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US2058786A - Light protective wrapper - Google Patents

Light protective wrapper Download PDF

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Publication number
US2058786A
US2058786A US51305831A US2058786A US 2058786 A US2058786 A US 2058786A US 51305831 A US51305831 A US 51305831A US 2058786 A US2058786 A US 2058786A
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US
United States
Prior art keywords
light
paper
quinine
light protective
protective
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
Inventor
Dudley H Grant
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.)
Stanco Inc
Original Assignee
Stanco Inc
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 Stanco Inc filed Critical Stanco Inc
Priority to US51305831 priority Critical patent/US2058786A/en
Application granted granted Critical
Publication of US2058786A publication Critical patent/US2058786A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04Coating
    • C08J7/0427Coating with only one layer of a composition containing a polymer binder
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2301/00Characterised by the use of cellulose, modified cellulose or cellulose derivatives
    • C08J2301/06Cellulose hydrate
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2401/00Characterised by the use of cellulose, modified cellulose or cellulose derivatives
    • 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]
    • Y10T428/31971Of carbohydrate
    • Y10T428/31975Of cellulosic next to another carbohydrate
    • Y10T428/31978Cellulosic next to another cellulosic
    • Y10T428/31986Regenerated or modified

Definitions

  • wrappers of paper, cloth, transparent films of cellulose or hydroxycellulose made by precipitation from viscose, cuprammonium or other cellulose solutions), gelatine, acetylcellulose, nitrocellulose, pyroxylin or other thin flexible material, such as are used to wrap commodities which may be injuriously affected by sunlight .or other actinic light, may be rendered wholly or partially impervious to such light by means of substantially colorless substances having the property of absorbing light waves of short wave length.
  • the following substances may, for example, be used in the preparation of light protective wrappers according to the present invention: quinine and its salts, aesculin, methyl esters of naphthalene carboxylic acids, salts of naphthol sulfonic acids, phthalic acid salts, and in. general protective substance to the solvent used in the manufacture of the pyroxylin material.
  • Such or similar methods may be used with other thin 40 flexible materials to incorporate the light protective ingredient.
  • one or more layers containing the protective substance may also be used.
  • the amount of the ingredient added depends on the substance and also on the degree of light protection desired and correspondingly may be varied within large limits.
  • Example 1 Sheets of paper preferably the translucent paper known in the trade as glassine, are coated on one 'or both sides with a lacquer composed 5 approximately as follows:
  • Per cent FYIOXylin 3 Amyl acetate or other medium boiling solvent. 5-25 10 Aesculin 0.5-5 Monoethyl ether of ethylene glycol or other blending agent 3-10 Ethyl acetate, acetone or other low boiling solvent 10-30 15 Castor oil or other plasticizer 2- 5 Benzol, toluol, naphtha or other diluent 30-70
  • aesculin in the above example may be substituted quinine alkaloid, quinine ricinoleate, linoleate or other quinine salt compatible with the lacquer film, phenanthrene, anthracene, or other substances of the types specified above.
  • Example 2 In the manufacture of thin sheets of cellulose or hvdroxycellulose by regeneration (coagula-' tion) from solutions of viscose, some of the lightprotective materials specified above may be incorporated with the viscose solution before 00- 'agulation. Among such substances may be mentioned the sodium salts of carboxylic or sulfonic acids derived from naphthalene, anthracene; phenanthrene, fiuorene and other conjugated hydrocarbons. '35
  • the transparent sheets of regenerated cellulose or hydroxycellulose, after washing and drying, may also be coated with lacquers as described in Example 1.
  • Example 3 V 40 1% to 20%. The sizing solution is then applied to paper or cloth.
  • Example 5 Transparent films, wrappers, caps, capsules, etc., made of gelatine, gelatine-glycerine, formaldehyde-gelatine or chromated gelatine have water-soluble protective substances such as quinine bisuli'ate, sodium naphthalene sulfonates or other salts of sulfonic or carboxylic acids of conjugated hydrocarbons, added to the gelatine solution in amounts of 1% to 30% before drying coagulating or exposing to light.
  • water-soluble protective substances such as quinine bisuli'ate, sodium naphthalene sulfonates or other salts of sulfonic or carboxylic acids of conjugated hydrocarbons
  • Example 6 To paper pulp in the heater is added a solution capable of furnishing a water-insoluble lightprotective substance of the classes mentioned above, when such solution is decomposed by subsequent addition of another reagent such as acid or alkali, and the protective substance is thereupon precipitated in intimate contact with the paper fiber, remaining in the finished paper.
  • a solution capable of furnishing a water-insoluble lightprotective substance of the classes mentioned above, when such solution is decomposed by subsequent addition of another reagent such as acid or alkali, and the protective substance is thereupon precipitated in intimate contact with the paper fiber, remaining in the finished paper.
  • another reagent such as acid or alkali
  • water-insoluble protective substances of acid nature such as naphthalene carboxylic acids
  • naphthalene carboxylic acids may be precipitated in the pulp by adding their alkali salts to the pulp and then acidifying it with hydrochloric or other acid.
  • Subsequent acidification then precipitates the carboxylic acids mixed with rosin acids, which aid in their fixation in the paper fiber.
  • 15 lbs. of sodium naphthalene beta-carboxylate and 20 lbs. of sodium resinate are dissolved in water containing 1,000 lbs. of paper stock in the beater.

