KR20230151496A - Kit and Method for sustained production of Chlorine dioxide gas - Google Patents
Kit and Method for sustained production of Chlorine dioxide gas Download PDFInfo
- Publication number
- KR20230151496A KR20230151496A KR1020230054371A KR20230054371A KR20230151496A KR 20230151496 A KR20230151496 A KR 20230151496A KR 1020230054371 A KR1020230054371 A KR 1020230054371A KR 20230054371 A KR20230054371 A KR 20230054371A KR 20230151496 A KR20230151496 A KR 20230151496A
- Authority
- KR
- South Korea
- Prior art keywords
- acid
- chlorine dioxide
- dioxide gas
- sustained
- chlorite
- Prior art date
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- 239000004155 Chlorine dioxide Substances 0.000 title claims abstract description 113
- 235000019398 chlorine dioxide Nutrition 0.000 title claims abstract description 113
- 238000000034 method Methods 0.000 title claims abstract description 26
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- LDXJRKWFNNFDSA-UHFFFAOYSA-N 2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]ethanone Chemical compound C1CN(CC2=NNN=C21)CC(=O)N3CCN(CC3)C4=CN=C(N=C4)NCC5=CC(=CC=C5)OC(F)(F)F LDXJRKWFNNFDSA-UHFFFAOYSA-N 0.000 description 1
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- 241000193738 Bacillus anthracis Species 0.000 description 1
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- QDHHCQZDFGDHMP-UHFFFAOYSA-N Chloramine Chemical compound ClN QDHHCQZDFGDHMP-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 239000005761 Dimethomorph Substances 0.000 description 1
- PDQAZBWRQCGBEV-UHFFFAOYSA-N Ethylenethiourea Chemical compound S=C1NCCN1 PDQAZBWRQCGBEV-UHFFFAOYSA-N 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 229920002581 Glucomannan Polymers 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000005802 Mancozeb Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- WINXNKPZLFISPD-UHFFFAOYSA-M Saccharin sodium Chemical compound [Na+].C1=CC=C2C(=O)[N-]S(=O)(=O)C2=C1 WINXNKPZLFISPD-UHFFFAOYSA-M 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 208000024780 Urticaria Diseases 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- WFDXOXNFNRHQEC-GHRIWEEISA-N azoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC(OC=2C(=CC=CC=2)C#N)=NC=N1 WFDXOXNFNRHQEC-GHRIWEEISA-N 0.000 description 1
- SXDBWCPKPHAZSM-UHFFFAOYSA-M bromate Inorganic materials [O-]Br(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-M 0.000 description 1
- SXDBWCPKPHAZSM-UHFFFAOYSA-N bromic acid Chemical compound OBr(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 230000000711 cancerogenic effect Effects 0.000 description 1
- 239000000828 canola oil Substances 0.000 description 1
- 235000019519 canola oil Nutrition 0.000 description 1
- 229920003123 carboxymethyl cellulose sodium Polymers 0.000 description 1
- 229940105329 carboxymethylcellulose Drugs 0.000 description 1
- 229940063834 carboxymethylcellulose sodium Drugs 0.000 description 1
- 231100000357 carcinogen Toxicity 0.000 description 1
- 239000003183 carcinogenic agent Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000002781 deodorant agent Substances 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 231100000676 disease causative agent Toxicity 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 239000003651 drinking water Substances 0.000 description 1
- 235000020188 drinking water Nutrition 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 235000013373 food additive Nutrition 0.000 description 1
- 239000002778 food additive Substances 0.000 description 1
- 244000053095 fungal pathogen Species 0.000 description 1
- 229940046240 glucomannan Drugs 0.000 description 1
- 229960001031 glucose Drugs 0.000 description 1
- 235000001727 glucose Nutrition 0.000 description 1
- 159000000011 group IA salts Chemical class 0.000 description 1
- 229940093915 gynecological organic acid Drugs 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 235000012907 honey Nutrition 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical compound ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- ICIWUVCWSCSTAQ-UHFFFAOYSA-M iodate Chemical compound [O-]I(=O)=O ICIWUVCWSCSTAQ-UHFFFAOYSA-M 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 244000144972 livestock Species 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- NNKVPIKMPCQWCG-UHFFFAOYSA-N methamidophos Chemical compound COP(N)(=O)SC NNKVPIKMPCQWCG-UHFFFAOYSA-N 0.000 description 1
- LPUQAYUQRXPFSQ-DFWYDOINSA-M monosodium L-glutamate Chemical compound [Na+].[O-]C(=O)[C@@H](N)CCC(O)=O LPUQAYUQRXPFSQ-DFWYDOINSA-M 0.000 description 1
- 239000004223 monosodium glutamate Substances 0.000 description 1
- 235000013923 monosodium glutamate Nutrition 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 229920001542 oligosaccharide Polymers 0.000 description 1
- 150000002482 oligosaccharides Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 230000010152 pollination Effects 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000036632 reaction speed Effects 0.000 description 1
- 239000003340 retarding agent Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
- 229940032147 starch Drugs 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229960004793 sucrose Drugs 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B11/00—Oxides or oxyacids of halogens; Salts thereof
- C01B11/02—Oxides of chlorine
- C01B11/022—Chlorine dioxide (ClO2)
- C01B11/023—Preparation from chlorites or chlorates
- C01B11/024—Preparation from chlorites or chlorates from chlorites
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01K—ANIMAL HUSBANDRY; CARE OF BIRDS, FISHES, INSECTS; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
- A01K51/00—Appliances for treating beehives or parts thereof, e.g. for cleaning or disinfecting
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
- A61L2/16—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor using chemical substances
- A61L2/20—Gaseous substances, e.g. vapours
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2101/00—Chemical composition of materials used in disinfecting, sterilising or deodorising
- A61L2101/02—Inorganic materials
- A61L2101/06—Inorganic materials containing halogen
- A61L2101/08—Elemental halogen
Abstract
본 발명은 위험한 고농도 가스 발생없이 장기간에 걸쳐 서방형으로 이산화염소 가스를 발생하기 위한 발생 방법에 관한 것이다. 본 발명의 서방형 이산화염소 가스 발생 방법을 이용하는 경우 꿀벌 군집의 감염관리를 위해 꿀벌의 손상 없는 저농도로 이산화염소 가스를 생산할 수 있어 봉군의 교체시까지 장기간 소독의 목적을 달성할 수 있다.The present invention relates to a generation method for generating chlorine dioxide gas in a sustained manner over a long period of time without generating dangerously high concentrations of gas. When using the sustained-release chlorine dioxide gas generation method of the present invention, chlorine dioxide gas can be produced at a low concentration without damaging the bees for infection control of the bee colony, thereby achieving the purpose of long-term disinfection until the colony is replaced.
Description
본 발명은 이산화염소 가스를 수개월간 서방형으로 발생하기 위한 발생 키트 및 방법에 관한 것이다.The present invention relates to a generation kit and method for generating chlorine dioxide gas in a sustained manner for several months.
종래 아염소산 나트륨을 포함하는 수용액이나, 겔제에 자외선을 조사하면 이산화염소가 발생된다는 점은 잘 알려져 있었다(특허문헌 1). 그러나 순수한 물에 아염소산 나트륨을 용해시킨 수용액에 자외선을 조사하면 반응이 너무 느리고 이산화염소의 생산량이 적어 소독 또는 멸균이 가능할 정도의 농도로 이산화염소를 발생시킬 수는 없었다. 또한, 아염소산 나트륨과 구연산 등의 산을 접촉시키면 이산화염소가 생성된다는 점도 잘 알려져 있었으나(특허문헌 2), 아염소산 나트륨과 구연산을 접촉시키는 방법은 한번 반응이 시작되면 중단할 수 없고, 구연산 대신 황산이나 염산을 사용할 경우에는 위험하고, 자칫 반응이 과도하게 진행되어 폭발의 위험이 있다. 따라서, 안전하게 저농도로 이산화염소 가스를 생산 방법이 필요하였다. Conventionally, it was well known that chlorine dioxide is generated when an aqueous solution or gel containing sodium chlorite is irradiated with ultraviolet rays (Patent Document 1). However, when an aqueous solution of sodium chlorite dissolved in pure water was irradiated with ultraviolet rays, the reaction was too slow and the production of chlorine dioxide was low, so chlorine dioxide could not be generated at a concentration sufficient to enable disinfection or sterilization. In addition, it was well known that chlorine dioxide is generated when sodium chlorite is brought into contact with an acid such as citric acid (Patent Document 2), but the method of contacting sodium chlorite with citric acid cannot be stopped once the reaction begins, and citric acid is used instead of citric acid. Using sulfuric acid or hydrochloric acid is dangerous, and there is a risk of explosion if the reaction progresses excessively. Therefore, a method for safely producing chlorine dioxide gas at low concentration was needed.
