Method of producing inorganic-organic plastic materials
专利摘要:
1421894 Porous cement compositions BAYER AG 1 March 1974 [17 May 1973] 9318/74 Addition to 1385605 Heading C1H [Also in Division C3] A quick-setting cement may be added to a reaction mixture for producing a macroscopically homogeneous inorganic-organic plastics composite material, the reaction mixture comprising (1) an aqueous sodium or potassium silicate solution and/or an aqueous silica sol and (2) a non-ionic organic prepolymer which contains reactive groups capable of polyaddition and/or polycondensation and/or polymerization and at least one non-ionic hydrophilic group, and optionally an agent which hardens the silicates, e.g. urea, HCHO and its condensates. The prepolymer (2) is most preferably an isocyanate group-containing polyurethane prepolymer and in Examples 9 and 10 such a prepolymer is mixed with a quick-setting cement and subsequently an aqueous sodium silicate solution, and with the aid of a blowing agent the reaction produces a finely porous foam. Reference has been directed by the Comptroller to Specification 1,186,771. 公开号:SU725568A1 申请号:SU2057668 申请日:1974-09-04 公开日:1980-03-30 发明作者:Дитерих Дитер;Маркуш Петер 申请人:Байер Аг (Фирма); IPC主号:
专利说明:
-4 - c: rac..j- 5c Vj; v4t is a tall form, o6pa 6pfaif andS Sny fpS wax, cf. meter 4x4x16 cm After 40 seconds after mixing, curing takes place, H & the material was still plastic and spreds formayatns After 5 Chg Y 11RrGG Yp1v & y. Up to 70 °, a solid like a stone similar to. Concrete, non-foamed inorganic. Rga: ni (tiche plaus TIch aki yi, ::;; material ( plastic), in which some f, ies-constants are determined. The raw density is 1530 / sg / l; the limit is .H10St. in static bending 11.3 l; g / sl 2; tLime limit for squeezing 19.4 n / sg / s 2. Item 2. 50 parts by weight of copolymer A is diluted with part of polyisocyanate colloidant T and the immediate mixture is mixed with a rapidly stirring mixer for 10 seconds with 300 parts of liquid SKslxfiii№tiiiSi: - X: S jif.-jA , -tK-K - i№; - i Ji la}. ““ “. whom glass of example 1. To the mixture used: ..;: Sew for 20 s 80 wt. h of fermiculite (maximal isec 200 kg / cm) and the entire mixture) Dakzt in pre-treated BpciKOM metal shape with dimensions 4X4X16; nd. The hardened 1 process begins after 40 seconds after preparation, after 5 minutes by heating 40 ° C, a continuous, solid, subbane is obtained; b: Noarga, single-grain wood. plastic. The material can be sawed, screwed up, threshed, it has excellent properties: And during firing. T, G, -: Play from this material; 1 cm thick, the jrfa flame of the Bunsen burner is reversed, the opposite of the old burner remains unchanged, and the side reversed. ; The flame is transformed into a ceramic surface. As a result of long-term resistance to fire, this Heopra-i organic organic platelet is of interest; it is of interest for the former; dB is important, you are in the field of construction. TGrim er 3. 100 weight. others with sulphonated polyphenylpolymethylene polyisodianate, which was obtained in anilineformaldehyde concentrate .. 1CbdSaRTsAy 1GbDsrd5st S6HHO after that, fasgenirovni and sul. %, viscosity, at 22 ° C, 1200 cP), displaces 7–20 wt.% g / 7ms- (p-trichloroethyl) phosphate and immediately after this displaces ic 300 the weight of an hour glass in 15. i ”according to the 1 K mixture 250 weight per hour of quartz muy (density 2.65 g / cm, grain size 0-30 mm (13 s), and the mixture, c a special liter, was a metallic metal cpa3MepdMk 4X4X16 hedgehog - .. The reaction mixture began to dissipate and hardened for 5 min to prepare it and cure by heating to 42 ° C until a non-porous nerve is obtained725568 4 - 5 5 6 6 masb1, cotrrnr mrnrr to remove .fory after 81 days after 2 days after fabrication. Some physical persons were identified. And; e values. Cheese, lottery. 1523 kg / m, pre; 1; I ate the goodness with static bending 11.7 kg / cm, the ultimate strength of irradiation and compression was 94.4 kg / cm. . Example 4. To 160 wt., Including sulphono-early P polyrzacyanate, obtained according to example 3, primeopivat 0.5 weight. h. triethylamine,; as a result, part of the sulfo. new group goes into the Hbie sulfolate group. TaiKoro kind of polyisocyanates through the month. 