WO1997031973A1 - Composite material and production of the composite material, and composite-material-containing resin composition and production of the resin composition - Google Patents
Composite material and production of the composite material, and composite-material-containing resin composition and production of the resin composition Download PDFInfo
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- WO1997031973A1 WO1997031973A1 PCT/US1997/003061 US9703061W WO9731973A1 WO 1997031973 A1 WO1997031973 A1 WO 1997031973A1 US 9703061 W US9703061 W US 9703061W WO 9731973 A1 WO9731973 A1 WO 9731973A1
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K7/00—Use of ingredients characterised by shape
Definitions
- the present invention is concerned with both a composite material used for mixing with an organic polymer material to improve mechanical properties, gas barrier properties, heat resistance, or transparency of the organic polymer material, and production of the composite material.
- the present invention is concerned with both a composite material containing silicate layers between which an ionomer is introduced, and production of the composite material.
- the present invention is also concerned with a composite-material-containing resin composition containing both an organic polymer material compatible to the ionomer and produced composite material, and production of the resin composition.
- Clay mineral/polyamide resin compositions characterized by, if necessary, treating silicate layers that make up swelling clay minerals with an alkvlamine swelling agent, then impregnating and polymerizing the monomers, were developed (Japanese Kokai Patent Application Nos. Sho 58[1983]-3521 1 and Sho 58[1983]-35542) as composite materials in order to solve the problems.
- a production method for the composite material employed in the following processes i.e., a contact process in which layered silicate was brought into contact with a swelling agent to make a composite that was swollen by polyamide contained in the monomer; a mixing process in which the produced composite was mixed with polyamide monomer; and polymerization process in which the mixture was heated to the required temperature to carry out polymerization (Japanese Kokai Patent Application No. Sho 62[1987]-74957). Because the production process contained a polymerization process it was not necessarily easy to make composite materials, and it was difficult to apply it to other than the polyamide.
- the purpose of the present invention is to provide a composite material consisting of both layered silicate and an organic polymer material, having thermal stability, containing silicate layers between which the distance is increased or which are not parallel each other, and to provide a production method for a good composite material which is easy and requires neither a process in which layered silicate is brought into contact with an alkylamine swelling agent or in which polymerization is carried out when a composite material having improved dispersibility either to increase the distance between the silicate layers or to make the layers be unparallel each other is made.
- the purpose of the present invention is to provide both a composite-material-containing resin composition that contains the composite materials and a production method for the composition.
- the purpose of the present invention is to provide a composite material consisting of both an ethylene ionomer and layered silicate, and production of the composite material, and a composite-material-containing resin composition that contains the composite material, and production of the composition.
- a production method for a composite material is characterized by dispersing, mixing, drying, and crushing a polar organic polymer that is either soluble or dispersible in water, and fusible with silicate layers in a polar solvent, to introduce the above-mentioned polar organic polymer to a layered silicate of the above-mentioned silicate layer.
- a production method for a composite material also is characterized by using an ionomer as the above-mentioned polar organic polymer.
- a production method for a composite material also is characterized by dispersing, mixing, drying, and crushing 100 parts by weight potassium ionomer made of potassium in which ethylene methacrylate copolymer is either partially or entirely neutralized, with 0.5-300 parts by weight silicate layers in water, to introduce potassium ionomer to a layered silicate of the above-mentioned silicate layers.
- a composite material is characterized by dispersing, mixing, drying, and crushing 100 parts by weight sodium ionomer that is made of ethylene methacrylate copolymer which is either partially or entirely neutralized with sodium and that can be soluble or dispersible in water, with 0.5-300 parts by weight silicate layers in water to introduce sodium ionomer to a layered silicate of the above-mentioned silicate layers.
- a composite material also is characterized by containing both a polar organic polymer that is either soluble or dispersible in water and fusible, and that is introduced between the above-mentioned silicate layers.
- a composite material also is characterized by compounding composite materials made by a production method described in any of Claims 1-4, composite materials described in Claim 5, and an organic polymer material compatible to the above-mentioned polar organic polymer to disperse and pack 0.05 part by weight or more of the above-mentioned silicate layers in 100 parts by weight of a mixture of the above-mentioned polar organic polymer and the above-mentioned organic polymer material.
- a composite-material-containing resin composition is characterized by containing a melted and kneaded material comprising composite materials made by one of the production methods described in Claims 1-4, or composite materials described in Claim 5, and an organic polymer material compatible with the above-mentioned polar organic polymer, and by containing both the above-mentioned polar organic polymer and 0.05 part by weight or more of the above-mentioned silicate layers to 100 parts by weight of the above-mentioned organic polymer material.
- Figure 1 explains the presence of both the layered silicate ( 1 ) and the ionomer (2) in each composite material made in Application Examples 1-3 of the present invention.
- Figure 2 explains the presence of both the layered silicate (1) and the ionomer (2) in each composite material made in Comparative Examples 1-4 of the present invention.
- Figure 3 shows an optical microscopic photograph of a composite material made in Application Example 4 of the present invention.
- (A) is a photograph with a magnification of 15 times.
- (B) is a photograph with a magnification of 40 times.
- Figure 4 shows an optical microscopic photograph of a composite material made in Application Example 5 of the present invention.
- (A) is a photograph with a magnification of 15 times.
- (B) is a photograph with a magnification of 40 times.
- Figure 5 shows an optical microscopic photograph of a composite material made in Application Example 6 of the present invention.
- (A) is a photograph with a magnification of 15 times.
- (B) is a photograph with a magnification of 40 times.
