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

Hydrogen Bonds01:04

Hydrogen Bonds

A hydrogen bond is formed when a weakly positive hydrogen atom already bonded to one electronegative atom (for example, the oxygen in the water molecule) is attracted to another electronegative atom from another polar molecule, such as water (H2O), hydrogen fluoride (HF), or ammonia (NH3). The huge electronegativity difference between the H atom (2.1) and the atom to which it is bonded (4.0 for an F atom, 3.5 for an O atom, or 3.0 for an N atom), combined with the very small size of an H atom...
Hydrogen Bonds00:26

Hydrogen Bonds

Hydrogen BondsHydrogen bonds are weak attractions between atoms that have formed other chemical bonds. One of these atoms is electronegative, like oxygen, and has a partial negative charge. The other is a hydrogen atom that has bonded with another electronegative atom and has a partial positive charge.Hydrogen Bonds Control the World!Because hydrogen has very weak electronegativity when it binds with a strongly electronegative atom, such as oxygen or nitrogen, electrons in the bond are...
Reduction of Alkenes: Catalytic Hydrogenation02:13

Reduction of Alkenes: Catalytic Hydrogenation

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 surface of...
Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation01:28

Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation

Unlike the easy catalytic hydrogenation of an alkene double bond, hydrogenation of a benzene double bond under similar reaction conditions does not take place easily. For example, in the reduction of stilbene, the benzene ring remains unaffected while the alkene bond gets reduced. Hydrogenation of an alkene double bond is exothermic and a favorable process. In contrast, to hydrogenate the first unsaturated bond of benzene, an energy input is needed; that is, the process is endothermic. This is...
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride01:26

Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride

Radical substitution reactions can be used to remove functional groups from molecules. The hydrogenolysis of alkyl halides is one such reaction, where the weak Sn–H bond in tributyltin hydride reacts with alkyl halides to form alkanes. Here, the reagent Bu3SnH yields tributyltin halide as a byproduct.
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation reactions,...
Radical Chain-Growth Polymerization: Chain Branching01:17

Radical Chain-Growth Polymerization: Chain Branching

The skeletal structure of polymers synthesized via radical polymerization is always branched. For example, the polymerization of ethylene by radical polymerization results in a low-density grade of polyethylene with a heavily branched skeletal structure. Here, the radical site abstracts hydrogen from the growing chain, and the radical site shifts from the end (a primary carbon center) to anywhere within the growing chain (a secondary carbon center). Consequently, the part of the chain from the...

You might also read

Related Articles

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

Sort by
Same author

Optimal Scanning Protocol of Whole-Brain CT Perfusion in Patients With Acute Ischemic Stroke.

Journal of computer assisted tomography·2025
Same author

A study on a clathrate-like transition for carbon dioxide + propane + water <i>via</i> molecular dynamics simulations.

Physical chemistry chemical physics : PCCP·2025
Same author

Cohesive and Adhesive Failure Mechanisms of CO<sub>2</sub>/Tetrahydrofuran Structure II Gas Hydrate Crystalline Cores through Hydraulic Yield Strength Measurements.

Langmuir : the ACS journal of surfaces and colloids·2025
Same author

Efficient Determination of Water/Ice Phase Diagram through Isenthalpic-Isobaric Molecular Dynamics Simulations.

The journal of physical chemistry. B·2025
Same author

Revision of an Abscess Drainage Catheter Malpositioned into the Inferior Vena Cava.

Journal of vascular and interventional radiology : JVIR·2025
Same author

Porous solids for energy applications.

The Journal of chemical physics·2024

Related Experiment Video

Updated: Jun 20, 2026

In Situ High Pressure Hydrogen Tribological Testing of Common Polymer Materials Used in the Hydrogen Delivery Infrastructure
10:01

In Situ High Pressure Hydrogen Tribological Testing of Common Polymer Materials Used in the Hydrogen Delivery Infrastructure

Published on: March 31, 2018

Increasing hydrogen storage capacity using tetrahydrofuran.

Takeshi Sugahara1, Joanna C Haag, Pinnelli S R Prasad

  • 1Division of Chemical Engineering, Graduate School of Engineering Science, Osaka University, Osaka, Japan.

Journal of the American Chemical Society
|September 29, 2009
PubMed
Summary

Researchers explored hydrogen storage in tetrahydrofuran (THF) hydrates, achieving 3.4 wt% capacity. This study demonstrates that hydrogen can occupy large cages in THF-promoted hydrates, contrary to previous findings.

More Related Videos

A Simple, Low-cost, and Robust System to Measure the Volume of Hydrogen Evolved by Chemical Reactions with Aqueous Solutions
06:32

A Simple, Low-cost, and Robust System to Measure the Volume of Hydrogen Evolved by Chemical Reactions with Aqueous Solutions

Published on: August 17, 2016

Supercritical Nitrogen Processing for the Purification of Reactive Porous Materials
09:05

Supercritical Nitrogen Processing for the Purification of Reactive Porous Materials

Published on: May 15, 2015

Related Experiment Videos

Last Updated: Jun 20, 2026

In Situ High Pressure Hydrogen Tribological Testing of Common Polymer Materials Used in the Hydrogen Delivery Infrastructure
10:01

In Situ High Pressure Hydrogen Tribological Testing of Common Polymer Materials Used in the Hydrogen Delivery Infrastructure

Published on: March 31, 2018

A Simple, Low-cost, and Robust System to Measure the Volume of Hydrogen Evolved by Chemical Reactions with Aqueous Solutions
06:32

A Simple, Low-cost, and Robust System to Measure the Volume of Hydrogen Evolved by Chemical Reactions with Aqueous Solutions

Published on: August 17, 2016

Supercritical Nitrogen Processing for the Purification of Reactive Porous Materials
09:05

Supercritical Nitrogen Processing for the Purification of Reactive Porous Materials

Published on: May 15, 2015

Area of Science:

  • Materials Science
  • Chemical Engineering
  • Energy Storage

Background:

  • Hydrogen storage in hydrates is crucial for clean energy applications.
  • The role of promoter molecules like tetrahydrofuran (THF) in hydrogen hydrate formation and storage capacity remains under investigation.
  • Previous studies suggested limitations in hydrogen occupancy within the large cages of promoter-based hydrates.

Purpose of the Study:

  • To investigate hydrogen storage capacity and cage occupancy in hydrogen hydrates promoted by tetrahydrofuran (THF).
  • To explore a novel preparation method for hydrogen-THF hydrates.
  • To determine the effect of THF concentration on hydrogen storage efficiency.

Main Methods:

  • A new preparation method involving mixing solid powdered THF with ice, followed by pressurization with hydrogen (70 MPa, 255 K).
  • Analysis using Raman microprobe spectroscopy.
  • Powder X-ray diffraction and gas volumetric analysis were employed to assess hydrogen storage.

Main Results:

  • Hydrogen storage capacity is strongly dependent on THF composition.
  • Contrary to prior reports, hydrogen molecules were observed to occupy large cages in THF+H(2) structure II hydrates at THF mole fractions below 0.01.
  • A maximum hydrogen storage capacity of approximately 3.4 wt% was achieved in the THF+H(2) hydrate system.

Conclusions:

  • This study successfully demonstrates the occupation of large cages by hydrogen in THF-promoted hydrates.
  • The findings challenge previous assumptions about promoter limitations in hydrogen hydrate cage occupancy.
  • The tunable effect of THF content offers potential for developing advanced hydrogen storage solutions for future scientific and practical applications.