SU682101A3 - Material for the preparation of stomatological models - Google Patents
Material for the preparation of stomatological modelsInfo
- Publication number
- SU682101A3 SU682101A3 SU731931272A SU1931272A SU682101A3 SU 682101 A3 SU682101 A3 SU 682101A3 SU 731931272 A SU731931272 A SU 731931272A SU 1931272 A SU1931272 A SU 1931272A SU 682101 A3 SU682101 A3 SU 682101A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- stomatological
- models
- preparation
- paste
- spz
- Prior art date
Links
- 239000000463 material Substances 0.000 title description 3
- 229960001957 stomatological preparations Drugs 0.000 title 1
- 239000000203 mixture Substances 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 3
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 2
- -1 poly di methylsiloxane Polymers 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- LFQCEHFDDXELDD-UHFFFAOYSA-N tetramethyl orthosilicate Chemical compound CO[Si](OC)(OC)OC LFQCEHFDDXELDD-UHFFFAOYSA-N 0.000 description 2
- 101150033248 AME1 gene Proteins 0.000 description 1
- 241001132374 Asta Species 0.000 description 1
- FYEHYMARPSSOBO-UHFFFAOYSA-N Aurin Chemical compound C1=CC(O)=CC=C1C(C=1C=CC(O)=CC=1)=C1C=CC(=O)C=C1 FYEHYMARPSSOBO-UHFFFAOYSA-N 0.000 description 1
- 241001060848 Carapidae Species 0.000 description 1
- 241001342895 Chorus Species 0.000 description 1
- 241000282326 Felis catus Species 0.000 description 1
- 241001397173 Kali <angiosperm> Species 0.000 description 1
- 101100096884 Rattus norvegicus Sult1e1 gene Proteins 0.000 description 1
- 241000124033 Salix Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- HAORKNGNJCEJBX-UHFFFAOYSA-N cyprodinil Chemical compound N=1C(C)=CC(C2CC2)=NC=1NC1=CC=CC=C1 HAORKNGNJCEJBX-UHFFFAOYSA-N 0.000 description 1
- OPTASPLRGRRNAP-UHFFFAOYSA-N cytosine Chemical compound NC=1C=CNC(=O)N=1 OPTASPLRGRRNAP-UHFFFAOYSA-N 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- UGCDBQWJXSAYIL-UHFFFAOYSA-N vat blue 6 Chemical compound O=C1C2=CC=CC=C2C(=O)C(C=C2Cl)=C1C1=C2NC2=C(C(=O)C=3C(=CC=CC=3)C3=O)C3=CC(Cl)=C2N1 UGCDBQWJXSAYIL-UHFFFAOYSA-N 0.000 description 1
- 238000004073 vulcanization Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
-
- 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
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/02—Polysilicates
-
- 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
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/14—Polysiloxanes containing silicon bound to oxygen-containing groups
- C08G77/16—Polysiloxanes containing silicon bound to oxygen-containing groups to hydroxyl groups
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Dental Preparations (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Adhesives Or Adhesive Processes (AREA)
Description
;54;; 54;
МАТЕРИАЛ ДЛЯMATERIAL FOR
СТО.МЛТОЛО П1 ЧЕСКИ XSTO.MLTOLO P1 CESKI X
ПОЛУЧЕНИЯ СЛЕПКОВOf getting blind
;.: ,: :: .. 1;,-и Г Г-rui р, г ;.:,: :: .. 1;, - and Г Г-rui р, г
(,У li. СИ;;И1(ПГ; . И ( 5 г ГИД )О1-.:иги кали , f:r,cr noj3o-u ой р 200 ПО; ц::;дного мптан)/-;), и 2500 г тогрэм г:гц г;силчката при н г у-ррр о .(, At li. SI ;; И1 (ПГ;. И (5 g ГИД) О1 -.: Kali fi, f: r, cr noj3o-u Oh p 200 PO; c ::; bottom mpan) / -;) , and 2500 g togrem g: Hz g; silchkata at n g y-rrr o.
И эту сусиенпию лобгтвл ют 1,2 г рс,1ммил-Н-стеауата , ра,;т )иого п полиэфирном , и ч которого удал ют газ. Смесь .чагр г::вают в обратном токе. 1 час. ооле зтого метанол ,ци сти.т:лиру1от на колонке с xopcujcft разде-пню цен способностью до пол;-:ой замены мето сигрупгты .And this susienpia is labeled with 1.2 g RS, 1 ml-H-steauate, pa, t) polyester, and from which the gas is removed. Mixture .chagr :: wate in reverse current. 1 hour. Gold, methanol, cyt. t: liraine from the column with the xopcujcft section of the price with the ability to the floor;
riocjie охлаждени ос;таток отдел ют F а .,еггрифуге .riocjie axle cooling; tatok separated F and.
