US20030139493A1

US20030139493A1 - Rubber mixtures for roller coatings

Info

Publication number: US20030139493A1
Application number: US10/354,665
Authority: US
Inventors: Erich Fuchs
Original assignee: Individual
Current assignee: Individual
Priority date: 1999-09-07
Filing date: 2003-01-30
Publication date: 2003-07-24
Also published as: EP1083197A3; CA2317318A1; DE19942743A1; JP2001151939A; US6538071B1; EP1083197A2

Abstract

This invention relates to a rubber mixture containing a nitrile rubber, a metal salt of an acrylate, a liquid acrylate and optionally other additives, a process for its preparation, and use for all types of molded articles, in particular roller coatings.

Description

FIELD OF THE INVENTION

BACKGROUND OF THE INVENTION

Rollers having a rubber coating are used in many fields, including the print and textile industry, in machines, such as, for example, fax machines and in the steel industry and paper industry.

Roller coatings are subjected to extreme stresses, particularly in the steel and paper industries. In such applications, the coatings are required to have a combination of the following properties:

low compression set;

low abrasion;

little swelling in the media used;

good resistance to heat and chemicals;

excellent adhesion to the metal surface under the coating; and/or

low build-up of heat under stress.

SUMMARY OF THE INVENTION

It has now been found that a rubber mixture which contains a nitrile rubber and, in addition, a metal salt of an acrylate and a liquid acrylate is particularly suitable as raw material for rubber coatings for rollers.

This application accordingly provides a rubber mixture, containing

a) one or more nitrite rubbers

b) one or more metal salts of an acrylate

c) one or more liquid acrylates, optionally applied to a carrier, and

d) optionally other additives and/or fillers.

Nitrite rubbers are meant to be diene-(meth)acrylonitrile copolymers. The preferred dienes here are isoprene and, in particular, butadiene. The copolymers have a content of copolymerized acrylonitrile units and/or methacrylonitrile units of 5 to 60 wt. %, preferably 10 to 50 wt. %.

Moreover, the term explicitly includes hydrogenated nitrite rubbers. According to this invention, “hydrogenated nitrite rubber” or “HNBR” means nitrite rubbers, the C═C double bonds of which are selectively (that is, without hydrogenation of the C≡N triple bond) partially or completely hydrogenated. Preferred hydrogenated nitrile rubbers are those having a degree of hydrogenation, based on the C═C double bonds originating from the butadiene, of at least 75%, preferably of at least 95%, in particular of at least 98%. The degree of hydrogenation can be determined by NMR spectroscopy and IR spectroscopy.

The hydrogenation of nitrite rubber is known: U.S. Pat. No. 3,700,637, DE-A 2,539,132, DE-A 3,046,008, DE-A 3,046,251, DE-A 3,227,650, DE-A 3,329,974, EP-A 111,412, FR-B 2,540,503. Hydrogenated nitrite rubbers are distinguished by having high tensile strength, low abrasion, low residual deformation after compressive stress and tensile load and good resistance to oil, but primarily by a notable resistance to thermal and oxidative influences. Accordingly, hydrogenated nitrite rubbers are preferred in this invention.

Suitable nitrite rubbers generally have Mooney viscosities (DIN 53 523, ML 1+4) of 25 to 100 Mooney units, in particular 40 to 80 Mooney units.

The addition of metal salts of an acrylate to mixtures containing nitrile rubbers is known. Suitable acrylates may be unsubstituted or substituted. Methacrylates are an example of substituted acrylates.

The person skilled in the art knows of suitable acrylates from EP-A1 0,319,320, in particular page 3, lines 16 to 35; from U.S. Pat. No. 5,208,294, in particular column 2, lines 25 to 40 and from U.S. Pat. No. 4,983,678, in particular column 2, lines 45 to 62. Zinc acrylate, zinc diacrylate and zinc dimethylacrylate, in particular, are mentioned there.

It may be advantageous to use the metal salt of the acrylate together with a scorch retarder. Suitable examples here are hindered phenols, such as methyl-substituted aminoalkylophenols, in particular 2,6-ditert.-butyl-4-(dimethylamino)phenol.

The liquid acrylate may be any acrylate which is known to the person skilled in the art and is in liquid form at room temperature.

Trimethylolpropane trimethacrylate (TRIM), butanediol dimethacrylate (BDMA) and ethylene glycol dimethacrylate (EDMA) are particularly preferred.

