Green diesel production via deoxygenation of triolein catalysed by nickel-molybdenum-supported catalysts
View abstract on PubMed
Summary
This summary is machine-generated.Catalytic deoxygenation of triolein efficiently produces hydrocarbons using NiO-MoO2/CeO2 catalysts under vacuum. Cerium dioxide (CeO2) support enhances diesel-rich fuel production via solvent-free methods.
Area Of Science
- Catalysis
- Green Chemistry
- Materials Science
Background
- Triolein, a triglyceride, is a potential feedstock for biofuel production.
- Catalytic deoxygenation offers a sustainable route to convert triglycerides into valuable hydrocarbons.
- Optimizing catalyst performance and reaction conditions is crucial for efficient deoxygenation.
Purpose Of The Study
- To investigate the catalytic deoxygenation of triolein into hydrocarbons.
- To evaluate the performance of NiO/CeO2, MoO2/CeO2, and NiO-MoO2/CeO2 catalysts.
- To determine optimal reaction conditions for maximizing hydrocarbon yield and n-C17 selectivity.
Main Methods
- Solvent-free deoxygenation of triolein using various metal oxide catalysts supported on CeO2.
- Reactions conducted under partial vacuum conditions.
- Systematic variation of reaction temperature, time, catalyst loading, and pressure.
Main Results
- NiO-MoO2/CeO2 demonstrated superior performance, achieving 65% hydrocarbon yield and 37% n-C17 selectivity.
- Optimal conditions (340 °C, 1 h, 15 wt% catalyst, 10 mbar) yielded 77% hydrocarbon and 58% n-C17 selectivity.
- CeO2 support proved more effective than Al2O3, SiO2, and ZSM-5 for diesel-rich fuel production.
Conclusions
- The synergistic effect between Ni-Mo and CeO2 enhances deoxygenation while suppressing cracking.
- CeO2 is a highly promising support for solvent-free catalytic deoxygenation of triolein.
- This process offers a viable pathway for producing diesel-rich fuels from renewable resources.
Related Concept Videos
Catalytic hydrogenation of alkenes is a transition-metal catalyzed reduction of the double bond using molecular hydrogen to give alkanes. The mode of hydrogen addition follows syn stereochemistry.
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Alkenes are converted to 1,2-diols or glycols through a process called dihydroxylation. It involves the addition of two hydroxyl groups across the double bond with two different stereochemical approaches, namely anti and syn. Dihydroxylation using osmium tetroxide progresses with syn stereochemistry.
Syn Dihydroxylation Mechanism
The reaction comprises a two-step mechanism. It begins with the addition of osmium tetroxide across the alkene double bond in a concerted manner forming a...
Alkenes undergo reduction by the addition of molecular hydrogen to give alkanes. Because the process generally occurs in the presence of a transition-metal catalyst, the reaction is called 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...
In addition to the oxymercuration–demercuration method, which converts the alkenes to alcohols with Markovnikov orientation, a complementary hydroboration-oxidation method yields the anti-Markovnikov product. The hydroboration reaction, discovered in 1959 by H.C. Brown, involves the addition of a B–H bond of borane to an alkene giving an organoborane intermediate. The oxidation of this intermediate with basic hydrogen peroxide forms an alcohol.
Borane as a reagent is very reactive, as the...
The presence of a catalyst affects the rate of a chemical reaction. A catalyst is a substance that can increase the reaction rate without being consumed during the process. A basic comprehension of a catalysts’ role during chemical reactions can be understood from the concept of reaction mechanisms and energy diagrams.
The illustrated image represents the reaction diagrams for an endothermic chemical process progressing in the absence (red curve) and presence (blue curve) of a catalyst.
Both...
In ozonolysis, ozone is used to cleave a carbon–carbon double bond to form aldehydes and ketones, or carboxylic acids, depending on the work-up.
Ozone is a symmetrical bent molecule stabilized by a resonance structure.
Ozonolysis proceeds through an oxidative cleavage reaction. The first step is the electrophilic addition of ozone across the alkene double bond, forming an unstable molozonide intermediate, which reacts further to form a carbonyl and a carbonyl oxide. These intermediates...

