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Related Concept Videos

Hydration of Cement01:24

Hydration of Cement

Hydration of cement is a chemical reaction between cement particles and water. This process occurs primarily through two mechanisms: through-solution and topochemical. In the through-solution process, anhydrous compounds dissolve into their constituents, hydrates form in the solution, and then precipitate from the supersaturated solution. The topochemical process involves solid-state reactions at the cement particle surface. The through-solution process dominates the topochemical process at the...
Strength and Heat of Hydration01:29

Strength and Heat of Hydration

The hydration of cement is an exothermic reaction in which heat is generated as cement hydrates. This heat of hydration is critical to cement's strength development. The rate at which this heat is generated affects the temperature rise, with a majority of the heat being released early in the hydration process, half within the first three days, and about 75% within the first week.
The heat of hydration for each cement compound is significant; for instance, tricalcium aluminate (C3A) and...
Transition Zone01:28

Transition Zone

The transition zone in concrete is a critical area where aggregate meets cement paste, marked by a distinct porosity and weakness compared to the surrounding material. The adhesion around the aggregates is primarily due to Van Der Waals forces. The voids within this zone influence its robustness; initially, it is less durable than the surrounding bulk mortar due to larger voids. Initially, when concrete is compacted, a higher water-cement ratio near the aggregates leads to the formation of...
Aldehydes and Ketones with Water: Hydrate Formation01:20

Aldehydes and Ketones with Water: Hydrate Formation

An oxygen-based nucleophile, like water, can undergo addition reactions with aldehydes and ketones. The reaction leads to the formation of hydrates, also referred to as 1,1-diols or geminal diols.
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,...
Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration02:34

Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration

The rate of acid-catalyzed hydration of alkenes depends on the alkene's structure, as the presence of alkyl substituents at the double bond can significantly influence the rate.
Carbonation Shrinkage01:24

Carbonation Shrinkage

Atmospheric CO2 penetrates the concrete's pores and, in the presence of moisture, forms carbonic acid, which then reacts with calcium hydroxide in the hydrated cement, forming calcium carbonate. This process reduces the concrete's volume and is termed carbonation shrinkage.
The concrete's permeability is slightly reduced as calcium carbonate produced during the reaction fills its pores. Furthermore, its strength is slightly enhanced as the water released during the reaction facilitates the...

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Updated: May 9, 2026

Methane Hydrate Crystallization on Sessile Water Droplets
08:46

Methane Hydrate Crystallization on Sessile Water Droplets

Published on: May 26, 2021

Cage occupancy and structural changes during hydrate formation from initial stages to resulting hydrate phase.

Judith M Schicks1, Manja Luzi-Helbing

  • 1Helmholtz Centre Potsdam GFZ German Research Centre for Geosciences, Section 4.2: Inorganic and Isotope Geochemistry, Telegrafenberg, 14473 Potsdam, Germany. schick@gfz-potsdam.de

Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy
|July 23, 2013
PubMed
Summary

This study reveals methane (CH4) initially fills small hydrate cavities during mixed gas hydrate formation. Early hydrate phases differ from steady-state ones in cavity occupancy and composition.

Keywords:
5(12) CavitiesHydrate formation kineticsMixed gas hydratesRaman spectroscopy

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Area of Science:

  • Geochemistry
  • Materials Science
  • Physical Chemistry

Background:

  • Hydrate formation mechanisms lack molecular-level experimental understanding.
  • Initial cavity formation and occupancy in mixed gas hydrates are under-investigated.

Purpose of the Study:

  • To investigate time-dependent hydrate formation and kinetics.
  • To understand initial cavity formation and guest molecule occupancy in mixed gas hydrates.

Main Methods:

  • Time-dependent Raman spectroscopy was employed.
  • Hydrate formation was studied from ice and various gas mixtures (CH4, CH4-CO2, CH4-H2S, CH4-C3H8, CH4-iso-C4H10, CH4-neo-C5H12).
  • Experiments were conducted under constant pressure, temperature, and feed gas composition.

Main Results:

  • Methane (CH4) incorporation into 5(12) cavities is the initial step in all investigated systems.
  • Early-stage hydrate phases exhibit distinct cavity occupancy and guest ratios compared to steady-state phases.
  • Differences in small and large cavity occupancy were observed between initial and steady-state hydrate phases.

Conclusions:

  • The study provides molecular-level insights into initial mixed gas hydrate formation.
  • Initial hydrate formation pathways differ significantly from steady-state conditions.
  • Raman spectroscopy is effective for studying dynamic hydrate formation processes.