Styrene

Styrene is an aromatic hydrocarbon with a benzene ring attached to a vinyl group, making it an important reactive building block in organic and industrial chemistry. Its carbon-carbon double bond undergoes chain-growth addition polymerization, often initiated by heat, light, or chemical initiators, to link monomers into polystyrene and related copolymers. This reactivity supports production of plastics, foams, coatings, and synthetic rubbers, while controlled polymerization helps tune material properties such as strength, flexibility, and thermal behavior. Studying styrene connects molecular structure, reaction kinetics, and polymer design, providing a foundation for understanding how small organic molecules become useful materials.

Styrene - Related Videos

Education

JoVE Science Education - Chemistry

Photochemical Initiation Of Radical Polymerization Reactions

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2023

Source: David C. Powers, Tamara M. Powers, Texas A&M In this video, we will carry out the photochemically initiated polymerization of styrene to generate polystyrene, which is an important commodity plastic. We will learn the fundamentals of photochemistry and use simple photochemistry to initiate radical polymerization reactions. Specifically, in this module we will examine the photochemistry of benzoyl peroxide and its role as a photo-initiator of styrene polymerization reactions. In the...

Research

JoVE Journal - Chemistry

Grafting Multiwalled Carbon Nanotubes with Polystyrene to Enable Self-Assembly and Anisotropic Patchiness

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Cited by 5 •

2018

A procedure for the synthesis of polystyrene-grafted multiwalled carbon nanotubes using successive chemical modification steps to selectively introduce the polymer chains to the sidewalls and their self-assembly via anisotropic patchiness is presented.

Research

JoVE Journal - Biochemistry
Free Sample

Rapid Assessment of Membrane Protein Quality by Fluorescent Size Exclusion Chromatography

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Cited by 2 •

2023

The present protocol describes a procedure to perform fluorescent size exclusion chromatography (FSEC) on membrane proteins to assess their quality for downstream functional and structural analysis. Representative FSEC results collected for several G-protein coupled receptors (GPCRs) under detergent-solubilized and detergent-free conditions are presented.

Procedure for Fabricating Biofunctional Nanofibers

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Cited by 1 •

2012

An efficient approach for preparing nanofibers decorated with functional groups capable of specifically interacting with proteins is described. The approach first requires the preparation of a polymer functionalized with the appropriate functional group. The functional polymer is fabricated into nanofibers by electrospinning. The effectiveness of the binding of the nanofibers with a protein is studied by confocal microscopy.

Magnetically Induced Rotating Rayleigh-Taylor Instability

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Cited by 5 •

2017

We present a protocol for preparing a two-layer density-stratified liquid that can be spun-up into solid body rotation and subsequently induced into Rayleigh-Taylor instability by applying a gradient magnetic field.

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