RSC Advances  

High efficiency hydrocracking degradation of mixed polyolefin polymers is achieved under mild circumstances by Ni-based catalysts supported on Hbeta.

Heat treatment changes the carbon structure, increasing the degree of graphitization and defects. Methane molecules gradually decompose at the graphitized edges of the carbon material (BAY clusters) to form ordered carbon and hydrogen.

Advanced oxidation techniques based on peroxysulfate activation have been paid much attention owing to their excellent performance in degrading stubborn pollutants in water.

The utilization of magnetic nanoparticles in the fields of science and technology has gained considerable popularity.

The cracking of propane molecules via a thermal cracking process, a base-catalyzed process, and a strong-base-catalyzed process was studied by means of catalyst characterization and evaluation of catalyst performance.

The 75In₂O₃–25ZrO₂ forms a solid solution structure, and can achieve 28% CO₂ conversion and 96% CO selectivity during a 200 h-test.

Catalytic hydrogenolysis of 5-hydroxymethylfurfural (HMF) to 2,5-dimethylfuran (DMF) has become a hot topic in the bioenergy field in recent years.

In situ phase transformation is achieved from single-phase Co₃O₄ to CoO/CoP hybrid phases, which acts as a highly efficient electrocatalyst for the hydrogen evolution reaction.

The impact of the active catalyst particle size on the CO₂ hydrogenation and product selectivity is presented using MOF-derived Fe-based catalytic system.

An efficient, green method for one-pot three-component synthesis of pyrimido[1,2-a]benzimidazole and 1-(benzothiazolylamino)methyl-2-naphthol derivatives using a new nanoporous catalyst ZnO@SO₃H@Tropine is reported. Advantages include, but are not limited to, simple work-up and high yields.

Zn doping promotes the formation of oxygen vacancy, which anchors and disperses Ba.

Different reaction routes with the influence of hydrogen bonding and without hydrogen bonding.

A defect-healed layered precursor of FER-type zeolite exhibited enhanced iron atom insertion in more homogeneous environments.

The superior catalytic performance of Pd nanocatalysts in AlOOH-80 is attributed to solid surface frustrated Lewis pairs (ssFLP), which enhance hydrogen gas dissociation, improve Pd nanocatalyst hydrogenation, and result in high catalytic activity of Pd/AlOOH-80.

Assessment of the performance of linear and nonlinear regression-based methods for estimating in situ catalytic CO₂ transformations employing TiO₂/Cu coupled with hydrogen exfoliation graphene (HEG) has been investigated.

We report the synthesis of xNi–yFe/γ-Al₂O₃ catalysts which were applied to the reductive amination of polypropylene glycol (PPG) for the preparation of polyether amine (PEA).

Four distinct CeO₂ catalysts featuring varied morphologies (nanorods, nanocubes, nanoparticles, and nano spindle-shaped) were synthesized through a hydrothermal process and subsequently employed in the oxidation of dichloromethane (DCM).

Interfacial Lewis acid–base pairs are commonly found in ZrO₂-supported metal catalysts due to the facile generation of oxygen vacancies of ZrO₂.

In this work, the effect of alkaline earth metal modification on the catalytic performance of activated carbon supported Cu was investigated.

Sulfur-doped activated carbon has proved to be a promising metal-free catalyst for persulfate (PDS) catalytic activation for the oxidation of aqueous refractory organics.

An efficient route for the construction of acridine-1,8-diones using Fe₃O₄@SiO₂ core/shell functionalized by sulfonated gallic acid as a robust heterogeneous catalyst.

The multicomponent synthesis of 2,4,6-trisubstituted pyridine via acceptorless alcohol dehydrogenation using ammonium acetate as a nitrogen source catalyzed by hydroxyapatite-supported palladium nanoparticles as a heterogeneous catalyst.

Single-atom Pt or Pd incorporated porous CeO₂ nanoparticles was prepared through one-step flash-combustion technique. The prepared catalysts exhibited high activity in the hydrogenation of cyclohexene under solvent-free conditions.

This is a process for producing xanthene and acridine derivatives. It uses copper metal catalysts supported by de-alumination zeolite-NaY. The process is conducted in a single pot and solvent-free conditions and does not require toxic reagents.