Title of Invention

ORGANSOILANE MASTERBATCH

Abstract Organosilane masterbatch comprising 2-20 parts by weight of rubber such as herein described, 0-60 parts by weight of filler, 5-55 parts by weigh of organosilane such as herein described and 0-10 parts by weight of dispersing agent.
Full Text Organosilane masterbatch
The present invention relates to organosilane masterbatch,
a process for their preparation and their use in rubber
mixtures.
It is known that organosilane preparation consist of or
consist essentially of 30 to 60 weight-% of one or more
organosilanes and 70 to 40 weight-% of carbon blacks (US
4,128,438) .
Disadvantages of the known organosilane preparation is the
high bead abrasion of the granulate in case of transport
and the difficult incorporation into rubber compounds.
It is furthermore known that unvulcanized elastomer
compositions are prepared in a multi-stage process
comprising in an early stage of the multi-stage process,
substantially dispersing particulate filler selected from
modified carbon blacks and sulfur crosslinking agent into
sulfur crosslinkable hydrocarbon elastomer to produce a
substantially unvulcanized elastomer to produce a
substantially unvulcanized elastomer masterbatch, the
sulfur crosslinking agent comprising sulfur or sulfur done
effective to crosslink the hydrocarbon elastomer, and ther
producing the substantially unvulcanized elastomer
composition in at least one subsequent stage of the multi-
stage process, comprising mechanical working of the
masterbatch (US 5,916,956).
Disadvantage of the known elastomer compositions is the
high rubber content which is in the case of different
rubbers in the masterbatch and the final product a
limitation of the compound.
The object of the present invention is to develop a new
organosilane masterbatch with a low bead abrasion in case

of transport, a good dispersion in rubber compounds and a
low content of rubber.
The invention provides an organosilane masterbatch
comprising
(a) 2-20 parts by weight, preferably 2 to 9 parts by
weight, especially prefered 2 to 5 parts by weight, of
rubber,
(b) 0-60 parts by weight, preferably 30 to 60 parts by
weight, especially prefered 40 to 55 parts by weight, of
filler,
(c) 5-55 parts by weight, preferably 15 to 55 parts by
weight, especially prefered 45 to 55 parts by weight, of
organosilane and
(d) 0-10 parts by weight, preferably 0.5 to 5 parts by
weight, especially prefered 0.5 to 1.5 parts by weight, of
dispersing agent.
The rubber may comprise naturally occurring rubber (NR),
polybutadiene (PB), polyisoprene (IR), isobutylene/isoprene
copolymers (IIR), butadiene/acrylonitrile copolymers with
acrylonitrile contents of 5 to 60, preferably 10 to 50 wt.%
(NBR), ethylene/propylene/diene copolymers (EPDM),
styrene/butadiene copolymers (E-SBR or S-SBR) and mixtures
of these rubbers. Synthetic rubbers are described, for
example, in W. Hofmann, Kautschuktechnologie [Rubber
Technology], Genter Verlag, Stuttgart 1980.
The filler may comprise carbon blacks.
The carbon blacks may comprise ASTM carbon blacks, flame
blacks, furnace blacks, channel blacks or gas blacks,
rubber or pigment blacks or carbon black mixtures,
preferably CORAX N 121, CORAX N 110, CORAX N 2 42, CORAX N
234, CORAX N 220, CORAX N 375, CORAX N 356, CORAX 347,
CORAX N 339, CORAX N 332, CORAX N 330, CORAX N 326, CORAX N
550, CORAX N 539, CORAX N 683, CORAX N 660, CORAX N 774,
CORAX N 7 65, CORAX N 650, CORAX N 7 62, DUREX 0, CORAX 3,
CORAX 4, CORAX 9, CORAX P, PRINTEX P, CORAX S 315, CK 3,

