Performance Evaluation of a Nylon-like Polyester Tire Cord Combining the Characteristics of Nylon and Polyester.

A nylon-like polyester tire cord, which combined the characteristics of nylon and polyester tire cords, was designed as the carcass reinforcement material used to meet the increasing demands of the tire industry for performance and impact on the environment. Tires' carcass construction plays a crucial role in affecting handling performance and ride comfort. Small changes in the carcass component can lead to significant improvements in the total tire/vehicle performance. This study evaluated the performance of nylon-like polyester and nylon 6 motorcycle tires. The results showed that the nylon-like polyester tire passed all indoor tests, and post-cure inflation (PCI) could be eliminated, resulting in energy and cost savings. The rolling resistance coefficient of the nylon-like polyester tire was reduced by 6.8% compared to that of the nylon 6 control tire, which could save fuel and have a positive impact on the environment. Nylon-like polyester tire cord extracted from the experimental tire possessed a higher modulus compared to that of nylon 6 tire cord, which could lead to better handling and ride comfort performance. Morphological pictures showed that both nylon-like polyester and nylon 6 cords extracted from tires had a good rubber coverage and comparable adhesion properties.

A tert-Butyldiphenylsilyl-Containing Polyimide-Based Chemosensor for Sequential Detection of Fluoride Ions and Trace Water in Organic Solvents.

A tert-butyldiphenylsilyl-containing polyimide (PI-OSi) has been established as a colorimetric and ratiometric chemosensor for rapid detecting fluoride ions (F-). The UV-vis absorbance ratio value (A322/A288) of PI-OSi in a DMF solution displays a wide linear range change to F- concentrations with a detection limit (DL) value of 2.13 µM. Additionally, adding incremental amounts of F- to a DMF solution of PI-OSi shows an immediate color change to yellow and finally to green from colorless. More interestingly, the resulting PI-OSi plus F- system (PI-OSi·F) could detect trace water in DMF. The A292/A322 value of PI-OSi·F almost linearly increases with low water content, which suggests convenient quantitative sensing of trace water content in DMF. The DL value of PI-OSi·F for sensing water in DMF is determined to be 0.00149% (v/v). The solution color of PI-OSi·F returns to colorless when the water content increases, indicating that PI-OSi·F can conveniently estimate water content in DMF by naked-eye detection. The detection mechanisms confirmed by an 1H NMR study and a DFT calculation involve a F--induced desilylation reaction of PI-OSi to form phenolate anion followed by protonation with trace water. Finally, PI-OSi film was fabricated for the colorimetric detection of F- and water in CH3CN.

Density Functional Simulation Study of Surface Wettability of Coal Molecules with Different Degrees of Defects.

To explore the adsorption mechanism of H2O molecules on the surfaces of defective coal molecules and perfect bituminous coal molecules, the energy band structure, electronic density of states, electrostatic potential, and front orbitals on the surfaces of three coal molecule models were investigated using quantum chemical density functional theory (DFT) simulations. The adsorption energy and Mulliken charge layout of H2O molecules with the surfaces of defective coal molecules and perfect bituminous coal molecules were similarly investigated. The results of the DFT calculations showed that the widths of the forbidden bands of the defective coal molecular surfaces were narrower, and the electrostatic potential values were smaller. In addition, they each had an increased conduction band near the Fermi energy level, a larger electronic density of states near the Fermi energy level, and a higher electron activity and electron density than those of the perfect bituminous coal molecular surface. While stable adsorption of H2O molecules occurred on the surfaces of the single-vacancy-defective coal molecules, double-vacancy-defective coal molecules, and perfect bituminous coal molecules, the adsorption energy values were -39.401, -30.002, and -29.844 kJ/mol for the more stable configurations, corresponding to -0.022, -0.013, and -0.011 electrons gained by H2O molecules, respectively. Wettability improved with the appearance of defects, and the order of improvement was single-vacancy-defective coal molecule > double-vacancy-defective coal molecule > no-defect coal molecule.

Modified Fabrication of Perovskite-Based Composites and Its Exploration in Printable Humidity Sensors.

Organic perovskites are promising optoelectronic semiconductor materials with photoelectric applications. It is known that the luminescence of perovskites is highly sensitive to hydron molecules due to its low moisture resistance of crystal structure, indicating its potential application on humidity-sensing. Herein, a novel perovskite-based compound (PBC) with minimal defects was developed to promote the photoluminescence performance via optimization of the drying method and precursor constitutions. Perovskite materials with good structural integrity and enhanced fluorescence performance up to four times were obtained from supercritical drying. Moreover, the hydrophilic polymer matrix, polyethylene oxide (PEO), was added to obtain a composite of perovskite/PEO (PPC), introducing enhanced humidity sensitivity and solution processibility. These perovskite/PEO composites also exhibited long-term stability and manifold cycles of sensitivity to humidity owing to perovskite encapsulation by PEO. In addition, this precursor solution of perovskite-based composites could be fancily processed by multiple methods, including printing and handwriting, which demonstrates the potential and broaden the applications in architecture decoration, logos, trademarks, and double encryption of anti-fake combined with humidity.