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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)
  • Paper (AREA)

Description

Patented Oct. 27,. 1936 PATENT OFFICE LIGHT PROTECTIVE WRAPPER Dudley H. Grant, Berkeley Heights, N. J., assignor to Stanco Inc., a corporationof Delaware No Drawing.
Application February 2, 1931, Serial No. 513,058
. 2 Claims. (01. 91-68) This invention relates to light protective wrappers and the process of making the same and will be fully understood from the following description.
I have discovered that wrappers of paper, cloth, transparent films of cellulose or hydroxycellulose (made by precipitation from viscose, cuprammonium or other cellulose solutions), gelatine, acetylcellulose, nitrocellulose, pyroxylin or other thin flexible material, such as are used to wrap commodities which may be injuriously affected by sunlight .or other actinic light, may be rendered wholly or partially impervious to such light by means of substantially colorless substances having the property of absorbing light waves of short wave length.
The following substances may, for example, be used in the preparation of light protective wrappers according to the present invention: quinine and its salts, aesculin, methyl esters of naphthalene carboxylic acids, salts of naphthol sulfonic acids, phthalic acid salts, and in. general protective substance to the solvent used in the manufacture of the pyroxylin material. Such or similar methods may be used with other thin 40 flexible materials to incorporate the light protective ingredient. Laminated sheets of two or more layers of the same or difierent materials,
one or more layers containing the protective substance, may also be used.
. The amount of the ingredient added depends on the substance and also on the degree of light protection desired and correspondingly may be varied within large limits.
The following examples will serve to illustrate 60 my process and the method of carrying it out.
Example 1 Sheets of paper, preferably the translucent paper known in the trade as glassine, are coated on one 'or both sides with a lacquer composed 5 approximately as follows:
Per cent FYIOXylin 3 Amyl acetate or other medium boiling solvent. 5-25 10 Aesculin 0.5-5 Monoethyl ether of ethylene glycol or other blending agent 3-10 Ethyl acetate, acetone or other low boiling solvent 10-30 15 Castor oil or other plasticizer 2- 5 Benzol, toluol, naphtha or other diluent 30-70 For aesculin in the above example may be substituted quinine alkaloid, quinine ricinoleate, linoleate or other quinine salt compatible with the lacquer film, phenanthrene, anthracene, or other substances of the types specified above.
Example 2 In the manufacture of thin sheets of cellulose or hvdroxycellulose by regeneration (coagula-' tion) from solutions of viscose, some of the lightprotective materials specified above may be incorporated with the viscose solution before 00- 'agulation. Among such substances may be mentioned the sodium salts of carboxylic or sulfonic acids derived from naphthalene, anthracene; phenanthrene, fiuorene and other conjugated hydrocarbons. '35
The transparent sheets of regenerated cellulose or hydroxycellulose, after washing and drying, may also be coated with lacquers as described in Example 1.
Example 3 V 40 1% to 20%. The sizing solution is then applied to paper or cloth.
Example 5 Transparent films, wrappers, caps, capsules, etc., made of gelatine, gelatine-glycerine, formaldehyde-gelatine or chromated gelatine have water-soluble protective substances such as quinine bisuli'ate, sodium naphthalene sulfonates or other salts of sulfonic or carboxylic acids of conjugated hydrocarbons, added to the gelatine solution in amounts of 1% to 30% before drying coagulating or exposing to light.
