Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
  • C08G64/18—Block or graft polymers
  • C08G64/183—Block or graft polymers containing polyether sequences
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
  • C08G64/20—General preparatory processes
  • C08G64/30—General preparatory processes using carbonates
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10S428/00—Stock material or miscellaneous articles
  • Y10S428/913—Material designed to be responsive to temperature, light, moisture
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
  • Y10S430/146—Laser beam
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/21—Circular sheet or circular blank
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/31504—Composite [nonstructural laminate]
  • Y10T428/31507—Of polycarbonate

Definitions

• This invention relates to polycarbonate technology, and more particularly to the development of optical quality polycarbonates.
• Optical data-recording media including optical disks as exemplified by compact audio disks and CD-ROM disks used in computers, have become a major means of storing data and making it available.
• the data on an optical disk are read by a plane polarized laser beam and a polarization-sensitive detection scheme. For this reason, it is necessary to minimize polarization-dependent effects on these laser beams upon passage through the disk.
• birefringence i.e., the difference between indices of refraction for light polarized in perpendicular directions. Birefringence leads to phase retardation between different polarization components of the laser beam, thereby reducing readability.
• Birefringence results from several sources, including the chemical nature of the raw material from which the disk is fabricated, the degree of molecular orientation therein and thermal stresses in a fabricated plastic optical disk.
• the observed birefringences of a disk are therefore determined by the molecular structure, which determines the intrinsic birefringence, and the processing conditions, which can create thermal stresses and orientation of the polymer chains.
• bisphenol A polycarbonates which are the principal ones currently being produced, are characterized by very high positive intrinsic birefringence, "bisphenol A” being the common name of 2,2-bis(4-hydroxyphenyl)propane.
• homopolycarbonates comprising units derived from spiro(bis)indanes, especially 6,6'-dihdyroxy-3,3,3',3'-tetramethyl-1 , 1 '-spiro(bis)indane, hereinafter designated "SBI”, have negative intrinsic birefringences, owing to the molecular structure. of the SBI unit and conformation in said homopolymers.
• a class of copolycarbonates having low intrinsic birefringence is disclosed, for example, in US Patent 4,552,949.
• Said copolycarbonates comprise structural units derived from bisphenol A and SBI.
• SBI polycarbonates are deficient in such areas as processability and ductility, as demonstrated, for example, by very high glass transition temperatures (Tg).
• Tg glass transition temperatures
• VBR vertical birefringence
• the vertical birefringence parameter is characteristic of optical disks specifically and cannot be related directly to polycarbonates in bulk.
• a related parameter which may be determined for a bulk polycarbonate is its stress optical coefficient in the glass phase, Cg.
• the Cg value for bisphenol A polycarbonate is 72, while that of a bisphenol A-SBI copolycarbonate containing 72 mole percent SBI units is 26.
• the present invention is based on the discovery of a class of copolycarbonates which have the desired physical and are expected to have the desired optical properties.
• Said copolycarbonates contain bisphenol-derived, spiro(bis)indane-derived and polyoxyalkylene glycol-derived structural units. Also provided is a method for their preparation which involves melt reaction with staged monomer addition, and articles made from said copolycarbonates.
• copolycarbonates comprising:
• each of A 1 and A 2 is a divalent aromatic radical and Y is a single bond or a bridging radical wherein one or two atoms separate A 1 from A 2 ;
• each R 1 is independently a C 2 . 6 divalent aliphatic radical and x is in the range of about 2-50;
• R 2 is C alkyl and n is 0 or 1 ;
• copolycarbonate comprising at least 4% by weight of units of formula II and at least about 10 mole percent of units of formula III.
• Another aspect of the invention is a method for preparing a copolycarbonate as describe above which comprises:
• Still another aspect of the invention is optical information storage media comprising a copolycarbonate as described above.
• the bisphenol carbonate structural units of formula I in the copolycarbonates of this invention may be considered as derived from bisphenols of the formula HO-A 1 -Y-A 2 -OH.
• a 1 and A 2 typically represent unsubstituted phenylene or substituted derivatives thereof.
• the bridging radical suitable as Y is most often a hydrocarbon group and particularly a saturated group such as methylene, cyclohexylidene or isopropylidene, although non- hydrocarbon groups such as oxygen, sulfur, sulfoxy or sulfone may be present.
• the most preferred bisphenol carbonate units are derived from bisphenol A, in which each of A 1 and A 2 is p-phenylene and Y is isopropylidene.
• the polyoxyalkylene carbonate units of formula II are typically derived from polyoxyalkylene glycols in which the alkylene groups contain 2-6 and preferably 2-4 carbon atoms, such as polyethylene glycol and polypropylene glycol.
• the value of x is in the range of about 2-50, and most often such that the molecular weight of the structural unit of formula II is in the range of about 100-5,000.
• polyoxyalkylene glycols of higher molecular weight will permit the use of smaller weight percentages thereof to produce essentially equivalent effects on properties.
• the R 2 groups may be such lower alkyl radicals as methyl, ethyl, n-propyl or isopropyl.
• the preferred units, however, are SBI units in which each n is 0.
