EP1049831A1 - Bennutzung von nylonfilmen als trockenreinigungsbeutel - Google Patents

Bennutzung von nylonfilmen als trockenreinigungsbeutel

Info

Publication number
EP1049831A1
EP1049831A1 EP99902342A EP99902342A EP1049831A1 EP 1049831 A1 EP1049831 A1 EP 1049831A1 EP 99902342 A EP99902342 A EP 99902342A EP 99902342 A EP99902342 A EP 99902342A EP 1049831 A1 EP1049831 A1 EP 1049831A1
Authority
EP
European Patent Office
Prior art keywords
nylon
copolymer
bag
film
blend
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.)
Withdrawn
Application number
EP99902342A
Other languages
English (en)
French (fr)
Inventor
James F. Insel
Carl E. Altman
Jeffrey D. Moulton
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Honeywell International Inc
Original Assignee
AlliedSignal Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by AlliedSignal Inc filed Critical AlliedSignal Inc
Publication of EP1049831A1 publication Critical patent/EP1049831A1/de
Withdrawn legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06FLAUNDERING, DRYING, IRONING, PRESSING OR FOLDING TEXTILE ARTICLES
    • D06F43/00Dry-cleaning apparatus or methods using volatile solvents
    • D06F43/007Dry cleaning methods
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06FLAUNDERING, DRYING, IRONING, PRESSING OR FOLDING TEXTILE ARTICLES
    • D06F43/00Dry-cleaning apparatus or methods using volatile solvents
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65DCONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D29/00Sacks or like containers made of fabrics; Flexible containers of open-work, e.g. net-like construction
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/18Manufacture of films or sheets
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L77/00Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L77/00Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
    • C08L77/02Polyamides derived from omega-amino carboxylic acids or from lactams thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L77/00Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
    • C08L77/06Polyamides derived from polyamines and polycarboxylic acids
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06FLAUNDERING, DRYING, IRONING, PRESSING OR FOLDING TEXTILE ARTICLES
    • D06F95/00Laundry systems or arrangements of apparatus or machines; Mobile laundries 
    • D06F95/002Baskets or bags specially adapted for holding or transporting laundry; Supports therefor
    • D06F95/004Bags; Supports therefor
    • D06F95/006Bags for holding the laundry during washing

Definitions

  • This invention relates to films for use in dry cleaning bags for in-home use.
  • the bag is formed of a nylon film composition selected from the group consisting of (a) a blend comprising at least one nylon homopolymer and at least one nylon copolymer and (b) at least one nylon copolymer.
  • the nylon homopolymer is nylon 6, nylon 66 or a mixture of nylon 6 and 66
  • the nylon copolymer is a nylon 6/66 copolymer, a nylon 6/12 copolymer or a mixture of such copolymers.
  • a plastic bag for use in dry cleaning wherein the bag is formed from a film selected from the group consisting of (a) a blend comprising at least one nylon homopolymer and at least one nylon copolymer and (b) at least one nylon copolymer, with the preferred nylon homopolymers and copolymers being those mentioned in the previous sentence.
  • the nylon composition may also contain additives such as heat stabilizers, plasticizers, extrusion aids, pigments, and the like.
  • Bags formed from such nylon compositions are resistant to hot spots in a home dryer, and are soft, flexible and heat stable.
  • the nylon composition used in this invention comprises a blend of at least one nylon homopolymer and at least one nylon copolymer.
  • the nylon homopolymer is selected from the group consisting of nylon 6, nylon 66 and mixtures thereof.
  • nylon homopolymers can be prepared in any conventional manner.
  • nylon 6 can be prepared by the condensation of epsilon-caprolactam, and nylon 66 from the hexamethylene diamine (or a salt thereof) and adipic acid.
  • nylon 6 the preferred nylon, such polymer typically has a number average molecular weight as measured in formic acid in the range of about 15,000 to about 40,000, preferably in the range of about 25,000 to about 35,000.
  • the nylon 6 may be washed, unwashed, or partially washed.
  • the nylon 6 may have balanced end groups, or be monofunctionally or difunctionally terminated.
  • nylon 66 polymers of film forming molecular weight are preferred.
  • the composition used in this invention further comprises at least one nylon copolymer.
  • the preferred copolymer is poly(epsiloncaprolactam-hexamethylene adipamide) copolymer (which is herein also referred to as nylon 6/66 copolymer).
  • the nylon 6/66 copolymer may be formed by any conventional means known to the art, including but not limited to processes wherein suitable monomeric constituents, i.e. caprolactam, hexamethylene diamine, and adipic acid are reacted to form a copolymer. In a further conventional manner, a salt of hexamethylene diamine, and adipic acid is added to caprolactam, and these constituents are reacted to form a copolymer.
  • suitable monomeric constituents i.e. caprolactam, hexamethylene diamine, and adipic acid
  • the relative proportion of nylon 6 to nylon 66 components in the copolymer may vary widely, with the proportion of nylon 6 segments comprising any amount between 0.1% to 99.9% of the nylon 6/66 copolymer structure.
  • the nylon 6/66 copolymer may be either a block type copolymer or a random type copolymer.
  • the nylon 6 segments of the nylon 6/66 copolymer comprises between 10% and 35% by weight, most preferably the nylon 6 comprises between 20% and 30% by weight of the nylon 6/66 copolymer, with the nylon 66 segments comprising the remaining amounts.
  • the nylon 6/66 copolymer preferably has a number average molecular weight as measured in a 95% sulfuric acid solution, in the range of about 15,000 to about 40,000, preferably in the range of about 20,000 to about 35,000.
  • the nylon 6/66 copolymer may be washed, unwashed or partially washed.
  • nylon 6/12 copolymer which can be prepared from caprolactam and lauryl lactam, and the relative proportions of nylon 6 segments to nylon 12 segments can likewise vary widely. As pointed out above, mixtures of two or more copolymers may also be employed.
  • the relative ratio of the nylon homopolymer to the nylon copolymer may be varied over a broad range so that the nylon homopolymer comprises between about 0.01% to about 99.99% of the sum of the weights of the nylon homopolymer and nylon copolymer of the film composition. It is to be understood that the relative ratio of the nylon homopolymer to the nylon copolymer in a composition may be purposely varied and selected so to produce a film having particular desired physical properties.
  • the compositions comprise from about 40 to about 80% by weight of nylon homopolymer and correspondingly from about 60 to about 20% by weight of nylon copolymer, and more preferably about 55 to about 75% by weight of nylon homopolymer and correspondingly from about 45 to about 25% by weight of nylon copolymer, especially where the nylon homopolymer is nylon 6 and the nylon copolymer is nylon 6/66.
  • the films can be formed only from a nylon copolymer, such as nylon 6/66 and nylon 6/12 and mixtures thereof, with the nylon 6/66 being presently preferred.
  • the films of this invention may contain conventional additives such as coloring agents (e.g., dyes or pigments), lubricants, mold release agents, flame retardants, fibrous and paniculate fillers and reinforcing agents, ultraviolet and other light stabilizers, heat stabilizers, extrusion aids, plasticizers, nucleating agents, and other conventional additives.
  • Blending or mixing of the constituents which comprise the film compositions may be by any effective means which preferably results in uniform dispersion. All of the constituents may be mixed simultaneously or separately by a blender, kneader, roll, extruder, or the like in order to assure a uniform blend of the constituents. In the alternative, the nylon homopolymer and the nylon copolymer may be blended or mixed by mixer, blender, kneader, roll, extruder, or the like in order to assure a uniform blend of the constituents and resultant mixture is melt-kneaded with the remaining constituents in an extruder to make a uniform blend.
  • a common method is to melt-knead a previously dry-blended composition further in a heated extruder provided with a single-screw, or in a heated extruder provided with a single-screw, or in the alternative, a plurality of screws, extrude the uniform composition into strands, and subsequently chop the extruded strands into pellets.
  • the dry-blended composition is provided to a film forming apparatus which comprises a heat extruder having at least a single screw, which heated extruder melts the constituents of the dry-blended composition and forms a film therefrom through a film die.
  • the film compositions may be formed into films by conventional methods using conventional film forming apparatus.
  • Conventional methods include the production of films by blown film techniques, by extruding the film through a film forming die and optionally casting the film, calendering, and forming a film forming composition into a billet and subsequently skiving a film from a billet.
  • a film forming composition is melt blended in an extruder to form an extrudate which is then extruded through a film forming die onto a casting roll.
  • the film forming apparatus may be one which is referred to in the art as a blown film apparatus and includes a circular die head through which the film composition is forced and formed into a film bubble, which is ultimately collapsed and formed into a film.
  • the films may optionally be stretched or orientated in any direction if so desired.
  • the film may be stretched in either the direction coincident with the direction of movement of the film being withdrawn from the casting roll, also referred to in the art as the machine direction, or in a direction which is perpendicular to the machine direction, and referred to in the art as the transverse direction, or in both the machine direction and the transverse direction.
  • the films formed by any of the above methods may be of any thickness desired and includes those which have thicknesses less than 100 mils.
  • the films Preferably, the films have a thickness in the range of about 0.1 mil and about 10 mils; most preferably the films have a thickness between about 1 mils and about 5 mils. While such thicknesses are preferred as providing a readily flexible film, it is to be understood that other film thicknesses may be produced to satisfy a particular need.
  • the above-described films are characterized by being soft and flexible as well as heat stable, so that bags formed from these films have the same attributes which are particularly desirable in bags used in home dry cleaning processes.
  • These films may be formed into bags by any conventional technique. For example, when made by a blown film process the bubble could be collapsed and one end heat sealed, leaving the other end open. Or a flat cast film can be centerfolded and the sides and one end heat sealed. Obviously other techniques can be used to form the bags.
  • These bags may be provided with conventional closing means which are used to enclose the contents prior to use.
  • bags formed from the above-described films are used in a process of cleaning fabrics, especially clothes, such as in a typical home dryer.
  • the soiled clothes are placed in the bag together with one or more cleansing agents and the open end(s) of the bag is secured.
  • the cleansing agent may be incorporated into a carrier, such as a non-woven fiber sheet.
  • the bag is then placed into the drum of a conventional automatic clothes dryer. When the clothes dryer is started, the drum is rotated and hot air is introduced in the dryer.
  • the amount of time which the bag remains in the dryer is dependent upon a number of factors, such as the amount of clothes, their degree of soilness, the effectiveness of the cleansing agent, the temperature in the dryer and similar considerations. Typical times may range, for example, from about 5 minutes to about 40 minutes at air temperatures in the range of about 50 to about 400 °C, for example.
  • the bags can be used with any conventional clothes dryer, such as electric, natural gas or propane gas dryers.
  • the bags are resistant to hot spots which may occur during the operation of the dryer. As a result, the bag material does not melt during the dry cleaning operation in the dryer.
  • the films of this invention are soft and flexible, as well as heat stable.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Polymers & Plastics (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Organic Chemistry (AREA)
  • Textile Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Mechanical Engineering (AREA)
  • Materials Engineering (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Polyamides (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
EP99902342A 1998-01-16 1999-01-18 Bennutzung von nylonfilmen als trockenreinigungsbeutel Withdrawn EP1049831A1 (de)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US7129598P 1998-01-16 1998-01-16
US71295P 1998-01-16
US22672899A 1999-01-07 1999-01-07
US226728 1999-01-07
PCT/US1999/001042 WO1999036610A1 (en) 1998-01-16 1999-01-18 Use of nylon films in home dry cleaning bags

