Method for the preparation of pentafluorophenylacrylate polymer
Granted 25 Oct 2005 · 1 office action
Assignee: National Chung-Shan Institute of Science and Technology
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Attorney: Attorney · Log in to unlock
Inventors: Shean-Jeng Jong, Chang-Chih Lin, Yu-Sheng Lin · Examiner: Robert D. Harlan · AU 1713 · TC 1700
Life of the application
9 dated eventsAbstract
A method for synthesizing a pentafluorophenyl acrylate polymer includes bulk polymerizing a pentafluorophenyl acrylate monomer in the presence of a free radical initiator. The reactant mixture was subjected to an ultrasonication treatment, so that the mixing of the initiator and the monomer is enhanced; carried out the bulk polymerization at 25-99° C. for a period of time, and at 100-200° C. under a vacuum pressure for another period of time to complete the bulk polymerization, so that residue amounts of the initiator, unreacted monomer and oligomer of the monomer are reduced in the resulting reaction mixture.
Description
7 parts›FIELD OF THE INVENTION
The present invention is related to a process for preparing a pentafluorophenyl acrylate polymer, and in particular to a process for preparing a pentafluorophenyl acrylate polymer by bulk polymerization.
›BACKGROUND OF THE INVENTION
Acrylate polymer is a highly transparent polymer and is suitable for use as a material for making long distance optical telecommunication products. However, C—H bonds of the acrylate polymer will absorb signals having a wavelength of 1.2-1.6 μm used in the telecommunication, which results in an optical loss. Halogen-containing acrylates having a less number of C—H bond have been developed and used, as a replacement of the acrylate polymer, for making improved optical telecommunication products in terms of a lower optical loss. Pentafluorophenyl acrylate polymer is one of these halogen-containing acrylates.
There are two methods for preparing the pentafluorophenyl acrylate polymer, which are solution polymerization and bulk polymerization. EP 0824096 (1998) discloses a process for bulk polymerizing pentafluorophenyl acrylate monomer in an organic solvent a free radical initiator. In Example 25 of EP 0824096, 3.48 g of pentafluorophenyl acrylate (FW=252.15, 13.8 mmoles), 12.2 mg of AIBN (2,2′-azobisisobutyronitrile, FW=164.21, 0.074 mmoles) were dissolved in 17.3 ml of 2-butanone (methyl ethyl ketone) in a 50 ml three-necked flask, provided with a magnetic stirring bar, vacuum/nitrogen line, and an oil bath. After careful degassing of the reaction mixture to expell oxygen, the polymerisation was started by heating and stirring the flask's contents to about 60° C. under the exclusion of atmospheric oxygen. After 20 hours, the polymerization was discontinued, the solvent was almost completely removed by means of a rotary evaporator, the residue was redissolved in 6.5 ml of tetrahydrofurane, and the dissolved polymer was recovered through precipitation in methanol (75 ml) and filtration through a G4 glass filter. After drying in order to remove residual methanol/tetrahydrofurane (20 hours, 40° C., in vacuo), 2.3 g of poly(pentafluorophenyl)acrylate were obtained (yield about 66%) (Mw=35,800; Mn=13,415, polydispersity 2.7). The process disclosed in this European patent application not only requires the use of organic solvents in the polymerization and purification steps, but the process per se is complicated.
FR 2623510 (1989) and J. Fluorine Chem., 97, 191 (1999) both disclose bulk polymerizations of pentafluorophenyl acrylate polymer. The former uses AIBN as a initiator and dodecane thiol as a chain transfer agent, and the latter uses a photoinitiator and a thermal radical initiator to undergo a two-stage reaction. Even though these two prior art processes do not use an organic solvent, and are easier to be carried out, the polymerization products contain unreacted monomer and polymers of low polymerization degree, which deteriorate the thermal properties and quality of the polymerization products. As a result, the processing ability of the polymerization products prepared by these two prior art processes is adversely affected.
