JPH0452148B2 - - Google Patents
Info
- Publication number
- JPH0452148B2 JPH0452148B2 JP61280246A JP28024686A JPH0452148B2 JP H0452148 B2 JPH0452148 B2 JP H0452148B2 JP 61280246 A JP61280246 A JP 61280246A JP 28024686 A JP28024686 A JP 28024686A JP H0452148 B2 JPH0452148 B2 JP H0452148B2
- Authority
- JP
- Japan
- Prior art keywords
- acid
- copper
- alum
- compound
- weight
- 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 - Lifetime
Links
- 239000002253 acid Substances 0.000 claims description 20
- 229940037003 alum Drugs 0.000 claims description 15
- 150000001875 compounds Chemical class 0.000 claims description 14
- 239000005749 Copper compound Substances 0.000 claims description 13
- -1 ascorbic acid compound Chemical class 0.000 claims description 13
- 150000001880 copper compounds Chemical class 0.000 claims description 13
- 150000007524 organic acids Chemical class 0.000 claims description 12
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Natural products OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims description 11
- 235000010323 ascorbic acid Nutrition 0.000 claims description 7
- 229960005070 ascorbic acid Drugs 0.000 claims description 7
- 239000011668 ascorbic acid Substances 0.000 claims description 7
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 claims description 6
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- 229940093915 gynecological organic acid Drugs 0.000 claims description 2
- 235000005985 organic acids Nutrition 0.000 claims description 2
- 239000001384 succinic acid Substances 0.000 claims 1
- 230000001877 deodorizing effect Effects 0.000 description 21
- 239000007864 aqueous solution Substances 0.000 description 11
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 10
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 5
- 229910021529 ammonia Inorganic materials 0.000 description 5
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 5
- 239000010949 copper Substances 0.000 description 5
- 229910052802 copper Inorganic materials 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- DNJIEGIFACGWOD-UHFFFAOYSA-N ethanethiol Chemical compound CCS DNJIEGIFACGWOD-UHFFFAOYSA-N 0.000 description 4
- 239000001530 fumaric acid Substances 0.000 description 4
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 4
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 3
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- OMPIYDSYGYKWSG-UHFFFAOYSA-N 2-(2-ethoxy-2-oxoethyl)-2-hydroxybutanedioic acid Chemical compound CCOC(=O)CC(O)(C(O)=O)CC(O)=O OMPIYDSYGYKWSG-UHFFFAOYSA-N 0.000 description 2
- KPGXRSRHYNQIFN-UHFFFAOYSA-N 2-oxoglutaric acid Chemical compound OC(=O)CCC(=O)C(O)=O KPGXRSRHYNQIFN-UHFFFAOYSA-N 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- JJLJMEJHUUYSSY-UHFFFAOYSA-L Copper hydroxide Chemical compound [OH-].[OH-].[Cu+2] JJLJMEJHUUYSSY-UHFFFAOYSA-L 0.000 description 2
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 2
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
- LCTONWCANYUPML-UHFFFAOYSA-N Pyruvic acid Chemical compound CC(=O)C(O)=O LCTONWCANYUPML-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 150000007824 aliphatic compounds Chemical class 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 description 2
- QTMDXZNDVAMKGV-UHFFFAOYSA-L copper(ii) bromide Chemical compound [Cu+2].[Br-].[Br-] QTMDXZNDVAMKGV-UHFFFAOYSA-L 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 2
- 238000004817 gas chromatography Methods 0.000 description 2
- HHLFWLYXYJOTON-UHFFFAOYSA-N glyoxylic acid Chemical compound OC(=O)C=O HHLFWLYXYJOTON-UHFFFAOYSA-N 0.000 description 2
- MNUOZFHYBCRUOD-UHFFFAOYSA-N hydroxyphthalic acid Natural products OC(=O)C1=CC=CC(O)=C1C(O)=O MNUOZFHYBCRUOD-UHFFFAOYSA-N 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 235000019645 odor Nutrition 0.000 description 2