- Figure 6 shows a transmission electromicrograph photograph of a composite material made in Application Example 6 of the present invention (magnification: about 70,000 times)
- Figure 7 shows an optical microscopic photograph of a composite material made in Comparative Example 5 of the present invention.
- A is a photograph with magnification of 15 times.
- B is a photograph with a magnification of 40 times.
- Figure 8 shows a transmission electromicrograph of a composite material made in Application Example 7 of the present invention (magnification: about 100 times).
- Figure 9 shows a transmission electromicrograph of a composite material made in Comparative Example 6 of the present invention (magnification: about 100 times).
- organic polymer material (A) Specific conditions include being soluble or dispersible in water and being fusible.
- organic polymer material (A) examples include ionomers made by partially or entirely neutralizing methacrylic acid in a random copolymer of ethylene and methacrylic acid with an alkali metal or alkaline-earth metal. Because potassium has good dispersibility in water, it is especially suitable. However, other metals typically used in making ionomers, including metals such as sodium or magnesium, which are either dispersible or soluble in water, can be used.
- a composite material containing an ionomer that is introduced between the silicate layers making up the layered silicate can be made by mixing an aqueous silicate dispersion, made by dispersing 0.5-300 parts by weight layered silicate in water with an aqueous polymer dispersion made by dispersing 100 parts by weight ionomer in water, drying, and crushing the mixture. It can be verified by both the peak position and intensity measured by wide-angled X-rays that the produced composite material contains ionomer introduced between the silicate layers.
- Organic polymer material (B) kneaded with a composite material must be compatible with organic polymer material (A), and must be able to be melted and kneaded. Compatibility means either complete compatibility or good affinity at the interface. If there is no compatibility, it is difficult to disperse silicate layers of layered silicate in a final material during the kneading process.
- organic polymer material (B) examples include random copolymers of ethylene and methacrylic acid; ionomers of random copolymer of ethylene and methacrylic acid partially or entirely neutralized particularly with metals such as sodium, magnesium or zinc; polyesters such as polybutylene terephthalate or polyethylene terephthalate; and polyamides such as nylon 6 or nylon 66.
- ethylene ionomer the problem of transparency of the ethylene ionomer being damaged, can be solved by adding an inorganic filler to the ethylene ionomer while at the same time improving the mechanical properties.
- Layered silicate should be dispersed and filled in amounts of 0.05 parts by weight or more in 100 parts by weight of a combination of organic polymer materials (A) and (B). When there is less than 0.05 part by weight, unsatisfactory effects result from the filling. When there are more than 300 parts by weight to 100 parts by weight of a combination of organic polymer materials (A) and (B), poor dispersion results.
- a silicate layer of layered silicate used for the present invention has a thickness of 7-15 A, and is formed with magnesium silicate or aluminum silicate.
- examples include smectite clay minerals such as montmorillonite, saponite, beidellite, nontronite, hectorite, or stevensite, vermiculite, halloysite, and mica. They can be either natural or synthetic. Swelling fluorine mica can be included in the examples. Smectite layered silicate is especially suitable.
- Any conventional method may be used for stirring, drying, and crushing, which are carried out in the production method for a composite material of the present invention.
- Any conventional method may be used for compounding a composite material with organic polymer material (B).
- a biaxial kneader rotation in the same direction or in the different direction
- a Yabusu kneader is suitable.
- Whether the distance between silicate layers is increased in a composite-material-containing resin composition or whether a composite material having improved dispersibility effective for making the layers unparallel to each other is formed or not is decided by visual observation of the transparency using an optical microscope and by observation using a transmission electron microscope if necessary.
- Powder montmorillonite (Kunipia® F made by Kunimine Kogyo K.K.) ( 1.0 g) was added to water ( 100 g); then, the mixture was stirred for about 3 hours to make an aqueous silicate dispersion.
- Aqueous poly(ethylene-methacrylic acid) potassium salt (MKD100 made by Du Pont-Mitsui Polychemicals Co., Ltd.) dispersion was diluted to disperse the poly(ethylene-methacrylic acid) potassium salt (1.0 g) in water (100 g), then stirred for about 1 hour to make an aqueous polymer dispersion.
- the produced aqueous polymer dispersion was slowly mixed with an aqueous silicate dispersion, then stirred for about 2 hours. Then, the mixture was completely dried in a pan on a hot plate at about 150°C to make a composite material consisting of layered silicate to polymer with combination ratio of 1 : 1. The produced composite material was crushed in a mortar.
- Synthetic smectite powder (Smecton® SA made by Kunimine Kogyo K.K.) (1.0 g) was added to water (100 g), then stirred for about 3 hours to make an aqueous silicate dispersion.
- Aqueous poly(ethylene-methacrylic acid) potassium salt (MKD100 made by Du Pont-Mitsui Polychemicals Co., Ltd.) dispersion was diluted to disperse the poly(ethylene-methacrylic acid) potassium salt ( 1.0 g) in water (100 g), then stirred for about 1 hour to make an aqueous polymer dispersion.
- the produced aqueous polymer dispersion was slowly mixed with the aqueous silicate dispersion: then, the mixture was stirred for about 2 hours. Then, the mixture was dried in a pan on a hot plate at 150°C to make a composite material of layered silicate and polymer with a combination ratio of 1 : 1. The produced composite material was crushed in a mortar.
- Montmorillonite powder (Kunipia® F made by Kunimine Kogyo K.K.) (1.0 g) was added to water (100 g); then, the mixture was stirred for about 3 hours to make an aqueous silicate dispersion.
