Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – Polymers from only ethylenic monomers or processes of...
Reexamination Certificate
1996-12-20
2002-12-03
Lipman, Bernard (Department: 1713)
Synthetic resins or natural rubbers -- part of the class 520 ser
Synthetic resins
Polymers from only ethylenic monomers or processes of...
C428S402000
Reexamination Certificate
active
06489419
ABSTRACT:
DESCRIPTION
The invention relates to non-free flowable (non-pourable) molding powders of a suspension polymer with units of tetrafluoroethylene and 0.01 to 1% by weight, preferably 0.02 to 0.5% by weight, of units of at least one perfluoro(alkyl-vinyl) ether with an alkyl group of 1 to 4 carbon atoms, preferably n-perfluoropropyl, having a bulk density of at least 450 g/l, obtainable by grinding the primary particles to an average particle diameter d
50
of 10 to 50 &mgr;m, preferably 15 to 25 &mgr;m, in particular is about 20 &mgr;m, and reagglomerating these particles in water to give a non-dusting agglomerate having a particle diameter d
50
of about 30 to about 100 &mgr;m, preferably about 40 to about 90 &mgr;m.
The invention furthermore relates to a process for the preparation of a non-free flowable, non-dusting molding powder having a bulk density of at least 450 g/l and an agglomerate diameter d
50
of about 30 to about 100 &mgr;m preferably about 40 to about 90 &mgr;m which comprises grinding a suspension polymer with units of tetrafluoroethylene and 0.01 to 1% by weight of units of at least one perfluoro(alkyl-vinyl) ether with an alkyl group of 1 to 4 carbon atoms to a particle diameter d
50
of 10 to 50 &mgr;m and agglomerating the particles in water.
The invention furthermore relates to the use of the molding powders according to the invention in compression molding.
As is known, polytetrafluoroethylene (PTFE) can be prepared by aqueous free radical polymerization by two different processes, that is to say suspension and emulsion polymerization. These two processes naturally lead to polymers which differ fundamentally in morphological terms. As a consequence, the two processes also require fundamentally different working up and processing methods.
The emulsion polymers comprise largely regular, spherical latex particles having a diameter of about 100 to 300 nm, which are agglomerated by a precipitation process to give a so-called paste powder having an average particle diameter of 400 to 700 &mgr;m. The specific surface area of such paste powders is 10 to 25 m
2
/g. These paste powders are further processed by the so-called paste extrusion process to give liners, tubes, hoses and tapes. The characteristic of paste extrusion is that shaping is carried out by forming a paste of the paste powder with gasoline (benzine) or other liquids which are water-immiscible but wet PTFE, using a paste extruder at far below the melting point of the PTFE. This shaping extrusion is usually followed by sintering at temperatures significantly above the melting point of the PTFE. PTFE emulsion polymers therefore cannot be processed as thermoplastics because of their exceptionally high melt viscosity of up to a few 100 GPas.
PTFE suspension polymers also cannot be processed as thermoplastics because of their high melt viscosity. Special processing techniques based on the method of metallurgical compaction sintering have therefore been developed. For this compaction sintering, the suspension polymer must be converted into a molding powder which can be employed.
For this purpose, the suspension polymer, which is obtained in coarse, irregularly shaped grains having a diameter of up to 1500 &mgr;m is first finely ground to a particle diameter of about 10 to 50 &mgr;m, preferably by dry grinding, in particular in an air mill. The ground material is also irregularly shaped. The molding powder thus produced is therefore not free-flowable and cannot be metered adequately for automatic processing by compaction. The bulk density is about 300 to 400 g/l.
This non-free flowable molding powder is chiefly compacted to cylinders or hollow cylinders under pressures of up to about 500 bar. These unsintered preforms (green compacts) are then sintered and commodity articles such as skived films or sealing rings are then produced by mechanical processing. To achieve high-grade final properties, the molding powder must have an adequate deformability during the production of the green compact, so that the primary particles can be packed densely against one another without inclusions of air and the green compact thus has an adequate so-called green strength for further processing.
In addition to being unusable for automatic processing by compaction and the difficulties in reliable filling of molds, the non-free flowable molding powder has the further disadvantage of a low bulk density. This means that larger shaping units are necessary. Another disadvantage is to be seen in the dusting during the production of the green compact. Dusting necessitates greater expenditure on keeping the processing unit clean, since PTFE dust is regarded as toxic, especially in connection with smoking.
There has therefore been no lack of attempts to eliminate the disadvantages mentioned. Thus, processes which render the molding powder free-flowing (pourable) and easier to meter by agglomeration processes have been developed. The known agglomeration processes essentially comprise agglomerating the non-free flowable molding powder to more or less regularly shaped granule grains, the average particle diameter of which is between 100 and 600 &mgr;m, by a suitable mechanical treatment in a usually two-phase liquid system (comprising water and a solvent of limited water-miscibility which wets the PTFE, such as gasolines and fluorochlorohydrocarbons). These granule grains are distinguished by a smooth surface and a certain grain stability for their handling and transportation. The free-flowing molding powders thus produced have a high bulk density, usually above 800 g/l, do not dust and accordingly offer considerable advantages over the non-free flowable molding powder.
However, these advantages are at the expense of a significant deterioration in the profile of properties. Thus, the tear strength and dielectric strength are significantly reduced, and the sintered articles have a higher content of voids, that is to say more pores up to so-called “pinholes”. The cause of the deterioration in properties is the necessarily poorer compactibility and deformability of the free-flowing powder due to the agglomeration. Thus, for example, the contour lines of the granule grain can be clearly detected in 100 &mgr;m thick skived films under a microscope at 20-fold magnification in phase contrast.
The change in properties by granulation of a PTFE molding powder is shown in the following Table 1, the abbreviations here and in the following having the meanings given below:
BD: Bulk density according to DIN 53466 or ISO 12086 in g/l
d
50
: Average particle diameter in &mgr;m, measured with a laser particle measuring instrument from Sympatec (Clausthal-Zellerfeld, Germany)
TS: Tear strength in N/mm
2
, according to DIN 53457 or ISO 12086, test specimens: strips 15 mm wide
EB: Elongation at break in %, determined according to DIN 53457 or ISO 12086
DS: Dielectric strength in kV/mm, according to DIN 53481, measurement arrangement ball (diameter 20 mm)/plate (diameter 50 mm)
TABLE 1
Properties of
Powder
100 &mgr;m skived
properties
films
BD
d
50
TS
EB
DS
Molding
non-free
380
18
42
480
110
powder,
flowable
crude
Molding
free-
830
450
32
360
80
powder,
flowable
agglomerated
The deterioration in properties seems inherent to the system, since the particle stability required impedes dense packing of the primary particles and of the granule grains during compaction. This deterioration in properties is also observed during granulation of a molding powder of “modified” PTFE, although to a lesser extent. “Modified” PTFE is understood as meaning a polymer which comprises low contents of comonomers, but in which the main property of the PTFE of not being processable as a thermoplastic is retained. The suspension polymers of tetrafluoroethylene employed according to the invention, with 0.01 to 1% by weight of units of at least one perfluoro(alkyl-vinyl) ether are such “modified” polytetrafluoroethylenes. One characteristic of the modified suspension polymers is their lower melt viscosity by about one to two orders of magnitude, which enables them to be w
Hintzer Klaus
Löhr Gernot
Sulzbach Reinhard Albert
3M Innovative Properties Company
Harts Dean M.
Lilly James V.
Lipman Bernard
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