|Publication number||USRE30699 E|
|Application number||US 06/026,381|
|Publication date||Aug 4, 1981|
|Filing date||Apr 2, 1979|
|Priority date||Apr 2, 1979|
|Publication number||026381, 06026381, US RE30699 E, US RE30699E, US-E-RE30699, USRE30699 E, USRE30699E|
|Original Assignee||J. M. Huber Corporation|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (14), Non-Patent Citations (1), Referenced by (5), Classifications (5)|
|External Links: USPTO, USPTO Assignment, Espacenet|
This invention relates to polyurethane polymer compositions containing finely divided amino organosilane modified kaolin clay fillers.
The present application is a continuation-in-part of applicant's copending application Ser. No. 269,695, filed Apr. 1, 1963, now Patent No. 3,290,165, entitled, "Surface Modified Pigments," which in turn is a continuation-in-part of applicant's application Ser. No. 189,321, filed Apr. 23, 1962, entitled, "Surface Modified Pigments," now abandoned.
Polyurethane polymer compositions can be formed from a variety of polymers, l.e., thermosetting gums, thermoplastic polymers and liquid or casting polymers. The preparations for various classes and grades of polyurethanes are well known in the art and need not be detailed here; however, the general reaction by which they are formed is by a chain extension process rather than the usual polymerization reaction. In this process a relatively short chain polymer, either a polyester or a polyether, is reacted with an organic diisocyanate to form long chain urethane polymer. The process variations and polymerization variations caused thereby result in a multitude of compositions all broadly falling in one of the three classes mentioned.
The polyurethanes have several outstanding properties which make them desirable products, chief among them is abrasion resistance, good low temperature characteristics, good resistance to heat deterioration, ozone cracking, weathering, and oil or solvent swelling.
Thermosetting gum vulcanizates have a variety of uses in conveyor belts, roll covers, sandblast-hose tubes and other applications where good abrasion resistance is needed.
Thermoplastic resins can be processed on standard extrusion, injection molding, and transfer molding equipment. These resins are useful in small parts such as mallet heads, sprocket gears, adhesive coatings and unsupported sheetings such as fuel tanks, tarpaulins and chute liners.
Liquid polyurethane valcanizates exhibit good abrasion resistance, non-marking and a wide range of hardnesses. These products have use in large rolls for the steel industry, fork lift truck wheels, ladies toplifts, ball-joint seals, automotive seals, potting compounds, conveyor belts, V-belts, and tank linings.
Despite the fact that the polyurethanes have outstanding properties and are suitable for a large variety of uses, industry is constantly attempting to improve them by various means. Properties which are desirable to improve are modulus, tear resistance, hardness and abrasion resistance. In many cases reinforcing fillers have been tried but on the whole, while some improvements resulted, the degradation of other properties resulted and a completely satisfactory filler has not been found.
It is an object of this invention to provide solid polyprethane vulcanizates and thermoplastic resin compositions containing reinforcing fillers of modified kaolin clays.
Other objects and advantages will be apparent from the following specification.
I have discovered that kaolin clay modified with saturated amino organosilanes are reinforcing fillers for polyurethane polymers and impart improved properties to them. Particularly, modulus and tear resistance are improved with little, if any, degradation of other important properties.
The kaoline clays which are suitable as substrates for the modifier are refined clays of the rubber and paper grades.
The modified kaolin clays can be prepared by dissolving the desired amount of amino organosilane in a suitable solvent, adding the pigment and heating until the reaction is complete. The amount of modifier added depends upon the specific modifier used and the intended polymer to be reinforced. Generally from 1% to 3% by weight of the modifier is sufficient for most purposes.
A particularly useful process for modifying the kaolin clay involves spray drying kaolin slurries having one or more of the amino organosilanes dispersed therein. The spray drying process effects a uniform distribution of the modifier on the kaolin. Another satisfactory method of modifying the kaolin involves dissolving the desired amount of amino organosilane in a suitable solvent, adding the kaolin and heating until the reaction is complete.