• copolycarbonates of the invention comprise at least 4% and preferably about 5-20% by weight of units of formula II and at least about 10 and preferably about 15-40% of units of formula III. It is in these preferred ranges that the most desired optical properties are believed to exist.
• copolycarbonates cannot be prepared interfacially (i.e., by the reaction of phosgene with dihydroxy reagents in a mixed aqueous-organic system, under basic conditions) by reason of the relative lack of reactivity of polyoxyalkylene glycols under such conditions. They may, however, be prepared by a melt polymerization reaction between the corresponding bisphenols and polyoxyalkylene glycols and a diaryl carbonate, most often diphenyl carbonate.
• the second aspect of the invention is a preferred melt polymerization method in which the polyoxyalkylene glycol is introduced following the formation of an oligomer comprising units of formulas I and III, by melt polymerization of the bisphenols. This sequential polymerization procedure is believed to promote incorporation of units of formula II as single-unit rather than multi-unit blocks.
• the preparation method may include the use of at least one transesterification catalyst.
• Suitable catalysts include many basic materials known in the art to be useful for this purpose, particularly alkali metal hydroxides, tetraalkylammonium hydroxides, tetraalkylphosphonium hydroxides and hexaalkylguanidinium bisphenolates of the type disclosed in US Patent 5,756,843, the disclosure of which is incorporated by reference herein. The latter are illustrated by the compound containing one hexaethylguanidinium cation, three protons and two bisphenol A dianions.
• alkali metal hydroxide such as sodium hydroxide in combination with a tetraalkylammonium hydroxide, tetraalkylphosphonium hydroxide or hexaalkylguanidinium bisphenolate.
• step A of the method of the invention the reaction mixture comprising diaryl carbonate and bisphenols and, usually, catalyst is heated in an inert atmosphere such as nitrogen, with effective agitation such as stirring, at temperatures above about 170°C, the temperature being progressively increased until one or more values in the range of about 170-230°C are attained.
• Reaction pressures are typically decreased with the increase in temperature.
• step B the polyoxyalkylene glycol is introduced and heating is continued at temperatures in the range of about 180-325°C.
• the polycarbonate thus obtained may be isolated by conventional procedures.
• copolycarbonates of the invention are their expected low Cg values.
• Cg values for bisphenol A polycarbonate and an SBI-bisphenol A copolycarbonate containing 72 mole percent SBI units are 72 and 26, respectively.
• the value for a bisphenol A-polyethylene glycol (mol. wt. 400) copolycarbonate containing 5 mole percent polyethylene glycol units is 42.
• the copolycarbonates of the invention are expected to have values even lower than 42, and perhaps lower than 26.
• Birefringence is determined from retardation, which is measured using a linearly polarized laser and a photoelastic modulator.
• the retardation in the polarization produced by an optical disk is analyzed using a detection scheme consisting of a linear polarizer and a lock-in amplifier.
• the retardation for light normally incident on a disk and that when the laser is incident at a known (non- normal) angle are used to determine the VBR.
• optical information storage media of the invention include such articles as audio disks, laser disks, optical disk memories and magnetoooptical disks to which information may be written and from which it may be read by laser.
• Such media may be produced from the copolycarbonates of the invention by art-recognized means.
• copolycarbonates of the invention is illustrated by the following examples. All parts are by weight. Molecular weights were determined by gel permeation chromatography relative to polystyrene.
• the reactors were heated to 180°C with stirring and were allowed to equilibrate for 5-10 minutes. There were then added, with continued stirring, 600 ⁇ l of a 0.221 M aqueous tetramethylammonium hydroxide solution and 500 ⁇ l of a 0.001 M aqueous sodium hydroxide solution. Heating at 180°C was continued for 5 minutes, after which the temperature was increased to 210°C and the pressure decreased to 180 torr, whereupon phenol began to distill from the mixtures.
• the reactors were returned to atmospheric pressure by nitrogen gas introduction and then opened to the atmosphere, all at 210°C, and various amounts of a polyethylene glycol (PEG) were added to the reaction mixture via syringe.
• PEG polyethylene glycol
• the reactors were resealed, allowed to equilibrate at 210°C for 10 minutes.
• the pressure was decreased to 100 torr and heating at 210°C was continued for 45 minutes.
• Polymerization was continued at 240°C/15 torr (45 minutes), 270°C/2 torr (100 minutes) and 300°C/0.2 torr (10 minutes).
• the polymers were then removed from the reactors, cooled, quenched with phosphorous acid in methylene chloride/methanol and dried. The results are given in the following table.

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• Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Organic Chemistry (AREA)
• Polyesters Or Polycarbonates (AREA)
• Optical Record Carriers And Manufacture Thereof (AREA)

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• 1998
  • 1998-08-07 US US09/131,218 patent/US6042920A/en not_active Expired - Lifetime
• 1999
  • 1999-06-10 DE DE1999624996 patent/DE69924996T2/de not_active Expired - Fee Related
  • 1999-06-10 JP JP2000563719A patent/JP2002522584A/ja not_active Withdrawn
  • 1999-06-10 WO PCT/US1999/013239 patent/WO2000008089A1/en not_active Ceased
  • 1999-06-10 EP EP99928585A patent/EP1100841B1/en not_active Expired - Lifetime
  • 1999-07-26 AR ARP990103670 patent/AR021458A1/es not_active Application Discontinuation

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