- 239000000123 paper Substances 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- ZUDZWKJBYZAGBS-QWWZWVQMSA-N (2r,3r)-4-ethoxy-2,3-dihydroxy-4-oxobutanoic acid Chemical compound CCOC(=O)[C@H](O)[C@@H](O)C(O)=O ZUDZWKJBYZAGBS-QWWZWVQMSA-N 0.000 description 1
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- RBNPOMFGQQGHHO-UHFFFAOYSA-N -2,3-Dihydroxypropanoic acid Natural products OCC(O)C(O)=O RBNPOMFGQQGHHO-UHFFFAOYSA-N 0.000 description 1
- PJFQKDBQOXFCAI-UHFFFAOYSA-N 1,2-dihydroxyethane-1,1,2-tricarboxylic acid Chemical compound OC(=O)C(O)C(O)(C(O)=O)C(O)=O PJFQKDBQOXFCAI-UHFFFAOYSA-N 0.000 description 1
- TYEYBOSBBBHJIV-UHFFFAOYSA-N 2-oxobutanoic acid Chemical compound CCC(=O)C(O)=O TYEYBOSBBBHJIV-UHFFFAOYSA-N 0.000 description 1
- OXTNCQMOKLOUAM-UHFFFAOYSA-N 3-Oxoglutaric acid Chemical compound OC(=O)CC(=O)CC(O)=O OXTNCQMOKLOUAM-UHFFFAOYSA-N 0.000 description 1
- ZQHYXNSQOIDNTL-UHFFFAOYSA-N 3-hydroxyglutaric acid Chemical compound OC(=O)CC(O)CC(O)=O ZQHYXNSQOIDNTL-UHFFFAOYSA-N 0.000 description 1
- OAKURXIZZOAYBC-UHFFFAOYSA-N 3-oxopropanoic acid Chemical compound OC(=O)CC=O OAKURXIZZOAYBC-UHFFFAOYSA-N 0.000 description 1
- 229940090248 4-hydroxybenzoic acid Drugs 0.000 description 1
- SJZRECIVHVDYJC-UHFFFAOYSA-N 4-hydroxybutyric acid Chemical compound OCCCC(O)=O SJZRECIVHVDYJC-UHFFFAOYSA-N 0.000 description 1
- MGTZCLMLSSAXLD-UHFFFAOYSA-N 5-oxohexanoic acid Chemical compound CC(=O)CCCC(O)=O MGTZCLMLSSAXLD-UHFFFAOYSA-N 0.000 description 1
- WDJHALXBUFZDSR-UHFFFAOYSA-N Acetoacetic acid Natural products CC(=O)CC(O)=O WDJHALXBUFZDSR-UHFFFAOYSA-N 0.000 description 1
- WZUKKIPWIPZMAS-UHFFFAOYSA-K Ammonium alum Chemical compound [NH4+].O.O.O.O.O.O.O.O.O.O.O.O.[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O WZUKKIPWIPZMAS-UHFFFAOYSA-K 0.000 description 1
- OCUCCJIRFHNWBP-IYEMJOQQSA-L Copper gluconate Chemical compound [Cu+2].OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O.OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O OCUCCJIRFHNWBP-IYEMJOQQSA-L 0.000 description 1
- 229910021589 Copper(I) bromide Inorganic materials 0.000 description 1
- 229910021591 Copper(I) chloride Inorganic materials 0.000 description 1
- 229910021595 Copper(I) iodide Inorganic materials 0.000 description 1
- 229910021590 Copper(II) bromide Inorganic materials 0.000 description 1
- CIWBSHSKHKDKBQ-DUZGATOHSA-N D-araboascorbic acid Natural products OC[C@@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-DUZGATOHSA-N 0.000 description 1
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 1
- RBNPOMFGQQGHHO-UWTATZPHSA-N D-glyceric acid Chemical compound OC[C@@H](O)C(O)=O RBNPOMFGQQGHHO-UWTATZPHSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- DSLZVSRJTYRBFB-UHFFFAOYSA-N Galactaric acid Natural products OC(=O)C(O)C(O)C(O)C(O)C(O)=O DSLZVSRJTYRBFB-UHFFFAOYSA-N 0.000 description 1
- IAJILQKETJEXLJ-UHFFFAOYSA-N Galacturonsaeure Natural products O=CC(O)C(O)C(O)C(O)C(O)=O IAJILQKETJEXLJ-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 239000002211 L-ascorbic acid Substances 0.000 description 1
- 235000000069 L-ascorbic acid Nutrition 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- NUSORQHHEXCNQC-UHFFFAOYSA-N [Cu].N1C(C=C2N=C(C=C3NC(=C4)C=C3)C=C2)=CC=C1C=C1C=CC4=N1 Chemical compound [Cu].N1C(C=C2N=C(C=C3NC(=C4)C=C3)C=C2)=CC=C1C=C1C=CC4=N1 NUSORQHHEXCNQC-UHFFFAOYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000003172 aldehyde group Chemical group 0.000 description 1
- IAJILQKETJEXLJ-QTBDOELSSA-N aldehydo-D-glucuronic acid Chemical compound O=C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)C(O)=O IAJILQKETJEXLJ-QTBDOELSSA-N 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- HWXBTNAVRSUOJR-UHFFFAOYSA-N alpha-hydroxyglutaric acid Natural products OC(=O)C(O)CCC(O)=O HWXBTNAVRSUOJR-UHFFFAOYSA-N 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- 235000011124 aluminium ammonium sulphate Nutrition 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 235000011126 aluminium potassium sulphate Nutrition 0.000 description 1
