CA1184728A - Continuous process for the agglomeration of ptfe powders in a liquid medium, and modified ptfe powder obtained thereby - Google Patents
Continuous process for the agglomeration of ptfe powders in a liquid medium, and modified ptfe powder obtained therebyInfo
- Publication number
- CA1184728A CA1184728A CA000410946A CA410946A CA1184728A CA 1184728 A CA1184728 A CA 1184728A CA 000410946 A CA000410946 A CA 000410946A CA 410946 A CA410946 A CA 410946A CA 1184728 A CA1184728 A CA 1184728A
- Authority
- CA
- Canada
- Prior art keywords
- stage
- powder
- agglomerated
- average
- 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.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/12—Powdering or granulating
-
- 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
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/12—Powdering or granulating
- C08J3/16—Powdering or granulating by coagulating dispersions
-
- 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
- C08J2327/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers
- C08J2327/02—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment
- C08J2327/12—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
- C08J2327/18—Homopolymers or copolymers of tetrafluoroethylene
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Dispersion Chemistry (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
Abstract of the disclosure:
A process for the continuous agglomeration of granular tetrafluoroethylene polymer powders which cannot be processed from the melt to give molding powders having a high bulk density, an improved powder flow and particle stability and a narrow particle size distribution is described. In this process, the powder to be agglomer-ated is first introduced uniformly into a pretreatment stage and is dispersed and pre-agglomerated in this stage in the liquid agglomeration medium, composed of water and an organic liquid capable of wetting polytetrafluoro-ethylene, is then agglomerated to the desired average particle diameter in an agglomeration stage and is finally treated further in an after-treatment stage in order to develop the final shape of the particles.
Finally, the powder is separated from the liquid medium and is dried. This makes it possible to obtain, in an economical manner and with excellent processing properties, high-grade agglomerated molding powders of such tetra-fluoroethylene polymers, in particular of such polymers which have been modified with small quantities of per-fluoro-(alkyl-vinyl) ethers.
A process for the continuous agglomeration of granular tetrafluoroethylene polymer powders which cannot be processed from the melt to give molding powders having a high bulk density, an improved powder flow and particle stability and a narrow particle size distribution is described. In this process, the powder to be agglomer-ated is first introduced uniformly into a pretreatment stage and is dispersed and pre-agglomerated in this stage in the liquid agglomeration medium, composed of water and an organic liquid capable of wetting polytetrafluoro-ethylene, is then agglomerated to the desired average particle diameter in an agglomeration stage and is finally treated further in an after-treatment stage in order to develop the final shape of the particles.
Finally, the powder is separated from the liquid medium and is dried. This makes it possible to obtain, in an economical manner and with excellent processing properties, high-grade agglomerated molding powders of such tetra-fluoroethylene polymers, in particular of such polymers which have been modified with small quantities of per-fluoro-(alkyl-vinyl) ethers.
Description
L7~
The invention relates to 2 process for the continu ous production of an agglomerated molding po~der from a granular_rln~melt-fa~ ble tetrafluoroethylene polvm~r uri~ary-powd-er ~~-n--wh-ic~~~~t~e'~~~~~~~~~`
. _ ~ _ _ . . _ . _ . _ . .
S average particle diameter d~o of the primary particles ;s ~0 to 80 ~m~ in a liquid medium which passes ~hrough the ~hole process and consists of ~ater and an organiç
liquid ~hich ;s capable of wetting such a tetrafluoroethy-lene polymer and is soluble in ~ater to ehe extent of ~0 not more than 15X by weight, the weight/volume ratio of primary powder to organic liquid being 7:1 to 1.3:1 and the volume/volume ratio of organic liquid to ~ater being 1:1.4 to 1:50, with mechanical agitation at temperatures of 5 to 90C. The invention also relates to an agglomerated molding po~Jder composed of a-non-m~It-abri-ca~'~ë'_tetraf'~uoroe hvlene po1vmer _ =
and has a specific surface area of 0.5 to 4 m2/g, as __ _ __ _ . _ measured by the BET metho`d.
As is known, because of their extremely high melt viscosity, ~hich does not permit the formation of a meLt in the customary sense, it is only possible to~process polytetrafluoroethylene powders ~abbrev;ated below to PTF for the homopolymer) further to give molded articles by special techniques, similar to those of po~der metallurgy~ Equivalent to them in this respect .
are those tetrafLuoroethylene polymers which contain smal~
quantities of a comonomer, in ~os~ cases a ~Luorine-con-taining comonomer ~hich~ in this sense~ is in most cases t knoun as a ~od;fying agent, i. being necessary to adjus~
this quantity to a Level so Lo~ that the transition to a copolymer ~hich can be processed from the melt, ie.
a 2rue thermoplastic~ is not yet reachedO
Tuo types of PTFE powders are used in further processing, namely so-called fine powders, prepared by 10 emuLsion polymer;zat;onr and so-called granular powders, prepared by suspension polymerizationO these t~o types dif~ering ~rom one another in principle in their particle structure, specific surface area and their po~der and pro-cessing properties and also ;n their fields of use. ~he 15 present inven~ion is concerned ~ith po~ders of the l2st-men-tioned type, ~hich are usu~lly processed by methods ~hich inc~ude metering into a mold~ compression to give a preform and sintering the latter, the metering~ in part;cular, being carried out substantially automatically. These methods 20 set high requirementsr in particuLar~ for the bulk density, the pourability and the particle size d;stribution, ~hich should be as narro~ as poss;ble~ of such a molding powder.
~ hese propert;es can only be achieved in rare and except;onal cases~ using very special polymerizat;on ~ 25 techniques, by crude polymers, such as are produced direct-ly from the polymerization process. In addition, these polymers have an excessively high compactness`of the parti-Cle5 and are therefore not suitable for compression-sin--terin~ processing, ouing to their inadequate moldability 7~
- 2nd their lo~ particle surface area. ~hen such crude po~ymers, ~hich, in the polym~ri~at on processes generally employed, are produced at particle sizes ~ithin the range from 300 to 3,000 ~Im~ are finely ground, ~hich is in ~ost cases necessary, in order to reduce the average par~i-cle size, large proportions of fibrous particles are formed, ~hereby the pcwdex fl~w and the bulk density are very considerably adversely affected.
It has therefore been known for a long time to 10 improve the processability of such granu~ar PTFE molding powders by so-called agglomera~ion processes ~occasionally also described as granulation processes) in agi~ated liquid media by the action of mechanical forces. Liquid agglo-~eration media of this type which have been described are 15 water (US Patent 3,36~,615 and US Patent 3,766,133), or-~an;c l;qu;ds capable of wetting PTFE (US Patent 3,265,679) am;no-substituted and/or hydroxyl-substituted alkanes ~US Patent 3,532,782) or mi~tures of water and organic liquids which are substantially insoluble in water ~US
20 Patent 3,527,857 and US Patent 3,781,258). An agglomera-tion of particles in the dry state has also been described ~US Patent 3,766,133).
All these processes are designed as discontinuous pcocesses, ie. the batchwise charging, the agglomeration 25 and the discharging of the product from a single treatment vessel take place successively. A simple conversion of such an agglomeration process into a ful ly continuous opera~ion runs into con$iderable difficulties, since ~he quality of the agglomerated PTFE 00lding powder obtained .
, J%
faLls off rapidly. This is probably due to the fact that, in the course thereof~ the mechanical agitation required for the agglomeration superimposes itself in an undesirable ~anner onto the flo~ ~otion of the po~der suspPnded in S the liquid medium as a continuum, as a result of ~hich port;ons of product are discharged ~hich hav no~
yet passed through the agglomeration process to reach full "maturity" and therefore do not yet have the proper~
,!ties desired, uhich then impairs the pattern of properties 10 of the entire product.
On the other hand, a fully continuous process ~ou~d be very desirable for economic reasons, if it were possible to adjust the properties of the agglomerated PTFE powders produced thereby to those obtained from dis-1~ continuous pro~essesO or even to i~prove them further,and if it ~ere also possible to produce the agglomerated PTFE po~der in a uniform product quality. Some processes ~hich have been disclosed hitherto, in which reference has been made to the possibility of continuous operation 20 or ~hich operate completely continuously~ are still uery unsatisfactory in this respect. Thus, US Patent 3,597,405 describes a method of continuous agglomeration in a vessel ;n wh;ch, using discs rotating at h;gh speed, drum treat-ment ~s carried out on a powder which has been merely 25 moistened ~lith ~ater and an organic liquid. The disadvan-tages of this procedure are ~he low capacity of the vessel, necessary to avoid the forma~ion of oversize particles as a result of excessive mutual contact be.~een particles, and also the blockages ~hich occur in the initial grinding and screening carried out in a moist conditiDn~ The -forma-tion of a fairly large proportion of oversize part;cles cannot, ho~ever~ be prevented; the resulting bulk density -~s relati~ely ~ow (`~00 9/l)- German Offenlegungsschrift 5 2,218,240 and US Paten~ 4~123,606 describe a two-stage procedure ~h;ch is similar in princip~ and in ~hich a higher sp~cific stirring eneryy is used in the first stage than in the subsequent second agglomerating stage, as a result of ~hich a fairly hard shell is stated to be 10 produced sn the outer surface of the agglomPrate. ALthough ~arrying-out the process described in Germ~n Offenlegungs-schrift 2,Z18,24û results in a reduction oF the fine frac-tion~ the coarse fraction in the second stage is increased in an undesirable manner as a result of mutual contact 15 betueen the partic~es at low stirring ~nergies. This disad-yantage is overcome by the improvement described in US
Patent 4,123,60~, by fractionating the coarse traction by screening and recycling it after it has passed through an additional comminution stage~ However, it proves to 20 be a disadvantage in this procedure that the wet screening o'F the agglomerate, ~hich is moist ~Jith ~ater and ~etted with gasoline, results in blockage caused by the parti~les of agglomerate, ~h;ch contain gasoline and~are therefore ~ery soFt~ Furthermore~ it is necessary 25 to pass a not inconsiderable part of the product through this comminution plant and thus to recycle it. The object of prov;ding a fully continuous agglomeration process For po-iders composed of non-~elt~fabricable TFE polymers .. .
_ ~ _ ~ .. . .. _ _ _ ~ . . . _ . . .. . .. . . .. _ . .. .. . _ . .. _ _ . .. .. .. ~ . _ . _ .
which forms' the sub ject_ of the pre~
7~2 sent invention~ has, therefore, not yet been soLved ;n a satisfactory manner, acçording to the state of the art.
This objeet is achieved in accordance uith the invention by a process of the type mentioned initially, ~hich comprises pass;ng the primary powder, together ~ith the ~iquid mediu~, through a three-stage cascade in ~Ihich~
~nitially, the primary po~der, the water and the organic ~;quid, in the ratio mentioned, ~0 a) are continuous~y introduced into a pretreatment stage fi5led ~ith the l;quid medium and are moved forward in the former stage, where the primary po~der is first drawn in a conveying zone into the liquid medium, and is suspend-e~ in the latter, by means of a stirring eLement uhich ~5 effects the conveyance, then arrives in a directLy adjacen~
dispersing zone and is there converted, by the action of a stirring element having a dispersing action ~;thi~
the range of the specific stirring energy applied, into a form which is essentially uniformly finely distributed within the liquid medium, then arrives in a directLy adja-cent homogen;zing zone and is pre-agglomerated therP by the action of a turbine-shaped stirring element to give secondary particles having an average particle diameter d50 of about 100 to about 4no ,um, ~he pretreatment stage being passed through at an average dwe~l time of 3 to 30 minutes and the specific stirring energy introduced there being 5 to 100 w/l, this pretreated suspension then b) passes through an agglomeration stage in which the pre-agglomerated primary`powder is further a~glomerated ~34L7~ !3 .. ~
by the gentle action of stirring elements ~hich~ ~ithin ~he range of specific stirrin~ energy applied~ exe t essen-tialLy no co~minuting action, producing an adequate contact bet~een particles in the liquid n~edium~ to give a powder havin~ tertiary particles of an average particle diameter dso of 150 to 1,000 ~m, ~he agglomeration stage being passed through at an average d~ell time of 5 to 50 m;nutes and the specific stirring energy introduced there bein~
The invention relates to 2 process for the continu ous production of an agglomerated molding po~der from a granular_rln~melt-fa~ ble tetrafluoroethylene polvm~r uri~ary-powd-er ~~-n--wh-ic~~~~t~e'~~~~~~~~~`
. _ ~ _ _ . . _ . _ . _ . .
S average particle diameter d~o of the primary particles ;s ~0 to 80 ~m~ in a liquid medium which passes ~hrough the ~hole process and consists of ~ater and an organiç
liquid ~hich ;s capable of wetting such a tetrafluoroethy-lene polymer and is soluble in ~ater to ehe extent of ~0 not more than 15X by weight, the weight/volume ratio of primary powder to organic liquid being 7:1 to 1.3:1 and the volume/volume ratio of organic liquid to ~ater being 1:1.4 to 1:50, with mechanical agitation at temperatures of 5 to 90C. The invention also relates to an agglomerated molding po~Jder composed of a-non-m~It-abri-ca~'~ë'_tetraf'~uoroe hvlene po1vmer _ =
and has a specific surface area of 0.5 to 4 m2/g, as __ _ __ _ . _ measured by the BET metho`d.
As is known, because of their extremely high melt viscosity, ~hich does not permit the formation of a meLt in the customary sense, it is only possible to~process polytetrafluoroethylene powders ~abbrev;ated below to PTF for the homopolymer) further to give molded articles by special techniques, similar to those of po~der metallurgy~ Equivalent to them in this respect .
are those tetrafLuoroethylene polymers which contain smal~
quantities of a comonomer, in ~os~ cases a ~Luorine-con-taining comonomer ~hich~ in this sense~ is in most cases t knoun as a ~od;fying agent, i. being necessary to adjus~
this quantity to a Level so Lo~ that the transition to a copolymer ~hich can be processed from the melt, ie.
a 2rue thermoplastic~ is not yet reachedO
Tuo types of PTFE powders are used in further processing, namely so-called fine powders, prepared by 10 emuLsion polymer;zat;onr and so-called granular powders, prepared by suspension polymerizationO these t~o types dif~ering ~rom one another in principle in their particle structure, specific surface area and their po~der and pro-cessing properties and also ;n their fields of use. ~he 15 present inven~ion is concerned ~ith po~ders of the l2st-men-tioned type, ~hich are usu~lly processed by methods ~hich inc~ude metering into a mold~ compression to give a preform and sintering the latter, the metering~ in part;cular, being carried out substantially automatically. These methods 20 set high requirementsr in particuLar~ for the bulk density, the pourability and the particle size d;stribution, ~hich should be as narro~ as poss;ble~ of such a molding powder.
~ hese propert;es can only be achieved in rare and except;onal cases~ using very special polymerizat;on ~ 25 techniques, by crude polymers, such as are produced direct-ly from the polymerization process. In addition, these polymers have an excessively high compactness`of the parti-Cle5 and are therefore not suitable for compression-sin--terin~ processing, ouing to their inadequate moldability 7~
- 2nd their lo~ particle surface area. ~hen such crude po~ymers, ~hich, in the polym~ri~at on processes generally employed, are produced at particle sizes ~ithin the range from 300 to 3,000 ~Im~ are finely ground, ~hich is in ~ost cases necessary, in order to reduce the average par~i-cle size, large proportions of fibrous particles are formed, ~hereby the pcwdex fl~w and the bulk density are very considerably adversely affected.
It has therefore been known for a long time to 10 improve the processability of such granu~ar PTFE molding powders by so-called agglomera~ion processes ~occasionally also described as granulation processes) in agi~ated liquid media by the action of mechanical forces. Liquid agglo-~eration media of this type which have been described are 15 water (US Patent 3,36~,615 and US Patent 3,766,133), or-~an;c l;qu;ds capable of wetting PTFE (US Patent 3,265,679) am;no-substituted and/or hydroxyl-substituted alkanes ~US Patent 3,532,782) or mi~tures of water and organic liquids which are substantially insoluble in water ~US
20 Patent 3,527,857 and US Patent 3,781,258). An agglomera-tion of particles in the dry state has also been described ~US Patent 3,766,133).
All these processes are designed as discontinuous pcocesses, ie. the batchwise charging, the agglomeration 25 and the discharging of the product from a single treatment vessel take place successively. A simple conversion of such an agglomeration process into a ful ly continuous opera~ion runs into con$iderable difficulties, since ~he quality of the agglomerated PTFE 00lding powder obtained .
, J%
faLls off rapidly. This is probably due to the fact that, in the course thereof~ the mechanical agitation required for the agglomeration superimposes itself in an undesirable ~anner onto the flo~ ~otion of the po~der suspPnded in S the liquid medium as a continuum, as a result of ~hich port;ons of product are discharged ~hich hav no~
yet passed through the agglomeration process to reach full "maturity" and therefore do not yet have the proper~
,!ties desired, uhich then impairs the pattern of properties 10 of the entire product.
