US3912758A - Polythioether impression material - Google Patents

Polythioether impression material Download PDF

Info

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
Authority
US
United States
Prior art keywords
parts
weight
component
catalyst
polymer
Prior art date
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.)
Expired - Lifetime
Application number
US437234A
Inventor
Benjamin Weaver
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Manufacturers Hanover Trust Co
Original Assignee
Sybron Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Sybron Corp filed Critical Sybron Corp
Priority to US437234A priority Critical patent/US3912758A/en
Application granted granted Critical
Publication of US3912758A publication Critical patent/US3912758A/en
Assigned to KERR MANUFACTURING COMPANY, A CORP OF DE. reassignment KERR MANUFACTURING COMPANY, A CORP OF DE. ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: SYBRON CORPORATION
Assigned to MANUFACTURERS HANOVER TRUST COMPANY reassignment MANUFACTURERS HANOVER TRUST COMPANY ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: BARNSTEAD COMPANY, BOTHNIA HOLDINGS, INC., ERIE SCIENTIFIC COMPANY, KERR MANUFACTURING COMPANY, MEXOSERV COMPANY, NALGE COMPANY, ORMCO CORPORATION, SAC/BARNSTEAD, INC., SAC/CK, INC., SAC/ERIE, INC., SAC/KERR, INC., SAC/NALGE, INC., SAC/ORMCO, INC., SAC/RESIDUAL, INC., SAC/THERMO-BARN, INC., SAC/THERMOLYNE, INC., THERMOLYNE CORPORATION, THERMOLYNE HOLDINGS, INC.
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G75/00Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
    • C08G75/02Polythioethers
    • C08G75/04Polythioethers from mercapto compounds or metallic derivatives thereof
    • C08G75/045Polythioethers from mercapto compounds or metallic derivatives thereof from mercapto compounds and unsaturated compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K6/00Preparations for dentistry
    • A61K6/90Compositions for taking dental impressions
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F291/00Macromolecular compounds obtained by polymerising monomers on to macromolecular compounds according to more than one of the groups C08F251/00 - C08F289/00
    • C08F291/14Macromolecular 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.

Landscapes

  • 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

A colorable, pleasant smelling, quick setting, putty-like polythioether polymer material formed by reacting a mercaptan and a diacrylate with the aid of a peroxide catalyst.