꿀벌은 잘 알려진 바와 같이 식물의 수분작용에 중요한 역할을 수행하므로, 생태계의 유지에 매우 중요한 역할을 한다. 그러나 꿀벌은 진균, 세균, 바이러스 등 다양한 원인체에 의한 질병에 매우 취약하고, 농작물의 생산성 향상 목적의 방제용 농약, 살충제 등의 화학물질이 오히려 꿀벌에 작용하여 꿀벌의 군집에 큰 피해를 입히는 경우가 빈번하게 발생한다. 특히 최근에는 꿀벌의 봉군 붕괴 이상(colony collapse disorder, CCD)이라는 현상이 미국, 캐나다, 유럽, 남미 지역 및 아시아 등지에서 나타나고 있으며, 이러한 봉군 붕괴 이상은 명확한 원인은 밝혀지지 않았으나, 꿀벌에 만연하는 각종 질병과 해충, 세균 및 바이러스 병원체의 등장이 복합적으로 작용하여 나타나는 것으로 알려졌다. 따라서, 꿀벌 자체에는 해가 없으면서도 꿀에 잔류하지 않고 소독 효과가 우수한 소독제 개발이 필요하다. As is well known, bees play an important role in the pollination of plants and thus play a very important role in maintaining the ecosystem. However, bees are very vulnerable to diseases caused by various pathogens such as fungi, bacteria, and viruses, and there are cases where chemicals such as pesticides and insecticides used for control purposes to improve crop productivity actually act on bees and cause great damage to bee colonies. Occurs frequently. In particular, recently, a phenomenon called colony collapse disorder (CCD) in honey bees has been appearing in the United States, Canada, Europe, South America, and Asia. Although the cause of this colony collapse disorder has not been clearly identified, various diseases that are prevalent in honey bees are occurring. It is known that the emergence of diseases, pests, bacteria, and viral pathogens occurs in a complex manner. Therefore, there is a need to develop a disinfectant that is not harmful to the bees themselves and has excellent disinfection effects without remaining in honey.
대한민국 특허 제10-1315260호(특허문헌 3)는 이산화염소 기체를 이용한 낭충봉아부패병 등의 전염성 질병의 예방 및 치료를 위한 소독장치를 개시하고 있다. 이산화염소는 10% 이상의 농도에서 폭발하여 보관이나 운반이 불가하므로, 상기 특허는 알칼리성 염과 반응시켜 안정화시킨 안정화 이산화염소를 자외선과 반응시키면 안전하게 이산화염소 기체가 발생되고 소독 효과가 우수함을 개시한 바 있다. 그러나 상기 장치는 전기 장치를 포함하므로 관리에 어려움이 있어 상업화에 실패하였다. Republic of Korea Patent No. 10-1315260 (Patent Document 3) discloses a disinfection device for preventing and treating infectious diseases such as cystic bud rot using chlorine dioxide gas. Since chlorine dioxide explodes at a concentration of 10% or more and cannot be stored or transported, the above patent discloses that when stabilized chlorine dioxide, which has been stabilized by reacting with an alkaline salt, is reacted with ultraviolet rays, chlorine dioxide gas is safely generated and the disinfection effect is excellent. there is. However, since the above device includes an electrical device, it is difficult to manage and has failed to be commercialized.
또한, 종래 아염소산 수용액에 구연산을 첨가하는 방법은 매우 폭발적으로 이산화염소 발생이 일어나나, 수용액 내에 이산화염소가 용해되어 생성된 가스가 서서히 방출되면서 가스 발생량이 줄어들어 최장 2주 정도면 가스 발생이 종료되어 버리는 문제가 있었다(도 4 참조). In addition, the conventional method of adding citric acid to an aqueous chlorous acid solution generates chlorine dioxide very explosively, but as the gas generated by dissolving chlorine dioxide in the aqueous solution is gradually released, the amount of gas generation decreases, and the gas generation ends in about two weeks at most. There was a problem that the problem occurred (see Figure 4).
따라서 전기 장치를 포함하지 않으면서도 저농도에서 장기간 안정적으로 이산화염소 기체를 발생시킬 수 있는 방법 및 키트의 개발이 필요한 실정이다. Therefore, there is a need to develop a method and kit that can stably generate chlorine dioxide gas at low concentration for a long period of time without including an electric device.
상술한 바와 같이, 꿀벌의 전염성 질환을 예방 또는 치료하기 위한 안전하고 장기적으로 사용이 용이한 소독방법의 개발이 필요한 실정이다. 특히 꿀벌은 다른 가축과는 다르게 감염병 발생시 이환된 꿀벌만을 격리하는 것이 불가능하고, 감염된 꿀벌에서 원인체 전부를 제거하는 것이 불가하므로, 꿀벌 집단의 감염관리를 위해서는 꿀벌 집단 전부에 대한 소독이 가능한 환경을 조성하고 상기 환경을 벌의 평균 수명인 60일 이상 지속해 주어 병원체에 의해 감염되지 않은 봉군으로 세대교체가 될 수 있도록 유도할 필요가 있다. As described above, there is a need to develop a disinfection method that is safe and easy to use over a long period of time to prevent or treat infectious diseases in bees. In particular, unlike other livestock, it is impossible to isolate only infected bees when an infectious disease occurs in honey bees, and it is impossible to remove all causative agents from infected bees. Therefore, in order to control infection in the bee population, an environment in which the entire bee population can be disinfected must be created. It is necessary to maintain the above environment for more than 60 days, which is the average lifespan of bees, to encourage generational replacement with bees that are not infected by pathogens.
따라서, 본 발명자들은 꿀벌의 군집 관리를 위하여 사용이 간편하면서도 안전하게 장기간 지속적으로 이산화염소 가스 생산이 가능한 방법 및 장치를 개발하고자 예의 연구 노력하였다. 그 결과 아염소산 나트륨을 포함하는 겔 조성물에 히드록시기(-OH group)를 포함하는 유기물, 및 유기산을 첨가할 경우 이산화염소가 낮은 농도로 장기간 생성되는 것을 확인하고, 본 발명을 완성하게 되었다. Therefore, the present inventors made extensive research efforts to develop a method and device that is easy to use and can safely produce chlorine dioxide gas continuously for a long period of time for honey bee colony management. As a result, it was confirmed that chlorine dioxide was generated at a low concentration for a long period of time when an organic material containing a hydroxy group (-OH group) and an organic acid were added to a gel composition containing sodium chlorite, and the present invention was completed.
따라서, 본 발명의 목적은 (a) 아염소산염, (b) 당류, (c) 겔화제 또는 점증제, 및 (d) 산을 포함하는 서방성 이산화염소 가스 발생 키트를 제공하는 것이다.Accordingly, an object of the present invention is to provide a sustained-release chlorine dioxide gas generation kit comprising (a) chlorite, (b) saccharide, (c) gelling agent or thickening agent, and (d) acid.
본 발명의 다른 목적은 a) 아염소산염을 포함하는 용기에 b) 당류, 및 산을 포함하는 분말제를 첨가하는 단계를 포함하는 이산화염소 가스의 지연 발생방법을 제공하는 것이다. Another object of the present invention is to provide a method for delayed generation of chlorine dioxide gas, which includes the steps of a) adding a powder containing saccharide and acid to a container containing chlorite and b) adding a powder containing saccharide and acid.
본 발명의 일 양태에 따르면, 본 발명은 다음을 포함하는 이산화염소 가스 발생 키트를 제공한다:According to one aspect of the present invention, the present invention provides a chlorine dioxide gas generation kit comprising:
(a) 아염소산염, (b) 당류, (c) 겔화제 또는 점증제, 및 (d) 산.(a) chlorite, (b) sugar, (c) gelling or thickening agent, and (d) acid.
본 발명의 상기 아염소산염은 당류와 반응하여 이산화염소 가스를 장기간 꾸준히 발생시키는 특징이 있다. 상기 당류의 종류는 하기 표 1에 나열된 것일 수 있으나, 이에 한정되는 것은 아니다. 그러나, 상기 제1제와 제2제의 반응은 반응의 시작시간을 특정할 수 없다는 문제가 있다. 또한, 교반을 시킬 경우에는 폭발할 위험성이 있다. The chlorite of the present invention has the characteristic of continuously generating chlorine dioxide gas for a long period of time by reacting with sugars. The types of sugars may be those listed in Table 1 below, but are not limited thereto. However, the reaction between the first and second agents has a problem in that the start time of the reaction cannot be specified. Additionally, there is a risk of explosion if stirred.
이에 본 발명자들은 키트에 산을 포함시켜, 아염소산염과 빠르게 반응을 시작할 수 있도록 하였다. 그 결과, 산과 아염소산염의 반응에 의해 이산화염소 가스가 신속하게 생성되었고, 이산화염소 가스는 다시 아염소산염과 당류와의 반응을 촉진하였다. 이에 따라 산은 아염소산염과 신속히 반응하여 이산화염소 가스 발생 반응의 시점을 통제할 수 있고, 상기 겔화제 또는 점증제로는 이산화염소의 발생을 지연시켜 장기간 서방형으로 이산화염소 가스를 발생시킬 수 있다는 특징이 있다.Accordingly, the present inventors included acid in the kit to quickly initiate a reaction with chlorite. As a result, chlorine dioxide gas was quickly generated by the reaction between acid and chlorite, and chlorine dioxide gas further promoted the reaction between chlorite and sugars. Accordingly, the acid reacts quickly with chlorite to control the timing of the chlorine dioxide gas generation reaction, and the gelling agent or thickener delays the generation of chlorine dioxide and can generate chlorine dioxide gas in a sustained manner for a long period of time. there is.
