JPS62175741A

JPS62175741A - 色素画像の光堅牢化方法

色素画像の光堅牢化方法

Info

Publication number: JPS62175741A
Authority: JP; Japan
Prior art keywords: group; groups; represented; general formula; alkyl
Prior art date: 1986-01-29
Legal status : Granted

Application number

JP1756886A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0581029B2 (enExample

Inventor

Toyoki Nishijima

豊喜西嶋

Kaoru Onodera

薫小野寺

Current Assignee

Konica Minolta Inc

Original Assignee

Konica Minolta Inc

Priority date

1986-01-29

Filing date

1986-01-29

Publication date

1987-08-01

1986-01-29 Application filed by Konica Minolta Inc filed Critical Konica Minolta Inc

1986-01-29 Priority to JP1756886A priority Critical patent/JPS62175741A/ja

1987-08-01 Publication of JPS62175741A publication Critical patent/JPS62175741A/ja

1993-11-11 Publication of JPH0581029B2 publication Critical patent/JPH0581029B2/ja

Status Granted legal-status Critical Current

Links

238000000034 method Methods 0.000 title claims description 48
230000002708 enhancing effect Effects 0.000 title 1
-1 silver halide Chemical class 0.000 claims abstract description 261
125000000217 alkyl group Chemical group 0.000 claims abstract description 116
125000003118 aryl group Chemical group 0.000 claims abstract description 84
229910052709 silver Inorganic materials 0.000 claims abstract description 76
239000004332 silver Substances 0.000 claims abstract description 76
239000000463 material Substances 0.000 claims abstract description 49
239000003795 chemical substances by application Substances 0.000 claims abstract description 35
125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 27
150000004696 coordination complex Chemical class 0.000 claims abstract description 23
238000006243 chemical reaction Methods 0.000 claims abstract description 19
125000001424 substituent group Chemical group 0.000 claims description 104
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 31
239000003960 organic solvent Substances 0.000 claims description 14
238000009835 boiling Methods 0.000 claims description 13
239000000126 substance Substances 0.000 claims description 12
238000005562 fading Methods 0.000 abstract description 15
238000004040 coloring Methods 0.000 abstract description 11
238000002845 discoloration Methods 0.000 abstract description 3
230000003647 oxidation Effects 0.000 abstract description 3
238000007254 oxidation reaction Methods 0.000 abstract description 3
239000010410 layer Substances 0.000 description 71
239000000839 emulsion Substances 0.000 description 59
239000000975 dye Substances 0.000 description 56
150000001875 compounds Chemical class 0.000 description 47
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 42
125000000623 heterocyclic group Chemical group 0.000 description 32
125000003545 alkoxy group Chemical group 0.000 description 29
125000004429 atom Chemical group 0.000 description 28
125000005843 halogen group Chemical group 0.000 description 25
KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 23
125000004432 carbon atom Chemical group C* 0.000 description 21
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 20
125000004104 aryloxy group Chemical group 0.000 description 19
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 19
239000002245 particle Substances 0.000 description 19
150000003839 salts Chemical class 0.000 description 19
238000000576 coating method Methods 0.000 description 18
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 17
239000011248 coating agent Substances 0.000 description 16
125000003342 alkenyl group Chemical group 0.000 description 15
125000004453 alkoxycarbonyl group Chemical group 0.000 description 15
229910052799 carbon Inorganic materials 0.000 description 15
229910052751 metal Inorganic materials 0.000 description 15
239000002184 metal Substances 0.000 description 15
230000000694 effects Effects 0.000 description 14
108010010803 Gelatin Proteins 0.000 description 13
239000002253 acid Substances 0.000 description 13
229910052731 fluorine Inorganic materials 0.000 description 13
229920000159 gelatin Polymers 0.000 description 13
239000008273 gelatin Substances 0.000 description 13
235000019322 gelatine Nutrition 0.000 description 13
235000011852 gelatine desserts Nutrition 0.000 description 13
239000003381 stabilizer Substances 0.000 description 13
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 13
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 12
PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 12
239000010931 gold Substances 0.000 description 12
229910052737 gold Inorganic materials 0.000 description 12
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 12
125000002252 acyl group Chemical group 0.000 description 11
229910052801 chlorine Inorganic materials 0.000 description 11
125000004093 cyano group Chemical group *C#N 0.000 description 11
125000001624 naphthyl group Chemical group 0.000 description 11
125000000565 sulfonamide group Chemical group 0.000 description 11
125000004421 aryl sulphonamide group Chemical group 0.000 description 10
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 10
125000004149 thio group Chemical group *S* 0.000 description 10
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 9
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 9
239000002585 base Substances 0.000 description 9