Description

United States Patent Weaver 1 1 Oct. 14, 1975 54] POLYTHIOETHERIMPRESSION 3,751,399 /1973 bee etal 32/15 MATERIAL OTHER PUBLICATIONS Inventor: Benjamin Weaver, Detroit, Mich.
Sybron Corporation, Rochester, N .Y.
Filed: Jan. 28, 1974 Appl. No.: 437,234
Assignee:
References Cited UNITED STATES PATENTS 6/1951 Knock et a1. 32/107 10/1967 Sheard 260/791 5/ 1973 Berenbaum et a1 260/79.1
Anderson Applied Dental Matls., (3rd ed.), (Blackwell Sci. Pub.), (Oxford, 0 England), (1967), pp. 217-219.
Combe Notes on Dental Matls., (Churchill Livingstone), (London), (1972), pp. 141-442.
Primary Examiner-M. J. Welsh Assistant Examiner-H. H. Fletcher Attorney, Agent, or Firm--'Iheodore B. Roessel; Papan Devnani ABSTRACT A colorable, pleasant smelling, quick setting, puttylike polythioether polymer material formed by reacting a mercaptan and a diacr'ylate with the aid of a peroxide catalyst.
5 Claims, No Drawings POLYTIIIOETHER IMPRESSION MATERIAL BACKGROUND OF THE INVENTION The present invention relates to a dental impression material and more particularly to a polythioether impression material. In current practice 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. When mixed, usually with a spatula on a paper pad a polymerizable material is formed which the dentist applies to the teeth to produce a custom dental tray. When set, 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, however, 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.
The drawbacks of the prior art are overcome in the present invention by providing an impression material which is lead-free, pleasant smelling, quick setting, and colorable.
SUMMARY OF THE INVENTION OBJECTS OF THE INVENTION 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.
DETAILED DESCRIPTION OF THE INVENTION 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. 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.
Some examples of 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.
Along with the mercaptan terminated polymer and acrylic monomers the use of appropriate fillers is 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. As in most elastomeric applications particle size and surface behavior are important considerations in filler selection.
The 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. We have also found that 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. 1
These components are formed into two pastes, one containing primarily the base and the other the catalyst. The catalyst component in addition includes the metal peroxide.
A typical base component formed according to the present invention would include:
Mercaptan Polymer (LP-2) 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:
Plasticizer TP-680 70.00 parts by wt. Triethylolamine 5.00 parts by wt. CaO 100.00 parts by wt. Filler (Silica) 190.00 pans by wt. Mineral Oil 15.00 parts by wt.
In order to form a dental impression material according to the present invention, 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:
Polymercaptzm 100.00 parts by weight ZnS 23.00 parts by weight 5 Trimethylol 2.00 parts by weight propane triacrylate parts by weight Hexane diol diacrylate r 2.00 parts by weight Water 1.50 parts by weight Catalyst v i Calcium peroxide 100.00 parts by weight Magnesium oxide 10.00 parts by weight Zinc oxide 100.00 parts by weight Plasticizer (TP-680) 175.00 parts by weight Mineral oil 5.00 parts by weight Silicone Oil 1000 parts by weight Thus, it should be appreciated that the present invention accomplishes its intended objectives in providing a dental impression material which smells good, is aesthetically pleasant, colorable, easy to handle, and sets in 1 /2 minutes instead of 6 minutes thereby saving a dentists time. In addition it is so easy to form a custom tray it saves an additional visit by the patient to the dentist.
Ideally, 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.
Having described the invention in detail, what is 30 claimed as new is:
1. An impression material formed by polymerization by mixing together two paste like components:
a. component one comprising;
i. an acrylate monomer selected from a group consisting of hexanediol diacrylate, polyethylene glycol diacrylate and trimethylolpropane triacrylate,
ii. a mercaptan terminated polymer of molecular weight 1000-4000, having mercaptan groups available for crosslinking with said monomer, and
iii. said acrylate monomer making up about 6 parts by weight and said polymer making up about 100 parts by weight of component one;
b. component two comprising;
i. alpha methyl styrene oligomer as plasticizer,
ii. a peroxide catalyst for initiating a reaction between said polymer and monomer of component one;
iii. triethylolamine as accelerator for reaction;
iv. said plasticizer making up 70 parts by weight,
peroxide catalyst 100 parts by weight and triethylolamine 5 parts by weight of component two;
and a I c. components one and two each further comprising 190-200 parts by weight a filler and 10-15 parts by weight mineral oil.
2. Material of claim 1 wherein the filler is silica.
3. Material of claim 1 wherein thecatalyst is calcium peroxide.
4. Material of claim 1 wherein saidmaterial contains a perfume.
5. Material of claim 1 wherein said material contains a pigment.
speeding the UNITED STATES PATENT QFFICE CERTIFICATE OF CORRECTION Patent No. 3,912,758 Dated October 14, 1975 Ben 'amin Weaver Inventor-(s) 3 It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:
Column line 57, change "1/2" to 1 1/2 Column 2; line 15, after "two" insert (2) I line 27, change "'aci'ylated" to acrylate M1 Column 3, line 55, the entire equation should be deleted 0 I Bigncd and Scaled this twentieth D y f January 1976 [SEAL] Arrest:
RUTH C. MASON C. MARSHALL DANN Arresting Office Commissioner of Patents and Trademarks

Claims (5)

