US3912758A - Polythioether impression material - Google Patents
Polythioether impression material Download PDFInfo
- Publication number
- US3912758A US3912758A US437234A US43723474A US3912758A US 3912758 A US3912758 A US 3912758A US 437234 A US437234 A US 437234A US 43723474 A US43723474 A US 43723474A US 3912758 A US3912758 A US 3912758A
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- US
- United States
- Prior art keywords
- parts
- weight
- component
- catalyst
- polymer
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- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/02—Polythioethers
- C08G75/04—Polythioethers from mercapto compounds or metallic derivatives thereof
- C08G75/045—Polythioethers from mercapto compounds or metallic derivatives thereof from mercapto compounds and unsaturated compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/90—Compositions for taking dental impressions
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F291/00—Macromolecular compounds obtained by polymerising monomers on to macromolecular compounds according to more than one of the groups C08F251/00 - C08F289/00
- C08F291/14—Macromolecular compounds obtained by polymerising monomers on to macromolecular compounds according to more than one of the groups C08F251/00 - C08F289/00 on to sulfur-containing macromolecules
Definitions
- the present invention relates to a dental impression material and more particularly to a polythioether impression material.
- a two paste system containing polymeric mercaptan, plasticizers, sulfur, lead peroxide and a filler is used by dentists to take impressions of patients teeth. Such impressions are used by the dentist to make crowns, dentures, or the like.
- a polymerizable material is formed which the dentist applies to the teeth to produce a custom dental tray.
- the polymerized material is removed and this custom dental tray used as a mold in making the crown or denture.
- the two paste system of the prior art has a relatively long setting time and the fact that the material contains lead may make it somewhat objectionable to the dentist. Furthermore the prior art mixture is an unsightly brown color and has an offensive odor due to the presence of low molecular weight sulfur compounds. For these reasons, putting such a material into the patients mouth and the taking of a dental impression, often proved to be an unpleasant and traumatic experience. During the time the impression is being taken the patient must keep his mouth steady and immobile and since the curing time of the prior art material is six minutes it is difficult for the patient to do this.
- One object of the invention is to provide a polymeric impression material which can be admixed and is aesthetically pleasing.
- Another object of the invention is toprovide a ploythioether dental impression material.
- a further object of the present invention is to provide a dimensionally stable dental impression material which has a pleasant odor and which can be given any color.
- Yet another object is to provide a dental impression material capable of hardening in approximately [2 minutes.
- the polythioether polymer material of this invention is used for making impression and imprints and serves as a mold from which a similar article could be reproduced.
- the polymer In the uncured stage the polymer has a puttylike consistency. An impression of a shape or a contour is made upon it. Upon curing the polymer hardens and retains the impression.
- the polymeric material has non-adhering properties and releases itself easily from the object whose impression is made.
- the polythioether impression material of the invention is a polymeric system based on the use of: (l) a mercaptan terminated polymer, more specifically a mercaptan terminated bis(oxyethylene)methane containing disulfide linkage with a small amount of thio groups in the chain, having a molecular weight of 4,000; (2) a di, tri or tetra-acrylate monomer such as hexane diol diacrylate or polyethyleneglycol diacrylate or trimethylolpropane triacrylate; and (3) a peroxide preferably calcium peroxide.
- the mercaptan terminated polymer suitable for use in the present invention will in general have a functionality of two or greater and will be of a high molecular weight but still liquid and fluid. It may also contain various amounts of mercapto groups in the chain for crosslinking purposes.
- the polymers should have molecular weights ranging from l0004000 and may contain various percentages of mercapto groups on the molecular chain.
- the mercapto groups are available for crosslinking the acrylic monomers. Many polymers meeting this description are commercially available. We have found products manufactured by Thiokol Chemical Co. under the trade name LP-Z, LP-33, etc. to be particularly useful.
- di, tri and tetra acrylated monomers and polymers are propylene glycol diacrylate, butylene glycol diacrylate, hexane diol diacrylate, tri methylol propane triacrylate, pentaerythritol tetraacrylate, and polyethylene glycol diacrylate.
- Properties of the polymerizable system will depend upon the acrylate chosen and the amount used. Functionality of acrylates is chosen to get optimum physical properties in the finished custom dental tray which is used as the mold. With the increase in functionality physical properties such as hardness, and rigidity increases. The excessive amounts lead to shorter pot life, brittleness and higher shrinkage.
