Synthesis of novel thermotropic liquid crystalline polymers by a reactive extrusion process

The syntheses of new thermotropic liquid crystalline polymers (TLCPs) were carried out via the polyaddition reactions of diepoxy-containing mesogens and a monoamine (1-naphthylamine). Both bulk polymerization and reactive extrusion were tested. The reaction between the two epoxy rings on the mesogen...

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Published inRSC advances Vol. 9; no. 22; pp. 12189 - 12194
Main Authors Oh, Kyunghwan, Kim, Hoyeon, Seo, Yongsok
Format Journal Article
LanguageEnglish
Published England Royal Society of Chemistry 17.04.2019
The Royal Society of Chemistry
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Abstract The syntheses of new thermotropic liquid crystalline polymers (TLCPs) were carried out via the polyaddition reactions of diepoxy-containing mesogens and a monoamine (1-naphthylamine). Both bulk polymerization and reactive extrusion were tested. The reaction between the two epoxy rings on the mesogen unit and the primary amine produces a thermotropic liquid crystalline polymer in the extruder. The amine group combines with the two epoxy rings in a single step via a polyaddition reaction to produce thermotropic liquid crystalline polymers without the formation of any by-products. Both polymers were found to exhibit nematic mesophase characteristics, which were examined by using polarized optical microscopy. The new thermotropic liquid crystalline polymers obtained with the bulk reaction have high molecular weights, whereas the polymers synthesized by using reactive extrusion have low molar mass due to their short residence times in the extruder. All the synthesized TLCPs were found to exhibit high thermal stability. Their decomposition temperatures were found to be above 350 °C, but their melting temperatures are low (below 250 °C). The liquid crystalline structures of the TLCPs were verified by performing 2D X-ray diffraction measurements. Scanning electron micrographs of the drawn polymer fibers show that the orientation of their morphologies lies predominantly along the direction of the fibers. The polymers synthesized with the reactive extrusion process have the same physical properties as those obtained with the bulk polyaddition reaction. This observation demonstrates the feasibility of the mass production of new TLCPs through reactive extrusion. The syntheses of new thermotropic liquid crystalline polymers (TLCPs) were carried out via the polyaddition reactions of diepoxy-containing mesogens and a monoamine (1-naphthylamine).
AbstractList The syntheses of new thermotropic liquid crystalline polymers (TLCPs) were carried out the polyaddition reactions of diepoxy-containing mesogens and a monoamine (1-naphthylamine). Both bulk polymerization and reactive extrusion were tested. The reaction between the two epoxy rings on the mesogen unit and the primary amine produces a thermotropic liquid crystalline polymer in the extruder. The amine group combines with the two epoxy rings in a single step a polyaddition reaction to produce thermotropic liquid crystalline polymers without the formation of any by-products. Both polymers were found to exhibit nematic mesophase characteristics, which were examined by using polarized optical microscopy. The new thermotropic liquid crystalline polymers obtained with the bulk reaction have high molecular weights, whereas the polymers synthesized by using reactive extrusion have low molar mass due to their short residence times in the extruder. All the synthesized TLCPs were found to exhibit high thermal stability. Their decomposition temperatures were found to be above 350 °C, but their melting temperatures are low (below 250 °C). The liquid crystalline structures of the TLCPs were verified by performing 2D X-ray diffraction measurements. Scanning electron micrographs of the drawn polymer fibers show that the orientation of their morphologies lies predominantly along the direction of the fibers. The polymers synthesized with the reactive extrusion process have the same physical properties as those obtained with the bulk polyaddition reaction. This observation demonstrates the feasibility of the mass production of new TLCPs through reactive extrusion.
The syntheses of new thermotropic liquid crystalline polymers (TLCPs) were carried out via the polyaddition reactions of diepoxy-containing mesogens and a monoamine (1-naphthylamine). Both bulk polymerization and reactive extrusion were tested. The reaction between the two epoxy rings on the mesogen unit and the primary amine produces a thermotropic liquid crystalline polymer in the extruder. The amine group combines with the two epoxy rings in a single step via a polyaddition reaction to produce thermotropic liquid crystalline polymers without the formation of any by-products. Both polymers were found to exhibit nematic mesophase characteristics, which were examined by using polarized optical microscopy. The new thermotropic liquid crystalline polymers obtained with the bulk reaction have high molecular weights, whereas the polymers synthesized by using reactive extrusion have low molar mass due to their short residence times in the extruder. All the synthesized TLCPs were found to exhibit high thermal stability. Their decomposition temperatures were found to be above 350 °C, but their melting temperatures are low (below 250 °C). The liquid crystalline structures of the TLCPs were verified by performing 2D X-ray diffraction measurements. Scanning electron micrographs of the drawn polymer fibers show that the orientation of their morphologies lies predominantly along the direction of the fibers. The polymers synthesized with the reactive extrusion process have the same physical properties as those obtained with the bulk polyaddition reaction. This observation demonstrates the feasibility of the mass production of new TLCPs through reactive extrusion.
