JP3252000B2 - Urinary stone inhibitor and method for urinary stone prevention - Google Patents

Urinary stone inhibitor and method for urinary stone prevention

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Publication number
JP3252000B2
JP3252000B2 JP03123893A JP3123893A JP3252000B2 JP 3252000 B2 JP3252000 B2 JP 3252000B2 JP 03123893 A JP03123893 A JP 03123893A JP 3123893 A JP3123893 A JP 3123893A JP 3252000 B2 JP3252000 B2 JP 3252000B2
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JP
Japan
Prior art keywords
urinary stone
weight
acid
inhibitor
phosphonic acid
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 - Fee Related
Application number
JP03123893A
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Japanese (ja)
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JPH06218392A (en
Inventor
和樹 高谷
Original Assignee
シントーファイン株式会社
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Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明はトイレの便器や排水管の
スケール防止剤、及び防止方法に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a scale inhibitor for toilets and drainage pipes of toilets, and a method for preventing scale.

【0002】[0002]

【従来の技術】水洗式トイレの普及によりトイレの環境
も改善されてきたが特に男子用トイレの場合、便器およ
び排水管内に溜った尿と洗浄水の混合排水のPHが上昇
することにより、尿中のカルシュウムイオンとリン酸イ
オンが反応して出来るリン酸カルシュウムの溶解性が低
下し、リン酸カルシュウムが有機物と共に便器内や排水
管に析出して尿石となる。一担付着した尿石は簡単に取
れないため、その量は少しずつ多くなり悪臭原因や、排
水管が詰まる原因になる。そのため従来から固体酸、昇
華性物質、界面活性剤、キレート剤からなる成形体を便
器内へ設置し、洗浄水中のPHを5.0〜8.5に抑制
する方法や前記方法に金属キレート剤であるNTA(ニ
トリロトリ酢酸)、EDTA(エチレンジアミン四酢
酸)などのアミノポリカルボン酸類、又はそれらのナト
リュウムやアンモニュウム塩等を併用し、尿中のカルシ
ュウムイオンを水可溶性の金属化合物とし、尿石の溶解
性を高める方法等が提案されている。
2. Description of the Related Art With the spread of flush toilets, the environment of toilets has been improved. In particular, in the case of men's toilets, the pH of urine and washing water mixed in a toilet and a drainpipe rises, resulting in an increase in urine. The solubility of calcium phosphate formed by the reaction of calcium ions and phosphate ions in the inside decreases, and calcium phosphate precipitates together with organic substances in toilets and drain pipes to form urine stone. Since the urine stones that have adhered to them cannot be easily removed, their amount gradually increases, causing odors and clogging of drain pipes. For this reason, conventionally, a molded body composed of a solid acid, a sublimable substance, a surfactant, and a chelating agent has been installed in a toilet bowl, and a method of suppressing the pH of washing water to 5.0 to 8.5 or a metal chelating agent by the method described above. Aminopolycarboxylic acids such as NTA (Nitrilotriacetic acid) and EDTA (Ethylenediaminetetraacetic acid), or their sodium and ammonium salts, etc. are used in combination to convert calcium ions in urine into water-soluble metal compounds and dissolve uroliths There have been proposed methods and the like for improving the performance.

【0003】[0003]

