Improved hydrogenation kinetics of timn1.52 alloy coated with palladium through electroless deposition

The deterioration of hydrogen charging performances resulting from the surface chemical action of electrophilic gases such as CO2 is one of the prevailing drawbacks of TiMn1.52 materials. In this study, we report the effect of autocatalytic Pd deposition on the morphology, structure, and hydrogenation kinetics of TiMn1.52 alloy. Both the uncoated and Pd-coated materials were characterized using scanning electron microscopy/energy dispersive spectroscopy (SEM/EDS) and X-ray diffraction (XRD). XRD analyses indicated that TiMn1.52 alloy contains C14-type Laves phase without any second phase, while the SEM images, together with a particle size distribution histogram, showed a smooth non-porous surface with irregular-shaped particles ranging in size from 1 to 8 µm. The XRD pattern of Pd-coated alloy revealed that C14-type Laves phase was still maintained upon Pd deposition. This was further supported by calculated crystallite size of 29 nm for both materials. Furthermore, a Sieverts-type apparatus was used to study the kinetics of the alloys after pre-exposure to air and upon vacuum heating at 300 ◦C. The Pd-coated AB2 alloy exhibited good coating quality as confirmed by EDS with enhanced hydrogen absorption kinetics, even without activation. This is attributed to improved surface tolerance and a hydrogen spillover mechanism, facilitated by Pd nanoparticles. Vacuum heating at 300 ◦C resulted in removal of surface barriers and showed improved hydrogen absorption performances for both coated and uncoated alloys

Hydrogen storage behaviours of high entropy alloys: A Review

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Improvement of hydriding kinetics of LaNi5-type metal alloy through substitution of nickel with tin followed by palladium deposition

Hydrogen absorption performances of LaNi5 alloy are sensitive to the surface reactions with poisonous gases, such as oxygen, readily forming oxides/hydroxides. In this study, we report the studies on the hydrogen absorption behaviour of AB5-type hydrogen storage alloys, formed by LaNi(5–x)Snx (X = 0.2) followed by electroless Pd deposition. The uncoated and Pd-coated materials were characterized using scanning electron microscopy/energy dispersive spectroscopy (SEM/EDS), atomic absorption spectroscopy (AAS), X-ray diffraction (XRD) and Brunauer–Emmet–Teller. XRD analyses indicated that both LaNi5 and LaNi4.8Sn0.2 alloys crystallize in CaCu5-type crystal structure, while SEM analysis and particle size distribution histograms showed increment in particle size upon Sn incorporation. Palladium particles on the surface of the materials were detected by AAS and EDS analyses. Furthermore, substitution of a small fraction of Ni by Sn leads to an increase in hydrogen absorption capacity even without activation. Moreover, a decrease in hydrogen absorption rate was observed for LaNi4.8Sn0.2 alloy and this was related to an increment in the crystalline unit cell volume. Kinetic curves of Pd-coated alloys show superior absorption kinetics compared to their uncoated counterparts due to high affinity of Pd for hydroge

Polyaniline-Based Nanocomposites for Environmental Remediation

With growth in civilisation and industrialisation, there is an increase in the release of toxic heavy metal ions and dyes into water system, which is of public concern. As a result, appropriate treatment methods have to be implemented in order to mitigate and prevent water pollution. The discovery of nanotechnology has led to the development and utilisation of various nanoadsorbent for the removal of pollutants from water. PANI nanostructures and nanocomposites are noble adsorbents that have gained popularity in addressing water pollution issues and have been reported in literature. In this chapter, the main focus is on the synthesis of PANI nanocomposites and nanostructures and their application as efficient adsorbents for water treatment. Detailed discussions on different synthetic routes and characterisation have been dedicated to applications of these materials and are compared for the adsorptive removal of heavy metal ions and dyes from water

Highlighting the Importance of Characterization Techniques Employed in Adsorption Using Metal–Organic Frameworks for Water Treatment

