Synthesis of Fe(III)-IIPs (Ion Imprinted Polymers): Comparing Different Concentrations of HCl and HNO3 Solutions in the Fe(III) Polymer Extraction Process for Obtaining the Largest Cavities in Fe(III)-IIPs

Q2 Pharmacology, Toxicology and Pharmaceutics
Novianty Novianty, J. Edianta, Jorena Jorena, Khairul Saleh, A. Bama, E. Koriyanti, M. Ariani, I. Royani
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Abstract

This study was conducted to synthesize Fe (III)-IIPs by free radical polymerization using the cooling-heating method. Cooling processat -5◦C for 1 hour, as well as heating at 75◦C, 80◦C, and 85◦C maintained for 3 hours, 2 hours and 1 hour, respectively. The Fe (III)-IIPs synthesis process involved Fe(NO3)3 with an average diameter of 18.23 nm, methacrylic acid (MAA), ethylene glycol dimethacrylate (EGDMA), benzoyl peroxide (BPO) and ethanol, each of which plays a role as an analyte, functional monomer, cross-linker, initiator, and porogen. The result of the polymerization process was a polymer containing ions namely Fe(III) polymer. The ions need to be removed by the extraction process to produce Fe(III)-IIPs, which act as absorbents. Furthermore, the extraction process is very influential in the process of losing ions and the formation of cavities or templates in the polymer body. The number of cavities formed tends to affect the ability of Fe(III)-IIPs to identify the target ion which has similar physical and chemical properties to the shape of the Fe(III)-IIPs cavity. The extraction process was carried out on Fe(III) polymer samples using HCl and HNO3 solutions with varying concentrations of 3 M and 6 M, respectively. The transmission percentage of FTIR analysis showed that for samples of Fe(III)-IIPs HCl 3 M and 6 M were 94.258% and 95.666%, while for Fe(III)-IIPs HNO3 3 M and 6 M were 92.735%, respectively. The largest percentage was shown in the 6 M HCl IIPs sample, which indicated that there were several ions lost from the polymer body after the extraction process. This is also reinforced by the results of the SEM analysis processed with Matlab, which showed 498 cavities with a distribution of voids on a scale of <100 nm, totaling 470.
Fe(III)-IIPs(离子印迹聚合物)的合成:比较不同浓度HCl和HNO3溶液在Fe(III)聚合物萃取过程中获得的最大空腔
本研究采用冷却-加热的自由基聚合方法合成了Fe(III)-IIPs。冷却过程at-5◦在摄氏度下加热1小时,并在75度下加热◦C、 80◦C、 和85◦C分别维持3小时、2小时和1小时。Fe(III)-IIPs的合成过程涉及平均直径为18.23nm的Fe(NO3)3、甲基丙烯酸(MAA)、二甲基丙烯酸乙二醇酯(EGDMA)、过氧化苯甲酰(BPO)和乙醇,它们各自起着分析物、功能单体、交联剂、引发剂和成孔剂的作用。聚合过程的结果是含有离子的聚合物,即Fe(III)聚合物。离子需要通过萃取过程去除,才能产生Fe(III)-IIP,它起到吸收剂的作用。此外,萃取过程在聚合物主体中离子损失和空腔或模板形成的过程中非常有影响。形成的空腔的数量往往会影响Fe(III)-IIP识别目标离子的能力,该目标离子具有与Fe(Ⅲ)-IIP空腔形状相似的物理和化学性质。提取过程分别使用浓度为3M和6M的HCl和HNO3溶液对Fe(III)聚合物样品进行。FTIR分析的透射比表明,Fe(III)-IIPs样品的HCl 3M和6M分别为94.258%和95.666%,而Fe(III。在6M HCl IIPs样品中显示了最大的百分比,这表明在提取过程后,聚合物主体中损失了几个离子。用Matlab处理的SEM分析结果也加强了这一点,该结果显示498个空腔的空隙分布在<100nm的范围内,总计470个。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Science and Technology Indonesia
Science and Technology Indonesia Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
CiteScore
1.80
自引率
0.00%
发文量
72
审稿时长
8 weeks
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