On the other hand, a fully continuous process ~ou~d be very desirable for economic reasons, if it were possible to adjust the properties of the agglomerated PTFE powders produced thereby to those obtained from dis-1~ continuous pro~essesO or even to i~prove them further,and if it ~ere also possible to produce the agglomerated PTFE po~der in a uniform product quality. Some processes ~hich have been disclosed hitherto, in which reference has been made to the possibility of continuous operation 20 or ~hich operate completely continuously~ are still uery unsatisfactory in this respect. Thus, US Patent 3,597,405 describes a method of continuous agglomeration in a vessel ;n wh;ch, using discs rotating at h;gh speed, drum treat-ment ~s carried out on a powder which has been merely 25 moistened ~lith ~ater and an organic liquid. The disadvan-tages of this procedure are ~he low capacity of the vessel, necessary to avoid the forma~ion of oversize particles as a result of excessive mutual contact be.~een particles, and also the blockages ~hich occur in the initial grinding and screening carried out in a moist conditiDn~ The -forma-tion of a fairly large proportion of oversize part;cles cannot, ho~ever~ be prevented; the resulting bulk density -~s relati~ely ~ow (`~00 9/l)- German Offenlegungsschrift 5 2,218,240 and US Paten~ 4~123,606 describe a two-stage procedure ~h;ch is similar in princip~ and in ~hich a higher sp~cific stirring eneryy is used in the first stage than in the subsequent second agglomerating stage, as a result of ~hich a fairly hard shell is stated to be 10 produced sn the outer surface of the agglomPrate. ALthough ~arrying-out the process described in Germ~n Offenlegungs-schrift 2,Z18,24û results in a reduction oF the fine frac-tion~ the coarse fraction in the second stage is increased in an undesirable manner as a result of mutual contact 15 betueen the partic~es at low stirring ~nergies. This disad-yantage is overcome by the improvement described in US
Patent 4,123,60~, by fractionating the coarse traction by screening and recycling it after it has passed through an additional comminution stage~ However, it proves to 20 be a disadvantage in this procedure that the wet screening o'F the agglomerate, ~hich is moist ~Jith ~ater and ~etted with gasoline, results in blockage caused by the parti~les of agglomerate, ~h;ch contain gasoline and~are therefore ~ery soFt~ Furthermore~ it is necessary 25 to pass a not inconsiderable part of the product through this comminution plant and thus to recycle it. The object of prov;ding a fully continuous agglomeration process For po-iders composed of non-~elt~fabricable TFE polymers .. .
_ ~ _ ~ .. . .. _ _ _ ~ . . . _ . . .. . .. . . .. _ . .. .. . _ . .. _ _ . .. .. .. ~ . _ . _ .
which forms' the sub ject_ of the pre~
7~2 sent invention~ has, therefore, not yet been soLved ;n a satisfactory manner, acçording to the state of the art.
This objeet is achieved in accordance uith the invention by a process of the type mentioned initially, ~hich comprises pass;ng the primary powder, together ~ith the ~iquid mediu~, through a three-stage cascade in ~Ihich~
~nitially, the primary po~der, the water and the organic ~;quid, in the ratio mentioned, ~0 a) are continuous~y introduced into a pretreatment stage fi5led ~ith the l;quid medium and are moved forward in the former stage, where the primary po~der is first drawn in a conveying zone into the liquid medium, and is suspend-e~ in the latter, by means of a stirring eLement uhich ~5 effects the conveyance, then arrives in a directLy adjacen~
dispersing zone and is there converted, by the action of a stirring element having a dispersing action ~;thi~
the range of the specific stirring energy applied, into a form which is essentially uniformly finely distributed within the liquid medium, then arrives in a directLy adja-cent homogen;zing zone and is pre-agglomerated therP by the action of a turbine-shaped stirring element to give secondary particles having an average particle diameter d50 of about 100 to about 4no ,um, ~he pretreatment stage being passed through at an average dwe~l time of 3 to 30 minutes and the specific stirring energy introduced there being 5 to 100 w/l, this pretreated suspension then b) passes through an agglomeration stage in which the pre-agglomerated primary`powder is further a~glomerated ~34L7~ !3 .. ~
by the gentle action of stirring elements ~hich~ ~ithin ~he range of specific stirrin~ energy applied~ exe t essen-tialLy no co~minuting action, producing an adequate contact bet~een particles in the liquid n~edium~ to give a powder havin~ tertiary particles of an average particle diameter dso of 150 to 1,000 ~m, ~he agglomeration stage being passed through at an average d~ell time of 5 to 50 m;nutes and the specific stirring energy introduced there bein~
2 to 30 ~I/l, this suspension then 10 c) is passed through an after-treatment stage in ~hich, by maintaining ~n average dwell time of 6 to 60 minutes and by the act;on of a mu~ti-bladed stirring element ~hich introduces a specific stirring energy of 5 to 30 ~/l into the suspension, the final formation of the partlcle shape 15 take~ place ~Jithout a further essential change in the average pa~ticle size, and finalLy d~ ;s d;scharged continua~ly from the after-treatment stage, and the agglomerated powder is separated from ~he Iiquid medium in a known manner.
The starting materials for the process according to the invention are the granular suspension polymers of tetrafluoroeth~lene which are prepared in a kno~n manner and ~hich are obtained, in the presence of catalysts ~h;ch form free radicals, by customary processes such 25 as ~ere firs. disclosed in US Patent 2,393,967 and have s;nce been modified in many ~ays. The suspension polymeri-zat;on can also be carried ou~ in the presence of modifyin~
comonomers. Such modifying comonomers are ~ell kno~in to those skilled in the art. They inc~ude, for example, .
2~
perfluoroalkenes having 3 to 6 C atoms, such as, in parti-cular, hexafluoropropylene, and also perfluoro-talkyL-v;nyl) ethers having perfluoroalkyL groups containing 1 to 4 C atoms, such as, in particular, perfluQro-~n-pro-pyl-vinyl) ether, and also ethylenica~ly unsaturated mono-mers uhich also contain~ in addition tD fluorine, other ~roups, such as, for example, ch~orine or h~drogen~ such as, for example, chlorotrifluoroethylene~ The preparation of such suspension polymers is described, for example, in US Patents 3,331,822, 4,0~8,134 and 4,078,13~, in Bri-tish Patent 1,116,210 and in German Offenlegungsschrift 2,325,562.
According~y, the expression "non=melt-fabr~icable-TF~~
.. . .. . ~ ,, olY~exs" embraces_both the homo~o1 mer __ _ _ __ ____ of tetrafluoroethylene and also copo~ymers in which the ~od;fy;ng comonomer is present in such smaLl proportions that the characteristicn-non-me~ a~-ricable~
;s ret~ined. Mod;fied TFE polymers of th;s type have an apparent melt v;scosity of ~0.1 Gpa s, often of ~ 1 Gpa s, it being possible for this value to increase in the case of mod;fied polymers to values around 100 Gpa s or higher, and in the case of the homopolymer to values of 900 Gpa s.
The expression ~~'non-melt-fabric-a~lé~ relates~~in~~~~~~~-~-~~~ --~-~-this context to the customary methods of processing true thermoplastics. The apparent melt visçosity tshear vis-cosity) is determined by ehe method ~creep test) of Ajroldi et al, ~escribed in J. appl. Polym. Sci., 14 (1970~, pages 79 e~ seq~ This method is described in more deta;l in US Patent 4,030,802, column 9~ line 46, to column 10, line 41~ In the measurements in this App~ication~ ~he method uas modified as fo~lo~s- determination of elonga-tion at 350C; test specimen 0.25 cm wide~ D~S sm thick and having a measured length of ~.5 cm on elongation.
Before the sgglomeration according to the inven-~ion, the powders are subjected in a known manner to f;ne-srinding in order to reduce their average ~article size to the desired range of 100 ~m, which is generalLy effec-ted in a ha~mer mil~, an air jet mill or the like. The 10 powders thus obtained from said non-me1t-fabric~ble IFE
~~~~~-po-lyme~rs~wITr~bè designate~ pri-~ ~~~ ~ ~ ~~ ~ ~--~
_ _ _, _ . . . , _ . _ _ mary po~ders below. They are in an unsintered form.
As suspension polymers~ they have a speci~ic surface area of 0.5 to 4 m2/g, preferably 1 to 2.8 m2/g.
15 This property s also retained in the agglomerated produc~
of the process according to the invention. ~he specific surface area mentioned is determined by the method of Brunauer, Emmet and Teller, described in J. Amer. Chem.
Soc. 60 (1938), page 309 ~BET method). Even if, as a 20 result of the grinding, these primary powders have a cer-Sain proportion of fibrous particles, they have in prin-ciple, as suspension polymers, a granular morphology and differ fundamen~ally in this respect from emulsion polym~rs ~Ihiich have been prepared in the presence of such Large 25 quantities of emulsifier that they remain in a colloidal dispersion in the aqueous medium after the completion of the polymerization. The so called ,ine po~ders obtained from such colloidal dispersions by precipitation are com~
posed of agglomerates of colloidal primary particles havin~
%~
an aYerage particle diameter of about Q.l to 0.5 ~m.
They ha~!e a specific surface area ~hich is usually greater than ~ ~2/9, and in general~ as is known to those skilled in the art, they cannot be shaped by the abovementioned techniques, nor could they be even if they contained modifying agents.
The organic liquid present in the liquid medium ~ithin the scope of the continuous process according to the invention should be able to ~et the TFE polymer primary po~der ~hich cannot be processed from the melt and~ as far as possible, should r,ot be miscible with the ~ater ~th;ch is present at the same time, ;e. this organic liquid shouLd, at the selected operating temperature of the pro-cess, ~ithin the range described below, have a surface tension of not more than about 4Q mN/m and should be solu-ble in water .o the extent of not more than 15X by ~ejsht,preferably not more than 2% by weiQht. Organic liquids of this type and suitable for such agglomeration processes are well known to those skilled in the art, so that a list of examples will be sufficient~
The ~oLlowing may be mentioned as examples:
Alkanes and cycloalkanes~ such as pentane, hexane or cyc~ohexane, aromatic hydrocarborls, such as benzene, toluene or xylene, mixtures of hydrocarbons, such as gaso-line or kerocene fractions and mixtures thereof within a suitable boiling range~ halogenated hydrocarbons, such as perchloroethylene, trichLoroethylene, chloroform or ch~orobenzene, or fluorinated chlorinated hydrocarbons or fluorochlorocarbons, such as, ~or exampleJ trifluorotri-ch~oroethane~
7~
~ 12 -Ti~e continuous process according to the inven~ion ~hich is descr;bed beio~ is carried out at temp-eratures of S to ~DC~ preferably 15 to 70C
and~ particularly preferablyO at 30 to 60~C. Depending on the operating temperat~re selected~ the organic liquid ment;oned should have a boiling point which is at least ~0C, preferably at ~east 20C, higher thas) this selec-ted operating temperature. Advantageously, the boiling point should not exceed 150C - although this is possib~e in principle - since the removal of the organic solven~
from the agglomerated powder formed is then rendered diffi-sult~
The second constituent of the liquid agglomerating ~e~ium is ~ater, ~Ihich is advantageously used in a deio-n;7ed form The mixing rat;o bet~een parts by volume of or~anicl;quid and parts by volume of uater is 1:1.4 ~o 1:50, preferably 1:4 to 1:25.
In the cont;nuous process according to the inven-tion~ the primary powder to be agglomerated, ~hich hasan average particle dso f 20 to 80 ~m, preferably 20 to 50 ~Jmt passes through, in series, a three-stage cascade.
The terms cascade and stage used here are ;ntended to describe spaces of different treatment action which are advantageously housed in separate vessels, although ~his is not absolutely necessary. The term zone within the pretreatment stage is~ on the other hand, to be under-stood as meaning treatment spaces which are admittedly not absolutely necessariiy located in the same vesselr but are certainly advantageously so arranged, the spaces of action of these 20nes being at ~east in contact ~ith one another, but pre~erably ov~rlapping s(ightly.
~he vessel comprising the pretreatmen~ stage is S first ~illed with the liqu;d medium, and preferably also with the primary powder suspended therein, for exampte by f;rst carryin~ out discontinuousty, until the steady state of a continuum has been reached, the process described below in the manner in ~hich it takes place 1~ in the pretreatment stage. The same procedure can also be follo~/ed in the succeeding stages. In this pretreatment stage, ~h;ch is housed in a vessel of elongated shape ~hich is preferably arranged vertically and through which the flow is vertical, the primary po~lder, the water and the organ;c liquid are metered in care~ully and ur,iformly in the selected prop~rtions. Unif~rm metering of ~he primary powder onto the surface of the a~itated liqu;d - medium is of great importance for the process according to the invention. It is advantageous to employ a metering hopper equipped ~ith a discharging device havin~ an equali~
z;ng action. A metering hopper of this type is described, for example, in 6erman Patent 1,531,934~ From the outlet of this metering bunker, the primary poh~der to be nletered ;n passes, either direct or via a storage vessel, to a feeding device~ for example a vibratory chute, from ~hich it is then con~eyed into the pretreatment stage~
The t~o components of the liquid med;um, namely, the organic liquid and the water~ can be added separately.
Preferabl~, however~ these t~lo components are introduced - lb -in a premixed form, ~hich can be effected, for example, ~n a static mixer in the inlet line or in a stock Yesse~
equipped ~lith a s~irrer, and, specifically~ ~hey are pre-ferably introduced into ~he conveying zone or into the region of the latter ~hich overLaps ~ith ~he dispersing ~one~ The ra~io between the organic liquid and wa~er and also that between organic liquid and primary po~der, hich ;s set ~hen metering into the pretreatment stage, is maintained throughout the ~hole o~ the process according to the invention; subsequent metering of a component ;sjgenerally not necessary, un~ess it is necessary to compensate for losses of organic li~uid ~hich can take place as a consequence of ~orking at temperatures near the boiling point of th;s organic liquid.
The ratio se~ in this metering bet~een pri~ary powder and organic ~iquid ~parts by ~eight to corresponding parts by volume, for example kilograms/liters or a multiple thereof~ is 7:1 to 1.3:1, preferably 4 1 to 1.6:1.
In the conveying zone, the powder ~hieh has been applied to the sur~ace of the liquid in the pretreatment stage comes under the influence of a stirring element which effects conveyance ;n the direction of flow of the continuum, as a result of which the po~der ;s dra~ln into the liquid medium and becomes suspended in the latter. Propeller stirrers of all known embodiments are pre-eminently suit-able as such stirring elements which effect conveyance, but inclined blade stirrers with obliquely mounted b~ades or vanes of a rectangular shape, if appropriate sambered, in a propeller`like arrangement are secondarily - ~5 ~
suit~ble. Under the influence of such conveying stirrer e~ements~ the suspended primary powder arr1ves in the direc~ly adjoining dispersing zone and there cornes in~o the region of action o, a stirring eLement which e~erts a dispersing action in the pretreatment stage, uithin the range of the specific stirr;ng energy applied. A
st;rring element of th;s type, having a dispersing ac~ion, 7S pre~erab~y shaped in the form of a disc and has, ~or !example in the peripheral region of the disc, angular elements, such as teeth or rectanguLar blades, mounted tan-gent;ally on both sides. In addition to such stirring ~ements of the type of the so-called dispersing disc, it is also possible to use, for example, so~salled disc stirrers in ~hich angular elements of this type are mount~d 15 radially orl both sides o, the plane of ;he disco In this dispersing .one, the powder is brought into a tate in ~h ich it is essentially un;~orm~y finely distribu-ted ~ithin the ~iquid medium, being in this finely distri-buted state still for the most part in the primary partic(e size. An intimate contact is also set up with the organic liquid which is finely distributed in the water, as a result of ~hich substantial proportions of this organic l~quid are absor~ed by the po~der. This hornogeniz;ny process is completed in the homogenizing zone`directly adjacent thereto, and, at the sarne tirne, a pre-ag~lomera-tion sets in, in which average particle sizes d50 of about 100 to about 400 ~m are reached in these resulting secondary particles - depending on the average particle ~ize of the pr;mary powder and on the temperature and 7~
composi~ion of the ~iquid medium. This îs effected by st;rrin~ e~e~ents ~hich are preferab~y cons~ructed as turbine-shaped stirr;ng elements, in the extended meaning of these ~ords. These preferably include stirring eLements ~n the embodiment of an open or closed turbine, ie. a turbine ~hi h ;s coJered on one side or two sides, but~
for exampie, the so-called double centrifugal stirrer is a~so suitable. Sinçe the homogenizing zone and the dis-'persing zone overlap to a certain extent, and also supple-~0 ment one another, in their action on the primary powder~and also, in particular, in relation to preventing the ~ormation of oversize particles or the coMminution of oversize particles which have already been formed, the stirring equipment employed in the homogenizing zone ran d~SO be used ,n the dispers;ng ~one if its dispersiny action is adequate.
In order to safe~uard the action o~ this stirring, the entire pretreatment stage is equipped with an adeq~ate num~er of flow breakers, unless the stirring elements of the individual zonesr ~hich are preferably mounted on a common shaft~ are arranged excentricaLly in the vessel of the pretreatment stage. An average dwell time of the suspension in thP whole pretreatment stage of 3 to 30, pre~erably 5 to ~5, m;notes, should be pro~ided; the ~pecific st;rring energy introduced amounts to a total of 5 to 100, preferably 10 to 60, lJ/l of suspension~
The product lea~ing the pretreatment stage has a bulk density which is already distinct~y higher, bùt is st;ll no. adequatef and a powder flo~ and particle . ~ ' ' 72~
- ~7 -stabili~y ~hich are still far from adequate. It îs now introdueed intQ the agglomerat;on stage, durin~ ~hich ~he actual for~at;on of the agglomerate takes place. The pre-agglo~era~ed particles are further agglomerated here, in a vessel of elongated shape which is preferably Mounted verticallyO by gentle action applied by stirring element~
~hich, in the range of specific stirring energy applied~
exert essentialLy no comminuting action, ~hile producing 'an adequate contact between the particles in the liquid medium, to g;ve a po~der which is suspen~ed in the liquid medium and has tertiary part;cles of an average particle diameter d~ of 150 to 1,000 ~m, in the course of ~hich the desired degree of agglomeration is already reached.