본 발명의 일 구현예에 있어서, 상기 아염소산염은 아염소산 나트륨, 아염소산 칼륨, 아염소산 리튬, 아염소산 칼슘, 아염소산 마그네슘, 및 아염소산 바륨으로 이루어진 군으로부터 선택되는 1종 이상의 것이나, 이에 한정되는 것은 아니다.In one embodiment of the present invention, the chlorite is one or more selected from the group consisting of sodium chlorite, potassium chlorite, lithium chlorite, calcium chlorite, magnesium chlorite, and barium chlorite, but is limited thereto. It doesn't work.
본 발명의 일 구현예에 있어서, 상기 아염소산염은 1 내지 15%, 1 내지 10%, 1 내지 9%, 1 내지 8%, 1 내지 7%, 1 내지 6%, 1 내지 5%, 2 내지 15%, 2 내지 10%, 2 내지 9%, 2 내지 8%, 2 내지 7%, 2 내지 6%, 2 내지 5%, 3 내지 15%, 3 내지 10%, 3 내지 9%, 3 내지 8%, 3 내지 7%, 3 내지 6%, 3 내지 5%, 4 내지 15%, 4 내지 10%, 4 내지 9%, 4 내지 8%, 4 내지 7%, 4 내지 6%, 4 내지 5%, 5 내지 15%, 5 내지 10%, 5 내지 9%, 5 내지 8%, 5 내지 7%, 또는 5 내지 6%의 중량으로 포함될 수 있으나, 이에 한정되는 것은 아니다.In one embodiment of the present invention, the chlorite is 1 to 15%, 1 to 10%, 1 to 9%, 1 to 8%, 1 to 7%, 1 to 6%, 1 to 5%, 2 to 2%. 15%, 2 to 10%, 2 to 9%, 2 to 8%, 2 to 7%, 2 to 6%, 2 to 5%, 3 to 15%, 3 to 10%, 3 to 9%, 3 to 8%, 3 to 7%, 3 to 6%, 3 to 5%, 4 to 15%, 4 to 10%, 4 to 9%, 4 to 8%, 4 to 7%, 4 to 6%, 4 to It may be included in an amount of 5%, 5 to 15%, 5 to 10%, 5 to 9%, 5 to 8%, 5 to 7%, or 5 to 6% by weight, but is not limited thereto.
본 발명의 일 구현예에 있어서, 상기 아염소산염은 이산화염소 가스의 전구물질이다.In one embodiment of the present invention, the chlorite is a precursor of chlorine dioxide gas.
본 발명의 상기 아염소산염을 포함하는 제제는 수용액 형태로 제공될 수 있고, 또는 겔의 형태로 제공될 수 있다. The formulation containing the chlorite of the present invention may be provided in the form of an aqueous solution, or may be provided in the form of a gel.
본 발명의 일 구현예에 있어서, 상기 당류는 단당류, 이당류, 당 알코올, 또는 이들의 조합일 수 있다.In one embodiment of the present invention, the saccharide may be a monosaccharide, a disaccharide, a sugar alcohol, or a combination thereof.
본 발명의 일 구현예에 있어서, 상기 단당류는 포도당, 과당, 갈락토오스 또는 이들의 조합일 수 있다.In one embodiment of the present invention, the monosaccharide may be glucose, fructose, galactose, or a combination thereof.
본 발명의 일 구현예에 있어서, 상기 단당류는 0.05 내지 5%, 0.05 내지 4%, 0.05 내지 3.5%, 0.05 내지 3%, 0.05 내지 2.5%, 0.05 내지 2%, 0.05 내지 1.5%, 0.05 내지 1%, 0.05 내지 0.9%, 0.05 내지 0.8%, 0.05 내지 0.7%, 0.05 내지 0.6%, 0.05 내지 0.5%, 0.05 내지 0.4%, 0.05 내지 0.35%, 0.05 내지 0.3%, 0.05 내지 0.25%, 0.05 내지 0.2%, 0.1 내지 5%, 0.1 내지 4%, 0.1 내지 3.5%, 0.1 내지 3%, 0.1 내지 2.5%, 0.1 내지 2%, 0.1 내지 1.5%, 0.1 내지 1%, 0.1 내지 0.9%, 0.1 내지 0.8%, 0.1 내지 0.7%, 0.1 내지 0.6%, 0.1 내지 0.5%, 0.1 내지 0.4%, 0.1 내지 0.35%, 0.1 내지 0.3%, 0.1 내지 0.25%, 또는 0.1 내지 0.2%의 중량으로 포함될 수 있으나, 이에 한정되는 것은 아니다. In one embodiment of the present invention, the monosaccharide is 0.05 to 5%, 0.05 to 4%, 0.05 to 3.5%, 0.05 to 3%, 0.05 to 2.5%, 0.05 to 2%, 0.05 to 1.5%, 0.05 to 1%. %, 0.05 to 0.9%, 0.05 to 0.8%, 0.05 to 0.7%, 0.05 to 0.6%, 0.05 to 0.5%, 0.05 to 0.4%, 0.05 to 0.35%, 0.05 to 0.3%, 0.05 to 0.25%, 0.05 to 0. 2 %, 0.1 to 5%, 0.1 to 4%, 0.1 to 3.5%, 0.1 to 3%, 0.1 to 2.5%, 0.1 to 2%, 0.1 to 1.5%, 0.1 to 1%, 0.1 to 0.9%, 0.1 to 0.8 %, 0.1 to 0.7%, 0.1 to 0.6%, 0.1 to 0.5%, 0.1 to 0.4%, 0.1 to 0.35%, 0.1 to 0.3%, 0.1 to 0.25%, or 0.1 to 0.2% by weight. It is not limited.
본 발명의 일 구현예에 있어서, 상기 이당류는 수크로스, 말토오스, 트레할로스, 락토오스, 또는 이들의 조합일 수 있다. In one embodiment of the present invention, the disaccharide may be sucrose, maltose, trehalose, lactose, or a combination thereof.
본 발명의 일 구현예에 있어서, 상기 이당류는 1 내지 10%, 1 내지 9%, 1 내지 8%, 1 내지 7%, 1 내지 6%, 1 내지 5%, 1 내지 4%, 2 내지 10%, 2 내지 9%, 2 내지 8%, 2 내지 7%, 2 내지 6%, 2 내지 5%, 2 내지 4%, 3 내지 10%, 3 내지 9%, 3 내지 8%, 3 내지 7%, 3 내지 6%, 3 내지 5%, 또는 3 내지 4%의 중량으로 포함될 수 있으나, 이에 한정되는 것은 아니다.In one embodiment of the present invention, the disaccharide is 1 to 10%, 1 to 9%, 1 to 8%, 1 to 7%, 1 to 6%, 1 to 5%, 1 to 4%, 2 to 10%. %, 2 to 9%, 2 to 8%, 2 to 7%, 2 to 6%, 2 to 5%, 2 to 4%, 3 to 10%, 3 to 9%, 3 to 8%, 3 to 7 %, 3 to 6%, 3 to 5%, or 3 to 4% by weight, but is not limited thereto.
본 발명의 일 구현예에 있어서, 상기 이당류는 아염소산이 단당류와 초기에 반응한 이후에 주된 반응을 이끄는 주반응제이다.In one embodiment of the present invention, the disaccharide is the main reactant that drives the main reaction after chlorous acid initially reacts with the monosaccharide.
본 발명의 일 구현예에 있어서, 상기 당 알코올은 에틸렌글리콜, 글리세롤, 에리스리톨, 솔비톨, 만니톨, 자일리톨, 이노시톨, 또는 이들의 조합일 수 있다.In one embodiment of the present invention, the sugar alcohol may be ethylene glycol, glycerol, erythritol, sorbitol, mannitol, xylitol, inositol, or a combination thereof.
본 발명의 구체적인 구현예에 있어서, 상기 당 알코올은 1 내지 10%, 1 내지 9%, 1 내지 8%, 1 내지 7%, 1 내지 6%, 1 내지 5%, 1 내지 4%, 2 내지 10%, 2 내지 9%, 2 내지 8%, 2 내지 7%, 2 내지 6%, 2 내지 5%, 2 내지 4%, 3 내지 10%, 3 내지 9%, 3 내지 8%, 3 내지 7%, 3 내지 6%, 3 내지 5%, 또는 3 내지 4%의 중량으로 포함될 수 있으나, 이에 한정되는 것은 아니다.In specific embodiments of the present invention, the sugar alcohol is 1 to 10%, 1 to 9%, 1 to 8%, 1 to 7%, 1 to 6%, 1 to 5%, 1 to 4%, 2 to 2%. 10%, 2 to 9%, 2 to 8%, 2 to 7%, 2 to 6%, 2 to 5%, 2 to 4%, 3 to 10%, 3 to 9%, 3 to 8%, 3 to It may be included in an amount of 7%, 3 to 6%, 3 to 5%, or 3 to 4% by weight, but is not limited thereto.
