The Journey of Phenolics from the First Spark to Advanced Materials

The emergence, historical and recent developments of phenolic resins are reviewed. The history of the invention of the first man made plastics and a short bibliography of the inventor Leo H. Baekeland is provided. Moreover, the basic chemistry of phenol-formaldehyde resins, as synthesis of resol and novolak, their structures, variations, and curing are discussed. Modification of these resins and molecular designs for specific applications in retro perspective are highlighted. This review also provides a comprehensive account on the development of benzoxazine resins as an alternative to classical phenolics. In addition to the benzoxazine synthesis and their curing mechanism, special monomers and polybenzoxazine precursors as curable thermoplastics are reviewed. Besides classical chemicals, the potential of renewables for phenolic resin production is also highlighted. Finally, the relative advantages and disadvantages of these systems are discussed and their future potentials are presented.     

The Effect of Hydrothermal Aging on the Low-Velocity Impact Behavior of Multi-Walled Carbon Nanotubes Reinforced Carbon Fiber/Epoxy Composite Pipes

Chemical transmission lines, petroleum and natural gas lines, pressure vessels, and pipes used in thermal facilities are expected to maintain their mechanical properties for many years without being damaged and not to be corroded in working conditions. The composite materials are the right candidate for these harsh conditions due to their superior properties. Reinforcement of nanoadditives to composite materials improves both the mechanical properties and the resistance to environmental conditions, thereby increasing the lifetime. In this study, multi-walled carbon nanotube (MWCNT) reinforced [±?55°] carbon fiber/epoxy composite pipes produced with filament wound method were used. It was hydrothermally aged in 80 °C distilled water for 1, 2, 3 weeks in order to examine the effect of environmental conditions. In order to investigate its resistance against loads that may occur in working conditions, ring tensile tests (ASTM D 2290–16 procedure A), and low-velocity impact tests at 5, 10, 15 J, energy levels were carried out. The effect of hydrothermal aging on neat and MWCNT added epoxy composite had been examined by considering the aging period. Consequently, the impact resistance of neat and MWCNT added samples decreased with the aging process. Besides, tangential tensile strength loss was 17% in MWCNT reinforced sample and 13% in the neat sample.

     

Incorporation of pyridinic and graphitic N to Ni@CNTs: As a competent electrocatalyst for hydrogen evolution reaction

Cheap production of hydrogen (H₂) from eco-friendly routes is preeminent for solving future energy challenges. This study explores the hydrogen evolution reaction (HER) activity of nickel (Ni) nanoparticles and nitrogen doped carbon nanotubes (NiNCNTs), which are fabricated by a cheap and one-step pyrolysis method. The most active catalyst synthesized at 800°C exhibits an overpotential of 0.244 V to reach a current density of 10 mA cm⁻², Tafel slope of 93.3 mV dec⁻¹ and a satisfactory 10 hours stability. Low resistance and large ECSA value of the sample also favor the competent response for HER in alkaline media. The robust HER activity of the catalyst is as a result of the nickel nanoparticles which are the active spots of reaction; while the presence of well-developed nitrogen containing carbon nanotubes with large content of pyridinic and graphitic nitrogen may provide high-electron density and feasible routes for its transportation to deliver an outstanding HER performance.     

Predicting catastrophic temperature changes based on past events via a CNN-LSTM regression mechanism

Neural Computing and Applications - The modelling and prediction of extreme temperature changes in enclosed compartments is a domain with applications ranging from residential fire alarms,...     

In Situ Liquid-Cell TEM Observation of Multiphase Classical and Nonclassical Nucleation of Calcium Oxalate

Calcium oxalate (CaOx) is the major phase in kidney stones and the primary calcium storage medium in plants. CaOx can form crystals with different lattice types, water contents, and crystal structures. However, the conditions and mechanisms leading to nucleation of particular CaOx crystals are unclear. Here, liquid-cell transmission electron microscopy and atomistic molecular dynamics simulations are used to study in situ CaOx nucleation at different conditions. The observations reveal that rhombohedral CaOx monohydrate (COM) can nucleate via a classical pathway, while square COM can nucleate via a non-classical multiphase pathway. Citrate, a kidney stone inhibitor, increases the solubility of calcium by forming calcium-citrate complexes and blocks oxalate ions from approaching calcium. The presence of multiple hydrated ionic species draws additional water molecules into nucleating CaOx dihydrate crystals. These findings reveal that by controlling the nucleation pathways one can determine the macroscale crystal structure, hydration state, and morphology of CaOx.     

Fabrication and Characterization of Nanostructured AACVD Thin Films on 316L SS as Surface Protective Layers in Simulated Body Fluid

Metallurgical and Materials Transactions A - The surface of implant materials is one of the most significant factors for controlling the interaction between biomaterials and bone tissues. Hence,...     

An experimental study for determination of the effects of machining parameters on surface roughness in electrical discharge machining (EDM)

Electrical discharge machining (EDM) is a non-traditional production method that has been widely used in the production of dies throughout the world in recent years. The most important performance measure in EDM is the surface roughness; among other measures material removal and tool wear rates could be listed. In this study, experiments were performed to determine parameters effecting surface roughness. The data obtained for performance measures have been analyzed using the design of experiments methods. A considerably profound equation is obtained for the surface roughness using power, pulse time, and spark time parameters. The results are discussed.     

Chemical Design of Palladium‐Based Nanoarchitectures for Catalytic Applications

Palladium (Pd) plays an important role in numerous catalytic reactions, such as methanol and ethanol oxidation, oxygen reduction, hydrogenation, coupling reactions, and carbon monoxide oxidation. Creating Pd‐based nanoarchitectures with increased active surface sites, higher density of low‐coordinated atoms, and maximized surface coverage for the reactants is important. To address the limitations of pure Pd, various Pd‐based nanoarchitectures, including alloys, intermetallics, and supported Pd nanomaterials, have been fabricated by combining Pd with other elements with similar or higher catalytic activity for many catalytic reactions. Herein, recent advances in the preparation of Pd‐based nanoarchitectures through solution‐phase chemical reduction and electrochemical deposition methods are summarized. Finally, the trend and future outlook in the development of Pd nanocatalysts toward practical catalytic applications are discussed.