Shear behavior of a shear thickening fluid-impregnated aramid fabrics at high shear rate

Shear-thickening fluid-impregnated aramid (STF-im-AR) fabrics have been manufactured for advanced soft body armor applications for which they provide improved ballistic and stab resistances. It is not yet clear whether or not such improvements can be attributed solely to the STF. In this study, the rate-dependent behavior of an STF-im-AR fabric was investigated at the fabric level, using uniaxial tensile, bias-extension, and picture-frame tests. Rate-dependent behavior of the STF-im-AR fabric was observed during uniaxial tensile testing; however, the effect of the STF treatment was slight and consistent with only the inherent effect of the polymeric nature of its constituent fibers. The shear rigidity of the STF-im-AR fabric increased, due to the presence of the STF and the sensitivity of the fabric's shear stiffness to changes in the shear strain rate also increased slightly. This rate-sensitive shear stiffness of STF-im-AR fabrics may contribute to improved ballistic and stab resistances

Detoxification Properties of Guanidinylated Chitosan Against Chemical Warfare Agents and Its Application to Military Protective Clothing

This study investigates the detoxification properties of guanidinylated chitosan against chemical warfare agents and its application to the preparation of military protective clothing. Guanidinylated chitosan was synthesized by chitosan guanidinylation with cyanamide. The detoxification properties of the guanidinylated chitosan were then evaluated using a chemical warfare agent simulant, called diisopropylfluorophosphate (DFP). Cotton fabric was treated with 1 wt.% of guanidinylated chitosan in acetic acid and water solution using the simple and conventional textile treatment method of pad–dry–cure. The detoxification properties of the guanidinylated chitosan-treated cotton fabric were evaluated to investigate the application of guanidinylated chitosan to the preparation of military protective clothing. Subsequently, 71.3% of DFP was hydrolyzed to non-hazardous diisopropylhydrogenphosphate (DHP) in 2 h because of the base organocatalytic activity of 0.02 g guanidinylated chitosan itself. Moreover, 60.1% of DFP was hydrolyzed by the catalytic activity of the guanidinylated chitosan-treated cotton fabric, which contained only 0.0002 g of guanidinylated chitosan. This result shows that the guanidinylated chitosan itself has detoxification properties for hydrolyzing DFP to DHP, and its detoxification properties can be more efficient when applied to cotton fabric because it showed 84.3% of the detoxification properties with only 1 wt.% of guanidinylated chitosan. For the first time, this study shows that guanidinylated chitosan has considerable detoxification properties and can be used as an agent to prepare protective clothing

Facile Fabric Detoxification Treatment Method Using Microwave and Polyethyleneimine Against Nerve Gas Agents

Generally, detoxification fabrics are defined as fabrics that remove or inhibit the production of toxic compounds, especially chemical warfare agents such as nerve gas agents. They are usually prepared using a complicated and time-consuming method. This study suggests a facile treatment method for preparing detoxification fabrics against nerve gas agents using polyethyleneimine and microwave curing. The detoxification properties of polyethyleneimine and microwave-treated polypropylene nonwoven fabric were evaluated using diisopropylfluoro-phosphate, which is a nerve agent simulant. The treated polypropylene fabric decontaminated 53.6% of diisopropylfluorophosphate (DFP) in 2 h at 32 °C, and the half-life of DFP on the surface of the treated fabric was 122 min. The result indicates that the treated fabric can act as a basic organocatalyst for the DFP hydrolysis and has a shorter half-life owing to the large number of amine groups. Therefore, the facile treatment method has the potential for use in the preparation of detoxification fabrics

Effect of slitting of carbon fiber-reinforced plastic strip on flexural properties of reinforced concrete

In this study, reinforced concrete was manufactured by attaching a carbon fiber reinforced plastic (CFRP) strips to the surface of the concrete. Strips with the same total area were slitted into one, two, three, four, and six pieces and attached to the upper, lower, and side parts of the concrete. The flexural strength and fracture toughness of the reinforced concrete were investigated. As the number of slits in the strip increased, for the upper reinforcement, the flexural strength gradually increased from 7.88 MPa to 11.21 MPa; for the lower reinforcement, the flexural strength increased significantly from 7.88 MPa to 26.48 MPa and then gradually increased to 33.90 MPa; and for the side reinforcement, the flexural strength increased from 7.12 MPa to 13.96 MPa and then gradually decreased. In the adhesive fracture toughness test, the fracture toughness energy significantly increased from 142.38 J m ^−2 to 516.63 J m ^−2 as the contact area between the adhesive and the strip increased. Therefore, in reinforcing concrete using a CFRP strip, it was confirmed that the reinforcement effect was enhanced when the strip was slit and then attached