- ZEMWIYASLJTEHQ-UHFFFAOYSA-J aluminum;sodium;disulfate;dodecahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.O.O.[Na+].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O ZEMWIYASLJTEHQ-UHFFFAOYSA-J 0.000 description 1
- 239000003429 antifungal agent Substances 0.000 description 1
- 229940121375 antifungal agent Drugs 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 229940072107 ascorbate Drugs 0.000 description 1
- LCPUDZUWZDSKMX-UHFFFAOYSA-K azane;hydrogen sulfate;iron(3+);sulfate;dodecahydrate Chemical compound [NH4+].O.O.O.O.O.O.O.O.O.O.O.O.[Fe+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O LCPUDZUWZDSKMX-UHFFFAOYSA-K 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 229930002875 chlorophyll Natural products 0.000 description 1
- 235000019804 chlorophyll Nutrition 0.000 description 1
- ATNHDLDRLWWWCB-AENOIHSZSA-M chlorophyll a Chemical compound C1([C@@H](C(=O)OC)C(=O)C2=C3C)=C2N2C3=CC(C(CC)=C3C)=[N+]4C3=CC3=C(C=C)C(C)=C5N3[Mg-2]42[N+]2=C1[C@@H](CCC(=O)OC\C=C(/C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)[C@H](C)C2=C5 ATNHDLDRLWWWCB-AENOIHSZSA-M 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 229940116318 copper carbonate Drugs 0.000 description 1
- 229940108925 copper gluconate Drugs 0.000 description 1
- BWFPGXWASODCHM-UHFFFAOYSA-N copper monosulfide Chemical compound [Cu]=S BWFPGXWASODCHM-UHFFFAOYSA-N 0.000 description 1
- 229910000365 copper sulfate Inorganic materials 0.000 description 1
- OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical compound [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 description 1
- BERDEBHAJNAUOM-UHFFFAOYSA-N copper(I) oxide Inorganic materials [Cu]O[Cu] BERDEBHAJNAUOM-UHFFFAOYSA-N 0.000 description 1
- XTVVROIMIGLXTD-UHFFFAOYSA-N copper(II) nitrate Chemical compound [Cu+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O XTVVROIMIGLXTD-UHFFFAOYSA-N 0.000 description 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- NKNDPYCGAZPOFS-UHFFFAOYSA-M copper(i) bromide Chemical compound Br[Cu] NKNDPYCGAZPOFS-UHFFFAOYSA-M 0.000 description 1
- DOBRDRYODQBAMW-UHFFFAOYSA-N copper(i) cyanide Chemical compound [Cu+].N#[C-] DOBRDRYODQBAMW-UHFFFAOYSA-N 0.000 description 1
- LSXDOTMGLUJQCM-UHFFFAOYSA-M copper(i) iodide Chemical compound I[Cu] LSXDOTMGLUJQCM-UHFFFAOYSA-M 0.000 description 1
- OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 description 1
- WMYBXRITVYIFCO-UHFFFAOYSA-N copper;2-hydroxybutanedioic acid Chemical compound [Cu].OC(=O)C(O)CC(O)=O WMYBXRITVYIFCO-UHFFFAOYSA-N 0.000 description 1
- RLSHUBNQSDLPAG-UHFFFAOYSA-L copper;2-oxopentanedioate Chemical compound [Cu+2].[O-]C(=O)CCC(=O)C([O-])=O RLSHUBNQSDLPAG-UHFFFAOYSA-L 0.000 description 1
- FSQAIQPPCOCRAX-UHFFFAOYSA-L copper;2-oxopropanoate Chemical compound [Cu+2].CC(=O)C([O-])=O.CC(=O)C([O-])=O FSQAIQPPCOCRAX-UHFFFAOYSA-L 0.000 description 1
- FSHOIESIOHHWIA-UHFFFAOYSA-L copper;4-hydroxy-3,4-dioxobutanoate Chemical compound [Cu+2].OC(=O)C(=O)CC([O-])=O.OC(=O)C(=O)CC([O-])=O FSHOIESIOHHWIA-UHFFFAOYSA-L 0.000 description 1
- GEZOTWYUIKXWOA-UHFFFAOYSA-L copper;carbonate Chemical compound [Cu+2].[O-]C([O-])=O GEZOTWYUIKXWOA-UHFFFAOYSA-L 0.000 description 1
- UVVWIYVATLQAFM-UHFFFAOYSA-I copper;tripotassium;18-(2-carboxylatoethyl)-20-(carboxylatomethyl)-12-ethenyl-7-ethyl-3,13,17-trimethyl-8-(oxidomethylidene)-17,18-dihydroporphyrin-21-ide-2-carboxylate Chemical compound [K+].[K+].[K+].[Cu+2].C1=C([N-]2)C(C)=C(C([O-])=O)C2=C(CC([O-])=O)C(C(C2C)CCC([O-])=O)=NC2=CC(C(=C2C=C)C)=NC2=CC\2=NC1=C(CC)C/2=C\[O-] UVVWIYVATLQAFM-UHFFFAOYSA-I 0.000 description 1
