AU2002254058A1 - Solid surface sheet materials containing synthetic MICA - Google Patents
Solid surface sheet materials containing synthetic MICAInfo
- Publication number
- AU2002254058A1 AU2002254058A1 AU2002254058A AU2002254058A AU2002254058A1 AU 2002254058 A1 AU2002254058 A1 AU 2002254058A1 AU 2002254058 A AU2002254058 A AU 2002254058A AU 2002254058 A AU2002254058 A AU 2002254058A AU 2002254058 A1 AU2002254058 A1 AU 2002254058A1
- Authority
- AU
- Australia
- Prior art keywords
- synthetic
- solid surface
- weight
- mica
- surface sheet
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Description
SOLID SURFACE SHEET MATERIALS CONTAINING SYNTHETIC
MICA
BACKGROUND OF THE INVENTION
This invention relates to solid surface sheet material having improved physical and aesthetic properties. More particularly, the invention relates to providing solid surface sheet material comprised of highly filled acrylic resin containing a controlled amount of a selected synthetic mica.
US patent 4,480,060 discloses composite pressed boards containing at least 50% mica mixed with an organic resin such as epoxy, polyi ide, melamine or phenolic resin. The boards are useful in electrical applications and have an opaque, lusterless appearance.
International Publication W098/38244, published 3 September 1998 discloses products said to contain oriented pearlescent flakes of mica.
The inclusion of natural occurring mica with resins and fillers in preparing composite materials is disclosed in general terms in a number of publications .
SUMMARY OF THE INVENTION
The subject invention provides a solid surface sheet material having excellent physical properties and a lustrous, sparkling appearance which comprises an acrylic resin, from about 20 to about 75% by weight of a filler, based on the total weight of the material, and from about 0.1 to about 5% by weight of a selected synthetic mica based on total weight of the material .
DETAILED DESCRIPTION OF THE INVENTION
The resins useful in the present invention are not specially limited as long as they can be formed into a solid surface material by curing. Examples of useful acrylic resins include various kinds of conventional acrylic group monomers, acrylic group partial polymers, vinyl monomers for copolymerization other than acrylic group monomers, or oligomers . As the arylic group monomer, (meth) acrylic ester is preferable .
Δ particularly good and especially preferred polymer which meets all of the above properties is poly (methyl methacrylate). In a castable composition, it is often introduced as a sirup of polymer in methyl methacrylate monomer. Methods of preparing such a sirup are described in the prior art. Another method of preparing a sirup is to simply dissolve polymer in the monomer. This latter method is quite useful for adjusting viscosity of the castable composition since molecular weight of polymer as well as concentration can be varied in such a way as to control the rheology.
The amount of fluid polymerizable constituent required in the castable composition is at least 30% by volume. Methyl methacrylate monomer is preferred as a major constituent.
Other monomers useful as fluid polymerizable constituents are alkyl acrylates and methacrylates in which the alkyl groups can be from 1 - 18 carbon atoms, but preferably 1-4 carbon atoms. Suitable acrylic monomers are methyl acrylate; ethyl acrylate and methacrylate; n-propyl and i-propyl acrylates and methacrylates; n-butyl, 2-butyl, i-butyl and t-butyl acrylates and methacrylates; 2-ethylhexyl acrylate and methacrylate; cyclohexyl acrylate and methacrylate; o ega-hydroxyalkyl acrylates and methacrylates; N,N-
dialkylaminoalkyl acrylates and methacrylates; N-[t- butyl] aminoethyl acrylate and methacrylate.
Other unsaturated monomers include such compounds as bis- [beta-chloroethyl] vinylphosphonate; styrene; vinyl acetate; acrylonitrile; methacrylonitrile; acrylic and methacrylic acids; 2-vinyl- and 4- vinylpyridines; maleic acid, maleic anhydride and esters of maleic acid; acryl amide and methacrylamide; itaconic acid, itaconic anhydride and esters of itaconic acid and multifunctional monomers for crosslinking purposes such as unsaturated polyesters; alkylene diacrylates and dimethacrylates; allyl acrylate and methacrylate; N-hydroxymethylacrylamide and N-hydroxymethylmethacrylamide; N, N ' -methylene diacrylamide and dimethacrylamide; glycidyl acrylate and methacrylate; diallyl phthalate; divinylbenzene; divinyltoluene; trimethylolpropane triacrylate and trimethacrylate; pentaerythritol tetraacrylate and tetramethacrylate; triallyl citrate and triallyl cyanurate.
