The recycling of scarce elements such as platinum-group metals is becoming crucial due to their growing importance in current and emerging applications. In this sense, the recovery of palladium and rhodium from a spent auto-catalyst by leaching in HCl/CuCl media was studied, aiming at assessing the kinetic performance as well as the influence of some processing factors, and the behaviour of contaminant metals. Based on a kinetic model developed for the present case, the influence of temperature was evaluated and the corresponding values of activation energy were estimated as 60.1 ± 4.1 kJ mol for Pd and 44.3 ± 7.3 kJ mol for Rh, indicating the relevance of the chemical step rather than diffusion. This finding was corroborated by the non-significant influence of the stirring velocity. The reaction orders were estimated for each leaching reagent: for HCl, values of 2.1 ± 0.1 for Pd and 1.0 ± 0.3 for Rh were obtained; for Cu the obtained values were 0.42 ± 0.04 for Pd and 0.36 ± 0.06 for Rh. Without any significant loss of efficiency, solutions with higher metal concentrations were obtained using lower liquid/solid ratios, such as 5 L/kg. The main contaminant in solution was aluminum, and its leaching was found to be very dependent on the temperature and acid concentration.
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http://dx.doi.org/10.1080/09593330.2018.1563635 | DOI Listing |
Int J Biol Macromol
December 2024
Department of Chemistry, University of Saskatchewan, 110 Science Place, Saskatoon S7N 5C9, SK, Canada. Electronic address:
Precious metal recovery from secondary sources has received significant attention due to the reduced availability of precious metals from conventional sources. Herein, chitosan (CHT) was modified via cross-linking with glutaraldehyde (glu) to yield CHT-glu adsorbents with improved physicochemical and adsorption properties with precious metal ions (Au(III) and Pd(II)). CHT-glu adsorbents were prepared at variable glu ratios and characterized via complementary spectral (IR, C solids NMR, XPS) and thermogravimetry methods.
View Article and Find Full Text PDFHeliyon
December 2024
Department of Chemistry, College of Engineering and Physical Sciences, Khalifa University of Science and Technology, Abu Dhabi, P.O. Box 127788, United Arab Emirates.
Suzuki-Miyaura coupling (SMC), a crucial C-C cross-coupling reaction, is still associated with challenges such as high synthetic costs, intricate work-ups, and contamination with homogeneous metal catalysts. Research intensely focuses on strategies to convert homogeneous soluble metal catalysts into insoluble powder solids, promoting heterogeneous catalysis for easy recovery and reuse as well as for exploring greener reaction protocols. Metal-Organic Frameworks (MOFs), recognized for their high surface area, porosity, and presence of transition metals, are increasingly studied for developing heterogeneous SMC.
View Article and Find Full Text PDFEnviron Res
December 2024
Yanshan Earth Critical Zone and Surface Fluxes Research Station, College of Resources and Environment, University of Chinese Academy of Sciences, Beijing, 100049, China. Electronic address:
N-termini Cyano group (CN) in metal hexacyanoferrates (MHCF) have been identified as specific-affinity sites for palladium (Pd), but C-termini CN do not effectively serve as Pd adsorption sites due to their stronger bonds with the metal ligands (M), which reduces the activity and density of CN. Herein, the optimization of directional coordination of cyano group C/N-termini by modulating the electronic structure of the M (Fe, Co, and Ni) in MHCF was investigated to reinforce the Pd recovery. Spectroscopic analyses and DFT calculations revealed that NiHCF exhibited N-site mono-coordination, whereas CoHCF displayed C-site mono-coordination due to spin-exchange interactions, leading to the strengthened N-Co bonds and weakened Fe-C bonds.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2024
State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources, School of Chemistry and Pharmaceutical Sciences, Guangxi Normal University, Guilin 541004, China; Guangxi Key Laboratory of Environmental Pollution Control Theory and Technology, Guilin 541004, China; Guangxi Key Laboratory of Environmental Processes and Remediation in Ecologically Fragile Regions, Guilin 541004, China. Electronic address:
A new nanopalladium surface molecularly imprinted covalent organic framework (MICOF) catalytic probe (Pd@TpPa) for enrofloxacin (ENR) was synthesized by molecular imprinting technology, using 1,3,5-triformylphloroglucinol (Tp) and p-phenylenediamine (Pa) as monomers, ENR as the template molecule, and palladium nanoparticles (PdNP) as the core of nanocatalytic probe. This nanoprobe not only specifically recognizes ENR but also catalyzes the cupric tartrate-glucose (GL) indicator reaction. The amino groups in TpPa replace the tartrate ions, forming a new complex with Cu.
View Article and Find Full Text PDFACS Omega
December 2024
Departamento de Química Analítica, Instituto de Química, Universidade Federal do Rio de Janeiro, Rio de Janeiro 21941-853, Brazil.
One of the main challenges in animal breeding systems is determining estradiol (E2) in livestock samples as simple and minimally invasive as possible, Thus, a nonenzymatic biosensor screen-printed electrode (SPE) was developed by modifying nanohybrid palladium nanoparticles (PdNPs), and carbon dots anchored on a nanosilica particle (PdNPs/C.dots/SiO), denominated SPE/PdNPs/C.dots/SiO, and successfully tested for the direct detection of estradiol in livestock samples.
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