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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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Citations
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Journal ArticleDOI

Electrochemical and Photoelectrochemical Water Oxidation for Hydrogen Peroxide Production

TL;DR: This review of recent developments for the EC/PEC H 2 O 2 production from water oxidation, including fundamental aspect, benchmarking activity evaluation, material/catalyst selection, and strategies for increasing selectivity, efficiency, and accumulation is reviewed.
Journal ArticleDOI

Periodic Trends in Olefin Epoxidation over Group IV and V Framework-Substituted Zeolite Catalysts: A Kinetic and Spectroscopic Study.

TL;DR: Observations show that more electrophilic active-oxygen species are more reactive and selective for epoxidations of electron-rich olefins and explain why Ti-based catalysts have been identified as the most active among early transition metals for these reactions.
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Ionic liquid-enhanced immobilization of biosynthesized Au nanoparticles on TS-1 toward efficient catalysts for propylene epoxidation

TL;DR: In this article, the authors proposed a method to use the National Natural Science Foundation of China (NNGF) to support the research of the Doctoral Program of Higher Education (DPHE).
Journal ArticleDOI

Electrochemical degradation of phenol by in situ electro-generated and electro-activated hydrogen peroxide using an improved gas diffusion cathode

TL;DR: In this article, an improved gas diffusion electrode constructed by carbon black and PTFE was designed to improve H2O2 productivity, and the diaphragm electrolytic device was then used to degrade phenol without adding any catalyst.
Journal ArticleDOI

Highly Selective Hydrogen Peroxide Electrosynthesis on Carbon: In Situ Interface Engineering with Surfactants

TL;DR: In this paper, Cationic surfactants were used as an in situ kinetic promoter for the oxygen-to-peroxide reaction on a carbon black electrode, achieving a peroxide yield above 90% (up to 95.2%) across a > 0.8 V window in alkaline media.
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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