Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – Polymerizing in tubular or loop reactor
Reexamination Certificate
2000-11-30
2002-02-19
Teskin, Fred (Department: 1713)
Synthetic resins or natural rubbers -- part of the class 520 ser
Synthetic resins
Polymerizing in tubular or loop reactor
C526S065000, C526S342000, C526S347000
Reexamination Certificate
active
06348549
ABSTRACT:
The present invention relates to a process for the production of vinylaromatic polymers, optionally containing an ethylenically unsaturated nitrile.
More specifically, the present invention relates to a process for the production of copolymers based on &agr;-methylstyrene and acrylonitrile (&agr;-SAN) with a mass-continuous process.
In mass-continuous processes for the production of vinylaromatic polymers, such as polystyrene (PS), SAN (styrene-acrylonitrile copolymers), &agr;-SAN, two types of reactors are used: PFR (Plug Flow Reactor) or CFSTR (Continuous Flow Stirred Tank Reactor).
PFR refers to one or more substantially cylindrical reaction containers in series, wherein the mixture of monomers enters the first reaction container with a conversion which is practically zero (<5-10%), it converts along the reactor and, if present, in the subsequent ones, and is then discharged at the desired conversion, generally 60-80%. Processes which use this type of technology are described, for example, in U.S. Pat. Nos. 2,769,804, 2,989,517 and 4,328,186 or in European patent 752,268.
CFSTR are reactors with homogeneous mixing in which the reaction mixture composition is the same in any point of the reactor and the conversion at the outlet is equal to that inside. Processes which use this type of technology are described, for example, in U.S. Pat. Nos. 2,769,804 and 3,954,722 or in German patents 2,809,180 and 3,626,319.
The use of PFR or CFSTR reactors in the polymerization of vinylaromatic polymers has both advantages and drawbacks. For example, the advantages of the PFR reactor can be summarized in process stability, also under gel effect conditions, the possibility of defining an optimum thermal profile, by varying the temperature along the reactor, and the possibility of using up the initiator inside the reactor, thus avoiding degradation problems of the polymer in the subsequent stripping phase of the monomers and residual solvents at a high temperature.
The disadvantages of PFR reactors, on the other hand, essentially consist in the wide molecular weight distribution of the vinylaromatic polymer produced, the high formation of oligomers of the phenyl tetraline type, owing to the unfavorable reaction selectivity and composition heterogeneity for non-“azeotropic” SAN and &agr;-SAN copolymers.
The disadvantages of the PFR reactor can be overcome with the use of CFSTR reactors which allow the production of vinylaromatic polymers with a narrow molecular weight distribution, a low formation of oligomers of the phenyl tetraline type for conversions of the monomers higher than 50% and composition homogeneity for SAN and &agr;-SAN copolymers.
Unfortunately, CFSTR reactors also have various disadvantages which can be overcome with the use of PFR reactors. The two reactors are therefore entirely complementary to each other. Combining a CFSTR reactor and a PFR reactor in a polymerization process of vinylaromatic polymers, has proved to be not very convenient as the sum of the advantages is negatively compensated by the sum of the disadvantages.
In this situation, to find a process for the production of vinylaromatic polymers which allows the advantages of both types of reactor to be exploited without also being subjected to the disadvantages, would prove to be of enormous industrial interest. The Applicant has succeeded in finding this process.
The object of the present invention therefore relates to a mass-continuous process for the production of vinylaromatic polymers, which comprises feeding a reaction mixture containing at least one vinylaromatic monomer to at least one tubular reactor of the PFR type and operating with a recycling ratio, referring to recycling flow-rate/feeding flow-rate, of less than 4.
It has been found, in fact, that the running of a PFR with a low recycling ratio also allows the advantages of CFSTR reactors to be exploited. It is therefore possible with the process of the present invention:
i. to obtain vinylaromatic polymers having good composition homogeneity and a narrow molecular weight distribution;
ii. to obtain complete consumption of the initiator leaving the reactor;
iii. to handle the polymerization with extremely reduced instability and with easily control under gel effect conditions;
iv. to reduce the formation of oligomers of the phenyl tetraline type for conversions of over 50% of the outgoing monomers;
v. to optimize the reaction thermal profile.
