JPS6244072B2 - - Google Patents

Info

Publication number

JPS6244072B2

JPS6244072B2 JP58094971A JP9497183A JPS6244072B2 JP S6244072 B2 JPS6244072 B2 JP S6244072B2 JP 58094971 A JP58094971 A JP 58094971A JP 9497183 A JP9497183 A JP 9497183A JP S6244072 B2 JPS6244072 B2 JP S6244072B2

Authority

JP

Japan

Prior art keywords

weight

compound

alkyl group

heater

yarn

Prior art date

1983-05-31

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

• Espacenet
• Global Dossier
• Discuss

• 150000001875 compounds Chemical class 0.000 claims description 83
• 239000011737 fluorine Substances 0.000 claims description 82
• 229910052731 fluorine Inorganic materials 0.000 claims description 82
• -1 perfluoroalkyl sulfonic acid Chemical compound 0.000 claims description 74
• 150000003839 salts Chemical class 0.000 claims description 57
• 238000012545 processing Methods 0.000 claims description 49
• 238000000034 method Methods 0.000 claims description 36
• 229920001515 polyalkylene glycol Polymers 0.000 claims description 34
• 125000004432 carbon atom Chemical group C* 0.000 claims description 28
• 239000000314 lubricant Substances 0.000 claims description 22
• 229910052751 metal Inorganic materials 0.000 claims description 20
• 239000002184 metal Substances 0.000 claims description 20
• 238000005979 thermal decomposition reaction Methods 0.000 claims description 20
• 238000010438 heat treatment Methods 0.000 claims description 18
• 125000000217 alkyl group Chemical group 0.000 claims description 16
• 230000004580 weight loss Effects 0.000 claims description 15
• LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 9
• 229920000728 polyester Polymers 0.000 claims description 8
• 125000005010 perfluoroalkyl group Chemical group 0.000 claims description 7
• 230000008569 process Effects 0.000 claims description 7
• BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 7
• 125000002091 cationic group Chemical group 0.000 claims description 6
• 150000003014 phosphoric acid esters Chemical class 0.000 claims description 6
• QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 5
• 125000003118 aryl group Chemical group 0.000 claims description 5
• 229910052757 nitrogen Inorganic materials 0.000 claims description 5
• 125000000129 anionic group Chemical group 0.000 claims description 4
• 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 4
• 239000000919 ceramic Substances 0.000 claims description 4
• 125000001153 fluoro group Chemical group F* 0.000 claims description 4
• 238000003672 processing method Methods 0.000 claims description 4
• JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 3
• 150000001767 cationic compounds Chemical class 0.000 claims description 3
• 239000003513 alkali Substances 0.000 claims description 2
• 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
• 239000003795 chemical substances by application Substances 0.000 description 55
• 239000000835 fiber Substances 0.000 description 42
• 230000000694 effects Effects 0.000 description 33
• 239000010802 sludge Substances 0.000 description 29
• 238000012546 transfer Methods 0.000 description 24
• 238000004140 cleaning Methods 0.000 description 21
• 239000000203 mixture Substances 0.000 description 19
• 229920003171 Poly (ethylene oxide) Polymers 0.000 description 18
• 230000000052 comparative effect Effects 0.000 description 16
• 150000002222 fluorine compounds Chemical class 0.000 description 16
• 229910019142 PO4 Inorganic materials 0.000 description 15
• 235000021317 phosphate Nutrition 0.000 description 15
• 239000010452 phosphate Substances 0.000 description 14
• GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 13
• IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 12
• 229910052700 potassium Inorganic materials 0.000 description 12
• 239000002253 acid Substances 0.000 description 11
• 239000011591 potassium Substances 0.000 description 11
• QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 10
• 238000011109 contamination Methods 0.000 description 10
• RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
• KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 10
• ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 9
• 238000011156 evaluation Methods 0.000 description 9
• 125000004435 hydrogen atom Chemical group [H]* 0.000 description 9
• 238000003754 machining Methods 0.000 description 9