Even if the action of a single such stirring element can be adequate in so e cases, it is preferable, because of the more uniform ac~ion, to e~ploy at least t~o such stir-rin~ elements, there be;ng no upper critical limit if the vesse~ has an adequate length. For reasons of economy ;
and design, ho~lever, the number of these stirring elements is usually limited to 8, preferably 6, depending on the ~ength of the vessel. Their individual re~ions of action should at least touch one another, and preferably overlap.
If ~hey are - preferably - mounted concentrically, it is also necessary to provide an adequate number of flow breakers here. The specific stirring energy introduced by this stirring equ;pment should be 2 to 30, preferably S to 20, W/l; the average d~ell time in stage b~ should be 5 to 50, preferably ~ to 20~ m;nutes. Stirring elements ~hich do not have a comminuting action in this region are, ~ lL8~7;~
~ ~8 pr~ferably, alL types of propeller stirrers, but atso inclined blade stirrers~ inclined paddle stirrers or cross-paddle stirrer~ and combinations of such s~irrers can a~so be employed. The product leaving tlle agglomer-ation stage not only already has the degree of agglomer-ation ~hich is desired and adequate, but also has the desired narro~ particle size distribution, but its bulk density~ p~r flow and particle stability are not !yet complete~y adequate. In order to improve these and to establish the pattern of properties finally, the sus~
pended and agglomerated po~der from the agglomeration s.aae b) ;s fed to an after-treatment stage s~. ALthough the processes taking place in the ind;vidual stages cannot be explained in the fwllest detai~ it is nevertheless ~5 assumed that a rounding and dens,fica.ior, o, the agglomêr-at~d particles formed takes place in the after-treatmen.
stage ~ithout significant alteration in the average par-t;cle dia~eter dso of the a~ lomerates being effected.
This after-treatment stage takes place in a long, straight vessel, advantageously having a length to diameter ratio of at least 2:1, it being possible to reach very high ratios of th;s kind~ such as, for example, 25:1, prefer-ably 10:1, in a singlc vessel, or even up to 50:1 (total length to diameter~, if the after-treatment stage is divided into several vessels of the said type arranged in series. This vessel or these vessels can be mounted vertically, but this makes it necessary to introduce flow-delay;ng elements. A horizontal arran3ement is preferred - particularly in the case of a single long vessel. In this vcss2l there is a multi bladed sti,rring element, - formcd from a large n~mber of stirrer rings arranged in ' - series preferably on one shaft - each of these s~irrer rin~s ~eing composed of at least 3 and not more than 8 5 preferably not more than 6, blades and these stirring blades having a configuration of the type o~ a disc s~irrer, ie. having a rectangular shape and their,rectangular planes being arranged radiaLly on the shaft. A slightly ' inclined position in relation to the shaft is poss;ble~
The number of these serially arranged stirrer biade rings of the type of a disc stirrer depends on the length of the vessel, and the ;nterspace between two su'ch rings should not exceed the width of the stirrer blades. If several vessels are arranged in series, it is also possible to have an assembly on separate shafts~ each of ~hich is effective for one of these vessels, In the ~hole after-treatment stage~ a specific stirring energy of 5 to 30, preferably 10 to 20, W/l is i~troduced; the dwe~l time is 6 to ~0, preferaoly 10 to 20, minutes.
After passing through the after-treatment stage c), the agglomerate suspended in the liquid medium is uithdrawn continuousl~ and fed to a continuously operatin~
filtering device in order to separate the agglomerated powder from the bulk of the water and ~rom,part of the organic liquid, and such a filtering device should, if poss;ble, permit the recvvery of the organic liquid employed. The removal of the remainder of the water and of the remaining organic solvent is effected by drying, 723~
preferably in seYeral successive ~rying stages and, if appropriate, using a vacuum, it being necessary for the drying to be carried out at temperatu;es belo~ the crystal-lite melting point~ and it is advantageously carried out at a temperature at leas~ 50C aboYe the boiling point of the organic liquid e~ployed. The dryin~ is preferably effected at a temperature of 25 to 300C - in the case - of stagewise drying this temperature is preferably employed in the last stage.
hfter the drying~ the coarse fraction, ie. over~
~;ze particles having a diameter 1,500 um, is removed by means of suitable screening. In the product of the pro-cess according to the invention, this coarse fraction is not more than 4X by ~eight~ but is very frequently b&low 1X by wêi5ht~ a percën.agê which car, scarcely bc ach ev2d in the discontinuous process. The temperature for the whole continuous agglomeration process according to the inventionO Nhich can be selected ~ithin the abovement~ned range, is preferably kept approximately constant from stage a) to stage b) within a controllable width of variation. Differing temperatures are possible, in ~hich case it is preferable to have an increase in temperature ;n the direction of ftow.
Customary fillers, in an amount of 1 to 60% by ~eight, can be m;xed into the primary powder before it ;s metered into the pretreatment stage a). Examples of fillers of this type are glass fibers ~hich, if appropriate, have been treated ~ith customary water-repelling agents, powdered carbon, g~aphite, molybdenum ~ulfide, bron~e, 7~
2~
asb~stos and the like~ Thes~ fillers are mixed homo-geneously in a dry state into the primary po~lder in a prem;xing vessel, before metering into the process accord-ing to the invention takes place. The said uater repelling agentsO such as, for example, silane couplin~ agents, can, if appropriate, also be added to the agglomeration pro-cess ;n the pretreatment stage~ In the course of the ~gglomeration the filler is incorporated homogeneously into the agglomerat2d particles.
In a preferred embodiment of the process, a part o~ the pretreated suspension, after it has passed through the homo~enization z~ne in the pretreatment stage, is extracted from the flo~ and returned via a circulating line to the pretreatment stage, if appropriate by means of a pu~p, uhich can perhaps also contribute ar addit,onal comminuting and/or homogenizin~ action~ The ratio of the fraction recycled to that passing through ;s preferably between 1:1 and 5:1.
The process according to the invention for the agglomerat;on of non-mëlt-fabricab~e TFE ~olymër ~owdérs _ _ _ ,, . _ _ . . , _ _ ...... . _ .. ..
~ ` màkes~i~~~possIbl~e~~~o~~produce,~~~in~~a~~~-~ ~~~~~--~~-~ ~~~ ~~~
_ _ _ .. .. _ _ . .... . _. _ _ . ._ ~ __ _ ..
continuous procedure, agglomerated powders of this type, ~he product propert;es of uhich are at least of equal rank u;th, but in some cases far superior to, the powders 2S orig;nating from discontinuous processesn The a3~lomer-at~s are obtained in a unifor~ product quality, especially ;n respect of their bulk density, their narro~l particle size distribu~ion, their improved'''w~e.r'~~low' ~an~ t~eir particle ~~ -- ~ --~ ~~
stability~ The process according to the invention is~
' 7~8 ho~ever, considerabLy more econo~ical and cost-advantageous to operate than discont;nuous processes; it offers the possi~i~ity of automa~ic control in who~e or in part~
In addit;on numerous manual ~orking stages are avoided, 5 so that the risk of spotlike impurities ;s virtualLy excluded. Th;s fact is of very particular importance in the case of TFE poly~ers, since such inlpurities can occur as visible black spots ~hen the product ;s sintered, and - add;tiona~ly, for exa~ple, effect the ~ormation of elec-lD trical pores and thus reduce the dielectric s~rength of insu(ations~
It has already been stated many times in the ~iterature that modified TFE polymers ~ere subjected to an agglomeration process. tlo~ever~ it has been ~ound that, particlllarly in ths case of p&rfluorinated ethers as mod;fying agents, it is only possible by such~pro~esses to obtain products ~hich are not equivalent to the unmodified polymers belonging to the state of the art, particularly in regàrd to thcir px~er-~l~w~~ their bulk density and their particle stabilîty. It has become possible, by the process accord;ng to the invention, for the first time to prepare, with the same advantageous properties, such 1FE polymers which have been modified ~ith per-fluorinated e~hers.
- The invention also relates, therefore, to ag~lomer-ated moldin~ po~ders composed of particles of a non=melt~
~ ~ ~cabIe _etrafluoroethylene PqlYmer = = __ ~~~~ ~rhich has a specific surface area, determined by . _.. _ _ . .
the BET method~ of 0.5 to ~ m~/g and which `~ ~18~L7~3 ~ 23 -a~ contains 0.001 to 1X by ~eight ~f copolymerized units of a perf luorinated vinyt e~her oF the formula t F~-C F-O-X
in ~hich X denotes a perfluoroalkyl radisal having 1 to 4 C atoms or a radical of the formula F,C
F ~ ~ F
~ CF3 n ~
and n is 0 to 1~ and also conta;ns copolymerized units of tetrafluoroethy~ene, b) is composed essentially of agg~omerates having an average particle diameter d50 of 150 ~o 1,000 ~m which naYe been b~iit up from primary partie~es having ar average particle diameter d50 of 20 to ~0 ~m and ~hich possess a spheroida~ form and a uniform, dense surface, c) has a bulk density of at least 700 g/l, d~ has a po~ flo~ time of 8.0 to 4.0 seconds/50 g at an ~verage agglomerate diâmeter dso of 150 to 250 ~m and of 4.0 to 1.5 seconds/50 9 at an agglomera~e diameter d50 of 250 to 1,000 ~m, e) has a particle stability of ~.0 to 4.D seconds 50 g at ar, average agglomerate diameter d50 of 150 to 250 ~m and of 4.0 to 1.8 seconds/S0 g at an aggLomerate diameter dso of 250 to ?, ~mf and f) has a proport;on of more than 50% by ~eight of agglomerates having a particle size diameter ~hich is at least 0~7 times and not more than 1.3 times the average , .
~ .
~L8~L72~
particle d;ameter dso, 9~ ~herein a molded article prepared therefrom has a ~elding factor of at least 0~60, and h) the pore count, measured at a voltage of 5,000 as electrical defects on a veneer-cut film 2DO,um thick prepared ~rom the agglomerated moLding po~der, is not more tha~ tS pores~m2.
The said po~ders preferably contain a proportion of 0.01 to 0.5X by ~eight o~ ~he said perfluorinated 1~ ethers, and have an average part;cle diameter of the agglomerates of 150 to 800 ~m, in particular 25a to 750 ~Imt an avera~e particle diameter of the primary part;cLes in the agglomerates of 20 to 50 ~m, a bulk density of 700 to 1,000~ in particular 800 to 1,000, 9/1~ a ~ot~er flo-~ t~ oî
~.0 to 3.0 secon~s;50 g at d50 o~ 150 to 250 ~m and Gf
The starting materials for the process according to the invention are the granular suspension polymers of tetrafluoroeth~lene which are prepared in a kno~n manner and ~hich are obtained, in the presence of catalysts ~h;ch form free radicals, by customary processes such 25 as ~ere firs. disclosed in US Patent 2,393,967 and have s;nce been modified in many ~ays. The suspension polymeri-zat;on can also be carried ou~ in the presence of modifyin~
comonomers. Such modifying comonomers are ~ell kno~in to those skilled in the art. They inc~ude, for example, .
2~
perfluoroalkenes having 3 to 6 C atoms, such as, in parti-cular, hexafluoropropylene, and also perfluoro-talkyL-v;nyl) ethers having perfluoroalkyL groups containing 1 to 4 C atoms, such as, in particular, perfluQro-~n-pro-pyl-vinyl) ether, and also ethylenica~ly unsaturated mono-mers uhich also contain~ in addition tD fluorine, other ~roups, such as, for example, ch~orine or h~drogen~ such as, for example, chlorotrifluoroethylene~ The preparation of such suspension polymers is described, for example, in US Patents 3,331,822, 4,0~8,134 and 4,078,13~, in Bri-tish Patent 1,116,210 and in German Offenlegungsschrift 2,325,562.
According~y, the expression "non=melt-fabr~icable-TF~~
.. . .. . ~ ,, olY~exs" embraces_both the homo~o1 mer __ _ _ __ ____ of tetrafluoroethylene and also copo~ymers in which the ~od;fy;ng comonomer is present in such smaLl proportions that the characteristicn-non-me~ a~-ricable~
;s ret~ined. Mod;fied TFE polymers of th;s type have an apparent melt v;scosity of ~0.1 Gpa s, often of ~ 1 Gpa s, it being possible for this value to increase in the case of mod;fied polymers to values around 100 Gpa s or higher, and in the case of the homopolymer to values of 900 Gpa s.
The expression ~~'non-melt-fabric-a~lé~ relates~~in~~~~~~~-~-~~~ --~-~-this context to the customary methods of processing true thermoplastics. The apparent melt visçosity tshear vis-cosity) is determined by ehe method ~creep test) of Ajroldi et al, ~escribed in J. appl. Polym. Sci., 14 (1970~, pages 79 e~ seq~ This method is described in more deta;l in US Patent 4,030,802, column 9~ line 46, to column 10, line 41~ In the measurements in this App~ication~ ~he method uas modified as fo~lo~s- determination of elonga-tion at 350C; test specimen 0.25 cm wide~ D~S sm thick and having a measured length of ~.5 cm on elongation.
Before the sgglomeration according to the inven-~ion, the powders are subjected in a known manner to f;ne-srinding in order to reduce their average ~article size to the desired range of 100 ~m, which is generalLy effec-ted in a ha~mer mil~, an air jet mill or the like. The 10 powders thus obtained from said non-me1t-fabric~ble IFE
~~~~~-po-lyme~rs~wITr~bè designate~ pri-~ ~~~ ~ ~ ~~ ~ ~--~
_ _ _, _ . . . , _ . _ _ mary po~ders below. They are in an unsintered form.
As suspension polymers~ they have a speci~ic surface area of 0.5 to 4 m2/g, preferably 1 to 2.8 m2/g.
15 This property s also retained in the agglomerated produc~
of the process according to the invention. ~he specific surface area mentioned is determined by the method of Brunauer, Emmet and Teller, described in J. Amer. Chem.
Soc. 60 (1938), page 309 ~BET method). Even if, as a 20 result of the grinding, these primary powders have a cer-Sain proportion of fibrous particles, they have in prin-ciple, as suspension polymers, a granular morphology and differ fundamen~ally in this respect from emulsion polym~rs ~Ihiich have been prepared in the presence of such Large 25 quantities of emulsifier that they remain in a colloidal dispersion in the aqueous medium after the completion of the polymerization. The so called ,ine po~ders obtained from such colloidal dispersions by precipitation are com~
posed of agglomerates of colloidal primary particles havin~
%~
an aYerage particle diameter of about Q.l to 0.5 ~m.
They ha~!e a specific surface area ~hich is usually greater than ~ ~2/9, and in general~ as is known to those skilled in the art, they cannot be shaped by the abovementioned techniques, nor could they be even if they contained modifying agents.
The organic liquid present in the liquid medium ~ithin the scope of the continuous process according to the invention should be able to ~et the TFE polymer primary po~der ~hich cannot be processed from the melt and~ as far as possible, should r,ot be miscible with the ~ater ~th;ch is present at the same time, ;e. this organic liquid shouLd, at the selected operating temperature of the pro-cess, ~ithin the range described below, have a surface tension of not more than about 4Q mN/m and should be solu-ble in water .o the extent of not more than 15X by ~ejsht,preferably not more than 2% by weiQht. Organic liquids of this type and suitable for such agglomeration processes are well known to those skilled in the art, so that a list of examples will be sufficient~
The ~oLlowing may be mentioned as examples:
Alkanes and cycloalkanes~ such as pentane, hexane or cyc~ohexane, aromatic hydrocarborls, such as benzene, toluene or xylene, mixtures of hydrocarbons, such as gaso-line or kerocene fractions and mixtures thereof within a suitable boiling range~ halogenated hydrocarbons, such as perchloroethylene, trichLoroethylene, chloroform or ch~orobenzene, or fluorinated chlorinated hydrocarbons or fluorochlorocarbons, such as, ~or exampleJ trifluorotri-ch~oroethane~
7~
~ 12 -Ti~e continuous process according to the inven~ion ~hich is descr;bed beio~ is carried out at temp-eratures of S to ~DC~ preferably 15 to 70C
and~ particularly preferablyO at 30 to 60~C. Depending on the operating temperat~re selected~ the organic liquid ment;oned should have a boiling point which is at least ~0C, preferably at ~east 20C, higher thas) this selec-ted operating temperature. Advantageously, the boiling point should not exceed 150C - although this is possib~e in principle - since the removal of the organic solven~
from the agglomerated powder formed is then rendered diffi-sult~
The second constituent of the liquid agglomerating ~e~ium is ~ater, ~Ihich is advantageously used in a deio-n;7ed form The mixing rat;o bet~een parts by volume of or~anicl;quid and parts by volume of uater is 1:1.4 ~o 1:50, preferably 1:4 to 1:25.
In the cont;nuous process according to the inven-tion~ the primary powder to be agglomerated, ~hich hasan average particle dso f 20 to 80 ~m, preferably 20 to 50 ~Jmt passes through, in series, a three-stage cascade.
The terms cascade and stage used here are ;ntended to describe spaces of different treatment action which are advantageously housed in separate vessels, although ~his is not absolutely necessary. The term zone within the pretreatment stage is~ on the other hand, to be under-stood as meaning treatment spaces which are admittedly not absolutely necessariiy located in the same vesselr but are certainly advantageously so arranged, the spaces of action of these 20nes being at ~east in contact ~ith one another, but pre~erably ov~rlapping s(ightly.
