CA2090905A1 - Thermoplastic microspheres, process for their preparation and use of the microspheres - Google Patents
Thermoplastic microspheres, process for their preparation and use of the microspheresInfo
- Publication number
- CA2090905A1 CA2090905A1 CA002090905A CA2090905A CA2090905A1 CA 2090905 A1 CA2090905 A1 CA 2090905A1 CA 002090905 A CA002090905 A CA 002090905A CA 2090905 A CA2090905 A CA 2090905A CA 2090905 A1 CA2090905 A1 CA 2090905A1
- Authority
- CA
- Canada
- Prior art keywords
- microspheres
- chlorine
- free aliphatic
- blowing agent
- aliphatic fluorocarbon
- 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.)
- Abandoned
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/32—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof from compositions containing microballoons, e.g. syntactic foams
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J13/00—Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided for; Making microcapsules or microballoons
- B01J13/02—Making microcapsules or microballoons
- B01J13/06—Making microcapsules or microballoons by phase separation
- B01J13/14—Polymerisation; cross-linking
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
- C08J9/12—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
- C08J9/14—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent organic
- C08J9/143—Halogen containing compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/18—Fireproof paints including high temperature resistant paints
- C09D5/185—Intumescent paints
Abstract
Abstract Thermoplastic microspheres, unexpanded or expanded, which contain chlorine-free aliphatic fluorocarbons or fluoro-hydrocarbons. Chlorine-free aliphatic fluorocarbons or fluorohydrocarbons are used as blowing agent at the produc-tion of expandable thermoplastic microspheres. Expanded microspheres containing these blowing agents have very low densities. The use of the specific blowing agents also gives other advantages, especially with regard to fire and insulation properties and the microspheres are thus especially suitable for use in fire-resistant paints and insulation materials.
Description
209~0~
Thermoplastic microspheres, process for their preparation and use of the microspheres The present invention relates to thermoplastic microspheres and more particularly to such microspheres containing special blowing agents. The invention also relates to preparation of the microspheres and the use of these.
Expandable and expanded thermoplastic microspheres are used in a great number of fields, for example as fillers in polymers, paints, plastisols, paper, cable insulation etc, and have been produced on a commercial scale for several years. Expandable thermoplastic micro-spheres are principally prepared according to the process disclosed in the US patent 3615972. The microspheres are thus conventionally prepared by suspension polymerisation of a liquid monomer or monomer mixture containing a con-densed blowing agent which is dispersed in an aqueous~ phase containing a suspending agent and polymerisation i~itiator.
The microspheres obtained after the polymerisation consist of a polymer shell which encapsulates the li~uid, volatile blowing agent. The spheres expand by heatin~ to a -tempera-ture above the boiling point of the blowing agent and above the softening point of the polymer.
At the production of expandable thermoplastic micro-spheres hydrocarbons such as n-butane, isobutane, iso-pentane and neopentane are conventionally used, and e-specially isobutane and isopentane which give microspheres with very good expansion capability. The commercially available microsphere product Expancel(R) contains iso-butane as blowing agent and has a polymer shell of a co-polymer of vinylidene chloride and acrylonitrile. Other blowing agents than pure hydrocarbons have been suggested for use in the preparation of microspheres. In the above mentioned ~S patent 3615972 it is, for example, mentioned that certain chlorofluorocarbons can be used, but these have, however, not been used commercially. Chlorofluoro-carbons do not give the microspheres satisfactory expansion properties and they also have other disadvantages.
.
2Q9~
According to the present invention it has been found that aliphatic fluorocarbons and fluorohydrocarbons are excellent blowing agents for microspheres and give spheres with very good expansion properties. Expanded microspheres containing aliphatic fluorocarbons and fluorohydrocarbons have densities of corresponding magnitude as those contain-ing isobutane and isopentane. The use o~ the specific blowing agents also lead to other advantages, particularly with regard to fire properties and insulation properties.
The present invention thus relates to thermoplastic microspheres containing chlorine-free aliphatic fluoro-carbons and fluorohydrocarbons as further defined in the claims. The invention also relates to a method for the production of the microspheres and to the use of these as additives/fillers in products for which heat insulation capacity and/or fire resistance are of importance.
The basis for the present invention is thus the use of chlorine-free aliphatic fluorocarbons and Eluorohydro-carbons as blowing agent in the production of expandable thermoplastic microspheres. The expandable thermoplastic microspheres encapsulates the volatile chlorine-free aliphatic fluorocarbons and fluorohydrocarbons in liquid form in a shell of polymerized ethylenically unsaturated monomer or mixture of ethylenically unsaturated monomers.
When the expandable microspheres are heated to temperatures above the boiling point of the blowing agent and above the softening point of the polymer the propellant is volatil-ized and the microspheres expand which results in micro-spheres having a substantially increased diameter and which contain the blowing agent in gas form.
The microspheres according to the present invention contains chlorine-free aliphatic fluorocarbons and/or fluorohydrocarbons. These can make up the whole amount of blowing agent but it is also within the scope of the invention that the microspheres contain these blowing agents in combination with other per se conventionally used blowing agents such as n-butane, lsobutane, isopentane and neopentane and preferably in combination with isobutane or .
