WO2003040048A2 - Method for utilising silica soot from quartz glass production - Google Patents
Method for utilising silica soot from quartz glass production Download PDFInfo
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- WO2003040048A2 WO2003040048A2 PCT/NO2002/000406 NO0200406W WO03040048A2 WO 2003040048 A2 WO2003040048 A2 WO 2003040048A2 NO 0200406 W NO0200406 W NO 0200406W WO 03040048 A2 WO03040048 A2 WO 03040048A2
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- Prior art keywords
- silica
- silica soot
- parts
- weight
- soot
- Prior art date
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 title claims abstract description 171
- 239000000377 silicon dioxide Substances 0.000 title claims abstract description 69
- 239000004071 soot Substances 0.000 title claims abstract description 66
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 34
- 238000000034 method Methods 0.000 title claims abstract description 19
- 239000000565 sealant Substances 0.000 claims abstract description 43
- 239000002699 waste material Substances 0.000 claims abstract description 15
- 229920002379 silicone rubber Polymers 0.000 claims abstract description 9
- 239000011521 glass Substances 0.000 claims abstract description 6
- 229910021485 fumed silica Inorganic materials 0.000 claims description 35
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 14
- 239000004590 silicone sealant Substances 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- 239000000945 filler Substances 0.000 claims description 11
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- 239000000463 material Substances 0.000 claims description 9
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 8
- 238000009472 formulation Methods 0.000 claims description 8
- 239000004945 silicone rubber Substances 0.000 claims description 6
- 239000003054 catalyst Substances 0.000 claims description 5
- 230000001698 pyrogenic effect Effects 0.000 claims description 5
- 239000004589 rubber sealant Substances 0.000 claims description 5
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 4
- 230000002209 hydrophobic effect Effects 0.000 claims description 4
- 229920001021 polysulfide Polymers 0.000 claims description 4
- 239000012763 reinforcing filler Substances 0.000 claims description 4
- 239000004971 Cross linker Substances 0.000 claims description 3
- 239000002318 adhesion promoter Substances 0.000 claims description 3
- 230000007062 hydrolysis Effects 0.000 claims description 3
- 238000006460 hydrolysis reaction Methods 0.000 claims description 3
- 239000000049 pigment Substances 0.000 claims description 3
- 239000004014 plasticizer Substances 0.000 claims description 3
- 241000500881 Lepisma Species 0.000 claims description 2
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 claims 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 229920000642 polymer Polymers 0.000 claims 1
- 239000000654 additive Substances 0.000 abstract description 3
- 239000003973 paint Substances 0.000 abstract description 3
- 239000000123 paper Substances 0.000 abstract description 3
- 229920001944 Plastisol Polymers 0.000 abstract description 2
- 238000000576 coating method Methods 0.000 abstract description 2
- 239000002537 cosmetic Substances 0.000 abstract description 2
- 239000003814 drug Substances 0.000 abstract description 2
- 239000005350 fused silica glass Substances 0.000 abstract description 2
- 239000004999 plastisol Substances 0.000 abstract description 2
- 229920005989 resin Polymers 0.000 abstract description 2
- 239000011347 resin Substances 0.000 abstract description 2
- 230000000996 additive effect Effects 0.000 abstract 1
- 239000002994 raw material Substances 0.000 description 6
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 5
- 229910052710 silicon Inorganic materials 0.000 description 5
- 239000010703 silicon Substances 0.000 description 5
- 229920004482 WACKER® Polymers 0.000 description 4
- 239000004148 curcumin Substances 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 229910000077 silane Inorganic materials 0.000 description 4
- 238000011084 recovery Methods 0.000 description 3
- 239000013008 thixotropic agent Substances 0.000 description 3
- MVODTGURFNTEKX-UHFFFAOYSA-N 2-bromo-n-(2-bromoethyl)-n-(thiophen-2-ylmethyl)ethanamine;hydrobromide Chemical compound Br.BrCCN(CCBr)CC1=CC=CS1 MVODTGURFNTEKX-UHFFFAOYSA-N 0.000 description 2
- -1 Acryl Chemical group 0.000 description 2
- 229910002012 Aerosil® Inorganic materials 0.000 description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 238000009435 building construction Methods 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- YDPIJJUIHRPFAN-UHFFFAOYSA-N hydroxyimino(methyl)silane Chemical compound C[SiH]=NO YDPIJJUIHRPFAN-UHFFFAOYSA-N 0.000 description 2