【発明が解決しようとする課題】しかしながらPHを抑
制する固体酸の錠剤を便器の中に置いて洗浄水で有効成
分を溶解することによるPHを抑制する方法の場合、例
えば水溶性の酸性物質(スルファミン酸)、昇華性物質
(パラジクロルベンゼン)、非イオン系界面活性剤から
なる男子用便器の尿石防止剤の有効濃度は400〜50
0ppmでありそれ以下になると効果は著しく低下す
る。従って1箇(80〜100g)又は、2箇(約50
g/1箇)の錠剤を設置し、1回の洗浄水全量4〜5リ
ットルを流してその液のPHを制御することによる尿石
防止機能は充分ではない。また、金属キレート剤、例え
ばEDTA等ポリアミノカルボン酸類の併用も有効であ
るが、1回の溶出量を400〜500ppmにしなけれ
ばならないため、錠剤中の含有量を極端に多くしなけれ
ば有効期間が短くなる。また、溶出量が400〜500
ppm以上になると、浄化槽の活性汚泥菌への悪影響が
ある等の問題がある。
However, in the case of a method of suppressing PH by placing a tablet of a solid acid that suppresses PH in a toilet bowl and dissolving the active ingredient with washing water, for example, a water-soluble acidic substance ( Sulfamic acid), a sublimable substance (paradichlorobenzene), and a non-ionic surfactant, the effective concentration of the urinary stone inhibitor in a urinal for men is 400 to 50.
When the content is 0 ppm or less, the effect is significantly reduced. Therefore, one (80-100 g) or two (about 50 g)
g / 1 tablet), and the urine stone prevention function by controlling the pH of the liquid by flowing a total of 4 to 5 liters of washing water at one time is not sufficient. Further, a combination use of a metal chelating agent, for example, a polyaminocarboxylic acid such as EDTA is also effective. However, since the dissolution amount at one time must be 400 to 500 ppm, the effective period is required unless the content in the tablet is extremely increased. Be shorter. In addition, the elution amount is 400 to 500
If the amount is not less than ppm, there is a problem that the activated sludge in the septic tank is adversely affected.

【0004】[0004]

【課題を解決するための手段】本発明者は、前記問題点
を解決すべく鋭意研究の結果、従来の酸によりPHを抑
制する方法および金属キレートによる溶解性を向上させ
る方法とは全く作用機構が異なるスレシュホールド効果
により尿石の付着を防止する方法を見出した。すなわ
ち、ホスホン酸、ホスホン酸のアルキル金属塩又は、ホ
スホン酸のアンモニュウム塩は加水分解に対する安定性
が良く、カルシュウムなどの過飽和溶液からの沈澱が化
学等量以下のインヒビターによって防止されるスレシュ
ホールド効果が大きいことを見出した。すなわち、カル
シュウムイオン濃度に対し化学等量的にはるかに少ない
濃度でリン酸カルシュウムを主体とする尿石の付着を防
止しようとするものであり、カルシュウムイオン濃度に
対し有効成分を化学等量的に低い濃度で用い、スレシュ
ホールド効果により一担生成する沈澱の生成速度を著し
く抑制し、さらに沈澱の結晶構造に歪を与えることによ
り、尿石付着を防止しようとするものである。本発明は
ホスホン酸及び/又はホスホン酸のアルキル金属塩及び
/又は、ホスホン酸のアンモニュウム塩を有効成分とし
て含有する尿石防止剤およびこの尿石防止剤を便器内に
添加又は設置する尿石防止方法である。本発明の有効成
分であるホスホン酸、ホスホン酸のアルキル金属塩又
は、ホスホン酸のアンモニュウム塩としては、アミノト
リ(メチレンホスホン酸)、1−ヒドロキシエチリデン
−1,1−ジホスホン酸、エチレンジアミンテトラ(メ
チレンホスホン酸)、ジエイレントリアミンペンタ(メ
チレンホスホン酸)などであるが、これらのみに限定さ
れるものではない。
Means for Solving the Problems The present inventor has made intensive studies to solve the above problems, and as a result, the mechanism of action is completely different from the conventional method of suppressing PH with an acid and improving the solubility with a metal chelate. Found a method of preventing the adhesion of urinary stones by different threshold effects. That is, phosphonic acid, an alkyl metal salt of phosphonic acid, or an ammonium salt of phosphonic acid have good stability against hydrolysis, and have a threshold effect in which precipitation from a supersaturated solution such as calcium is prevented by a chemical equivalent or less of an inhibitor. I found it great. In other words, it is intended to prevent the adhesion of uric stone mainly composed of calcium phosphate at a concentration much smaller than the calcium ion concentration in a stoichiometrically equivalent manner. When used at a low concentration, the rate of formation of the precipitate formed by the threshold effect is remarkably suppressed, and the crystal structure of the precipitate is distorted to prevent the adhesion of urolith. The present invention relates to a uremic inhibitor containing a phosphonic acid and / or an alkyl metal salt of a phosphonic acid and / or an ammonium salt of a phosphonic acid as an active ingredient, and a urolith preventer in which the urolith inhibitor is added or installed in a toilet bowl. Is the way. Examples of the phosphonic acid, an alkyl metal salt of the phosphonic acid, or an ammonium salt of the phosphonic acid which are the active ingredients of the present invention include aminotri (methylenephosphonic acid), 1-hydroxyethylidene-1,1-diphosphonic acid, ethylenediaminetetra (methylenephosphonic acid). Acid), diylenetriaminepenta (methylenephosphonic acid), and the like, but are not limited thereto.