In order to achieve an improved incorporation, it may be advantageous to use the liquid acrylate bound to a carrier. Examples of suitable carriers are silicates, precipitated silicas, clays, carbon black, talc or polymers. In general, mixtures containing 5 to 50 wt. % carrier are used.

Other suitable additives include those known to the person skilled in the art, for example, vulcanization activators, in particular metal oxides, such as zinc oxide or magnesium oxide, antidegradants, such as alkyl-substituted diphenylamines, mercaptobenzimidazoles, unsaturated ethers, such as Vulkazon® AFD (Bayer AG, D) or cyclic, unsaturated acetals, such as Vulkazon® AFS/LG (Bayer AG, D). The following may also be mentioned as additives:

plasticizers, in particular carboxylic esters, as well as sebacic acid and its derivatives or trimellitic acid and its derivatives

processing aids, in particular stearic acid and its derivatives, such as zinc stearate, or polymers, such as poly(ethylene vinyl acetate) (Levapren® from Bayer AG, D) or poly(ethylene vinyl acrylate)VAMAC® from DuPont).

It may also be advantageous to introduce fillers into the rubber mixture according to the present invention. These may be non-reinforcing or reinforcing.

Examples of fillers which may be mentioned are:

carbon blacks, such as MT, GPF, SRF blacks and primarily FEF blacks;

metal oxides, such as titanium dioxide (primarily as white pigment);

silicates, such as sodium aluminium silicate;

silicas, in particular precipitated silicas;

To improve the abrasion, so-called active fillers in accordance with the DIN 66131 are preferred, published, for example, on page 535 of “Handbuch für die Gummiindustrie”, Bayer AG, 1992, Leverkusen.

Clays, mica, talc.

In addition, it may be advantageous to use extra activators in order to improve the adhesion between filler and rubber, such as, for example, silanes, such as Silquest® RC-1 (Union Carbide, US). Pigments may also be added.

The quantities of the individual components of the mixture depend on the intended use of the mixture and can be determined by a few preliminary tests.

The materials are generally used in the following quantities (in each case, in phr=per hundred parts of rubber):

metal salt of an acrylate: 10 to 120 phr, preferably 10 to 85 phr, most preferably, 20 to 65 phr,

liquid acrylate: 5 to 80 phr, preferably 20 to 60 phr, in each case calculated without carrier,

antidegradant: 0 to 4 phr,

retarder: 0 to 2 phr,

metal oxides, such as ZnO: 0 to 30 phr,

fillers: 0 to 150 phr, preferably active fillers,

plasticizer: 0 to 20 phr,

processing aids: 0 to 2 phr.

The invention also provides crosslinkable mixtures containing the rubber mixtures according to the present invention, as well as a process for the preparation of the rubber mixtures according to the present invention and of cross-linkable rubber mixtures, characterized in that the components are mixed in a mixing unit.

In order to produce crosslinkable mixtures from the mixtures according to the present invention, crosslinking agents are added to the rubber mixtures according to the present invention. Peroxide systems are suitable crosslinking agents.

Preferred peroxide systems include dialkyl peroxides, ketal peroxides, aralkyl peroxides, peroxide ethers, peroxide esters, such as, for example: di-tert.-butyl peroxide, bis(tert.-butylperoxyisopropyl)benzene, dicumyl peroxide, 2,5-dimethyl-2,5-di(tert.-butylperoxy)hexane, 2,5-dimethyl-2,5-di(tert.-butylperoxy)-3-hexene, 1,1-bis(tert.-butylperoxy)-3,3,5-trimethylcyclohexane, benzoyl peroxide, tert.-butyl cumyl peroxide and tert.-butyl perbenzoate.

The quantities of peroxide are within the range of 1 to 10 phr, preferably within the range of 4 to 8 phr, based on rubber. The cross-linking can be effected at temperatures of 100° C. to 200° C., preferably 130° C. to 180° C., optionally at a pressure of 10 to 200 bar. Subsequent to the crosslinking, the vulcanizates can be post-cured by being stored at elevated temperature.

The peroxides can advantageously also be used in polymer-bound form. Appropriate systems are commercially available, for example, Poly-Dispersion® T (VC) D-40 P from Rhein Chemie Rheinau GmbH, D (=polymer-bound di-tert.-butylperoxyisopropylbenzene).

The crosslinking can also be achieved by high-energy radiation.

Crosslinking according to the present invention means that less than 10 wt. %, preferably less than 5 wt. %, based on rubber, is extractable during extraction for 10 hours in a Soxhlet attachment with toluene as extracting agent.

