US3655326A - Acetylation of textile articles of cellulose - Google Patents
Acetylation of textile articles of cellulose Download PDFInfo
- Publication number
- US3655326A US3655326A US874366A US3655326DA US3655326A US 3655326 A US3655326 A US 3655326A US 874366 A US874366 A US 874366A US 3655326D A US3655326D A US 3655326DA US 3655326 A US3655326 A US 3655326A
- Authority
- US
- United States
- Prior art keywords
- acetylation
- bath
- acetic anhydride
- cellulose
- percent
- 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
Links
- 239000004753 textile Substances 0.000 title claims abstract description 23
- 229920002678 cellulose Polymers 0.000 title claims description 17
- 239000001913 cellulose Substances 0.000 title claims description 17
- 230000021736 acetylation Effects 0.000 title abstract description 50
- 238000006640 acetylation reaction Methods 0.000 title abstract description 50
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 claims abstract description 114
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 claims abstract description 54
- 238000000034 method Methods 0.000 claims abstract description 31
- 235000011056 potassium acetate Nutrition 0.000 claims abstract description 27
- 239000004627 regenerated cellulose Substances 0.000 claims abstract description 15
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 14
- -1 alkali metal acetate Chemical class 0.000 claims abstract description 14
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 92
- 238000001035 drying Methods 0.000 claims description 7
- 229920001407 Modal (textile) Polymers 0.000 claims description 6
- 239000007864 aqueous solution Substances 0.000 claims description 6
- 229920003043 Cellulose fiber Polymers 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 2
- 239000003054 catalyst Substances 0.000 abstract description 6
- 239000000470 constituent Substances 0.000 abstract description 6
- 239000012345 acetylating agent Substances 0.000 abstract description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- 238000004090 dissolution Methods 0.000 description 9
- 239000000835 fiber Substances 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 5
- 239000003085 diluting agent Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 229920002301 cellulose acetate Polymers 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000002759 woven fabric Substances 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- LUTSRLYCMSCGCS-BWOMAWGNSA-N [(3s,8r,9s,10r,13s)-10,13-dimethyl-17-oxo-1,2,3,4,7,8,9,11,12,16-decahydrocyclopenta[a]phenanthren-3-yl] acetate Chemical compound C([C@@H]12)C[C@]3(C)C(=O)CC=C3[C@@H]1CC=C1[C@]2(C)CC[C@H](OC(=O)C)C1 LUTSRLYCMSCGCS-BWOMAWGNSA-N 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
- D06M13/184—Carboxylic acids; Anhydrides, halides or salts thereof
- D06M13/188—Monocarboxylic acids; Anhydrides, halides or salts thereof
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F2/00—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof
- D01F2/24—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof from cellulose derivatives
- D01F2/28—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof from cellulose derivatives from organic cellulose esters or ethers, e.g. cellulose acetate
Definitions
- ABSTRACT The heterogeneous acetylation of regenerated cellulose textile articles is carried out using acetic anhydride as the acetylating agents and an alkali metal acetate, especially potassium acetate, as catalyst at l00135 C., keeping the acetic anhydride content of the acetylation bath above 95 percent by weight, and also keeping the constituent filaments of the articles at constant length.
- the process is quick and thus suitable for continuous operation, and avoids mutual cohesion of the filaments as a result of softening or partial solution.
- the invention relates to the production of textile articles of cellulose acetate by acetylation of textile articles of regenerated cellulose, without going through the stage of dissolving the cellulose.
- This method of acetylation, in which the structures are preserved, is generally called heterogeneous acetylation.
- the present invention provides a new process of heterogeneous acetylation which makes it possible, without using a diluent, to acetylate textile articles of regenerated cellulose up to a combined acetic acid content between 50 percent and 62.5 percent without partial dissolution of the acetylated articles, and in less than 10 minutes.
- the process of the invention comprises treating textile articles of regenerated cellulose, at a temperature between 100 C. and 135 C., and in the presence of an alkali metal acetate, with a bath containing more than 95 percent by weight of acetic anhydride, keeping the acetic anhydride content constantly above 95 percent by weight by removing impurities formed and introducing fresh acetic anhydride, and maintaining the constituent filaments of the articles at a substantially constant length throughout the treatment.
- the acetylation can be carried out on various cellulose textile articles, for example yarns, tows, woven fabrics or knitted fabrics of regenerated cellulose which does not possess a fibrillar structure, or of Polynosic regenerated cellulose having a fibrillar and oriented micro-structure. It can be carried out discontinuously but because the time required for the acetylation is short it is particularly advantageous to carry out the process continuously.
- Potassium acetate is preferably employed as the alkali metal acetate catalyst and is used in aknown manner; preferably, it is incorporated in the textile articles before the acetylation by passing them continuously through an aqueous solution, preferably saturated, of the potassium acetate, and then drying them with hot air, for example at a temperature of 150 to 180 C. for 1 to 2 minutes.
- the impregnated articles preferably contain to 180 g. of potassium acetate per 100 g. of cellulose.
- the bath used for the acetylation must contain more than percent by weight of acetic anhydride, and preferably contains 99 percent of acetic anhydride and 1 percent of acetic acid.
