Recyclable Thermoplastic Elastomer from Furan Functionalized Hairy Nanoparticles with Polystyrene Core and Polydimethylsiloxane Hairs.

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Title: Recyclable Thermoplastic Elastomer from Furan Functionalized Hairy Nanoparticles with Polystyrene Core and Polydimethylsiloxane Hairs.
Authors: Uddin, Md Hanif1 (AUTHOR) muddin@cau.edu, Alshali, Sultan1 (AUTHOR), Alqurashi, Esam1 (AUTHOR), Alyoubi, Saber1 (AUTHOR), Walters, Natalia1 (AUTHOR), Khan, Ishrat M.1 (AUTHOR) ikhan@cau.edu
Source: Polymers (20734360). Nov2024, Vol. 16 Issue 22, p3117. 15p.
Subjects: Linear polymers, Coupling reactions (Chemistry), Thermoplastic elastomers, Glass transition temperature, Addition polymerization, Crosslinked polymers, Polymer networks
Abstract: Polymers synthesized with end-of-life consideration allow for recovery and reprocessing. "Living-anionic polymerization (LAP)" and hydrosilylation reaction were utilized to synthesize hair-end furan functionalized hairy nanoparticles (HNPs) with a hard polystyrene (PS) core and soft polydimethylsiloxane (PDMS) hairs via a one-pot approach. The synthesis was carried out by first preparing the living core through crosslinking styrene with divinylbenzene using sec-butyl lithium, followed by the addition of the hexamethylcyclotrisiloxane (D3) monomer to the living core. The living polymer was terminated by dimethylchlorosilane to obtain the HNPs with Si-H functional end groups. The furan functionalization was carried out by the hydrosilylation reaction between the Si-H of the functionalized HNP and 2-vinyl furan. Additionally, furan functionalized polystyrene (PS) and polydimethylsiloxane (PDMS) were also synthesized by LAP. 1H NMR and ATR-IR spectra confirmed the successful synthesis of the target polymers. Differential scanning calorimetry showed two glass transition temperatures indicative of a polydimethylsiloxane soft phase and a polystyrene hard phase, suggesting that the HNPs are microphase separated. The furan functionalized HNPs form thermo-reversible networks upon crosslinking with bismaleimide (BMI) via a Diels−Alder coupling reaction. The kinetics of the forward Diels–Alder reaction between the functionalized polymer and BMI were studied at three different temperatures: 50 °C, 60 °C, and 70 °C by UV–Vis spectroscopy. The activation energy for the furan functionalized HNPs reaction with the bismaleimide was lower compared to the furan functionalized polystyrene and polydimethylsiloxane linear polymers. The crosslinked polymer network formed from the Diels−Alder forward reaction dissociates at around 140–154 °C, and the HNPs are recovered. The recovered HNPs can be re-crosslinked at 50 °C. The results suggest that furan functionalized HNPs are promising building blocks for preparing thermo-reversible elastomeric networks. [ABSTRACT FROM AUTHOR]
Copyright of Polymers (20734360) is the property of MDPI and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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  Data: Recyclable Thermoplastic Elastomer from Furan Functionalized Hairy Nanoparticles with Polystyrene Core and Polydimethylsiloxane Hairs.
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  Data: <searchLink fieldCode="AR" term="%22Uddin%2C+Md+Hanif%22">Uddin, Md Hanif</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> muddin@cau.edu</i><br /><searchLink fieldCode="AR" term="%22Alshali%2C+Sultan%22">Alshali, Sultan</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Alqurashi%2C+Esam%22">Alqurashi, Esam</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Alyoubi%2C+Saber%22">Alyoubi, Saber</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Walters%2C+Natalia%22">Walters, Natalia</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Khan%2C+Ishrat+M%2E%22">Khan, Ishrat M.</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> ikhan@cau.edu</i>
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  Data: <searchLink fieldCode="JN" term="%22Polymers+%2820734360%29%22">Polymers (20734360)</searchLink>. Nov2024, Vol. 16 Issue 22, p3117. 15p.