The synthetic mica useful in providing the products of this invention are fluoro-phlogopites such as KMg 3 (AlSi 3 O 10)F 2- They are described in detail and a process for their preparation is disclosed in US patent 5,094,852 which is incorporated herein by reference. Other useful forms of synthetic include fluoro-tetrasilicicmica (KMg2.5Si4Oιo) F2, sodium-fluoro- tetrasilicicmica (NaMg2.5 Li (SiOι0) F2 , sodium- taeniolite (NaMg22Li (Si4Oιo) F2 , and fluoro-hectorite Naι/3Mg8/3Liι3(Si4Oιo) F2.
Fillers useful in the present invention include, for example, aluminum trihydrate, calcium carbonate, barium sulfate, Bayer hydrate, magnesium hydroxide, talc, wolastonite, as a list that is not exhaustive and not intended to limit the invention. Fillers can
be present in effective amounts from as low as about 20% by weight to about 75% by weight. Preferably, amounts from 30 to 67% by weight are used.
It is known to include in solid surface materials other additives such as pigments, dyes, flame retardant agents, parting agents, fluidizing agents, viscosity control agents, curing agents (chemical and thermal), antioxidants, toughening agents and the like as known to those of ordinary skill in the art. Solid surface materials of this invention can be prepared by cell cast, continuous casting or by reactive extrusion using a multi-feeder twin-screw extruder equipped with vacuum and a sheet die of proper dimensions. The sheets produced can be transferred either onto a double belt press or into an oven for curing. The preferred method is continuous casting. The production of filled poly (methyl methacrylate) compositions is well known in the art, see for instance US patents 3,847,865; 4,413,089; and 4,406,662, which are hereby incorporated by reference. Light pressure may be needed for maintaining sheet gauge or profile during curing. The resulting solid surface material is thermoformable . The invention can be further understood by reference to the following examples in which parts and percentages are by weight unless otherwise indicated.
EXAMPLES Example 1
Alumina trihydrate, approximately 60% by weight, was mixed with ingredients a. through f . as shown in Table 1 at a temperature of 27-29 deg C. After mixing for 1 minute, approximately 0.3 parts per hundred of water (based on the weight of the sirup) was added to the mixture. The mixture was then evacuated under vacuum (24-25in Hg) using a pump and a suitable
condensing vapor trap. At 3 minutes and 4 minutes into the evacuation, small amounts of calcium hydroxide and ethylene glycol dimercaptoacetate (GDMA) were added by syringe . After 5 minutes of total mixing and evacuation, the mixture was poured into a container of square design to form a layer of approximately " thickness and allowed to cure.
One control article (Control A) and four "synthetic mica containing" articles were made using the described procedure. In Control A, the pearlescent pigment was a 22% solids dispersion of natural mica (muscovite) in butylmethacrylate (BMA) . Articles 1-4 used a synthetic fluoro-phlogopite mica (SH-100) purchased from TOPY Industries (dry) with an adjustment in sirup to account for the residual BMA.
