US2902336A - Process for the production of amylose articles by extrusion of aqueous sodium hydroxide solution thereof into concentrated aqueous ammonium sulphate solution - Google Patents
Process for the production of amylose articles by extrusion of aqueous sodium hydroxide solution thereof into concentrated aqueous ammonium sulphate solution Download PDFInfo
- Publication number
- US2902336A US2902336A US768071A US76807158A US2902336A US 2902336 A US2902336 A US 2902336A US 768071 A US768071 A US 768071A US 76807158 A US76807158 A US 76807158A US 2902336 A US2902336 A US 2902336A
- Authority
- US
- United States
- Prior art keywords
- amylose
- solution
- ammonium sulphate
- sodium hydroxide
- articles
- 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
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 title claims description 24
- 229920000856 Amylose Polymers 0.000 title claims description 22
- 238000000034 method Methods 0.000 title claims description 10
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 title claims description 9
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 238000001125 extrusion Methods 0.000 title description 4
- 239000000243 solution Substances 0.000 description 19
- 230000015271 coagulation Effects 0.000 description 13
- 238000005345 coagulation Methods 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 238000009987 spinning Methods 0.000 description 7
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 6
- 239000001166 ammonium sulphate Substances 0.000 description 6
- 235000011130 ammonium sulphate Nutrition 0.000 description 6
- 239000000835 fiber Substances 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 239000012153 distilled water Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920000945 Amylopectin Polymers 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
- 230000005593 dissociations Effects 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- PXXKQOPKNFECSZ-UHFFFAOYSA-N platinum rhodium Chemical compound [Rh].[Pt] PXXKQOPKNFECSZ-UHFFFAOYSA-N 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000011800 void material Substances 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
- D01F9/00—Artificial filaments or the like of other substances; Manufacture thereof; Apparatus specially adapted for the manufacture of carbon filaments
Definitions
- the invention relates to a process for the production of articles of manufacture, such as films and fibres, from amylose.
- amylose films can be made by means of casting process.
- Processes of such a type whereby an amylose solution is prepared by dissolving amylose in water e.g. with the aid of a complex forming agent or in an aqueous solution of an aldehyde such as for example formaldehyde, and wherein this solution is cast on a support on which it is dried, are relatively expensive, chiefly because the drying and coagulation rates are limited, and the process is consequently rather slow.
- amylose dissolved in an aqueous sodium hydroxide solution when extruded into a concentrated aqueous ammonium sulphate solution, coagulates almost instantaneously, whereby a fairly strong, very resilient film or fibre is obtained, which is eminently free supporting and therefore very transportable.
- the spinning rate may serve; for the coagulation rate is so high that it is hardly measurable in itself.
- spinning rates up to about 50 metres per minute were reached, whilst with casting processes rates of not more than 4 to 5 metres per minute could be reached.
- Extrusion can be done through an opening of a round or rectangular or polygonal shape so that fibres or films and the like are formed.
- the concentration of the ammonium sulphate in the coagulation bath is exceedingly important. With concentrations of 30 percent by weight and lower, the spinning rate is only a few metres a minute. With a concentration of 40%, however, this rate is already about 35 rn./minute, and in a saturated aqueous solution of ammonium sulphate spinning rates of up to 50 mjrninute could be realized.
- a very suitable extrusion bath contains NH OH and more than 30 percent by weight of ammonium sulphate.
- the films and fibres obtained by coagulation can be freed of the inorganic compounds they had taken up, by washing with a suitable solvent, in which the amylose is not soluble, as for example a mixture of water and alcohol or more generally mixtures of water and organic water soluble substances, and subsequently dried.
- a suitable solvent in which the amylose is not soluble, as for example a mixture of water and alcohol or more generally mixtures of water and organic water soluble substances, and subsequently dried.
- Amylose films have the advantage of consisting of easily digestible material, and are therefore eminently suitable for packing food, as these films can be consumed with the packed product.
- Example 224 g. of air-dry commercial amylose in powder form (moisture content 12% by weight) was dispersed in 1070 g. of air-free distilled water at a temperature of 20 C. whilst stirring vigorously.
