US596662A - Oskar nagel - Google Patents

Oskar nagel Download PDF

Info

Publication number
US596662A
US596662A US596662DA US596662A US 596662 A US596662 A US 596662A US 596662D A US596662D A US 596662DA US 596662 A US596662 A US 596662A
Authority
US
United States
Prior art keywords
solvent
pyroxylin
nitrocellulose
oskar
nagel
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
Publication date
Application granted granted Critical
Publication of US596662A publication Critical patent/US596662A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D101/00Coating compositions based on cellulose, modified cellulose, or cellulose derivatives
    • C09D101/08Cellulose derivatives
    • C09D101/16Esters of inorganic acids
    • C09D101/18Cellulose nitrate

Definitions

  • My invention relates to the manufacture of compounds'of pyroxylin by the use of a new solvent for nitrocellulose, which acts substantially in the'same manner as does gum-camphor I have discovered that the crystalline body formed by passing dry hydrochloric-acid gas through dry turpentine may be employed as a solvent for nitrocellulose either just as it is produced by passing the gas through the turpentine or after it has been subsequently treated to remove the hydrochlorid.
  • hydrochlorinated turpene (C H HGL)
  • camphene The body O H remaining after the hydrochlorid has been distilled 01f, as by the use of lime, is known as camphene.
  • either of these bodies may be used as a solvent for nitrocellulose in the same manner.
  • Persons skilled in the art of producing pyroxylin compounds will readily understand the manner of working this solvent with pyroxylin, as there is no essential diiference between it and the mode of working gum-oamphor.
  • hydrochlorinated turpene or the camphene may first be dissolved by any suitable solventas, for instance, the ethyl alcohol and ether above mentioned--and the nitrocellulose then added and that any of the known solvents for nitrocellulose or camphor may be employed.
  • any suitable solventas for instance, the ethyl alcohol and ether above mentioned--and the nitrocellulose then added and that any of the known solvents for nitrocellulose or camphor may be employed.
  • my newly-discovered solvent may be employed as a substitute for camphor in any of the known ways of using camphor for nitrocellulose, and the hydrochlorinated turpene and camphene may be mixed together and used as a solvent.
  • Iclaim- 1 The process of manufacturing pyroxylin compounds consisting of combining with nitrocellulose, a solvent consisting of the crystalline product produced by passing hydrochloric-acid gas through turpentine, substantially as set forth.