239000000084 colloidal system Substances 0.000 description 9
238000011161 development Methods 0.000 description 9
230000018109 developmental process Effects 0.000 description 9
239000011737 fluorine Substances 0.000 description 9
125000002887 hydroxy group Chemical group [H]O* 0.000 description 9
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 9
125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 9
239000000243 solution Substances 0.000 description 9
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 8
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 8
125000004414 alkyl thio group Chemical group 0.000 description 8
125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 8
125000005110 aryl thio group Chemical group 0.000 description 8
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 8
229910052794 bromium Inorganic materials 0.000 description 8
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 8
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 8
239000000460 chlorine Substances 0.000 description 8
230000000052 comparative effect Effects 0.000 description 8
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 8
239000006185 dispersion Substances 0.000 description 8
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 8
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 8
238000012545 processing Methods 0.000 description 8
206010070834 Sensitisation Diseases 0.000 description 7
239000006096 absorbing agent Substances 0.000 description 7
125000004423 acyloxy group Chemical group 0.000 description 7
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Natural products OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 7
239000013078 crystal Substances 0.000 description 7
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 7
230000006866 deterioration Effects 0.000 description 7
XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 7
230000008313 sensitization Effects 0.000 description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 6
SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 6
125000004422 alkyl sulphonamide group Chemical group 0.000 description 6
125000003368 amide group Chemical group 0.000 description 6
125000005161 aryl oxy carbonyl group Chemical group 0.000 description 6
125000004391 aryl sulfonyl group Chemical group 0.000 description 6
BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 6
150000001721 carbon Chemical group 0.000 description 6
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 6
150000002430 hydrocarbons Chemical group 0.000 description 6
229910052739 hydrogen Inorganic materials 0.000 description 6
125000005740 oxycarbonyl group Chemical group [*:1]OC([*:2])=O 0.000 description 6
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 6
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 6
230000008569 process Effects 0.000 description 6
125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 description 6
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 5
125000004442 acylamino group Chemical group 0.000 description 5
229910052783 alkali metal Inorganic materials 0.000 description 5
125000002947 alkylene group Chemical group 0.000 description 5
125000000304 alkynyl group Chemical group 0.000 description 5
239000007844 bleaching agent Substances 0.000 description 5
125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 description 5
125000001309 chloro group Chemical group Cl* 0.000 description 5
229910052736 halogen Inorganic materials 0.000 description 5
HNQIVZYLYMDVSB-UHFFFAOYSA-N methanesulfonimidic acid Chemical group CS(N)(=O)=O HNQIVZYLYMDVSB-UHFFFAOYSA-N 0.000 description 5
239000000203 mixture Substances 0.000 description 5
229910052757 nitrogen Inorganic materials 0.000 description 5
125000002958 pentadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 5
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 5
239000002904 solvent Substances 0.000 description 5
229910052717 sulfur Inorganic materials 0.000 description 5
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 5
JKRNNIGZNCVVHA-UHFFFAOYSA-N 2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate;trimethylazanium Chemical compound C[NH+](C)C.C[NH+](C)C.C[NH+](C)C.C[NH+](C)C.[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O JKRNNIGZNCVVHA-UHFFFAOYSA-N 0.000 description 4
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical group NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 description 4
ZGTMUACCHSMWAC-UHFFFAOYSA-L EDTA disodium salt (anhydrous) Chemical compound [Na+].[Na+].OC(=O)CN(CC([O-])=O)CCN(CC(O)=O)CC([O-])=O ZGTMUACCHSMWAC-UHFFFAOYSA-L 0.000 description 4
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 4
125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 4
150000007513 acids Chemical class 0.000 description 4
125000005115 alkyl carbamoyl group Chemical group 0.000 description 4
125000005153 alkyl sulfamoyl group Chemical group 0.000 description 4
125000004390 alkyl sulfonyl group Chemical group 0.000 description 4
125000003277 amino group Chemical group 0.000 description 4
125000005116 aryl carbamoyl group Chemical group 0.000 description 4
238000004061 bleaching Methods 0.000 description 4
125000004989 dicarbonyl group Chemical group 0.000 description 4
125000001153 fluoro group Chemical group F* 0.000 description 4