The compounds used to modify the kaolin clays can be depicted by the formula: ##STR1## wherein R1 is hydrogen, alkyl, aryl, cycloalkyl, or alkylaryl; R2 is hydrogen, alkyl, aryl, cycloalkyl, or alkylaryl; R3 is hydrogen, lower alkyl, aryl, lower alkylaryl, or lower arylalkyl; R4 is hydrogen, lower alkyl, aryl, lower alkylaryl, or lower arylalkyl; R5 is hydrogen, lower alkyl, aryl, lower alkylaryl, or lower arylalkyl; and X is alkylene, alkylene containing secondary amino nitrogen, alkylene containing tertiary amino nitrogen, arylene, arylene containing secondary amino nitrogen, arylene containing tertiary amino nitrogen, alkylarylene, alkylarylene containing secondary amino nitrogen, alkylarylene containing tertiary amino nitrogen, arylalkylene, arylalkylene containing secondary amino nitrogen, arylalkylene containing tertiary amino nitrogen, cycloalkylene, cycloalkylene containing secondary amino nitrogen and cycloalkylene containing tertiary amino nitrogen. Some of these amino organosilanes are disclosed along with methods for their preparation in U.S. Patents Nos. 2,832,754, 2,930,809, 3,007,957, and 3,020,302. Commercially available amino organo silanes useful in the practice of this invention include "A-1100," a gamma-aminopropyltriethoxy silane (GAPTS), and "Y-2967," an amino organosilane which is a modified gamma-aminopropyltriethoxy silane, sold by Union Carbide Corporation, New York, N.Y., "Z-6020," a diamino functional silane, sold by Dow Corning Corporation, Midland, Michigan.
Representative commercially available polyurethane polymers suitable for use in this invention are "Vibrathane 5003," a thermosetting gum which is cross-linked, produced by Naugatuck Chemical Division of U.S. Rubber Company; "Elastothane 455," a thermosetting gum which is cross-linked, produced by Thiokol; "Genthane S," a cross-linked thermosetting gum produced by General Chemical; "Estane," a thermoplastic resin produced by B. F. Goodrich Chemical; "Texin," a thermoplastic resin produced by Mobay; "Multrathane," a liquid polymer produced by Mobay; "Cyanoprene 4590," a liquid polymer produced by American Cyanamid; "Adiprene L," produced by Du Pont; "Vibrathane 6000," produced by Naugatuck; and "Neothane," produced by Goodyear.
In the following formulations the gums were mill-mixed or Banbury-mixed and the thermoplastic resins were mill-mixed and injection molded.
The following formulations illustrate this invention.
______________________________________ Parts______________________________________Vibrathane 5003 100Stearic acid 0.25Dicup 40C (polymerizing agent) 5Filler (modified clay) 60______________________________________
The compounds were mixed on a 6 inch by 12 inch laboratory mill and cured for 30 minutes at 307° F., except for the NBS abrasion test where the cure was for 60 minutes at 307° F.
The data tabulated in Table I indicates the results when 1%, 2% and 3% by weight of GAPTS modified kaolin clay and 1% by weight Silicone Z-6020 modified kaolin clay is the filler.
TABLE I__________________________________________________________________________ 1% 2% 3% 1% GAPTS GAPTS GAPTS Z-6020 Control Kaolin on Kaolin on Kaolin on Kaolin on Kaolin__________________________________________________________________________Parts Filler/100 parts Polymer None 60 60 60 60 60Tensile, p.s.i. 3,500 (1) 3,920 3,600 3,840 3,270Stress 300%, p.s.i. 1,040 (1) 2,600 3,390 -- 2,520Elongation, percent 440 (1) 470 350 265 365Shore A Hardness 58 -- 74 74 74 73NBS Abrasion, percent of Standard 100 -- 89 134 157 193Minutes Cured at 305° F. 30 30 30 30 30 60__________________________________________________________________________ 1 No cure.
______________________________________ Parts______________________________________ Texin 480A 100 Modified clay 20______________________________________
The resin was molded at 390°-410° F. and post cured at 110° C. for 24 hrs. The results are tabulated in Table II.
TABLE II______________________________________ 1% Con- Kao- GAPTS trol lin on Kaolin______________________________________Parts Filler/100 parts Polymer None 20 20Stress 300%, p.s.i. 1,720 2,170 2,430Tensile, p.s.i. 5,700 2,540 2,620Elongation, percent 640 510 400Shore A Hardness 75 78 78NBS Abrasion, percent of Standard 100 77 92.5______________________________________
______________________________________ Parts______________________________________ Texin 480A 100 Modified clay 20______________________________________
The resin was molded at 390°-410° F. and was not post cured. The results are shown in Table III.