- 238000009533 lab test Methods 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 239000013307 optical fiber Substances 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 238000005204 segregation Methods 0.000 description 2
- 229910021487 silica fume Inorganic materials 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 229920005573 silicon-containing polymer Polymers 0.000 description 2
- VXEGSRKPIUDPQT-UHFFFAOYSA-N 4-[4-(4-methoxyphenyl)piperazin-1-yl]aniline Chemical compound C1=CC(OC)=CC=C1N1CCN(C=2C=CC(N)=CC=2)CC1 VXEGSRKPIUDPQT-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 241001085205 Prenanthella exigua Species 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 229910021486 amorphous silicon dioxide Inorganic materials 0.000 description 1
- 229920005549 butyl rubber Polymers 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 238000010891 electric arc Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- IZDPBPIQKQJYFB-UHFFFAOYSA-N ethenyl(hydroxyimino)silane Chemical compound ON=[SiH]C=C IZDPBPIQKQJYFB-UHFFFAOYSA-N 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000003349 gelling agent Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 238000009854 hydrometallurgy Methods 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 235000021190 leftovers Nutrition 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000011344 liquid material Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 238000009853 pyrometallurgy Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 150000003376 silicon Chemical class 0.000 description 1
- 239000005049 silicon tetrachloride Substances 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/03—Printing inks characterised by features other than the chemical nature of the binder
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds
- C08K3/36—Silica
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/43—Thickening agents
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/10—Materials in mouldable or extrudable form for sealing or packing joints or covers
- C09K3/1006—Materials in mouldable or extrudable form for sealing or packing joints or covers characterised by the chemical nature of one of its constituents
- C09K3/1018—Macromolecular compounds having one or more carbon-to-silicon linkages
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G7/00—Selection of materials for use in image-receiving members, i.e. for reversal by physical contact; Manufacture thereof
- G03G7/0006—Cover layers for image-receiving members; Strippable coversheets
- G03G7/002—Organic components thereof
- G03G7/0026—Organic components thereof being macromolecular
- G03G7/0033—Natural products or derivatives thereof, e.g. cellulose, proteins
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/06—Lead-acid accumulators
- H01M10/08—Selection of materials as electrolytes
- H01M10/10—Immobilising of electrolyte
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
-
- 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
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
Definitions
- This invention relates to a method of utilising silica soot from the quartz glass production. More specific, this invention is a method for utilising the pure silica soot, which is collected in the off-gas filter in the production of optical fibre raw material quartz glass cylinder ingots.
- the group of fine silica materials consists of micro-silica, precipitated silica and fumed silica.
- Micro-silica stems from the production of silicon metal in electric arc furnaces. It has a specific surface area of approx. 10-30 m 2 /g and is mainly applied in the concrete business.
- the precipitated silica is produced in a hydrometallurgical process, has a specific surface area in the range of 90-600 m 2 /g and is used as reinforcement filler to silicon rubber and plastic as well as filler in paper and paints.
- Fumed silica is produced in a pyrometallurgical process, has a specific surface area in the range of 100-800 m /g and is used as a pseudoplastic and thixotropic property agent in resins, as a rheological property agent in plastisols, to reduce the water absorption of printing ink, viscosity control and thixotropic agent in paints and coatings, as thickener and gelling agent in rechargeable batteries, in chemical-mechanical polishing, as a reinforcing filler in silicon elastomers, as reinforcing and rheological properties agent in joint sealant, in electrophotographic toners and developers as well as in cosmetics, pharmaceuticals and foods.
- Silica soot stems from the production of high purity fused quartz glass for e g the optical fibre industry.
- the first step of the quartz glass produced can be to produce silica soot in a flame hydrolysis process, in which silicon tetrachloride and various volatile reactants are introduced to an oxygen/hydrogen flame.
- the product of this process takes a physical form of fine particles and these are usually designated as silica "soot".