【0005】有効成分を便器内に一定濃度になるよう流
す方法としては、有効成分を常法により固形にした尿石
防止剤を便器内に設置し洗浄水で溶解する方法と、液体
状の有効成分を水溶液とした尿石防止剤とし、これを自
動添加装置で洗浄水中の濃度が一定になるよう添加する
方法がある。固形状の尿石防止剤は有効成分を10〜9
5重量%、好ましくは70〜30重量%、パラジクロル
ベンゼン、トリアルキルトリオキ酸(炭素数3〜6のア
ルキル基)などの昇華性物質を10〜90重量%、好ま
しくは70〜30重量%、非イオン系界面活性剤(HL
B12〜20)5〜50重量%、好ましくは50〜30
重量%含有するのが望ましい。その他必要に応じ香料、
着色剤、成形付与剤などを添加する事が出来る。またホ
スホン酸の水溶性を良くする目的で少量のアルカリ性物
質を添加する事もできる。また、非イオン系界面活性剤
のかわりにポリエチレングリコールを用いてもよい。本
発明においては、1回の洗浄水中の有効成分濃度が1〜
100ppmになるよう昇華性物質、水溶性物質、その
他添加剤の量を調整すればよいため、固形化のための割
合は記述内容のみに限定されるものではない。水溶液の
尿石防止剤は、ホスホン酸、及びそのアルキル金属塩又
はアンモニウム塩の一定高濃度水溶液にするのみで使用
することができるが、その濃度はトイレに設置した添加
装置の添加量調整機能、洗浄水量などをもとに、洗浄水
中の有効成分濃度が1〜100ppmになるように変え
ることが出来る。また、清涼感、清潔感を与える目的で
必要に応じ香料、着色剤を添加することが望ましい。
[0005] As a method of flowing the active ingredient into the toilet so as to have a constant concentration, there are a method of disposing the active ingredient solidified by a usual method in a toilet bowl and dissolving the same with washing water. There is a method in which a component is used as an aqueous solution of a urinary stone inhibitor, and this is added by an automatic addition device so that the concentration in the washing water becomes constant. Solid urinary stone inhibitors contain 10-9 active ingredients
5% by weight, preferably 70 to 30% by weight, 10 to 90% by weight, preferably 70 to 30% by weight of a sublimable substance such as paradichlorobenzene, trialkyltrioxoic acid (an alkyl group having 3 to 6 carbon atoms). , Nonionic surfactants (HL
B12-20) 5-50% by weight, preferably 50-30% by weight
It is desirable to contain by weight. Other perfume as needed,
A coloring agent, a forming agent and the like can be added. Also, a small amount of an alkaline substance can be added for the purpose of improving the water solubility of the phosphonic acid. Further, polyethylene glycol may be used instead of the nonionic surfactant. In the present invention, the concentration of the active ingredient in one wash water is 1 to
Since the amounts of the sublimable substance, the water-soluble substance, and other additives may be adjusted to 100 ppm, the ratio for solidification is not limited to the description. The urinary stone inhibitor of the aqueous solution can be used only by making it a constant high-concentration aqueous solution of phosphonic acid, and its alkyl metal salt or ammonium salt. The concentration of the active ingredient in the washing water can be changed so as to be 1 to 100 ppm based on the washing water amount and the like. In addition, it is desirable to add a fragrance and a coloring agent as needed for the purpose of giving a refreshing feeling and a clean feeling.

