Non-Destructive Infrared Thermographic Curing Analysis of Polymer Composites

M. Rahman, Javier Becerril, Dipannita Ghosh, Nazmul Islam, A. Ashraf
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Abstract

Infrared (IR) thermography is a non-contact method of measuring temperature that analyzes the infrared radiation emitted by an object. Properties of polymer composites are heavily influenced by the filler material, filler size, and filler dispersion, and thus thermographic analysis can be a useful tool to determine the curing and filler dispersion. In this study, we investigated the curing mechanisms of polymer composites at the microscale by capturing real-time temperature using an IR Thermal Camera. Silicone polymers with fillers of Graphene, Graphite powder, Graphite flake, and Molybdenum disulfide (MoS2) were subsequently poured into a customized 3D printed mold for thermography. The nanocomposites were microscopically heated with a Nichrome resistance wire, and real-time surface temperatures were measured using different Softwares. This infrared thermal camera divides the target area into 640 × 480 pixels, allowing measurement and analysis of the sample with a resolution of 65 micrometers. Depending on the filler material, the temperature rises to a certain maximum point before curing, and once curing is complete, polymer composites exhibit a rapid temperature change indicating a transition from viscous fluid to solid. MoS2, Polydimethylsiloxane (PDMS) without filler, and PDMS with larger filler are ranked in order of maximum constant temperature. PDMS (without filler) cures in 500s, while PDMS-Graphene and PDMS Graphite Powder cure in about 800s. The curing time for PDMS Graphite flake is slightly longer (950s), while MoS2 is around 520s. Therefore, this technique can indicate the influence of fillers on the curing of composites at the microscale, which is difficult to achieve by conventional methods such as differential scanning calorimetry. This nondestructive, low-cost, fast infrared thermography can be used to analyze the properties of polymer composites with different fillers and dispersion qualities in a variety of applications including precision additive manufacturing and quality control of curable composite inks.
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聚合物复合材料的无损红外热成像固化分析
红外热像仪是一种非接触式测量温度的方法,它分析物体发出的红外辐射。聚合物复合材料的性能很大程度上受填料、填料尺寸和填料分散的影响,因此热成像分析可以作为确定固化和填料分散的有用工具。在这项研究中,我们利用红外热像仪实时捕捉温度,研究了聚合物复合材料在微观尺度下的固化机理。随后,将填充石墨烯、石墨粉、石墨片和二硫化钼(MoS2)的硅树脂聚合物倒入定制的3D打印模具中进行热成像。用镍铬合金电阻丝对纳米复合材料进行显微加热,并使用不同的软件实时测量表面温度。该红外热像仪将目标区域划分为640 × 480像素,允许以65微米的分辨率对样品进行测量和分析。根据填充材料的不同,在固化前温度会上升到某一最大值,一旦固化完成,聚合物复合材料就会出现快速的温度变化,表明从粘性流体到固体的转变。二硫化钼、无填料的聚二甲基硅氧烷(PDMS)和填料较多的聚二甲基硅氧烷(PDMS)的最大恒温性能依次为:PDMS(无填料)在500秒内固化,而PDMS-石墨烯和PDMS石墨粉在800秒左右固化。PDMS石墨片的固化时间稍长(950s),而MoS2的固化时间在520s左右。因此,该技术可以在微观尺度上表明填料对复合材料固化的影响,这是差示扫描量热法等常规方法难以实现的。这种无损、低成本、快速的红外热成像技术可用于分析具有不同填料和分散质量的聚合物复合材料的性能,包括精密增材制造和可固化复合油墨的质量控制。
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