~he vessel comprising the pretreatmen~ stage is S first ~illed with the liqu;d medium, and preferably also with the primary powder suspended therein, for exampte by f;rst carryin~ out discontinuousty, until the steady state of a continuum has been reached, the process described below in the manner in ~hich it takes place 1~ in the pretreatment stage. The same procedure can also be follo~/ed in the succeeding stages. In this pretreatment stage, ~h;ch is housed in a vessel of elongated shape ~hich is preferably arranged vertically and through which the flow is vertical, the primary po~lder, the water and the organ;c liquid are metered in care~ully and ur,iformly in the selected prop~rtions. Unif~rm metering of ~he primary powder onto the surface of the a~itated liqu;d - medium is of great importance for the process according to the invention. It is advantageous to employ a metering hopper equipped ~ith a discharging device havin~ an equali~
z;ng action. A metering hopper of this type is described, for example, in 6erman Patent 1,531,934~ From the outlet of this metering bunker, the primary poh~der to be nletered ;n passes, either direct or via a storage vessel, to a feeding device~ for example a vibratory chute, from ~hich it is then con~eyed into the pretreatment stage~
The t~o components of the liquid med;um, namely, the organic liquid and the water~ can be added separately.
Preferabl~, however~ these t~lo components are introduced - lb -in a premixed form, ~hich can be effected, for example, ~n a static mixer in the inlet line or in a stock Yesse~
equipped ~lith a s~irrer, and, specifically~ ~hey are pre-ferably introduced into ~he conveying zone or into the region of the latter ~hich overLaps ~ith ~he dispersing ~one~ The ra~io between the organic liquid and wa~er and also that between organic liquid and primary po~der, hich ;s set ~hen metering into the pretreatment stage, is maintained throughout the ~hole o~ the process according to the invention; subsequent metering of a component ;sjgenerally not necessary, un~ess it is necessary to compensate for losses of organic li~uid ~hich can take place as a consequence of ~orking at temperatures near the boiling point of th;s organic liquid.
The ratio se~ in this metering bet~een pri~ary powder and organic ~iquid ~parts by ~eight to corresponding parts by volume, for example kilograms/liters or a multiple thereof~ is 7:1 to 1.3:1, preferably 4 1 to 1.6:1.
In the conveying zone, the powder ~hieh has been applied to the sur~ace of the liquid in the pretreatment stage comes under the influence of a stirring element which effects conveyance ;n the direction of flow of the continuum, as a result of which the po~der ;s dra~ln into the liquid medium and becomes suspended in the latter. Propeller stirrers of all known embodiments are pre-eminently suit-able as such stirring elements which effect conveyance, but inclined blade stirrers with obliquely mounted b~ades or vanes of a rectangular shape, if appropriate sambered, in a propeller`like arrangement are secondarily - ~5 ~
suit~ble. Under the influence of such conveying stirrer e~ements~ the suspended primary powder arr1ves in the direc~ly adjoining dispersing zone and there cornes in~o the region of action o, a stirring eLement which e~erts a dispersing action in the pretreatment stage, uithin the range of the specific stirr;ng energy applied. A
st;rring element of th;s type, having a dispersing ac~ion, 7S pre~erab~y shaped in the form of a disc and has, ~or !example in the peripheral region of the disc, angular elements, such as teeth or rectanguLar blades, mounted tan-gent;ally on both sides. In addition to such stirring ~ements of the type of the so-called dispersing disc, it is also possible to use, for example, so~salled disc stirrers in ~hich angular elements of this type are mount~d 15 radially orl both sides o, the plane of ;he disco In this dispersing .one, the powder is brought into a tate in ~h ich it is essentially un;~orm~y finely distribu-ted ~ithin the ~iquid medium, being in this finely distri-buted state still for the most part in the primary partic(e size. An intimate contact is also set up with the organic liquid which is finely distributed in the water, as a result of ~hich substantial proportions of this organic l~quid are absor~ed by the po~der. This hornogeniz;ny process is completed in the homogenizing zone`directly adjacent thereto, and, at the sarne tirne, a pre-ag~lomera-tion sets in, in which average particle sizes d50 of about 100 to about 400 ~m are reached in these resulting secondary particles - depending on the average particle ~ize of the pr;mary powder and on the temperature and 7~
composi~ion of the ~iquid medium. This îs effected by st;rrin~ e~e~ents ~hich are preferab~y cons~ructed as turbine-shaped stirr;ng elements, in the extended meaning of these ~ords. These preferably include stirring eLements ~n the embodiment of an open or closed turbine, ie. a turbine ~hi h ;s coJered on one side or two sides, but~
for exampie, the so-called double centrifugal stirrer is a~so suitable. Sinçe the homogenizing zone and the dis-'persing zone overlap to a certain extent, and also supple-~0 ment one another, in their action on the primary powder~and also, in particular, in relation to preventing the ~ormation of oversize particles or the coMminution of oversize particles which have already been formed, the stirring equipment employed in the homogenizing zone ran d~SO be used ,n the dispers;ng ~one if its dispersiny action is adequate.
In order to safe~uard the action o~ this stirring, the entire pretreatment stage is equipped with an adeq~ate num~er of flow breakers, unless the stirring elements of the individual zonesr ~hich are preferably mounted on a common shaft~ are arranged excentricaLly in the vessel of the pretreatment stage. An average dwell time of the suspension in thP whole pretreatment stage of 3 to 30, pre~erably 5 to ~5, m;notes, should be pro~ided; the ~pecific st;rring energy introduced amounts to a total of 5 to 100, preferably 10 to 60, lJ/l of suspension~
The product lea~ing the pretreatment stage has a bulk density which is already distinct~y higher, bùt is st;ll no. adequatef and a powder flo~ and particle . ~ ' ' 72~
- ~7 -stabili~y ~hich are still far from adequate. It îs now introdueed intQ the agglomerat;on stage, durin~ ~hich ~he actual for~at;on of the agglomerate takes place. The pre-agglo~era~ed particles are further agglomerated here, in a vessel of elongated shape which is preferably Mounted verticallyO by gentle action applied by stirring element~
~hich, in the range of specific stirring energy applied~
exert essentialLy no comminuting action, ~hile producing 'an adequate contact between the particles in the liquid medium, to g;ve a po~der which is suspen~ed in the liquid medium and has tertiary part;cles of an average particle diameter d~ of 150 to 1,000 ~m, in the course of ~hich the desired degree of agglomeration is already reached.
Even if the action of a single such stirring element can be adequate in so e cases, it is preferable, because of the more uniform ac~ion, to e~ploy at least t~o such stir-rin~ elements, there be;ng no upper critical limit if the vesse~ has an adequate length. For reasons of economy ;
and design, ho~lever, the number of these stirring elements is usually limited to 8, preferably 6, depending on the ~ength of the vessel. Their individual re~ions of action should at least touch one another, and preferably overlap.
If ~hey are - preferably - mounted concentrically, it is also necessary to provide an adequate number of flow breakers here. The specific stirring energy introduced by this stirring equ;pment should be 2 to 30, preferably S to 20, W/l; the average d~ell time in stage b~ should be 5 to 50, preferably ~ to 20~ m;nutes. Stirring elements ~hich do not have a comminuting action in this region are, ~ lL8~7;~
~ ~8 pr~ferably, alL types of propeller stirrers, but atso inclined blade stirrers~ inclined paddle stirrers or cross-paddle stirrer~ and combinations of such s~irrers can a~so be employed. The product leaving tlle agglomer-ation stage not only already has the degree of agglomer-ation ~hich is desired and adequate, but also has the desired narro~ particle size distribution, but its bulk density~ p~r flow and particle stability are not !yet complete~y adequate. In order to improve these and to establish the pattern of properties finally, the sus~
pended and agglomerated po~der from the agglomeration s.aae b) ;s fed to an after-treatment stage s~. ALthough the processes taking place in the ind;vidual stages cannot be explained in the fwllest detai~ it is nevertheless ~5 assumed that a rounding and dens,fica.ior, o, the agglomêr-at~d particles formed takes place in the after-treatmen.
stage ~ithout significant alteration in the average par-t;cle dia~eter dso of the a~ lomerates being effected.
This after-treatment stage takes place in a long, straight vessel, advantageously having a length to diameter ratio of at least 2:1, it being possible to reach very high ratios of th;s kind~ such as, for example, 25:1, prefer-ably 10:1, in a singlc vessel, or even up to 50:1 (total length to diameter~, if the after-treatment stage is divided into several vessels of the said type arranged in series. This vessel or these vessels can be mounted vertically, but this makes it necessary to introduce flow-delay;ng elements. A horizontal arran3ement is preferred - particularly in the case of a single long vessel. In this vcss2l there is a multi bladed sti,rring element, - formcd from a large n~mber of stirrer rings arranged in ' - series preferably on one shaft - each of these s~irrer rin~s ~eing composed of at least 3 and not more than 8 5 preferably not more than 6, blades and these stirring blades having a configuration of the type o~ a disc s~irrer, ie. having a rectangular shape and their,rectangular planes being arranged radiaLly on the shaft. A slightly ' inclined position in relation to the shaft is poss;ble~
The number of these serially arranged stirrer biade rings of the type of a disc stirrer depends on the length of the vessel, and the ;nterspace between two su'ch rings should not exceed the width of the stirrer blades. If several vessels are arranged in series, it is also possible to have an assembly on separate shafts~ each of ~hich is effective for one of these vessels, In the ~hole after-treatment stage~ a specific stirring energy of 5 to 30, preferably 10 to 20, W/l is i~troduced; the dwe~l time is 6 to ~0, preferaoly 10 to 20, minutes.
After passing through the after-treatment stage c), the agglomerate suspended in the liquid medium is uithdrawn continuousl~ and fed to a continuously operatin~
filtering device in order to separate the agglomerated powder from the bulk of the water and ~rom,part of the organic liquid, and such a filtering device should, if poss;ble, permit the recvvery of the organic liquid employed. The removal of the remainder of the water and of the remaining organic solvent is effected by drying, 723~
preferably in seYeral successive ~rying stages and, if appropriate, using a vacuum, it being necessary for the drying to be carried out at temperatu;es belo~ the crystal-lite melting point~ and it is advantageously carried out at a temperature at leas~ 50C aboYe the boiling point of the organic liquid e~ployed. The dryin~ is preferably effected at a temperature of 25 to 300C - in the case - of stagewise drying this temperature is preferably employed in the last stage.
hfter the drying~ the coarse fraction, ie. over~
~;ze particles having a diameter 1,500 um, is removed by means of suitable screening. In the product of the pro-cess according to the invention, this coarse fraction is not more than 4X by ~eight~ but is very frequently b&low 1X by wêi5ht~ a percën.agê which car, scarcely bc ach ev2d in the discontinuous process. The temperature for the whole continuous agglomeration process according to the inventionO Nhich can be selected ~ithin the abovement~ned range, is preferably kept approximately constant from stage a) to stage b) within a controllable width of variation. Differing temperatures are possible, in ~hich case it is preferable to have an increase in temperature ;n the direction of ftow.
Customary fillers, in an amount of 1 to 60% by ~eight, can be m;xed into the primary powder before it ;s metered into the pretreatment stage a). Examples of fillers of this type are glass fibers ~hich, if appropriate, have been treated ~ith customary water-repelling agents, powdered carbon, g~aphite, molybdenum ~ulfide, bron~e, 7~
2~
asb~stos and the like~ Thes~ fillers are mixed homo-geneously in a dry state into the primary po~lder in a prem;xing vessel, before metering into the process accord-ing to the invention takes place. The said uater repelling agentsO such as, for example, silane couplin~ agents, can, if appropriate, also be added to the agglomeration pro-cess ;n the pretreatment stage~ In the course of the ~gglomeration the filler is incorporated homogeneously into the agglomerat2d particles.
In a preferred embodiment of the process, a part o~ the pretreated suspension, after it has passed through the homo~enization z~ne in the pretreatment stage, is extracted from the flo~ and returned via a circulating line to the pretreatment stage, if appropriate by means of a pu~p, uhich can perhaps also contribute ar addit,onal comminuting and/or homogenizin~ action~ The ratio of the fraction recycled to that passing through ;s preferably between 1:1 and 5:1.
The process according to the invention for the agglomerat;on of non-mëlt-fabricab~e TFE ~olymër ~owdérs _ _ _ ,, . _ _ . . , _ _ ...... . _ .. ..
~ ` màkes~i~~~possIbl~e~~~o~~produce,~~~in~~a~~~-~ ~~~~~--~~-~ ~~~ ~~~
_ _ _ .. .. _ _ . .... . _. _ _ . ._ ~ __ _ ..
continuous procedure, agglomerated powders of this type, ~he product propert;es of uhich are at least of equal rank u;th, but in some cases far superior to, the powders 2S orig;nating from discontinuous processesn The a3~lomer-at~s are obtained in a unifor~ product quality, especially ;n respect of their bulk density, their narro~l particle size distribu~ion, their improved'''w~e.r'~~low' ~an~ t~eir particle ~~ -- ~ --~ ~~
stability~ The process according to the invention is~
' 7~8 ho~ever, considerabLy more econo~ical and cost-advantageous to operate than discont;nuous processes; it offers the possi~i~ity of automa~ic control in who~e or in part~
In addit;on numerous manual ~orking stages are avoided, 5 so that the risk of spotlike impurities ;s virtualLy excluded. Th;s fact is of very particular importance in the case of TFE poly~ers, since such inlpurities can occur as visible black spots ~hen the product ;s sintered, and - add;tiona~ly, for exa~ple, effect the ~ormation of elec-lD trical pores and thus reduce the dielectric s~rength of insu(ations~
It has already been stated many times in the ~iterature that modified TFE polymers ~ere subjected to an agglomeration process. tlo~ever~ it has been ~ound that, particlllarly in ths case of p&rfluorinated ethers as mod;fying agents, it is only possible by such~pro~esses to obtain products ~hich are not equivalent to the unmodified polymers belonging to the state of the art, particularly in regàrd to thcir px~er-~l~w~~ their bulk density and their particle stabilîty. It has become possible, by the process accord;ng to the invention, for the first time to prepare, with the same advantageous properties, such 1FE polymers which have been modified ~ith per-fluorinated e~hers.
- The invention also relates, therefore, to ag~lomer-ated moldin~ po~ders composed of particles of a non=melt~
~ ~ ~cabIe _etrafluoroethylene PqlYmer = = __ ~~~~ ~rhich has a specific surface area, determined by . _.. _ _ . .
the BET method~ of 0.5 to ~ m~/g and which `~ ~18~L7~3 ~ 23 -a~ contains 0.001 to 1X by ~eight ~f copolymerized units of a perf luorinated vinyt e~her oF the formula t F~-C F-O-X
in ~hich X denotes a perfluoroalkyl radisal having 1 to 4 C atoms or a radical of the formula F,C
F ~ ~ F
~ CF3 n ~
and n is 0 to 1~ and also conta;ns copolymerized units of tetrafluoroethy~ene, b) is composed essentially of agg~omerates having an average particle diameter d50 of 150 ~o 1,000 ~m which naYe been b~iit up from primary partie~es having ar average particle diameter d50 of 20 to ~0 ~m and ~hich possess a spheroida~ form and a uniform, dense surface, c) has a bulk density of at least 700 g/l, d~ has a po~ flo~ time of 8.0 to 4.0 seconds/50 g at an ~verage agglomerate diâmeter dso of 150 to 250 ~m and of 4.0 to 1.5 seconds/50 9 at an agglomera~e diameter d50 of 250 to 1,000 ~m, e) has a particle stability of ~.0 to 4.D seconds 50 g at ar, average agglomerate diameter d50 of 150 to 250 ~m and of 4.0 to 1.8 seconds/S0 g at an aggLomerate diameter dso of 250 to ?, ~mf and f) has a proport;on of more than 50% by ~eight of agglomerates having a particle size diameter ~hich is at least 0~7 times and not more than 1.3 times the average , .
~ .
~L8~L72~
particle d;ameter dso, 9~ ~herein a molded article prepared therefrom has a ~elding factor of at least 0~60, and h) the pore count, measured at a voltage of 5,000 as electrical defects on a veneer-cut film 2DO,um thick prepared ~rom the agglomerated moLding po~der, is not more tha~ tS pores~m2.
The said po~ders preferably contain a proportion of 0.01 to 0.5X by ~eight o~ ~he said perfluorinated 1~ ethers, and have an average part;cle diameter of the agglomerates of 150 to 800 ~m, in particular 25a to 750 ~Imt an avera~e particle diameter of the primary part;cLes in the agglomerates of 20 to 50 ~m, a bulk density of 700 to 1,000~ in particular 800 to 1,000, 9/1~ a ~ot~er flo-~ t~ oî
~.0 to 3.0 secon~s;50 g at d50 o~ 150 to 250 ~m and Gf
3~0 to 1.5 seconds/50 g at d50 of 250 to 1,00C ~m, and a particle stability of 6.0 to 3.0 seconds~50~ at dso of 150 to 250 ~m and of 3.0 to 1.8 at dso f 250 to 1,000 ~m~
The proportion of agglomerated particles hav;ng a diameter ~ithin 0~7 times to 1.3 ~;mes the average particle dia-~ete~ dso ;s preferably 50 to 75, particularly preferen-tially 60 to 75, X by ~eight, the ~elding factor is pre-~erably 0.6 to 1~0, particularly preferably 0.80 to 1.0, and the pore count is 15 to 0~ preferably 6 to 0, pores/m2. They also have a deformat;on under load~
d~term;ned as specified in ASTM D-621 on test specimens prepared therefrom, of not more than 15 (do~n to 5), pre-ferably 12 to 5, ~.
