CN1969633A - Monophyletic solid disinfectant of chlorine dioxide and preparation method thereof - Google Patents
Monophyletic solid disinfectant of chlorine dioxide and preparation method thereof Download PDFInfo
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- CN1969633A CN1969633A CN 200610102230 CN200610102230A CN1969633A CN 1969633 A CN1969633 A CN 1969633A CN 200610102230 CN200610102230 CN 200610102230 CN 200610102230 A CN200610102230 A CN 200610102230A CN 1969633 A CN1969633 A CN 1969633A
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- sodium
- chlorine dioxide
- tartrate
- percarbonate
- niter cake
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Abstract
The invention discloses a monobasic solid chlorine dioxide sanitizer and making method, which comprises the following steps: a. weighing raw material with 16-19% sodium chlorite, 3-4% sodium percarbonate, 35-38% sodium bisulfate, 25-31% sodium tartrate, 5-6.2% citrate and/or amidosulfonic acid and 8.6-10.2% sodium bicarbonate; adding sodium percarbonate, sodium bisulfate, sodium tartrate and sodium bicarbonate in the drier to dry at 100-140 deg.c; b. blending sodium chlorite, sodium tartrate, sodium percarbonate and sodium bicarbonate in the sealed container evenly; c. adding sodium bisulfate, citrate and/or amidosulfonic acid to mix evenly; d. packing composition bag by bag.
Description
Technical field
The present invention relates to a kind of disinfection sanitizer, specifically a kind of Monophyletic solid disinfectant of chlorine dioxide and preparation method thereof.
Background technology
Monophyletic solid disinfectant of chlorine dioxide be by the active ingredient sodium chlorite is coated, the means of passivation make active ingredient and solid acid does not but react with putting a place, mix the generation chlorine dioxide with water during use and the purpose that realizes sterilizing.The difference of coating, passivation means will directly influence production cost of products and serviceability.CN1439268 discloses a kind of solid chlorine dioxide disinfectant of doing clad material with organic polymer, it at first will carry out the preparation of clad material, again institute's prepared material is coated on active ingredient sodium chlorite outer surface, complex process not only, and equipment drops into high, cause production cost to improve, thereby reduced its exploitativeness and promotional value.And, owing to introduced the organic polymers such as polyvinyl alcohol of biological degradability difference, the destruction that long-term use can cause ecotope.The disclosed solid chlorine dioxide disinfectant of CN1104610A, because the covering poorly water-soluble that uses, drop into result of use when using in the water and influence finished product, also cause the solid insoluble ratio rising of disinfectant on the other hand, and the covering after the thawing also can cause water pollution.CN1238130A uses the chloride of alkali metal or alkaline earth metal to make passivator, utilize its water imbibition to reach drying purpose, to guarantee that mixing preceding sodium chlorite and solid acid with water does not react, but because the passivator water imbibition of using is strong, cause the disinfectant poor stability, holding time is short, especially one opens bag, loses efficacy soon.
Summary of the invention
Purpose of the present invention be exactly to provide that a kind of preparation technology is easy, the Monophyletic solid disinfectant of chlorine dioxide of good stability, good water solubility and preparation method thereof.
The present invention is achieved by the following technical solutions: solid chlorine dioxide disinfectant is made up of the material of following portions by weight:
Sodium chlorite 16-19, SODIUM PERCARBONATE 3-4,
Niter cake 35-38, sodium tartrate 25-31,
Citric acid and/or sulfamic acid 5-6.2, sodium bicarbonate 8.6-10.2.
Solid chlorine dioxide disinfectant of the present invention is active ingredient with the sodium chlorite, with the niter cake is activator, sodium tartrate is a passivator, citric acid and/or sulfamic acid are buffer, SODIUM PERCARBONATE is the absorption stabilizing agent, sodium bicarbonate is a blowing agent, makes made solid chlorine dioxide disinfectant good stability, and the holding time was more than 2 years.When meeting water, sodium tartrate is soluble in water, loses passivation, and citric acid and/or sulfamic acid transfer to sour environment with solution, and sodium chlorite and niter cake react, and produces chlorine dioxide.Meanwhile, the sodium bicarbonate that is dissolved in the water rapidly can produce a large amount of carbonic acid gas bubbles, in the process that bubble is overflowed, solution is played stirring action, thereby quickens the generation of chlorine dioxide.
Sodium chlorite is stable alkaline matter under drying regime among the present invention, in water body with the niter cake generation chlorine dioxide that reacts.The suitable amount ranges of sodium chlorite is 16-19.Consumption is lower than 16, can reduce the concentration of chlorine dioxide, does not reach bactericidal effect, and consumption is higher than 19, can reduce the stability of finished product.