- Aqueous poly(ethylene-methacrylic acid) sodium salt (Chemipearl® S-100 made by Mitsui Petrochemical Industries, Ltd.) dispersion was diluted to disperse poly(ethylene-methacrylic acid) sodium salt (3.0 g) in water (100 g), then stirred for about 1 hour to make an aqueous polymer dispersion.
- the produced aqueous polymer dispersion was slowly mixed with the aqueous silicate dispersion, then stirred for about 2 hours. Then, the mixture was completely dried in a pan on a hot plate at about 150°C to make a composite material consisting of layered silicate to polymer with the combination ratio of 1 :3. The produced composite material was crushed in a mortar.
- Powder Smecton® SA only 7.5 4000
- 1 represents a silicate layer of layered silicate
- 2 represents an ionomer.
- silicate layers 1 are not parallel to each other, and ionomer 2 is introduced between the silicate layers extended in the various directions.
- silicate layers 1 are parallel, the distance between the layers is not increased, and ionomer 2 is not introduced between the layers nor present in the outside of the layered silicate particles.
- Kunipia® F/poly(ethylene-me ⁇ acrylic acid) potassium salt powder composite material weight ratio: 1/1 (80 g).
- the material was dry-blended with pellets of poly(ethylene-methacrylic acid) zinc salt (Himilan® 1706 made by Du Pont-Mitsui Polychemicals Co., Ltd.) (920 g); then, the mixture was compounded using a biaxial kneader (same direction, TEM 35 made by Toshiba Kikai).
- Kunipia® F was contained in the produced composite material in an amount of 4 wt%. Its transparency was visually observed by an optical microscope and it was photographed (Figure 3).
- Kunipia® F (40 g) was made. It was dry-blended with pellets of polyethylene-methacryiic acid zinc salt (Himilan® 1707 made by Du Pont-Mitsui Polychemicals Co., Ltd.) (960 g); then, the mixture was compounded using a biaxial kneader (same direction, TEM 35 made by Toshiba Kikai). Kunipia® F was contained in the produced composite material in an amount of 4 wt%. Its transparency was visually observed by an optical microscope and it was photographed (Figure 7).
- Layered silicate is dispersed better using a Kunipia® F/poly(ethylene-methacrylic acid) potassium salt powder composite material with a weight ratio equal to 1/3 in a final composite material than using a Kunipia® F/poly(ethylene-methacrylic acid) potassium salt powder composite material with a weight ratio equal to 1/1.
- Application Example 7
- Kunipia F (4 g) was made. It was dry-blended with pellets of poly(ethylene-methacrylic acid) zinc salt (Himilan® 1707 made by Du Pont-Mitsui Polychemicals Co., Ltd.) (96 g); then, the mixture was compounded using a biaxial kneader (same direction, TEM 35 made by Toshiba Kikai).
- Kunipia® F was contained in the produced composite material in an amount of 4 wt%. Its transparency was visually observed by an optical microscope and it was photographed (Figure 9).
- Layered silicate can be added to a polymer by an easy production method while maintaining transparency, if the polymer satisfies specific conditions, such as ionomer content. The reason for this is that the distance between the silicate layers is increased and the polymer is introduced so that the silicate layers can be well dispersed in the polymer.
Abstract
A composite material of layered silicate and organic polymer, (as shown in the figure wherein (1) is layered silicate and (2) is ionomer) having heat stability, and containing silicate layers that are not parallel and between which the distance is increased; a production method for a composite material utilizing no polymerization but dispersion of layered silicate in organic polymer materials other than amide; a composite-material-containing resin composition containing the composite material; and a production method for the resin composition, are provided. Particularly, a composite material is made by dispersing, mixing, drying, and crushing 100 parts by weight ionomer made of ethylene methacrylate copolymer that is partially or entirely neutralized by alkali metal or alkaline-earth metal with at least 0.05 parts by weight of layered silicate in water to introduce the ionomer into a layered silicate of the silicate layers.
Description
TITLE COMPOSITE MATERIAL AND PRODUCTION OF THE COMPOSITE MATERIAL, AND COMPOSITE-MATERIAL-CONTAINING RESIN COMPOSITION AND PRODUCTION OF THE RESIN COMPOSITION
This patent application claims priority to Japanese Patent Application Nos. 8-65355 and 8-302368, which is incorporated herein by reference.
Field nf the Invention The present invention is concerned with both a composite material used for mixing with an organic polymer material to improve mechanical properties, gas barrier properties, heat resistance, or transparency of the organic polymer material, and production of the composite material. In detail, the present invention is concerned with both a composite material containing silicate layers between which an ionomer is introduced, and production of the composite material. The present invention is also concerned with a composite-material-containing resin composition containing both an organic polymer material compatible to the ionomer and produced composite material, and production of the resin composition.
Background
Development of a composite material containing silicate layers between which an ionomer was introduced was attempted, and is described in Chuzo Kato (Polymer, 1970, Vol. 19, No. 222, pp. 758-764) and Chuzo Kato and Kazuyuki Kuroda (Clay Science, 1986, Vol. 26, No. 4, pp. 292-305). However, it was difficult to introduce an organic polymer material to a silicate layer in order to increase the distance between the layers, and to make the layers unparallel with each other to disperse clay minerals.
Clay mineral/polyamide resin compositions characterized by, if necessary, treating silicate layers that make up swelling clay minerals with an alkvlamine swelling agent, then impregnating and polymerizing the monomers, were
developed (Japanese Kokai Patent Application Nos. Sho 58[1983]-3521 1 and Sho 58[1983]-35542) as composite materials in order to solve the problems.
