Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
  • C08L83/04—Polysiloxanes
  • C08L83/08—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C25/00—Surface treatment of fibres or filaments made from glass, minerals or slags
  • C03C25/10—Coating
  • C03C25/104—Coating to obtain optical fibres
  • C03C25/106—Single coatings
• • 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
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
  • C08G18/40—High-molecular-weight compounds
  • C08G18/61—Polysiloxanes
• • 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
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
  • C08G18/81—Unsaturated isocyanates or isothiocyanates
  • C08G18/8141—Unsaturated isocyanates or isothiocyanates masked
  • C08G18/815—Polyisocyanates or polyisothiocyanates masked with unsaturated compounds having active hydrogen
  • C08G18/8158—Polyisocyanates or polyisothiocyanates masked with unsaturated compounds having active hydrogen with unsaturated compounds having only one group containing active hydrogen
  • C08G18/8175—Polyisocyanates or polyisothiocyanates masked with unsaturated compounds having active hydrogen with unsaturated compounds having only one group containing active hydrogen with esters of acrylic or alkylacrylic acid having only one group containing active hydrogen
• • 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
  • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
  • C08G77/04—Polysiloxanes
  • C08G77/38—Polysiloxanes modified by chemical after-treatment
  • C08G77/382—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon
  • C08G77/388—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon containing nitrogen
• • 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
  • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
  • C08G77/04—Polysiloxanes
  • C08G77/38—Polysiloxanes modified by chemical after-treatment
  • C08G77/382—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon
  • C08G77/392—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon containing sulfur
• • 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]
  • Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
  • Y10T428/31609—Particulate metal or metal compound-containing
  • Y10T428/31612—As silicone, silane or siloxane

Definitions

• This invention relates to radiation-curable liquid coating compositions which cure to form coatings which maintain their flexibility at temperatures as low as about -40°C. to -60°C. , and to optical glass fibers coated therewith. 10 Background Art
• Radiation-curable liquid coating compositions are well known, and many of these involve diacrylate- ter inated polyurethane oligomers. However, these known compositions may, under some conditions, be relatively 15 hard when cured. In these cases, one can dilute the diac- r late-terminated polyurethane with a large proportion of radiation-curable monomer of low T (glass transition temp- erature) so that radiation exposure ' will cure the coating and produce a soft layer instead of a hard one. However, 20 these soft layers have little strength and, hence, are not useful for coating optical fibers.
• glass fiber has become impor ⁇ tant for the transmission of beams of light used for communication. These must be coated to protect the fiber 25 surface against abrasion. The coating must also be able to resist microbending when the coated fiber is cabled and also when the coated fiber is subjected to large changes in temperature. These complex character ⁇ istics demand an unusual coating, namely, one which is 30 both soft and tough. Moreover, this toughness must be achieved without introducing stiffness which would cause microbending when the coating contracts at low tempera ⁇ ture.
• One effort to provide radiation-curable coatings having these properties is the subject of prior appli- 35 cation Serial No. 170,148, filed July 18, 1980, butthere the properties begin to fall off when exceptionally low
• OM PI temperatures are encountered. It is desired to extend the range of low temperature which can be sustained without encountering unacceptable stiffness.
• optical glass filament is prime coated with a liquid, polyethylenic- ally unsaturated, radiation-curable resin constituted by an organic polysiloxane having from 2 to 6 reactive side chains each of which carry a functional group providing one reactive site which is preferably selected from the group consisting of hydroxyl, amine, mercaptan, carboxyl or glycidyl, and said functional group having been reacted to provide a single radiation-curable mono ⁇ ethylenically unsaturated side chain which preferably contains an acrylic or methacrylic group.
• the polysiloxane derivative is a polyacrylate or polymethacrylate, terms which are used here to identify a plurality of
• the unique properties desired herein are obtained by having the described polysiloxane possess about one such monoethylenically unsaturated side chain for every 500 to 5,000 units of molecular weight.
• the organic polysiloxanes used herein include known compounds which are available in commerce.
• the polysiloxane backbone is substituted with organic radi ⁇ cals, some of which are inert, and here methyl, phenyl, or a mixture thereof is preferred, and some of which are reactive, like hydroxy propyl or hydroxy polyoxypropyl, which illustrate the side chain providing the hydroxy functional group which is the preferred group providing a single reactive site in the previous description of the organic polysiloxane.
• the reactive organic radical may be joined to the silicon atoms of the polysiloxane backbone through oxygen, but it is preferred to have it joined to the silicon atoms by a direct carbon to silicon bond. This is because the direct carbon to silicon bond is more re ⁇ sistant to hydrolysis.
• the prime coatings of this inven ⁇ tion are soft and it is preferred to topcoat them.
• the topcoating supplies improved hydrolysis resistance as well as improved abrasion protection, so the use of a topcoat minimizes the significance of hydrolysis resist ⁇ ance just as it minimizes the importance of toughness in the prime coating. Nonetheless, when the prime coating is hydrolysis-resistant and when it possesses good tough ⁇ ness as well as having a low modulus of elasticity which is retained at low temperature, the best overall proper ⁇ ties are obtained.
• the functional group providing the single reactive site can be supplied by any organic radical
• aliphatic radicals are preferred, especially those which are saturated and which contain, except for the reactive functional group, only carbon and hydrogen, or carbon, hydrogen and oxygen.
• the preferred reactive side chains are saturated aliphatic hydrocarbon groups con ⁇ taining from two to four carbon atoms, especially 2-hydroxy propyl, and polyoxyalkylene ethers in which the alkylene group contains from two to four carbon atoms,•such as hydroxy polyoxypropyl.
• Polyesters and polyether polyesters may be used in place of the more pre ⁇ ferred polyethers noted above.
• a suitable polyester would be the reaction product of two moles of ethylene glycol or propylene glycol, with one mole of adipic acid or phthalic acid. This reaction product provides a diol which can be joined to the polysiloxane by one of its two hydroxy groups, leaving the other hydroxy group available to react with a compound which brings in the single ethylenically unsaturated group.
• the reactive side chain can be provided by an aromatic group such as the hydroxyethyl phenyl group.
• glycine a carboxy amine
• glycine a carboxy amine
• second ⁇ ary amines are preferred because only one reactive func ⁇ tional site is provided
• primary amines are effectively monofunctional when reacted with isocyanates, so they can be used and reacted with a monoethylenically unsaturated monoisocyanate, like the reaction product of 2-hydroxy- ethyl acrylate with 2,4-toluene diisocyanate or iso- phorone diisocyanate which contain one isocyanate group which is far more reactive than the other so that equi- molar proportions of reactants will provide the desired monoisocyanate.
• Mercaptan functionality is illustrated in the ex ⁇ amples. It can also be provided by reacting a dithiol, like 1,6-hexane dithiol or an hydroxy thiol, such as 1-hydroxy, 6-thiol hexane with a silanol-terminated polysiloxane.
• glycidyl functionality can be employed in the glycidoxy propyl group since glycidoxy propyl-functional polysiloxanes are available in com ⁇ merce. These can be reacted with acrylic acid to form a single acrylate ester group, the hydroxy group genera ⁇ ted by the reaction being nonreactive under the condi ⁇ tions which enable ester formation with the glycidyl group.
• the radiation-cured coatings of this invention in which the number of reac ⁇ tive side chains, the requirement that these be effec- tively monoreactive, and the spacing of the groups provided by the molecular weight per reactive group, are both soft and physically tough.
• These charactaristics are not generally useful in coatings, but they provide useful prime coatings for the optical glass filament.
• These prime coatings possess a low modulus of elasticity which stays low at low temperatures. A room temperature modulus of 300 psi is typical in the present invention.
• OMPI At -60°C. the modulus in a typical example increases to only about 1000. This is a very small increase in modulus for such a large reduction in temperature.
• This inven ⁇ tion contemplates cured coatings which have a modulus of elasticity at room temperature and at -60°C. which are below 3000, preferably below 2000.
• the preferred modulus at -60°C. is between 400 - 1500.
• optical glass filament One purpose of coating optical glass filament is to protect the surface of the filament before it might be abraded, and it is therefore preferred to apply the coating to the glass filament as it is initially formed. This _is itself conventional.
• the optical glass has the form of a continuous filament, but it is commonly referred to as a fiber, so these words are used inter ⁇ changeably herein.
• overcoat the prime-coated filament of this invention it is also preferred to overcoat the prime-coated filament of this invention to provide additional abrasion and/or hydrolysis protection, but this is also conven ⁇ tional, and the overcoats which may be used form no part of this invention.
• the radiation used to provide the cure may be of diverse type, such as beta rays, electron beam and actinic radiation, but ultra ⁇ violet light is preferred because it is very rapid and does not significantly damage the optical glass filament.
• ultraviolet light is to be used, the initiators and/or photosensitizers normally used for this purpose
• OMPI _ will be employed herein, such as about 3% by weight of diethoxy acetophenone. Since ultraviolet light is pre ⁇ ferred, acrylic unsaturation is best, but since the radiation character can vary, so can the specific charac- ter of the unsaturation. Other useful ethylenic unsatura- tions are illustrated by itaconic, crotonic, allylic, vinylic, etc. These are in addition to the methacralic unsaturation, provided by reaction with methacrylic acid or 2-hydroxyethyl methacrylate, which has been noted previously. Itaconic or crotonic unsaturation may be introduced by using the corresponding acids in place of acrylic acid. Allylic unsaturation may be introduced using allyl alcohol in place of 2-hydrox ethyl acrylate. Vinylic unsaturation may be introduced using hydroxy butyl vinyl ether in place of 2-hydrox ethyl acrylate.
• the coating composition consist of the radiation-curable polysiloxane deriva ⁇ tives described herein
• small amounts up to about 15% of the total weight of the ' composition, but desirably ho more than about 5% of the composition, may be constituted by other materials, such as dissolved resins, like melamine-formaldehyde condensates or unsaturated poly ⁇ esters made from ethylene glycol, adipic acid and crotonic acid, radiation-curable monomers like 2-hydroxyeth l acrylate, or solvents like acetone. Since ultraviolet cure is preferred, liquid mono- or poly-acrylates may be added to adjust viscosity or for ancillary purpose.
• Example 1 Into a reaction vessel fitted with a stirrer and gas inlet tube is placed one mole (222 gms) of isophorone diisocyanate.
• Example 2 The product of Example 2 is converted into an ultraviolet curable composition by the addition of 3% by weight of the photoinitiator diethoxy acetophenone (no photosensitizer is needed) . The product is then filtered through a 1 micron filter to remove particles
• the liquid coating composition is coated upon freshly formed glass filament of optical quality and the freshly coated filament is irradiated with 5 ultraviolet light to cure the coating.
• This coating is normally overcoated, which forms no part of this invention.
• the prime coating has a very low modulus of 300 psi and, at -60°C. , the modulus only increased to 1100 psi. 10 Note 1 - The Dow Corning product 1248 may be used.
• Example 5 Charge to a flask equipped with a stirrer, reflux condenser and a dropping funnel 3 moles (666 grams) of isophorone diisocyanate and 3 grams of dibutyl tin dilaurate.
• toluene diisocyanate Two moles of toluene diisocyanate are placed into a suitable reaction vessel. To this is added 5.7 grams of dibutyltindilaurate. The mixture is heated to 90°C. while one mole of a mercaptopropyldimethyl terminated polydimethylsiloxane having an average molecular weight of 2500 is added slowly. The reaction is continued at about 90°C. until there is no evidence of free SH groups by infrared spectrophotographic analysis. The reaction mixture is then cooled to 60°C. and two moles of hydroxy- ethyl acrylate and 3 grams of phenothiazine are added. The reaction is continued at 60°C. - 65°C. until no free isocyanate groups remain as determined by infrared spectophotographic analysis.
• This product is a radiation- curable coating composition and can be made sensitive to ultraviolet light by the addition of 3% by weight of diethoxyacetophenone.

