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用于大幅面增材制造的光聚合物配方中的光引发剂选择与浓度

Photoinitiator Selection and Concentration in Photopolymer Formulations towards Large-Format Additive Manufacturing.

作者信息

Stiles Alex, Tison Thomas-Allan, Pruitt Liam, Vaidya Uday

机构信息

Bredesen Center for Interdisciplinary Research, University of Tennessee, Middle Drive, Knoxville, TN 37996, USA.

Tickle College of Engineering, University of Tennessee, Middle Drive, Knoxville, TN 37996, USA.

出版信息

Polymers (Basel). 2022 Jul 1;14(13):2708. doi: 10.3390/polym14132708.

Abstract

Photopolymers are an attractive option for large-format additive manufacturing (LFAM), because they can be formulated from structural thermosets and cure rapidly in ambient conditions under low-energy ultraviolet light-emitting diode (UV LED) lamps. Photopolymer cure is strongly influenced by the depth penetration of UV light, which can be limited in the 2-4 mm layer thicknesses typical of LFAM. Photoinitiator (PI) systems that exhibit photobleaching have proven useful in thick-section cure applications, because they generate a photoinitiation wavefront, but this effect is time-dependent. This study investigates the light transmission and through-thickness cure behavior in (meth)acrylate photopolymer formulations with the photobleaching initiator bis(2,4,6-trimethylbenzoyl)-phenylphosphine oxide (BAPO). Utilizing an optical model developed by Kenning et al., lower concentrations (0.1 wt% to 0.5 wt%) of BAPO were predicted to yield rapid onset of photoinitiation. In situ cure measurements under continuous UV LED irradiation of 380 mW/cm showed that a 0.1 wt% concentration of BAPO achieved peak polymerization rate within 2.5 s at a 3-mm depth. With only 1 s of irradiation at 1.7 W/cm intensity, the 0.1 wt% BAPO formulation also achieved the highest level of cure of the formulas tested. For an irradiation dose of 5.5 J/cm at a duration of 3.7 s, cured polymer specimens achieved a flexural strength of 108 MPa and a flexural modulus of 3.1 GPa. This study demonstrates the utility of optical modeling as a potential screening tool for new photopolymer formulations, primarily in identifying an upper limit to PI concentration for the desired cure depth. The results also show that photobleaching provides only a limited benefit for LFAM applications with short (1.0 s to 3.7 s) UV irradiation times and indicate that excess PI concentration can inhibit light transmission even under extended irradiation times up to 60 s.

摘要

光聚合物是大幅面增材制造(LFAM)的一个有吸引力的选择,因为它们可以由结构热固体制备而成,并在低能量紫外发光二极管(UV LED)灯的环境条件下快速固化。光聚合物的固化受到紫外光深度穿透的强烈影响,在LFAM典型的2-4毫米层厚中,这种穿透可能会受到限制。已证明表现出光漂白的光引发剂(PI)体系在厚截面固化应用中很有用,因为它们会产生光引发波前,但这种效应是随时间变化的。本研究调查了含有光漂白引发剂双(2,4,6-三甲基苯甲酰基)-苯基氧化膦(BAPO)的(甲基)丙烯酸酯光聚合物配方中的光传输和全厚度固化行为。利用肯宁等人开发的光学模型,预测较低浓度(0.1 wt%至0.5 wt%)的BAPO会使光引发迅速开始。在380 mW/cm的连续UV LED照射下进行的原位固化测量表明,0.1 wt%浓度的BAPO在3毫米深度处2.5秒内达到峰值聚合速率。在1.7 W/cm强度下仅照射1秒,0.1 wt% BAPO配方也达到了所测试配方的最高固化水平。对于持续3.7秒、照射剂量为5.5 J/cm的情况,固化的聚合物试样达到了108 MPa的弯曲强度和3.1 GPa的弯曲模量。本研究证明了光学建模作为新光聚合物配方潜在筛选工具的实用性,主要用于确定所需固化深度的PI浓度上限。结果还表明,对于紫外线照射时间较短(1.0秒至3.7秒)的LFAM应用,光漂白仅提供有限的益处,并表明即使在长达60秒的延长照射时间下,过量的PI浓度也会抑制光传输。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ecd/9268840/d9a05d5c2d7f/polymers-14-02708-g001.jpg

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