GB2083099A - A shaped form or formed mass of microspheres - Google Patents
A shaped form or formed mass of microspheres Download PDFInfo
- Publication number
- GB2083099A GB2083099A GB8127635A GB8127635A GB2083099A GB 2083099 A GB2083099 A GB 2083099A GB 8127635 A GB8127635 A GB 8127635A GB 8127635 A GB8127635 A GB 8127635A GB 2083099 A GB2083099 A GB 2083099A
- Authority
- GB
- United Kingdom
- Prior art keywords
- microspheres
- plastic
- microns
- shaped form
- diameter
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
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- 229910052787 antimony Inorganic materials 0.000 description 1
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- 239000010425 asbestos Substances 0.000 description 1
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Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16L—PIPES; JOINTS OR FITTINGS FOR PIPES; SUPPORTS FOR PIPES, CABLES OR PROTECTIVE TUBING; MEANS FOR THERMAL INSULATION IN GENERAL
- F16L59/00—Thermal insulation in general
- F16L59/08—Means for preventing radiation, e.g. with metal foil
-
- 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
- B01J13/20—After-treatment of capsule walls, e.g. hardening
- B01J13/22—Coating
-
- 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
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/28—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties
-
- 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
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/50—Catalysts, in general, characterised by their form or physical properties characterised by their shape or configuration
- B01J35/51—Spheres
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C49/00—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor
- B29C49/0042—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor without using a mould
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C49/00—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor
- B29C49/42—Component parts, details or accessories; Auxiliary operations
- B29C49/46—Component parts, details or accessories; Auxiliary operations characterised by using particular environment or blow fluids other than air
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C70/00—Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts
- B29C70/58—Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts comprising fillers only, e.g. particles, powder, beads, flakes, spheres
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- C03—GLASS; MINERAL OR SLAG WOOL
- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B19/00—Other methods of shaping glass
- C03B19/10—Forming beads
- C03B19/107—Forming hollow beads
- C03B19/1075—Forming hollow beads by blowing, pressing, centrifuging, rolling or dripping
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- C—CHEMISTRY; METALLURGY
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- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B37/00—Manufacture or treatment of flakes, fibres, or filaments from softened glass, minerals, or slags
- C03B37/01—Manufacture of glass fibres or filaments
- C03B37/02—Manufacture of glass fibres or filaments by drawing or extruding, e.g. direct drawing of molten glass from nozzles; Cooling fins therefor
- C03B37/022—Manufacture of glass fibres or filaments by drawing or extruding, e.g. direct drawing of molten glass from nozzles; Cooling fins therefor from molten glass in which the resultant product consists of different sorts of glass or is characterised by shape, e.g. hollow fibres, undulated fibres, fibres presenting a rough surface
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B14/00—Use of inorganic materials as fillers, e.g. pigments, for mortars, concrete or artificial stone; Treatment of inorganic materials specially adapted to enhance their filling properties in mortars, concrete or artificial stone
- C04B14/02—Granular materials, e.g. microballoons
- C04B14/04—Silica-rich materials; Silicates
- C04B14/22—Glass ; Devitrified glass
- C04B14/24—Glass ; Devitrified glass porous, e.g. foamed glass
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B20/00—Use of materials as fillers for mortars, concrete or artificial stone according to more than one of groups C04B14/00 - C04B18/00 and characterised by shape or grain distribution; Treatment of materials according to more than one of the groups C04B14/00 - C04B18/00 specially adapted to enhance their filling properties in mortars, concrete or artificial stone; Expanding or defibrillating materials
- C04B20/10—Coating or impregnating
- C04B20/1055—Coating or impregnating with inorganic materials
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- 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
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16L—PIPES; JOINTS OR FITTINGS FOR PIPES; SUPPORTS FOR PIPES, CABLES OR PROTECTIVE TUBING; MEANS FOR THERMAL INSULATION IN GENERAL
- F16L59/00—Thermal insulation in general
- F16L59/06—Arrangements using an air layer or vacuum
- F16L59/065—Arrangements using an air layer or vacuum using vacuum
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F24—HEATING; RANGES; VENTILATING
- F24S—SOLAR HEAT COLLECTORS; SOLAR HEAT SYSTEMS
- F24S80/00—Details, accessories or component parts of solar heat collectors not provided for in groups F24S10/00-F24S70/00
- F24S80/50—Elements for transmitting incoming solar rays and preventing outgoing heat radiation; Transparent coverings
- F24S80/52—Elements for transmitting incoming solar rays and preventing outgoing heat radiation; Transparent coverings characterised by the material
- F24S80/525—Elements for transmitting incoming solar rays and preventing outgoing heat radiation; Transparent coverings characterised by the material made of plastics
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F24—HEATING; RANGES; VENTILATING
- F24S—SOLAR HEAT COLLECTORS; SOLAR HEAT SYSTEMS
- F24S80/00—Details, accessories or component parts of solar heat collectors not provided for in groups F24S10/00-F24S70/00
- F24S80/50—Elements for transmitting incoming solar rays and preventing outgoing heat radiation; Transparent coverings
- F24S80/56—Elements for transmitting incoming solar rays and preventing outgoing heat radiation; Transparent coverings characterised by means for preventing heat loss
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C49/00—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor
- B29C49/42—Component parts, details or accessories; Auxiliary operations
- B29C49/46—Component parts, details or accessories; Auxiliary operations characterised by using particular environment or blow fluids other than air
- B29C2049/4602—Blowing fluids
- B29C2049/4605—Blowing fluids containing an inert gas, e.g. helium
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C49/00—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor
- B29C49/42—Component parts, details or accessories; Auxiliary operations
- B29C49/46—Component parts, details or accessories; Auxiliary operations characterised by using particular environment or blow fluids other than air
- B29C2049/4602—Blowing fluids
- B29C2049/4605—Blowing fluids containing an inert gas, e.g. helium
- B29C2049/4608—Nitrogen
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C49/00—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor
- B29C49/42—Component parts, details or accessories; Auxiliary operations
- B29C49/46—Component parts, details or accessories; Auxiliary operations characterised by using particular environment or blow fluids other than air
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
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- B29C49/00—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor
- B29C49/42—Component parts, details or accessories; Auxiliary operations
- B29C49/46—Component parts, details or accessories; Auxiliary operations characterised by using particular environment or blow fluids other than air
- B29C2049/4602—Blowing fluids
- B29C2049/465—Blowing fluids being incompressible
- B29C2049/4655—Blowing fluids being incompressible water
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C49/00—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor
- B29C49/42—Component parts, details or accessories; Auxiliary operations
- B29C49/46—Component parts, details or accessories; Auxiliary operations characterised by using particular environment or blow fluids other than air
- B29C2049/4602—Blowing fluids
- B29C2049/465—Blowing fluids being incompressible
- B29C2049/4664—Blowing fluids being incompressible staying in the final article
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2105/00—Condition, form or state of moulded material or of the material to be shaped
- B29K2105/06—Condition, form or state of moulded material or of the material to be shaped containing reinforcements, fillers or inserts
- B29K2105/16—Fillers
- B29K2105/165—Hollow fillers, e.g. microballoons or expanded particles
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- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B2203/00—Fibre product details, e.g. structure, shape
- C03B2203/10—Internal structure or shape details
- C03B2203/14—Non-solid, i.e. hollow products, e.g. hollow clad or with core-clad interface
- C03B2203/16—Hollow core
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/40—Solar thermal energy, e.g. solar towers
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- Ceramic Engineering (AREA)
- Physics & Mathematics (AREA)
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- Structural Engineering (AREA)
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- Polymers & Plastics (AREA)
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Description
1
SPECIFICATION
A shaped form or formed mass including microspheres The present invention relates to a shaped or formed mass including hollow microspheres made from organic film forming materials. Such a shaped or formed mass is useful in making panels, wall- board etcetera, having good thermal insulation properties.
In accordance with the present invention, there is provided a shaped form or formed mass of cemented or bonded together hollow organic film forming material microspheres having a diameter of 200 to 10,000 microns and having a wall thickness of 0.1 to 1,000 microns, wherein said microspheres are free of latent solid or liquid blowing gas materials or gases and the walls of said microspheres are sub- stantially free of holes, relatively thinned wall portions or sections and bubbles.
In the present Specification, the term -organic film forming material" is to be understood to include natural and synthetic resins and synthetic plastics materials which are capable of forming a film.
Also in accordance with the invention, there is provided a shaped form or formed mass of cemented or bonded together filamented, hollow organic film forming material microspheres having a diameter of 500 to 6000 microns and having a wall thickness of 0.5 to 400 microns, wherein said microspheres are connected to each other by filament portions which are continuous with the microspheres and are of the same organic film forming material from which the microspheres are made.
Such hollow plastic microspheres may have a thin reflecitve metal coating deposited on the inner wall surface of the microsphere.
The shaped or formed mass may be used in the manufacture of improved insulation materials for use in construction of homes, factories and office buildings and in the manufacture of products in which heat barriers are desired or necessary.
As stated, thin plastics filaments may connect adj- acent microspheres.
The hollow microspheres described herein, depending on their diameter and theirwall thickness and the particular composition from which they are made, are capable of withstanding relatively high external pressures andlor weight. Hollow plastic microspheres can be made that are resistant to relatively high temperatures and stable to many chemical agents and weathering conditions. These characteristics make the microspheres suitable for a wide variety of uses.
In recent years the substantial increases in costs of basic materials such as plastics, cement, asphalt and the like has encouraged development and use of filler materials to reduce the amount and cost of the basic materials used and the weight of the finished materials.
The substantial increases in the energy costs of heating and cooling has encouraged the development of new and better insulation materials and many new insulation materials and insulating sys- GB 2 083 099 A 1 tems using the new materials have been developed in an attempt to satisfy these needs.
One of the newly suggested filler materials and insulating materials utilizes hollow plastic micros- pheres. The known methods for producing hollow plastic microspheres, however, have not been successful in producing microspheres of uniform size or uniform thin walls which makes it very difficult to produce filler and insulation materials of controlled and predictable physical and chemical characteristics and quality. Also, the relatively high cost and the relatively small size of the prior art microspheres has limited their use.
One of the existing methods of producing hollow plastic microspheres, for example, as disclosed in the Veatch et ai U.S. Patent 2,797,201, is to disperse a liquid or solid gas-phase precursor material in a plastic material to be blown to form the microspheres. The plastic material containing the solid or liquid gas-phase precursor enclosed therein is then heated to convert the solid or liquid gas-phase precursor material into a gas and is further heated to expand the gas and produce the hollow plastic microsphere containing there in the expanded gas. This process is, understandably, difficult to control and inherently produces plastic microspheres of random size and wall thickness, microspheres with walls that have sections or portions of the walls that are relatively thin, walls that have holes, small trapped bub- bles, trapped or dissolved solvents or gases, any one or more of which will result in a substantial weakening of the microspheres, and a substantial proportion of the microspheres which are not suitable for use and must be scrapped or recycled.
Further, the use of conventional fiberglass insulation is being questioned in the light of the recently discovered possibility that fiberglass of certain particle size may be carcinogenic in the same or similar manner as asbestos. The use of polyurethane foams, urea-formaldehyde foams and polystyrene foams as insulating materials have recently been criticized because of their dimensional and chemical instability, for example, a tendency to shrink and to evolve the blowing gases such as Freon and to evolve unreacted gases such as formaldehyde.
In addition, in some applications, the use of low density microspheres presents a serious problem because they are difficult to handle since they are readily eluriated and tend to blow about. In situa- tions of this type, the filamented microspheres of the present invention provide a convenient and safe method of handling the microspheres.
Thus, the known methods for producing hollow plastic microspheres have therefore not been suc- cessful in producing microspheres of uniform size or uniform thin walls or in producing hollow plastic microspheres of controlled and predictable physical and chemical characteristics, quality and strength or at low cost.
The hollow plastics microspheres specifically disclosed herein are made by forming a liquid film of thermoplastic or thermosetting plastic composition across a coaxial blowing nozzle, applying a gas or a gas containing dispersed metal particles andlor a gaseous organo metal compound at a positive pres- 2 sure to the inner surface of the plastic film to blow the film and form an elongated cylinder shaped liquid film of plastic which is closed at its outer end. A balancing gas pressure is provided in the area of the blowing nozzle into which the elongated cylinder shaped liquid plastic film is blown.
A transverse jet is used to direct an entraining fluid over and around the blowing nozzle at an angle to the axis of the blowing nozzle. The entraining fluid as it passes over and around the blowing nozzle and the elongated cylinder fluid dynamically induces a pulsating or fluctuating pressure field at the opposite or lee side of the blowing nozzle in the wake or shadow of the blowing nozzle. The fluctuating pressure field has regular periodic oscillations similar to those of a flag flapping in a breeze. The transverse jet entraining fluid can also be pulsed at regular intervals to assist in controlling the size of the microspheres and in separating the microspheres from the blowing nozzle and the distance or spacing between microspheres. The entraining fluid envelops and acts asymmetrically on the elongated cylinder and causes the cylinderto flap, fold, pinch and close-off at its inner end at a point proximate to the coaxial blowing nozzle. The continued movement of the entraining fluid over the elongated cylinder produces asymmetric fluid drag forces on the cylinder and closes and detaches the elongated cylinder from the coaxial blowing nozzle to have it fall from the blowing nozzle. The surface tension forces of the plastic act on the entrained elongated cylinder and cause the cylinder to seek a minimum surface area and to form a spherical shape.
