US2195930A - Production of artificial threads, filaments, bands, films, or the like containing proteins - Google Patents
Production of artificial threads, filaments, bands, films, or the like containing proteins Download PDFInfo
- Publication number
- US2195930A US2195930A US156006A US15600637A US2195930A US 2195930 A US2195930 A US 2195930A US 156006 A US156006 A US 156006A US 15600637 A US15600637 A US 15600637A US 2195930 A US2195930 A US 2195930A
- Authority
- US
- United States
- Prior art keywords
- product
- bath
- filaments
- acid
- bands
- 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
- 102000004169 proteins and genes Human genes 0.000 title description 22
- 108090000623 proteins and genes Proteins 0.000 title description 22
- 238000004519 manufacturing process Methods 0.000 title description 17
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 60
- 239000000047 product Substances 0.000 description 40
- 230000001376 precipitating effect Effects 0.000 description 35
- 239000002253 acid Substances 0.000 description 28
- 235000018102 proteins Nutrition 0.000 description 21
- 125000003118 aryl group Chemical group 0.000 description 18
- 238000000034 method Methods 0.000 description 18
- 238000009987 spinning Methods 0.000 description 16
- 239000003292 glue Substances 0.000 description 14
- 150000001447 alkali salts Chemical class 0.000 description 13
- 239000007859 condensation product Substances 0.000 description 13
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 13
- 239000000126 substance Substances 0.000 description 12
- 150000007513 acids Chemical class 0.000 description 11
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 9
- 102000011632 Caseins Human genes 0.000 description 7
- 108010076119 Caseins Proteins 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 6
- -1 hydroxy, amino Chemical group 0.000 description 6
- 239000005018 casein Substances 0.000 description 5
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 5
- 235000021240 caseins Nutrition 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 4
- 150000003460 sulfonic acids Chemical class 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- IULJSGIJJZZUMF-UHFFFAOYSA-N 2-hydroxybenzenesulfonic acid Chemical compound OC1=CC=CC=C1S(O)(=O)=O IULJSGIJJZZUMF-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 229940080237 sodium caseinate Drugs 0.000 description 2
- 239000001117 sulphuric acid Substances 0.000 description 2
- 235000011149 sulphuric acid Nutrition 0.000 description 2
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 2
- 239000011686 zinc sulphate Substances 0.000 description 2
- 235000009529 zinc sulphate Nutrition 0.000 description 2
- BGLLQCPSNQUDKF-UHFFFAOYSA-N 1,2,3,4-tetrahydronaphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)CCCC2=C1 BGLLQCPSNQUDKF-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 241001494479 Pecora Species 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 150000001454 anthracenes Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 125000001309 chloro group Chemical class Cl* 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- IIXGBDGCPUYARL-UHFFFAOYSA-N hydroxysulfamic acid Chemical class ONS(O)(=O)=O IIXGBDGCPUYARL-UHFFFAOYSA-N 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- CYGSXDXRHXMAOV-UHFFFAOYSA-N o-cresol hydrogen sulfate Chemical compound CC1=CC=CC=C1OS(O)(=O)=O CYGSXDXRHXMAOV-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 235000020183 skimmed milk Nutrition 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical class NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- 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
- D01F4/00—Monocomponent artificial filaments or the like of proteins; Manufacture thereof
Definitions
- This invention relates to the production of artificial threads, filaments, bands, films or the like containing proteins. It is known to spin into threads alkaline spinning solutions containing casein or other proteins by employing spinning baths containing acid. The artificial threads made in this way have, however, little value as substitutes for textile fibres since they possess only very low strength.
- the present invention accordingly comprises a process for the production of artificial threads, 35 filaments, bands, films or the like containing proteins from solutions of alkali salts of protein by bringing the said solution into contact with an acid precipitating bath which process consists in incorporating in the precipitating bath a proportion of a substance which has a precipitating action on glue solutions and a tanning action on the freshly produced artificial product and thereafter subjecting the said artificial prodnot to hardening with formaldehyde or the like.
- the thread, filament, band, film or the like may be subjected to tension whiie still in the acid bath.
- the tanning substances added to the precipitating bath may consist of condensation products of aromatic and hydroaromatic sulfonic acids and aldehydes and include in particular the water soluble methylene compounds resultifig from the condensation of aromatic and hydroaromatic sulfonic acids or their hydroxy, amino In Germany August 4, 1936 or chlorine derivatives and the like with aldehydes for example formaldehyde.
