# Preparation and characterization of HfOC/SiOC composite powders and fibermats via the polymer pyrolysis route

**Authors:** Arijit Roy, Paul Owiredu, Gurpreet Singh

PMC · DOI: 10.1039/d5ra02006a · 2025-05-09

## TL;DR

This paper describes a new ceramic composite combining HfOC and SiOC, offering high-temperature resilience and oxidation resistance through a polymer pyrolysis method.

## Contribution

A novel HfOC/SiOC composite is synthesized via polymer pyrolysis, enhancing oxidation resistance and ceramic yield.

## Key findings

- The composite showed a 78 wt% polymer-to-ceramic yield at 800 °C and 74 wt% at 1200 °C.
- The HfOC/SiOC fibermat exhibited only 6% linear shrinkage during oxidation testing at 800 °C.
- The composite outperformed carbon-rich SiOC and carbon fibermats in oxidation resistance.

## Abstract

We report on the synthesis and characterization of HfOC/SiOC ceramic composite powders and electrospun fibermats, which integrate the high-temperature resilience of HfOC with the oxidation resistance of silicon oxycarbide (SiOC). The composites were fabricated through a polymer-pyrolysis route by integrating 1,3,5,7-tetramethyl, 1,3,5,7-tetravinyl cyclotetrasiloxane (4-TTCS), a precursor source for SiOC, and a commercial HfC precursor in a 1 : 1 ratio by mass. First, the HfC precursor was heated to 70 °C to drive off water molecules, followed by its blending with the liquid phase 4-TTCS and cross-linking at a moderate temperature (160–400 °C). This was followed by pyrolysis at three different temperatures – 800, 1000, and 1200 °C in an inert argon atmosphere. The composite ceramic was comprehensively characterized by the use of electron microscopy for particle and fiber morphology, X-ray diffraction for the evolution of various ceramic phases, and a range of spectroscopies to document the change in molecular vibrations or the evolution of the functional groups and molecular bonding in preceramic polymer during cross-linking and ceramization. The crosslinked polymer-to-ceramic yield for powder samples was observed to be as high as approximately 78 wt% when pyrolyzed at 800 °C, and 74 wt% when pyrolyzed at 1200 °C. The oxidation test performed at 800 °C in stagnant air for the fibermat pyrolyzed at 1000 °C indicated a linear shrinkage of 6% for the HfOC/SiOC composite. This represents an improvement over the carbon rich-SiOC fibermat which exhibited a mass loss of 71 wt% and a linear shrinkage of nearly 19%, while the neat carbon fibermat was completely burned off under similar conditions.

Synthesis and characterization of a HfOC/SiOC ceramic composite.

## Linked entities

- **Chemicals:** 1,3,5,7-tetramethyl, 1,3,5,7-tetravinyl cyclotetrasiloxane (PubChem CID 75706), HfC (PubChem CID 5281416)

## Full-text entities

- **Chemicals:** polymer (MESH:D011108), argon (MESH:D001128), 4-TTCS (-), water (MESH:D014867), carbon (MESH:D002244), 1,3,5,7-tetramethyl, 1,3,5,7-tetravinyl cyclotetrasiloxane (MESH:C507689)

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12063723/full.md

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Source: https://tomesphere.com/paper/PMC12063723