KR102473847B1 - A molded article for water quality improvement comprising activated carbon - Google Patents
A molded article for water quality improvement comprising activated carbon Download PDFInfo
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- KR102473847B1 KR102473847B1 KR1020220097135A KR20220097135A KR102473847B1 KR 102473847 B1 KR102473847 B1 KR 102473847B1 KR 1020220097135 A KR1020220097135 A KR 1020220097135A KR 20220097135 A KR20220097135 A KR 20220097135A KR 102473847 B1 KR102473847 B1 KR 102473847B1
- Authority
- KR
- South Korea
- Prior art keywords
- weight
- oxygen
- parts
- activated carbon
- water
- Prior art date
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- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 title claims abstract description 80
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims abstract description 44
- 239000004568 cement Substances 0.000 claims abstract description 25
- 239000004576 sand Substances 0.000 claims abstract description 11
- 235000007164 Oryza sativa Nutrition 0.000 claims description 39
- 235000009566 rice Nutrition 0.000 claims description 39
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 claims description 29
- 238000003763 carbonization Methods 0.000 claims description 24
- 239000006087 Silane Coupling Agent Substances 0.000 claims description 19
- NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate group Chemical group C(C=C)(=O)[O-] NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 13
- 238000010000 carbonizing Methods 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 5
- 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 claims description 4
- 239000005539 carbonized material Substances 0.000 claims description 4
- 125000003700 epoxy group Chemical group 0.000 claims description 4
- 238000000227 grinding Methods 0.000 claims description 3
- 240000007594 Oryza sativa Species 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract description 67
- 239000001301 oxygen Substances 0.000 abstract description 67
- 229910052760 oxygen Inorganic materials 0.000 abstract description 67
- 239000000203 mixture Substances 0.000 abstract description 37
- 230000000844 anti-bacterial effect Effects 0.000 abstract description 28
- 241000251468 Actinopterygii Species 0.000 abstract description 10
- 230000008635 plant growth Effects 0.000 abstract description 9
- 241000894006 Bacteria Species 0.000 abstract description 6
- 244000052616 bacterial pathogen Species 0.000 abstract description 6
- 239000000843 powder Substances 0.000 abstract description 5
- 239000007788 liquid Substances 0.000 abstract description 4
- 241000195628 Chlorophyta Species 0.000 abstract 2
- 239000004927 clay Substances 0.000 abstract 1
- 241000209094 Oryza Species 0.000 description 38
- 238000001179 sorption measurement Methods 0.000 description 26
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 18
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 17
- 229920001577 copolymer Polymers 0.000 description 17
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 11
- 239000001569 carbon dioxide Substances 0.000 description 9
- 229910002092 carbon dioxide Inorganic materials 0.000 description 9
- 239000011261 inert gas Substances 0.000 description 9
- 239000000463 material Substances 0.000 description 9
- 229910052757 nitrogen Inorganic materials 0.000 description 8
- 241000195493 Cryptophyta Species 0.000 description 7
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 6
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 239000010902 straw Substances 0.000 description 6
- -1 KClO 4 ) Chemical compound 0.000 description 5
- 238000002347 injection Methods 0.000 description 5
- 239000007924 injection Substances 0.000 description 5
- 239000000178 monomer Substances 0.000 description 5
- XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 description 4
- 230000001737 promoting effect Effects 0.000 description 4
- 239000004484 Briquette Substances 0.000 description 3
- 230000000845 anti-microbial effect Effects 0.000 description 3
- 229910052786 argon Inorganic materials 0.000 description 3
- 239000010883 coal ash Substances 0.000 description 3
- 230000001877 deodorizing effect Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000001307 helium Substances 0.000 description 3
- 229910052734 helium Inorganic materials 0.000 description 3
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 229910052754 neon Inorganic materials 0.000 description 3
- GKAOGPIIYCISHV-UHFFFAOYSA-N neon atom Chemical compound [Ne] GKAOGPIIYCISHV-UHFFFAOYSA-N 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 238000000748 compression moulding Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- AXZAYXJCENRGIM-UHFFFAOYSA-J dipotassium;tetrabromoplatinum(2-) Chemical compound [K+].[K+].[Br-].[Br-].[Br-].[Br-].[Pt+2] AXZAYXJCENRGIM-UHFFFAOYSA-J 0.000 description 2
- 238000007599 discharging Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000010903 husk Substances 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 229910001487 potassium perchlorate Inorganic materials 0.000 description 2
- 238000010298 pulverizing process Methods 0.000 description 2
- 239000010420 shell particle Substances 0.000 description 2
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 2
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- FEUFEGJTJIHPOF-UHFFFAOYSA-N 2-butyl acrylic acid Chemical compound CCCCC(=C)C(O)=O FEUFEGJTJIHPOF-UHFFFAOYSA-N 0.000 description 1
- WROUWQQRXUBECT-UHFFFAOYSA-N 2-ethylacrylic acid Chemical compound CCC(=C)C(O)=O WROUWQQRXUBECT-UHFFFAOYSA-N 0.000 description 1
- FYZUENZXIZCLAZ-UHFFFAOYSA-N 2-methylhept-2-enoic acid Chemical compound CCCCC=C(C)C(O)=O FYZUENZXIZCLAZ-UHFFFAOYSA-N 0.000 description 1
- YWZKHUXXEKYLCD-UHFFFAOYSA-N 2-methylidenedodecanoic acid Chemical compound CCCCCCCCCCC(=C)C(O)=O YWZKHUXXEKYLCD-UHFFFAOYSA-N 0.000 description 1
- JJYWRQLLQAKNAD-UHFFFAOYSA-N 2-methylpent-2-enoic acid Chemical compound CCC=C(C)C(O)=O JJYWRQLLQAKNAD-UHFFFAOYSA-N 0.000 description 1
- BZSXEZOLBIJVQK-UHFFFAOYSA-N 2-methylsulfonylbenzoic acid Chemical compound CS(=O)(=O)C1=CC=CC=C1C(O)=O BZSXEZOLBIJVQK-UHFFFAOYSA-N 0.000 description 1
- CJAQSQCRHBLDGZ-UHFFFAOYSA-N 2-methyltridec-2-enoic acid Chemical compound CCCCCCCCCCC=C(C)C(O)=O CJAQSQCRHBLDGZ-UHFFFAOYSA-N 0.000 description 1
- DOYKFSOCSXVQAN-UHFFFAOYSA-N 3-[diethoxy(methyl)silyl]propyl 2-methylprop-2-enoate Chemical compound CCO[Si](C)(OCC)CCCOC(=O)C(C)=C DOYKFSOCSXVQAN-UHFFFAOYSA-N 0.000 description 1
- LZMNXXQIQIHFGC-UHFFFAOYSA-N 3-[dimethoxy(methyl)silyl]propyl 2-methylprop-2-enoate Chemical compound CO[Si](C)(OC)CCCOC(=O)C(C)=C LZMNXXQIQIHFGC-UHFFFAOYSA-N 0.000 description 1
- URDOJQUSEUXVRP-UHFFFAOYSA-N 3-triethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CCO[Si](OCC)(OCC)CCCOC(=O)C(C)=C URDOJQUSEUXVRP-UHFFFAOYSA-N 0.000 description 1
- KBQVDAIIQCXKPI-UHFFFAOYSA-N 3-trimethoxysilylpropyl prop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C=C KBQVDAIIQCXKPI-UHFFFAOYSA-N 0.000 description 1