The syntheses of new thermotropic liquid crystalline polymers (TLCPs) were carried out via the polyaddition reactions of diepoxy-containing mesogens and a monoamine (1-naphthylamine). Both bulk polymerization and reactive extrusion were tested. The reaction between the two epoxy rings on the mesogen unit and the primary amine produces a thermotropic liquid crystalline polymer in the extruder. The amine group combines with the two epoxy rings in a single step via a polyaddition reaction to produce thermotropic liquid crystalline polymers without the formation of any by-products. Both polymers were found to exhibit nematic mesophase characteristics, which were examined by using polarized optical microscopy. The new thermotropic liquid crystalline polymers obtained with the bulk reaction have high molecular weights, whereas the polymers synthesized by using reactive extrusion have low molar mass due to their short residence times in the extruder. All the synthesized TLCPs were found to exhibit high thermal stability. Their decomposition temperatures were found to be above 350 °C, but their melting temperatures are low (below 250 °C). The liquid crystalline structures of the TLCPs were verified by performing 2D X-ray diffraction measurements. Scanning electron micrographs of the drawn polymer fibers show that the orientation of their morphologies lies predominantly along the direction of the fibers. The polymers synthesized with the reactive extrusion process have the same physical properties as those obtained with the bulk polyaddition reaction. This observation demonstrates the feasibility of the mass production of new TLCPs through reactive extrusion. The syntheses of new thermotropic liquid crystalline polymers (TLCPs) were carried out via the polyaddition reactions of diepoxy-containing mesogens and a monoamine (1-naphthylamine).
The syntheses of new thermotropic liquid crystalline polymers (TLCPs) were carried out via the polyaddition reactions of diepoxy-containing mesogens and a monoamine (1-naphthylamine). Both bulk polymerization and reactive extrusion were tested. The reaction between the two epoxy rings on the mesogen unit and the primary amine produces a thermotropic liquid crystalline polymer in the extruder. The amine group combines with the two epoxy rings in a single step via a polyaddition reaction to produce thermotropic liquid crystalline polymers without the formation of any by-products. Both polymers were found to exhibit nematic mesophase characteristics, which were examined by using polarized optical microscopy. The new thermotropic liquid crystalline polymers obtained with the bulk reaction have high molecular weights, whereas the polymers synthesized by using reactive extrusion have low molar mass due to their short residence times in the extruder. All the synthesized TLCPs were found to exhibit high thermal stability. Their decomposition temperatures were found to be above 350 °C, but their melting temperatures are low (below 250 °C). The liquid crystalline structures of the TLCPs were verified by performing 2D X-ray diffraction measurements. Scanning electron micrographs of the drawn polymer fibers show that the orientation of their morphologies lies predominantly along the direction of the fibers. The polymers synthesized with the reactive extrusion process have the same physical properties as those obtained with the bulk polyaddition reaction. This observation demonstrates the feasibility of the mass production of new TLCPs through reactive extrusion.
The syntheses of new thermotropic liquid crystalline polymers (TLCPs) were carried out via the polyaddition reactions of diepoxy-containing mesogens and a monoamine (1-naphthylamine). Both bulk polymerization and reactive extrusion were tested. The reaction between the two epoxy rings on the mesogen unit and the primary amine produces a thermotropic liquid crystalline polymer in the extruder. The amine group combines with the two epoxy rings in a single step via a polyaddition reaction to produce thermotropic liquid crystalline polymers without the formation of any by-products. Both polymers were found to exhibit nematic mesophase characteristics, which were examined by using polarized optical microscopy. The new thermotropic liquid crystalline polymers obtained with the bulk reaction have high molecular weights, whereas the polymers synthesized by using reactive extrusion have low molar mass due to their short residence times in the extruder. All the synthesized TLCPs were found to exhibit high thermal stability. Their decomposition temperatures were found to be above 350 °C, but their melting temperatures are low (below 250 °C). The liquid crystalline structures of the TLCPs were verified by performing 2D X-ray diffraction measurements. Scanning electron micrographs of the drawn polymer fibers show that the orientation of their morphologies lies predominantly along the direction of the fibers. The polymers synthesized with the reactive extrusion process have the same physical properties as those obtained with the bulk polyaddition reaction. This observation demonstrates the feasibility of the mass production of new TLCPs through reactive extrusion. The syntheses of new thermotropic liquid crystalline polymers (TLCPs) were carried out via the polyaddition reactions of diepoxy-containing mesogens and a monoamine (1-naphthylamine).
