Fabrication of silver nanoparticles dispersed in palm oil using laser ablation

In this study we used a laser ablation technique for preparation of silver nanoparticles. The fabrication process was carried out by ablation of a silver plate immersed in palm oil. A pulsed Nd:YAG laser at a wavelength of 1064 nm was used for ablation of the plate at different times. The palm coconut oil allowed formation of nanoparticles with very small and uniform particle size, which are dispersed very homogeneously within the solution. The obtained particle sizes for 15 and 30 minute ablation times were 2.5 and 2 nm, respectively. Stability study shows that all of the samples remained stable for a reasonable period of time.     

Numerical analysis of the influence of two-phase flow mass and heat transfer on n-heptane autoignition

This paper investigates the influence of liquid fuel presence on the autoignition of n-heptane/air mixtures over a wide range of conditions encountered in internal combustion engines. To this end, evaporating droplet physics and skeletal chemistry mechanisms are simultaneously solved considering a homogeneous constant-pressure reactor. A skeletal mechanism is introduced to account for specific kinetics behavior in the Negative Temperature Coefficient (NTC) region. The impact of mass and heat source terms during evaporation is emphasized by comparing a two-phase flow scenario with a purely gaseous case. The competition between fuel vapor availability and the evaporation-induced gas temperature decrease is specific to two-phase flow autoignition. On the one hand, droplet evaporation delay restricts the gaseous local fuel/air equivalence ratio and consequently the kinetics runaway. On the other hand, temperature reduction due to evaporation may either reduce or enhance chemical reactivity, depending on the local thermodynamic conditions lying either inside or outside the NTC region. By simultaneously accounting for evaporation source terms and skeletal chemistry, we can reproduce the already experimentally observed transformation of the NTC region into a Zero Temperature Coefficient (ZTC) region depending on thermodynamic conditions and droplet size. The ZTC phenomenon appears when combustion heat-release starts before complete droplet evaporation. Since the ZTC behavior can be captured using the point source approach, in which droplets are considered only as zero-dimensional source terms of mass and energy, the present results pave the way for future exploration of NTC chemistry in sprays with a direct numerical simulation of discrete particles considering detailed chemistry and turbulent flows.     

Structure and Dynamic Mechanical Properties of Melt Intercalated Polyamide 6—Montmorillonite Nanocomposites

Summary: Polymer‐layered silicate nanocomposites (PLSN), based on polyamide 6 (PA6) and montmorillonite (MMT) modified with an octadecylammonium salt, were produced via melt compounding in a co‐rotating twin‐screw extruder. Wide angle X‐ray diffraction (WAXD) and TEM revealed a PLSN containing 3.3% by weight (wt.‐%) of MMT to exhibit a mixed exfoliated/intercalated morphology, consisting mainly of individual silicate lamellae together with some intercalated stacks, resulting in a mean value of 1.8 lamellae per particle. In contrast, a PLSN containing a higher level of 7.2 wt.‐% MMT exhibited a more ordered intercalated structure, consisting mainly of a distribution of lamellae stacks with a mean value of 3.8 lamellae per particle. The dispersion of MMT in the PLSN generated very large polymer–filler interfacial areas, resulting in significant increase in the volume of constrained PA6 chain segments. Consequently, significant changes in the ratio of α/γ crystallites and in the thermal behaviour of the matrix PA6 were observed during WAXD, DSC and dynamic‐mechanical thermal analysis (DMTA) studies of the PLSN. In particular, damping data from DMTA showed relaxations between T_g and T_m resulting from amorphous polymer chain segments constrained at the polymer–filler interface, indicating the formation of a continuous phase of constrained polymer. In contrast, a PA6 microcomposite formed using unmodified MMT generated much lower polymer–filler interfacial area, with most of the MMT residing within large, poorly wetted aggregates. Consequently, changes to the thermal behaviour of the matrix PA6 were much less significant than those induced in the PLSN.