- a solution of 50 g. of sodium hydroxide in 156 g. of air-free distilled water was added whilst stirring vigorously. After three more hours of stirring a solution was obtained, in which no undissolved amylose had been left.
- the solution was subsequently filtered over a vacuum filter through filtering cloth with a high mesh-number. This solution was kept in vacuum for 24 hours, in order to remove dissolved gases if any.
- the solution thus obtained was optically void and contained 13.2% by weight of amylose and 3.3% by weight of NaOH, and had a viscosity of 10002000 centipoises.
- the solution was extruded from a spinnerette of platinum rhodium with 30 apertures, each of which having a diameter of 0.100 mm., into a spinning bath of 30 C., consisting of a solution of ammonium sulphate in distilled water, which solution contained 43-44% by weight of (NH SO).
- the fibres which were formed were led through the bath for about 2 seconds and subsequently wound on a bobbin (at a rate of about 45 m./ minute)
- the closing of the spinning solution was 3.8 cm. a minute; the filaments obtained had, after washing and drying, a denier of 3.3.
- an amylose film can be produced at approximately the same rate.
- Impurities may influence the properties of the fibres and films obtained to a large extent.
- ammonium sulphate should be removed as completely as possible. This can be done by thorough washing.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Artificial Filaments (AREA)
- Spinning Methods And Devices For Manufacturing Artificial Fibers (AREA)
Description
United States Patent Pieter Hiemstra, Veendam, and Johannes Muetgeert, Delft, Netherlands, assignors to Coiiperatieve Verkoopen Productievereniging Van Aardappelmeel en Derivaten Avebe G.A., Veendam, Netherlands Application October 20, 1958 Serial No. 768,071
Claims priority, application Netherlands October 22, 1957 3 Claims. (Cl. 18--54) No Drawing.
The invention relates to a process for the production of articles of manufacture, such as films and fibres, from amylose.
It is known that amylose films can be made by means of casting process. Processes of such a type, whereby an amylose solution is prepared by dissolving amylose in water e.g. with the aid of a complex forming agent or in an aqueous solution of an aldehyde such as for example formaldehyde, and wherein this solution is cast on a support on which it is dried, are relatively expensive, chiefly because the drying and coagulation rates are limited, and the process is consequently rather slow.
Attempts have been made at making fibres and films from an amylose solution by extrusion into a coagulation bath, but none of the attempts that have so far been made have yielded any useful results. In some cases, as for example by extruding amylose, which had been dissolved in an aqueous sodium hydroxide solution, into an acid bath as coagulation bath, a fibre or film was obtained by gelation, but the amylose film or fibre which had coagulated in this manner was so weak as to be practically untransportable.
It has now been found that amylose dissolved in an aqueous sodium hydroxide solution, when extruded into a concentrated aqueous ammonium sulphate solution, coagulates almost instantaneously, whereby a fairly strong, very resilient film or fibre is obtained, which is eminently free supporting and therefore very transportable.
As a measure for the coagulation rate the spinning rate may serve; for the coagulation rate is so high that it is hardly measurable in itself. In applying the process according to the invention spinning rates up to about 50 metres per minute were reached, whilst with casting processes rates of not more than 4 to 5 metres per minute could be reached.
Extrusion can be done through an opening of a round or rectangular or polygonal shape so that fibres or films and the like are formed.
The concentration of the ammonium sulphate in the coagulation bath is exceedingly important. With concentrations of 30 percent by weight and lower, the spinning rate is only a few metres a minute. With a concentration of 40%, however, this rate is already about 35 rn./minute, and in a saturated aqueous solution of ammonium sulphate spinning rates of up to 50 mjrninute could be realized.
Hereby a pH value of between 7.5 and 8.0 is automatically established in the coagulation bath. In extruding a solution of amylose in aqueous sodium hydroxide the following reaction takes place in the spinnnig bath:
ice
By the high concentration of NH,+ ions the dissociation of the NH OH which has been formed is pushed back and the above-mentioned pH value is reached automatically.