~0~09a~
isopentane. The amount of other blowing agent than fluoro-carbons or fluorohydrocarbons should suitably not exceed 50~ by weight and preferably not exceed 25% in order to utili~e the advantages obtained with fluorocarbons and fluorohydrocarbons. The greatest advantages with regard to fire and insulation are of course obtained when the entire amount of blowing agent is made up from fluorocarbons or fluorohydrocarbons. However, mixtures with other blowing agents can be advantageous for example to compensate for high pressures during polymerisation when the utilized fluorocarbon or fluorohydrocarbon has a lower boiling point.
The -thermoplastic shell of the microspheres is made up from polymers or copolymers of ethylenically unsaturated monomers. Examples of suitable monomers are vinyl chloride, vinylidene chloride, acrylonitrile, methacrylonitrile, acrylic esters, methacrylic esters, styrene etc, and mixtures of two or more of these. Preferred microspheres have a shell based on a copolymer containing acrylonitrile and then particularly copolymers of acrylonitrile and vinylidene chloride and/or methyl methacrylate and/or methacrylonitrile. These copolymers can for example contain 30 to 80% by weight o~ acrylonitrile, 0 to 70% by weight of vinylidene chloride and/or 0 to 50% by weight of methyl methacrylate and/or methacrylonitrile. The shell of the microspheres can be cross-linked or not cross-linked.
The expandable microspheres can be prepared in per se known manner by suspension polymerisation of the monomers using conventional polymerisation initiators such as dialkyl peroxides, diacyl peroxides, peroxy esters, peroxy dicarbonates and azo compounds. The polymerisable monomer or monomer mixture, the condensed blowing agent, optional cross-linking agent and the initiator are suspended in an aqueous medium containing suspending agent in a reaction vessel. As cross-linking agents divinylbenzene, ethylene glycol dimethacrylate, triethylene glycol d`imethacrylate, triallyl isocyanate etc, can for example be used. Usually a powder stabilizer, such as colloidal silicic acid, is used , ~ -4 2~9~
as suspending agent. The powder stabilizer is usually used in combination with a so-called co-stabilizer, such as for example polyethylene oxide, polyethyleneimine, tetramethyl-ammonium hydroxide, condensation products of diethanolamine and adipic acid, condensation products of urea and form-aldehyde. The powder stabilizer is usually used in an amount of from about 3 to about 10% by weight, based on the monomer, while the co-stabilizer usually is used in an amount of some tenth %.
The blowing agent, the chlorine-free aliphatic fluorocarbons and fluorohydrocarbons and optional other blowing agents, as stated earlier, is usually used in amounts of from about 10 to about 70~ by weight, based on total monomer weight, so that they make up from about 10 to about 45% of the weight of the produced expandable micro-spheres. The process e~uipment used for the polymerisation is decisive for the choice of the chlorine-free aliphatic fluorocarbons and fluorohydrocarbons since a too low boiling point for these gives rise to too high pressures during the polymeri.sation process. The boiling point should usually not be lower than -40C and preferably not lower than -20C. The upper limit for the boiling point of the compounds is in the first hand dependent on the monomer composition, since the boiling point of the compounds shall be below the softening point for the polymer in question in order to carry out expansion of the microspheres. Generally the boiling point of the compounds should thus not exceed 60C and as a rule not exceed 40C. As examples of fluoro-carbons and fluorohydrocarbons which can be used can be mentioned CH2FCF3, CH3CHF2, CH3CH2F, CF3CF2cF3~
CF3CF2CF2CF3~ CYC1-C4F8, CF3(CF2)3CF3 and CF3CHFCF3. 2H-heptafluoropropane ~ CF3-CHF-CF3) iS especially suitable.
The polymerisation can be carried out in per se known manner and usually polymerisation temperatures of from about 40C to about 70C are used and the polymerisate is normally post-treated by filtration, washing and dewater-ing. The particle size for the unexpanded spheres, and thus also for the expanded spheres, can vary within wide limits . .
:
Thermoplastic microspheres, process for their preparation and use of the microspheres The present invention relates to thermoplastic microspheres and more particularly to such microspheres containing special blowing agents. The invention also relates to preparation of the microspheres and the use of these.
Expandable and expanded thermoplastic microspheres are used in a great number of fields, for example as fillers in polymers, paints, plastisols, paper, cable insulation etc, and have been produced on a commercial scale for several years. Expandable thermoplastic micro-spheres are principally prepared according to the process disclosed in the US patent 3615972. The microspheres are thus conventionally prepared by suspension polymerisation of a liquid monomer or monomer mixture containing a con-densed blowing agent which is dispersed in an aqueous~ phase containing a suspending agent and polymerisation i~itiator.
The microspheres obtained after the polymerisation consist of a polymer shell which encapsulates the li~uid, volatile blowing agent. The spheres expand by heatin~ to a -tempera-ture above the boiling point of the blowing agent and above the softening point of the polymer.