CORAX XE-1, PRINTEX L, PRINTEX L 6, CORAX L 29, PRINTEX
XE2, FARBRUSS FW 200, FARBRUSS FW 2, FARBRUSS FW 2 V,
FARBRUSS FW 1, FARBRUSS FW 18, SPEZIALRUSS 6, FARBRUSS S
170, FARBRUSS S 160, SPEZIALRUSS 5, SPEZIALRUSS 4,
SPEZIALRUSS 4A, PRINTEX 150 T, PRINTEX U, PRINTEX V,
PRINTEX 140 U, PRINTEX 140 V, PRINTEX 95, PRINTEX 90,
PRINTEX 85, PRINTEX 80, PRINTEX 75, SPECIALRU.beta. 550,
PRINTEX 55, PRINTEX 45, PRINTEX 40, PRINTEX 60, PRINTEX XE
2, PRINTEX L 6, PRINTEX L, PRINTEX 300, PRINTEX 30, PRINTEX
3, SPEZIALRUSS 350, PRINTEX 35, SPEZIALRUSS 250, PRINTEX
25, PRINTEX 200, PRINTEX A, SPEZIALRUSS 100, PRINTEX G,
FLAMMRUSS 101, all made by Degussa AG, described in
"Information fur die Gummiindustrie" ("Information for the
Rubber Industry"), Degussa AG, PT 39-4-05-1287 Ha and
"Pigment Blacks" Degussa AG PT 80-0-11-10 86 Ha. The carbon
blacks may optionally also contain heteroatoms such as e.g.
Si.
The filler may comprise glass fibres and glass fibre
products (mats, strands) or microsize glass spheres.
The organosilane may comprise organosilane of the formula I
Z-A-Sx-A-Z (I)
in which
x is a number from 1 to 12, preferably 1 to 8, particularly
preferably 2 to 6,
Z is equal to SiX2X3 and
X1, X2, X3 can each mutually independently denote hydrogen
(-H),
halogen or hydroxy (-OH),
an alkyl substituent, preferably methyl or ethyl,
alkenyl acid substituent, for example acetoxy R-(C=O)O-,
or a substituted alkyl or alkenyl acid substituent, for
example oximato R12C=NO-,
a linear or branched hydrocarbon chain with 1-6 carbon
atoms,

a cycloalkyl radical with 5-12 carbon atoms,
a benzyl radical or a halogen- or alkyl-substituted phenyl
radical,
alkoxy groups, preferably (C1-C4) or (C12-C16) alkoxy,
particularly preferably methoxy or ethoxy, with linear or
branched hydrocarbon chains with (C1-6) atoms,
a cycloalkoxy group with (C5-12) atoms,
a halogen- or alkyl-substituted phenoxy group or
a benzyloxy group,
A is a (C1-C16) , preferably (C1-C4) , branched or unbranched,
saturated or unsaturated, aliphatic, aromatic or mixed
aliphatic/aromatic divalent hydrocarbon group.
The following compounds can for example be used as
organosilane having the general formula (I):
[(MeO)3Si(CH2)3]2S, [(MeO)3Si(CH2)3]2S2, [ (MeO) 3Si (CH2) =] 2S3,
[(MeO)3Si(CH2)3]2S4, [(MeO)3Si(CH2)3]2S5, [ (MeO) 3Si (CH2) 3] 2S6,
[(MeO)3Si(CH2)3]2S7, [(MeO)3Si(CH2)3]2S8, [ (MeO) 3Si (CH2) 3] 2S9,
[ (MeO)3Si(CH2)3]2S10, [ (MeO) 3Si (CH2) 3] 2S11, [ (MeO) 3Si (CH2) 3] 2S12,
[ (MeO)3Si(CH2)3]2S, [ (EtO) 3Si (CH2) 3] 2S2, [ (EtO) 3Si (CH2) 3] 2S3,
[(EtO)3Si(CH2)3]2S4, [(EtO)3Si(CH2)3]2S5, [ (EtO) 3Si (CH2) 3] 2S6,
[(EtO)3Si(CH2)3]2S7, [(EtO)3Si(CH2)3]2S8, [ (EtO) 3Si (CH2) 3] 2S9,
[ (EtO)3Si(CH2)3]2S10, [ (EtO)3Si(CH2)3]2S11, [ (EtO) 3Si (CH2) 3] 2S12,
[ (C3H7O)3Si(CH2)3]2S, [ (C3H7O)3Si(CH2)3]2S2,
[ (C3H7O) 3Si (CH2) 3] 2S3, [ (C3H7O) 3Si (CH2) 3] 2S4,
[ (C3H7O)3Si(CH2)3]2S5, [ (C3H7O)3Si(CH2)3]2S6,
[ (C3H7O)3Si(CH2)3]2S7, [ (C3H7O)3Si(CH2)3]2S8,
[ (C3H7O) 3Si (CH2) 3] 2S9, [ (C3H7O) 3Si (CH2) 3] 2S10,
[ (C3H7O)3Si(CH2)3]2S11 or [ (C3H7O) 3Si (CH2) 3] 2S12 .
The organosilane may comprise organosilane of the formula
II
Z-A-Y (II)
in which
Z and A have the same meaning as in formula (I) and