• 239000000126 substance Substances 0.000 description 9
• 238000007792 addition Methods 0.000 description 8
• 238000004519 manufacturing process Methods 0.000 description 8
• 229910052708 sodium Inorganic materials 0.000 description 8
• 239000011734 sodium Substances 0.000 description 8
• HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 7
• 150000007513 acids Chemical class 0.000 description 7
• 239000012190 activator Substances 0.000 description 7
• 229910052783 alkali metal Inorganic materials 0.000 description 7
• 125000002947 alkylene group Chemical group 0.000 description 7
• 125000004429 atom Chemical group 0.000 description 7
• 150000002148 esters Chemical class 0.000 description 7
• 125000003709 fluoroalkyl group Chemical group 0.000 description 7
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 7
• 239000003921 oil Substances 0.000 description 7
• NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 6
• 229910001220 stainless steel Inorganic materials 0.000 description 6
• 239000010935 stainless steel Substances 0.000 description 6
• 238000012360 testing method Methods 0.000 description 6
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
• 229910021529 ammonia Inorganic materials 0.000 description 5
• 229960003237 betaine Drugs 0.000 description 5
• 238000000354 decomposition reaction Methods 0.000 description 5
• 235000014113 dietary fatty acids Nutrition 0.000 description 5
• 239000000194 fatty acid Substances 0.000 description 5
• 229930195729 fatty acid Natural products 0.000 description 5
• 150000008040 ionic compounds Chemical class 0.000 description 5
• 239000000463 material Substances 0.000 description 5
• 238000005259 measurement Methods 0.000 description 5
• XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 5
• 238000009987 spinning Methods 0.000 description 5
• OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
• ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 4
• QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 4
• LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
• YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 4
• DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
• OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
• BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 4
• 230000015572 biosynthetic process Effects 0.000 description 4
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 4
• 230000007423 decrease Effects 0.000 description 4
• 230000008021 deposition Effects 0.000 description 4
• ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 4
• 239000000839 emulsion Substances 0.000 description 4
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
• 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
• 230000003647 oxidation Effects 0.000 description 4
• 238000007254 oxidation reaction Methods 0.000 description 4
• 229920001451 polypropylene glycol Polymers 0.000 description 4
• 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
• WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 4
• 239000007787 solid Substances 0.000 description 4
• 150000003460 sulfonic acids Chemical class 0.000 description 4
• 150000003467 sulfuric acid derivatives Chemical class 0.000 description 4
• YEAMHXDZHZNOQE-UHFFFAOYSA-N 1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluoro-n-propyloctane-1-sulfonamide Chemical compound CCCNS(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F YEAMHXDZHZNOQE-UHFFFAOYSA-N 0.000 description 3
• QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 3
• QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical compound [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 3
• ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
• 238000005299 abrasion Methods 0.000 description 3
• 238000009825 accumulation Methods 0.000 description 3
• 150000003973 alkyl amines Chemical class 0.000 description 3
• 150000001555 benzenes Chemical class 0.000 description 3
• 125000006267 biphenyl group Chemical group 0.000 description 3
• 229910052799 carbon Inorganic materials 0.000 description 3
• 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 3
• 150000002169 ethanolamines Chemical class 0.000 description 3
• 239000002563 ionic surfactant Substances 0.000 description 3
• 230000007246 mechanism Effects 0.000 description 3
• 238000002844 melting Methods 0.000 description 3
