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Related Concept Videos

Polymers02:34

Polymers

The word polymer is derived from the Greek words “poly” which means “many” and “mer” which means “parts”. Polymers are long chains of molecules composed of repeating units of smaller molecules, known as monomers. They either occur naturally, such as DNA and proteins, or can be constructed synthetically, like plastics. They have varied structural characteristics, such as linear chains, branched chains, or complex networks, that contribute to the properties that they exhibit. Additionally,...
Radical Chain-Growth Polymerization: Mechanism01:09

Radical Chain-Growth Polymerization: Mechanism

The radical chain-growth polymerization mechanism consists of three steps: initiation, propagation, and termination of polymerization. The polymerization initiates when a free radical generated from the radical initiator adds to the unsaturated bond in the monomer. The unpaired electron of the free radical and one π electron in the unsaturated bond creates a σ bond between the free radical and the monomer. As a result, the other π electron in the unsaturated bond converts this species into the...
Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

The cationic polymerization mechanism consists of three steps: initiation, propagation, and termination. In the initiation step of the polymerization process, the π bond of a monomer gets protonated by the Lewis acid catalyst, which is formed from boron trifluoride and water. The protonation of the π bond generates a carbocation stabilized by the electron‐donating group. In the propagation step, the π bond of the second monomer acts as a nucleophile and attacks the generated carbocation,...
Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

Step-growth or condensation polymerization is a stepwise reaction of bi or multifunctional monomers to form long-chain polymers. As all the monomers are reactive, most of the monomers are consumed at the early stages of the reaction to form small chains of reactive oligomers, which then combine to form long polymer chains in the late stages. Hence, the reaction has to proceed for a long time to achieve high molecular weight polymers.
Many natural and synthetic polymers are produced by...
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...
Types of Step-Growth Polymers: Polyesters01:20

Types of Step-Growth Polymers: Polyesters

The introduction of polyesters has brought major development to the textile industry. The wrinkle-free behavior of polyester blends has eliminated the need for starching and ironing clothes.
Polyesters are commonly prepared from terephthalic acid and ethylene glycol; the crude product is known as poly(ethylene terephthalate) or PET. However, polyesters are synthesized industrially by transesterification of dimethyl terephthalate with ethylene glycol at 150 °C. The two reactants and the polymer...

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Ethylene Polymerizations Using Parallel Pressure Reactors and a Kinetic Analysis of Chain Transfer Polymerization
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Published on: November 27, 2015

Polymerization kinetics of pre-heated composite.

M Daronch1, F A Rueggeberg, M F De Goes

  • 1Department of Dental Materials, School of Dentistry, University of São Paulo, São Paulo, SP, Brazil.

Journal of Dental Research
|December 24, 2005
PubMed
Summary

This study examined how pre-warming affects the polymerization of a dental composite material. The researchers found that increasing the temperature before light exposure improved the rate and extent of monomer conversion. The effect was stronger at the surface than at 2-mm depth. The time to reach the maximum polymerization rate did not change with temperature but was faster at the surface. The study suggests that pre-warming allows more of the reaction to occur before the material solidifies. These findings may help improve the performance of dental composites in clinical settings. The researchers propose that pre-warming could be a useful technique to optimize polymerization efficiency.

Keywords:
dental materialsphoto-activated compositesmonomer conversionpolymerization behavior

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Area of Science:

  • Dental materials science
  • Polymer chemistry in clinical applications

Background:

Current understanding of polymerization behavior in dental composites is limited by the lack of data on how pre-heating affects reaction dynamics. Prior research has shown that temperature influences the rate of monomer conversion in dimethacrylate-based systems. However, the specific impact of pre-polymerization temperature on both surface and subsurface polymerization remains unclear. No prior work had resolved how depth affects the timing and extent of polymerization. Existing studies focus on room-temperature conditions, which may not reflect clinical scenarios where pre-warming is used. This gap motivated the need to explore how temperature gradients influence polymerization kinetics. That uncertainty drove the investigation into whether pre-warming could optimize material performance. No prior work had resolved the relationship between pre-warming and vitrification in dental composites.

Purpose Of The Study:

The aim of this study was to investigate how pre-polymerization temperature and exposure duration affect the polymerization kinetics of a dental composite. The specific problem addressed is the lack of data on how temperature gradients influence the rate and extent of monomer conversion at different depths. The motivation for this study stems from the clinical use of pre-warmed composites to improve handling and flow. The researchers propose that pre-warming could enhance polymerization efficiency. The study focused on a commercial photo-activated composite to ensure clinical relevance. The researchers propose that depth plays a significant role in polymerization behavior. The study sought to quantify the impact of temperature on real-time conversion and maximum conversion rate. The researchers propose that pre-warming may allow more of the reaction to occur before vitrification.

Main Methods:

The researchers used a temperature-controlled stage to pre-set composite samples between 3 and 60 degrees Celsius. A diamond-attenuated-total-reflectance unit was used to monitor real-time polymerization. Composite was exposed to light from a quartz-tungsten-halogen curing unit for 5, 10, 20, or 40 seconds. Infrared spectra were collected to calculate polymerization parameters. Real-time conversion was determined from the spectral data. Maximum conversion rate and time to reach that rate were also calculated. Conversion at the point of maximum rate was analyzed for depth differences. The study compared surface and 2-mm depth polymerization behavior.

Main Results:

Pre-warming the composite increased the maximum polymerization rate and overall monomer conversion. The effect was more pronounced at the surface than at 2-mm depth. Time to achieve maximum rate did not change with temperature. However, the surface reached maximum rate faster than the 2-mm depth. Conversion at the point of maximum rate increased with higher pre-polymerization temperatures. This suggests more of the reaction occurred before vitrification at higher temperatures. The surface showed significantly greater conversion than the 2-mm depth. The study found that pre-warming allowed for more efficient polymerization before the material solidified.

Conclusions:

The authors suggest that pre-warming dental composites may enhance polymerization efficiency. They propose that surface polymerization benefits more from pre-warming than deeper layers. The study suggests that higher temperatures allow more of the reaction to occur before vitrification. The researchers propose that depth affects the timing of maximum conversion rate. The study suggests that pre-warming could improve clinical outcomes by increasing monomer conversion. The authors suggest that pre-warming may be a useful technique to optimize composite performance. The study suggests that temperature gradients influence the extent of polymerization at different depths. The researchers propose that further work is needed to explore the clinical implications of these findings.

According to the authors, pre-warming increases the maximum polymerization rate, especially at the surface.

The study shows that the surface reaches maximum rate faster than the 2-mm depth, regardless of temperature.

The researchers propose that higher conversion at this point allows more of the reaction to occur before vitrification.

The study used infrared spectra from a diamond-attenuated-total-reflectance unit to calculate conversion values.

The authors suggest that higher pre-polymerization temperatures allow more of the reaction to occur before the material solidifies.

The researchers propose that pre-warming may improve composite performance by increasing monomer conversion.