A composite material made by mixing resin that contained the polyamide with silicate layers making up the layered silicate and having both thickness of 7-12 A (angstrom) and a distance between the layers of 30 A or more, then ion-bonding a part of a polyamide polymer chain to the silicate layers, was reported as a composite material made by ion-bonding a part of the polyamide polymer chain to the silicate layers (Japanese Kokai Patent Application No. Sho 62[1987]-74957). A production method for the composite material employed in the following processes, i.e., a contact process in which layered silicate was brought into contact with a swelling agent to make a composite that was swollen by polyamide contained in the monomer; a mixing process in which the produced composite was mixed with polyamide monomer; and polymerization process in which the mixture was heated to the required temperature to carry out polymerization (Japanese Kokai Patent Application No. Sho 62[1987]-74957). Because the production process contained a polymerization process it was not necessarily easy to make composite materials, and it was difficult to apply it to other than the polyamide. A composite-material-containing resin composition having a distance between the layers of 30 A or more, making the layers unparallel to each other, and made by compounding polyamide with a layered silicate/alkylamine swelling agent composite material made by dispersing both layered silicate and an alkylamine swelling agent in water, then drying, was reported (U.S. Patent No. 5,385,776). However, because an alkylamine swelling agent having a low molecular weight was contained in the final products, poor thermal stability was obtained. Because increasing the distance between the layers 30 A or more makes the layers unparallel to each other, it was difficult to make a composite-material-containing resin composition having improved dispersibility.
Problems to be solved by the invention
Development of production methods for a composite material involving no polymerization process and using organic polymer materials other than polyamide which can disperse layered silicate was desired. The purpose of the present invention is to provide a composite material consisting of both layered silicate and an organic polymer material, having thermal stability, containing silicate layers between which the distance is increased or which are not parallel each other, and to provide a production method for a good composite material which is easy and requires neither a process in which layered silicate is brought into contact with an alkylamine swelling agent or in which polymerization is carried out when a composite material having improved dispersibility either to increase the distance between the silicate layers or to make the layers be unparallel each other is made.
The purpose of the present invention is to provide both a composite-material-containing resin composition that contains the composite materials and a production method for the composition.
In detail, the purpose of the present invention is to provide a composite material consisting of both an ethylene ionomer and layered silicate, and production of the composite material, and a composite-material-containing resin composition that contains the composite material, and production of the composition.
Summary of Invention
Research was undertaken by the inventors to solve the problems, and it was found that a composite material of both layered silicate and an organic polymer material, made with a process involving no polymerization, able to be used for various types of resin, having improved dispersibility that either increases the distance between silicate layers or makes the layers unparallel to each other, could be made in a simple production process by selecting both organic polymer material (A), satisfying specific conditions as an organic polymer material making up a composite material with layered silicate, and organic polymer material (B), which is kneaded with the composite material, and a production method for a
composite-material-containing resin composition that contains the composite material.
Therefore, a production method for a composite material is characterized by dispersing, mixing, drying, and crushing a polar organic polymer that is either soluble or dispersible in water, and fusible with silicate layers in a polar solvent, to introduce the above-mentioned polar organic polymer to a layered silicate of the above-mentioned silicate layer.
A production method for a composite material also is characterized by using an ionomer as the above-mentioned polar organic polymer. A production method for a composite material also is characterized by dispersing, mixing, drying, and crushing 100 parts by weight potassium ionomer made of potassium in which ethylene methacrylate copolymer is either partially or entirely neutralized, with 0.5-300 parts by weight silicate layers in water, to introduce potassium ionomer to a layered silicate of the above-mentioned silicate layers.
A composite material is characterized by dispersing, mixing, drying, and crushing 100 parts by weight sodium ionomer that is made of ethylene methacrylate copolymer which is either partially or entirely neutralized with sodium and that can be soluble or dispersible in water, with 0.5-300 parts by weight silicate layers in water to introduce sodium ionomer to a layered silicate of the above-mentioned silicate layers.
A composite material also is characterized by containing both a polar organic polymer that is either soluble or dispersible in water and fusible, and that is introduced between the above-mentioned silicate layers. A composite material also is characterized by compounding composite materials made by a production method described in any of Claims 1-4, composite materials described in Claim 5, and an organic polymer material compatible to the above-mentioned polar organic polymer to disperse and pack 0.05 part by weight or more of the above-mentioned silicate layers in 100 parts by weight of a mixture of the above-mentioned polar organic polymer and the above-mentioned organic polymer material.
A composite-material-containing resin composition is characterized by containing a melted and kneaded material comprising composite materials made by one of the production methods described in Claims 1-4, or composite materials described in Claim 5, and an organic polymer material compatible with the above-mentioned polar organic polymer, and by containing both the above-mentioned polar organic polymer and 0.05 part by weight or more of the above-mentioned silicate layers to 100 parts by weight of the above-mentioned organic polymer material.
Brief Description of Figures
Figure 1 explains the presence of both the layered silicate ( 1 ) and the ionomer (2) in each composite material made in Application Examples 1-3 of the present invention.
Figure 2 explains the presence of both the layered silicate (1) and the ionomer (2) in each composite material made in Comparative Examples 1-4 of the present invention.