1 is fully stabilized for HbiMH .VK storage. If, to the usual trading, non-modifying product, to the bathroom polyphenyl or ethylene-polyethylene, add ra.vnoe Kritichestvie triethylamine, then. its viscosity quickly increases, and after a week it hardens, and it cannot be reused. The effect with the application of partially neutralized sulphonated scholiisocyanate is. higher reactivity with liquid glass, this leads to a more rapid solidification of the reaction mixture and, as a result, to a shorter mold time, nor ..: ..;, E.slii prov1e; dnt. rtsyt, written in Example 3., when using the partially neutralized with triethylamine .ttoliisocyanate, the reaction time. Significantly shortened. With other similar .h. And T.aiKOM recipes, the same mixing for creation is already starting in 35 seconds; by 1; when heated to 80 ° C, a sample is obtained, solid as a stone, which, after 30 seconds, is obtained from the mold. The indicated physical constants were determined after 2 days g / after 1 ready. The density of the cheese is 156, the static bending strength is 19.9 kg / sl1, the compressive strength. 105 kg / cm. :: Example 5. 100 wt. including sulfonated pris isocyanate according to example 3, p is reduced to 100 weight. including polyisocyanate yomyoint 1. To this 57 add patTi op 400 weight. including liquid glass according to example 1, in which a preliminary list) 0.4 parts by weight: .4. emulsifier (50% aqueous solution of Na-salt of sulfochlorinated paafine, merzolate). . , ... After pererem | shi.ani for 15 s (with the help of a baktr) pscha1vt; Ёks itddal-kn) 5 s mixed .140 weight. chalk (yd. web., 8; bulk weight 920 g /., ich.chichina parts um and zhidkupea HilHOh.Httyip smvs poured into a metal FRPMu with sizes 4x4x16 ate. Through 5. Inc .; beginning; wda {b1 ) with atverDe.nie, through, 8 Zhm “temp1n: etauru ydd“ -, ... „.„ l Jl Jl; J fliypy IODimyut to C, which is 50 min. .-..- out of shape. Through 2 yes dirvddel. And some physical properties | VA. Cheese density is 1367 and the limit of strength in static. Bend: 21.7 kg / cm; Compressive strength 142kg / cm. PRI me r 6. 100 weight. part of the sulphonated isocyanate floor according to example 3. is mixed using a rapidly rotating messenger for 20 s with 300 weight, part of the liquid of the glass of example 1. As a result, a whitish, opaque, liquid, homogeneous, which can recycle in 10 minutes This mixture is laminated to wood chip plates (16 mm) ≥ mm thick. NeorGa | Nikeoko-organic coating mass begins to cure 15 minutes after preparation, after 1 h it is completely cured. After 1 day, the mass turns into a solid, like a stone, having a good adhesion coating. In the experiment conducted for SravBöni, the untreated and finished plates were introduced into the flame of a laboratory bunsenob burner. While the raw plate is burned out after 7 minutes, the sandwich laminast under the same experimental conditions is kept for 12 minutes. Laying the layers not only increases the IHO duration of resistance against the effect of organic fire on fire, but also prevents the spread of fire on the surface and therefore presents an excellent material for protective protection against fire. I, Invention formula The method of obtaining organic orthopedic plastics from the interaction 20-70% aqueous solution of alkali metal and alkaline earth metal silicates and / or 20-50% aqueous siliceous sol with an organic prepolymer containing terminal MCO-pr-upa, in suitable filler, and that, in order to reduce the strength, elasticity and incombustibility of the final product, 3 as an organic prepolymer, a compound is used at least with one ionic group and / or one non-ionic hydrophilic group, and the weight ratio between the prepolymer and alkali or alkaline earth metal silicate and / or siliceous sol is from 1: 99 to 70: 30. The source of information taken into account during the eco-review: 1. USSR author's certificate 260883, cl. C 08 G 18/14, 10/27/65 (protoTim).