- this silica soot is heated to or slightly above its melting point.
- silica soot particles fuse with one another and create a quartz glass material without voids.
- some of the silica soot particles escape the sintering process trough the furnace off-gas system and must be collected in the off-gas cleansing filter.
- this silica soot, collected in the off-gas filter has mainly been considered as a waste material which has been pelletized and put on the municipal rubbish heap.
- This solution of the waste slurry problem is unfortunate, both from an economical and environmental point of view. Especially when considering that the silicon soot are leftovers from one of the commercially available purest raw material, and thus constitute a valuable material which is well suited to be applied as raw material in a number of industrial applications.
- the objective of this invention is to eliminate the waste disposal by utilising the silica soot as a raw material in other industrial applications.
- Another objective of this invention is to provide a method for using the silica soot as a substitute to fumed and precipitated silica.
- silica soot is a very pure X-ray amorphous silicon dioxide (SiO2) which is physiologically inert.
- silica soot may be utilised as a substitute for conventional fumed silica and/or precipitated silica as an active reinforcing filler and thixotropic agent in a variety of applications.
- Table 1 which compares a set of properties of a conventional fumed silica sold under the name acker HDK® H 15 and silica soot. Both materials have a bright white colour with light reflection above 94%.
- silica soot is a waste material which is very cheap compared to a highly purified raw material such as fumed silica or precipitated silica. And it is fairly obvious that the environment will also benefit when a waste materiel is given the opportunity of being utilised as a raw material in other industrial processes.
- the Silica Soot is a pyrogenic silica with a specific area (BET) of ca 50 m 2 /g.
- BET specific area
- TOTAL 100,00 110,00 Sealants with a total movement capacity of 25% are classified according to their modulus into two types:
- Type HM high modulus tensile modulus E 100 at 23 °C > 0,4 N/mm 2 at - 20 °C > 0,6 N/mm 2
- the tested transparent/opalescent silicone sealant fulfil the requirements of ISO 11600 for high modulus sealants with a total movement capacity of 25 % and is design as: Sealant ISO 11600 F - 25 HM Because of the lower specific area the amount of pyrogenic Silica Soot is about three times higher to have a non sag type sealant. Due to this effect it is possible to incorporate more silica into the sealant.
- the whitish colour of the pyrogenic Silica Soot is suitable for the production of transparent/translucent silicone sealants.
- Acrylic sealants with Silica Soot has been produced and tested according to ISO F/DIS 116600 : 2001 Building construction- Jointing products-Sealants- Classification and requirements in order to find out if the in acrylic sealants widely used pyrogenic silica Aerosil R 972 can be replaced by Silica Soot.
- the Silica Soot is a pyrogenic silica with a specific area (BET) of ca 50 m 2 /g.
- the pyrogenic Silica Soot with a specific surface area (BET) of 47.9 m 2 /g was used instead of a pyrogenic hydrophobic silica Aerosil R 972 with a BET surface area of 110 m 2 /g in a acrylic water-based sealant.
- Acrylic sealants with a total movement capacity of 12,5 % are classified according to their modulus into two types:
- the tested acrylic sealants correspond to a sealant with mainly elastomeric properties.
- the preconditioning was carried out according to method B of DIN EN 28 340.
- Test according to ISO F/DIS 11600:2001 The test of the adhesion and cohesion properties was carried out according to the test conditions described in the test procedures.
- the tested acrylic sealant fulfill the requirements of ISO F/DIS 11600:2001 for elastomeric sealants with a total movement capacity of 12,5 % and is design as: Sealant ISO 11600 F - 12,5 E
- Silicone rubber is often produced from dimethyl-dichlorine-silane, in a process where the chlorine ions are exchanged with oxygen through hydrolysis until the whole material is polymerised.
- a number of additives are added to the liquid material to provide it with the ideal rheological properties and also the necessary mechanical strength as well as a smooth surface.
- additives are among others; filler, plasticizer, adhesion promoter, crosslinker, and cure catalyst.
- Fumed silica e g the above mentioned Wacker HDK® H 15, is the most commonly used filler in silicone rubber. Normally approximately 8-10% fumed silica is added as filler material.