Shear storage modulus (G′) versus temperature data for the matrix PA6, the 5T and 10T PLSN and the 5P microcomposite.     

n-Hexane hydroisomerization over Zr-modified bicontinuous lamellar silica mordenite supported Pt as highly selective catalyst: Molecular hydrogen generated protonic acid sites and optimization

Zr-modified bicontinuous lamellar silica mordenite supported Pt catalysts were synthesized using the zirconyl chloride oxahydrate as the precursor for Zr species by the incipient wetness impregnation method. The influence of zirconium loading on the properties of Zr-modified HM@KCC-1 catalysts for n-hexane isomerization were studied. The results of XRD and lattice structure from IR study indicated that increasing zirconium loading did not change the properties of catalysts. The IR study with pre-adsorbed 2,6-dimethylpyridine as a probe molecule affirmed that increasing zirconium loading could increase the Lewis acid sites. The generation of protonic acid sites which were active in n-hexane hydroisomerization was mainly from molecular hydrogen through a hydrogen spill-over mechanism as established by in situ-IR study. The results for the catalytic testing indicated that PtZr/HM@KCC-1 catalyst was highly selective in n-hexane hydroisomerization due to abundant permanent Lewis acid sites for its promotive effect in the generation of protonic acid sites. However, the incorporation of excessive zirconium amount up to 10 wt percent loading led to a decline in the amount of protonic acid sites generated, thus reduced the hydroisomerization performance in the process. The optimum conditions for hydroisomerization of n-hexane over Pt5Zr/HM@KCC-1 were reaction temperature of 293 °C, treatment temperature of 474 °C and F/W of 502 mL/g.min with the predicted value for isomer yield of 83.9%.     

Evaluation of Quaternized polyvinyl alcohol/graphene oxide-based membrane towards improving the performance of air-breathing passive direct methanol fuel cells

Graphene oxide (GO) nanosheets are introduced to a Quaternized polyvinyl alcohol (QPVA) polymer matrix to obtain an anion exchange membranes (AEMs) for application of fuel cells. QPVA/GO nanocomposite membranes provide desirable properties such as low fuel uptake and permeability, excellent ionic conductivity, and cell performance, all of which are favorable for AEMs based on our previous works. Passive direct methanol fuel cells (DMFCs) are recognized as suitable technologies for use in portable devices. Nevertheless, the commercialization of DMFCs remains restricted due to a number of issues related to the conventional membrane; one of these issues is high fuel crossover problems due to high fuel uptake and permeability of Nafion membrane. This study aimed to expand the potential applications of QPVA/GO nanocomposite membranes in air-breathing passive DMFCs. The ionic conductivity, methanol uptakes (MUs), and permeabilities of self-synthesis QPVA/GO nanocomposites are examined to evaluate the ability to operate in methanol atmosphere. At 30°C, the ionic conductivity of the membranes reached 1.74 × 10⁻² S cm⁻¹. The MUs and permeabilities were as low as 35% and 7.6 × 10⁻⁷ cm² s⁻¹, respectively. The performance of air-breathing passive DMFCs bearing QPVA/GO nanocomposite membrane is much higher compared to conventional membranes. The maximum power density of air-breathing passive DMFCs was achieved 27.2 mW cm⁻² under the optimum condition of 2 M methanol + 4 M KOH at 70°C. Single-cells could be sustained for 1000 hours. This article is the first to optimize and highlight the performance air-breathing passive DMFCs by using a QPVA-based membrane.     

Preparation of asymmetric polysulfone/polyimide blended membranes for CO<Subscript>2</Subscript> separation

Asymmetric Flat sheet polysulfone-polyimide (PSF-PI) blended polymeric membranes (with PI content from 5–20%) have been fabricated following phase inversion technique. The membranes have been thoroughly characterized by the measurement of porosity, mechanical properties and also by SEM, FTIR and DSC analyses. With the increase in the PI content, the mechanical properties of the membranes, like Young’s modulus, tensile strength and elongation at break, increased. SEM investigations revealed that the surfaces of fabricated blended membranes possessed adequate homogeneity and their cross-sections showed non-porous top and diminutive porous substructure. From DSC analyses it has been observed that different compositions of the blended membranes exhibited single glass transition temperatures, implying proper compatibility of the polymers. The permeance of CO₂ and CH₄ through the membrane increased with the increase in PI content and it gradually decreased with the increase in the feed pressure in the range of 2–10 bar. Under the present investigation, the membrane with 20% PI content exhibited the maximum selectivity for the separation of CO₂/CH₄ gas mixes.     

