GB1455667A - Insoluble and infusible cured phenol-aldehyde resin fibres and production thereof - Google Patents
Insoluble and infusible cured phenol-aldehyde resin fibres and production thereofInfo
- Publication number
- GB1455667A GB1455667A GB2387274A GB2387274A GB1455667A GB 1455667 A GB1455667 A GB 1455667A GB 2387274 A GB2387274 A GB 2387274A GB 2387274 A GB2387274 A GB 2387274A GB 1455667 A GB1455667 A GB 1455667A
- Authority
- GB
- United Kingdom
- Prior art keywords
- fibres
- aqueous
- phenol
- pva
- acid
- 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
Links
- 239000007864 aqueous solution Substances 0.000 abstract 9
- 229920002451 polyvinyl alcohol Polymers 0.000 abstract 8
- 239000011734 sodium Substances 0.000 abstract 6
- 229920003987 resole Polymers 0.000 abstract 5
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 abstract 4
- 239000004327 boric acid Substances 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- 238000010438 heat treatment Methods 0.000 abstract 4
- 239000002253 acid Substances 0.000 abstract 3
- 230000001112 coagulating effect Effects 0.000 abstract 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 abstract 2
- 229910021538 borax Inorganic materials 0.000 abstract 2
- 150000001639 boron compounds Chemical class 0.000 abstract 2
- GRWZHXKQBITJKP-UHFFFAOYSA-N dithionous acid Chemical compound OS(=O)S(O)=O GRWZHXKQBITJKP-UHFFFAOYSA-N 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 150000007522 mineralic acids Chemical class 0.000 abstract 2
- 229920003986 novolac Polymers 0.000 abstract 2
- 150000007524 organic acids Chemical class 0.000 abstract 2
- 238000006116 polymerization reaction Methods 0.000 abstract 2
- 229920005989 resin Polymers 0.000 abstract 2
- 239000011347 resin Substances 0.000 abstract 2
- 235000010339 sodium tetraborate Nutrition 0.000 abstract 2
- TXUICONDJPYNPY-UHFFFAOYSA-N (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate Chemical compound C1CC2CC(=O)C=C(C)C2(C)C2C1C1CCC(OC(=O)CCCCCC)C1(C)CC2 TXUICONDJPYNPY-UHFFFAOYSA-N 0.000 abstract 1
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 abstract 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 abstract 1
- 101100348008 Caenorhabditis elegans nas-2 gene Proteins 0.000 abstract 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical group OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 abstract 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 abstract 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 abstract 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical class OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 abstract 1
- 229910021626 Tin(II) chloride Inorganic materials 0.000 abstract 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 abstract 1
- 238000010306 acid treatment Methods 0.000 abstract 1
- 239000003929 acidic solution Substances 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- 150000001299 aldehydes Chemical class 0.000 abstract 1
- 239000001132 aluminium potassium sulphate Substances 0.000 abstract 1
- 235000011126 aluminium potassium sulphate Nutrition 0.000 abstract 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid group Chemical group C(C1=CC=CC=C1)(=O)O WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract 1
- 229910052810 boron oxide Inorganic materials 0.000 abstract 1
- 150000001642 boronic acid derivatives Chemical class 0.000 abstract 1
- 239000000701 coagulant Substances 0.000 abstract 1
- 229920001577 copolymer Polymers 0.000 abstract 1
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 abstract 1
- 230000032050 esterification Effects 0.000 abstract 1
- 238000005886 esterification reaction Methods 0.000 abstract 1
- 238000006266 etherification reaction Methods 0.000 abstract 1
- 239000003063 flame retardant Substances 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- RCHKEJKUUXXBSM-UHFFFAOYSA-N n-benzyl-2-(3-formylindol-1-yl)acetamide Chemical compound C12=CC=CC=C2C(C=O)=CN1CC(=O)NCC1=CC=CC=C1 RCHKEJKUUXXBSM-UHFFFAOYSA-N 0.000 abstract 1
- VGTPKLINSHNZRD-UHFFFAOYSA-N oxoborinic acid Chemical compound OB=O VGTPKLINSHNZRD-UHFFFAOYSA-N 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 abstract 1
- 229920002689 polyvinyl acetate Polymers 0.000 abstract 1
- 239000011118 polyvinyl acetate Substances 0.000 abstract 1