The a~glomerated molding po~ders according to the ~ ~18~
~nvent;on, ~hich are composed of particles of a tetra-fluoroethylene polymer which cannot be processed from the melt, and uhich have the said content of copolymerized units of the perfluorinated vinyi ethers indicated, are dis-S tinguished, a~ove all, by very ~ood elec-trical insulation properties. Thus~ they have a surprisingly hi~h elec~
tricaL breakdo~n strength, which manifests itself, above a~l, in the number of pores counted per square ~eter of a veneer-cut fiLm 200 ~m thick. Whereas in the case of agglomerated molding powders of tetrafluoroethylene, ie.
those containin~ no modifyin~ agent, a considerabLe decre~se in the pore count, compared with the finely ground starting powder~ takes place as an undesirable consequence of the a~glomeration process, this is the case only to a very small extent in the ag~lomeration ~eading to the ~odif;ed molding po~ders accordin~ to the ;nvention. The agglomerated molding powders according to the ;nvention, wh;ch contain the said perfluorinated vinyl ethers as ~od;~ying agents, are therefore far superior in this respect to the conventional molding powders ~hich have been a~lomerated but not modified.
The finely divided, agglomerated molding powders ~up to 240 ~m~ which a`re obtained by the process accord-ing to the invention are particularly suitable for the production of veneer-cut films for isostatic compression molding and for the production of sheets. The aggLomer-ates of somewhat coarser part;cle si~e ~above 250 ~M) are employed in ~he automatic compression molding of thin-~alled components, such as, for example~ sheets, rods and ~ 26 -tu~es, but also for ram extrusion (for example in the lo~ pressure range)~
The foLlo~ing rethods of determina~ion have been - used in connection w;th this invention:
1) ~~verage particle diameter (d50) .. . . . _ .
The d tertnination is effected by sieve analysis as specified by DIN Standard 53,477, in a vibration time o~ 10 minutes, the coarse fract'ion having particle dia-meters ~1,5001um being left out account in determining the average particle diameter dso.
23 Determination of the coarse fract;on The coarse materia~ is removed by screening using a 1~500 ,um sieve and the ~raction is quoted in % by ueight ~table ~I).
t5 3) Bulk der1sity 1'he determination is carried out as specified in ~IN Standard 53,468, after removing the coarse fraction ~having a particle d;ameter greater than 1,500 ~m).
Powder ~l:ow .: .
A polytetrafluoroethylene-coated aluminum funnel having an internal diameter ~at the top) of 74 mm, an internal diameter ~at the bottom) of 12 mm and a hei~ht - , of 89 mm is fastened to a commercially available vibrator in such a ~ay that the distance from the motor casing of the vibrator to the center of the funnel is 90 to 100 mm.
S0 ~ of product are plac,ed in the funr,el, t'he vibrator is s~itched on at an amplitude of vibration of 0.1 to 1 mm and ~he time from releasing the funnel aperture until the funnel has run ;tself completely empty is measured. The "` ~ 72~3 ~ ~7 ~
chorter the flo~ time, the better the p~er flow of the po~der 1he coarse fraction >1,500 ~m is removed before ~easuring the pourability.
S) Part_icle stability S 50 g of po~der are placed in an aluminum beaker hav~ng an internal diameter of 100 mm and a height of 750 mmS and are stirred for 5 r,1inutes at 200 r.p~m. The stirrer, which is e~uipped with t~o vanes, is aligned via a pin and a corresponding recess in the base of the beaker.
The distance from the lo~er edge of the stirrer blade to the base is 1~ mm. The stirrer blades have a thickness of 1.5 mm, a ~idth of 25 mm and a length of 46 mm and are inclined at an an~le of 45 to the stirrer shaft and at an an~le of 90 to one another~ The edges of the vane blade~ are slightly rounded. Approx7mateLy 0.1 9 ~, aluminum oxide is added to the product before stirring is be~un in order to aYoid the development of an electro-static charge. In this determination too, the coarse particles 1,500 ~nl are removed beforehand. The powder flow, as defined under 4), of the product wh;ch has been stirred in the aluminum beaker is then measured. This valwe of powder ~low, obtained after exposure to mechanical stress, is used as a measure of the particle stab-~lity. Compar;ng the powder flow - values of the powder ~5 before and after the stirring treatment provides infor-mation as to ho~J far the part;cles have been destroyed in the course of the exposure to mechanical stress.
The proportion of agglomerated particles hav;ng a diameter ~ithin 0~7 times to 1.3 ~;mes the average particle dia-~ete~ dso ;s preferably 50 to 75, particularly preferen-tially 60 to 75, X by ~eight, the ~elding factor is pre-~erably 0.6 to 1~0, particularly preferably 0.80 to 1.0, and the pore count is 15 to 0~ preferably 6 to 0, pores/m2. They also have a deformat;on under load~
d~term;ned as specified in ASTM D-621 on test specimens prepared therefrom, of not more than 15 (do~n to 5), pre-ferably 12 to 5, ~.
The a~glomerated molding po~ders according to the ~ ~18~
~nvent;on, ~hich are composed of particles of a tetra-fluoroethylene polymer which cannot be processed from the melt, and uhich have the said content of copolymerized units of the perfluorinated vinyi ethers indicated, are dis-S tinguished, a~ove all, by very ~ood elec-trical insulation properties. Thus~ they have a surprisingly hi~h elec~
tricaL breakdo~n strength, which manifests itself, above a~l, in the number of pores counted per square ~eter of a veneer-cut fiLm 200 ~m thick. Whereas in the case of agglomerated molding powders of tetrafluoroethylene, ie.
those containin~ no modifyin~ agent, a considerabLe decre~se in the pore count, compared with the finely ground starting powder~ takes place as an undesirable consequence of the a~glomeration process, this is the case only to a very small extent in the ag~lomeration ~eading to the ~odif;ed molding po~ders accordin~ to the ;nvention. The agglomerated molding powders according to the ;nvention, wh;ch contain the said perfluorinated vinyl ethers as ~od;~ying agents, are therefore far superior in this respect to the conventional molding powders ~hich have been a~lomerated but not modified.
The finely divided, agglomerated molding powders ~up to 240 ~m~ which a`re obtained by the process accord-ing to the invention are particularly suitable for the production of veneer-cut films for isostatic compression molding and for the production of sheets. The aggLomer-ates of somewhat coarser part;cle si~e ~above 250 ~M) are employed in ~he automatic compression molding of thin-~alled components, such as, for example~ sheets, rods and ~ 26 -tu~es, but also for ram extrusion (for example in the lo~ pressure range)~
The foLlo~ing rethods of determina~ion have been - used in connection w;th this invention:
1) ~~verage particle diameter (d50) .. . . . _ .
The d tertnination is effected by sieve analysis as specified by DIN Standard 53,477, in a vibration time o~ 10 minutes, the coarse fract'ion having particle dia-meters ~1,5001um being left out account in determining the average particle diameter dso.
23 Determination of the coarse fract;on The coarse materia~ is removed by screening using a 1~500 ,um sieve and the ~raction is quoted in % by ueight ~table ~I).
t5 3) Bulk der1sity 1'he determination is carried out as specified in ~IN Standard 53,468, after removing the coarse fraction ~having a particle d;ameter greater than 1,500 ~m).
Powder ~l:ow .: .
A polytetrafluoroethylene-coated aluminum funnel having an internal diameter ~at the top) of 74 mm, an internal diameter ~at the bottom) of 12 mm and a hei~ht - , of 89 mm is fastened to a commercially available vibrator in such a ~ay that the distance from the motor casing of the vibrator to the center of the funnel is 90 to 100 mm.
S0 ~ of product are plac,ed in the funr,el, t'he vibrator is s~itched on at an amplitude of vibration of 0.1 to 1 mm and ~he time from releasing the funnel aperture until the funnel has run ;tself completely empty is measured. The "` ~ 72~3 ~ ~7 ~
chorter the flo~ time, the better the p~er flow of the po~der 1he coarse fraction >1,500 ~m is removed before ~easuring the pourability.
S) Part_icle stability S 50 g of po~der are placed in an aluminum beaker hav~ng an internal diameter of 100 mm and a height of 750 mmS and are stirred for 5 r,1inutes at 200 r.p~m. The stirrer, which is e~uipped with t~o vanes, is aligned via a pin and a corresponding recess in the base of the beaker.
The distance from the lo~er edge of the stirrer blade to the base is 1~ mm. The stirrer blades have a thickness of 1.5 mm, a ~idth of 25 mm and a length of 46 mm and are inclined at an an~le of 45 to the stirrer shaft and at an an~le of 90 to one another~ The edges of the vane blade~ are slightly rounded. Approx7mateLy 0.1 9 ~, aluminum oxide is added to the product before stirring is be~un in order to aYoid the development of an electro-static charge. In this determination too, the coarse particles 1,500 ~nl are removed beforehand. The powder flow, as defined under 4), of the product wh;ch has been stirred in the aluminum beaker is then measured. This valwe of powder ~low, obtained after exposure to mechanical stress, is used as a measure of the particle stab-~lity. Compar;ng the powder flow - values of the powder ~5 before and after the stirring treatment provides infor-mation as to ho~J far the part;cles have been destroyed in the course of the exposure to mechanical stress.
4~
6) ~ f ~h~ ~roport;on by weight of the particl-es having 0.7 times to 1.3 times_the diameter of the_~s~ value This is effected by calculating the 0.7 times value and t~e 1.3 times ~alue ~ro~ the d50 value by multiplication and determining the proportion by ~eiQht by plotting the points in a cumulative curve.
7~ ~etermination_of the perfluoro-~alkylvinyl) ether tPAY~) conten.
; ~O The PAV content of the polymers prepared in accordance ~Jith the invention can be deter~,ned by a mass ba~ance by measuring the total quantity fed to the reactor, less the quantity of monomeric PAVE remaining in the re-actor after the polymerization.
~5 An analy~ical me~hod ~sing IR ~pectroscopy is also availa~le for determining the perfluoro-tpropyl vinyl) e.her content in the polymer and is described in detall in German Offenlegungsschrift 2,416,452 8) S~ecific stirring energy 2û The power input of the stirring e~ements in watts is measured at various speeds of rotation, in each case ~:hile the vessel is emptyA The ~iquid medium, of the quantity and type req~ired in accordance with the pro-cess accord;ng to the invent;on for the steady state of a continuum, is then added and the measurement is repeated.
The specific st;rring energy for a g;ven stirrer speed of rotation is then calculated as follows:
.
7~3 -- 2g -- pecific stirring energy ~W/1~ = Lt~ L(e~pty)~W) c~pac;ty ~l;ter~
where L~fUll) and L~emp~y) are the po~ér inputs in ~atts measured at a specific speed of rotat;on in the full and empty condition of the vessel.
~ Specific surface area This is determined us;ng an apparatus of the hreatron type ~manufacturer: Leybold, Cologne) by the ; ~ethod of S. Brunauer, P. Emmet and E. Teller; see J. Amer~ Chem. Soc. 60 ~19383, page 309 (8ET method).
10) Pore count A solid cylindrical biock of the agglomerated moLding po~der having a diameter of 100 mm and a height of t20 mm ;s prepared by compression moLding in a cylin-dr;cal m~ld under a pressur? of 35 N/mm2~ This block is then sintered by first brSn~ing it to a tempera.ure of 380~ at a ra~e of heating of ~5C~hour, keeping ;t at this temperature for 4 hours and then cooling it at a rate of 45C/hour A film 200 ~m th;ck ;s then veneer-cut from th;s block. Th;s veneer-cut f;lm, wh;ch ;s 120 mm ~Jide and 200 ~m th;ck, is passed over a system of rollers, along an aluminum foil to ~hich a direct current potential of 5,000 volts is applied. The opposite roller is earthed.
1 In2 oF the Film is measured. The pore count is recorded by means of a counting mechan;sm. The result is quoted 2~ in nu~ber of pores/m2.
11) Deformation under load This is determined as specified in ASTM-D 621 at 20C
on circular test specimens havin~ a diameter of 10 mm and 8~72~
and a thickness of ~0 mmO
12) ~elding factor .
Solid cylinders of the agglomerate~ molding powder having a diameter of 45 mm and a len~th of 45 mm (weight 150 g) are compression molded under a pressure of of 15 N/rnm2. Two each of these cylinders are sin-t~red uithout loading in a glass tube of 4~ mm diameter, as follows:
8 hours, heat;ng up from 20 to 380C at a linear rate of 1D heating of 45QC/hour, this temperature bein0 maintained for 4 hours, and 8 hours' coolin~ from 33~C to 20C at a ~inear rate of cooling of 45C/hour.
This s~nt~ring and cooling process is repeated.
Test specimens having a diameter of Z0 mm in the center (outside the region of clamping) are turned from the ~elded articles thus obtained. Comparison specimens ~hich are not ~elcled (ie. are compression molded from the out-set ;n the full length of 90 mm~ are prepared in an identi-cal manner. These test specimens are subjected to a ten-sile test in order to determine the tensile strength atbreak, following the guid elines of DIN Standard 53,455 and ~orking at a drawing speed of 30 mm/minute. The ~elding factGr is the quotient of the tensile force at break of the welded sample, divided by the tensile force at break o~ the non-welded sample.
Th~ invention is illus~rated by means of the ~ollowing examples-Example 1 Completely deionized water, gasoline tboiling . i . .
2 !3 point 80 to 110C) and finely gr~und tetrafluoroethylene poly~er po~der, modified w;th 300 ppm of perfluoro-~propyl vinyl) ether, were fed continuousLyJ uhile stirring, to a vertically mounted, cylindrical 30-liter vessel o~ elong-ated design equipped ~ith t~o flow ~reakers. The water, ~hich had been preheated to 50C, and the gasoline had previously been homogenized in the line via a static mixer and ~ere introduced via a dip tube into the vicinity of the dispersing disc. The ,inely ground tetrafluoroethyl-1~ ene polymer po~der, the data of which are specified inTable I~ was introduced into the vessel from above, via a vibratory chute, from a metering bunker. The ratio of organic liquid to water and of primary powder to organic liquid can be seen in each case in Table I. Three stir-~5 ring elements, each havins a diameter 0.~5 times the dia-meter of the vesseL, ~ere located on a common stirrer shaft.
In the upper third (the conveying stage) there ~as a three-bladed propeller stirrer, ;n the central third there was a so~called dispersing disc, on the circumference of rlhich b~ade-shaped teeth were mounted on the disc on botn sides, and in the lower third there was a double turbine. During the ~hole test, the stirrin~ energy in this pretreatment vessel was 29 W/l and the average d~ell time was 6 minutes. After being discharged from this pretreatment vessel, the suspension passed to another vertically mounted, elongated and cylindrical 55-l capacity vessel ~hich had tvo flo~ breakers (agglomeration zone) and on the stirrer shaft of which four three-bladed pro-pe~ler stirrers having a diameter of 0.5 tim~s ~he diameter o~ the vessel were moun~ed at uniform intervals~ The stirring po~ler during the test ~as here 10 ~Jl. After be;ng discharged from the homogenization ~one the suspension then passed into a horizontal!y mounted, cylindrical vessel of 8Q liters capacity and having a length to diameter ratio of 10:1. The stirriny element used here uas a stirring element mounted on a common shaft and comprising 48 s~irrer rings composed in each-case of four-bladed disc stirrers having rectangular stirring blades 1 cm wide. The st;rring po~er of this after-treatment zone was 16 W/l. The temperature ~as kept at 50C through out all the stages of the process. ~he ndividual vessels - ~ere instaLled at dif~erent heights, so that flow took p~ace under the influence of gravity, and they ~Jere con-nected ~lith one anoth0r by short lengths of piping. Thevessels were kept at a constant level of fillin~ during the test by addin~ the components un;form~y and cont;n-uously and by discharging the suspension from the last stirred vessel to the drying apparatus at a controlled rate.
The removal of the gasoline and the water uas effected in a multi-stage, continuous drying process, ~ith recovery of the yasoline, temperatures of 260 to 290C
be;ng used. The powder thus obtained ~as then conveyed v;a a cool;ng zone to a v;bratory screen hav;n~ a mesh ~idth of 1,500 ~m, ~here the remoYal of the coarse mat-erial took place. The properties of the produc~ ob.ained and also those of the products of the succeeding examples are recorded in Tables II and III.
The variations in the process carried out in Examples 2 to 16 uhich follo~, in respect of starting 0aterial ~primary po~der~, Ser,lperatureO aver2ge dwell time and spec;fic stirring energy ;n the indi~idual stages are shoi~n in Table I~ The fo(lo~ing ad~itional variations in
6) ~ f ~h~ ~roport;on by weight of the particl-es having 0.7 times to 1.3 times_the diameter of the_~s~ value This is effected by calculating the 0.7 times value and t~e 1.3 times ~alue ~ro~ the d50 value by multiplication and determining the proportion by ~eiQht by plotting the points in a cumulative curve.
7~ ~etermination_of the perfluoro-~alkylvinyl) ether tPAY~) conten.
; ~O The PAV content of the polymers prepared in accordance ~Jith the invention can be deter~,ned by a mass ba~ance by measuring the total quantity fed to the reactor, less the quantity of monomeric PAVE remaining in the re-actor after the polymerization.
~5 An analy~ical me~hod ~sing IR ~pectroscopy is also availa~le for determining the perfluoro-tpropyl vinyl) e.her content in the polymer and is described in detall in German Offenlegungsschrift 2,416,452 8) S~ecific stirring energy 2û The power input of the stirring e~ements in watts is measured at various speeds of rotation, in each case ~:hile the vessel is emptyA The ~iquid medium, of the quantity and type req~ired in accordance with the pro-cess accord;ng to the invent;on for the steady state of a continuum, is then added and the measurement is repeated.