Mesotartaric acid sodium of the present invention uses as passivator, and under drying regime, it mixes with sodium chlorite, can make the independent respectively existence of sodium chlorite and niter cake, citric acid and/or sulfamic acid, with putting a place chemical reaction does not take place.The suitable amount ranges of sodium tartrate is 25-31, and consumption is lower than 25, can reduce the stability of finished product, and content is higher than 31 reactivities that can excessively suppress niter cake, reduces conversion ratio.
Niter cake uses as activator among the present invention, and molten water is acid and the sodium chlorite generation chlorine dioxide that reacts.The suitable consumption of niter cake is 35-38, is lower than 35 and can causes conversion ratio to reduce; Be higher than 38 and make reaction too fierce, the chlorine dioxide duration of generation is short, reduces the lasting effect of sterilizing.
SODIUM PERCARBONATE is used as the absorption stabilizing agent among the present invention, is storing or the haulage stage, and when having a small amount of chlorine dioxide to produce in the medicament, this component can be a sodium chlorite with its absorbing and reducing, thus the stabilization of playing.Its suitable amount ranges is 3-4, and content is lower than stability and the safety that 3 meetings influence this finished product, and content is higher than 4 can reduce the activity ratio of niter cake and the conversion ratio of chlorine dioxide.
Citric acid and/or sulfamic acid among the present invention use as buffer, have buffering, complexing, chelating, anti-oxidant synergy and catalytic action.Its suitable amount ranges is 5-6.2, in this scope, can store safely under the drying regime, then solution can be transferred to the proper acidic environment when meeting water, thereby the chemical reaction that produces chlorine dioxide is normally carried out.Citric acid and sulfamic acid can use separately, also can mix use by arbitrary proportion.The preferential citric acid that uses separately.
Produce carbon dioxide when the sodium bicarbonate that uses among the present invention is met water, in the process that bubble is overflowed, solution is played stirring action, increase the dissolution velocity of medicament, quicken the generation of chlorine dioxide at water body.Suitable consumption is 8.6-10.2, the low effect that increases dissolution velocity that do not reach of content, and high chlorine dioxide can being taken out of of content influences bactericidal effect.
Monophyletic solid disinfectant of chlorine dioxide of the present invention uses as passivator with sodium tartrate, the environmental pollution that organic covering causes and the shortcoming of wax covering poorly water-soluble have been avoided using, compared with prior art, the present invention not only preparation technology is easy, and finished product all dissolvings in water body, water-soluble is 100%.Because the present invention does not use in the prior art the extremely strong desiccant of water imbibition such as employed magnesium sulfate to do passivator, has avoided opening a defective that lost efficacy fast in the bag back.The present invention makes the stability of finished product, safety obviously improve owing to selected unique activator and passivator, and period of storage was brought up to 2 years by 1 year.As blowing agent, solution is played stirring action with sodium bicarbonate, the carbon dioxide that is produced is nonpoisonous and tasteless, can accelerate the dissolution velocity of finished product in water, quickens the generation of chlorine dioxide.The present invention makes conversion ratio up to 99.5% owing to selected proper raw material and suitable ratio range, because the conversion ratio height, residual chlorite is few, thereby the various fields such as sterilization fresh-keeping of town and country preferably drinking water, food processing, food and drink fruits and vegetables.
Solid chlorine dioxide disinfectant of the present invention is made as follows:
A. after each component being weighed in proportion, wherein SODIUM PERCARBONATE, niter cake, sodium tartrate, sodium bicarbonate placed respectively in the warm air drier, under 100-140 ℃ of temperature, dry;
B. sodium chlorite, sodium tartrate, SODIUM PERCARBONATE and sodium bicarbonate are mixed in closed container;
C. in said vesse, add niter cake, citric acid and/or sulfamic acid, mixing;
D. with packing composition bag by bag.
The bake out temperature of above-mentioned a in the step is advisable to be no more than 140 ℃, in order to avoid raw material is by gelatinization; Be preferably 110-130 ℃, more preferably 120 ℃.Got final product in 30-40 minute 120 ℃ of general down oven dry, low excessively as temperature, then can cause drying time long, reduce production efficiency.
Embodiment
Below by embodiment the present invention is further described.
