专利摘要:

公开号:SU1011054A3
申请号:SU792777107
申请日:1979-06-19
公开日:1983-04-07
发明作者:Мейер Никола;Фулон Раймон
申请人:Сосьете Шимик Де Шарбоннаж С.А. (Фирма);
IPC主号:
专利说明:

SP
4 The invention relates to boric anhydride based solutions used as curing agents for resole phenol formaldehyde resins. A known curing agent for phenol-formaldehyde resins, including boric anhydride and hexamethylenetetramine. 3 However, the polymer pressing capacity, including this hardener, will have a low cure rate. Closest to the proposed technical essence and the achieved result is a hardener for rezol phenol-formaldehyde resins, including boric anhydride. Boric anhydride is introduced into the press in the form of a powder; therefore, the use of a hardener is associated with technological difficulties arising from the simultaneous introduction into the form of liquid and solid components included in a polymer press composition. In addition, the disadvantage of the known hardener is the need for accurate dosing of solid components, namely boric anhydride. The purpose of the invention is to simplify and speed up the preparation process {| polymeric press composition. This goal is achieved by the fact that the hardener for phenolic resins phenol-formaldehyde resins, including boric anhydride, contains an acidic component selected from the group: sulfuric acid, Vl-toluenesulfonic acid, a mixture of sulfuric and I-toluenesulfur acids at a weight ratio of 5 - 3, and an organic solvent selected from the group: trimethylborate, methylal, methanol, with the following ratio of components, weight .; Boric anhydride 10.6-27.3 Acidic componentM, 3-42, i Organic solvent Else The hardener is prepared according to the following technology. Boric anhydride in powder form is added with stirring at rooms. temperature in a variety of solvents, including a mixture of the acid component and an organic solvent. The prepared hardener is a clear solution. The solubility of boric anhydride in sulfuric acid, in organic solvents, e.g. methylal, methanol, ethanol, dipropyleneglycol and trimethyl borate, as well as in a mixture of organic solvents, e.g. five%. Therefore, the listed solvents are not used separately for the preparation of the proposed hardener. To increase the solubility of boric anhydride, a mixture of the acid component with organic solvents is used as a solvent. The data on the solubility of boric anhydride at room temperature in a mixture of the acid component with organic solvents are given in Table. 1. The compositions used as a hardener for resole phenol-formaldehyde resins are listed in Table 2. As rezol phenol-formaldehyde resin use resols, which are obtained by condensation of phenol and formaldehyde in the presence of caustic soda, followed by. By neutralizing the resulting product to pH 7 and drying in vacuo to obtain the desired viscosity. The conditions for the condensation of the resols are given in table. 3. Resol P is used in pure form; the R / 2 resol is diluted with methanol (5 parts of methanol per 100 parts of the resol) to obtain a product that has 8 P bones at 20 ° C, termed R; Resol R.-5 is diluted with dipropylene glycol (12 parts per 100 parts of Resol) to obtain a product having a C-. Bone 15 P at 20 ° C, named R, given in Table. 3 amounts of dry extract are obtained by drying g of the corresponding resole for 3 hours at C. Different resols are mixed with hardening agent solutions according to the examples in the table. 2. The mixture is kept at and measured during its existence in the form at the indicated temperature (Table 4). Resole R-ij together with hardener according to the table. 2 can be used to teach glass fiber reinforced laminates to be made by simultaneous insertion.
components using the method of injection or impregnation. In all cases, the resulting products. you have good homogeneity and surface finish.
Thus, the selection and ratio of components in the proposed hardener allows one to think over solutions with a high concentration of boric anhydride, which accelerates and simplifies the process of preparing a polymeric press composition based on rezol phenol-formaldehyde resin at a very high curing rate. ,four. Hardener compositions for rezol Table2 phenol-formaldehyde
Methanol SN.ON
Paratoluenesulfonating acid ....
