PL29439B3 - A method of producing waterproof cellulose fibers. - Google Patents
A method of producing waterproof cellulose fibers. Download PDFInfo
- Publication number
- PL29439B3 PL29439B3 PL29439A PL2943936A PL29439B3 PL 29439 B3 PL29439 B3 PL 29439B3 PL 29439 A PL29439 A PL 29439A PL 2943936 A PL2943936 A PL 2943936A PL 29439 B3 PL29439 B3 PL 29439B3
- Authority
- PL
- Poland
- Prior art keywords
- fibers
- aldehydes
- solution
- cellulose fibers
- aliphatic
- Prior art date
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- 238000000034 method Methods 0.000 title claims description 8
- 229920003043 Cellulose fiber Polymers 0.000 title claims description 4
- -1 aliphatic aldehydes Chemical class 0.000 claims description 11
- 239000000835 fiber Substances 0.000 claims description 11
- 150000001299 aldehydes Chemical class 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 5
- 239000007859 condensation product Substances 0.000 claims description 4
- 239000000047 product Substances 0.000 claims description 4
- 230000002378 acidificating effect Effects 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 229940037003 alum Drugs 0.000 claims 1
- 238000002844 melting Methods 0.000 claims 1
- 230000008018 melting Effects 0.000 claims 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 239000004310 lactic acid Substances 0.000 description 3
- 235000014655 lactic acid Nutrition 0.000 description 3
- 229920000297 Rayon Polymers 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 235000013877 carbamide Nutrition 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- FJLUATLTXUNBOT-UHFFFAOYSA-N 1-Hexadecylamine Chemical compound CCCCCCCCCCCCCCCCN FJLUATLTXUNBOT-UHFFFAOYSA-N 0.000 description 1
- GKFPQWDKGDLIIE-UHFFFAOYSA-N 2,3-bis(4-methylpentyl)phenol Chemical compound C(CCC(C)C)C=1C(=C(C=CC1)O)CCCC(C)C GKFPQWDKGDLIIE-UHFFFAOYSA-N 0.000 description 1
- CYEJMVLDXAUOPN-UHFFFAOYSA-N 2-dodecylphenol Chemical compound CCCCCCCCCCCCC1=CC=CC=C1O CYEJMVLDXAUOPN-UHFFFAOYSA-N 0.000 description 1
- BQACOLQNOUYJCE-FYZZASKESA-N Abietic acid Natural products CC(C)C1=CC2=CC[C@]3(C)[C@](C)(CCC[C@@]3(C)C(=O)O)[C@H]2CC1 BQACOLQNOUYJCE-FYZZASKESA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 208000006558 Dental Calculus Diseases 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
- WRNOAELBRPKVHC-UHFFFAOYSA-N dodecylurea Chemical compound CCCCCCCCCCCCNC(N)=O WRNOAELBRPKVHC-UHFFFAOYSA-N 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Natural products OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 1
- XMYQHJDBLRZMLW-UHFFFAOYSA-N methanolamine Chemical compound NCO XMYQHJDBLRZMLW-UHFFFAOYSA-N 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- POULHZVOKOAJMA-UHFFFAOYSA-N methyl undecanoic acid Natural products CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 1
- LCTOXAHEDJCUII-UHFFFAOYSA-N n-carbamoyloctadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NC(N)=O LCTOXAHEDJCUII-UHFFFAOYSA-N 0.000 description 1
- LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- GJNDMSSZEBNLPU-UHFFFAOYSA-N octadecylurea Chemical compound CCCCCCCCCCCCCCCCCCNC(N)=O GJNDMSSZEBNLPU-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
Description
