Full Recycling and Re-Use of Bio-Based Epoxy Thermosets: Chemical and Thermomechanical Characterization of the Recycled Matrices

被引:20
作者
Dattilo, Sandro [1 ]
Cicala, Gianluca [2 ,3 ]
Riccobene, Paolo Maria [1 ]
Puglisi, Concetto [1 ]
Saitta, Lorena [2 ]
机构
[1] CNR IPCB, Via Paolo Gaifami 18, I-95126 Catania, Italy
[2] Univ Catania, Dept Civil Engn & Architecture, Viale Andrea Doria 6, I-95125 Catania, Italy
[3] INSTM UDR CT, Viale Andrea Doria 6, I-95125 Catania, Italy
关键词
bio-based epoxy resin; chemical recycling; recyclable epoxy; recycled matrices re-use; thermomechanical properties; CARBON FIBRE/EPOXY COMPOSITES; FIBER-REINFORCED POLYMERS; UNSATURATED POLYESTER; CURED EPOXY; RESIN; DEGRADATION; SOLVOLYSIS; DECOMPOSITION; RECOVERY; TECHNOLOGIES;
D O I
10.3390/polym14224828
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
High performances of thermosets deriving from their covalent intermolecular cross-link bonds result in their low recyclability hindering the full exploitation of a truly circular approach for cured thermosets. In this experimental work, the recyclability of a bio-based fully recyclable epoxy resin using a mild chemical recycling process was demonstrated. The recycled polymer obtained was fully characterized to ascertain its structure and properties. MALDI (Matrix-Assisted Laser Desorption/Ionization), GPC (Gel Permeation Chromatography) and NMR (Nuclear Magnetic Resonance) spectroscopy to determine the chemical structure of the recycled polymer were used. The thermomechanical properties of the cured virgin network and of the recycled product obtained were measured by DSC (Differential Scanning Calorimetry) and DMA (Dynamic Mechanical Analysis). Thermogravimetric analysis of the recycled polymer was also performed. The recycled polymer was transformed into a polyurethane by reacting it with an isocyanate. The synthetized polyurethane obtained therefrom was thoroughly characterized by thermogravimetric analysis. This approach proved the possibility to up-scale the recycled product making it available for novel applications exploiting its re-use.
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页数:16
相关论文
共 53 条
[1]  
[Anonymous], 2000, OFFICIAL J EUROPEAN, V269, P34, DOI DOI 10.1016/J.JCLEPRO.2010.02.014
[2]   Recovery of value-added chemicals by solvolysis of unsaturated polyester resin [J].
Arturi, Katarzyna R. ;
Sokoli, Hulya U. ;
Sogaard, Erik G. ;
Vogel, Frederic ;
Bjelic, Saga .
JOURNAL OF CLEANER PRODUCTION, 2018, 170 :131-136
[3]   Decomposition behavior of epoxy-resin systems cured by diamines [J].
Barral, L ;
Cano, J ;
López, J ;
López-Bueno, I ;
Nogueira, P ;
Abad, MJ ;
Ramírez, C .
EUROPEAN POLYMER JOURNAL, 2000, 36 (06) :1231-1240
[4]   Recycling of Carbon Fiber-Reinforced Composites-Difficulties and Future Perspectives [J].
Borjan, Dragana ;
Knez, Zeljko ;
Knez, Masa .
MATERIALS, 2021, 14 (15)
[5]   Polyols and Polyurethanes Prepared from Epoxidized Soybean Oil Ring-Opened by Polyhydroxy Fatty Acids with Varying OH Numbers [J].
Chen, Ruqi ;
Zhang, Chaoqun ;
Kessler, Michael R. .
JOURNAL OF APPLIED POLYMER SCIENCE, 2015, 132 (01)
[6]   Hybrid composites manufactured by resin infusion with a fully recyclable bioepoxy resin [J].
Cicala, G. ;
Pergolizzi, E. ;
Piscopo, F. ;
Carbone, D. ;
Recca, G. .
COMPOSITES PART B-ENGINEERING, 2018, 132 :69-76
[7]   Green synthesis of flexible polyurethane foams from liquefied lignin [J].
Cinelli, Patrizia ;
Anguillesi, Irene ;
Lazzeri, Andrea .
EUROPEAN POLYMER JOURNAL, 2013, 49 (06) :1174-1184
[8]   An approach to chemical recycling of epoxy resin cured with amine using nitric acid [J].
Dang, WR ;
Kubouchi, M ;
Yamamoto, S ;
Sembokuya, H ;
Tsuda, K .
POLYMER, 2002, 43 (10) :2953-2958
[9]   An Efficient Method of Recycling of CFRP Waste Using Peracetic Acid [J].
Das, Mohan ;
Chacko, Rinu ;
Varughese, Susy .
ACS SUSTAINABLE CHEMISTRY & ENGINEERING, 2018, 6 (02) :1564-1571
[10]   From Vegetable Oils to Polyurethanes: Synthetic Routes to Polyols and Main Industrial Products [J].
Desroches, Myriam ;
Escouvois, Maxime ;
Auvergne, Remi ;
Caillol, Sylvain ;
Boutevin, Bernard .
POLYMER REVIEWS, 2012, 52 (01) :38-79