- HWDGVJUIHRPKFR-UHFFFAOYSA-I copper;trisodium;18-(2-carboxylatoethyl)-20-(carboxylatomethyl)-12-ethenyl-7-ethyl-3,8,13,17-tetramethyl-17,18-dihydroporphyrin-21,23-diide-2-carboxylate Chemical compound [Na+].[Na+].[Na+].[Cu+2].N1=C(C(CC([O-])=O)=C2C(C(C)C(C=C3C(=C(C=C)C(=C4)[N-]3)C)=N2)CCC([O-])=O)C(=C([O-])[O-])C(C)=C1C=C1C(CC)=C(C)C4=N1 HWDGVJUIHRPKFR-UHFFFAOYSA-I 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 229960003280 cupric chloride Drugs 0.000 description 1
- 235000019855 cupric citrate Nutrition 0.000 description 1
- 239000011641 cupric citrate Substances 0.000 description 1
- 229960004643 cupric oxide Drugs 0.000 description 1
- 229940045803 cuprous chloride Drugs 0.000 description 1
- KRFJLUBVMFXRPN-UHFFFAOYSA-N cuprous oxide Chemical compound [O-2].[Cu+].[Cu+] KRFJLUBVMFXRPN-UHFFFAOYSA-N 0.000 description 1
- 229940112669 cuprous oxide Drugs 0.000 description 1
- 239000002781 deodorant agent Substances 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- WOWBFOBYOAGEEA-UHFFFAOYSA-N diafenthiuron Chemical compound CC(C)C1=C(NC(=S)NC(C)(C)C)C(C(C)C)=CC(OC=2C=CC=CC=2)=C1 WOWBFOBYOAGEEA-UHFFFAOYSA-N 0.000 description 1
- PEVJCYPAFCUXEZ-UHFFFAOYSA-J dicopper;phosphonato phosphate Chemical compound [Cu+2].[Cu+2].[O-]P([O-])(=O)OP([O-])([O-])=O PEVJCYPAFCUXEZ-UHFFFAOYSA-J 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 235000010350 erythorbic acid Nutrition 0.000 description 1
- 239000004318 erythorbic acid Substances 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 235000013373 food additive Nutrition 0.000 description 1
- 239000002778 food additive Substances 0.000 description 1
- 238000004108 freeze drying Methods 0.000 description 1
- DSLZVSRJTYRBFB-DUHBMQHGSA-N galactaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)C(O)=O DSLZVSRJTYRBFB-DUHBMQHGSA-N 0.000 description 1
- 229940074391 gallic acid Drugs 0.000 description 1
- 235000004515 gallic acid Nutrition 0.000 description 1
- 239000000174 gluconic acid Substances 0.000 description 1
- 235000012208 gluconic acid Nutrition 0.000 description 1
- 229940097043 glucuronic acid Drugs 0.000 description 1
- 229960004275 glycolic acid Drugs 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 150000002506 iron compounds Chemical class 0.000 description 1
- 229940026239 isoascorbic acid Drugs 0.000 description 1
- 125000000468 ketone group Chemical group 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229940050271 potassium alum Drugs 0.000 description 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 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 229940107700 pyruvic acid Drugs 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 235000011127 sodium aluminium sulphate Nutrition 0.000 description 1
- 229940079841 sodium copper chlorophyllin Drugs 0.000 description 1
- 235000013758 sodium copper chlorophyllin Nutrition 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000004763 sulfides Chemical class 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- STDMRMREKPZQFJ-UHFFFAOYSA-H tricopper;2-hydroxypropane-1,2,3-tricarboxylate Chemical compound [Cu+2].[Cu+2].[Cu+2].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O STDMRMREKPZQFJ-UHFFFAOYSA-H 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Landscapes
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
Description
(産業上の利用分野)
本発明は新規な脱臭剤に関し、更に詳しくは、
(A)ミヨウバン、(B)銅化合物、(C)オキシカルボン酸
化合物、オキソカルボン酸化合物、エチレンジア
ミン四酢酸、コハク酸、フマル酸から選ばれる有
機酸及び(D)アスコルビン酸化合物を有効成分とす
る新規な脱臭剤に関する。
(従来の技術)
ミヨウバンは、顔料をはじめとして、医薬品、
浄水剤、食品添加物、化粧品原料、製紙用各種触
媒等の種々の用途に利用されており、なかでも最
近、脱臭剤としての利用が注目されてきている。
しかし、ミヨウバンの水溶液をアンモニア等の塩
基臭の脱臭に用いると沈殿が生じてしまい安定性
に劣り、またミヨウバン単独では脱臭性能に劣る
といつた問題があつた。
これらの問題に対し、ミヨウバンに有機酸を配
合して安定性を向上させる方法やミヨウバンに銅
化合物を配合して脱臭性能を向上させる方法が提
起されている。しかし、ミヨウバンに有機酸と銅
化合物を併用すると有機酸が銅化合物に対して阻
害作用を示し、優れた脱臭効果が得られないとい
う問題点があつた。
