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Hydrogen Peroxide Synthesis: An Outlook beyond the Anthraquinone Process

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TLDR
The direct synthesis of H 2O2 from O2 and H2 using a variety of catalysts, and the factors influencing the formation and decomposition of H2O2 are examined in detail in this Review.
Abstract
Hydrogen peroxide (H2O2) is widely used in almost all industrial areas, particularly in the chemical industry and environmental protection. The only degradation product of its use is water, and thus it has played a large role in environmentally friendly methods in the chemical industry. Hydrogen peroxide is produced on an industrial scale by the anthraquinone oxidation (AO) process. However, this process can hardly be considered a green method. It involves the sequential hydrogenation and oxidation of an alkylanthraquinone precursor dissolved in a mixture of organic solvents followed by liquid–liquid extraction to recover H2O2. The AO process is a multistep method that requires significant energy input and generates waste, which has a negative effect on its sustainability and production costs. The transport, storage, and handling of bulk H2O2 involve hazards and escalating expenses. Thus, novel, cleaner methods for the production of H2O2 are being explored. The direct synthesis of H2O2 from O2 and H2 using a variety of catalysts, and the factors influencing the formation and decomposition of H2O2 are examined in detail in this Review.

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Potential implications of hydrogen peroxide in the pathogenesis and therapeutic strategies of gliomas

TL;DR: The potential cellular and molecular roles of H 2 O 2 in gliomagenesis are discussed and the potential implications in radiotherapy and chemotherapy and in the ongoing challenges of current glioma treatment are explored.
Journal ArticleDOI

Durability and surface chemistry of horizontally aligned CNT films as electrodes upon electrolysis of acidic aqueous solution

TL;DR: In this paper, a simple and effective method of electrochemical functionalization of horizontally aligned CNT films in diluted HCl and H2SO4 solutions upon their electrolysis under a constant current mode was devised, which was able to cause notable generation of carbonoxygen and carbon chlorine functional groups on the CNT film anodes as proven by EDX, XPS, and Raman spectroscopy.
Journal ArticleDOI

Unexpected formation of a novel pyridinium-containing catecholate ligand and its manganese(III) complex.

TL;DR: Manganese(III), which represents the first complex of this ligand class to be structurally characterized by X-ray diffraction, is active in the catalytic reduction of dioxygen to hydrogen peroxide under ambient conditions and turnover frequencies (TOFs) >10,000 h(-1) can be obtained.
Journal ArticleDOI

Catalytic hydrogenation of 2-ethylanthraquinone using an in situ synthesized Pd catalyst

TL;DR: In this paper, an in situ synthesized Pd catalyst with an egg-shell structure was employed to catalyze the hydrogenation of 2-ethylanthraquinone in a fixed bed.
Journal ArticleDOI

Towards selective catalytic oxidations using in-situ generated H2O2

TL;DR: In this paper, a series of mesoporous SiO2-supported monometallic and bimetallic DMAP-stabilised Au and Pd nanoparticles were used as catalysts in the selective epoxidation of a probe alkene (cyclohexene) using H2O2 as an oxidising agent.
References
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Journal ArticleDOI

Titanium dioxide photocatalysis

TL;DR: A review of the current progress in the area of TiO 2 photocatalysis, mainly photocatalytic air purification, sterilization and cancer therapy is discussed in this paper.

Titanium dioxide as photocatalysis

TL;DR: A review of the current progress in the area of TiO 2 photocatalysis, mainly photocatalytic air purification, sterilization and cancer therapy is discussed in this article.
Journal ArticleDOI

Titanium-containing mesoporous molecular sieves for catalytic oxidation of aromatic compounds

TL;DR: The use of the templating approach to synthesize mesoporous silica-based molecular sieves partly substituted with titanium—large-pore analogues of titanium silicalite find that these materials show selective catalytic activity towards the oxidation of 2,6-ditert-butyl phenol to the corresponding quinone and the conversion of benzene to phenol.
Book

Gas-liquid reactions

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