- tanning substances which may be employed in the precipitating bath, the following specific compounds may be mentioned, di-
- the tanning substance may also consist of an aromatic sulphonic acid including the monoor polysulphonic acids of aromatic or hydroaromatic hydrocarbons or of monoor polysulphonic acids of oxygen-containing derivatives of aromatic or hydroaromatic hydrocarbons.
- the monoor polysulphonic acids may further be employed in the form of their compounds with aliphatic alcohols. There may also be employed sulphonic acids of aromatic or hydroaromatic monoor polyhydroxy compounds, of keto-compounds, or of carboxylic acids. Examples of the above substances are naphthalene-sulphonic acid, tetraline-sulphonic acid, toluene-isopropyl-sulphonic acid, phenol-sulphonic acid, cyclohexanone-sulphonic acid, benzoic-sulphonic acid and so forth. Such substances have a. different action in the precipitating bath from that of free aldehydes since they do not attack the amino groups of the protein. 1
- the spinning bath may also contain a soluble salt or a mixture of soluble salts and these salts may include for example the sulphates of sodium, am-
- the acid concentration of the precipitating bath may vary between wide limits and this conv centration may be controlled either by neutraliscarbo-hydrates such as glycerol, sugar and the like, or mineral or organic acids.
- the sulphonic acids of the monoor polyhydroxy compounds have the advantage of a higher solubility when salts are present-
- These added substances also possess the advantage that they are simple and cheap to manufacture, and even at lowconcentrations they have a tanning action which is even superior to that of the condensation products mentioned above.
- the freshly spun thread has an appreciabiy increased strength and the rate of drawing ofi may thus be increased.
- Threads, filaments, bands, films or like artificial products obtained in accordance with the present invention are firmer than those prepared in the normal precipitating baths sothat a higher .degree of stretching may be applied thereto, this stretching resulting in a more pronounced orientation of the micells and in the production of products possessing greater strength.
- Example I A 17.5% solution of sodium caseinate is spun into a spinning bath consisting of 20% zinc sulphate, 1% sulphuric acid and 5% of the neutralised condensation product obtained by the action of half a molecule of formaldehyde on one. molecule of cresyl sulphonic acid.
- the casein solution is spun with a total titre of 250 denier from a spinning nozzle having 0 holes each of a diameter of mu. After the thread has travelled through a distance of about 60 centimetres in the spinning bath a tension of for example 25 grams is allowed to act upon it and a considerable increase in strength is thereby obtained.
- a tension of for example 25 grams is allowed to act upon it and a considerable increase in strength is thereby obtained.
- the thread is subsequently hardened with a 10% solution of formaldehyde and is then washed and dried at a moderate temperature. Hardening may take place immediately after spinning or at a later stage.
- the product is flexible and has a strength which even exceeds that of sheeps wool.
- Casein obtained from skim milk is dissolved in 14% ammonia water to form a 16% casein solution.
- This solution is spun at 45 C. in a spinning bath containing 10% by weight of sodium sulphate, 10% by weight of zinc sulphate, 3% by weight of sulphuric acid and 3% by weight of cresol sulphonic acid.
- the initial tension which may be applied to the thread in the spinning process if the abovementioned sulphonic acid is employed in the spinning bath is greater than that which can be used if the sulphonic acid is not present. This increased tension results in an increased rate of spinning.
- a process for the production of proteincontaining artificial threads, filaments, bands and the like which comprises extruding a solution of an alkali salt of a protein into an acid precipitating bath containing at least one substance selected from the group consisting of aromatic and hydroaromatic acids and the condensation products of aromatic and hydroaromatic sulphonic acids with aldehydes, for exerting a glue precipitating action and for tanning the formed product, tensioning said product while in said bath and finally treating the product with a hardening agent.
- a process for the production of proteincontaining artificial threads, filaments, bands and the like which comprises extruding a solution of an alkali salt of a protein into an acid precipitating bath containing at least one substance selected from the group consisting of arcmatic and hydroaromatic acids and the condensation products of aromatic and hydroaromatic sulphonic acids with aldehydes, for exerting a glue precipitating action and for tanning the formed product, tensioning said product while in said bath and finally hardening the product by treatment with an aldehyde.
- a process for the production of proteincontaining artificial threads, filaments, bands and the like which comprises extruding a solution of an alkali salt of casein into an acid precipitating bath containing at least one substance selected from the group consisting of aromatic and hydroaromatic acids and the condensation products of aromatic and hydroaromatic sulphonic acids with aldehydes, for exerting a glue precipitating action and for tanning the formed product, tensioning said product while in said bath and finally hardening the product by treatment with an aldehyde.