The optimal quantity of crosslinking agent is easily determined by preliminary experiments.

Any apparatus for mixing rubbers which is known to the person skilled in the art may be used as the mixing apparatus, in particular internal mixer, open mills and screw-type machines.

Here, care should be taken to ensure that the rubber is not degraded during the mixing procedure. It may be advantageous to cool the mixture during the mixing procedure. In order to avoid scorch, the peroxide is frequently added as the last component, optionally in a separate mixing procedure.

The invention also provides the use of the rubber mixtures according to the present invention for the production of all types of molded articles, in particular coatings for rollers, most particularly rollers for the paper, textiles, printing and steel industries.

Rollers generally consist of a metal core having a variable diameter, metal cores with a diameter of 1 to 5 m being preferred. The metal core generally consists of steel of various compositions, onto which the crosslinkable rubber mixture is drawn by means of conventional prior art methods and subsequently cross-linked. A good adhesion of coating to metal and inside the coating is crucial here. It may be advantageous to improve the adhesion of coating to metal by means of adhesion promoters, such as dispersions/solutions of halogenated polymers, optionally with crosslinking agents/fillers/pigments. These substances are commercially available.

The rubber mixtures according to the present invention are particularly suitable for use on rollers, as in the crosslinked condition they combine an excellent hardness in the range above 20 Shore D (DIN 53 505), even at elevated service temperatures, with a good resistance to abrasion, heat, water and chemicals. This balanced range of properties is not achieved in prior art. The rubber mixtures according to the present invention are, of course, also suitable for the production of other molded articles, such as profiles, belts, rings, seals, damping elements, etc.

Accordingly, molded articles, in particular rollers and belts, obtainable using a rubber mixture according to the present invention are also provided by the invention.

To the person skilled in the art, it is a trivial matter to modify specifically the properties of the mixtures according to the present invention by adding other polymers, such as BR, NR, IIR, IR, EPDM, EPM, CR, SBR, AEM, ACM or fluoropolymers.

The following Examples are intended to illustrate the invention, without thereby limiting it.

EXAMPLES

A. Methods of Measurement



	Residual double-bond content	IR spectroscopy
	Mooney viscosity	ASTM D 1646
	(ML 1 + 4 (100° C.))	(given in Mooney units)
	Volatile constituents (wt. %)	ASTM D 1416
	Ash content (wt. %)	ASTM D 1416
	Acrylonitrile (ACN) content	in accordance with the
	(wt. % bound in the polymer)	instructions below.

B. Brief Description of the Method

In the analysis, the rubber is pyrolyzed at 900° C. on a catalyst in a stream of oxygen. The unused oxygen is absorbed on a copper reduction reactor and the NO[0065] _xgases formed are reduced to nitrogen. Then the CO₂present in the stream of sample gas is withdrawn in an Na₂CO₃/NaOH trap and the water present in the stream of sample gas is withdrawn in an MgClO₄trap. The change in the thermal conductivity of the stream of sample gas compared with the stream of carrier gas is a measure of the nitrogen content of the sample.

C. Equipment

Protein analyzer, product of Fisons, Model NA 2000 [0066]
Microbalance, product of Sartorius, Model Micro [0067]
Analytical unit, product of Digital, Model DECpc Lpx 433 dx, with interfaces to the NA 2000 and balance interface, and the software EAGER 200 [0068]

D. Chemicals and Solvents

Methionine, product of Hekatech [0069]

E. Constituents of Formulation



Therban ® C 3467	Bayer AG	HNBR with 5.5% RDB
		34% ACN, 68 Mooney
		units
Zinkoxyd Aktiv	Bayer AG	active zinc oxide
Scorchguard ® O	Rhein Chemie Rheinau	magnesium oxide paste
	GmbH
Naugard 445	Uniroyal	subst. diphenylamine
Vulkanox ® ZMB 2	Bayer AG	zinc methylmercapto-
		benzimidazole
Tronox ® R-UF	Kerr-McGee Pigments	titanium dioxide, rutile
	GmbH & Co. KG	type
Vulkasil ® S	Bayer AG	precipitate silica
Vulkasil ® A 1	Bayer AG	sodium aluminum silicate
Sartomer SR633	Sartomer	zinc diacrylate with
		retarder additive
TRIM SR-350	Sartomer	trimethylolpropane
		trimethacrylate
Rhenofit ® TRIM/S	Rhein Chemie Rheinau	trimethylolpropane
	GmbH	trimethacrylate 70%
		bonded to silica 30%
BDMA ATM	Ancomer	butanediol dimethacrylate
Ethanox 703	Albemarle, BE	2,6-ditert.-butyl-4-(di-
		methylamino)phenol
Poly-Dispersion ®	Rhein Chemie Rheinau	di(tert.-butylperoxy-iso-
T (VC) D-40 P	GmbH	propyl)benzene, poly-
		merically bonded

