The Physical and Morphological Properties of Kenaf/ Epoxy Fibres in Coating Treatment Process

Natural fibre is an economical material that often used in various applications due to its low in density, non-abrasiveness in processing and biodegradable. But, its usage in various applications is still limited due to the low in overall properties. The acceptable method to improve the properties of the fibres is by chemical treatment method that is costly, meticulous process and high energy demand. Thus, a new, simple and cost-effective fibre coating treatment method was developed which was able to improve the physical and morphological properties that open a new path for natural based materials to be used in a more robust application. In this study, the physical and morphological properties of various coated Kenaf fibres were analysed to comprehend the cutting behaviour of coated fibres after subjected to the pulverisation process. The Kenaf fibres were individually immersed in 1:4, 1:5 and 1:6 epoxy to acetone coating solutions prior cured, and pulverised consecutively using 5 mm, 1 mm, 0.5 mm and 0.25 mm mesh sizes aperture. The morphological characteristic was analysed using polarised optical and scanning electron microscope. The result showed that 1:6 coating ratio solution able to effectively coat the fibres’ aspect ratio that forming individual coated fibre which in long length pulverised fibres. Moreover, the low viscous 1:6 solution able to penetrate inside fibre structure that supported by density and fibre cross-section analysis compare to the other solutions. In future, this analysis is crucial to give insight on the coated fibres behaviour after subjected to the mechanical means of cutting process that later relates to the reinforcing mechanism in the composite samples.

Fatigue Performance of Type I Fibre Bragg Grating Strain Sensors

Although fibre Bragg gratings (FBGs) offer obvious potential for use in high-density, high-strain sensing applications, the adoption of this technology in the historically conservative aerospace industry has been slow. There are several contributing factors, one of which is variability in the reported performance of these sensors in harsh and fatigue prone environments. This paper reports on a comparative evaluation of the fatigue performance of FBG sensors written according to the same specifications using three different grating manufacturing processes: sensors written in stripped and re-coated fibres, sensors written during the fibre draw process and sensors written through fibre coating. Fatigue cycling of the fibres is provided by a customized electro-dynamically actuated loading assembly designed to provide high frequency and amplitude loading. Pre- and post-fatigue microscopic analysis and high-resolution transmission and reflection spectra scanning are conducted to investigate the fatigue performance of FBGs, the failure regions of fibres as well as any fatigue-related effects on the spectral profiles. It was found that because of the unique fabrication method, the sensors written through the fibre coating, also known as trans-jacket FBGs, show better fatigue performance than stripped and re-coated FBGs with greater control possible to tailor the optical reflection properties compared to gratings written in the draw tower. This emerging method for inscription of Type I gratings opens up the potential for mass production of higher reflectivity, apodised sensors with dense or complex array architectures which can be adopted as sensors for harsh environments such as in defence and aerospace industries.

Development of a SiNx-Based Barrier Coating for SiC Fibres

Uncoated SiC fibres in SiC/SiC composites manufactured by the liquid-silicon infiltration (LSI) process show a strong degradation as a result of silicon attack. The goal of this research is the development of a SiNx-based fibre coating, which acts as a barrier against the liquid silicon. The coating is applied by means of low-pressure chemical vapour deposition (LPCVD) utilising the gaseous precursors silane (SiH4) and ammonia (NH3) on a commercial SiC multifilament yarn. The result is an amorphous fibre coating with an increasing coating thickness and a variable chemical composition from the middle of the yarn to the edges. The coated fibres exhibit a reduced characteristic Weibull strength in comparison to the uncoated fibres. In order to examine the stability of the films, the coated fibres undergo a heat treatment at 1450 °C in different environments (vacuum, argon and nitrogen). In all environments, the amorphous SiNxcoatings crystallise to the trigonal Si3N4. Depending on the coating thickness cracks and defects develop. However, the best results and the lowest amount of damaging occurs during the treatment in nitrogen.

