JPS5850793B2 - How to dissolve solid chlorine agent - Google Patents
How to dissolve solid chlorine agentInfo
- Publication number
- JPS5850793B2 JPS5850793B2 JP3808380A JP3808380A JPS5850793B2 JP S5850793 B2 JPS5850793 B2 JP S5850793B2 JP 3808380 A JP3808380 A JP 3808380A JP 3808380 A JP3808380 A JP 3808380A JP S5850793 B2 JPS5850793 B2 JP S5850793B2
- Authority
- JP
- Japan
- Prior art keywords
- chlorine
- tablets
- solid chlorine
- drug solution
- chlorine agent
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 title claims description 33
- 239000000460 chlorine Substances 0.000 title claims description 33
- 229910052801 chlorine Inorganic materials 0.000 title claims description 33
- 239000007787 solid Substances 0.000 title claims description 12
- 239000003795 chemical substances by application Substances 0.000 title claims description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 21
- 239000003814 drug Substances 0.000 claims description 19
- 229940079593 drug Drugs 0.000 claims description 19
- 238000000034 method Methods 0.000 claims description 17
- 239000000126 substance Substances 0.000 claims description 8
- 239000000243 solution Substances 0.000 description 19
- 210000002700 urine Anatomy 0.000 description 13
- 239000002351 wastewater Substances 0.000 description 9
- 238000005406 washing Methods 0.000 description 3
- 230000000249 desinfective effect Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- CEJLBZWIKQJOAT-UHFFFAOYSA-N dichloroisocyanuric acid Chemical compound ClN1C(=O)NC(=O)N(Cl)C1=O CEJLBZWIKQJOAT-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 230000001954 sterilising effect Effects 0.000 description 2
- 238000004659 sterilization and disinfection Methods 0.000 description 2
- YRIZYWQGELRKNT-UHFFFAOYSA-N 1,3,5-trichloro-1,3,5-triazinane-2,4,6-trione Chemical compound ClN1C(=O)N(Cl)C(=O)N(Cl)C1=O YRIZYWQGELRKNT-UHFFFAOYSA-N 0.000 description 1
- ZKQDCIXGCQPQNV-UHFFFAOYSA-N Calcium hypochlorite Chemical compound [Ca+2].Cl[O-].Cl[O-] ZKQDCIXGCQPQNV-UHFFFAOYSA-N 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- -1 alkali metal salts Chemical class 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 229950009390 symclosene Drugs 0.000 description 1
Description
【発明の詳細な説明】
本発明は固型塩素剤の溶解方法に関するものであり、そ
の目的とする処は航空機、列車船舶などの使用頻度の高
い水洗便所における採尿の消毒に好適な方法を提供する
ことにある。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for dissolving a solid chlorine agent, and its purpose is to provide a method suitable for disinfecting urine collected in frequently used flush toilets of aircraft, trains, ships, etc. It's about doing.
この種の従来技術としては、例えば特公昭432858
7号公報に記載されているように、垂直状薬筒に固型塩
素剤の錠剤を充填し、その下端開口部において連続的に
流れている汚水と接触する方法あるいは例えば特公昭4
6−31511号公報に記載されているように、採尿あ
るいはその洗滌水に固型塩素剤を直接混合して汚水を消
毒する方法である。As this type of conventional technology, for example, Japanese Patent Publication No. 432858
As described in Publication No. 7, a method in which solid chlorine tablets are filled in a vertical cartridge and comes into contact with continuously flowing wastewater at the opening at the bottom end of the cartridge, or for example,
As described in Japanese Patent No. 6-31511, this is a method of disinfecting wastewater by directly mixing a solid chlorine agent with collected urine or its washing water.
然し乍ら前者の方法にあっては、薬剤に対する接触時間
が瞬時であってほとんどの装置において必要な塩素濃度
に達しないものであり、後者の方法にあっては、汚水の
流量変化に応じて処理液中の塩素濃度に極端なバラツキ
を生じていづれも完全な殺菌消毒を期待できない。However, in the former method, the contact time with the chemical is instantaneous, and most equipment does not reach the required chlorine concentration, whereas in the latter method, the treatment liquid is adjusted according to changes in the flow rate of wastewater. Complete sterilization cannot be expected due to extreme variations in the chlorine concentration inside.