- FXTXRXXCMFFRTL-UHFFFAOYSA-N 4-ethyl-2-methylideneoctanoic acid Chemical compound CCCCC(CC)CC(=C)C(O)=O FXTXRXXCMFFRTL-UHFFFAOYSA-N 0.000 description 1
- GHMRLAGSBJPPDG-UHFFFAOYSA-N 5-ethyl-2-methylnon-2-enoic acid Chemical compound CCCCC(CC)CC=C(C)C(O)=O GHMRLAGSBJPPDG-UHFFFAOYSA-N 0.000 description 1
- UIERETOOQGIECD-UHFFFAOYSA-N Angelic acid Natural products CC=C(C)C(O)=O UIERETOOQGIECD-UHFFFAOYSA-N 0.000 description 1
- 241000254173 Coleoptera Species 0.000 description 1
- 241000234435 Lilium Species 0.000 description 1
- 241000237502 Ostreidae Species 0.000 description 1
- 239000011398 Portland cement Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 239000003463 adsorbent Substances 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
- 239000002956 ash Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- ASGKDLGXPOIMTM-UHFFFAOYSA-N diethoxy-methyl-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](C)(OCC)OCC)CCC2OC21 ASGKDLGXPOIMTM-UHFFFAOYSA-N 0.000 description 1
- FUXUUPOAQMPKOK-UHFFFAOYSA-N diethoxy-methyl-[2-(oxiran-2-ylmethoxy)ethyl]silane Chemical compound CCO[Si](C)(OCC)CCOCC1CO1 FUXUUPOAQMPKOK-UHFFFAOYSA-N 0.000 description 1
- PQOOHYQAWSVSJD-UHFFFAOYSA-N diethoxy-methyl-[3-(7-oxabicyclo[4.1.0]heptan-4-yl)propyl]silane Chemical compound C1C(CCC[Si](C)(OCC)OCC)CCC2OC21 PQOOHYQAWSVSJD-UHFFFAOYSA-N 0.000 description 1
- OTARVPUIYXHRRB-UHFFFAOYSA-N diethoxy-methyl-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CCO[Si](C)(OCC)CCCOCC1CO1 OTARVPUIYXHRRB-UHFFFAOYSA-N 0.000 description 1
- SLQTWNAJXFHMHM-UHFFFAOYSA-N dimethoxy-methyl-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](C)(OC)OC)CCC2OC21 SLQTWNAJXFHMHM-UHFFFAOYSA-N 0.000 description 1
- PWPGWRIGYKWLEV-UHFFFAOYSA-N dimethoxy-methyl-[2-(oxiran-2-ylmethoxy)ethyl]silane Chemical compound CO[Si](C)(OC)CCOCC1CO1 PWPGWRIGYKWLEV-UHFFFAOYSA-N 0.000 description 1
- RWHQSBVLPQVZPR-UHFFFAOYSA-N dimethoxy-methyl-[3-(7-oxabicyclo[4.1.0]heptan-4-yl)propyl]silane Chemical compound C1C(CCC[Si](C)(OC)OC)CCC2OC21 RWHQSBVLPQVZPR-UHFFFAOYSA-N 0.000 description 1
- WHGNXNCOTZPEEK-UHFFFAOYSA-N dimethoxy-methyl-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](C)(OC)CCCOCC1CO1 WHGNXNCOTZPEEK-UHFFFAOYSA-N 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- XQHAGELNRSUUGU-UHFFFAOYSA-M lithium chlorate Chemical compound [Li+].[O-]Cl(=O)=O XQHAGELNRSUUGU-UHFFFAOYSA-M 0.000 description 1
- MHCFAGZWMAWTNR-UHFFFAOYSA-M lithium perchlorate Chemical compound [Li+].[O-]Cl(=O)(=O)=O MHCFAGZWMAWTNR-UHFFFAOYSA-M 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 235000020636 oyster Nutrition 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- VKJKEPKFPUWCAS-UHFFFAOYSA-M potassium chlorate Chemical compound [K+].[O-]Cl(=O)=O VKJKEPKFPUWCAS-UHFFFAOYSA-M 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- BAZAXWOYCMUHIX-UHFFFAOYSA-M sodium perchlorate Chemical compound [Na+].[O-]Cl(=O)(=O)=O BAZAXWOYCMUHIX-UHFFFAOYSA-M 0.000 description 1
- 229910001488 sodium perchlorate Inorganic materials 0.000 description 1
- 230000004936 stimulating effect Effects 0.000 description 1
- UIERETOOQGIECD-ONEGZZNKSA-N tiglic acid Chemical compound C\C=C(/C)C(O)=O UIERETOOQGIECD-ONEGZZNKSA-N 0.000 description 1
- UDUKMRHNZZLJRB-UHFFFAOYSA-N triethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OCC)(OCC)OCC)CCC2OC21 UDUKMRHNZZLJRB-UHFFFAOYSA-N 0.000 description 1
- RWJUTPORTOUFDY-UHFFFAOYSA-N triethoxy-[2-(oxiran-2-ylmethoxy)ethyl]silane Chemical compound CCO[Si](OCC)(OCC)CCOCC1CO1 RWJUTPORTOUFDY-UHFFFAOYSA-N 0.000 description 1
- NLKPPXKQMJDBFO-UHFFFAOYSA-N triethoxy-[3-(7-oxabicyclo[4.1.0]heptan-4-yl)propyl]silane Chemical compound C1C(CCC[Si](OCC)(OCC)OCC)CCC2OC21 NLKPPXKQMJDBFO-UHFFFAOYSA-N 0.000 description 1
- JXUKBNICSRJFAP-UHFFFAOYSA-N triethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCOCC1CO1 JXUKBNICSRJFAP-UHFFFAOYSA-N 0.000 description 1
- UZIAQVMNAXPCJQ-UHFFFAOYSA-N triethoxysilylmethyl 2-methylprop-2-enoate Chemical compound CCO[Si](OCC)(OCC)COC(=O)C(C)=C UZIAQVMNAXPCJQ-UHFFFAOYSA-N 0.000 description 1
- DQZNLOXENNXVAD-UHFFFAOYSA-N trimethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OC)(OC)OC)CCC2OC21 DQZNLOXENNXVAD-UHFFFAOYSA-N 0.000 description 1
- ZNXDCSVNCSSUNB-UHFFFAOYSA-N trimethoxy-[2-(oxiran-2-ylmethoxy)ethyl]silane Chemical compound CO[Si](OC)(OC)CCOCC1CO1 ZNXDCSVNCSSUNB-UHFFFAOYSA-N 0.000 description 1
- DBUFXGVMAMMWSD-UHFFFAOYSA-N trimethoxy-[3-(7-oxabicyclo[4.1.0]heptan-4-yl)propyl]silane Chemical compound C1C(CCC[Si](OC)(OC)OC)CCC2OC21 DBUFXGVMAMMWSD-UHFFFAOYSA-N 0.000 description 1
- UOKUUKOEIMCYAI-UHFFFAOYSA-N trimethoxysilylmethyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)COC(=O)C(C)=C UOKUUKOEIMCYAI-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B13/00—Oxygen; Ozone; Oxides or hydroxides in general
- C01B13/02—Preparation of oxygen
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B32/00—Carbon; Compounds thereof
- C01B32/30—Active carbon
- C01B32/312—Preparation
- C01B32/318—Preparation characterised by the starting materials
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B32/00—Carbon; Compounds thereof
- C01B32/30—Active carbon
- C01B32/354—After-treatment
- C01B32/382—Making shaped products, e.g. fibres, spheres, membranes or foam
Abstract
Description
본 발명은 활성탄을 포함하는 산소발생 조성물에 관한 것으로, 더욱 상세하게는 시멘트, 모래, 활성탄, 황토 및 물을 포함하는 산소발생 조성물에 관한 것이다.The present invention relates to an oxygen-generating composition containing activated carbon, and more particularly, to an oxygen-generating composition containing cement, sand, activated carbon, loess and water.
산소를 발생하는 물질은 비행기의 기내 압력이 떨어지는 비상상황, 화재 발생으로 인한 긴급대피가 필요한 상황, 밀폐된 공간에서 장시간의 작업이 요구되는 상황 등의 경우에 산소를 공급하기 위한 용도로 사용되고 있다.Oxygen-generating materials are used for supplying oxygen in emergency situations where in-flight pressure drops, emergency evacuation due to fire, and long-term work required in an enclosed space.
산소를 발생하는 물질로는 과염소산리튬(lithium perchlorate, LiClO4), 염소산리튬(lithium chlorate, LiClO3), 과염소산나트륨(sodium perchlorate, NaClO4), 염소산나트륨(sodium chlorate, NaClO3), 과염소산칼륨(potassium perchlorate, KClO4), 염소산칼륨(potassium chlorate, KClO3) 등이 있으며, 이러한 물질들은 전기적인 방법이나 화학적인 방법으로 열을 가하면 분해하면서 염(salt)과 산소를 발생하는 것으로 알려져 있다.Materials that generate oxygen include lithium perchlorate (LiClO 4 ), lithium chlorate (LiClO 3 ), sodium perchlorate (NaClO 4 ), sodium chlorate (NaClO 3 ), potassium perchlorate ( There are potassium perchlorate, KClO 4 ), potassium chlorate (KClO 3 ), and the like, and these materials are known to generate salt and oxygen while decomposing when heated by an electrical or chemical method.
그러나 기존의 산소발생 물질은 산소 발생 과정에서 과도한 열을 발생하게 되어 산소발생 성형체가 서로 융합되는 현상이 나타나고, 강한 산화반응으로 표면 경화가 발생하여 내부의 산소발생 물질이 반응하지 못하는 문제점이 있다. However, conventional oxygen generating materials generate excessive heat in the oxygen generating process, which causes oxygen generating molded bodies to fuse with each other, and surface hardening occurs due to a strong oxidation reaction, so that the oxygen generating material inside does not react.
