In solar heating, ventilation, and air conditioning (HVAC), communications are designed to create new 3D mathematical models that address the flow of rotating Sutterby hybrid nanofluids exposed to slippery and expandable seats. The heat transmission investigation included effects such as copper and graphene oxide nanoparticles, as well as thermal radiative fluxing. The activation energy effect was used to investigate mass transfer with fluid concentration. The boundary constraints utilized were Maxwell speed and Smoluchowksi temperature slippage. With the utilization of fitting changes, partial differential equations (PDEs) for impetus, energy, and concentricity can be decreased to ordinary differential equations (ODEs). To address dimensionless ODEs, MATLAB’s Keller box numerical technique was employed. Graphene oxide Copper/engine oil (GO-Cu/EO) is taken into consideration to address the performance analysis of the current study. Physical attributes, for example, surface drag coefficient, heat move, and mass exchange are mathematically processed and shown as tables and figures when numerous diverse factors are varied. The temperature field is enhanced by an increase in the volume fraction of copper and graphene oxide nanoparticles, while the mass fraction field is enhanced by an increase in activation energy.

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This work entails a detailed modeling and experimental study for the oxidation kinetics of acetaldehyde (CH3CHO) and its interaction with NO x . The ignition behavior of CH3CHO/O2/Ar has been investigated in a shock tube over the temperature range of 1149 to 1542 K, with equivalence ratios of 0.5 and 1.0 and pressures near 1.2 bar. Absorbance–time profiles of acetaldehyde were recorded using a mid-IR laser during the autoignition measurements. A comprehensive kinetic model has been developed to quantitatively predict the oxidation of acetaldehyde and its interaction with NO x . The kinetic model has been validated using experimental data of this work and available literature data from shock tube, plug flow, and jet-stirred reactors, freely propagating, and burner-stabilized premixed flames. For better accuracy of the kinetic model, the thermochemistry of 14 important species in the acetaldehyde submechanism was calculated using ab initio methods. The heat of formation of these species was computed using atomization and isodesmic reaction schemes. For the first time, this modeling study examines the effect of NO on acetaldehyde oxidation behavior over a wide range of experimental conditions. In most cases, the proposed kinetic model captures the experimental trends remarkably well. Interestingly, the doping of NO in CH3CHO did not perturb the NTC behavior of CH3CHO in contrast to other fuels, such as n-heptane and dimethyl ether. However, for flow reactor conditions at 1 atm, doping with 504 ppm of NO was found to promote the reactivity of acetaldehyde by lowering the onset temperature for CH3CHO oxidation by ∼140 K. The hydroxyl radical is the main cause of this shift, which originates from the NO + HO2 = OH + NO2 reaction. Further evolution of hydroxyl radicals occurs via the “NO–NO2” looping mechanism and expedites the reactivity of the system. This experimental and modeling work sheds new light on acetaldehyde oxidation behavior and its interaction with NO x under combustion-relevant conditions.

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