Functional cellulose fibers via polycarboxylic acid/carbon nanotube composite coating

In this study, carbon nanotubes (CNTs) were stabilized on a cotton surface using 1,2,3,4-butanetetracarboxylic acid (BTCA) as a crosslinking agent and sodium hypophosphite as a catalyst. The influence of CNTs on the performance of the cellulose fiber was investigated using a Raman spectrophotometer, thermogravimetric analyzer, a scanning electron microscope, electrical contacting equipment, and an electromagnetic field detector. The possible interactions between CNTs, a crosslinking agent, and cellulose functional groups at the surface were elucidated by Raman spectroscopy. The results indicate that the stabilized CNTs modify the surface of the fibers and increase the functionality and thermal stability of the substrate. SEM showed a uniform coating of CNTs on the fiber surface.     

Risk-Based Design of Flood Control Systems Considering Multiple Dependent Uncertainties

Due to random behavior of flood events and inaccuracies in measurements, design, analysis, and operation of flood control systems are subjected to several uncertainties. An important aspect in developing stochastic models for evaluating and analyzing more than one uncertainty is the dependence or independence of them. In flood control projects, hydrologic, hydraulic, geotechnical, and economic uncertainties are important considerations. In this paper, a stochastic Monte-Carlo simulation – optimization modeling approach is described for risk-based design of flood control levees (as a common structural flood control measure): considering multiple dependent uncertainties. It has been applied to the Leaf River reach in Hattiesburg, Mississippi for testing and evaluation of modeling results. Unlike a deterministic model that yields just one set of values for system dimensions, the stochastic model solution gives a range of values for each of them. One of the major reasons for limited field application of uncertainty analysis is difficulties in performing the modeling results in real world contexts. For closing the gap between theory and reality, design charts are developed in this study. This helps decision makers in identifying design values with desired and accepted risks.     

Performance of quaternized poly(vinyl alcohol)-based electrolyte membrane in passive alkaline DEFCs application: RSM optimization approach

Direct ethanol fuel cells (DEFCs) have emerged as potential tools for producing sustainable energy for portable devices due to their high energy density and their safe and nontoxic fuel source. However, the main problem of DEFCs is the sluggish oxidation of ethanol and fuel crossover from the anode side to the cathode side. Nafion membranes are commonly used as the electrolyte membrane in DEFCs, but they have a high production cost and high ethanol permeability. Thus, this work studies the performance of an alternative electrolyte membrane that is based on a quaternized poly(vinyl alcohol) (QPVA) polymer in passive alkaline DEFCs. The composition of the QPVA-based membranes was optimized with potassium hydroxide (KOH) as an ion charge carrier and by the inorganic filler graphene oxide (GO). The membrane properties were influenced by KOH and GO. The effect of these two parameters on the performance of the QPVA-based membranes was investigated for its ion-exchange capacity and ionic conductivity and selectivity using the response surface methodology to optimize the membrane composition. The QPVA-based membranes were characterized by Fourier transform infrared spectroscopy, X-ray diffraction, and field emission scanning electron microscope. The membrane properties were influenced by KOH concentration doping and GO filler loading, which affect the membrane selectivity and, consequently, the overall performance of the passive alkaline DEFCs. Finally, the maximum power density of the passive DEFCs was improved from 5.8 to 11.3 W cm⁻² at 30 °C, 13.7 mW cm⁻² at 60 °C, and 19.3 mW cm⁻² at 90 °C, respectively, in ambient air. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47526.