US1858993A - Process for producing cellulose esters - Google Patents

Process for producing cellulose esters Download PDF

Info

Publication number
US1858993A
US1858993A US302138A US30213828A US1858993A US 1858993 A US1858993 A US 1858993A US 302138 A US302138 A US 302138A US 30213828 A US30213828 A US 30213828A US 1858993 A US1858993 A US 1858993A
Authority
US
United States
Prior art keywords
cellulose
swelling
acid
fibres
swollen
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
US302138A
Inventor
Heberlein Georges
Bodmer Albert
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.)
Heberlein and Co AG
Original Assignee
Heberlein and Co AG
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 Heberlein and Co AG filed Critical Heberlein and Co AG
Application granted granted Critical
Publication of US1858993A publication Critical patent/US1858993A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08BPOLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B1/00Preparatory treatment of cellulose for making derivatives thereof, e.g. pre-treatment, pre-soaking, activation
    • C08B1/02Rendering cellulose suitable for esterification

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biochemistry (AREA)
  • Materials Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)

Description

Patented May 17, 1932 STATES PATENT oFFicE GEORGES HEBERLEIN AND ALBERT BODMER, OF WATTWIL, SWITZERLAND, ASSIGNOBS TO HEBERLEIN & 00., A G., F 'WA'I'TWIL, SWITZERLAND, A CORPORATION OF SWITZ PROCESS FOR PRODUCING GELLULOSE ESTEIRS No Drawing. Application filed August 25, 1928, Serial No. 302,138, and in Germany September 30, 1927.
This invention relates to a process for producing cellulose esters.
The object of the invention is to effect esterification of the cellulose in a more expeditious and efiective manner.
It has been known that the reaction in the esterification of cellulose is a slow one; and in order to improve same in the case of acetyl cellulose it has been proposed to first convert the cellulose by a pretreatment into hydro-cellulose by treating the cellulose with very dilute sulphuric acid (3% sulphuric acid) and then drying and heating the cellulose. The resulting hydro-cellulose was then acetylized by treating it with acetic anhydride in the presence of sulphuric acid. According to said known treatment the sulphuric acid was too weak to bring about a swelling action of the cellulose fibre, i. e., too
weak to act as a swelling means for the fibres; but the heating of the fibres when dry was required to convert the cellulose into hydrocellulose, i. e., to effect a hydrolyzation of the cellulose.
undesirable as it changes the cellulose structurally in a manner to effect a certain destruction or disintegration in the cellulose which is undesirable in the treatment, since it results in a substantially useless or a very 3o inferior product for the production of artificial silk, films, etc. This process was therefore given up.
We have discovered that the esterification of cellulose can be accomplished in a rapid and uniform manner if instead of hydrolyzing the cellulose fibres (such for example as cotton fibres) as heretofore proposed, the fibres are pretreated so as to cause them to swell, and while in the swollen state they are subjected to the action of the reagent or reagents. The object of the swelling action is to bring about a physical change in the fibres such as to render the material thereof more readily accessible to the reagent. .The swelling should be carried out preferably without hydrolyzation, and in any event without substantial hydrolyzation, it being desirable where an acid swelling agent is used for the pretreatment, to effect the swelling in such manner as to avoid, if possible, any hy- This. hydrolyzation, however, is.
drolyzation of the fibres. It is also important that the swollen condition of the fibres is maintained until the esterifying reagent is applied, and that undesirable coagulation of the swollen fibres should not take place before the esterifying reagent is applied.
Further objects and advantages of the invention will more fully appear from the following description of some preferred methods of carrying out the invention.
As suitable swelling agents there may be used such of the known or usual swelling agents as are of an acid character or of a socalled neutral character; as distinguished from those of an alkaline character. For example there may be used concentrated mineral acids such as sulphuric, phosphoric, nitric, hydrochloric or the like, either separately or in mixtures; also salts having swelling properties, such for example as zinc chloride, calcium thiocyanate, etc. While these salts are not in a strict technical sense exactly neutral, yet for the purpose of this invention they may be regarded as neutral in comparison to the acid swelling agents and to the 7 alkaline swelling agents such as -caustic and Schweitzers solution. Alkaline swelling agents are to be avoided because if they are used, then when the swollen fibres are treated with the esterifying mixture, which is acid, 30 there will take place a momentary coagulation, and hence a destruction of the desired swollen state of the fibres. Alkaline swelling agents are therefore not usable unless some means should be provided whereby this re- 5 sulting undesirable coagulation could be overcome.
The character and strengths of the various swelling agents, the duration of treatment of various kinds of cellulosic fibres thereby, etc., to effect swelling without detri mental efi'ect to the particular fibres treated, are now all well understood and need not, be detailed. Those skilled in the art also now known that when acid swelling agents are used on cellulosic fibres, that if the swelling action is'permitted to continue after the swelling of the fibres has taken eflect, the undesirable hydrolyzation may take place; and care should be taken to stop the action of the acid swelling agent in time to avoid, if possible, any hydrolyzation of the fibres.
As is known, the strength of the agent, the character of the fibres, and other factors and conditions will come into consideration in determining the permissible length of the swelling treatment in each case, so that no' go this mixture upon the fibres, the fibres after water or organic solvents having been swollen can be washed out so that the residue of swelling agent is reduced to an uninJurious quantity or is removed altogether. The swelling agent can be washed out by as for instance alcohol, glacial acetic acid, or acetone. The washing means can be removed in any suitable manner as for example by squeezing out or centrifuging the fibres, etc.; but drying must be avoided.
upon by the reagents.
The esterification of the swollen fibres is carried out in known manner as for example with concentrated organic acid, acid anhydrides, acid chlorides or reagents having a similar action, and if necessary or desirable utilizing therewith a catalizer. After the reaction has taken place the mass is poured P into water or into a precipitating bath and the converted cellulose is isolated. The primary esters that are formed may also be converted into the more readily soluble secondary products in well known manner by means of partial saponification or transformation. The products that are obtained may be dissolved in the usual solvents, for example, acetone, chloroform, pyridin, etc.; and out of this solution artificial silk, films or lacquers can be produced. The production of moulded structures may also be effected by means of direct coagulation of the said mass.