150000002367 halogens Chemical class 0.000 description 4
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 4
230000006872 improvement Effects 0.000 description 4
229910052742 iron Inorganic materials 0.000 description 4
239000007788 liquid Substances 0.000 description 4
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 4
125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
QWOKKHXWFDAJCZ-UHFFFAOYSA-N octane-1-sulfonamide Chemical group CCCCCCCCS(N)(=O)=O QWOKKHXWFDAJCZ-UHFFFAOYSA-N 0.000 description 4
150000007524 organic acids Chemical class 0.000 description 4
125000004430 oxygen atom Chemical group O* 0.000 description 4
125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 4
125000005499 phosphonyl group Chemical group 0.000 description 4
150000003014 phosphoric acid esters Chemical class 0.000 description 4
238000010791 quenching Methods 0.000 description 4
230000000171 quenching effect Effects 0.000 description 4
230000009467 reduction Effects 0.000 description 4
210000002784 stomach Anatomy 0.000 description 4
238000006467 substitution reaction Methods 0.000 description 4
NVBFHJWHLNUMCV-UHFFFAOYSA-N sulfamide Chemical compound NS(N)(=O)=O NVBFHJWHLNUMCV-UHFFFAOYSA-N 0.000 description 4
238000012360 testing method Methods 0.000 description 4
CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 3
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 3
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
125000004448 alkyl carbonyl group Chemical group 0.000 description 3
125000005129 aryl carbonyl group Chemical group 0.000 description 3
239000012964 benzotriazole Substances 0.000 description 3
125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 3
239000011230 binding agent Substances 0.000 description 3
239000003086 colorant Substances 0.000 description 3
125000000392 cycloalkenyl group Chemical group 0.000 description 3
SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 3
230000005611 electricity Effects 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
229940093915 gynecological organic acid Drugs 0.000 description 3
125000005842 heteroatom Chemical group 0.000 description 3
239000001257 hydrogen Substances 0.000 description 3
230000002209 hydrophobic effect Effects 0.000 description 3
125000005462 imide group Chemical group 0.000 description 3
125000002960 margaryl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 description 3
125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
CMWTZPSULFXXJA-VIFPVBQESA-N naproxen Chemical group C1=C([C@H](C)C(O)=O)C=CC2=CC(OC)=CC=C21 CMWTZPSULFXXJA-VIFPVBQESA-N 0.000 description 3
235000005985 organic acids Nutrition 0.000 description 3
125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 description 3
239000000049 pigment Substances 0.000 description 3
229910000027 potassium carbonate Inorganic materials 0.000 description 3
239000011241 protective layer Substances 0.000 description 3
230000001235 sensitizing effect Effects 0.000 description 3
235000015170 shellfish Nutrition 0.000 description 3
125000004469 siloxy group Chemical group [SiH3]O* 0.000 description 3
230000003595 spectral effect Effects 0.000 description 3
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 3
239000011593 sulfur Substances 0.000 description 3
125000004434 sulfur atom Chemical group 0.000 description 3
125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
229910052724 xenon Inorganic materials 0.000 description 3
FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 3
PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 2
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
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 2
QECVIPBZOPUTRD-UHFFFAOYSA-N N=S(=O)=O Chemical group N=S(=O)=O QECVIPBZOPUTRD-UHFFFAOYSA-N 0.000 description 2
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
239000004698 Polyethylene Substances 0.000 description 2
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 2
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical group NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
238000010521 absorption reaction Methods 0.000 description 2
229960000583 acetic acid Drugs 0.000 description 2
239000013543 active substance Substances 0.000 description 2
239000000654 additive Substances 0.000 description 2
230000002411 adverse Effects 0.000 description 2
239000003513 alkali Substances 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
229910021529 ammonia Inorganic materials 0.000 description 2
125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 2
239000002216 antistatic agent Substances 0.000 description 2
125000003710 aryl alkyl group Chemical group 0.000 description 2
125000005199 aryl carbonyloxy group Chemical group 0.000 description 2
125000001231 benzoyloxy group Chemical group C(C1=CC=CC=C1)(=O)O* 0.000 description 2
125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
XZOWIJDBQIHMFC-UHFFFAOYSA-N butanamide Chemical compound CCCC(N)=O.CCCC(N)=O XZOWIJDBQIHMFC-UHFFFAOYSA-N 0.000 description 2
125000004744 butyloxycarbonyl group Chemical group 0.000 description 2
239000001913 cellulose Substances 0.000 description 2
229920002678 cellulose Polymers 0.000 description 2
239000003610 charcoal Substances 0.000 description 2
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