- GRLPQNLYRHEGIJ-UHFFFAOYSA-J potassium aluminium sulfate Chemical compound [Al+3].[K+].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O GRLPQNLYRHEGIJ-UHFFFAOYSA-J 0.000 abstract 1
- 239000001103 potassium chloride Substances 0.000 abstract 1
- 239000001508 potassium citrate Substances 0.000 abstract 1
- 229960002635 potassium citrate Drugs 0.000 abstract 1
- QEEAPRPFLLJWCF-UHFFFAOYSA-K potassium citrate (anhydrous) Chemical compound [K+].[K+].[K+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O QEEAPRPFLLJWCF-UHFFFAOYSA-K 0.000 abstract 1
- 235000011082 potassium citrates Nutrition 0.000 abstract 1
- KMUONIBRACKNSN-UHFFFAOYSA-N potassium dichromate Chemical compound [K+].[K+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O KMUONIBRACKNSN-UHFFFAOYSA-N 0.000 abstract 1
- JVUYWILPYBCNNG-UHFFFAOYSA-N potassium;oxido(oxo)borane Chemical compound [K+].[O-]B=O JVUYWILPYBCNNG-UHFFFAOYSA-N 0.000 abstract 1
- 238000007127 saponification reaction Methods 0.000 abstract 1
- 239000011780 sodium chloride Substances 0.000 abstract 1
- 239000004289 sodium hydrogen sulphite Substances 0.000 abstract 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 abstract 1
- 239000004328 sodium tetraborate Substances 0.000 abstract 1
- 239000001119 stannous chloride Substances 0.000 abstract 1
- 235000011150 stannous chloride Nutrition 0.000 abstract 1
- -1 sulphites Chemical class 0.000 abstract 1
- DHCDFWKWKRSZHF-UHFFFAOYSA-L thiosulfate(2-) Chemical compound [O-]S([S-])(=O)=O DHCDFWKWKRSZHF-UHFFFAOYSA-L 0.000 abstract 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 abstract 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 abstract 1
- 229920003169 water-soluble polymer Polymers 0.000 abstract 1
- 238000002166 wet spinning Methods 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G8/00—Condensation polymers of aldehydes or ketones with phenols only
- C08G8/38—Block or graft polymers prepared by polycondensation of aldehydes or ketones onto macromolecular compounds
-
- 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
- D01F6/94—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 other polycondensation products
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Artificial Filaments (AREA)
Abstract
1455667 Phenol-aldehyde resin fibres JAPAN EXLAN CO Ltd 29 May 1974 [29 May 1973 22 Nov 1973 26 Nov 1973 (2) 11 Dec 1973 (2)] 23872/74 Heading B5B [Also in Division C3] Insoluble and infusible, flame retardant phenol-aldehyde resin fibres are produced by curing fibres comprising 30-98% wt. of a crosslinkable phenol-aldehyde resin and 70-2% wt. of a water-soluble polymer (PVA) containing at least 50 mol. per cent of vinyl alcohol units. The phenol-aldehyde resin may be a resol or a mixture of a resol and a novolac resin. The PVA polymer preferably has a degree of polymerization of 500-2500 and may be prepared by hydrolysis of polyvinyl acetate or a copolymer of vinyl acetate, or by etherification, esterification or formalization of a part of the hydroxyl groups of the vinyl alcohol polymer thus obtained. The fibres are produced by first preparing an aqueous solution consisting of the cross-linkable phenol-aldehyde resin and PVA in the above percentage amounts, wet-spinning the aqueous solution and then curing the wetspun fibres, generally by heating above 60‹ C. and/or by acid treatment and/or by treatment with an acid and aldehyde. The aqueous solution is spun into an aqueous coagulating bath preferably containing at least one of the following coagulants: (NH 4 ) 2 SO 4 , Na 2 SO 4 , K 2 SO 4 , ZnSO 4 , CuSO 4 , FeSO 4 , MgSO 4 , (Al) 2 (SO 4 ) 3 , NH 4 NO 3 , NaNO 3 , KNO 3 , Al(NO 3 ) 3 , NaCl, KCl, Na 3 PO 4 , aluminium potassium sulphate, potassium bichromate and potassium citrate; and optionally at least one boron compound capable of forming boric ester bonds with the hydroxyl groups of the phenol/aldehyde resin and/or PVA, e.g. boric acid, metaboric acid, boron oxide, borates and metaborates; and optionally at least one reducing compound, e.g. sulphites, bisulphites, hydrosulphite, thiosulphate, bisulphite addition compounds of HCHO, hydroxylamine and stannous chloride. The coagulating bath is preferably made acid by addition of an inorganic and/or organic acid. In general the wet-spun fibres may be treated before or after curing with an inorganic and/or organic acid, or with an aqueous acidic solution containing either a boron compound or a reducing compound, which improves the colour