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Nanocatalysis using metal nanoparticles constitutes one of the emerging technologies for destructive oxidation of organics such as dyes. This paper deals with the degradation of acid red-26 (AR-26), an azo dye by hexacyanoferrate (abbreviated as HCF) (III) using iridium nanoparticles. UV-vis spectroscopy has been employed to obtain the details of the oxidative degradation of the selected dye. The effect of various operational parameters such as HCF(III) concentration, pH, initial dye concentration, catalyst and temperature was investigated systematically at the λ, 507 nm, of the reaction mixture. Degradation kinetics follows the first order kinetic model with respect to AR-26 and Ir nano concentrations, while with respect to the HCF(III) concentration reaction it follows first order kinetics at lower concentrations, tending towards zero order at higher concentrations. Thermodynamic parameters have been calculated by studying the reaction rate at four different temperatures. The UV-vis, high performance liquid chromatography (HPLC), liquid chromatography-mass spectrometry (LC-MS) analysis of degradation products showed the formation of carboxylic acid and substituted carboxylic acids as major degradation products, which are simple and less hazardous compounds. The big advantage of the present method is the recovery and reuse of iridium nanoparticles. Moreover, turnover frequencies for each catalytic cycle have been determined, indicating the long life span of Ir nanoparticles. Thus, the finding is a novel and highly economical alternative for environmental safety against pollution by dyes, and extendable for other contaminants as well.
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http://dx.doi.org/10.2166/wst.2016.330 | DOI Listing |
Adv Mater
September 2025
Department of Neurosurgery, Qilu Hospital and Shandong Key Laboratory of Brain Health and Function Remodeling, Institute of Brain and Brain-Inspired Science, Jinan Microecological Biomedicine Shandong Laboratory, Cheeloo College of Medicine, Shandong University, 107 Wenhua Xi Road, Jinan, Shandong,
Innate immunity is crucial in orchestrating the brain immune response, however, glioblastoma multiforme (GBM) has evolved sophisticated mechanisms to evade innate immune surveillance, posing significant challenges for current immunotherapies. Here, a therapeutic strategy is reported that aims at reactivating innate immune responses in GBM via targeted induction of mitochondrial stress, thereby enhancing tumor immunogenicity. Specifically, innate immune-stimulating nanoparticles (INSTNA) are developed, encapsulating positively charged iridium-based complexes (Ir-mito) and small interfering RNA against Methylation-Controlled J protein (si-MCJ) to attenuate mitochondrial respiration.
View Article and Find Full Text PDFNat Commun
September 2025
State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry, Jilin University, Changchun, China.
The dynamic reconstruction of oxygen evolution electrocatalysts dictates their performance, yet conventional Ir-based materials face an inherent activity-stability trade-off due to surface amorphization into hydrous IrO phases accompanied by lattice oxygen mechanisms. Here, we uncover a distinct reconstruction pathway for supported Ir nanoparticles, where a TiO@Ti substrate drives a bulk phase transition from metallic Ir to crystalline rutile IrO during electrocatalysis. Unlike surface-limited amorphization, this support-guided crystallization shifts the reaction mechanism from involving lattice oxygen mechanism to the complete adsorbate evolution mechanism, as confirmed by mechanistic and structural analyses.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2025
State Key Laboratory of Synergistic Chem-Bio Synthesis, School of Chemistry and Chemical Engineering, Frontiers Science Center for Transformative Molecules, State Key Laboratory of Micro-Nano Engineering Science, Shanghai Jiao Tong University, Shanghai, 200240, China.
Although being considered as a promising alternative to iridium-based catalysts in proton exchange membrane water electrolysis (PEM-WE), cost-effective ruthenium (Ru)-based anodic catalysts generally lack sufficient stability for harsh operating conditions. Here, we developed a facile method to fabricate erect nanoarrays of interweaved nanorods of zirconium-doped ruthenium oxide (ZrRuO) for long-term industrial-level oxygen evolution reaction (OER). This is accomplished by the spontaneous and abundant accumulation of Ru nanoparticles and Zr ions in pyridine-rich micellar brushes through coordination interactions, followed by direct calcination in air.
View Article and Find Full Text PDFAnal Chim Acta
October 2025
College of Chemistry and Materials Engineering, Anhui Science and Technology University, Bengbu, 233030, PR China; Anhui Province Quartz Sand Purification and Photovoltaic Glass Engineering Research Center, Chuzhou, 233100, PR China. Electronic address:
Exploring the internal relationship between the structure and properties of AIE-active iridium complexes and their applications have been great significance. It is imperative to acknowledge that the precise control of nanoparticle morphology and particle size of organic molecules in solutions remains elusive, while comprehending the luminescent mechanisms of self-assembled aggregates continues to present a challenge. The previously work proposed that solvent-induced amphiphilic molecules could enhance the self-assembly properties of iridium complexes, but the influence of ligands' hydrophilic-lipophilic interactions on the AIE characteristics of iridium complexes remained unclear.
View Article and Find Full Text PDFAdv Mater
August 2025
MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, Guangdong Basic Research Center of Excellence for Functional Molecular Engineering, School of Chemistry, Sun Yat-Sen University, Guangzhou, 510275, P. R. China.
The clinical translation of photodynamic therapy (PDT) faces dual challenges of tumor hypoxia and antioxidant defense mechanisms. To address these limitations, herein tumor microenvironment (TME)-adaptive nanoparticles are rationally designed that enable oxygen-independent PDT while reprogramming immunosuppressive TME. An Ir(III) complex (Ir1) is engineered to achieve copper-mediated and glutathione (GSH)-activated switching of photodynamic modes from oxygen-dependent Type II to hypoxia-tolerant Type I PDT via coordination-induced modulation of electron transfer.
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