Figure 3 shows an optical microscopic photograph of a composite material made in Application Example 4 of the present invention. (A) is a photograph with a magnification of 15 times. (B) is a photograph with a magnification of 40 times. Figure 4 shows an optical microscopic photograph of a composite material made in Application Example 5 of the present invention. (A) is a photograph with a magnification of 15 times. (B) is a photograph with a magnification of 40 times. Figure 5 shows an optical microscopic photograph of a composite material made in Application Example 6 of the present invention. (A) is a photograph with a magnification of 15 times. (B) is a photograph with a magnification of 40 times. Figure 6 shows a transmission electromicrograph photograph of a composite material made in Application Example 6 of the present invention (magnification: about 70,000 times)
Figure 7 shows an optical microscopic photograph of a composite material made in Comparative Example 5 of the present invention. (A) is a photograph with magnification of 15 times. (B) is a photograph with a magnification of 40 times.
Figure 8 shows a transmission electromicrograph of a composite material made in Application Example 7 of the present invention (magnification: about 100 times).
Figure 9 shows a transmission electromicrograph of a composite material made in Comparative Example 6 of the present invention (magnification: about 100 times).
Application of the invention
Specific conditions of organic polymer material (A) include being soluble or dispersible in water and being fusible. An organic polymer material able to form a composite material containing organic polymer material (A), which is introduced between the silicate layers by mixing and dispersing either an aqueous solution or an aqueous dispersion of organic polymer material (A) with an aqueous silicate dispersion made by dispersing layered silicate in water, followed by drying then crushing the mixture, must be chosen.
Detailed examples of organic polymer material (A) include ionomers made by partially or entirely neutralizing methacrylic acid in a random copolymer of ethylene and methacrylic acid with an alkali metal or alkaline-earth metal. Because potassium has good dispersibility in water, it is especially suitable. However, other metals typically used in making ionomers, including metals such as sodium or magnesium, which are either dispersible or soluble in water, can be used.
A composite material containing an ionomer that is introduced between the silicate layers making up the layered silicate can be made by mixing an aqueous silicate dispersion, made by dispersing 0.5-300 parts by weight layered silicate in water with an aqueous polymer dispersion made by dispersing 100 parts by weight ionomer in water, drying, and crushing the mixture. It can be verified by both the peak position and intensity measured by wide-angled X-rays that the produced composite material contains ionomer introduced between the silicate layers. Organic polymer material (B) kneaded with a composite material must be compatible with organic polymer material (A), and must be able to be melted and kneaded. Compatibility means either complete compatibility or good affinity at
the interface. If there is no compatibility, it is difficult to disperse silicate layers of layered silicate in a final material during the kneading process.
Examples of organic polymer material (B) include random copolymers of ethylene and methacrylic acid; ionomers of random copolymer of ethylene and methacrylic acid partially or entirely neutralized particularly with metals such as sodium, magnesium or zinc; polyesters such as polybutylene terephthalate or polyethylene terephthalate; and polyamides such as nylon 6 or nylon 66. In the case of using an ethylene ionomer, the problem of transparency of the ethylene ionomer being damaged, can be solved by adding an inorganic filler to the ethylene ionomer while at the same time improving the mechanical properties.
Layered silicate should be dispersed and filled in amounts of 0.05 parts by weight or more in 100 parts by weight of a combination of organic polymer materials (A) and (B). When there is less than 0.05 part by weight, unsatisfactory effects result from the filling. When there are more than 300 parts by weight to 100 parts by weight of a combination of organic polymer materials (A) and (B), poor dispersion results.
A silicate layer of layered silicate used for the present invention has a thickness of 7-15 A, and is formed with magnesium silicate or aluminum silicate. Examples include smectite clay minerals such as montmorillonite, saponite, beidellite, nontronite, hectorite, or stevensite, vermiculite, halloysite, and mica. They can be either natural or synthetic. Swelling fluorine mica can be included in the examples. Smectite layered silicate is especially suitable.
Any conventional method may be used for stirring, drying, and crushing, which are carried out in the production method for a composite material of the present invention. Any conventional method may be used for compounding a composite material with organic polymer material (B). However, it is desired to use a kneader having a strong compounding power for transmitting mechanical dispersibility to a composite material and which results in better dispersion of layered silica when organic polymer material (A) has good compatibility to organic polymer material (B). Either a biaxial kneader (rotation in the same direction or in the different direction) or a Yabusu kneader is suitable.
Whether the distance between silicate layers is increased in a composite-material-containing resin composition or whether a composite material having improved dispersibility effective for making the layers unparallel to each other is formed or not is decided by visual observation of the transparency using an optical microscope and by observation using a transmission electron microscope if necessary.
Examples
The present invention is explained with application examples. However, the present invention is not specifically limited by said application examples.
Application Example 1
Powder montmorillonite (Kunipia® F made by Kunimine Kogyo K.K.) ( 1.0 g) was added to water ( 100 g); then, the mixture was stirred for about 3 hours to make an aqueous silicate dispersion. Aqueous poly(ethylene-methacrylic acid) potassium salt (MKD100 made by Du Pont-Mitsui Polychemicals Co., Ltd.) dispersion was diluted to disperse the poly(ethylene-methacrylic acid) potassium salt (1.0 g) in water (100 g), then stirred for about 1 hour to make an aqueous polymer dispersion. The produced aqueous polymer dispersion was slowly mixed with an aqueous silicate dispersion, then stirred for about 2 hours. Then, the mixture was completely dried in a pan on a hot plate at about 150°C to make a composite material consisting of layered silicate to polymer with combination ratio of 1 : 1. The produced composite material was crushed in a mortar.
