Surfaces of carbon fibre roving were modified by means of a low temperature plasma treatment to improve their bonding with mineral fines; the latter serving as an inorganic fibre coating for the improved mechanical performance of carbon reinforcement in concrete matrices. Variation of the plasma conditions, such as gas composition and treatment time, was accomplished to establish polar groups on the carbon fibres prior to contact with the suspension of mineral particles in water. Subsequently, the rovings were implemented in a fine concrete matrix and their pull-out performance was assessed. Every plasma treatment resulted in increased pull-out forces in comparison to the reference samples without plasma treatment, indicating a better bonding between the mineral coating material and the carbon fibres. Significant differences were found, depending on gas composition and treatment time. Microscopic investigations showed that the samples with the highest pull-out force exhibited carbon fibre surfaces with the largest areas of hydration products grown on them. Additionally, the coating material ingresses into the multifilament roving in these specimens, leading to better force transfer between individual carbon filaments and between the entire roving and surrounding matrix, thus explaining the superior mechanical performance of the specimens containing appropriately plasma-treated carbon roving.

This article reports the successful manufacturing of hybrid yarns from virgin staple CF (40 or 60 mm) or recycled staple CF (rCF) by mixing with polyamide 6 (PA 6) fibers of defined length. The hybrid yarns are produced using an optimized process route of carding, drawing, and flyer machine. Furthermore, the influence of CF length, CF type (i.e. virgin or rCF), CF volume content, and twist of the yarn are also investigated regarding the tensile properties of unidirectionally laid (UD) thermoplastic composites. The results show that CF length, yarn twist, and CF content of composites play a big role on the tensile properties of thermoplastic composites. From the comparison of tensile strength of UD composites produced from 40 and 60mm virgin staple CF, it can be seen that the increase of yarn twist decreases the tensile strength. However, the effect of twist on the tensile properties of UD composites manufactured from 40mm virgin staple CF is insignificant. The tensile strength of UD thermoplastic composites manufactured from the hybrid yarn with 40 and 60mm virgin staple CF and rCF is found to be 771 ± 100, 838 ± β1, and 801 ± 53.4 MPa, respectively, in the case of 87 T/m containing 50 volume% CF.

The availability of a considerable amount of waste carbon fiber (CF) and the increased pressure to recycle/reuse materials at the end of their life cycle have put the utilization of recycled CF (rCF) under the spotlight. This article reports the successful manufacturing of hybrid yarns consisting of staple CF cut from virgin CF filament yarn and polyamide 6 fibers of defined lengths (40 and 60 mm). Carding and drawing are performed to prepare slivers with improved fiber orientation and mixing for the manufacturing of hybrid yarns. The slivers are then spun into hybrid yarns on a flyer machine. The investigations reveal the influence of fiber length and mixing ratio on the quality of the card web, slivers and on the strength of the hybrid yarns. The findings based on the results of this research work will help realize value-added products from rCF on an industrial scale in the near future.

The Joule heating of carbon fiber-based textiles enables an energy- and cost-efficient processing of carbon fiber reinforced thermoplastic parts. This article introduces a new method to pass direct current into a dry, not pre-consolidated hybrid yarn textile based on recycled carbon fibers and polyamide 6 fibers. The aim is to melt polyamide fibers, subsequently impregnate carbon fibers, and finally consolidate the material to form a composite part in a single process step. To increase the reliability of this technology, the electrical properties and the behavior of the material during the heating process must be thoroughly investigated. It will be addressed how the material is characterized during the process and how the changing resistivity of the textile affects the current flow between the electrodes to generate intrinsic heat. Moreover, a method to determine the effective material resistivity by finite element simulation on the fiber scale based on a CT scan is presented. Thus, a validated material model with respect to the temperature development in the textile based on ρ = ρ (T) was established.