Затем избыточное ксзличество тетраметилсиликата полностью отдел ют .цистилл цией л вакууме при непрерывном пересмешив ании остатка. Температура M THH;viaJiьна . Получают полужидкий остатс К синего цвета. В зависимости от свойств егО псремаииаают с раз/:;: ным к од и ч SCT в ом ди бути л;д1 л аурин ат а олова, дл пр :дани отверждаюы х CBofCTjj дог-:олн - телfcno ддобавл ют неCKviLbKO пропей гоп тератид иди по.г; метилсиликата, i:,-;/; прида;п:м более густоп конс;; сте1 аки доба : п .;т 12 ;/ коллоидной Д1 уокиси KpeMiniH при непрерыпгаом переме1иивании ,Then, excess tetramethyl silicate is completely separated by cyclization under vacuum with continuous stirring of the residue. Temperature M THH; viaJi on. A semi-liquid blue K is obtained. Depending on its properties, it is preemptive with times of:::: one to one SCT in ohm di-buti l; d1 l aurin ata tin, for the pr: hardened CBofCTj jy:: - telfcno to add non-CKviLbKO hop teratis go by; methyl silicate, i:, -; /; d; n: m more dense cons ;; Ste1 aki doba: p. T 12; / colloidal D1 uokisi KpeMiniH with continuous movement,
I: Р и м е Р 2 .I: R and e R 2.
а) г пасть., состо.чщей -из 35% W . W -ди: идроксипо;-(идиме -и силокс;ан л с 2 з чость о 20000 спз при температуре 20 С и ЬэЧ: КЕАрпевог о гк рамка, замешивают |; ;:а1е-тем с 0,8 г отверди сдч , при го г лонного ov:i:::aiii: м сч;оообом . Смесь у7:к М11;Зир ;от г:ри 1 омнатHOF томтюрамуре з тече/мги v-c миг. Пот учаОг эласиг ;л 1И л1тoin j:i, имеюIi-iH тг ерде-:;ть ,a) d mouth., consisting of-35% W. W –di: iroxipo ;-( idimene-and silox; anl with 2 components of 20,000 centipoise at a temperature of 20 ° C and LEC: KEArpevog about the frame, knead |;;: with a hollow ov: i ::: aiii: m, m; ooob. Mix y7: to M11; Zir; from g: Re: 1 omnHHOT tomuramur from leaking / mgi vc instant.Participating elasig; l 1I l1toin j: i, I have Ii-iH tg herede - :; t,
б)10 г пасты, ;;ocTO :ue i из 35% W, h - ди гидр он си го 1КДГ .С /г, л:: локсан г: с ЕЯЗ остью 12000 ;:: и i;-- без::ОДНОГО гипсоБОгч;- ПО.); ::;;: а : амешивают как в примере 1 с ., :: Oj-i) ердите:; b) 10 g of paste, ;; ocTO: ue i from 35% W, h - dihydrogen on 1 Cd. C / g, l :: loksan g: with EYAZ awn 12000; :: and i; - without: : ONE drywall; - ON.); :: ;;: a: mixed as in example 1 p., :: Oj-i) go to ;;
Материал эласгги :. и имеет твер-з ) 10 г пасты, состо :;:ек из 35 димeтилпoJ иcилокеаноного слтирта с BH3KocTJ io 12000 сгг зарцезсзго порО:;1ка, 3 аме1;;изаю J с О,;- г -., :it;p/u, тел . Пос/ге зазермюнин аниз апии эдастичный продукт имсет твердость по Шору 58.Elasggi material:. and has a hard h) 10 g of paste, consisting of:;: ek from 35 dimethylpolyozoic and orange slit with BH3KocTJ io 12000 crg of the chorus scorpus:; 1ka, 3 am1 ;; izayu J with O,; - g -.,: it; p / u, tel. Pos / ge zazhermyunin aniz apii edastic product imset Shore hardness 58.
г) Пос/те замешыраш: насты притeл -.jepjiocTb IovoBoro продхкта и tiiopy 57.d) Pos / those zamesyrash: Nasti pritel -.jepjiocTb IovoBoro products and tiiopy 57.
