CH674925A5 - - Google Patents
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- Publication number
- CH674925A5 CH674925A5 CH2902/87A CH290287A CH674925A5 CH 674925 A5 CH674925 A5 CH 674925A5 CH 2902/87 A CH2902/87 A CH 2902/87A CH 290287 A CH290287 A CH 290287A CH 674925 A5 CH674925 A5 CH 674925A5
- Authority
- CH
- Switzerland
- Prior art keywords
- polymer
- methyl methacrylate
- methacrylate
- composition according
- ester
- Prior art date
Links
- 239000000203 mixture Substances 0.000 claims description 115
- 229920000642 polymer Polymers 0.000 claims description 54
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 52
- -1 methacrylate ester Chemical class 0.000 claims description 34
- 239000007788 liquid Substances 0.000 claims description 26
- 229920001577 copolymer Polymers 0.000 claims description 24
- 239000002245 particle Substances 0.000 claims description 21
- 239000000178 monomer Substances 0.000 claims description 20
- 150000001451 organic peroxides Chemical class 0.000 claims description 14
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims description 13
- 239000003431 cross linking reagent Substances 0.000 claims description 13
- DNZPLHRZXUJATK-UHFFFAOYSA-N 2-sulfanylidene-5-[[5-[2-(trifluoromethyl)phenyl]furan-2-yl]methyl]-1,3-diazinane-4,6-dione Chemical compound FC(F)(F)C1=CC=CC=C1C(O1)=CC=C1CC1C(=O)NC(=S)NC1=O DNZPLHRZXUJATK-UHFFFAOYSA-N 0.000 claims description 12
- 150000002148 esters Chemical class 0.000 claims description 10
- 150000002734 metacrylic acid derivatives Chemical class 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 8
- 239000000470 constituent Substances 0.000 claims description 8
- HTKIZIQFMHVTRJ-UHFFFAOYSA-N 5-butyl-1,3-diazinane-2,4,6-trione Chemical compound CCCCC1C(=O)NC(=O)NC1=O HTKIZIQFMHVTRJ-UHFFFAOYSA-N 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 6
- KCWWCWMGJOWTMY-UHFFFAOYSA-N 1-benzyl-5-phenyl-1,3-diazinane-2,4,6-trione Chemical compound O=C1C(C=2C=CC=CC=2)C(=O)NC(=O)N1CC1=CC=CC=C1 KCWWCWMGJOWTMY-UHFFFAOYSA-N 0.000 claims description 5
- 239000004342 Benzoyl peroxide Substances 0.000 claims description 5
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical group C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 claims description 5
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 claims description 5
- 235000019400 benzoyl peroxide Nutrition 0.000 claims description 5
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 claims description 5
- HNYOPLTXPVRDBG-UHFFFAOYSA-N barbituric acid Chemical compound O=C1CC(=O)NC(=O)N1 HNYOPLTXPVRDBG-UHFFFAOYSA-N 0.000 claims 1
- MELGLHXCBHKVJG-UHFFFAOYSA-N dimethyl(dioctyl)azanium Chemical compound CCCCCCCC[N+](C)(C)CCCCCCCC MELGLHXCBHKVJG-UHFFFAOYSA-N 0.000 claims 1
- 239000011342 resin composition Substances 0.000 claims 1
- 238000006116 polymerization reaction Methods 0.000 description 66
- 229920005989 resin Polymers 0.000 description 51
- 239000011347 resin Substances 0.000 description 51
- 230000000052 comparative effect Effects 0.000 description 42
- 239000011505 plaster Substances 0.000 description 35
- 239000012265 solid product Substances 0.000 description 28
- 229910052751 metal Inorganic materials 0.000 description 26
- 239000002184 metal Substances 0.000 description 26