F. Preparation of the Mixtures

The mixtures were prepared in an internal mixer GK 1.5 E product of Krupp Elasto-mertechnik, Hamburg). Cooling-water temperature 50° C.; rotor speed 50 rpm; ram pressure 6 bar; proportion of internal mixer filled 70-80%, based on the volume of the mixing compartment. [0071]
Mixing procedure: The rubber is placed in the internal mixer. After an operating time of 1 minute, the remaining constituents are added. The internal mixer emptied at a batch temperature of >125° C. The peroxide is subsequently mixed on a roll mill (Krupp Elastomertechnik; diameter 200 mm, working width 350 mm) at a cooling-water temperature of 40° C. [0072]

The sheets for the determination of the mechanical properties were cross-linked/vulcanized under the stated conditions, between Teflon sheets, in a vulcanizing press (Krupp Elastomertechnik).



	Properties:

Value:	Dimension	Test Standard:

ML-1 + 4/	Mooney units	Mooney viscosity	DIN 53525 Part 3
100° C.
MS-T5/120°, and	min	Mooney pre-	DIN 53525 Part 4
140° C.		vulcanization
		behavior (time
		for 5 Mooney
		units above
		minimum)
MDR rheometer	S'd Nm	Course of	DIN 53529 Part 3
minimum, or		vulcanization.
maximum or		Torque-
MAX − Min		minimum-
		maximum or
		difference
		max./min.
T10, T50, T80,	min	Time for 10%,
T90		50%, 80%, 90%
		of full cure
F	MPa	Tensile strength	DIN 53504
D	%	elongation at	DIN 53504
		break
S xxx	MPa	Tensile strength	DIN 53504
		at xxx %
		elongation
H	Shore A/D	Hardness	DIN 53505
E	%	Rebound	DIN 53512
		resilience
Abrasion	cmm	Abrasion	DIN 53516
Compression set	%	Compression set	DIN 53517
			Sample II
Hot-air aging		Aging in hot air
delta F, delta D,	%, or Shore	Change in tensile	DIN 53508
delta H	A/D	strength,
		elongation at
		break, hardness
Distilled water		Immersion in
		distilled water
delta F, delta D,	%, or Shore D	Change in tensile,	DIN 53521
delta H, delta G		strength,
		elongation at
		break, hardness
		weight

G. Testing of the Mixtures

Example 1



	Parts

Example 1
Therban C 3467		100
Sartomer SR 633		60
Rhenofit TRIM/S		57
Naugard 445		2
Poly-Dispersion T (VC) D-40 P		6
Ethanox 703		1
Properties of the mixtures
ML-1 + 4/100° C.	(Mooney units)	24
		120/140° C.
MS-T5/120° C.	(min)	>45/>45
MDR Rheometer 170° C./
operating time 45 min
MINIMUM	(S'dNm)	0.3
MAXIMUM		160.4
MAX − MIN		160.1
T 10	(min)	3.5
T 50		6.8
T 80		11.6
T 90		15.2
Vulcanization 170° C. (min)		17
F	(MPa)	20.3
D	(%)	110
S 20	(MPa)	12.8
S 50	(MPa)	15.9
S 100	(MPa)	20.5
H 23° C.	(Sh. A)	97
H 23° C.	(Sh. D)	55
Vulcanization 170° C. (min)		23
Abrasion DIN 53516 (cmm)		63
Example 2
Therban C 3467		100
Zinkoxyd aktiv		2
Scorchguard O		2
Vulkasil S		20
Vinylsilane (1)		3
Naugard 445		2
Vulkanox ZMB-2		0.5
Tronox R-UF		3
Rhenofit TRIM/S		57
Sartomer SR 633 (3)		60
Ethanox 703		1
Poly-Dispersion T (VC) D-40 P		6
Properties of the mixture
ML-1 + 4/100 C.	(Mooney units)	37
MS-T5/135 C.	(min)	43.2
MDR Rheometer 152° C./
operating time 180 min.
MINIMUM	(S'dNm)	0.9
MAXIMUM		195.7
MAX − MIN		194.9
T 10	(min)	8.7
T 50		11.4
T 80		14.4
T 90		16.2
Vulcanization 90 min 152° C.
F	(MPa)	20.8
D	(%)	46
S 20	(MPa)	17.3
S 50	(MPa)	21.3
S 100	(MPa)	—
H 23° C.	(Sh. A)	99
H 23° C.	(Sh. D)	69
Hot-air aging 21 d 100° C.
Δ F	(%)	+22
ΔD	(%)	−20
Δ U	(Sh. D)	+3