Y is SH, SCN, S-C(O)-X1, a straight-chain, branched or
cyclic (C1-C18) alkyl, for example methyl, ethyl, n-propyl,
n-butyl, n-pentyl, n-hexyl, isopropyl or tert-butyl,
(C1-C5) alkoxy, for example methoxy, ethoxy, propoxy,
butoxy, isopropoxy, isobutoxy or pentoxy,
halogen, for example fluorine, chlorine, bromine or iodine,
hydroxy, nitrile, (C1-C4) haloalkyl, -NO2, (C1-C8)
thioalkyl, -NH2, -NHR1, -NR1R2, alkenyl, allyl, vinyl, aryl
or (C7-C16) aralkyl.
The following compounds can for example be used as
organosilane having the general formula (II):
(EtO)3-Si-(CH2)3-H, (MeO)3-Si-(CH2)3-H, (EtO) 3-Si- (CH2) 8-H,
(MeO)3-Si-(CH2)8-H, (EtO) 3-Si-(CH2) 16-H, (MeO) 3-Si-(CH2) 16-H,
(Me)3Si-(OMe), ( (Et) 3Si-(OMe) , (C3H7) 3Si-(OMe) ,
(C6H5)3Si-(OMe) , (Me)3Si-(OEt) , ( (Et) 3Si-(OEt) ,
(C3H7)3Si-(OEt) , (C6H5)3Si-(OEt) , (Me) 3Si-(OC3H7) ,
((Et)3Si-(OC3H7) , (C3H7)3Si-(OC3H7) , (C6H5) 3Si- (OC3H7) ,
(Me)3SiCl, ((Et)3SiCl, (C3H7)3SiCl, (C6H5) 3SiCl, Cl3-Si-CH2-
CH=CH2, (MeO)3-Si-CH2-CH=CH2, (EtO) 3-Si-CH2-CH=CH2, Cl3-Si-
CH=CH2, (MeO) 3-Si-CH=CH2, (EtO) 3-Si- (CH2) 3-SH or (EtO)3-Si-
CH=CH2.
Examples of organosilanes which can be used in the
invention include
3,3'-bis(trimethoxysilylpropyl) disulfide,
3,3'-bis(triethoxysilylpropyl) tetrasulfide,
3,3'-bis(trimethoxysilylpropyl) tetrasulfide,
2,2'-bis(triethoxysilylethyl) tetrasulfide,
3,3'-bis(trimethoxysilylpropyl) trisulfide,
3,3'-bis(triethoxysilylpropyl) trisulfide,
3,3'-bis(trimethoxysilylpropyl) hexasulfide,
2, 2'-bis(methoxy diethoxy silyl ethyl) tetrasulfide,
2,2'-bis(tripropoxysilylethyl) pentasulfide,
bis(trimethoxysilylmethyl) tetrasulfide,
2, 2'-bis(methyl dimethoxysilylethyl) trisulfide,
2,2'-bis(methyl ethoxypropoxysilylethyl) tetrasulfide,

