化学
过氧化氢
天然橡胶
甲酸
甲醛
试剂
热稳定性
亚硝酸钠
傅里叶变换红外光谱
过氧化物
核化学
高分子化学
活化能
有机化学
化学工程
工程类
作者
Kraiwut Wisetkhamsai,Weerawat Patthaveekongka,Wanvimon Arayapranee
出处
期刊:Polymers
[MDPI AG]
日期:2023-02-19
卷期号:15 (4): 1031-1031
被引量:7
标识
DOI:10.3390/polym15041031
摘要
Liquid natural rubber (LNR), a depolymerized natural rubber (NR) consisting of shorter chains, was prepared via oxidative degradation using NaNO2 and H2O2 degrading agents in the presence of HCOOH. The influence of reagent concentrations, temperature, and reaction time on the number-average molecular weight (Mn) was studied. Results showed the higher concentration of H2O2 and HCOOH employed faster degradative rates. However, a higher concentration of NaNO2 decreased the Mn reduction. Prolonged reaction time and high temperature resulted in a product with low Mn. FTIR spectra indicated the synthesized LNR contained hydroxyl end groups resulting from the breaking of the NR chains at an acidic pH, whereas a carboxyl terminated LNR was formed at an alkaline pH. SEM micrographs showed the latex particles of LNR were spherical and smaller compared to NR. The experimental results showed the reaction orders of [H2O2], [HCOOH], and [NaNO2] were 1.58, 0.79, and −0.65, respectively. In addition, the pre-exponential factor and activation energy were 1.04 × 109 M−1.72 t−1 and 78.66 kJ/mol, respectively. Based on TGA analysis, the thermal stability of the rubber depended on its Mn. The LNR containing functional end groups exhibited thermal instability and could be a starting material for many applications.
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