Embodiment 1
A. take by weighing sodium chlorite 16g in proportion, SODIUM PERCARBONATE 3g, niter cake 35g, sodium tartrate 25g, citric acid 6.2g, sodium bicarbonate 10.2g.SODIUM PERCARBONATE, niter cake, sodium tartrate, sodium bicarbonate are placed respectively in the warm air drier, under 120 ℃, dried respectively 35 minutes.
B. sodium tartrate, SODIUM PERCARBONATE and sodium bicarbonate after will drying and sodium chlorite stirred in closed container 30 minutes, mixing.
C. in said vesse, add niter cake, citric acid, continue to stir 30 minutes to mixing;
D. gains tested, weigh, bag distribution packaging, sealing get final product.
Embodiment 2
A. take by weighing sodium chlorite 19g in proportion, SODIUM PERCARBONATE 4g, niter cake 36g, sodium tartrate 31g, citric acid 5g, sodium bicarbonate 8.6g.SODIUM PERCARBONATE, niter cake, sodium tartrate, sodium bicarbonate are placed respectively in the warm air drier, under 100 ℃, dried respectively 45 minutes.
B. sodium tartrate, SODIUM PERCARBONATE and sodium bicarbonate after will drying and sodium chlorite stirred in closed container 30 minutes, mixing.
C. in said vesse, add niter cake, citric acid, continue to stir 30 minutes to mixing;
D. gains tested, weigh, bag distribution packaging, sealing get final product.
Embodiment 3
A. take by weighing sodium chlorite 17g in proportion, SODIUM PERCARBONATE 3.3g, niter cake 38g, sodium tartrate 29g, amino acid 5.4g, sodium bicarbonate 9.2g.SODIUM PERCARBONATE, niter cake, sodium tartrate, sodium bicarbonate are placed respectively in the warm air drier, under 110 ℃, dried respectively 40 minutes.
B. sodium tartrate, SODIUM PERCARBONATE and sodium bicarbonate after will drying and sodium chlorite stirred in closed container 30 minutes, mixing.
C. in said vesse, add niter cake, amino acid, continue to stir 30 minutes to mixing;
D. gains tested, weigh, bag distribution packaging, sealing get final product.
Embodiment 4
A. take by weighing sodium chlorite 18g in proportion, SODIUM PERCARBONATE 3.6g, niter cake 37g, sodium tartrate 27g, citric acid 3.2g, amino acid 2.6g, sodium bicarbonate 9.8g.SODIUM PERCARBONATE, niter cake, sodium tartrate, sodium bicarbonate are placed respectively in the warm air drier, under 130 ℃, dried respectively 30 minutes.
B. sodium tartrate, SODIUM PERCARBONATE and sodium bicarbonate after will drying and sodium chlorite stirred in closed container 30 minutes, mixing.
C. in said vesse, add niter cake, citric acid, amino acid, continue to stir 30 minutes to mixing;
D. gains tested, weigh, bag distribution packaging, sealing get final product.
Claims (2)
1, a kind of Monophyletic solid disinfectant of chlorine dioxide is characterized in that being made up of the material of following portions by weight: sodium chlorite 16-19, SODIUM PERCARBONATE 3-4, niter cake 35-38, sodium tartrate 25-31, citric acid and/or sulfamic acid 5-6.2, sodium bicarbonate 8.6-10.2.
2, the preparation method of the described Pickering disinfection agent of chlorine dioxide of claim 1 is characterized in that making as follows:
A. after each component being weighed in proportion, wherein SODIUM PERCARBONATE, niter cake, sodium tartrate, sodium bicarbonate placed respectively in the warm air drier, under 100-140 ℃ of temperature, dry;
B. sodium chlorite, sodium tartrate, SODIUM PERCARBONATE and sodium bicarbonate are mixed in closed container;
C. in said vesse, add niter cake, citric acid and/or sulfamic acid, mixing;
D. with packing composition bag by bag.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2006101022304A CN100391343C (en) | 2006-12-06 | 2006-12-06 | Monophyletic solid disinfectant of chlorine dioxide and preparation method thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2006101022304A CN100391343C (en) | 2006-12-06 | 2006-12-06 | Monophyletic solid disinfectant of chlorine dioxide and preparation method thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1969633A true CN1969633A (en) | 2007-05-30 |
| CN100391343C CN100391343C (en) | 2008-06-04 |
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| CNB2006101022304A Expired - Fee Related CN100391343C (en) | 2006-12-06 | 2006-12-06 | Monophyletic solid disinfectant of chlorine dioxide and preparation method thereof |
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Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101143225B (en) * | 2007-10-17 | 2010-07-28 | 艾雪莉 | Air purifying agent and its preparing process |
| CN101595891B (en) * | 2008-06-05 | 2012-09-05 | 廖伟凯 | Chlorine dioxide composition with selective antioxidation |
| US8992831B2 (en) | 2009-09-25 | 2015-03-31 | E. I. Du Pont De Nemours And Company | Stabilized chlorine dioxide to preserve carbohydrate feedstocks |
| CN106367230A (en) * | 2015-07-20 | 2017-02-01 | 修建东 | Reverse osmosis membrane acid sterilizing scale removing powder solid cleaning agent |
| CN106489931A (en) * | 2016-09-08 | 2017-03-15 | 天津博锐开元环保科技有限公司 | It is used as sodium chlorite gel and its preparation technology of disinfectant |
| CN107593762A (en) * | 2017-09-29 | 2018-01-19 | 广州闪电生物科技有限公司 | A kind of antiseptic solution and sterilization method |
| CN107691471A (en) * | 2017-09-29 | 2018-02-16 | 广州闪电生物科技有限公司 | Antiseptic solution and sterilization method |
| CN111436456A (en) * | 2020-05-09 | 2020-07-24 | 南京协心健康科技有限公司 | Chlorine dioxide solution spray and preparation method thereof |
| CN113207903A (en) * | 2021-04-21 | 2021-08-06 | 清远海贝生物技术有限公司 | Chlorine dioxide effervescent tablet and preparation method and application thereof |
| CN114027319A (en) * | 2021-12-15 | 2022-02-11 | 佛山市南海东方澳龙制药有限公司 | Chlorine dioxide disinfectant and preparation method thereof |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101755732A (en) * | 2009-11-09 | 2010-06-30 | 张家口市净宇天成化工有限公司 | Composite solid activating agent of novel stable chlorine dioxide solution |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1023205C (en) * | 1989-06-23 | 1993-12-22 | 栾和林 | Preparation method of chlorine dioxide and control box |
| CN1138948A (en) * | 1995-06-29 | 1997-01-01 | 叶中良 | Mildew preventing method of grains |
| CN1209970C (en) * | 2003-03-28 | 2005-07-13 | 河北科技大学 | Solid stable chlorinedioxide antiseptics and preparation thereof |
-
2006
- 2006-12-06 CN CNB2006101022304A patent/CN100391343C/en not_active Expired - Fee Related
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101143225B (en) * | 2007-10-17 | 2010-07-28 | 艾雪莉 | Air purifying agent and its preparing process |
| CN101595891B (en) * | 2008-06-05 | 2012-09-05 | 廖伟凯 | Chlorine dioxide composition with selective antioxidation |
| US8992831B2 (en) | 2009-09-25 | 2015-03-31 | E. I. Du Pont De Nemours And Company | Stabilized chlorine dioxide to preserve carbohydrate feedstocks |
| US9504710B2 (en) | 2009-09-25 | 2016-11-29 | E I Du Pont De Nemours And Company | Stabilized chlorine dioxide to preserve carbohydrate feedstocks |
| CN106367230A (en) * | 2015-07-20 | 2017-02-01 | 修建东 | Reverse osmosis membrane acid sterilizing scale removing powder solid cleaning agent |
| CN106489931A (en) * | 2016-09-08 | 2017-03-15 | 天津博锐开元环保科技有限公司 | It is used as sodium chlorite gel and its preparation technology of disinfectant |
| CN107593762A (en) * | 2017-09-29 | 2018-01-19 | 广州闪电生物科技有限公司 | A kind of antiseptic solution and sterilization method |
| CN107691471A (en) * | 2017-09-29 | 2018-02-16 | 广州闪电生物科技有限公司 | Antiseptic solution and sterilization method |
| CN107593762B (en) * | 2017-09-29 | 2020-10-27 | 广州闪电生物科技有限公司 | Disinfecting solution and disinfecting method |
| CN111436456A (en) * | 2020-05-09 | 2020-07-24 | 南京协心健康科技有限公司 | Chlorine dioxide solution spray and preparation method thereof |
| CN113207903A (en) * | 2021-04-21 | 2021-08-06 | 清远海贝生物技术有限公司 | Chlorine dioxide effervescent tablet and preparation method and application thereof |
| CN114027319A (en) * | 2021-12-15 | 2022-02-11 | 佛山市南海东方澳龙制药有限公司 | Chlorine dioxide disinfectant and preparation method thereof |
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| Publication number | Publication date |
|---|---|
| CN100391343C (en) | 2008-06-04 |
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Granted publication date: 20080604 Termination date: 20101206 |