Quench nozzles where the plastic is thermoplastic and heating nozzles where the plastic is thermosetting are disposed below and on either side of the blowing nozzle and direct cooling or heating fluid at and into contact with the plastic microspheres to rapidly cool or heat and cure and solidify the plastic and form a harden, smooth hollow plastic microsphere. Where a thermosetting plastic is used, the microspheres are heated and cured and the cured plastic microspheres can be subsequently cooled.
The microspheres can be made from a low heat conductivity plastic composition and can contain a low heat conductivity gas. The microspheres, can also be made to contain a thin metal coating deposited on the inner wall surface of the microspheres. The metal coating, depending on its thickness, can be transparent or reflective. The use of a reflective metal coating improves the insulating and heat reflecting characteristics of the microspheres.
The plastics microspheres disclosed. herein can be used to form a heat barrier by using them to fill void spaces between existing walls or other spaces and by forming them into sheets or other shaped forms to be used as insulation barriers. When used to form insulation barriers, the interstices between the microspheres can be filled with a low heat conductivity gas, a foam or other material all of which increase the heat insulation characteristics of the materials made from the microspheres.
In one embodiment of the invention, the microspheres are coated with an adhesive or foam filler and flattened to an oblate spheroid or a generally cellular 130 GB 2 083 099 A 2 shape. The microspheres are held in the flattened position until the adhesive hardens andlor cures after which the microspheres retain their flattened shape. The use of the flattened microspheres sub- stantially reduces the volume of the interstices between the microspheres and significantly improves the thermal insulating characteristics of the microspheres.
The microspheres can be made from plastics compositions selected for their desired optical and chemical properties and for the particular gaseous material to be contained therein.
Where a gas containing dispersed metal particles is used to blow the microspheres, a metal layer is deposited on the innerwall surface of the microsphere as a thin metal coating. Where a gaseous organo metal compound is used to deposit the metal layers, a gaseous organo metal compound is used as orwith the blowing gas to blow the microspheres.
The organo metal compound can be decomposed just priorto blowing the microspheres or afterthe microspheres are formed by, for example, subjecting the blowing gas or the microspheres to heat andlor an electrical discharge.
The filamented microspheres are made in a manner such that they are connected or attached to each other by a thin continuous plastic filament. The fi lamented microspheres can be flattened to produce the oblate spheroids. The filaments interrupt and reduce the area of wall to wall contact between the microspheres and reduce the thermal conductivity between the walls of the microspheres. The filamented microspheres also assist in handling and preventing scattering of microspheres, particularly where very small diameter microspheres or low density microspheres are produced. The fi lamented microspheres have a distinct advantage over the simple addition of filaments in that the continuous filaments do not tend to settle in the systems in which they are used.
The present invention overcomes many of the problems associated with prior attempts to produce hollow plastic microspheres. The process and apparatus of the present invention allows the pro- duction of hollow plastic microspheres having predetermined characteristics such that improved filler materials and insulating materials and insulating systems can be designed, manufactured and tailor made to suit a particular desired use. The diameter and wall thickness uniformity, and the thermal, strength and chemical resistance characteristics of the plastic rnicrospheres can be determined by carefully selecting the plastic and constituents of the plastic composition and controlling the blowing gas pressure and temperature, and the temperature, viscosity and thickness of the liquid plastic film f rom which the microspheres are formed. The inner vorume of the microspheres may contain an inert low heat conductivity gas used to blow the microsphere.
The hollow plastic microspheres of the present invention can have a transparent metal coating deposited on the inner wall surface thereof which allows visual light to pass,through the microspheres but reflects and traps infrared radiations. The hollow plastic microspheres can also have a low emissivity - 4 3 reflective metal coating deposited on the inner wal I surface of the microsphere which effectively reflects visual light and radiant heat energy.
The process and apparatus of the present inven- tion provide a practical and economical means by which hollow plastic microspheres having a high heat insulation efficiency can be utilized to prepare a relatively low cost efficient insulating material for common every day uses. The present invention also allows the economic production of hollow plastic microspheres from plastic compositions which incorporates a metallic radiation barrier and can be used as an insulation material.
The process and apparatus of the present inven tion, as compared to the prior art processes of using a latent liquid or solid blowing agent, can be conducted at higher temperatures since there is no included expandible andlor decomposable blowing agent used. The ability to use higher blowing temp- eratures results in for particular plastic compositions a lower viscosity for the plastic composition which allows surface tension forces to produce significantly greater uniformity in wall thickness, sphericity and diameter of the microspheres produced.
The present invention also allows the use of a wide variety of blowing gases andlor blowing gas materials. In accordance with the present invention, a wide variety of gaseous material blowing gas can be encapsulated, i.e. it is no longer required to use a latent liquid or solid blowing agent as the blowing gas.
The apparatus and process of the present inven tion provide for the production of hollow plastic mic rospheres at economic prices and in large quantities.
The process and apparatus of the present invention allows the production of hollow plastic micros pheres having predetermined diameters, wall thick nesses, strength and resistance to chemical agents and weathering and gas permeability such that superior systems can be designed, manufactured and tailor made to suit a particular desired use.
The present invention as illustrated in the attached drawings represent exemplary forms of the method and apparatus for making microspheres for use in and as filler materials and for use in and as insulat ing materials.
The Figure 1 of the drawings shows in cross section an apparatus having multiple coaxial blow ing nozzle means for supplying the gaseous material for blowing hollow plastic microspheres, a trans- 115 verse jet providing an entraining fluid to assist in the formation and detachment of the microspheres from the blowing nozzles, and means for supplying a quench or heating fluid to cool or heat the micros pheres. 120 The Figure 2 of the drawings is an enlarged detailed cross-section of the nozzle means of apparatus shown in Figure 1.
The Figure 3 of the drawings is a detailed cross section of a modified form of the nozzle means shown in Figure 2 in which the lower end of the nozzle means is tapered inwardly.
The Figure 3a of the drawings is a detailed cross section of a modified transverse jet entraining means having a flattened orifice opening and the GB 2 083 099 A 3 Figure 3 nozzle means.
The Figure 3b of the drawings is a top plane view of the modified transverse jet entraining means and the nozzle means illustrated in Figure 3a of the draw- ings.
The Figure 3c of the drawings illustrates the use of the apparatus of Figure 3b to make filamented hollow plastic microspheres.
The Figure 4 of the drawings is a detailed cross- section of a modified form of the nozzle means shown in Figure 2 in which the lower portion of the nozzle is enlarged.
The Figure 5 of the drawings shows a crosssection of an end view of a flat plate solar energy collector using the hollow plastic microspheres of the present invention.
The Figure 6 of the drawings shows a crosssection of an end view of a tubular solar energy collector using the hollow plastic microspheres of the present invention.
The Figure 7 of the drawings shows a crosssection of spherical shaped hollow plastic microspheres made into a formed panel.
The Figure 7a of the drawings shows a cross- section of oblate spheroid shaped hollow plastic microspheres made into a formed panel.
The Figure 7b of the drawings shows a crosssection of oblate spheroid shaped hollow plastic filamented microspheres made into a formed panel in which the filaments interrupt the microsphere wall to wall contact.
The invention will be described with reference to the accompanying Figures of the drawings wherein like numbers designate like parts throughoutthe several views.
Referring to Figures 1 and 2 of the drawings, there is illustrated a vessel 1, made of suitable container material heated, as necessary, by means not shown for holding a liquid plastic 2. The bottom floor 3 of vessel 1 contains a plurality of openings 4 through which liquid plastic 2 is fed to coaxial blowing nozzles 5. The coaxial blowing nozzle 5 can be made separately or can be formed by a downward extension of the bottom 3 of vessel 1. The coaxial blowing nozzle 5 consists of an inner nozzle 6 having an orifice 6a for a blowing gas and an outer nozzle 7 having an orifice 7a for liquid plastic. The inner nozzle 6 is disposed within and coaxial to outer nozzle 7 to form annular space 8 between nozzles 6 and 7, which annular space provides a flow path for liquid plastic. The orifice 6a of inner nozzle 6 terminates at or a short distance above the plane of orifice 7a of outer nozzle 7.
The liquid plastic 2 at about atmospheric pressure or at elevated pressure flows downwardly through annular space 8 and fills the area between orifice 6a and 7a. The surface tension forces in the liquid plastic 2 from a thin liquid plastic film 9 across orifices 6a and 7a.
A blowing gas 10 andlor blowing gas containing dispersed metal particles, which is at or below ambient temperature or which is heated by means not shown to about the temperature of the liquid plastic and which is at a pressure above the liquid plastic pressure at the blowing nozzle, is fed through 4 GB 2 083 099 A 4 distribution conduit 11 and inner coaxial nozzle 6 and brought into contact with themnersurface of the liquid plastic fl lm 9. The blowing gas exerts a positive pressure on the liquid plastic film to blow and distend the film outwardly to form an elongated cylinder shaped liquid film 12 of plastic filled with the blowing gas. The elongated cylinder 12 is closed at its outer end and is connected at its inner end to outer nozzle 7 at the peripheral edge of orifice 7a. A balancing pressure of a gas or of an inert gas, i.e. a slightly lower pressure, is provided in the area of the blowing nozzle into which the elongated cylinder shaped liquid film is blown. The illustrated coaxial nozzle can be used to produce microspheres having diameters three to five times the size of the inside diameter of orifice 7a and is useful in blowing low viscosity plastic materials.
A transverse jet 13 is used to direct an inert entraining fluid 14, which is at about, below or above the temperature of the liquid plastic 2. The entraining fluid 14 is fed through distribution conduit 15, nozzle 13 and transverse jet nozzle orifice 13a and directed atthe coaxial blowing nozzle 5. The transverse jet 13 is aligned to direct the flow of entraining fluid 14 over and around blowing nozzle 7 in the microsphere forming region at and behind the orifice 7a. The entraining fluid 14 as it passes over and around blowing nozzle 5 fluid dynamically induces a pulsating or fluctuating pressure field in the entraining fluid 14 at the opposite or tee side of blowing nozzle 5 in its wake or shadow.
The entraining fluid 14 envelops and acts on the elongated cylinder 12 in such a manner as to and causes the cylinder to flap, fold, pinch and close-off at its inner end at a point 16 proximate to the orifice 7a of outer nozzle 7. The continued movement of the entraining fluid 14 over the elongated cylinder 12 produces fluid drag forces on the cylinder 12 and detaches it from the orifice 7a of the outer nozzle 7 to allow the cylinderto fall. The surface tension forces 105 of the liquid plastic act on the entrained, falling elongated cylinder 12 and cause the cylinder to seek a minimum surface area and to form a spherical shape hollow plastic microsphere 17.
Quench or heating nozzles 18 having orifices 18a are disposed below and on both sides of coaxial blowing nozzle 5 and direct cooling or heating fluid 19 at and into contact with the liquid plastic microsphere 17 to rapidly cool or heat and cure and solidify the liquid plastic and form a smooth, hardened, hollow plastic microsphere. The quench or heating fluid 19 also serves to carrythe hollow plastic microspheres away from the coaxial blowing nozzle 5. Sufficient heating and curing time can be provided by using a heated fluidized bed, heated liquid carrier or belt carrier system for the thermosetting hollow plastic microspheres to cure and harden the microspheres with substantially little or no distortion or effect on the size or shape of the microspheres.
Where the plastic is thermosetting, the heated and cured plastic microspheres can be subsequently cooled. The solidified and hardened hollow plastic microspheres are collected by suitable means not shown.
The Figure 3 of the drawings illustrates a preferred 130 embodiment of the inventiQn in which the lower portion of the outer coaxial nozzle 7 is tapered downwardly and inwardly at 21. This embodiment as in the previous embodiment comprises coaxial blow- ing nozzle 5 which consists of inner nozzle 6 with orifice 6a and outer nozzle 6 with orifice 7a'. The figure of the drawings also shows elongated cylinder shaped liquid film 12 with a pinched portion 16.
The use of the tapered nozzle 21 construction was foundto substantially assist in the formation of a thin plastic film 9'in the area between orifice 6a of inner nozzle 6 and orifice 7a'of outer nozzle 7. The inner wall surface 22 of the taper portion 21 of the outer nozzle 7 when pressure is applied to liquid plastic 2 forces the liquid plastic 2 to squeeze through a fine gap formed between the outer edge -of orifice 6a i.e. the outer edge of the inner nozzle 6, and the inner surface 22 to form the thin liquid plastic film 9'across orifices 6a and M. The formation of the liquid plastic film 9'does not in this embodiment rely solely on the surface tension properties of the liquid plastic. The illustrated coaxial nozzle can be used to produce microspheres having diameters three to five times the size of the diameter of orifice 7a of coaxial nozzle 7 and allows making microspheres of smaller diameterthan those made using the Figure 2 apparatus and is particularly useful in blowing high viscosity plastic materials.