The specific st;rring energy for a g;ven stirrer speed of rotation is then calculated as follows:
.
7~3 -- 2g -- pecific stirring energy ~W/1~ = Lt~ L(e~pty)~W) c~pac;ty ~l;ter~
where L~fUll) and L~emp~y) are the po~ér inputs in ~atts measured at a specific speed of rotat;on in the full and empty condition of the vessel.
~ Specific surface area This is determined us;ng an apparatus of the hreatron type ~manufacturer: Leybold, Cologne) by the ; ~ethod of S. Brunauer, P. Emmet and E. Teller; see J. Amer~ Chem. Soc. 60 ~19383, page 309 (8ET method).
10) Pore count A solid cylindrical biock of the agglomerated moLding po~der having a diameter of 100 mm and a height of t20 mm ;s prepared by compression moLding in a cylin-dr;cal m~ld under a pressur? of 35 N/mm2~ This block is then sintered by first brSn~ing it to a tempera.ure of 380~ at a ra~e of heating of ~5C~hour, keeping ;t at this temperature for 4 hours and then cooling it at a rate of 45C/hour A film 200 ~m th;ck ;s then veneer-cut from th;s block. Th;s veneer-cut f;lm, wh;ch ;s 120 mm ~Jide and 200 ~m th;ck, is passed over a system of rollers, along an aluminum foil to ~hich a direct current potential of 5,000 volts is applied. The opposite roller is earthed.
1 In2 oF the Film is measured. The pore count is recorded by means of a counting mechan;sm. The result is quoted 2~ in nu~ber of pores/m2.
11) Deformation under load This is determined as specified in ASTM-D 621 at 20C
on circular test specimens havin~ a diameter of 10 mm and 8~72~
and a thickness of ~0 mmO
12) ~elding factor .
Solid cylinders of the agglomerate~ molding powder having a diameter of 45 mm and a len~th of 45 mm (weight 150 g) are compression molded under a pressure of of 15 N/rnm2. Two each of these cylinders are sin-t~red uithout loading in a glass tube of 4~ mm diameter, as follows:
8 hours, heat;ng up from 20 to 380C at a linear rate of 1D heating of 45QC/hour, this temperature bein0 maintained for 4 hours, and 8 hours' coolin~ from 33~C to 20C at a ~inear rate of cooling of 45C/hour.
This s~nt~ring and cooling process is repeated.
Test specimens having a diameter of Z0 mm in the center (outside the region of clamping) are turned from the ~elded articles thus obtained. Comparison specimens ~hich are not ~elcled (ie. are compression molded from the out-set ;n the full length of 90 mm~ are prepared in an identi-cal manner. These test specimens are subjected to a ten-sile test in order to determine the tensile strength atbreak, following the guid elines of DIN Standard 53,455 and ~orking at a drawing speed of 30 mm/minute. The ~elding factGr is the quotient of the tensile force at break of the welded sample, divided by the tensile force at break o~ the non-welded sample.
Th~ invention is illus~rated by means of the ~ollowing examples-Example 1 Completely deionized water, gasoline tboiling . i . .
2 !3 point 80 to 110C) and finely gr~und tetrafluoroethylene poly~er po~der, modified w;th 300 ppm of perfluoro-~propyl vinyl) ether, were fed continuousLyJ uhile stirring, to a vertically mounted, cylindrical 30-liter vessel o~ elong-ated design equipped ~ith t~o flow ~reakers. The water, ~hich had been preheated to 50C, and the gasoline had previously been homogenized in the line via a static mixer and ~ere introduced via a dip tube into the vicinity of the dispersing disc. The ,inely ground tetrafluoroethyl-1~ ene polymer po~der, the data of which are specified inTable I~ was introduced into the vessel from above, via a vibratory chute, from a metering bunker. The ratio of organic liquid to water and of primary powder to organic liquid can be seen in each case in Table I. Three stir-~5 ring elements, each havins a diameter 0.~5 times the dia-meter of the vesseL, ~ere located on a common stirrer shaft.
In the upper third (the conveying stage) there ~as a three-bladed propeller stirrer, ;n the central third there was a so~called dispersing disc, on the circumference of rlhich b~ade-shaped teeth were mounted on the disc on botn sides, and in the lower third there was a double turbine. During the ~hole test, the stirrin~ energy in this pretreatment vessel was 29 W/l and the average d~ell time was 6 minutes. After being discharged from this pretreatment vessel, the suspension passed to another vertically mounted, elongated and cylindrical 55-l capacity vessel ~hich had tvo flo~ breakers (agglomeration zone) and on the stirrer shaft of which four three-bladed pro-pe~ler stirrers having a diameter of 0.5 tim~s ~he diameter o~ the vessel were moun~ed at uniform intervals~ The stirring po~ler during the test ~as here 10 ~Jl. After be;ng discharged from the homogenization ~one the suspension then passed into a horizontal!y mounted, cylindrical vessel of 8Q liters capacity and having a length to diameter ratio of 10:1. The stirriny element used here uas a stirring element mounted on a common shaft and comprising 48 s~irrer rings composed in each-case of four-bladed disc stirrers having rectangular stirring blades 1 cm wide. The st;rring po~er of this after-treatment zone was 16 W/l. The temperature ~as kept at 50C through out all the stages of the process. ~he ndividual vessels - ~ere instaLled at dif~erent heights, so that flow took p~ace under the influence of gravity, and they ~Jere con-nected ~lith one anoth0r by short lengths of piping. Thevessels were kept at a constant level of fillin~ during the test by addin~ the components un;form~y and cont;n-uously and by discharging the suspension from the last stirred vessel to the drying apparatus at a controlled rate.
The removal of the gasoline and the water uas effected in a multi-stage, continuous drying process, ~ith recovery of the yasoline, temperatures of 260 to 290C
be;ng used. The powder thus obtained ~as then conveyed v;a a cool;ng zone to a v;bratory screen hav;n~ a mesh ~idth of 1,500 ~m, ~here the remoYal of the coarse mat-erial took place. The properties of the produc~ ob.ained and also those of the products of the succeeding examples are recorded in Tables II and III.
The variations in the process carried out in Examples 2 to 16 uhich follo~, in respect of starting 0aterial ~primary po~der~, Ser,lperatureO aver2ge dwell time and spec;fic stirring energy ;n the indi~idual stages are shoi~n in Table I~ The fo(lo~ing ad~itional variations in
5 the experimental condition uere carried out in the course of these examples:
Examp~es 2, 4, 5 and ~
A double centrifugal stirrer instead of a double turb;ne ~as installed in the homosenization zone in the vesse~ of the pretreatment stage~
Example 3 In the vessel of the agglomeration stage there were only three propeller stirrers, mounted at uniform interva~s on the stirrer shaft.
Examplc 7 The gasoline and the water ~ere added to the pre~reatment stage without premix;ng; mixing took place solely in the common feed line.
Example 9 A r~ecycle line, leading back to the pretreatment stage~ branched off the connectin~ ~ine between the pre-treatment stage and the ag~lomeration stageO At this point 3 parts by volume of the suspended product leaving the pretreatment staqe were recycled by means o-~ a pump into this pretreatment stage, ~Ihile 1 part flo~ed into ~he agglomeration stage~
ExampLe 11 A double centrifugal stirrer instead of the dis-persin~ disc was installed in the dispersing zone of ~he 4 ~'Z~
pre~rea~ment s~age~
ExampLe 1Z
_ . .
The product was dried at 150C.
Example 14 S The product ~as dried at 160C.
Example 15 Before bein~ metered into the aggLomerization process, th~ primary powder ~as homogeneously mixed~ in ~the dry state, uith 15X by weight of desized glass fibers ta~erage length S0 ~m and diameter 15 ~o 25 ~m).
Example 16 Before the agglomerization process, the primary po~der was homogeneousLy mixed with 10% by weight of charcoal powder ~as speci~ied in DIN 80).
7~
1) It~JaU~ ~iUIJJ.~S ~ ~ ~ ~ u~ o a dS
~sa~nul~) a~l~ c~ c~ , ~ c~ co ~ c~, arp a6eJall~ ~ ~ ~, ~ ~ ,_ c~ ,_ ,_ C~ .
3~ln~eJad~al o~ ~ o ~ o c~ c~ o o o~ ~ o c_ u~
(1/~) 16Jaua 6UI.lJl~s ~ o .~ o o ~ o o ~ u~ U~
ads _~
~lsa~nul~) a~
Il> . O~ C~ O~ CJ~ C~
lla~p a6eJa~\V ~ ~ ` ' c~
v, I
~ ~o ) O ~ O ~ O O O O O O u~ ~ o aJn~J~d~al ~ c~ ~ c~. = ~ c~ ~ u~
(I/t'.) -16Jaua ~UIJJl~S a~ 2 ~, ~ . c~ "~
,~~IJI~ads ~ v ~ CJI . `~, ~
~lsa~nu.c~ ac J C~lla~lp a6eJaAV ~ o o ~ ~ o e o ~ o ~ ~ _r ~ o~ o o o o ~ ~
a.~n~eJad~al ~ '~' ~ '`' ~ ~ '`' ~ ~ ~' ~ ~' ~ ;
( I ~6 ) cu~ o o c~ o o o o o o ~ o o l~lsuap ~In~ ~ ~ ~ c~ ~ ~ ~ ~ c'~
~(un/) 05p ,~ o o o o O o u~ c~ ~ c~ o o~ o~
.~
c~plnhll .
~lue6Jol~lapnod ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~
E ~JeulJd Jo OT~IIJ ~ o U~ o ~ ô U~ c-- u~ o O co ~ o , ~ a~n loA/~ u,6 1 aM ~ c~i #~ dd u a6e 6UI~JIpo~ Jo g c~ O O O o O g c~ 0 0 ~,A~l~uenb) ad~l ~ s~ c-~ T 0, C~ O " ~ C'~
W .
Ja~e~l pue plnbl~ ~ ,_ ~ c~ r .~ O
ue6Jo uaal\~aq ............ .... ..... : .. .. ..
a~nlol~ ~q ol~e~ ~ ,~ * o p~nbll JO ~Jn~N o = ~ ~ ~ o S~l ~ ~ O ~ ~--V ~
o'Q~ dLlex3 ~`~ ~ ~ '~ ` C-- ~ C~ ~ ~ r .
7~3 .
_ ~b .
/n) ~6~:aua 6UIJJ~s ol;~laads "(sa~nu~c) a~l~, ~ ~
a~p aSeJaAy . ' ~o) 2 n~eJad ( I/R ) ~5Ja~a 6UI_~J~s . .
t oa ds ,_ (Sa~nulu) awl~ o~
anp a6eJaAy (~0) o c~ ' a~n~eJadual ~ ~
( 1/11) ISJaua 5UIJJl~s 0~ c~
~IJ ~ad .~
C _ . ', ~, (sa~nu~uj awl:~
<a llanp a6e.-a~y ~ v~
_, ~
c (~0) o o n~e~ladcal . ;.
o~ o~
~}suap ~ S
L (~n/) ~p u~
~ ptnhll tue6Jo/Jap~lod .. .. L
.n~ el~l Jd J o O t ~ ~J ~ t--- '~aunloAl~46ta~ o ~3*~* (Jdd ut o o _ ~ua5e 6ut,t;~pow ~o o o~ o ~
a~ I ~ ue n b ) a d ~1 ~ ~o a~en pue plnb~ I o o ~ v ~:~tue6~1o uaaH~aq .. ~ .~ " L
,aunlo/\ ~q o~eu * ~ cDt O
.,1 C _I _ 4- . -plnbll ~ o 0 JO aJn~eN a cc~ ~ G
' N a I d~ e x 3 ~
o ~J
o ~
.
~: ~ Q
CJ ~ ~ ~J O r, ~ ~r~ ~) ~ N ~ J O
~ E D
~ _ ., J ~
O
Ll~ O ~ O ~`J U~ `O ~ `O ~J Ir~ Ir~ C~ C) O ~J ~ ~ ~ r~ N
Vl .1 ~
V~
a~ C
.6 Ll'~
L~ ~ ~ o 3~ . 'O N t^) r~ 3 N N ~ N t~l 1 L C) V~
_~
~ C
E
~ ~ ~ ~n J ~ O 0 3 ~-- co ~ N P~ CO ~ N ~ ~ J C
u~ E ?~ ~ O O O t~i OO O O O ~ ~ ~ O
v v 1~ U~ t~ L. _O
t¢ ~- A
l_ o ~' ~, . .. ~
r- , Ot~ooO~U~oOOOOOOU~o CO CO O` ~ ~ ~ O ~') CO ~ Il~ Ul ~ O` O' ~I
Cl~ CO r- CO ~ ~ 00 DO CO CO CO co oo 1 C ~ E cO 8 coO v~ o~ o u~ 8 ~ C~ ~ ~ N 1~ r~ N ~ N ~ ~ . I~ I~ r-- ~
O ' ..
~'J
'~ ~. ~1 ~ ~ ~ ~ CO O` O ~ N ~) ~ u `.0 n . ~ ~_ ~ "_ ,,, . ~
UJ . ~.
7~
38 _ ~V~
~ L~
_~ C U~ O U'~ O O O O O U~ O C O O O U`. C~
S ~ .
. .
V~ P~) O ~ ~ L~ 1 0 ~ O r~
-~ OOOOOOOOOOOO~OOO
O ~ O N O ~ ~ O N 00 ~-- O - O ~
..~....,..~. ..
~ o o o n o o o o o o o o o o o o ~ ~ V~
~ ~ o ~ 00 ~ o ~ o o U~ o ~o ~ ~ U~ U~ ~ oo U~
~_1 ~.> Q ~ Ul 00 0 ~ J O CO ~
~ ~ !7 U~ `O ~
U- ~ `:
~ ' C ~
~ L. ~ ~ ~ ~ t~J~ ~ N~ ) N t~ N N
~_ Y~
. ~
~IB
~ O U~ `O 0~ ~ U~ ~ ~ t~ U~ , ~o z ~ .
L O O O u~ ~ O u~ 1 O O O ~
O O` O O" O` I`~ I~ O O r-- ~0 CO O` O` CO
3 ~ ~- O - O O O O O ~ O O O O O O
. .- - .
, - _ ~
Z
E , ~_ ~_ e_ ~ ~ ~
. , LU . ~ ~, .
'
Examp~es 2, 4, 5 and ~
A double centrifugal stirrer instead of a double turb;ne ~as installed in the homosenization zone in the vesse~ of the pretreatment stage~
Example 3 In the vessel of the agglomeration stage there were only three propeller stirrers, mounted at uniform interva~s on the stirrer shaft.
Examplc 7 The gasoline and the water ~ere added to the pre~reatment stage without premix;ng; mixing took place solely in the common feed line.
Example 9 A r~ecycle line, leading back to the pretreatment stage~ branched off the connectin~ ~ine between the pre-treatment stage and the ag~lomeration stageO At this point 3 parts by volume of the suspended product leaving the pretreatment staqe were recycled by means o-~ a pump into this pretreatment stage, ~Ihile 1 part flo~ed into ~he agglomeration stage~
ExampLe 11 A double centrifugal stirrer instead of the dis-persin~ disc was installed in the dispersing zone of ~he 4 ~'Z~
pre~rea~ment s~age~
ExampLe 1Z
_ . .
The product was dried at 150C.
Example 14 S The product ~as dried at 160C.
Example 15 Before bein~ metered into the aggLomerization process, th~ primary powder ~as homogeneously mixed~ in ~the dry state, uith 15X by weight of desized glass fibers ta~erage length S0 ~m and diameter 15 ~o 25 ~m).
Example 16 Before the agglomerization process, the primary po~der was homogeneousLy mixed with 10% by weight of charcoal powder ~as speci~ied in DIN 80).
7~
1) It~JaU~ ~iUIJJ.~S ~ ~ ~ ~ u~ o a dS
~sa~nul~) a~l~ c~ c~ , ~ c~ co ~ c~, arp a6eJall~ ~ ~ ~, ~ ~ ,_ c~ ,_ ,_ C~ .
3~ln~eJad~al o~ ~ o ~ o c~ c~ o o o~ ~ o c_ u~
(1/~) 16Jaua 6UI.lJl~s ~ o .~ o o ~ o o ~ u~ U~
ads _~
~lsa~nul~) a~
Il> . O~ C~ O~ CJ~ C~
lla~p a6eJa~\V ~ ~ ` ' c~
v, I
~ ~o ) O ~ O ~ O O O O O O u~ ~ o aJn~J~d~al ~ c~ ~ c~. = ~ c~ ~ u~
(I/t'.) -16Jaua ~UIJJl~S a~ 2 ~, ~ . c~ "~
,~~IJI~ads ~ v ~ CJI . `~, ~
~lsa~nu.c~ ac J C~lla~lp a6eJaAV ~ o o ~ ~ o e o ~ o ~ ~ _r ~ o~ o o o o ~ ~
a.~n~eJad~al ~ '~' ~ '`' ~ ~ '`' ~ ~ ~' ~ ~' ~ ;
( I ~6 ) cu~ o o c~ o o o o o o ~ o o l~lsuap ~In~ ~ ~ ~ c~ ~ ~ ~ ~ c'~
~(un/) 05p ,~ o o o o O o u~ c~ ~ c~ o o~ o~
.~
c~plnhll .