Distilled water 90° C.
Δ F	(%)	7 d	+1
		14 d	+1
Δ D	(%)	7 d	+22
		14 d	+17
Δ H	(Sh. A)	7 d	−1
		14 d	−1
Δ U	(Sh. D)	7 d	−7
		14 d	−9
Δ G	(%)	7 d	+2.5
		14 d	+1.7

Vulcanization 180 min. 152° C.
Abrasion DIN 53516 (cmm)	129

Although the invention has been described in detail in the foregoing for the purpose of illustration, it is to be understood that such detail is solely for that purpose and that variations can be made therein by those skilled in the art without departing from the spirit and scope of the invention except as it may be limited by the claims. [0075]

Claims

What is claimed is:

1. A rubber mixture comprising:

a) at least one nitrile rubber;

b) at least one metal salt of an acrylate;

c) at least one liquid acrylate, optionally applied to a carrier, and

d) optionally other additives and/or fillers.

2. A rubber mixture according to claim 1, wherein said at least one nitrile rubber is selected from the group consisting of NBR, partially hydrogenated NBR and completely hydrogenated NBR or mixtures of two or more of these.

3. A rubber mixture according to claim 1, wherein said at least one metal salt of an acrylate is a zinc diacrylate or a zinc dimethylacrylate or a mixture.

4. A rubber mixture according to claim 1, wherein the liquid acrylate is butanediol dimethacrylate or trimethylolpropane trimethacrylate or a mixture.

5. A rubber mixture according to claim 1, wherein said rubber mixture also contains a siliceous filler, carbon black, zinc oxide, magnesium oxide or a mixture of two or more of these components.

A rubber mixture according to claim 1, wherein said rubber mixture contains vulcanization retarders and/or vulcanization accelerators.

A cross-linkable rubber mixture comprising a rubber mixture, wherein said rubber mixture comprises:

a) at least one nitrile rubber;

b) at least one metal salt of an acrylate;

c) at least one liquid acrylate, optionally applied to a support, and

d) optionally other additives and/or fillers.

8. A crosslinkable rubber mixture according to claim 7 wherein said at least one nitrile rubber is selected from the group consisting of NBR, partially hydrogenated NBR and completely hydrogenated NBR or mixtures of two or more of these.

9. A crosslinkable rubber mixture according to claim 7, wherein said at least one metal salt of an acrylate is a zinc diacrylate or a zinc dimethylacrylate or a mixture.

10. A crosslinkable rubber mixture according to claim 7, wherein the liquid acrylate is butanediol dimethacrylate or trimethylolpropane trimethacrylate or a mixture.

11. A crosslinkable rubber mixture according to claim 7, wherein said rubber mixture also contains a siliceous filler, carbon black, zinc oxide, magnesium oxide or a mixture of two or more of these components.

12. A crosslinkable rubber mixture according to claim 7, wherein said rubber mixture contains vulcanization retarders and/or vulcanization accelerators.

13. A process for the preparation of a rubber mixture comprising the step of mixing in a mixing unit:

a) at least one nitrile rubber;

b) at least one metal salt of an acrylate;

c) at least one liquid acrylate,, optionally applied to a carriers and

d) optionally other additives and/or fillers.

14. A process according to claim 13, wherein said mixture is crosslinked.

15. A process according to claim 14, wherein said mixture is crosslinked with a peroxide.

16. A molded article comprising a rubber mixture comprising

a) at least one nitrile rubber;

b) at least one metal salt of an acrylate;

c) at least one liquid acrylate, optionally applied to a carrier, and

d) optionally other additives and/or fillers.

17. A coating for a roller comprising a rubber mixture comprising:

a) at least one nitrile rubber;

b) at least one metal salt of an acrylate;

c) at least one liquid, acrylate, optionally applied to a support and

d) optionally other additives and/or fillers.