(発明が解決しようとする問題点)
そこで本発明者らは従来技術に見られるこれら
の欠点を解決すべく鋭意検討を重ねた結果、(A)ミ
ヨウバン、(B)銅化合物及び(C)オキシカルボン酸化
合物、オキソカルボン酸化合物、エチレンジアミ
ン四酢酸、コハク酸、フマル酸から選ばれる有機
酸からなる組成物に(D)アスコルビン酸化合物を配
合すると、ミヨウバンの安定性を改善し、かつ、
銅化合物の機能を損なうことのなく優れた脱臭性
能を有することを見い出し、本発明を完成するに
到つた。
(問題点を解決するための手段)
かくして本発明によれば(A)ミヨウバン100重量
部に対して、(B)銅化合物0.01〜100重量部、(C)オ
キシカルボン酸化合物、オキソカルボン酸化合
物、エチレンジアミン四酢酸、コハク酸、フマル
酸から選ばれる有機酸5〜100重量部、(D)アスコ
ルビン酸化合物5〜100重量部、及び必要に応じ
て(E)水を含有、新規なして成る脱臭剤が提供され
る。
本発明で用いられる(A)成分のミヨウバンの具体
例としては、カリウムミヨウバン、焼ミヨウバ
ン、アンモニウムミヨウバン、ナトリウムミヨウ
バン、鉄ミヨウバン等が挙げられる。
(B)成分の銅化合物は無機酸塩、水酸化物、硫化
物、有機酸塩、錯体、酸化物のいずれでもよく、
その具体例として、例えば、硫酸銅、硝酸銅、塩
化第一銅、塩化第二銅、臭化第一銅、臭化第二
銅、ヨウ化第一銅、炭酸銅、水酸化第二銅、硫化
第二銅、シアン化銅、酢酸銅、クエン酸第二銅、
グルコン酸銅、リンゴ酸銅、グルオキシル酸銅、
2−ケトグルタル酸銅、ピルビン酸銅、オキサロ
酢酸銅、ピロリン酸銅、銅クロロフイル、銅クロ
ロフイリンナトリウム、銅クロロフイリンカリウ
ム、フタロシアニン銅、銅ポルフイリン、酸化第
一銅、酸化第二銅などが挙げられる。なかでもコ
ストや入手の容易性から無機酸塩が、安定性の面
からは錯体が好んで使用される。
(C)成分の有機酸、オキシカルボン酸化合物、オ
キソカルボン酸化合物、エチレンジアミン四酢酸
(EDTA)、コハク酸及びフマル酸から選ばれる
有機酸であり、なかでもオキシカルボン酸化合
物、オキソカルボン酸化合物が賞用される。
かかるオキシカルボン酸化合物は分子中に水酸
基とカルボキシル基をそれぞれ一つ以上含有する
オキシカルボン酸またはその水溶性塩であり、そ
の具体例として、例えば乳酸、ヒドロキシ酢酸、
ヒドロキシ酪酸、リンゴ酸、酒石酸、グリセリン
酸、クエン酸、α−メチルリンゴ酸、β−ヒドロ
キシグルタル酸、デソキサル酸、酒石酸モノエチ
ル、クエン酸モノエチル、グルコン酸、ガラクタ
ル酸、グルクロン酸、ケトグルコン酸、サリチル
酸、p−ヒドロキシ安息香酸、没食子酸、ヒドロ
キシフタル酸などのごとき脂肪族または芳香族化
合物、これらのナトリウム塩、カリウム塩、アン
モニウム塩などのごとき水溶性塩が例示される。
なかでも脂肪族化合物が賞用される。
またオキソカルボン酸化合物は、分子中にアル
デヒド基またはケト基とカルボキシル基をそれぞ
れ一つ以上含有するオキソカルボン酸またはその
水溶性塩であり、その具体例として、例えばグリ
オキシル酸、マロンアルデヒド酸、スクシンアル
デヒド酸、ピルビン酸、2−ケト酪酸、4−アセ
チル酪酸、2−ケトグルタル酸、4−ケト−n吉
草酸、アセト酢酸、オキソマロン酢酸、アセトン
ジカルボン酸などのごとき化合物、これらのナト
リウム塩、カリウム塩、アンモニウム塩などの如
き水溶性塩が例示される。
(D)成分のアスコルビン酸化合物の例としては、
L−アスコルビン酸、エリソルビン酸、及びその
アルカリ金属塩などがあげられる。
なお、本発明においては上記銅化合物が有機酸
銅又はアスコルビン酸銅である場合は、別途上記
(C)又は(D)成分を加えなくとも銅と(C)又は(D)成分を
含んでいるものとする。
本発明における各化合物の配合比は目的物の要
求性能に応じて適宜選択しうるが、通常は(A)成分
のミヨウバン100重量部に対し、(B)成分の銅化合
物が0.01〜100重量部好ましくは0.02〜50重量部
の範囲である。(C)成分の有機酸は5〜100重量部
の範囲であり、また(D)成分のアスコルビン酸化合
物は5〜100重量部の範囲である。
(B)成分の使用量が過度に少ないと脱臭性能が劣
る場合があり、逆に過度に多いと毒性の面で好ま
しくない場合がある。
また、(C)成分の使用量が過度に少ないとミヨウ
バンの安定性に劣るうえ、アンモニア等の塩基臭
の脱臭に適用した場合に沈殿が生成する場合があ
り、逆に過度に多いと経済性に劣る場合がある。
一方、(D)成分の使用量が過度に少ないと銅化合
物の機能に対して有機酸が示す阻害効果を抑えら
れず脱臭性能に劣る場合があり、逆に過度に多い
と経済性に劣る場合がある。
また、本発明の効果を損なわない限りであれば
既存の脱臭剤、殺菌剤、防カビ剤等と併用した
り、顔料、着色剤、安定剤、酸化防止剤等の各種
添加剤を必要に応じて添加することができる。
本発明における脱臭剤の調製方法は特に制限さ
れるものではなく、例えば各成分を均一に溶解し
水溶液にする方法、該水溶液を凍結乾燥、粉霧乾
燥等により乾燥化する方法、結晶粉末を均一に混
合する方法等が挙げられる。
又、脱臭剤の性状も特に制限されるものではな
く、例えば水溶液、粉末、錠剤にして単独で用い
る他、必要に応じて水溶液を紙、布、発泡シー
ト、バルプ、繊維等の含浸塗布可能な物質及び無
機担体に含浸、塗布、担持させて用いることもで
きる。本発明で用いられる無機担体は該脱臭剤が
担持可能なものであれば特に制限されるものでは
なく、具体例としては、活性炭、アルミナ、シリ
カゲル、ゼオライト、クレー、ベントナイト、ケ
イソウ土、酸性白土等が挙げられる。無機担体の
形状は、粉末、粒状、針状、繊維状等があるが特
に制限されるものではない。含浸、塗布、担持さ
せる場合、対象となる部材に対する脱臭剤の使用
量は特に制限はなく、用途及び使用方法等に応じ
て異なるが、通常固形分として10〜20重量%の範
囲である。使用量が過度に少ないと機能が不充分
である場合があり、逆に過度に多い場合には経済
性に劣る場合がある。
(発明の効果)
かくして本発明によれば、ミヨウバンの安定性
を改善し、かつその銅化合物の機能を損なうこと
のなく優れた脱臭性能を有する新規な脱臭剤を得
ることができる。
(実施例)
以下に実施例を挙げて本発明をさらに具体的に
説明する。なお、実施例及び比較例中の部及び%
は特に断りのない限り重量基準である。
実施例 1
第1表に示した(A)、(B)、(C)及び(D)成分、及び2
価鉄化合物を所定の割合で用い蒸留水を加え溶解
して、全体が100gの水溶液に成るように調製し、
この時のPHを測定した。
なお、表中の100部は約7gに相当する。次に
各種水溶液20gを50mlビーカーに入れ、2.8%ア
ンモニア水溶液を加えていき、沈殿が生成したと
きのPHを測定した。
まだ、各種水溶液50mgを100ml三角フラスコに
入れて密栓した後、エチルメルカプタン(0.5
g/3N2)1mlを加え、ガスクロマトグラフ
イーにて30分後の気相部分のエチルメルカプタン
量を経時的に定量し、メルカプタン脱臭性能の評
価とした。結果を合せて第1表に示す。
(Industrial Application Field) The present invention relates to a novel deodorizer, and more specifically,
The active ingredients are (A) alum, (B) a copper compound, (C) an oxycarboxylic acid compound, an oxocarboxylic acid compound, an organic acid selected from ethylenediaminetetraacetic acid, succinic acid, and fumaric acid, and (D) an ascorbic acid compound. Regarding a new deodorizer. (Conventional technology) Alum is used for pigments, pharmaceuticals,
It is used for a variety of purposes, including water purifiers, food additives, cosmetic raw materials, and various catalysts for paper manufacturing, and recently, its use as a deodorizing agent has been attracting attention.