본 발명의 일 구현예에 있어서, 상기 당알코올은 아염소산염이 단당류와 초기에 반응한 이후에 주된 반응을 이끄는 주반응제이다.In one embodiment of the present invention, the sugar alcohol is the main reactant that leads the main reaction after the chlorite is initially reacted with the monosaccharide.
본 발명의 일 구현예에 있어서, 상기 겔화제 또는 점증제는 한천, 곤약분말, 카라기난, 펙틴, 젤라틴, 전분, 로커스트콩검, 타라검, 구아검, 젤란검, 잔탄검, 타마린드검, 아라비아검, 셀룰로오스검, 카제인나트륨, 알긴산나트륨, 덱스트란, 덱스트린, 카르복시메틸셀룰로오스, 또는 이들의 조합을 포함할 수 있다.In one embodiment of the present invention, the gelling agent or thickening agent is agar, konjac powder, carrageenan, pectin, gelatin, starch, locust bean gum, tara gum, guar gum, gellan gum, xanthan gum, tamarind gum, gum Arabic. , cellulose gum, sodium caseinate, sodium alginate, dextran, dextrin, carboxymethylcellulose, or a combination thereof.
본 발명의 구체적인 구현예에 있어서, 상기 겔화제 또는 점증제는 1 내지 10%, 1 내지 9%, 1 내지 8%, 1 내지 7%, 1 내지 6%, 1 내지 5.5%, 1 내지 5%, 1 내지 4%, 1 내지 3%, 1 내지 2%, 1 내지 1.5%, 1.1 내지 10%, 1.1 내지 9%, 1.1 내지 8%, 1.1 내지 7%, 1.1 내지 6%, 1.1 내지 5.5%, 1.1 내지 5%, 1.1 내지 4%, 1.1 내지 3%, 1.1 내지 2%, 1.1 내지 1.5%, 1.2 내지 10%, 1.2 내지 9%, 1.2 내지 8%, 1.2 내지 7%, 1.2 내지 6%, 1.2 내지 5.5%, 1.2 내지 5%, 1.2 내지 4%, 1.2 내지 3%, 1.2 내지 2%, 1.2 내지 1.5%, 1.3 내지 10%, 1.3 내지 9%, 1.3 내지 8%, 1.3 내지 7%, 1.3 내지 6%, 1.3 내지 5.5%, 1.3 내지 5%, 1.3 내지 4%, 1.3 내지 3%, 1.3 내지 2%, 1.3 내지 1.5%, 1.5 내지 10%, 1.5 내지 9%, 1.5 내지 8%, 1.5 내지 7%, 1.5 내지 6%, 1.5 내지 5.5%, 1.5 내지 5%, 1.5 내지 4%, 1.5 내지 3%, 1.5 내지 2%, 2 내지 10%, 2 내지 9%, 2 내지 8%, 2 내지 7%, 2 내지 6%, 2 내지 5.5%, 2 내지 5%, 2 내지 4%, 2 내지 3%, 3 내지 10%, 3 내지 9%, 3 내지 8%, 3 내지 7%, 3 내지 6%, 3 내지 5.5%, 3 내지 5%, 3 내지 4%, 4 내지 10%, 4 내지 9%, 4 내지 8%, 4 내지 7%, 4 내지 6%, 4 내지 5.5%, 4 내지 5%, 5.5 내지 10%, 5.5 내지 9%, 5.5 내지 8%, 5.5 내지 7%, 또는 5.5 내지 6%, 5 내지 10%, 5 내지 9%, 5 내지 8%, 5 내지 7%, 5 내지 6%, 또는 5 내지 5.5%의 중량으로 포함될 수 있으나, 이에 한정되는 것은 아니다. In specific embodiments of the present invention, the gelling agent or thickening agent is 1 to 10%, 1 to 9%, 1 to 8%, 1 to 7%, 1 to 6%, 1 to 5.5%, 1 to 5%. , 1 to 4%, 1 to 3%, 1 to 2%, 1 to 1.5%, 1.1 to 10%, 1.1 to 9%, 1.1 to 8%, 1.1 to 7%, 1.1 to 6%, 1.1 to 5.5% , 1.1 to 5%, 1.1 to 4%, 1.1 to 3%, 1.1 to 2%, 1.1 to 1.5%, 1.2 to 10%, 1.2 to 9%, 1.2 to 8%, 1.2 to 7%, 1.2 to 6% , 1.2 to 5.5%, 1.2 to 5%, 1.2 to 4%, 1.2 to 3%, 1.2 to 2%, 1.2 to 1.5%, 1.3 to 10%, 1.3 to 9%, 1.3 to 8%, 1.3 to 7% , 1.3 to 6%, 1.3 to 5.5%, 1.3 to 5%, 1.3 to 4%, 1.3 to 3%, 1.3 to 2%, 1.3 to 1.5%, 1.5 to 10%, 1.5 to 9%, 1.5 to 8% , 1.5 to 7%, 1.5 to 6%, 1.5 to 5.5%, 1.5 to 5%, 1.5 to 4%, 1.5 to 3%, 1.5 to 2%, 2 to 10%, 2 to 9%, 2 to 8% , 2 to 7%, 2 to 6%, 2 to 5.5%, 2 to 5%, 2 to 4%, 2 to 3%, 3 to 10%, 3 to 9%, 3 to 8%, 3 to 7% , 3 to 6%, 3 to 5.5%, 3 to 5%, 3 to 4%, 4 to 10%, 4 to 9%, 4 to 8%, 4 to 7%, 4 to 6%, 4 to 5.5% , 4 to 5%, 5.5 to 10%, 5.5 to 9%, 5.5 to 8%, 5.5 to 7%, or 5.5 to 6%, 5 to 10%, 5 to 9%, 5 to 8%, 5 to 7 %, 5 to 6%, or 5 to 5.5% by weight, but is not limited thereto.
본 발명의 일 구현예에 있어서, 상기 겔화제 또는 점증제는 아염소산과의 반응을 지연시키는 지연반응제이다.In one embodiment of the present invention, the gelling agent or thickening agent is a retarding agent that delays the reaction with chlorous acid.
본 발명의 일 구현예에 있어서, 상기 키트는 겔화촉진제를 포함한다.In one embodiment of the present invention, the kit includes a gelation accelerator.
본 발명의 구체적인 구현예에 있어서, 상기 겔화촉진제는 염화마그네슘, 염화칼륨, 염화칼슘, 염화나트륨, 또는 이들의 조합이나, 이에 한정되는 것은 아니다.In a specific embodiment of the present invention, the gelation accelerator is magnesium chloride, potassium chloride, calcium chloride, sodium chloride, or a combination thereof, but is not limited thereto.
본 발명의 일 구현예에 있어서, 상기 산은 유기산, 무기산, 또는 이들의 혼합물이다.In one embodiment of the present invention, the acid is an organic acid, an inorganic acid, or a mixture thereof.
본 발명의 구체적인 구현예에 있어서, 상기 유기산은 젖산, 아세트산, 포름산, 구연산, 옥살산, 아스코르브산, 글루쿠론산, 말레산, 숙신산, 벤조산, 타르타르산, 푸마르산, 프로피온산, 글루탐산, 아스파르트산, 부티르산, 또는 이들의 조합을 포함하는 것이나, 이에 한정되는 것은 아니다. In a specific embodiment of the present invention, the organic acid is lactic acid, acetic acid, formic acid, citric acid, oxalic acid, ascorbic acid, glucuronic acid, maleic acid, succinic acid, benzoic acid, tartaric acid, fumaric acid, propionic acid, glutamic acid, aspartic acid, butyric acid, or It includes, but is not limited to, combinations of these.
본 발명의 구체적인 구현예에 있어서, 상기 무기산은 염산, 인산, 황산, 질산, 또는 이들의 조합을 포함하는 것이나, 이에 한정되는 것은 아니다.In a specific embodiment of the present invention, the inorganic acid includes hydrochloric acid, phosphoric acid, sulfuric acid, nitric acid, or a combination thereof, but is not limited thereto.