д)После 3 аме1;:из а:п.1 тз::.. : i.ii, 0,6 г oiB ердител Г :;15 рдост i; ::/,:. затора iici iilor)y 5 у .d) After 3 AME1;: from a: p.1 of the TS :: ..: i.ii, 0.6 g oiB Herditel G:; 15 of the cost i :: /,:. mash iici iilor) y 5 y.
е)10 г пасты из i-:;i ариеп о:.-о пор::на , сод:1ержаи1ей 6% W// -J;H r-ivipi:)--:-)поли ,циметило;;локоана с р л:; к ос-г у,н: 12300 спз и 2;. Vv W - дм f-и лрсксиполиметилсилокса:-а с а :-:. IjOO сп:еe) 10 g of paste from i - :; i ariep about: .- about then :: on, sod: 1 6% W // -J; H r-ivipi:) - :-) poly, tsimetilo ;; locoan c p l :; to OS-g y, n: 12300 spz and 2 ;. Vv W - dm f-and lrskypolymethylsilox: -a with a: - :. IjOO sp: e
замеишвают обычн1:им с: -.обом с О.Н i отвердитед , в i OTOpi.;i liytMiH vi 31; но добавл ют - - етр1К-:ил:-ил:: ::а-:-а иthey note the usual 1: it with: -.obom with O.N i hardened, in i OTOpi.; i liytMiH vi 31; but they add - - ether1K-: il: -yl :: :: a -: - a and
(Ч4(P4
2 :г ;г--:Тил или кат а . Чер-:.; 10 MIH п:-;с:(. зарер11;рни ву/:кан з ации трердо сть эластомера по Шору составл ет 48, а спуст 16 час она равна 57. Если не 0,8 г от вегодител , а 0,6 г, то через 10 мин после заверj иени вулканизации твердость продукта по Пору составд ет 47, а через 16 чао .цостигает посто нной величинь; 55 .2: g; g -: Thil or cat a. Cher -:.; 10 MIH n: -; s: (. Zarer; 1): the strain of Shore elastomer can be 48, and after 16 hours it is 57. If not 0.8 g from the delinquent, but 0.6 g then 10 minutes after the completion of vulcanization, the hardness of the product at Poru is 47, and after 16 hours, a constant value is reached; 55.
ПримерExample
г пасты, состо - Q niefi из V,W -ди 1и дрок си поли ди метилсилоксана с в зкостью 20000 спз при 20с и 65% кварцевой , перемеши0 ,8 г отвердител , состо тего из 10% дибутиддилаурината адова и 90% диметслксибутоксиполиизопропокси силоксана , а котором бутЬксиполиизопропоксигруппы имеют мол.в. 1900. Через 4- 6 мин продукт вулканизируют. Он обладает эластичными свойствами.g of paste, consisting of Q niefi from V, W-di 1i, and drok si poly di methylsiloxane with a viscosity of 20,000 centipoise at 20 s and 65% quartz, stirring, 8 g of hardener, consisting of 10% hell dibutidyl dialurinate and 90% dimethyl oxo butoxy depolypoxy siloxane, and which the butxypolyisopropoxy groups have a mol.v. 1900. After 4-6 minutes, the product is vulcanized. It has elastic properties.