The syntheses of new thermotropic liquid crystalline polymers (TLCPs) were carried out via the polyaddition reactions of diepoxy-containing mesogens and a monoamine (1-naphthylamine). Both bulk polymerization and reactive extrusion were tested. The reaction between the two epoxy rings on the mesogen unit and the primary amine produces a thermotropic liquid crystalline polymer in the extruder. The amine group combines with the two epoxy rings in a single step via a polyaddition reaction to produce thermotropic liquid crystalline polymers without the formation of any by-products. Both polymers were found to exhibit nematic mesophase characteristics, which were examined by using polarized optical microscopy. The new thermotropic liquid crystalline polymers obtained with the bulk reaction have high molecular weights, whereas the polymers synthesized by using reactive extrusion have low molar mass due to their short residence times in the extruder. All the synthesized TLCPs were found to exhibit high thermal stability. Their decomposition temperatures were found to be above 350 °C, but their melting temperatures are low (below 250 °C). The liquid crystalline structures of the TLCPs were verified by performing 2D X-ray diffraction measurements. Scanning electron micrographs of the drawn polymer fibers show that the orientation of their morphologies lies predominantly along the direction of the fibers. The polymers synthesized with the reactive extrusion process have the same physical properties as those obtained with the bulk polyaddition reaction. This observation demonstrates the feasibility of the mass production of new TLCPs through reactive extrusion.The syntheses of new thermotropic liquid crystalline polymers (TLCPs) were carried out via the polyaddition reactions of diepoxy-containing mesogens and a monoamine (1-naphthylamine). Both bulk polymerization and reactive extrusion were tested. The reaction between the two epoxy rings on the mesogen unit and the primary amine produces a thermotropic liquid crystalline polymer in the extruder. The amine group combines with the two epoxy rings in a single step via a polyaddition reaction to produce thermotropic liquid crystalline polymers without the formation of any by-products. Both polymers were found to exhibit nematic mesophase characteristics, which were examined by using polarized optical microscopy. The new thermotropic liquid crystalline polymers obtained with the bulk reaction have high molecular weights, whereas the polymers synthesized by using reactive extrusion have low molar mass due to their short residence times in the extruder. All the synthesized TLCPs were found to exhibit high thermal stability. Their decomposition temperatures were found to be above 350 °C, but their melting temperatures are low (below 250 °C). The liquid crystalline structures of the TLCPs were verified by performing 2D X-ray diffraction measurements. Scanning electron micrographs of the drawn polymer fibers show that the orientation of their morphologies lies predominantly along the direction of the fibers. The polymers synthesized with the reactive extrusion process have the same physical properties as those obtained with the bulk polyaddition reaction. This observation demonstrates the feasibility of the mass production of new TLCPs through reactive extrusion.
Author Seo, Yongsok
Kim, Hoyeon
Oh, Kyunghwan
AuthorAffiliation School of Materials Science and Engineering
College of Engineering
RIAM
Seoul National University
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Cites_doi 10.1016/0032-3861(95)91561-K
10.1016/S0032-3861(98)00684-3
10.1016/j.polymer.2005.06.117
10.1016/j.polymer.2005.06.084
10.1021/ma00200a046
10.1080/00222357908080906
10.1039/c3py01717f
10.1016/0032-3861(95)91560-T
10.1002/anie.201300872
10.1016/0032-3861(94)90506-1
10.1021/la051918c
10.1021/ma00037a001
10.1351/pac197648030317
10.3139/217.940266
10.1002/anie.201300371
