This paper reports the facile one-pot synthesis of glycidol via the transesterification of glycerol with dimethyl carbonate using KNO/AlO nanoparticles as supporting catalysts. KNO/AlO nanoparticles were prepared by the impregnation method. XRD and FT-IR analyses indicated an interaction between KNO and AlO that enabled the decomposition of KNO during the process and resulted in the formation of KAlO, the Al-O-K group, and KO. KO was recognized as one of the active sites of the catalyst. SEM results indicated the high performance of the supporting catalyst, as the catalytic activity depended on both the number of catalytic active sites and their distribution. The yield of glycidol was 64% at the expense of 95% glycerol under moderate reaction conditions (120 min, 1 atm, and 70 °C). The nanocatalyst prepared at 800 °C with a loading amount of 30% KNO was the most efficient for the synthesis of glycidol. Furthermore, the catalyst was recovered and reused without a loss of efficiency even after the fourth recycling. A plausible mechanism for the one-pot synthesis of glycidol has also been proposed.
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http://dx.doi.org/10.1021/acsomega.2c02381 | DOI Listing |
Polymers (Basel)
November 2024
User Convenience Technology R&D Department, Korea Institute of Industrial Technology (KITECH), Ansan-si 15588, Republic of Korea.
Herein, a novel glycidyl carbamate functional epoxy resin (GCE) is synthesized by the additional reaction of the isocyanate group of tolylene diisocyanate (TDI) with the hydroxyl group of hydroxyl-terminated polybutadiene (HTPB) and glycidol. The successful synthesis of the GCE is confirmed by FT-IR and H NMR spectroscopy. Furthermore, a dual-curing adhesive system is developed using acrylic acid and trimethylolpropane triacrylate with varying GCE contents, and its adhesive performance is assessed by testing adhesive strength, pencil hardness, and surface energy.
View Article and Find Full Text PDFMaterials (Basel)
November 2024
Center for Microelectronics and Nanotechnology, Institute of Materials Engineering, University of Rzeszow, Al. Rejtana 16, 35-959 Rzeszow, Poland.
Three methods of cellulose-derived polyol synthesis were elaborated. The suitable substrates were (hydroxypropyl)cellulose or cellulose, which were hydroxyalkylated in reactions with glycidol and ethylene carbonate in triethylene glycol or in water. The products were characterized by IR, H NMR, and MALDI ToF spectroscopies.
View Article and Find Full Text PDFMacromol Rapid Commun
November 2024
Donostia International Physics Center (DIPC), Paseo Manuel Lardizábal 4, Donostia-San Sebastián, 20018, Spain.
In the present study, low molecular weight cyclic polyglycidol is used as a macroinitiator for hypergrafting glycidol and producing cyclic graft hyperbranched polyglycerol (cPG-g-hbPG) in the molecular weight range of 10-10 g mol. Linear graft hyperbranched polyglycerol (linPG-g-hbPG) and hyperbranched polyglycerol (hbPG) are prepared as reference samples. This creates a family of hbPG structures with cyclic, linear, and star cores, allowing to evaluate their properties in solution and in bulk.
View Article and Find Full Text PDFACS Sustain Chem Eng
October 2024
Departamento de Bioquimica y Biologia Molecular B e Inmunologia. Facultad de Quimica, Universidad de Murcia, E-30100 Murcia, Spain.
A sustainable approach for CO capture and chemo-enzymatic transformation into bis(cyclic carbonate) esters from CO, glycidol, and organic anhydrides under solvent-free conditions has been demonstrated. The chemo-enzymatic process is based on two consecutive catalytic steps, which can be executed through separated operations or within a one-pot combo system, taking advantage of the synergic effects that emerge from integrating ionic liquid (IL) technologies and biocatalysts. In a first step, lipase-catalyzed transesterification and esterification reactions of different diacyl donors (e.
View Article and Find Full Text PDFMolecules
September 2024
Medical College, University of Rzeszow, 1a Warzywna Street, 35-310 Rzeszow, Poland.
In this study, we hypothesized that biotinylated and/or glycidol-flanked fourth-generation polyamidoamine (PAMAM G4) dendrimers could be a tool for efficient drug transport into glioma and liver cancer cells. For this purpose, native PAMAM (G4) dendrimers, biotinylated (G4B), glycidylated (G4gl), and biotinylated and glycidylated (G4Bgl), were synthesized, and their cytotoxicity, uptake, and accumulation in vitro and in vivo were studied in relation to the transport mediated by the sodium-dependent multivitamin transporter (SMVT). The studies showed that the human temozolomide-resistant glioma cell line (U-118 MG) and hepatocellular carcinoma cell line (HepG2) indicated a higher amount of SMVT than human HaCaT keratinocytes (HaCaTs) used as a model of normal cells.
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