5,5'-bis(dimethoxymethylsilylpentyl) trisulfide,
3,3'-bis(trimethoxysilyl-2-methoxypropyl) tetrasulfide,
5,5'-bis(triethoxysilylpentyl) tetrasulfide,
4,4'-bis(triethoxysilylbutyl) tetrasulfide,
3,3'-bis(diethoxymethylsilylpropyl) trisulfide,
bis(triethoxysilylmethyl) tetrasulfide,
3,3'-bis(dimethylethoxysilylpropyl) tetrasulfide,.
3,3'-bis(dimethylmethoxysilylpropyl) tetrasulfide,
3,3'-bis(dimethylethoxysilylpropyl) disulfide,
3,3'-bis(dimethylmethoxysilylpropyl) disulfide,
3-mercaptopropyltriethoxysilane,
3-mercaptopropyltrimethoxysilane,
3,3'-bis(dodecanyldiethoxysilylpropyl) tetrasulfide,
3,3'-bis(didodecanylethoxysilylpropyl) tetrasulfide,
3,3'-bis(hexadecanyldiethoxysilylpropyl) tetrasulfide,
3,3'-bis(dihexadecanylethoxysilylpropyl) tetrasulfide,
3,3'-bis(dodecanyldiethoxysilylpropyl) disulfide,
3,3'-bis(didodecanylethoxysilylpropyl) disulfide,
3,3'-bis(hexadecanyldiethoxysilylpropyl) disulfide,
3,3'-bis(dihexadecanylethoxysilylpropyl) disulfide,
3-triethoxysilyl-1-propylthiooctoate,
3-trimethoxysilyl-1-propylthiooctoate,
3-triethoxysilyl-1-propylthiohexanoate,
3-trimethoxysilyl-1-propylthiohexanoate,
3-triethoxysilyl-1-propylthiobenzoate,
3-trimethoxysilyl-1-propylthiobenzoate or
3-thiocyanatopropyltriethoxysilane.
The organosilane may comprise Si 69, Si 108, Si 116, Si
118, Si 203, Si 208, Si 230, Si 264, Si 75 or Si 266, all
made by Degussa AG.
The organosilane may be a mixture of organosilanes.
The dispersing agent may comprise of all such additives
used in the rubber industry, preferably Struktol WB16 or
Struktol WB212, all made by Schill & Seilacher AG,
Moorfleeter Strasse 28, 22113 Hamburg, Germany.

The organosilane masterbatch may comprise silicone oil.
The organosilane masterbatch can consist of
(a) 2-20 parts by weight, preferably 2 to 9 parts by
weight, especially prefered 2 to 5 parts by weight, of
rubber,
(b) 0-60 parts by weight, preferably 30 to 60 parts by
weight, especially prefered 40 to 55 parts by weight, of
filler,
(c) 5-55 parts by weight, preferably 15 to 55 parts by
weight, especially prefered 45 to 55 parts by weight, of
organosilane and
(d) 0-10 parts by weight, preferably 0.5 to 5 parts by
weight, especially prefered 0.5 to 1.5 parts by weight, of
dispersing agent.
The invention also provides a process for the production of
organosilane masterbatch according to the invention, which
is characterized in that the rubber, filler, organosilane
and dispersing agent are mixed in a banbury or kneader,
extruded and cut into pieces.
The pieces can be cooled on a conveyor system.
The mixing in the banbury or kneader can be carried out at
temperatures from 20° to 100°C, preferably from 60° to
80°C. The mixing period can be from 1 to 20 minutes,
preferably from 5 to 15 minutes.
The extrusion can be carried out in conventional extruding
machine.
The present invention also provides rubber mixtures, which
are characterised in that they contain organosilane
masterbatch according to the invention.
The organosilane masterbatch according to the invention may
be used in quantities of 0.1 to 20 wt. %, relative to the
quantity of rubber used.

The rubber compounds according to the invention can be used
for producing mouldings, for example, for the production of
pneumatic tyres, tyre treads, cable coverings, flexible
tubes, drive belts, conveyor belts, roller coatings, tyres,
shoe soles, washers and damping elements.
The organosilane masterbatch according to the invention
have the advantage that the bead abrasion is low in case of
transport, the dispersion into rubber is well and the
rubber content is very low.
Example 1
Organonsilane masterbatch
There are weighed into a 75 1 Banbury 4 kg of E-SBR, 45 kg
of N 330, 50 kg of Si 69 and 1 kg of Struktol WB212. All
ingredients are mixed for 10 minutes below 80°C.
Afterwards the organosilane masterbatch is extruded in a
conventional extruder at temperature lower than 80°C.
The extrudated organosilane masterbatch is cut into pieces
of approx 0.5 cm and then cooled on a conveyor system.
The organosilane masterbatch has no fine content unlike X
50-S (approx 15%).
Example 2
The organosilane masterbatch of Example 1 is tested in a NR
radial truck tread compound. The unit phr here means parts
by weight relative to 100 parts of rubber used. The
formulation used for the rubber compounds is stated in
Table 1 below.