At the production of expandable thermoplastic micro-spheres hydrocarbons such as n-butane, isobutane, iso-pentane and neopentane are conventionally used, and e-specially isobutane and isopentane which give microspheres with very good expansion capability. The commercially available microsphere product Expancel(R) contains iso-butane as blowing agent and has a polymer shell of a co-polymer of vinylidene chloride and acrylonitrile. Other blowing agents than pure hydrocarbons have been suggested for use in the preparation of microspheres. In the above mentioned ~S patent 3615972 it is, for example, mentioned that certain chlorofluorocarbons can be used, but these have, however, not been used commercially. Chlorofluoro-carbons do not give the microspheres satisfactory expansion properties and they also have other disadvantages.
.
2Q9~
According to the present invention it has been found that aliphatic fluorocarbons and fluorohydrocarbons are excellent blowing agents for microspheres and give spheres with very good expansion properties. Expanded microspheres containing aliphatic fluorocarbons and fluorohydrocarbons have densities of corresponding magnitude as those contain-ing isobutane and isopentane. The use o~ the specific blowing agents also lead to other advantages, particularly with regard to fire properties and insulation properties.
The present invention thus relates to thermoplastic microspheres containing chlorine-free aliphatic fluoro-carbons and fluorohydrocarbons as further defined in the claims. The invention also relates to a method for the production of the microspheres and to the use of these as additives/fillers in products for which heat insulation capacity and/or fire resistance are of importance.
The basis for the present invention is thus the use of chlorine-free aliphatic fluorocarbons and Eluorohydro-carbons as blowing agent in the production of expandable thermoplastic microspheres. The expandable thermoplastic microspheres encapsulates the volatile chlorine-free aliphatic fluorocarbons and fluorohydrocarbons in liquid form in a shell of polymerized ethylenically unsaturated monomer or mixture of ethylenically unsaturated monomers.
When the expandable microspheres are heated to temperatures above the boiling point of the blowing agent and above the softening point of the polymer the propellant is volatil-ized and the microspheres expand which results in micro-spheres having a substantially increased diameter and which contain the blowing agent in gas form.
The microspheres according to the present invention contains chlorine-free aliphatic fluorocarbons and/or fluorohydrocarbons. These can make up the whole amount of blowing agent but it is also within the scope of the invention that the microspheres contain these blowing agents in combination with other per se conventionally used blowing agents such as n-butane, lsobutane, isopentane and neopentane and preferably in combination with isobutane or .
~0~09a~
isopentane. The amount of other blowing agent than fluoro-carbons or fluorohydrocarbons should suitably not exceed 50~ by weight and preferably not exceed 25% in order to utili~e the advantages obtained with fluorocarbons and fluorohydrocarbons. The greatest advantages with regard to fire and insulation are of course obtained when the entire amount of blowing agent is made up from fluorocarbons or fluorohydrocarbons. However, mixtures with other blowing agents can be advantageous for example to compensate for high pressures during polymerisation when the utilized fluorocarbon or fluorohydrocarbon has a lower boiling point.
The -thermoplastic shell of the microspheres is made up from polymers or copolymers of ethylenically unsaturated monomers. Examples of suitable monomers are vinyl chloride, vinylidene chloride, acrylonitrile, methacrylonitrile, acrylic esters, methacrylic esters, styrene etc, and mixtures of two or more of these. Preferred microspheres have a shell based on a copolymer containing acrylonitrile and then particularly copolymers of acrylonitrile and vinylidene chloride and/or methyl methacrylate and/or methacrylonitrile. These copolymers can for example contain 30 to 80% by weight o~ acrylonitrile, 0 to 70% by weight of vinylidene chloride and/or 0 to 50% by weight of methyl methacrylate and/or methacrylonitrile. The shell of the microspheres can be cross-linked or not cross-linked.
The expandable microspheres can be prepared in per se known manner by suspension polymerisation of the monomers using conventional polymerisation initiators such as dialkyl peroxides, diacyl peroxides, peroxy esters, peroxy dicarbonates and azo compounds. The polymerisable monomer or monomer mixture, the condensed blowing agent, optional cross-linking agent and the initiator are suspended in an aqueous medium containing suspending agent in a reaction vessel. As cross-linking agents divinylbenzene, ethylene glycol dimethacrylate, triethylene glycol d`imethacrylate, triallyl isocyanate etc, can for example be used. Usually a powder stabilizer, such as colloidal silicic acid, is used , ~ -4 2~9~
as suspending agent. The powder stabilizer is usually used in combination with a so-called co-stabilizer, such as for example polyethylene oxide, polyethyleneimine, tetramethyl-ammonium hydroxide, condensation products of diethanolamine and adipic acid, condensation products of urea and form-aldehyde. The powder stabilizer is usually used in an amount of from about 3 to about 10% by weight, based on the monomer, while the co-stabilizer usually is used in an amount of some tenth %.