Example 6 Example 7 To paper pulp in the heater is added a solution capable of furnishing a water-insoluble lightprotective substance of the classes mentioned above, when such solution is decomposed by subsequent addition of another reagent such as acid or alkali, and the protective substance is thereupon precipitated in intimate contact with the paper fiber, remaining in the finished paper. For example, to 1,000 lbs. of paper stock inthe pulp state in the beater is added '10 lbs. of quinine hydrochloride dissolved in water. To the mixture is then added an amount of sodium resinate, stearate, etc., equivalent to the quinine salt or in slight excess, thereby precipitating quinine resinate, stearate, etc., in the pulp. For sodium resinate or stearate may be substituted any alkali salt of an acid of which the quinine salt is insoluble in water.
Similarly, water-insoluble protective substances of acid nature, such as naphthalene carboxylic acids, may be precipitated in the pulp by adding their alkali salts to the pulp and then acidifying it with hydrochloric or other acid. In this case. I find it advantageous to combine the sodium salts of naphthalene carboxylic acids (or carboxylic acids of other conjugated hydrocarbons) with sodium resinate. Subsequent acidification then precipitates the carboxylic acids mixed with rosin acids, which aid in their fixation in the paper fiber. For example, 15 lbs. of sodium naphthalene beta-carboxylate and 20 lbs. of sodium resinate are dissolved in water containing 1,000 lbs. of paper stock in the beater. After thorough mixing, 2 gallons, or a suitable slight excess, of hydrochloric acid is gradually added. In either case, when the pulp passes to the paper machine, it retains the light-protective substance intimatelymixed with the fiber, and remaining in the finished paper.
Having thus described my invention and the method of carrying it out what I claim is:
1. A thin, flexible transparent wrapper of regenerated cellulose, for articles tending to deteriorate if subjected to actinic light, said wrapper comprising a colorless substance adapted to prevent the passage of objectionable amounts of such light, in which the colorless substance is a coating having the following approximate composition:
Per cent Pyroxylin 3 Amyl acetate or other medium boiling solvent 5-25 Colorless absorber of actinic light 0.5- 5 Monoethyl ether of ethylene glycol or other blending agent Ethyl acetate, acetone or other low boiling solvent 10-30 Castor oil or other plasticizer. 2- 5 Benzol, toluol, naphtha or other diluent 30-70 2. A wrapper according to claim 1 in which the colorless absorber of actinic light is aesculin.
DUDLEY H. GRANT.
US51305831 1931-02-02 1931-02-02 Light protective wrapper Expired - Lifetime US2058786A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2418818A (en) * 1941-08-14 1947-04-15 Rile Coe Filter Process Inc Packaging material and process covered thereby
US2598506A (en) * 1947-04-09 1952-05-27 Rile Coe Filter Process Inc Packaged dairy products and process thereof
US2600093A (en) * 1947-04-09 1952-06-10 Rile Coe Filter Process Inc Packaged bakery products and process thereof
US2631499A (en) * 1945-07-23 1953-03-17 Rile Coe Filter Process Inc Selected light transmission and protective materials
US2749252A (en) * 1951-10-31 1956-06-05 Philco Corp Method of applying an organic film to a phosphor layer

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2418818A (en) * 1941-08-14 1947-04-15 Rile Coe Filter Process Inc Packaging material and process covered thereby
US2631499A (en) * 1945-07-23 1953-03-17 Rile Coe Filter Process Inc Selected light transmission and protective materials
US2598506A (en) * 1947-04-09 1952-05-27 Rile Coe Filter Process Inc Packaged dairy products and process thereof
US2600093A (en) * 1947-04-09 1952-06-10 Rile Coe Filter Process Inc Packaged bakery products and process thereof
US2749252A (en) * 1951-10-31 1956-06-05 Philco Corp Method of applying an organic film to a phosphor layer

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