Пример г пасты, состо дей из 35% W , w -диг ид роксиполидиметилсилоксана с в зкостью 12000 спз и 6у1 безводного отожл ен Kfjro гипсов-ого порошка замешивают с 0,8 г отаердител , состо щегО из 10% ,Ш-1 бутил илаурин ата олова и 90% метоК си Э т ОК сиди бу.Т окон ПчЗЛНИ 3 ОПр ОПОКСИ силоксана , в которо-м бутоксиполиизопропокси группы имеют мод в, 1900. При -гемпературе 37 С смесь отверждаетс в эластичную массу,An example of a paste consisting of 35% W, w-dig iroxyphoxypolydimethylsiloxane with a viscosity of 12,000 sps and 6y1 anhydrous annealed Kfjro gypsum powder is kneaded with 0.8 g of operder, consisting of 10%, W-1 butyl ilaurin ATA tin and 90% of metoc si e t OK sit bu.T windows PZZLNI 3 OPR OPOKSI siloxane, in which the butoxypolyisopropoxy group have a mode in, 1900. At 37 ° C, the mixture cures to an elastic mass,
11 Р и е Р 5 . 1U г r:a-j-ibi. ее сто 1;: (й из 35б полид1- мети.:сид(1.сан--дио .:о1 с :в зкостью . спз и юза; цевого порслгка, замеи:ива :т с 0,8 г ,-ди-;-1:1л , соеС-.ще1-о из 59% дибутидi:H- ;;iypHH ата ол;:йа, 2% аэроси;:а, 0,12% {-едами: --В-С1еары о, и 9z,88% тримето; : с и бу-;- Oi-c си и з оиропокси си J; ан а, а котором бугоксиизопропокеигруппа имеет11 R and e P 5. 1U r r: a-j-ibi. it is one hundred;; (th of 35b polyd1-methi.: sid (1.san - dio.: o1 s: viscosity. spz and yuz; a valuable servant, note: willow: t with 0.8 g, -di -; - 1: 1l, soEС -.shche1-o of 59% dibutidi: H- ;; iypHH ata ol;: ya, 2% of aeroi;: a, 0.12% {-feeds: - B-Steary o , and 9z, 88% of trimeto;: s and bu -; - Oi-c b and z oiropoxy ci J; an a, and of which the bugoxy-isopropegroup has
;:со;,у;;т ::осл-. :jy.::K аки з ации имеет твердость 58 по iiiopv /-.,;: co;, y ;; t :: Osl. : jy. :: K aki ztation has a hardness of 58 to iiiopv / -.,
; :- и :-1 е Р о. 10 г Пс;с: ; c:j.е-г::5 и;ей из иолидиметилсилоксандио .-ia с в зкое-тьк 12000 спз и 79% : 3 -;.рцеаого гкзроигка, заме1лившм1 с 0,7 г отверд1-1 тел , состо ;„его из 10% дибутилди.г;аурината олова, 50% диметиддиОуток оии . о пр опок си си дан а и 40% -гриметокситрибутоксиизопропоксидиоидоксана . Смесь отверждаетсч за несл л .пько минут 53 водб; при в эласти чный вулк аи и з ат .; : - and: -1 e P o. 10 g Ps; with:; c: j.е-г :: 5 и; to her from iolidimethylsiloxandio.-ia with viscous-ing to 12000 spz and 79%: 3 - ;. pceic acid, replacing 1 with 0.7 g hardened 1-1 bodies, state; „ it is from 10% dibutyl-dg; tin aurinate, 50% dimetidide; About pr opok Si Si Dan a and 40% -grimethoxytributoxy-isopropoxydioxidoxane. The mixture hardens for 5 minutes for carrying Vodb; when in elastic volc ai and s am.
П Р и м е Р . 10 г ;асты, со- г-илси.;; -:сан а с Ci,,;; амеииза т кэ -Jein-s:.. J -U:H с 0,0 г ..:-.:-ве;.; .cro из 4,55 дибутилд; 11лоза, 3,0% те-. : т;-леи гти гтоли -,.-гил.-:илик.гга, и 00, 5PRIme R. 10 g; asta, co-glysi .; -: San and with Ci ,, ;; ame iiz t ke -Jein-s: .. J-U: H with 0.0 g.: -.: - ve;.; .cro from 4.55 dibutild; 11loza, 3.0% of those. : t; -lei gti gtoli -, .- gil .-: ork.gga, and 00, 5
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2223937A DE2223937C3 (en) | 1972-05-17 | 1972-05-17 | Hardening of cold-curing polysiloxane impression compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
SU682101A3 true SU682101A3 (en) | 1979-08-25 |
Family
ID=5845068
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU731931272D SU953970A3 (en) | 1972-05-17 | 1973-05-17 | Material for making stomatological models |
SU731931272A SU682101A3 (en) | 1972-05-17 | 1973-05-17 | Material for the preparation of stomatological models |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU731931272D SU953970A3 (en) | 1972-05-17 | 1973-05-17 | Material for making stomatological models |
Country Status (19)