The blowing agent, the chlorine-free aliphatic fluorocarbons and fluorohydrocarbons and optional other blowing agents, as stated earlier, is usually used in amounts of from about 10 to about 70~ by weight, based on total monomer weight, so that they make up from about 10 to about 45% of the weight of the produced expandable micro-spheres. The process e~uipment used for the polymerisation is decisive for the choice of the chlorine-free aliphatic fluorocarbons and fluorohydrocarbons since a too low boiling point for these gives rise to too high pressures during the polymeri.sation process. The boiling point should usually not be lower than -40C and preferably not lower than -20C. The upper limit for the boiling point of the compounds is in the first hand dependent on the monomer composition, since the boiling point of the compounds shall be below the softening point for the polymer in question in order to carry out expansion of the microspheres. Generally the boiling point of the compounds should thus not exceed 60C and as a rule not exceed 40C. As examples of fluoro-carbons and fluorohydrocarbons which can be used can be mentioned CH2FCF3, CH3CHF2, CH3CH2F, CF3CF2cF3~
CF3CF2CF2CF3~ CYC1-C4F8, CF3(CF2)3CF3 and CF3CHFCF3. 2H-heptafluoropropane ~ CF3-CHF-CF3) iS especially suitable.
The polymerisation can be carried out in per se known manner and usually polymerisation temperatures of from about 40C to about 70C are used and the polymerisate is normally post-treated by filtration, washing and dewater-ing. The particle size for the unexpanded spheres, and thus also for the expanded spheres, can vary within wide limits . .
:
2~9a5 and is selected with regard to the desired properties of the finished product. At the polymarisation the particle size is controlled mainly by tne composition of the poly-merisation mixture and the degree of stirring. 1 ~m to 1 mm, preferably 2 ~m to 0.5 mm and especially 5 ~m to 50 ~m can be mentioned as examples of particles sizes of un-expanded spheres.
The expandable spheres are expanded by heating to a temperature which gives rise to softening of the polymer shell and volatilization of the propellant whereby the particles expand to a diameter substantially larger than the diameter for the unexpanded particles and the expansion can be carried out in per se known manners. The spheres can for example be dried and expanded by dispersing the un-expanded spheres in an inert liquid, atomization of the dispersion and bringing this in contact with a warm inert gas stream. Another suitable manner for expansion is disclosed in the European patent applicatlon 03~8372.
According to this process the expandable microspheres are first dried to a certain dry content and then expanded by heating, eg by IR-heating. The expansion temperature is set by the boiling point of the blowing agent and the softening point of the shell-polymer and is usually within the range of from about 70C to about 140C. It has been found that the blowing agents used according to the present invention give at least as good expansion as the commercially used blowing agents isobutane and isopentane and thereby give expanded microspheres with about the same densities as those which are commercially acceptable. ThiS is in con-trast to chlorofluorocarbons and chlorofluorohydrocarbonswhich give substantially inferior expansion, which is believed to be due to their interference at the polymer-isation, and expanded microspheres which have densities about 3 to about 7 times higher than when isobutane or isopentane is used. Compared with isobutane and isopentane 2H-heptafluoropropane, for example, is also advantageous since it is non-combustible which is of importance both at the production and the use of the microspheres. Since the .
:
2 1~ ~ ~ 9 ~ ~
compounds are non-combustible problems with dust explosions in connection with drying of expandable as well as o~
expanded spheres are reduced. ~nother advantage in com-parison with isobutane and isopentane is that for example 2H-heptafluoropropane has substantially lower thermal conductivity which broadens the fields of application for the microspheres. Compared with chlorofluorocarbons the present fluorocarbons and fluorohydrocarbons are also advantageous since they do not have any ozone degrading effect.
Expandable and expanded thermoplastic microspheres have a large number of applications. The use of unexpanded microspheres is based on the expansion capability of the spheres and they are then expanded in situ in the mate-rials in which they are incorporated when these materialsare heated. As some examples of such use can be mentioned printing inks for the production of relief print on paper and textiles, fillers in paper and board and Eoaming of Eor example PVC-plastisol. At the use of expanded microspheres the low densit~ and filling effect of the spheres are utilized and they can for example be used as fillers in paints, putty, polymers and resins such as polyester, polyurethane, epoxy resins, composite materials based on polymers, paper, insulation materials etc.. The micro-spheres of the present invention can be used for the samepurposes for which microspheres are generally used. The present microspheres are particularly suitable for use in products for which fire resistance and thermal insulating capacity are of importance since the microspheres are advantageous in such applications since they contain chlorine-free fluorocarbons and fluorohydrocarbons, such as 2H-heptafluoropropane, which are non-combustible and which have low thermal conductivity. The present invention thus also relates to use of the microspheres in fire-resistant paints and in insulation materials. In fire-resistant paints the microspheres are used as fillers/`additives. The unexpanded microspheres are advantageously used in fire-resistant paints since they expand at heating and thereby 2 ~
give an insulating layer which protects the substrate. When the temperature becomes so high that the microspheres break the non-combustible blowing agent is released and the fire is retarded. As concerns insulation materials the entire product can be made up from microspheres, for economical reasons the microspheres are, however, also in this application as a rule used as ~illers/additives. As examples of insulation materials wherein the microspheres can be used are jointing compounds for, among other things, cable entries, where good insulation and fire-resistant properties are desired.