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  Data: <searchLink fieldCode="DE" term="%22Linear+polymers%22">Linear polymers</searchLink><br /><searchLink fieldCode="DE" term="%22Coupling+reactions+%28Chemistry%29%22">Coupling reactions (Chemistry)</searchLink><br /><searchLink fieldCode="DE" term="%22Thermoplastic+elastomers%22">Thermoplastic elastomers</searchLink><br /><searchLink fieldCode="DE" term="%22Glass+transition+temperature%22">Glass transition temperature</searchLink><br /><searchLink fieldCode="DE" term="%22Addition+polymerization%22">Addition polymerization</searchLink><br /><searchLink fieldCode="DE" term="%22Crosslinked+polymers%22">Crosslinked polymers</searchLink><br /><searchLink fieldCode="DE" term="%22Polymer+networks%22">Polymer networks</searchLink>
– Name: Abstract
  Label: Abstract
  Group: Ab
  Data: Polymers synthesized with end-of-life consideration allow for recovery and reprocessing. "Living-anionic polymerization (LAP)" and hydrosilylation reaction were utilized to synthesize hair-end furan functionalized hairy nanoparticles (HNPs) with a hard polystyrene (PS) core and soft polydimethylsiloxane (PDMS) hairs via a one-pot approach. The synthesis was carried out by first preparing the living core through crosslinking styrene with divinylbenzene using sec-butyl lithium, followed by the addition of the hexamethylcyclotrisiloxane (D3) monomer to the living core. The living polymer was terminated by dimethylchlorosilane to obtain the HNPs with Si-H functional end groups. The furan functionalization was carried out by the hydrosilylation reaction between the Si-H of the functionalized HNP and 2-vinyl furan. Additionally, furan functionalized polystyrene (PS) and polydimethylsiloxane (PDMS) were also synthesized by LAP. 1H NMR and ATR-IR spectra confirmed the successful synthesis of the target polymers. Differential scanning calorimetry showed two glass transition temperatures indicative of a polydimethylsiloxane soft phase and a polystyrene hard phase, suggesting that the HNPs are microphase separated. The furan functionalized HNPs form thermo-reversible networks upon crosslinking with bismaleimide (BMI) via a Diels−Alder coupling reaction. The kinetics of the forward Diels–Alder reaction between the functionalized polymer and BMI were studied at three different temperatures: 50 °C, 60 °C, and 70 °C by UV–Vis spectroscopy. The activation energy for the furan functionalized HNPs reaction with the bismaleimide was lower compared to the furan functionalized polystyrene and polydimethylsiloxane linear polymers. The crosslinked polymer network formed from the Diels−Alder forward reaction dissociates at around 140–154 °C, and the HNPs are recovered. The recovered HNPs can be re-crosslinked at 50 °C. The results suggest that furan functionalized HNPs are promising building blocks for preparing thermo-reversible elastomeric networks. [ABSTRACT FROM AUTHOR]
– Name: AbstractSuppliedCopyright
  Label:
  Group: Ab
  Data: <i>Copyright of Polymers (20734360) is the property of MDPI and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
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      – Type: doi
        Value: 10.3390/polym16223117
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      – Code: eng
        Text: English
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        PageCount: 15
        StartPage: 3117
    Subjects:
      – SubjectFull: Linear polymers
        Type: general
      – SubjectFull: Coupling reactions (Chemistry)
        Type: general
      – SubjectFull: Thermoplastic elastomers
        Type: general
      – SubjectFull: Glass transition temperature
        Type: general
      – SubjectFull: Addition polymerization
        Type: general
      – SubjectFull: Crosslinked polymers
        Type: general
      – SubjectFull: Polymer networks
        Type: general
    Titles:
      – TitleFull: Recyclable Thermoplastic Elastomer from Furan Functionalized Hairy Nanoparticles with Polystyrene Core and Polydimethylsiloxane Hairs.
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            NameFull: Uddin, Md Hanif
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              Text: Nov2024
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              Y: 2024
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