Najdluzszy czas trwania patentu do 30 sierpnia 1954 r.W patencie nr 29077 opisany jest spo¬ sób wytwarzania nieprzemakalnych wló¬ kien celulozowych, wedlug którego wlók¬ na te napawa sie zwiazkami, zawierajacy¬ mi co najmniej jedna alifatyczna lub cy- kloalifatyczna reszte utworzona z co naj¬ mniej czterech atomów wegla i mogacymi reagowac z aldehydami, a nastepnie na ob¬ robione w ten sposób wlókna dziala sie je¬ dnoczesnie lub pózniej aldehydami alifa¬ tycznymi. Jako zwiazki, wchodzace w re¬ akcje z aldehydami, mozna stosowac: ami¬ ny tluszczowe lub aminy kwasów tluszczo¬ wych, jak dodecyloamine, heksadecyloami- ne, oktadecyloamine, oktadecenyloamine, amine kwasu abietynowego, amine kwasu laurynowego, .steiarioyliometylo- lub ibuty- loamine, stearoylooktadecyloamine, lub moczniki, podstawione alkylami, np. mocz¬ nik jednoizobutylowy, mocznik jednodode- cylowy, mocznik jednooktadecylowy, mocz¬ nik stearoylowy, lub tez etery imin albo amidyny kwasów tluszczowych. Prócz po¬ wyzej wspomnianych zwiazków mozna sto-scwac równiez pochodne fenolu, np. fenol dodecylowy, fenol dwuizoheksylowy. Za¬ miast wymienionych produktów mozna stosowac ich produkty przemiany z alde¬ hydami alifatycznymi, np. ich zwiazki me- tylolowe. W razie stosowania tych produk¬ tów, staje sie zbyteczne w róznych przy¬ padkach traktowanie nastepnie aldehydem mrówkowym, wystarcza wtedy tylko o- grzewanie dodatkowe.Wynalazek niniejszy dotyczy dalszego rozwiniecia i ulepszenia wspomnianego sposobu. Wedlug wynalazku powyzej wspo¬ mnianych zwiazków, jako takich lub jako produktów ich kondensacji z aldehydami, dodaje sie do roztworów przedzalniczych, sluzacych do wytwarzania wlókien celulo¬ zowych. Wlókna, wytworzone z tych roz¬ tworów, w celu spotegowania dzialania hydrofobowego mozna ewentualnie obra¬ biac dodatkowo aldehydami alifatyczny¬ mi.Sposób moze byc przeprowadzany np. tak, ze do roztworu przedzalniczego doda¬ je sie powyzej wspomnianych cial lub pro¬ duktów ich kondensacji z aldehydami w postaci mozliwie drobnej rozproszyny, przy czym rozproszenie to mozna osiagnac za pomoca odpowiedniej obróbki wstepnej w maszynie homogenizujacej lub przez u- zycis odpowiednich emulgatorów. Roztwór przedzalniczy przedzie sie do kapieli Mullera, to jest do kapieli kwasnej, zawie¬ rajacej kwas siarkowy i siarczan isodowy, albo przedzie sie^ w inny sposób znany, przy którym stosuje sie dwie kapiele prze¬ dzalnicze. Wlókna, wytworzone w ten spo¬ sób, poddaje sie ewentualnie po wysusze¬ niu dzialaniu aldehydów. Tego rodzaju dzialanie aldehydami staje sie zbyteczne, gdy do roztworu przedzalniczego dodano juz produktów kondensacji opisanych zwiazków z aldehydami. Po wysuszeniu wlókna poddaje sie dodatkowemu ogrzewa¬ niu, najkorzystniej w srodowisku kwas¬ nym. Ogrzewanie dodatkowe mozna usku¬ teczniac np. w temperaturze 110°. Jako srodowisko kwasne moga sluzyc, np. kwas octowy, kwas mlekowy i kwasy podo¬ bne.Przyklad I. Do 5 kg roztworu wiskozy o zawartosci 7,5% celulozy i 6,5% NaOH wprowadza sie 250 cm3 10%-owej emulsji metyloloaminy kwasu stearynowego. Roz¬ twór ten przedzie sie w sposób zwykly do kapieli Mullera. Wlókna, otrzymane w ten sposób, traktuje sie w stanie wilgotnym lub wysuszonym roztworem 1%-owego roz¬ tworu kwasu mlekowego, suszy w tempe- rturze 50 — 60° i pozwala dojrze¬ wac w ciagu godziny w temperaturze 110°.Przyklad II. Do 5 kg roztworu wisko¬ zy, zawierajacego 7,5% celulozy i 6,5% NaOH dodaje sie 250 g 10%-owej emulsji amidu kwasu stearynowego. Wlókna, wy¬ przedzone z tego roztworu do kapieli Mul¬ lera, obrabia sie 30%rowym roztworem aldehydu mrówkowego i suszy lub poddaje dzialaniu par aldehydu mrówkowego w ciagu 10 godzin i suszy w temperaturze 110°.Przyklad III. Wlókna z poczatku wy¬ twarza sie i obrabia tak, jak opisano w przykladzie II. Wysuszone wlókna obra¬ bia sie nastepnie 1%-owym roztworem kwasu mlekowego, a nastepnie poddaje dojrzewaniu w ciagu 1 godziny. PLThe longest term of the patent until August 30, 1954. Patent No. 29077 describes a method of making waterproof cellulose fibers, according to which these fibers are infused with compounds containing at least one