- the silicone rubber is somewhat heavier.
- the additional weight might reduce the price in the market.
- the loss of transparency will make silica soot useful only in coloured silicone sealer applications.
- sealants Another class of sealants is polysulphide rubber sealants, a two component sealant comprising a liquid polysulphide elastomer and a curing agent.
- Such sealants often contain calcium carbonate and have encountered problems with segregation. These problems can be solved by replacing the calcium carbonate filler with silica soot. This is a surprising effect since it is known that conventional fumed silica gives a too large viscosity of the sealant.
- Silica soot has been mixed with water to a slicker in the soot/water weight ratio 1 : 1. The mixture got stiff after a few hours. After nine months it is still set, showing no signs of segregation. A touch with e g a brush brings it back to the fluid state. Left to rest the mixture get stiff again. This indicates that silica soot is an excellent viscosity control and thixotropic agent.
- silica soot from the production quartz glass as a replacement of filler materials in other sealants, such as for instance acrylic sealants, butyl rubber sealants etc., and in other types of products such as for instance urethane prepolymers etc.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- General Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- General Physics & Mathematics (AREA)
- Manufacturing & Machinery (AREA)
- Electrochemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Sealing Material Composition (AREA)
- Glass Compositions (AREA)
Abstract
This invention relates to method of utilising a waste material from quartz glass production. More specific, this invention relates to a method for utilising the so-called silica soot, which stems from the fused quartz glass production, as an additive in other industrial processes such as production of resins, plastisols, printing ink, paints and coatings, rechargeable batteries, silicon elastomers, joint sealant, electrophotographics toners and developers as well as in cosmetics, pharmaceuticals and paper.
Description
Method for utilising silica soot from quartz glass production
This invention relates to a method of utilising silica soot from the quartz glass production. More specific, this invention is a method for utilising the pure silica soot, which is collected in the off-gas filter in the production of optical fibre raw material quartz glass cylinder ingots.
Background
The group of fine silica materials consists of micro-silica, precipitated silica and fumed silica.
Micro-silica stems from the production of silicon metal in electric arc furnaces. It has a specific surface area of approx. 10-30 m2/g and is mainly applied in the concrete business.
The precipitated silica is produced in a hydrometallurgical process, has a specific surface area in the range of 90-600 m2/g and is used as reinforcement filler to silicon rubber and plastic as well as filler in paper and paints. Fumed silica is produced in a pyrometallurgical process, has a specific surface area in the range of 100-800 m /g and is used as a pseudoplastic and thixotropic property agent in resins, as a rheological property agent in plastisols, to reduce the water absorption of printing ink, viscosity control and thixotropic agent in paints and coatings, as thickener and gelling agent in rechargeable batteries, in chemical-mechanical polishing, as a reinforcing filler in silicon elastomers, as reinforcing and rheological properties agent in joint sealant, in electrophotographic toners and developers as well as in cosmetics, pharmaceuticals and foods. It is also used in paper to enhance opacity, reflection, printing, pitch adhesion on rollers, retention aid and to give a smooth surface and enhanced friction. Silica soot stems from the production of high purity fused quartz glass for e g the optical fibre industry. The first step of the quartz glass produced can be to produce silica soot in a flame hydrolysis process, in which silicon tetrachloride and various volatile reactants are introduced to an oxygen/hydrogen flame. The product of this process takes a physical form of fine particles and these are usually designated as silica "soot". In the second step of the quartz glass production this silica soot is heated to or slightly above its melting point. The silica soot particles fuse with one another and create a quartz glass material without voids. However, some of the silica soot particles escape the sintering process trough the furnace off-gas system and must be collected in the off-gas cleansing filter. Up till now, this silica soot, collected in the off-gas filter, has mainly been considered as a waste material which has been pelletized and put on the municipal rubbish heap.
This solution of the waste slurry problem is unfortunate, both from an economical and environmental point of view. Especially when considering that the silicon soot are leftovers from one of the commercially available purest raw material, and thus constitute a valuable material which is well suited to be applied as raw material in a number of industrial applications.
