Related Experiment Video
Updated: Jun 26, 2025

A Microfluidic Approach for the Study of Ice and Clathrate Hydrate Crystallization
Published on: August 18, 2022
Can Aluminum Cations Promote Nucleation for THF Hydrate Growth?
Randeep Ravesh1, Ayaj A Ansari1, P K Panigrahi1
1Gas Hydrate Laboratory, Department of Mechanical Engineering, Indian Institute of Technology Kanpur, 208016 Kanpur, India.
Aluminum chloride (AlCl3) significantly accelerates tetrahydrofuran (THF) hydrate nucleation, crucial for cold storage technology. This study confirms AlCl3
Area of Science:
- Materials Science
- Chemical Engineering
- Physical Chemistry
Background:
- Tetrahydrofuran (THF) hydrate nucleation is vital for cold storage applications.
- Previous research suggested aluminum complexes promote clathrate hydrate nucleation.
Purpose of the Study:
- To investigate if aluminum salts, specifically AlCl3, can promote THF hydrate nucleation.
- To evaluate the influence of cation type (charge/radius ratio) using NaCl and MgCl2.
- To understand the nucleation mechanism through pH and Raman spectroscopy.
Main Methods:
- Measuring induction time in a stirred reactor across various subcoolings and AlCl3 concentrations (0.05-2 wt%).
- Comparing salt premixed in solution versus direct injection.
- Analyzing temperature rise as an indicator of hydrate formation.
- Conducting pH and Raman spectroscopy measurements.
Main Results:
- AlCl3 reduced THF hydrate induction time by 92.2% at 0.05 wt% concentration compared to pure water.
- Direct injection of AlCl3 resulted in nearly instantaneous nucleation.
- MgCl2 and NaCl did not exhibit a similar nucleation-promoting effect.
Conclusions:
- Aluminum salts, particularly AlCl3, effectively promote THF hydrate nucleation.
- The cation type plays a significant role in nucleation promotion.
- AlCl3 offers a promising approach for enhancing THF hydrate-based cold storage technologies.
More Related Videos
12:30Synthesis of a Thiol Building Block for the Crystallization of a Semiconducting Gyroidal Metal-sulfur Framework
Published on: April 9, 2018
05:50Facile Preparation of Ultrafine Aluminum Hydroxide Particles with or without Mesoporous MCM-41 in Ambient Environments
Published on: May 11, 2017
Related Concept Videos
Aldehydes and Ketones with Water: Hydrate Formation
The formation of hydrates is a reversible reaction. Hydrate formation is influenced by steric and electronic factors accompanying the alkyl substituents on the carbonyl group: The rate of hydrate formation increases with a decrease in the number of alkyl groups attached to the carbonyl carbon. Hence,...
Alkynes to Aldehydes and Ketones: Acid-Catalyzed Hydration
Analogous to alkenes, alkynes also undergo acid-catalyzed hydration. While the addition of water to an alkene gives an alcohol, hydration of alkynes produces different products such as aldehydes and ketones.
Acid-Catalyzed Hydration of Alkenes
Acid Halides to Alcohols: LiAlH4 Reduction
The mechanism proceeds in three steps. First, the nucleophilic hydride ion attacks the carbonyl carbon of the acid halide to form a tetrahedral intermediate. Next, the carbonyl group is re-formed, and the halide ion departs as a leaving group, generating an aldehyde. A second nucleophilic attack by the hydride yields an alkoxide ion, which, upon protonation, gives a primary alcohol as...
Electrophilic Addition to Alkynes: Halogenation
Halogenation is another class of electrophilic addition reactions where a halogen molecule gets added across a π bond. In alkynes, the presence of two π bonds allows for the addition of two equivalents of halogens (bromine or chlorine). The addition of the first halogen molecule forms a trans-dihaloalkene as the major product and the cis isomer as the minor product. Subsequent addition of the second equivalent yields the tetrahalide.
Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration