DE1794380C3 - Use of chrysotile asbestos as a thixotropic thickener. Eliminated from: 1619771 - Google Patents
Use of chrysotile asbestos as a thixotropic thickener. Eliminated from: 1619771Info
- Publication number
- DE1794380C3 DE1794380C3 DE1794380A DE1794380A DE1794380C3 DE 1794380 C3 DE1794380 C3 DE 1794380C3 DE 1794380 A DE1794380 A DE 1794380A DE 1794380 A DE1794380 A DE 1794380A DE 1794380 C3 DE1794380 C3 DE 1794380C3
- Authority
- DE
- Germany
- Prior art keywords
- asbestos
- chrysotile asbestos
- thickener
- chrysotile
- rpm
- 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.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K7/00—Use of ingredients characterised by shape
- C08K7/02—Fibres or whiskers
- C08K7/04—Fibres or whiskers inorganic
- C08K7/14—Glass
-
- 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
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/06—Solidifying liquids
-
- 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
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K7/00—Use of ingredients characterised by shape
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K7/00—Use of ingredients characterised by shape
- C08K7/02—Fibres or whiskers
- C08K7/04—Fibres or whiskers inorganic
- C08K7/10—Silicon-containing compounds
- C08K7/12—Asbestos
-
- 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
- C09D7/44—Combinations of two or more thickening agents
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M113/00—Lubricating compositions characterised by the thickening agent being an inorganic material
- C10M113/12—Silica
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/10—Compounds containing silicon
- C10M2201/102—Silicates
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/10—Compounds containing silicon
- C10M2201/105—Silica
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2290/00—Mixtures of base materials or thickeners or additives
- C10M2290/10—Thickener
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/02—Bearings
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/015—Dispersions of solid lubricants
- C10N2050/02—Dispersions of solid lubricants dissolved or suspended in a carrier which subsequently evaporates to leave a lubricant coating
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/10—Semi-solids; greasy
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Inorganic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Engineering & Computer Science (AREA)
- Detergent Compositions (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Lubricants (AREA)
- Processing Of Solid Wastes (AREA)
Description
Die Verwendung von Asbest als Verdickungsmittel zur Herstellung von Schmierfetten aus Schmierölen ist an sich bereits bekannt, beispielsweise aus der USA.-Patentschrift 3 010 896 sowie aus einem Aufsatz von C. J. B ο η e r, »Manufacture and Application of Lubricating Greases«.The use of asbestos as a thickener in the manufacture of lubricating greases from lubricating oils is already known per se, for example from US Pat. No. 3,010,896 and from an article by C. J. B ο η e r, “Manufacture and Application of Lubricating Greases ".
Es wurde nunmehr gefunden, daß ein erheblich verbessertes Verdickungsmittel für Flüssigkeiten, beispielsweise zur Herstellung von thixotropen Schmierfetten oder thixotropen Anstrichfarben bzw. ähnlichen Zusammensetzungen, erhalten wird, wenn man Chrysotilasbest einer Vermahlung in einer Strahlmühle unterwirft. Nach der Behandlung in der Strahlmühle liegt der Asbest in Form von feinen Fasern vor, «deren Durchmesser im kolloidalen Bereich Hegt.It has now been found that a vastly improved thickening agent for liquids, for example for the production of thixotropic lubricating greases or thixotropic paints or similar Compositions obtained by subjecting chrysotile asbestos to a jet mill subject. After treatment in the jet mill, the asbestos is in the form of fine fibers, «Whose diameter lies in the colloidal range.
Die Chrysotilasbest-Fasern lassen sich dadurch herstellen, daß man unter Überdruck und bei einer Temperatur zwischen Raumtemperatur und 650° C einen bewegten Körper aus in einem gasförmigen Medium suspendierten Asbestteilchen herstellt und in diesen kontinuierlich weiteres gasförmiges Medium in mehreren Strömen mit einer Temperatur in dem genannten Bereich und hoher Geschwindigkeit unter Erzeugung starker Turbulenz in dem Körper und damit unter Zerkleinerung der suspendierten Teilchen einführt, die zerkleinerten Asbestteilchen zusammen mit dem gasförmigen Medium kontinuierlich abzieht und die feinen Asbestteilchen von dem Suspendierungsgas abtrennt. Als Suspendierungsmedium werden Luft und Dampf bevorzugt.The chrysotile asbestos fibers can be produced by being under positive pressure and at a temperature a moving body in a gaseous medium between room temperature and 650 ° C produces suspended asbestos particles and in these continuously further gaseous medium in several Flowing at a temperature in said range and at a high speed with generation introduces strong turbulence in the body and thus with comminution of the suspended particles that Crushed asbestos particles together with the gaseous medium continuously withdraws and the fine Separating asbestos particles from the suspending gas. Air and steam are used as the suspending medium preferred.
Zum Zerkleinern der Asbestteilchen eignen sich Strahlmühlen bekannter Art. Bevorzugt wird eine Strahlmühle, in welcher verhältnismäßig große Teilchen in einem Gasmedium suspendiert und um eine innen angeordnete Basis gewirbelt werden und in den Wirbelkörper weiteres Gas unter Erzeugung von Turbulenz in dem Körper und unter Zerkleinerung und Zerreibung der Teilchen eingeführt wird.Jet mills of a known type are suitable for comminuting the asbestos particles. One is preferred Jet mill, in which relatively large particles are suspended in a gas medium and around a internally arranged base are swirled and further gas is generated in the vertebral body by turbulence in the body and with crushing and attrition of the particles.
Die Strahlmühle wird bei der Verwendung von Luft als gasförmigem Mahlmedium zweckmäßig mit einem Druck von etwa 7 bis 35 und vorzugsweise 7 bis 21 kg/cm2 (über Atmosphärendruck) betrieben. Die Turbulenz erzeugende zusätzliche Luft kann mit einem Druck von eiwa 7 bis 35 kg/cm2, vorzugsweise etwa 10,5 bis 17,5 kg/cm-, in den die Asbestteilchen enthaltenden Wirbelkörper eingeführt werden. Vorzugsweise findet Luft von Raumtemperatur Verwendung. Die durchschnittliche Teilchengröße kann durch Regulierung der Luftgeschwindigkeit und -temperatur sowie der Zuführgeschwindigkeit für den Asbest variiert werden. Das Produkt kann auf beliebige Weise von dem Suspendierungsmedium abgetrennt werden; vor-When using air as the gaseous grinding medium, the jet mill is expediently operated at a pressure of about 7 to 35 and preferably 7 to 21 kg / cm 2 (above atmospheric pressure). The additional air generating turbulence can be introduced into the vertebral body containing the asbestos particles at a pressure of about 7 to 35 kg / cm 2, preferably about 10.5 to 17.5 kg / cm 2. Air at room temperature is preferably used. The average particle size can be varied by regulating the air speed and temperature as well as the feed rate for the asbestos. The product can be separated from the suspending medium in any manner; before-
Herstellung von
strahlvermahlenem ChrysotilasbestProduction of
jet-milled chrysotile asbestos
In eine handelsübliche Strahlmühle mit einem Mahlkammerdurchmesser von 20,3 cm wurden durch einen Venturiinjektor (mit Druckluft von 10,5 bis 17,5 kg/cm2) Chrysotilasbestleilchen mit einer Geschwindigkeit von etwa 25 g/min eingeführt. In den in der Strahlmühle gebildeten Wirbelkörper aus Asbes;-teilchen wurde zur Erzeugung einer turbulenten Masse Luft von Raumtemperatur mit einem Druck von etwa 21 kg/cm2 eingeblasen. Die feinteiligen Asbestfasern wurden in einem Sackfänger von dem Luftstrom abgetrennt.Chrysotile asbestos particles were introduced into a commercially available jet mill with a grinding chamber diameter of 20.3 cm through a venturi injector (with compressed air from 10.5 to 17.5 kg / cm 2 ) at a rate of about 25 g / min. Air at room temperature with a pressure of about 21 kg / cm 2 was blown into the vortex body of asbes; particles formed in the jet mill to generate a turbulent mass. The finely divided asbestos fibers were separated from the air flow in a bag catcher.
Einzelheiten über Art und Menge der Ausgangsmaterialien sind in den nachfolgenden Tabellen 1 und 2 angegeben.Details of the type and amount of the starting materials are given in Tables 1 and 2 below specified.
Die Teilchengröße des Ausgangsmaterials ist nur insofern begrenzt, als das Material sich in den Venturiinjektor einführen lassen muß. Zu große Asbestteilchen können zur Verringerung der Faserlänge auf den erforderlichen Bereich einer Vorbehandlung unterworfen werden.The particle size of the feedstock is only limited in that the material can get into the venturi injector must have imported. Asbestos particles that are too large can reduce the fiber length on the required area to be subjected to a pretreatment.
Beispiel 2
Verdickung von PolyesternExample 2
Thickening of polyesters
Als Harz wurde ein flüssiges Polyesterharz mit einer Viskosität von 150 bis 20OcP bei 250C (gemessen im Brookfield-Viskosimeter mit einer Spindel Nr. 2 bei 20 U/min) und einem auf 41 % eingestellten Styrolgehalt verwendet. Als Verdickungsmittel wurden die nach Beispiel 1 hergestellten Chrysotilasbest-Fasern eingesetzt. Der Polyester wurde mit dem Verdickungsmittel vermischt und die Viskositätserhöhung bei 6 U/min und 60 U/min wurde im Brookfield-Viskosimeter gemessen. Die Viskosität des verdickten Harzes wurde dabei sofort und nach 7 Tagen Lagerung bei 38° C bestimmt. Das Absetzvermögen der verdickten Polyesterharze wurde durch Messen der überstehenden Flüssigkeit ermittelt.As the resin, a liquid polyester resin having a viscosity of 150 was to 20OcP at 25 0 C (measured in a Brookfield viscometer using a spindle no. 2 / min at 20 rpm) was used and one set at 41% styrene content. The chrysotile asbestos fibers produced according to Example 1 were used as thickening agent. The polyester was mixed with the thickener and the increase in viscosity at 6 rpm and 60 rpm was measured in a Brookfield viscometer. The viscosity of the thickened resin was determined immediately and after storage at 38 ° C. for 7 days. The settling power of the thickened polyester resins was determined by measuring the supernatant liquid.
Beispiel 3
Verdickung von PolyepoxidenExample 3
Thickening of polyepoxides
Als Harz wurde ein flüssiges Polyepoxid mit einer Viskosität von 400 bis 60OcP bei 25°C und mit einem Epoxidäquivalent von 175 bis 200 verwendet. Die Verdickungswirkung der nach Beispiel 1 hergestellten feinteiligen Chrysotilasbestfasern wurde wie im Beispiel 2 bestimmt. Die Ergebnisse finden sich in der nachfolgenden Tabelle 2.The resin used was a liquid polyepoxide with a viscosity of 400 to 60OcP at 25 ° C and with an epoxy equivalent of 175 to 200 is used. The thickening effect of the prepared according to Example 1 finely divided chrysotile asbestos fibers were determined as in Example 2. The results can be found in the following table 2.
794794
Chrysotil-AsbestKind of used
Chrysotile asbestos
100 Teiie
PolyesterParts thickener each
100 parts
polyester
6 U/minimmediately gf
6 rpm
:rnessen
60 U/minviscosity in el
: rnessen
60 rpm
nach
7 Tagen
6 U/min»
after
7 days
6 rpm
überstehende Flüssigkeit
nach 7 TagenAbseGvermogeo,%
supernatant liquid
after 7 days
qualität FM-3Arizona filter
quality FM-3
Asbest 7D5Quebec Lake-
Asbestos 7D5
CoalingaCalifornian
Coalinga
blauer KrokydolithSouth African
blue crocidolite
·) Teilweise durch Säurebehandlung entfasert.·) Partly defibrated by acid treatment.
Art des verwendeten
Chrysotil-AsbestsKind of used
Chrysotile asbestos
Kalifornischer
CoalingaCalifornian
Coalinga
Teile Verdicker je 100 Teile PolyepoxidParts of thickener per 100 parts of polyepoxide
2,02.0
Viskosität in cP sofort gemessen U/min I 60 U/minViscosity in cP measured immediately rpm I 60 rpm
200200
34003400
nach 7 Tagen
bei 54° C
6 U/minafter 7 days
at 54 ° C
6 rpm
12 60012 600
Absetzvermögen, %Deductibility,%
überstehendeprotruding
Flüssigkeitliquid
nach 7 Tagenafter 7 days
4,24.2
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US56908766A | 1966-08-01 | 1966-08-01 |
Publications (3)
Publication Number | Publication Date |
---|---|
DE1794380A1 DE1794380A1 (en) | 1973-08-09 |
DE1794380B2 DE1794380B2 (en) | 1973-12-20 |
DE1794380C3 true DE1794380C3 (en) | 1974-07-18 |
Family
ID=24274054
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE1619771A Expired DE1619771C3 (en) | 1966-08-01 | 1967-07-29 | Use of a mixture of chrysotile asbestos and silicon dioxide to thicken liquids |
DE1794380A Expired DE1794380C3 (en) | 1966-08-01 | 1967-07-29 | Use of chrysotile asbestos as a thixotropic thickener. Eliminated from: 1619771 |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE1619771A Expired DE1619771C3 (en) | 1966-08-01 | 1967-07-29 | Use of a mixture of chrysotile asbestos and silicon dioxide to thicken liquids |
Country Status (3)
Country | Link |
---|---|
DE (2) | DE1619771C3 (en) |
GB (1) | GB1146926A (en) |
SE (1) | SE319117B (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU6465580A (en) * | 1980-02-29 | 1981-09-03 | W.R. Grace & Co. | Silica/fibrous polyolefin thickening agents |
-
1967
- 1967-07-03 GB GB30595/67A patent/GB1146926A/en not_active Expired
- 1967-07-25 SE SE10843/67*A patent/SE319117B/xx unknown
- 1967-07-29 DE DE1619771A patent/DE1619771C3/en not_active Expired
- 1967-07-29 DE DE1794380A patent/DE1794380C3/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
DE1619771C3 (en) | 1974-04-04 |
GB1146926A (en) | 1969-03-26 |
DE1794380A1 (en) | 1973-08-09 |
DE1794380B2 (en) | 1973-12-20 |
DE1619771B2 (en) | 1973-08-23 |
SE319117B (en) | 1969-12-22 |
DE1619771A1 (en) | 1970-07-30 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
C3 | Grant after two publication steps (3rd publication) | ||
E77 | Valid patent as to the heymanns-index 1977 | ||
8339 | Ceased/non-payment of the annual fee |