Development and Characterisation of Phenolic Resin Based Liquid Silicon Infiltrated SiC/SiC Composites with SiNx Fibre Coating

SiC/SiC ceramics consist of silicon carbide fibres embedded in a silicon carbide matrix. As an alternative to classic CVI and PIP routes, Liquid Silicon Infiltration (LSI) was chosen as a technique with short process times to obtain composites with low porosity. Silicon carbide composites show good thermal shock resistance, a low coefficient of thermal expansion and excellent physical and chemical stability at elevated temperatures and are therefore regarded as promising candidates for various applications in jet engines and in power engineering. To build up the matrix, different phenolic resin based carbon precursors were infiltrated in fibre preforms and thermally cured, pyrolysed and siliconized. The aim is to obtain a high carbon yield during pyrolysis and to control the pore morphology in a way that the following liquid silicon infiltration leads to a complete reaction of the carbon matrix with silicon to SiC. The siliconization behaviour and conversion into SiC in dependence of pore morphology and chosen precursor is analysed.At the same time a functional fibre coating has to be developed which protects the fibres from liquid silicon and simultaneously provides a weak fibre matrix bonding. A LPCVD-SiNx fibre coating has been chosen and is investigated in fibre composites especially in terms of protection and reactivity in different atmospheres during pyrolysis and siliconization.

Quantitative and enantioselective analysis of monoterpenes from plant chambers and in ambient air using SPME

A headspace solid-phase microextraction (HS-SPME) and gas chromatography/mass spectrometry (GC/MS) system has been developed for quantifying enantiomeric and nonenantiomeric monoterpenes in plant chamber studies and ambient air. Performance of this system was checked using a capillary diffusion system to produce monoterpene standards. The adsorption efficiency, competitive adsorption and chromatographic peak resolution of monoterpene enantiomer pairs were compared for three SPME fibre coatings: 75 μm Carboxen-PDMS (CAR-PDMS), 50/30 μm divinylbenzene-carboxen-polydimethylsiloxane (DVB-CAR-PDMS) and 65 μm divinylbenzene-polydimethylsiloxane (DVB-PDMS). Key parameters such as the linearity and reproducibility of the SPME system have been investigated in this work. The best compromise between the enantiomeric separation of monoterpenes and competitive adsorption of the isoprenoids on the solid SPME fibre coating was found for DVB-PDMS fibres. The optimum conditions using DVB-PDMS fibres were applied to measure the exchange rates of monoterpenes in the emission of Quercus ilex using a laboratory whole plant enclosure under light and dark conditions, as well as in ambient air. With 592 and 223 ng m−2 s−1 respectively, β-myrcene and limonene were the predominant monoterpenes in the emission of Q. ilex. These values were closely comparable to those obtained using a zNose and cartridge GC-FID systems.

Quantitative and enantioselective analysis of monoterpenes from plant chambers and in ambient air using SPME

A solid-phase microextraction (HS-SPME) and gas chromatography/mass spectrometry (GC/MS) system has been developed for quantifying enantiomeric and nonenantiomeric monoterpenes in plant chamber studies and ambient air. Performance of this system was checked using a capillary diffusion system to produce monoterpene standards. The adsorption efficiency, competitive adsorption and chromatographic peak resolution of monoterpene enantiomer pairs were compared for three SPME fibre coatings: 75 μm Carboxen-PDMS (CAR-PDMS), 50/30 μm, divinylbenzene-carboxen-polydimethylsiloxane (DVB-CAR-PDMS) and 65 μm divinylbenzene-polydimethyl-siloxane (DVB-PDMS). Key parameters such as the linearity and reproducibility of the SPME system have been investigated in this work. The best compromise between the enantiomeric separation of monoterpenes and competitive adsorption of the isoprenoids on the solid SPME fibre coating was found for DVB-PDMS fibres. The optimum conditions using DVB-PDMS fibres were applied to measure the exchange rates of monoterpenes in the emission of Quercus ilex using a laboratory whole plant enclosure under light and dark conditions, as well as in ambient air. With 592 and 223 ng m−2 s−1, respectively, β-myrcene and limonene were the predominant monoterpenes in the emission of Q. ilex. These values were closely comparable to those obtained using a zNose and cartridge GC-FID systems.