- a process for the production of proteincontaining artificial threads, filaments, bands and the like which comprises extruding a solution of an alkali salt of a protein into an acid precipitating bath containing a condensation product of an' aromatic sulphonic acid and an aldehyde, for everting a glue precipitating action and for tanning the formed product, tensioning said product while in said bath and finally hardening the product by treatment with formaldehyde and the like.
- a process for the production of proteincontaining artificial threads, filaments, bands and the like which comprises extruding a solution of an alkali salt of a protein into an acid precipitating bath containing a condensation product of an hydroxy aromatic sulphonic acid and an aldehyde, for exerting a glue precipitating action and for tanning the formed product, tensioning said product while in said bath and finally hardening the product by treatment with formaldehyde and the like.
- a process for the production of protein-containing artificial threads, filaments, bands and the like which comprises extruding a solution of an alkali salt of a protein into an acid precipitating bath containing a hydroaromatic sulphonic acid, for exerting a glue precipitating action and for tanning the formed product. tensioning said product while in said bath and finally hardening the product by treatment with formaldehyde and the like.
- a process for the production of protein-containing artificial threads, filaments, bands and the like which comprises extruding a solution of an alkali salt of a protein into an acid precipitating bath containing an oxyhydroaromatic sulphonic acid, for exerting a glue precipitating action and. for tanning the formed product, tensioning said product while in 'said bath and finally hardening the product by treatment with formaldehyde and the like.
- a process for the production of proteincontaining artificial threads, filaments, bands and the like which comprises extruding a solution of an alkali salt of a protein into an acid precipitating bath containing cyclohexanone-sulphonic acid, for exerting a glue precipitating action and for tanning the formed product, tensioning said product while in said bath and finally hardening the product by treatment with formaldehyde and the like.
- a process for the production of proteincontaining artificial threads, filaments, bands and the like which comprises extruding a solution of an alkali salt of a protein into an acid precipitating bath containing an aromatic sulphonic acid, for exerting a glue precipitating action and for tanning the formed product, tensioning said product while in said bath and finally hardening the product by treatment with formaldehyde and the like.
- a process for the production of proteincontaining artificial threads, filaments, bands and the like which comprises extruding a solution of an alkali salt of a protein into an acid precipitating bath containing an aromatic monosulphonic acid, for exerting a glue precipitating action and for tanning the formedproduct, tensioning said product while in said bath and finally hardening the product by treatment with formaldehyde and the like.
- a process for the production of proteincontaining artificial threads, filaments, bands and the like which comprises extruding a solution of an alkali salt of a protein into an acid precipitating bath containing cresyl sulphonic acid, for exerting a glue precipitating action and for tanning the formed product, tensioning said product while in said bath and finally hardening the product by treatment with formaldehyde and the like.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Artificial Filaments (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE499769X | 1936-08-04 |
Publications (1)
Publication Number | Publication Date |
---|---|
US2195930A true US2195930A (en) | 1940-04-02 |
Family
ID=6545519
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US156006A Expired - Lifetime US2195930A (en) | 1936-08-04 | 1937-07-27 | Production of artificial threads, filaments, bands, films, or the like containing proteins |
Country Status (5)
Country | Link |
---|---|
US (1) | US2195930A (en(2012)) |
BE (1) | BE422506A (en(2012)) |
FR (1) | FR823962A (en(2012)) |
GB (1) | GB499769A (en(2012)) |
NL (1) | NL46479C (en(2012)) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2519978A (en) * | 1945-10-11 | 1950-08-22 | Jack J Press | Generated proteins and process for preparation thereof |
US2576576A (en) * | 1946-04-19 | 1951-11-27 | American Cyanamid Co | Lubricated thread |
US3123653A (en) * | 1960-09-20 | 1964-03-03 | Method of producing a tubular collagen casing |
-
0
- BE BE422506D patent/BE422506A/xx unknown
- NL NL46479D patent/NL46479C/xx active
-
1937
- 1937-07-06 FR FR823962D patent/FR823962A/fr not_active Expired
- 1937-07-27 US US156006A patent/US2195930A/en not_active Expired - Lifetime
- 1937-07-27 GB GB20822/37A patent/GB499769A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2519978A (en) * | 1945-10-11 | 1950-08-22 | Jack J Press | Generated proteins and process for preparation thereof |
US2576576A (en) * | 1946-04-19 | 1951-11-27 | American Cyanamid Co | Lubricated thread |
US3123653A (en) * | 1960-09-20 | 1964-03-03 | Method of producing a tubular collagen casing |
Also Published As
Publication number | Publication date |
---|---|
GB499769A (en) | 1939-01-27 |
NL46479C (en(2012)) | |
FR823962A (fr) | 1938-01-29 |
BE422506A (en(2012)) |
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