ES2639807T3 - Cuerpo moldeado celulósico tridimensional, procedimiento para su fabricación y su uso - Google Patents
Cuerpo moldeado celulósico tridimensional, procedimiento para su fabricación y su uso Download PDFInfo
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- ES2639807T3 ES2639807T3 ES14838769.9T ES14838769T ES2639807T3 ES 2639807 T3 ES2639807 T3 ES 2639807T3 ES 14838769 T ES14838769 T ES 14838769T ES 2639807 T3 ES2639807 T3 ES 2639807T3
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- 238000004519 manufacturing process Methods 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- 239000011258 core-shell material Substances 0.000 abstract description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 229960005489 paracetamol Drugs 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 239000011049 pearl Substances 0.000 description 4
- 239000011324 bead Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- 229920000433 Lyocell Polymers 0.000 description 2
- LFTLOKWAGJYHHR-UHFFFAOYSA-N N-methylmorpholine N-oxide Chemical compound CN1(=O)CCOCC1 LFTLOKWAGJYHHR-UHFFFAOYSA-N 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 238000001291 vacuum drying Methods 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 235000019888 Vivapur Nutrition 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 239000013256 coordination polymer Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000004584 weight gain Effects 0.000 description 1
- 235000019786 weight gain Nutrition 0.000 description 1
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- C—CHEMISTRY; METALLURGY
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- C08B1/00—Preparatory treatment of cellulose for making derivatives thereof, e.g. pre-treatment, pre-soaking, activation
- C08B1/003—Preparation of cellulose solutions, i.e. dopes, with different possible solvents, e.g. ionic liquids
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- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
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- A—HUMAN NECESSITIES
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
- A61K31/167—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the nitrogen of a carboxamide group directly attached to the aromatic ring, e.g. lidocaine, paracetamol
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- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
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- C08B15/02—Oxycellulose; Hydrocellulose; Cellulosehydrate, e.g. microcrystalline cellulose
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- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/12—Powdering or granulating
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- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/12—Powdering or granulating
- C08J3/126—Polymer particles coated by polymer, e.g. core shell structures
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- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
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- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
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- C08L1/02—Cellulose; Modified cellulose
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- 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
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
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- A61K2800/20—Chemical, physico-chemical or functional or structural properties of the composition as a whole
- A61K2800/28—Rubbing or scrubbing compositions; Peeling or abrasive compositions; Containing exfoliants
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- A61K2800/65—Characterized by the composition of the particulate/core
- A61K2800/654—The particulate/core comprising macromolecular material
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- C08J2301/00—Characterised by the use of cellulose, modified cellulose or cellulose derivatives
- C08J2301/02—Cellulose; Modified cellulose
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- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/14—Polymer mixtures characterised by other features containing polymeric additives characterised by shape
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- Polymers & Plastics (AREA)
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- Pharmacology & Pharmacy (AREA)
- Materials Engineering (AREA)
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- Birds (AREA)
- Pain & Pain Management (AREA)
- Crystallography & Structural Chemistry (AREA)
- Dermatology (AREA)
- Textile Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- Cosmetics (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Treatment Of Liquids With Adsorbents In General (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Artificial Filaments (AREA)
- Medicinal Preparation (AREA)
- Materials For Medical Uses (AREA)
Abstract
Cuerpo moldeado celulósico tridimensional, que presenta una estructura de núcleo-envolvente ópticamente detectable, en donde la envolvente presenta una mayor densidad y una menor cristalinidad que el núcleo y el núcleo presenta una estructura similar a una esponja, caracterizado por que la envolvente presenta una densidad relativa del 65% al 85%y el núcleo presenta una densidad relativa del 20% al 60%-referido a la celulosa compacta-, el espesor de la envolvente oscila entre 50 μ 200 μa relación de espesor de la envolvente y el diámetro total del cuerpo moldeado oscila entre 1:5 y 1:50 y la relación de los semiejes del cuerpo moldeado no supera 3:1.
Description
5
10
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20
25
30
Tabla 1
- V1
- V2 V3 V4 V5 V6
- Diámetro de orificio [mm]
- 1,0 1,5 1,5 1,5 1,5 1,5
- Número de revoluciones de la cuchilla [rpm]
- 4500 3000 3000 3000 3000 3000
- Temperatura del baño de precipitación [°C]
- 30 50 50 50 50 10
- Baño de presentación de NMMO concentrado [% en peso]
- 20 34,5 38,9 42 44,6 0
- Espesor de la piel [μm] – valor medio
- 114,7 89,0 85,0 75,2 53,6 182,2
- Espesor de la piel [μm] – desviación estándar
- 20,1 14,7 4,2 7,7 8,0 35,3
Las perlas celulósicas fabricadas mediante la granuladora sumergida fueron precipitadas en agua completamente desalinizada (agua VE) y seguidamente sometidas a lavado en una columna con agua VE caliente a una temperatura de 80°C. El lavado fino tuvo lugar con lejía de sosa (pH 11). Después del lavado con lejía de sosa se lavaron las pequeñas esferas con agua a una temperatura de 80°C bajo pH neutro y se sometieron a centrifugación hasta una humedad residual de aproximadamente el 70% en peso.
La estructura de las partículas nunca secadas de los ensayos V1 a V6 fue examinada bajo un microscopio óptico ( tipo Zeiss Discovery.V12, Olympus DP71). En este caso se comprobó que todas las partículas presentan una destacada estructura de núcleo y envuelta. La Figura 1 muestra como ejemplo partícula de V6.
Mediante el software AnalySIS 5.0 de Olympus se midió el espesor de la envuelta, efectuándose y promediándose cinco mediciones. Los resultados se han recopilado también en la Tabla 1. Se encontró una manifiesta dependencia del espesor de la envolvente con respecto a las condiciones de regeneración. Al aumentar la concentración de NMMO en el baño de precipitación, junto con una elevación de la temperatura, disminuye el espesor de la capa externa.
Además, se puede reconocer que la piel exterior es transparente, mientras que el interior de las pequeñas esferas es blanco. Esto demuestra de manera unívoca la diferente estructuración del material. La capa transparente es muy densa, mientras que, en cambio, la capa interior de las perlas celulósicas presenta una estructura de tipo esponja. En el ejemplo 5 puede encontrarse una caracterización detallada de la estructura del núcleo-envuelta.
Ejemplo 2 -Carga con sustancia activa
20 g de perlas celulósicas nunca secadas V1 del Ejemplo 1 (68,3% en peso de humedad residual) fueron añadidos a 40 ml de un paracetamol (Merck) al 5% en peso regulado a una temperatura de 30°C en solución p.A. de etanol. Esta suspensión fue sometida a agitación a 100 rpm durante 120 min. Se filtraron las perlas celulósicas cargadas y se lavaron subsiguientemente con 10 ml de agua VE completamente desalinizada y a continuación se secaron en un gabinete de secado al vacío a 40°C, 150 mbar durante aproximadamente 8 h. El peso total de las perlas celulósicas secadas era de 5,6915 g. La carga de las perlas celulósicas con paracetamol era del 8,48% en peso (aumento de peso).
Como sustancias comparativas se utilizaron los siguientes materiales: Tencel® CP 4 (Polvo de celulosa esférico, fabricante: Lenzing AG), Tencel® Gel (suspensión de celulosa, Lenzing AG) y Vivapur 105 (MCC, Fabricante, J. R & Söhne). A partir de ellos también se prepararon suspensiones con paracetamol en etanol de manera análoga a las perlas celulósicas de acuerdo con la invención, manteniéndose siempre constante la relación entre la celulosa y el paracetamol. Sin embargo, los materiales comparativos no fueron secados en el gabinete de secado en vacío, por cuanto que, debido a las partículas finas, esto habría conducido a la formación de grumos, sino mediante la secadora de rociado Büchi B290. En la Tabla 2 se han resumido las propiedades de las partículas cargadas.
10
Claims (1)
-
imagen1 imagen2
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ATA794/2013A AT515180B1 (de) | 2013-10-15 | 2013-10-15 | Dreidimensionaler cellulosischer Formkörper, Verfahren zu seiner Herstellung und seine Verwendung |
| AT7942013 | 2013-10-15 | ||
| PCT/AT2014/000202 WO2015054711A2 (de) | 2013-10-15 | 2014-11-14 | Dreidimensionaler cellulosischer formkörper, verfahren zu seiner herstellung und seine verwendung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2639807T3 true ES2639807T3 (es) | 2017-10-30 |
Family
ID=52544214
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES14838769.9T Active ES2639807T3 (es) | 2013-10-15 | 2014-11-14 | Cuerpo moldeado celulósico tridimensional, procedimiento para su fabricación y su uso |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US10093790B2 (es) |
| EP (1) | EP3058022B1 (es) |
| JP (1) | JP6511441B2 (es) |
| KR (1) | KR20170071444A (es) |
| CN (1) | CN105829351B (es) |
| AT (1) | AT515180B1 (es) |
| DK (1) | DK3058022T3 (es) |
| ES (1) | ES2639807T3 (es) |
| PL (1) | PL3058022T3 (es) |
| WO (1) | WO2015054711A2 (es) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AT515174B1 (de) | 2013-10-15 | 2019-05-15 | Chemiefaser Lenzing Ag | Cellulosesuspension, Verfahren zu ihrer Herstellung und Verwendung |
| AT517020B1 (de) | 2015-02-06 | 2020-02-15 | Chemiefaser Lenzing Ag | Recycling von cellulosischen Kunstfasern |
