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Biowaste chicken eggshell powder as a potential cure modifier for epoxy/anhydride systems: competitiveness with terpolymer-modified calcium carbonate at low loading levels

机译:生物废物鸡蛋壳粉可作为环氧/酸酐体系的潜在固化改性剂:在低负载量下与三元共聚物改性的碳酸钙具有竞争力

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Biowaste chicken eggshell (ES) powder was applied as a potential cure modifier in epoxy/anhydride systems. Cure behaviour and kinetics of composites filled with very low content (0.1 wt% based on epoxy resin) of ES, calcium carbonate (CaCO3), and terpolymer-modified fillers, mES and mCaCO3, were discussed comparatively. Surface analysis was performed by X-ray photoelectron spectroscopy. Cure kinetics was investigated by differential (Friedman) and integral (Ozawa and Kissinger–Akahira–Sunose) isoconversional methods using dynamic differential scanning calorimetry (DSC) data. Overall, protein precursors naturally existing in the structure of pristine ES facilitated crosslinking of epoxy and hardener of anhydride with functional groups resulting from terpolymer attachment to CaCO3 particles. Accelerated/hindered cure was observed depending on the filler type and surface characteristics, as investigated via the autocatalyticon-catalytic nature of reactions and comparison of activation energy values of four types of composites. An enhanced cure was identified for composites containing untreated ES, which could be inferred on account of the lower competitive cure of carboxyl groups in the terpolymer backbone with epoxy compared to peptide groups existing in microporous pristine ES. On the other hand, mCaCO3 revealed low values of activation energy compared to pristine CaCO3, but still of the same order as ground biowaste ES.
机译:Biowaste鸡蛋壳(ES)粉末被用作环氧/酸酐体系中潜在的固化改性剂。填充极低含量(基于环氧树脂的0.1 wt%)的ES,碳酸钙(CaCO 3 )和三元共聚物改性填料的复合材料的固化行为和动力学,对mES和mCaCO 3 进行了比较讨论。表面分析通过X射线光电子能谱进行。使用动态差示扫描量热法(DSC)数据,通过微分(Friedman)和积分(Ozawa和Kissinger–Akahira–Sunose)等转换方法研究了固化动力学。总体而言,天然存在于原始ES结构中的蛋白质前体可促进三元共聚物与CaCO 3 颗粒的附着,从而使环氧树脂和酸酐的固化剂具有官能团。通过 反应的自催化/非催化性质以及四种类型复合材料的活化能值的比较,观察到加速/受阻的固化取决于填料的类型和表面特性。对于含有未处理ES的复合材料,已确定了增强的固化性,这可以归因于与微孔原始ES中存在的肽基相比,三元共聚物主链中羧基与环氧的竞争性固化性较低。另一方面,与原始CaCO 3 相比,mCaCO 3 的活化能值较低,但仍为与地面生物废物ES的顺序相同。

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