Object of the Invention
The objective of this invention is to eliminate the waste disposal by utilising the silica soot as a raw material in other industrial applications.
Another objective of this invention is to provide a method for using the silica soot as a substitute to fumed and precipitated silica.
Brief description of the invention
The objects of this invention can be achieved by what is described in the appended claims and/or in the following description.
The objectives of this invention can be obtained by exploiting the fact that silica soot is a very pure X-ray amorphous silicon dioxide (SiO2) which is physiologically inert. Thus silica soot may be utilised as a substitute for conventional fumed silica and/or precipitated silica as an active reinforcing filler and thixotropic agent in a variety of applications. This can for instance be seen from Table 1 which compares a set of properties of a conventional fumed silica sold under the name acker HDK® H 15 and silica soot. Both materials have a bright white colour with light reflection above 94%.
Table 1 Comparison of silica soot and fumed silica of type Wacker HDK® H IS
Wacker Silica soot
HDK® H 15
Surface area according to BET (m2/g) 120+20 50±10
SiO2-content (%) 99,8 99,9
Moisture (%) <0,6 0,5
Loss of ignition (%) <2,0 <0,01 pH-value 4,0-4,8 2,8-3,9
HCL-content (%) <0,02 0,02
Al2O3-content (%) <0,05 0,02
Fe2O3-content (%) <0,005 <0,01
C-content (%) <2,0 0,03
From Table 1, one has that silica soot is purer than Wacker HDK® H 15 while the surface area of silica soot is approx. half the size of the Wacker material. Thus for some applications where the surface area is the dominating property, one has to use roundabout twice the quantity of silica soot when substituting fumed silica. Obviously, when the ratio of the surface area of silicon soot and the fumed or precipitated silica is different from the ratio of the example shown in Table 1 , the quantity ratio of silicon soot/substituted silicon should be the adjusted accordingly.
However, even if one has to substitute fumed silica with larger amounts of silica soot, there is still considerable economical benefits involved since silica soot is a waste material which is very cheap compared to a highly purified raw material such as fumed silica or precipitated silica. And it is fairly obvious that the environment will also benefit when a waste materiel is given the opportunity of being utilised as a raw material in other industrial processes.
Detailed description of the invention
The invention will now be described in more detail by way of examples of preferred embodiments. This should not be constructed as a limitation of the invention.
Example 1 Production of silicone sealant Silicon sealants with Silica Soot has been produced and tested according to ISO
116600 Building construction-Sealants-Classification and requirements in order to find out if the in silicone sealants widely used pyrogenic silica can be replaced by Silica Soot.
As described, the Silica Soot is a pyrogenic silica with a specific area (BET) of ca 50 m2/g. When incorporated in transparent formulations of silicone sealants the sealant appears opalescent.
The pyrogenic Silica Soot with a specific surface area (BET) of 47.9 m2/g was used instead of a pyrogenic silica with a BET surface area of 150 m /g in a transparent (tr) and a pigment containing formulation (pig). Exchanging pyrogenic silica in a silicone sealant formulation with oxin-cure by Silica Soot the following compositions have been obtained:
Table 2 Transparent/opalescent silicone-sealant (parts by weight)
Formulation Si-tr-1 Si-tr-2
Silicone-polymer MG 50 000 58,00 58,00
Silicon-oil 1000 27,00 27,00
MOS Methyloximino-Silane 4,00 4,00
NOS Vinyloximino-Silane 1,30 1,30
HDK V 15 Wacker 9,23
Silica Soot 35,00
Silane 3024 AMMO 0,40 0,40
Catalyst DBTA 0,07 0,07
TOTAL 100,00 125,77
For the exchange of the pyrogenic silica the sealants have been tested according to:
ISO 11600 Building construction - Sealants, Classification and requirements (1993) construction sealants (F)
Table 3 Pigment-containing silicone-sealant (parts by weight)
Formulation Si-pig-1 Si-pig-2
Silicone-polymer MG 50 000 38,00 38,00
Silicon-oil 1000 20,50 20,50
MOS Methyloximino-Silane 3,50 3,50
NOS Ninyloximino-Silane 0,90 0,90
HDK N 15 Wacker 5,00
Silica Soot 15,00 ■ calsium carbonate Omyacarb 5 GU 30,00 30,00
Silane 3024 AMMO 0,50 0,50
Titandioxide-paste 1,50 1,50
Catalyst DBTA 0,10 0,10
TOTAL 100,00 110,00
Sealants with a total movement capacity of 25% are classified according to their modulus into two types:
Type LM (low modulus) tensile modulus E 100 at 23 °C ≤ 0,4 N/mm2 at - 20 °C < 0,6 N/mm2
Type HM (high modulus) tensile modulus E 100 at 23 °C > 0,4 N/mm2 at - 20 °C > 0,6 N/mm2
(E 100: Tensile modulus at 100% elongation)
If either at 23 °C or at -20 °C the tensile modulus is higher than the type LM given values, the sealant is designed as Type HM. The results of the tests are given in the tables 4 and 5 :
Table 4 Test results of transparent/opalescent silicone sealants
In the above described laboratory tests it could be confirmed that the pyrogenic Silica Soot can be used in silicone sealants by replacing the widely used pyrogenic silica with a specific surface area of 150 m2/g.