따라서 공기 중이나 물속에 서서히 산소를 배출하여 물속의 산소농도를 장기간 동안 증가시킬 수 있고, 세균이나 박테리아 등에 대한 항균성을 나타내며, 녹조를 제거하고 오염수를 정화할 수 있는 산소발생 조성물의 개발이 필요하다. Therefore, it is necessary to develop an oxygen-generating composition that can increase the oxygen concentration in water for a long period of time by gradually releasing oxygen into the air or water, exhibits antibacterial properties against germs or bacteria, and can remove algae and purify contaminated water. .
본 발명은 상기 종래 기술의 문제점을 해결하기 위한 것으로서, 공기 중이나 물속에 서서히 산소를 배출하여 물속의 산소농도를 장기간 동안 증가시킬 수 있고, 세균이나 박테리아 등에 대한 항균성을 나타내며, 녹조를 제거하고 오염수를 정화할 수 있으며, 식물의 성장을 촉진할 수 있는 산소발생 조성물을 제공하는데 그 목적이 있다. The present invention is to solve the problems of the prior art, and can increase the oxygen concentration in the water for a long period of time by gradually discharging oxygen into the air or water, exhibit antibacterial properties against germs or bacteria, remove algae and polluted water It is an object of the present invention to provide an oxygen generating composition capable of purifying and promoting the growth of plants.
또한 본 발명은 액체 상태, 분말 상태, 성형체 등으로 제조되어 양식장, 어항 등에 산소를 공급하는 용도로 사용되거나 녹조제거 및 수질개선을 위한 용도를 사용되거나 화분, 농작물 등에 식물성장을 촉진하는 용도로 사용되는 산소발생 조성물을 제공하는 것을 목적으로 한다. In addition, the present invention is manufactured in a liquid state, powder state, molded body, etc., and is used for supplying oxygen to fish farms, fish tanks, etc., used for removing algae and improving water quality, or used for promoting plant growth in pots, crops, etc. It is an object of the present invention to provide an oxygen generating composition.
상기와 같은 목적을 달성하기 위하여 본 발명은 시멘트, 모래, 활성탄, 황토 및 물을 포함하는 산소발생 조성물을 제공한다.In order to achieve the above object, the present invention provides an oxygen generating composition including cement, sand, activated carbon, loess and water.
본 발명의 일실시예에 있어서, 상기 조성물은 시멘트 100중량부에 대하여 모래 70~120중량부, 활성탄 5~30중량부, 황토 5~20중량부 및 물 1~20중량부를 포함하는 것을 특징으로 한다. In one embodiment of the present invention, the composition comprises 70 to 120 parts by weight of sand, 5 to 30 parts by weight of activated carbon, 5 to 20 parts by weight of loess, and 1 to 20 parts by weight of water based on 100 parts by weight of cement. do.
본 발명의 일실시예에 있어서, 상기 조성물은 아크릴레이트기 함유 실란 커플링제, 2-하이드록시에틸 아크릴레이트(HEA) 및 2-하이드록시에틸 메타크릴레이트(HEMA)의 공중합체 1~10중량부를 추가로 포함하는 것을 특징으로 한다. In one embodiment of the present invention, the composition comprises 1 to 10 parts by weight of a copolymer of an acrylate group-containing silane coupling agent, 2-hydroxyethyl acrylate (HEA) and 2-hydroxyethyl methacrylate (HEMA) It is characterized in that it further includes.
본 발명의 일실시예에 있어서, 상기 활성탄은 (a) 왕겨를 탄화하여 1차 탄화물을 제조하는 1차 탄화단계;In one embodiment of the present invention, the activated carbon may include (a) a first carbonization step of carbonizing rice hulls to produce a first carbonized material;
(b) 상기 1차 탄화물을 탄화하여 2차 탄화물을 제조하는 2차 탄화단계;(b) a secondary carbonization step of carbonizing the primary carbide to produce a secondary carbide;
(c) 상기 2차 탄화물을 탄화하여 3차 탄화물을 제조하는 3차 탄화단계; 및(c) a tertiary carbonization step of carbonizing the secondary carbide to produce a tertiary carbide; and
(d) 상기 3차 탄화물을 분쇄하는 단계를 포함하는 방법에 의하여 제조되는 것을 특징으로 한다. (d) characterized in that it is produced by a method comprising the step of grinding the tertiary carbide.
또한 본 발명은 상기 산소발생 조성물을 포함하는 성형체를 제공한다.In addition, the present invention provides a molded article containing the oxygen generating composition.
본 발명은 공기 중이나 물속에 서서히 산소를 배출하여 물속의 산소농도를 장기간 동안 증가시킬 수 있고, 세균이나 박테리아 등에 대한 항균성을 나타내며, 녹조를 제거하고 오염수를 정화할 수 있으며, 식물의 성장을 촉진할 수 있는 산소발생 조성물을 제공할 수 있다. The present invention can increase the oxygen concentration in the water for a long period of time by slowly discharging oxygen into the air or water, exhibit antibacterial properties against germs or bacteria, remove algae and purify contaminated water, and promote plant growth. It is possible to provide an oxygen generating composition capable of
또한 본 발명은 액체 상태, 분말 상태, 성형체 등으로 제조되어 양식장, 어항 등에 산소를 공급하는 용도로 사용되거나 녹조제거 및 수질개선을 위한 용도를 사용되거나 화분, 농작물 등에 식물성장을 촉진하는 용도로 사용되는 산소발생 조성물을 제공할 수 있다. In addition, the present invention is manufactured in a liquid state, powder state, molded body, etc., and is used for supplying oxygen to fish farms, fish tanks, etc., used for removing algae and improving water quality, or used for promoting plant growth in pots, crops, etc. It is possible to provide an oxygen generating composition that is.
이하 실시예를 바탕으로 본 발명을 상세히 설명한다. 본 발명에 사용된 용어, 실시예 등은 본 발명을 보다 구체적으로 설명하고 통상의 기술자의 이해를 돕기 위하여 예시된 것에 불과할 뿐이며, 본 발명의 권리범위 등이 이에 한정되어 해석되어서는 안 된다.The present invention will be described in detail based on the following examples. The terms, examples, etc. used in the present invention are merely exemplified to explain the present invention in more detail and help the understanding of those skilled in the art, and the scope of the present invention should not be construed as being limited thereto.
본 발명에 사용되는 기술 용어 및 과학 용어는 다른 정의가 없다면 이 발명이 속하는 기술 분야에서 통상의 지식을 가진 자가 통상적으로 이해하고 있는 의미를 나타낸다.Technical terms and scientific terms used in the present invention represent meanings commonly understood by those of ordinary skill in the art to which this invention belongs, unless otherwise defined.
본 발명은 시멘트, 모래, 활성탄, 황토 및 물을 포함하는 산소발생 조성물에 관한 것이다.The present invention relates to an oxygen generating composition comprising cement, sand, activated carbon, loess and water.
상기 조성물은 시멘트 100중량부에 대하여 모래 70~120중량부, 활성탄 5~30중량부, 황토 5~20중량부 및 물 1~20중량부를 포함할 수 있다. The composition may include 70 to 120 parts by weight of sand, 5 to 30 parts by weight of activated carbon, 5 to 20 parts by weight of loess, and 1 to 20 parts by weight of water, based on 100 parts by weight of cement.
상기 시멘트는 조성물을 결합시키는 바인더로 작용하며, 포틀랜드 시멘트, 슬래그 시멘트, 알루미나 시멘트, 석고 시멘트, 플라스틱 시멘트 등의 공지의 시멘트가 제한 없이 사용될 수 있다. The cement acts as a binder binding the composition, and known cements such as Portland cement, slag cement, alumina cement, gypsum cement, and plastic cement may be used without limitation.
상기 모래는 산소배출특성 및 내구성을 향상시키기 위하여 사용되며, 시멘트 100중량부에 대하여 70~120중량부 사용되는 것이 바람직하다. The sand is used to improve oxygen release characteristics and durability, and is preferably used in an amount of 70 to 120 parts by weight based on 100 parts by weight of cement.
모래의 함량이 상기 수치범위를 만족하는 경우 산소배출특성, 항균성, 흡착성 및 내구성이 극대화될 수 있다. When the content of sand satisfies the above numerical range, oxygen release characteristics, antibacterial properties, adsorption properties, and durability can be maximized.
상기 활성탄은 산소배출특성, 항균성 및 흡착성을 향상시키기 위하여 사용되며, 시멘트 100중량부에 대하여 5~30중량부 사용되는 것이 바람직하다. The activated carbon is used to improve oxygen release characteristics, antibacterial properties and adsorption, and is preferably used in an amount of 5 to 30 parts by weight based on 100 parts by weight of cement.