Attempts at accelerating the process by adding an acid to the coagulation bath did not bring about the desired result. It is true that coagulation in a bath of the type where acid is added is very swift, but the film or fibre thus obtained is very weak and its transportation and further working up is very difiicult. It would seem, therefore that a high H+-ion concentration is unfavourable for obtaining a strong amylose gel in the coagulation bath.
A very suitable extrusion bath contains NH OH and more than 30 percent by weight of ammonium sulphate.
Naturally, the films and fibres obtained by coagulation, can be freed of the inorganic compounds they had taken up, by washing with a suitable solvent, in which the amylose is not soluble, as for example a mixture of water and alcohol or more generally mixtures of water and organic water soluble substances, and subsequently dried.
Amylose films have the advantage of consisting of easily digestible material, and are therefore eminently suitable for packing food, as these films can be consumed with the packed product.
Example 224 g. of air-dry commercial amylose in powder form (moisture content 12% by weight) was dispersed in 1070 g. of air-free distilled water at a temperature of 20 C. whilst stirring vigorously. To the viscous mass thus obtained a solution of 50 g. of sodium hydroxide in 156 g. of air-free distilled water was added whilst stirring vigorously. After three more hours of stirring a solution was obtained, in which no undissolved amylose had been left.
The solution was subsequently filtered over a vacuum filter through filtering cloth with a high mesh-number. This solution was kept in vacuum for 24 hours, in order to remove dissolved gases if any.
The solution thus obtained was optically void and contained 13.2% by weight of amylose and 3.3% by weight of NaOH, and had a viscosity of 10002000 centipoises.
The solution was extruded from a spinnerette of platinum rhodium with 30 apertures, each of which having a diameter of 0.100 mm., into a spinning bath of 30 C., consisting of a solution of ammonium sulphate in distilled water, which solution contained 43-44% by weight of (NH SO The fibres which were formed were led through the bath for about 2 seconds and subsequently wound on a bobbin (at a rate of about 45 m./ minute) The closing of the spinning solution was 3.8 cm. a minute; the filaments obtained had, after washing and drying, a denier of 3.3.
If, instead of a spinnerette with round apertures, a slot having a width of 0.1 mm. is used for extruding the spinning solution, an amylose film can be produced at approximately the same rate.
Impurities may influence the properties of the fibres and films obtained to a large extent. In order to obtain the greatest possible strength, ammonium sulphate should be removed as completely as possible. This can be done by thorough washing.
It proved to be possible, however, to replace part of the amylose by amylopectin without exerting a distinctly unfavourable influence on the properties of the films.
What we claim is:
1. In a process for the production of articles of manufacture such as fibres and films from amylose, the step of dissolving amylose in an aqueous sodium hydroxide solution and extruding this solution into a concentrated aqueous ammonium sulphate'solution.
2. The process according to claim 1, wherein the coagulation bath, in addition to more than 30% sy Weight of '(NH )2SO also contains 'NH OH.