【0006】[0006]

【実施例】【Example】

(実施例1〜6、比較例1〜8)新鮮な尿を、尿約20
0ミリリットル(1人1回分の量)に対し、水道水約2
リットル(1回の洗浄水量)の割合で希釈したものを、
140ミリリットルのガラスビンに100ミリリットル
入れ表1のとおりそれぞれの有効成分を各濃度になるよ
う添加し、24時間ごとに液を入れ換える操作を1ケ月
繰り返し、試験前後のビンの重量変化を調べた。その結
果は表1のとおりホスホン酸、及びそれらのナトリュウ
ム塩及びアンモニウム塩は低濃度でも優れた効果を示し
た。
(Examples 1 to 6 and Comparative Examples 1 to 8)
0 ml (per person), about 2 tap water
What was diluted at the rate of liter (one washing water amount)
An operation of adding 100 ml into a 140 ml glass bottle, adding each active ingredient to each concentration as shown in Table 1, and replacing the solution every 24 hours was repeated for one month, and the weight change of the bottle before and after the test was examined. As a result, as shown in Table 1, phosphonic acids and their sodium salts and ammonium salts showed excellent effects even at low concentrations.

【0007】[0007]

【表1】 [Table 1]

【0008】(注1)いずれの成分も200ppm以下
の濃度では添加前後でPH変化はなかった。また、貯蔵
前後のPH変化は各試料共同じ傾向であった。 (注2)ビンに付着した成分と、実際の尿石を赤外分光
分析、及びケイ光X線分析を行い比較したところ、殆ど
同じであった。 (注3)評価基準(尿石付着重量/mmg) ◎:5以下 ○:6〜10 △:11〜20
×:21以上
(Note 1) At any concentration of 200 ppm or less, there was no change in pH before and after the addition of each component. The pH change before and after storage had the same tendency in each sample. (Note 2) Infrared spectroscopic analysis and fluorescent X-ray analysis were performed on the components adhering to the bottle and the actual urine stone, and the results were almost the same. (Note 3) Evaluation criteria (weight of urinary calculus / mmg) :: 5 or less ○: 6 to 10 △: 11 to 20
×: 21 or more

【0009】実施例7 エチレンジアミンテトラ(メチレンホスホン酸)50重
量部、ポリエチレングリコール(分子量6000)10
重量部、パラジクロルベンゼン40重量部を粉砕混合し
たもの80gを加圧成形し、直径50mmの半円柱状の
成形体を作成した。 実施例8 エチレンジアミンテトラ(メチレンホスホン酸)50重
量部、非イオン系界面活性剤(HLB18.5)10重
量部、パラジクロルベンゼン40重量部を粉砕混合した
もの80gを加圧成形し、直径50mmの半円柱状の成
形体を作成した。 実施例9 エチレンジアミンテトラ(メチレンホスホン酸)50重
量部、非イオン系界面活性剤7重量部、ステアリルアル
コール3重量部、パラジクロルベンゼン40重量部を粉
砕混合したもの80gを加圧成形し直径50mmの半円
柱状の成形体を作成した。 実施例10 エチレンジアミンテトラ(メチレンホスホン酸)50重
量部、トリアルキルトリオキ酸(アルキル基の炭素数
3)38重量部、ステアリン酸カルシュウム2重量部を
粉砕混合したもの80gを加圧成形し、直径50mmの
半円柱状の成形体を作成した。 比較例9 スルファミン酸を有効成分として含有する市販品成形
体。
Example 7 50 parts by weight of ethylenediaminetetra (methylenephosphonic acid), 10 of polyethylene glycol (molecular weight: 6000)
80 g of a mixture obtained by pulverizing and mixing 40 parts by weight of p-dichlorobenzene and 40 parts by weight of p-dichlorobenzene was subjected to pressure molding to prepare a semi-cylindrical molded body having a diameter of 50 mm. Example 8 50 g of ethylenediaminetetra (methylenephosphonic acid), 10 parts by weight of a nonionic surfactant (HLB 18.5), and 40 parts by weight of paradichlorobenzene were pulverized and mixed. A semi-cylindrical shaped body was prepared. Example 9 80 g of a mixture obtained by pulverizing and mixing 50 parts by weight of ethylenediaminetetra (methylenephosphonic acid), 7 parts by weight of a nonionic surfactant, 3 parts by weight of stearyl alcohol, and 40 parts by weight of p-dichlorobenzene was subjected to pressure molding to form a powder having a diameter of 50 mm. A semi-cylindrical shaped body was prepared. Example 10 80 g of a mixture obtained by pulverizing and mixing 50 parts by weight of ethylenediaminetetra (methylenephosphonic acid), 38 parts by weight of trialkyltrioxoic acid (the number of carbon atoms in the alkyl group is 3) and 2 parts by weight of calcium stearate was subjected to pressure molding. A 50 mm semi-cylindrical shaped body was prepared. Comparative Example 9 A commercially available molded article containing sulfamic acid as an active ingredient.