- the molecular weight of acrylate can affect rigidity, elasticity, as well as working time.
- High molecular weight acrylates such as polyethylene diacrylate produce soft elastic, non-rigid polymers. Hexane diol diacrylate produces polymers having increased hardness and rigidity. Tri acrylates would produce corresponding results depending upon molecular weight. For our purposes we have found that an excess of stoichiometric equivalents is desirable, although less amounts can be used if modifications are desirable in the work ing characteristics.
- fillers are quite necessary to reinforce the set material.
- Many fillers known in the elastomeric field could be used, such as: calcium carbonate, calcium oxide, magnesium oxide, magnesium sulfate, strontium sulfate, barium sulfate, titanium dioxide, zinc oxide, zinc sulfate, zinc sulfide, zinc chloride, aluminum oxide, silica, antimony oxides, tin oxides, and others.
- particle size and surface behavior are important considerations in filler selection.
- plasticizers are used to control the consistency of the hand moldable putty.
- a number of plasticizers are available for use, depending upon particular properties desired. We have found a low molecular weight liquid styrene polymer to be quite useful as a plasticizer.
- Suitable plasticizers are those having the viscosity in the range 2000-50000 cps at ambient tempera- Color, Gardner v 2.5 Viscosity at 77F.. poise 120-200 Volatility 2 hrs. at 311F.- .557: Volatility 4 hrs. at 31 1F. 1.29%
- Flash point F open cup Fire point F. open cup 300 maximum 350 maximum Pour point F 50 Refractive lndex 1.58 Sp. G. at 77F. 1.03
- Metal peroxides are utilized as reactive components. These include zinc peroxide, tin peroxide, antimony peroxide, lead peroxide, manganese peroxide, barium peroxide, strontium peroxide, calcium peroxide, magnesium peroxide, and others.
- hydroperoxides such as cumene hydroperoxide can be useful. For our purposes we have found calcium peroxide to be most desirable because of its good reactivity, good handling, acceptable color and low potential toxicity. Water and amines such as triethylolamine can be further used to accelerate the reaction and improve the physical properties.
- the catalyst component in addition includes the metal peroxide.
- a typical base component formed according to the present invention would include:
- Mercaptan Polymer 100.00 parts by wt. Hexane Diol Diacrylate 6.00 parts by wt. Filler (silica) 200.00 parts by wt. Mineral Oil 10.00 parts by wt. Perfume trace parts by wt. Pigment trace parts by wt. Water 2.00 parts by wt.
- the catalyst component typically would include:
- two parts of the base is admixed with one part of the catalyst.
- the base and catalyst can be mixed together in the hands and when molded and set, produce a rigid high durometer material having a hardness of 75-80 on a Shore A durometer.
- the material sets in l minutes and because of absence of low molecular weight sulfur compounds it is void of offensive odor.
- the ratio of base to catalyst could be varied to control the setting time between [-5 minutes. An increase in the catalyst amount shortens the time.
- Another successful formula for these components would include:
- the polymeric material is most suited as a dental impression material. It could also be used in making reproductions of carvings and sculptures. The impression material is applied on the surface of the sculpture and removed upon hardening. This matrix could then be used to make more copies of the sculpture.
- a. component one comprising
- an acrylate monomer selected from a group consisting of hexanediol diacrylate, polyethylene glycol diacrylate and trimethylolpropane triacrylate,
- mercaptan terminated polymer of molecular weight 1000-4000, having mercaptan groups available for crosslinking with said monomer
- component two comprising
- a peroxide catalyst for initiating a reaction between said polymer and monomer of component one;
- peroxide catalyst 100 parts by weight and triethylolamine 5 parts by weight of component two;
- I c. components one and two each further comprising 190-200 parts by weight a filler and 10-15 parts by weight mineral oil.