The invention is further illustrated in the following examples which, however, are not intended to limit the same. Parts and per cent relate to parts by weight and per cent by weight respectively, unless otherwise stated~
xample 1 125 parts of water were mixed with 5.5 parts of 1 molar NaOH-solution and 10 parts oE 10~ acetic aclcl solu-tion, 6 parts of 40% colloidal sillclc acld, 0.5 parts of a condensation product of diethanolamlne and adipic acid and 0.5 parts of dicetyl peroxydicarbo~ate and charged to a 15 1 reactor e~uipped with stirrer. The reactor was sealed and evacuated. A mixture of 0.3 parts of divinylbenzene, 7 parts of methylmethacrylate, 32 parts of acrylonitrile, 32 parts of vinylidene chloride and 29 parts of 2H-hepta-fluoropropane were then charged. The polymerisation mixture was stirred at 850 rpm during 60 minutes. After homogeniz-ation the rotation speed was lowered to 400 rpm and the mixture was then heated to 55C and polymerized at this temperature for 8 hours. The obtained polymerisate was washed and dewatered. The unexpanded microspheres had an average particle size, by weight, of 16 ~m. The micro-spheres were dried and their expansion capacity was invest-igated by means of thermomechanical analysis. They were found to have the same expansion capacity and temperature resistance as if isobutane or isopentane had been used, ie a density of about 17 kg/m3 was reached.
2 0 ~ 0 ~
Comparative Exam~les 2a) - 2c) The process according to ~xample 1 was repeated with other blowing agents.
2a) Instead of 2H-heptafluoropropane 12 parts of isopentane were used. The dried microspheres had a density below 20 kg/m3.
2b) Instead of 2~-heptafluoropropane 30 parts of trichloro-fluoromethane were used. The dried microspheres had a dens-ity of about 60 kg/m3.
2c) Instead of 2H-heptafluoropropane 30 parts of l,1-di-chloro-2,2,2-trifluoroetha~e were used. The dried micro-spheres had a density of about 100 kg/m3.
Example 3 For evaluation of the heat insulation capacity of products produced from microspheres according to the invention a plate having the dimenslons 300x~00x20 rnm was produced. This was produced by spreading dry unexpanded microspheres, prepared according to Example 1, in a mould which was then sealed and placed in an oven where it was allowed to stand during ~5 minutes at a temperature of 135C. The obtained plate had a density o~ 40 kg/m3. The heat conductivity was measured to 0.0235 ~/mC. For a plate produced in the same manner from microspheres containing isobutane as the blowing agent the measured heat conduct-ivi-ty was 0.0275 W/mC. A clearly improved insulation capability was thus obtained with microspheres according to the invention containing 2H-heptafluoropropane as blowing agent.
The expandable spheres are expanded by heating to a temperature which gives rise to softening of the polymer shell and volatilization of the propellant whereby the particles expand to a diameter substantially larger than the diameter for the unexpanded particles and the expansion can be carried out in per se known manners. The spheres can for example be dried and expanded by dispersing the un-expanded spheres in an inert liquid, atomization of the dispersion and bringing this in contact with a warm inert gas stream. Another suitable manner for expansion is disclosed in the European patent applicatlon 03~8372.
According to this process the expandable microspheres are first dried to a certain dry content and then expanded by heating, eg by IR-heating. The expansion temperature is set by the boiling point of the blowing agent and the softening point of the shell-polymer and is usually within the range of from about 70C to about 140C. It has been found that the blowing agents used according to the present invention give at least as good expansion as the commercially used blowing agents isobutane and isopentane and thereby give expanded microspheres with about the same densities as those which are commercially acceptable. ThiS is in con-trast to chlorofluorocarbons and chlorofluorohydrocarbonswhich give substantially inferior expansion, which is believed to be due to their interference at the polymer-isation, and expanded microspheres which have densities about 3 to about 7 times higher than when isobutane or isopentane is used. Compared with isobutane and isopentane 2H-heptafluoropropane, for example, is also advantageous since it is non-combustible which is of importance both at the production and the use of the microspheres. Since the .
:
2 1~ ~ ~ 9 ~ ~
compounds are non-combustible problems with dust explosions in connection with drying of expandable as well as o~
expanded spheres are reduced. ~nother advantage in com-parison with isobutane and isopentane is that for example 2H-heptafluoropropane has substantially lower thermal conductivity which broadens the fields of application for the microspheres. Compared with chlorofluorocarbons the present fluorocarbons and fluorohydrocarbons are also advantageous since they do not have any ozone degrading effect.
