EP0411493A2 - Synthetic yarn and related production procedure - Google Patents
Synthetic yarn and related production procedure Download PDFInfo
- Publication number
- EP0411493A2 EP0411493A2 EP90114443A EP90114443A EP0411493A2 EP 0411493 A2 EP0411493 A2 EP 0411493A2 EP 90114443 A EP90114443 A EP 90114443A EP 90114443 A EP90114443 A EP 90114443A EP 0411493 A2 EP0411493 A2 EP 0411493A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- yarn
- polyester
- polyamide
- copolymer
- phase
- 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.)
- Ceased
Links
- 238000000034 method Methods 0.000 title claims abstract description 14
- 238000004519 manufacturing process Methods 0.000 title description 3
- 229920000728 polyester Polymers 0.000 claims abstract description 25
- 239000004952 Polyamide Substances 0.000 claims abstract description 21
- 229920002647 polyamide Polymers 0.000 claims abstract description 20
- 238000009987 spinning Methods 0.000 claims abstract description 13
- 239000004744 fabric Substances 0.000 claims abstract description 11
- 238000004043 dyeing Methods 0.000 claims abstract description 8
- 229920001577 copolymer Polymers 0.000 claims abstract description 6
- 239000004753 textile Substances 0.000 claims abstract description 6
- 238000002156 mixing Methods 0.000 claims description 5
- 238000005516 engineering process Methods 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims description 3
- 230000003542 behavioural effect Effects 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 description 9
- 238000001125 extrusion Methods 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 6
- 238000001035 drying Methods 0.000 description 5
- 238000001816 cooling Methods 0.000 description 4
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 3
- 229920001410 Microfiber Polymers 0.000 description 3
- 238000010622 cold drawing Methods 0.000 description 3
- 235000019253 formic acid Nutrition 0.000 description 3
- 239000003658 microfiber Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 229920002292 Nylon 6 Polymers 0.000 description 2
- VQLYBLABXAHUDN-UHFFFAOYSA-N bis(4-fluorophenyl)-methyl-(1,2,4-triazol-1-ylmethyl)silane;methyl n-(1h-benzimidazol-2-yl)carbamate Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1.C=1C=C(F)C=CC=1[Si](C=1C=CC(F)=CC=1)(C)CN1C=NC=N1 VQLYBLABXAHUDN-UHFFFAOYSA-N 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 238000009941 weaving Methods 0.000 description 2
- 241000239290 Araneae Species 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 229920005601 base polymer Polymers 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000012768 molten material Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 238000004448 titration Methods 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
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/88—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds
- D01F6/90—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds of polyamides
-
- 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
- D01F6/88—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds
- D01F6/92—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds of polyesters
-
- 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
- D01F8/00—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
- D01F8/04—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers
- D01F8/12—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers with at least one polyamide as constituent
-
- 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
- D01F8/00—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
- D01F8/04—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers
- D01F8/14—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers with at least one polyester as constituent
Definitions
- the present invention concerns a new synthetic continuous filament yarn obtained by extruding a polyamide/polyester copolymer.
- Synthetic yarns are generally produced by melting down a polymer and extruding it through a multi-holed spinneret and then solidifying the obtained filaments. After extrusion, the yarns undergo a drawing or texturising process.
- Whether the drawing is hot or cold depends on the type of polymer making up the yarn; cold drawing normally in the case of polyamide, hot drawing normally in the case of polyester.
- the yarns prepared by the general method described above have shrinking and dyeing properties and a specific textile behaviour well known to all.
- the aim of the present invention is to obtain a synthetic continuous filament yarn which has both polyamide and polyester characteristics and in which the properties described above can be varied, according to the reciprocal proportions of the two components, in such a way as to make them suitable for special articles (such as technical articles, textiles for sails and textiles for electric motor covers) as well as for fabrics in general (such as for clothing and soft furnishings).
- the yarn, subject of the invention is obtained by means of a procedure which involves mixing the two components during the spinning phase in order to obtain the copolymer.
- Spinning takes place at temperatures generally ranging from 250° to 320°C; that is, between the normal thermal profiles of polyamide and polyester.
- the pick-up is then either drawn or texturised. Drawing may be done cold (using the technology typical of polyamide) or hot (using the technology typical of polyester), depending on the proportions of the individual components.
- Cold drawing is carried out at ambient temperature; hot drawing at between 80° and 170°C.
- the drawn yarn subject of the present invention has varying shrinking and dyeing properties and textile behaviour. For example, 50% shrinkage can be obtained if so desired.
- the texturisation phase does not change the properties of the yarn except, of course, in terms of morphology.
- the problem of the spinner is to find a system which allows the temperature and speeds of spinning and picking-up to be adjusted to the various stages.
- Our mixing method can be carried out by means of all known and used mixing systems, the most common being: - volumetric dosers for chips or powders; - gravimetric dosers for chips or powders; - weight-volumetric dosers for the injection of molten material.
- the product obtained by using the method of the present invention is an above-average quality yarn.
- the product obtained by means of the method of the present invention has properties which are superior to those of products produced by previous methods.
- the resulting product will have different dyeing, tactile and shrinking characteristics.
- polyamide melts in formic acid.
- a fabric made partially or wholly with this yarn is immersed in formic acid, part of the polyamide content is lost and this results in a fabric which has a different weight and feel from that of the untreated raw material.
- various dyeing effects can be obtained by varying the length of time in which the formic acid is left to act.
- this yarn can be drawn by using either polyamide (cold drawing) or polyester (hot drawing) technologies, with clear-cut differences in terms of behaviour. These differences not only relate to the well-known differences in dyeability produced by the two techniques but also to the possibility of managing (or rather, controlling) the mechanical behaviour (shrinkage) of the yarn for the successive fixing phase.
- this characteristic of the yarn could find appropriate technical application in yarns of fabrics for clothing or soft furnishings, where the characteristics mentioned above could lead to lower weaving costs (because the yarn is shrunk during the subsequent finishing phase of the completed fabric, reaching the desired compactness downstream of the weaving process) or could give the finished product a different and more original appearance (thanks to the effects of shrinking and dyeing).
- microfibres are individual fibres with a count of less than 1 denier making up a continuous filament or tufted yarn.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Artificial Filaments (AREA)
- Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
Abstract
Description
- The present invention concerns a new synthetic continuous filament yarn obtained by extruding a polyamide/polyester copolymer.
- Synthetic yarns are generally produced by melting down a polymer and extruding it through a multi-holed spinneret and then solidifying the obtained filaments. After extrusion, the yarns undergo a drawing or texturising process.
- Whether the drawing is hot or cold depends on the type of polymer making up the yarn; cold drawing normally in the case of polyamide, hot drawing normally in the case of polyester.
- The yarns prepared by the general method described above have shrinking and dyeing properties and a specific textile behaviour well known to all.
- The aim of the present invention is to obtain a synthetic continuous filament yarn which has both polyamide and polyester characteristics and in which the properties described above can be varied, according to the reciprocal proportions of the two components, in such a way as to make them suitable for special articles (such as technical articles, textiles for sails and textiles for electric motor covers) as well as for fabrics in general (such as for clothing and soft furnishings).
- This aim is reached by the creation of a synthetic continuous filament yarn composed of varying reciprocal percentages of polyamide and polyester: from 1% to 99% of polyamide and from 99% to 1% of polyester.
- The yarn, subject of the invention, is obtained by means of a procedure which involves mixing the two components during the spinning phase in order to obtain the copolymer. Spinning takes place at temperatures generally ranging from 250° to 320°C; that is, between the normal thermal profiles of polyamide and polyester. The pick-up is then either drawn or texturised. Drawing may be done cold (using the technology typical of polyamide) or hot (using the technology typical of polyester), depending on the proportions of the individual components.
- Cold drawing is carried out at ambient temperature; hot drawing at between 80° and 170°C.
- According to the type of drawing adopted, the drawn yarn subject of the present invention has varying shrinking and dyeing properties and textile behaviour. For example, 50% shrinkage can be obtained if so desired.
- The texturisation phase does not change the properties of the yarn except, of course, in terms of morphology.
- The invention will now be explained by referring to some examples of manufacture relating to PES/PAM spinning by means of the extrusion and pick-up of the partially oriented yarn (POY) obtained by mixing polyester and polyamide 6 during the polymer fusion phase.
- The following polymers are used:
- a) Polyester (PES): the base polymer was a full lustre polymer with an intrinsic viscosity η (ETA)/20°C = 0.640 DL⁻¹. Before entering the extrusion phase, this polymer was dried in a continuous plant until chip residual humidity was 30/40 ppm (depending on the length of time in the plant).
The drying plant was a MIAG-type countercurrent vertical tower whose crystalliser was separate from the drier. - b) Polyamide (nylon 6): the base polyester polymer was mixed with a full lustre chip (PAM) whose relative viscosity, determined in 96% sulphuric acid at 20°C, was η (ETA) rel 20°C = 2.70.
This polyamide was previously batch-dried in nitrogen until the residual humidity of the chips was 400 ppm. - The problem of the spinner is to find a system which allows the temperature and speeds of spinning and picking-up to be adjusted to the various stages.