- 238000002474 experimental method Methods 0.000 description 25
- 238000000034 method Methods 0.000 description 16
- 239000000047 product Substances 0.000 description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- 229920001187 thermosetting polymer Polymers 0.000 description 14
- 235000011837 pasties Nutrition 0.000 description 12
- 239000011159 matrix material Substances 0.000 description 10
- 238000012360 testing method Methods 0.000 description 9
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 8
- 238000002156 mixing Methods 0.000 description 8
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 7
- 239000004575 stone Substances 0.000 description 7
- 239000001993 wax Substances 0.000 description 7
- 239000000843 powder Substances 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 230000008602 contraction Effects 0.000 description 5
- 238000005259 measurement Methods 0.000 description 5
- 150000002978 peroxides Chemical class 0.000 description 5
- VDYWHVQKENANGY-UHFFFAOYSA-N 1,3-Butyleneglycol dimethacrylate Chemical compound CC(=C)C(=O)OC(C)CCOC(=O)C(C)=C VDYWHVQKENANGY-UHFFFAOYSA-N 0.000 description 4
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 4
- 150000007656 barbituric acids Chemical class 0.000 description 4
- JBIROUFYLSSYDX-UHFFFAOYSA-M benzododecinium chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 JBIROUFYLSSYDX-UHFFFAOYSA-M 0.000 description 4
- WLCFKPHMRNPAFZ-UHFFFAOYSA-M didodecyl(dimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCC WLCFKPHMRNPAFZ-UHFFFAOYSA-M 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 4
- 239000003112 inhibitor Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- GHMRLAGSBJPPDG-UHFFFAOYSA-N 5-ethyl-2-methylnon-2-enoic acid Chemical compound CCCCC(CC)CC=C(C)C(O)=O GHMRLAGSBJPPDG-UHFFFAOYSA-N 0.000 description 3
- JMHWNJGXUIJPKG-UHFFFAOYSA-N CC(=O)O[SiH](CC=C)OC(C)=O Chemical compound CC(=O)O[SiH](CC=C)OC(C)=O JMHWNJGXUIJPKG-UHFFFAOYSA-N 0.000 description 3
- 230000001788 irregular Effects 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- JZXVADSBLRIAIB-UHFFFAOYSA-N 2-pyrrolidin-2-ylethanol Chemical compound OCCC1CCCN1 JZXVADSBLRIAIB-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- OKKRPWIIYQTPQF-UHFFFAOYSA-N Trimethylolpropane trimethacrylate Chemical compound CC(=C)C(=O)OCC(CC)(COC(=O)C(C)=C)COC(=O)C(C)=C OKKRPWIIYQTPQF-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 210000000481 breast Anatomy 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000001055 chewing effect Effects 0.000 description 2
- 150000001805 chlorine compounds Chemical class 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000011049 filling Methods 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 229910001385 heavy metal Chemical class 0.000 description 2
- 150000002736 metal compounds Chemical class 0.000 description 2
- 210000000214 mouth Anatomy 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- WRXCBRHBHGNNQA-UHFFFAOYSA-N (2,4-dichlorobenzoyl) 2,4-dichlorobenzenecarboperoxoate Chemical compound ClC1=CC(Cl)=CC=C1C(=O)OOC(=O)C1=CC=C(Cl)C=C1Cl WRXCBRHBHGNNQA-UHFFFAOYSA-N 0.000 description 1
- OXYKVVLTXXXVRT-UHFFFAOYSA-N (4-chlorobenzoyl) 4-chlorobenzenecarboperoxoate Chemical compound C1=CC(Cl)=CC=C1C(=O)OOC(=O)C1=CC=C(Cl)C=C1 OXYKVVLTXXXVRT-UHFFFAOYSA-N 0.000 description 1
