A new strategy to synthesize degradable polystyrene of ultra-high molecular weight

Jianhan Li; Hongjun Yang; Qimin Jiang; Jiang Li; Bibiao Jiang; Xiaoqiang Xue; Sridhar Komarneni; Wenyan Huang

doi:10.1039/d4cc05166a

journal article Open Access Jan 01, 2025

A new strategy to synthesize degradable polystyrene of ultra-high molecular weight

Jianhan Li Hongjun Yang

Qimin Jiang

Jiang Li

Bibiao Jiang

Xiaoqiang Xue Sridhar Komarneni

Wenyan Huang

Chemical Communications Vol. 61 No. 18 pp. 3692-3695 · Royal Society of Chemistry (RSC)

View at Publisher Save 10.1039/d4cc05166a

Abstract

Degradation or recycling of styrene-copolymers whose main chains are saturated carbon chains is very difficult under natural conditions.

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References

37

[1]

Khuong J. Am. Chem. Soc. (2005) 10.1021/ja0448667

[2]

Jiang Polym. Int. (2001) 10.1002/1097-0126(200101)50:1<63::aid-pi561>3.0.co;2-l

[3]

Wu Acta Polymerica Sinica (2001)

[4]

Yang Chem. J. Chin. Univ. (1993)

[5]

A metal-free method for ultra-high molecular weight polyacrylonitrile under dimethyl sulfoxide

Guanchun Rui, Qiang Lv, Tianyu Wu et al.

Polymer 2021 10.1016/j.polymer.2020.123245

[6]

Con Microelectron. Eng. (2012) 10.1016/j.mee.2012.07.005

[7]

Banerjee Macromol. Chem. Phys. (2014) 10.1002/macp.201300741

[8]

Ciftci ACS Macro Lett. (2016) 10.1021/acsmacrolett.6b00460

[9]

Hyun Kim RSC Adv. (2017) 10.1039/c6ra25848d

[10]

Gutiérrez Process Saf. Environ. Prot. (2016) 10.1016/j.psep.2015.12.004

[11]

Abdel-Hakim Polym. Test. (2021) 10.1016/j.polymertesting.2021.107215

[12]

Oh J. Am. Chem. Soc. (2022) 10.1021/jacs.2c01411

[13]

Lu e-Polym. (2021) 10.1515/epoly-2021-0037

[14]

Pfäffli Scand. J. Work, Environ. Health (1978) 10.5271/sjweh.2744

[15]

Dement’ev J. Anal. Appl. Pyrolysis (2019) 10.1016/j.jaap.2019.05.001

[16]

Ho Crit. Rev. Biotechnol. (2018) 10.1080/07388551.2017.1355293

[17]

Wang Sci. Total Environ. (2024) 10.1016/j.scitotenv.2024.172243

[18]

Carter Macromolecules (2023) 10.1021/acs.macromol.3c00571

[19]

Li Angew. Chem., Int. Ed. (2024)

[20]

Delplace Nat. Chem. (2015) 10.1038/nchem.2343

[21]

Tardy Chem. Rev. (2017) 10.1021/acs.chemrev.6b00319

[22]

50th Anniversary Perspective: There Is a Great Future in Sustainable Polymers

Deborah K. Schneiderman, Marc A. Hillmyer

Macromolecules 2017 10.1021/acs.macromol.7b00293

[23]

Beckerab Chem. Soc. Rev. (2018) 10.1039/c8cs00531a

[24]

Tardy Angew. Chem., Int. Ed. (2017) 10.1002/anie.201707043

[25]

Pesenti ACS Macro Lett. (2020) 10.1021/acsmacrolett.0c00676

[26]

Jackson Polym. Chem. (2020) 10.1039/d0py00446d

[27]

Wickel Macromolecules (2003) 10.1021/ma034551w

[28]

Jackson Materials (2020) 10.3390/ma13102325

[29]

Gil Macromolecules (2022) 10.1021/acs.macromol.2c00651

[30]

Kiel J. Am. Chem. Soc. (2022) 10.1021/jacs.2c05374

[31]

Zhang J. Am. Chem. Soc. (2022) 10.1021/jacs.1c10359

[32]

Zhang Matter (2021) 10.1016/j.matt.2021.01.014

[33]

Albanese ACS Macro Lett. (2023) 10.1021/acsmacrolett.3c00204

[34]

Choi Adv. Funct. Mater. (2022)

[35]

Lipoates as building blocks of sulfur-containing branched macromolecules

Houliang Tang, Nicolay V. Tsarevsky

Polymer Chemistry 2015 10.1039/c5py01005e

[36]

Zhang Sci. Adv. (2018) 10.1126/sciadv.aat8192

[37]

Deng Angew. Chem., Int. Ed. (2020) 10.1002/anie.201913893

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Details

Published: Jan 01, 2025
Vol/Issue: 61(18)
Pages: 3692-3695
License: View

Authors

J

Jianhan Li