- Our mixing method can be carried out by means of all known and used mixing systems, the most common being:
- volumetric dosers for chips or powders;
- gravimetric dosers for chips or powders;
- weight-volumetric dosers for the injection of molten material. - For example, it is possible to use a spinning plant composed of:
- a) a PES/PAM dosing system: a volumetric doser capable of releasing the correct proportion of chips of the two polymers directly into the mouth of the extruder; once the weight of the chips to be dosed from each of the mouths of the doser has been established, an electronic control device ensures that the system continues to keep tile input given to the desired dosage ratio;
- b) a horizontal, 90 mm diameter ⌀ Barmag extruder with five heating zones and an LTM system in front of the auger;
- c) a static mixer for homogenising the molten mass, equipped with two heating zones which can be used in the case that greater homogeneity is to be given to the final product;
- d) a heated molten polymer distribution spider;
- e) a Barmag SP spinning plant composed of: 1) steam-heated diathermic oil spinning heads; 2) sixteen 2.4 cc titration pumps; 3) 32 spinneret packages, each composed of a spinneret, a pre-spinneret with flow distributors, a metal grid filter, a metal sand container and a baffle for the sand container;
- f) a cooling chamber with an air flow perpendicular to the path of the thread;
- g) an enzyme catalyser located at the base of the cooling chamber, consisting of distribution nozzles and 0.06 cc/revolution dosing pumps;
- h) if necessary, interlacing machines before the pick-up;
- i) a Barmag SW4SLD lapping machine with a feeding godet, a drawing frame roller and a grooved roller.
- PES/PAM spinning of a 30 filament (85% polyester and 15% polyamide) 135 dtx POY destined for texturisation with a final count of 78 dtx.
- The table below shows some of the parameters adopted during the various working phases:
TABLE 1 WORKING PARAMETERS 30 filaments 135 dtx % polyamide - 15% DRYING PES drying air temperature 165° C Time spent in drier 6 hours EXTRUSION Extruder head pressure 130 kgp/cm² Temperature: Zone 1 270° C Temperature: Zone 2 270° C Temperature: Zone 3 270° C Temperature: Zone 4 270° C Temperature: Zone 5 270° C Mixer temperature Zone 1 270° C Mixer temperature Zone 2 270° C Spinning boiler temperature 282° C FILTRATION AND SPINNERET Circular spinneret diameter 100 mm Number of holes 30 Extrusion speed 16.8 m/i Capillary diameter 0.30 mm Capillary height 0.60 mm PAK pressure 110 kgp/cm² COOLING Temperature 22° C Speed at outlet 0.9 m/sec Relative humidity 50% ENZYMATION % Emulsion 12% Dosing pump capacity 0.06 cc/rev Dosing pump revolutions/minute 20 rpm INTERLACING AND PICKUP Interlacer air pressure 3.0 atm Pick-up speed 3190 m/m - The product obtained by using the method of the present invention is an above-average quality yarn.
- Using the same procedure as in Example 1, PES/PAM spinning of a 30 filament (85% polyester and 15% polyamide) 280 dtx POY destined for texturisation with a final count of 165 dtx.
- The table below shows some of the parameters adopted during the various working phases:
TABLE 2 WORKING PARAMETERS 30 filaments 280 dtx % polyamide - 15% DRYING PES drying air temperature 165° C Time spent in drier 3 hours EXTRUSION Extruder head pressure 130 kgp/cm² Temperature: Zone 1 285° C Temperature: Zone 2 285° C Temperature: Zone 3 285° C Temperature: Zone 4 280° C Temperature: Zone 5 280° C Mixer temperature Zone 1 285° C Mixer temperature Zone 2 285° C Spinning boiler temperature 292° C FILTRATION AND SPINNERET Circular spinneret diameter 100 mm Number of holes 30 Extrusion speed 34.8 m/i Capillary diameter 0.30 mm Capillary height 0.60 mm PAK pressure 120 kgp/cm² COOLING Temperature 22° C Speed at outlet 1.2 m/sec Relative humidity 50% ENZYMATION % Emulsion 12% Dosing pump capacity 0.06 cc/rev Dosing pump revolutions/minute 35 rpm INTERLACING AND PICKUP Interlacer air pressure 3.0 atm Pick-up speed 3190 m/m - Also in this case, it appears that the product obtained by means of the method of the present invention has properties which are superior to those of products produced by previous methods.
- It is obvious that it is possible to spin different compositions of the two products by appropriately modifying speeds and temperature.
- In each case, the resulting product will have different dyeing, tactile and shrinking characteristics.
- More details concerning each of the aspects characterising the said yarn are given below.