10.1039/C6PY00086J
10.1039/C7RA02809A
10.1016/S0032-3861(98)00257-2
10.1039/b9py00358d
10.1016/S0032-3861(98)00685-5
10.1021/ma961343d
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Notes Electronic supplementary information (ESI) available: Synthesis details of the mesogenic epoxides, the polymerization process and the table of NMR peak positions. See DOI
10.1039/c8ra10410g
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References Oh (C8RA10410G-(cit19)/*[position()=1]) 2017; 7
Kantor (C8RA10410G-(cit24)/*[position()=1]) 1992; 25
Mossey-Lesczak (C8RA10410G-(cit20)/*[position()=1]) 2011
Enikolopiyan (C8RA10410G-(cit21)/*[position()=1]) 1976; 48
Ryu (C8RA10410G-(cit26)/*[position()=1]) 1994; 9
Seo (C8RA10410G-(cit10)/*[position()=1]) 2006; 8
(C8RA10410G-(cit2)/*[position()=1]) 2001
(C8RA10410G-(cit3)/*[position()=1]) 2016
Seo (C8RA10410G-(cit14)/*[position()=1]) 1995; 36
Zhu (C8RA10410G-(cit25)/*[position()=1]) 2007; 45
Tschierske (C8RA10410G-(cit1)/*[position()=1]) 2013; 52
Seo (C8RA10410G-(cit9)/*[position()=1]) 1997; 30
Krishwaswamy (C8RA10410G-(cit18)/*[position()=1]) 1999; 40
San Jose (C8RA10410G-(cit6)/*[position()=1]) 2014; 5
Zhang (C8RA10410G-(cit8)/*[position()=1]) 2016; 7
Seo (C8RA10410G-(cit13)/*[position()=1]) 1999; 40
Chena (C8RA10410G-(cit27)/*[position()=1]) 2005; 46
Seo (C8RA10410G-(cit15)/*[position()=1]) 1995; 36
Blanco (C8RA10410G-(cit22)/*[position()=1]) 2005; 46
Burrell II (C8RA10410G-(cit5)/*[position()=1]) 1979; 7
Donald (C8RA10410G-(cit4)/*[position()=1]) 2006
Seo (C8RA10410G-(cit12)/*[position()=1]) 1999; 40
Lee (C8RA10410G-(cit16)/*[position()=1]) 1994; 35
(C8RA10410G-(cit17)/*[position()=1]) 1993
Fleischmann (C8RA10410G-(cit11)/*[position()=1]) 2013; 52
Watanabe (C8RA10410G-(cit23)/*[position()=1]) 1989; 22
Sato (C8RA10410G-(cit7)/*[position()=1]) 2010; 1
References_xml – issn: 2016
  publication-title: Liquid Crystalline Polymers: Vol 1-Structure and Chemistry
– issn: 2001
  publication-title: Thermotropic Liquid Crystal Polymers: Thin Polymerization, Characterization, Blends, and Applications
– issn: 2011
  end-page: p125-152
  publication-title: Liquid Crystalline Compounds and Polymers as Materials of the XXI Century from Syntheses to Applications
  doi: Mossey-Lesczak Locharska
– issn: 1993
  publication-title: Thermotropic Liquid Crystal Polymer Blends
– issn: 2006
  publication-title: Liquid Crystalline Polymers (Cambridge Solid State Science)
  doi: Donald Windle Hanna
– volume: 36
  start-page: 525
  year: 1995
  ident: C8RA10410G-(cit15)/*[position()=1]
  publication-title: Polymer
  doi: 10.1016/0032-3861(95)91561-K
– volume-title: Liquid Crystalline Polymers (Cambridge Solid State Science)
  year: 2006
  ident: C8RA10410G-(cit4)/*[position()=1]
– volume: 45
  start-page: 800
  year: 2007
  ident: C8RA10410G-(cit25)/*[position()=1]
  publication-title: J. Polym. Sci., Part A-1: Polym. Chem.
– volume: 40
  start-page: 4483
  year: 1999
  ident: C8RA10410G-(cit12)/*[position()=1]
  publication-title: Polymer
  doi: 10.1016/S0032-3861(98)00684-3
– volume: 46
  start-page: 7989
  year: 2005
  ident: C8RA10410G-(cit22)/*[position()=1]
  publication-title: Polymer
  doi: 10.1016/j.polymer.2005.06.117
– volume: 46
  start-page: 8624
  year: 2005
  ident: C8RA10410G-(cit27)/*[position()=1]
  publication-title: Polymer
  doi: 10.1016/j.polymer.2005.06.084
– volume-title: Liquid Crystalline Compounds and Polymers as Materials of the XXI Century from Syntheses to Applications
  year: 2011
  ident: C8RA10410G-(cit20)/*[position()=1]
– volume-title: Liquid Crystalline Polymers: Vol 1-Structure and Chemistry
  year: 2016
  ident: C8RA10410G-(cit3)/*[position()=1]
– volume: 22
  start-page: 4083
  year: 1989
  ident: C8RA10410G-(cit23)/*[position()=1]
  publication-title: Macromolecules
  doi: 10.1021/ma00200a046
– volume: 7
  start-page: 137
  year: 1979
  ident: C8RA10410G-(cit5)/*[position()=1]
  publication-title: J. Macromol. Sci. Rev. Macromol.