~lue6Jol~lapnod ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~
E ~JeulJd Jo OT~IIJ ~ o U~ o ~ ô U~ c-- u~ o O co ~ o , ~ a~n loA/~ u,6 1 aM ~ c~i #~ dd u a6e 6UI~JIpo~ Jo g c~ O O O o O g c~ 0 0 ~,A~l~uenb) ad~l ~ s~ c-~ T 0, C~ O " ~ C'~
W .
Ja~e~l pue plnbl~ ~ ,_ ~ c~ r .~ O
ue6Jo uaal\~aq ............ .... ..... : .. .. ..
a~nlol~ ~q ol~e~ ~ ,~ * o p~nbll JO ~Jn~N o = ~ ~ ~ o S~l ~ ~ O ~ ~--V ~
o'Q~ dLlex3 ~`~ ~ ~ '~ ` C-- ~ C~ ~ ~ r .
7~3 .
_ ~b .
/n) ~6~:aua 6UIJJ~s ol;~laads "(sa~nu~c) a~l~, ~ ~
a~p aSeJaAy . ' ~o) 2 n~eJad ( I/R ) ~5Ja~a 6UI_~J~s . .
t oa ds ,_ (Sa~nulu) awl~ o~
anp a6eJaAy (~0) o c~ ' a~n~eJadual ~ ~
( 1/11) ISJaua 5UIJJl~s 0~ c~
~IJ ~ad .~
C _ . ', ~, (sa~nu~uj awl:~
<a llanp a6e.-a~y ~ v~
_, ~
c (~0) o o n~e~ladcal . ;.
o~ o~
~}suap ~ S
L (~n/) ~p u~
~ ptnhll tue6Jo/Jap~lod .. .. L
.n~ el~l Jd J o O t ~ ~J ~ t--- '~aunloAl~46ta~ o ~3*~* (Jdd ut o o _ ~ua5e 6ut,t;~pow ~o o o~ o ~
a~ I ~ ue n b ) a d ~1 ~ ~o a~en pue plnb~ I o o ~ v ~:~tue6~1o uaaH~aq .. ~ .~ " L
,aunlo/\ ~q o~eu * ~ cDt O
.,1 C _I _ 4- . -plnbll ~ o 0 JO aJn~eN a cc~ ~ G
' N a I d~ e x 3 ~
o ~J
o ~
.
~: ~ Q
CJ ~ ~ ~J O r, ~ ~r~ ~) ~ N ~ J O
~ E D
~ _ ., J ~
O
Ll~ O ~ O ~`J U~ `O ~ `O ~J Ir~ Ir~ C~ C) O ~J ~ ~ ~ r~ N
Vl .1 ~
V~
a~ C
.6 Ll'~
L~ ~ ~ o 3~ . 'O N t^) r~ 3 N N ~ N t~l 1 L C) V~
_~
~ C
E
~ ~ ~ ~n J ~ O 0 3 ~-- co ~ N P~ CO ~ N ~ ~ J C
u~ E ?~ ~ O O O t~i OO O O O ~ ~ ~ O
v v 1~ U~ t~ L. _O
t¢ ~- A
l_ o ~' ~, . .. ~
r- , Ot~ooO~U~oOOOOOOU~o CO CO O` ~ ~ ~ O ~') CO ~ Il~ Ul ~ O` O' ~I
Cl~ CO r- CO ~ ~ 00 DO CO CO CO co oo 1 C ~ E cO 8 coO v~ o~ o u~ 8 ~ C~ ~ ~ N 1~ r~ N ~ N ~ ~ . I~ I~ r-- ~
O ' ..
~'J
'~ ~. ~1 ~ ~ ~ ~ CO O` O ~ N ~) ~ u `.0 n . ~ ~_ ~ "_ ,,, . ~
UJ . ~.
7~
38 _ ~V~
~ L~
_~ C U~ O U'~ O O O O O U~ O C O O O U`. C~
S ~ .
. .
V~ P~) O ~ ~ L~ 1 0 ~ O r~
-~ OOOOOOOOOOOO~OOO
O ~ O N O ~ ~ O N 00 ~-- O - O ~
..~....,..~. ..
~ o o o n o o o o o o o o o o o o ~ ~ V~
~ ~ o ~ 00 ~ o ~ o o U~ o ~o ~ ~ U~ U~ ~ oo U~
~_1 ~.> Q ~ Ul 00 0 ~ J O CO ~
~ ~ !7 U~ `O ~
U- ~ `:
~ ' C ~
~ L. ~ ~ ~ ~ t~J~ ~ N~ ) N t~ N N
~_ Y~
. ~
~IB
~ O U~ `O 0~ ~ U~ ~ ~ t~ U~ , ~o z ~ .
L O O O u~ ~ O u~ 1 O O O ~
O O` O O" O` I`~ I~ O O r-- ~0 CO O` O` CO
3 ~ ~- O - O O O O O ~ O O O O O O
. .- - .
, - _ ~
Z
E , ~_ ~_ e_ ~ ~ ~
. , LU . ~ ~, .
'
Claims (11)
OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. A process for the continuous production of an agglomerated molding powder from a granular non-melt-fabricable tetrafluoroethylene polymer primary powder in which the average particle diameter d50 of the primary particles is 20 to 80 µm, in a liquid medium which passes through the whole process and consists of water and an organic liquid which is capable of wetting such a tetrafluoroethylene polymer and is soluble in water to the extent of not more than 15% by weight the weight/
volume ratio of primary powder to organic Liquid being 7:1 to 1.3:1 and the volume/volume ratio of organic liquid to water being 1:1.4 to 1:50, with mechanical agitation at temperatures of 5 to 90°C, which comprises passing the primary powder, together with the liquid medium, through a three-stage cascade in which, initially, the primary powder, the water and the organic liquid, in the ratio mentioned, a) are continuously introduced into a pretreatment stage filled with the liquid medium and are moved forward in the former, where the primary powder is first drawn in a conveying zone into the liquid medium, and is suspended in the latter, by means of a stirring element which effects the conveyance, then arrives in a directly adjacent dispersing zone and is there converted, by the action of a stirring element having a dispersing action within the range of the specific stirring energy applied, into a form which is essentially uniformly finely distributed within the liquid medium, then arrives in a directly adjacent homogenizing zone and is pre-agglomerated there by the action of a turbine-shaped stirring element to give sec-ondary particles having an average particle diameter d50 of about 100 to about 400 µm, the pretreatment stage being passed through at an average dwell time of 3 to 30 minutes and the specific stirring energy introduced there being 5 to 100 W/1, this pretreated suspension then b) passes through an agglomeration stage in which the pre-agglomerated primary powder is further agglomerated by the gentle action of stirring elements which, within the range of specific stirring energy applied, exert essentially no commenting action, producing an adequate contact between particles in the liquid medium, to give a powder having tertiary particles of an average particle diameter d50 of 150 to 1,000 µm, the agglomeration stage being passed through at an average dwell time of 5 to 50 minutes and the specific stirring energy introduced there being 2 to 30 W/1, this suspension then c) is passed through an after-treatment stage in which, by maintaining an average dwell time of 6 to 60 minutes and by the action of a multi-bladed stirrer elm-ment which introduces a specific stirring energy of 5 to 30 W/1 into the suspension, the final formation of the particle shape takes place without a further essential change in the average particle size, and finally is discharged continually from the after-treatment stage, and the agglomerated powder is separated from the liquid medium.
volume ratio of primary powder to organic Liquid being 7:1 to 1.3:1 and the volume/volume ratio of organic liquid to water being 1:1.4 to 1:50, with mechanical agitation at temperatures of 5 to 90°C, which comprises passing the primary powder, together with the liquid medium, through a three-stage cascade in which, initially, the primary powder, the water and the organic liquid, in the ratio mentioned, a) are continuously introduced into a pretreatment stage filled with the liquid medium and are moved forward in the former, where the primary powder is first drawn in a conveying zone into the liquid medium, and is suspended in the latter, by means of a stirring element which effects the conveyance, then arrives in a directly adjacent dispersing zone and is there converted, by the action of a stirring element having a dispersing action within the range of the specific stirring energy applied, into a form which is essentially uniformly finely distributed within the liquid medium, then arrives in a directly adjacent homogenizing zone and is pre-agglomerated there by the action of a turbine-shaped stirring element to give sec-ondary particles having an average particle diameter d50 of about 100 to about 400 µm, the pretreatment stage being passed through at an average dwell time of 3 to 30 minutes and the specific stirring energy introduced there being 5 to 100 W/1, this pretreated suspension then b) passes through an agglomeration stage in which the pre-agglomerated primary powder is further agglomerated by the gentle action of stirring elements which, within the range of specific stirring energy applied, exert essentially no commenting action, producing an adequate contact between particles in the liquid medium, to give a powder having tertiary particles of an average particle diameter d50 of 150 to 1,000 µm, the agglomeration stage being passed through at an average dwell time of 5 to 50 minutes and the specific stirring energy introduced there being 2 to 30 W/1, this suspension then c) is passed through an after-treatment stage in which, by maintaining an average dwell time of 6 to 60 minutes and by the action of a multi-bladed stirrer elm-ment which introduces a specific stirring energy of 5 to 30 W/1 into the suspension, the final formation of the particle shape takes place without a further essential change in the average particle size, and finally is discharged continually from the after-treatment stage, and the agglomerated powder is separated from the liquid medium.
2. The process as claimed in claim 1, wherein a dispersing disc equipped with blade-shaped elements project ing on both sides at the peripheral circumference is used.
3. The process as claimed in claim 1, wherein, after passing through the homogenization zone, a part of the pretreated suspension is recycled to the pretreatment stage.
4. The process as claimed in claim l claim 2 or claim 3 wherein the after-treatment stage is carried out in a horizontally mounted, elongated stirred vessel having a length to diameter ratio of at least 2:1.
5. The process as claimed in claim 1 claim 2 or claim 3, wherein the pretreatment stage a) is passed through at an average dwell time of 5 to 15 minutes and the specific stirring energy introduced is 10 to 60 W/l.
6. The process as claimed in claim l claim 2 or claim 3, wherein the agglomeration stage b) is passed through at an average dwell time of 8 to 20 minutes and the stirring energy introduced is 5 to 20 W/1.
7. The process as claimed in claim l claim 2 or claim 3 wherein the after-treatment stage c) is passed through at an average dwell time of 10 to 20 minutes and the stirring energy introduced is 10 to 20 W/l.
8. The process as claimed in claim l, claim 2 or claim 3 wherein 2 to 60% by weight of customary fillers are added to the primary powder before it is introduced into the pretreatment stage.
An agglomerated molding powder composed of particles of a non-melt-fabricabie tetrafluoroethylene polymer which-has a specific surface are, as measured by the BET method, of 0.5 to 4 m2/g and which a) contains 0.001 to 1X by weight of copolymerized units of a perfluorinated vinyl ether of the formula CF2=CF-0-X
in which X denotes a perfluoroalkyl radical having 1 to 4 C atoms or a radical of the formula and n is 0 to 1, and also contains copolymerized units of tetrafLuoroethylene, b) is composed essentially of agglomerates having an average particle diameter d50 of 150 to 1,000 µm which have been built up from primary particles having an average particle diameter d50 of 20 to 80 µm and which possess a spheroidal form and a uniform, dense surface, c) has a bulk density of at least 700 g/1, d) has a flow time of 8.0 to 4.0 seconds/50 g at an average agglomerate diameter d50 of 150 to 250 µm and of 470 to 1.5 seconds/50 9 at an agglomerate diameter d50 of 250 to 1,000 µm, e) has a particle stability of 8.0 to 4.0 seconds/
50 g at an average agglomerate diameter d50 of 150 to 250 µm and of 4.0 to 1.8 seconds/50 9 at an agglomerate diameter d50 of 250 to 1,000 µm, and f) has a proportion of more than 50% by weigh of agglomerates having a particle size diameter which is at least 0.7 times and not more than 1.3 times the average particle diameter d50, g) wherein a molded article prepared therefrom has a welding factor of at least 0.60, and h) the pore count, measured at a voltage of 5,000 V
as electrical defects on a veneer-cut film 200 µm thick prepared from the agglomerated molding powder, is not more than 15 pores/m2.
in which X denotes a perfluoroalkyl radical having 1 to 4 C atoms or a radical of the formula and n is 0 to 1, and also contains copolymerized units of tetrafLuoroethylene, b) is composed essentially of agglomerates having an average particle diameter d50 of 150 to 1,000 µm which have been built up from primary particles having an average particle diameter d50 of 20 to 80 µm and which possess a spheroidal form and a uniform, dense surface, c) has a bulk density of at least 700 g/1, d) has a flow time of 8.0 to 4.0 seconds/50 g at an average agglomerate diameter d50 of 150 to 250 µm and of 470 to 1.5 seconds/50 9 at an agglomerate diameter d50 of 250 to 1,000 µm, e) has a particle stability of 8.0 to 4.0 seconds/
50 g at an average agglomerate diameter d50 of 150 to 250 µm and of 4.0 to 1.8 seconds/50 9 at an agglomerate diameter d50 of 250 to 1,000 µm, and f) has a proportion of more than 50% by weigh of agglomerates having a particle size diameter which is at least 0.7 times and not more than 1.3 times the average particle diameter d50, g) wherein a molded article prepared therefrom has a welding factor of at least 0.60, and h) the pore count, measured at a voltage of 5,000 V
as electrical defects on a veneer-cut film 200 µm thick prepared from the agglomerated molding powder, is not more than 15 pores/m2.
10. An agglomerated molding powder as claimed in claim 9 which a) contains 0.01 to 0.5% by weight of copolymerized units of a perfluorinated vinyl ether of the formula CF2=CF-0-X
in which X denotes a perfluoroalkyl radical having 1 to C atoms or a radical of the formula and n is 0 to 1, and also contains copolymerized units of tetrafluoroethylene, b) is composed essentially of agglomerates having an average particle diameter d50 of 150 to 800 µm which have been built up from primary particles having an average particle diameter d50 of 20 to 80 µm and which possess a spheroidal form and a uniform, dense surface, c) has a bulk density of at least 800 g/l, d) has a flow time of 6.0 to 3.0 seconds/50 g at an average agglomerate diameter d50 of 150 to 250 µm and of 3.0 to 1.5 seconds/50 g at an agglomerate diameter d50 of 250 to 1,000 µm, e) has a particle stability of 6.0 to 3.0 seconds/
50 g at an average agglomerate diameter d50 of 150 to 250 µm and of 3.0 to 1.8 seconds/50 g at an agglomerate diameter of d50 of 250 to 1,000 µm and f) has a proportion of more than 60% by weight of agglomerates having a particle diameter which is at least 0.7 times and note more than 1.3 times the average particle diameter d50, and g) wherein a molded article prepared therefrom has a welding factor of at least 0.80 and h) the pore count measured at a voltage of 5,000 V
as electrical defects on a veneer-cut film 200 µm thick pre-pared from the agglomerated molding powder is not more than 6 pores/m2.
in which X denotes a perfluoroalkyl radical having 1 to C atoms or a radical of the formula and n is 0 to 1, and also contains copolymerized units of tetrafluoroethylene, b) is composed essentially of agglomerates having an average particle diameter d50 of 150 to 800 µm which have been built up from primary particles having an average particle diameter d50 of 20 to 80 µm and which possess a spheroidal form and a uniform, dense surface, c) has a bulk density of at least 800 g/l, d) has a flow time of 6.0 to 3.0 seconds/50 g at an average agglomerate diameter d50 of 150 to 250 µm and of 3.0 to 1.5 seconds/50 g at an agglomerate diameter d50 of 250 to 1,000 µm, e) has a particle stability of 6.0 to 3.0 seconds/
50 g at an average agglomerate diameter d50 of 150 to 250 µm and of 3.0 to 1.8 seconds/50 g at an agglomerate diameter of d50 of 250 to 1,000 µm and f) has a proportion of more than 60% by weight of agglomerates having a particle diameter which is at least 0.7 times and note more than 1.3 times the average particle diameter d50, and g) wherein a molded article prepared therefrom has a welding factor of at least 0.80 and h) the pore count measured at a voltage of 5,000 V
as electrical defects on a veneer-cut film 200 µm thick pre-pared from the agglomerated molding powder is not more than 6 pores/m2.