Due to their excellent strength, rigidity, and damping properties, as well as low weight, carbon fiber reinforced composites (CFRCs) are being widely used for load bearing structures. On the other hand, with an increased demand and usage of CFRCs, effective methods to re-use waste carbon fiber (CF) materials, which are recoverable either from process scraps or from end-of-life components, are attracting increased attention. In this paper, hybrid yarns consisting of waste staple CF (40 and 60 mm) and polyamide 6 staple fibers (60 mm) are manufactured on a DREF-3000 friction spinning machine with various process parameters, such as spinning drum speed, suction air pressure, and core–sheath ratio. The relationship between different textile physical properties of the hybrid yarns, such as tensile strength, elongation, and evenness with different spinning parameters, core–sheath ratio, and input CF length is revealed.

Surfaces of carbon fibre roving were modified by means of a low temperature plasma treatment to improve their bonding with mineral fines; the latter serving as an inorganic fibre coating for the improved mechanical performance of carbon reinforcement in concrete matrices. Variation of the plasma conditions, such as gas composition and treatment time, was accomplished to establish polar groups on the carbon fibres prior to contact with the suspension of mineral particles in water. Subsequently, the rovings were implemented in a fine concrete matrix and their pull-out performance was assessed. Every plasma treatment resulted in increased pull-out forces in comparison to the reference samples without plasma treatment, indicating a better bonding between the mineral coating material and the carbon fibres. Significant differences were found, depending on gas composition and treatment time. Microscopic investigations showed that the samples with the highest pull-out force exhibited carbon fibre surfaces with the largest areas of hydration products grown on them. Additionally, the coating material ingresses into the multifilament roving in these specimens, leading to better force transfer between individual carbon filaments and between the entire roving and surrounding matrix, thus explaining the superior mechanical performance of the specimens containing appropriately plasma-treated carbon roving.

Carbon fiber (CF) must be protected from thermal oxidation for high temperature application because of its low thermo-oxidative stability above 450°C in air. CF is now increasingly being used as a reinforcing material in the construction industry. A thermal and oxidation resistant coating is necessary for CF-reinforced concrete (CFRC) composites in order to satisfy a high level of safety standard in the case of fire. New types of pre-ceramic coatings, such as Tyranno® polymer (Si–Ti based pre-ceramic) and SiO₂ sol–gel, have been deposited on CF filament yarn by means of a wet chemical continuous dip coating method. The results of surface analyses, e.g. scanning electron microscopy, X-ray photoelectron spectroscopy, and infrared spectroscopy, showed the changes in topographical properties of CF caused by the coatings. Thermogravimetric analysis proved that the high temperature (up to 800°C) oxidation stability of CF was considerably improved due to the coatings. Tensile test results indicated that the strength of CF yarn at 20°C was increased by up to 80% with the coatings. Thermo-mechanical properties were also enhanced up to 600°C. CF yarn retains its original strength and elasticity modulus, i.e. the stiffness at 700°C, with a Tyranno® polymer coating.

This contribution will introduce carbon-reinforced concrete components (so-called carbon concrete composites, or C³) with sensor functionalities for innovative building envelopes. For a continuous in situ structural monitoring, these textile-reinforced concrete components are equipped with textile sensor networks consisting of resistive carbon fiber sensors (CFSs), which are integrated into the carbon fiber non-crimp fabrics of the concrete reinforcement by multiaxial warp-knitting. The in situ CFSs, consisting of 1 k or 50 k carbon fiber roving with added staple fiber/multifilament dielectric cladding, are later integral to the load-distributing elements of the concrete component, and elongations within these are easy to record with good correlation to ohmic resistance changes. Gage factors of k = 0.52–1.23 at linearity deviations of ALin=4.0–8.7% are feasible. This allows a monitoring of C³ building envelopes for structural mechanical changes caused by physical changes within the component through mechanical or thermal loads or deformation and cracks.

