US2290193A - Laminated glass - Google Patents

Laminated glass Download PDF

Info

Publication number
US2290193A
US2290193A US112995A US11299536A US2290193A US 2290193 A US2290193 A US 2290193A US 112995 A US112995 A US 112995A US 11299536 A US11299536 A US 11299536A US 2290193 A US2290193 A US 2290193A
Authority
US
United States
Prior art keywords
phthalate
tributyl phosphate
phosphate
plastic
alkyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US112995A
Inventor
Kirkpatrick Arnold
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Monsanto Chemicals Ltd
Monsanto Chemical Co
Original Assignee
Monsanto Chemicals Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Monsanto Chemicals Ltd filed Critical Monsanto Chemicals Ltd
Priority to US112995A priority Critical patent/US2290193A/en
Application granted granted Critical
Publication of US2290193A publication Critical patent/US2290193A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B17/00Layered products essentially comprising sheet glass, or glass, slag, or like fibres
    • B32B17/06Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
    • B32B17/10Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
    • B32B17/10005Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing
    • B32B17/1055Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/10Esters; Ether-esters
    • C08K5/12Esters; Ether-esters of cyclic polycarboxylic acids
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31551Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
    • Y10T428/31634Next to cellulosic
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31551Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
    • Y10T428/31645Next to addition polymer from unsaturated monomers
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31551Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
    • Y10T428/31645Next to addition polymer from unsaturated monomers
    • Y10T428/31649Ester, halide or nitrile of addition polymer