활성탄의 함량이 상기 수치범위를 만족하는 경우 산소배출특성, 항균성 및 흡착성이 극대화될 수 있다. When the content of activated carbon satisfies the above numerical range, oxygen release characteristics, antibacterial properties, and adsorption properties can be maximized.
상기 활성탄은 (a) 왕겨를 탄화하여 1차 탄화물을 제조하는 1차 탄화단계;The activated carbon includes (a) a first carbonization step of carbonizing rice hulls to produce a first carbonized material;
(b) 상기 1차 탄화물을 탄화하여 2차 탄화물을 제조하는 2차 탄화단계;(b) a secondary carbonization step of carbonizing the primary carbide to produce a secondary carbide;
(c) 상기 2차 탄화물을 탄화하여 3차 탄화물을 제조하는 3차 탄화단계; 및(c) a tertiary carbonization step of carbonizing the secondary carbide to produce a tertiary carbide; and
(d) 상기 3차 탄화물을 분쇄하는 단계를 포함하는 방법에 의하여 제조될 수 있다. (d) it can be produced by a method comprising the step of grinding the tertiary carbide.
상기 (a) 단계는 왕겨를 탄화하여 1차 탄화물을 제조하는 1차 탄화단계로서, 100℃에서 300℃까지 승온하고, 300℃에서 30분~3시간 유지하여 왕겨를 1차 탄화할 수 있다. The step (a) is the first carbonization step of carbonizing rice hull to produce primary carbonized material. The temperature is raised from 100 ° C. to 300 ° C., and maintained at 300 ° C. for 30 minutes to 3 hours to first carbonize rice hull.
상기 1차 탄화단계는 비활성 기체 하에 수행될 수 있으며, 상기 비활성 기체로는 질소, 아르곤, 네온, 헬륨 등이 사용될 수 있다. The first carbonization step may be performed under an inert gas, and nitrogen, argon, neon, helium, or the like may be used as the inert gas.
상기 비활성 기체는 10㎖/min~100㎖/min의 속도로 주입될 수 있으며, 주입속도가 상기 수치범위를 만족하는 경우 산소배출특성, 항균성, 흡착성 등이 극대화될 수 있다. The inert gas may be injected at a rate of 10 ml/min to 100 ml/min, and when the injection rate satisfies the above numerical range, oxygen emission characteristics, antibacterial properties, adsorption properties, and the like can be maximized.
상기 1차 탄화단계는 왕겨 내에 포함된 수분, 휘발성 성분, 불순물 등을 제거할 수 있다. The first carbonization step may remove moisture, volatile components, impurities, etc. contained in the rice hull.
상기 1차 탄화단계의 승온속도는 1℃/min~10℃/min 인 것이 바람직하고, 승온속도가 상기 수치범위를 만족하는 경우 산소배출특성, 항균성, 흡착성 등이 극대화될 수 있다. The heating rate of the first carbonization step is preferably 1 ° C./min to 10 ° C./min. When the heating rate satisfies the numerical range, oxygen release characteristics, antibacterial properties, adsorption properties, and the like can be maximized.
또한 본 발명은 활성탄의 원료로 왕겨 및 쌀겨를 동시에 사용할 수 있으며, 왕겨 및 쌀겨의 중량비는 100:1~20 인 것이 바람직하다. In addition, in the present invention, rice hull and rice bran may be simultaneously used as raw materials for activated carbon, and the weight ratio of rice hull and rice hull is preferably 100:1 to 20.
왕겨 및 쌀겨의 중량비가 상기 수치범위를 만족하는 경우 산소배출특성, 항균성, 흡착성 등이 극대화될 수 있다. When the weight ratio of rice husk and rice husk satisfies the above numerical range, oxygen release characteristics, antibacterial properties, adsorption properties, and the like can be maximized.
아울러 본 발명은 활성탄의 원료로 왕겨, 쌀겨 및 볏짚을 동시에 사용할 수 있으며, 왕겨, 쌀겨 및 볏짚의 중량비는 100:1~20:1~10 인 것이 바람직하다. In addition, in the present invention, rice hull, rice bran, and rice straw may be simultaneously used as raw materials for activated carbon, and the weight ratio of rice hull, rice bran, and rice straw is preferably 100:1 to 20:1 to 10.
왕겨, 쌀겨 및 볏짚의 중량비가 상기 수치범위를 만족하는 경우 산소배출특성, 항균성, 흡착성 등이 극대화될 수 있다. When the weight ratio of rice hull, rice hull, and rice straw satisfies the above numerical range, oxygen release characteristics, antibacterial properties, adsorption properties, and the like can be maximized.
또한 본 발명은 활성탄의 원료로 왕겨, 쌀겨, 볏짚 및 톱밥을 동시에 사용할 수 있으며, 왕겨, 쌀겨, 볏짚 및 톱밥의 중량비는 100:1~20:1~10:1~5 인 것이 바람직하다. In addition, rice hull, rice bran, rice straw, and sawdust may be simultaneously used as raw materials for activated carbon in the present invention, and the weight ratio of rice hull, rice bran, rice straw, and sawdust is preferably 100:1 to 20:1 to 10:1 to 5.
왕겨, 쌀겨, 볏짚 및 톱밥의 중량비가 상기 수치범위를 만족하는 경우 산소배출특성, 항균성, 흡착성 등이 극대화될 수 있다. When the weight ratio of rice hull, rice hull, rice straw, and sawdust satisfies the above numerical range, oxygen release characteristics, antibacterial properties, adsorption properties, and the like can be maximized.
상기 (b) 단계는 상기 1차 탄화물을 탄화하여 2차 탄화물을 제조하는 2차 탄화단계로서, 300℃에서 600℃까지 승온하고, 600℃에서 30분~3시간 유지하여 2차 탄화를 수행할 수 있다. The step (b) is a secondary carbonization step of carbonizing the primary carbide to produce a secondary carbide. can
상기 2차 탄화단계는 비활성 기체 하에 수행될 수 있으며, 상기 비활성 기체로는 질소, 아르곤, 네온, 헬륨 등이 사용될 수 있다. The second carbonization step may be performed under an inert gas, and nitrogen, argon, neon, helium, or the like may be used as the inert gas.
상기 비활성 기체는 10㎖/min~100㎖/min의 속도로 주입될 수 있으며, 주입속도가 상기 수치범위를 만족하는 경우 산소배출특성, 항균성, 흡착성 등이 극대화될 수 있다. The inert gas may be injected at a rate of 10 ml/min to 100 ml/min, and when the injection rate satisfies the above numerical range, oxygen emission characteristics, antibacterial properties, adsorption properties, and the like can be maximized.
상기 2차 탄화단계의 승온속도는 1℃/min~10℃/min 인 것이 바람직하고, 승온속도가 상기 수치범위를 만족하는 경우 산소배출특성, 항균성, 흡착성 등이 극대화될 수 있다. The temperature increase rate of the second carbonization step is preferably 1 ° C / min to 10 ° C / min, and when the temperature increase rate satisfies the above numerical range, oxygen release characteristics, antibacterial properties, adsorption properties, etc. can be maximized.
상기 2차 탄화단계는 수증기 또는 이산화탄소를 주입할 수 있으며, 상기 수증기 또는 이산화탄소는 0.1㎖/h~0.5㎖/h 의 속도로 주입될 수 있으며, 주입속도가 상기 수치범위를 만족하는 경우 산소배출특성, 항균성, 흡착성 등이 극대화될 수 있다. In the second carbonization step, steam or carbon dioxide may be injected, and the steam or carbon dioxide may be injected at a rate of 0.1 ml / h to 0.5 ml / h, and when the injection rate satisfies the above numerical range, oxygen emission characteristics , antimicrobial activity, adsorption, etc. can be maximized.
상기 수증기 또는 이산화탄소는 왕겨 내에 포함된 유기물, 무기물 등을 제거하여 활성탄의 기공 및 비표면적을 증가시킬 수 있다. The steam or carbon dioxide can increase the pores and specific surface area of the activated carbon by removing organic and inorganic substances contained in the rice hull.
상기 (c) 단계는 상기 2차 탄화물을 탄화하여 3차 탄화물을 제조하는 3차 탄화단계로서, 600℃에서 900℃까지 승온하고, 900℃에서 30분~3시간 유지하여 3차 탄화를 수행할 수 있다. The step (c) is a tertiary carbonization step of carbonizing the secondary carbide to produce a tertiary carbide. can
상기 3차 탄화단계는 비활성 기체 하에 수행될 수 있으며, 상기 비활성 기체로는 질소, 아르곤, 네온, 헬륨 등이 사용될 수 있다. The third carbonization step may be performed under an inert gas, and nitrogen, argon, neon, helium, or the like may be used as the inert gas.
