Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – At least one aryl ring which is part of a fused or bridged...
Reexamination Certificate
2000-07-07
2004-03-16
Shosho, Callie (Department: 1714)
Synthetic resins or natural rubbers -- part of the class 520 ser
Synthetic resins
At least one aryl ring which is part of a fused or bridged...
C524S457000, C524S567000, C524S805000
Reexamination Certificate
active
06706803
ABSTRACT:
The present invention relates to a process for obtaining halogenated polymers having good thermal stability.
Specifically the present invention relates to a process for obtaining chlorotrifluoroethylene (CTFE) polymers having substantially no discoloration, combined with a good thermal stability.
The chlorotrifluoroethylene (PCTFE) polymers according to the process of the present invention contain at least 80% by moles of CTFE and the complement to 100 being one or more fluorinated monomers, preferably the complement to 100 is formed of one or more perfluorinated monomers.
The polymers obtained in the process of the invention are to be used for manufacturing pipes, sheets, films and other articles having the advantages indicated below.
More specifically it is known in the prior art that the CTFE homopolymer is a fluorinated resin having excellent chemical resistance with good properties of impermeability to gases and vapours, more specifically to oxygen, nitrogen and water vapour, which make this resin the most suitable material for the extrusion in films for the pharmaceutical packaging industry.
For the above mentioned applications, it is desirable to use a PCTFE having good thermal stability and substantially no discoloration, allowing a wide processing window, i.e. high temperatures and long residence times in extrusion such that the PCTFE does not undergo discoloration without substantial weight loss. This wide processing window allows to obtain articles having complex shapes which require long residence times and high temperatures. In particular, the availaibility of a PCTFE with a wide processing window could allow the processing of polymers of high molecular weight and therefore to manufacture articles with improved mechanical properties from those PCTFE's of low molecular weight.
It is therefore desirable to have available an efficient industrial polymerization process, i.e. with yields not lower than about 10 g/(lxh) (g of polymer/l of water·h), thermodynamically stable latexes and absence of polymer buildup in the polymerization reactor, which allows the PCTFE synthesis of different viscosity values, in particular high molecular weight PCTFE's, having good thermal stability combined with substantial no discoloration.
The Applicant has unexpectedly and surprisingly found an efficient process for obtaining the above PCTFE's.
It is therefore an object of the present invention a process for the synthesis of chlorotrifluoroethylene (PCTFE) (co)polymers, containing at least 80% by moles of CTFE, being the complement to 100 one or more fluorinated monomers, preferably the complement to 100 is formed of one or more perfluorinated monomers, characterized in that the reaction medium comprises (per)fluoropolyoxyalkylene microemulsions wherein the fluorinated surfactant is salified with sodium and/or potassium and an inorganic potassium and/or sodium initiator.
The (per)fluoropolyoxyalkylene microemulsions according to the present invention are obtainable following the methods described in U.S. Pat. No. 4,864,006, in the name of the Applicant, herein incorporated by reference.
The fluorinated surfactants of the microemulsions according to the present invention are selected from the products of general formula
R
f
, —X
−
M
+
wherein R
f
, is a C
5
-C
14
(per)fluoroalkyl chain, or a (per)fluoropolyoxyalkylene chain, X
−
is —COO
−
or —SO
3
−
, M
+
is selected between Na
+
and K
+
, preferably K
+
.
According to the present invention, potassium inorganic initiators are preferred, potassium persulphate is still more preferred.
The process of the invention is carried out at a temperature betwen 0° C. and 150° C., preferably between 10° C. and 70° C. The reaction pressure is generally in the range 3-80 bar, preferably 4-20 bar.
The amount of the radical usable initiator is the standard one for the copolymerization of fluorinated olefinic monomers, and is generally in the range 0.003%-10% by weight with respect to the total amount of (co)polymerized monomers.
The control of the molecular weight of the fluorinated polymers of the invention can be carried out in various ways.
Preferred are those by a suitable dosage of the radical initiator in polymerization and the selection of the synthesis temperature. To obtain the polymers of the invention having high molecular weight, i.e. having MFI lower than 15 g/10′, a low synthesis temperature (10° C.-50° C.) combined with a low concentration of free radicals coming from the initiator is preferred. To obtain the invention polymers having low molecular weight, i.e. having a MFI higher than 5 g/10′, a high synthesis temperature (60° C.-80° C.) combined with a high concentration of free radicals coming from the initiator, is preferred.
Another way to control the molecular weight is the use of chain transfer agents, these can be halogenated hydrocarbons, for example chloroform or HCFC 123 and ethane or methane. The transfer agent is fed to the reactor at the beginning of the reaction, or in a continuous way or in discrete amounts during the polymerization. The used chain transfer agent amount can range within rather wide limits, depending on the reaction temperature and the molecular weight target. Generally, such amount ranges from 0.001 to 5% by weight, preferably from 0.05 to 1% by weight, with respect to the total amount of monomers fed to the reactor.
In the process according to the present invention the presence of liquid CTFE in the reaction medium, in order to obtain high productivity (R
p
) in g/(lxh), is preferred.
A further object of the present invention are chlorotrifluoroethylene (PCTFE) (co)polymers, obtainable by the above described process, containing at least 80% by moles of CTFE, being the complement to 100 one or more fluorinated monomers, preferably the complement to 100 being one or more perfluorinated monomers.
The chlorotrifluoroethylene (PCTFE) (co)polymers of the invention are characterized in that the CTFE homopolymer, having a MFI of about 25 g/10′, does not show discoloration, as defined below, and a global very reduced weight loss by thermogravimetric analysis.
The preferable (co)polymers of the invention are the thermoplastic ones.
The CTFE homopolymers with MFI of about 25 g/10′, obtained according to the present invention, have a weight loss which is approximately the half of the weight loss of the CTFE homopolymers obtained in emulsion.
Besides the efficiency confirmation of the process object of the present invention is mainly given by the high productivity yield and by the absence of polymer buildup in autoclave.
This low weight loss of the polymers of the invention combined with absence of discoloration allows to obtain manufactured articles of complex shape and with substantial absence of defects, mainly bubbles. For example, the presence of bubbles in the extruded film makes it unusable, since the main PCTFE characteristic is the impermeability.
Among the fluorinated monomers, we can mention hexafluoropropylene, hexafluoroisobutylene, vinilydenfluoride, tetrafluoroethylene, fluorinated ethers such as perfluoroalkylvinylethers, for example perfluoroethylvinylether, perfluoromethylvinylether, preferably perfluoropropylvinyl-ether, or mixtures thereof,
The viscosity of CTFE (co)polymers according to the present invention is defined by the Melt Flow Index measure (MFI) at 265° C. and 10 Kg load according to the ASTM D 1238-88 method.
The discoloration is determined through the observation of the strands obtained after 20, 40 and 60 minutes of residence time of the polymer in the MFI machine at 265° C. Discoloration means the coloration of the extruded polymer. The product not showing discoloration is colourless or white. Polymers showing discoloration are generally yellowish or brown. The skilled in the art is able to determine whether the polymer shows or not discoloration also by using methods measuring the colour index such as for example white index or yellow index.
The thermal stability is subsequently controlled, i
Abusleme Julio A.
Manzoni Claudia
Arent Fox Kintner & Plotkin & Kahn, PLLC
Ausimont S.p.A.
Shosho Callie
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