aliphatic or cycloaliphatic residue made of at least one Less than four carbon atoms which can react with aldehydes, and then the fibers thus treated are treated simultaneously or subsequently with aliphatic aldehydes. As compounds to react with aldehydes, the following may be used: fatty amines or fatty acid amines, such as dodecylamine, hexadecylamine, octadecylamine, octadecenylamine, abietic acid amine, lauric acid amine, sterioybutyliomethyl- or i-amine. loamine, stearoylooctadecylamine or ureas, substituted with alkyls, for example monisobutyl urea, monododecyl urea, monooctadecyl urea, stearoyl urea or also imine ethers or fatty acid amidines. In addition to the above-mentioned compounds, phenol derivatives can also be used, for example, dodecyl phenol, diisohexyl phenol. Instead of the products mentioned, their transformation products with aliphatic aldehydes, for example their methylol compounds, can be used. In the case of using these products, it becomes superfluous in various cases to subsequently treat with formaldehyde, and then only additional heating is sufficient. The present invention relates to the further development and improvement of said process. According to the invention, the abovementioned compounds, as such or as their condensation products with aldehydes, are added to pre-limiting solutions for the production of cellulose fibers. The fibers produced from these solutions can optionally be additionally treated with aliphatic aldehydes in order to increase the hydrophobic effect. The method can be carried out, for example, by adding the above-mentioned bodies or their condensation products to the pre-limiting solution. with the aldehydes in the form of as fine a dispersion, this dispersion can be achieved by suitable pretreatment in a homogenizing machine or by the use of suitable emulsifiers. The pre-solution will pass to a Muller bath, that is, an acid bath containing sulfuric acid and sodium sulfate, or it will pass through the method known in the art where two pre-treatment baths are used. The fibers produced in this way are, if appropriate, subjected to the action of aldehydes after drying. Such treatment with aldehydes becomes superfluous when the condensation products of the described compounds with the aldehydes have already been added to the pre-quenching solution. After drying, the fibers are subjected to additional heating, most preferably in an acidic environment. Supplementary heating may be effected, for example, at a temperature of 110 °. As an acidic medium, for example, acetic acid, lactic acid and similar acids can serve. Example I. To 5 kg of a viscose solution containing 7.5% cellulose and 6.5% NaOH, 250 cm3 of a 10% methylolamine emulsion are added stearic acid. This solution will pass in the usual manner to the Muller bath. The fibers thus obtained are treated in a wet or dried state with a 1% solution of lactic acid, dried at 50-60 ° and allowed to mature for an hour at 110 °. Example II. 250 g of a 10% strength emulsion of stearic acid amide are added to a 5 kg solution of viscose containing 7.5% cellulose and 6.5% NaOH. The fibers, separated from this muller bath solution, are treated with a 30% solution of tartar formaldehyde and dried or treated with formaldehyde vapors for 10 hours and dried at 110 °. Example III. The fibers are initially prepared and processed as described in Example II. The dried fibers are then treated with a 1% solution of lactic acid and then matured for 1 hour. PL
Claims (3)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL29439B3 true PL29439B3 (en) | 1940-12-31 |
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