The diameter of the microsphere is determined by the diameter of orifice 7a'. This apparatus allows the use of larger inner diameters of outer nozzle 7 and larger inner diameters of inner nozzle 6, both of which reduce the possibility of plugging of the coaxial nozzles when in use. These features are particu- larly advantageous when the blowing gas contains dispersed metal particles andlor the plastic compositions contain additive material particles.
The Figures 3a and 3b of the drawings illustrate another preferred embodiment of the invention in which the outer portion of the transverse jet 13 is flattened to form a generally rectangular or oval shaped orifice opening 13a. The orifice opening 13a can be disposed at an angle relative to a line drawn through the central axis of coaxial nozzle 5. The preferred angle, however, is that as illustrated in the drawing. That is, at an angle of about 90'to the central axis of the coaxial nozzle 5.
The use of the flattened transverse jet entraining fluid was found, at a given velocity, to concentrate the effect of the fluctuating pressure field and to increase the amplitude of the pressure fluctuations induced in the region of the formation of the hollow microspheres at the opposite or lee side of the blowing nozzle 5. By the use of the flattened transversejet and increasing the amplitude of the pressure fluctuations, the pinching action exerted on the cylinder 12 is increased. This action facilitates the closing off of the cylinder 12 at its inner pinched end 16 and detaching of the cylinder 13 from the orifice 7a of the center nozzle 7.
The Figure 3c of the drawings illustrates another preferred embodiment of the present invention in which a high viscosity plastic material is used to blow hollow plastic filamented microspheres. 1 n this Figure, the elongated shaped cylinder 12 and plastic microspheres 17a, 17b and 17c are connected to each other by thin plastic filaments 17d. As can be seen in the drawing, as microspheres 17a, 17b and 17c progress away from blowing nozzle 5 surface tension forces act on the elongated cylinder 12 to effect the gradual change of the elongated shaped cylinder 12 to the generally spherical shape 17a, more spherical shape 17b and finally the spherical shape microsphere 17c. The same surface tension forces cause a gradual reduction in the diameter of the connecting filaments 17d, as the distance between the microspheres and filaments and the blowing nozzle 5 increases. The hollow plastic microspheres 17a, 17b and 17cthat are obtained are connected by thin filament portions 17d that are substantially of equal length and that are continuous with the plastic microspheres.
The operation of the apparatus illustrated in Figures 3,3a, 3b and 3c otherwise than discussed above is similar to that discussed with regard to Figures 1 and 2 of the drawings.
The Figure 4 of the drawing illustrates an embodiment of the invention in which the lower portion of the coaxial nozzle 7 is provided with a bulbous member 23 which imparts to the outer nozzle 7 an expanded spherical shape. This embodiment as in the previous embodiments comprises coaxial blowing nozzle 5 which consists of inner nozzle 6 with orifice 6a and outer nozzle 7 with orifice 7a. The Fig- ure of the drawings also shows elongated cylinder shaped liquid film 12 with the pinched portion 16.
The use of the bulbous spherical shaped member 23 is found for a given velocity of entraining fluid 14 (Figure 2) to substantially increase the amplitude of the pressure fluctuations included in the region of the formation of the hollow microspheres at the opposite or lee side of the blowing nozzle 5. Bythe use of the bulbous member 23 and increasing the amplitude of the pressure fluctuations, the pinching action exerted on the elongated cylinder 12 is increased. This action facilitates the closing off of the cylinder 12 at its inner pinched end 16 and detaching the cylinder 12 from the orifice 7a of the outer nozzle 7.
In still another embodiment of the invention which is also illustrated in Figure 4 of the drawings, a beater bar 24 can be used to assist in detaching the cylinder 12 from orifice 7a. The beater bar 24 is attached to a spindle, not shown, which is caused to rotate in a manner such that the beater bar 24 is brought to bear upon the pinched portion 16 of the elongated cylinder 12 and to thus facilitate the closing off of the cylinder 12 at its inner pinched end 16 and detaching the cylinder 12 from the orifice 7a of outer nozzle 7.
The embodiments of the invention illustrated in the Figures 2 to 4 can be used singly or in various combinations as the situations may require. The entire apparatus can be enclosed in a high pressure containment vessel, not shown, which allows the process to be carried out at elevated pressures.
The Figure 5 of the drawings illustrates the use of the hollow plastic microspheres of the present invention in the construction of a fiat platesolar energy collector 29. The drawing shows a cross- GB 2 083 099 A 5 section taken from an end view of the solar collector. The outer cover member 30 protects the solar collector from the weather elements. The cover 30 can be made from clear glass or plastic. The cover member 30 can also be made from several layers of light transparent hollow plastic microspheres of this invention bonded togetherwith a transparent polyacrylate or polymethyl acrylate resin to form a transparent cover. There is disposed below and parallel to cover 30 a black coated flat metal plate absorber 31 to which there is bonded to the bottom surface thereof a multiplicity of evenly spaced heat exchange medium 32 containing tubes 33. The heat exchange medium can, for example, be water and the tubes 33 are interconnected by conventional means not shown to allow for the flow of the heat exchange medium 32 through the tubes 33. In order to minimize heat loss from the solar collector and increase its efficiency, the space between the outer cover 30 and the f lat plate absorber 31 can also be filled with a bed of light transparent hollow plastic microspheres 34 of the present invention. The solar collector 29 has an inner cover member 35 by means of which the collector can be attached to a roof 36 of a home. To further decrease the heat loss of the solar collector and increase its efficiency, the space between the lower surface of the flat plate absorber 31 and the inner cover member 35 can be filled with reflective hollow plastic microspheres 39 containing on the inner wall surface thereof a visible light and infrared radiation reflective metal coating. The end members 37 and 38 of the solar collector 29 close-off the top and bottom edges of the collector.
The construction and operation of the flat plate solar collector are otherwise essentially the same as the know flat plate solar collector.
The Figure 6 of the drawings illustrates the use of the hollow plastic microspheres of the present invention in the construction of a tubular solar energy collector 43. The drawing shows a crosssection taken from an end view of the solar collector. The outer cover member 44 can be made from clear glass or plastic. The cover member 44 can also be made from several layers of light transparent hollow plastic microspheres of this invention bonded togetherwith a transparent polyester or polyolefin resin to form a transparent cover. There is disposed below and parallel to cover 30 a double pipe tubular member 45. The tubular member 45 consists of an inner feed tube 46 and an outer return tube 47. The heat exchange medium 48, for example water, is fed through inner feed tube 46, passes to one end of the tube where it reverses its direction of flow, by means not shown, and the heat exchange medium 49 (return) passes back through the return tube 47. The inner feed tube 46 is coaxial to the outer return tube 47. The outer return tube 47 has on its outer surface a black heat absorbing coating. The heat exchange medium in passing through feed tube 46 and return tube 47 is heated.
The tubular collector 43 has outer parallel side covers 50 and a lower outer curved cover portion 51. The lower curved cover portion 51 is concentric with the innertube 46 and outer tube 47. The inner sur- face of the lower portion 51 is coated with a reflect- 6 ing material 52 such that the sun's rays are reflected and concentrated in the direction of the black heat absorbing surface coating of return tube 47. In order to minimize heat loss from the solar collector and increase its efficiency, the entire area between the outer covers 44, 50 and 51 and the return tube 47 can be filled with a bed of the visible light transparent hollow plastic microspheres 54 of the present invention.
The tubular solar collector 43 is normally mounted in groups in a manner such that they intercept the movement of the sun across the sky. The sun's rays pass through the transparent microspheres 54 and impinged directly on the outer side of the return tube 47 and are reflected by reflector 52 and impinged on the lower side of return tube 47.
The construction and operation of the tubular solar collector are otherwise essentially the same as the known tubular solar collectors.
The Figure 7 of the drawings illustrates the use of the hollow plastic microspheres of the present invention in the construction of a formed panel 61. The panel contains multiple layers of uniform sized plastic microspheres 62. The microspheres can have a thin deposited layer 63 of a reflecting metal deposited on their inner wall surface. The internal volume of the microspheres can be filled with a low heat conductivity gas 64 and the interstices 65 between the microspheres can be filled with the same gas or a low heat conductivity foam containing a low heat conductivity gas. The facing surface 66 can be coated with a thin layer of plaster suitable for subsequent sizing and painting andfor covering with wall paper. The backing surface 67 can be coated with the same or different plastic from which the microspheres are made to form a vapor barrier or with plaster or with both materials.
The Figure 7a of the drawings illustrates the use of the hollow plastic microspheres of the present invention in the construction of a formed panel 71. The panel contains multiple layers of uniform sized flattened oblate spheroid or rectangular shaped microspheres 72. The oblate spheroid shaped microspheres can have an inner thin deposited layer 73 of a reflective metal. The internal volume of the microsphere can be filled with a low heat conductivity gas 74. The flattened configuration of the microspheres substantially reduces the volume of the insterstices between the microspheres which can be filled with a low heat conductivity foam 75. The facing 76 can be coated with a thin layer of plaster suitable for subsequent sizing and painting andfor covering with wall paper. The backing surface 77 can be coated with the same or different plastic from which the micros- pheres are made to form a vapor barrier or with plaster or with both materials.
The Figure 7b of the drawings illustrates an embodiment of the formed wall panel of Figure 7a in which filamented hollow microspheres connected by very thin plasfic filaments 78 are used. The thin plastic filaments 78 are formed between adjacent microspheres when and as the microspheres are blown and join the microspheres together. The connecting filaments 78 in the formed panel interrupt the wall to wall contact, i.e. the contact between the 130 GB 2 083 099 A 6 microspheres and serve to substantially reduce the conduction heat transfer between adjacent microspheres. The use of filamented microspheres to provide the interrupting filaments is particularly advan- tageous and preferred because the filaments are positively evenly distributed, cannot settle, are sup plied in the desired controlled amount, and in the formed panel provide an interlocking structure which serves to strengthen the formed panel. The facing 76, as before, can be coated with a thin layer of plaster suitable for subsequent sizing and painting andfor covering with wall paper. The backing surface 77 can be coated with the same or different plastic. from which the microspheres are made to form a vapor barrier or with plaster or with both materials. ORGANIC FILM FORMING MA TERIAL AND PLASTIC COMPOSITIONS The organic film forming material and compositions and particularly the plastic compositions from which the hollow plastic microspheres of the present invention are made can be widely varied to obtain the desired physical characteristics for blowing and forming, cooling or heating and curing the microspheres and the desired heat insulating, strength, gas permeability and light trasmission characteristics of the plastic microspheres produced.
The plastic compositions can be selected to have a low heat conductivity and sufficient strength when hardened, solidified and cured to support a substan- tial amount of external pressure or weight. The constituents of the plastic compositions can vary widely, depending on their intended use and can include naturally occurring resins as well as synthetically produced plastic materials.
The constituents of the plastic compositions can be selected and blended to have high resistance to corrosive gaseous materials, high resistance to gaseous chemical agents, high resistance to alkali and weather, low susceptibility to diffusion of gase- ous materials into and out of the plastic microspheres, and to be substantially free of trapped gas bubbles or dissolved gases in the walls of the microspheres which can form bubbles and to have sufficient strength when cured, hardened and solidified to withstand external pressure andlor weight.
The microspheres of the present invention are capable of contacting adjacent microspheres without significant wear or deterioration at the points of contact and are resistant to deterioration from exposure to moisture, heat andlor weathering.
The plastic. compositions that can be used to form microspheres of the present invention include thermosetting and thermoplastic materials such as polyethylene, polypropylene, polystyrene,.polyesf ters, polyurethanes, plychloro-trifluoro ethylene, polyvinyl fluoride, polyvinylidene, polymethyl methacrylate acetyl, phenol-formaldehyde resins and silicone and polycarbonate resins. The plastic compositions also include organic materials such as cellulose acetate, cellulose acetate-butyrate, and cellulose acetate- propionate. The plastic compositions may consist essentially of the plastic material or may contain the plastic material dissolved or dispersed in a suitable solvent.
Thermoplastic synthetic resins that can be used 51 1 7 GB 2 083 099 A 7 are polyvinyl resins, i.e. polyvinyl alcohol (water- or organic solventsoluble), polyvinyl chloride, copolymers of vinyl chloride and vinyl acetate, polyvinyl butyral, polystyrene, polyvinylidene chloride, acrylic resins such as polymethyl methacry- 70 late, polyallyl, polyethylene, and polyamide (nylon) resins.
Thermosetting resins that can be used are those in the thermoplastic water- or organic solvent-soluble stage of partial polymerization, the resins being converted after or during formation of the microspheres into a more or less fully polymerized solventinsoluble stage. Other useful resins are alkyd, polysiloxane, phenol-formaldehyde, urea- formaldehyde and melamine-formaldehyde resins.
Natural film forming materials are also included within the scope of the form, including soybean protein, zein protein, alginates, and cellulose in solution as cellulose xanthate or cuprammonium cellulose.