Definitions

  • the present invention relates to safety glass and more particularly to plastic products for use as intermediate sheets or layers between the glass sheets of such laminated glass.
  • a modifying agent for use with the customary plastic bases of such intermediate sheets which modifying agent imparts to the plastic base an exceptional flexibility at low temperatures and which agent is characterized by great stability to light, water resistance, retentivity in the plastic composition, and exceptional miscibility with the other components of the plastic composition.
  • the plastic sheet must possess permanently brilliant transparency and be smooth and tough.
  • the present invention is based in part on the discovery that certain alkyl phosphates, for example, tributyl phosphate, import to cellulose acetate, cellulose nitrate and other plastic substances an extraordinary degree of flexibility in comparison with the amount of alkyl phosphate added and that this flexibility is retained at low temperatures.
  • alkyl phosphates for example, tributyl phosphate
  • import to cellulose acetate, cellulose nitrate and other plastic substances an extraordinary degree of flexibility in comparison with the amount of alkyl phosphate added and that this flexibility is retained at low temperatures.
  • the proportion of alkyl phosphate which can be retained in such compositions is too small to produce films of satisfactory flexibility for many purposes.
  • compositions containing dimethyl phthalate are not especially flexible at low temperatures, the addition of tributyl phosphate imparts this property thereto.
  • the tributyl phosphate appears to transmit to other plasticizers not especially characterized thereby, an improved flexibility without impairing other desirable qualities.
  • Tributyl phosphate 60 125-164 2.
  • Tributyl phosphate 75 118-196 8.
  • Dimethyl phthalate 60 33 4.
  • Dimethyl phthalate 75 15-26 5.
  • Diethyl phthalate 60 50-74 6.
  • Diethyl phthalate 75 95-124 7.
  • Tributyl phosphate 30 d i m e t h y l phthalate 30 28-32 8.
  • Tributyl phosphate 37 dimethyl phthalate 37 125-146 9.
  • Ethyl phthalyl ethyl glycolate 60.- 4 18. Ethyl phthalyl ethyl glycolate 75 3 19. Tributyl p h o s p h a t e 30 ethyl phthalyl ethyl glycolate 30 28-34 20. Tributyl p h o s p h a t e 37 ethyl phthalyl ethyl glycolate 37 90-138
  • the light resistance, water resistance, fire resistance, flexibility at room temperature (20 C.), and transparency were exceptionally good.
  • compositions numbered 1 and 2 there was slight exudation showing a slight lack of retentivity of the tributyl phosphate.
  • compositions numbered 10, 16 and 20 Very slight exudation was noted also in compositions numbered 10, 16 and 20. It will be noted that the flexibility at the low temperature (number of bends) of the mixture with tributyl phosphate is greater in every case than the composition without the tributyl phosphate and in most cases is greater than the flexibility which would result from the use of tributyl phosphate alone.
  • compositions numbered 48, 49 and 50 do not show the advantageous efiects produced when alkyl phosphates are admixed. Compositions numbered 24, 25 and 31 stweated, this indicating a slight lack of retentiv- 1 y.
  • the tributyl phosphate described hereinabove is the normal butyl derivative and is particularly useful as the plasticizer in intermediate plastic sheets in the production of safety glass.
  • triethyl phosphate is characterized by not as great an ability to impart flexibility which is permanent at low temperatures to the resulting plastic composition, but it can be used with some success in partially replacing tributyl phosphate in some compositions.
  • Triethyl phosphate is too soluble in water and too easily decomposed to be entirely satisfactory for the uses contemplated herein, especially when used alone or to replace predominant proportions of tributyl or higher alkyl phosphates.
  • Triphenyl or tricresyl phosphates are not as advantageous for use in accordance with this invention as are the alkyl phosphates; celluloslc compositions made therewith are characterized by poor light stability and poor flexibility at low temperatures.
  • plasticizers which can be used in the same manner as diethyl phthalate'as specified above, that is, those which are used in admixture with the alkyl phosphates to produce the advantageous results of this invention, include such varied plasticizer as phthalates, for example, dibutyl and diamyl phthalate; glycolates,
  • plasticizers for example, methyl or ethyl phthalyl ethyl glycolate; toluenesulfonamides and similar plasticizers.
  • the plasticizers are preferably those which are light stable and miscible with the alkyl phosphate as well as with the plastic.
  • plasticizers of the invention are adapted is limited only by the compatibility of the plasticizer with the plastic.
  • the industry is largely restricted to the utilization of cellulose acetate, smaller amounts of cellulose nitrate and the newer vinyl resins such, for example, as Formvar" and Gelva.” -To the plasticization of these materials the invention is especially applicable.
  • any particular plasticizer mixture which are used in the preparation of the plastic compositions of the invention may be varied considerably.
  • 90 parts of tributyl phosphate and 10 parts of diethyl phthalate are usable to obtain other ranges of properties.
  • similar variations of proportions can be made to produce compositions for specific purposes.
  • the method of incorporating the plasticizer into the plastic composition presents no features new to the art. Any of the standard methods, such as kneading with or without the aid of heat, solution in mutual solvents or similar procedures may be used.
  • composition which comprises incorporating uniformly with said composition a modifying substance consisting of a neutral alkyl phthalate ester selected from the group consisting of neutral dialkyl phthalate esters having not more than five carbon atoms in each alkyl group and neutral alkyl esters of phthalyl glycclic acid having not more than two carbon atoms in each alkyl group.
  • a neutral alkyl phthalate ester selected from the group consisting of neutral dialkyl phthalate esters having not more than five carbon atoms in each alkyl group and neutral alkyl esters of phthalyl glycclic acid having not more than two carbon atoms in each alkyl group.
  • Safety glass including in combination a plurality of sheets of glass bonded together through the medium of a plastic composition as defined in claim 2.
  • Safety glass including in combination a plurality of sheets of glass bonded together through the medium of a plastic composition as defined in claim 3.
  • Safety glass including in combination a plurality of sheets of glass bonded together through the medium of a plastic composition as defined in claim 4.
  • Safety glass including in combination a plurality of sheets of glass bonded together through the medium of a plastic composition as defined in claim 5.
  • Safety glass including in combination a plurality of sheets of glass bonded together through the medium of a plastic composition as defined in claim 6.
  • Safety glass including in combination a plurality of sheets of glass bonded through the medium of a plastic composition as defined in claim 'I.
  • a transparent, rubbery sheet comprising 100 parts of a polyvinyl formaldehyde acetal resin and, as an elasticizer therefor, at least parts, approximately, of an alkyl phthalyl ethyl glycolate in which the alkyl group contains less than 3 carbon atoms.