- WCCUCVYMWMWXAG-UHFFFAOYSA-N 1-cyclohexyl-5-ethyl-1,3-diazinane-2,4,6-trione Chemical compound O=C1C(CC)C(=O)NC(=O)N1C1CCCCC1 WCCUCVYMWMWXAG-UHFFFAOYSA-N 0.000 description 1
- GDOBGDUGIFUCJV-UHFFFAOYSA-N 2,2-dimethylbutane;2-methylprop-2-enoic acid Chemical compound CCC(C)(C)C.CC(=C)C(O)=O.CC(=C)C(O)=O.CC(=C)C(O)=O GDOBGDUGIFUCJV-UHFFFAOYSA-N 0.000 description 1
- OPLCSTZDXXUYDU-UHFFFAOYSA-N 2,4-dimethyl-6-tert-butylphenol Chemical compound CC1=CC(C)=C(O)C(C(C)(C)C)=C1 OPLCSTZDXXUYDU-UHFFFAOYSA-N 0.000 description 1
- HJLBNEMRPGSWOR-UHFFFAOYSA-N 2-methyl-4-(oxolan-2-yl)but-2-enoic acid Chemical compound OC(=O)C(C)=CCC1CCCO1 HJLBNEMRPGSWOR-UHFFFAOYSA-N 0.000 description 1
- RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-UHFFFAOYSA-N 0.000 description 1
- MEKATFFSLMQMRX-UHFFFAOYSA-N 3-cyclohexyl-2-methylprop-2-enoic acid Chemical compound OC(=O)C(C)=CC1CCCCC1 MEKATFFSLMQMRX-UHFFFAOYSA-N 0.000 description 1
- XOJWAAUYNWGQAU-UHFFFAOYSA-N 4-(2-methylprop-2-enoyloxy)butyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCOC(=O)C(C)=C XOJWAAUYNWGQAU-UHFFFAOYSA-N 0.000 description 1
- FMTLDVACNZDTQL-UHFFFAOYSA-N 5-ethyl-1,3-diazinane-2,4,6-trione Chemical compound CCC1C(=O)NC(=O)NC1=O FMTLDVACNZDTQL-UHFFFAOYSA-N 0.000 description 1
- HTEHILLCBQWTLP-UHFFFAOYSA-N 5-phenyl-1,3-diazinane-2,4,6-trione Chemical compound O=C1NC(=O)NC(=O)C1C1=CC=CC=C1 HTEHILLCBQWTLP-UHFFFAOYSA-N 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000002730 additional effect Effects 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- DDXLVDQZPFLQMZ-UHFFFAOYSA-M dodecyl(trimethyl)azanium;chloride Chemical class [Cl-].CCCCCCCCCCCC[N+](C)(C)C DDXLVDQZPFLQMZ-UHFFFAOYSA-M 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000011152 fibreglass Substances 0.000 description 1
- 238000007542 hardness measurement Methods 0.000 description 1
- 238000013007 heat curing Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 210000002200 mouth mucosa Anatomy 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- DXGLGDHPHMLXJC-UHFFFAOYSA-N oxybenzone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 DXGLGDHPHMLXJC-UHFFFAOYSA-N 0.000 description 1
- NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 125000005498 phthalate group Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000001029 thermal curing Methods 0.000 description 1
- 238000012719 thermal polymerization Methods 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
Classifications
-
- 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
- C08F265/00—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00
- C08F265/04—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00 on to polymers of esters
- C08F265/06—Polymerisation of acrylate or methacrylate esters on to polymers thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/80—Preparations for artificial teeth, for filling teeth or for capping teeth
- A61K6/884—Preparations for artificial teeth, for filling teeth or for capping teeth comprising natural or synthetic resins
- A61K6/887—Compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
Landscapes
- Health & Medical Sciences (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Plastic & Reconstructive Surgery (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Dental Preparations (AREA)