- This can be done by means of a simple polyester dye, a simple polyamide dye or by using both. In each case, the results will be different in terms of colour and intensity, and these results can be varied by changing the proportions of the two products in the composition of the yarn.
- It should be noted that polyamide melts in formic acid. When a fabric made partially or wholly with this yarn is immersed in formic acid, part of the polyamide content is lost and this results in a fabric which has a different weight and feel from that of the untreated raw material. Furthermore, various dyeing effects can be obtained by varying the length of time in which the formic acid is left to act.
- The use of such yarns, handled with imagination by an expert technician, provides the opportunity for greater creativity in an extremely wide range of fields, particularly that of fabrics for clothing or soft furnishings.
- As previosly stated, this yarn can be drawn by using either polyamide (cold drawing) or polyester (hot drawing) technologies, with clear-cut differences in terms of behaviour. These differences not only relate to the well-known differences in dyeability produced by the two techniques but also to the possibility of managing (or rather, controlling) the mechanical behaviour (shrinkage) of the yarn for the successive fixing phase.
- In practice, it is possible to obtain varying degrees of shrinkage (from almost zero to about 50%) according to the proportion of the two components in the final composition and according to whether the yarn is hot or cold drawn.
- In practice, this characteristic of the yarn could find appropriate technical application in yarns of fabrics for clothing or soft furnishings, where the characteristics mentioned above could lead to lower weaving costs (because the yarn is shrunk during the subsequent finishing phase of the completed fabric, reaching the desired compactness downstream of the weaving process) or could give the finished product a different and more original appearance (thanks to the effects of shrinking and dyeing).
- It is well known that two similar fabrics (one made of 100% polyamide and the other of 100% polyester) have a completely different "feel".
- Fabrics made from the new yarn fall between these two extremes in accordance with the different proportions of the two components.
- Furthermore, it is possible to obtain a yarn (and therefore a fabric) which is softer to the touch and more similar to those composed of microfibres, with obvious savings in terms of production.
- As is known, microfibres are individual fibres with a count of less than 1 denier making up a continuous filament or tufted yarn.
- In our case, without needing to produce microfibre threads and while maintaining a higher individual fibre count, a higher-quality, softer "feel" can be obtained.
Claims (6)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT8921394A IT8921394A0 (en) | 1989-07-31 | 1989-07-31 | SYNTHETIC YARN AND RELATED PRODUCTION PROCEDURE. |
IT2139489 | 1989-07-31 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0411493A2 true EP0411493A2 (en) | 1991-02-06 |
EP0411493A3 EP0411493A3 (en) | 1991-05-15 |
Family
ID=11181107
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP19900114443 Ceased EP0411493A3 (en) | 1989-07-31 | 1990-07-27 | Synthetic yarn and related production procedure |
Country Status (2)
Country | Link |
---|---|
EP (1) | EP0411493A3 (en) |
IT (1) | IT8921394A0 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6090494A (en) * | 1998-03-09 | 2000-07-18 | E. I. Du Pont De Nemours And Company | Pigmented polyamide shaped article incorporating free polyester additive |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1126126A (en) * | 1965-07-31 | 1968-09-05 | Teijin Ltd | Spinning process for fibres consisting of polyamides and polyesters |
DE2037742A1 (en) * | 1969-08-28 | 1971-03-11 | Allied Chemical Corp , New York, NY (VStA) | Device for extrusion molding of polymer masses from several components |
DE2063440A1 (en) * | 1970-12-23 | 1972-07-06 | J.H. Benecke Gmbh, 3001 Vinnhorst | Mixed component fibers made from polymer blends using the melt spinning process |
-
1989
- 1989-07-31 IT IT8921394A patent/IT8921394A0/en unknown
-
1990
- 1990-07-27 EP EP19900114443 patent/EP0411493A3/en not_active Ceased
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1126126A (en) * | 1965-07-31 | 1968-09-05 | Teijin Ltd | Spinning process for fibres consisting of polyamides and polyesters |
DE2037742A1 (en) * | 1969-08-28 | 1971-03-11 | Allied Chemical Corp , New York, NY (VStA) | Device for extrusion molding of polymer masses from several components |
DE2063440A1 (en) * | 1970-12-23 | 1972-07-06 | J.H. Benecke Gmbh, 3001 Vinnhorst | Mixed component fibers made from polymer blends using the melt spinning process |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6090494A (en) * | 1998-03-09 | 2000-07-18 | E. I. Du Pont De Nemours And Company | Pigmented polyamide shaped article incorporating free polyester additive |
Also Published As
Publication number | Publication date |
---|---|
IT8921394A0 (en) | 1989-07-31 |
EP0411493A3 (en) | 1991-05-15 |
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