The plastic compositions disclosed in Veatch et al U.S. Patent 2,797,201 and the Morehouse, Jr. U.S. Patent 3,615,972 can also be used in carrying out the present invention and the disclosures of said patents are accordingly incorporated herein in their entirety by reference.
There may be added to the plastic compositions chemical agents or additives which effect the viscosity of the compositions or of the surface film of the microsphere in order to obtain the desired vis- cosities needed to obtain a stable film for blowing the microspheres. Suitable chemical agents are materials that act as solvents forthe plastic compositions. The solvents that are used will, of course, depend on the solubility in the solvent of the plastic composition used. Water, alcohols, ethers, esters, organic acids, hydrocarbons and chlorinated hydrocarbons can be used as solvents. To assist in the blowing and formation of the plastic microspheres, surface active agents, such as colloidal particles of insoluble substances and viscosity stabilizers can be added to the plastic composition as additives. These additives can affect the viscosity of the surface film of the microsphere to stabilize the film during film formation.
A distinct and advantageous feature of the present invention is that latent solid or latent liquid blowing gases are not used or required and that the microspheres that are produced are free of latent solid or latent liquid blowing gas materials or gases.
Additional plastic compositions suitable for use in the present invention are:
Thermoplastic resins: Epoxy resins, phenolformaldehyde resins, and Melmac; Other resin compositions are: Elvanol, silicones, and Teflon.
For a more specific description of the above plastic and resin compositions see Zimmerman and Lavine, "Handbook of Material Trade Names-, Vols. 1-1V, 1953-1965.
The plastic compositions of the present invention are formulated to have a relatively narrow temperature difference between the liquid temperature and the plastic hardening temperature (thermoplastic) or a relatively narrow temperature difference between the liquid temperature and the thermosetting and 1 curing temperature. The plastic compositions are formulated such that they have a high rate of viscosity increase with the hardening temperature or the thermosetting temperature such that the microsphere walls will solidify, harden and strengthen before the blowing gas within the sphere decreases in volume and pressure a sufficient amount to cause the microsphere to collapse. Where it is desirous to maintain a positive pressure in the contained volume of the microspheres, the permeability of the contained gases can be decreased in the manner discussed below.
The use of Saran plastic compositions is found to produce microspheres that are useful as filler mater- ials. The polystyrene plastic compositions can be used to make microspheres for use as improved insulating materials. The polyethylene plastic compositions can be advantageously used to make microspheres for use as filler materials in plastic mold- ing compositions. The polypropylene plastic compositions can be used to make microspheres for use as aggregate in concrete.
The plastic compositions from which the hollow plastic microsphere can be made are, depending on the particular plastic materials used, to some degree permeable to the gas materials used to blow the microspheres andlor to the gases present in the medium surrounding the microspheres. The gas permeability of the plastic compositions can be reduced and/or substantially eliminated by the addition, prior to blowing the microspheres, to the plastic composition of very small inert laminar planeorientable additive material particles. Suitable additive particles are mica, graphite and aluminum leaf powders. When any one or more of these laminar plane-orientable additive material particles are added to a plastic composition prior to the blowing and formation of the hollow plastic microspheres, the process of making the microsphere aligns the laminar particles, as the plastic film is stretched in passing, i.e. extruded, through the conical blowing nozzle, with the walls of the hollow plastic microsphere and normal to the gas diffusion direction. The presence of the laminar plane particles in the mic- rosphere walls substantially diminishes the gas permeability of the plastic film. The sizes of the additive particles are advantageously selected to be less than one-half the thickness of the wall of the microspheres. The gas permeability of certain plastics may be further diminished or reduced by subjecting the microspheres to ionization radiation to promote cross-linking of the plastic molecules. BLOWING GAS The hollow plastic microspheres used to make insulating materials can be blown with an inert gas or gas containing dispersed metal particles or a mixture thereof. The gases that are used to blow the microspheres are selected to have a low heat conductivity and generally involve heavy molecules which do not transfer heat readily. Suitable blowing gases can be argon, xenon, Freon gases, nitrogen and sulfur dioxide. The blowing gas is selected to have the desired internal pressure when cooled to ambient temperatures. Blowing gases can also be selected that react with the plastic microspheres, e.g.
8 GB 2 083 099 A 8 to assist in the hardening andfor curing of the microspheres or to make the microsphere less permeable to the contained blowing gases. For certain uses, oxygen or air can be used as or added to the blowing gas.
A blowing gas containing dispersed metal particles can be used to obtain in the contained volume of the microsphere a deposit of a thin metal coating on the inner wall surface of the hollow plastic micros- phere. The thickness of metal coating deposited will determine whetherthe metal coating is transparent or reflective of visible light. The blowing gases can also be selected to react with the deposited thin metal layer to obtain desired characteristics in the metal layer. For example, to reduce the thermal conductivity of the metal layer.
The metal used to coat the inner wall surface of the hollow plastic microspheres is selected to have the desired emissivity, low heat conduction characteris- tics, and to adhere to the inner wall surface of the plastic microspheres. The thickness and the nature of the deposited metal coating will depend to some extent upon the metal, the particle size of the metal used, the size of the microsphere and the amount of dispersed metal particles used.
The dispersed metal particle size can be 25A to 1 O,OOOA, preferably 50A to 5,OOOA and more preferably 100Ato 1,OOOA. A sufficient amount of the metal is dispersed in the blowing gas to obtain the desired thickness of the deposited metal. The dispersed metal particles can advantageously be provided with an electrostatic charge to assist in depositing them on the inner wall surface of the microspheres.
Metal particles such as aluminum, silver, nickel, zinc, antimony, barium, cadmium, cesium, bismuth, selenium, lithium, magnesium, potassium, and gold can be used. Aluminum, zinc and nickel, however, are preferred. Dispersed metal oxide particles can in a similar manner be used to obtain similar effects to that of the metals. In addition, the metal oxide particles can be used to produce a deposited film of lower heat conductivity characteristics.
The thin metal coating can also be deposited on the inner wall surface of the microsphere by using as or with blowing gas organo metal compounds that are gases at ambient temperatures or that become gases on heating. Of the organo metal compounds available, the organo carbonyl compounds are preferred. Suitable organo metal carbonyl compounds are nickel and iron.
The organo metal compounds can be decomposed by heating just prior to blowing the microspheres to obtain finely dispersed metal particles and a decomposition gas or product. The decomposition gas, if present, can be used to assist in blowing the microspheres. The dispersed metal particles from decomposition of the organo metal compound, as before, deposit to form the thin metal layer. Alternatively, the microsphere, after being formed and con- taining the gaseous organo metal compound blowing gas, can be subjected to "electrical dischargemeans which decomposes the organo metal compound to form the finely dispersed metal particles and the decomposition gas or product.
The thickness of the deposited metal layer will depend primarily on the partial pressure of the gaseous organo metal blowing gas and the inside diameter of the microsphere.
An auxiliary blowing gas, e.g. an inert blowing gas, can be used to dilute the gaseous organo metal compound blowing gas in order to control the thickness of the deposited metal layer. There can also be used as an auxiliary blowing gas, a gas that acts as a catalyst or hardening agent for the plastic composi- tions. The addition of the catalyst or hardening agent to the blowing gas prevents contact of the catalyst or hardening agent with the plastic composition until a time just before the microsphere is formed.
The entraining fluid, e.g. an inert entraining fluid, can be a gas at a high or low temperature and can be selected to react with or be inert to the plastic composition. Suitable entraining fluids are nitrogen, air, steam and argon. A gaseous catalyst for the plastic can also be included in the entraining fluid.
The quench of heating fluid can be a liquid, a liquid dispersion or a gas. Suitable quench or heating fluids are steam, a fine water spray, air, nitrogen or mixtures thereof. The selection of a specific quench or heating fluid and quench or heating temperature depends to some extent on the plastic composition from which the microspheres are made and the blowing gas temperature and pressure. PROCESS CONDITIONS The organic film forming materials andlor plastic compositions of the present invention are in a liquid-fluid form at the desired blowing temperature and during the blowing operation. The liquid plastic composition can be at a temperature of about O'C. to about 400'C., preferably 100C. to 3000C. and more preferably 20'C. to 200'C_ depending on the constituents and state of polymerization of, for example, the plastic composition. The plastic composition at the blowing temperature is liquid, fluid and flows easily. The liquid plastic just prior to the blowing operation can have a viscosity of 0.10 to 600 poises, usually 10 to 350 poises and more usually 30 to 200 poises.
Where the process is used to make non-filamented microspheres, the liquid plastic just prior to the blowing operation can have a viscosity of 0.1 to 200 poises, preferably 0. 5 to 100 poises, and more preferably 5.0 to 50 poises.
Where the process is used to make filamented microspheres, the liquid plastic just prior to the blowing operation can have a viscosity of 50 to 600 poises, preferably 100 to 400 poises, and more preferably 150 to 300 poises. The viscosity can be measured by conventional means, e.g. using a Broofield viscometer.
A critical feature of the present invention is that the formation of the hollow plastic microspheres, can be carried out at low viscosities relative to the viscosities heretofore used in the prior art processes that utilized latent liquid or solid blowing agents dis- persed throughout or contained in the plastic compositions used to blow the microspheres. Because of the ability to utilize comparatively low viscosities, applicant is able to obtain hollow plastic microspheres, the walls of which are f ree of any entrapped or dissolved gases or bubbles. With the low vis- - v 9 cosities used by applicant, any entrapped or dissoi ved gases diffuse out and escape from the plastic film surface during the bubble formation. With the high viscosities required to be used in the prior are processes, any dissolved gaseous bubbles are trapped in the walls of the plastic microspheres as they are formed because of the high viscosities required to be used.
The liquid plastic fed to the coaxial blowing nozzle can be at about ambient pressure or can be at an elevated pressure. The liquid plastic feed can be at a pressure of 1 to 20,000 p.s.i.g., usually 3 to 10,000 p.s.i.g. and more usually 5 to 5,000 p.s.i.g.
Where the process is used to make microspheres for use as insulating materials and in insulating systems, for use in syntactic foam systems and as filler materials in general, the liquid plastic fed to the coaxial blowing nozzle can be at a pressure of 1 to 1, 000 p.s.i.g., preferably at 3 to 100 p.s.i.g., and more preferably at 5 to 50 p.s.i.g.
The liquid plastic is continuously fed to the coaxial blowing nozzle during the blowing operation to pre vent premature breaking and detaching of the elongated cylinder shaped liquid plastic film as it is being formed by the blowing gas.
The blowing gas or gaseous material blowing gas will be at about the same temperature as the liquid plastic being blown. The blowing gas or gaseous material blowing gas temperature can, however, be at a higher temperature than the liquid plastic to assist in maintaining the fluidity of the hollow liquid plastic microsphere during the blowing operation or can be at a lower temperature than the liquid plastic to assist in the solidification and hardening of the hollow liquid plastic microsphere as it is formed. The pressure of the blowing gas or gaseous material blowing gas is sufficient to blow the microsphere and will be slightly above the pressure of liquid plastic film at the orifice 7a of the outer nozzle 7. The blowing gas pressure will also depend on and be slightly above the ambient pressure external to the blowing nozzle.
The temperatures of the gaseous material blowing gases will depend on the blowing gas used and the viscosity-temperatureshear relationship for the plastic materials used to make the microspheres.
The pressure of the blowing gas or gaseous material blowing gas is sufficient to blow the microsphere and will be slightly above the pressure of liquid plas- tic at the orifice 7a of the outer nozzle 7. Depending on the gaseous material to be encapsulated within the hollow plastic microspheres, the blowing gas or the gaseous material can be at a pressure of 1 to 20,000 p. s.i.g., usually 3 to 10,000 p.s.i.g. and more usually 5 to 5,000 p.s.i.g.
The blowing gas or gaseous material blowing gas can also be at a pressure of 1 to 1,000 p.s.i.g., preferably 3 to 100 p.s.i.g. and more preferably 5 to 50 P.S.i.g.
Where the process is used to make microspheres for use as insulating materials and in insulating systems, for use in syntactic foam systems and as filler materials in general, the blowing gas or gaseous material blowing gas can be at a pressure of 1 to 125 p.s.i.g., preferably at2 to 100 p.s.i.g. and more pref- GB 2 083 099 A 9 erably at 5 to 30 p.s.i.g.
The pressure of the blowing gas containing dispersed meta: particles alone andlor in combination with the principle blowing gas is sufficient to blow the microsphere and the combined gas pressure will be slightly above the pressure of the liquid plastic at the orifice 7a of the outer nozzle 7. The pressure of the combined mixture of the blowing gases will also depend on and be slightly above the ambient pres- sure external to the blowing nozzle.
The ambient pressure external to the blowing nozzle can be at about atmospheric pressure or can be at subatmospheric or super-atmospheric pressure. The ambient pressure external to the blowing nozzle will be such that it substantially balances, but is slightly less than the blowing gas pressure.
The transverse jet entraining fluid which is directed over and around the coaxial blowing nozzle to assist in the formation and detaching of the hol- low liquid plastic microsphere from the coaxial blowing nozzle can have a linear velocity in the region of microsphere formation of 1 to 120 ft/see, usually 5 to 80 ft/see and more usually 10 to 60 ft/sec.
