Bulk radical polymerization using a batch reactor

• US 5,637,646 A
• Filed: 12/14/1995
• Issued: 06/10/1997
• Est. Priority Date: 12/14/1995
• Status: Expired due to Term

• Current Assignee: Minnesota Mining and Manufacturing Co (3M Company)
• Original Assignee: Minnesota Mining and Manufacturing Co (3M Company)
• Inventors: Ellis, Mark F.
• Primary Examiner(s): ZEMEL, IRINA SOPJIA
• Application Number:
  US08/572,310
• Time in Patent Office: 544 Days
• Field of Search: 525/309, 526/88, 526/307.7, 526/328.5
• US Class Current: 525/309
• CPC Class Codes: C08F 2/02 Polymerisation in bulk

Abstract

The present invention provides a method for the polymerization of free-radically polymerizable vinyl monomers in a batch reactor under essential adiabatic conditions.

Claims

1. A method of free radically polymerizing vinyl monomers comprising the steps of:

(a) providing a mixture comprising;

(i) free radically (co)polymerizable vinyl monomers;

(ii) optional chain transfer agent;

(iii) optional crosslinking agent;

(iv) at least one thermal free-radical initiator;

(v) optionally polymer comprising polymerized free radically polymerizable monomers;

in a batch reactor;

(b) deoxygenating the mixture if the mixture is not already deoxygenated, wherein step (b) can optionally at least partially overlap with step (c);

(c) heating the mixture to a sufficient temperature to generate sufficient initiator free radicals from at least one thermal free radical initiator so as to initiate polymerization;

(d) allowing the mixture to polymerize under essentially adiabatic conditions to yield an at least partially polymerized mixture;

(e) optionally heating the mixture to generate free radicals from some or all of any initiator that has not generated initiator free radicals, followed by allowing the mixture to polymerize under essentially adiabatic conditions to yield a further polymerized mixture; and

(f) optionally repeating step (e) one or more times;

(g) optionally cooling the mixture;

(h) adding to the mixture in the batch reactor at least one thermal free radical initiator wherein the initiator(s) of step (h) can be the same or different than the initiator(s) of step (a), optionally free radically polymerizable monomers, optionally crosslinking agents, optionally chain transfer agent(s), optionally polymer comprising polymerized free radically polymerizable monomers, wherein the mixture optionally has a temperature below that which would generate initiator free radicals from the initiator(s) added in step (h);

(i) deoxygenating the mixture if the mixture is not already deoxygenated;

(j) optionally heating the mixture to generate initiator free radicals from at least one initiator to further polymerize the mixture if the mixture has a temperature below that which would generate initiator free radicals from the initiator(s) in step (h);

(k) allowing the mixture to further polymerize under essentially adiabatic conditions to yield a further polymerized mixture;

(l) optionally heating the mixture to generate free radicals from some or all of any initiator that has not generated initiator free radicals, followed by allowing the mixture to polymerize under essentially adiabatic conditions to yield a further polymerized mixture;

(m) optionally repeating step (l) one or more times;

(n) optionally repeating steps (g) through (m) one or more times.

2. The method of claim 1 wherein the free radically polymerizable monomer is selected from the group consisting of acrylate monomers.

3. The method of claim 1 wherein the free radically polymerizable monomer is selected from the group consisting of monofunctional unsaturated acrylate esters of a non-tertiary alkyl alcohol, wherein the alkyl group contains about 1 to about 18 carbon atoms.

4. The method of claim 1 wherein the free radically polymerizable monomer is selected from the group consisting of isooctyl acrylate, isononyl acrylate, 2-ethylhexyl acrylate, decyl acrylate, dodecyl acrylate, n-butyl acrylate, hexyl acrylate, octadecyl acrylate, methyl acrylate, ethyl acrylate, butyl acrylate, methyl methacrylate, N-butyl methacrylate, N-vinyl pyrrolidone, N,N-dimethyl acrylamide, acrylic acid, and mixtures thereof.

5. The method of claim 1 wherein the free radically polymerizable monomer is selected from the group consisting of monoalkenyl aromatic monomers, vinyl ester monomers, and mixtures thereof.

6. The method of claim 1 wherein the mixture further comprises about 0 to about 5 percent by weight of a chain transfer agent based upon the total weight of the monomers.