of the fibres. In Examples 1-7 aqueous solutions of PVA having a degree of saponification of 78-99À9 mol. per cent and a degree of polymerization of 1750 and phenol-HCHO resol resin alone or in admixture with a phenol- HCHO novolac are wet-spun into aqueous coagulating baths containing Na 2 SO 4 and either boric acid or borax or potassium metaborate and optionally H 2 SO 4 . The fibres obtained are cold-drawn, heat-treated, washed and dried, and then cured by heating. In Examples 8, 9 aqueous solutions of the resol and PVA are wet spun into aqueous baths containing Na 2 SO 4 , H 2 SO 4 and either sodium hydrogen sulphite or hydrosulphite. In Examples 10, 11 and 14 aqueous solutions of the resol resin and PVA are wet spun into aqueous baths of NaS 2 O 4 , H 2 SO 4 and boric acid and the resulting fibres are cold-drawn and then crosslinked by heating. The cured fibres are then either treated with any of the following acids: H 2 SO 4 , benzoic, acetic, succinic, lactic, oxalic, maleic, malonic, H 3 PO 4 , or HCl, or are treated with an aqueous solution of boric acid or sodium borate. In Examples 12, 13 the uncured fibres of Example 10 are either treated with an aqueous solution of Na 2 SO 4 and H 2 SO 4 and then cured or are first cured by heating and then treated with aqueous p-toluene sulphonic acid. In Example 17 the crosslinked fibres of Example 10 are treated with aqueous solutions of any of the following reducing compounds: NaHSO 3 , Na 2 S 2 O 4 , SnCl 2 or with aqueous HCl alone and together with NaHSO 3 .
Applications Claiming Priority (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6010373A JPS5634648B2 (en) | 1973-05-29 | 1973-05-29 | |
JP13149773A JPS5082314A (en) | 1973-11-22 | 1973-11-22 | |
JP13291573A JPS5127775B2 (en) | 1973-11-26 | 1973-11-26 | |
JP13291673A JPS5127776B2 (en) | 1973-11-26 | 1973-11-26 | |
JP13911673A JPS5088327A (en) | 1973-12-11 | 1973-12-11 | |
JP13911573A JPS5128732B2 (en) | 1973-12-11 | 1973-12-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1455667A true GB1455667A (en) | 1976-11-17 |
Family
ID=27550773
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2387274A Expired GB1455667A (en) | 1973-05-29 | 1974-05-29 | Insoluble and infusible cured phenol-aldehyde resin fibres and production thereof |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1455667A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103409841A (en) * | 2013-07-30 | 2013-11-27 | 中原工学院 | Preparation method of boric acid modified high-ortho phenolic fiber |
US8765829B2 (en) | 2005-09-08 | 2014-07-01 | Kingspan Holdings (Irl) Limited | Phenolic foam |
CN109183187A (en) * | 2018-07-27 | 2019-01-11 | 中原工学院 | A method of the high ortho phenolic fiber of boron modification is prepared using wet spinning |
CN109208115A (en) * | 2018-07-27 | 2019-01-15 | 中原工学院 | A method of epoxy-modified high ortho position thermosetting phenolic fiber is prepared using wet spinning |
CN109208116A (en) * | 2018-07-27 | 2019-01-15 | 中原工学院 | A method of high ortho position thermosetting phenolic fiber is prepared using wet spinning |
-
1974
- 1974-05-29 GB GB2387274A patent/GB1455667A/en not_active Expired
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8765829B2 (en) | 2005-09-08 | 2014-07-01 | Kingspan Holdings (Irl) Limited | Phenolic foam |
CN103409841A (en) * | 2013-07-30 | 2013-11-27 | 中原工学院 | Preparation method of boric acid modified high-ortho phenolic fiber |
CN103409841B (en) * | 2013-07-30 | 2015-11-04 | 中原工学院 | Preparation method of boric acid modified high ortho phenolic fiber |
CN109183187A (en) * | 2018-07-27 | 2019-01-11 | 中原工学院 | A method of the high ortho phenolic fiber of boron modification is prepared using wet spinning |
CN109208115A (en) * | 2018-07-27 | 2019-01-15 | 中原工学院 | A method of epoxy-modified high ortho position thermosetting phenolic fiber is prepared using wet spinning |
CN109208116A (en) * | 2018-07-27 | 2019-01-15 | 中原工学院 | A method of high ortho position thermosetting phenolic fiber is prepared using wet spinning |
CN109208116B (en) * | 2018-07-27 | 2021-03-16 | 中原工学院 | A method for preparing high-ortho-thermosetting phenolic fibers by wet spinning |
Also Published As
Publication number | Publication date |
---|---|
DE2425558B2 (en) | 1976-07-15 |
DE2425558A1 (en) | 1974-12-19 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PCNP | Patent ceased through non-payment of renewal fee |