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用于立体光刻的银纳米复合材料的合成:纳米颗粒的原位形成

Synthesis of Silver Nanocomposites for Stereolithography: In Situ Formation of Nanoparticles.

作者信息

Valencia Luisa M, Herrera Miriam, de la Mata María, de León Alberto S, Delgado Francisco J, Molina Sergio I

机构信息

Departamento de Ciencia de los Materiales e Ingeniería Metalúrgica y Química Inorgánica, IMEYMAT, Facultad de Ciencias, Universidad de Cádiz, Campus Río San Pedro, s/n, Puerto Real, 11510 Cádiz, Spain.

出版信息

Polymers (Basel). 2022 Mar 15;14(6):1168. doi: 10.3390/polym14061168.

DOI:10.3390/polym14061168
PMID:35335499
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8948828/
Abstract

Additive Manufacturing (AM) offers remarkable advantages in relation to traditional methods used to obtain solid structures, such as the capability to obtain customized complex geometries adapted to individual requirements. The design of novel nanocomposites suitable for AM is an excellent strategy to widen the application field of these techniques. In this work, we report on the fabrication of metal/polymer nanocomposites with enhanced optical/electrical behaviour for stereolithography (SLA). In particular, we analyse the in situ generation of Ag nanoparticles (NPs) from Ag precursors (AgNO and AgClO) within acrylic resins via SLA. Transmission electron microscopy (TEM) analysis confirmed the formation of Ag NPs smaller than 5 nm in all nanocomposites, providing optical activity to the materials. A high density of Ag NPs with a good distribution through the material for the larger concentration of AgClO precursor tested was observed, in contrast to the isolated agglomerations found when the precursor amount was reduced to 0.1%. A significant reduction in the electrical resistivity up to four orders of magnitude was found for this material compared to the unfilled resin. However, consumption of part of the photoinitiator in the formation process of the Ag NPs contributed to a reduction in the polymerization degree of the resin and, consequently, degraded the mechanical properties of the nanocomposites. Experiments with longer curing times showed that, for the higher AgClO concentrations tested, post-curing times of 300 min allowed an 80% degree of polymerization to be achieved. These conditions turned these materials into promising candidates to obtain solid structures with multifunctional properties.

摘要

与用于制造实体结构的传统方法相比,增材制造(AM)具有显著优势,例如能够获得适应个体需求的定制复杂几何形状。设计适用于增材制造的新型纳米复合材料是拓宽这些技术应用领域的绝佳策略。在这项工作中,我们报道了用于立体光刻(SLA)的具有增强光学/电学性能的金属/聚合物纳米复合材料的制备。具体而言,我们分析了通过SLA在丙烯酸树脂中由银前驱体(AgNO₃和AgClO₄)原位生成银纳米颗粒(NPs)的过程。透射电子显微镜(TEM)分析证实,所有纳米复合材料中均形成了尺寸小于5nm的银纳米颗粒,赋予了材料光学活性。对于测试的较高浓度的AgClO₄前驱体,观察到材料中分布良好的高密度银纳米颗粒,而当前驱体用量降至0.1%时,则发现孤立的团聚体。与未填充的树脂相比,这种材料的电阻率显著降低了多达四个数量级。然而,在银纳米颗粒形成过程中部分光引发剂的消耗导致树脂聚合度降低,从而降低了纳米复合材料的机械性能。较长固化时间的实验表明,对于测试的较高AgClO₄浓度,300分钟的后固化时间可实现80%的聚合度。这些条件使这些材料成为获得具有多功能特性的实体结构的有前途的候选材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9ed/8948828/1609920057d7/polymers-14-01168-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9ed/8948828/de5af61a101e/polymers-14-01168-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9ed/8948828/cb53fedb1c34/polymers-14-01168-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9ed/8948828/eb63b12a0beb/polymers-14-01168-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9ed/8948828/a8f31796648f/polymers-14-01168-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9ed/8948828/83da6ffd08ea/polymers-14-01168-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9ed/8948828/d872f8c16631/polymers-14-01168-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9ed/8948828/1609920057d7/polymers-14-01168-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9ed/8948828/de5af61a101e/polymers-14-01168-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9ed/8948828/cb53fedb1c34/polymers-14-01168-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9ed/8948828/eb63b12a0beb/polymers-14-01168-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9ed/8948828/a8f31796648f/polymers-14-01168-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9ed/8948828/83da6ffd08ea/polymers-14-01168-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9ed/8948828/d872f8c16631/polymers-14-01168-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9ed/8948828/1609920057d7/polymers-14-01168-g007.jpg

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