- acetic anhydride is consumed and acetic acid formed; part of this acetic acid combines with potassium acetate in the bath to yield a complex compound of potassium acetate and acetic acid.
- the acetic anhydride content of the acetylation bath can be maintained above 95 percent by any continuously operating system which allows acetic anhydride to be replaced at the rate at which it is consumed, and the acetic acid produced by the acetylation to be removed, either in the form of free acid or in the form of a complex compound of potassium acetate and acetic acid.
- free acetic anhydride is introduced into the acetylation bath, and an equivalent amount of the bath is continuously withdrawn throughout the duration of the treatment.
- the acetylated articles are treated according to known processes to free them from unreacted acetic anhydride, free acetic acid and the complex compound of potassium acetate and acetic acid with which they may still be contaminated. This can be done, for example, by treating them first with benzene to remove the acetic anhydride and then with water to remove any acetic acid and its complex compound with potassium acetate, and finally drying them in an oven at a temperature of about 100 C.
- the acetylated articles can alternatively be treated, as they leave the acetylation bath, with a stream of hot air at a temperature between and 150 C. for a period which can be between 2 and 7 minutes so as to evaporate the acetic anhydride, then washed with water to remove any acetic acid and its complex compound with potassium acetate, and finally dried in an oven at a temperature of about 1 10 C.
- the acetylated articles so obtained have suffered no partial dissolution while passing through the acetylation bath, andsubstantially retain the mechanical properties of the initial cellulose articles.
- Woven fabrics treated according to the invention or prepared from yarns obtained according to the invention have a good rub resistance, especially if their combined acetic acid content is above 55 percent. They can be washed very easily and their dyeing affinity for plastosoluble dyestuffs is excellent.
- EXAMPLE 1 A continuous treatment is carried out on a tow of continuous Polynosic cellulose filaments having the following characteristics: gauge per strand: 1.06 dtex (0.96 denier); total gauge: 6,700 dtex (6,000 den); tenacity per strand; 5.4 g.; elongation at break 15 percent.
- This tow initially passes into a saturated aqueous solution of potassium acetate at 25 C. After drying at 150 C. in air for 2 minutes, it contains g. of potassium acetate per 100 g. of dry cellulose.
- the tow impregnated with potassium acetate thereafter passes for 3 minutes through an acetic anhydride bath maintained at 130 C.
- the devices for driving the tow on entering and leaving the acetylation bath are adjusted to the same speed so that the tow retains a constant length in the acetylation bath.
- the bath used for the acetylation initially contains 99 percent by weight of acetic anhydride and 1 percent by weight of acetic acid. Its acetic anhydride content is kept at 96 percent throughout the operation by continuously adding acetic anhydride and withdrawing an equivalent amount of acetylation bath.
- the tow After issuing from the acetylation bath, the tow is first washed with benzene and then with water to remove completely the uncombined acetic anhydride and the catalyst present in the tow, and is finally dried by means of a stream of hot air at 1 C. for about 4 minutes.
- the tow treated in this way has suffered no partial dissolution and individual filaments do not stick; it has a combined acetic acid content of 55.8 percent, a gauge per strand of 1.64 dtex 1.48 denier), a tenacity per strand of 4.6 g. and an elongation at break of 16.8 percent; thus its mechanical characteristics are close to those of the initial tow.
- the tow is initially impregnated with potassium acetate, then dried and thereafter acetylated at constant length according to the process described in Example 1, varying the amount of potassium acetate taken up by the tow as well as the duration and temperature of the acetylation.
- the tow On leaving the acetylation bath the tow, which has suffered no partial dissolution and whose fibers do not stick, is dried by means of a stream of hot air at 130 C. for about 3 minutes, washed with water and finally dried at 110 C. for about 4 minutes.
- the Table below indicates, for each of these Examples, the amount of potassium acetate with which the tow is impregnated before acetylation, the temperature and duration of the acetylation, and the combined acetic acid content and mechanical characteristics of the tow after acctylation.
- EXAMPLES 8 TO 12 A continuous treatment is carried out by the same process as in Examples 2 to 7, on a tow of Polynosic cellulose filaments having the following characteristics: gauge per strand: 1.56 dtex, (1.40 denier); total gauge: 20,000 dtex (18,000 denier); tenacity per strand: 7.7 g; elongation at break: 16.8 percent.
- the Table below shows, for each of these Examples, the amount of potassium acetate with which the tow is impregnated before acetylation, the temperature and duration of the acetylation, and the combined acetic acid content and mechanical characteristics of the tow after acetylation.
- a process for the production of cellulose acetate textile articles having a combined acetic acid content of 50-625 percent by the heterogeneous acetylation of regenerated cellulose textile articles which comprises treating the said regenerated cellulose textilc articles at a temperature of 100-l35 C.