The tested transparent/opalescent silicone sealant fulfil the requirements of ISO 11600 for high modulus sealants with a total movement capacity of 25 % and is design as: Sealant ISO 11600 F - 25 HM
Because of the lower specific area the amount of pyrogenic Silica Soot is about three times higher to have a non sag type sealant. Due to this effect it is possible to incorporate more silica into the sealant.
The whitish colour of the pyrogenic Silica Soot is suitable for the production of transparent/translucent silicone sealants.
Example 2: Production of water based acrylic sealant
Acrylic sealants with Silica Soot has been produced and tested according to ISO F/DIS 116600 : 2001 Building construction- Jointing products-Sealants- Classification and requirements in order to find out if the in acrylic sealants widely used pyrogenic silica Aerosil R 972 can be replaced by Silica Soot.
As described, the Silica Soot is a pyrogenic silica with a specific area (BET) of ca 50 m2/g.
The pyrogenic Silica Soot with a specific surface area (BET) of 47.9 m2/g was used instead of a pyrogenic hydrophobic silica Aerosil R 972 with a BET surface area of 110 m2/g in a acrylic water-based sealant.
Exchanging pyrogenic silica in an acrylic sealant formulation by Silica Soot the following compositions have been obtained:
For the exchange of the pyrogenic silicas the sealants have been tested according to: ISO F/DIS 11600:2001, Building construction - Jointing products - Sealants, Classification and requirements construction sealants (F)
Table 6 Formulation water based acrylic sealants (parts by weight)
- Class 12,5 E elastomeric type Elastic recovery > 40%
- Class 12,5 P plastic type Elastic recovery < 40%
The tested acrylic sealants correspond to a sealant with mainly elastomeric properties.
The following tests given in table 7 have been carried out:
Table 7 Test program
No. Test Test according to
1 Elastic recovery ISO 7389
2 Tensile properties at maintained extension ISO 8340
3 Adhesion-cohesion properties at varible temperature ISO 9047
Adhesion-cohesion properties
4 under at maintained extension ISO 10590 after water immersion
5 Change of volume ISO 10563
6 Resistance to flow ISO 7390
7 Secant tensile modulus at 60 % and 100 % elongation ISO 8339
8 Dynamic viscosity ISO 3219
The tests of the adhesion and cohesion properties have been carried out with test specimens of mortar coated with acrylic based primer DISBON 486 Acryl Tiefgrund. The sealant was applied after 30 min drying time of the primer.
The preconditioning was carried out according to method B of DIN EN 28 340.
Test according to ISO F/DIS 11600:2001 : The test of the adhesion and cohesion properties was carried out according to the test conditions described in the test procedures.
Test of dynamic viscosity: The dynamic viscosity of the sealants have been tested with the Haake rotavisco with cone and plate according to ISO 3219 at 23 °C. Using the system PK5-1,0 wiyh a share speed from 0 to 50 s"1 the hysteresis was determined.