Correlation between Pitch Impregnation Pressure and Pore Sizes of Graphite Block

This study aimed to investigate the effect of impregnation pressure on the decrease in porosity of impregnated bulk graphite. The correlation between pitch impregnation behavior and the pore sizes of the bulk graphite block was studied to determine the optimal impregnation pressure. The densities and porosities of the bulk graphite before and after pitch impregnation under various pressures between 10 and 50 bar were evaluated based on the Archimedes method and a mercury porosimeter. The density increased rates increased by 1.93–2.44%, whereas the impregnation rate calculated from the rate of open porosity decreased by 15.15–24.48%. The density increase rate and impregnation rate were significantly high when the impregnation pressures were 40 and 50 bar. Compared with impregnation pressures of 10, 20, and 30 bar, the minimum impregnatable pore sizes with impregnation pressures of 40 and 50 bar were 30–39 and 24–31 nm, respectively. The mercury intrusion porosimeter analysis results demonstrated that the pressure-sensitive pore sizes of the graphite blocks were in the range of 100–4500 nm. Furthermore, the ink-bottle-type pores in this range contributed predominantly to the effect of impregnation under pressure, given that the pitch-impregnated-into-ink-bottle-type pores were difficult to elute during carbonization

Polymer Concentration and Liquid—Liquid Demixing Time Correlation with Porous Structure of Low Dielectric Polyimide in Diffusion-Driven Phase Separation

Porous polyimide (PI) films are a promising low-k dielectric material for high-frequency data transmission with low signal attenuation. Pores are generated by non-solvent induced phase separation (NIPS) during phase inversion of polymer solution via non-solvent accumulation and solvent diffusion. In this study, aromatic PI was employed as a matrix for NIPS, and the influence of polymer concentration and liquid—liquid demixing time on the morphology of pores in the PI films was investigated. This ensured control over the porous structure of the PI film and provided desirable dielectric properties in a broad frequency range of 100 Hz–30 MHz (1.99 at 30 MHz) and thermal stability (Td5% > 576 °C, Tg > 391 °C). This study addresses the effect of polymer concentration and coagulation time on the morphology and physical properties of PI sponge films and provides guidance on the design and optimization of architectures for polymeric materials requiring pore modification

Self-Cleaning Polyester Fabric Prepared with TiOF₂ and Hexadecyltrimethoxysilane

In this study, self-cleaning polyester (PET) fabrics were prepared using TiOF2 and hexadecyltrimethoxysilane(HDS) treatment. TiOF2 was synthesized via direct fluorination of a precursor TiO2 at various reaction temperatures. The prepared PET fabrics had superior photocatalytic self-cleaning properties compared with anatase TiO2/HDS-treated PET fabrics under UV and sunlight with 98% decomposition of methylene blue. TiOF2/HDS-treated PET fabrics also had superior superhydrophobic self-cleaning properties compared with anatase TiO2/HDS-treated PET fabrics with a 161° water contact angle and 6° roll-off angle. After the self-cleaning tests of the non-dyed TiOF2/HDS-treated PET fabrics, we prepared dyed TiOF2/HDS-treated PET fabrics to test practical aspects of the treatment method. These PET fabrics were barely stained by tomato ketchup; even when stained, they could be self-cleaned within 4 h. These results suggest that practical self-cleaning PET fabrics with superhydrophobicity and photocatalytic degradation could be prepared using TiOF2/HDS-treatment

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Pyro-polymerization of organic pigments for superior lithium storage

Design of high energy density lithium storage materials is one of the everlasting issues in energy storage systems to realize a fully clean and sustainable energy grid. Here, 2,9-dimethyl quinacridone was selected as a precursor to prepare carbon-based electrode via low temperature heat-treatment process from 750 degrees C to 1050 degrees C. The pyro-polymerization of 2,9-dimethyl quinacridone induced a distinctive morphological transformation from rice husk-shaped 2,9-dimethyl quinacridone to carbon nanofibers. Electrode fabricated from pigment derived carbon nanofibers (PCNF) pyrolyzed at 750 degrees C maintained 878 mAh g-1 at a current density of 1 A g-1 and good Coulombic efficiency up to 98% after 1000 cycles. Furthermore, it delivered 337 mAh g-1 at a high current density of 25 A g-1. The superior performance was attributed to the stable structure of pristine 2,9-dimethyl quinacridone giving high thermal stability and crystallinity owing to well-defined pi-pi and hydrogen bonding interactions, thus rendering a stable microstructure with a large d-spacing of (002) plane of 3.580 angstrom, as well as efficient surface redox reactions. Density functional theory calculations indicated that the large interlayer distance could facilitate fast lithium ion insertion/extraction because of a similar to 38% lower energy barrier for lithium ion insertion than compared with graphite. (C) 2021 Elsevier Ltd. All rights reserved