11. An agglomerated molding powder as claimed in claim 9 or claim 10 wherein the copolymerized units of the perfluorinated vinyl ether are units of per-fluoro-(n-propyl-vinyl) ether.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE3135598A DE3135598A1 (en) | 1981-09-09 | 1981-09-09 | "CONTINUOUS PROCESS FOR AGGLOMING PTEE POWDERS IN LIQUID MEDIUM, AND MODIFIED PTEE POWDER OBTAINED FROM THEM" |
DEP3135598.6 | 1981-09-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1184728A true CA1184728A (en) | 1985-04-02 |
Family
ID=6141149
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA000410946A Expired CA1184728A (en) | 1981-09-09 | 1982-09-08 | Continuous process for the agglomeration of ptfe powders in a liquid medium, and modified ptfe powder obtained thereby |
Country Status (6)
Country | Link |
---|---|
US (2) | US4439385A (en) |
EP (1) | EP0074096B1 (en) |
JP (2) | JPS5865722A (en) |
BR (1) | BR8205249A (en) |
CA (1) | CA1184728A (en) |
DE (2) | DE3135598A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102011078766A1 (en) | 2011-07-06 | 2013-01-10 | Leibniz-Institut Für Polymerforschung Dresden E.V. | Processing polytetrafluoroethylene comprises e.g. mixing non-flowing polytetrafluoroethylene-raw material with low-boiling or high-boiling liquid or liquid mixture, grinding and drying mixture or sedimented polytetrafluoroethylene |
Families Citing this family (65)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61136525A (en) * | 1984-12-07 | 1986-06-24 | Du Pont Mitsui Fluorochem Co Ltd | Bonded article of modified polytetrafluoroethylene molding |
EP0265924B2 (en) * | 1986-10-29 | 1998-04-22 | Kanegafuchi Kagaku Kogyo Kabushiki Kaisha | Uniform polymer particles |
JPH02175727A (en) * | 1988-12-28 | 1990-07-09 | Kagawa Atsuko | Production of ultrafine composite material |
JP2701434B2 (en) * | 1989-03-14 | 1998-01-21 | ダイキン工業株式会社 | Continuous production method of wet powder of polytetrafluoroethylene |
US5977295A (en) * | 1990-03-12 | 1999-11-02 | Daikin Industries, Ltd | Continuous process for preparing polytetrafluoroethylene wet powder |
US5149334A (en) * | 1990-04-02 | 1992-09-22 | The Procter & Gamble Company | Absorbent articles containing interparticle crosslinked aggregates |
US5124188A (en) * | 1990-04-02 | 1992-06-23 | The Procter & Gamble Company | Porous, absorbent, polymeric macrostructures and methods of making the same |
US5492962A (en) * | 1990-04-02 | 1996-02-20 | The Procter & Gamble Company | Method for producing compositions containing interparticle crosslinked aggregates |
US5180622A (en) * | 1990-04-02 | 1993-01-19 | The Procter & Gamble Company | Absorbent members containing interparticle crosslinked aggregates |
US5300565A (en) * | 1990-04-02 | 1994-04-05 | The Procter & Gamble Company | Particulate, absorbent, polymeric compositions containing interparticle crosslinked aggregates |
EP0583481B1 (en) * | 1992-02-05 | 1999-11-10 | Daikin Industries, Ltd. | Polytetrafluoroethylene powder for molding |
US5433906A (en) * | 1993-07-09 | 1995-07-18 | General Motors Corporation | Composite of small carbon fibers and thermoplastics and method for making same |
DE4331971A1 (en) * | 1993-09-21 | 1995-03-23 | Hoechst Ag | Polytetrafluoroethylene micropowder, its manufacture and use |
US5868724A (en) * | 1993-10-22 | 1999-02-09 | The Procter & Gamble Company | Non-continuous absorbent cores comprising a porous macrostructure of absorbent gelling particles |
US5713881A (en) * | 1993-10-22 | 1998-02-03 | Rezai; Ebrahim | Non-continuous absorbent composites comprising a porous macrostructure of absorbent gelling particles and a substrate |
US5536264A (en) * | 1993-10-22 | 1996-07-16 | The Procter & Gamble Company | Absorbent composites comprising a porous macrostructure of absorbent gelling particles and a substrate |
US5372766A (en) * | 1994-03-31 | 1994-12-13 | The Procter & Gamble Company | Flexible, porous, absorbent, polymeric macrostructures and methods of making the same |
JP3671435B2 (en) * | 1994-07-22 | 2005-07-13 | ダイキン工業株式会社 | High molecular weight fluorine-based molten resin fine powder, molded product thereof, and production method thereof |
US5502161A (en) * | 1994-12-21 | 1996-03-26 | Ici Americas Inc. | Method for the production of free-flowing tetrafluoroethylene polymer molding powders |
AU4869796A (en) * | 1995-02-21 | 1996-09-11 | Serrot Corporation | Fabric mesh reinforced monolithic thermoplastic membrane |
JPH0952955A (en) * | 1995-08-11 | 1997-02-25 | Daikin Ind Ltd | Production of modified polytetrafluoroethylene granular powder |
WO1997017392A1 (en) * | 1995-11-09 | 1997-05-15 | Daikin Industries, Ltd. | Granulated powder of filled polytetrafluoroethylene for molding and process for the production thereof |
DE19547907A1 (en) * | 1995-12-21 | 1997-06-26 | Dyneon Gmbh | Non-drizzle molded powder made from modified polytetrafluoroethylene |
EP1004426A4 (en) * | 1997-03-17 | 2000-06-28 | Daikin Ind Ltd | Method of bonding and molding modified polytetrafluoroethylene moldings |
CN1090081C (en) † | 1997-03-19 | 2002-09-04 | 大金工业株式会社 | Molded polytetrafluoroethylene article and method of production thereof |
US6518349B1 (en) * | 1999-03-31 | 2003-02-11 | E. I. Du Pont De Nemours And Company | Sprayable powder of non-fibrillatable fluoropolymer |
US6482979B1 (en) | 1999-12-22 | 2002-11-19 | Dyneon Llc | Perfluorinated acid fluorides and preparation thereof |
DE60119282T2 (en) * | 2000-06-01 | 2007-04-19 | 3M Innovative Properties Co., Saint Paul | PROCESS FOR THE PRODUCTION OF VERY PURE FLUOROPOLYMERS |
US7125941B2 (en) * | 2001-03-26 | 2006-10-24 | 3M Innovative Properties Company | Aqueous emulsion polymerization process for producing fluoropolymers |
WO2002088206A2 (en) | 2001-05-02 | 2002-11-07 | 3M Innovative Properties Company | Emulsifier free aqueous emulsion polymerization process for making fluoropolymers |
EP1432744B2 (en) * | 2001-05-02 | 2014-10-01 | 3M Innovative Properties Company | Aqueous emulsion polymerization in the presence of ethers as chain transfer agents to produce fluoropolymers |
US6737489B2 (en) | 2001-05-21 | 2004-05-18 | 3M Innovative Properties Company | Polymers containing perfluorovinyl ethers and applications for such polymers |
US7045571B2 (en) * | 2001-05-21 | 2006-05-16 | 3M Innovative Properties Company | Emulsion polymerization of fluorinated monomers |
US7279522B2 (en) | 2001-09-05 | 2007-10-09 | 3M Innovative Properties Company | Fluoropolymer dispersions containing no or little low molecular weight fluorinated surfactant |
US6870020B2 (en) * | 2002-04-30 | 2005-03-22 | E. I. Du Pont De Nemours And Company | High vinyl ether modified sinterable polytetrafluoroethylene |
ITMI20021383A1 (en) * | 2002-06-21 | 2003-12-22 | Dry Doughy S R L | PROCEDURE AND ADDITIVE FOR THE COALITION AND DRY MIXING OF POWDERS UP TO ARRIVING THE SHEETING |
RU2342403C2 (en) * | 2002-10-31 | 2008-12-27 | Зм Инновейтив Пропертиз Компани | Polymerisation in aqueous emulsion without emulsifiers to obtain copolymers of fluorated olefin and hydrocarbon olefin |
AU2003289359A1 (en) * | 2002-12-19 | 2004-07-14 | Asahi Glass Company, Limited | Tetrafluoroethylene copolymer |
EP1441014A1 (en) * | 2003-01-22 | 2004-07-28 | 3M Innovative Properties Company | Aqueous fluoropolymer dispersion comprising a melt processible fluoropolymer and having a reduced amount of fluorinated surfactant |
DE60336400D1 (en) * | 2003-10-24 | 2011-04-28 | 3M Innovative Properties Co | Aqueous dispersions of polytetrafluoroethylene particles |
EP1533325B1 (en) * | 2003-11-17 | 2011-10-19 | 3M Innovative Properties Company | Aqueous dispersions of polytetrafluoroethylene having a low amount of fluorinated surfactant |
ATE433350T1 (en) * | 2004-03-01 | 2009-06-15 | 3M Innovative Properties Co | METHOD FOR COATING AN OBJECT WITH A PLASTIC DISPERSION CONTAINING FLUORINE |
ATE534876T1 (en) * | 2004-09-21 | 2011-12-15 | Iglesias Vives Joan | METHOD AND MACHINE FOR SINTERING AND/OR DRYING POWDER MATERIALS USING INFRARED RADIATION |
US7495051B2 (en) * | 2004-09-27 | 2009-02-24 | 3M Innovative Properties Company | Nanocomposite and method of making the same |
GB2427170A (en) * | 2005-06-17 | 2006-12-20 | 3M Innovative Properties Co | Fluoropolymer film having glass microspheres |
US20080015304A1 (en) | 2006-07-13 | 2008-01-17 | Klaus Hintzer | Aqueous emulsion polymerization process for producing fluoropolymers |
GB0514398D0 (en) * | 2005-07-15 | 2005-08-17 | 3M Innovative Properties Co | Aqueous emulsion polymerization of fluorinated monomers using a fluorinated surfactant |
GB0525978D0 (en) * | 2005-12-21 | 2006-02-01 | 3M Innovative Properties Co | Fluorinated Surfactants For Making Fluoropolymers |
US20070025902A1 (en) * | 2005-07-15 | 2007-02-01 | 3M Innovative Properties Company | Recovery of fluorinated carboxylic acid from adsorbent particles |
GB0514387D0 (en) * | 2005-07-15 | 2005-08-17 | 3M Innovative Properties Co | Aqueous emulsion polymerization of fluorinated monomers using a perfluoropolyether surfactant |
GB0523853D0 (en) | 2005-11-24 | 2006-01-04 | 3M Innovative Properties Co | Fluorinated surfactants for use in making a fluoropolymer |
GB2430437A (en) * | 2005-09-27 | 2007-03-28 | 3M Innovative Properties Co | Method of making a fluoropolymer |
US7728087B2 (en) | 2005-12-23 | 2010-06-01 | 3M Innovative Properties Company | Fluoropolymer dispersion and method for making the same |
US20070276103A1 (en) * | 2006-05-25 | 2007-11-29 | 3M Innovative Properties Company | Fluorinated Surfactants |
US7754795B2 (en) * | 2006-05-25 | 2010-07-13 | 3M Innovative Properties Company | Coating composition |
US8119750B2 (en) | 2006-07-13 | 2012-02-21 | 3M Innovative Properties Company | Explosion taming surfactants for the production of perfluoropolymers |
US7678859B2 (en) * | 2006-09-14 | 2010-03-16 | 3M Innovative Properties Company | Preparation and stabilization of fluoropolymer dispersions |
CN100376609C (en) * | 2006-12-25 | 2008-03-26 | 山东东岳高分子材料有限公司 | Dry method of particles in suspending resin of poluterrafluoroethylenel |
US20100084343A1 (en) * | 2007-02-16 | 2010-04-08 | Mader Brian T | System and process for the removal of fluorochemicals from water |
US20080264864A1 (en) * | 2007-04-27 | 2008-10-30 | 3M Innovative Properties Company | PROCESS FOR REMOVING FLUORINATED EMULSIFIER FROM FLUOROPOLMER DISPERSIONS USING AN ANION-EXCHANGE RESIN AND A pH-DEPENDENT SURFACTANT AND FLUOROPOLYMER DISPERSIONS CONTAINING A pH-DEPENDENT SURFACTANT |
GB0716421D0 (en) | 2007-08-23 | 2007-10-03 | 3M Innovative Properties Co | Method of preparing fluoropolymers by aqueous emulsion polymerization |
US8754176B2 (en) * | 2009-03-31 | 2014-06-17 | Daikin Industries, Ltd. | Low molecular weight polytetrafluoroethylene powder and preparation method therefor |
EP2810958B1 (en) * | 2012-02-02 | 2016-11-30 | Asahi Glass Company, Limited | Method for producing polytetrafluoroethylene fine powder |
US11084895B2 (en) | 2013-11-29 | 2021-08-10 | Daikin Industries, Ltd. | Modified polytetrafluoroethylene fine powder and uniaxially stretched porous body |
GB201807544D0 (en) | 2018-05-09 | 2018-06-20 | 3M Innovative Properties Co | Fluoropolymers with very low amounts of a fluorinated alkanoic acid or its salts |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1061227A (en) * | 1963-11-28 | 1967-03-08 | Ogilvie Flour Mills Company Lt | Process and apparatus for preparing free-flowing and readily dispersible products from finely powdered materials |
US3527857A (en) * | 1965-10-26 | 1970-09-08 | Hoechst Ag | Process for preparing polytetrafluoroethylene-containing powder |
US3597405A (en) * | 1966-04-21 | 1971-08-03 | Daikin Ind Ltd | Polytertrafluoroethylene powder and method for making the same |
JPS5221011B1 (en) * | 1971-04-14 | 1977-06-08 | ||
JPS5032098B2 (en) * | 1972-08-09 | 1975-10-17 | ||
US4123606A (en) * | 1977-09-21 | 1978-10-31 | E. I. Du Pont De Nemours And Company | Deagglomeration process |
DE2744244C3 (en) * | 1977-10-01 | 1981-01-08 | Hoechst Ag, 6000 Frankfurt | Thermally pretreated tetrafluoroethylene polymer powder, which cannot be processed from the melt and modified with a perfluorinated monomer, and a process for the production of powders from tetrafluoroethylene polymers which cannot be processed from the melt and have a high bulk density and good flowability |
US4241137A (en) * | 1977-11-22 | 1980-12-23 | Daikin Kogyo Co., Ltd. | Process for preparing polytetrafluoroethylene granular powder |
DE2949908A1 (en) * | 1979-12-12 | 1981-06-19 | Hoechst Ag, 6230 Frankfurt | GIANT POWDER POWDER WITH IMPROVED PROPERTIES BASED ON TETRAFLUORETHYLENE POLYMERS AND METHOD FOR THE PRODUCTION THEREOF |
DE3110193A1 (en) * | 1980-06-06 | 1982-09-30 | Hoechst Ag, 6000 Frankfurt | Improved process for the preparation of modified tetrafluoroethylene polymer powder having high bulk density and good flow properties |
-
1981
- 1981-09-09 DE DE3135598A patent/DE3135598A1/en not_active Withdrawn
-
1982
- 1982-09-01 US US06/413,716 patent/US4439385A/en not_active Expired - Lifetime
- 1982-09-03 DE DE8282108130T patent/DE3270126D1/en not_active Expired
- 1982-09-03 EP EP82108130A patent/EP0074096B1/en not_active Expired
- 1982-09-08 JP JP57155337A patent/JPS5865722A/en active Granted
- 1982-09-08 BR BR8205249A patent/BR8205249A/en unknown
- 1982-09-08 CA CA000410946A patent/CA1184728A/en not_active Expired
-
1987
- 1987-03-03 US US07/021,168 patent/US4774304A/en not_active Expired - Lifetime
-
1990
- 1990-12-19 JP JP2403738A patent/JPH0776274B2/en not_active Expired - Lifetime
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102011078766A1 (en) | 2011-07-06 | 2013-01-10 | Leibniz-Institut Für Polymerforschung Dresden E.V. | Processing polytetrafluoroethylene comprises e.g. mixing non-flowing polytetrafluoroethylene-raw material with low-boiling or high-boiling liquid or liquid mixture, grinding and drying mixture or sedimented polytetrafluoroethylene |
Also Published As
Publication number | Publication date |
---|---|
US4774304A (en) | 1988-09-27 |
EP0074096A3 (en) | 1983-09-14 |
JPS5865722A (en) | 1983-04-19 |
BR8205249A (en) | 1983-08-16 |
EP0074096B1 (en) | 1986-03-26 |
DE3270126D1 (en) | 1986-04-30 |
US4439385A (en) | 1984-03-27 |
DE3135598A1 (en) | 1983-03-17 |
JPH05186605A (en) | 1993-07-27 |
JPH0776274B2 (en) | 1995-08-16 |
JPH0339105B2 (en) | 1991-06-12 |
EP0074096A2 (en) | 1983-03-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA1184728A (en) | Continuous process for the agglomeration of ptfe powders in a liquid medium, and modified ptfe powder obtained thereby | |
US3766133A (en) | Polytetrafluoroethylene filled and unfilled molding powders and theirpreparation | |
US3674736A (en) | Process for the preparation of pigmented polymer powders of controlled particle shape and size and size distribution and product | |
CA1054288A (en) | Process for agglomeration of filled polytetrafluoroethylene using aminosilane or silicone resin adjuvant | |
US4143110A (en) | Method of agglomerating polytetrafluoroethylene powder | |
CA1212810A (en) | Method of finishing thermoplastic granules | |
CA1212811A (en) | Finishing of rotational molding grade resin | |
US3915916A (en) | Process for reducing filler loss | |
US4123606A (en) | Deagglomeration process | |
KR19990036238A (en) | Preparation of Modified Polytetrafluoroethylene Granular Powder | |
US5216068A (en) | Process for producing an agglomerated molding powder composed of polytetrafluoroethylene and hydrophobic fillers | |
US3781258A (en) | Polytetrafluoroethylene powder and method of preparation thereof | |
CA1050686A (en) | Manufacture of a pulverulent plasticised rubber-filler mixture | |
EP0175769A1 (en) | Polyethylene molding composition and process. | |
EP1857492B1 (en) | Process for producing filler-containing polytetrafluoroethylene granule | |
US2895939A (en) | Method for coating rubber in granular form with impalpable resinous vinyl aromatic polymer dusts | |
US5411213A (en) | Method for treatment of solid materials | |
US4241137A (en) | Process for preparing polytetrafluoroethylene granular powder | |
US3154530A (en) | Preparation of polyethylene powders | |
US5156343A (en) | Process for preparing polytetrafluoroethylene granular powder | |
US3532782A (en) | Polytetrafluoroethylene granular powder and process for its manufacture | |
US3980596A (en) | Process for reducing filler loss | |
US3857813A (en) | Incorporation of reinforcing fibers into olefin polymers | |
EP1213321B1 (en) | Polytetrafluoroethylene agglomerated product and its molded product | |
EP0690781A4 (en) | Process and apparatus for production of free flowing polytetrafluoroethylene molding pellets |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
MKEC | Expiry (correction) | ||
MKEX | Expiry |