Expandable and expanded thermoplastic microspheres have a large number of applications. The use of unexpanded microspheres is based on the expansion capability of the spheres and they are then expanded in situ in the mate-rials in which they are incorporated when these materialsare heated. As some examples of such use can be mentioned printing inks for the production of relief print on paper and textiles, fillers in paper and board and Eoaming of Eor example PVC-plastisol. At the use of expanded microspheres the low densit~ and filling effect of the spheres are utilized and they can for example be used as fillers in paints, putty, polymers and resins such as polyester, polyurethane, epoxy resins, composite materials based on polymers, paper, insulation materials etc.. The micro-spheres of the present invention can be used for the samepurposes for which microspheres are generally used. The present microspheres are particularly suitable for use in products for which fire resistance and thermal insulating capacity are of importance since the microspheres are advantageous in such applications since they contain chlorine-free fluorocarbons and fluorohydrocarbons, such as 2H-heptafluoropropane, which are non-combustible and which have low thermal conductivity. The present invention thus also relates to use of the microspheres in fire-resistant paints and in insulation materials. In fire-resistant paints the microspheres are used as fillers/`additives. The unexpanded microspheres are advantageously used in fire-resistant paints since they expand at heating and thereby 2 ~
give an insulating layer which protects the substrate. When the temperature becomes so high that the microspheres break the non-combustible blowing agent is released and the fire is retarded. As concerns insulation materials the entire product can be made up from microspheres, for economical reasons the microspheres are, however, also in this application as a rule used as ~illers/additives. As examples of insulation materials wherein the microspheres can be used are jointing compounds for, among other things, cable entries, where good insulation and fire-resistant properties are desired.
The invention is further illustrated in the following examples which, however, are not intended to limit the same. Parts and per cent relate to parts by weight and per cent by weight respectively, unless otherwise stated~
xample 1 125 parts of water were mixed with 5.5 parts of 1 molar NaOH-solution and 10 parts oE 10~ acetic aclcl solu-tion, 6 parts of 40% colloidal sillclc acld, 0.5 parts of a condensation product of diethanolamlne and adipic acid and 0.5 parts of dicetyl peroxydicarbo~ate and charged to a 15 1 reactor e~uipped with stirrer. The reactor was sealed and evacuated. A mixture of 0.3 parts of divinylbenzene, 7 parts of methylmethacrylate, 32 parts of acrylonitrile, 32 parts of vinylidene chloride and 29 parts of 2H-hepta-fluoropropane were then charged. The polymerisation mixture was stirred at 850 rpm during 60 minutes. After homogeniz-ation the rotation speed was lowered to 400 rpm and the mixture was then heated to 55C and polymerized at this temperature for 8 hours. The obtained polymerisate was washed and dewatered. The unexpanded microspheres had an average particle size, by weight, of 16 ~m. The micro-spheres were dried and their expansion capacity was invest-igated by means of thermomechanical analysis. They were found to have the same expansion capacity and temperature resistance as if isobutane or isopentane had been used, ie a density of about 17 kg/m3 was reached.
2 0 ~ 0 ~
Comparative Exam~les 2a) - 2c) The process according to ~xample 1 was repeated with other blowing agents.
2a) Instead of 2H-heptafluoropropane 12 parts of isopentane were used. The dried microspheres had a density below 20 kg/m3.
2b) Instead of 2~-heptafluoropropane 30 parts of trichloro-fluoromethane were used. The dried microspheres had a dens-ity of about 60 kg/m3.
2c) Instead of 2H-heptafluoropropane 30 parts of l,1-di-chloro-2,2,2-trifluoroetha~e were used. The dried micro-spheres had a density of about 100 kg/m3.
Example 3 For evaluation of the heat insulation capacity of products produced from microspheres according to the invention a plate having the dimenslons 300x~00x20 rnm was produced. This was produced by spreading dry unexpanded microspheres, prepared according to Example 1, in a mould which was then sealed and placed in an oven where it was allowed to stand during ~5 minutes at a temperature of 135C. The obtained plate had a density o~ 40 kg/m3. The heat conductivity was measured to 0.0235 ~/mC. For a plate produced in the same manner from microspheres containing isobutane as the blowing agent the measured heat conduct-ivi-ty was 0.0275 W/mC. A clearly improved insulation capability was thus obtained with microspheres according to the invention containing 2H-heptafluoropropane as blowing agent.
Claims (14)
1. Thermoplastic microspheres having a shell of polymerized ethylenically unsaturated monomer or mixture of ethylenically unsaturated monomers which encapsulates a blowing agent, characterized in that the blowing agent comprises a chlorine-free aliphatic fluorocarbon or fluoro-hydrocarbon.
2. Microspheres according to claim 1, characterized in that the microspheres are unexpanded and contain the chlorine-free aliphatic fluorocarbon or fluorohydrocarbon in liquid form.
3. Microspheres according to claim 1, characterized in that the microspheres are expanded and contain the chlorine-free aliphatic fluorocarbon or fluorohydrocarbon in gas form.
4. Microspheres according to any of the preceding claims, characterized in that the chlorine-free aliphatic fluorocarbon or fluorohydrocarbon has a boiling point of not lower than -40°C.
5. Microspheres according to claim 4, characterized in that the chlorine-free aliphatic fluorocarbon or fluoro-hydrocarbon is 2H-heptafluoropropane.
6. Microspheres according to any of the preceding claims, characterized in that the entire amount of blowing agent is a chlorine-free aliphatic fluorocarbon or fluoro-hydrocarbon.
7. Microspheres according to any of claims 1 to 5, characterized in that the blowing agent is made up from chlorine-free aliphatic fluorocarbon or fluorohydrocarbon in combination with not more than 50% by weight of a blowing agent selected from the group n-butane, isobutane, isopentane and neopentane.