Table 1: Articles 1 Control A, Articles 2-5 Synthetic
Mica
(1) (2) (3) (4) (5)
Confrol A Synthetic Synthetic Synthetic Synthetic Article #1 Article #2 Article #3 Article #4 a. Alumina Trihydrate (ATH)* 59.9% 59.9% 60.0% 59.7% 60.3% b. Sirup (24% PMMA in 31.8% 34.2% 34.2% 34.2% 34.2% MMA) c. MMA Monomer 2.9% 2.9% 2.9% 2.9% 2.9% d. PMA 25 paste ( t- 0.9% 0.9% 0.9% 0.9% 0.9% butylperoxy maleic acid) e. Trimethylol propane 0.3% 0.3% 0.3% 0.3% 0.3% trimethacrylate (TRIM)
Dioctyl sodium 0.1% 0.1% 0.1% 0.1% 0.1% sulfosuccinate
Phosphated propylene glycol 0.1% 0.1% 0.1% 0.1% 0.1% methacrylate h. Ca(OH)2 Slurry (34% in 0.3% 0.3% 0.3% 0.3% 0.3% sirup)
Ethylene glycol dimercapto 0.1% 0.1% 0.1% 0.1% 0.1% acetate (GDMA)
J- Distilled Water 0.1% 0.1% 0.1% 0.1% 0.1% k. Yellow Pigment Dispersion # 0 0..44%% 0.4% 0.4% 0.4% 0.4% PC-9Y139 (0.1% in Sirup)
1. White Pigment Dispersion # 0.2% 0.2% 0.2% 0.2% 0.2% PC-11W1185 ** m. Muscovite Natural Pearl 3.0% - - - - Dispersion # PC-9Z319 ** n. Synthetic Pearl Flake - 0.6% 0.5% 0.8% 0.2%
#SH100 (Ultimica by TOPY)
Total: 100% 100% 100% 100%, 100%
* From Alcan, particle size 40 micons ** from Perm Color Corp.
Samples 1-4 were tested on a Series IX Automated Materials Testing System (Instron Corporation v4.06) for strength and flexibility. The results of the testing are tabulated in Table 2. It will be noted that the structures containing synthetic mica support greater loads (lbs) and stresses (psi) prior to yield and increased force (energy) to break. In addition to increased strength, it was also noted that samples 2-4
displayed greater visual pearlescence than the control despite the lower levels of mica pigment (solids basis) . Samples 2-5 were also found to be free of objectionable reddish- brown contamination present in the control sample and in the mica supplied by EM Industries (Ruby muscovite) .
Table 2: Flexural 3-Pont Bend Analysis of Samples 1-5:
Stress Force to Strain @ Load at
@ Yield Modulus to Break Break Yield
Specimen (psi) (psi) (lbs-in) (%) (lbs)
Sample 1 (Control A) 8502 1276541 1.8 0.72 45.98
Sample 2 (Synthetic Article #1) 9634 1239000 2.6 0.88 51.02 Sample 3 (Synthetic Article #2) 10240 1257000 2.9 0.93 54.27
Sample 4 (Synthetic Article #3) 9846 1286000 2.7 0.87 52.21
Sample 5 (Synthetic Article #4) 9378 1223000 2.4 0.85 49.23
Average of Triplicate Readings shown
Example 2
Articles #5, #6, and Control B were prepared using equivalent methods to that as described above for Example 1, except that large scale, commercial continuous casting equipment and techniques were employed as described in U.S. patents Nos. 3,570,056 and 3,600,490 which are hereby incorporated by reference. Pigment flows were adjusted to achieve near equal color, pearlescence and appearance.
Table 3: Process Conditions and Formulations for Control B, Articles 5 and 6
(6) (7) (8) Control B Synthetic Synthetic Article #5 Article #6 a. Alumina Trihydrate (ATH)* 60.0% 60.0% 60.0% b. Sirup (24% PMMA in MMA) 32.2% 34.1% 34.3% c. MMA Monomer 2.6% 2.2% 2.2% d. PMA 25 paste ( t-butylperoxy 0.8% 0.8% 0.8% maleic acid) e. Trimethylol propane 0.3% 0.3% 0.3% trimethacrylate (TRIM) f. Dioctyl sodium sulfosuccinate 0.2% 0.2% 0.2% g. Phosphated propylene glycol 0.1% 0.1% 0.1% methacrylate h. Ca(OH)2 Slurry (34% in sirup) 0.3% 0.3% 0.3% i. Ethylene glycol dimercapto acetate 0.1% 0.1% 0.1% (GDMA) j. Distilled Water 0.1% 0.1% 0.1% k. Yellow Pigment Dispersion # PC- 0.3% 0.4% 0.5% 9Y139 (0.2% in Sirup) **
1. White Pigment Dispersion # PC- 0.2% 0.2% 0.2% l lW1185 (90% in Sirup)** m. Muscovite Natural Pearl 3.0% - -
Dispersion # PC-9Z319 (22% in BMA) ** n. Synthetic Pearl Flake Dispersion # - 1.0% 1.0% PC-9Z412 (22% in BMA) **
Total: 100% 100% 100% * particle size 40 mm, from Alcan ** from Perm Color Corp.