Description

UNITED STATES PATENT OFFICE.
OSKAR NAGEL, OFVIENNA, AUSTRIA-HUNGARY.
MANUFACTURE OF COMPOUNDS OF PYROXYLIN.
SPECIFICATION forming part of Letters Patent No. 596,662, dated January 4, 1898. Application filed February 3 1896. $eria1 No. 577,942- (No specimens.)
To all whom it may concern.-
Be it known that I, OSKAR NAGEL, a subject of the Emperor of Austria-Hungary, residing at Vienna, Austria-Hungary, have invented a certain new and useful Improvement in the Manufacture of Compounds of Pyroxylin, of which the following is a specification.
My invention relates to the manufacture of compounds'of pyroxylin by the use of a new solvent for nitrocellulose, which acts substantially in the'same manner as does gum-camphor I have discovered that the crystalline body formed by passing dry hydrochloric-acid gas through dry turpentine may be employed as a solvent for nitrocellulose either just as it is produced by passing the gas through the turpentine or after it has been subsequently treated to remove the hydrochlorid. The crystalline body produced by passing dry hydrochloric-aoid gas through anhydrous turpentine is known as hydrochlorinated turpene, (C H HGL) The body O H remaining after the hydrochlorid has been distilled 01f, as by the use of lime, is known as camphene. Either of these bodies may be used as a solvent for nitrocellulose in the same manner. Persons skilled in the art of producing pyroxylin compounds will readily understand the manner of working this solvent with pyroxylin, as there is no essential diiference between it and the mode of working gum-oamphor. However, as an example I will state that I prefer to dissolve the nitrocellulose in a suitable solventas, for instance, ethyl alcohol and etherin the proportions usually employed for dissolving nitrocellulose in the'manufacture of pyroxylin compoundsthat is to say, two parts of ethyl alcohol and eight parts of ether to dissolve ten parts of pyroxylin, all by weight. When the pyroxolin has been thoroughly dissolved, I add thereto in the usual way five parts, or about half of the weight of the pyroxylin, of the hydrochlorinated turpene or camphene. The compound may then be worked in the ordinary way to convert it intoa solid mass. I need not describe the mode of doing this, as it is well-known in the art. 1
I may also combine my new solvent with the nitrocellulose or pyroxylin by what is known as the dry process. In so doing I employ ten parts of pyroxylin to about half that weight of camphene or hydrochlorinated turpene. This is done by mixing the'bodies while in a ground state and then subjecting them to heat and pressure, whereby the turpene chlorid or camphene becomes a solvent without the aid of a liquid menstruum.
It will be understood by those skilled in the art that the hydrochlorinated turpene or the camphene may first be dissolved by any suitable solventas, for instance, the ethyl alcohol and ether above mentioned--and the nitrocellulose then added and that any of the known solvents for nitrocellulose or camphor may be employed. In fact my newly-discovered solvent may be employed as a substitute for camphor in any of the known ways of using camphor for nitrocellulose, and the hydrochlorinated turpene and camphene may be mixed together and used as a solvent.
I'have not found it necessary to add gumcamphor to aid the action of my newly-discovered solvent; but the addition of the same, if one chooses to add it, does not harm the product or interfere with the action of my solvent.
Iclaim- 1. The process of manufacturing pyroxylin compounds consisting of combining with nitrocellulose, a solvent consisting of the crystalline product produced by passing hydrochloric-acid gas through turpentine, substantially as set forth.
2. The process of manufacturing pyroxylin compounds consisting of combining with nitrocellulose the hydrochlorinated turpene (O I-I HOl) or camphene (C H as a solvent, substantially as set forth.
3. The process of manufacturing pyroxylin compounds consisting of combining with nitrocellulose hydorchlorinated turpene (G H H01) or camphene (C H as a solvent in connection with a liquid menstruum, substantially as set forth.
This specification signed and witnessed this 1st day of February, 1896.
OSKAR NAGEL.
Witnesses:
EUGENE CONRAN, J OHN RTAYLOR.
US596662D Oskar nagel Expired - Lifetime US596662A (en)

Publications (1)

Publication Number Publication Date
US596662A true US596662A (en) 1898-01-04

Family

ID=2665308

Family Applications (1)

Application Number Title Priority Date Filing Date
US596662D Expired - Lifetime US596662A (en) Oskar nagel

Country Status (1)

Country Link
US (1) US596662A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070149129A1 (en) * 2005-12-22 2007-06-28 Arnab Das Methods and apparatus for communicating transmission backlog information

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070149129A1 (en) * 2005-12-22 2007-06-28 Arnab Das Methods and apparatus for communicating transmission backlog information

Similar Documents

Publication Publication Date Title
US596662A (en) Oskar nagel
US718670A (en) Pyroxylin compound.
US1213369A (en) Explosive and method of producing same.
US600556A (en) Pyroxylin compound
US1041115A (en) Compound of acetyl cellulose and process of making such compound.
US494791A (en) Process of making pyroxyline compounds and their products
US710648A (en) Process of making acetyl chlorid.
US622292A (en) Transparent pyroxylin composition of matter
US852915A (en) Process of treating casein and compound obtained therefrom.
US282488A (en) Alexander bohbinger
US741554A (en) Pyroxylin compound.
US767943A (en) Process of dissolving nitrated cellulose.
US1653010A (en) Nitrocellulose lacquer
US552209A (en) Pyroxyline compound
US287972A (en) Compound for stiffening hats
US1067785A (en) Non-inflammable cellulose compound and method of making same.
US1089241A (en) Process for the synthetic preparation of ammonia from its constituents.
US658846A (en) Artificial oil of jasmin.
US1245476A (en) Non-inflammable cellulose compound and process of making the same.
US1199798A (en) Non-inflammable cellulose compound.
US1188797A (en) Plastic composition.
US647764A (en) Plastic compound.
US269343A (en) John h
US1207782A (en) Production of anhydrous hydrosulfites from aqueous hydrosulfite solutions.
US410209A (en) Charles robert schupphaus