3. The process according to claim 1 wherein the coagulation bath has a pH value of 7.5-8.
References Cited in the file of this patent UNITED STATES PATENTS Levey Nov. 15, 1938 Reid et a1. Jan. 31, 1950 Horsak Oct. 9, 1951 Wolfi et a1 Sept. 2, 1952 Muetgurt et al Feb. 11, 1958 Wimmer Sept. 23, .1958
Claims (1)
1. IN A PROCESS FOR THE PRODUCTION OF ARTICLES OF MANUFACTURE SUCH AS FIBRES AND FILMS FROM AMYLOSE, THE STEP OF DISSOLVING AMYLOSE IN AN AQUEOUS SODIUM HYDROXIDE SOLUTION AND EXTRUDING THIS SOLUTION INTO A CONCENTRATED AQUEOUS AMMONIUM SULPHATE SOLUTION.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL2902336X | 1957-10-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2902336A true US2902336A (en) | 1959-09-01 |
Family
ID=19876242
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US768071A Expired - Lifetime US2902336A (en) | 1957-10-22 | 1958-10-20 | Process for the production of amylose articles by extrusion of aqueous sodium hydroxide solution thereof into concentrated aqueous ammonium sulphate solution |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2902336A (en) |
Cited By (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2999032A (en) * | 1958-01-29 | 1961-09-05 | Vasco Ind Corp | Process for the preparation of amylose solutions |
| US3030667A (en) * | 1959-10-05 | 1962-04-24 | American Viscose Corp | Method of preparing amylose film, tubing, and the like |
| US3108891A (en) * | 1961-04-24 | 1963-10-29 | Owens Corning Fiberglass Corp | Amylaceous forming size compositions |
| US3188237A (en) * | 1960-12-29 | 1965-06-08 | American Machinery And Foundry | Activation of amylose |
| DE2713311A1 (en) * | 1976-03-25 | 1977-09-29 | Nat Starch Chem Corp | METHOD FOR MANUFACTURING PAPER, CARDBOARD OR CARDBOARD |
| US4139699A (en) * | 1976-03-25 | 1979-02-13 | National Starch And Chemical Corporation | Water insensitive starch fibers and a process for the production thereof |
| US4243480A (en) * | 1977-10-17 | 1981-01-06 | National Starch And Chemical Corporation | Process for the production of paper containing starch fibers and the paper produced thereby |
| US4340442A (en) * | 1978-11-06 | 1982-07-20 | Champion International Corporation | Starch fibrids useful in enhancing the physical properties of paper, and process of preparing same |
| US4755397A (en) * | 1986-12-24 | 1988-07-05 | National Starch And Chemical Corporation | Starch based particulate encapsulation process |
| US4812445A (en) * | 1987-02-06 | 1989-03-14 | National Starch And Chemical Corporation | Starch based encapsulation process |
| US4853168A (en) * | 1987-12-23 | 1989-08-01 | National Starch And Chemical Corporation | Process for spinning starch fibers |
| US5430140A (en) * | 1992-07-16 | 1995-07-04 | Ems-Inventa Ag | Starch intermediate product, a process for producing a starch intermediate product, and a process for further processing of a starch intermediate product |
| US5866251A (en) * | 1992-10-16 | 1999-02-02 | Eridania Beghin-Say | Device and process for the production of fibrious starch materials |
| US20030203196A1 (en) * | 2000-11-27 | 2003-10-30 | Trokhan Paul Dennis | Flexible structure comprising starch filaments |
| US6709526B1 (en) | 1999-03-08 | 2004-03-23 | The Procter & Gamble Company | Melt processable starch compositions |
| US6723160B2 (en) | 2002-02-01 | 2004-04-20 | The Procter & Gamble Company | Non-thermoplastic starch fibers and starch composition for making same |
| US20040183238A1 (en) * | 2001-09-06 | 2004-09-23 | James Michael David | Process for making non-thermoplastic starch fibers |
| US6811740B2 (en) | 2000-11-27 | 2004-11-02 | The Procter & Gamble Company | Process for making non-thermoplastic starch fibers |
| US6955850B1 (en) | 2004-04-29 | 2005-10-18 | The Procter & Gamble Company | Polymeric structures and method for making same |
| US20050244635A1 (en) * | 2004-04-29 | 2005-11-03 | The Procter & Gamble Company | Polymeric structures and method for making same |
