DE1101347B - Process for the flame-retardant finishing of light fabrics, which consist entirely or mainly of cellulose - Google Patents
Process for the flame-retardant finishing of light fabrics, which consist entirely or mainly of celluloseInfo
- Publication number
- DE1101347B DE1101347B DEA24851A DEA0024851A DE1101347B DE 1101347 B DE1101347 B DE 1101347B DE A24851 A DEA24851 A DE A24851A DE A0024851 A DEA0024851 A DE A0024851A DE 1101347 B DE1101347 B DE 1101347B
- Authority
- DE
- Germany
- Prior art keywords
- plasticizer
- chlorine
- flame
- cellulose
- mainly
- 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.)
- Pending
Links
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/244—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of halogenated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K13/00—Use of mixtures of ingredients not covered by one single of the preceding main groups, each of these compounds being essential
- C08K13/02—Organic and inorganic ingredients
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
DEUTSCHESGERMAN
Die vorliegende Erfindung betrifft ein Verfahren zur flammfesten Ausrüstung von leichten Geweben, insbesondere von Wäschestücken für Frauen und Kinder, z. B. von leichten Baumwollgeweben, wie Flannelette.The present invention relates to a method for the flame-retardant finishing of light fabrics, in particular of laundry items for women and children, e.g. B. of light cotton fabrics such as flannelette.
Es ist das Ziel der Erfindung, trotz der Imprägnierung mit dem flarnmfestmachenden Antimontrioxyd die damit verbundene Versteifung durch. Zusatz von Weichmachern zu kompensieren, wobei aber die Waschfestigkeit der Imprägnierung nicht verlorengehen darf.It is the aim of the invention, in spite of the impregnation with the flame-proofing antimony trioxide associated stiffening by. To compensate for the addition of plasticizers, but with the washing resistance the impregnation must not be lost.
Dies wird erreicht, indem man die leichten Gewebe mit einer wäßrigen Suspension imprägniert, die, bezogen auf Feststoffe der Dispersion, 10 bis 20% Antimontrioxyd, 30 bis 50 °/0 Weichmacher und im übrigen Polyvinylchlorid oder ähnliche Polymerisate, wie Polyvinylidenchlorid oder Mischpolymerisate aus Vinylchlorid und Vinylidenchlorid oder Gemische dieser Polymerisate, enthält. In dieser Dispersion soll der Weichmacher aus nicht chlorhaltigen Weichmachern und bis zu 50% chlorhaltigem Weichmacher bestehen, und der Chlorgehalt des Weichmachergemisches soll mindestens 15 Gewichtsprozent, vorzugsweise mindestens 20 Gewichtsprozent Chlor betragen.This is achieved by impregnating the light fabric with an aqueous suspension containing, based on the solids of the dispersion, 10 to 20% of antimony trioxide, 30 to 50 ° / 0 plasticizers and the rest of polyvinyl chloride or similar polymers such as polyvinylidene chloride or copolymers of vinyl chloride and vinylidene chloride or mixtures of these polymers. In this dispersion, the plasticizer should consist of non-chlorine-containing plasticizers and up to 50% chlorine-containing plasticizer, and the chlorine content of the plasticizer mixture should be at least 15 percent by weight, preferably at least 20 percent by weight, chlorine.
Die imprägnierten Gewebe werden zur Fixierung der Imprägnierung bei etwa 110 bis 15O0C behandelt.The impregnated fabrics are treated to fix the impregnation at about 110 to 15O 0 C.
Die bisher vorgeschlagenen Massen erteilen den behandelten Geweben eine gewisse Steifheit. Dies ist bei schweren Geweben, z. B. Segeltuch, nicht zu beanstanden und kann sogar vorteilhaft sein. Eine solche Imprägnierung ist aber bei leichten Baumwollgeweben, wie Flannelette, die für die Herstellung von Kleidungsstücken, insbesondere für Frauen und Kinder, verwendet werden, vollständig unbrauchbar.The masses proposed so far give the treated fabrics a certain stiffness. This is at heavy tissues, e.g. B. canvas, not objectionable and can even be beneficial. Such an impregnation but with light cotton fabrics, such as flannelettes, which are used for the production of garments, especially used for women and children, completely unusable.
