Effects of upholstery materials on the burning behavior of real‐scale residential upholstered furniture mock‐ups

Fire spread and growth on real‐scale four cushion mock‐ups of residential upholstered furniture (RUF) were investigated with the goal of identifying whether changes in five classes of materials (barrier, flexible polyurethane foam, polyester fiber wrap, upholstery fabric, and sewing thread), referred to as factors, resulted in statistically significant changes in burning behavior. A fractional factorial experimental design plus practical considerations yielded a test matrix with 20 material combinations. Experiments were repeated a minimum of two times. Measurements included fire spread rates derived from video recordings and heat release rates (HRRs). A total of 13 experimental parameters (3 based on the videos and 10 on the HRR results), referred to as responses, characterized the measurements. Statistical analyses based on Main Effects Plots (main effects) and Block Plots (main effects and factor interactions) were used. The results showed that three of the factors resulted in statistically significant effects on varying numbers of the 13 responses. The Barrier and Fabric factors had the strongest main effects with roughly comparable magnitudes. Foam was statistically significant for fewer of the responses and its overall strength was weaker than for Barrier and Fabric. No statistically significant main effects were identified for Wrap or Thread. Multiple two‐term interactions between factors were identified as being statistically significant. The Barrier*Fabric interaction resulted in the highest number of and strongest statistically significant effects. The existence of two‐term interactions means that it will be necessary to consider their effects in approaches designed to predict the burning behavior of RUF.     

Segmental Baffles as a Means of Improving the Heat Transfer Efficiency of Air Coolers

Chemical and Petroleum Engineering - A comparative analysis of the main types of air coolers (ACs) is presented. Their advantages and disadvantages are indicated along with the main approaches for...     

In Between the $$LQG/H_{2}$$ - and $$H_{\infty } $$ -Control Theories

Automation and Remote Control - In this survey, we discuss various approaches to control theory that have arisen in the recent decades and reflect the desire to reach a trade-off between the $$LQG...     

A benzoate coprecipitation route for synthesizing nanocrystalline GDC powder with lowered sintering temperature

Electrolyte powders with low sintering temperature and high-ionic conductivity can considerably facilitate the fabrication and performance of solid oxide fuel cells (SOFCs). Gadolinia-doped ceria (GDC) is a promising electrolyte for developing intermediate- and low-temperature (IT and LT) SOFCs. However, the conventional sintering temperature for GDC is usually above 1200 °C unless additives are used. In this work, a nanocrystalline powder of GDC, (10 mol% Gd dopant, Gd_0.1Ce_0.9O_1.95) with low-sintering temperature has been synthesized using ammonium benzoate as a novel, environmentally friendly and cost-effective precursor/precipitant. The synthesized benzoate powders (termed washed- and non-washed samples) were calcined at a relatively low temperature of 500 °C for 6 h. Physicochemical characteristics were determined using thermal analysis (TG/DTA), Raman spectroscopy, FT-IR, SEM/EDX, XRD, nitrogen absorptiometry, and dilatometry. Dilatometry showed that the newly synthesized GDC samples (washed and non-washed routes) start to shrink at temperatures of 500 and 600 °C (respectively), reaching their maximum sintering rate at 650 and 750 °C. Sintering of pelletized electrolyte substrates at the sintering onset temperature for commercial GDC powder (950 °C) for 6 h, showed densification of washed- and non-washed samples, obtaining 97.48 and 98.43% respectively, relative to theoretical density. The electrochemical impedance spectroscopy (EIS) analysis for the electrolyte pellets sintered at 950 °C showed a total electrical conductivity of 3.83 × 10^?2 and 5.90 × 10^?2 S cm^?1 (under air atmosphere at 750 °C) for washed- and non-washed samples, respectively. This is the first report of a GDC synthesis, where a considerable improvement in sinterability and electrical conductivity of the product GDC is observed at 950 °C without additives addition.     

Low-cost and high-performance 3D printed YBCO superconductors

High-performance YBCO 123 (YBa₂Cu₃O_7-x) bulk superconductor samples were produced using the 3D printing paste-extrusion technique. The YBCO powder obtained after sintering a pre-mixture of Y₂O₃, BaCO₃ and CuO powders at 950 °C was used in the formulation of pastes for extrusion in a 3D freeform printer. The 3D samples printed from pastes containing the pre-mixture powders were sintered, while those produced using the YBCO powder were not. X-ray diffraction (XRD), energy dispersive spectroscopy (EDS) and Raman analysis all confirmed the YBCO phase after sintering, both in the powder and in the samples made with the pre-mixture. Scanning electron microscopy (SEM) images revealed powder grains of heterogeneous size and geometry, as well as grain aggregation, in the sintered samples. Superconducting quantum interference device (SQUID) measurements taken within a fixed magnetic range revealed that the printed pieces have a typical magnetization temperature of 92 K, reaching ?1.43 emu/g and ?1.59 emu/g respectively a zero-field-cooled magnetization (ZFC) for sintered and non-sintered printed samples.     