상기 비활성 기체는 10㎖/min~100㎖/min의 속도로 주입될 수 있으며, 주입속도가 상기 수치범위를 만족하는 경우 산소배출특성, 항균성, 흡착성 등이 극대화될 수 있다. The inert gas may be injected at a rate of 10 ml/min to 100 ml/min, and when the injection rate satisfies the above numerical range, oxygen emission characteristics, antibacterial properties, adsorption properties, and the like can be maximized.
상기 3차 탄화단계의 승온속도는 1℃/min~10℃/min 인 것이 바람직하고, 승온속도가 상기 수치범위를 만족하는 경우 산소배출특성, 항균성, 흡착성 등이 극대화될 수 있다. The temperature increase rate of the tertiary carbonization step is preferably 1 ° C / min to 10 ° C / min, and when the temperature increase rate satisfies the above numerical range, oxygen release characteristics, antibacterial properties, adsorption properties, etc. can be maximized.
상기 3차 탄화단계는 수증기 또는 이산화탄소를 주입할 수 있으며, 상기 수증기 또는 이산화탄소는 0.5㎖/h~1㎖/h 의 속도로 주입될 수 있으며, 주입속도가 상기 수치범위를 만족하는 경우 산소배출특성, 항균성, 흡착성 등이 극대화될 수 있다. In the third carbonization step, steam or carbon dioxide may be injected, and the steam or carbon dioxide may be injected at a rate of 0.5 ml / h to 1 ml / h, and when the injection rate satisfies the above numerical range, oxygen emission characteristics , antimicrobial activity, adsorption, etc. can be maximized.
상기 수증기 또는 이산화탄소는 왕겨 내에 포함된 유기물, 무기물 등을 제거하여 활성탄의 기공 및 비표면적을 증가시킬 수 있다. The steam or carbon dioxide can increase the pores and specific surface area of the activated carbon by removing organic and inorganic substances contained in the rice hull.
또한 본 발명은 수증기 및 이산화탄소를 동시에 사용할 수 있으며, 수증기 및 이산화탄소의 부피비는 60~80:20~40 인 것이 바람직하다. In addition, in the present invention, steam and carbon dioxide can be used simultaneously, and the volume ratio of steam and carbon dioxide is preferably 60 to 80:20 to 40.
수증기 및 이산화탄소의 부피비가 상기 수치범위를 만족하는 경우 산소배출특성, 항균성, 흡착성 등이 극대화될 수 있다. When the volume ratio of water vapor and carbon dioxide satisfies the above numerical range, oxygen release characteristics, antibacterial properties, adsorption properties, and the like can be maximized.
상기 (d) 단계는 상기 3차 탄화물을 분쇄하는 단계로서, 제조된 3차 탄화물을 냉각한 후, 공지의 분쇄수단을 사용하여 분쇄함으로써, 일정한 크기의 활성탄을 수득할 수 있다. The step (d) is a step of crushing the tertiary carbide. Activated carbon having a certain size can be obtained by cooling the prepared tertiary carbide and then pulverizing the tertiary carbide using a known crushing means.
상기 분쇄된 활성탄은 공지의 건조수단을 통하여 건조될 수 있으며, 이를 통해 활성탄의 수분함량을 조절할 수 있다. The pulverized activated carbon may be dried through a known drying means, through which the moisture content of the activated carbon may be adjusted.
또한 본 발명은 상기 (d) 단계 이후에, 상기 활성탄의 표면을 아크릴레이트기 함유 실란 커플링제, 2-하이드록시에틸 아크릴레이트(HEA) 및 2-하이드록시에틸 메타크릴레이트(HEMA)의 공중합체로 처리할 수 있으며, 상기 공중합체는 활성탄의 흡착특성 및 결합력을 향상시킬 수 있다. In addition, in the present invention, after the step (d), the surface of the activated carbon is coated with a silane coupling agent containing an acrylate group, a copolymer of 2-hydroxyethyl acrylate (HEA) and 2-hydroxyethyl methacrylate (HEMA) It can be treated with, and the copolymer can improve the adsorption properties and bonding strength of activated carbon.
상기 아크릴레이트기 함유 실란 커플링제로는 3-메타크릴록시프로필메틸디메톡시실란, 3-메타크릴록시프로필트리메톡시실란, 3-메타크릴록시프로필메틸디에톡시실란, 3-메타크릴록시프로필트리에톡시실란, 3-아크릴록시프로필트리메톡시실란, 메타크릴록시메틸트리에톡시실란, 메타크릴록시메틸트리메톡시실란 등이 있다. The acrylate group-containing silane coupling agent includes 3-methacryloxypropylmethyldimethoxysilane, 3-methacryloxypropyltrimethoxysilane, 3-methacryloxypropylmethyldiethoxysilane, 3-methacryloxypropyltri ethoxysilane, 3-acryloxypropyltrimethoxysilane, methacryloxymethyltriethoxysilane, methacryloxymethyltrimethoxysilane and the like.
상기 아크릴레이트기 함유 실란 커플링제, 2-하이드록시에틸 아크릴레이트(HEA) 및 2-하이드록시에틸 메타크릴레이트(HEMA)의 중량비는 2~10:100:20~50인 것이 바람직하며, 상기 수치범위에서 결합력 및 흡착특성이 극대화될 수 있다. The weight ratio of the acrylate group-containing silane coupling agent, 2-hydroxyethyl acrylate (HEA) and 2-hydroxyethyl methacrylate (HEMA) is preferably 2 to 10:100:20 to 50, and the above numerical values In the range, binding force and adsorption characteristics can be maximized.
상기 공중합체는 활성탄 100중량부에 대하여 2~10중량부 사용되며, 함량이 2중량부 미만인 경우 첨가의 효과가 미미하고, 10중량부를 초과하는 경우 비표면적이 저하된다.The copolymer is used in an amount of 2 to 10 parts by weight based on 100 parts by weight of activated carbon. When the content is less than 2 parts by weight, the effect of addition is insignificant, and when the content exceeds 10 parts by weight, the specific surface area is reduced.
또한 본 발명은 상기 (d) 단계 이후에, 상기 활성탄의 표면을 아크릴레이트기 함유 실란 커플링제, 아크릴산계 모노머, 2-하이드록시에틸 아크릴레이트(HEA) 및 2-하이드록시에틸 메타크릴레이트(HEMA)의 공중합체로 처리할 수 있으며, 상기 공중합체는 활성탄의 흡착특성 및 결합력을 향상시킬 수 있다. In addition, in the present invention, after step (d), the surface of the activated carbon is treated with an acrylate group-containing silane coupling agent, an acrylic acid monomer, 2-hydroxyethyl acrylate (HEA) and 2-hydroxyethyl methacrylate (HEMA) ), and the copolymer can improve adsorption properties and bonding strength of activated carbon.
상기 아크릴산계 모노머는 아크릴산, 메타크릴산, 카르복실 에틸아크릴레이트, 카르복실 에틸메타크릴레이트, 카르복실 펜틸아크릴레이트, 카르복실 펜틸메타크릴레이트, 이타콘산, 말레인산, 푸마르산, 메틸 아크릴산, 에틸 아크릴산, 부틸 아크릴산, 2-에틸 헥실 아크릴산, 데실아크릴산, 메틸 메타크릴산, 에틸 메타크릴산, 부틸 메타크릴산, 2-에틸 헥실 메타크릴산, 데실메타크릴산 등이 있다. The acrylic acid-based monomers include acrylic acid, methacrylic acid, carboxyl ethyl acrylate, carboxyl ethyl methacrylate, carboxyl pentyl acrylate, carboxyl pentyl methacrylate, itaconic acid, maleic acid, fumaric acid, methyl acrylic acid, ethyl acrylic acid, Butyl acrylic acid, 2-ethylhexyl acrylic acid, decyl acrylic acid, methyl methacrylic acid, ethyl methacrylic acid, butyl methacrylic acid, 2-ethylhexyl methacrylic acid, decyl methacrylic acid and the like.
상기 아크릴레이트기 함유 실란 커플링제, 아크릴산계 모노머, 2-하이드록시에틸 아크릴레이트(HEA) 및 2-하이드록시에틸 메타크릴레이트(HEMA)의 중량비는 2~10:30~60:100:20~50 인 것이 바람직하다. The weight ratio of the silane coupling agent containing an acrylate group, acrylic acid monomer, 2-hydroxyethyl acrylate (HEA) and 2-hydroxyethyl methacrylate (HEMA) is 2 to 10:30 to 60:100:20 to 50 is preferred.