However, when an alum aqueous solution is used to deodorize basic odors such as ammonia, it causes precipitation and is poor in stability, and alum alone has problems in that it has poor deodorizing performance. In order to solve these problems, methods have been proposed in which the stability is improved by adding an organic acid to alum, and the deodorizing performance is improved by adding a copper compound to alum. However, when alum is used in combination with an organic acid and a copper compound, the organic acid exhibits an inhibitory effect on the copper compound, resulting in a problem in that excellent deodorizing effects cannot be obtained. (Problems to be Solved by the Invention) Therefore, the present inventors have conducted intensive studies to solve these drawbacks seen in the prior art, and have found that (A) alum, (B) copper compounds, and (C) oxy When (D) an ascorbic acid compound is blended into a composition consisting of an organic acid selected from carboxylic acid compounds, oxocarboxylic acid compounds, ethylenediaminetetraacetic acid, succinic acid, and fumaric acid, the stability of alum is improved, and
The present inventors have discovered that copper compounds have excellent deodorizing performance without impairing their functions, and have completed the present invention. (Means for Solving the Problems) Thus, according to the present invention, (A) 100 parts by weight of alum, (B) 0.01 to 100 parts by weight of a copper compound, (C) an oxycarboxylic acid compound, an oxocarboxylic acid compound , 5 to 100 parts by weight of an organic acid selected from ethylenediaminetetraacetic acid, succinic acid, and fumaric acid, (D) 5 to 100 parts by weight of an ascorbic acid compound, and optionally (E) water. agent is provided. Specific examples of alum as component (A) used in the present invention include potassium alum, burnt alum, ammonium alum, sodium alum, iron alum, and the like. The copper compound of component (B) may be any of inorganic acid salts, hydroxides, sulfides, organic acid salts, complexes, and oxides,
Specific examples include copper sulfate, copper nitrate, cuprous chloride, cupric chloride, cuprous bromide, cupric bromide, cuprous iodide, copper carbonate, cupric hydroxide, Cupric sulfide, copper cyanide, copper acetate, cupric citrate,
copper gluconate, copper malate, copper gluoxylate,
Examples include copper 2-ketoglutarate, copper pyruvate, copper oxaloacetate, copper pyrophosphate, copper chlorophyll, sodium copper chlorophyllin, potassium copper chlorophyllin, copper phthalocyanine, copper porphyrin, cuprous oxide, cupric oxide, etc. . Among these, inorganic acid salts are preferred from the viewpoint of cost and availability, and complexes are preferred from the viewpoint of stability. Component (C) is an organic acid selected from organic acids, oxycarboxylic acid compounds, oxocarboxylic acid compounds, ethylenediaminetetraacetic acid (EDTA), succinic acid, and fumaric acid, and among them, oxycarboxylic acid compounds and oxocarboxylic acid compounds are Awarded. Such oxycarboxylic acid compounds are oxycarboxylic acids or water-soluble salts thereof containing one or more hydroxyl groups and one or more carboxyl groups in the molecule, and specific examples thereof include lactic acid, hydroxyacetic acid,
Hydroxybutyric acid, malic acid, tartaric acid, glyceric acid, citric acid, α-methylmalic acid, β-hydroxyglutaric acid, desoxalic acid, monoethyl tartrate, monoethyl citrate, gluconic acid, galactaric acid, glucuronic acid, ketogluconic acid, salicylic acid, Examples include aliphatic or aromatic compounds such as p-hydroxybenzoic acid, gallic acid, and hydroxyphthalic acid, and water-soluble salts thereof such as sodium salts, potassium salts, and ammonium salts.