TABLE III______________________________________ 0.25% 0.5% 1% GAPTS GAPTS GAPTS Con- Kao- on on on trol lin Kaolin Kaolin Kaolin______________________________________Parts Filler/100 0 20 20 20 20parts PolymerStress 300%, p.s.i. 1,090 1,680 1,725 1,735 1,720Tensile, p.s.i. 4,380 4,470 3,340 4,250 4,400Elongation, 610 640 560 655 595percentShore A Hardness 85 88 88 88 88______________________________________
______________________________________ Parts______________________________________Estane 5701 100Barium stearate 3Modified clay 25 or 50______________________________________
The resin was molded 5' at 350° F. held in the mold under pressure until the temperature dropped below 200° F. The results are tabulated in Table IV.
TABLE IV______________________________________ Con- Kaolin plus trol Kaolin 1% Z 6020______________________________________Parts Filler/100 parts Polymer 0 25 50 25 50300% Modulus, p.s.i. 1,220 1,580 1,640 2,840 3,300ASTM Test "Die" C, lbs./in 410 500 300 560 580NBS Abrasion Index, percent 492 521 720 1,285 16.72NBS Abrasion Shore A 82 90 92 90 92______________________________________
______________________________________ Parts______________________________________Estane 5701 100Barium stearate 3Filler 25, 50 or 100______________________________________
The polymer batch was treated as in Example IV. The results are shown in Table V.
TABLE V__________________________________________________________________________ Kaolin Kaolin Kaolin Kaolin Kaolin Kaolin Kaolin Kaolin Con- Kao- plus 2% plus 2% plus 3% plus 1% Kao- plus 2% plus 1% Kao- plus plus 1% trol lin GAPTS GAPTS GAPTS Z 6020 lin GAPTS Z 6020 lin GAPTS Z__________________________________________________________________________ 6020Parts Filler/100 parts 0 25 25 25 25 25 50 50 50 100 100 100Polymer200% Modulus, p.s.i. 860 -- -- -- -- -- 1,700 3,500 3,740 -- -- --300% Modulus, p.s.i. 1,440 1,780 2,940 3,260 3,040 3,000 -- -- -- -- -- --Shore A Hardness 88 93 91 92 91 91 94 94 95 97 97 97NBS Abrasion, Index 460 641 827 703 641 746 624 936 568 334 553 575__________________________________________________________________________
______________________________________ Parts______________________________________Estane 5701 100Barium Stearate 3Pigment 25 or 50______________________________________
The recipe was treated the same as in Example IV. The results are shown in Table VI.
TABLE VI______________________________________ Kaolin Kaolin plus plus Con- Kao- 2% 1% trol lin GAPTS Z-6020______________________________________Parts Filler/100 None 25 50 25 50 25 50parts Polymer300% Modulus, 1,220 1,580 1,640 2,880 3,600 2,840 3,300p.s.i.ASTM Tear "Die 410 500 500 550 480 560 580C," lbs./inNBS Abrasion, 492 521 720 1,015 1,411 1,285 1,672Index percentNBS Abrasion, 82 90 92 90 91 90 92Shore A Hardness______________________________________
______________________________________ Parts______________________________________Estane 5701 100Barium Stearate 3Filler 10, 20, 60 or 100______________________________________
The recipe was treated as in Example IV. The results are shown in Table VII.
TABLE VII__________________________________________________________________________ Con- Kaolin Plus Kao- Kaolin Plus Kao- -trol 1% Z-6020 lin 1% Z-6020 lin__________________________________________________________________________Parts Filler/100 parts Polymer 0 10 20 20 60 100 100300% Modulus, p.s.i. 1,280 2,040 2,740 1,640 3,420 -- 2,040ASTM Tear "Die C," lbs./in 420 500 600 530 540 406 510NBS Abrasion, Index percent 570 867 1,095 957 1,722 1,465 717NBS Abrasion, Shore A 84 85 89 89 94 95 95__________________________________________________________________________
______________________________________ Parts______________________________________Adiprene L-100 100Methylene-bis-orthochloraniline 11Pigment 20______________________________________
The mixture was cured for 180 minutes at 212° F. The results are shown in Table VIII.