Mit dem Ausdruck »nicht chlorhaltige Weichmacher« ist jeder beliebige Weichmacher gemeint, der üblicherweise bei der Herstellung von Polyvinylchlorid verwendet wird. Solche Weichmacher können brennbar sein, wie z. B. Dioctylphthalat und Dioctylsebacat.The term "non-chlorine-containing plasticizer" means any plasticizer that is customary used in the manufacture of polyvinyl chloride. Such plasticizers can be flammable be, such as B. dioctyl phthalate and dioctyl sebacate.
Als chlorhaltige Weichmacher sind vorzugsweise chlorierte Paraffine oder chloriertes Diphenyl zu verwenden.Chlorinated paraffins or chlorinated diphenyl should preferably be used as chlorinated plasticizers.
Die Verwendung eines chlorhaltigen Stoffes als Bestandteil des Weichmachers hat zwei Vorteile:Using a chlorine-containing substance as a component of the plasticizer has two advantages:
1. Da er selbst nicht brennbar ist, gestattet er die Einverleibung eines höheren Gehaltes an Weichmachern in die Masse, als es sonst zulässig wäre, so daß die Ausrüstung, die dem Gewebe erteilt ist, bei gleichzeitiger Flammfestigkeit eine weichere ist.1. Since it is not flammable itself, it allows the incorporation of a higher content of plasticizers to the extent that it would otherwise be permissible, so that the equipment given to the fabric is a softer one with simultaneous flame retardancy.
2. Die obenerwähnten chlorhaltigen Weichmacher verleihen dem Textilgut eine weichere Ausrüstung als äquivalente Mengen anderer nicht brennbarer Weichmacher, wie Tritolylphosphat.2. The above-mentioned chlorine-containing softeners give the textile a softer finish than equivalent amounts of other non-flammable plasticizers such as tritolyl phosphate.
Im folgenden sind Beispiele von erfindungsgemäß anzuwendenden feuerhemmenden Massen angeführt. Mit diesen Massen ausgerüstetes Gewebe behielt seine feuerhemmende Eigenschaft und seinen weichen Griff, auchExamples of fire-retardant compositions to be used according to the invention are given below. With Fabric finished with these measures retained its fire-retardant property and its soft hand, too
Verfahren zur öammfesten AusrüstungProcedure for flame-proof equipment
von leichten Geweben,of light fabrics,
die ganz oder zum wesentlichen Teilwhich in whole or in part
aus Cellulose bestehenconsist of cellulose
Anmelder:Applicant:
Associated Lead Manufacturers Limited,
LondonAssociated Lead Manufacturers Limited,
London
Vertreter: Dipl.-Ing. G. Weinhausen, Patentanwalt,
München 22, Widenmayerstr. 46Representative: Dipl.-Ing. G. Weinhausen, patent attorney,
Munich 22, Widenmayerstr. 46
Beanspruchte Priorität:
Großbritannien vom 9. Mai 1955Claimed priority:
Great Britain 9 May 1955
Norman John Read, Greenford, MiddlesexNorman John Read, Greenford, Middlesex
(Großbritannien),
ist als Erfinder genannt worden(Great Britain),
has been named as the inventor
nach wiederholtem Waschen und Reiben und auch nachdem es einer chemischen Reinigung unterworfen war. In allen Beispielen sind die Mengen Gewichtsmengen.after repeated washing and rubbing, and also after being dry-cleaned was. In all examples the amounts are amounts by weight.