Description

Patented July 21, 1942 F F ACE LAMINATED GLASS Arnold Kirkpatrick, Webster Groves, Mo., assignor to Monsanto Chemical Company, St. Louis, Mo., a corporation of Delaware No Drawing. Application November 27, 1936, Serial No. 112,995
14 Claims.
The present invention relates to safety glass and more particularly to plastic products for use as intermediate sheets or layers between the glass sheets of such laminated glass.
The imperfections of present-day safety glass are well known. Changes such as darkening, loss of transparency, crystallization and embrittlement of the intermediate plastic sheets of safety glass in normal use occur after short periods. It is recognized that these imperfections of the intermediate sheet are not entirely inherent in the cellulose nitrate or acetate or other material that is the base of the plastic composition; rather, the imperfections are largely attributable to those substances, particularly plasticizers, which are added to modify the properties of the base to impart to the composition suitable characteristics which permits its use for safety glass.
It is an object of the present invention to provide a plastic composition for use as the intermediate sheet in safety glass production, which composition isimproved particularly in regard to flexibility at low temperatures. Thus, it is an object of the invention to provide a modifying agent for use with the customary plastic bases of such intermediate sheets, which modifying agent imparts to the plastic base an exceptional flexibility at low temperatures and which agent is characterized by great stability to light, water resistance, retentivity in the plastic composition, and exceptional miscibility with the other components of the plastic composition. Furthermore, the plastic sheet must possess permanently brilliant transparency and be smooth and tough.
Other objects and advantages of the invention will be more apparent from the description which follows.
It is known that when alkyl phosphates, such as tributyl phosphate, are used as plasticizers, discoloration by the action of light is to a large extent prevented. The proportion of such a plasticizer which can be retained in any individual plastic composition, however, is rather limited.
The present invention is based in part on the discovery that certain alkyl phosphates, for example, tributyl phosphate, import to cellulose acetate, cellulose nitrate and other plastic substances an extraordinary degree of flexibility in comparison with the amount of alkyl phosphate added and that this flexibility is retained at low temperatures. However, the proportion of alkyl phosphate which can be retained in such compositions is too small to produce films of satisfactory flexibility for many purposes. It was found that when tributyl phosphate is admixed with an equal proportion of diethyl phthalate or other plasticizer a greater proportion of the mixture can be incorporated into and retained by the composition without any sacrifice of the desirable light resistance and flexibility at low temperatures inherent in the alkyl phosphate and that products of greater flexibility result than can be obtained without this admixture. Thus the presence of the alkyl phosphates has been found to have a synergistic efiect or action with respect to the plastic when used in conjunction with alkyl phthalate and aryl sulfonamide plasticizers. This effect is illustrated in the results of tests which are set forth hereinafter. Whereas compositions containing dimethyl phthalate are not especially flexible at low temperatures, the addition of tributyl phosphate imparts this property thereto. Thus, in admixture the tributyl phosphate appears to transmit to other plasticizers not especially characterized thereby, an improved flexibility without impairing other desirable qualities.
Several methods of applying the discovery, which are suggestive of many other applications, are illustrated in greater detail in the following description.
The following examples are typical of the effect produced on a resin resulting from the condensation of formaldehyde with a partially hydrolyzed vinyl ester polymer. A commercial resin of this type, known as Formvar," was used with the indicatedparts by weight of the various plasticizing substances and mixtures; the proportions represent parts by weight of the substances to parts of the resin. Uniform thin sheets of the plastic composition were made, the sheets being approximately 0.025 inch in thickness, and these were subjected to bending tests while at a temperature of -20 F. (-29 C.). The number of bends, each bend consisting of a bend through an angle of and back to the original position, which the composition could withstand without cracking, is taken to be a measure of the flexibility of me composition at that temperature.
Table IFormvar" resin Bends at 20 F.