权利要求:
Claims (1) [1] Claim A method of producing inorganic-organic plastics by reacting a 20-70% aqueous solution of silicates of alkali and alkaline earth metals and / or 20-50% aqueous' siliceous sol with an organic prepolymer containing terminal NCO groups in the presence of a filler, characterized in that, in order to increase the strength, elasticity and incombustibility of the final product, a compound with at least one ionic group and / or one nonionic hydrophilic group is used as an organic prepolymer, moreover, by weight the wear between the prepolymer and the silicate of alkali or alkaline earth metals and / or siliceous sol is from 1: 99 to 70: 30. Source of information taken into account during the examination / '' 1. USSR copyright certificate 260883, cl. C 08 G 18/14, 10.27.65 (prototype). 4 'Compiled by S. Purin
类似技术:
公开号 | 公开日 | 专利标题 SU725568A1|1980-03-30|Method of producing inorganic-organic plastic materials US5112405A|1992-05-12|Lightweight concrete building product EP0280971B1|1991-09-04|High strength cured cement article and process for manufacturing the same US4659385A|1987-04-21|Building material manufacturing from fly ash US4640715A|1987-02-03|Mineral binder and compositions employing the same US3983081A|1976-09-28|Inorganic-organic composition US4686252A|1987-08-11|Process for preparing a building and/or construction material, a polymer modified aqueous dispersion, and use thereof for the preparation of a building and/or construction material JP3946332B2|2007-07-18|Use of nonionic water-dispersible polyisocyanates as concrete additives JP4092020B2|2008-05-28|Water dispersible or water soluble polyurethanes as additives for building materials JP2008502572A|2008-01-31|Composition and use of a new sprayable phosphate cement combined with styrofoam. HU176469B|1981-03-28|Method for producing organic-inorganic plastic mateirals EP0692464B1|2002-06-19|Cement type kneaded molded article having high bending strength and compressive strength, and method of production thereof DE2227147C3|1979-10-18|Homogeneous inorganic-organic ionomer-polysilicic acid-gel composite material present as colloidal xerosol US3649317A|1972-03-14|Shrinkage compensating cement US1951691A|1934-03-20|Manufacture of porous plaster EP0786439A1|1997-07-30|Polymer-modified ready-to-use cement mortar JPH10291852A|1998-11-04|Ceramic composition hardenable at ordinary temperature JP3584723B2|2004-11-04|Manufacturing method of hardened cement KR102342008B1|2021-12-22|Manufacturing method of precast geopolymer concrete member EP0027816A1|1981-05-06|Cementitious materials with resin binder JP4301076B2|2009-07-22|Cement composition CZ83993A3|1994-02-16|The use of melamine and glyoxylic acid condensation products as an ingredient in hydraulic binding agents US3373048A|1968-03-12|Hardening accelerated portland cement JP3378965B2|2003-02-17|Method for improving strength of hardened cement JP2004224698A5|2005-08-04|
同族专利:
公开号 | 公开日 JPS5418719B2|1979-07-10| SU725568A3|1980-03-30| GB1421894A|1976-01-21| FR2229734B2|1977-09-09| DE2325090B2|1980-03-20| SE416056B|1980-11-24| CA1064199A|1979-10-09| BE811623R|1974-08-27| LU68889A1|1974-01-29| AU6643074A|1975-09-11| PL93447B1|1977-05-30| CA1064200A|1979-10-09| CH610341A5|1979-04-12| DE2325090C3|1980-11-06| US4097422A|1978-06-27| US4052347A|1977-10-04| FR2229734A2|1974-12-13| ATA171974A|1977-02-15| ES423822A2|1977-07-01| HU169478B|1976-12-28| IT1048267B|1980-11-20| NL7402835A|1974-11-19| AT339614B|1977-10-25| DE2325090A1|1974-11-28| BR7401539D0|1974-12-03| JPS5019885A|1975-03-03| DD108105A5|1974-09-05|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题 US1999382A|1932-06-13|1935-04-30|Grasselli Chemical Co|Refractory material for use in metal castings and process