Effects of incorporating polycaprolactone and flax fiber into glycerol-plasticized pea starch

The environmental menace associated with the existing eco-unfriendly conventional plastics prompted the exploration of natural polymers such as starch for the development of biodegradable plastics. These efforts have seen starch used in various ways, one of which is in the processing of thermoplasti...

Full description

Bibliographic Details
Main Author: Fabunmi, Olayide Oyeyemi
Other Authors: Tabil, Lope G.
Format: Others
Language:en
Published: University of Saskatchewan 2008
Subjects:
Online Access:http://library.usask.ca/theses/available/etd-12122008-150652/
id ndltd-USASK-oai-usask.ca-etd-12122008-150652
record_format oai_dc
collection NDLTD
language en
format Others
sources NDLTD
topic Starch
Polycaprolactone
Flax fiber
Composites
Biodegradable
spellingShingle Starch
Polycaprolactone
Flax fiber
Composites
Biodegradable
Fabunmi, Olayide Oyeyemi
Effects of incorporating polycaprolactone and flax fiber into glycerol-plasticized pea starch
description The environmental menace associated with the existing eco-unfriendly conventional plastics prompted the exploration of natural polymers such as starch for the development of biodegradable plastics. These efforts have seen starch used in various ways, one of which is in the processing of thermoplastic starch (TPS). Thermoplastic starch (also known as plasticized starch) is the product of the interaction between starch and a plasticizer in the presence of thermomechanical energy. While starch blends with conventional plastics only yield products that biofragment, thermoplastic starch (TPS) offers a completely biodegradable option. However, it is limited in application due to its weak mechanical strength and poor moisture resistance. To this end, the objective of this study was to determine the effects of incorporating polycaprolactone (PCL) and flax fiber into glycerol-plasticized pea starch. The effects of processing moisture content on the physical properties of glycerol-plasticized pea starch were also evaluated. The physical properties investigated included morphology, tensile properties, moisture absorption, and thermal properties.<p> Accordingly, two thermoplastic pea starch mixtures containing 9.3 and 20% processing moisture contents were prepared while maintaining starch (pea starch) and glycerol in ratio 7:3 by weight (dry basis). Polycaprolactone was then compounded at 0, 10, 20, 30, and 40% by weight in the solid phase with the TPS mixtures to determine the effects of processing moisture content and PCL incorporation on the physical properties of glycerol-plasticized pea starch. This experiment was structured as a 2 x 5 factorial completely randomized design at 5% level of significance. Subsequently, PCL and flax fiber were compounded with the TPS mixture containing 20% processing moisture to determine the effects of PCL (0, 20, and 40% wt) and flax fiber (0, 5, 10, and 15% wt) incorporation on the physical properties of glycerol-plasticized pea starch. This was structured as a 3 x 4 factorial completely randomized design at 5% level of significance. All the samples were compressed at 140°C for 45 min under 25000-kg load. The compression-molded samples were characterized using scanning electron microscopy (SEM), tensile test, moisture absorption test, and differential scanning calorimetry (DSC) techniques.<p> The tensile fracture surfaces showed a moisture-induced fundamental morphological difference between the two TPSs. The TPS prepared at 20% processing moisture content revealed complete starch gelatinization, thus, exhibiting a rather continuous phase whereas the TPS prepared at 9.3% processing moisture content revealed instances of ungelatinized and partly gelatinized pea starch granules. Consequently, the tensile strength, yield strength, Youngs modulus, and elongation at break increased by 208.6, 602.6, 208.5, and 292.0%, respectively at 20% processing moisture content. The incorporation of PCL reduced the degree of starch gelatinization by interfering with moisture migration during compression molding due to its (PCL) hydrophobicity. At both processing moisture levels of 9.3 and 20%, PCL incorporation had significant impacts on the tensile properties of the plasticized pea starch. Flax fiber incorporation also increased the tensile strength, yield strength, and Youngs modulus while concomitantly reducing the elongation at break of the plasticized pea starch. In the TPS/PCL/flax fiber ternary composites, both PCL and flax fiber improved the tensile strength by acting as independent reinforcing materials as no PCL-fiber interfacial bonding was observed. Maximum tensile strength of 11.55 MPa was reached at 10% flax fiber and 40% PCL reinforcement. While the PCL-TPS interfacial interaction was poor, some degree of TPS-flax fiber interfacial bonding was noticed due to their chemical similarity.<p> TPS prepared at 20% moisture showed more moisture affinity than that prepared at 9.3% moisture. The moisture absorption of TPS dropped progressively with the addition of hydrophobic PCL. Fiber incorporation also reduced moisture absorption by the plasticized pea starch. PCL-fiber incorporation also yielded improved moisture resistance vis-à-vis pure TPS. Finally, the TPS processed at 9.3% moisture exhibited higher thermal stability than that processed at 20%. Individual components of the composites retained their respective thermal properties, thus, implying thermodynamic immiscibility.
author2 Tabil, Lope G.
author_facet Tabil, Lope G.
Fabunmi, Olayide Oyeyemi
author Fabunmi, Olayide Oyeyemi
author_sort Fabunmi, Olayide Oyeyemi
title Effects of incorporating polycaprolactone and flax fiber into glycerol-plasticized pea starch
title_short Effects of incorporating polycaprolactone and flax fiber into glycerol-plasticized pea starch
title_full Effects of incorporating polycaprolactone and flax fiber into glycerol-plasticized pea starch
title_fullStr Effects of incorporating polycaprolactone and flax fiber into glycerol-plasticized pea starch
title_full_unstemmed Effects of incorporating polycaprolactone and flax fiber into glycerol-plasticized pea starch
