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Related Concept Videos

Van der Waals Equation01:10

Van der Waals Equation

The ideal gas law is an approximation that works well at high temperatures and low pressures. The van der Waals equation of state (named after the Dutch physicist Johannes van der Waals, 1837−1923) improves it by considering two factors.
First, the attractive forces between molecules, which are stronger at higher densities and reduce the pressure, are considered by adding to the pressure a term equal to the square of the molar density multiplied by a positive coefficient a. Second, the volume...
Osmotic Pressure01:26

Osmotic Pressure

Osmosis is a process where solvent molecules move toward a solution through a semipermeable membrane. As the solution dilutes due to the entry of solvent, it expands. This expansion increases the hydrostatic pressure of the solution. When the hydrostatic pressure equals the osmotic pressure, osmosis stops.Osmotic pressure, denoted by Π, is the minimum pressure needed to prevent the solvent from passing into the solution by osmosis. The van 't Hoff equation calculates the osmotic pressure of an...
Molecular Weight of Step-Growth Polymers01:08

Molecular Weight of Step-Growth Polymers

Step growth polymerization involves bi or multifunctional monomers. Bifunctional monomers react to form linear step growth polymers, whereas multifunctional monomers react to form non-linear or branched polymers.
As the step-growth polymerization involves step-wise condensation of monomers, the molecular weight also builds up eventually. Consequently, high molecular weight polymers are obtained at the late stages of the polymerization, where 99% of monomers have been consumed.
The extent of the...
Clausius-Clapeyron Equation02:35

Clausius-Clapeyron Equation

The equilibrium between a liquid and its vapor depends on the temperature of the system; a rise in temperature causes a corresponding rise in the vapor pressure of its liquid. The Clausius-Clapeyron equation gives the quantitative relation between a substance’s vapor pressure (P) and its temperature (T); it predicts the rate at which vapor pressure increases per unit increase in temperature.
The Van der Waals Equation01:26

The Van der Waals Equation

The ideal gas law is based on two simplifying assumptions: first, that there are no intermolecular attractions between gas molecules, and second, that the volume occupied by the molecules themselves is negligible compared with the volume of the container. However, these assumptions don't hold up under all conditions - specifically, at high pressures and low temperatures, as gas tends to deviate from ideal gas behavior.The van der Waals equation is an enhanced version of the ideal gas law,...
Determination of Molar Masses of Polymers II01:27

Determination of Molar Masses of Polymers II

Polymer samples typically consist of macromolecular chains with a distribution of lengths, resulting in a range of molar masses rather than a single discrete value. Conventional descriptors such as the number-average molar mass and weight-average molar mass quantify this distribution but do not fully capture polymer behavior in solution..The viscosity-average molar mass provides a more realistic description of polymer behavior in solution because it accounts for the enhanced contribution of...

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Confocal Imaging of Confined Quiescent and Flowing Colloid-polymer Mixtures
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Density functional approach for modeling CO2 pressurized polymer thin films in equilibrium.

Manish Talreja1, Isamu Kusaka, David L Tomasko

  • 1William G. Lowrie Department of Chemical and Biomolecular Engineering, The Ohio State University, 140 West 19th Avenue, Columbus, Ohio 43210, USA.

The Journal of Chemical Physics
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Polymer density functional theory reveals how carbon dioxide (CO(2)) affects polymer thin film properties. CO(2) presence and film thickness alter surface tension and interface width, with end-segment segregation observed.

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Published on: September 26, 2016

Area of Science:

  • Materials Science
  • Physical Chemistry
  • Computational Physics

Background:

  • Polymer thin films are crucial in various applications.
  • Understanding their interfacial properties with gases like carbon dioxide (CO(2)) is essential.
  • CO(2) interactions can significantly alter polymer film behavior.

Purpose of the Study:

  • To analyze equilibrium density profiles and interfacial properties of polymer thin films in the presence of CO(2).
  • To investigate the effects of CO(2) and film thickness on surface tension, CO(2) adsorption, and interface width.
  • To explore the influence of polymer chain length on these interfacial characteristics.

Main Methods:

  • Utilized polymer density functional theory (DFT) for theoretical analysis.
  • Calculated equilibrium density profiles and interfacial parameters.
  • Introduced a novel 'Delta profiles' method to quantify end-segment segregation.

Main Results:

  • Observed changes in surface tension, CO(2) surface excess adsorption, and interface width due to CO(2) presence and increasing film thickness.
  • Established an inverse linear relationship between interfacial properties and polymer chain length.
  • Provided evidence of end-segment segregation towards the interface, enhanced by CO(2) and chain length.

Conclusions:

  • CO(2) significantly influences the interfacial properties of polymer thin films.
  • End-segment segregation is a key phenomenon, quantifiable with the new Delta profile method.
  • The findings offer qualitative trends comparable to experimental and simulation studies, particularly for systems like octacosane-CO(2) near critical points.