US2071462A - Film - Google Patents

Film Download PDF

Info

Publication number
US2071462A
US2071462A US713770A US71377034A US2071462A US 2071462 A US2071462 A US 2071462A US 713770 A US713770 A US 713770A US 71377034 A US71377034 A US 71377034A US 2071462 A US2071462 A US 2071462A
Authority
US
United States
Prior art keywords
film
cellulose
mixture
alcohols
grams
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
US713770A
Other languages
English (en)
Inventor
Hagedorn Max
Ossenbrunner Armin
Wilmanns Gustav
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.)
GAF Chemicals Corp
Original Assignee
Agfa Ansco Corp
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 Agfa Ansco Corp filed Critical Agfa Ansco Corp
Application granted granted Critical
Publication of US2071462A publication Critical patent/US2071462A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00Photosensitive materials
    • G03C1/76Photosensitive materials characterised by the base or auxiliary layers
    • G03C1/795Photosensitive materials characterised by the base or auxiliary layers the base being of macromolecular substances

Definitions

  • Our present invention relates to photographic film and more particularly to such a film with an improved support.
  • phosphoric acid esters of an alcohol which is derived from a fatty acid such as trioctylphosphate, diisoamylbutylphosphate, diethylphosphate, or butylphosphate
  • softening agents have no dissolving action on cellulose derivatives and in contradistinction to the softening agents having a dissolving action on cellulose have a more favorable influence on the mechanical properties of the films made from cellulose derivatives.
  • softening agents having no dissolving action on cellulose ester and which are derived from vegetable oils containing the glycerides of fatty acids having from 8 tol l carbon atoms are particularly suited as softening agents for cellulose esters for the manufacture of supports of photographic films.
  • oils are, for'instance, cocoa nut oil, palm nut oil, and laurel-oil.
  • esters of the mixture of fatty acids obtained by saponification of the glycerides with a monovalent alcohol the esters of the alcohols obtained from the oils by simultaneous saponification and hydrogenation with aliphatic acids, or aromatic acids, or halogen hydracids, or phosphoric acid; the ethers of the aforesaid alcohols.
  • the softening agents are suitable for the ;manufacture of supports for photographic films they must not contain strongly smelling compounds. For this reason, for instance, the esters of the mixture of fatty acids from the above mentioned oils with methyl alcohol or ethyl al 3 cohol are not suitable.
  • the esters of such a fatty acid and propyl alcohol or a higher alcohol preferably an alcohol having more than 5 carbon atoms.
  • the separation of compounds of low molecular weight which yield strongly smelling constituents may be effected by distillation in the vacuum before or 7 after conversion of the oils into their derivatives. For the same reason the nitriles of fatty "acids are useless.
  • softeners for nitrocellulose.
  • the mixtures of softening agents are suitable for the preparation of films from cellulose nitrate and for films from organic cellulose ester, for instance, cellulose acetate; cellulose nitroacetate, cellulose acetobutyrate, cellulose butyrate and other technically useful cellulose esters. It is clear that not all of the products have the same action. A few experiments will be sufficient to ascertain which of the softeners suggested have the best effect for films made of a certain cellulose ester or a mixture of cellulose esters, to render it elastic and resistant to mechanical strain.
  • the conversion products of fatty acids with more than 14 carbon atoms have no longer the same good properties as softeners than have the conversion products of fatty acids with a number of carbon atoms between 8 and 14. Mixtures, containing a large amount of such fatty acids should therefore not be employed for the purpose in question.
  • the softeners for the manufacture of support for photographic films according to this invention can also be used in admixture with the softeners hitherto known for this purpose and even then an improved product will be obtained.
  • Example 1 -20 parts of nitrocellulose containing 12.2 per cent of nitrogen are dissolved in 100 parts of a'mixture consisting of 8 parts of acetone and 2 parts of ethyl alcohol while adding 2 parts of amyl ester of the acids from laurel oil containing 8 to 14 carbon atoms.
  • the solution is cast in known manner to form a film of 0.130 mm. thickness.
  • the process'of manufacturing a support for photographic layers which comprises dissolving cellulose acetate containing 56 per cent of acetic acid in a mixture of methylene chloride, chloroform and amylalcohol; adding as a softening agent diphenylphosphate havingthe last hydrogen atom'esterified by the alcohols containing 8 to 14 carbon atoms obtainable from cocoa nut oil, and triphenylphosphate and casting the solution to form a film.
  • a support for photographic layers comprising celluloseacetate containing 56 per cent of acetic acid and diphneylphosphate having the last hydrogen atom esterified by the alcohols containing 8 to 14 carbon atoms obtainable from cocoa nut oil. and triphenylphosphate.

Landscapes

  • Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • General Physics & Mathematics (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)
US713770A 1933-03-04 1934-03-02 Film Expired - Lifetime US2071462A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEI46681D DE683061C (de) 1933-03-04 1933-03-04 Herstellung photographischer Schichttraeger aus Cellulosederivaten

Publications (1)

Publication Number Publication Date
US2071462A true US2071462A (en) 1937-02-23

Family

ID=6477131

Family Applications (1)

Application Number Title Priority Date Filing Date
US713770A Expired - Lifetime US2071462A (en) 1933-03-04 1934-03-02 Film

Country Status (5)

Country Link
US (1) US2071462A (hu)
BE (1) BE401736A (hu)
DE (1) DE683061C (hu)
FR (1) FR769485A (hu)
GB (1) GB426023A (hu)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2464784A (en) * 1945-08-09 1949-03-22 Gen Aniline & Film Corp Film forming solution of cellulose acetate

Also Published As

Publication number Publication date
GB426023A (en) 1935-03-26
BE401736A (hu)
FR769485A (fr) 1934-08-27
DE683061C (de) 1939-10-28

Similar Documents

Publication Publication Date Title
US2139369A (en) Plastic compositions
US2465915A (en) Stabilized cellulose esters and ethers
US2071462A (en) Film
US2093464A (en) Cellulose esters containing succinyl groups and process of making same
US2126460A (en) Preparation of cellulose esters containing dicarboxylic acid radicals
US1668946A (en) Process of reacetylating cellulose acetate
US2497135A (en) Polymeric sulfurous acid esters
US3000747A (en) Ester of 2,2 dimethyl-hydracrylic acid, 3 hydroxy 2,2 dimethylpropyl ester and resinous materials plasticized therewith
US2023485A (en) Preparation of esters derived from dicarboxylic acids and polyhydroxy compounds
US2107202A (en) Glycerol monolactate triacetate and process of making same
US1309980A (en) Hants t
US1818108A (en) Process of manufacturing celluloid-like masses
US2253064A (en) Cellulosic compositions of matter containing organic ester amides
US2170030A (en) Preparation of mixed dicarboxylic acid esters of polyhydroxy compounds and monohydroxy alcohols
US2253821A (en) Plasticized organic solvent soluble cellulosic film
US2102016A (en) Method of separating an organic acid ester of cellulose from its reaction mixture
US1848155A (en) Esters of secondary butyl alcohol
US1388472A (en) Plastic compound and process
US1704283A (en) Soluble halogen substituted cellulosic organic acid esters
US2029925A (en) Cellulose organic ester compositions containing a propionyl ester of glycerol
US1957868A (en) Cellulose acetate composition
US2101994A (en) Preparation of cellulose acetate propionate butyrate
US1600700A (en) Cellulose-ester plastic and solution
US2383897A (en) alpha-naphthylmethyl esters of hydroxy-aliphatic acids
US3100717A (en) Ultraviolet light stabilized cellulose ester plastic composition