Gamma Irradiation-Based Free Radical Grafting of N-Hydroxyethyl Acrylamide onto Poly[(R)-3-hydroxybutyrate].

IF 4.1 3区 化学 Q2 POLYMER SCIENCE
Cole Walchle, Céline Chaléat, Paul Lant, Bronwyn Laycock, Steven Pratt, Samuel Lawless
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引用次数: 0

Abstract

This work demonstrates successful grafting of N-hydroxyethyl acrylamide (HEAA) onto poly[(R)-3-hydroxybutyrate] (P[(R)-3HB]), up to 156 wt.% using 60Co gamma irradiation (10.1 kGy) and a 1:4 P[(R)-3HB]:HEAA molar ratio in ethyl acetate. The resulting N-hydroxyethyl acrylamide-grafted poly[(R)-3-hydroxybutyrate] (P3HB-HEAA) was comprehensively characterized using FTIR, NMR, SEM, DSC, TGA/DTG, tensile testing, and water uptake, and exhibited striking property changes relative to the native polymer. The modified material showed a Tg of 124°C, reduced melting enthalpy (ΔHm = 12 J/g), increased Td,10 and Td,50 of 260°C and 340°C, respectively, increased elongation at break (ɛ = 65%), increased toughness (by 378%), exceptional water absorption capacity (610 wt.%), a markedly less ordered surface structure compared to the starting materials. These changes indicate formation of a less crystalline, highly hygroscopic, hydrogel-like system. HEAA grafting generated a biphasic architecture comprising a semicrystalline, structurally robust, P[(R)-3HB] backbone coupled with an amorphous, hydrogel-like HEAA surface layer, yielding a potentially biodegradable polymer with enhanced hydration capacity. The structure retains structural integrity while enabling substantial water uptake properties not accessible with either component alone. Combining mechanical strength with tuneable hydration behavior, HEAA-grafted P[(R)-3HB] expands the functional and commercial potential of P[(R)-3HB] into applications requiring simultaneous structural integrity, controlled swelling, and potential biocompatibility.

γ辐照自由基接枝n-羟乙基丙烯酰胺在聚[(R)-3-羟基丁酸盐]上的研究。
这项工作证明了n -羟乙基丙烯酰胺(HEAA)成功地接枝到聚[(R)-3-羟基丁酸盐](P[(R)-3HB])上,使用60Co伽马辐射(10.1 kGy)和1:4 P[(R)-3HB]:HEAA的摩尔比在乙酸乙酯中达到156 wt.%。通过FTIR、NMR、SEM、DSC、TGA/DTG、拉伸测试和吸水测试等手段对n -羟乙基丙烯酰胺接枝聚[(R)-3-羟基丁酸酯](P3HB-HEAA)进行了全面表征,结果表明,与天然聚合物相比,n -羟乙基丙烯酰胺接枝聚[(R)-3-羟基丁酸酯](P3HB-HEAA)的性能发生了显著变化。改性后的材料Tg为124℃,熔融焓降低(ΔHm = 12 J/g), Td分别在260℃和340℃时增加10和50,断裂伸长率增加(r = 65%),韧性增加(378%),吸水率增加(610 wt.%),表面结构明显不如初始材料有序。这些变化表明形成了一个较少结晶的、高度吸湿的、类似水凝胶的体系。HEAA接枝产生了一种双相结构,包括半结晶的、结构坚固的P[(R)-3HB]骨架与无定形的、类似水凝胶的HEAA表面层,产生了一种具有增强水化能力的潜在可生物降解聚合物。该结构保留了结构的完整性,同时具有单独使用任何一种组件都无法获得的大量吸水性能。结合机械强度和可调节的水化行为,heaa接枝的P[(R)-3HB]将P[(R)-3HB]的功能和商业潜力扩展到需要同时具有结构完整性、控制肿胀和潜在生物相容性的应用中。
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来源期刊
Macromolecular Rapid Communications
Macromolecular Rapid Communications 工程技术-高分子科学
CiteScore
7.70
自引率
6.50%
发文量
477
审稿时长
1.4 months
期刊介绍: Macromolecular Rapid Communications publishes original research in polymer science, ranging from chemistry and physics of polymers to polymers in materials science and life sciences.
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