Abstract:Lignin samples fractionated from microwave liquefied switchgrass were applied in the preparation of semirigid polyurethane (PU) foams without purification. The objective of this study was to elucidate the influence of lignin in the PU matrix on the morphological, chemical, mechanical, and thermal properties of the PU foams. The scanning electron microscopy (SEM) images revealed that lignin with 5 and 10% content in the PU foams did not influence the cell shape and size. The foam cell size became larger by incr… Show more
“…The shoulder of -C=O may appear due to the intermolecular H bonding in polymer structure. These transitions of IR bands strongly established the synthesis of polyurethane sample [6,[16][17][18]. Other noticeable bands in IR spectra of synthesized CPUF were symmetric and antisymmetric bands of aliphatic -CH at 2933 cm -1 and 2855 cm -1 , aromatic C=C stretching band at 1645 cm -1 and 1595 cm -1 , and multiple stretching bands of ester C-O at 1064 cm -1 , 1160 cm -1 , and 1214 cm -1 .…”
Section: Resultsmentioning
confidence: 63%
“…Polyurethane is an exclusive class of synthetic polymers which contains urethane link (-NHCOO). It is well known for versatile applications from cushioning to coatings due to tunable properties [6][7][8]. Polyurethane foams are extensively involved in water treatment processes, directly and indirectly [9].…”
A number of physical, chemical, and biological technologies have been developed to address the issue of synthetic dyes in wastewater. One of the important chemical methods involves reduction of these stringent pollutants into less hazardous products. In this study, a cross-linked polyurethane foam (CPUF) was prepared from toluene diisocyanate (TDI), tetraethylenepentamine (TEPA), and polycaprolactone diol (PCL; Mw: 1000 g/mole). To avoid harmful reducing agents, ecofriendly reduction of methylene blue (MB) was executed with CPUF as catalyst where ascorbic acid and fresh juice extracts were applied as reducing agents. The FTIR and SEM analysis confirmed the chemical composition and porous morphology of CPUF, respectively. The 100% reduction of MB was recorded in just 15 minutes with ascorbic acid and CPUF, while similar result was obtained in 37 minutes in blank experiment composed of only MB and ascorbic acid. Thus, catalytic role of CPUF in reduction process was proved. Fresh fruit extracts also participated in the reduction process, but rate of reaction was accelerated in the presence of CPUF. The reusability study of the catalyst supported its stability and efficiency. All the successful reduction processes followed 1st-order kinetics with highest apparent rate constant for ascorbic acid. Furthermore, phytotoxicity evaluation proved safe reduction of MB with 60% germination index. Hence, it can be concluded that catalytic role of CPUF has been established with safe and biodegradable reducing agents which can be extended to other redox processes.
“…The shoulder of -C=O may appear due to the intermolecular H bonding in polymer structure. These transitions of IR bands strongly established the synthesis of polyurethane sample [6,[16][17][18]. Other noticeable bands in IR spectra of synthesized CPUF were symmetric and antisymmetric bands of aliphatic -CH at 2933 cm -1 and 2855 cm -1 , aromatic C=C stretching band at 1645 cm -1 and 1595 cm -1 , and multiple stretching bands of ester C-O at 1064 cm -1 , 1160 cm -1 , and 1214 cm -1 .…”
Section: Resultsmentioning
confidence: 63%
“…Polyurethane is an exclusive class of synthetic polymers which contains urethane link (-NHCOO). It is well known for versatile applications from cushioning to coatings due to tunable properties [6][7][8]. Polyurethane foams are extensively involved in water treatment processes, directly and indirectly [9].…”
A number of physical, chemical, and biological technologies have been developed to address the issue of synthetic dyes in wastewater. One of the important chemical methods involves reduction of these stringent pollutants into less hazardous products. In this study, a cross-linked polyurethane foam (CPUF) was prepared from toluene diisocyanate (TDI), tetraethylenepentamine (TEPA), and polycaprolactone diol (PCL; Mw: 1000 g/mole). To avoid harmful reducing agents, ecofriendly reduction of methylene blue (MB) was executed with CPUF as catalyst where ascorbic acid and fresh juice extracts were applied as reducing agents. The FTIR and SEM analysis confirmed the chemical composition and porous morphology of CPUF, respectively. The 100% reduction of MB was recorded in just 15 minutes with ascorbic acid and CPUF, while similar result was obtained in 37 minutes in blank experiment composed of only MB and ascorbic acid. Thus, catalytic role of CPUF in reduction process was proved. Fresh fruit extracts also participated in the reduction process, but rate of reaction was accelerated in the presence of CPUF. The reusability study of the catalyst supported its stability and efficiency. All the successful reduction processes followed 1st-order kinetics with highest apparent rate constant for ascorbic acid. Furthermore, phytotoxicity evaluation proved safe reduction of MB with 60% germination index. Hence, it can be concluded that catalytic role of CPUF has been established with safe and biodegradable reducing agents which can be extended to other redox processes.
