Ecofriendly Multifunctional Monodisperse Spherical Polymer Colloids from Hyperbranched Poly(p-phenyl ester) Phenol AITranslate
Abstract AITranslate
Multifunctional, monodisperse, and hyperbranched poly(p-phenyl ester) phenol (HPPEP) colloids are prepared using commercially available inexpensive monomers (i.e., terephthaloyl chloride (A2) and phloroglucinol (B3)) via a simple condensation polymerization reaction (A2 + B3) at room temperature. Because of their symmetrical, rigid, highly branched, and cross-linked structure and the presence of the terminal phenolic units, the formation of highly monodisperse HPPEP colloids (coefficient of variation < 1.6%) can be realized under trimethylamine base conditions without any emulsifier (or surfactants) and expensive catalyst. Owing to their rigid aromatic and cross-linked structure, the HPPEP colloids exhibit excellent thermal, chemical, and mechanical resistances. Furthermore, the phenolic surface groups of HPPEP colloids enable the generation of highly negative surface charges (−60 mV) and catalytic protons (0.26 mmol H+/g) while enhancing surface functionality by chemically binding to red, green, and blue fluorescent dye molecules. Through carbonization, HPPEP colloids can be directly transformed into monodisperse porous carbon spheres with a large surface area (as,BET = 644.99 m2 g–1). Moreover, the HPPEP colloids can fully decompose into environmentally benign monomers after being exposed to an alkali environment.
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DOI:https://doi.org/10.1021/acsapm.2c00098
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Multifunctional, monodisperse, and hyperbranched poly(p-phenyl ester) phenol (HPPEP) colloids are prepared using commercially available inexpensive monomers (i.e., terephthaloyl chloride (A2) and phloroglucinol (B3)) via a simple condensation polymerization reaction (A2 + B3) at room temperature. Because of their symmetrical, rigid, highly branched, and cross-linked structure and the presence of the terminal phenolic units, the formation of highly monodisperse HPPEP colloids (coefficient of variation < 1.6%) can be realized under trimethylamine base conditions without any emulsifier (or surfactants) and expensive catalyst. Owing to their rigid aromatic and cross-linked structure, the HPPEP colloids exhibit excellent thermal, chemical, and mechanical resistances. Furthermore, the phenolic surface groups of HPPEP colloids enable the generation of highly negative surface charges (−60 mV) and catalytic protons (0.26 mmol H+/g) while enhancing surface functionality by chemically binding to red, green, and blue fluorescent dye molecules. Through carbonization, HPPEP colloids can be directly transformed into monodisperse porous carbon spheres with a large surface area (as,BET = 644.99 m2 g–1). Moreover, the HPPEP colloids can fully decompose into environmentally benign monomers after being exposed to an alkali environment.
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| GB/T 7714-2015 | [1] Yeshin Lee, HyeIn Jung, YeonIm Jang, et al. ACS Applied Polymer Materials, 2022(4). DOI:10.1021/acsapm.2c00098. |
| MLA | [1] Yeshin Lee, et al., ACS Applied Polymer Materials, no. 4, 2022, https://doi.org/10.1021/acsapm.2c00098. |
| APA | [1] Yeshin Lee, HyeIn Jung, YeonIm Jang, & ByeongKwan An. (2022). ACS Applied Polymer Materials(4). https://doi.org/10.1021/acsapm.2c00098 |
| IEEE | [1] Yeshin Lee, HyeIn Jung, YeonIm Jang, and ByeongKwan An, ACS Applied Polymer Materials, no. 4, 2022, doi: 10.1021/acsapm.2c00098. keywords: {polymer colloid;ecofriendly;monodisperse;surfactantfree;porous carbon sphere} |
