based catalyst and fossil-derived isocyanate precursors toward the formulation of a more sustainable polyurethane thermosetting resins (PUs), emulating the performance of a fully fossil-based one employed in industrial encapsulation of optoelectronics. A mixed Bi-Zn catalyst and a 71 % bio-based isocyanate are exploited at this aim through multivariate chemometric approaches, namely Design of Experiment (DoE). DoE allows us to investigate the effect of different formulation factors on selected parameters, such as the film flexibility and transparency or the gel time.
View Article and Find Full Text PDFInt J Biol Macromol
January 2025
College of Materials and Energy, South China Agricultural University, Guangzhou 510642, Guangdong, China.
Isocyanate-free polyurethane adhesives have attracted considerable attention as a promising environmentally friendly alternative. However, their progress has been hindered by insufficient bonding performance and weak solvent resistance, as well as the laborious synthesis processes involved. Herein, we successfully synthesized a high-performance lignin-based non-isocyanate adhesives (LNIPUs-G) through a one-pot strategy that combines the polycondensation of carbonate groups with polyether amines and aldehyde-amine chemistry.
View Article and Find Full Text PDFACS Sustain Chem Eng
December 2024
Chemical Engineering Department, University of Castilla-La Mancha, Institute of Chemical and Environmental Technology, ITQUIMA, Avda. Camilo José Cela s/n, 13004 Ciudad Real, Spain.
The isocyanate-derived fraction resulting as the bottom phase from the split-phase glycolysis of conventional polyurethane flexible foams has been given a new life based on the formation of amine-based polymers (polyureas and polyamides). For that purpose, the bottom phase was first hydrolyzed, producing toluenediamine and diethylene glycol, and further subjected to controlled vacuum distillation in order to recover both products separately. The hydrolysis reaction and the separation process conditions were determined and optimized, obtaining products with a purity comparable to that of commercial ones.
View Article and Find Full Text PDFPolymers (Basel)
October 2024
School of Polymer Science and Engineering, Qingdao University of Science and Technology, Qingdao 266042, China.
Polyurethane (PU) plays a critical role in elastomers, adhesives, and self-healing materials. We selected the most commonly used aromatic isocyanates, 4,4'-methylene diphenyl diisocyanate (MDI) and tolylene-2,4-diisocyanate (TDI), and the most commonly used aliphatic isocyanates, hexamethylene diisocyanate (HDI), isophorone diisocyanate (IPDI), and dicyclohexylmethane-4,4'-diisocyanate (HMDI), as raw materials, combined with polytetramethylene ether glycol (PTMG) and 1,4-butanediol (BDO) to successfully synthesize five PU materials. The effects of isocyanate structure on polymerization rate, hydrogen bonding, thermal properties, phase separation, wettability, self-healing performance, adhesion, and mechanical properties were systematically investigated.
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