Iskalieva Asylzat, Yesmurat Mateyev, Al Azzam Khaldun M, Ainakulova Dana, Yerbolat Yerzhanov, Negim El-Sayed, Ibrahim Mohamad Nasir Mohamad, Gulzhakhan Yeligbayeva
School of Chemical Engineering, Kazakh-British Technical University, Str. Tole bi, 59, Almaty 050000, Kazakhstan.
«LF COMPANY» LLP, Zhambyl Region, Village Named after B. Momyshuly, Zhibek Zholy Str., 3b, Almaty 080300, Kazakhstan.
Polymers (Basel). 2023 Jul 26;15(15):3165. doi: 10.3390/polym15153165.
Blend copolymers (PVA/S) were grafted with polyethylene glycol methyl methacrylate (PEGMA) with different ratios. Potassium persulfate was used as an initiator. The blend copolymer (PVA/S) was created by combining poly(vinyl alcohol) (PVA) with starch (S) in various ratios. The main idea was to study the effect of different ratios of the used raw materials on the biodegradability of plastic films. The resulting polymers (PVA/S/PEGMA) were analyzed using FTIR spectroscopy to investigate the hydrogen bond interaction between PVA, S, and PEGMA in the mixtures. TGA and SEM analyses were used to characterize the polymers (PVA/S/AA). The biodegradability and mechanical properties of the PVA/S/PEGMA blend films were evaluated. The findings revealed that the mechanical properties of the blend films are highly influenced by PEGMA. The time of degradation of the films immersed in soil and Coca-Cola increases as the contents of PVA and S and the molecular weight (MW) of PEGMA increase in the terpolymer. The M8 sample (PVA/S/PEGMA in the ratio of 3:1:2, respectively) with a MW of 950 g/mol produced the lowest elongation at break (67.5%), whereas M1 (PVA/S/PEGMA in the ratio of 1:1:1, respectively) with a MW of 300 g/mol produced the most (150%). The film's tensile strength and elongation at break were improved by grafting PEGMA onto the blending polymer (PAV-b-S). and increased when the PEGMA MW increased from 300 to 950. (48.4 °C) and (190.9 °C) were the lowest in M1 (300), while (84.8 °C) and (190.9 °C) were greatest in M1 (950) at 209.3 °C. The increased chain and molecular weight of PEGMA account for the increase in and of the copolymers.
将不同比例的聚乙二醇甲基丙烯酸甲酯(PEGMA)接枝到共混聚合物(PVA/S)上。以过硫酸钾作为引发剂。共混聚合物(PVA/S)是通过将聚乙烯醇(PVA)与淀粉(S)按不同比例混合而成。主要目的是研究所用原材料的不同比例对塑料薄膜生物降解性的影响。使用傅里叶变换红外光谱(FTIR)对所得聚合物(PVA/S/PEGMA)进行分析,以研究混合物中PVA、S和PEGMA之间的氢键相互作用。热重分析(TGA)和扫描电子显微镜(SEM)分析用于表征聚合物(PVA/S/AA)。对PVA/S/PEGMA共混薄膜的生物降解性和机械性能进行了评估。研究结果表明,共混薄膜的机械性能受PEGMA的影响很大。随着三元共聚物中PVA和S的含量以及PEGMA分子量(MW)的增加,浸泡在土壤和可乐中的薄膜的降解时间增加。分子量为950 g/mol的M8样品(PVA/S/PEGMA比例分别为3:1:2)的断裂伸长率最低(67.5%),而分子量为300 g/mol的M1样品(PVA/S/PEGMA比例分别为1:1:1)的断裂伸长率最高(150%)。通过将PEGMA接枝到共混聚合物(PAV-b-S)上,薄膜的拉伸强度和断裂伸长率得到了提高。当PEGMA分子量从300增加到950时,拉伸强度和断裂伸长率增加。在209.3℃时,M1(300)的起始分解温度(48.4℃)和最大分解温度(190.9℃)最低,而M1(950)的起始分解温度(84.8℃)和最大分解温度(190.9℃)最高。PEGMA链和分子量的增加导致了共聚物起始分解温度和最大分解温度的升高。