  doi: 10.1080/00222357908080906
– volume: 5
  start-page: 3737
  year: 2014
  ident: C8RA10410G-(cit6)/*[position()=1]
  publication-title: Polym. Chem.
  doi: 10.1039/c3py01717f
– volume-title: Thermotropic Liquid Crystal Polymers: Thin Polymerization, Characterization, Blends, and Applications
  year: 2001
  ident: C8RA10410G-(cit2)/*[position()=1]
– volume: 36
  start-page: 515
  year: 1995
  ident: C8RA10410G-(cit14)/*[position()=1]
  publication-title: Polymer
  doi: 10.1016/0032-3861(95)91560-T
– volume: 52
  start-page: 8828
  year: 2013
  ident: C8RA10410G-(cit1)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201300872
– volume: 35
  start-page: 519
  year: 1994
  ident: C8RA10410G-(cit16)/*[position()=1]
  publication-title: Polymer
  doi: 10.1016/0032-3861(94)90506-1
– volume-title: Thermotropic Liquid Crystal Polymer Blends
  year: 1993
  ident: C8RA10410G-(cit17)/*[position()=1]
– volume: 8
  start-page: 3062
  year: 2006
  ident: C8RA10410G-(cit10)/*[position()=1]
  publication-title: Langmuir
  doi: 10.1021/la051918c
– volume: 25
  start-page: 2789
  year: 1992
  ident: C8RA10410G-(cit24)/*[position()=1]
  publication-title: Macromolecules
  doi: 10.1021/ma00037a001
– volume: 48
  start-page: 317
  year: 1976
  ident: C8RA10410G-(cit21)/*[position()=1]
  publication-title: Pure Appl. Chem.
  doi: 10.1351/pac197648030317
– volume: 9
  start-page: 266
  year: 1994
  ident: C8RA10410G-(cit26)/*[position()=1]
  publication-title: Int. Polym. Process.
  doi: 10.3139/217.940266
– volume: 52
  start-page: 8810
  year: 2013
  ident: C8RA10410G-(cit11)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201300371
– volume: 7
  start-page: 3013
  year: 2016
  ident: C8RA10410G-(cit8)/*[position()=1]
  publication-title: Polym. Chem.
  doi: 10.1039/C6PY00086J
– volume: 7
  start-page: 29772
  year: 2017
  ident: C8RA10410G-(cit19)/*[position()=1]
  publication-title: RSC Adv.
  doi: 10.1039/C7RA02809A
– volume: 40
  start-page: 701
  year: 1999
  ident: C8RA10410G-(cit18)/*[position()=1]
  publication-title: Polymer
  doi: 10.1016/S0032-3861(98)00257-2
– volume: 1
  start-page: 891
  year: 2010
  ident: C8RA10410G-(cit7)/*[position()=1]
  publication-title: Polym. Chem.
  doi: 10.1039/b9py00358d
– volume: 40
  start-page: 4441
  year: 1999
  ident: C8RA10410G-(cit13)/*[position()=1]
  publication-title: Polymer
  doi: 10.1016/S0032-3861(98)00685-5
– volume: 30
  start-page: 2978
  year: 1997
  ident: C8RA10410G-(cit9)/*[position()=1]
  publication-title: Macromolecules
  doi: 10.1021/ma961343d
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Snippet The syntheses of new thermotropic liquid crystalline polymers (TLCPs) were carried out via the polyaddition reactions of diepoxy-containing mesogens and a...
The syntheses of new thermotropic liquid crystalline polymers (TLCPs) were carried out the polyaddition reactions of diepoxy-containing mesogens and a...
The syntheses of new thermotropic liquid crystalline polymers (TLCPs) were carried out via the polyaddition reactions of diepoxy-containing mesogens and a...
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SubjectTerms Bulk polymerization
byproducts
Chemical synthesis
Chemistry
Crystal structure
Crystallinity
Electron micrographs
epoxides
Extrusion
light microscopy
Liquid crystal polymers
Liquid crystals
liquids
Mass production
Mesophase
molecular weight
Morphology
NMR
Nuclear magnetic resonance
Optical microscopy
Physical properties
Polymerization
Polymers
temperature
Thermal stability
X-ray diffraction
Title Synthesis of novel thermotropic liquid crystalline polymers by a reactive extrusion process
URI https://www.ncbi.nlm.nih.gov/pubmed/35515872
https://www.proquest.com/docview/2215762751
https://www.proquest.com/docview/2237545634
https://www.proquest.com/docview/2661081159
https://pubmed.ncbi.nlm.nih.gov/PMC9063539
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