| US7029620B2 (en) | 2000-11-27 | 2006-04-18 | The Procter & Gamble Company | Electro-spinning process for making starch filaments for flexible structure |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2137171A (en) * | 1936-09-25 | 1938-11-15 | Harold A Levey | Composite carbohydrate films |
| US2495767A (en) * | 1946-08-09 | 1950-01-31 | Reid John David | Preparation of fibers from carboxymethylcellulose |
| US2570449A (en) * | 1946-01-19 | 1951-10-09 | Horsak Drahomir | Method of production of synthetic material from starch or starch containing substances |
| US2608723A (en) * | 1950-08-01 | 1952-09-02 | Ivan A Wolff | Process for the production of amylose films |
| US2822581A (en) * | 1954-04-22 | 1958-02-11 | Avebe Coop Verkoop Prod | Amylose films |
| US2853414A (en) * | 1953-12-02 | 1958-09-23 | American Sugar Refining Co | Water-insoluble complex of quaternary ammonium salt, a heavy-metal oxide, and an organic colloid and method of preparing same |
-
1958
- 1958-10-20 US US768071A patent/US2902336A/en not_active Expired - Lifetime
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2137171A (en) * | 1936-09-25 | 1938-11-15 | Harold A Levey | Composite carbohydrate films |
| US2570449A (en) * | 1946-01-19 | 1951-10-09 | Horsak Drahomir | Method of production of synthetic material from starch or starch containing substances |
| US2495767A (en) * | 1946-08-09 | 1950-01-31 | Reid John David | Preparation of fibers from carboxymethylcellulose |
| US2608723A (en) * | 1950-08-01 | 1952-09-02 | Ivan A Wolff | Process for the production of amylose films |
| US2853414A (en) * | 1953-12-02 | 1958-09-23 | American Sugar Refining Co | Water-insoluble complex of quaternary ammonium salt, a heavy-metal oxide, and an organic colloid and method of preparing same |
| US2822581A (en) * | 1954-04-22 | 1958-02-11 | Avebe Coop Verkoop Prod | Amylose films |
Cited By (43)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2999032A (en) * | 1958-01-29 | 1961-09-05 | Vasco Ind Corp | Process for the preparation of amylose solutions |
| US3030667A (en) * | 1959-10-05 | 1962-04-24 | American Viscose Corp | Method of preparing amylose film, tubing, and the like |
| US3188237A (en) * | 1960-12-29 | 1965-06-08 | American Machinery And Foundry | Activation of amylose |
| US3108891A (en) * | 1961-04-24 | 1963-10-29 | Owens Corning Fiberglass Corp | Amylaceous forming size compositions |
| US4139699A (en) * | 1976-03-25 | 1979-02-13 | National Starch And Chemical Corporation | Water insensitive starch fibers and a process for the production thereof |
| JPS52118009A (en) * | 1976-03-25 | 1977-10-04 | Nat Starch Chem Corp | Process for making paper admixed with starch fiber and paper made thereof |
| DE2713311A1 (en) * | 1976-03-25 | 1977-09-29 | Nat Starch Chem Corp | METHOD FOR MANUFACTURING PAPER, CARDBOARD OR CARDBOARD |
| US4243480A (en) * | 1977-10-17 | 1981-01-06 | National Starch And Chemical Corporation | Process for the production of paper containing starch fibers and the paper produced thereby |
| US4340442A (en) * | 1978-11-06 | 1982-07-20 | Champion International Corporation | Starch fibrids useful in enhancing the physical properties of paper, and process of preparing same |
| US4755397A (en) * | 1986-12-24 | 1988-07-05 | National Starch And Chemical Corporation | Starch based particulate encapsulation process |
| US4812445A (en) * | 1987-02-06 | 1989-03-14 | National Starch And Chemical Corporation | Starch based encapsulation process |
| US4853168A (en) * | 1987-12-23 | 1989-08-01 | National Starch And Chemical Corporation | Process for spinning starch fibers |
| US5430140A (en) * | 1992-07-16 | 1995-07-04 | Ems-Inventa Ag | Starch intermediate product, a process for producing a starch intermediate product, and a process for further processing of a starch intermediate product |