›SUMMARY OF THE INVENTION
The present invention provides a process for preparing a pentafluorophenyl acrylate polymer by bulk polymerizing a pentafluorophenyl acrylate monomer in the presence of a radical initiator. The reaction mixture is subjected to an ultrasonication treatment, so that the mixing of the initiator and the monomer is enhanced. The bulk polymerization is carried out at a first temperature of 25-200° C. for a first period of time, and at a second temperature of 25-200° C. and higher than the first temperature under a vacuum pressure for a second of time to complete the bulk polymerization, so that residue amounts of the initiator, unreacted monomer and oligomer of the monomer are reduced in the resulting product mixture, and thus the processing ability of the resulting product mixture is improved.
Preferably, said radical initiator is 2,2′-azobisisobutyronitrile.
Preferably, an amount of said radical initiator used in the reaction mixture ranges from 0.001 to 1 mole, and more preferably 0.006 mole, per mole of the pentafluorophenyl acrylate monomer.
Preferably, said second temperature ranges from 100 to 200° C., said vacuum pressure ranges from 0.1 to 30 mmHg, and said second period of time ranges from 4 to 36 hours. More preferably, said second temperature is about 140° C., said vacuum pressure is about 0.3 mmHg, and said second period of time is about 12 hours.
Preferably, said first temperature ranges from 25 to 99° C., and said first period of time ranges from 4 to 36 hours. More preferably, said first temperature is about 60° C., and said first period of time is about 12 hours.
›BRIEF DESCRIPTION OF THE DRAWING
FIG. 1 shows transmission percentages (% T) of the polymerization product prepared in Example 1 of the present invention at various wavelengths (nm).
›DETAILED DESCRIPTION OF THE INVENTION
The invention of the present application provides a process for bulk polymerizing pentafluorophenyl acrylate monomer in the presence of a radical initiator. The initiator is a solid and substantially not soluble in the monomer. The inventors of the present application use an ultrasonication treatment at the beginning of the polymerization to break the initiator particles and to enhance the mixing of the initiator and the monomer, so that the bulk polymerization can undergo more uniformly. The bulk polymerization is carried out at a first temperature of 25-200° C. for a first period of time, and at a second temperature of 25-200° C. and higher than the first temperature under a vacuum pressure for a second of time to complete the bulk polymerization. The higher second temperature can assure the decomposition and the exhaustion the initiator. In addition, the vacuum pressure applied within the second period of time can reduce the residue amounts of the initiator, if any, unreacted monomer and oligomer of the monomer in the resulting product mixture.
The present invention will be better understood from the following examples which are for illustration and nor for limitation of the scope of the present invention.
›EXAMPLE 1
0.006 g (0.036 mmol) of AIBN was added to 1.74 g (6 mmol) pentafluorophenyl acrylate monomer, and the resulting mixture was subjected to an ultrasonication treatment for 1.5 minute. The mixture was then heated at 60° C. for 12 hours under a nitrogen atmosphere, and heated at 140° C. and under a vacuum pressure of 0.3 mmHg for another 12 hours to obtain a transparent product. It can be seen from FIG. 1 that the transmission percentages (% T) of the product is about 80% or higher within 200-1700 nm wavelength.
The average molecular weight of the product was measured by gel permeation chromatography (GPC), and the results are listed as follows:
The product was subjected to thermogravimetric analysis (TGA), and the results indicate that the weight loss is 1.6% at 277° C., and 5% weight loss is at 344° C.
›CONTROL EXAMPLE
0.006 g (0.036 mmol) of AIBN was added to 1.74 g (6 mmol) pentafluorophenyl acrylate monomer, and the resulting mixture was subjected to an ultrasonication treatment for 1.5 minute. The mixture was then heated at 60° C. for 24 hours under a nitrogen atmosphere to obtain a transparent product.
The product was subjected to thermogravimetric analysis (TGA), and the results indicate that the weight loss is 5.1% at 272° C., and 10.2% at 344° C.
In comparison with Control Example, the product prepared in Example 1 exhibits significantly superior thermal properties.
›Tables in the description — 1
| Mn* | Mw* | Mp* | (polydispersity) |
| 26379 | 89254 | 132091 | 3.28 |
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5 codes- C08F220/22
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