- Process according to claim 4 in which the process is carried out continuously be passing the regenerated cellulose textile articles through a bath of an aqueous solution of the alkali metal acetate, drying them, passing them into the acetic anhydride bath while keeping their dimensions substantially constant, removing them from the bath, and freeing them substantially from unreacted acetic anhydride, and from the complex salt of acetic acid and potassium acetate which is formed in the process.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Artificial Filaments (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR172765 | 1968-11-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3655326A true US3655326A (en) | 1972-04-11 |
Family
ID=8656548
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US874366A Expired - Lifetime US3655326A (en) | 1968-11-06 | 1969-11-05 | Acetylation of textile articles of cellulose |
Country Status (11)
Country | Link |
---|---|
US (1) | US3655326A (en(2012)) |
AT (1) | AT297657B (en(2012)) |
BE (1) | BE741322A (en(2012)) |
BR (1) | BR6913866D0 (en(2012)) |
CH (1) | CH1646569D (en(2012)) |
DE (1) | DE1955931A1 (en(2012)) |
ES (1) | ES373233A1 (en(2012)) |
FR (1) | FR1590866A (en(2012)) |
GB (1) | GB1254796A (en(2012)) |
NL (1) | NL6916310A (en(2012)) |
RO (1) | RO55880A (en(2012)) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5427852A (en) * | 1993-07-09 | 1995-06-27 | Rhone-Poulenc Rhodia Aktiengesellschaft | Filter tow and method for its manufacture as well as tobacco smoke filter element and method for its manufacture |
CN109485735A (zh) * | 2018-10-25 | 2019-03-19 | 深圳大学 | 纤维素酯及其制备方法和应用 |
WO2020082294A1 (zh) * | 2018-10-25 | 2020-04-30 | 深圳大学 | 纤维素酯及其制备方法和应用 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1546211A (en) * | 1922-02-01 | 1925-07-14 | American Cellulose & Chemical | Manufacture of products containing cellulose |
US1930895A (en) * | 1930-02-13 | 1933-10-17 | Chem Ind Basel | Cellulose esters and process of making same |
US2348001A (en) * | 1941-10-24 | 1944-05-02 | Nat Vulcanized Fibre Company | Acetylation of cellulose |
US3037902A (en) * | 1960-12-22 | 1962-06-05 | Rayonier Inc | Partial acetylation of cellulose |
US3215490A (en) * | 1959-10-02 | 1965-11-02 | Rhodiaceta | Process of acetylating a specific kind of regenerated cellulose and recovering ingredients from the used acetylating bath |
-
0
- CH CH1646569D patent/CH1646569D/xx unknown
-
1968
- 1968-11-06 FR FR172765A patent/FR1590866A/fr not_active Expired
-
1969
- 1969-10-29 NL NL6916310A patent/NL6916310A/xx unknown
- 1969-11-03 BR BR213866/69A patent/BR6913866D0/pt unknown
- 1969-11-03 RO RO61448A patent/RO55880A/ro unknown
- 1969-11-05 BE BE741322D patent/BE741322A/xx unknown
- 1969-11-05 US US874366A patent/US3655326A/en not_active Expired - Lifetime
- 1969-11-05 GB GB54344/69A patent/GB1254796A/en not_active Expired
- 1969-11-06 AT AT1044769A patent/AT297657B/de not_active IP Right Cessation
- 1969-11-06 DE DE19691955931 patent/DE1955931A1/de active Pending
- 1969-11-06 ES ES373233A patent/ES373233A1/es not_active Expired
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1546211A (en) * | 1922-02-01 | 1925-07-14 | American Cellulose & Chemical | Manufacture of products containing cellulose |
US1930895A (en) * | 1930-02-13 | 1933-10-17 | Chem Ind Basel | Cellulose esters and process of making same |
US2348001A (en) * | 1941-10-24 | 1944-05-02 | Nat Vulcanized Fibre Company | Acetylation of cellulose |
US3215490A (en) * | 1959-10-02 | 1965-11-02 | Rhodiaceta | Process of acetylating a specific kind of regenerated cellulose and recovering ingredients from the used acetylating bath |
US3037902A (en) * | 1960-12-22 | 1962-06-05 | Rayonier Inc | Partial acetylation of cellulose |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5427852A (en) * | 1993-07-09 | 1995-06-27 | Rhone-Poulenc Rhodia Aktiengesellschaft | Filter tow and method for its manufacture as well as tobacco smoke filter element and method for its manufacture |
CN109485735A (zh) * | 2018-10-25 | 2019-03-19 | 深圳大学 | 纤维素酯及其制备方法和应用 |
WO2020082294A1 (zh) * | 2018-10-25 | 2020-04-30 | 深圳大学 | 纤维素酯及其制备方法和应用 |
Also Published As
Publication number | Publication date |
---|---|
AT297657B (de) | 1972-04-10 |
ES373233A1 (es) | 1971-12-16 |
NL6916310A (en(2012)) | 1970-05-11 |
BE741322A (en(2012)) | 1970-05-05 |
CH1646569D (en(2012)) | |
RO55880A (en(2012)) | 1973-11-20 |
BR6913866D0 (pt) | 1973-01-16 |
DE1955931A1 (de) | 1970-06-11 |
FR1590866A (en(2012)) | 1970-04-20 |
GB1254796A (en) | 1971-11-24 |
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