8. Microspheres according to any of the preceding claims, characterized in that the shell is based on a copolymer of acrylonitrile with vinylidene chloride and/or methyl methacrylate and/or methacrylonitrile.
9. A process for the production of thermoplastic microspheres by polymerisation of an ethylenically un-saturated monomer or a mixture of ethylenically unsaturated monomers in aqueous suspension in the presence of a blowing agent, characterized in that the blowing agent comprises a chlorine-free aliphatic fluorocarbon or fluorohydrocarbon.
10. A process according to claim 9, characterized in that the chlorine-free aliphatic fluorocarbon or fluoro-hydrocarbon has a boiling point of not lower than -40°C.
11. A. process according to claim 10, characterized in that the chlorine-free aliphatic fluorocarbon or fluoro-hydrocarbon is 2H-heptafluoropropane.
12. Use of expandable or expanded thermoplastic microspheres having a shell of polymerized ethylenically unsaturated monomer or mixture of ethylenically unsaturated monomers which encapsulates a blowing agent comprising a chlorine-free aliphatic fluorocarbon or fluorohydrocarbon in fire-resistant paints and insulation materials.
13. Use according to claim 12, whereby the chlorine-free aliphatic fluorocarbon or fluorohydrocarbon in the microspheres is 2H-heptafluoropropane.
14. Use according to claim 12 or 13, whereby the whole amount of blowing agent is made up from chlorine-free aliphatic fluorocarbon or fluorohydrocarbon.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE9200704A SE9200704L (en) | 1992-03-06 | 1992-03-06 | Thermoplastic microspheres, process for their preparation and use of the microspheres |
| SE9200704-6 | 1992-03-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2090905A1 true CA2090905A1 (en) | 1993-09-07 |
Family
ID=20385547
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002090905A Abandoned CA2090905A1 (en) | 1992-03-06 | 1993-03-03 | Thermoplastic microspheres, process for their preparation and use of the microspheres |
Country Status (6)
| Country | Link |
|---|---|
| EP (1) | EP0559254A1 (en) |
| JP (1) | JPH0649260A (en) |
| KR (1) | KR930019739A (en) |
| AU (1) | AU641101B1 (en) |
| CA (1) | CA2090905A1 (en) |
| SE (1) | SE9200704L (en) |
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| SE510857C2 (en) * | 1994-11-14 | 1999-06-28 | Casco Products Ab | Coating composition based on polyvinyl chloride plastisol containing thermoplastic microspheres |
| US6559213B2 (en) | 1995-03-16 | 2003-05-06 | Henkel-Teroson Gmbh | Plastisol composition |
| CN1104266C (en) * | 1995-11-10 | 2003-04-02 | 特瑞托恩研究和发展有限公司 | Ball and manufacture thereof |
| US5786095A (en) * | 1996-07-03 | 1998-07-28 | H.B. Fuller Licensing & Financing, Inc. | Inorganic based intumescent system |
| US6919111B2 (en) | 1997-02-26 | 2005-07-19 | Fort James Corporation | Coated paperboards and paperboard containers having improved tactile and bulk insulation properties |
| SE513860C2 (en) * | 1998-01-16 | 2000-11-20 | Glasis Holding Ab | Fire-resistant board and method of making it |
| DE69920664T3 (en) * | 1998-01-26 | 2008-09-25 | Kureha Corp. | EXPANDABLE MICROBALLETS AND MANUFACTURING METHOD THEREFOR |
| JP4291510B2 (en) | 1998-03-13 | 2009-07-08 | 松本油脂製薬株式会社 | Thermally expandable microcapsules and methods of use |
| DE19812123A1 (en) * | 1998-03-19 | 1999-09-30 | Blanco Gmbh & Co Kg | Casting compounds for the production of sanitary molded parts with more than one visible side |
| AUPQ118399A0 (en) * | 1999-06-24 | 1999-07-22 | Selleys Pty Limited | Novel composition container apparatus and process |
| JP2002120510A (en) * | 2000-07-27 | 2002-04-23 | Bridgestone Corp | Safe tire, complex and expandable composition used for it, and manufacturing method of safe tire |
| DE10130888A1 (en) | 2001-06-27 | 2003-01-30 | Henkel Teroson Gmbh | Adhesion promoter for plastisols |
| DE10239631A1 (en) * | 2002-08-23 | 2004-03-04 | Carcoustics Tech Center Gmbh | Insulating structural part for heat and noise insulation, has fire resistant coating, ceramic adhesive, expandable microhollow ceramic spheres and heat expanding propellant |
| JP2004155999A (en) * | 2002-11-08 | 2004-06-03 | Sekisui Chem Co Ltd | Thermally expandable microcapsule |
| TWI299101B (en) * | 2003-01-30 | 2008-07-21 | Sipix Imaging Inc | High performance capsules for electrophoretic displays |