The results of the tests are given in table 8 :
Table 8 Test result water-based acrylic sealant
1) E 60: secant tensile modulus at 60%o elongation
2) E 100: secant tensile modulus at 100%> elongation
In the above described laboratory tests it could be confirmed that the pyrogenic Silica Soot can be used in water-based acrylic dispersion sealants by replacing the widely used pyrogenic silica with a specific surface area of 110 m2/g.
The tested acrylic sealant fulfill the requirements of ISO F/DIS 11600:2001 for elastomeric sealants with a total movement capacity of 12,5 % and is design as: Sealant ISO 11600 F - 12,5 E
Production of silicone rubber sealant
Silicone rubber is often produced from dimethyl-dichlorine-silane, in a process where the chlorine ions are exchanged with oxygen through hydrolysis until the whole material is polymerised. A number of additives are added to the liquid material to provide it with the ideal rheological properties and also the necessary mechanical strength as well as a smooth surface. Such additives are among others; filler, plasticizer, adhesion promoter, crosslinker, and cure catalyst. Fumed silica, e g the above mentioned Wacker HDK® H 15, is the most commonly used filler in silicone rubber. Normally approximately 8-10% fumed silica is added as filler material.
Trials have shown that by adding 20% silica soot in stead of 8-10% fumed silica, a silicone rubber sealant with almost the same properties is achieved. The rheological properties, the mechanical strength and the rubber surface arc excellent. Yet two properties are different:
The silicone rubber is somewhat heavier.
The transparency has decreased; it has become "milky".
The additional weight might reduce the price in the market. The loss of transparency will make silica soot useful only in coloured silicone sealer applications.
Polysulphide rubber sealant
Another class of sealants is polysulphide rubber sealants, a two component sealant comprising a liquid polysulphide elastomer and a curing agent. Such sealants often contain calcium carbonate and have encountered problems with segregation. These problems can be solved by replacing the calcium carbonate filler with silica soot. This is a surprising effect since it is known that conventional fumed silica gives a too large viscosity of the sealant.
Thixotropy agent
Silica soot has been mixed with water to a slicker in the soot/water weight ratio 1 : 1. The mixture got stiff after a few hours. After nine months it is still set, showing no signs of segregation. A touch with e g a brush brings it back to the
fluid state. Left to rest the mixture get stiff again. This indicates that silica soot is an excellent viscosity control and thixotropic agent.
It is also possible to employ silica soot from the production quartz glass as a replacement of filler materials in other sealants, such as for instance acrylic sealants, butyl rubber sealants etc., and in other types of products such as for instance urethane prepolymers etc.
Claims
1. A method for producing silicone sealants by oxin-curing of a conventional sealant formulation comprising an filler, plasticizer, adhesion promoter, crosslinker, and cure catalyst, until an ideal rheological strength and mechanical strength is achieved, characterised in that the reinforcing filler and rheological properties agent is silica soot waste from quarts glass production instead of conventional pyrogenic silica.
2. A method according to claim 1, characterised in that the ratio (parts by weight times BET for silica soot)/
(parts by weight times BET for pyrogenic silica) is in the range of <0.8, 1.5>, preferably in the range of <0.9, 1.3>.
3. A method according to claim 2, characterised in that in the case of producing a transparent/opalescent silicone-sealant, the ratio (parts by weight times BET for silica soot)/ (parts by weight times BET for pyrogenic silica) is in the range of <0.9, 1.0>.
4. A method according to claim 2, characterised in that in the case of producing a pigment-containing silicone- sealant, the ratio (parts by weight times BET for silica soot)/ (parts by weight times BET for pyrogenic silica) is in the range of <1.15, 1.25>.
5. A method for producing a viscosity control and thixotropy agent, characterised in that silica soot and water is admixed in an 1 : 1 weight ratio in a slicker.
6. A method for producing water based acrylic sealants according to a conventional manufacturing method, characterised in that the conventionally used pyrogenic hydrophobic silica is replaced with silica soot waste from quarts glass production.
7. A method according to claim 6, characterised in that the ratio (parts by weight silica soot)/ (parts by weight pyrogenic hydrophobic silica) is in the range of <0.8, 1.5>, preferably in the range of <0.9, 1.3>.