According to the process of the present invention, it is possible to obtain the desired results with a single PFR reactor having at least two thermostat-regulation zones or with several PFR in series having a recycling ratio of less than 4 from the last to the first PFR.
Any vinylaromatic monomer can be used in the process object of the present invention. The traditional vinylaromatic monomer is styrene but other styrene monomers can be used, having one or more hydrogen atoms substituted with C
1
-C
4
alkyl or aryl radicals, a halogen or nitro radical such as, for instance, methylstyrene, &agr;-methylstyrene, mono-, di-, tri-, tetra-, penta-chloro styrene and the corresponding &agr;-methylstyrenes, styrenes alkylated in the nucleus and the corresponding &agr;-methylstyrenes such as ortho- and para-methylstyrene, ortho- and para-ethylstyrene, ortho- and para-methyl-&agr;-methylstyrene, etc., either alone or mixed with each other and/or with styrene.
The vinylaromatic monomer can be mixed with an ethylenically unsaturated nitrile such as acrylonitrile or methacrylonitrile, for example in quantities ranging from 5 to 60% by weight with respect to the total weight of monomers, or, as an alternative, to the ethylenically unsaturated nitrile or, in addition to this, mixed with other ethylenically unsaturated monomers in such quantities that the vinylaromatic monomer is present in a concentration of over 40% by weight.
Examples of ethylenically unsaturated monomers are alkyl or cycloalkyl esters of acrylic or methacrylic acid in which the alkyl or cycloalkyl group respectively contain from 1 to 4 carbon atoms and from 4 to 10 carbon atoms such as methylacrylate, methylmethacrylate, ethylacrylate, ethylmethacrylate, butylmethacrylate, cyclohexylmethacrylate, etc. Other ethylenically unsaturated monomers are ethylene, propylene, maleic anhydride, etc.
An inert solvent, which acts as diluent, is added to the mixture to be polymerized, in a quantity of not more than 20% and preferably from 5 to 15% by weight with respect to the mixture to be polymerized. Examples of suitable inert solvents are aromatic hydrocarbons, as etilbenzene ketones, esters and nitriles which are liquid at the polymerization temperature. In addition to ethylbenzene mentioned above, toluene, xylenes or their mixtures can be used as aromatic hydrocarbons. Examples of ketones are 2-butanone, methylethylketone, cyclohexanone, etc. Other examples of solvents which are particularly suitable for the present process are ethyl acetate and acetonitrile.
The polymerization initiators are the conventional ones which are generally used in the polymerization of styrene. As an example, organic peroxides such as dibenzoyl peroxide, ter-butyl peroctoate, ter-butyl perbenzoate, di-ter-butyl peroxide, 1,1′-di-terbutyl peroxycyclohexane, 1,1′-di-terbutyl peroxy-3,3,5-trimethylcyclohexane, or azo-derivatives such as 2,2′-azobis(isobutyronitrile), 2,2′-azomethylbutyronitrile), etc., can be mentioned.
These catalysts are added in a quantity of less than 1% by weight with respect to the monomers, generally from 0.005 to 0.5%.
Finally, the reaction mixture can contain conventional additives which are used in the polymerization of vinylaromatic monomers such as, for example, antioxidants, stabilizers, lubricants, release agents, etc. Among these additives chain transfer agents are particularly important as it is by means of these that the molecular weight of the polymer is regulated. Examples of chain transfer agents are mercaptans containing from 4 to 18 carbon atoms such as, for example, n-butyl mercaptan, n-octyl mercaptan, ter-dodecyl merca
LandOfFree
Process for the production of vinylaromatic polymers,... does not yet have a rating. At this time, there are no reviews or comments for this patent.
If you have personal experience with Process for the production of vinylaromatic polymers,..., we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Process for the production of vinylaromatic polymers,... will most certainly appreciate the feedback.
Profile ID: LFUS-PAI-O-2985198