Country | Link |
---|---|
JP (1) | JPS5334213B2 (en) |
AR (1) | AR197987A1 (en) |
AT (1) | AT330457B (en) |
BE (1) | BE799579A (en) |
CA (1) | CA1015489A (en) |
CH (1) | CH588277A5 (en) |
DD (1) | DD103810A5 (en) |
DE (1) | DE2223937C3 (en) |
ES (1) | ES414807A1 (en) |
FR (1) | FR2185006B1 (en) |
GB (1) | GB1425607A (en) |
HU (1) | HU166511B (en) |
IT (1) | IT1004533B (en) |
NL (1) | NL7306895A (en) |
PL (1) | PL91586B1 (en) |
RO (1) | RO66222A (en) |
SE (1) | SE7306935L (en) |
SU (2) | SU953970A3 (en) |
ZA (1) | ZA733323B (en) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4007153A (en) * | 1975-06-19 | 1977-02-08 | General Electric Company | Silicone dental impression compositions |
DE3104721C2 (en) * | 1981-02-10 | 1983-01-13 | Langer, Hans-Georg, 8021 Taufkirchen | Method and device for taking impressions for dentures |
JPS58128762A (en) * | 1982-01-27 | 1983-08-01 | Fujitsu Ltd | Semiconductor device |
JPS5912964A (en) * | 1982-07-15 | 1984-01-23 | Otsuka Chem Co Ltd | Polyorganosiloxane composition |
JPS608361A (en) * | 1983-06-29 | 1985-01-17 | Shin Etsu Chem Co Ltd | Condensed silicone rubber composition |
DE3681274D1 (en) * | 1986-02-06 | 1991-10-10 | Dentsply Gmbh, 7750 Konstanz, De | Improved wettability silicone dental impression material |
DE3838587A1 (en) * | 1988-11-14 | 1990-05-17 | Espe Stiftung | POLYETHER IMPRESSION MATERIAL, METHOD FOR PRODUCING IT AND ITS USE |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE549810A (en) * | 1955-07-27 | |||
FR1210265A (en) * | 1957-10-21 | 1960-03-08 | Dow Corning | silicate-siloxane elastomers |
-
1972
- 1972-05-17 DE DE2223937A patent/DE2223937C3/en not_active Expired
-
1973
- 1973-05-15 AT AT425773A patent/AT330457B/en not_active IP Right Cessation
- 1973-05-16 DD DD170869A patent/DD103810A5/xx unknown
- 1973-05-16 HU HUTE713A patent/HU166511B/hu unknown
- 1973-05-16 SE SE7306935A patent/SE7306935L/sv unknown
- 1973-05-16 GB GB2337873A patent/GB1425607A/en not_active Expired
- 1973-05-16 BE BE131148A patent/BE799579A/en unknown
- 1973-05-16 ZA ZA733323A patent/ZA733323B/en unknown
- 1973-05-16 ES ES414807A patent/ES414807A1/en not_active Expired
- 1973-05-17 RO RO7374821A patent/RO66222A/en unknown
- 1973-05-17 NL NL7306895A patent/NL7306895A/xx not_active Application Discontinuation
- 1973-05-17 SU SU731931272D patent/SU953970A3/en active
- 1973-05-17 SU SU731931272A patent/SU682101A3/en active
- 1973-05-17 CA CA171,727A patent/CA1015489A/en not_active Expired
- 1973-05-17 JP JP5513273A patent/JPS5334213B2/ja not_active Expired
- 1973-05-17 AR AR248084A patent/AR197987A1/en active
- 1973-05-17 FR FR7317993A patent/FR2185006B1/fr not_active Expired
- 1973-05-17 CH CH707573A patent/CH588277A5/xx not_active IP Right Cessation
- 1973-05-17 IT IT68434/73A patent/IT1004533B/en active
- 1973-05-17 PL PL1973162630A patent/PL91586B1/pl unknown
Also Published As
Publication number | Publication date |
---|---|
ZA733323B (en) | 1974-04-24 |
AT330457B (en) | 1976-07-12 |
FR2185006B1 (en) | 1977-09-02 |
RO66222A (en) | 1979-03-15 |
DD103810A5 (en) | 1974-02-12 |
PL91586B1 (en) | 1977-03-31 |
DE2223937C3 (en) | 1975-02-13 |
ES414807A1 (en) | 1976-02-01 |
SU953970A3 (en) | 1982-08-23 |
CH588277A5 (en) | 1977-05-31 |
ATA425773A (en) | 1975-09-15 |
GB1425607A (en) | 1976-02-18 |
DE2223937A1 (en) | 1973-12-06 |
FR2185006A1 (en) | 1973-12-28 |
JPS5334213B2 (en) | 1978-09-19 |
CA1015489A (en) | 1977-08-09 |
NL7306895A (en) | 1973-11-20 |
JPS4948753A (en) | 1974-05-11 |
BE799579A (en) | 1973-09-17 |
SE7306935L (en) | 1973-11-19 |
HU166511B (en) | 1975-03-28 |
AR197987A1 (en) | 1974-05-24 |
IT1004533B (en) | 1976-07-20 |
DE2223937B2 (en) | 1974-06-20 |
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