| US5514790A (en) * | 1992-07-16 | 1996-05-07 | Ems-Inventa Ag | Starch intermediate product, a process for producing a starch intermediate product, and a process for further processing of a starch intermediate product |
| US5866251A (en) * | 1992-10-16 | 1999-02-02 | Eridania Beghin-Say | Device and process for the production of fibrious starch materials |
| US7041369B1 (en) | 1999-03-08 | 2006-05-09 | The Procter & Gamble Company | Melt processable starch composition |
| US7524379B2 (en) | 1999-03-08 | 2009-04-28 | The Procter + Gamble Company | Melt processable starch compositions |
| US9458556B2 (en) | 1999-03-08 | 2016-10-04 | The Procter & Gamble Company | Fiber comprising polyvinylpyrrolidone |
| US20040132873A1 (en) * | 1999-03-08 | 2004-07-08 | The Procter & Gamble Company | Melt processable starch compositions |
| US8764904B2 (en) | 1999-03-08 | 2014-07-01 | The Procter & Gamble Company | Fiber comprising starch and a high polymer |
| US8168003B2 (en) | 1999-03-08 | 2012-05-01 | The Procter & Gamble Company | Fiber comprising starch and a surfactant |
| US7938908B2 (en) | 1999-03-08 | 2011-05-10 | The Procter & Gamble Company | Fiber comprising unmodified and/or modified starch and a crosslinking agent |
| US6709526B1 (en) | 1999-03-08 | 2004-03-23 | The Procter & Gamble Company | Melt processable starch compositions |
| US7704328B2 (en) | 1999-03-08 | 2010-04-27 | The Procter & Gamble Company | Starch fiber |
| US7666261B2 (en) | 1999-03-08 | 2010-02-23 | The Procter & Gamble Company | Melt processable starch compositions |
| US6811740B2 (en) | 2000-11-27 | 2004-11-02 | The Procter & Gamble Company | Process for making non-thermoplastic starch fibers |
| US7029620B2 (en) | 2000-11-27 | 2006-04-18 | The Procter & Gamble Company | Electro-spinning process for making starch filaments for flexible structure |
| US20030203196A1 (en) * | 2000-11-27 | 2003-10-30 | Trokhan Paul Dennis | Flexible structure comprising starch filaments |
| US20040183238A1 (en) * | 2001-09-06 | 2004-09-23 | James Michael David | Process for making non-thermoplastic starch fibers |
| US7276201B2 (en) | 2001-09-06 | 2007-10-02 | The Procter & Gamble Company | Process for making non-thermoplastic starch fibers |
| US7025821B2 (en) | 2002-02-01 | 2006-04-11 | The Procter & Gamble Company | Non-thermoplastic starch fibers and starch composition for making same |
| US6723160B2 (en) | 2002-02-01 | 2004-04-20 | The Procter & Gamble Company | Non-thermoplastic starch fibers and starch composition for making same |
| US20040149165A1 (en) * | 2002-02-01 | 2004-08-05 | The Procter & Gamble Company | Non-thermoplastic starch fibers and starch composition for making same |
| US6802895B2 (en) | 2002-02-01 | 2004-10-12 | The Procter & Gamble Company | Non-thermoplastic starch fibers and starch composition for making same |
| US20050076809A1 (en) * | 2002-02-01 | 2005-04-14 | Mackey Larry Neil | Non-thermoplastic starch fibers and starch composition for making same |
| US7744791B2 (en) | 2004-04-29 | 2010-06-29 | The Procter & Gamble Company | Method for making polymeric structures |
| US7754119B2 (en) | 2004-04-29 | 2010-07-13 | The Procter & Gamble Company | Method for making polymeric structures |
| US6955850B1 (en) | 2004-04-29 | 2005-10-18 | The Procter & Gamble Company | Polymeric structures and method for making same |
| US20050244634A1 (en) * | 2004-04-29 | 2005-11-03 | The Procter & Gamble Company | Polymeric structures and method for making same |
| US8623246B2 (en) | 2004-04-29 | 2014-01-07 | The Procter & Gamble Company | Process of making a fibrous structure |
| US20050244635A1 (en) * | 2004-04-29 | 2005-11-03 | The Procter & Gamble Company | Polymeric structures and method for making same |
| US9017586B2 (en) | 2004-04-29 | 2015-04-28 | The Procter & Gamble Company | Polymeric structures and method for making same |
| US6977116B2 (en) | 2004-04-29 | 2005-12-20 | The Procter & Gamble Company | Polymeric structures and method for making same |
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