Landscapes

• Chemical & Material Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Organic Chemistry (AREA)
• Health & Medical Sciences (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• General Chemical & Material Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• General Life Sciences & Earth Sciences (AREA)
• Engineering & Computer Science (AREA)
• Geochemistry & Mineralogy (AREA)
• Materials Engineering (AREA)
• Macromonomer-Based Addition Polymer (AREA)
• Paints Or Removers (AREA)
• Silicon Polymers (AREA)
• Surface Treatment Of Glass Fibres Or Filaments (AREA)
• Other Air-Conditioning Systems (AREA)
• Compositions Of Macromolecular Compounds (AREA)

Priority Applications (1)

Applications Claiming Priority (1)

Publications (1)

Family

ID=23574234

Family Applications (1)

Country Status (5)

Cited By (16)

Families Citing this family (27)

Citations (12)

Family Cites Families (4)

• 1982
  • 1982-07-19 US US06/398,161 patent/US4496210A/en not_active Expired - Lifetime
• 1983
  • 1983-07-19 EP EP83902605A patent/EP0113779B1/en not_active Expired
  • 1983-07-19 JP JP58502661A patent/JPS59501381A/ja active Granted
  • 1983-07-19 WO PCT/US1983/001094 patent/WO1984000424A1/en not_active Ceased
  • 1983-07-19 DE DE8383902605T patent/DE3369199D1/de not_active Expired

Patent Citations (12)

Non-Patent Citations (1)

Also Published As

Similar Documents

Legal Events