“…Various lignocellulosic biomass types such as poplar, southern pine, bamboo, bagasse, agricultural residues, and lignin have been microwave liquefied in alcohol solvents to produce PU foams. As shown in Figure 2, under different liquefaction conditions (the mass ratio of bagasse flour and biocomponent polyhydric alcohol was 1 : 2, 1 : 3, and 1 : 4 and the temperature was 125°C and 150°C), all the synthesized PU foams were of rigid type and the foam was darker in color with the addition of the liquefied bagasse [49,60,[74][75][76][77][78][79][80]. The properties of the fabricated biobased foams from microwave-liquefied products were largely dependent on the biomass type, heating methods, and liquefaction conditions.…”
Section: Integrated Utilization Of Liquefied Liquidmentioning
confidence: 99%
“…The poor thermal stability is mainly because the molecular weight of the microwave liquefaction product of corn stover is lower than that of the conventional liquefied product, resulting in a decrease in the degree of crosslinking of the synthesized polyurethane [26]. The application of the proper amount (less than 10%) of lignin fractionated from the microwave-assisted liquefied switchgrass into the PU matrix could improve the performances of PU foams in the apparent density, mechanical strength, and thermal stability [79]. By adding 20% biopolyol from microwave-liquefied rape straw, the biofoam cell diameter decreased by 90% compared with the PU without biopolyol from rape straw and the foam cell became more International Journal of Polymer Science homogenous and finer, and the PU foams exhibited extremely low thermal conductivity and excellent mechanical strength.…”
Section: Integrated Utilization Of Liquefied Liquidmentioning
Microwave-assisted liquefaction is regarded as a promising thermochemical approach to produce renewable and sustainable chemicals and materials from lignocellulosic biomass. Agricultural and forest residues as sources of lignocellulosic biomass have great potential in this regard. With process optimizations, several biomass types have been subjected to liquefaction in different solvents with various catalysts. The products from recent microwave liquefaction with and without further fractionation have been thoroughly analyzed and used for the synthesis of biomaterials. Renewable chemicals, polyurethane foams with partial use of renewable raw materials, and phenolic resins have been the main products from microwave-liquefied products. Further research on microwave liquefaction mechanisms and scalable production should be enhanced to fully evaluate the economic and environmental benefits. This work presents an overview on achievements using liquefaction in combination with microwave energy to convert lignocellulosic biomass into value-added products and chemicals.
“…Catalysts were involved in most of the lignin liquefaction reactions in hydrogen donor solvents with microwave heating. The catalysts mostly used for the microwave assisted lignin liquefaction could be generally divided into homogeneous and heterogeneous catalysts [20,21,26,46,[49][50][51][52][53][54][55][56]. Several studies reported the application of homogeneous catalysts in the microwave assisted lignin liquefaction in hydrogen donor solvents, which could be generally grouped into acid/base catalysts and/or metal salts.…”
Lignin, a renewable source of aromatic chemicals in nature, has attracted increasing attention due to its structure and application prospect. Catalytic solvolysis has developed as a promising method for the production of value-added products from lignin. The liquefaction process is closely associated with heating methods, catalysts and solvents. Microwave assisted lignin liquefaction in hydrogen donor solvent with the presence of catalysts has been confirmed to be effective to promote the production of liquid fuels or fine chemicals. A great number of researchers should be greatly appreciated on account of their contributions on the progress of microwave technology in lignin liquefaction. In this study, microwave assisted liquefaction of lignin in a hydrogen donor solvent is extensively overviewed, concerning the effect of different solvents and catalysts. This review concludes that microwave assisted liquefaction is a promising technology for the valorization of lignin, which could reduce the reaction time, decrease the reaction temperature, and finally fulfill the utilization of lignin in a relatively mild condition. In the future, heterogeneous catalysts with high catalytic activity and stability need to be prepared to achieve the need for large-scale production of high-quality fuels and value-added chemicals from lignin.
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