Application Example 2
Synthetic smectite powder (Smecton® SA made by Kunimine Kogyo K.K.) (1.0 g) was added to water (100 g), then stirred for about 3 hours to make an aqueous silicate dispersion. Aqueous poly(ethylene-methacrylic acid) potassium salt (MKD100 made by Du Pont-Mitsui Polychemicals Co., Ltd.) dispersion was diluted to disperse the poly(ethylene-methacrylic acid) potassium salt ( 1.0 g) in water (100 g), then stirred for about 1 hour to make an aqueous polymer dispersion. The produced aqueous polymer dispersion was slowly mixed with the
aqueous silicate dispersion: then, the mixture was stirred for about 2 hours. Then, the mixture was dried in a pan on a hot plate at 150°C to make a composite material of layered silicate and polymer with a combination ratio of 1 : 1. The produced composite material was crushed in a mortar.
Comparative Example 1
The same process used in Application Example 1 was used to make a composite material of Kunipia® F made by Kunimine Kogyo K.K. and sodium polyacrylate in a 1 : 1 ratio.
Comparative Example 2
The same process used in Application Example 2 was used to make a composite material of Smecton® SA made by Kunimine Kogyo K.K. and sodium polyacrylate in a 1 : 1 ratio.
Comparative Example 3
The same process used in Application Example 1 was used to make a composite material of Kunipia® F made by Kunimine Kogyo K.K. and polyethylene imine in a 1 :1 ratio.
Comparative Example 4
The same process used in Application Example 2 was used to make a composite material of Smecton® SA made by Kunimine Kogyo K.K. and polyethylene imine in a 1 : 1 ratio.
Application Example 3
Montmorillonite powder (Kunipia® F made by Kunimine Kogyo K.K.) (1.0 g) was added to water (100 g); then, the mixture was stirred for about 3 hours to make an aqueous silicate dispersion. Aqueous poly(ethylene-methacrylic acid) sodium salt (Chemipearl® S-100 made by Mitsui Petrochemical Industries, Ltd.) dispersion was diluted to disperse poly(ethylene-methacrylic acid) sodium salt (3.0 g) in water (100 g), then stirred for about 1 hour to make an aqueous polymer
dispersion. The produced aqueous polymer dispersion was slowly mixed with the aqueous silicate dispersion, then stirred for about 2 hours. Then, the mixture was completely dried in a pan on a hot plate at about 150°C to make a composite material consisting of layered silicate to polymer with the combination ratio of 1 :3. The produced composite material was crushed in a mortar.
X-ray analysis
X-ray analysis was carried out for the produced composite materials. Results are shown in Table I.
Table I
Sample Peak position Peak intensity
Powder Kunipia® F only 7.4 5000
Powder Smecton® SA only 7.5 4000
Application Example 1 Unable to detect
Application Example 2 Unable to detect
Comparative Example 1 7.0 5000
Comparative Example 2 8.0 1500
Comparative Example 3 6.8 2000
Comparative Example 4 6.5 1500
Application Example 3 Unable to detect
Note: unable to detect = peak intensity of less than 1000 cps
As seen in Table I, peaks (1000 cps or more) were not observed at 2Θ up to 10°. So, it is verified that either potassium salt or sodium salt of poly(ethylene-methacrylic acid) was introduced between the silicate layers of the layered silicate to make the silicate layers unparallel to each other, so that the silicate layers could be dispersed. Because peaks of the composite materials made in Comparative Examples 1 and 2 had both the same position and intensity as those of peaks of either Kunipia® F or Smecton® SA powder, neither sodium polyacrylate nor polyethylene imine was introduced between the silicate layers. Both Figures 1 and 2 show the structures. In Figures 1 and 2, 1 represents a
silicate layer of layered silicate, and 2 represents an ionomer. In Figure 1 , which shows the shape of each composite material made in Application Examples 1-3, silicate layers 1 are not parallel to each other, and ionomer 2 is introduced between the silicate layers extended in the various directions. In Figure 2, which shows the shape of each composite material made in Comparative Examples 1-4, silicate layers 1 are parallel, the distance between the layers is not increased, and ionomer 2 is not introduced between the layers nor present in the outside of the layered silicate particles.
Application Example 4
The same method used in Application Example 1 was used to make a Kunipia® F/poly(ethylene-meϋ acrylic acid) potassium salt powder composite material (weight ratio: 1/1) (80 g). The material was dry-blended with pellets of poly(ethylene-methacrylic acid) zinc salt (Himilan® 1706 made by Du Pont-Mitsui Polychemicals Co., Ltd.) (920 g); then, the mixture was compounded using a biaxial kneader (same direction, TEM 35 made by Toshiba Kikai). Kunipia® F was contained in the produced composite material in an amount of 4 wt%. Its transparency was visually observed by an optical microscope and it was photographed (Figure 3).
Application Example 5
The same process used in Application Example 1 was used to make a Kunipia® F/poly(ethylene-methacrylic acid) potassium salt powder composite material (weight ratio = 1/3) (160 g). The material was dry-blended with pellets of poly(ethylene-methacrylic acid) zinc salt (Himilan® 1706 made by Du
Pont-Mitsui Polychemicals Co., Ltd.) (840 g); then, the mixture was compounded using a biaxial kneader (same direction, TEM 35 made by Toshiba Kikai). Kunipia® F was contained in the produced composite material in an amount of 4 wt%. Its transparency was visually observed by an optical microscope and it was photographed (Figure 4).
Application Example 6
The same process used in Application Example 1 was used to make a Smecton® SA/poly(ethylene-methacrylic acid) potassium salt powder composite material (weight ratio = 1/1) (80 g). The material was dry-blended with pellets of ρoly(ethylene-methacrylic acid) zinc salt (Himilan® 1706 made by Du
Pont-Mitsui Polychemicals Co., Ltd.) (840 g); then, the mixture was compounded using a biaxial kneader (same direction, TEM 35 made by Toshiba Kikai). Kunipia® F was contained in the produced composite material in an amount of 4 wt%. Its transparency was visually observed by an optical microscope and it was photographed (Figure 5). Transmission electromicrographs were taken (Figure 6).
