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High Modulus and High Strength C/C-SiC Ceramic Matrix Composites by Fiber-Matrix Interface Tailoring via Modification of Fiber Surface and Matrix Precursor - Kerafam 2

High Modulus and High Strength C/C-SiC Ceramic Matrix Composites by Fiber-Matrix Interface Tailoring via Modification of Fiber Surface and Matrix Precursor - Kerafam 2
通过纤维表面和基体前驱体改性实现纤维基体界面定制的高模量和高强度 C/C-SiC 陶瓷基复合材料 - Kerafam 2
批准号:
277680365
负责人:
Professor Dr. Michael R. Buchmeiser
金额:
$0.0万
依托单位国家:
德国
项目类别:
Research Grants
财政年份:
2015
资助国家:
德国
项目状态:
已结题
起止时间:
2014-12-31 至 2022-12-31

项目摘要

项目成果

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中文摘要
翻译
基于先前KeraFaM项目中获得的知识,KeraFaM 2旨在使C/C- sic材料的机械性能更接近标准和高性能纤维的理论极限。到目前为止,获得了以下见解:•通过精确剪裁纤维-基质键合(FMB),可以实现在硅化过程中防止纤维转化的保护。这可以防止纤维基体分层(FMD),并有利于纤维束之间的分割裂纹(SC),从而产生由SiC基体分隔的致密C/C块。所得C/C- sic复合材料的力学性能低于理论极限。纤维性能利用率低的原因是C/C块结构有利于纤维束的拉出。•碳化后观察到的样品的裂纹结构的形成已经在树脂固化期间开始。•基体树脂的选择影响微观结构。树脂之间的本质区别是酚醛和溶剂含量。•项目中使用的超高模量(UHM)纤维由于其脆性,在退浆后无法进行加工。•不同fmb在热解过程中的微裂纹形成可以采用有限元法(FEM)进行建模。斯图加特DLR、登肯多夫DITF和奥格斯堡大学实验物理学主席的陶瓷复合材料和结构团队之间的合作在KeraFaM期间被证明是互补和有效的。基于这次成功的合作,KeraFaM 2将实现以下目标:•为了提高C/C模块的光纤利用率,打算进行子结构设计。这可以通过多层上浆来实现。这种尺寸是用来获得更明确的FMB剪裁,并保护纤维从转换。在第二种方法中,将产生微孔c -基质。这两个概念都倾向于单纤维拉拔而不是光纤束拉拔。•从树脂固化阶段开始进行交联反应分析、原位声发射分析和纳米ct检查,以了解微观结构的形成。这将最终导致更好地控制微观结构和得到的C/C- sic复合材料性能。•fe模型将通过考虑实验获得的材料参数来改进,以便真实地代表不同FMB值下的微观结构发展。所得到的模型将通过声发射分析和扫描电镜测量进行验证。•通过改变基体树脂中芳香族化合物的比例,评估基体树脂中酚类含量对炭化后残余碳质量、收缩率和微观结构的影响。•为了允许进一步加工并防止纤维转化为SiC, UHM纤维将通过在接收的浆料上施加额外的浆料来进行改性。
英文摘要
Based on the knowledge gained in the previous KeraFaM project, KeraFaM 2 aims to bring the mechanical properties of C/C-SiC materials closer to the theoretical limits expected from standard and high performance fibers.So far, the following insights were obtained:•Protection of the fibers against conversion during the siliconisation can be achieved by precise tailoring of the fiber-matrix-bonding (FMB). This prevents fiber-matrix-delamination (FMD) and favors segmentation cracks (SC) between fiber bundles, resulting in dense C/C-blocks separated by SiC matrix. Mechanical properties of the resulting C/C-SiC composites are below the theoretical limits. The low utilization rate of fiber properties is attributed to the C/C block structure favoring a fiber bundle pullout.•The formation of the crack structure of the samples observed after carbonization does already start during curing of the resin.•The choice of matrix resin influences the microstructure. The essential difference between the resins are the phenolic and solvent content.•The Ultra High Modulus (UHM) fibers used during the project could not be processed after desizing due to their brittleness.•The micro crack formation for different FMBs during pyrolysis can be modeled employing the Finite Element Method (FEM).The collaboration between the team ceramic composites and structures at the DLR in Stuttgart, the DITF in Denkendorf and the chair of experimental physics 2 at the University of Augsburg has proven to be complementery and effective during KeraFaM. Based on this successful collaboration, the following goals will be pursued in KeraFaM 2:•To raise the fiber utilization rate substructuring of the C/C blocks is intended. This could be achieved by a multilayer sizing. This sizing is used to obtain a more defined tailoring of the FMB and to protect the fibers from conversion. In a second approach a microporous C-matrix will be produced. Both concepts are expected to favor single fiber pullout over fiber bundle pullout.•Analysis of cross-linking reactions, in situ acoustic emissions analysis and nano-CT examination starting at the curing stage of the resin addresses understanding of the microstructure formation. This will ultimately lead to better control of the microstructure and the resulting C/C-SiC composite properties.•The FE-Model will be refined by taking into account experimentally obtained material parameters in order to realistically represent microstructure development for different FMB values. The resulting model will be validated by acoustic emissions analysis and SEM measurements.•The impact of phenolic content of the matrix resins on residual carbon mass, shrinkage and microstructure after carbonization will be evaluated varying the proportion of aromatic compounds of the matrix resin.•To allow further processing and to protect fibers from conversion to SiC, UHM fibers will be modified by applying an additional sizing on top of the as-received sizing.
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