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Prof. Amal EZZ ELDIN DentaL biomaterials 2012

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Presentation on theme: "Prof. Amal EZZ ELDIN DentaL biomaterials 2012"— Presentation transcript:

1 Prof. Amal EZZ ELDIN DentaL biomaterials 2012
Elastomeric Impression Materials Prof. Amal EZZ ELDIN DentaL biomaterials 2012

2 Elastomeric Impression Materials
Rubber-like in nature *polymers (ADA No. 19: Non Aqueous Elastomers). They are synthetic rubber and formed by chemical reaction. The process of changing the elastomeric base into final rubber-like material known as polymerization They offer potential solution to two main problems of hydrocolloids Poor tear strength Poor dimensional stability Uses: .Impression for crown and bridge. Impression for Partial and complete denture.

3 Classification Elastic Polysulfides Polyethers -Hydrocolloids
Non-aqueous elastomers Condensation silicone Addition silicone

4 Characteristics or Elastomeric Impression Materials
Base Packaged as a paste in a tube, as a cartridge, or as putty in a jar. Catalyst Also known as the accelerator, is packaged as a paste in a tube, as a cartridge, or as a liquid in a bottle with a dropper top.

5 Forms of Elastomeric Materials
Light-bodied Also referred to as syringe type, or wash type. This material is used because of its ability to flow in and about the details of the prepared tooth. A special syringe, or extruder, is used to place the light-bodied material on and immediately around the prepared teeth. Light body Heavy body

6 Forms of Elastomeric Materials- cont’d
Regular and heavy-bodied Often referred to as tray‑type materials, they are much thicker. As the names imply, they are used to fill the tray. Their stiffness helps to force the light‑bodied material into close contact with the prepared teeth and surrounding tissues to ensure a more accurate impression of the details of a preparation.

7 Elastomers Setting reaction: Polymerization for Chain-lengthening & Cross-linking Condensation polymerization Polysulphide Condensation silicone Additional polymerization Additional silicone Cationic polymerization Polyether

8 Polysulfide

9 Polysulphides BASE CATALYST Lead dioxide(PbO2) Dibutyl pthalate
Polysulphide polymer Copper carbonate Titanium carbonate Or silica as filler materials. BASE CATALYST Lead dioxide(PbO2) Dibutyl pthalate Sulphur

10 Polysulfide A polyfunctional mercaptan or polysulfide polymer
Terminal S-H Chain-lengthening 1 mol% Pendent S-H Cross-link Initiated by an oxidizing agent such as lead dioxide. By-product = H2O Exothermic reaction

11 Reaction: condensation polymerization
Terminal and pendant groups of polymer are oxidized by lead dioxide  chain extension of terminal SH gp and cross linking of pendant gp. Polysulphide polymer + lead dioxide  polysulphide rubber + lead oxide + H2O ….. Exothermic 3-4°C.  in molecular weight Paste  rubber.

12 As % filler increase viscosity increases
Base: three consistencies low: syringe light body Medium regular High: tray Heavy body As % filler increase viscosity increases

13 Lead dioxide: is dark brown to gray brown in colour and toxic.
So substituted by hydrated Cu(OH)2  green mix

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15 light body heavy body

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17 Properties of clinical interest
Setting time: 8-14 minutes this is one of the problem that we don’t use it very much as it is annoying for the pt to put the impression inside the pt mouth for more than 10 min. Higher tear strength than hydrocolloids Accuracy improves if impression is poured within 30 minutes (after 30min water can be produced and evaporate changing its shape. very unpleasant taste and odor this is another reason why we don’t use if often. Messy ( can stain clothes ) Can be irritant to oral mucosa For all these reasons, Polysulfides have been largely replaced by other rubber materials

18 Important notice To help you study go to the following web site
Good luck


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