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Organic Chemistry (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Dental Preparations (AREA)
Abstract
Description
Claims (5)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US437234A US3912758A (en) | 1974-01-28 | 1974-01-28 | Polythioether impression material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US437234A US3912758A (en) | 1974-01-28 | 1974-01-28 | Polythioether impression material |
Publications (1)
Publication Number | Publication Date |
---|---|
US3912758A true US3912758A (en) | 1975-10-14 |
Family
ID=23735617
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US437234A Expired - Lifetime US3912758A (en) | 1974-01-28 | 1974-01-28 | Polythioether impression material |
Country Status (1)
Country | Link |
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US (1) | US3912758A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4698385A (en) * | 1984-02-23 | 1987-10-06 | Rohm And Haas Company | Binder for high solids ambient cure coatings |
US4728712A (en) * | 1985-06-11 | 1988-03-01 | Products Research & Chemical Corp. | Method of producing mercaptan terminated polymers with increased reactivity and reduced odor |
EP0366977A2 (en) * | 1988-11-04 | 1990-05-09 | THERA Patent GmbH & Co. KG Gesellschaft für industrielle Schutzrechte | Visible light curable dental materials |
US20040028624A1 (en) * | 2001-05-17 | 2004-02-12 | Kettenbach Gmbh & Co. Kg. | Chemically curing dental bleaching material |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2558139A (en) * | 1947-08-26 | 1951-06-26 | L D Caulk Company | Dental material and method |
US3349047A (en) * | 1965-10-22 | 1967-10-24 | Thiokol Chemical Corp | Curable liquid polysulfide resin stably admixed with calcium peroxide |
US3736301A (en) * | 1971-08-20 | 1973-05-29 | M Berenbaum | Curable polysulfide polymers |
US3751399A (en) * | 1971-05-24 | 1973-08-07 | Lee Pharmaceuticals | Polyacrylate resin compositions |
-
1974
- 1974-01-28 US US437234A patent/US3912758A/en not_active Expired - Lifetime
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2558139A (en) * | 1947-08-26 | 1951-06-26 | L D Caulk Company | Dental material and method |
US3349047A (en) * | 1965-10-22 | 1967-10-24 | Thiokol Chemical Corp | Curable liquid polysulfide resin stably admixed with calcium peroxide |
US3751399A (en) * | 1971-05-24 | 1973-08-07 | Lee Pharmaceuticals | Polyacrylate resin compositions |
US3736301A (en) * | 1971-08-20 | 1973-05-29 | M Berenbaum | Curable polysulfide polymers |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4698385A (en) * | 1984-02-23 | 1987-10-06 | Rohm And Haas Company | Binder for high solids ambient cure coatings |
US4728712A (en) * | 1985-06-11 | 1988-03-01 | Products Research & Chemical Corp. | Method of producing mercaptan terminated polymers with increased reactivity and reduced odor |
EP0366977A2 (en) * | 1988-11-04 | 1990-05-09 | THERA Patent GmbH & Co. KG Gesellschaft für industrielle Schutzrechte | Visible light curable dental materials |
EP0366977A3 (en) * | 1988-11-04 | 1991-01-30 | THERA Patent GmbH & Co. KG Gesellschaft für industrielle Schutzrechte | Visible light curable dental materials |
US20040028624A1 (en) * | 2001-05-17 | 2004-02-12 | Kettenbach Gmbh & Co. Kg. | Chemically curing dental bleaching material |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
AS | Assignment |
Owner name: KERR MANUFACTURING COMPANY, A CORP OF DE. Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:SYBRON CORPORATION;REEL/FRAME:004610/0363 Effective date: 19860731 Owner name: KERR MANUFACTURING COMPANY, A CORP OF DE., STATELE Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:SYBRON CORPORATION;REEL/FRAME:004610/0363 Effective date: 19860731 |
|
AS | Assignment |
Owner name: MANUFACTURERS HANOVER TRUST COMPANY Free format text: ASSIGNMENT OF ASSIGNORS INTEREST. ASSIGNS THE ENTIRE INTEREST;ASSIGNORS:SAC/THERMOLYNE, INC.;SAC/BARNSTEAD, INC.;SAC/THERMO-BARN, INC.;AND OTHERS;REEL/FRAME:004834/0513 Effective date: 19871020 Owner name: MANUFACTURERS HANOVER TRUST COMPANY,STATELESS Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:SAC/THERMOLYNE, INC.;SAC/BARNSTEAD, INC.;SAC/THERMO-BARN, INC.;AND OTHERS;REEL/FRAME:004834/0513 Effective date: 19871020 |