Samples 6-8 were tested on a Series IX Automated Materials Testing System (Instron Corporation v4.06) for strength and flexibility. The results of the testing are tabulated in Table 4. It will be noted that the structures containing synthetic mica support greater loads (lbs) and stresses (psi) prior to yield and increased force (energy) to break. Stain resistance (ANSI Z124 for Stain, Chemical, and
Cigarette resistance) was improved in addition to
Gardner Impact Performance and the ability of this product to resist discoloration at high temperatures using methods such as NEMA-LD-3.3.6. Improved weatherability was demonstrated in ASTM G24 using an Atlas Ci3000 weatherometer for products of this invention over those incorporating natural mica, e.g. reduced discoloration (dECIE94) at equivalent exposure conditions. In addition to increased strength, stain, temperature resistance, impact, and accelerated weatherability, extensive inspection of production found improved cleanliness of the synthetic formulation (reduced objectionable reddish- brown contamination) present in the control samples and in the natural mica formulations supplied by EM Industries (Ruby muscovite) . Improved production yields are achieved.
Table 4 : Analysis of Samples 6-
Sample 6 Sample 7 Sample 8
Natural Synthetic Synthetic
Appearance Color Absolute L' 89.91 90.36 a' -0.10 -0.23 b' 5.73 5.62
Flexural Properties
Instron/Sintech Stress (MPa) 58.8 73.5 74.8 (Room Temp) Modulus (MPa) 8759 9244 8305
Force to Break (J) 215 346 414
Strain at Break (%) 0.7360 0.9340 1.0590
Physical Properties
Hardness Rockwell 89.0 90.3 87.7 25 Item Stain Sanded finish 83 73 77 Gardner Impact (J) 7-9 9-11
L', a' and b' values were obtained employing a Gretag Macbeth® Coloreye® XTH Spectrophotometer using CIELAB: D65-10 RAV-SCI Geometry.
Claims (8)
1. A highly filled acrylic solid surface sheet material comprising an acrylic resin, from 20 to 75 % by weight of a filler and from 0.1 to 30% by weight of a synthetic mica.
