Investigating the Multistep Polymerization Reactions of DCPD with Grubbs’ First-Generation Catalyst

IF 4.4 2区 化学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY
Başak Özeroğlu*,  and , Necati Özkan*, 
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引用次数: 0

Abstract

Self-healing polymer composites using Grubbs’ first-generation (G1) catalyst and dicyclopentadiene (DCPD) as the healing monomer are widely used in self-healing applications. In such systems, DCPD released from ruptured microcapsules reacts with dispersed G1, enabling healing without external intervention. This study simulates the local DCPD–G1 interaction at the crack site using Differential Scanning Calorimetry (DSC) analysis, imitating self-healing conditions. The polymerization reactions of the DCPD–G1 system were systematically investigated using DSC, Dynamic Mechanical Analysis (DMA), kinetic modeling, Fourier Transform Infrared (FT-IR), and nuclear magnetic resonance (1H NMR) spectroscopy. One of the main outcomes of this work is the identification of three separate exothermic transitions in the DSC analysis. These results indicate that the polymerization follows a multistep pathway, starting with ROMP to form linear polydicyclopentadiene (L-PDCPD) and proceeding with cross-linking via olefin addition and metathesis reactions. DMA analysis, performed within temperature intervals identified in deconvoluted DSC peaks, further clarifies that the first process involves linear polymerization, while the second and third processes are associated with cross-linking reactions. A slight increase in glass transition temperature (Tg) and shear storage modulus (G′) in the first-process interval indicates linear PDCPD growth via increased molecular weight (Mw) and chain entanglements. In contrast, a sharp increase in Tg and G′ in the sample that passed through the second-process interval and a distinct stiffness increase at the onset of the third process (∼82 °C) indicate two distinct curing mechanisms. These findings are further supported by FT-IR analysis through the monitoring of the peaks at 972, 726, and 754 cm–1. Kinetic modeling (Šesták–Berggren) closely matches experimental data, validating this multistep polymerization reaction. The findings can clearly show the multistep polymerization process for G1 – catalyzed DCPD.

用Grubbs第一代催化剂研究DCPD的多步聚合反应
以Grubbs第一代(G1)催化剂和二环戊二烯(DCPD)为修复单体的自修复聚合物复合材料广泛应用于自修复领域。在这种系统中,从破裂的微胶囊中释放的DCPD与分散的G1发生反应,无需外部干预即可实现愈合。本研究采用差示扫描量热法(DSC)模拟裂纹部位局部DCPD-G1相互作用,模拟自愈条件。采用DSC、动态力学分析(DMA)、动力学建模、傅里叶变换红外(FT-IR)和核磁共振(1H NMR)等方法对DCPD-G1体系的聚合反应进行了系统的研究。这项工作的主要成果之一是在DSC分析中确定了三个独立的放热转变。这些结果表明,聚合遵循一个多步骤的途径,从ROMP开始形成线性聚双环戊二烯(L-PDCPD),然后通过烯烃加成和复分解反应进行交联。在反卷积DSC峰中确定的温度区间内进行的DMA分析进一步阐明了第一个过程涉及线性聚合,而第二个和第三个过程与交联反应有关。玻璃化转变温度(Tg)和剪切储存模量(G’)在第一道工序期间的轻微增加表明,PDCPD通过分子量(Mw)和链缠结的增加而线性生长。相比之下,样品中Tg和G′的急剧增加以及第三个过程开始时(~ 82°C)的明显刚度增加表明了两种不同的固化机制。通过监测972、726和754 cm-1处的峰,FT-IR分析进一步支持了这些发现。动力学模型(Šesták-Berggren)与实验数据密切匹配,验证了这种多步聚合反应。研究结果清楚地显示了G1催化的DCPD的多步聚合过程。
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来源期刊
CiteScore
7.20
自引率
6.00%
发文量
810
期刊介绍: ACS Applied Polymer Materials is an interdisciplinary journal publishing original research covering all aspects of engineering, chemistry, physics, and biology relevant to applications of polymers. The journal is devoted to reports of new and original experimental and theoretical research of an applied nature that integrates fundamental knowledge in the areas of materials, engineering, physics, bioscience, polymer science and chemistry into important polymer applications. The journal is specifically interested in work that addresses relationships among structure, processing, morphology, chemistry, properties, and function as well as work that provide insights into mechanisms critical to the performance of the polymer for applications.
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