- Polymerisation Methods In General (AREA)
- Polymerization Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61178958A JPS6335508A (ja) | 1986-07-31 | 1986-07-31 | 義歯床用樹脂組成物 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH674925A5 true CH674925A5 (d) | 1990-08-15 |
Family
ID=16057633
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH2902/87A CH674925A5 (d) | 1986-07-31 | 1987-07-29 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US4873269A (d) |
| JP (1) | JPS6335508A (d) |
| AU (1) | AU598005B2 (d) |
| BE (1) | BE1001319A3 (d) |
| CH (1) | CH674925A5 (d) |
| DE (1) | DE3725502C2 (d) |
| FR (1) | FR2602140B1 (d) |
| GB (1) | GB2193967B (d) |
| IT (1) | IT1222081B (d) |
| NL (1) | NL188501C (d) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH066608B2 (ja) * | 1985-08-06 | 1994-01-26 | 住友化学工業株式会社 | メタクリル酸エステル系重合体の製造方法 |
| JPH0625204B2 (ja) * | 1985-08-28 | 1994-04-06 | 住友化学工業株式会社 | ビニル系単量体の重合成形方法 |
| JPH0655655B2 (ja) * | 1987-03-06 | 1994-07-27 | 而至陶歯工業株式会社 | 歯科用樹脂の硬化方法 |
| US5183834A (en) * | 1989-04-05 | 1993-02-02 | Dentsply G.M.B.H. | Pasty dental veneer making composition |
| JPH0819173B2 (ja) * | 1990-09-14 | 1996-02-28 | テルモ株式会社 | 界面での重合を制御する重合開始剤組成物およびそれを含む硬化性組成物 |
| US5344902A (en) * | 1991-06-18 | 1994-09-06 | Occidental Research Corporation | Polymerization with initiator and quaternary ammonium salt |
| JP3034650B2 (ja) * | 1991-06-19 | 2000-04-17 | 株式会社ジーシー | 歯質用接着剤 |
| JPH05178714A (ja) * | 1991-11-13 | 1993-07-20 | G C Dentaru Prod:Kk | 歯科用樹脂の硬化方法 |
| US5252577A (en) * | 1992-03-06 | 1993-10-12 | Gillette Canada, Inc. | Methods of desensitizing teeth |
| US5328362A (en) * | 1992-03-11 | 1994-07-12 | Watson Sherman L | Soft resilient interocclusal dental appliance, method of forming same and composition for same |
| DE4233891A1 (de) * | 1992-10-08 | 1994-04-14 | Roehm Gmbh | Verfahren zum Verkleben von amorphen Kunststoffen |
| US5502087A (en) * | 1993-06-23 | 1996-03-26 | Dentsply Research & Development Corp. | Dental composition, prosthesis, and method for making dental prosthesis |
| IT1272191B (it) * | 1994-03-28 | 1997-06-16 | Bandini Srl | Composizione di materiale dentario a base di resine sintetiche con proprieta' antisettiche. |
| AU692520B2 (en) | 1994-05-16 | 1998-06-11 | Dentsply Detrey G.M.B.H. | Method of making a dental prosthesis and curable system |
| US5660817A (en) * | 1994-11-09 | 1997-08-26 | Gillette Canada, Inc. | Desensitizing teeth with degradable particles |
| JP3919925B2 (ja) * | 1997-08-07 | 2007-05-30 | 住友化学株式会社 | 樹脂組成物、その成形体及び成形体の製造方法 |
| US6605651B1 (en) * | 1998-09-09 | 2003-08-12 | Biomat Sciences, Inc. | Curing methods and material compositions having dental and other applications |
| US6254389B1 (en) | 1999-09-20 | 2001-07-03 | Marc Seghatol | Hand-held microwave intra-oral dental system |
| WO2000018191A1 (en) | 1998-09-18 | 2000-03-30 | Marc Seghatol | Microwave polymerization system for dentistry |
| JP4774696B2 (ja) * | 2004-07-20 | 2011-09-14 | 日産自動車株式会社 | 加工装置及び加工方法 |
| ATE532797T1 (de) | 2006-05-31 | 2011-11-15 | 3M Innovative Properties Co | Polymerisierbare zusammensetzungen enthaltend salze aus barbitursäure-derivaten |