l. Tributyl phosphate 60 125-164 2. Tributyl phosphate 75 118-196 8. Dimethyl phthalate 60 33 4. Dimethyl phthalate 75 15-26 5. Diethyl phthalate 60 50-74 6. Diethyl phthalate 75 95-124 7. Tributyl phosphate 30 d i m e t h y l phthalate 30 28-32 8. Tributyl phosphate 37 dimethyl phthalate 37 125-146 9. Tributyl p h o s p h a te 30 diethyl phthalate 30 40-58 10. Tributyl phosphate 37% diethyl phthalate 37 600-1170 11. Tributyl p h o s p h a t e 34 diethyl phthalate 40 120-218 12. Tributyl phosphate 37 dimethyl phthalate 18% diethyl phthalate 18% 190-232 13. Methyl phthalyl ethyl glycolate 60 5 l4. Methyl phthalyl ethyl glycolate 75 1 15. 'I'ributyl p h o s p h a t e 30 methyl phthalyl ethyl glycolate 30 18-23 16. 'I'ributyl phosphate 37% m e t h y l phthalyl ethyl glycolate 37 60-74 17. Ethyl phthalyl ethyl glycolate 60.- 4 18. Ethyl phthalyl ethyl glycolate 75 3 19. Tributyl p h o s p h a t e 30 ethyl phthalyl ethyl glycolate 30 28-34 20. Tributyl p h o s p h a t e 37 ethyl phthalyl ethyl glycolate 37 90-138 In all the above examples the light resistance, water resistance, fire resistance, flexibility at room temperature (20 C.), and transparency were exceptionally good. In compositions numbered 1 and 2 there was slight exudation showing a slight lack of retentivity of the tributyl phosphate. Very slight exudation was noted also in compositions numbered 10, 16 and 20. It will be noted that the flexibility at the low temperature (number of bends) of the mixture with tributyl phosphate is greater in every case than the composition without the tributyl phosphate and in most cases is greater than the flexibility which would result from the use of tributyl phosphate alone.
The following table represents typical results to be obtained when cellulose acetate is treated according to the invention. The conclusions are similar to those above, that is, the flexibility at room temperature is good, and the light resistance, water resistance, fire resistance, transparency, brilliance and such characteristics are exceptionally good.
Table IICeZZulose acetate Bends at -20 F.
21. Dimethyl phthalate 100 21 22. Dimethyl phthalate 125 1 23. Dimethyl phthalate 150 65-94 24. Diethyl phthalate 125 1 25. Diethyl phthalate 150 25-68 26. Methyl phthalyl ethyl glycolate 100 1 2'7. Ethyl phthalyl ethyl glycolate 100 1 28. Dimethyl phthalate 45 diethyl phthalate 55 1 29. Dimethyl phthalate 56 A; diethyl phthalate 68% 3 30. Dimethyl phthalate 67 A; diethyl phthalate 82 70-118 31. Tributyl phosphate 75 diethyl phthalate 75 32. Tributyl phosphate 75 dimethyl phthalate 37% diethyl phthalate 371 Tributyl phosphate 50 methyl phthalyl ethyl glycolate Tributyl phosphate 75 methyl phthalyl ethyl glycolate 75 Tributyl phosphate 75 methyl phthalyl ethyl glycolate 37 /2 ethyl phthalyl ethyl glycolate 37% Tributyl phosphate 37 methyl phthalyl ethyl glycolate 75 ethyl phthalyl ethyl glycolate 37%-" Tributyl phosphate 37 methyl phthalyl ethyl glycolate 37% ethyl phthalyl ethyl glycolate 75 Tributyl phosphate 37 methyl phthalyl ethyl glycolate 75 diethyl phthalate 37 /2 Tributyl phosphate 75 ethyl phthalyl ethylglycolate 75 Tributyl phosphate 75 methyl phthalyl ethyl glycolate 37%; diethyl phthalate 37% Tributyl phosphate 100 dimethyl phthalate 50 Tributyl phosphate 50 dimethyl phthalate 100 Tributyl phosphate 100 diethyl phthalate 50 Tributyl phosphate 50 diethyl phthalate 100 Tributyl phosphate 100 ethyl phthalyl ethyl glycolate 50 Tributyl phosphate 50 ethyl phthalyl ethyl glycolatc 100 Tributyl phosphate 100 .methyl phthalyl ethyl glycolate 100 Dimethyl phthalate 50 methyl phthalyl ethyl glycolate 100-- Dimethyl phthalate 75 methyl phthalyl ethyl glycolate 75 5 50. Dimethyl phthalate 1 It is to be observed that mixtures not containing alkyl phosphates (compositions numbered 48, 49 and 50) do not show the advantageous efiects produced when alkyl phosphates are admixed. Compositions numbered 24, 25 and 31 stweated, this indicating a slight lack of retentiv- 1 y.
The tributyl phosphate described hereinabove is the normal butyl derivative and is particularly useful as the plasticizer in intermediate plastic sheets in the production of safety glass. On the other hand, triethyl phosphate is characterized by not as great an ability to impart flexibility which is permanent at low temperatures to the resulting plastic composition, but it can be used with some success in partially replacing tributyl phosphate in some compositions. In the compositions described it is possible to substitute partially or completely the tributyl phosphate by other isomeric tributyl phosphates, or by tripropyl, triamyl, and trihexyl derivatives. Triethyl phosphate is too soluble in water and too easily decomposed to be entirely satisfactory for the uses contemplated herein, especially when used alone or to replace predominant proportions of tributyl or higher alkyl phosphates. Triphenyl or tricresyl phosphates are not as advantageous for use in accordance with this invention as are the alkyl phosphates; celluloslc compositions made therewith are characterized by poor light stability and poor flexibility at low temperatures.
The plasticizers which can be used in the same manner as diethyl phthalate'as specified above, that is, those which are used in admixture with the alkyl phosphates to produce the advantageous results of this invention, include such varied plasticizer as phthalates, for example, dibutyl and diamyl phthalate; glycolates,