Among them, aliphatic compounds are prized. Further, oxocarboxylic acid compounds are oxocarboxylic acids or water-soluble salts thereof containing one or more aldehyde groups or keto groups and one or more carboxyl groups in the molecule, and specific examples thereof include glyoxylic acid, malonaldehydic acid, succinic acid, Compounds such as cinaldehyde acid, pyruvic acid, 2-ketobutyric acid, 4-acetylbutyric acid, 2-ketoglutaric acid, 4-keto-nvaleric acid, acetoacetic acid, oxomalonacetic acid, acetonedicarboxylic acid, their sodium salts, potassium Examples include water-soluble salts such as salts and ammonium salts. Examples of the ascorbic acid compound of component (D) are:
Examples include L-ascorbic acid, erythorbic acid, and alkali metal salts thereof. In addition, in the present invention, when the above-mentioned copper compound is organic acid copper or ascorbate copper, the above-mentioned
It is assumed that copper and component (C) or (D) are included even if component (C) or (D) is not added. The blending ratio of each compound in the present invention can be appropriately selected depending on the required performance of the target product, but usually the copper compound (B) is 0.01 to 100 parts by weight per 100 parts by weight of the alum (A). Preferably it is in the range of 0.02 to 50 parts by weight. The organic acid as component (C) is in the range of 5 to 100 parts by weight, and the ascorbic acid compound as component (D) is in the range of 5 to 100 parts by weight. If the amount of component (B) used is too small, the deodorizing performance may be poor, while if it is too large, it may be unfavorable in terms of toxicity. In addition, if the amount of component (C) used is too small, the stability of alum will be poor, and when applied to deodorizing basic odors such as ammonia, a precipitate may be formed. It may be inferior to On the other hand, if the amount of component (D) used is too small, the inhibitory effect of the organic acid on the function of the copper compound may not be suppressed, resulting in poor deodorizing performance.On the other hand, if the amount used is too large, the economic efficiency may be poor. There is. In addition, as long as it does not impair the effects of the present invention, it may be used in combination with existing deodorizers, disinfectants, antifungal agents, etc., and various additives such as pigments, colorants, stabilizers, antioxidants, etc. may be added as necessary. can be added. The method for preparing the deodorizing agent in the present invention is not particularly limited, and examples include a method of uniformly dissolving each component to form an aqueous solution, a method of drying the aqueous solution by freeze drying, powder mist drying, etc. Examples include a method of mixing with Furthermore, the properties of the deodorizer are not particularly limited; for example, in addition to being used alone as an aqueous solution, powder, or tablet, the aqueous solution can be applied to impregnate paper, cloth, foam sheets, bulbs, fibers, etc. as necessary. It can also be used by impregnating, coating, or supporting a substance or an inorganic carrier. The inorganic carrier used in the present invention is not particularly limited as long as it can support the deodorizing agent, and specific examples include activated carbon, alumina, silica gel, zeolite, clay, bentonite, diatomaceous earth, acid clay, etc. can be mentioned. The shape of the inorganic carrier may be powder, granules, needles, fibers, etc., but is not particularly limited. When impregnating, coating, and supporting the target member, the amount of deodorizing agent used for the target member is not particularly limited and varies depending on the purpose and method of use, but is usually in the range of 10 to 20% by weight as a solid content. If the amount used is too small, the function may be insufficient, and on the other hand, if the amount used is too large, the economy may be poor. (Effects of the Invention) Thus, according to the present invention, it is possible to obtain a novel deodorizing agent that improves the stability of alum and has excellent deodorizing performance without impairing the function of its copper compound. (Example) The present invention will be described in more detail with reference to Examples below. In addition, parts and % in Examples and Comparative Examples
are based on weight unless otherwise specified. Example 1 Components (A), (B), (C) and (D) shown in Table 1, and 2
Prepare a valent iron compound in a predetermined ratio by adding distilled water and dissolving it so that the total amount becomes 100 g of an aqueous solution.
The pH at this time was measured. Note that 100 parts in the table corresponds to about 7 g. Next, 20 g of each aqueous solution was put into a 50 ml beaker, a 2.8% ammonia aqueous solution was added, and the pH was measured when a precipitate was formed. After putting 50mg of various aqueous solutions into a 100ml Erlenmeyer flask and sealing it tightly, add ethyl mercaptan (0.5
g/3N 2 ) was added, and the amount of ethyl mercaptan in the gas phase was determined over time using gas chromatography after 30 minutes to evaluate the mercaptan deodorizing performance. The results are shown in Table 1.
【表】【table】
【表】
第1表より、本発明例は安定性及び脱臭性に優
れていることがわかる。
実施例 2
第2表に示す各成分を所定の割合で用いて実施
例1と同様に脱臭剤水溶液を調製し、メルカプタ
ンの脱臭性能を測定した。
また、各種脱臭剤水溶液100mgを100ml三角フラ
スコに入れて密栓した後、2.8%アンモニア水溶
液50μを加え、ガスクロマトグラフイーにて10
分後の気相部分のアンモニア量を定量し、アンモ
ニア脱臭性能の評価とした。結果を合せて第2表
に示す。Table 1 shows that the examples of the present invention are excellent in stability and deodorizing properties. Example 2 An aqueous deodorizing solution was prepared in the same manner as in Example 1 using each component shown in Table 2 in a predetermined ratio, and the deodorizing performance of mercaptan was measured. In addition, after putting 100mg of various deodorizing aqueous solutions into a 100ml Erlenmeyer flask and sealing it, add 50μ of a 2.8% ammonia aqueous solution, and perform gas chromatography for 10 minutes.