본 발명의 구체적인 구현예에 있어서, 상기 산은 0.001 내지 2%, 0.001 내지 1.5%, 0.001 내지 1%, 0.001 내지 0.5%, 0.001 내지 0.4%, 0.001 내지 0.3%, 0.001 내지 0.2%, 0.001 내지 0.1%, 0.005 내지 2%, 0.005 내지 1.5%, 0.005 내지 1%, 0.005 내지 0.5%, 0.005 내지 0.4%, 0.005 내지 0.3%, 0.005 내지 0.2%, 0.005 내지 0.1%, 0.01 내지 2%, 0.01 내지 1.5%, 0.01 내지 1%, 0.01 내지 0.5%, 0.01 내지 0.4%, 0.01 내지 0.3%, 0.01 내지 0.2%, 0.01 내지 0.1%, 0.05 내지 2%, 0.05 내지 1.5%, 0.05 내지 1%, 0.05 내지 0.5%, 0.05 내지 0.4%, 0.05 내지 0.3%, 0.05 내지 0.2%, 또는 0.05 내지 0.1%의 중량으로 포함될 수 있으나, 이에 한정되는 것은 아니다.In specific embodiments of the present invention, the acid is 0.001 to 2%, 0.001 to 1.5%, 0.001 to 1%, 0.001 to 0.5%, 0.001 to 0.4%, 0.001 to 0.3%, 0.001 to 0.2%, 0.001 to 0.1%. , 0.005 to 2%, 0.005 to 1.5%, 0.005 to 1%, 0.005 to 0.5%, 0.005 to 0.4%, 0.005 to 0.3%, 0.005 to 0.2%, 0.005 to 0.1%, 0.01 to 2%, 0.01 to 1.5 % , 0.01 to 1%, 0.01 to 0.5%, 0.01 to 0.4%, 0.01 to 0.3%, 0.01 to 0.2%, 0.01 to 0.1%, 0.05 to 2%, 0.05 to 1.5%, 0.05 to 1%, 0.05 to 0.5% , 0.05 to 0.4%, 0.05 to 0.3%, 0.05 to 0.2%, or 0.05 to 0.1% by weight, but is not limited thereto.
본 발명의 구체적인 구현예에 있어서, 상기 이산화염소 가스 발생키트는(a) 아염소산염, (b) 포도당 및 수크로스, (c) 한천, 전분 및 잔탄검, (d) 아스코르브산을 포함하는 것일 수 있다. In a specific embodiment of the present invention, the chlorine dioxide gas generation kit may include (a) chlorite, (b) glucose and sucrose, (c) agar, starch and xanthan gum, and (d) ascorbic acid. there is.
본 발명의 일 구현예에 있어서, 상기 키트는 물품의 소독용, 물품의 탈취용, 또는 식물의 농약 제거용이나, 이에 한정되는 것은 아니다.In one embodiment of the present invention, the kit is for disinfecting items, deodorizing items, or removing pesticides from plants, but is not limited thereto.
도 6에 나타낸 바와 같이, 상기 키트는 살아있는 벌통에 적용이 가능하며, 상기 키트의 주변에 벌이 밀집해 있어도 벌에 아무런 해를 끼치지 않는다.As shown in Figure 6, the kit can be applied to live beehives, and does not cause any harm to bees even if bees are crowded around the kit.
본 발명의 아염소산염을 포함하는 제제는 용기에 담긴 상태로 제공될 수 있다. The preparation containing chlorite of the present invention may be provided in a container.
본 발명의 일 구현예에 있어서, 상기 당류는 분말 형태로 제공된다. In one embodiment of the present invention, the saccharide is provided in powder form.
본 발명의 일 구현예에 있어서, 상기 겔화제 또는 점증제는 분말 또는 겔의 형태로 제공된다. In one embodiment of the present invention, the gelling agent or thickening agent is provided in the form of powder or gel.
본 발명의 일 구현예에 있어서, 상기 산은 분말 또는 액상의 형태로 제공된다.In one embodiment of the present invention, the acid is provided in powder or liquid form.
본 발명의 실시예에서 입증된 바와 같이, 본 발명의 이산화염소 발생 키트의 구성제제를 접촉하면 수시간 후부터 이산화염소 가스가 발생된다. As demonstrated in the examples of the present invention, chlorine dioxide gas is generated several hours after contact with the components of the chlorine dioxide generating kit of the present invention.
상기 이산화염소 가스의 농도는 초기 1 내지 3일간은 0.5 내지 1 ppm의 농도가 유지되고, 3일 이후에는 60일 이상 0.03 내지 0.05 ppm의 농도를 유지할 수 있다. The concentration of the chlorine dioxide gas can be maintained at 0.5 to 1 ppm for the first 1 to 3 days, and after 3 days, the concentration can be maintained at 0.03 to 0.05 ppm for more than 60 days.
본 발명의 이산화염소는 미국환경보호청에 의해 음용수의 정수 처리시 발암물질인 트리할로메탄을 생성하지 않아 안전한 살균 소독제로 사용가능한 것으로 확인되었다. 또한 탄저균의 살균 및 소독에 사용된 바 있다. 상기 이산화염소는 또한 세계보건기구에 의해 식품첨가물 중 가장 안전한 기준인 A-1 등급을 받은 소독제이며, 미국식품의약품안전청 및 대한민국 식약처에서 과일, 채소, 식품 용기 등의 세척에 살균 목적으로 사용가능한 것으로 알려져 있다. The chlorine dioxide of the present invention has been confirmed by the U.S. Environmental Protection Agency to be used as a safe sterilizing disinfectant because it does not produce trihalomethane, a carcinogen, when purifying drinking water. It has also been used to sterilize and disinfect anthrax. The chlorine dioxide is also a disinfectant rated A-1, the safest standard among food additives by the World Health Organization, and can be used for sterilization purposes in washing fruits, vegetables, food containers, etc. by the U.S. Food and Drug Administration and the Korean Ministry of Food and Drug Safety. It is known that
본 발명의 이산화염소는 다른 염소계 소독제인 차아염소산(락스), 클로라민과는 달리, 소독과정에서 발생하는 트리할로메탄, 할로아세토니트릴, 할로아세틱애시드, 요오드산염, 브롬산염, 알데히드, 케톤, 벤젠 등의 유독한 부산물이 발생하지 않아 안전성이 높은 특징이 있다.Unlike other chlorine-based disinfectants such as hypochlorous acid (chlorox) and chloramine, the chlorine dioxide of the present invention removes trihalomethane, haloacetonitrile, haloacetic acid, iodate, bromate, aldehyde, ketone, and benzene generated during the disinfection process. It has a high level of safety as no toxic by-products are generated.
또한, 본 발명의 이산화염소는 다양한 세균 및 바이러스에 대하여 우수한 소독효과가 있다(Morino et al., Letters in Applied Microbiology 53, 628-634, 2011).In addition, the chlorine dioxide of the present invention has an excellent disinfection effect against various bacteria and viruses (Morino et al., Letters in Applied Microbiology 53, 628-634, 2011).
본 발명의 다른 일 양태에 따르면, 본 발명은 a) 아염소산염을 포함하는 용기에 b) 당류, 및 산을 포함하는 분말제를 첨가하는 단계를 포함하는 이산화염소 가스의 지연 발생방법을 제공한다:According to another aspect of the present invention, the present invention provides a method for delayed generation of chlorine dioxide gas comprising the steps of a) adding a powder containing saccharide and acid to a container containing chlorite and b):
본 발명의 일 구현예에 있어서, 상기 용기내 포함된 제형은 액상 또는 겔상일 수 있다.In one embodiment of the present invention, the dosage form contained in the container may be in a liquid or gel form.
본 발명의 일 구현예에 있어서, 상기 용기는 정제수를 포함한다. In one embodiment of the invention, the container contains purified water.
본 발명의 일 구현예에 있어서, 상기 i) 용기, ii) 분말제, 또는 iii) 용기 및 분말제는 겔화제 또는 점증제를 포함하는 것이다.In one embodiment of the present invention, i) the container, ii) the powder, or iii) the container and the powder contain a gelling agent or a thickening agent.
본 발명의 일 구현예에 있어서, 상기 용기는 개폐가 가능한 뚜껑을 구비하고, 뚜껑에는 용기 내에서 발생된 이산화염소 가스를 분출할 수 있는 구멍이 구비된 것이다.In one embodiment of the present invention, the container has a lid that can be opened and closed, and the lid is provided with a hole through which chlorine dioxide gas generated in the container can be ejected.
본 발명의 일 구현예에 있어서, 상기 이산화염소 가스의 발생방법은 10 내지 50℃의 기온 조건에서 사용되는 것이다. In one embodiment of the present invention, the method for generating chlorine dioxide gas is used under temperature conditions of 10 to 50°C.
본 발명의 일 구현예에 있어서, 상기 이산화염소 가스의 발생방법에서 사용되는 제제의 교체 주기는 2개월 내지 3개월이다. 본 발명의 방법에 이용되는 상기 키트는 지속기간이 꿀벌의 평균 수명인 60일 이상이므로 병원체에 의해 감염되지 않은 봉군으로 세대교체가 될 때까지 사용이 가능하다는 특징이 있다.In one embodiment of the present invention, the replacement cycle of the agent used in the method for generating chlorine dioxide gas is 2 to 3 months. The kit used in the method of the present invention has a duration of more than 60 days, which is the average lifespan of honey bees, so it can be used until a generation change occurs with a colony of bees that is not infected by pathogens.
본 발명의 일 구현예에 있어서, 상기 이산화염소 가스는 꿀벌의 세균, 바이러스, 또는 진균성 병원체를 소독하는 것이다.In one embodiment of the present invention, the chlorine dioxide gas disinfects bacteria, viruses, or fungal pathogens in bees.