• 230000008018 melting Effects 0.000 description 3
• 239000002480 mineral oil Substances 0.000 description 3
• 235000010446 mineral oil Nutrition 0.000 description 3
• 150000002790 naphthalenes Chemical class 0.000 description 3
• 229920000570 polyether Polymers 0.000 description 3
• 229920000139 polyethylene terephthalate Polymers 0.000 description 3
• 239000012261 resinous substance Substances 0.000 description 3
• 159000000000 sodium salts Chemical class 0.000 description 3
• 150000003871 sulfonates Chemical class 0.000 description 3
• 125000000542 sulfonic acid group Chemical group 0.000 description 3
• 125000005270 trialkylamine group Chemical group 0.000 description 3
• HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
• DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
• AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
• XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
• NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical group OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
• 239000004721 Polyphenylene oxide Substances 0.000 description 2
• GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
• 238000000862 absorption spectrum Methods 0.000 description 2
• WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
• 150000001298 alcohols Chemical class 0.000 description 2
• 125000003342 alkenyl group Chemical group 0.000 description 2
• 125000005037 alkyl phenyl group Chemical group 0.000 description 2
• 239000007864 aqueous solution Substances 0.000 description 2
• IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
• 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
• 150000007942 carboxylates Chemical class 0.000 description 2
• 230000008859 change Effects 0.000 description 2
• 238000006243 chemical reaction Methods 0.000 description 2
• 238000010924 continuous production Methods 0.000 description 2
• 238000007334 copolymerization reaction Methods 0.000 description 2
• 230000001419 dependent effect Effects 0.000 description 2
• 230000006866 deterioration Effects 0.000 description 2
• 150000001991 dicarboxylic acids Chemical class 0.000 description 2
• USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 2
• KCIDZIIHRGYJAE-YGFYJFDDSA-L dipotassium;[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] phosphate Chemical class [K+].[K+].OC[C@H]1O[C@H](OP([O-])([O-])=O)[C@H](O)[C@@H](O)[C@H]1O KCIDZIIHRGYJAE-YGFYJFDDSA-L 0.000 description 2
• 239000002612 dispersion medium Substances 0.000 description 2
• 150000004665 fatty acids Chemical class 0.000 description 2
• 229910052739 hydrogen Inorganic materials 0.000 description 2
• 239000001257 hydrogen Substances 0.000 description 2
• WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
• 239000012535 impurity Substances 0.000 description 2
• 238000002329 infrared spectrum Methods 0.000 description 2
• QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
• 238000012423 maintenance Methods 0.000 description 2
• 238000012986 modification Methods 0.000 description 2
• 230000004048 modification Effects 0.000 description 2
• 229910017464 nitrogen compound Inorganic materials 0.000 description 2
• 150000002830 nitrogen compounds Chemical class 0.000 description 2
• OQILCOQZDHPEAZ-UHFFFAOYSA-N octyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OCCCCCCCC OQILCOQZDHPEAZ-UHFFFAOYSA-N 0.000 description 2
• 125000006353 oxyethylene group Chemical group 0.000 description 2
• YFSUTJLHUFNCNZ-UHFFFAOYSA-N perfluorooctane-1-sulfonic acid Chemical compound OS(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F YFSUTJLHUFNCNZ-UHFFFAOYSA-N 0.000 description 2
• 230000035699 permeability Effects 0.000 description 2
• XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
• 239000005020 polyethylene terephthalate Substances 0.000 description 2
• 229920000642 polymer Polymers 0.000 description 2
• 238000006116 polymerization reaction Methods 0.000 description 2
• 229920001296 polysiloxane Polymers 0.000 description 2
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
• YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
• 150000003152 propanolamines Chemical class 0.000 description 2
• 238000000746 purification Methods 0.000 description 2
• 239000011347 resin Substances 0.000 description 2
• 229920005989 resin Polymers 0.000 description 2
• CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