Polymer STR 5L (ML1+4=70) is a natural rubber with a
Mooney viscosity 70 MU.
Corax N115 is an ASTM carbon black from Degussa AG.
Ultrasil 7000 GR is a readily dispersible precipitated
silica from Degussa AG with a BET surface area of 175 m2/g.

The product X 50 S is a 1:1 mixture of Si 69
(Bis(triethoxysilylpropyl)tetrasulfane) and of a HAF carbon
black from Degussa AG. Antilux 654 is antiozonant from
RheinChemie,Vulkanox 4020(6PPD)is antioxidants with
antiozonant effects from Bayer AG, and Vulkanox HS/LG(TMQ)
is antioxidants without antiozonant effects from Bayer AG.
Vulkacit NZ/EG and Vulkacit D are vulcanization
accelerators from Bayer AG.
The rubber mixtures are prepared in an internal mixer in
accordance with the mixing instructions in Table 2.










Comparison is made between truck tread compounds with and
without silane in typical NR truck tread compound (Table 4a
/4b). Compound 2 contains 9 phr of the organosilane
masterbatch made according to the invention (Example 1).
Compound 3 contain X 50-S which is a mixture of 50% Si69
and 50% HAF carbon black. As can be seen in the properties
(Compound 2), the use of the organosilane masterbatch of
the invention, improves modulus, abrasion, heat generation,
and don't have any dispersion problem, versus the reference
Compound 1. The improvements are comparable to those using
X 50-S (Compound 3).

We Claim:
1. Organosilane masterbatch comprising
(a) 2-20 parts by weight of rubber such as herein described,
(b)0-60 parts by weight of filler,
(c) 5-55 parts by weigh of organosilane such as herein described
and
(d)0-10 parts by weight of dispersing agent.
2. Organosilane masterbatch as claimed in claim 1 wherein the rubber
is emulsion styrene-butadiene rubber E-SBR or solution styrene-
butadiene rubber S-SBR.
3. Organosilane masterbatch as claimed in claim 1 wherein the filler
is carbon black.
4. Organosilane masterbatch as claimed in claim 1 wherein the
organosilane is one of the group of the organosilane of formula I
Z-A-Sx-A-Z (I)
in which
x is a number from 1 to 12,
Z is equal to SiX1X2X3 and
X1,X2,X3 can each mutually independently denote hydrogen (-H),
halogen or hydroxy (-OH),

an alkyl substituent -CnH2n+1,
alkenyl acid substituent -O(O=C)-CnH2n-1
a linear or branched hydrocarbon chain with 1-6 carbon atoms:
CnH2n+1 with n= 1-6
a cycloalkyl radical with 5-12 carbon atoms,
a benzyl radical or a halogen- or alkyl substituted phenyl radical: -
C6H(5_m)Rm with m = 1-5, R = CnH2n+1,
alkoxy groups with linear or branched hydrocarbon chains with
(C1-6) atoms,
a cycloalkoxy group with (C5_12) atoms,
a halogen- or alkyl-substituted phenoxy group or a benzyloxy
group,
A is a (C1-16) branched or unbranched, saturated or unsaturated,
aliphatic, aromatic or mixed aliphatic/aromatic divalent
hydrocarbon group or organosilane of formula II
Z-A-Y (II)
In which
Z and A have the same meaning as in formula (I) and
Y is SH, SCN, S-C(O)-X1, a straight-chain, branched or cyclic (Cr
C18) alkyl,
(C1-C5) alkoxy,
halogen, hydroxy, nitrile, (C1-C4) haloalkyl, -NO2, (C1-C8)
thioalkyl, -NH2, -NHR1, -NR1R2, alkenyl, allyl, vinyl, aryl or (C7-
C16) aralkyl.