title_sort effects of incorporating polycaprolactone and flax fiber into glycerol-plasticized pea starch
publisher University of Saskatchewan
publishDate 2008
url http://library.usask.ca/theses/available/etd-12122008-150652/
work_keys_str_mv AT fabunmiolayideoyeyemi effectsofincorporatingpolycaprolactoneandflaxfiberintoglycerolplasticizedpeastarch
_version_ 1716532589009829888
spelling ndltd-USASK-oai-usask.ca-etd-12122008-1506522013-01-08T16:33:40Z Effects of incorporating polycaprolactone and flax fiber into glycerol-plasticized pea starch Fabunmi, Olayide Oyeyemi Starch Polycaprolactone Flax fiber Composites Biodegradable The environmental menace associated with the existing eco-unfriendly conventional plastics prompted the exploration of natural polymers such as starch for the development of biodegradable plastics. These efforts have seen starch used in various ways, one of which is in the processing of thermoplastic starch (TPS). Thermoplastic starch (also known as plasticized starch) is the product of the interaction between starch and a plasticizer in the presence of thermomechanical energy. While starch blends with conventional plastics only yield products that biofragment, thermoplastic starch (TPS) offers a completely biodegradable option. However, it is limited in application due to its weak mechanical strength and poor moisture resistance. To this end, the objective of this study was to determine the effects of incorporating polycaprolactone (PCL) and flax fiber into glycerol-plasticized pea starch. The effects of processing moisture content on the physical properties of glycerol-plasticized pea starch were also evaluated. The physical properties investigated included morphology, tensile properties, moisture absorption, and thermal properties.<p> Accordingly, two thermoplastic pea starch mixtures containing 9.3 and 20% processing moisture contents were prepared while maintaining starch (pea starch) and glycerol in ratio 7:3 by weight (dry basis). Polycaprolactone was then compounded at 0, 10, 20, 30, and 40% by weight in the solid phase with the TPS mixtures to determine the effects of processing moisture content and PCL incorporation on the physical properties of glycerol-plasticized pea starch. This experiment was structured as a 2 x 5 factorial completely randomized design at 5% level of significance. Subsequently, PCL and flax fiber were compounded with the TPS mixture containing 20% processing moisture to determine the effects of PCL (0, 20, and 40% wt) and flax fiber (0, 5, 10, and 15% wt) incorporation on the physical properties of glycerol-plasticized pea starch. This was structured as a 3 x 4 factorial completely randomized design at 5% level of significance. All the samples were compressed at 140°C for 45 min under 25000-kg load. The compression-molded samples were characterized using scanning electron microscopy (SEM), tensile test, moisture absorption test, and differential scanning calorimetry (DSC) techniques.<p> The tensile fracture surfaces showed a moisture-induced fundamental morphological difference between the two TPSs. The TPS prepared at 20% processing moisture content revealed complete starch gelatinization, thus, exhibiting a rather continuous phase whereas the TPS prepared at 9.3% processing moisture content revealed instances of ungelatinized and partly gelatinized pea starch granules. Consequently, the tensile strength, yield strength, Youngs modulus, and elongation at break increased by 208.6, 602.6, 208.5, and 292.0%, respectively at 20% processing moisture content. The incorporation of PCL reduced the degree of starch gelatinization by interfering with moisture migration during compression molding due to its (PCL) hydrophobicity. At both processing moisture levels of 9.3 and 20%, PCL incorporation had significant impacts on the tensile properties of the plasticized pea starch. Flax fiber incorporation also increased the tensile strength, yield strength, and Youngs modulus while concomitantly reducing the elongation at break of the plasticized pea starch. In the TPS/PCL/flax fiber ternary composites, both PCL and flax fiber improved the tensile strength by acting as independent reinforcing materials as no PCL-fiber interfacial bonding was observed. Maximum tensile strength of 11.55 MPa was reached at 10% flax fiber and 40% PCL reinforcement. While the PCL-TPS interfacial interaction was poor, some degree of TPS-flax fiber interfacial bonding was noticed due to their chemical similarity.<p> TPS prepared at 20% moisture showed more moisture affinity than that prepared at 9.3% moisture. The moisture absorption of TPS dropped progressively with the addition of hydrophobic PCL. Fiber incorporation also reduced moisture absorption by the plasticized pea starch. PCL-fiber incorporation also yielded improved moisture resistance vis-à-vis pure TPS. Finally, the TPS processed at 9.3% moisture exhibited higher thermal stability than that processed at 20%. Individual components of the composites retained their respective thermal properties, thus, implying thermodynamic immiscibility. Tabil, Lope G. Panigrahi, Satyanarayan Maule, Charles P. Chang, Peter R. Wegner, Leon D. University of Saskatchewan 2008-12-19 text application/pdf http://library.usask.ca/theses/available/etd-12122008-150652/ http://library.usask.ca/theses/available/etd-12122008-150652/ en restricted I hereby certify that, if appropriate, I have obtained and attached hereto a written permission statement from the owner(s) of each third party copyrighted matter to be included in my thesis, dissertation, or project report, allowing distribution as specified below. I certify that the version I submitted is the same as that approved by my advisory committee. I hereby grant to University of Saskatchewan or its agents the non-exclusive license to archive and make accessible, under the conditions specified below, my thesis, dissertation, or project report in whole or in part in all forms of media, now or hereafter known. I retain all other ownership rights to the copyright of the thesis, dissertation or project report. I also retain the right to use in future works (such as articles or books) all or part of this thesis, dissertation, or project report.