본 발명의 일 구현예에 있어서, 상기 이산화염소 가스는 제초제를 제거하는 것이다. 상기 제초제는 만코제브(mancozeb), 에틸렌티오유레아(ethylenethiourea), 테부코나졸(tebuconzole), 아족시스트로빈(azoxystrobin), 다이메토몰프(dimethomorph), 메타미디도포스(methamidophos), 또는 이들의 조합이나, 이에 한정되는 것은 아니다.In one embodiment of the present invention, the chlorine dioxide gas removes herbicides. The herbicides include mancozeb, ethylenethiourea, tebuconzole, azoxystrobin, dimethomorph, metamidophos, or a combination thereof. , but is not limited to this.
본 발명은 종래의 초기 높은 가스 발생을 낮추고 보관이 짧은 이산화염소 가스를 장기간에 걸처 서방형으로 발생하기 위한 키트 및 방법을 제시한다. 본 발명의 이산화염소 발생 키트 및 발생방법을 이용하는 경우 고농도로 인한 유해성 없이 장기간 이산화염소 가스를 생산할 수 있어 봉군 전체에서 감염된 벌의 세대 교체시까지 안전하게 이산화염소 가스를 생산하여 공간 및 사물의 살균, 또는 소독의 목적을 달성할 수 있다.The present invention provides a kit and method for reducing the conventional initial high gas generation and generating chlorine dioxide gas, which has a short storage period, in a sustained manner over a long period of time. When using the chlorine dioxide generation kit and generation method of the present invention, chlorine dioxide gas can be produced for a long period of time without harm due to high concentration, and chlorine dioxide gas can be safely produced until the generation of infected bees is replaced in the entire colony to sterilize spaces and objects, or The purpose of disinfection can be achieved.
도 1은 본 발명의 키트의 제1제를 포함하는 용기에 분말 형태의 제2제 및 분말 형태의 제3제를 첨가한 사진을 나타낸다.
도 2는 본 발명의 제1제, 제2제, 및 제3제를 첨가한 후 3시간 후부터 77일간 이산화염소 농도를 측정한 결과를 나타낸 도이다.
도 3은 제1제, 제2제 제3제의 비율을 높여 100 입방미터 공간을 소독할 목적으로 제조하였으며, 이산화염소가 120일째 1 ppm 이상으로 발생하고 있는 도이다.
도 4는 종래의 구연산을 이용한 이산화염소 가스 발생을 구현하였으며 상온에서 최대 14일간 가스가 발생되고 중단된다.
도 5는 본 발명의 서방성 이산화염소 발생 키트 제품의 제조예를 나타낸 것이다.
도 6은 본 발명의 서방성 이산화염소 발생 키트 제품을 살아있는 벌통에 적용한 예이다. Figure 1 shows a photograph of the second agent in powder form and the third agent in powder form added to a container containing the first agent of the kit of the present invention.
Figure 2 is a diagram showing the results of measuring the chlorine dioxide concentration for 77 days starting 3 hours after adding the first, second, and third agents of the present invention.
Figure 3 shows that it was manufactured for the purpose of disinfecting a 100 cubic meter space by increasing the ratio of the first, second, and third agents, and that chlorine dioxide is generated at more than 1 ppm after 120 days.
Figure 4 illustrates the generation of chlorine dioxide gas using conventional citric acid, and gas is generated for up to 14 days at room temperature and then stopped.
Figure 5 shows a manufacturing example of the sustained-release chlorine dioxide generation kit product of the present invention.
Figure 6 is an example of applying the sustained-release chlorine dioxide generation kit product of the present invention to a living beehive.
이하, 실시예를 통하여 본 발명을 더욱 상세히 설명하고자 한다. 이들 실시예는 오로지 본 발명을 보다 구체적으로 설명하기 위한 것으로, 본 발명의 요지에 따라 본 발명의 범위가 이들 실시예에 의해 제한되지 않는다는 것은 당업계에서 통상의 지식을 가진 자에 있어서 자명할 것이다.Hereinafter, the present invention will be described in more detail through examples. These examples are only for illustrating the present invention in more detail, and it will be apparent to those skilled in the art that the scope of the present invention is not limited by these examples according to the gist of the present invention. .
실시예Example
본 명세서 전체에 걸쳐, 특정 물질의 농도를 나타내기 위하여 사용되는 "%"는 별도의 언급이 없는 경우, 고체/고체는 (중량/중량) %, 고체/액체는 (중량/부피) %, 그리고 액체/액체는 (부피/부피) %이다.Throughout this specification, “%” used to indicate the concentration of a specific substance means (weight/weight) % for solid/solid, (weight/volume) % for solid/liquid, and Liquid/liquid is (volume/volume) %.
실시예 1: 이산화염소 발생 시험 1 - 유기물 첨가Example 1: Chlorine dioxide generation test 1 - Addition of organic matter
유기물의 종류에 따른 아염소산 나트륨과의 반응성과 위험성을 확인하기 위하여 아염소산나트륨 23% 수용액에 표 1의 유기물을 첨가하여 상온 내지 냉장온도에서 반응성을 관찰하였다. 유기물의 종류 및 반응성 결과는 표 1에 나타내었다.In order to confirm the reactivity and risk with sodium chlorite according to the type of organic material, the organic materials in Table 1 were added to a 23% aqueous solution of sodium chlorite and the reactivity was observed at room temperature or refrigerated temperature. The types of organic substances and reactivity results are shown in Table 1.
반응 속도가 빠른(+++++) 유기물은 유기물 첨가 후 수시간 내지 수일 사이에서 비교적 빠르게 이산화염소 가스가 발생하기 시작하였고 반응도 비교적 빠르게 진행되었다. 반응 속도가 중간(+++)인 유기물은 유기물 첨가 후 수일 내지 수십일 사이에서 이산화염소 가스가 발생하기 시작하였고, 반응 속도도 빠른 유기물보다는 느리게 반응하였으며, 반응 속도가 느린(+) 유기물은 반응이 시작되는 시기를 특정하기 어렵고, 반응이 시작하여도 자세히 관찰해야 미세하게 이산화염소 가스가 발생하는 것을 관찰할 수 있었다. For organic materials with a fast reaction rate (+++++), chlorine dioxide gas began to be generated relatively quickly within a few hours to several days after the addition of the organic material, and the reaction proceeded relatively quickly. Organic materials with a medium (+++) reaction rate began to generate chlorine dioxide gas within a few days to tens of days after adding the organic material, and reacted more slowly than organic materials with a fast reaction rate, and organic materials with a slow (+) reaction rate reacted. It is difficult to specify when this begins, and even when the reaction begins, only a close observation is needed to observe the minute chlorine dioxide gas being generated.
또한, 반응 시작 시점은 유기물의 종류에 따라 달랐으나 공통적으로 반응이 시작되는 시점을 특정할 수 없었고, 다만 이산화염소 가스 발생 반응이 시작되면 반응이 빠른 물질은 빠르게 반응이 일어났고, 반응이 느린 물질은 느리게 반응하면서 가스 발생 지속시간이 길었다. In addition, the starting time of the reaction differed depending on the type of organic material, but the common starting point of the reaction could not be specified. However, once the chlorine dioxide gas generation reaction began, the fast-reacting substances reacted quickly, and the slow-reacting substances reacted quickly. reacted slowly and the duration of gas generation was long.
실시예 2: 이산화염소 발생 시험 2 - 유기물 및 유기산 첨가Example 2: Chlorine dioxide generation test 2 - Addition of organic matter and organic acid
본 발명자들은 상기 실시예 1로부터, 수용액 상태에서 아염소산 나트륨을 반응시킬 경우 반응 속도가 빠른 포도당을 첨가하는 경우 7일 내지 20일에 반응이 시작되고 반응이 시작되면 꾸준히 반응하지만, 종래 아염소산염에 유기산을 첨가하여 이산화염소를 발생시키는 방법에 비해서는 천천히 반응이 진행되는 특징을 확인하였다.From Example 1, the present inventors found that when reacting sodium chlorite in an aqueous solution and adding glucose, which has a fast reaction rate, the reaction starts in 7 to 20 days and reacts steadily once the reaction starts, but It was confirmed that the reaction proceeds slowly compared to the method of generating chlorine dioxide by adding an organic acid.
즉, 유기물을 첨가하면 유해성이 없는 수준의 농도로 장기간 이산화염소 가스를 발생시킬 수 있었으나, 이 경우 반응 시작이 너무 느렸고 반응의 시작 시기를 특정할 수 없어 실용성이 없음을 확인하고, 반응 시작을 촉진하기 위하여 소량의 유기산을 첨가하기로 하였다. In other words, it was possible to generate chlorine dioxide gas for a long period of time at a non-hazardous concentration by adding organic substances, but in this case, the start of the reaction was too slow and the start time of the reaction could not be specified, so it was confirmed that it was not practical, and the start of the reaction was confirmed to be impractical. It was decided to add a small amount of organic acid to promote it.