After several minutes, the amount of ammonia in the gas phase was quantified to evaluate the ammonia deodorizing performance. The results are shown in Table 2.
【表】【table】
【表】
実施例 3
実施例1で調製した実験番号1−2の脱臭剤水
溶液を第3表に示す各種担体に含浸させた後、減
圧乾燥させることにより固形分で10%の脱臭剤を
担持させた担持体を得た。
この担持体100mgを用いアンモニア及びメルカ
プタンの脱臭性能を実施例1及び2と同様に調べ
た。
また比較のため担体のみを用いた場合について
も同様に実験を行なつた。併わせて結果を第3表
に示す。[Table] Example 3 Various carriers shown in Table 3 were impregnated with the aqueous deodorant solution of Experiment No. 1-2 prepared in Example 1, and then dried under reduced pressure to support 10% deodorizer in terms of solid content. A carrier was obtained. Using 100 mg of this carrier, the deodorizing performance of ammonia and mercaptan was investigated in the same manner as in Examples 1 and 2. For comparison, a similar experiment was also conducted using only the carrier. The results are also shown in Table 3.
【表】
第3表より、本発明例は担体に担持させた場合
でも優れた脱臭性能を示すことがわかる。Table 3 shows that the examples of the present invention exhibit excellent deodorizing performance even when supported on a carrier.
Claims (1)
物0.01〜100重量部、(C)オキシカルボン酸化合物、
オキソカルボン酸化合物、エチレンジアミン四酢
酸、コハク酸及びフマル酸から選ばれる有機酸5
〜100重量部、(D)アスコルビン酸化合物5〜100重
量部、及び必要に応じて(E)水を配合して成る脱臭
剤。1 (A) 100 parts by weight of alum, (B) 0.01 to 100 parts by weight of a copper compound, (C) an oxycarboxylic acid compound,
Organic acids selected from oxocarboxylic acid compounds, ethylenediaminetetraacetic acid, succinic acid and fumaric acid5
~100 parts by weight, (D) 5 to 100 parts by weight of an ascorbic acid compound, and optionally (E) water.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61280246A JPS63132661A (en) | 1986-11-25 | 1986-11-25 | Deodorant |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61280246A JPS63132661A (en) | 1986-11-25 | 1986-11-25 | Deodorant |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63132661A JPS63132661A (en) | 1988-06-04 |
JPH0452148B2 true JPH0452148B2 (en) | 1992-08-21 |
Family
ID=17622334
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61280246A Granted JPS63132661A (en) | 1986-11-25 | 1986-11-25 | Deodorant |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63132661A (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE20210904U1 (en) * | 2002-07-19 | 2003-08-21 | Holzlehner Martin | Deodorant preparation for use on human skin |
JP5827814B2 (en) * | 2011-03-30 | 2015-12-02 | 理研香料ホールディングス株式会社 | Deodorant composition and foundry sand |
JP2013017582A (en) * | 2011-07-08 | 2013-01-31 | Matsumiya:Kk | Liquid deodorant |
CA2977038A1 (en) * | 2015-02-10 | 2016-08-18 | Kamin Llc | Organic acid or weak acid addition to alum to inhibit ammonia volatilization from poultry litter |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59132937A (en) * | 1983-01-20 | 1984-07-31 | Agency Of Ind Science & Technol | Deodorant |
JPS6066753A (en) * | 1983-09-24 | 1985-04-16 | 工業技術院長 | Composition containing ferric compound |
JPS60136506A (en) * | 1983-12-23 | 1985-07-20 | Takasago Corp | Deodorant |
JPS60142856A (en) * | 1983-12-21 | 1985-07-29 | 工業技術院長 | Powder composition of iron (ii) compound and its production |
JPS61106161A (en) * | 1984-10-31 | 1986-05-24 | 梶原 博文 | Solid deodorant composition |
JPS61154673A (en) * | 1984-12-28 | 1986-07-14 | 株式会社祥光化学研究所 | Deodorant |
JPS61181467A (en) * | 1985-02-08 | 1986-08-14 | 王子製紙株式会社 | Deodorant |
-
1986
- 1986-11-25 JP JP61280246A patent/JPS63132661A/en active Granted
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59132937A (en) * | 1983-01-20 | 1984-07-31 | Agency Of Ind Science & Technol | Deodorant |
JPS6066753A (en) * | 1983-09-24 | 1985-04-16 | 工業技術院長 | Composition containing ferric compound |
JPS60142856A (en) * | 1983-12-21 | 1985-07-29 | 工業技術院長 | Powder composition of iron (ii) compound and its production |
JPS60136506A (en) * | 1983-12-23 | 1985-07-20 | Takasago Corp | Deodorant |
JPS61106161A (en) * | 1984-10-31 | 1986-05-24 | 梶原 博文 | Solid deodorant composition |
JPS61154673A (en) * | 1984-12-28 | 1986-07-14 | 株式会社祥光化学研究所 | Deodorant |
JPS61181467A (en) * | 1985-02-08 | 1986-08-14 | 王子製紙株式会社 | Deodorant |
Also Published As
Publication number | Publication date |
---|---|
JPS63132661A (en) | 1988-06-04 |
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