Where the process is used to make non-filamented microspheres, the linear velocity of the transverse jet fluid in the region of microsphere formation can be 30 to 120 ft/sec, preferably 40 to 100 ft/sec and more preferably 50 to 80 ft/sec.
Where the process is used to make filamented microspheres, the linear velocity of the transverse jet fluid in the region of microsphere formation can be 1 to 50 ft/sec, preferably 5 to 40 ft/sec and more preferably 10 to 30 ft/sec.
Further, it is found (Figures 2 to 4) that pulsing the transverse jet entraining fluid at a rate of 2 to 1500 pulses/sec, preferably 50 to 1000 pulses/sec and more preferably 100 to 500 pulses/sec assists in controlling the diameter of the microspheres and detaching the microspheres from the coaxial blow- ing nozzle.
The distance between fi lamented microspheres depends to some extent on the viscosity of the plastic and the linear velocity of the transverse jet entraining fluid.
The entraining fluid can be at the same temperature as the fluid plastic being blown. The entraining fluid can, however, be at a higher temperature than the liquid plastic to assist in maintaining the fluidity of the hollow liquid plastic microsphere during the blowing operation or can be at a lower temperature than the liquid plastic to assist in the stabilization of the forming film and the solidification and hardening of the hollow liquid plastic microsphere as it is formed.
The quench or heating fluid is at a temperature such that it rapidly cools or heats the microspheres to solidify, harden and strengthen the liquidplastic before the inner gas pressure decreases to a value at which the plastic microsphere would collapse or burst the microsphere. The quench cooling fluid can be at a temperature of 0 to 200'R, usually 40 to 2000F. and more usually 50 to 100'17. The heating fluid can be at a temperature of 100 to 800'F_ usually 200 to 6000F. and more usually 300 to 500OR, depend- ing on the plastic composition.
GB 2 083 099 A 10 The quench cooling fluid very rapidly cools the outer liquid plastic surface of the microsphere with which it is in direct contact and more slowly cools the blowing gas enclosed within the microsphere because of the lower thermal conductivity of the gas. 70 This cooling process allows sufficient time for the plastic walls of the microspheres to strengthen before the gas is cooled and the pressure within the plastic microsphere is substantially reduced.
The time elapsed from commencement of the blowing of the plastic microspheres to the cooling and initial hardening of the microspheres can be.0001 to 60.0 seconds, preferably.001 0 to 30.0 seconds and more preferably 0.10 to 10.0 seconds.
Where a thermosetting plastic composition is used 80 to form the microsphere, the time elapsed from commencement of the blowing of the plastic microsphere to the heating and curing of the microsphere for it to have sufficient strength to maintain its size and shape can be 0.10 second to 30 minutes, preferably 1 second to 20 minutes and more preferably 10 seconds to 10 minutes.
The filamented microsphere embodiment of the invention provides a means by which the micros- pheres may be suspended and allowed to harden andlor cure without being brought into contact with any surface. The filamented microspheres are simply drawn on a blanket or drum and are suspended between the blowing nozzle and the blanket or drum fora sufficient period of time for them to harden a ndlor cure.
APPARA TUS Referring to Figures 1 and 2 of the drawings, the vessel 1 is constructed to maintain the liquid plastic at the desired operating temperatures. The liquid plastic 2 is fed to coaxial blowing nozzle 5. The coaxial blowing nozzle 5 consists of an inner nozzle 6 having an outside diameter of 0.32 to 0.010 inch, preferably 0.20 to 0.015 inch and more preferably 0.10 to 0.020 inch and an outer nozzle 7 having an inside diameter of 0. 420 to 0.020 inch, preferably 0.260 to 0.025 and more preferably 0.130 to 0.030 inch. The inner nozzle 6 and outer nozzle 7 form annular space 8 which provides a flow path through which the liquid plastic 2 is extruded. The distance 110 between the inner nozzle 6 and outer nozzle 7 can be 0.050 to 0.004 preferably 0.030 to 0.005 and more preferably 0.015 to 0.008 inch.
The orifice 6a of inner nozzle 6 terminates a short distance above the plane of orifice 7a of outer nozzle 115 7. The orifice 6a can.be spaced above orifice 7a at a distance of 0.001 to 0.125 inch, preferably 0.002 to 0.050 inch and more preferably 0.003 to 0.025 inch. The liquid plastic 2 flows downwardly and is extruded through annular space 8 and fills the area between orifice 6a and 7a. The orifices 6a and 7a can be made from stainless steel, platinum alloys, glass or fused alumina. Stainless steel, however, is preferred. The surface tension forces in the liquid plastic 2 form a thin liquid plastic film 9 across orifices 6a and 7a which has about the same or a smaller thickness as the distance of orifice 6a is spaced above orifice 7a. The liquid plastic film 9 can be 25 to 3175 microns, preferably 50 to 1270 microns, and more pref- erably 76 to 635 microns thick.
The Figure 2 blowing nozzle can be used to blow liquid plastic at relatively low viscosities, for example, of 10 to 60 poises and to blow hollow plastic microspheres of relatively thick wall size, for example, of 20 to 100 microns or more.
A blowing gas or gaseous material blowing gas is fed through inner coaxial nozzle 6 and brought into contact with the inner surface of liquid plastic film 9. The blowing gas or gaseous material blowing gas exerts a positive pressure on the liquid plastic film to blow and distend the film outwardly and downwardly to form an elongated cylinder shaped liquid film 12 of liquid plastic filled with the inert blowing gas or gaseous material blowing gas 10. The elongated cylinder 12 is closed at its outer end and is connected to outer nozzle 7 at the peripheral edge of orifice7a.
The transverse jet 13 is used to direct an inert entraining fluid 14 th rough nozzle 13 and transverse jet nozzle orifice 13a at the coaxial blowing nozzle 5. The coaxial blowing nozzle 5 has an outer diameter of 0.52 to 0.030 inch, preferably 0.36 to 0.035 inch and more preferably 0.140 to 0.040 inch.
The process of the present invention was found to be very sensitive to the distance of the transverse jet 13 from the orifice 7a of outer nozzle 7, the angle at which the transverse jet was directed at coaxial blowing nozzle 5 and the point at which a line drawn through the center axis of transverse jet 13 interse- cted with a line drawn through the center axis of coaxial nozzle 5. The transverse jet 13 is aligned to direct the flow of entraining fluid 14 over and around outer nozzle 7 in the microsphere forming region of the orifice 7a. The orifice 13a of transverse jet 13 is located a distance of 0.5 to 14 times, preferably 1 to 10 times and more preferably 1.5 to 8 times and still more preferably 1.5 to 4 times the outside diameter of coaxial blowing nozzle 5 away from the point of intersect of a line drawn along the center axis of transverse jet 13 and a line drawn along the center axis of coaxial blowing nozzle 5. The center axis of transverse jet 13 is aligned at an angle of 15 to 85', preferably 25 to 750 and more preferably 35 to 55' relative to the center axis of the coaxial blowing nozzle 5. The orifice 13a can be circular in shape and have an inside diameter of 0.32 to 0.010 inch, preferably 0.20 to 0.015 inch and more preferably 0.10 to 0.020 inch.
The line drawn through the center axis of transverse jet 13 intersects the line drawn through the center axis of coaxial blowing nozzle 5 at a poirt above the orifice 7a of outer nozzle 7 which is.5 to 4 times, preferably 1.0 to 3.5 times and more preferably 2 to 3 times the outside diameter of the coaxial blowing nozzle 5. The transverse jet entraining f luid acts on the elongated shaped cylinder 12 to flap and pinch it closed and to detach it from the orifice 7a ofthe outer nozzle 7 to allowthe cylinderto fall, i.e. be transported away from the outer nozzle 7 by the entraining fluid.
The transverse pet entraining fluid as it passes over and around the blowing nozzle fluid dynamically induces a periodic pulsating or fluctuating pressure field at the opposite or lee side of the blow- ing nozzle in the wake or shadow of the coaxial blow- 11 ing nozzle. A similar periodic pulsating or fluctuating pressure field can be produced by a pulsating sonic pressure field directed at the coaxial blowing nozzle. The entraining fluid assists in the formation and detaching of the hollow plastic microsphere from the coaxial blowing nozzle. The use of the transverse jet and entraining fluid in the manner described also discourages wetting of the outer wall surface of the coaxial blowing nozzle 5 by the fluid plastic being blown. The wetting of the outer wall disrupts and interfers with blowing the microspheres.
The quench or heating nozzles 18 are disposed below and on both sides of the coaxial blowing nozzle 5 a sufficient distance apart to allow the micros- pheres 17 to fall between the quench nozzles 18. The inside diameter of quench nozzle orifice 18a can be 0.1 to 0.75 inch, preferably 0.2 to 0.6 inch and more preferably 0.3 to 0.5 inch. The quench nozzles 18 direct cooling or heating fluid 19 at and into contact with the liquid plastic microspheres 17 at a velocity of 2 to 14, preferably 3 to 10 and more preferably 4 to 8 ft/sec to rapidly cool or heat and solidify the liquid plastic and form a hard, smooth hollow plastic microsphere.
The Figure 3 of the drawings illustrates a preferred 90 embodiment of the invention. It is found that in blowing high viscosity liquid plastic compositions that it is advantageous to immediately priorto blow ing the liquid plastic to provide by extrusion a very thin liquid plastic film for blowing into the elongated 95 cylinder shape liquid film 12. The thin liquid film 9'is provided by having the lower portion of the outer coaxial nozzle 7 tapered downwardly and inwardly at 21. The tapered portion 21 and inner wall surface 22 thereof can be at an angle of 15 to 75', 30 to 60' and 100 preferably about 45' relative to the center axis of coaxial blowing nozzle 5. The orifice 7a'can be 0.10 to 1.5 times, preferably 0.20 to 1.1 times and more preferably 0.25 to.8 times the inner diameter of orifice 6a of inner nozzle 6.
The thickness of the liquid plastic film 9'can be varied by adjusting the distance of orifice 6a of inner nozzle 6 above orifice 7a of outer nozzle 7 such that the distance between the peripheral edge of orifice 6a and the inner wall surface 22 of tapered nozzle 21 can be varied. By controlling the distance between the peripheral edge of orifice 6a and the inner wall surface 22 of the tapered nozzle to form a very fine gap and by controlling the pressure applied to feed the liquid plastic 2 through annular space 8 the liquid 115 plastic 2 can be squeezed or extruded through the very 'line gap to form a relativelythin liquid plastic film 9'.
The proper gap can best be determined by pres- sing the inner coaxial nozzle 6 downward with suffi- 120 cient pressure to completely block-off the flow of plastic, and to then very slowly raise the inner coaxial nozzle 6 until a stable system is obtained, i.e. until the microspheres are being formed.
The tapered nozzle construction illustrated in Fig- 125 ure 3 is as mentioned above the preferred embodiment of the invention. This embodiment can be used to blow plastic compositions at relatively high viscosities as well as to blow plastic compositions at the relatively low viscosities referred to with regard 130 GB 2 083 099 A 11 to Figure 2 of the drawings. The Figure 3 embodiment of the invention is of particular advantage in blowing the thin walled microspheres for use in or as insulating materials.
When blowing high or low viscosity plastic compositions, it was found to be advantageous to obtain the very thin liquid plastic film and to continue during the blowing operation to supply liquid plastic to the elongated cylinder shaped liquid film as it was formed. Where a high pressure is used to squeeze, i.e. extrude, the liquid plastic through the very thin gap, the pressure of the inert blowing gas or gaseous material blowing gas is generally less than the liquid plastic feed pressure, but slightly above the pressure of the liquid plastic at the coaxial blowing nozzle.
The tapered nozzle configuration of Figure 3 is also particularly useful in aligning the laminar planeorientable plastic additive materials. The passage of the plastic material through the fine or narrow gap serves to align the additive materials with the walls of the microspheres as the microspheres are being formed.
The Figures 3a and 3b of the drawings also illus trate a preferred embodiment of the invention in which the transverse jet 13 can be flattened to form a generally rectangular or oval shape. The orifice 13a can also be flattened to form a generally oval or rectangular shape. The width of the orifice can be 0.96 to 0.030 inch, preferably 0.60 to 0.045 inch and more preferably 0.030 to 0.060 inch. The height of the orifice can be 0.32 to 0.010 inch, preferably 0.020 to 0.015 inch and more preferably 0.10 to 0.20 inch.
With reference to Figure 3c of the drawings which illustrates an embodiment of the present invention in which a high viscosity plastic material is used to blow filamented hollow plastic microspheres, there is shown the formation of the uniforrn diameter microspheres spaced about equal distances apart. The numbered items in this drawing have the same means as discussed above with reference to Figures 1, 2,3,3a and 3b.