The accumulation of toxic heavy metal ions continues to be a global concern due to their adverse effects on the health of human beings and animals. Adsorption technology has always been a preferred method for the removal of these pollutants from wastewater due to its cost-effectiveness and simplicity. Hence, the development of highly efficient adsorbents as a result of the advent of novel materials with interesting structural properties remains to be the ultimate objective to improve the adsorption efficiencies of this method. As such, advanced materials such as metal–organic frameworks (MOFs) that are highly porous crystalline materials have been explored as potential adsorbents for capturing metal ions. However, due to their diverse structures and tuneable surface functionalities, there is a need to find efficient characterization techniques to study their atomic arrangements for a better understanding of their adsorption capabilities on heavy metal ions. Moreover, the existence of various species of heavy metal ions and their ability to form complexes have triggered the need to qualitatively and quantitatively determine their concentrations in the environment. Hence, it is crucial to employ techniques that can provide insight into the structural arrangements in MOF composites as well as their possible interactions with heavy metal ions, to achieve high removal efficiency and adsorption capacities. Thus, this work provides an extensive review and discussion of various techniques such as X-ray diffraction, Brunauer–Emmett–Teller theory, scanning electron microscopy and transmission electron microscopy coupled with energy dispersive spectroscopy, and X-ray photoelectron spectroscopy employed for the characterization of MOF composites before and after their interaction with toxic metal ions. The review further looks into the analytical methods (i.e., inductively coupled plasma mass spectroscopy, ultraviolet-visible spectroscopy, and atomic absorption spectroscopy) used for the quantification of heavy metal ions present in wastewater treatment

Ethylenediamine functionalized waste polyethylene terephthalate-derived metal-organic framework for adsorption of palladium ions from aqueous solutions

The recovery of palladium metal is essential in order to meet its growing global demand and also to address water pollution crisis. Herein, MIL-101(Cr)/ED was fabricated from waste polyethylene terephthalate (PET) bottles and modified using ethylenediamine (ED) to retrieve divalent palladium (Pd(II)) metal ions from aqueous environment. The successful grafting of ED moieties onto MIL-101(Cr) was established by the appearance of broad bands at around 2800–3300 cm−1 on the Fourier transform infrared spectrum which was supported by the increase in binding energy using density functional theory. The adsorption experiments revealed that higher Pd(II) ion intake occurred using 30 mg of MIL-101(Cr)/ED in acidic media of pH = 3.0. The data fit better on the Langmuir isotherm with the correlation coefficient (R2) 0.9089. At 25 °C, the MIL-101(Cr)/ED achieved a substantial enhancement in the intake capacities of 454.2 mg.g−1. Kinetics data demonstrated to comply with pseudo-second order, achieving a rapid rate of Pd(II) adsorption by the MIL-101(Cr)/ED in less than 3 min given by the rate constant k2 = 0.02065 g.mg−1.min−1. The MIL-101(Cr)/ED has high affinity for Pd(II) ions as more than 80% removal was achieved even in presence of other ions. These observations revealed the potential utilization of MIL-101(Cr)/ED as an adsorbent to efficiently extract Pd(II) ions from wastewater

Improved Hydrogenation Kinetics of TiMn1.52 Alloy Coated with Palladium through Electroless Deposition

The deterioration of hydrogen charging performances resulting from the surface chemical action of electrophilic gases such as CO2 is one of the prevailing drawbacks of TiMn1.52 materials. In this study, we report the effect of autocatalytic Pd deposition on the morphology, structure, and hydrogenation kinetics of TiMn1.52 alloy. Both the uncoated and Pd-coated materials were characterized using scanning electron microscopy/energy dispersive spectroscopy (SEM/EDS) and X-ray diffraction (XRD). XRD analyses indicated that TiMn1.52 alloy contains C14-type Laves phase without any second phase, while the SEM images, together with a particle size distribution histogram, showed a smooth non-porous surface with irregular-shaped particles ranging in size from 1 to 8 µm. The XRD pattern of Pd-coated alloy revealed that C14-type Laves phase was still maintained upon Pd deposition. This was further supported by calculated crystallite size of 29 nm for both materials. Furthermore, a Sieverts-type apparatus was used to study the kinetics of the alloys after pre-exposure to air and upon vacuum heating at 300 °C. The Pd-coated AB2 alloy exhibited good coating quality as confirmed by EDS with enhanced hydrogen absorption kinetics, even without activation. This is attributed to improved surface tolerance and a hydrogen spillover mechanism, facilitated by Pd nanoparticles. Vacuum heating at 300 °C resulted in removal of surface barriers and showed improved hydrogen absorption performances for both coated and uncoated alloys