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

基本信息

项目摘要

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.
基于之前KeraFaM项目中获得的知识,KeraFaM 2旨在使C/C-SiC材料的力学性能更接近标准和高性能纤维所期望的理论极限。到目前为止,获得了以下见解:·通过精确定制纤维-基体-粘合(FMB),可以实现在硅化过程中保护纤维免受转化。这防止了纤维-基体-分层(FMD)并有利于纤维束之间的分段裂纹(SC),从而导致由SiC基体分离的致密C/C块。所得C/C-SiC复合材料的力学性能低于理论极限。纤维性能的低利用率归因于有利于纤维束拔出的C/C嵌段结构。·碳化后观察到的样品裂纹结构的形成在树脂固化过程中已经开始。·基体树脂的选择影响微结构。树脂之间的本质区别在于酚和溶剂含量。·项目中使用的超高模量(UHM)纤维由于其脆性而无法在退浆后进行加工。·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。在KeraFaM期间,斯图加特DLR的陶瓷复合材料和结构团队,Denkendorf的DITF和奥格斯堡大学实验物理2主席之间的合作已被证明是互补和有效的。基于这次成功的合作,KeraFaM 2将追求以下目标:·为了提高光纤利用率,打算对C/C块进行子结构化。这可以通过多层施胶来实现。这种施胶用于获得更明确的FMB定制并保护纤维免于转化。在第二种方法中,将产生微孔C-基质。预计这两种概念都有利于单根光纤拔出,而不是光纤束拔出。·从树脂固化阶段开始的交联反应分析、原位声发射分析和纳米CT检查解决了对微观结构形成的理解。这将最终导致更好地控制微观结构和C/C-SiC复合材料的性能。·将通过考虑实验获得的材料参数来细化FE模型,以真实地表示不同FMB值的微观结构发展。生成的模型将通过声发射分析和SEM测量进行验证。·通过改变基体树脂中芳香族化合物的比例,评估基体树脂中的酚含量对碳化后残余碳质量、收缩率和微观结构的影响。·为了允许进一步加工并保护纤维不转化为SiC,UHM纤维将通过在收到的上浆剂上施加额外的上浆剂来改性。

项目成果

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Professor Dr. Michael R. Buchmeiser其他文献

Professor Dr. Michael R. Buchmeiser的其他文献

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{{ truncateString('Professor Dr. Michael R. Buchmeiser', 18)}}的其他基金

High Oxidation State Tungsten Oxo, Tungsten Thio, and Tungsten Imido Alkylidene NHC Complexes for Olefin Metathesis of Functional Olefins
高氧化态氧化钨、硫代钨和亚氨基亚烷基钨 NHC 配合物用于功能性烯烃的烯烃复分解
  • 批准号:
    319116190
  • 财政年份:
    2016
  • 资助金额:
    --
  • 项目类别:
    Research Grants
Functional Group Tolerant Olefin Metathesis Catalysts Based on N-Heterocyclic Carbene Complexes of High Oxidation State Molybdenum Imido Alkylidenes
基于高氧化态亚氨基钼亚烷基N-杂环卡宾配合物的官能团耐受性烯烃复分解催化剂
  • 批准号:
    271749009
  • 财政年份:
    2015
  • 资助金额:
    --
  • 项目类别:
    Research Grants
Polymerization Catalysts for the Reversible Switching Between Vinyl Insertion and Ring-Opening Metathesis Polymerization
用于乙烯基插入和开环复分解聚合之间可逆转换的聚合催化剂
  • 批准号:
    226688656
  • 财政年份:
    2012
  • 资助金额:
    --
  • 项目类别:
    Research Grants
Metathesis under Biphasic Conditions Using Monolithic-Supported Ionic Liquids
使用整体支撑离子液体在双相条件下进行复分解
  • 批准号:
    136355964
  • 财政年份:
    2010
  • 资助金额:
    --
  • 项目类别:
    Research Grants
Regio- and Stereoselective Cyclopolymerization of Functional 1,6-Heptadiynes and 1,5-Hexadiynes: Rationalizing Catalyst Activity with Monomer Structure
功能性 1,6-庚二炔和 1,5-己二炔的区域和立体选择性环聚合:通过单体结构合理化催化剂活性
  • 批准号:
    41694162
  • 财政年份:
    2007
  • 资助金额:
    --
  • 项目类别:
    Research Grants
Novel photoactive transition metal catalysts for the UV-Light-Triggered Metathesis Polymerization of Functional Monomers
用于紫外光触发功能单体复分解聚合的新型光活性过渡金属催化剂
  • 批准号:
    25106151
  • 财政年份:
    2006
  • 资助金额:
    --
  • 项目类别:
    Research Grants
Monolithisch-geträgerte Metall-Nanocluster für katalytische Anwendungen
用于催化应用的整体支撑金属纳米团簇
  • 批准号:
    20805014
  • 财政年份:
    2006
  • 资助金额:
    --
  • 项目类别:
    Research Grants
Origin of Differences in Regioselectivity in the (Cyclo-) Polymerization of alpha, omega-Diynes and 1-Alkynes Between Tetra- and Penta-Coordinated Mo/W Imido/Oxo Alkylidene N-Heterocyclic Carbene Complexes and Implications for Ene-yne Metathesis
四配位和五配位Mo/W亚氨基/氧代亚烷基N-杂环卡宾配合物之间α、omega-二炔和1-炔烃的(环)聚合中区域选择性差异的起源及其对烯-炔复分解的影响
  • 批准号:
    449377332
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
    Research Grants

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