With reference to Figure 4 of the drawings which illustrates another embodiment of the invention, it was found that in blowing the liquid plastic to form the elongated cylinder shaped liquid film 12 that it was advantageous to increase the outer diameter of the lower portion coaxial blowing nozzle 5. One method of increasing the outer diameter of coaxial blowing nozzle 5 is by providing the lower portion of outer nozzle 7 with a bulbous member 23 which imparts to the lower portion of outer nozzle 7 a spherical shape. The use of the bulbous spherical shaped member 23 is found for a given velocity of the entraining fluid to substantially increase the amplitude of the pressure fluctuations induced in the region of the formation of the hollow microspheres. The diameter of the bulbous member 23 can be 1. 25 to 4 times, preferably 1.5 to 3 times and more preferably 1.75 to 2.75 times the diameter of the outer diameter of coaxial blowing nozzle 5. When using a bulbous member 23, the transverse jet 13 is generally aligned such that a line drawn through the center axis of transverse jet 13 will pass through the center of bulbous member 23.
12 The Figure 4 illustrates still another embodiment of the invention in which a beater bar 24 is used to facilitate detaching of the elongated cylinder shaped liquid film 12 from the orifice 7a of outer nozzle 7.
The beater bar 24 is attached to a spindle, not shown, which is caused to rotate in a manner such that the beater bar 24 is brought to bear upon the pinched portion 16 of the elongated cylinder 12. The beater bar 24 is set to spin at about the same rate as the formation of hollow microspheres and can be 2 to 1500, preferably 10 to 800 and more preferably 20 to 400 revolutions per second. The beater bar 24 can thus be used to facilitate the closing off of the cylinder 12 at its inner pinched end 16 and to detach the cylinder 12 from the orifice 7a of outer nozzle 7. DESCRIPTION OF THE MICROSPHERES
The hollow microspheres made in accordance with the present invention can be made from a wide variety of organic film forming materials and compositions particularly plastic compositions.
The hollow plastic microspheres made in accordance with the present invention can be made from suitable organic film forming compositions which are resistant to high temperatures and chemical attack and resistant to weathering as the situation may require.
The organic film forming compositions that can be used are those that have the necessary viscosities, as mentioned above, when being blown to form stable films and which have a rapid change from the molten or liquid state to the solid or hard state with a relatively narrow temperature change or within a relatively short cure time. That is, they change from liquid to solid within a relative narrowly defined temperature range andfor cure in a relatively short time.
The hollow plastic microspheres are substantially uniform in diameter and wall thickness, and depending on their composition and the blowing conditions are light transparent, translucent or opaque, soft or hard, and smooth or rough. The walls of the microspheres are free or substantially free of any holes, relatively thinned wall portions or sections, trapped gas bubbles, or sufficient amounts of dissolved gases or solvents to form bubbles. The micros- 110 pheres are also free of any latent solid or liquid blowing gas materials or gases. The preferred plastic compositions are those that are resistant to chemical attack, elevated temperatures weathering and diff u- sion of gases into andlor out of the microspheres. Where the blowing gases may decompose at ele vated temperatures, plastic compositions that are liquid below the decomposition temperature of the gases can be used.
The plastic microspheres can be made in various diameters and wall thickness, depending upon the desired end use of the microspheres. The microspheres can have an outer diameter of 200 to 10,000 microns, preferably 500 to 6,000 microns and more preferably 1,000 to 4,000 microns, The microspheres can have a wall thickness of 0.1 to 1,000 microns, preferably 0.5 to 400 microns and more preferably 1 to 100 microns.
The diameter and wall thickness of the hollow mic rospheres will of course affect the average bulk 130 GB 2 083 099 A 12 density of the microspheres. The microspheres can have an average bulk density of 0.2 to 15]blft3, usually 0.5 to 12 iblft3 and more usually 0. 75 to 9 lb/ft'. For use in a preferred embodiment to make low density insulating materials, the hollow plastic microspheres can have an average bulk density as low as 0.5 to 1.5, for example, about 1.0 lblftl.
The microspheres, because the walls are free or substantially free of any holes, thinned sections, trapped gas bubbles, and/or sufficient amount of dissolved gases or solvents to form bubbles and are substantially stronger than the microspheres heretofore produced.
The microspheres made from thermoplastic com- positions after being formed can be reheated to soften the plastic and enlarge the microspheres andior to improve the surface smoothness of the microspheres. On reheating, the internal gas pressure will increase and cause the microsphere to increase in size. After reheating to the desired size, for example, in a---shottower-, the microspheres are rapidly cooled to retain the increase in size.
Where the microspheres are formed in a manner such that they are connected by continuous thin plastic filaments, that is they are made in the form of filamented microspheres, the length of the connecting filaments can be 1 to 40, usually 2 to 20 and more usually 3 to 15 times the diameter of the microspheres. The diameter, that is the thickness of the connecting filaments, can be 115000 to 1110, usually 112500 to 1120 and more usually 111000 to 1130 of the diameter of the microspheres.
The microspheres can contain a gas at superatmospheric pressure, about ambient pressure or at partial vacuum.
Where the microspheres are used as insulating materials and in insulating systems, or in syntactic foam systems, or as filler material in general, the microspheres can have an outer diameter of 200 to 5,000, preferably 500 to 3,000 and more preferably 750 to 2000 microns. These microspheres can have a wall thickness of 0.1 to 500 microns, preferably 0.5 to 200 microns and more preferably 1 to 50 microns. These microspheres can have an average bulk density of 0.3 to 15 1b[ft3, preferably 0.5 to 10 IbIffi and more preferably 0.75 to 5.0 Ibiffi. These microspheres can have a contained gas pressure of 12 to 100 p.s.i.a., preferably 15 to 75 p.s.i.a. and more preferably 18 to 25 p.s.i.a.
In a preferred embodiment of the invention, the ratio of the diameterto the wall thickness of the microspheres is selected such that the microspheres are f'exible, i.e. can be deformed under pressure without breaking.
The microspheres can contain a thin metal layer deposited on the innerwall surface of the microsphere where the blowing gas contains dispersed metal particles. The thickness of the thin metal coating deposited on the inner wall surface of the mic- rosphere will depend on the amount and particle size of the dispersed metal particles or partial pressure of organo metal blowing gas that are used and the diameter of the microsphere. The thickness of the thin metal coating can be 25 to 1 O,OOOA, preferably 50 to 5,OOOA and more preferably 100 to 1,OOOA.
j 3 13 GB 2 083 099 A 13 1 when it is desired that the deposited metal coating be transparent to light, the coating should be less than 1 OOA and preferably less than BOA. The trans parent rnetal coated microspheres can have a depo sited metal coating 25 to 95A and preferably 50 to BOA thick. These microspheres, though transparent to visible light, are substantially reflective of infrared radiation.
When it is desired that the deposited metal coating be reflective to light, the coating can be more than 1 OOA and preferably more than 150A thick. The reflective metal coated microspheres can have a deposited metal coating 105 to 600A, preferably 150 to 400A and more preferably 150 to 250A thick.
The thermal heat conductivity characteristics of heat barriers made from the microspheres can be f urther improved by partially flattening the micros pheres into an oblate spheroid or generally rectan gular shape. The thermal conductivity of the oblate spheroids is further improved by mixing with the oblate spheroids thin plastic filaments. The filaments are preferably provided in the form of the filamented microspheres.
The filamented microspheres can as they are formed be drawn and laid on a conveyor belt or drum. A sufficient amount of tension can be main tained on the filamented microspheres as they are drawn to stretch them into the oblate spheroid shape. The filamented microspheres are maintained in that shapefor a sufficient period oftime to harden and cure. After hardening of the filamented oblate spheroids, they can be laid in a bed, an adhesive andlorfoam can be added and the filamented mic rospheres can be made into, e.g. a four by eight formed panel. The panel can be 114 to 3 inches in thickness, for example, 112, 1, 1 112 or 2 inches in thickness.
The thermal properties of the microspheres can also be improved by filling the interstices between 410 the microspheres with a low thermal conductivity gas, finely divided inert particles, e.g. lamp black, a low conductivity foam, e.g. polyurethane, or polyole fin resin foam.
The hollow plastic microspheres of the present -1.5 invention can be used to design systems having improved insulating characteristics. Where hollojj microspheres are used in which the contained.fol umehas a low heat conductivity gas, systems can be designed in which the thermal conductivity car, be R5 to Rg, 'for example, R8 per inch.
Where hollow plastic microspheres are used ha-v ing a loliv heat conductivity gas and a low emissivity, reflective metal coating deposited on the inner wall sunace thereof are used, systems cart be designed in which the thermal conductivity can be R7 o RI 2, for - example, R10 per inch.
Where an insulating system containing filarnented oblate spheroids and a reflective metal coating deposited on the inner wall sur,ace of the micros phere are used, systems can be designed in which the thermal conductivity can be R9 to R16, for exam ple R1 4 per inch.
The microspheres can also be used as heat bar riers by filling spaces between existing wails or other void spaces or can be made into sheets or other 130 shaped forms by cementing the microspheres together with a suitable resin or other adhesive or by fusing the microspheres together and can be used in new construction.
When the hollow plastic microspheres are massed together to form a heat barrier, there is reduced heat transfer by solid conduction because of the point to point contact between adjacent spheres and the low conductivity of the plastic material used to form the spheres. There is little heat transfer by convection because the characteristic dimensions of the voids between the packed spheres are below that necessary to initiate convection. There is little heat transfer by gas conduction within the spheres when there is a low heat conductivity gas in the enclosed volume. Where there is a low emissivity, highly reflective metal layer deposited on the inner wall surface of the microspheres, there is substantially little radiant beat transfer because of the highly reflective metal layer on the inner wall surface of the spheres. A primary mode of heat transfer remaining, therefore, is by gas conduction in the interstices or voids between the microspheres. The overall conductivity of the system is lower than that of the voids gas because the voids gas occupies only a fraction of the volume of the total system, and because conduction paths through the voids gas are attenuated by the presence of the low conductivity microspheres and the filaments. The use of a low heat conductivity gas andlor a foam containing a low heat conductivity gas to fill the interstices between the microspheres further reduces the thermal conductivity of a bed of the microspheres.
The hollow plastic microspheres of the present invention have a distinct advantage of being strong and capable of supporting a substantial amount of weight. They can thus be used to make simple inexpensive self-supporting or load bearing systems.
The following examples are used to illustrate the invention.
EXAMPLES
The Examples 1-7 are illustrative of the use of the present invention to make insulating materials andlor systems.
Example 1
A thermoplastic composition comprising the following constituents is used to make hollow plastic microspheres:
Polyethylene polymer The plastic composition is heated to form a fluid plastic having a viscosity of 10 to 20 poises at the blowing nozzle.
The liquid plastic is fed to the apparatus of Figures 1 and 2 of the drawings. The liquid plastic passes through annular space 8 of blowing nozzle 5 and forms a thin liquid plastic film across the orifices 6a and 7a. The blowing nozzle 5 has an outside diameter of 0.040inch and orifice 7a has an inside diameter of 0. 030 inch. The thin liquid molten plastic film has a diameter of 0.030 inch and a thickness of 0.005 inch. A heated blowing gas consisting of argon or a low heat conductivity gas at a positive pressure is applied to the inner surface of the liquid plastic film causing the film to distend downwardly into a elongated cylinder shape with its outer end closed and its 14 GB 2 083 099 A 14 inner end attached to the outer edge of orifice 7a.
The transverse jet is used to direct an entraining fluid which consists of heated nitrogen over and around the blowing nozzle 5. The transverse jet is aligned at an angle of 35 to 500 relative to the blowing nozzle and a line drawn through the center axis of the transverse jet intersects a line drawn through the center axis of the blowing nozzle 5 at a point 2 to 3 times the outside diameter of the coaxial blowing nozzle 5 above the orifice 7a.
The entrained falling elongated cylinders assume a spherical shape, are cooled to about ambient temperature by a cool quench fluid consisting of a fine water spray which quickly cools, solidifies and hardens the plastic microspheres.
Uniform sized, smooth, hollow plastic microspheres having a 2000 to 3000 micron diameter, a 20 to 40 micron wall thickness and filled with argon or a low heat conductivity gas are obtained. The micros- pheres are closely examined and the walls are found 85 to be free of any trapped gas bubbles.
Example 2
A thermosetting plastic composition comprising a mixture of 50% by weight acrylonitrile and 50% by weight vinylidene chloride and a suitable catalyst is used to make hollow plastic microspheres.
The plastic composition mixture at the blowing nozzle has a viscosity of ten poises.
The liquid plastic mixture is heated and is fed to the apparatus of Figures 1 and 3 of the drawings. The 95 liquid plastic is passed through annular space 8 of blowing nozzle 5 and into tapered portion 21 of outer nozzle 7. The liquid plastic under pressure is squeezed and extruded through a fine gap formed between the outer edge of orifice 6a and the inner surface 22 of the tapered portion 21 of outer nozzle 7 and forms a thin liquid plastic film across the orifices 6a and M. The blowing nozzle 5 has an outside diameter of 0.04 inch and orifice 7a' has an inside diameter of 0.01 inch. The thin liquid plastic film has a diameter of 0. 01 inch and thickness of 0.003 inch. A heated blowing gas consisting of argon or a low heat conductivity gas at a positive pressure is applied to the inner surface of the liquid plastic film causing the film to distend outwardly into an elongated cylinder shape with its outer end closed and its inner end attached to the outer edge of orifice 7a'.