• 150000005846 sugar alcohols Polymers 0.000 description 2
• 229940124530 sulfonamide Drugs 0.000 description 2
• 238000004381 surface treatment Methods 0.000 description 2
• 239000004094 surface-active agent Substances 0.000 description 2
• DLYUQMMRRRQYAE-UHFFFAOYSA-N tetraphosphorus decaoxide Chemical compound O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 2
• HFLXWLZPQHZKJR-SCSAIBSYSA-N (4S)-2,2,3,3,4-pentafluoro-4-[fluoro(1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctylsulfonyl)amino]pentanedioic acid Chemical compound OC(=O)C(F)(F)C(F)(F)[C@@](F)(C(O)=O)N(F)S(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F HFLXWLZPQHZKJR-SCSAIBSYSA-N 0.000 description 1
• PXGZQGDTEZPERC-UHFFFAOYSA-N 1,4-cyclohexanedicarboxylic acid Chemical compound OC(=O)C1CCC(C(O)=O)CC1 PXGZQGDTEZPERC-UHFFFAOYSA-N 0.000 description 1
• WPIOBXGJZUSKGK-UHFFFAOYSA-N 16-methylheptadecyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCCCCCCCCCCCCCCCC(C)C WPIOBXGJZUSKGK-UHFFFAOYSA-N 0.000 description 1
• BIMGNSFDPAFWTK-UHFFFAOYSA-N 2-(ethylsulfonylamino)acetic acid Chemical compound CCS(=O)(=O)NCC(O)=O BIMGNSFDPAFWTK-UHFFFAOYSA-N 0.000 description 1
• MPNXSZJPSVBLHP-UHFFFAOYSA-N 2-chloro-n-phenylpyridine-3-carboxamide Chemical compound ClC1=NC=CC=C1C(=O)NC1=CC=CC=C1 MPNXSZJPSVBLHP-UHFFFAOYSA-N 0.000 description 1
• IKVCSHRLYCDSFD-UHFFFAOYSA-N 2-hexadecanoyloxyethyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCCOC(=O)CCCCCCCCCCCCCCC IKVCSHRLYCDSFD-UHFFFAOYSA-N 0.000 description 1
• UFMBOFGKHIXOTA-UHFFFAOYSA-N 2-methylterephthalic acid Chemical compound CC1=CC(C(O)=O)=CC=C1C(O)=O UFMBOFGKHIXOTA-UHFFFAOYSA-N 0.000 description 1
• LLLVZDVNHNWSDS-UHFFFAOYSA-N 4-methylidene-3,5-dioxabicyclo[5.2.2]undeca-1(9),7,10-triene-2,6-dione Chemical compound C1(C2=CC=C(C(=O)OC(=C)O1)C=C2)=O LLLVZDVNHNWSDS-UHFFFAOYSA-N 0.000 description 1
• VAGKJPNNRZBGEE-UHFFFAOYSA-N C1(=C(C(=C(C(=C1F)F)F)F)C(=O)S)C(=C(C(C(C(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)F)F Chemical compound C1(=C(C(=C(C(=C1F)F)F)F)C(=O)S)C(=C(C(C(C(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)F)F VAGKJPNNRZBGEE-UHFFFAOYSA-N 0.000 description 1
• GQDQDXGNOIUQQK-UHFFFAOYSA-N C1(=C(C(=C(C(=C1F)F)F)F)F)C(F)(P(=O)(O)O)SC(=C(C(C(C(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)F)F Chemical compound C1(=C(C(=C(C(=C1F)F)F)F)F)C(F)(P(=O)(O)O)SC(=C(C(C(C(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)F)F GQDQDXGNOIUQQK-UHFFFAOYSA-N 0.000 description 1
• GEXAOTGASRCRBM-UHFFFAOYSA-N C1(=C(C(=C(C(=C1F)F)F)F)F)C(OC(=C(C(C(C(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)F)F)(F)P(=O)(O)O Chemical compound C1(=C(C(=C(C(=C1F)F)F)F)F)C(OC(=C(C(C(C(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)F)F)(F)P(=O)(O)O GEXAOTGASRCRBM-UHFFFAOYSA-N 0.000 description 1
• DXDCSTONYYVVBA-UHFFFAOYSA-N C1(=C(C(=C(C(=C1S(=O)(=O)O)F)F)F)F)OC(=C(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)F)F Chemical compound C1(=C(C(=C(C(=C1S(=O)(=O)O)F)F)F)F)OC(=C(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)F)F DXDCSTONYYVVBA-UHFFFAOYSA-N 0.000 description 1
• 239000004471 Glycine Substances 0.000 description 1
• QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 1
• WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
• KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 1
• ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Natural products OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
• 239000004698 Polyethylene Substances 0.000 description 1
• 239000002202 Polyethylene glycol Substances 0.000 description 1
• ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
• WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
• YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 1
• COGKUZILVBRCSE-UHFFFAOYSA-N [bis(1,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,9-heptadecafluoronon-1-enoxy)-phenylmethyl]phosphonic acid Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)=C(F)OC(P(O)(=O)O)(OC(F)=C(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)C1=CC=CC=C1 COGKUZILVBRCSE-UHFFFAOYSA-N 0.000 description 1
• 239000000853 adhesive Substances 0.000 description 1
• 230000001070 adhesive effect Effects 0.000 description 1
• 239000001361 adipic acid Substances 0.000 description 1
• 235000011037 adipic acid Nutrition 0.000 description 1
• 230000001476 alcoholic effect Effects 0.000 description 1
