2019
DOI: 10.1016/j.fuproc.2018.11.001
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Synergy effects of basic graphitic-C3N4 over acidic Al2O3 for a liquid-phase decarboxylation of naphthenic acids

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Cited by 17 publications
(4 citation statements)
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“…The formation of complete metal oxide for a catalyst is obtained via the calcination step [7]. The Ca/Cu(10:90)/Al2O3 catalyst calcined at temperatures of 900, 1000 and 1100°C was used to aid the removal process and, the data is portrayed in Fig.…”
Section: Effect Of Different Calcination Temperatures Of Catalystmentioning
confidence: 99%
See 1 more Smart Citation
“…The formation of complete metal oxide for a catalyst is obtained via the calcination step [7]. The Ca/Cu(10:90)/Al2O3 catalyst calcined at temperatures of 900, 1000 and 1100°C was used to aid the removal process and, the data is portrayed in Fig.…”
Section: Effect Of Different Calcination Temperatures Of Catalystmentioning
confidence: 99%
“…Crude oil with a TAN value above 0.5 and 1.0 mgKOH/g is classified as acidic and highly acidic oil, respectively [3]. Many researchers have conducted different approaches, for instance, caustic washing, catalytic decarboxylation and catalytic esterification for removal of NA from acidic crude oil [5,6,7]. However, these technologies suffered from some drawbacks, such as the development of emulsion that is difficult to be treated, and requirement for a higher temperature of reaction with a slower reaction process.…”
Section: Introductionmentioning
confidence: 99%
“…The development of transition-metal-free protocols for synthesizing value-added products from abundant feedstock supplies is a central topic in organic synthesis. Alkanes, alkenes, and carboxylic acids are abundantly available in nature, petrochemical, and pharmaceutical industries. Converting these materials into high-value carbonyl compounds is a desirable and cost-effective approach. However, most reported methods for this transformation rely on transition-metal-based catalysts or require harsher reaction conditions or toxic oxidants. , , Visible-light photoredox catalysis has emerged as a powerful tool for sustainable organic synthesis. ,,, Initially, expensive transition-metal photocatalysts (such as Ir or Ru complexes) or photounstable organic dyes were often employed for catalytic conversions. In recent years, heterogeneous photocatalytic systems have gained significant interest in organic synthesis and energy storage applications. Notably, mesoporous graphitic carbon nitride (mpg-CN) has attracted attention in the field of photochemistry due to its stability, large surface area, and recyclability. , With a band gap of 2.7 eV, mpg-CN possesses similar properties to many homogeneous photocatalysts . Thus, the direct utilization of mpg-CN catalysts for converting readily available feedstock materials into value-added functional groups under low-energy visible light irradiation is highly desirable yet relatively unexplored.…”
Section: Introductionmentioning
confidence: 99%
“…The first approach, referred to as a physical method for naphthenic acid removal, includes adsorption, solvent and ionic liquid extractions, and neutralization . The second approach, known as a chemical method for naphthenic acid removal, involves esterification, thermal decomposition, and catalytic decomposition. Naphthenic acid is easily decomposed into hydrocarbons, carbon dioxide, carbon monoxide, and water in the presence of a catalyst, especially the zeolite catalyst. Under the same experimental conditions, the catalytic conversion of naphthenic acid over the zeolite catalyst is higher than the thermal conversion and catalytic conversion over basic oxides …”
Section: Introductionmentioning
confidence: 99%