Structural,ferroelectric, magnetic and magnetoelectric properties of (1-x) Ba0.85Ca0.15Zr0.1Ti0.9O3 -x La0.67Sr0.33MnO3 lead-free magnetoelectric composites

The influence of an additional La_0.67Sr_0.33MnO₃ (LSMO) magnetic phase on the structural, ferromagnetic, ferroelectric, and magnetoelectric properties of Ba_0.85Ca_0.15Zr_0.1Ti_0.9O₃ (BCZT) ferroelectric phase was studied for composites of (1-x)BCZT -xLSMO (x = 0, 25, 50, 75 and 100%). The ferroelectric BCZT sample showed a perovskite single phase formation with a tetragonal crystal structure of the P4mm space group, and the magnetic phase of LSMO presented a rhombohedral crystal structure of R3c space group as shown by XRD. The composite sample with 25% LSMO exhibited large ferroelectric and piezoelectric properties with remnant, saturation polarization, and coercive electric field P_r ~7.74 μC/cm², P_s ~11.69 μC/cm² and E_C ~12.22 kV/cm with a piezoelectric coefficient d₃₃ ~ 231 pC/N. The magnetic characterization for the composites showed that the sample containing 75% of LSMO revealed the highest remnant, saturation magnetization, and coercive field of M_r ~1.358 emu/g, M_s ~19.17 emu/g, and H_C ~33.19 Oe, respectively. Moreover, it revealed the largest magnetoelectric coupling coefficient α_ME ~2.51 mV/cm.Oe with high coupling quality at a lower applied magnetic field. The results highlight the value of these composites as lead-free room temperature magnetoelectric sensors and actuators.     

Crack-free caustic magnesia-bonded refractory castables

A growing interest in designing high-alumina MgO-bonded refractory castables has been identified in recent years due to the magnesia ability to react: (i) with water at the initial processing stages of these materials (inducing the precipitation of brucite phase) or (ii) with alumina, giving rise to in situ MgAl₂O₄ generation at high temperatures. Nevertheless, despite the great potential of caustic magnesia to be used as a binder in such systems due to its high reactivity, it is still a challenge to control the hydration reaction rate of this oxide and the negative effects derived from the expansive feature of Mg(OH)₂ formation. Thus, this work evaluated the incorporation of different contents of aluminum hydroxyl lactate (AHL) into caustic magnesia-bonded castables, aiming to control the brucite precipitation during the curing and drying steps of the prepared samples, resulting in crack-free refractories. The designed compositions were characterized via flowability, setting behavior, X-ray diffraction, cold flexural strength, porosity, permeability and thermogravimetric measurements. According to the results, instead of Mg(OH)₂, hydrotalcite-like phases [Mg₆Al₂(OH)₁₆(OH)₂.4.5H₂O and Mg₆Al₂(OH)₁₆(CO₃)·4H₂O] were the main hydrated phases identified in the AHL-containing compositions. The addition of 1.0 wt% of aluminum hydroxyl lactate to the designed castable proved to be, so far, the best option for this magnesia source, resulting in the development of a crack-free refractory with enhanced properties and greater spalling resistance under heating.     

Review on recent advances of zinc substituted cobalt ferrite nanoparticles: Synthesis characterization and diverse applications

Researchers have taken a prodigious consideration in characterizing and synthesizing zinc substituted cobalt ferrite nanoparticles because of their substantial applications across diverse technological and industrial fields. Zinc substituted cobalt ferrite nanoparticles are a class of lenient magnetic nanomaterials, which have potentially high magnetic, optical, electrical, and dielectric properties. These properties include a high value of permeability, low power losses, permittivity, saturation magnetization, coercivity, resistivity, and other beneficial properties that make them promise candidates for applications in various fields. These ferrites are also used in biomedical areas such as MRI and cancer treatments. In electronic fields, zinc substituted cobalt ferrite nanoparticles are used to make transducers, transformers, biosensors, and sensors. Apart from these advantages, they are found in our everyday electronic and electrical appliances like LED bulb, refrigerator, mobile charger, TV, microwave oven, juicer, washing machine, mixer, iron, printer, laptop, mobile, desktop, etc. Hence, the current review reports some properties of these spinel ferrites and emphasizes the different synthesis techniques that can be used to prepare them. Afterward, the impact of dopant on the materials' properties, the characterization techniques, and the momentous application in the present era have been well discussed.     

Efficient sunlight and UV photocatalytic degradation of Methyl Orange,Methylene Blue and Rhodamine B,using Citrus×paradisi synthesized SnO2 semiconductor nanoparticles

In this work, tin dioxide (SnO2) Nanoparticles (NPs) were synthesized through green synthesis, using Citrus × paradisi extract as a stabilizing (capping). The extract concentrations used were 1, 2 and 4% in relation to the aqueous solution. The resulting SnO2 NPs were used for the degradation of Methyl Orange (MO), Methylene Blue (MB) and Rhodamine B (RhB), under both solar and UV radiation. The NPs were characterized via Attenuated Total Reflectance Infrared Spectroscopy (ATR-IR), X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM-SAED), the Brunauer-Emmett-Teller (BET) theory, Ultraviolet to Visible spectroscopy (UV–Vis), and Photoluminescence spectroscopy (PL); while the photocatalytic degradation was evaluated using UV-VIS. The results showed that the Citrus × paradisi extract is a good medium for the formation of SnO2 NPs. These NPs presented quasi-spherical morphology, particle sizes of 4–8 nm, with a rutile phase crystalline structure, and with banned gap of 2.69 at 3.28 eV. The NPs had excellent photocatalytic properties under solar radiation, degrading 100% of the OM in 180 min. Furthermore, under UV radiation, 100% degradation of the three dyes was achieved in a short time; 20 min for MO, and 60 min for MB and RhB. Therefore, green synthesis is a feasible medium for the formation of SnO2 NPs with good photocatalytic properties.