for making the same| US2505353A|1947-06-13|1950-04-25|Us Rubber Co|Microporous resin| US2946112A|1956-07-10|1960-07-26|Koppers Co Inc|Process of producing light weight aggregate| US3004921A|1958-06-11|1961-10-17|Argus Chem|Preparation of colloidal dispersions of fine-particle size silica hydrogel in polyols| GB884153A|1959-01-30|1961-12-06|Ici Ltd|Polyurethane compositions| US3024209A|1959-05-27|1962-03-06|Minerals & Chem Philipp Corp|Polyurethane foam containing inorganic pigment coated with polymeric material| US3224899A|1961-08-17|1965-12-21|Christopher L Wilson|Wettable polyurethane sponge| GB1080590A|1964-12-28|1967-08-23|Bayer Ag|Polyurethanes| AT267888B|1966-07-29|1969-01-27|Marquet & Cie Noel|Process for the production of new polyester-based foams with improved properties| DE1694096A1|1966-12-13|1971-08-26|Bayer Ag|Process for the production of water vapor permeable, porous areas| US3607822A|1967-03-23|1971-09-21|Takeda Chemical Industries Ltd|Thixotropical polyurethane compositions| GB1186771A|1967-05-12|1970-04-02|Conteki Dev Ltd|Silicious Products| US3716502A|1970-11-27|1973-02-13|Inmont Corp|Elastomeric thermoplastic polyester polyurethane compositions stabilized against hydrolysis| US3740743A|1971-03-29|1973-06-19|Columbia Broadcasting Sys Inc|Character generating apparatus for television titling| US3764365A|1972-01-21|1973-10-09|Gen Tire & Rubber Co|Adhesion improving agent for urethane coatings on rubber| US3812619A|1972-05-03|1974-05-28|Grace W R & Co|Horticultural foam structures and method| US3812618A|1972-05-03|1974-05-28|Grace W R & Co|Seed-foam-fabric composite| US3975316A|1972-05-04|1976-08-17|Thiokol Corporation|Curing liquid polyurethane prepolymers| US3833386A|1972-07-07|1974-09-03|Grace W R & Co|Method of prepairing porous ceramic structures by firing a polyurethane foam that is impregnated with inorganic material| DE2359606C3|1973-11-30|1980-01-17|Bayer Ag, 5090 Leverkusen|Process for the production of an inorganic-organic polymer-polysilicic acid gel composite material in the form of a colloidal xerosol|US4153768A|1976-03-04|1979-05-08|Blount David H|Organic hydroxy silicates utilized as curing agents for polyurethane prepolymers| USRE31340E|1970-09-11|1983-08-09|Process for the production of polysolid| US4072637A|1972-06-14|1978-02-07|Blount David H|Process for the production of polyurethane resins and foams utilizing silico-formic acid| DE2359607C2|1973-11-30|1982-12-09|Bayer Ag, 5090 Leverkusen|Process for the production of an inorganic-organic composite material| DE2366240C3|1973-11-30|1982-03-11|Bayer Ag, 5090 Leverkusen|Organic-inorganic composite plastics| DE2359610C3|1973-11-30|1981-09-17|Bayer Ag, 5090 Leverkusen|Process for the production of flexible, organic-inorganic composite plastics with a low calorific value and improved fire behavior| US4136238A|1974-12-21|1979-01-23|Metallgesellschaft A.G.|Non-flammable and optionally electrically conductive organo-silicate polymers and process for preparing same| DE2512170C3|1975-03-20|1981-06-11|Bayer Ag, 5090 Leverkusen|Process for the production of optionally foam-shaped, hard inorganic-organic composite material| DE2542288C2|1975-09-23|1988-12-01|Chemie-Anlagenbau Bischofsheim Gmbh, 4500 Osnabrueck, De| JPS52102395A|1976-02-25|1977-08-27|Onishi Sumiko|Process for producing glass foam pf| DE2734690A1|1977-08-02|1979-02-08|Bayer Ag|PROCESS FOR THE PRODUCTION OF INORGANIC-ORGANIC PLASTICS| USRE31946E|1979-03-06|1985-07-16|Bergwerksverband Gmbh|Process for consolidating and sealing off geological and artificially deposited rock and earth formations| DE2908746C2|1979-03-06|1983-08-11|Bayer Ag, 5090 Leverkusen|Process for consolidating and sealing geological and poured rock and earth