The transverse jet is used to direct an entraining fluid which consists of heated nitrogen over and around the blowing nozzle. The transverse jet isaligned at an angle of 35 to 500 relative to the blowing nozzle and a line drawn through the center axis of the transverse jet intersects a line drawn through the center axis of the blowing nozzle 5 at a point 2 to 3 times the outside diameter of the coaxial blowing nozzle 5 above orifice M.
The entrained failing elongated cylinders filled with the blowing gas quickly assume a spherical shape. The microspheres are contracted with a heat- ing fluid consisting of heated nitrogen which sol idifies, hardens and begins to cure the liquid plastic.
Uniform sized, smooth, hollow plastic microspheres having an about 800 to 900 micron diameter, a 8 to 20 micron wall thickness and an internal pressure of 12 p.s.i.a. are obtained. The microspheres are examined and are found to be free of any trapped gas bubbles. Example 3 A thermosetting composition comprising a mix- ture of 90% by weight methyl methacrylate and 10% by weight styrene and a suitable catalyst is used to make low emissivity, reflective hollow plastic microspheres.
The plastic composition mixture has a viscosity of ten poises at the blowing nozzle.
The liquid plastic mixture is fed to the apparatus of Figures 1 and 3 of the drawings. The liquid plastic is heated to and is passed through annular space 8 of. the blowing nozzle 5 and into tapered portion 21 of outer nozzle 7. The liquid plastic under pressure is squeezed through a fine gap formed between the outer edge of orifice 6a and the inner surface 22 of the tapered portion 21 of outer nozzle 7 and forms a thin liquid plastic film across the orifices 6a and 7a'. The blowing nozzle 5 has an outside diameter of 0.05 inch and orifice 7a' has an inside diameter of 0.03 inch. The thin liquid plastic film has a diameter of 0. 03 inch and a thickness of 0.01 inch. A heated blowing gas consisting of argon or a low heat conductiv- ity gas and containing finely dispersed aluminum particles 0.03 to 0.05 micron size and at a positive pressure is applied to the inner surface of the liquid plastic film causing the film to distend outwardly into an elongated cylinder shape with its outer end closed and its inner end attached to the outer edge of orifice 7a'.
The transverse jet is used to direct an inert entraining fluid which consists of heated nitrogen gas over and around the blowing nozzle. The transverse jet is aligned at an angle of 35 to 50'relative to the blowing nozzle and a line drawn through the center axis of the transversejet intersects a line drawn through the center axis of the blowing nozzle 5 at a point 2 to 3 times the outside diameter of the coaxial blowing nozzle 5 above orifice 7a'.
The entrained failing elongated cylinders filled with the blowing gas containing the dispersed aluminum particles quickly assume a spherical shape. The microspheres are contacted with a heat- ing fluid consisting of heated nitrogen which quickly solidifies, hardens and begins to cure the liquid plastic. The dispersed aluminum particles are deposited on and adhere to the inner wall surface of the plastic microsphere.
Uniform sized, smooth, hollow plastic microspheres, having an about 3000 to 4000 micron diameter, a 30 to 40 micron wall thickness and having a low emissivity, reflective aluminum metal coating 600A to 1000A thick and an internal contained pressure of 12 p.s.i.a. are obtained. The microspheres are examined and are found to be free of any trapped gas bubbles. Example 4 An efficient flat plate solar energy collector, as illustrated in Figure 5 of the drawings, is constructed using the plastic microsphere of the present invention as an improved insulating material.
In accordance with the present invention, the area between the outer cover and the upper surface of the black coated metal absorber plate is filled to a depth J1 t of about one inch with transparent plastic microspheres made by the method of Example 2 of about 800 micron diameter, 10 micron wall thickness and having an internal contained pressure of 10 p.s.i.a. These microspheres are transparent to visible light.
The area between the lower surface of the black coated metal absorber plate and the inner cover member is filled to a depth of about 1 112 inches with the reflective plastic microspheres made by the method of Example 3 of about 3000 micron diameter, 30 micron wall thickness and having a thin low emissivity, reflective aluminum metal coating 700A thick and an internal contained pressure of 12 p.s.i.a. Example 5 An efficient tubular solar energy collector, as illustrated in Figure 6 of the drawings, is constructed using the plastic microspheres of the present invention as an improved insulating material.
In accordance with the present invention, the vol- ume between the outer cover, the sides and the lower curved portion and the double pipe tubular member is filled with transparent plastic microspheres made by the method of Example 2 to provide an about one inch layer of transparent plastic mic- rospheres completely around the double pipe tubular member. The transparent plastic microspheres are 800 microns in diameter, have a wall thickness of 10 microns and an internal contained pressure of 12 p.s.i.a. These microspheres are transparentto visible light. Example 6 The Figure 7 of the drawings illustrates the use of the hollow plastic microspheres of the present invention in the construction of a one-inch thick formed wall panel. The wall panel contains multiple 100 layers of uniform size plastic microspheres made by the method of Example 3 of the invention. The mic rospheres have an about 3000 micron diameter, 30 micron wall thickness and a thin, low emissivity aluminum metal coating 700A thick deposited on the 105 inner wall surface of the microsphere. The internal volume of the microspheres is filled with a low heat conductivity gas, e.g. Freon-1 1, and the interstices between the microspheres is filled with a low heat conductivity foam containing Freon-1 1 gas. The microspheres are treated with a thin adhesive coating of a similar composition to that from which the plastic microspheres were made and formed into a 718 inch thick layer. The adhesive is allowed to cure to form a semi-rigid wallboard. The facing surface of the wallboard is coated with an about 118 inch thick plaster which is suitable for subsequent sizing and painting andlor covering with wall paper. The backing surface of the panel is coated with an about 1116 inch coating of the same plastic composition from which the microspheres are made. The final panels are allowed to cure. The cured panels form strong wall panels which can be sawed and nailed and readily used in construction of new homes. Several sections of the panels are tested and found to have a R value of 12 per inch. Example 7 The Figure 7b of the drawings illusrates the use of the hollow plastic microspheres of the present invention in the construction of a formed wall panel GB 2 083 099 A 15 one-inch thick. The wall panel contains hollow plastic microspheres made by the method of Example 3. The microspheres have a diameter of about 3000 micron, 30 micron wall thickness and a low emissiv- ity aluminum metal coating 700A thick deposited on the inner wall surface of the microsphere. The microspheres are coated with an adhesive of similar composition to that from which the microspheres are made. A layer of microspheres about two inches thick is pressed and flattened between two flat plates to form the microspheres into an oblate spheroid or a general rectangular shape in which the ratio of the height to length of the flattened microspheres is 1:1 The flattened microspheres form a layer about 718 inch thick and are held in this position until the adhesive coating on the microspheres cure after which microspheres retain their flattened shape. The internal volume of the microspheres is filled with a low heat conductivity gas, e.g. Freon-1 1. The flattened configuration of the microspheres substantially reduces the volume of the interstices between the microspheres and any volume that remains is filled with a low heat conductivity foam containing Freon-1 1 gas. The facing surface of the wallboard is about 118 inch plaster which is suitable for subsequent sizing and painting andlor covering with wall paper. The backing of the wall panel is about 1116 inch coating of the plastic from which the microspheres are made. The panels are cured and form strong wall panels which can be sawed and nailed and readily used in construction on new homes. One of the important effects of compressing the microspheres is to significantly reduce the volume of the interstices between the microspheres to substantially reduce the heat loss by convection. Several sections of the panel are tested and found to have a R value of 10 per inch.
The formed panel of Examples 6 and 7 can also be made to have a density gradient in the direction of the front to back of the panel. Where the panel is used indoors the surface facing the room can be made to have a relatively high density and high strength, by increasing the proportion of resin or other binderto microspheres. The surface facing the outside can be made to have relatively low density and a high insulation barrier effect by having a high proportion of microspheres to resin or binder. For example, the front one third of the panel can have an average density of about two to three times that of the average density of the center third of the panel. The density of the back one third of the panel can be about one-half to one-third that of the centerthird of the panel. Where the panels are used on the outside of a house, the sides of the panel can be reversed, i.e. the high density side can face outward.
The shaped forms and formed masses of the present invention have many uses including tile manufacture of improved insulating materials, insulated louvers and synthetic construction board materials.
The hollow microspheres embodied in the masses can be produced from high melting temperature andforfire resistant plastic compositions and when used as a component in building construction retard the development and expansion of fires.
The microspheres can be bonded together by sin- 16 GB 2 083 099 A 16 tering or resin adhesives. The construction materials made from the microspheres can be pre-formed or made at the construction site.
The microspheres may be adhered together with known adhesives or binders to produce semi- or rigid cellulartype materials for use in maufacturing various products or in construction. The micros pheres, because they can be made from very stable plastic compositions, are not subject to degradation by outgassing, aging, moisture, weathering or biological attack. The hollow plastic microspheres when used in manufacture of improved insulating materials can advantageously be used alone or in combination with fiberglass, styrofoam, polyurethane foam, phenol-formaldehyde foam, organic and inorganic binders.
The microspheres of the present invention can be used to make insulating material tapes and insulat ing, wall board and ceiling tiles. The microspheres can also advantageously be used in plastic or resin boat construction to produce high strength hull andlor hulls which themselves are buoyant.
The plastic compositions can also be selected to produce microspheres that will be selectively permeable to specific gases andfor organic molecules.
The plastic compositions used in making the mic rospheres can be transparent, translucent or opa que. A suitable coloring material can be added to the plastic compositions to aid in identification of mic rospheres of specified size andfor wall thickness.
A process for making microspheres as described herein can also be carried out in a centrifuge apparatus in which the coaxial blowing nozzles are disposed in the outer circumferential surface of the centrifuge. Liquid plastics is fed into the centrifuge and because of centrifugal forces rapidly coats and wets the inner wall surface of the outerwall of the centrifuge. The liquid plastics is fed into the outer coaxial nozzle. The inlet to the inner coaxial nozzle is disposed above the coating of liquid plastics. The blowing gas is as before fed into the inner coaxial nozzle. The transverse jet entraining fluid is provided by transverse jets mounted on the outer surface of the rotating bowl.
An external gas can be directed along the longitud inal axis of the centrifuge to assist in removing the microspheres from the vicinity of the centrifuge as they are formed. Quench and heating fluids can be provided as before.
It will be understood that various changes and modifications may be made in the invention and that the scope thereof is not to be regarded as limited to the details of the embodiments which have been particularly described and illustrated herein. 120
Claims (48)
1. A shaped form or formed mass of cemented or bonded together hollow organic film forming mater ial microspheres having a diameter of 200 to 10,000 microns and having a wall thickness of 0.1 to 1,000 microns, wherein said microspheres are free of latent solid or liquid blowing gas materials or gases and the walls of said microspheres are substantially free of holes, relatively thinned wall portions or sec tions and bubbles.
2. A shaped form or formed mass of cemented or bonded together hollow organic film forming mater ial microspheres of substantially uniform diameter of 500 to 6,000 microns and of substantially uniform wall thickness of 0.5 to 400 microns, wherein said microspheres are free of latent solid or liquid blowing gas materials or gases and the walls of said microspheres are substantially free of holes, relatively thinned wall portions or sections and bubbles.
3. The shaped form or formed mass of microspheres of Claim 2 wherein the microspheres are cemented together by fusion or sintering or are bonded together with an organic or inorganic bonding agent or adhesive.
4. The shaped form or formed mass of microspheres of Claim 2 wherein the microspheres comprise a filler material.
5. The microspheres of Claim 4 having a contained gas pressure of 15 to 75 p.s.i.a.
6. The shaped form or formed mass of microspheres of Claim 3 formed into a thin sheet or panel.
7. The microspheres of Claim 6 having deposited on the inner wall surfaces thereof a thin metal coating of 50 to 5000A thick.
8. A shaped form or formed mass of cemented or bonded together filamented, hollow organic film forming material microspheres having a diameter of 200 to 10,000 microns and having a wall thickness of 0.1 to 1000 microns, wherein said microspheres are connected to each other by filament portions which are continuous with the microspheres and are of the same organic film forming material from which the microspheres are made.
9. A shaped form or formed mass of cemented or bonded together filamented, hollow organic film forming material microspheres having a diameter of 500 to 6000 microns and having a wall thickness of 0.5 to 400 microns, wherein said microspheres are connected to each other by filament portions which are continuous with the microspheres and are of the same organic film forming material from which the microspheres are made.
10. The shaped form or formed mass of microspheres of Claim 9 wherein the microspheres are cemented together by fusion or sintering or are bonded together with an organic or inorganic bonding agent or adhesive.
11. The microspheres of Claim 10 wherein the length of the connecting filaments is substantially equal and is 2 to 20 times the diameter of the microspheres.
12. The microspheres of Claim 10 wherein the length of the connecting filaments is substantially equal and the diameterof the connecting filamentd if 112500 to 1120 the diameter of the microspheres.
