Microstructured fiber interface coatings for composites
11565977 · 2023-01-31
Assignee
Inventors
- Richard Wesley Jackson (Mystic, CT, US)
- Ying She (East Hartford, CT, US)
- Gajawalli V. Srinivasan (South Windsor, CT, US)
Cpc classification
C04B2235/5228
CHEMISTRY; METALLURGY
D06M11/79
TEXTILES; PAPER
C04B2235/524
CHEMISTRY; METALLURGY
C04B2235/5232
CHEMISTRY; METALLURGY
C04B35/80
CHEMISTRY; METALLURGY
C04B2235/76
CHEMISTRY; METALLURGY
D06M11/74
TEXTILES; PAPER
C04B35/195
CHEMISTRY; METALLURGY
C04B35/62897
CHEMISTRY; METALLURGY
International classification
C04B35/80
CHEMISTRY; METALLURGY
C04B35/628
CHEMISTRY; METALLURGY
D06M11/74
TEXTILES; PAPER
Abstract
Disclosed is a coated ceramic fiber including a silicon carbide coating layer adjacent to the ceramic fiber and a silicon dioxide coating layer adjacent to the silicon carbide coating layer, wherein the silicon dioxide coating layer forms micro cracks after a crystal structure transformation. The coated ceramic fiber may be included in a composite material having a ceramic matrix.
Claims
1. A coated ceramic fiber comprising: a silicon carbide coating layer adjacent to the ceramic fiber, a portion of the silicon carbide layer oxidized to form amorphous silicon dioxide, and a silicon dioxide coating layer adjacent to the silicon carbide coating layer, the silicon dioxide coating layer including the amorphous silicon dioxide, an additional coating layer adjacent to the silicon dioxide coating layer; wherein the silicon dioxide coating layer forms micro cracks after a crystal structure transformation; wherein the additional coating layer does not include silicon carbide; and wherein the silicon dioxide coating layer includes silicon dioxide in β cristobalite form which forms micro cracks after transforming to α cristobalite form.
2. The coated ceramic fiber of claim 1, wherein the silicon dioxide coating layer has a thickness of 50 nm to 10,000 nm.
3. The coated ceramic fiber of claim 1, wherein the silicon carbide coating layer has a thickness of 1000 nm to 20,000 nm.
4. A composite material comprising: a ceramic matrix material and a plurality of ceramic fibers embedded within the ceramic matrix material; wherein the plurality of ceramic fibers comprise a multi-layer interface coating and the multi-layer interface coating comprises a silicon carbide coating layer adjacent to the plurality of ceramic fibers, a portion of the silicon carbide layer oxidized to form amorphous silicon dioxide, and a silicon dioxide coating layer deposited onto the silicon carbide coating layer, the silicon dioxide coating layer including the amorphous silicon dioxide, an additional coating layer adjacent to the silicon dioxide coating layer; wherein the silicon dioxide coating layer forms micro cracks after a crystal structure transformation; wherein the additional coating layer does not include silicon carbide; and wherein the silicon dioxide coating layer includes silicon dioxide in β cristobalite form which forms micro cracks after transforming to α cristobalite form.
5. The composite material of claim 4, wherein the silicon dioxide coating layer has a thickness of 50 nm to 10,000 nm.
6. The composite material of claim 4, wherein the silicon carbide coating layer has a thickness of 1000 nm to 20,000 nm.
7. The coated ceramic fiber of claim 1, wherein the additional coating layer comprises zirconium or zirconium boride or combinations thereof.
8. The composite material of claim 4, wherein the additional coating layer comprises zirconium or zirconium boride or combinations thereof.
9. A method for forming a multi-layer interface coating onto a ceramic fiber comprising: depositing a silicon carbide coating layer onto the fiber, oxidizing a portion of the silicon carbide coating layer to form an amorphous silicon dioxide coating layer, and depositing an additional coating layer on the silicon dioxide coating layer; and crystallizing the amorphous silicon dioxide layer to beta cristobalite; wherein the additional coating layer does not include silicon carbide; and wherein the beta cristobalite forms micro cracks in the silicon dioxide coating layer after transforming to a cristobalite form.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1) The following descriptions should not be considered limiting in any way. With reference to the accompanying drawings, like elements are numbered alike:
(2) The FIGURE shows a representative interface coating and method of making.
DETAILED DESCRIPTION
(3) A detailed description of one or more embodiments of the disclosed apparatus and method are presented herein by way of exemplification and not limitation with reference to the FIGURE.