| JP7223006B2 (ja) * | 2018-07-26 | 2023-02-15 | 株式会社日本触媒 | セルロースモノリスの製法および該方法によって得られるセルロースモノリス |
| US20230407225A1 (en) * | 2020-10-30 | 2023-12-21 | Corning Incorporated | Methods and systems for production of cell culture scaffolds |
Family Cites Families (55)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AT101779B (de) | 1923-07-07 | 1925-11-25 | Bleichert & Co Adolf | Verfahren zum Befördern und Verlegen von Rohrleitungen auf stark geneigten Geländeteilen. |
| US2543928A (en) * | 1946-06-08 | 1951-03-06 | Olin Ind Inc | Method of producing cellulose pellets |
| US2593786A (en) * | 1947-06-19 | 1952-04-22 | Olin Ind Inc | Regenerated cellulose pellets |
| DE907051C (de) | 1949-11-01 | 1954-02-11 | Rayonier Inc | Verfahren zur Herstellung von Viskose aus Baumwolle, insbesondere Linters |
| AT287905B (de) | 1968-09-20 | 1971-02-10 | Chemiefaser Lenzing Ag | Verfahren zur Herstellung von Faden aus regenerierter Cellulose |
| US4946953A (en) | 1986-10-16 | 1990-08-07 | Kanebo, Ltd. | Fine cellulose particles and process for production thereof employing coagulated viscose |
| JP2627642B2 (ja) | 1988-06-11 | 1997-07-09 | チッソ株式会社 | 粉末化粧料 |
| AT392972B (de) | 1988-08-16 | 1991-07-25 | Chemiefaser Lenzing Ag | Verfahren zur herstellung von loesungen von cellulose sowie einrichtung zur durchfuehrung des verfahrens |
| US5328603A (en) * | 1990-03-20 | 1994-07-12 | The Center For Innovative Technology | Lignocellulosic and cellulosic beads for use in affinity and immunoaffinity chromatography of high molecular weight proteins |
| US5331801A (en) | 1992-01-24 | 1994-07-26 | Eco Fibre Canada Inc. | Recycled yarns from textile waste and the manufacturing process therefor |
| ATA53792A (de) | 1992-03-17 | 1995-02-15 | Chemiefaser Lenzing Ag | Verfahren zur herstellung cellulosischer formkörper, vorrichtung zur durchführung des verfahrens sowie verwendung einer spinnvorrichtung |
| US6010594A (en) | 1993-03-03 | 2000-01-04 | Ahlstrom Machinery Corporation | Method of bleaching pulp with chlorine-free chemicals wherein a complexing agent is added immediately after an ozone bleach stage |
| US5447603A (en) | 1993-07-09 | 1995-09-05 | The Dow Chemical Company | Process for removing metal ions from liquids |
| US5369861A (en) | 1994-01-21 | 1994-12-06 | Burlington Industries, Inc. | Process for recycling denim waste |
| US5481864A (en) | 1994-07-11 | 1996-01-09 | Wright; Herbert J. | Cloth scrap recycling method |
| AT401392B (de) | 1994-09-05 | 1996-08-26 | Chemiefaser Lenzing Ag | Verfahren zur herstellung eines cellulosischen formkörpers |
| DE4444245C1 (de) | 1994-12-13 | 1996-07-04 | Hoechst Ag | Verfahren zum Recycling von gefärbten, cellulosischen Abfallprodukten zu Fasern |
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-
2013
- 2013-10-15 AT ATA794/2013A patent/AT515180B1/de not_active IP Right Cessation
-
2014
- 2014-11-14 DK DK14838769.9T patent/DK3058022T3/da active
- 2014-11-14 CN CN201480056149.XA patent/CN105829351B/zh not_active Expired - Fee Related
- 2014-11-14 WO PCT/AT2014/000202 patent/WO2015054711A2/de not_active Ceased
- 2014-11-14 PL PL14838769T patent/PL3058022T3/pl unknown
- 2014-11-14 EP EP14838769.9A patent/EP3058022B1/de not_active Not-in-force
- 2014-11-14 US US15/027,923 patent/US10093790B2/en not_active Expired - Fee Related
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- 2014-11-14 ES ES14838769.9T patent/ES2639807T3/es active Active
- 2014-11-14 JP JP2016524151A patent/JP6511441B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| AT515180B1 (de) | 2016-06-15 |
| US10093790B2 (en) | 2018-10-09 |
| JP2016538367A (ja) | 2016-12-08 |
| WO2015054711A2 (de) | 2015-04-23 |
| AT515180A1 (de) | 2015-06-15 |
| WO2015054711A3 (de) | 2015-07-16 |
| JP6511441B2 (ja) | 2019-05-15 |
| DK3058022T3 (da) | 2017-10-02 |
| KR20170071444A (ko) | 2017-06-23 |
| EP3058022B1 (de) | 2017-06-14 |
| US20160257806A1 (en) | 2016-09-08 |
| CN105829351B (zh) | 2019-05-10 |
| CN105829351A (zh) | 2016-08-03 |
| PL3058022T3 (pl) | 2017-11-30 |
| EP3058022A2 (de) | 2016-08-24 |
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