贻贝表面改性与阴离子开环聚合相结合制备高效去除刚果红的SiO2复合材料

Jinjiu Zhu , Ke Wang , Shuhui Fan , Aoxing Ouyang , Jiawei Gu , Jianwen Tian , Meiying Liu , Fengjie Deng , Xiaoyong Zhang , Yen Wei
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引用次数: 0

摘要

二氧化硅纳米颗粒由于其易于合成、可调节的形态特征和可定制的表面化学特性而成为废水修复的有希望的候选者。这些特点使各种水生污染物的有效隔离。原始二氧化硅纳米颗粒的吸附能力往往表现出较低的效率,主要是由于缺乏有效的分子结合相互作用所必需的靶向功能部分。本研究采用2,3-环氧丙基三甲基氯化铵(PTAC)作为功能单体来设计二氧化硅纳米结构,通过贻贝启发化学和可控阴离子聚合的协同整合,引入了一种创新的纳米颗粒表面工程方法。合成的SiO2复合材料(称为SiO2- pda - ptac)的结构和形态性能通过各种技术得到了证实。进行了大量的实验室研究,以评估合成材料对刚果红(CR)的吸附能力。结果表明,SiO2-PDA-PTAC复合物的吸附能力显著提高,其中SiO2-PDA-PTAC复合物的最大吸附能力为131.30 mg/g,约为未改性二氧化硅(32.48 mg/g)的四倍。热力学分析证实了吸附过程的自发性质,其特征是正熵变和吸热行为。实验数据与建立的理论模型具有良好的相关性,拟二级动力学(R2 = 0.9918)和Langmuir等温线(R2 = 0.9993)均具有较高的回归系数。在SiO2-PDA-PTAC与CR之间的各种相互作用中,静电相互作用在吸附过程中起着关键作用。通过连续的再生循环,SiO2-PDA-PTAC保持了可观的吸附效率,在实际应用中表现出优异的可重复使用性和稳定性,突出了其在废水处理中的实际应用潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preparation of SiO2 composites for efficient removal of Congo red via the combination of mussel-inspired surface modification and anionic ring-opening polymerization
SiO2 nanoparticles have emerged as promising candidates for wastewater remediation due to their facile synthesis, tunable morphological characteristics, and customizable surface chemistry. These features enable effective sequestration of various aquatic contaminants. The adsorption capability of pristine silica nanoparticles frequently demonstrates poor efficiency, primarily due to the absence of targeted functional moieties essential for effective molecular binding interactions. This research introduces an innovative approach for nanoparticle surface engineering through the synergistic integration of mussel-inspired chemistry and controlled anionic polymerization, employing 2,3-epoxypropyltrimethylammonium chloride (PTAC) as the functional monomer to engineer silica nanostructures. The structural and morphological properties of resultant SiO2 composites (designated as SiO2-PDA-PTAC) were confirmed by various techniques. Quantities of laboratory investigations were conducted to assess the adsorption capacity of Congo red (CR) of the synthesized materials. The findings demonstrated a remarkable improvement in adsorption capability, where SiO2-PDA-PTAC hybrid achieved a maximum capacity of 131.30 mg/g—approximately four times higher than that of unmodified silica (32.48 mg/g). Thermodynamic analysis confirmed the spontaneous nature of the adsorption process, characterized by positive entropy changes and endothermic behavior. The experimental data exhibited excellent correlation with established theoretical models, showing high regression coefficients for both pseudo-second-order kinetics (R2 = 0.9918) and Langmuir isotherm (R2 = 0.9993). Among various interactions between SiO2-PDA-PTAC and CR, electrostatic interaction played critical roles in adsorption process. SiO2-PDA-PTAC maintained substantial adsorption efficiency through successive regeneration cycles, demonstrating excellent reusability and stability in practical applications, highlighting their potential for practical applications in wastewater treatment.
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