1. AN IMPRESSION MATERIAL FORMED BY POLYMERIZATION BY MIXING TOGETHER TWO PASTE LIKE COMPONENTS: A. COMPONENT ONE COMPRISING, I. AN ACRYLATE MONOMER SELECTED FROM A GROUP CONSISTING OF HEXANEDIOL DIACRYLATE, POLYETHYLENE GLYCOL DIACRYLATE AND TRIMETHYLOLPROPANE TRIACRYLATE, II. A MERCAPTAN TERMINATED POLYMER OF MOLECULAR WEIGHT 1000-4000, HAVING MERCAPTAN GROUPS AVAILABLE FOR CROSSLINKED WITH SAID MONOMER, AND III. SAID ACRYLATE MONOMER MAKING UP ABOUT 6 PARTS BY WEIGHT AND SAID POLYMER MAKING UP ABOUT 100 PARTS BY WEIGHT OF COMPONENT ONE, B. COMPONENT TWO COMPRISING, I. ALPHA METHYL STYRENE OLIGOMER AS PLASTICIZER, II. A PERIOXIDE CATALYST FOR INITIATING A REACTION BETWEEN SAID POLYMER AND MONOMER OF COMPONENT ONE, III. TRIETHYLOLAMINE AS ACCELERATOR FOR SPEEDING THE REACTION, 1V. SAID PLASTICIZER MAKING UP 70 PARTS BY WEIGHT, PERIOXIDE CATALYST 100 PARTS BY WEIGHT AND TRIETHYLOLAMINE 5 PARTS BY WEIGHT OF COMPONENT TWO, AND C. COMPONENTS ONE AND TWO EACH FURTHER COMPRISING 190-200 PARTS BY WEIGHT A FILLER AND 10-15 PARTS BY WEIGHT MINERAL OIL.
2. Material of claim 1 wherein the filler is silica.
3. Material of claim 1 wherein the catalyst is calcium peroxide.
4. Material of claim 1 wherein said material contains a perfume.
5. Material of claim 1 wherein said material contains a pigment.
US437234A 1974-01-28 1974-01-28 Polythioether impression material Expired - Lifetime US3912758A (en)

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
US (1) US3912758A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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

Patent Citations (4)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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

Similar Documents

Publication Publication Date Title
US4468202A (en) Method for making dental impressions
US4543063A (en) Elastomeric impression material for tooth and supporting structure duplication
US5753781A (en) Blended polycaprolactone thermoplastic molding composition
US3829973A (en) Dental and surgical bonding-filling material
JP4344946B2 (en) Curable acrylate polymer composition characterized by improved bending properties
CN105722494B (en) Impact-modified denture base composition
JP3454980B2 (en) Silicone composition for dental impression
Chaing Polymers in the service of prosthetic dentistry
JPS6339564B2 (en)
US3912758A (en) Polythioether impression material
JP2007512115A (en) How to mold dental products
US3084436A (en) Polymers prepared by polymerizing a mixture of esters in the presence of a vinyl stearate-vinyl acetate copolymer, and a denture therewith
US3923754A (en) Curing of liquid polythiopolymercaptan polymers
JP2007051116A (en) Room temperature curing resin for dental use
US4759798A (en) Process for the preparation of dental-technical, dental-medical and medical molding and lining materials
US5718924A (en) Fluoride releasing biomaterials
May et al. A narrative review of different types and processing methods of acrylic denture base material
JPH08169806A (en) Dental adhesive composition
Tanveer Biomaterials for maxillofacial prosthetic rehabilitation
CA1256237A (en) Substance for the preparation of plastic and/or hard substances for dental-technical, (dental)medical and related purposes, process for its production and the use thereof
JP3481070B2 (en) Soft rebase material mounting kit
GB2114142A (en) Elastomeric moulding compositions
CA2223367A1 (en) Hydrophilic silicone dental impression composition
SU704610A1 (en) Material for making dentures
JP3489899B2 (en) Dental composition

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