5. Organosilane masterbatch as claimed in claim 4 wherein the
organosilane is
3,3'-bis(trimethoxysilylpropyl) disulfide,
3,3' -bis(triethoxysilylpropyl) tetrasulfide,
3,3 '-bis(trimethoxysilylpropyl) tetrasulfide,
2,2' -bis(triethoxysilylpropyl) tetrasulfide,
3,3 '-bis(trimethoxysilylpropyl) trisulfide,
3,3 '-bis(triethoxysilylpropyl) trisulfide,
3,3 '-bis(trimethoxysilylpropyl) hexasulfide,
2,2"-bis(methoxy diethoxy silyl ethyl) tetrasulfide,
2,2'-bis(tripropoxysilylethyl)pentasulfide,
bis (trimethoxysilylmethyl) tetrasulfide,
2,2'-bis(methyl dimethoxysilylethyl) trisulfide,
2,2'-bis(methyl ethoxypropoxysilylethyl) tetrasulfide,
5,5' -bis(dimethoxymethylsilylpentyl) trisulfide,
3,3 '-bis(trimethoxysilyl-3-methoxypropyl) tetrasulfide,
5,5 '-bis(triethoxysilylpentyl) tetrasulfide,
4,4'-bis(triethoxysilylbutyl) tetrasulfide,
3,3 '-bis(diethoxymethylsilylpropyl) trisulfide,
bis (triethoxysilylmethyl) tetrasulfide,
3,3 '-bis(dimethylethoxysilylpropyl) tetrasulfide,
3,3' -bis(dimethylmethoxysilylpropyl) tetrasulfide,
3,3'-bis(dimethylethoxysilylpropyl) disulfide,

3,3'-bis(dimethylmethoxysilylpropyl) disulfide,
3 -mercaptopropyltriethoxy silane,
3-mercaptopropyltrimethoxysilane,
3,3' -bis(dodecanyldiethoxysilylpropyl) tetrasulfide,
3,3 '-bis(didodecanylethoxysilylpropyl) tetrasulfide,
3,3 '-bis(hexadecanyldiethoxysilylpropyl) tetrasulfide,
3,3' -bis(dihexadecanylethoxysilylpropyl) tetrasulfide,
3,3'-bis(dodecanyldiethoxysilylpropyl) disulfide,
3,3' -bis(didodecanylethoxysilylpropyl) disulfide,
3,3 '-bis(hexadecanyldiethoxysilylpropyl) disulfide,
3,3' -bis(dihexadecanylethoxysilylpropyl) disulfide,
3 -triethoxy silyl-1 -propylthiooctoate,
3-trimethoxysilyl-1 -propy lthiooctoate,
3-triethoxy silyl-1 -propylthiohexanoate,
3-trimethoxysilyl-1 -propylthiohexanoate,
3-triethoxysilyl-1 -propylthiobenzoate,
3-trimethoxysilyl-1 -propylthiobenzoate or
3-thiocyanatopropyltriethoxysilane.
6. A process for the production of organosilane masterbatch as

claimed in claim 1, wherein the rubber, filler, organosilane and
dispersing agent are mixed in a banbury or kneader, extruded and
cut into pieces.

Organosilane masterbatch comprising 2-20 parts by weight of rubber such as
herein described, 0-60 parts by weight of filler, 5-55 parts by weigh of
organosilane such as herein described and 0-10 parts by weight of dispersing
agent.

Documents:

204-kol-2004-granted-abstract.pdf

204-kol-2004-granted-claims.pdf

204-kol-2004-granted-correspondence.pdf

204-kol-2004-granted-description (complete).pdf

204-kol-2004-granted-examination report.pdf

204-kol-2004-granted-form 1.pdf

204-kol-2004-granted-form 18.pdf

204-kol-2004-granted-form 2.pdf

204-kol-2004-granted-form 26.pdf

204-kol-2004-granted-form 3.pdf

204-kol-2004-granted-form 5.pdf

204-kol-2004-granted-gpa.pdf

204-kol-2004-granted-reply to examination report.pdf

204-kol-2004-granted-specification.pdf

204-kol-2004-granted-translated copy of priority document.pdf


Patent Number 230197
Indian Patent Application Number 204/KOL/2004
PG Journal Number 09/2009
Publication Date 27-Feb-2009
Grant Date 25-Feb-2009
Date of Filing 26-Apr-2004
Name of Patentee DEGUSSA AG.
Applicant Address BENNIGSENPLATZ 1, DE-40474 DÜSSELDORF
Inventors:
# Inventor's Name Inventor's Address
1 WU, LU-LIANG 4TH FL. NO. 7.LANE 165 SEC. 1, HSING SHENG S.RD., TAIPEI, TAIWAN
PCT International Classification Number B61
PCT International Application Number N/A
PCT International Filing date
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 03 010 018.4 2003-05-02 EUROPEAN UNION