Comparative Example 5
Kunipia® F (40 g) was made. It was dry-blended with pellets of polyethylene-methacryiic acid zinc salt (Himilan® 1707 made by Du Pont-Mitsui Polychemicals Co., Ltd.) (960 g); then, the mixture was compounded using a biaxial kneader (same direction, TEM 35 made by Toshiba Kikai). Kunipia® F was contained in the produced composite material in an amount of 4 wt%. Its transparency was visually observed by an optical microscope and it was photographed (Figure 7).
Optical microscopic photograph and electronmicrographs
As seen in both optical microscopic photographs and electromicrographs, in the case of dispersing layered silicate alone in poly(ethylene-methacrylic acid) zinc salt, large lumps were observed, and poor transparency was obtained. In the case of dispersing a layered silicate/poly(ethylene-methacrylic acid) potassium salt composite material in poly(ethylene-methacrylic acid) zinc salt, no large lumps were observed and good transparency was obtained. Layered silicate is dispersed better using a Kunipia® F/poly(ethylene-methacrylic acid) potassium salt powder composite material with a weight ratio equal to 1/3 in a final composite material than using a Kunipia® F/poly(ethylene-methacrylic acid) potassium salt powder composite material with a weight ratio equal to 1/1.
Application Example 7
The same process used in Application Example 3 was used to make a Kunipia® F/poly(ethylene-methacrylic acid) potassium salt powder composite material (weight ratio = 1/3) (16 g). The material was dry-blended with pellets of poly(ethylene-methacrylic acid) zinc salt (Himilan® 1707 made by Du
Pont-Mitsui Polychemicals Co., Ltd.) (84 g); then, the mixture was compounded using a biaxial kneader (same direction, TEM 35 made by Toshiba Kikai). Kunipia® F was contained in the produced composite material in an amount of 4 wt%. Its transparency was visually observed by an optical microscope and it was photographed (Figure 8).
Comparative Example 6
Kunipia F (4 g) was made. It was dry-blended with pellets of poly(ethylene-methacrylic acid) zinc salt (Himilan® 1707 made by Du Pont-Mitsui Polychemicals Co., Ltd.) (96 g); then, the mixture was compounded using a biaxial kneader (same direction, TEM 35 made by Toshiba Kikai).
Kunipia® F was contained in the produced composite material in an amount of 4 wt%. Its transparency was visually observed by an optical microscope and it was photographed (Figure 9).
Electromicrograph
As seen in the electromicrographs, in the case of dispersing layered silicate alone in poly(ethylene-methacrylic acid) zinc salt, large lumps were observed, and poor transparency resulted. In the case of dispersing layered silicate/poly(ethylene-methacrylic acid) sodium salt composite material in poly(ethylene-methacrylic acid) zinc salt, no large lumps were observed, and good transparency resulted.
Effect of the invention
Layered silicate can be added to a polymer by an easy production method while maintaining transparency, if the polymer satisfies specific conditions, such as ionomer content. The reason for this is that the distance between the silicate layers is increased and the polymer is introduced so that the silicate layers can be well dispersed in the polymer.
Claims
1. Production of a composite material, characterized by dispersing, mixing, drying, and crushing a polar organic polymer material that is either soluble or dispersible in water and fusible with silicate layers in a polar solvent to introduce the polar organic polymer to a layered silicate of the silicate layers.
2. Production of a composite material described in Claim 1, characterized by using an ionomer as the polar organic polymer.
3. Production of a composite material, characterized by dispersing, mixing, drying, and crushing 100 parts by weight potassium ionomer in which ethylene methacrylate copolymer is either partially or entirely neutralized with potassium, with 0.5-300 parts by weight silicate layers in water to introduce the potassium ionomer to a layered silicate of the silicate layers.
4. Production of a composite material, characterized by dispersing, mixing, drying, and crushing 100 parts by weight sodium ionomer which ethylene methacrylate copolymer is either partially or entirely neutralized with sodium and that can be soluble or dispersible in water, with 0.5-300 parts by weight silicate layers in water to introduce sodium ionomer to a layered silicate of the silicate layers.
5. A composite material characterized by containing both a polar organic polymer that is either soluble or dispersible in water and fusible, and that is introduced between the silicate layers.
6. Production of a composite-material-containing resin composition, characterized by compounding all of a composite material made by a production method described in any of Claims 1-4, a composite material described in Claim 5, and an organic polymer material compatible with the polar organic polymer to disperse and pack at least 0.05 part by weight of the silicate layers in 100 parts by weight of a mixture of the polar organic polymer and the organic polymer material.