Sulfuric acid
Boric anhydride
27.3
Condensation conditions for the used resole phenol-formaldehyde resins
, 47
42.4
24.3 5.4
17.9
10.6
26.2
27.1
itablice
The composition and properties of the polymer binder
t a b l and 14 a C
权利要求:
Claims (1)
[1]
Hardener for resolving phenol-formaldehyde resins, including boric anhydride, characterized in that, in order to simplify and accelerate the preparation of the polymer press composition, it additionally contains an acid component selected from the group: sulfuric acid, and “toluenesulfonic acid a mixture of sulfuric and h-toluenesulfonic acid in a weight ratio of 5.4: 24.3, and an organic solvent selected from the group: trimethylboron T, methylal, methanol, in the following ratio, wt.%:: '.
!; Boric anhydride. 10.6-27.3
Acid component 17.9-42.4 Organic solvent: t Else
类似技术:
公开号 | 公开日 | 专利标题
SU1011054A3|1983-04-07|Curing agent for resol phenol formaldehyde resins
US2471631A|1949-05-31|Furfuryl alcohol-phenol aldehyde resinous products and method of making the same
US2566851A|1951-09-04|Phenolic intercondensation resins and methods of making same
Zhao et al.2000|Fast advancement and hardening acceleration of low condensation alkaline phenol‐formaldehyde resins by esters and copolymerized urea. II. Esters during resin reaction and effect of guanidine salts
GB726782A|1955-03-23|Cation exchange resins
ES8103124A1|1981-02-16|Low shrink acid curing compositions for furan cements and process for their preparation.
GB768125A|1957-02-13|Improvements in or relating to resinous compositions comprising a glycidyl polyetherand a phenol-formaldehyde resin
US5650478A|1997-07-22|Liquid binding agents
ES8605843A1|1985-12-16|Mixture for the preparation of acid-resistant sealants and impregnated products, method for their preparation and their use.
DE1233606B|1967-02-02|Process for the preparation of polymeric boron compounds
SU1024479A1|1983-06-23|Binder for glass fiber plastic
JPS6112714A|1986-01-21|Production of linear cresol novolak resin of high molecular weight
KR830008760A|1983-12-14|Binder composition and method for producing molded article thereof
US4615737A|1986-10-07|Impregnation composition for thermochemical modification of wood and process for preparing same
JPS5692908A|1981-07-28|High-molecular novolak type substituted phenolic resin, its preparation and application
US2279499A|1942-04-14|Process of combining hardenable phenol-aldehyde condensation products with air-drying fatty oils
DE1086043B|1960-07-28|Process for the production of molded, infusible and insoluble synthetic resins
GB798174A|1958-07-16|Process for curing epoxy ethers
SU117451A1|1957-11-30|The method of obtaining phenolic urea formaldehyde resins
US3265652A|1966-08-09|Resin binders
SU371262A1|1973-02-22|POLYMER COMPOSITION
SU1657517A1|1991-06-23|Binding agent for glass-reinforced plastic
DE2914315C2|1982-06-03|Process for the production of phenol-formaldehyde resins of the resol type
SU1024475A1|1983-06-23|Polymeric binder
US3014007A|1961-12-19|Composition comprising an epoxy resin, an aniline-formaldehyde resin, a liquid polysulfide polymer and a phenolic curing accelerator
同族专利:
公开号 | 公开日
AT555T|1982-01-15|
FR2434118A1|1980-03-21|
FI791941A|1979-12-20|
EP0006373B1|1982-01-13|
EP0006373A1|1980-01-09|
US4272403A|1981-06-09|
DK149330C|1986-10-06|
BR7903784A|1980-02-05|
FR2434118B1|1981-03-20|
JPS551899A|1980-01-09|
CA1117514A|1982-02-02|
JPS5730861B2|1982-07-01|
NO792017L|1979-12-20|
NO151370B|1984-12-17|
DE2961813D1|1982-02-25|
DK149330B|1986-05-05|
US4323667A|1982-04-06|
DK253979A|1979-12-20|
NO151370C|1985-03-27|
FI67206B|1984-10-31|
FI67206C|1985-02-11|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题

US2230564A|1941-02-04|Manufacture of condensation |
US1884747A|1929-01-10|1932-10-25|Du Pont|Plastic composition|
US2177420A|1935-12-05|1939-10-24|Ig Farbenindustrie Ag|Water-soluble condensation products|
US2413777A|1941-04-07|1947-01-07|California Research Corp|Hydrocarbon conversion|
GB646093A|1948-04-21|1950-11-15|Stephen Frederick Pearce|Improved moulding compositions|
US3306860A|1962-05-03|1967-02-28|Archer Daniels Midland Co|Liquid boric acid suspension, method and products|
US3298973A|1963-10-10|1967-01-17|Union Carbide Corp|Phenolic foam compositions|
DE1544771A1|1965-02-09|1970-04-02|Dynamit Nobel Ag|Process for improving the glow resistance of mats and molded bodies made of glass and / or mineral wool bound with phenol-formaldehyde resins|
US3347916A|1965-10-11|1967-10-17|Pennsalt Chemical Corp|Process for preparing nu-formyl compounds using boric acid as catalyst|
FR1524731A|1966-05-28|1968-05-10|Sir Soc Italiana Resine Spa|Phenolic resins useful as binders for foundry sands|
US4111911A|1968-06-06|1978-09-05|Dynamit Nobel Aktiengesellschaft|Method of hardening liquid resols|
FR2016760A1|1968-06-06|1970-05-15|Dynamit Nobel Ag|
GB1272566A|1968-10-01|1972-05-03|Bp Chem Int Ltd|Friction elements|
US3679710A|1970-05-18|1972-07-25|Reichhold Chemicals Inc|Method of isomerizing 4-cyclo-hexene-1,2-dicarboxylic acid anhydrides|
NL178784C|1973-10-09|1986-05-16|Stamicarbon|PROCESS FOR MANUFACTURING BUILDING ELEMENTS FROM A MINERAL RAW MATERIAL AND A PHENOL RESIN.|
FR2331587B1|1975-11-12|1980-04-04|Comptoir Plastiques|
DE2646145A1|1975-11-12|1977-05-26|Comptoir Des Plastiques S A|ARTICLES MADE OF PHENOLIC RESIN AND PROCESS FOR THEIR PRODUCTION|
FR2352021B2|1976-05-19|1980-11-21|Comptoir Plastiques|FR2481294B1|1980-04-24|1985-05-10|Charbonnages Ste Chimique|
FR2481194B1|1980-04-24|1982-03-19|Charbonnages Ste Chimique|
FR2505852B1|1981-05-15|1985-09-20|Charbonnages Ste Chimique|PROCESS FOR THE CONTINUOUS MANUFACTURE OF QUICK SET PHENOLIC FOAMS|
US4478958A|1981-07-10|1984-10-23|Kopper Company, Inc.|Method for preparing phenolic foams using anhydrous aryl sulfonic acid catalysts|
US4480068A|1981-09-14|1984-10-30|Fiberglas Canada Inc.|High temperature resistant binders|
US4539338A|1982-07-09|1985-09-03|Koppers Company, Inc.|Phenol formaldehyde resoles for making phenolic foam|
GB2137214B|1983-03-29|1986-04-23|Hitco|Resoles containing metal atoms|
US4585837A|1983-03-29|1986-04-29|Hitco|Resoles containing zirconium metal atoms|
US4650840A|1983-03-29|1987-03-17|Hitco|Tungsten containing resoles|
FR2557581B1|1983-12-30|1986-08-14|Charbonnages Ste Chimique|PROCESS FOR CURING PHENOLIC RESINS|
US5032431A|1990-02-06|1991-07-16|Georgia-Pacific Resins, Inc.|Glass fiber insulation binder|
US5290843A|1993-04-29|1994-03-01|Georgia-Pacific Resins, Inc.|Phenolic resins for reinforced composites|
EP3956729A1|2019-04-16|2022-02-23|Basf Se|Composition for avoiding pattern collapse when treating patterned materials with line-space dimensions of 50 nm or below comprising a boron-type additive|
法律状态:
优先权:
申请号 | 申请日 | 专利标题
FR7818279A|FR2434118B1|1978-06-19|1978-06-19|
[返回顶部]