7. The method of claim 6 wherein the chain transfer agent is selected from the group consisting of carbon tetrabromide, hexanebromoethane, bromotrichloromethane, 2-mercaptoethanol, t-dodecylmercaptan, n-octal mercaptan, isooctylthioglycoate, 3-mercapto-1,2-propanediol, cumene, and mixtures thereof.

8. The method of claim 1 wherein the mixture comprises about 0 to about 10 percent by weight of a non-copolymerizable crosslinking agent based upon the total weight of the mixture.

9. The method of claim 1 wherein the mixture further comprises about 0 to about 2 percent by weight of a copolymerizable crosslinking agent based on the total weight of the mixture.

10. The method of claim 3 wherein the copolymerizable crosslinking agent is 4-acryloxybenzophenone.

11. The method of claim 1 wherein the mixture comprises about 0 to about 50 percent by weight of the polymer based upon the total weight of the monomer plus the polymer.

12. The method of claim 1 wherein the initiator(s) are selected from the group consisting of organic peroxides, organic hydroperoxides, azo-group initiators, and mixtures thereof.

13. The method of claim 1 wherein the initiator(s) are selected from the group consisting of benzoyl peroxide, di-t-amyl peroxide, di-cumyl peroxide, t-amyl hydroperoxide, t-butyl hydroperoxide, 2,2'"'"'-azobis(2,4-dimethylpentanenitrile), 2,2'"'"'-azobis (2-methylpropanenitrile), 2,2'"'"'-azobis(cyclohexanecarbonitrile), 2,2'"'"'-azobis(2-methylbutanenitrile), t-butyl peroxy benzoate, and mixtures thereof.

14. The method of claim 1 wherein more than one initiator is present in the mixture of step (a).

15. The method of claim 1 wherein 1 to 5 different initiators are present in the mixture of step (a), 1 to 5 different initiators are present in step (h), and 1 to 5 different initiators are present in each repeat of steps (g) through (m) when step (n) is included.

16. The method of claim 1 wherein 2 to 5 different initiators are present in the mixture of step (a), 2 to 5 different initiators are present in step (h), and 2 to 5 different initiators are present in each repeat of steps (g) through (k) when step (1) is included.

17. The method of claim 1 wherein when more than one initiator is included in the mixture, and the value of ##EQU11## the negative value of the first derivative of the concentration of initiator i with respect to time, for at least one initiator i in a series of n initiators ordered by lowest temperature to highest temperature for each initiator i which produces a one-hour half life, wherein i <

n-1, n>

1, and i =1, . . . ,n, decreases to about 10% of its maximum value, the value of ##EQU12## for the next initiator in the series has increased to at least about 20% of its maximum value, as the reaction temperature increases due to essentially adiabatic polymerization, wherein n is the number of initiators and t is time.

18. The method of claim 1 wherein when more than one initiator is used, and the value of ##EQU13## the negative value of the first derivative of the concentration of initiator i with respect to time, for at least one initiator i in a series of initiators where i>

1, n >

1, and where i=1, . . . ,n, reaches about 30% of its maximum value, the previous initiator in the series of initiators ordered by lowest temperature to highest temperature for each initiator i which produces a one-hour half life, has already reached its maximum value of ##EQU14## as the reaction temperature increases due to essentially adiabatic polymerization, wherein n is the number of initiators and t is time.

19. The method of claim 1 wherein total amount of all the initiator(s) used is in the mixture ranges from about 0.0005 weight % to about 0.5 weight % based on the total weight of the monomer(s).

20. The method of claim 1 wherein total amount of all the initiator(s) used is in the mixture ranges from about 0.001 weight % to about 0.1 weight % based on the total weight of the monomer(s).

21. The method of claim 1 wherein the free radically (co) polymerizable vinyl monomers comprise about 1 to about 30 percent by weight of a macromonomer.

22. A pressure sensitive adhesive prepared according to the method of claim 1.

23. The method of claim 1 wherein the free radically (co)polymerizable vinyl monomers comprise a macromonomer of a formula

X--(Y_n)--Z

wherein

X is a vinyl group copolymerizable with other monomer(s) in the reaction mixture;

Y is a divalent linking group;

where n can be zero or one; and

Z is a monovalent polymeric moiety having a glass transition temperature, T_g, greater than about 20°

C., and a weight average molecular weight in the range of about 2,000 to about 30,000 and being essentially unreactive under copolymerization conditions.

24. The method of claim 1 wherein polymerization is conducted under adiabatic conditions.