2. The material of claim 1 wherein the acrylic resin is polymethylmethacrylate .
3. The material of claim 1 wherein the synthetic mica is present in an amount from 0.1 to 5% by weight.
4. The material of claim 3 wherein said filler is present in an amount from 30 to 67% by weight.
5. The material of claim 4 wherein the filler is aluminum trihydrate.
6. The material of claim 5 wherein the synthetic mica is a synthetic fluoro-phlogopite .
7. The material of claim 6 wherein the fluoro- phlogopite is KMg3 (AlSi3Oι0) F2.
8. A highly filled acrylic solid surface sheet material comprising polymethylmethacrylate resin, from 30 to 67% by weight aluminum trihydrate and from 0.1 to 5% by weight of synthetic fluoro-phlogopite mica.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/794,812 | 2001-02-27 | ||
US09/794,812 US6515060B2 (en) | 2001-02-27 | 2001-02-27 | Solid surface sheet materials containing synthetic mica |
PCT/US2002/006072 WO2002068514A2 (en) | 2001-02-27 | 2002-02-27 | Solid surface sheet materials containing synthetic mica |
Publications (2)
Publication Number | Publication Date |
---|---|
AU2002254058A1 true AU2002254058A1 (en) | 2003-03-06 |
AU2002254058B2 AU2002254058B2 (en) | 2006-06-08 |
Family
ID=25163752
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU2002254058A Ceased AU2002254058B2 (en) | 2001-02-27 | 2002-02-27 | Solid surface sheet materials containing synthetic MICA |
Country Status (10)
Country | Link |
---|---|
US (1) | US6515060B2 (en) |
EP (1) | EP1368417A2 (en) |
JP (1) | JP4037758B2 (en) |
KR (1) | KR20030080037A (en) |
AU (1) | AU2002254058B2 (en) |
BR (1) | BR0207622A (en) |
CA (1) | CA2432951A1 (en) |
MX (1) | MXPA03007652A (en) |
NZ (1) | NZ526889A (en) |
WO (1) | WO2002068514A2 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20080264303A1 (en) | 2007-04-24 | 2008-10-30 | The Diller Corporation | Solid surface product containing oriented reflective particles and method of making same |
US20080274343A1 (en) * | 2007-05-01 | 2008-11-06 | The Diller Corporation | Thick solid surface laminate product and method of making same |
US8114924B2 (en) * | 2008-02-21 | 2012-02-14 | E. I. Du Pont De Nemours And Company | Pearlescent slurry concentrate for acrylic sheet |
WO2023133021A1 (en) * | 2022-01-10 | 2023-07-13 | Dupont Safety & Construction | Method for producing electrical circuitry on filled organic polymers |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3600490A (en) | 1969-07-23 | 1971-08-17 | Du Pont | Process of forming a ripple-free structure from a polymerizable material that shrinks upon polymerization |
US3570056A (en) | 1969-07-24 | 1971-03-16 | Du Pont | Multi-colored plastic building product and its manufacture |
US3847865A (en) | 1972-04-28 | 1974-11-12 | Du Pont | Use of alumina trihydrate in a polymethyl methacrylate article |
US4406662A (en) * | 1982-03-05 | 1983-09-27 | E. I. Du Pont De Nemours And Company | Heat transfer printing on a filled polymethyl methacrylate article |
US4413089A (en) | 1982-03-10 | 1983-11-01 | E. I. Du Pont De Nemours And Company | Use of iron oxide pigments in a polymethyl methacrylate article |
US4480060A (en) | 1983-01-27 | 1984-10-30 | Corning Glass Works | Mica-resin composite material |
DE3865763D1 (en) | 1987-01-26 | 1991-11-28 | Shiseido Co Ltd | ARTIFICIAL Mica POWDER, METHOD FOR THE PRODUCTION AND COSMETICS THAT CONTAIN THIS POWDER. |
JPH0720652B2 (en) * | 1988-03-24 | 1995-03-08 | 株式会社クラレ | Acrylic resin extruded plate having pearl luster and method for producing the same |
JPH0693161A (en) * | 1992-06-18 | 1994-04-05 | Sakamoto Yakuhin Kogyo Kk | Marble-grain injection molding material |
US5741355A (en) * | 1995-01-27 | 1998-04-21 | Topy Industries, Limited | Pearlescent pigment, and paint composition, cosmetic material, ink and plastics blended with the new pearlescent pigment |
CA2251893C (en) * | 1997-02-17 | 2007-05-01 | Doppel Co., Ltd. | Noctilucent or fluorescent artificial stone |
EP0963401A1 (en) | 1997-02-28 | 1999-12-15 | International Paper Company | Particle filled resinous product of improved appearance |
US5947804A (en) | 1998-04-27 | 1999-09-07 | Ryobi North America, Inc. | Adjustable eccentricity orbital tool |
-
2001
- 2001-02-27 US US09/794,812 patent/US6515060B2/en not_active Expired - Lifetime
-
2002
- 2002-02-27 NZ NZ526889A patent/NZ526889A/en unknown
- 2002-02-27 BR BR0207622-5A patent/BR0207622A/en not_active Application Discontinuation
- 2002-02-27 WO PCT/US2002/006072 patent/WO2002068514A2/en active IP Right Grant
- 2002-02-27 KR KR10-2003-7011192A patent/KR20030080037A/en not_active Application Discontinuation
- 2002-02-27 AU AU2002254058A patent/AU2002254058B2/en not_active Ceased
- 2002-02-27 MX MXPA03007652A patent/MXPA03007652A/en not_active Application Discontinuation
- 2002-02-27 CA CA002432951A patent/CA2432951A1/en not_active Abandoned
- 2002-02-27 JP JP2002568019A patent/JP4037758B2/en not_active Expired - Fee Related
- 2002-02-27 EP EP02723268A patent/EP1368417A2/en not_active Withdrawn
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