TABLE VIII______________________________________ Kaolin Plus 1% Control Kaolin Z-6020______________________________________Parts Filler/100 parts Polymer 0 20 20300% Modulus, p.s.i. 1,530 -- 1,940Tensile, p.s.i. 2,570 1,310 2,710 -Elongation, Percent 495 285 480 5Shore A Hardness 87 88 90ASTM Tear "Die C," lbs./in 450 408 505NBS Abrasion, Index Percent 224 126 194______________________________________
The examples and data indicate that when the modified kaolin clays useful in this invention are used as fillers in thermosetting gum polyurethanes increases in modulus, hardness and abrasion resistance occur. The remaining properties of the polymer remain within acceptable levels. When these fillers are used to reinforce thermoplastic resins, increases in modulus, tear resistance, and abrasion resistance occur while the remaining polymer properties remain within acceptable levels. When these modified kaolin clay fillers are used to reinforce liquid polymers, increases in modulus, tensile strength, hardness, and tear resistance occur while the remaining properties of the polyurethane remain within acceptable levels. In all the polymers tested the general level of performance of the modified kaolins was superior to the unmodified kaolins.
The foregoing is illustrative only and additional modifications may be made without departing from the substance of the invention as defined in the appended claims.
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US2742378 *||Aug 2, 1952||Apr 17, 1956||Gen Tire & Rubber Co||Fillers having vinyl siloxane groups bonded to the surface thereof and copolymers thereof with ethylenically unsaturated polymerizable monomers|
|US2832754 *||Jan 21, 1955||Apr 29, 1958||Union Carbide Corp||Alkoxysilylpropylamines|
|US3015569 *||Nov 26, 1958||Jan 2, 1962||Interchem Corp||Treatment of pigments|
|US3029209 *||Aug 12, 1959||Apr 10, 1962||Minerals & Chem Philipp Corp||Polyurethane foams filled with organophilic kaolin clay and method for making same|
|US3150109 *||Aug 1, 1961||Sep 22, 1964||Minerals & Chem Philipp Corp||Filled polyurethane foams and method for making same|
|US3158519 *||Jun 30, 1960||Nov 24, 1964||Owens Corning Fiberglass Corp||Continuous process for producing molding compounds|
|US3168389 *||Dec 28, 1960||Feb 2, 1965||Pittsburgh Plate Glass Co||Silane forming size and glass fiber strands threated therewith for resin reinforcement|
|US3227675 *||May 1, 1963||Jan 4, 1966||Huber Corp J M||Silane-treated clay reinforced resin compositions|
|US3328339 *||Aug 28, 1963||Jun 27, 1967||Monsanto Co||Reinforced plastics containing base treated, calcined particulate fillers and organosilane coupling agents|
|US3350345 *||Dec 21, 1962||Oct 31, 1967||Exxon Research Engineering Co||Bonded rubber-siliceous materials and process of producing same|
|US3364050 *||Jun 22, 1964||Jan 16, 1968||Tetra Pak Ab||Method of treating a cut edge and its adjacent portion in a porous sheet material|
|US3388144 *||Jul 15, 1965||Jun 11, 1968||Dow Corning||Polymercaptoorgano and polyhydroxyorgano silanes and siloxanes|
|US3392182 *||Feb 12, 1964||Jul 9, 1968||Goldschmidt Ag Th||Novel organosilicon compounds and process for their preparation|
|US3419517 *||Jun 24, 1966||Dec 31, 1968||Monsanto Co||Reinforced polyamides and process of preparation thereof|
|1||*||Jellinek et al., Silane Finishes for Fibrous Glass, 1957, Presentation before the Society of Plastic Industries, Union Carbide Corp.|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US5693696 *||Jan 16, 1996||Dec 2, 1997||Mcp Industries, Inc.||Modified polyurethane including filler and method of manufacture thereof|
|US6420456 *||May 21, 1998||Jul 16, 2002||Bayer Inc.||Process for hydrophobicizing particles, and their use as fillers in polymer masterbatches|
|US6808808||Jan 14, 2003||Oct 26, 2004||Freeman Gary M||Coating composition containing surface treated clay mixture, the surface treated clay mixture used therefor, and methods of their use|
|US9260613||Jul 14, 2010||Feb 16, 2016||Imerys Minerals Limited||Clear coating compositions comprising particulate inorganic mineral|
|US20040138339 *||Jan 14, 2003||Jul 15, 2004||Freeman Gary M.||Coating composition containing surface treated clay mixture, the surface treated clay mixture used therefor, and methods of their use|
|U.S. Classification||524/262, 524/445|