Die Masse bestand aus 44 Gewichtsteilen Polyvinylchlorid-Latex (52% Polyvinylchlorid und 48% Wasser), 44,6 Teilen Weichmacher, bestehend aus einem Gemisch gleicher Gewichtsmengen Dioctylphthalat und 65%igem chloriertem Diphenyl (als 65%ige wäßrige Emulsion) und 11,4 Teilen Antimontrioxyd. Die Masse wurde unter Verwendung von 4 Teilen einer 60%igen Paste von Dioctymatriumsulfosuccinat als Emulgiermittel und als Emulsionsstabilisator von 2 Teilen einer 2%igen wäßrigen Lösung von Natriumcarboxymethylcellulose in Wasser emulgiert.The mass consisted of 44 parts by weight of polyvinyl chloride latex (52% polyvinyl chloride and 48% water), 44.6 parts of plasticizer, consisting of a mixture of equal amounts by weight of dioctyl phthalate and 65% strength chlorinated diphenyl (as a 65% aqueous emulsion) and 11.4 parts of antimony trioxide. The crowd was taking Use of 4 parts of a 60% paste of dioctymodium sulfosuccinate as an emulsifier and as Emulsion stabilizer of 2 parts of a 2% aqueous solution of sodium carboxymethyl cellulose in Water emulsified.
Es können hierbei auch Weichmachermischungen aus 75% Dioctylphthalat und 25% chloriertem Diphenyl oder aus 66% Dioctylphthalat und 34% chloriertem Diphenyl verwendet werden.Plasticizer mixtures of 75% dioctyl phthalate and 25% chlorinated diphenyl can also be used here or from 66% dioctyl phthalate and 34% chlorinated diphenyl can be used.
Ein Gemisch aus 362 Teilen Dioctylphthalat und 362 Teilen chloriertem Paraffin mit 45% Chlor, enthaltend 2 Teile Dioctyhiatriumsuccinat, wurde mitContaining a mixture of 362 parts of dioctyl phthalate and 362 parts of chlorinated paraffin with 45% chlorine 2 parts of Dioctyhiatriumsuccinat, was with
109 529/664109 529/664
367 Teilen Sb2O3 zermahlen und dann mit 2057 Teilen Polyvinylchlorid-Latex (vgl. Beispiel 1) und 500 Teilen Wasser mit 5 Teilen einer 60%igen Paste von Dioctylnatriumsuccinat in Wasser und 25 Teilen einer 2°/0igen wäßrigen Lösung von Natriumcarboxymethylcellulose emulgiert.367 parts Sb 2 O ground 3 and then with 2057 parts of polyvinyl chloride latex (see. Example 1) and 500 parts of water with 5 parts of a 60% paste of dioctyl sodium succinate in water and 25 parts of a 2 ° / 0 aqueous solution of sodium carboxymethylcellulose emulsified.
Die Emulsion wurde entsprechend der im Beispiel 2 angeführten hergestellt aus 2057 Teilen Polyvinylchlorid-Latex (vgl. Beispiel 1), 544 Teilen Dioctylphthalat, 180 Teilen chloriertem Paraffin mit 54% Chlor und 367 Teilen Antimantrioxyd.The emulsion was prepared from 2057 parts of polyvinyl chloride latex in accordance with that given in Example 2 (See. Example 1), 544 parts of dioctyl phthalate, 180 parts of chlorinated paraffin with 54% chlorine and 367 parts of antimony trioxide.
Die nach den vorstehenden Beispielen hergestellte Emulsion kann, falls es gewünscht ist, vor dem Aufbringen auf das Gewebe mit Wasser verdünnt werden. Sie kann aufgebracht werden, indem man das Gewebe in die Dispersion eintaucht und anschließend die überschüssige Flüssigkeit mit einem Wringer entfernt. Nach der Behandlung wird das Gewebe durch Erhitzen in einem Ofen auf etwa 110 bis 1500C behandelt. Die Erhitzungszeit hängt von der Feuchtigkeitsmenge ab, die in den Geweben zurückgehalten wird, und kann von etwa 2 bis 10 Minuten variieren.The emulsion prepared according to the above examples can, if desired, be diluted with water prior to application to the fabric. It can be applied by dipping the fabric into the dispersion and then removing the excess liquid with a wringer. After the treatment, the fabric is treated by heating it to about 110 to 150 ° C. in an oven. The heating time depends on the amount of moisture retained in the fabrics and can vary from about 2 to 10 minutes.
