Alkoxysilyl-containing adhesive sealants with intrinsically reduced viscosity

US2016304666A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2016304666-A1
Application numberUS-201415035902-A
CountryUS
Kind codeA1
Filing dateOct 23, 2014
Priority dateNov 18, 2013
Publication dateOct 20, 2016
Grant date

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Abstract

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The present invention provides specific alkoxylation products, a process for preparing them, compositions which comprise these alkoxylation products, and the use thereof.

First claim

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1 . An alkoxylation product having intrinsically reduced viscosity, the alkoxylation product comprising the formula (I) M i D j T k Q l UR u AP v   formula (I), where the fragments M, D, T and Q are linked not to one another but instead with one another via the groups UR and/or AP, and the groups UR and AP are linked not to one another but instead with one another, correspondingly, via the fragments M, D, T or Q, i=0 to 16, j=0 to 10, k=0 to 6, l=0 to 4, u=0 to 17, v=0 to 6, with the proviso that i+j+k+l>=1, M independently at each occurrence is an oxygen-radical-carrying hydrocarbon radical having a minimum numerical molar mass of 88 g/mol, which may optionally be interrupted by heteroatoms, or is a radical of the formula (Ia) or of the formula (Ib) or of the formula (Ic) with where a=0 to 1000, b=1 to 1000, c=0 to 1000, d=0 to 1000, w=an integer from 0 to 1000, x=0 to 1000, y=an integer from 0 to 500, e=1 to 10, f=0 to 2, g=1 to 3, with the proviso that g+f=3 and g is at least 1, h=0 to 10 and with the proviso that the various monomer units of the fragments with the indices a, b, c, d, w, x and y may be constructed blockwise among one another or else are subject to a statistical distribution and, moreover, are freely permutable among one another, it being disallowed for each of the groups with the indices w and y to follow itself or the other respective group, and where R 1 =independently at each occurrence a saturated or unsaturated, linear or branched organic hydrocarbon radical which may comprise O, S and/or N as heteroatoms, R 2 =independently at each occurrence an alkyl group having 1 to 8 carbon atoms, R 3 =independently at each occurrence an alkyl group having 1 to 8 carbon atoms, R 4 =independently at each occurrence a hydrogen radical, an alkyl group having 1 to 20 carbon atoms, or an aryl or alkaryl group, or R 4 and one of the radicals R 5 may together form a ring which includes the atoms bonded to R 4 and R 5 , this ring containing 5 to 8 carbon atoms, R 5 =independently at each occurrence a hydrogen radical or an alkyl group having 1 to 8 carbon atoms, R 6 , R 7 =independently at each occurrence a hydrogen radical, an alkyl group having 1 to 20 carbon atoms, an aryl or alkaryl group, and/or alkoxy group, R 11 =independently at each occurrence a saturated or unsaturated alkyl group having 1 to 24 carbon atoms, whose chain may be interrupted by oxygen and may further carry functional groups such as, for example, carboxyl groups optionally esterified with alcohols such as, for example, methanol, ethanol, propanol, butanol or hexanol, hydroxyl groups optionally esterified with acids such as acetic acid, butyric acid or (meth)acrylic acid, or the polymers of (meth)acrylic acid, or an aryl group having 6 to 20 carbon atoms, or an alkaryl group having 7 to 30, R 12 =independently at each occurrence a saturated or unsaturated, aliphatic or aromatic hydrocarbon radical having 2 to 30 C atoms, whose chain may be interrupted by oxygen and may further carry functional groups such as, for example, carboxyl groups or hydroxyl groups, it being possible for the carboxyl groups to be esterified optionally with alcohols, preferably with methanol, ethanol, propanol, butanol or hexanol, and for the hydroxyl groups to be esterified optionally with acids, preferably with acetic acid, neodecanoic acid or butyric acid, and/or an alkaryl group having 7 to 30, with the proviso that there must be at least one branched structural element present, R 13 , R 14 =independently at each occurrence hydrogen and/or an organic radical, preferably alkyl, alkenyl, alkylidene, alkoxy, aryl