formations| US4273908A|1979-05-07|1981-06-16|Blount David H|Process for the production of poly (polyisocyanate-polyol-alkali metal silicate solid| US4355118A|1981-01-09|1982-10-19|Mobay Chemical Corporation|Process for the production of inorganic-organic compositions| CA1153500A|1981-01-09|1983-09-06|Miltiadis I. Iliopulos|Process for the production of inorganic-organiccompositions| JPS58175360A|1983-03-17|1983-10-14|Sanyo Electric Co Ltd|Picture and character printer| JPS6357448B2|1983-11-21|1988-11-11|Nichias Corp| US4572862A|1984-04-25|1986-02-25|Delphic Research Laboratories, Inc.|Fire barrier coating composition containing magnesium oxychlorides and high alumina calcium aluminate cements or magnesium oxysulphate| CA1248679A|1984-05-21|1989-01-10|Peter C. Gaa|Aqueous dispersion, internally silylated anddispersed polyurethane resins, and process forproducing same and surfaces containing same| DE3421086C2|1984-06-06|1987-09-10|Kvt Kunststoffverfahrenstechnik Gmbh & Co| DE3421085C1|1984-06-06|1985-10-31|F. Willich GmbH & Co, 4600 Dortmund|Process for solidifying and sealing coal and / or rock and earth formations| US4900359A|1984-06-25|1990-02-13|Lisa Concrete Inc.|Cellular concrete| US4741782A|1984-11-07|1988-05-03|Resource Technology, Inc.|Process for forming a light-weight aggregate| DE3538791A1|1985-10-31|1987-05-07|Webac Chemie Gmbh|Process for hardening of waterglass solutions and hardening system for this purpose| JPH0678520B2|1986-04-08|1994-10-05|清水建設株式会社|Water stop method for concrete structure| DE3626048A1|1986-08-01|1988-02-11|Bayer Ag|REINFORCED PLASTERBOARDS| JPH0699654B2|1987-02-16|1994-12-07|ダイニツク株式会社|Coating composition for ink fixing layer| DE3738934C2|1987-11-17|1989-10-19|Pelikan Ag, 3000 Hannover, De| JPH01187242A|1988-01-22|1989-07-26|Michio Otsuka|Wall-making stuff made of earth and vegetable materials, and its manufacture| US4904522A|1988-07-26|1990-02-27|Mobay Corporation|Process for the production of fiberglass mats| AU6522290A|1989-09-29|1991-04-28|Research Corporation Technologies, Inc.|Process for making a lightweight cellular inorganic material| JP2603367B2|1991-01-22|1997-04-23|株式会社常盤電機|Coating composition| US5191012A|1991-03-28|1993-03-02|Miles Inc.|Aqueous dispersions of encapsulated polyisocyanates| DE4121153C2|1991-06-26|2000-01-13|Polinvent K F T|Polysilicic acid-polyisocyanate materials, composite materials and foams and a process for their production| EP0524505B1|1991-07-26|1996-11-13|Matsushita Electric Industrial Co., Ltd.|Foamed plastic and method of manufacturing the same| US5876134A|1992-02-14|1999-03-02|The Gillette Company|Foam grip| US5260344A|1992-03-13|1993-11-09|Asahi Glass Company, Ltd.|Open cell rigid isocyanurate foams and method for producing the same and vacuum heat insulating layer by use of the same| JPH05320646A|1992-05-26|1993-12-03|Denki Kagaku Kogyo Kk|Flame-resisting grout for binding rock bed| US5183505A|1992-05-27|1993-02-02|Concrete Technology, Inc.|Cellular concrete| AT165590T|1992-12-09|1998-05-15|Victor Alexander Milles|METHOD FOR PRODUCING A MATERIAL CONTAINING SILICONE AND MATERIALS PRODUCED THEREOF| US5462699A|1993-04-02|1995-10-31|Fireblock International, Inc.|Fire retardant materials and methods of use thereof| GB9613113D0|1996-06-21|1996-08-28|Ecc Int Ltd|Granular materials| DE19654429A1|1996-12-24|1998-06-25|Bayer Ag|Water-dispersible polyisocyanate mixtures as additives for concrete| US5817860A|1998-03-20|1998-10-06|Essex Specialty Products, Inc.|Polyurethane prepolymer compositions, foams made therefrom and methods of making each thereof| DE19840640A1|1998-09-05|2000-03-16|Isovac Ingenieurgesellschaft M|Insulating housing, especially for refrigerator and/or energy storage device| US6488762B1|2000-10-30|2002-12-03|Advanced Materials Technologies, Llc|Composition of materials for use in cellular lightweight concrete and methods thereof| DE10119818B4|2001-04-23|2005-04-07|Strobel, Klaus, Dipl.