13. The shaped form or formed mass of microspheres of Claim 9 wherein the microspheres com-"' prise a filler material.
14. The shaped form or formed mass of micros- pheres of Claim 10 formed into a thin sheet or panel.
15. A shaped form or formed mass of cemented or bonded together hollow plastic microspheres having a diameter of 200 to 10,000 microns and having a wall thickness of 0.1 to 1,000 microns, wherein said microspheres are free of latent solid or liquid blow- 1 1 1 17 GB 2 083 099 A 17 ing gas materials or gases and the walls of said mic rospheres are substantially free of holes, relatively thinned wall portions or sections and bubbles.
16. A shaped form or formed mass of cemented or bonded together hollow plastic microspheres of substantially uniform diameter of 500 to 6,000 mic rons and of substantially uniform wall thickness of 0.5 to 400 microns, wherein said microspheres are free of latent solid or liquid blowing gas materials or gases and the walls of said microspheres are sub stantially free of holes, relatively thinned wall por tions or sections and bubbles.
17. The shaped form or formed mass of micros pheres of Claim 16 wherein the microspheres are cemented together by fusion or sintering or are bonded together with an organic on inorganic bond ing agent or adhesive.
18. The microspheres of Claim 17 having a thin metal coating deposited on the innerwali surfaces of the microspheres consisting of a layer of dispersed 85 metal particles 50 to 5000A thick.
19. The microspheres of Claim 17 having a diameterof 500 to 3000 microns and a wall thickness of 0.5 to 200 microns.
20. The microspheres of Claim 17 having an average bulk density of 0.5 to 12 lb/ft3.
21. The shaped form or formed mass of micros pheres of Claim 16 wherein the microspheres com prise a filler material.
22. The microspheres of Claim 21 having a contained gas pressure of 15 to 75 p.s.i.a.
23. The shaped form or formed mass of microspheres of Claim 21 wherein the shaped form or formed mass comprises said microspheres and a member selected from the group consisting of plastics, resins, concrete and asphalt.
24. The shaped form or formed mass of microspheres of Claim 17 formed into a thin sheet or panel.
25. The microspheres of Claim 24 having deposted on the inner wall surfaces thereof a thin metal coating 100to 1000Athick.
26. The microspheres of Claim 25 wherein the deposited metal is less than 1 OOA thick and is trans parent to visible light.
27, The microspheres of Claim 25 wherein the 110 deposited metal is more than 100A thick and is reflective of visible light.
28. The microspheres of Claim 24 having an oblate spheroid shape.
29. The plastic microspheres of Claim 24 wherein 115 there is deposited on the inner wall surfaces a thin metal transparent coating 25 to 90A thick.
30. The plastic microspheres of Claim 24 wherein there is deposited on the inner wall surfaces thereof a thin metal reflective coating 105 to 600A thick.
31. The microspheres of Claim 24 wherein the microspheres have deposited on the inner wall surfaces thereof a thin metal coating 150 to 250A thick.
32. The microspheres of Claim 24 wherein the microspheres have deposited on the inner wall surfaces thereof a thin metal coating 150 to 40M thick.
33. A shaped form or formed mass of cemented or bonded together filamented, hollow plastic microspheres having a diameter of 200 to 10, 000 mic- rons and having a wall thickness of 0.1 to 1000 mic- rons, wherein said microspheres are connected to each other by filament portions which are continuous with the microspheres and are of the same organic film forming material from which the mic- rospheres are made.
34. A shaped form or formed mass of cemented or bonded together fi lamented, hollow plastic m icrospheres having a diameter of 500 to 6000 microns and having a wall thickness of 0.5 to 400 microns, wherein said microspheres are connected to each other by filament portions which are continuous with the microspheres and are of the same organic film forming material from which the microspheres are made.
35. The shaped form or formed mass of micros pheres of Claim 34 wherein the microspheres are cemented together by fusion or sintering or are bonded together with an organic or inorganic bond ing agent or adhesive.
36. The shaped form or bonded mass of micros pheres of Claim 34 wherein the microspheres com prise a filler material.
37. The microspheres of Claim 36 having a con tained gas pressure of 15 to 75 p.s.i.a.
38. The shaped form or formed mass of micros pheres of Claim 36 wherein the shaped form or formed mass comprises said microspheres and a member selected from the group consisting of plas tics, resins, concrete and asphalt.
39. The shaped form or formed mass of micros pheres of Claim 35 formed into a thin sheet or panel.
40. The microspheres of Claim 39 having depo sited on the inner wall surfaces thereof a thin metal coating 50 to 5000A thick.
41. The microspheres of Claim 40 wherein the deposited metal is less than 100A thick and is trans parent to visible light.
42. The microspheres of Claim 40 wherein the deposited metal is more than 1 OOA thick and is reflective of visible light.
43. The microspheres of Claim 39 having an oblate spheroid shape.
44. The microspheres of Claim 35 wherein the length of the connecting filaments is substantially equal and is 2 to 20 times the diameter of the mic rospheres.
45. The microspheres of Claim 35 wherein the length of the connecting filaments is substantially equal and the diameter of the connecting filament is 112500 to 1120 the diameter of the microspheres.
46. A formed panel comprising amass of fi lamented hollow, organic film forming material microspheres and an adhesive binder for said microspheres, said microspheres having a diameter of 500 to 6000 microns and a wail thickness of 0.5 to 400 microns, wherein said microspheres are connected to each other by filament portions which are continuous with the microspheres and are of the same organic film forming material from which the microspheres are made.
47. A tape comprising amass of filamented hollow, organic film forming material microspheres, an adhesive binder for said microspheres, a backing for said microspheres and an adhesive for said tape, said microspheres having a diameter of 500 to 6000 is GB 2 083 099 A 18 microns and a wall thickness of 0.5 to 400 microns, wherein said microspheres are connected to each other by filamented portions which are continuous with the microspheres and are of the same organic film forming material from which the microspheres are made.
48. A composition comprising asphalt and a mass of filamented hollow, organic film forming material microspheres, said microspheres having a diameterof 500 to 6000 microns and a wall thickness of 0.5 to 400 microns, wherein said microspheres are connected to each other by filamented portions which are continuous with the microspheres and are of the same organic film forming material from which the microspheres are made.
Printed for Her Majesty's Stationery Office by The Tweeddale Press Ltd-Berwick-upon-Tweed, 1982. Published atthe Patent Office,25 Southampton Buildings, London,WC2A lAY, from which copies may be obtained.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US93712378A | 1978-08-28 | 1978-08-28 | |
US94464378A | 1978-09-21 | 1978-09-21 | |
US5929679A | 1979-07-20 | 1979-07-20 |
Publications (2)
Publication Number | Publication Date |
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GB2083099A true GB2083099A (en) | 1982-03-17 |
GB2083099B GB2083099B (en) | 1983-04-27 |
Family
ID=27369619
Family Applications (4)
Application Number | Title | Priority Date | Filing Date |
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GB7943902A Expired GB2042963B (en) | 1978-08-28 | 1979-08-17 | Method and apparatus for producing hollow plastic microspheres |
GB8127636A Expired GB2081877B (en) | 1978-08-28 | 1979-12-28 | A solar energy collector |
GB8127634A Expired GB2082190B (en) | 1978-08-28 | 1979-12-28 | Hollow plastics microspheres |
GB8127635A Expired GB2083099B (en) | 1978-08-28 | 1979-12-28 | A shaped form or formed mass of microspheres |
Family Applications Before (3)
Application Number | Title | Priority Date | Filing Date |
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GB7943902A Expired GB2042963B (en) | 1978-08-28 | 1979-08-17 | Method and apparatus for producing hollow plastic microspheres |
GB8127636A Expired GB2081877B (en) | 1978-08-28 | 1979-12-28 | A solar energy collector |
GB8127634A Expired GB2082190B (en) | 1978-08-28 | 1979-12-28 | Hollow plastics microspheres |
Country Status (4)
Country | Link |
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EP (1) | EP0018410A1 (en) |
CA (1) | CA1150017A (en) |
GB (4) | GB2042963B (en) |
WO (1) | WO1980000426A1 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2398296A (en) * | 2003-01-23 | 2004-08-18 | Bj Services Co | Cement containing a polymer encapsulated expandable material |
US7543642B2 (en) | 2003-01-24 | 2009-06-09 | Halliburton Energy Services, Inc. | Cement compositions containing flexible, compressible beads and methods of cementing in subterranean formations |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0226738B1 (en) * | 1978-08-28 | 1989-06-14 | TOROBIN, Leonard B. | Filamented, hollow microspheres and applications thereof |
CA1287459C (en) * | 1986-10-01 | 1991-08-13 | Mukesh Jain | Process for the preparation of hollow microspheres |
CA1329461C (en) * | 1987-04-14 | 1994-05-17 | Alcan International Limited | Process of producing aluminum and titanium nitrides |
US8316842B2 (en) | 2004-08-24 | 2012-11-27 | Natan Guryevskiy | Solar heat collector |
US20130020049A1 (en) | 2011-07-18 | 2013-01-24 | Architectural Applications P.C. | Architectural heat and moisture exchange |
DE202015009384U1 (en) | 2014-10-20 | 2017-05-10 | Architectural Applications P.C. | Rain cover with integrated heat and moisture exchanger |
CN112592244B (en) * | 2020-12-18 | 2022-11-25 | 大同市农产品质量安全检验检测中心 | Vegetable organic fertilizer and preparation method thereof |
Family Cites Families (14)
Publication number | Priority date | Publication date | Assignee | Title |
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US948541A (en) * | 1908-03-23 | 1910-02-08 | Clyde J Coleman | Heat-insulating wall. |
US1871792A (en) * | 1925-03-02 | 1932-08-16 | Aluminum Co Of America | Treatment of metallic oxides |
US2187432A (en) * | 1935-11-11 | 1940-01-16 | Milton A Powers | Process and apparatus for the manufacture of insulating material |
US2907626A (en) * | 1958-01-15 | 1959-10-06 | Bjorksten Res Lab Inc | Metal coating of glass fibers at high speeds |
US3186812A (en) * | 1961-06-08 | 1965-06-01 | Owens Illinois Glass Co | Method and apparatus for forming hollow glass articles |
US3226285A (en) * | 1962-01-04 | 1965-12-28 | Mencher Alexander | Modified plastic tubing |
US3365315A (en) * | 1963-08-23 | 1968-01-23 | Minnesota Mining & Mfg | Glass bubbles prepared by reheating solid glass partiles |
US3421873A (en) * | 1966-03-17 | 1969-01-14 | Jerome A Burgman | Method and apparatus for producing an intermittently hollow glass filament |
US3607169A (en) * | 1968-11-07 | 1971-09-21 | Exxon Research Engineering Co | Method for producing evacuated glass microspheres |
ZA718171B (en) * | 1971-01-12 | 1972-09-27 | Lavorazione Mat Plast | Synthetic resin laminate and its manufacturing process |
JPS495722A (en) * | 1972-04-28 | 1974-01-18 | ||
US3955956A (en) * | 1975-08-06 | 1976-05-11 | Midland Glass Company, Inc. | Process for producing glass articles |
JPS5911540B2 (en) * | 1976-06-21 | 1984-03-16 | セントラル硝子株式会社 | Inorganic fiber manufacturing method and device |
DE2649472A1 (en) * | 1976-10-29 | 1978-05-03 | Schoell Guenter | TRANSPARENT THERMAL INSULATION |
-
1979
- 1979-08-17 WO PCT/US1979/000622 patent/WO1980000426A1/en unknown
- 1979-08-17 GB GB7943902A patent/GB2042963B/en not_active Expired
- 1979-08-27 CA CA000334619A patent/CA1150017A/en not_active Expired
- 1979-12-28 GB GB8127636A patent/GB2081877B/en not_active Expired
- 1979-12-28 GB GB8127634A patent/GB2082190B/en not_active Expired
- 1979-12-28 GB GB8127635A patent/GB2083099B/en not_active Expired
-
1980
- 1980-03-25 EP EP79901297A patent/EP0018410A1/en not_active Withdrawn
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2398296A (en) * | 2003-01-23 | 2004-08-18 | Bj Services Co | Cement containing a polymer encapsulated expandable material |
GB2398296B (en) * | 2003-01-23 | 2007-04-25 | Bj Services Co | Polymer shell encapsulated gas as a cement expansion additive |
US7494544B2 (en) | 2003-01-23 | 2009-02-24 | Bj Services Company | Polymer shell encapsulated gas as a cement expansion additive |
US7543642B2 (en) | 2003-01-24 | 2009-06-09 | Halliburton Energy Services, Inc. | Cement compositions containing flexible, compressible beads and methods of cementing in subterranean formations |
Also Published As
Publication number | Publication date |
---|---|
GB2082190B (en) | 1983-04-13 |
GB2042963A (en) | 1980-10-01 |
GB2082190A (en) | 1982-03-03 |
GB2081877B (en) | 1983-05-25 |
GB2081877A (en) | 1982-02-24 |
GB2083099B (en) | 1983-04-27 |
WO1980000426A1 (en) | 1980-03-20 |
CA1150017A (en) | 1983-07-19 |
GB2042963B (en) | 1983-03-09 |
EP0018410A1 (en) | 1980-11-12 |
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Legal Events
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PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 19950817 |