8. A method according to claim 7, characterised in that the ratio (parts by weight silica soot)/ (parts by weight pyrogenic hydrophobic silica) is in the range of <0.95, 1.05>.
9. A method for producing silicone rubber sealant by hydrolysis of dimethyl - dichlorine-silane until complete polymerisation, where the formed polymer is admixed with filler, plasticizer, adhesion promoter, cross linker, and cure catalyst until an ideal rheological strength and mechanical strength is achieved, characterised in that the reinforcing filler and rheological properties agent is silica soot waste from quarts glass production instead of conventional fumed silica.
10. A method according to claim 9, characterised in that the ratio (parts by weight silica soot)/ (parts by weight fumed silica) is in the range of <1.5, 2.5>, preferably in the range of <1.8,
2.2>.
11. A method for poly-sulphide rubber sealants according to a conventional manufacturing method, characterised in that the conventionally used calcium carbonate filler is replaced with silica soot waste from quarts glass production.
12. Use of a waste fraction comprising silica soot from the production of quartz glass as a viscosity control and/or thixotropy agent.
13. Use of a waste fraction comprising silica soot from the production of quartz glass as a viscosity control and/or thixotropy agent by admixture with water in a weight ratio of approximately 1 : 1.
14. Use of a waste fraction comprising silica soot from the production quartz glass as a substitute for fumed silica in industrial processes.
15. Use of a waste fraction comprising silica soot from the production quartz glass as a substitute for precipitated silica in industrial processes.
16. Use of a waste fraction comprising silica soot from the production quartz glass as a substitute for calcium carbonate as a filler material in polysulphide rubber sealants.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU2002339762A AU2002339762A1 (en) | 2001-11-07 | 2002-11-06 | Method for utilising silica soot from quartz glass production |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10154531 | 2001-11-07 | ||
| DE10154531.2 | 2001-11-07 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2003040048A2 true WO2003040048A2 (en) | 2003-05-15 |
| WO2003040048A3 WO2003040048A3 (en) | 2003-10-16 |
Family
ID=7704822
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/NO2002/000406 WO2003040048A2 (en) | 2001-11-07 | 2002-11-06 | Method for utilising silica soot from quartz glass production |
Country Status (3)
| Country | Link |
|---|---|
| AU (1) | AU2002339762A1 (en) |
| DE (1) | DE10251909A1 (en) |
| WO (1) | WO2003040048A2 (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005095503A1 (en) * | 2004-03-05 | 2005-10-13 | Degussa Ag | Silicone rubber |
| WO2008012641A3 (en) * | 2006-07-28 | 2008-05-22 | Litokol S R L | White mixture for applying a coating |
| US7659328B2 (en) | 2004-02-03 | 2010-02-09 | Degussa Ag | Silicone rubber |
| BE1024484B1 (en) * | 2016-12-01 | 2018-03-05 | Dl Chemicals Detaellenaere-Loosvelt N.V. | Silicone sealant of the oxime type and kit with sealant |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103214854B (en) * | 2013-03-26 | 2016-01-20 | 安徽瑞侃电缆科技有限公司 | A kind of Environment-friendlyfireproof fireproof control cable material and preparation method thereof |
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- 2002-11-07 DE DE10251909A patent/DE10251909A1/en not_active Withdrawn
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Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7659328B2 (en) | 2004-02-03 | 2010-02-09 | Degussa Ag | Silicone rubber |
| WO2005095503A1 (en) * | 2004-03-05 | 2005-10-13 | Degussa Ag | Silicone rubber |
| US9708458B2 (en) | 2004-03-05 | 2017-07-18 | Evonik Degussa Gmbh | Silicone rubber |
| WO2008012641A3 (en) * | 2006-07-28 | 2008-05-22 | Litokol S R L | White mixture for applying a coating |
| BE1024484B1 (en) * | 2016-12-01 | 2018-03-05 | Dl Chemicals Detaellenaere-Loosvelt N.V. | Silicone sealant of the oxime type and kit with sealant |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2003040048A3 (en) | 2003-10-16 |
| AU2002339762A1 (en) | 2003-05-19 |
| DE10251909A1 (en) | 2003-05-22 |
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