• 125000001931 aliphatic group Chemical group 0.000 description 1
• 150000001340 alkali metals Chemical class 0.000 description 1
• 150000004996 alkyl benzenes Chemical class 0.000 description 1
• 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
• 150000008052 alkyl sulfonates Chemical class 0.000 description 1
• 229910052782 aluminium Inorganic materials 0.000 description 1
• XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
• 125000003368 amide group Chemical group 0.000 description 1
• 125000003277 amino group Chemical group 0.000 description 1
• 150000003863 ammonium salts Chemical class 0.000 description 1
• 238000004458 analytical method Methods 0.000 description 1
• 239000003945 anionic surfactant Substances 0.000 description 1
• 239000003963 antioxidant agent Substances 0.000 description 1
• 230000003078 antioxidant effect Effects 0.000 description 1
• 125000003710 aryl alkyl group Chemical group 0.000 description 1
• YOALFLHFSFEMLP-UHFFFAOYSA-N azane;2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluorooctanoic acid Chemical compound [NH4+].[O-]C(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F YOALFLHFSFEMLP-UHFFFAOYSA-N 0.000 description 1
• 230000004888 barrier function Effects 0.000 description 1
• 235000015278 beef Nutrition 0.000 description 1
• 230000008901 benefit Effects 0.000 description 1
• 235000010290 biphenyl Nutrition 0.000 description 1
• 229920001400 block copolymer Polymers 0.000 description 1
• 238000003763 carbonization Methods 0.000 description 1
• 150000001734 carboxylic acid salts Chemical class 0.000 description 1
• 150000001735 carboxylic acids Chemical class 0.000 description 1
• 239000004359 castor oil Substances 0.000 description 1
• 235000019438 castor oil Nutrition 0.000 description 1
• 239000003086 colorant Substances 0.000 description 1
• 239000002131 composite material Substances 0.000 description 1
• 238000013329 compounding Methods 0.000 description 1
• 238000001816 cooling Methods 0.000 description 1
• 229920001577 copolymer Polymers 0.000 description 1
• 125000000753 cycloalkyl group Chemical group 0.000 description 1
• 125000005265 dialkylamine group Chemical group 0.000 description 1
• HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
• 239000000975 dye Substances 0.000 description 1
• 230000005611 electricity Effects 0.000 description 1
• 238000005516 engineering process Methods 0.000 description 1
• 125000001033 ether group Chemical group 0.000 description 1
• 150000002170 ethers Chemical class 0.000 description 1
• 238000002474 experimental method Methods 0.000 description 1
• 239000004744 fabric Substances 0.000 description 1
• ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
• 150000002334 glycols Chemical class 0.000 description 1
• XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
• 230000001771 impaired effect Effects 0.000 description 1
• 230000002401 inhibitory effect Effects 0.000 description 1
• 238000011835 investigation Methods 0.000 description 1
• 229910052742 iron Inorganic materials 0.000 description 1
• 239000007788 liquid Substances 0.000 description 1
• 229910052744 lithium Inorganic materials 0.000 description 1
• 239000006224 matting agent Substances 0.000 description 1
• 238000000691 measurement method Methods 0.000 description 1
• 239000002609 medium Substances 0.000 description 1
• 150000002739 metals Chemical class 0.000 description 1
• 239000010445 mica Substances 0.000 description 1
• 229910052618 mica group Inorganic materials 0.000 description 1
• 238000002156 mixing Methods 0.000 description 1
• VIJMMQUAJQEELS-UHFFFAOYSA-N n,n-bis(ethenyl)ethenamine Chemical compound C=CN(C=C)C=C VIJMMQUAJQEELS-UHFFFAOYSA-N 0.000 description 1
• KYTZHLUVELPASH-UHFFFAOYSA-N naphthalene-1,2-dicarboxylic acid Chemical compound C1=CC=CC2=C(C(O)=O)C(C(=O)O)=CC=C21 KYTZHLUVELPASH-UHFFFAOYSA-N 0.000 description 1
• SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
• 239000002736 nonionic surfactant Substances 0.000 description 1
• SBOJXQVPLKSXOG-UHFFFAOYSA-N o-amino-hydroxylamine Chemical compound NON SBOJXQVPLKSXOG-UHFFFAOYSA-N 0.000 description 1
• QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
• 150000007524 organic acids Chemical class 0.000 description 1
• 238000006864 oxidative decomposition reaction Methods 0.000 description 1
