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Related Concept Videos

Combustion Energy: A Measure of Stability in Alkanes and Cycloalkanes02:14

Combustion Energy: A Measure of Stability in Alkanes and Cycloalkanes

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The low reactivity in alkanes can be attributed to the non-polar nature of C–C and C–H σ bonds. Alkanes, therefore, were  initially termed as “paraffins,” derived from the Latin words: parum, meaning “too little,” and affinis, meaning “affinity.”
Alkanes undergo combustion in the presence of excess oxygen and high-temperature conditions to give carbon dioxide and water. A combustion reaction is the energy source in natural gas, liquified...
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Thermal and Photochemical Electrocyclic Reactions: Overview01:26

Thermal and Photochemical Electrocyclic Reactions: Overview

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Electrocyclic reactions are reversible reactions. They involve an intramolecular cyclization or ring-opening of a conjugated polyene. Shown below are two examples of electrocyclic reactions. In the first reaction, the formation of the cyclic product is favored. In contrast, in the second reaction, ring-opening is favored due to the high ring strain associated with cyclobutene formation.
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Reduction of Alkenes: Catalytic Hydrogenation02:13

Reduction of Alkenes: Catalytic Hydrogenation

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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...
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Hydroboration-Oxidation of Alkenes03:08

Hydroboration-Oxidation of Alkenes

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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.
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Diels–Alder vs Retro-Diels–Alder Reaction: Thermodynamic Factors01:31

Diels–Alder vs Retro-Diels–Alder Reaction: Thermodynamic Factors

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The Diels–Alder reaction is thermally reversible, meaning that the reaction reverts to the starting diene and dienophile under suitable temperatures. The forward reaction gives a cyclohexene derivative and is favored at low to medium temperatures. The reverse process, also called retro-Diels–Alder reaction, is a ring-opening process favored at high temperatures.
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Enthalpy and Heat of Reaction02:12

Enthalpy and Heat of Reaction

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Combustion, commonly known as burning, is a reaction in which a substance reacts with an oxidizing agent, which in most cases is molecular oxygen, to liberate energy in the form of heat, light, or sound. The heat of combustion is also known as the enthalpy of combustion. The energy released when one mole of a substance undergoes complete combustion at constant pressure is called molar heat of combustion. Combustion reactions are exothermic; that is, they release energy, and their ΔH sign...
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Updated: Mar 25, 2026

CO2 Photoreduction to CH4 Performance Under Concentrating Solar Light
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Solar photothermochemical alkane reverse combustion.

Wilaiwan Chanmanee1, Mohammad Fakrul Islam1, Brian H Dennis2

  • 1Department of Chemistry and Biochemistry, University of Texas at Arlington, Arlington TX 76019;

Proceedings of the National Academy of Sciences of the United States of America
|February 24, 2016
PubMed
Summary

This study demonstrates a novel photothermocatalytic process converting carbon dioxide (CO2) and water into valuable liquid hydrocarbons. Optimized conditions yield C5+ hydrocarbons, offering a sustainable route for fuel production.

Keywords:
CO2 reductionFischer–Tropschphotochemistrysolar fuelwater splitting

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Biomass Conversion to Produce Hydrocarbon Liquid Fuel Via Hot-vapor Filtered Fast Pyrolysis and Catalytic Hydrotreating
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A Toolkit to Enable Hydrocarbon Conversion in Aqueous Environments
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A Toolkit to Enable Hydrocarbon Conversion in Aqueous Environments
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A Toolkit to Enable Hydrocarbon Conversion in Aqueous Environments

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Area of Science:

  • Chemical Engineering
  • Catalysis
  • Renewable Energy

Background:

  • Growing demand for sustainable fuel sources.
  • Need for efficient carbon dioxide (CO2) utilization technologies.
  • Limitations of existing methods for hydrocarbon synthesis.

Purpose of the Study:

  • To develop a one-step, gas-phase photothermocatalytic process for synthesizing hydrocarbons from CO2 and water.
  • To investigate the influence of temperature, pressure, and reactant ratios on product distribution.
  • To assess the potential for producing drop-in liquid fuels.

Main Methods:

  • Utilized a flow photoreactor operating at elevated temperatures (180-200 °C) and pressures (1-6 bar).
  • Employed a 5% cobalt on titanium dioxide (TiO2) catalyst under UV irradiation.
  • Conducted a parametric study to optimize reaction conditions.

Main Results:

  • Successfully synthesized hydrocarbons (alkanes, aromatics, oxygenates) with carbon numbers (Cn) up to C13.
  • Identified optimal temperatures (>160 °C) and pressures for producing higher Cn products.
  • Achieved over 13% by mass of C5+ hydrocarbons, including octane, suitable as drop-in fuels.
  • Detected dioxygen in yields ranging from 64% to 150%.

Conclusions:

  • The demonstrated photothermocatalytic process offers a direct and potentially cost-effective method for producing liquid hydrocarbons from CO2 and water.
  • Further development with solar-spectrum-matched photocatalysts could enable a solar-driven process for sustainable fuel production.
  • The process integrates photochemical and thermochemical steps, utilizing concentrated solar energy for both intermediate generation and carbon-chain formation.