本発明者等はこのような事情に鑑み、乗物などの使用頻
度の高い水洗便所の採尿消毒を完全に実施しつる方法を
鋭意検討の結果、垂直状薬筒の下端部に水溜室を設けて
これに薬剤溶解液を間歇的に供給し、薬筒に活性塩素を
放出しうる固型塩素剤からなる錠剤を複数個充填し、水
溜室に供給の薬剤溶解液とこれに接する錠剤の重量比を
1:1〜100割合として薬液を形成し、これを乗物等
の採尿汚水に混合させることによって所期の目的を達成
しうろことを認めた。In view of these circumstances, the inventors of the present invention conducted extensive research into a method to completely sterilize urine collection in flush toilets that are frequently used in vehicles, etc., and as a result, created a water storage chamber at the bottom end of the vertical cartridge. A drug solution is intermittently supplied to this, a plurality of tablets made of a solid chlorine agent capable of releasing active chlorine are filled into the cartridge, and the weight ratio of the drug solution supplied to the water reservoir and the tablets in contact with it is It has been found that the intended purpose can be achieved by forming a medicinal solution at a ratio of 1:1 to 100 and mixing this with urine collected from vehicles, etc.
本発明方法によれば、薬筒の下端部に水溜室を設け、こ
れに薬剤溶解液を固型塩素錠剤に対し1〜1/10倍の
割合で間歇的に供給して薬筒内の固型塩素錠剤を溶解し
たものであるから、水溜室において薬剤溶解液を約5〜
15分間停溜させることによって固型塩素剤の飽和溶液
が形成され、これ以上薬剤溶解液を水溜室に留めても最
早塩素濃度の変化は生じないため、常に数千ppmの所
定塩素濃度の薬液が水溜室の大きさに応じて一定量づつ
得られるものであり、水洗便所の使用の都度水溜室内の
薬液を採尿汚水と混合し常に採尿汚水の要求塩素量に見
合う活性塩素を供給して完壁な殺菌消毒を行なうことが
できる。According to the method of the present invention, a water storage chamber is provided at the lower end of the cartridge, and a drug solution is intermittently supplied to this chamber at a ratio of 1 to 1/10 times the solid chlorine tablet. Since it is made by dissolving a type of chlorine tablet, the drug solution is poured into the water reservoir for about 5 to 50 minutes.
A saturated solution of solid chlorine agent is formed by standing for 15 minutes, and the chlorine concentration will no longer change even if the chemical solution is left in the reservoir chamber any longer, so the chemical solution always has a predetermined chlorine concentration of several thousand ppm. A certain amount of chlorine is obtained depending on the size of the water storage chamber, and each time the flush toilet is used, the chemical solution in the water storage chamber is mixed with collected urine wastewater to constantly supply active chlorine that matches the amount of chlorine required by the collected urine wastewater. Walls can be sterilized and disinfected.
本発明において使用し5る固型塩素剤は、次亜塩素酸カ
ルシウム、トリクロロイソシアヌル酸、ジクロロイソシ
アヌル酸及びそのアルカリ金属塩が代表的なものであり
、粉末状または粒状物を打錠圧500 kg/i以上を
もってタブレット化すれば良い。Typical solid chlorine agents used in the present invention are calcium hypochlorite, trichloroisocyanuric acid, dichloroisocyanuric acid, and their alkali metal salts, and powder or granules are compressed under a tableting pressure of 500 kg. /i or higher to make it into a tablet.
本発明方法の実施に当っては、第1図ないし第2図に示
したように垂直状薬筒1の下端部に縦長状のスリット2
,2・・・・・・を形成し、該薬筒1の側壁部に足踏ペ
ダル等の作動によって一定量の薬剤溶解液が供給される
導水口3を有し、下端部に縦溝4を穿設して薬筒より径
の犬なる外筒5を介在し、且つ外筒5の縦溝4の外周部
に傾斜状スリット6を有する鞘筒7を嵌合し、外筒5の
縦溝4と鞘筒7のスリット6の交差する位置を適宜な位
置に変化して薬筒内の錠剤8,8・・・・・・と水溜室
9内の薬剤溶解液の浸漬量を加減することができ、薬剤
溶解液とこれに接する錠剤の重量比が1:1を超えると
その供給間隔に時間的バラツキを生じた際には錠剤の過
度な溶解を生じ経済的でないのみならず循環式便所など
における貯水タンクの容量を増加して乗物等の消毒装置
として不向であり、逆に薬剤溶解液とこれに接する錠剤
の重量比が1:10より少ない場合には処理すべき採尿
汚水の要求塩素量に見合う量の薬液を形成することがで
きない。In carrying out the method of the present invention, as shown in FIGS.
, 2 . A sheath cylinder 7 having an inclined slit 6 is fitted to the outer periphery of the longitudinal groove 4 of the outer cylinder 5, and a sheath cylinder 7 having an inclined slit 6 is fitted to the outer circumference of the longitudinal groove 4 of the outer cylinder 5. The intersecting position of the groove 4 and the slit 6 of the sheath cylinder 7 is changed to an appropriate position to adjust the amount of immersion of the tablets 8, 8, etc. in the cartridge and the drug solution in the water reservoir 9. However, if the weight ratio of the drug solution and the tablets in contact with it exceeds 1:1, if there is a time variation in the supply interval, the tablets may be excessively dissolved, which is not only uneconomical but also requires a circulating system. It is not suitable for use as a sterilization device for vehicles, etc. by increasing the capacity of water storage tanks in toilets, etc. On the other hand, if the weight ratio of the drug solution and the tablets in contact with it is less than 1:10, the collected urine wastewater that should be treated is It is not possible to form a chemical solution in an amount corresponding to the required amount of chlorine.
本発明方法によって得られる数千ppm の塩素濃度を
有する薬剤は、採尿あるいは採尿とその洗滌水の混合液
に通常約200 ppm 以上の必要塩素量を供給しう
る割合で混合されるものである。The drug having a chlorine concentration of several thousand ppm obtained by the method of the present invention is mixed with the urine collection or a mixture of the urine collection and its washing water in a proportion capable of supplying the required amount of chlorine, usually about 200 ppm or more.
第3図は貯留型水洗便所に本発明方法を適応した例を示
す系統図であり、便器11に排泄された採尿は、水タン
ク10からの洗滌水によって固液分離機12に送られ、
固形物と分離された採尿汚水は貯留槽13に導かれ、他
方水タンク10から導かれた洗滌水の一部は、第1図な
いし第2図に示された構成を有する薬剤溶解装置14に
送られ、高塩素濃度の薬液として間歇的に貯留槽13に
送られ、消毒された採尿汚水は貯留槽13から適宜放流
されるものである。FIG. 3 is a system diagram showing an example in which the method of the present invention is applied to a storage type flush toilet, in which collected urine excreted into the toilet bowl 11 is sent to the solid-liquid separator 12 by flushing water from the water tank 10.
The collected urine wastewater separated from the solids is led to a storage tank 13, while a part of the washing water led from the water tank 10 is sent to a drug dissolving device 14 having the configuration shown in FIGS. 1 and 2. The collected urine wastewater is intermittently sent to the storage tank 13 as a chemical solution with a high chlorine concentration, and the sterilized collected urine wastewater is discharged from the storage tank 13 as appropriate.
以下実施例をもって本発明方法を具体的に説明する。The method of the present invention will be specifically explained below with reference to Examples.
実施例 1
薬筒1に顆粒状ジクロロイソシアヌル酸ナトリウムを面
圧約1000kg/−の圧力で打錠した直径30關、厚
さ10mm、重さ15rの錠剤8,8・・・・・・を複
数個整列して充填し、水溜室9における18℃の薬剤溶
解液と水に浸漬の錠剤2,2・・・・・・の重量比を約
1:2.5として水溜室内における薬液塩素濃度の経時
変化を測定したところ、その結果は第1表の通りであっ
た。Example 1 A plurality of tablets 8, 8, having a diameter of 30 mm, a thickness of 10 mm, and a weight of 15 r were compressed from granular sodium dichloroisocyanurate at a surface pressure of approximately 1000 kg/- in a cartridge 1. The drug solution chlorine concentration in the water reservoir chamber 9 was filled in a row, and the weight ratio of the drug solution at 18 °C and the tablets 2, 2, etc. immersed in water was approximately 1:2.5, and the chlorine concentration of the drug solution in the water reservoir chamber 9 was determined over time. When the changes were measured, the results were as shown in Table 1.
ごれらの試験によって本発明方法によれば約5〜15分
間で数千ppm 高塩素濃度の薬剤が形成されそれ以
上の長時間においても薬剤の塩素濃度はほとんど変わら
ないことが認められた。According to the test conducted by Goret et al., it was found that according to the method of the present invention, a drug with a high chlorine concentration of several thousand ppm was formed in about 5 to 15 minutes, and that the chlorine concentration of the drug hardly changed even after a longer period of time.
実施例 2
実施例1において、導水口3を通じて水溜室9に夫々7
5m1の薬剤溶解液を10分毎に供給し、水溜室9から
その都度溢流する薬液の塩素濃度を測定したところ、そ
の結果は第2表の通りであった。Embodiment 2 In Embodiment 1, each of
When 5 ml of drug solution was supplied every 10 minutes and the chlorine concentration of the drug solution overflowing from the water storage chamber 9 was measured each time, the results were as shown in Table 2.
これらの試験によって本発明方法によれば、極めて短時
間のうちには文一定した塩素濃度の薬液を定量的に形成
しうるものと認められた。These tests confirmed that the method of the present invention makes it possible to quantitatively form a chemical solution with a constant chlorine concentration within an extremely short period of time.
第1図は本発明方法の実施に適する薬剤溶解装置を示す
一部欠截縦断面図、第2図は同じく要部を示す斜視図、
第3図は本発明方法を貯留型水洗便所に応用した一例を
示す系統図であり、図中1は薬筒、2はスリット、3は
導水口、4は縦溝、5は外筒、6はスリット、7は鞘筒
、8は錠剤、9は水溜室を表わす。FIG. 1 is a partially cutaway vertical cross-sectional view showing a drug dissolving device suitable for carrying out the method of the present invention, and FIG. 2 is a perspective view similarly showing the main parts.
FIG. 3 is a system diagram showing an example of applying the method of the present invention to a storage type flush toilet. In the figure, 1 is a cartridge, 2 is a slit, 3 is a water inlet, 4 is a vertical groove, 5 is an outer cylinder, and 6 7 represents a slit, 7 represents a sheath cylinder, 8 represents a tablet, and 9 represents a water reservoir chamber.
Claims (1)
解液を間歇的に供給し、薬筒に活性塩素を放出しうる固
型塩素剤からなる錠剤を複数個充填し水溜室に供給の薬
剤溶解液とこれに接する錠剤の重量比を1:1〜100
割合として短時間のうちに所定の塩素濃度を有する薬液
を形成することを特徴とする固型塩素剤の溶解方法。1. A water reservoir is provided at the lower end of the vertical cartridge, a drug solution is intermittently supplied to this chamber, and a plurality of tablets made of a solid chlorine agent capable of releasing active chlorine are filled into the cartridge, and the reservoir chamber is filled with a plurality of tablets made of a solid chlorine agent capable of releasing active chlorine. The weight ratio of the supplied drug solution and the tablets in contact with it is 1:1 to 100.
A method for dissolving a solid chlorine agent, characterized by forming a chemical solution having a predetermined chlorine concentration in a relatively short period of time.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3808380A JPS5850793B2 (en) | 1980-03-24 | 1980-03-24 | How to dissolve solid chlorine agent |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3808380A JPS5850793B2 (en) | 1980-03-24 | 1980-03-24 | How to dissolve solid chlorine agent |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS56133092A JPS56133092A (en) | 1981-10-17 |
| JPS5850793B2 true JPS5850793B2 (en) | 1983-11-12 |
Family
ID=12515576
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3808380A Expired JPS5850793B2 (en) | 1980-03-24 | 1980-03-24 | How to dissolve solid chlorine agent |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5850793B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100354609B1 (en) * | 2000-06-29 | 2002-09-30 | 글로벌에너지텍주식회사 | The chlorine inputing machine to ch;orine disinfact in case simple water works |
-
1980
- 1980-03-24 JP JP3808380A patent/JPS5850793B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS56133092A (en) | 1981-10-17 |
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