As the materials to be treated, one may use any suitable cellulosic material or cellulosiccontaining substance capable of being acted For example, cellulosic fibres such as cotton may be used or other cellulosic material preferably in the form of finely divided fibrous material; but moderately reduced material may also be utilized such as wood splinters or the like, capable of being acted upon by the reagents; also paper pulp may be used.
Examples 1. Previously bleached cotton waste is introduced into sulphuric acid of 62% strength in the cold state, and is left therein for several minutes until swollen. The sulphuric acid is then drawn off and the surplus acid is pressed out, the remaining substance (swollen fibres) being then introduced into the esterifying mixture which may consist of 6 parts of acetic acid anhydride and 6 parts of glacial acetic acid, these parts being by weight with relation to the unit of weight of the dry cellulosic fibre. The temperature is maintained below about 40 C. by means of cooling. The reaction sets in very rapidly and is concluded in a quarter of an hour, whereupon the product can be isolated by precipitation in water.
2. Cleaned or purified loose cotton is allowed to swell for a quarter of an hour in nitric acid of 7 0% strength, whereupon most of the acid is removed by pressing. The residue of the nitric acid is then removed from the fibres by washing by means of glacial acetic acid,
whereupon the mass is pressed out again. Thereupon the esterifying mixture is caused to act on the mass while in the swollen state. This mixture may consist of 4: parts of acetic acid anhydride, 4: parts of glacial acetic acid and 0.15 parts of concentrated sulphuric acid, these parts being by weight with relation to the unit of weight of the dry cotton. The temperature is kept below about 30 C. and the reaction is completed in two hours. The esterify cellulose is now removed by precipitation in the usual manner.
As heretofore stated, coagulation or drying of the swollen goods should be avoided rior to the esterifying reaction and care should be taken to avoid detrimental hydrolyzation.
By the use of the term neutral character as used in the specification and claims to characterize the swelling agents, we wish to be understood as using the term in its broader sense, i. e., as meaning swelling agents which are substantially neutral in character, as contrasted with the decided acid or sour character of the acid swelling agents and as contrasted with the decided alkaline character of what are generally known as alkaline swelling agents, such for example as caustic acid and Schweitzers solution. Also, by the term suitable swelling agent as used in the claims, we wish to be understood as including swelling agents of acid and neutral character as herein mentioned, and also any other swelling agents of an acid or neutral character having similar action for the purpose.
Thus while we have described our improvements in detail and with respect to certain preferred forms, we do not desire to be limited to such details or forms since, as will be understood by those skilled in the art after understanding our invention, many changes and modifications may be made and the invention embodied in widely different forms which comprises producing a swelling action tion, treating said material with a reagent to esterify it.
Having thus described our invention, what we claim as new anddesire to secure by Let- 5 or more of the appended claims.
ters Patent, is:
1. Pprocess of producing cellulose esters in the cellulose withoutsubstantial production of hydrocellulose, and while it is in the swollen condition and not alkaline in reaction, treating said cellulose with a reagent to 2. Process of producing cellulose esters without; substantial production of hydro! cellulose, and while it is in swollen condition, treating said material with a reagent to 10. Process of producing acetyl cellulose ,which comprises treating cellulose with a strong mineral acid to swell the material without substantial "production of hydrocellulose, and while \it is in swollen condi- 'acetylize it. I I
In testimony whereof we have signed our names to this specification.
GEORGES HEBERLEIN} ALBERT BODMER.
which comprises swelling the cellulose without substantial production of hydrocellulose by treating it 'witha non-alkaline swelling agent and while-swollen treating said cellu lose with a,reagent to esterify it.
3. Process of producing cellulose esters which comprises treating thecellulose without substantial production of hydrocellulose with a non-alkaline swelling agent until the material is swollen, removing the excess swelling agent from the ccellulose and thereupon treating said swollen material with a reagent to esteri'fy it.
' 4. Process of producing cellulose esters 4 which comprises treating the cellulose without substantial production of hydrocellulose with a swelling agent to swell the same a d thereupon treating the swollencellulose with 5 a reagent to esterify it. o a
5. Process of producing-cellulose esters which comprises treating the cellulose without substantial production of hydrocellulose with a, swelling agent to swell the same, removing the excess swelling agent from the cellulose and theteupon treatingthe swollen cellulose with a reagent'to esterify it.
6. Process of producing cellulose esters which'comprises treating the cellulose without substantial production of hydrocellulose with a non-alkaline swelling agent until the material is swollen, washing the swollen celluloseland thereupon treating said cellulose with a reagent to esterify it.
7. Process of producing acetyl cellulose 4 esters which comprises treating the cellulose without substantial production of hydrocellulose with a swelling agent to swell the same,
removing the excess swelling $5 cellulose, then washing'the cellulose to removean additional amount of the swelling agent from tha agent therefrom, and thereupon treating the swollen material with a reagent to acetylize it.
8. As a product'of" manufacture, a cellulose ester made according to-the process of claim 1. v
9. Process of producing acyl cellulose which comprises treating cellulose with a strong mineral acid to swell the material I CERTIFICATE 01 commtmon :mm No. 1,858,993 ",Ma u', 1932. f
GEORGES mum ET AL.
' It ilsherebg cettified that error appears in the minted speciiicatibn at the above numbened patent requiring correction as follnwszL Page 1, line 95, for "known? read know; page Byline 51, claim 7, strike out the word "esters";' and that the said Letters Patent should be read with these cot ection therein that the same may conform, to" the record of the case in the Patent Offine'. Signed and sealed this 12th day of July, B 1932.
' Mr'J. Moore, Seal Acting Commissioner of'Patents,
US302138A 1927-09-30 1928-08-25 Process for producing cellulose esters Expired - Lifetime US1858993A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE1858993X 1927-09-30

Publications (1)

Publication Number Publication Date
US1858993A true US1858993A (en) 1932-05-17

Family

ID=7746394

Family Applications (1)

Application Number Title Priority Date Filing Date
US302138A Expired - Lifetime US1858993A (en) 1927-09-30 1928-08-25 Process for producing cellulose esters

Country Status (1)

Country Link
US (1) US1858993A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2484455A (en) * 1946-03-26 1949-10-11 Eastman Kodak Co Method of continuously esterifying cellulose
US2772944A (en) * 1953-03-27 1956-12-04 American Viscose Corp Process for the acetylation of regenerated cellulose fibers and product resulting therefrom
US2828304A (en) * 1954-11-18 1958-03-25 Eastman Kodak Co Method of preparing cellulose propionate isobutyrate

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2484455A (en) * 1946-03-26 1949-10-11 Eastman Kodak Co Method of continuously esterifying cellulose
US2772944A (en) * 1953-03-27 1956-12-04 American Viscose Corp Process for the acetylation of regenerated cellulose fibers and product resulting therefrom
US2828304A (en) * 1954-11-18 1958-03-25 Eastman Kodak Co Method of preparing cellulose propionate isobutyrate

Similar Documents

Publication Publication Date Title
US2243765A (en) Treatment of cellulosic textile materials
US1858993A (en) Process for producing cellulose esters
US4385172A (en) Prevention of hornification of dissolving pulp
US2478396A (en) Activation of cellulose for acylation
US2190445A (en) Regenerated cellulose ether product
US2074339A (en) Preparation of cellulosic material
US2848343A (en) Process for producing cellulose triesters
US2164416A (en) Process for the production of cellulosic products
US1911030A (en) Purification of cellulosic material
US2261237A (en) Manufacture of cellulose derivatives
US920828A (en) Process of making a cellulose material.
US2024381A (en) Esterification of cellulose
US2122572A (en) Manufacture of cellulose derivatives
GB399508A (en) Improvements in cellulosic materials
US1742611A (en) Cellulose esters and the manufacture thereof
US2071333A (en) Manufacture of organic esters of cellulose
US2426982A (en) Production of cellulose esters
US2512983A (en) Mixed cellulose esters and process of making same
US2138283A (en) Conditioning of wood pulp for nitration
US1925309A (en) Manufacture of cellulose esters
US2159015A (en) Manufacture of artificial materials
US1884802A (en) Inorganic cellulose esters and manufacture thereof
GB343712A (en) Improvements in or relating to processes for the production of organic acid esters of cellulose
US1697907A (en) Cellulosic material and product obtained therefrom
US1936189A (en) Manufacture of cellulose esters