상기 공중합체는 활성탄 100중량부에 대하여 2~10중량부 사용되며, 함량이 2중량부 미만인 경우 첨가의 효과가 미미하고, 10중량부를 초과하는 경우 비표면적이 저하된다.The copolymer is used in an amount of 2 to 10 parts by weight based on 100 parts by weight of activated carbon. When the content is less than 2 parts by weight, the effect of addition is insignificant, and when the content exceeds 10 parts by weight, the specific surface area is reduced.
상기 활성탄은 산소배출특성, 항균성, 흡착성, 불연성, 단열성, 소취특성 등이 우수하고 가격이 낮아 산소배출재, 불연재, 단열재, 흡착제, 촉매 등의 분야에 효과적으로 사용될 수 있다. The activated carbon has excellent oxygen emitting properties, antibacterial properties, adsorption properties, nonflammability, insulation properties, and deodorizing properties, and is inexpensive, so it can be effectively used in the fields of oxygen emitting materials, nonflammable materials, heat insulating materials, adsorbents, and catalysts.
상기 황토는 산소배출특성, 소취특성 및 항균성을 향상시키기 위하여 사용되며, 시멘트 100중량부에 대하여 5~20중량부 사용되는 것이 바람직하다. The ocher is used to improve oxygen release characteristics, deodorizing characteristics and antibacterial properties, and is preferably used in an amount of 5 to 20 parts by weight based on 100 parts by weight of cement.
황토의 함량이 상기 수치범위를 만족하는 경우 산소배출특성, 소취특성 및 항균성이 극대화될 수 있다. When the content of loess satisfies the above numerical range, oxygen emission characteristics, deodorizing characteristics and antibacterial properties can be maximized.
상기 물은 조성물의 농도를 조절하고, 조성물을 경화시키기 위한 것으로서, 물의 함량은 시멘트 100중량부에 대하여 1~20중량부인 것이 바람직하다. The water is used to adjust the concentration of the composition and harden the composition, and the water content is preferably 1 to 20 parts by weight based on 100 parts by weight of cement.
물의 함량이 상기 수치범위를 만족하는 경우 산소배출특성, 흡착성, 내구성 및 항균성이 극대화될 수 있다. When the water content satisfies the above numerical range, oxygen release characteristics, adsorption properties, durability and antibacterial properties can be maximized.
또한 상기 조성물은 아크릴레이트기 함유 실란 커플링제, 2-하이드록시에틸 아크릴레이트(HEA) 및 2-하이드록시에틸 메타크릴레이트(HEMA)의 공중합체를 추가로 포함할 수 있다. In addition, the composition may further include a silane coupling agent containing an acrylate group, a copolymer of 2-hydroxyethyl acrylate (HEA) and 2-hydroxyethyl methacrylate (HEMA).
상기 아크릴레이트기 함유 실란 커플링제, 2-하이드록시에틸 아크릴레이트(HEA) 및 2-하이드록시에틸 메타크릴레이트(HEMA)의 중량비는 2~10:100:20~50 인 것이 바람직하다. The weight ratio of the acrylate group-containing silane coupling agent, 2-hydroxyethyl acrylate (HEA) and 2-hydroxyethyl methacrylate (HEMA) is preferably 2 to 10:100:20 to 50.
상기 공중합체는 시멘트 100중량부에 대하여 1~10중량부 사용되는 것이 바람직하며, 공중합체의 함량이 상기 수치범위를 만족하는 경우 산소배출특성, 흡착성, 내구성 및 항균성이 극대화될 수 있다. It is preferable to use 1 to 10 parts by weight of the copolymer based on 100 parts by weight of cement, and when the content of the copolymer satisfies the above numerical range, oxygen release characteristics, adsorption properties, durability and antibacterial properties can be maximized.
또한 상기 조성물은 아크릴레이트기 함유 실란 커플링제, 아크릴산계 모노머, 2-하이드록시에틸 아크릴레이트(HEA) 및 2-하이드록시에틸 메타크릴레이트(HEMA)의 공중합체를 추가로 포함할 수 있다. In addition, the composition may further include a copolymer of an acrylate group-containing silane coupling agent, an acrylic acid monomer, 2-hydroxyethyl acrylate (HEA) and 2-hydroxyethyl methacrylate (HEMA).
상기 아크릴레이트기 함유 실란 커플링제, 아크릴산계 모노머, 2-하이드록시에틸 아크릴레이트(HEA) 및 2-하이드록시에틸 메타크릴레이트(HEMA)의 중량비는 2~10:30~60:100:20~50 인 것이 바람직하다. The weight ratio of the silane coupling agent containing an acrylate group, acrylic acid monomer, 2-hydroxyethyl acrylate (HEA) and 2-hydroxyethyl methacrylate (HEMA) is 2 to 10:30 to 60:100:20 to 50 is preferred.
상기 공중합체는 시멘트 100중량부에 대하여 1~10중량부 사용되는 것이 바람직하며, 공중합체의 함량이 상기 수치범위를 만족하는 경우 산소배출특성, 흡착성, 내구성 및 항균성이 극대화될 수 있다. It is preferable to use 1 to 10 parts by weight of the copolymer based on 100 parts by weight of cement, and when the content of the copolymer satisfies the above numerical range, oxygen release characteristics, adsorption properties, durability and antibacterial properties can be maximized.
또한 상기 조성물은 아크릴레이트기 함유 실란 커플링제, 에폭시기 함유 실란 커플링제, 비스페놀 A(BPA) 및 2-하이드록시에틸 아크릴레이트(HEA)를 반응시켜 제조되는 실란 커플링제 올리고머를 추가로 포함할 수 있다. In addition, the composition may further include a silane coupling agent oligomer prepared by reacting an acrylate group-containing silane coupling agent, an epoxy group-containing silane coupling agent, bisphenol A (BPA) and 2-hydroxyethyl acrylate (HEA). .
상기 에폭시기 함유 실란 커플링제로는 2-글리시독시에틸메틸디메톡시실란, 2-글리시독시에틸메틸디에톡시실란, 3-글리시독시프로필메틸디메톡시실란, 3-글리시독시프로필메틸디에톡시실란, 2-글리시독시에틸트리메톡시실란, 2-글리시독시에틸트리에톡시실란, 3-글리시독시프로필트리메톡시실란, 3-글리시독시프로필트리에톡시실란, 2-(3,4-에폭시시클로헥실)에틸메틸디메톡시실란, 2-(3,4-에폭시시클로헥실)에틸메틸디에톡시실란, 3-(3,4-에폭시시클로헥실)프로필메틸디메톡시실란, 3-(3,4-에폭시시클로헥실)프로필메틸디에톡시실란, 2-(3,4-에폭시시클로헥실)에틸트리메톡시실란, 2-(3,4-에폭시시클로헥실)에틸트리에톡시실란, 3-(3,4-에폭시시클로헥실)프로필트리메톡시실란, 3-(3,4-에폭시시클로헥실)프로필트리에톡시실란 등이 있다.The epoxy group-containing silane coupling agent includes 2-glycidoxyethylmethyldimethoxysilane, 2-glycidoxyethylmethyldiethoxysilane, 3-glycidoxypropylmethyldimethoxysilane, 3-glycidoxypropylmethyldiethoxy Silane, 2-glycidoxyethyltrimethoxysilane, 2-glycidoxyethyltriethoxysilane, 3-glycidoxypropyltrimethoxysilane, 3-glycidoxypropyltriethoxysilane, 2-(3 ,4-epoxycyclohexyl)ethylmethyldimethoxysilane, 2-(3,4-epoxycyclohexyl)ethylmethyldiethoxysilane, 3-(3,4-epoxycyclohexyl)propylmethyldimethoxysilane, 3-( 3,4-epoxycyclohexyl)propylmethyldiethoxysilane, 2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane, 2-(3,4-epoxycyclohexyl)ethyltriethoxysilane, 3- (3,4-epoxycyclohexyl)propyltrimethoxysilane, 3-(3,4-epoxycyclohexyl)propyltriethoxysilane, and the like.
상기 아크릴레이트기 함유 실란 커플링제, 에폭시기 함유 실란 커플링제, 비스페놀 A(BPA) 및 2-하이드록시에틸 아크릴레이트의 중량비는 2~10:100:10~30:20~50인 것이 바람직하다. The weight ratio of the acrylate group-containing silane coupling agent, the epoxy group-containing silane coupling agent, bisphenol A (BPA), and 2-hydroxyethyl acrylate is preferably 2 to 10:100:10 to 30:20 to 50.
