Related Experiment Video
Updated: Mar 7, 2026

Facile Preparation of Ultrafine Aluminum Hydroxide Particles with or without Mesoporous MCM-41 in Ambient Environments
Published on: May 11, 2017
β-alumina and green H2 production from discarded aluminum foil via a novel refined hydrolysis-calcination pathway
Afef Bouazizi1, Salah Jellali2, Imene Bekri-Abbes1
1Laboratory of Composite Materials and Clay Minerals, National Center of Materials Research, Borj Cedria Technopole, University of Carthage, Tunis, Tunisia.
Abstract:
The escalating generation of multilayer packaging waste presents significant environmental challenges due to their complex laminated structure comprising paperboard, polyethylene, and aluminum foil. This study presents a novel integrated hydrolysis-calcination pathway for complete valorization of Aluminun multilayer pakaging waste, achieving simultaneous production of green hydrogen and β-alumina solid electrolyte. Following hot water separation of the paperboard fraction, the LDPE/aluminum laminate undergoes alkaline hydrolysis, generating hydrogen gas with a yield of 97.5% (215 mL from 5.9 g waste) while preserving intact LDPE film for direct mechanical recycling. Kinetic analysis reveals that increasing NaOH concentration reduces activation energy from 26.2 kJ/mol (1M) to 12.7 kJ/mol (4M). The resulting sodium aluminate solution is transformed into pure β-alumina (NaAl₁₁O₁₇) phase via controlled precipitation at pH 9 and calcination at 1000°C. Comprehensive characterization (XRD, SEM-EDS, FTIR, TGA, photoluminescence) confirms good material quality suitable for advanced energy storage applications. This zero-waste process exemplifies circular economy principles, converting challenging multilayer packaging into four high-value products: renewable hydrogen fuel, advanced battery electrolyte material, recycled polymers, and cellulosic feedstock.
Related Concept Videos
Acid Halides to Alcohols: LiAlH4 Reduction
The mechanism proceeds in three steps. First, the nucleophilic hydride ion attacks the carbonyl carbon of the acid halide to form a tetrahedral intermediate. Next, the carbonyl group is re-formed, and the halide ion departs as a leaving group, generating an aldehyde. A second nucleophilic attack by the hydride yields an alkoxide ion, which, upon protonation, gives a primary alcohol as...
Hydroboration-Oxidation of Alkenes
Carboxylic Acids to Primary Alcohols: Hydride Reduction
Reduction of Alkenes: Catalytic Hydrogenation
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
Esters to Alcohols: Hydride Reductions
Lithium aluminum hydride is a source of hydride ions and functions as a nucleophile. The mechanism proceeds in three steps. Firstly, the nucleophilic hydride ion attacks the carbonyl carbon of the ester to form a tetrahedral intermediate. Subsequently, the carbonyl group re-forms,...
Alcohols from Carbonyl Compounds: Reduction
Catalytic hydrogenation is similar to the reduction of an alkene or alkyne by adding H2 across the pi bond in the presence of transition metal catalysts like Raney Ni, Pd–C, Pt, or Ru. Aldehydes and ketones can be reduced by this method, often under mild to moderate heat (25–100°C) and...