Publications (1)

Publication Number Publication Date
EP1049831A1 true EP1049831A1 (de) 2000-11-08

Family

ID=26752067

Family Applications (1)

Application Number Title Priority Date Filing Date
EP99902342A Withdrawn EP1049831A1 (de) 1998-01-16 1999-01-18 Bennutzung von nylonfilmen als trockenreinigungsbeutel

Country Status (7)

Country Link
EP (1) EP1049831A1 (de)
JP (1) JP2002509011A (de)
KR (1) KR20010034207A (de)
CN (1) CN1293726A (de)
AU (1) AU2234899A (de)
CA (1) CA2318155A1 (de)
WO (1) WO1999036610A1 (de)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU3382400A (en) * 1999-03-01 2000-09-21 Allied-Signal Inc. Use of nylon films in home dry cleaning and/or fabric refreshing bags
DE60032618T2 (de) * 1999-10-01 2007-11-15 The Procter & Gamble Company, Cincinnati Behälter zum Waschen von empfindlicher Wäsche in einer Waschmaschine
DE19957663A1 (de) * 1999-11-30 2001-05-31 Basf Ag Verfahren zur kontinuierlichen Herstellung von Copolyamiden, die auf einem Lactam (I), einem Diamin (II) und einer Dicarbonsäure (III) basieren
FR2938846B1 (fr) * 2008-11-24 2012-12-07 Rhodia Operations Composition polymere thermoplastique a base de polyamide

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3432253A (en) * 1966-04-27 1969-03-11 Peter Ray Dixon Fabric cleaning process
GB8923285D0 (en) * 1989-10-16 1989-12-06 Unilever Plc Fabric conditioning article
US5206309A (en) * 1991-03-06 1993-04-27 Allied Signal Inc. Heat stable film composition comprising polyepsiloncaprolactam
US5681355A (en) * 1995-08-11 1997-10-28 The Procter & Gamble Company Heat resistant dry cleaning bag

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO9936610A1 *

Also Published As

Publication number Publication date
WO1999036610A1 (en) 1999-07-22
AU2234899A (en) 1999-08-02
CN1293726A (zh) 2001-05-02
JP2002509011A (ja) 2002-03-26
KR20010034207A (ko) 2001-04-25
CA2318155A1 (en) 1999-07-22

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