상기 올리고머의 중량평균분자량은 5,000~50,000g/mol 인 것이 바람직하다. The oligomer preferably has a weight average molecular weight of 5,000 to 50,000 g/mol.
상기 올리고머는 시멘트 100중량부에 대하여 1~10중량부 사용되는 것이 바람직하며, 올리고머의 함량이 상기 수치범위를 만족하는 경우 산소배출특성, 흡착성, 내구성 및 항균성이 극대화될 수 있다. The oligomer is preferably used in an amount of 1 to 10 parts by weight based on 100 parts by weight of cement, and when the content of the oligomer satisfies the above numerical range, oxygen release characteristics, adsorption properties, durability and antibacterial properties can be maximized.
또한 상기 조성물은 석탄재를 추가로 포함할 수 있으며, 상기 석탄재는 시멘트 100중량부에 대하여 1~10중량부 사용되는 것이 바람직하다. In addition, the composition may further include coal ash, and the coal ash is preferably used in an amount of 1 to 10 parts by weight based on 100 parts by weight of cement.
석탄재의 함량이 상기 수치범위를 만족하는 경우 산소배출특성, 흡착성, 내구성 및 항균성이 극대화될 수 있다. When the content of the coal ash satisfies the above numerical range, oxygen emission characteristics, adsorption properties, durability and antibacterial properties can be maximized.
또한 상기 조성물은 연탄재를 추가로 포함할 수 있으며, 상기 연탄재는 시멘트 100중량부에 대하여 1~10중량부 사용되는 것이 바람직하다. In addition, the composition may further include a briquette material, and the briquette material is preferably used in an amount of 1 to 10 parts by weight based on 100 parts by weight of cement.
연탄재의 함량이 상기 수치범위를 만족하는 경우 산소배출특성, 흡착성, 내구성 및 항균성이 극대화될 수 있다. When the content of the briquette ash satisfies the above numerical range, oxygen release characteristics, adsorption properties, durability and antibacterial properties may be maximized.
또한 상기 조성물은 패각 입자를 추가로 포함할 수 있으며, 패각으로는 굴패각, 고동패각, 바지락패각, 백합패각, 전복패각 등이 제한 없이 사용될 수 있다. In addition, the composition may further include shell particles, and as shells, oyster shells, beetle shells, clam shells, lily shells, abalone shells, and the like may be used without limitation.
패각 입자의 함량은 시멘트 100중량부에 대하여 1~10중량부인 것이 바람직하며, 함량이 상기 수치범위를 만족하는 경우 산소배출특성, 흡착성, 내구성 및 항균성이 극대화될 수 있다. The content of shell particles is preferably 1 to 10 parts by weight based on 100 parts by weight of cement, and when the content satisfies the above numerical range, oxygen release characteristics, adsorption properties, durability and antibacterial properties can be maximized.
또한 본 발명은 상기 산소발생 조성물을 포함하는 성형체에 관한 것이다. In addition, the present invention relates to a molded article containing the oxygen generating composition.
상기 산소발생 조성물은 공기 중이나 물속에 서서히 산소를 배출하여 물속의 산소농도를 장기간 동안 증가시키거나 일정 농도 이상으로 유지시킬 수 있고, 세균이나 박테리아 등에 대한 항균성을 나타내며, 녹조를 제거하고 오염수를 정화할 수 있으며, 식물의 성장을 촉진할 수 있다. The oxygen-generating composition can increase the oxygen concentration in the water for a long period of time or maintain it above a certain concentration by gradually releasing oxygen into the air or water, exhibit antibacterial properties against germs or bacteria, remove algae, and purify polluted water. and can promote plant growth.
상기 산소발생 조성물은 액체 상태, 분말 상태, 성형체 등으로 제조되어 양식장, 어항 등에 산소를 공급하는 용도로 사용되거나 바다, 강, 하천 등의 녹조제거 및 수질개선을 위한 용도를 사용되거나 화분, 농작물 등에 식물성장을 촉진하는 용도로 사용될 수 있다. The oxygen-generating composition is manufactured in a liquid state, powder state, molded body, etc., and is used for supplying oxygen to fish farms, fish tanks, etc., or used for algae removal and water quality improvement in seas, rivers, rivers, etc., or used for pollen, crops, etc. It can be used for stimulating plant growth.
상기 성형체는 펠릿 형태, 막대 형태, 블록 형태(구, 원기둥, 원뿔, 각뿔, 육면체, 다면체 등) 등의 다양한 형상으로 제조되어 양식장, 어항 등에 투입되어 산소를 장기간 배출하여 물속의 용존산소량을 증가시킬 수 있고, 세균이나 박테리아 등에 대한 항균성을 나타내며, 수질을 개선할 수 있으며, 화분, 농작물 등에 식물성장을 촉진하는 용도로 사용될 수 있다. The molded body is manufactured in various shapes such as pellet form, rod form, block form (sphere, cylinder, cone, pyramid, hexahedron, polyhedron, etc.) and put into fish farms, fish tanks, etc. to discharge oxygen for a long period of time to increase the amount of dissolved oxygen in water It can exhibit antimicrobial properties against germs or bacteria, can improve water quality, and can be used for promoting plant growth in pollen, crops, etc.
상기 성형체는 상기 산소발생 조성물을 혼합한 후 압축 성형, 프레스 성형, 사출 성형, 압출 성형 등의 방법으로 제조될 수 있다. The molded article may be manufactured by mixing the oxygen generating composition and then compression molding, press molding, injection molding, extrusion molding, or the like.
또한 상기 제조된 성형체를 분쇄하여 분말 상태로 제조할 수 있다. In addition, the prepared molded body may be pulverized to be prepared in a powder state.
이하 실시예 및 비교예를 통해 본 발명을 상세히 설명한다. 하기 실시예는 본 발명의 실시를 위하여 예시된 것일 뿐, 본 발명의 내용이 하기 실시예에 의하여 한정되는 것은 아니다.The present invention will be described in detail through Examples and Comparative Examples below. The following examples are only exemplified for the practice of the present invention, and the content of the present invention is not limited by the following examples.
(실시예 1)(Example 1)
왕겨를 건조하고 불순물을 제거하여 탄화장치에 투입한 후, 100℃에서 300℃까지 5℃/min의 속도로 승온하고, 300℃에서 1시간 유지하여 왕겨를 1차 탄화하였다. 이때 질소를 50㎖/min 로 주입하였다. After drying the rice hull, removing impurities, and putting it into a carbonization device, the temperature was raised from 100 ° C to 300 ° C at a rate of 5 ° C / min, and maintained at 300 ° C for 1 hour to first carbonize the rice hull. At this time, nitrogen was injected at 50 ml/min.
상기 1차 탄화물을 300℃에서 600℃까지 5℃/min의 속도로 승온하고, 600℃에서 1시간 유지하여 2차 탄화를 수행하였다. 이때 질소를 50㎖/min 로 주입하면서, 수증기를 0.3㎖/h 로 주입하였다. The primary carbide was heated from 300 °C to 600 °C at a rate of 5 °C/min, and maintained at 600 °C for 1 hour to perform secondary carbonization. At this time, water vapor was injected at 0.3 ml/h while nitrogen was injected at 50 ml/min.
상기 2차 탄화물을 600℃에서 900℃까지 5℃/min의 속도로 승온하고, 900℃에서 1시간 유지하여 3차 탄화를 수행하였다. 이때 질소를 50㎖/min 로 주입하면서, 수증기를 0.7㎖/h 로 주입하였다. The secondary carbide was heated from 600 °C to 900 °C at a rate of 5 °C/min, and maintained at 900 °C for 1 hour to perform tertiary carbonization. At this time, water vapor was injected at 0.7 ml/h while nitrogen was injected at 50 ml/min.
상기 3차 탄화물을 냉각한 후 분쇄하여 활성탄을 제조하였다. The tertiary carbide was cooled and pulverized to prepare activated carbon.
시멘트 100중량부, 모래 100중량부, 상기 활성탄 15중량부, 황토 10중량부 및 물 10중량부를 혼합하여 산소발생 조성물을 제조하였다.An oxygen generating composition was prepared by mixing 100 parts by weight of cement, 100 parts by weight of sand, 15 parts by weight of the activated carbon, 10 parts by weight of loess, and 10 parts by weight of water.
(실시예 2)(Example 2)
왕겨 대신에, 왕겨 100중량부 및 쌀겨 10중량부를 사용하여 제조된 활성탄을 사용한 것을 제외하고는 실시예 1과 동일한 방법으로 산소발생 조성물을 제조하였다. An oxygen generating composition was prepared in the same manner as in Example 1, except that activated carbon prepared using 100 parts by weight of rice hull and 10 parts by weight of rice hull was used instead of rice hull.