• SNGREZUHAYWORS-UHFFFAOYSA-N perfluorooctanoic acid Chemical compound OC(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F SNGREZUHAYWORS-UHFFFAOYSA-N 0.000 description 1
• 239000003208 petroleum Substances 0.000 description 1
• 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
• 235000011007 phosphoric acid Nutrition 0.000 description 1
• 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
• 230000000704 physical effect Effects 0.000 description 1
• 239000000049 pigment Substances 0.000 description 1
• 229920000233 poly(alkylene oxides) Polymers 0.000 description 1
• 229920000768 polyamine Polymers 0.000 description 1
• 229920001748 polybutylene Polymers 0.000 description 1
• 229920000573 polyethylene Polymers 0.000 description 1
• 229920001223 polyethylene glycol Polymers 0.000 description 1
• 230000000379 polymerizing effect Effects 0.000 description 1
• 150000007519 polyprotic acids Polymers 0.000 description 1
• WWZBEXSHRVAXDY-UHFFFAOYSA-M potassium;2,3,4-tris(1,2,3,3,3-pentafluoroprop-1-enoxy)benzenesulfonate Chemical compound [K+].[O-]S(=O)(=O)C1=CC=C(OC(F)=C(F)C(F)(F)F)C(OC(F)=C(F)C(F)(F)F)=C1OC(F)=C(F)C(F)(F)F WWZBEXSHRVAXDY-UHFFFAOYSA-M 0.000 description 1
• OKOLYKRUWSHDMW-UHFFFAOYSA-M potassium;2,3-bis(1,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,9-heptadecafluoronon-1-enoxy)benzenesulfonate Chemical compound [K+].[O-]S(=O)(=O)C1=CC=CC(OC(F)=C(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)=C1OC(F)=C(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F OKOLYKRUWSHDMW-UHFFFAOYSA-M 0.000 description 1
• SJVZUJVRHXYCSP-UHFFFAOYSA-M potassium;octane-1-sulfonate Chemical compound [K+].CCCCCCCCS([O-])(=O)=O SJVZUJVRHXYCSP-UHFFFAOYSA-M 0.000 description 1
• 230000002265 prevention Effects 0.000 description 1
• KCXFHTAICRTXLI-UHFFFAOYSA-N propane-1-sulfonic acid Chemical class CCCS(O)(=O)=O KCXFHTAICRTXLI-UHFFFAOYSA-N 0.000 description 1
• 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
• 238000000197 pyrolysis Methods 0.000 description 1
• 229920005604 random copolymer Polymers 0.000 description 1
• 230000009467 reduction Effects 0.000 description 1
• 238000011160 research Methods 0.000 description 1
• 239000012260 resinous material Substances 0.000 description 1
• 229910052701 rubidium Inorganic materials 0.000 description 1
• IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 description 1
• 230000001568 sexual effect Effects 0.000 description 1
• 238000004513 sizing Methods 0.000 description 1
• 239000000779 smoke Substances 0.000 description 1
• 239000000344 soap Substances 0.000 description 1
• IUWVEVPHMRSHMP-UHFFFAOYSA-M sodium;1,1,2,2,3,3,4,4,5,5,6,6,7,7,7-pentadecafluoroheptane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F IUWVEVPHMRSHMP-UHFFFAOYSA-M 0.000 description 1
• UYCAUPASBSROMS-UHFFFAOYSA-M sodium;2,2,2-trifluoroacetate Chemical compound [Na+].[O-]C(=O)C(F)(F)F UYCAUPASBSROMS-UHFFFAOYSA-M 0.000 description 1
• 239000007921 spray Substances 0.000 description 1
• 238000005507 spraying Methods 0.000 description 1
• 239000003381 stabilizer Substances 0.000 description 1
• 230000000087 stabilizing effect Effects 0.000 description 1
• 238000010186 staining Methods 0.000 description 1
• 230000003068 static effect Effects 0.000 description 1
• 150000003456 sulfonamides Chemical class 0.000 description 1
• 230000002195 synergetic effect Effects 0.000 description 1
• 238000001308 synthesis method Methods 0.000 description 1
• 239000000057 synthetic resin Substances 0.000 description 1
• 229920003002 synthetic resin Polymers 0.000 description 1
• 239000000454 talc Substances 0.000 description 1
• 229910052623 talc Inorganic materials 0.000 description 1
• 150000005621 tetraalkylammonium salts Chemical class 0.000 description 1
• 239000004753 textile Substances 0.000 description 1
• 150000003568 thioethers Chemical class 0.000 description 1
• 125000005208 trialkylammonium group Chemical group 0.000 description 1
• 239000013638 trimer Substances 0.000 description 1
• CURCMGVZNYCRNY-UHFFFAOYSA-N trimethylazanium;iodide Chemical compound I.CN(C)C CURCMGVZNYCRNY-UHFFFAOYSA-N 0.000 description 1
• DCXXMTOCNZCJGO-UHFFFAOYSA-N tristearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 description 1
• 238000007514 turning Methods 0.000 description 1
• 238000011179 visual inspection Methods 0.000 description 1
• 239000001993 wax Substances 0.000 description 1
• 238000004804 winding Methods 0.000 description 1