-Ing.|A roller shutter case| WO2002087843A1|2001-04-30|2002-11-07|Orbseal Llc|Reinforcement for expandable compositions and methods for using the reinforcement| ES2385983T3|2003-03-17|2012-08-06|Tech-Wood International Ltd|Method to manufacture a reinforced plastic profile| US20050096411A1|2003-10-31|2005-05-05|Illinois Tool Works Inc.|Polyurethane adhesive for masonry construction| US9840066B2|2005-06-09|2017-12-12|United States Gypsum Company|Light weight gypsum board| US9802866B2|2005-06-09|2017-10-31|United States Gypsum Company|Light weight gypsum board| US7731794B2|2005-06-09|2010-06-08|United States Gypsum Company|High starch light weight gypsum wallboard| US20060281825A1|2005-06-11|2006-12-14|Je Kyun Lee|Microporous Polyisocyanate Based Hybrid Materials| US7670427B2|2007-06-06|2010-03-02|United States Gypsum Company|Very fast setting cementitious composition with high early-age compressive strength| US20090149574A1|2007-12-07|2009-06-11|Construction Research & Technology Gmbh|Iron Filled Urethane Cementitious Flooring Composition| WO2010102284A2|2009-03-06|2010-09-10|Parker Anthony A|Protein-containing emulsions and adhesives, and manufacture and use thereof| CA2753896C|2009-03-06|2018-08-28|Biopolymer Technologies, Ltd.|Protein-containing foams, manufacture and use thereof| KR100958736B1|2009-12-07|2010-05-18|주식회사 삼공사|Organic-inorganic hybrid transparent hydrogel complex for fire-retardant glass and fire-retardant glass assembly using the same, and the preparation method of said fire-retardant glass assembly| EP2576661B1|2010-06-07|2016-12-14|Evertree|Protein-containing adhesives, and manufacture and use thereof| EP2428499A1|2010-09-13|2012-03-14|Construction Research & Technology GmbH|Use of compounds containing aluminium and silicon for producing a hydrophilic material product| EP2439219A1|2010-10-06|2012-04-11|Sika Technology AG|Reduction of amount of Isocynate groups containing monomers in moisture curable Polyurethane compositions| KR20130124960A|2010-12-07|2013-11-15|바스프 에스이|Polyurethane composite| UA112183C2|2011-05-05|2016-08-10|Басф Се|Sawing unit| ES2624138T3|2011-08-26|2017-07-13|Construction Research & Technology Gmbh|Hydrophilic Building Material Products| US20150044483A1|2011-09-09|2015-02-12|Biopolymer Technologies, Ltd.|Protein-containing adhesives, and manufacture and use thereof| RU2621798C2|2011-09-09|2017-06-07|Эвертри|Protein-containing adhesives, their production and application| EP2880116B1|2012-07-30|2020-02-05|Evertree|Protein adhesives containing an anhydride, carboxylic acid, and/or carboxylate salt compound and their use| EP2746358A1|2012-12-21|2014-06-25|Basf Se|Polyurea silicate resin for wellbore application| CN109651578B|2018-12-12|2021-09-17|中昊北方涂料工业研究设计院有限公司|Ablation-resistant flame-retardant organic-inorganic resin and preparation thereof| CN110016115A|2019-03-07|2019-07-16|齐鲁交通发展集团有限公司建设管理分公司|A kind of grouting for water blocking material| CZ308477B6|2019-08-06|2020-09-09|First Point a.s.|Insulation material and a method of its production|
法律状态:
优先权:
[返回顶部]
申请号 | 申请日 | 专利标题 DE2325090A|DE2325090C3|1973-05-17|1973-05-17|Process for the production of an inorganic-organic polymer-polysilicic acid composite material in the form of a colloidal xerosol| 相关专利
Sulfonates, polymers, resist compositions and patterning process
Washing machine
Washing machine
Device for fixture finishing and tension adjusting of membrane
Structure for Equipping Band in a Plane Cathode Ray Tube
Process for preparation of 7 alpha-carboxyl 9, 11-epoxy steroids and intermediates useful therein an
国家/地区
|