This report deals with the influence of different sizing agents on carbon fiber (CF) heavy tows towards their impregnation with a geopolymer (GP) suspension and resulting properties of mineral-impregnated carbon-fiber composites (MCF) produced in an automated, continuous process. Three different commercial CFs were investigated after treatment with either thermoplastic, epoxy, or vinyl-ester sizing agents and then compared to unsized CFs. During impregnating, diverse yarn-spreading behavioral modes and degrees of wetness were observed, indicating different degrees of impregnation, both in quality and quantity. All sizing agents decreased the hydrophobic nature of unsized CFs significantly. Supported by microscopic investigation, water contact angle measurement, and thermal gravimetric and mercury intrusion porosity, the epoxy sizing showed the best fiber-matrix distribution over the cross-section and a dense microstructure. Moreover, in single-fiber pullout tests each sizing brought about a significant increase in maximum pullout force, indicating enhanced bond between fiber and matrix. This is attributed to more intense interaction in the interfacial region, fully corroborating the topological characteristics obtained in microscopic analysis. With higher interfacial bond strength, the thermoplastic sizing enabled the highest tensile properties of MCF despite slightly less impregnation quality in comparison with epoxy-sized samples.:Abstract Keywords 1. Introduction 2. Materials and methods 2.1. Raw materials 2.2. Preparation of the mineral-impregnated carbon fiber composites (MCF) 2.3. Single-fiber pullout tests 2.4. Characterization of fresh state properties of MCF 2.5. Mechanical testing of MCF 2.6. Analytical and morphological characterization 3. Results and discussion 3.1. Characterization of CF yarns 3.2. Characterization of yarn processing 3.3. Morphological and analytical characterization of MCF 3.4. Bending behavior of MCF 3.5. Pullout behavior of carbon fibers 3.6. Uniaxial tensile behavior of MCF 3.7. Microscopic analysis of the fracture surfaces of MCF 4. Summary and conclusions CRediT authorship contribution statement Declaration of Competing Interest Acknowledgment References