일 실시예로, 본 발명자들은 제1제로 아염소산 나트륨 0.3 g을 포함한 내알칼리성 한천을 이용하여 35 ml 겔 고형물로 제조하고; 제2제로 포도당 분말 0.5g, 잔탄검 0.5g; 제3제로 아스코르브산 0.02 g 을 한천 겔의 표면에 도포하였다. 그 결과, 한천 겔의 표면에서 서서히 반응하여 겔 전체가 이산화염소 가스를 서서히 방출하기 시작하였다. In one example, the present inventors used alkaline-resistant agar containing 0.3 g of sodium chlorite as a first agent to prepare a 35 ml gel solid; Second agent: 0.5g glucose powder, 0.5g xanthan gum; As a third agent, 0.02 g of ascorbic acid was applied to the surface of the agar gel. As a result, a slow reaction occurred on the surface of the agar gel, and the entire gel began to slowly release chlorine dioxide gas.
본 발명자들은 상기 이산화염소 발생 방법에 따른 이산화염소 발생 농도를 측정하기 위하여 125 L 들이 챔버(가로 50 cm*세로 50 cm*높이 50 cm)를 제작하고 위와 같은 방법으로 이산화염소 가스가 발생하도록 아염소산 나트륨 한천 겔에 구연산 및 포도당 분말을 첨가하고 1시간 후부터 7일마다 77일(11주)간 이산화염소의 농도를 측정하였다. The present inventors manufactured a 125 L chamber (width 50 cm*length 50 cm*height 50 cm) to measure the concentration of chlorine dioxide generated according to the chlorine dioxide generation method and produced chlorine dioxide gas in the same manner as above. Citric acid and glucose powder were added to the sodium agar gel, and the concentration of chlorine dioxide was measured every 7 days for 77 days (11 weeks) starting 1 hour later.
본 발명의 키트의 제1제를 포함하는 용기에 분말 형태의 제2제 및 분말 형태의 제3제를 첨가한 사진을 도 1에 나타내었다. Figure 1 shows a photograph of the second agent in powder form and the third agent in powder form added to a container containing the first agent of the kit of the present invention.
또한, 77일간 이산화염소 농도를 측정한 결과는 도 2에 나타내었다. Additionally, the results of measuring chlorine dioxide concentration for 77 days are shown in Figure 2.
도 2에 나타낸 바와 같이, 본 발명의 이산화염소 발생 키트의 제1제, 제2제 및 제3제를 접촉하면 수시간 후부터 이산화염소 가스가 발생되어 최고 0.5 ppm의 농도로 측정이 되었고, 수일 내로 점점 농도가 감소하여 77일 까지 약 0.03 내지 약 0.05 ppm 내외의 농도로 측정되는 것을 확인하였다. As shown in Figure 2, when the first, second, and third agents of the chlorine dioxide generation kit of the present invention are contacted, chlorine dioxide gas is generated several hours later and was measured at a maximum concentration of 0.5 ppm, and within a few days. It was confirmed that the concentration gradually decreased and was measured at around 0.03 to about 0.05 ppm by day 77.
감염된 봉군에서 알부터 성충까지 자라는데 걸리는 시간은 약 22일이고, 성충의 수명은 약 35일이므로, 봉군 전체를 소독하려면 60일 이상 장기간 소독이 필요하다. 상기 결과로부터, 본 발명의 키트를 이용하여 이산화염소 가스를 발생시키면, 낮은 농도의 이산화염소 가스를 발생하여 벌을 손상시키지 않으면서도 봉군이 교체되는 주기인 약 60일 이상으로 장기간 이산화염소를 발생시킬 수 있어 봉군 전체의 감염병 확산을 막고 충분한 소독 효과에 도달할 수 있음을 확인하였다. The time it takes for an infected swarm to grow from egg to adult is about 22 days, and the adult swarm's lifespan is about 35 days, so disinfection of the entire swarm requires long-term disinfection of more than 60 days. From the above results, when chlorine dioxide gas is generated using the kit of the present invention, a low concentration of chlorine dioxide gas is generated and chlorine dioxide can be generated for a long period of time, over about 60 days, which is the replacement cycle of the bees, without damaging the bees. It was confirmed that it was possible to prevent the spread of infectious diseases throughout the entire group and achieve sufficient disinfection effect.
실시예 3: 이산화염소 발생 시험 3Example 3: Chlorine dioxide generation test 3
본 발명자들은 제1제, 제2제, 및 제3제의 첨가 비율별로 이산화염소의 발생량이 어떻게 달라지는지를 확인하기 위하여 표 2와 같은 조건으로 이산화염소 발생 시험을 수행하였다.The present inventors performed a chlorine dioxide generation test under the conditions shown in Table 2 to determine how the amount of chlorine dioxide generated varies depending on the addition ratio of the first, second, and third agents.
상기 표 2에서 물, 한천, 및 아염소산나트륨 용액을 혼합하여 겔로 제조하였고, 구연산, 포도당, 및 잔탄검은 분말의 형태로 준비하여 겔 표면에 도포하였다.In Table 2, water, agar, and sodium chlorite solution were mixed to prepare a gel, and citric acid, glucose, and xanthan gum were prepared in the form of powder and applied to the gel surface.
상기 표 2에 나타낸 바와 같이, 대조군에서는 이산화염소가 발생하지 않았고, 유기물로 포도당만을 첨가한 실시예 3-1에서는 첨가 후 6일째에 일시적으로 이산화염소 가스가 발생한 후, 14일째부터 점점 이산화염소 가스의 발생이 일어났다.As shown in Table 2, no chlorine dioxide was generated in the control group, and in Example 3-1, in which only glucose was added as an organic material, chlorine dioxide gas was temporarily generated on the 6th day after addition, and then chlorine dioxide gas gradually increased from the 14th day. occurred.
구연산을 포함하는 실시예 3-2와 실시예 3-3은 이산화염소의 발생이 1일차부터 관찰되었으나, 6일까지만 이산화염소가 발생되었고, 그 이후에는 이산화염소의 발생이 확인되지 않았다. 한편, 잔탄검을 추가로 첨가한 실시예 3-3에서는 구연산만을 첨가한 실시예보다 이산화염소의 발생량이 더 많은 것을 알 수 있었다. In Examples 3-2 and 3-3 containing citric acid, the generation of chlorine dioxide was observed from the 1st day, but chlorine dioxide was generated only until the 6th day, and the generation of chlorine dioxide was not confirmed after that. Meanwhile, in Example 3-3 in which xanthan gum was additionally added, it was found that the amount of chlorine dioxide generated was greater than in the example in which only citric acid was added.
구연산 및 포도당을 포함하는 실시예 3-4과, 구연산을 포함하고, 포도당의 용량을 0.5 g으로 줄이고 잔탄검을 0.5 g 첨가한 실시예 3-5는, 둘 다 이산화염소의 발생이 1일차부터 관찰되었고 30일까지 지속적으로 이산화염소의 발생이 관찰되었다. 그러나, 포도당만 1 g을 첨가한 실시예 3-4는 포도당과 잔탄검을 각각 0.5 g 첨가한 실시예 3-5와 비교하여 초기에 이산화염소 발생량이 더 많았고, 상대적으로 급격하게 발생량이 감소하였다. 반면 포도당과 잔탄검을 각각 0.5 g 첨가한 실시예 3-5는 이산화염소 가스의 초기 발생량은 적었으나 상대적으로 더 높은 농도로 오랫동안 발생량이 유지되는 것을 확인하였다. In both Example 3-4, which contained citric acid and glucose, and Example 3-5, which contained citric acid, reduced the dose of glucose to 0.5 g, and added 0.5 g of xanthan gum, the generation of chlorine dioxide was observed from the first day. And the generation of chlorine dioxide was observed continuously for up to 30 days. However, in Example 3-4, in which only 1 g of glucose was added, the amount of chlorine dioxide generated initially was greater than in Example 3-5 in which 0.5 g of glucose and xanthan gum were added respectively, and the amount of chlorine dioxide generated decreased relatively rapidly. On the other hand, in Example 3-5, in which 0.5 g of glucose and xanthan gum were added, the initial amount of chlorine dioxide gas generated was small, but it was confirmed that the amount generated was maintained for a long time at a relatively higher concentration.
상기 결과로부터, 본 발명에서 제3제인 유기산과, 제2제인 유기물은 각각 아염소산 나트륨과 반응하여 이산화염소 가스를 발생함을 알 수 있었다. 따라서, 첨가된 유기산과 유기물의 양에 따라서 이산화염소 가스 발생량이 달라짐을 알 수 있었다. From the above results, it was found that in the present invention, the organic acid as the third agent and the organic material as the second agent each reacted with sodium chlorite to generate chlorine dioxide gas. Therefore, it was found that the amount of chlorine dioxide gas generated varies depending on the amount of organic acid and organic matter added.
또한, 구연산과 같은 유기산은 이산화염소 발생 반응을 개시하는 효과가 있는 것을 알 수 있었고, 표 1에서 반응속도가 빨랐던 포도당과 같은 유기물은 유기산 첨가에 의해 반응이 개시되면 포도당과 아염소산 나트륨의 반응이 가속화되어 보다 빠르게 이산화염소 가스를 발생시키는 것을 알 수 있었다. In addition, it was found that organic acids such as citric acid are effective in initiating the chlorine dioxide generation reaction, and in Table 1, for organic substances such as glucose, which had a fast reaction rate, when the reaction is initiated by the addition of the organic acid, the reaction between glucose and sodium chlorite is reduced. It was found that it was accelerated and chlorine dioxide gas was generated more quickly.