| EP1598405B1 (en) * | 2003-02-24 | 2014-10-01 | Matsumoto Yushi-Seiyaku Co., Ltd. | Thermoexpansible microsphere, process for producing the same and method of use thereof |
| US6872761B2 (en) | 2003-04-24 | 2005-03-29 | Henkel Kommanditgesellschaft Auf Aktien | Compositions for acoustic-damping coatings |
| MX2007011113A (en) * | 2005-03-11 | 2007-11-15 | Int Paper Co | Compositions containing expandable microspheres and an ionic compound, as well as methods of making and using the same. |
| DE102005017912A1 (en) | 2005-04-18 | 2006-10-19 | Henkel Kgaa | Low temperature hardening of 1-component polyurethane adhesives or sealants for bonding plastics especially in headlamp manufacture involves exposure to microwave irradiation |
| DE102006014190A1 (en) | 2006-03-24 | 2007-09-27 | Henkel Kgaa | Single component, hot-setting reactive composition, useful e.g. as an adhesive in automobile construction, comprises e.g. a liquid polyene, a block copolymer with a polyene block and a saturated block and/or a vulcanization system |
| DE102006016577A1 (en) | 2006-04-06 | 2007-10-11 | Henkel Kgaa | Adhesives / sealants based on liquid rubbers |
| EP2151456B1 (en) * | 2007-05-21 | 2012-07-11 | Matsumoto Yushi-Seiyaku CO., LTD. | Process for production of thermally expandable beads and application thereof |
| NZ714911A (en) | 2013-05-07 | 2020-09-25 | Xflam Pty Ltd | Processes for preparing foam composites |
| AU2014262384B2 (en) * | 2013-05-07 | 2017-06-29 | Xflam Pty Ltd | Foam composites |
| DE202013103055U1 (en) | 2013-07-10 | 2014-10-13 | Heimbach Gmbh & Co. Kg | The paper machine belt |
| DE102013226505A1 (en) | 2013-12-18 | 2015-06-18 | Henkel Ag & Co. Kgaa | Thermosetting rubber compositions with plastisol-like flow behavior |
| US10486128B2 (en) * | 2015-03-05 | 2019-11-26 | Matsumoto Yushi-Seiyaku Co., Ltd. | Heat-expandable microspheres and application thereof |
| CN105218714A (en) * | 2015-10-30 | 2016-01-06 | 浙江中天氟硅材料有限公司 | A kind of flame retardant microcapsule and its preparation method and application |
| EP3587465A1 (en) | 2018-06-27 | 2020-01-01 | Solvay Sa | Process for the preparation of a polyurethane foam |
| EP3696225B1 (en) | 2019-02-18 | 2021-11-10 | Eftec Nv | Plastisol composition suitable for sealing of metal parts |
| CN109989207A (en) * | 2019-04-15 | 2019-07-09 | 无锡市信文机械制造有限公司 | A kind of compound forming machine baking oven of Balance route temperature |
| EP3950800A1 (en) | 2020-08-03 | 2022-02-09 | Henkel AG & Co. KGaA | Improved corrosion resistance in rubber-based adhesives and sealants |
| WO2023007853A1 (en) * | 2021-07-29 | 2023-02-02 | 松本油脂製薬株式会社 | Thermally expandable microspheres, composition, and shaped body |
| CN116179137B (en) * | 2023-03-06 | 2023-10-13 | 广东德聚技术股份有限公司 | Low-water vapor transmittance moisture-curable polyurethane hot melt adhesive |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3615972A (en) * | 1967-04-28 | 1971-10-26 | Dow Chemical Co | Expansible thermoplastic polymer particles containing volatile fluid foaming agent and method of foaming the same |
| JPS59173132A (en) * | 1983-03-22 | 1984-10-01 | Matsumoto Yushi Seiyaku Kk | Solvent-resistant heat expansive microcapsule |
| US4563481A (en) * | 1984-07-25 | 1986-01-07 | The Dow Chemical Company | Expandable synthetic resinous thermoplastic particles, method for the preparation thereof and the application therefor |
| JPH03223346A (en) * | 1990-01-30 | 1991-10-02 | Asahi Chem Ind Co Ltd | Preparation of expandable vinylidene chloride resin particle |
| JPH03225182A (en) * | 1990-01-30 | 1991-10-04 | Asahi Chem Ind Co Ltd | Heat insulating material for refrigerator |
-
1992
- 1992-03-06 SE SE9200704A patent/SE9200704L/en not_active Application Discontinuation
-
1993
- 1993-02-05 EP EP93200325A patent/EP0559254A1/en not_active Withdrawn
- 1993-02-23 KR KR1019930002464A patent/KR930019739A/en not_active Application Discontinuation
- 1993-02-25 AU AU33775/93A patent/AU641101B1/en not_active Ceased
- 1993-03-03 CA CA002090905A patent/CA2090905A1/en not_active Abandoned
- 1993-03-04 JP JP5067313A patent/JPH0649260A/en active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| SE9200704L (en) | 1993-09-07 |
| AU641101B1 (en) | 1993-09-09 |
| JPH0649260A (en) | 1994-02-22 |
| EP0559254A1 (en) | 1993-09-08 |
| SE9200704D0 (en) | 1992-03-06 |
| KR930019739A (en) | 1993-10-18 |
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