The main goal of this dissertation was to show that the principle of atomic layer deposition (ALD) can be applied to “endless” fibers. A reactor of atomic layer deposition has been designed, especially for coating depositions onto meter long bundles of fibers. Aluminum oxide (alumina), titanium oxide (titania), double layers of alumina and titania, as well as aluminium phosphate have been deposited onto bundles of carbon fibers using the home-built reactor. Scanning electron microscopic (SEM) and transmission electron microscopic (TEM) images indicate that the coatings were uniform and conformal onto fiber surface. There was a good adhesion of the coatings to the fibers. Alumina has been deposited using two separate aluminum sources (aluminum trichloride and trimethylaluminum), and water as a source of oxygen. In case of alumina deposition using aluminum trichloride and water, initial deposition temperature was 500 °C. In these conditions, a part of the fiber bundle has been damaged. Thus, the deposition temperature was decreased to 300 °C and the fibers were unaffected. In addition, during this process hydrochloric acid is formed as a byproduct which is a corrosive substance and affects the reactor and there was a chloride impurity in the coatings. Thus, aluminum trichloride precursor was replaced by trimethylalumium. Alumina deposition onto carbon fibers using trimethylaluminum and water was carried out at a temperature of 77 °C. SEM images revealed that the fibers were unaffected and the coatings were uniform and conformal. Oxidation resistance of the carbon fibers was improved slightly after alumina deposition. Oxidation onset temperature of the uncoated fibers was about 630 °C. The resistance was linearly increased with the coating thickness (up to 660 °C) and getting saturated over a thickness of 120 nm. Titania coatings have been deposited using titanium tetrachloride and water. The physical appearances of the titania coatings were similar to the alumina coatings. The oxidation onset temperature of the titania coated carbon fibers was similar to the uncoated fibers but the rate of oxidation was decreased than the uncoated fibers. Two double layer coatings were deposited, alumina followed by titania (alumina/titania), and titania followed by alumina (titania/alumina). If the fibers were coated with the double layer of alumina/titania, they had almost same oxidation onset as alumina coated fibers but the rate of oxidation was decreased significantly compared to alumina coated fibers. This feature is independent of the thickness of the titania layers, at least in the regime investigated (50 nm alumina followed by 13 nm and 40 nm titania). On the other hand, the oxidation onset temperature of fibers coated with titania/alumina (20 nm titania /30 nm alumina) was approximately 750 °C. The fibers were burned completely when temperature was further increased to 900 °C and held another 60 minutes at 900 °C. This is significantly better than any other coating used in this dissertation. ALD of titania and alumina in principle was known beforehand, this dissertation here applies this knowledge for the first time to endless fibers. Furthermore, this dissertation shows for the first time that one can deposit aluminum phosphate via ALD (planar surface as well as fibers). Aluminum phosphate might be special interest in the fiber coating because it is a rather soft material and thus might be used to obtain a weak coupling between fiber and matrix in composites. Aluminum phosphate was deposited using trimethylaluminum and triethylphosphate as precursors. Energy dispersive X-ray spectroscopy and solid state nuclear magnetic resonance spectra confirmed that the coating comprises aluminum phosphate (orthophosphate as well as other stoichiometries). Scanning electron microscopic images revealed that coatings are uniform and conformal. In cases of alumina and titania, it was observed that the coatings were delaminated from the ends of cut fibers and thus formed of clear steps. On the other hand, for aluminum phosphate coating it was observed that the border between coating and underlying fiber often being smeared out and thus formed an irregular line. It seems in case aluminum phosphate cohesion is weaker than adhesion, thus it might be act a weak interface between fiber and matrix. Alumina, titania, and double layer microtubes have been obtained after selective removal of the underlying carbon fibers. The carbon fibers were selectively removed via thermal oxidation in air at temperatures exceeding 550 °C. SEM and TEM images indicate that the inner side of the tube wall has the same morphology like the fibers. In addition, it was observed that the individual microtubes were separated from their neighbors and they had almost uniform wall thicknesses. The longest tubes had a length of 30 cm. / Das Hauptziel dieser Dissertation bestand darin nachzuweisen, dass die Atomlagenabscheidung (engl. atomic layer deposition (ALD)) auf „endlose“ Fasern angewendet werden kann. Es wurde ein Reaktor zur Atomlagenabscheidung gestaltet, der speziell für die Beschichtung meterlanger Faserbündel geeignet ist. Aluminiumoxid, Titanoxid, Doppelschichten aus Aluminiumoxid und Titanoxid sowie Aluminiumphosphat wurden mit Hilfe des selbstgebauten Reaktors auf Kohlefaserbündel abgeschieden. Rasterelektronenmikroskopische (REM) und transmissionselektronenmikroskopische (TEM) Aufnahmen zeigten, dass die Beschichtung auf den Fasern einheitlich und oberflächentreu war. Des Weiteren wurde eine gute Adhäsion zwischen Beschichtung und Fasern beobachtet. Das Prinzip der Beschichtung mit Titanoxid und Aluminiumoxid mit Hilfe der ALD war bereits vorher bekannt und im Rahmen dieser Dissertation jedoch erstmals auf "endlose" Fasern angewendet. Des Weiteren wird in dieser Dissertation erstmals gezeigt, dass es möglich ist, Aluminiumphosphat mittels ALD abzuscheiden (sowohl auf planaren Oberflächen als auch auf Fasern). Aluminiumphosphat könnte von besonderem Interesse in der Faserbeschichtung sein, da es ein relativ weiches Material ist und könnte daher als eine Art „schwacher“ Verbindung zwischen Faser und Matrix in Kompositen dienen. Die Oxidationsbeständigkeit von beschichten Kohlefasern wurde im Vergleich zu unbeschichteten Fasern bis zu einem gewissen Grad erhöht. Monoschichten von Aluminiumoxid und Titanoxid waren dafür wenig effektiv. Aluminiumphosphatbeschichtete Fasern waren deutlich besser geeignet als die beiden anderen. Eine Doppelschicht aus Titanoxid gefolgt von Aluminiumoxid verbesserte die Oxidationsbeständigkeit nochmals deutlich gegenüber allen anderen Beschichtungen, die in dieser Dissertation verwendet wurden. Mikroröhren aus Aluminiumoxid, Titanoxid und Doppelschichten wurden durch die selektive Entfernung der zugrunde liegenden Kohlefasern erhalten. Einzelne Mikroröhren waren von benachbarten Röhren getrennt und sie weisen eine nahezu einheitliche Wanddicke auf.