반응속도가 상대적으로 느린 잔탄검과 같은 유기물과 포도당을 혼합하여 첨가하는 경우에는 포도당만 첨가한 경우보다 낮은 농도로 장시간 이산화염소 가스를 발생시키는 것에 미루어보아, 포도당은 먼저 빠르게 반응하고, 잔탄검은 뒤늦게 반응을 시작하는 것을 확인하였다. 따라서, 본 발명의 이산화염소 발생 키트 내지 방법은 반응이 빠른 유기물과 반응이 느린 유기물의 혼합 비율을 조절함으로써 반응속도와 키트의 사용기간을 쉽게 조절할 수 있음을 알 수 있었다. Considering that when glucose is mixed and added with an organic substance such as xanthan gum, which has a relatively slow reaction rate, chlorine dioxide gas is generated at a lower concentration for a longer period of time than when only glucose is added, glucose reacts quickly first, and xanthan gum reacts later. It was confirmed that the reaction had started. Therefore, it was found that the chlorine dioxide generation kit or method of the present invention can easily control the reaction rate and use period of the kit by adjusting the mixing ratio of the fast-reacting organic material and the slow-reacting organic material.
본 발명자들은 상기 실시예 3-5와 같은 비율 조건에서 제1제, 제2제 제3제의 용량을 높여 100 입방미터 공간을 소독할 목적으로 제조하였다. 도 3에 나타낸 바와 같이, 2021년 12월 13일에 제조한 이산화염소 가스 제조 키트에서, 4개월(120일)이 지난 2022년 4월 12일에도 1 ppm의 농도로 이산화염소 가스를 The present inventors manufactured it for the purpose of disinfecting a 100 cubic meter space by increasing the capacity of the first, second, and third agents under the same ratio conditions as in Example 3-5. As shown in Figure 3, in the chlorine dioxide gas production kit manufactured on December 13, 2021, chlorine dioxide gas was produced at a concentration of 1 ppm even on April 12, 2022, 4 months (120 days) later.
발생시키는 제품이 제조 가능하였다. The resulting product could be manufactured.
한편, 도 4는 종래의 구연산과 아염소산 나트륨 수용액을 이용한 이산화염소 가스 발생을 구현한 것으로 상온에서 최대 14일간 가스가 발생되고 발생이 중단되는 것을 나타낸다. Meanwhile, Figure 4 shows the implementation of chlorine dioxide gas generation using a conventional aqueous solution of citric acid and sodium chlorite, and shows that gas is generated for up to 14 days at room temperature and then the generation is stopped.
실시예 4: 서방성 이산화염소 발생 키트의 제조Example 4: Preparation of sustained-release chlorine dioxide generation kit
본 발명자들은 하기 표 3과 같은 구성으로 서방성 이산화염소 발생 키트 제품을 제조하였다. The present inventors manufactured a sustained-release chlorine dioxide generation kit product with the configuration shown in Table 3 below.
상기 제품의 용도는 상온의 신발장 등 밀폐공간, 빈벌통, 벌통, 소비 등의 물품에 대한 살균/소독제, 탈취제, 꿀벌의 전염성 질환의 예방 또는 치료용, 또는 식물의 농약 제거를 위한 키트로서 제작되었다.The intended use of the product is as a sterilizer/disinfectant and deodorant for closed spaces such as shoe racks at room temperature, empty bee hives, beehives, consumer goods, etc., for the prevention or treatment of infectious diseases in bees, or as a kit for removing pesticides from plants. .
본 발명의 제품 사진을 도 5에 나타내었다. 사용방법은 상기 정제수, 아염소산나트륨 및 한천을 포함하는 용기의 밀봉 포장을 제거하고, 용기 내에 아스코르브산, 포도당, 전분, 수크로스, 및 잔탄검을 포함하는 첨부된 스틱봉투 가루를 넣고 뚜껑을 닫으면 되고, 반응 결과 이산화염소 가스가 발생한다. A photo of the product of the present invention is shown in Figure 5. To use, remove the sealed packaging of the container containing the purified water, sodium chlorite, and agar, add the attached stick bag powder containing ascorbic acid, glucose, starch, sucrose, and xanthan gum into the container, and close the lid. As a result of the reaction, chlorine dioxide gas is generated.
상기 용기의 뚜껑에는 작은 구멍이 형성되어 있어 뚜껑을 닫아 놓아도 상기 구멍을 통하여 이산화염소 가스가 용기 외부로 서서히 분출된다. A small hole is formed in the lid of the container, so even when the lid is closed, chlorine dioxide gas is slowly emitted out of the container through the hole.
Claims (15)
(a) 아염소산염, (b) 당류, (c) 겔화제 또는 점증제, 및 (d) 산.
Sustained-release chlorine dioxide gas generation kit containing:
(a) chlorite, (b) sugar, (c) gelling or thickening agent, and (d) acid.
The sustained-release chlorine dioxide of claim 1, wherein the chlorite is one or more selected from the group consisting of sodium chlorite, potassium chlorite, lithium chlorite, calcium chlorite, magnesium chlorite, and barium chlorite. Gas generation kit.
The sustained-release chlorine dioxide gas generation kit according to claim 1, wherein the saccharide is a monosaccharide, a disaccharide, a sugar alcohol, or a combination thereof.
The sustained-release chlorine dioxide gas generation kit according to claim 1, wherein the monosaccharide is glucose, fructose, galactose, or a combination thereof.
The sustained-release chlorine dioxide gas generation kit according to claim 1, wherein the disaccharide is sucrose, maltose, trehalose, lactose, or a combination thereof.
The sustained-release chlorine dioxide gas generation kit of claim 1, wherein the sugar alcohol is ethylene glycol, glycerol, erythritol, sorbitol, mannitol, xylitol, inositol, or a combination thereof.
The method of claim 1, wherein the gelling agent or thickening agent is agar, konjac powder, carrageenan, pectin, gelatin, starch, locust bean gum, tara gum, guar gum, gellan gum, xanthan gum, tamarind gum, gum arabic, and cellulose gum. , sodium caseinate, sodium alginate, dextran, dextrin, carboxymethylcellulose, or a combination thereof, a sustained-release chlorine dioxide gas generation kit.
The sustained-release chlorine dioxide gas generation kit of claim 1, wherein the acid is an organic acid, an inorganic acid, or a mixture thereof.
The method of claim 8, wherein the organic acid is lactic acid, acetic acid, formic acid, citric acid, oxalic acid, ascorbic acid, glucuronic acid, maleic acid, succinic acid, benzoic acid, tartaric acid, fumaric acid, propionic acid, glutamic acid, aspartic acid, butyric acid, or a combination thereof. A sustained-release chlorine dioxide gas generation kit comprising:
The sustained-release chlorine dioxide gas generation kit according to claim 8, wherein the inorganic acid includes hydrochloric acid, phosphoric acid, sulfuric acid, nitric acid, or a combination thereof.
The sustained-release chlorine dioxide gas generation kit according to claim 1, wherein the kit is used for preventing or treating infectious diseases in bees, disinfecting articles, deodorizing articles, or removing pesticides from plants.
A method of delayed generation of chlorine dioxide gas comprising the step of adding a) a powder containing b) sugars and an acid to a container containing chlorite.
The method of claim 12, wherein the formulation contained in the container is in a liquid or gel form.
The method of claim 12, wherein i) the container, ii) the powder, or iii) the container and the powder contain a gelling agent or a thickening agent.
The method of claim 12, wherein the container has a lid that can be opened and closed, and the lid is provided with a hole through which chlorine dioxide gas generated in the container can be ejected.
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| PCT/KR2023/013214 WO2024090774A1 (en) | 2022-10-28 | 2023-09-05 | Sustained-release chlorine dioxide gas generation kit and method |
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| KR1020220051100 | 2022-04-25 | ||
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Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005224386A (en) | 2004-02-12 | 2005-08-25 | Daiichi Seidenki Kk | Apparatus for chlorine dioxide gas sterilization |
| KR101315260B1 (en) | 2011-11-04 | 2013-10-10 | 대한민국 | An apparatus and methods producing chlorine dioxide gas for prevention and treatment of honey bee diseases containing sacbrood |
| KR101807966B1 (en) | 2016-09-22 | 2017-12-11 | 주식회사 더원 | Device for making chlorine dioxide |
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2023
- 2023-04-25 KR KR1020230054371A patent/KR20230151496A/en unknown
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005224386A (en) | 2004-02-12 | 2005-08-25 | Daiichi Seidenki Kk | Apparatus for chlorine dioxide gas sterilization |
| KR101315260B1 (en) | 2011-11-04 | 2013-10-10 | 대한민국 | An apparatus and methods producing chlorine dioxide gas for prevention and treatment of honey bee diseases containing sacbrood |
| KR101807966B1 (en) | 2016-09-22 | 2017-12-11 | 주식회사 더원 | Device for making chlorine dioxide |
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