and/or aralkyl groups, or optionally R 13 and/or R 14 may also be absent, and, if R 13 and R 14 are absent, there is a C═C double bond instead of the radicals R 13 and R 14 ; the bridging fragment Z may be present or absent: if the bridging fragment Z is absent, then R 15 , R 16 =independently at each occurrence hydrogen and/or an organic radical, preferably alkyl, alkenyl, alkylidene, alkoxy, aryl and/or aralkyl groups, and, if one of the radicals R 13 or R 14 is absent, the respective germinal radical (i.e. R 15 if R 13 is absent, and R 16 if R 14 is absent) is an alkylidene radical, if the bridging fragment Z is present, then R 15 and R 16 =hydrocarbon radicals which are bridged cycloaliphatically or aromatically via the fragment Z, Z representing a divalent alkylene or alkenylene radical which may be further substituted, where R 17 =independently at each occurrence a linear or branched, saturated or unsaturated, optionally further substituted alkyl group having 1 to 30 carbon atoms, or an aryl or alkaryl group, where R 18 =a divalent linear or cyclic, saturated or unsaturated alkyl or aryl group which may be substituted, and, if j, k and l are each=0, then M must=formula (Ia); and where, for the fragments D, T and Q: D is a polyether radical PE with t being 2, T is a polyether radical PE with t being 3 and Q is a polyether radical PE with t being 4, where PE independently at each occurrence is a polyether radical with the formula -(D A ) t -D X , where t=2 to 4 and D X is a t-valent functional, saturated or unsaturated, linear or branched organic hydrocarbon radical which may comprise O, S, Si and/or N as heteroatoms, each of the radicals D A being bonded covalently to the radical D X , and where D A is a fragment of the formula (II) with a to h, w, x and y and R 2 to R 16 independently of one another as defined in formula (Ia), with the proviso that the sum of all the indices a from formula (Ia) and formula (II) must be greater than or equal to 1, characterized in that the sum of all the indices x from formula (Ia) and formula (II) must be greater than or equal to 1, UR independently at each occurrence are identical or different divalent radicals of the form —U-D C -U—, or a monovalent radical of the form D D -U—, or a trivalent radical of the form D E U 3 , or a tetravalent radical of the form D F U 4 , where U is a —C(O)—NH— group which is bonded via the nitrogen to D C , D E , D F or D D , and D C independently at each occurrence is a divalent substituted or unsubstituted, linear or branched, saturated or unsaturated hydrocarbon radical having 1 to 30 carbon atoms, selected from alkyl, alkenyl, aryl or alkaryl radicals, which may optionally be interrupted by heteroatoms such as O, N and/or S, and D D independently at each occurrence is a monovalent linear or branched, saturated or unsaturated hydrocarbon radical having 1 to 30 carbon atoms, selected from alkyl, alkenyl, aryl or alkaryl radicals, which may be interrupted by heteroatoms such as O, N and/or S and/or may carry further functional groups, and D E independently at each occurrence is a trivalent substituted or unsubstituted linear or branched, saturated or unsaturated hydrocarbon radical having 1 to 30 carbon atoms, selected from alkyl, alkenyl, aryl or alkaryl radicals, which may be interrupted by heteroatoms such as O, N and/or S and/o

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Classifications

  • and at least one isocyanate or isothiocyanate group linked to a secondary carbon atom of the cycloaliphatic ring, e.g. isophorone diisocyanate · CPC title

  • from polyethers · CPC title

  • C08G65/336Primary

    containing silicon · CPC title

  • containing silicon · CPC title

  • having alkylene polyamine groups · CPC title

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What does patent US2016304666A1 cover?
The present invention provides specific alkoxylation products, a process for preparing them, compositions which comprise these alkoxylation products, and the use thereof.
Who is the assignee on this patent?
Evonik Degussa Gmbh
What technology area does this patent fall under?
Primary CPC classification C08G65/336. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Oct 20 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).