Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Hydroboration-Oxidation of Alkenes03:08

Hydroboration-Oxidation of Alkenes

12.4K
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.
12.4K
Catalysis02:50

Catalysis

32.4K
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.
32.4K
Preparation of Alcohols via Addition Reactions02:15

Preparation of Alcohols via Addition Reactions

8.2K
Overview
The acid-catalyzed addition of water to the double bond of alkenes is a large-scale industrial method used to synthesize low-molecular-weight alcohols. An acidic atmosphere is required to allow the hydrogen in the water molecule to act as an electrophile and attack the double bond in an alkene. The addition of a proton to the double bond creates a carbocation intermediate. The proton preferentially bonds to the less substituted end of the double bond to create a more stable carbocation...
8.2K
Reduction of Alkenes: Catalytic Hydrogenation02:13

Reduction of Alkenes: Catalytic Hydrogenation

15.0K
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...
15.0K
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation02:17

Reduction of Alkenes: Asymmetric Catalytic Hydrogenation

4.0K
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...
4.0K
Oxidation of Alkenes: Syn Dihydroxylation with Potassium Permanganate02:21

Oxidation of Alkenes: Syn Dihydroxylation with Potassium Permanganate

18.3K
Alkenes can be dihydroxylated using potassium permanganate.  The method encompasses the reaction of an alkene with a cold, dilute solution of potassium permanganate under basic conditions to form a cis-diol along with a brown precipitate of manganese dioxide.
18.3K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Synthesis of Potent Vanin-1 Inhibitors Labelled With Carbon-14 and Deuterium.

Journal of labelled compounds & radiopharmaceuticals·2026
Same author

Life-course metabolic vulnerability and chronic kidney disease risk after early-life famine exposure in Middle-aged and older chinese adults.

The journals of gerontology. Series A, Biological sciences and medical sciences·2026
Same author

APRIL-targeted and dual BAFF/APRIL blockade in primary IgA nephropathy: a systematic review and meta-analysis of randomized placebo-controlled trials.

International urology and nephrology·2026
Same author

Comparison of the predictive value of mri-based cervical endplate bone quality (C-EBQ) score and cervical vertebral bone quality (C-VBQ) score for the progression of cervical disc degeneration.

European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society·2026
Same author

Zinc (d)-Tartrate Catalyzed Asymmetric Epoxide Ring Opening: Access to Enantioenriched β-Hydroxy Thiols and ADC Linker Compounds.

The Journal of organic chemistry·2026
Same author

Identification of MMP14 and FOS as key regulators of vascular smooth muscle cell senescence in diabetic kidney disease: A combined bioinformatics and experimental study.

Archives of gerontology and geriatrics·2026

Related Experiment Video

Updated: Apr 3, 2026

Chemical Precipitation Method for the Synthesis of Nb2O5 Modified Bulk Nickel Catalysts with High Specific Surface Area
08:13

Chemical Precipitation Method for the Synthesis of Nb2O5 Modified Bulk Nickel Catalysts with High Specific Surface Area

Published on: February 19, 2018

12.6K

Understanding the Conversion Routes of Butanol in Steam Reforming Over Nix/MgO Catalyst.

Yajing Wang1, Tingting Ji2, Bo Qu1

  • 1College of Chemistry and Chemical Engineering, Harbin Normal University, Harbin, China.

Chemistry, an Asian Journal
|April 2, 2026
PubMed
Summary

A reaction scheme for butanol steam reforming (BSR) over mesoporous Ni/MgO was proposed. Moderate Ni nanoparticle size (∼5.3 nm) on Ni$_{0.12}$/MgO showed the highest H$_{2}$ yield.

Keywords:
Butanol steam reformingNi catalysthydrogen productionreaction pathwayvarious Ni sizes

More Related Videos

Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction
10:57

Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction

Published on: April 10, 2018

19.4K
Tuning the Acidity of Pt/ CNTs Catalysts for Hydrodeoxygenation of Diphenyl Ether
09:21

Tuning the Acidity of Pt/ CNTs Catalysts for Hydrodeoxygenation of Diphenyl Ether

Published on: August 17, 2019

9.5K

Related Experiment Videos

Last Updated: Apr 3, 2026

Chemical Precipitation Method for the Synthesis of Nb2O5 Modified Bulk Nickel Catalysts with High Specific Surface Area
08:13

Chemical Precipitation Method for the Synthesis of Nb2O5 Modified Bulk Nickel Catalysts with High Specific Surface Area

Published on: February 19, 2018

12.6K
Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction
10:57

Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction

Published on: April 10, 2018

19.4K
Tuning the Acidity of Pt/ CNTs Catalysts for Hydrodeoxygenation of Diphenyl Ether
09:21

Tuning the Acidity of Pt/ CNTs Catalysts for Hydrodeoxygenation of Diphenyl Ether

Published on: August 17, 2019

9.5K

Area of Science:

  • Catalysis
  • Chemical Engineering
  • Materials Science

Background:

  • Butanol steam reforming (BSR) is a promising route for hydrogen production.
  • Understanding the reaction mechanism and the role of catalyst properties is crucial for optimizing BSR.

Purpose of the Study:

  • To propose a detailed reaction scheme for BSR over mesoporous Ni/MgO catalysts.
  • To investigate the effect of nickel (Ni) nanoparticle size on BSR performance.
  • To correlate catalyst properties with hydrogen yield.

Main Methods:

  • Synthesis of mesoporous Ni/MgO catalysts with varying Ni sizes (2.5–14.0 nm).
  • Characterization using Temperature Programmed Desorption (TPD), Temperature Programmed Surface Reaction (TPSR), and Diffuse Reflectance Infrared Fourier Transform Spectroscopy (DRIFTS).
  • Evaluation of catalytic activity in BSR, focusing on hydrogen (H$_{2}$) yield.

Main Results:

  • A two-pathway reaction mechanism for BSR was elucidated, involving butoxy and butyraldehyde intermediates.
  • Catalyst performance was found to be dependent on the geometric configuration and electronic properties of Ni active sites.
  • Ni$_{0.12}$/MgO, with an optimal Ni nanoparticle size of approximately 5.3 nm, exhibited the highest H$_{2}$ yield compared to catalysts with smaller or larger Ni sizes.

Conclusions:

  • The study provides a comprehensive understanding of the BSR reaction mechanism over Ni/MgO.
  • Nickel nanoparticle size is a critical factor influencing BSR activity and selectivity.
  • Optimized Ni nanoparticle size (∼5.3 nm) on Ni$_{0.12}$/MgO maximizes hydrogen production via BSR.