(실시예 3)(Example 3)
3-메타크릴록시프로필트리메톡시실란 5중량부, 2-하이드록시에틸 아크릴레이트(HEA) 100중량부 및 2-하이드록시에틸 메타크릴레이트(HEMA) 30중량부를 혼합하고 반응시켜 공중합체를 제조하였다. 5 parts by weight of 3-methacryloxypropyltrimethoxysilane, 100 parts by weight of 2-hydroxyethyl acrylate (HEA), and 30 parts by weight of 2-hydroxyethyl methacrylate (HEMA) were mixed and reacted to prepare a copolymer. did
활성탄을 상기 공중합체로 표면처리하였으며, 이때 활성탄 100중량부에 대하여 공중합체 5중량부를 사용하였다. Activated carbon was surface treated with the copolymer, and at this time, 5 parts by weight of the copolymer was used based on 100 parts by weight of the activated carbon.
상기 표면처리된 활성탄을 사용한 것을 제외하고는 실시예 1과 동일한 방법으로 산소발생 조성물을 제조하였다. An oxygen generating composition was prepared in the same manner as in Example 1, except that the surface-treated activated carbon was used.
(실시예 4)(Example 4)
3-메타크릴록시프로필트리메톡시실란 5중량부, 2-하이드록시에틸 아크릴레이트(HEA) 100중량부 및 2-하이드록시에틸 메타크릴레이트(HEMA) 30중량부를 혼합하고 반응시켜 공중합체를 제조하였다. 5 parts by weight of 3-methacryloxypropyltrimethoxysilane, 100 parts by weight of 2-hydroxyethyl acrylate (HEA), and 30 parts by weight of 2-hydroxyethyl methacrylate (HEMA) were mixed and reacted to prepare a copolymer. did
상기 공중합체 5중량부를 추가로 사용한 것을 제외하고는 실시예 1과 동일한 방법으로 산소발생 조성물을 제조하였다. An oxygen generating composition was prepared in the same manner as in Example 1, except that 5 parts by weight of the copolymer was additionally used.
(실시예 5)(Example 5)
3-메타크릴록시프로필트리메톡시실란 5중량부, 3-글리시독시프로필트리메톡시실란 100중량부, 비스페놀 A(BPA) 20중량부 및 2-하이드록시에틸 아크릴레이트(HEA) 30중량부를 혼합하고 반응시켜 올리고머를 제조하였다. 이때 상기 올리고머의 중량평균분자량은 30,000g/mol 이었다. 5 parts by weight of 3-methacryloxypropyltrimethoxysilane, 100 parts by weight of 3-glycidoxypropyltrimethoxysilane, 20 parts by weight of bisphenol A (BPA) and 30 parts by weight of 2-hydroxyethyl acrylate (HEA) Oligomers were prepared by mixing and reacting. At this time, the weight average molecular weight of the oligomer was 30,000 g/mol.
상기 올리고머 5중량부를 추가로 사용한 것을 제외하고는 실시예 1과 동일한 방법으로 산소발생 조성물을 제조하였다. An oxygen generating composition was prepared in the same manner as in Example 1, except that 5 parts by weight of the oligomer was additionally used.
(비교예 1)(Comparative Example 1)
왕겨를 100℃에서 900℃까지 5℃/min의 속도로 승온하고, 900℃에서 1시간 유지하여 왕겨를 탄화하였다. 이때 질소를 50㎖/min 로 주입하면서, 수증기를 0.3㎖/h 로 주입하였다. The rice hull was heated from 100 ° C to 900 ° C at a rate of 5 ° C / min, and maintained at 900 ° C for 1 hour to carbonize the rice hull. At this time, water vapor was injected at 0.3 ml/h while nitrogen was injected at 50 ml/min.
상기 탄화물을 냉각한 후 분쇄하여 활성탄을 제조하였다. Activated carbon was prepared by cooling the carbide and then pulverizing it.
상기 활성탄을 사용한 것을 제외하고는 실시예 1과 동일한 방법으로 산소발생 조성물을 제조하였다. An oxygen generating composition was prepared in the same manner as in Example 1, except that the activated carbon was used.
(비교예 2)(Comparative Example 2)
활성탄을 사용하지 않은 것을 제외하고는 실시예 1과 동일한 방법으로 산소발생 조성물을 제조하였다. An oxygen generating composition was prepared in the same manner as in Example 1, except that activated carbon was not used.
상기 실시예 및 비교예로부터 제조된 조성물을 압축 성형하여 육면체 형상의 성형체를 제조하였다. A molded body having a hexahedral shape was prepared by compression molding the compositions prepared in Examples and Comparative Examples.
하천수가 담긴 용기에 상기 성형체를 투입하였으며, 성형체를 투입한 1개월 후의 하천수의 탁도, BOD, COD, 총질소량 및 총인량을 측정하여 그 결과를 아래의 표 1에 나타내었다. The molded body was put into a container containing river water, and turbidity, BOD, COD, total nitrogen and total phosphorus of the river water were measured one month after the molded body was added, and the results are shown in Table 1 below.
(NTU)turbidity
(NTU)
(mg/L)BOD
(mg/L)
(mg/L)COD
(mg/L)
(mg/L)Total Nitrogen (TN)
(mg/L)
(mg/L)total phosphorus (TP)
(mg/L)
상기 표 1의 결과로부터, 실시예 1 내지 5는 산소배출특성 및 수질개선효과가 우수하며, 특히 실시예 2 내지 5는 상기 특성이 가장 우수하다. From the results of Table 1, Examples 1 to 5 are excellent in oxygen emission characteristics and water quality improvement effects, and in particular, Examples 2 to 5 are the most excellent in the above characteristics.
반면 비교예 1 및 2는 상기 특성이 실시예에 비하여 열등함을 알 수 있다. On the other hand, it can be seen that Comparative Examples 1 and 2 are inferior to those of Examples.
Claims (5)
상기 성형체는 시멘트 100중량부에 대하여 모래 70~120중량부, 활성탄 5~30중량부, 황토 5~20중량부, 상기 올리고머 1~10중량부 및 물 1~20중량부를 포함하고,
상기 활성탄은
(a) 왕겨를 탄화하여 1차 탄화물을 제조하는 1차 탄화단계;
(b) 상기 1차 탄화물을 탄화하여 2차 탄화물을 제조하는 2차 탄화단계;
(c) 상기 2차 탄화물을 탄화하여 3차 탄화물을 제조하는 3차 탄화단계; 및
(d) 상기 3차 탄화물을 분쇄하는 단계를 포함하는 방법에 의하여 제조되는 것을 특징으로 하는 수질개선용 성형체.
cement; sand; activated carbon; ocher; A silane coupling agent oligomer prepared by reacting an acrylate group-containing silane coupling agent, an epoxy group-containing silane coupling agent, bisphenol A (BPA), and 2-hydroxyethyl acrylate (HEA); And in the molded body for water quality improvement containing water,
The molded body contains 70 to 120 parts by weight of sand, 5 to 30 parts by weight of activated carbon, 5 to 20 parts by weight of loess, 1 to 10 parts by weight of the oligomer, and 1 to 20 parts by weight of water, based on 100 parts by weight of cement.
The activated carbon
(a) a first carbonization step of carbonizing rice hull to produce a first carbonized material;
(b) a secondary carbonization step of carbonizing the primary carbide to produce a secondary carbide;
(c) a tertiary carbonization step of carbonizing the secondary carbide to produce a tertiary carbide; and
(d) a molded body for water quality improvement characterized in that it is manufactured by a method comprising the step of grinding the tertiary carbide.
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KR20030002222A (en) * | 2001-06-30 | 2003-01-08 | 한국지질자원연구원 | Porous mineral media for wastewater treatment and manufacturing process of the same |
KR20030042250A (en) * | 2001-11-22 | 2003-05-28 | 이용교 | concrete structure |
KR20050025337A (en) * | 2002-07-26 | 2005-03-14 | 킴벌리-클라크 월드와이드, 인크. | Fluid storage material including particles secured with a crosslinkable binder composition |
KR101261365B1 (en) * | 2012-10-05 | 2013-05-06 | 김남순 | Solid support for forwastewater treatment |
KR101661516B1 (en) * | 2016-07-11 | 2016-09-30 | 필터로직 주식회사 | A complex filter and a method manufacturing the same |
KR20180085334A (en) | 2017-01-18 | 2018-07-26 | 김문배 | Oxygen generating composition |
KR20220081037A (en) | 2020-12-08 | 2022-06-15 | 캠아이티(주) | Oxygen generating composition and method for preparing the same |
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