for example, methyl or ethyl phthalyl ethyl glycolate; toluenesulfonamides and similar plasticizers. The plasticizers are preferably those which are light stable and miscible with the alkyl phosphate as well as with the plastic.
The range of plastic substances to which the plasticizers of the invention are adapted is limited only by the compatibility of the plasticizer with the plastic. For making safety glass the industry is largely restricted to the utilization of cellulose acetate, smaller amounts of cellulose nitrate and the newer vinyl resins such, for example, as Formvar" and Gelva." -To the plasticization of these materials the invention is especially applicable.
The proportions of any particular plasticizer mixture which are used in the preparation of the plastic compositions of the invention may be varied considerably. Preferably about equal parts of tributyl phosphate and diethyl phthalate are used but as little as parts of tributyl phosphate to 90 parts of diethyl phthalate are satisfactoryfor many purposes. On the other extreme, 90 parts of tributyl phosphate and 10 parts of diethyl phthalate are usable to obtain other ranges of properties. With other plasticizing substances similar variations of proportions can be made to produce compositions for specific purposes.
The method of incorporating the plasticizer into the plastic composition presents no features new to the art. Any of the standard methods, such as kneading with or without the aid of heat, solution in mutual solvents or similar procedures may be used.
Inasmuch as the specification comprises preferred embodiments of the invention it is to be understood that the invention is not limited thereto and that changes and modifications may be made therein without departing substantially from the invention, which is defined in the appended claims.
I claim:
1. The method of increasing the compatibility and retentivity of a trialkyl phosphate, the alkyl radicals of which contain more than two and not more than six carbon atoms, with an organic plastic substance characterized by a plurality of COC linkages and selected from the group consisting of cellulose derivatives, vinyl ester and vinyl acetal resins, and at the same time producing a synergistic increase in the flexibility at subatmospheric temperature conditions of such a. composition, which comprises incorporating uniformly with said composition a modifying substance consisting of a neutral alkyl phthalate ester selected from the group consisting of neutral dialkyl phthalate esters having not more than five carbon atoms in each alkyl group and neutral alkyl esters of phthalyl glycclic acid having not more than two carbon atoms in each alkyl group.
2. A plastic composition embodying an organic plastic substance characterized by a plurality of COC linkages and. selected from the group consisting of cellulose derivatives, vinyl ester and vinyl acetal resins, and embodying a mixture of two plasticizing substances, one of which is a trialkyl phosphate, the alkyl radicals of which contain more than two but not more than six carbon atoms, and the other of which is a phthalate ester selected from the group consisting of neutral dialkyl phthalate esters having not more than five carbon atoms in each alkyl group and neutral alkyl esters of phthalyl glycolic acid having not more than two carbon atoms in each alkyl group, whereby a degree of flexibility is imparted to the composition at subnormal temperature conditions as a result of the synergistic action of the two modifying substances that is not attainable by means of the presencein-the composition of the phthalate ester modifying substance without the trialkyl phosphate in a proportion corresponding to the total proportion of the mixture of the two modilying substances.
3. A plastic composition embodying an organic plastic substance characterized by a plurality of COC linkages and selected from the group consisting of cellulose derivatives, vinyl ester and vinyl acetal resins, and embodying a trialkyl phosphate, the alkyl radicals of which contain more than two but not more than six carbon atoms, in a proportion corresponding to more than 30 parts by weight of the trialkyl phosphate to parts by weight of the organic plastic substance, and embodying a phthalate ester selected from the group consisting of neutral dialkyl phthalate esters having not more than five carbon atoms in each alkyl group and neutral alkyl esters of phthalyl glycolic acid having not more than two carbon atoms in each alkyl group, in a proportion suflicient to impart to the plastic composition a degree of flexibility under subnormal temperature conditions without exudation of the trialkyl phosphate that is not attainable by means of the presence in the composition of the phthalate ester without the trialkyl phosphate in a proportion corresponding to the total proportion of the two plasticizing substances.
4. A plastic composition embodying a vinyl acetal resin and a mixture of two modifying substances, one of which is a neutral dialkyl phthalate ester having not more than five carbon atoms in each alkyl group, and the other of which is a trialkyl phosphate, the alkyl radicals of which latter substance contain more than two but not more than six carbon atoms, whereby a degree of flexibility under subnormal temperature conditions is imparted to the composition as a result of the synergistic action of the two modifying substances that is not attainable by means of the presence in the composition of the neutral alkyl phthalate ester modifying substance without the trialkyl phosphate in a proportion corresponding to the total proportion of the mixture of the two modifying substances.
5. A plastic composition embodying a polyvinyl acetal resin and embodying a mixture of two plasticizing substances, one of which is a trialkyl phosphate, the alkyl radicals of which contain more than two but not more than six carbon atoms, in a proportion corresponding to from 30 to 37 parts by weight to 100 parts by weight of the polyvinyl acetal resin, and the other of which is a phthalate ester selected from the group consisting of neutral dialkyl phthalate esters having not more than five carbon atoms in each alkyl group and neutral esters of phthalyl glycolic acid having not more than two carbon atoms in each alkyl group, in a proportion cor responding to from 30 to 37 parts by weight to 100 parts by weight of the polyvinyl acetal resin.
6. A plastic composition embodying a cellulose derivative and a mixture of two modifying substances, one of which is a neutral dialkyl phthalate ester having not more than five carbon atoms in each alkyl group, and the other of which is a trialkyl phosphate, the alkyl radicals of which latter substance contain more than two but not more than six carbon atoms, whereby a degree of flexibility under subnormal temperature conditions is imparted to the composition as a result of the synergistic action of the two modifying substances that is not attainable by means of the presence in the composition of the neutral alkyl phthalate ester modifying substance without the trialkyl phosphate in a proportion corresponding to the total proportion of the mixture of the two modifying substances.
'7. A plastic composition embodying cellulose acetate and embodying a mixture of two plasticizing substances, one of which is a trialkyl phosphate, the alkyl radicals of which contain more than two but not more than six carbon atoms, in a proportion corresponding to more than 50 parts by weight of the trialkyl phosphate to 100 parts of the cellulose acetate and the other of which is a phthalate ester selected from the group consisting of neutral dialkyl phthalate esters having not more than five carbon atoms in each alkyl group and neutral esters of phthalyl glycolic acid having not more than two carbon atoms in each alkyl group, in a proportion corresponding to more than parts by weight of the phthalate ester to 100 parts by weight of the cellulose acetate.
8. Safety glass including in combination a plurality of sheets of glass bonded together through the medium of a plastic composition as defined in claim 2.
9. Safety glass including in combination a plurality of sheets of glass bonded together through the medium of a plastic composition as defined in claim 3.
10. Safety glass including in combination a plurality of sheets of glass bonded together through the medium of a plastic composition as defined in claim 4.
11. Safety glass including in combination a plurality of sheets of glass bonded together through the medium of a plastic composition as defined in claim 5.
12. Safety glass including in combination a plurality of sheets of glass bonded together through the medium of a plastic composition as defined in claim 6.
13. Safety glass including in combination a plurality of sheets of glass bonded through the medium of a plastic composition as defined in claim 'I.
14. A transparent, rubbery sheet comprising 100 parts of a polyvinyl formaldehyde acetal resin and, as an elasticizer therefor, at least parts, approximately, of an alkyl phthalyl ethyl glycolate in which the alkyl group contains less than 3 carbon atoms.
ARNOLD KIRKPATRICK.
CERTIFICATE OF CORRECTION. Patent No. 2,290,195. July 21, 191m.
ARNOLD KIRKPATR ICK It is hereby certified that error appears in the printed specification of the above numbered patent requiring correction as follows: Page 1, first column, line 14.8, for the word "import" read -impart-; page 2 first column, line 19; for the numeral "514." read -55--; and that the said Letters Patent should be read with this correction therein that the same may conform to the record of the case in the Patent Office.
Signed and sealed this 25th day of August, A. D. 19142.
Henry Van Arsdale, (Seal) Acting Commissioner of Patents.
US112995A 1936-11-27 1936-11-27 Laminated glass Expired - Lifetime US2290193A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US112995A US2290193A (en) 1936-11-27 1936-11-27 Laminated glass

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US112995A US2290193A (en) 1936-11-27 1936-11-27 Laminated glass

Publications (1)

Publication Number Publication Date
US2290193A true US2290193A (en) 1942-07-21

Family

ID=22346985

Family Applications (1)

Application Number Title Priority Date Filing Date
US112995A Expired - Lifetime US2290193A (en) 1936-11-27 1936-11-27 Laminated glass

Country Status (1)

Country Link
US (1) US2290193A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2567327A (en) * 1947-02-21 1951-09-11 Celanese Corp Process of making pile fabric
US3388033A (en) * 1965-01-13 1968-06-11 Monsanto Co Laminated safety glass
US3406086A (en) * 1965-03-31 1968-10-15 Mobay Chemical Corp Transparent safety laminates and method of making same
US3793105A (en) * 1970-12-11 1974-02-19 Ici Ltd Glass laminates
US4361625A (en) * 1978-05-12 1982-11-30 Dynamit Nobel Aktiengesellschaft Plasticizer-containing films of partially acetalized polyvinyl alcohols

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2567327A (en) * 1947-02-21 1951-09-11 Celanese Corp Process of making pile fabric
US3388033A (en) * 1965-01-13 1968-06-11 Monsanto Co Laminated safety glass
US3406086A (en) * 1965-03-31 1968-10-15 Mobay Chemical Corp Transparent safety laminates and method of making same
US3793105A (en) * 1970-12-11 1974-02-19 Ici Ltd Glass laminates
US4361625A (en) * 1978-05-12 1982-11-30 Dynamit Nobel Aktiengesellschaft Plasticizer-containing films of partially acetalized polyvinyl alcohols

Similar Documents

Publication Publication Date Title
US2290193A (en) Laminated glass
US2032091A (en) Plasticized composition
US2720535A (en) Bis-(2-ethylhexyl) benzylphosphonate
US3579363A (en) Plasticized resin compositions
US2695279A (en) Vinyl plastic compositions and method of making the same
US3216840A (en) Cellulose ester article having reduced blushing
US2618568A (en) Self-extinguishing cellulose acetate molding compositions
US2372947A (en) Polyvinyl halide composition
US2156956A (en) Synthetic rubberlike compositions
US2360306A (en) Plastic polyvinyl acetal compositions
US1884619A (en) Derivatives of cellulose compositions of low inflammability containing cinnamic aciddibromide
US2327652A (en) Plastic composition for laminated glass interlayers
US2205420A (en) Safety glass
US2556420A (en) Use of pentavalent antimony compounds for stabilizing vinyl chloride resins
US2372980A (en) Cellulose derivative composition
US1969482A (en) Cellulose organic ester composition containing an ester of maleic acid
US2667504A (en) Trialkyl-1-benzoylpropane-1,2,3-tricarboxylates and process of preparing same
US2795566A (en) Resinous composition
US2510009A (en) Vinyl chloride resin plasticized with an aromatic hydrocarbon and stabilized by dypnone
US2511577A (en) Esters of anthracene acid adducts
US2253064A (en) Cellulosic compositions of matter containing organic ester amides
US2039744A (en) Cellulose organic ester composition containing an alpha-substituted phenylethyl alcohol
US2312963A (en) Plasticized polyvinyl acetal resin
US1942844A (en) Cellulose organic ester composition of matter containing an ester of dibromo succinic acid
US1933827A (en) Cellulose organic ester composition containing ethyl gamma-phenoxy butyrate