(4) Composites exhibit a significant amount of damage tolerance when under an applied load. In ceramic matrix composites (CMC) in particular, this damage tolerance is due to the formation of multiple matrix cracks that aid in the redistribution of stresses. However, the formation of matrix cracks can result in environmental exposure to the fiber and fiber interface coating. The fiber interface coating protects the fiber from the environmental exposure and provides a weak interface to allow for composite behavior.
(5) The multi-layer interface coating described herein provides a weak interface with the fiber to allow for composite behavior and also provides environmental protection. The multiple layers can prevent crack propagation from reaching the fibers and protect the fiber from environmental degradation. In particular, the silicon dioxide layer is a crystalline material which goes through a crystal structure transformation after a heat treatment or under conditions of normal use. The crystal structure transformation results in the presence of micro cracks which can deflect any matrix cracks from reaching the fiber.
(6) Referring now to the FIGURE a coated ceramic fiber for use in a composite is shown. The coated ceramic fiber includes ceramic fiber 12 and a multi-layer interface coating 22. The multi-layer interface coating 22 as shown includes three coating layers 24, 32 and 28. It should be appreciated that the additional coating layer 28 is optional. Exemplary ceramic fiber materials include silicon carbide, carbon, aluminum oxide, mullite, hafnium carbide, zirconium carbide, tantalum carbide, niobium carbide, boron carbide, titanium carbide, hafnium boride, zirconium boride, tantalum boride, niobium boride, titanium boride, and combinations thereof. Silicon carbide fibers have residual carbon which distinguishes the fibers compositionally from the silicon carbide coating layer which does not have carbon.
(7) The first interface layer 24 includes silicon carbide. A portion of the silicon carbide layer is oxidized to form amorphous silicon dioxide. The additional coating layer 28, may include silicon carbide, zirconium, zirconium boride or a combination thereof.
(8) The silicon carbide layer may have a thickness of 1000 nm to 20,000 nm, or, 2,000 nm to 10,000 nm. The silicon dioxide layer may have a thickness of 50 nm to 10,000 nm, or, 100 nm to 1,000 nm. The additional coating layer may have a thickness of 1000 nm to 20,000 nm, or, 2000 nm to 10,000 nm.
(9) The silicon carbide layer is deposited on the ceramic fiber by chemical vapor deposition (shown as step 110). The combination of the silicon carbide layer and the ceramic fiber are then heat treated in the presence of oxygen to oxidize a portion of the silicon carbide layer to form a silicon dioxide 30 (shown as step 120) which is initially amorphous.
(10) An additional coating layer or at least portion of the matrix is then deposited on the silicon dioxide layer (shown as step 130) by, for example, chemical vapor deposition, after which the fiber with the multilayer coating is subjected to a heat treatment (shown as step 140) to crystallize the silicon dioxide. Exemplary additional coating layer materials include zirconium, silicon carbide, zirconium boride or combinations thereof. Exemplary matrix materials include silicon carbide, aluminum oxide, mullite, cordierite, and combinations thereof.
(11) The heat treatment crystallizes the silicon dioxide 30 and forms beta-cristobalite 26 and upon cooling (shown as step 150) alpha-cristobalite 32 forms with a volume reduction which results in micro cracking. Exemplary heat treatment temperatures (step 140) 1200 to 1650° C., or, 1300 to 1600° C. Exemplary times for the heat treatment include 1 minute to 100 hours, or, 1 minutes to 50 hours.
(12) The micro cracks in the silicon dioxide coating layer provide protection to the fiber from matrix cracking by deflecting the cracks into the silicon dioxide layer. The first interlayer provides environmental protection to the fiber so the combination of layers results in a composite with more robust properties. The third layer, when present, protects the micro cracked second layer.
(13) The terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting of the present disclosure. As used herein, the singular forms “a”, “an” and “the” are intended to include the plural forms as well, unless the context clearly indicates otherwise. The term “adjacent to” is defined as being in contact with the underlying material. It will be further understood that the terms “comprises” and/or “comprising,” when used in this specification, specify the presence of stated features, integers, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, integers, steps, operations, element components, and/or groups thereof.
(14) While the present disclosure has been described with reference to an exemplary embodiment or embodiments, it will be understood by those skilled in the art that various changes may be made and equivalents may be substituted for elements thereof without departing from the scope of the present disclosure. In addition, many modifications may be made to adapt a particular situation or material to the teachings of the present disclosure without departing from the essential scope thereof. Therefore, it is intended that the present disclosure not be limited to the particular embodiment disclosed as the best mode contemplated for carrying out this present disclosure, but that the present disclosure will include all embodiments falling within the scope of the claims.