| JP5331697B2 (ja) * | 2007-09-13 | 2013-10-30 | サンメディカル株式会社 | 歯科用重合性組成物およびそのキット |
| US8217081B2 (en) * | 2009-04-07 | 2012-07-10 | The United States of America as represented by the Secretary of Commerce, the National Institute of Standards and Technology | Polymerizable biomedical composition |
| JP5653554B1 (ja) * | 2014-05-30 | 2015-01-14 | 株式会社松風 | 二成分混和型イオン徐放性義歯床用関連材料組成物 |
| CN106536578B (zh) * | 2014-07-22 | 2020-03-17 | 3M创新有限公司 | 自由基聚合方法和由此而得的制品 |
| WO2019189579A1 (ja) * | 2018-03-30 | 2019-10-03 | 三井化学株式会社 | 歯科材料用重合性組成物、該組成物から得られた歯科材料 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2987500A (en) * | 1957-05-03 | 1961-06-06 | Rossetti Carlo | Process for the production of polymethacrylic acid esters |
| DE1495520B2 (de) * | 1964-05-02 | 1970-06-25 | Deutsche Gold- U. Silber-Scheideanstalt, Vorm. Roessler, 6000 Frankfurt | Verfahren zum Polymerisieren |
| US4001939A (en) * | 1967-08-19 | 1977-01-11 | Kulzer & Co. Gmbh | Tooth-filling material based on synthetic plastics material |
| US4396476A (en) * | 1979-02-01 | 1983-08-02 | Dentsply Research & Development Corporation | Blend of cross-linked polymer, swelling monomer and cross-linking agent and curing process |
| DE3107577A1 (de) * | 1981-02-27 | 1982-09-16 | ESPE Fabrik pharmazeutischer Präparate GmbH, 8031 Seefeld | 1,2-6-thiadiazin-3,5-dion-1,1-dioxide und ihre verwendung |
| JPS61339A (ja) * | 1984-06-13 | 1986-01-06 | 株式会社 東洋化学研究所 | 加工容易な歯科用硬質レジンの使用方法 |
| JPS6176149A (ja) * | 1984-07-31 | 1986-04-18 | 木村 博 | 義歯床の製造方法 |
| JPS6178707A (ja) * | 1984-09-27 | 1986-04-22 | Toyo Kagaku Kenkyusho:Kk | 加工容易な歯科用硬質レジンの使用方法 |
| JPS61126007A (ja) * | 1984-11-22 | 1986-06-13 | Shiyoufuu:Kk | 歯科用修復組成物 |
| JPS62175410A (ja) * | 1986-01-29 | 1987-08-01 | Shiyoufuu:Kk | 歯科用修復材組成物 |
| JPS62175412A (ja) * | 1986-01-29 | 1987-08-01 | Shiyoufuu:Kk | 歯科用修復材組成物 |
-
1986
- 1986-07-31 JP JP61178958A patent/JPS6335508A/ja active Granted
-
1987
- 1987-07-07 US US07/070,701 patent/US4873269A/en not_active Expired - Lifetime
- 1987-07-21 IT IT21365/87A patent/IT1222081B/it active
- 1987-07-21 AU AU75990/87A patent/AU598005B2/en not_active Ceased
- 1987-07-23 FR FR8710475A patent/FR2602140B1/fr not_active Expired - Lifetime
- 1987-07-23 NL NLAANVRAGE8701740,A patent/NL188501C/xx not_active IP Right Cessation
- 1987-07-28 BE BE8700840A patent/BE1001319A3/fr not_active IP Right Cessation
- 1987-07-29 CH CH2902/87A patent/CH674925A5/fr not_active IP Right Cessation
- 1987-07-30 GB GB8718115A patent/GB2193967B/en not_active Expired
- 1987-07-31 DE DE3725502A patent/DE3725502C2/de not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| FR2602140A1 (fr) | 1988-02-05 |
| FR2602140B1 (fr) | 1991-10-31 |
| GB8718115D0 (en) | 1987-09-03 |
| GB2193967B (en) | 1989-12-13 |
| IT8721365A0 (it) | 1987-07-21 |
| AU7599087A (en) | 1988-02-04 |
| DE3725502A1 (de) | 1988-02-11 |
| JPH0460562B2 (d) | 1992-09-28 |
| JPS6335508A (ja) | 1988-02-16 |
| DE3725502C2 (de) | 1994-10-06 |
| US4873269A (en) | 1989-10-10 |
| BE1001319A3 (fr) | 1989-09-26 |
| NL188501B (nl) | 1992-02-17 |
| NL8701740A (nl) | 1988-02-16 |
| GB2193967A (en) | 1988-02-24 |
| AU598005B2 (en) | 1990-06-14 |
| NL188501C (nl) | 1992-07-16 |
| IT1222081B (it) | 1990-08-31 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased |