CS272884B1 - (3-cyclohexenylethyl) tris (2-aminoethoxy)silane - Google Patents

(3-cyclohexenylethyl) tris (2-aminoethoxy)silane Download PDF

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Publication number
CS272884B1
CS272884B1 CS124589A CS124589A CS272884B1 CS 272884 B1 CS272884 B1 CS 272884B1 CS 124589 A CS124589 A CS 124589A CS 124589 A CS124589 A CS 124589A CS 272884 B1 CS272884 B1 CS 272884B1
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CS
Czechoslovakia
Prior art keywords
silane
cyclohexenylethyl
aminoethoxy
tris
aminoethanol
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CS124589A
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Czech (cs)
Slovak (sk)
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CS124589A1 (en
Inventor
Stanislav Ing Florovic
Juraj Ing Forro
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Florovic Stanislav
Forro Juraj
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Application filed by Florovic Stanislav, Forro Juraj filed Critical Florovic Stanislav
Priority to CS124589A priority Critical patent/CS272884B1/en
Publication of CS124589A1 publication Critical patent/CS124589A1/en
Publication of CS272884B1 publication Critical patent/CS272884B1/en

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Abstract

The invention concerns (3-cyclohexenylethyl) tris (2-aminoethoxy) silane, suitable for modification of fillers for reinforcement of plastics. It can be prepared by the action of 2-aminoethanol on cyclohexenylethyltrisethoxysilane. By neutralisation by methanoic and acetic acid the corresponding salts can be produced.

Description

Vynález sa týká cyklohexenylsllanu vhodného ako promotoradhezie na úpravu plniv pre výstuž plastov.BACKGROUND OF THE INVENTION The present invention relates to cyclohexenylslanine useful as a promoter for the treatment of fillers for plastic reinforcement.

Za účelora zlepšenia adhezie plastov k roznym anorganickým substrátom, či ve formě vlákien, guličiek, tkanin, drtě a pod. sa uskutečňuje úprava fázového rozhrania róznymi vazbovými prostriedkami, tiež nazývanými promotory adhezie. Priemyselne je najpoužívanejší sposob aplikovat vazbové prostriedky z vodných systémov, hlavně s dovodu, že použitie organických rozpúštadiel je obmedzené, či už pre ich toxicitu, horlavosť a v neposlednom řade aj z ekonomických příčin.In order to improve the adhesion of plastics to various inorganic substrates or in the form of fibers, beads, fabrics, pulp and the like. the phase interface is adjusted by different binding means, also called adhesion promoters. In industrial terms, the most widely used method is to apply binding agents from aqueous systems, mainly because the use of organic solvents is limited, either because of their toxicity, flammability and, last but not least, for economic reasons.

Cyklohexenylsilany sú známe a aplikovat do vodných kompozici! je ich možné buď vo formě emulzií alebo solí v připadne dusíkatých derivátov. Nie je známy spósob ani deriváty, ktoré sa dajú aplikovat do vodných systémov jednoduchým rozpuštěním vo vodě.Cyclohexenylsilanes are known and applied to aqueous compositions! they are possible either in the form of emulsions or salts or nitrogen derivatives. There is no known method or derivatives which can be applied to aqueous systems by simple dissolution in water.

Zistili sme, že tieto problémy sa odstránxe pri použití derivátu cyklohexenylsllanu podía vynálezu.We have found that these problems are eliminated by using the cyclohexenylsilane derivative according to the invention.

Vynález popisuje (3-cyklohexenyletyl) tris (2-aminoetoxy) silan sumárneho vzorca C^HjiQ-jN-jSí a štruktúrneho vzorca IThe present invention provides (3-cyclohexenylethyl) tris (2-aminoethoxy) silane of the general formula C ^HjiQQ-jNN j a and structural formula I

-CCff2)2 - si(oc2H4Nír2)3 ftí a jeho adičné s kyselinou mravčou a octovou soli.-C ( c ) 2 ) 2 -si (oc 2 H 4 Ni 2 ) 3 is 3 and its addition with formic acid and acetic salts.

Přípravu je možné uskutočniť pósobením 2-aminoetanolu na cyklohexenyletyltrialkoxysilany za zvýšenej teploty a uvolnenia příslušného alkoholu. V případě potřeby je ich možné neutralizáciou kyselinou mravčou a octovou previest na příslušné soli so zníženou až neutrálnou bazicitou.The preparation can be carried out by reacting 2-aminoethanol to cyclohexenylethyltrialkoxysilanes at elevated temperature and liberating the corresponding alcohol. If necessary, they can be converted to the corresponding salts with reduced to neutral basicity by neutralization with formic acid and acetic acid.

Vynález je ďalej objasněný formou příkladu.The invention is further illustrated by way of example.

PříkladExample

Do reakčenj banky opatrenej chladičom, miešadlom a teplomerom sa předložilo 100 g cyklohexenyletyltrietoxysilanu a 67,3 g 2-aminoetanolu. Násada za miešania vyhriala na 150 °C kedy sa začal uvolňovat etylalkohol. Reakcia sa nechala prebiehat až ďo uvolnenia teoretického množstva alkoholu, pričom teplota vystúpila až na 190 °C. Připravený silan má mernú hmotnost 1 076,6 kg . m-^ mPa . s pri 20 °C a index lomu pri 20 °C je 1,4806. Neutralizáciu je možné uskutečňovat jednoduchým přidáním silanu do vody s příslušnou kyselinou. Podlá potřeby je ju možné uskutočňovat v molárnom pomere silan : kyselina, rovnajúcom sa 1 : 1 až 3, čím sa pripravia roztoky soli neobmedzene miešatelné s vodou.100 g of cyclohexenylethyltriethoxysilane and 67.3 g of 2-aminoethanol were charged to a reaction flask equipped with a condenser, stirrer and thermometer. The batch was heated to 150 ° C with stirring when ethyl alcohol began to be released. The reaction was allowed to proceed until the theoretical amount of alcohol was released, the temperature rising to 190 ° C. The prepared silane has a specific gravity of 1076.6 kg. m - 1 mPa. s at 20 ° C and the refractive index at 20 ° C is 1.4806. Neutralization can be accomplished by simply adding silane to water with the appropriate acid. If desired, it can be carried out in a silane: acid molar ratio of 1: 1 to 3 to prepare salt solutions which are freely miscible with water.

Claims (1)

(3-cyklohexenyletyl) tris (2-aminoetoxy) silan sumárneho vzorca Cj^Hj^OjNjSx a štruktúrneho vzorca(3-cyclohexenylethyl) tris (2-aminoethoxy) silane of the general formula C 1 H 4 O 2 O 3 N 3 S x and structural formula -(CH2)2 - Si(0C2H<tNH2)3 a jeho adičné soli s kyselinou marvčou a octovou.- (CH 2 ) 2 -Si (OC 2 H ? T NH 2 ) 3 and its addition salts with maric acid and acetic acid.
CS124589A 1989-02-27 1989-02-27 (3-cyclohexenylethyl) tris (2-aminoethoxy)silane CS272884B1 (en)

Priority Applications (1)

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CS124589A CS272884B1 (en) 1989-02-27 1989-02-27 (3-cyclohexenylethyl) tris (2-aminoethoxy)silane

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Application Number Priority Date Filing Date Title
CS124589A CS272884B1 (en) 1989-02-27 1989-02-27 (3-cyclohexenylethyl) tris (2-aminoethoxy)silane

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CS124589A1 CS124589A1 (en) 1990-06-13
CS272884B1 true CS272884B1 (en) 1991-02-12

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