Das erfindungsgemäße Verfahren kann auch auf alle leichten Gewebe angewendet werden, die aus Cellulosematerial bestehen oder einen wesentlichen Teil davon enthalten.The method according to the invention can also be applied to all light fabrics made of cellulose material exist or contain a substantial part thereof.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB355767X | 1955-05-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
DE1101347B true DE1101347B (en) | 1961-03-09 |
Family
ID=10379269
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DEA24850A Pending DE1154067B (en) | 1955-05-09 | 1956-05-07 | Process for the production of a stable, aqueous flame-retardant impregnation dispersion |
DEA24851A Pending DE1101347B (en) | 1955-05-09 | 1956-05-07 | Process for the flame-retardant finishing of light fabrics, which consist entirely or mainly of cellulose |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DEA24850A Pending DE1154067B (en) | 1955-05-09 | 1956-05-07 | Process for the production of a stable, aqueous flame-retardant impregnation dispersion |
Country Status (6)
Country | Link |
---|---|
BE (2) | BE547651A (en) |
CH (2) | CH355767A (en) |
DE (2) | DE1154067B (en) |
FR (2) | FR1149605A (en) |
GB (2) | GB791803A (en) |
NL (2) | NL111139C (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1619072B1 (en) * | 1965-02-18 | 1970-06-18 | Hooker Chemical Corp | Process for the flame retardancy of cellulose textiles or paper material |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3642531A (en) * | 1969-11-28 | 1972-02-15 | Dyna Therm Corp | Water based fire protective composition applied to electrical cable |
DE4403470A1 (en) * | 1994-02-04 | 1995-08-10 | Lueckenhaus Tech Textilien Gmb | Coated fabric made with coated synthetic filament warp yarn |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2536978A (en) * | 1949-12-07 | 1951-01-02 | American Cyanamid Co | Oil-in-water type emulsion for flameproofing fabrics |
US2591368A (en) * | 1947-01-22 | 1952-04-01 | Treesdale Lab And Textile Proc | Water-and flameproofing composition |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB603425A (en) * | 1942-10-22 | 1948-06-16 | Johnson & Johnson Great Britai | Improvements in and relating to flame-resistant coating or impregnating compositions |
US2536988A (en) * | 1949-12-07 | 1951-01-02 | American Cyanamid Co | Flame resistant and mildew resistant composition for cellulose fibers and fabrics |
-
0
- BE BE547652D patent/BE547652A/xx unknown
- BE BE547651D patent/BE547651A/xx unknown
- NL NL207019D patent/NL207019A/xx unknown
- NL NL111139D patent/NL111139C/xx active
-
1955
- 1955-05-09 GB GB10005/56A patent/GB791803A/en not_active Expired
- 1955-05-09 GB GB13388/55A patent/GB791802A/en not_active Expired
-
1956
- 1956-05-07 DE DEA24850A patent/DE1154067B/en active Pending
- 1956-05-07 DE DEA24851A patent/DE1101347B/en active Pending
- 1956-05-08 CH CH355767D patent/CH355767A/en unknown
- 1956-05-08 CH CH356437D patent/CH356437A/en unknown
- 1956-05-09 FR FR1149605D patent/FR1149605A/en not_active Expired
- 1956-05-09 FR FR1149604D patent/FR1149604A/en not_active Expired
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2591368A (en) * | 1947-01-22 | 1952-04-01 | Treesdale Lab And Textile Proc | Water-and flameproofing composition |
US2536978A (en) * | 1949-12-07 | 1951-01-02 | American Cyanamid Co | Oil-in-water type emulsion for flameproofing fabrics |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1619072B1 (en) * | 1965-02-18 | 1970-06-18 | Hooker Chemical Corp | Process for the flame retardancy of cellulose textiles or paper material |
Also Published As
Publication number | Publication date |
---|---|
DE1154067B (en) | 1963-09-12 |
FR1149605A (en) | 1957-12-30 |
NL111139C (en) | |
FR1149604A (en) | 1957-12-30 |
CH356437A (en) | 1961-08-31 |
NL207019A (en) | |
GB791802A (en) | 1958-03-12 |
CH355767A (en) | 1961-07-31 |
BE547651A (en) | |
BE547652A (en) | |
GB791803A (en) | 1958-03-12 |
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