7. A composite-material-containing resin composition characterized by containing a melted and kneaded material comprising composite material made by one of the production methods described in Claims 1-4, or composite material described in Claim 5, and an organic polymer material compatible with the polar organic polymer, and by containing both the polar organic polymer, and at least 0.05 parts by weight of the above-mentioned silicate layers to 100 parts by weight of the above-mentioned organic polymer material.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA 2245860 CA2245860A1 (en) | 1996-02-27 | 1997-02-27 | Composite material and production of the composite material, and composite-material-containing resin composition and production of the resin composition |
| EP97907906A EP0883647A1 (en) | 1996-02-27 | 1997-02-27 | Composite material and production of the composite material, and composite-material-containing resin composition and production of the resin composition |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6535596 | 1996-02-27 | ||
| JP8/65355 | 1996-02-27 | ||
| JP30236896A JPH09295810A (en) | 1996-02-27 | 1996-10-29 | Composite material and its production and composite material-containing resin composition and its production |
| JP8/302368 | 1996-10-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO1997031973A1 true WO1997031973A1 (en) | 1997-09-04 |
Family
ID=26406499
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US1997/003061 WO1997031973A1 (en) | 1996-02-27 | 1997-02-27 | Composite material and production of the composite material, and composite-material-containing resin composition and production of the resin composition |
Country Status (3)
| Country | Link |
|---|---|
| EP (1) | EP0883647A1 (en) |
| JP (1) | JPH09295810A (en) |
| WO (1) | WO1997031973A1 (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6071988A (en) * | 1996-12-31 | 2000-06-06 | Eastman Chemical Company | Polyester composite material and method for its manufacturing |
| US6084019A (en) * | 1996-12-31 | 2000-07-04 | Eastman Chemical Corporation | High I.V. polyester compositions containing platelet particles |
| US6162857A (en) * | 1997-07-21 | 2000-12-19 | Eastman Chemical Company | Process for making polyester/platelet particle compositions displaying improved dispersion |
| US6238793B1 (en) * | 1996-11-01 | 2001-05-29 | E. I. Du Pont De Nemours And Company | Method for production of a low density polyethylene-lamellar silicate composite material |
| US6337046B1 (en) | 1997-12-22 | 2002-01-08 | Eastman Chemical Company | Process for producing containers from polymer/platelet particle compositions |
| US6793592B2 (en) | 2002-08-27 | 2004-09-21 | Acushnet Company | Golf balls comprising glass ionomers, or other hybrid organic/inorganic compositions |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19919881A1 (en) * | 1999-04-30 | 2000-11-02 | Univ Stuttgart | Thermally stable proton conductive composite, for use in e.g. fuel cells, membrane separation, catalysis, electrolysis or electrochemical processes, comprises acid and/or organic base and layered and/or framework silicate |
| KR100733922B1 (en) * | 2004-12-03 | 2007-07-02 | 주식회사 엘지화학 | Article having barrier property |
| JP2007132442A (en) * | 2005-11-11 | 2007-05-31 | Kanto Auto Works Ltd | Jig for laser resin deposition |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4105709A (en) * | 1975-04-03 | 1978-08-08 | Asahi-Dow Limited | Polyamide compositions |
| US4739007A (en) * | 1985-09-30 | 1988-04-19 | Kabushiki Kaisha Toyota Chou Kenkyusho | Composite material and process for manufacturing same |
| US4889885A (en) * | 1987-03-04 | 1989-12-26 | Kabushiki Kaisha Toyota Chuo Kenkyusho | Composite material containing a layered silicate |
| US5164460A (en) * | 1990-05-30 | 1992-11-17 | Kabushiki Kaisha Toyota Chuo Kenkyusho | Polyimide composite material and process for producing the same |
| US5385776A (en) * | 1992-11-16 | 1995-01-31 | Alliedsignal Inc. | Nanocomposites of gamma phase polymers containing inorganic particulate material |
-
1996
- 1996-10-29 JP JP30236896A patent/JPH09295810A/en active Pending
-
1997
- 1997-02-27 EP EP97907906A patent/EP0883647A1/en not_active Withdrawn
- 1997-02-27 WO PCT/US1997/003061 patent/WO1997031973A1/en not_active Application Discontinuation
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4105709A (en) * | 1975-04-03 | 1978-08-08 | Asahi-Dow Limited | Polyamide compositions |
| US4739007A (en) * | 1985-09-30 | 1988-04-19 | Kabushiki Kaisha Toyota Chou Kenkyusho | Composite material and process for manufacturing same |
| US4889885A (en) * | 1987-03-04 | 1989-12-26 | Kabushiki Kaisha Toyota Chuo Kenkyusho | Composite material containing a layered silicate |
| US5164460A (en) * | 1990-05-30 | 1992-11-17 | Kabushiki Kaisha Toyota Chuo Kenkyusho | Polyimide composite material and process for producing the same |
| US5385776A (en) * | 1992-11-16 | 1995-01-31 | Alliedsignal Inc. | Nanocomposites of gamma phase polymers containing inorganic particulate material |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6238793B1 (en) * | 1996-11-01 | 2001-05-29 | E. I. Du Pont De Nemours And Company | Method for production of a low density polyethylene-lamellar silicate composite material |
| US6071988A (en) * | 1996-12-31 | 2000-06-06 | Eastman Chemical Company | Polyester composite material and method for its manufacturing |
| US6084019A (en) * | 1996-12-31 | 2000-07-04 | Eastman Chemical Corporation | High I.V. polyester compositions containing platelet particles |
| US6162857A (en) * | 1997-07-21 | 2000-12-19 | Eastman Chemical Company | Process for making polyester/platelet particle compositions displaying improved dispersion |
| US6359052B1 (en) * | 1997-07-21 | 2002-03-19 | Jack Wesley Trexler, Jr. | Polyester/platelet particle compositions displaying improved dispersion |
| US6337046B1 (en) | 1997-12-22 | 2002-01-08 | Eastman Chemical Company | Process for producing containers from polymer/platelet particle compositions |
| US6793592B2 (en) | 2002-08-27 | 2004-09-21 | Acushnet Company | Golf balls comprising glass ionomers, or other hybrid organic/inorganic compositions |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0883647A1 (en) | 1998-12-16 |
| JPH09295810A (en) | 1997-11-18 |
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