EP0715007B1 - Fibrides plastiques - Google Patents
Fibrides plastiques Download PDFInfo
- Publication number
- EP0715007B1 EP0715007B1 EP95117219A EP95117219A EP0715007B1 EP 0715007 B1 EP0715007 B1 EP 0715007B1 EP 95117219 A EP95117219 A EP 95117219A EP 95117219 A EP95117219 A EP 95117219A EP 0715007 B1 EP0715007 B1 EP 0715007B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- fibrets
- plastic
- follows
- polyester
- fibrids
- 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
Classifications
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
- D01D5/00—Formation of filaments, threads, or the like
- D01D5/26—Formation of staple fibres
-
- 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
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/58—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products
- D01F6/62—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyesters
Definitions
- the invention relates to plastic fibrids according to the Preamble of claim 1.
- Plastic fibrids are not spinnable and not more divisible pure fibers with irregular Fiber morphology. They are made up of the crystallites and probably also put together and put amorphous fiber parts represent the smallest fiber units Possible uses of these fibers are in recent years Years has risen sharply. In addition to the conventional Areas of application, such as in papermaking, can through the growing importance Product recyclability in other sales markets be opened up.
- Plastic fibrids made of polyethylene are known to date (HDPE, LLDPE) and polypropylene (PP). Getting produced the plastic fibrids in the flash spinning process.
- the plastics are mixed in a water-solvent mixture emulsified under pressure and temperature and spray the emulsion into a vacuum. It evaporates the solvent, the temperature drops sharply and the plastic is crystallized into fibrids transformed.
- Plastic fibrids made of polyacrylonitrile (PAN) or Polyaromatics and cellulose acetate are made from prefabricated splicable fibers.
- the way leads to the production of fibrids via foils or Staple fibers.
- the film is extruded, cut, stretched and mechanically fibrillated. Under the influence of heat, the film becomes many times the length stretched.
- the use of the fibrids is essentially oriented on the raw material properties of the starting plastics. In many cases, one is procedural Hydrophilicity is a prerequisite for the possible uses. To open up new applications or existing ones Applications with new product value enhancement Providing properties would be fibrids from others Plastics, especially polyester, are desirable. Try polyester-based fibrids according to the above to produce the described process did not lead to a result. Mechanical fibrillation does not apply because of the crystallization of the film Production in a separate step (fixation) out so that because of their crystallized state can no longer be spliced while due to missing suitable solvent the spinning process is not economically feasible.
- the invention is based, new task To create plastic fibrids.
- polyester-based fibrid preferably from a Polyephtalate esters
- the fibrids are characterized by the desired Fibril fineness and shortness of 0.1 to 5 mm at the Made from.
- the fibrids according to the invention are characterized in that they consist of a polyester which is injected as a low-viscosity jet into a shear field formed by liquid jets, torn apart by the liquid jets and formed into fibrids by cooling, crystallization and orientation.
- the polyester-based fibrids have a specific surface area of 1 to 10 m 2 / g and are dispersible in water without pretreatment.
- the melting point is between 200 - 260 ° C with good long-term heat resistance.
- the Polyester jet shows a after heating Viscosity below 200 pascals second, preferably below 100 (Pa ⁇ s).
- the low-viscosity polyester is under a pressure between 100 and 1000 bar high speed in the beam freely in one high-energy shear field sprayed. Form the shear field liquid or gaseous atomizing jets a center are aligned and with high kinetic Energy at pressures between 100 and 1000 bar on the Hit the polyester jet.
- Atomizing jets from cryogenic liquefied gases like the inert gases nitrogen and argon. Water too can be used at pressures above 100 bar.
- the one in the shear field with liquid nitrogen jets torn polyester forms on cooling, Crystallization and orientation fibrids.
- the polyester is melted in an extruder through a nozzle, which the polyester jet geometry determined, with a temperature of 100 ° C to 450 ° C. freely sprayed into the shear field.
- the spray pressure is at least 100 bar and will be related to his Maximum pressure, for example 1000 bar, only through limited technical and economic limits.
- the Nozzle system consists of flat jet or full jet nozzles, which at an angle of 30 to 150 ° to Polyester jet are arranged.
- the Polyester beam torn by the energy of the shear field and at the same time extremely cooled.
- the kinetic Energy of the atomizing medium preferably one liquefied inert gas, in particular nitrogen and the large temperature difference of up to 650 K. cause such a heavy load on the polyester, that it breaks down into fibrids.
- the resulting fibrids accumulate at the bottom of the reaction space. she can be removed through an opening in the reaction chamber become.
- the resulting nitrogen gas is replaced by a Filters and a cyclone into a fan Chimney and thus into the open or into a recovery cycle promoted.
- the one from the nozzle system of the shear field required nitrogen comes from one insulated tank via a high pressure pump in the liquid Condition and under high pressure in the nozzle system.
- the fibrids produced show clear variations in density and length of the individual fibril and lie in their free surface under that over emulsion or Dissolving the surfaces of manufactured products. she have more hidden surfaces.
- the controllability of fibril sizes is beyond that of the invention Process significantly expanded, so that a very fine Pulp can be achieved.
- Polyalkylene terephthalates belong to the group of Polyephtalate ester.
- Two different types of Polyalkylene terephthalates are polyethylene terephthalates (PET) and polybutylene terephthalate (PBT). PET and PBT are hard, stiff at room temperature, even at deep ones Cold temperatures impact resistant semi-crystalline Plastics with good sliding and abrasion behavior.
- PTP is very low viscosity at higher processing temperatures.
- Celanex Type 2000-2 Manufacturer: Hoechst AG Melt index MVI 250/2: 65 cm 3/10 min Density: 1.30 g / cm 3 Crystalline melting range: 200-225 ° C
- RT 40 A low-viscosity PTP type from Hoechst AG (RT 40) was divided into fribids in the shear field with cryogenic liquefied nitrogen.
- RT 40 The physical properties of RT 40 are listed below: Trade name: Impet Type: RT 40 Manufacturer: Hoechst AG Density: 1.3 g / cm 3 Crystalline melting range: 250-260 ° C Parameter: Acid base, terephthalic and isophthalic acid Trial material PET RT 40 temperature jet 340 ° C Zone 1 350 ° C Zone 2 310 ° C Zone 3 200 ° C Nitrogen nozzle Fl.str. 1.02 mm Plastic nozzle Vollstr. 0.47 mm Nitrogen pressure 250 bar Plastic printing 180 bar Spraying time 4-5 sec Sieve beam analysis: Mesh size in um PET 800 100% 630 98.4% 400 95.2% 250 74.4%
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Mechanical Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Artificial Filaments (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Lubricants (AREA)
- Spinning Methods And Devices For Manufacturing Artificial Fibers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Paper (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
Claims (8)
- Les fibres plastiques sont caractérisées ainsi:
elles sont composées d'un polyester qui, en tant que rayon pauvre en viscosité, est injecté dans un champ découpé formé de rayons liquides, cassé par les rayons liquides et formant par refroidessement, cristallisation et orientation des fibres d'une longueur de 0,1 à 5 mm. - Les fibres plastiques sont caractérisées ainsi:
le rayon de polyester présente une viscosité inférieure à 200 (Pa . s), de préférence inférieure à 100 (Pa . s). - Les fibres plastiques sont caractérisées ainsi:
Les fibres se composent d'un testeur de polyterephtalat, - Les fibres plastiques sont caractérisées ainsi:
Les fibres se composent de polyalklenterephtalat. - Les fibres plastiques sont caractérisées ainsi:
Les fibres se composent de polybutylenterephtalat. - Les fibres plastiques sont caracterisées ainsi:
Les fibres sont injectées dans le champ découpé formé de rayons liquides à une température au dessons de leur température de décomposition entre 100° C et 450° C et à une pression entre 100 et 1000 bar et sont cassées par les rayons liquides. - Les fibres plastiques sont d'après 1 ou 6 caractérisées ainsi:
Les rayons liquides sont formés d'un gaz liquéfié gelé d'azote ou d'argon. - Les fibres plastiques sont, d'après 1, 6 ou 7 caractérisées ainsi:
Les rayons liquides sont injectés à une pression entre 10 et 600 bar sur le rayon de polyester.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE4441801 | 1994-11-24 | ||
DE4441801A DE4441801C1 (de) | 1994-11-24 | 1994-11-24 | Polyesterfibride |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0715007A1 EP0715007A1 (fr) | 1996-06-05 |
EP0715007B1 true EP0715007B1 (fr) | 1999-02-03 |
Family
ID=6534016
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP95117219A Expired - Lifetime EP0715007B1 (fr) | 1994-11-24 | 1995-11-02 | Fibrides plastiques |
Country Status (8)
Country | Link |
---|---|
US (1) | US5695695A (fr) |
EP (1) | EP0715007B1 (fr) |
JP (1) | JPH08209440A (fr) |
AT (1) | ATE176505T1 (fr) |
DE (1) | DE4441801C1 (fr) |
ES (1) | ES2131740T3 (fr) |
FI (1) | FI955640A (fr) |
ZA (1) | ZA959840B (fr) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2247423A1 (fr) * | 1996-03-06 | 1997-09-12 | Mitsubishi Rayon Co., Ltd. | Fibres a base de fibrilles, leur procede de fabrication, buse de filage utilisee pour ce procede, et moulages obtenus a partir de ces fibres |
US6168733B1 (en) | 1998-08-31 | 2001-01-02 | Eastman Chemical Company | Method for forming discrete pellets from viscous materials |
DE19959532C1 (de) * | 1999-12-10 | 2001-10-04 | Seitz Schenk Filtersystems Gmb | Verfahren und Vorrichtung zur Herstellung von filtrationsaktiven Fasern |
US10945381B1 (en) | 2014-07-02 | 2021-03-16 | Outdoor Product Innovations, Inc. | Modular tools with detachable coupling |
WO2017196864A1 (fr) | 2016-05-09 | 2017-11-16 | North Carolina State University | Particules polymères de type fractal et leur utilisation dans diverses applications |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL246230A (fr) * | 1958-12-09 | |||
DE1934541A1 (de) * | 1969-07-08 | 1971-01-14 | Basf Ag | Verfahren und Vorrichtung zur Herstellung von Stapelfasern aus thermoplastischen Kunststoffen |
BE795724A (fr) * | 1972-02-25 | 1973-08-21 | Basf Ag | Procede et dispositif de fabrication de fibres courtes en matieres synthetiques thermoplastiques |
US4210615A (en) * | 1973-05-23 | 1980-07-01 | Basf Aktiengesellschaft | Manufacture of thermoplastics fibrids |
DE2363671C3 (de) * | 1973-12-21 | 1979-09-20 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Herstellung von Kurzfasern aus Niederdruckpolyäthylen |
DE2516561C3 (de) * | 1975-04-16 | 1979-10-11 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Herstellung von Fibrillen aus Polymerisaten |
DE2543824C3 (de) * | 1975-10-01 | 1980-05-14 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Herstellung von Fibrillen aus Poly(amid-imid)-harzen und die Fibrillen aus diesen Harzen |
DE2646332B2 (de) * | 1976-10-14 | 1979-04-12 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Herstellung von Fibrillen aus fluorhaltigen Polymerisaten |
US4128614A (en) * | 1977-05-20 | 1978-12-05 | Celanese Corporation | Halogenated aromatic polyester fibers prepared via dry-spinning having reduced spin-line static generation |
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 |
DE2947490A1 (de) * | 1979-11-24 | 1981-06-04 | Hoechst Ag, 6000 Frankfurt | Polyoxymethylenfibride und verfahren zu ihrer herstellung |
US4438172A (en) * | 1980-05-28 | 1984-03-20 | Toray Industries, Inc. | Heat retaining sheet |
US5482773A (en) * | 1991-07-01 | 1996-01-09 | E. I. Du Pont De Nemours And Company | Activated carbon-containing fibrids |
-
1994
- 1994-11-24 DE DE4441801A patent/DE4441801C1/de not_active Expired - Fee Related
-
1995
- 1995-11-02 ES ES95117219T patent/ES2131740T3/es not_active Expired - Lifetime
- 1995-11-02 AT AT95117219T patent/ATE176505T1/de not_active IP Right Cessation
- 1995-11-02 EP EP95117219A patent/EP0715007B1/fr not_active Expired - Lifetime
- 1995-11-20 ZA ZA959840A patent/ZA959840B/xx unknown
- 1995-11-21 JP JP7302674A patent/JPH08209440A/ja active Pending
- 1995-11-21 US US08/561,303 patent/US5695695A/en not_active Expired - Fee Related
- 1995-11-23 FI FI955640A patent/FI955640A/fi unknown
Also Published As
Publication number | Publication date |
---|---|
US5695695A (en) | 1997-12-09 |
ATE176505T1 (de) | 1999-02-15 |
FI955640A0 (fi) | 1995-11-23 |
DE4441801C1 (de) | 1996-06-05 |
ZA959840B (en) | 1996-05-29 |
JPH08209440A (ja) | 1996-08-13 |
EP0715007A1 (fr) | 1996-06-05 |
ES2131740T3 (es) | 1999-08-01 |
FI955640A (fi) | 1996-05-25 |
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