【0010】実施例7〜10の各サンプル1箇(80
g)に対し水道水4リットルを20秒流し、その水を均
一に攪拌後リン酸イオン濃度を測定して溶解性を調べ
た。その結果表2のとおり、有効成分目標濃度10pp
m以上溶解していた。
Each sample of Examples 7 to 10 (80
g), 4 liters of tap water was allowed to flow for 20 seconds, the water was stirred uniformly, and the phosphate ion concentration was measured to examine the solubility. As a result, as shown in Table 2, the active ingredient target concentration was 10 pp.
m or more.

【0011】[0011]

【表2】 [Table 2]

【0012】各実施例および比較例の尿石防止剤で1日
当たり約50人が使用する男子用トイレで約3ケ月間尿
石付着量をテストした。その結果は表3に示すとおりで
実施例のものは極めて少ない付着量であった。なお、固
形成形体のものは2週間ごとに新しいものと取り替え
た。液状のものについては、それぞれ有効成分の1重量
%水溶液を作り、自動添加装置で洗浄水の有効成分濃度
が10ppmになるよう設定した。尿石付着量は、30
メッシュステンレス製円筒状金網(7×10cm)をト
イレ洗浄水の溜水部に設置し、約3ケ月後に取り出し、
流水で簡単に洗浄し乾燥後の重量増加量を尿石付着量と
した。
The urinary stone deposits of each Example and Comparative Example were tested for about 3 months in a men's toilet used by about 50 people per day for about 3 months. The results are as shown in Table 3, and those of the examples had an extremely small amount of adhesion. The solid molded product was replaced with a new one every two weeks. For the liquid, a 1% by weight aqueous solution of the active ingredient was prepared, and the concentration of the active ingredient in the washing water was set to 10 ppm by an automatic addition device. Urinary stone adhesion is 30
A mesh stainless steel wire mesh (7 × 10 cm) was placed in the basin of the toilet flushing water and taken out after about 3 months.
The amount of weight increase after washing and drying with running water was defined as the urinary stone adhesion amount.

【0013】[0013]

【表3】 [Table 3]

【0014】[0014]

【発明の効果】本発明の尿石防止剤は従来の尿石防止剤
の約10倍以上も効果がある。また、ホスホン酸、及び
そのアルキル金属塩又はアンモニウム塩は防錆作用があ
るため、洗浄水の排水管の腐食の心配も無くなる。従っ
て本発明による経済的、公衆衛生的意義は大きい。
EFFECT OF THE INVENTION The urinary stone inhibitor of the present invention is about 10 times more effective than the conventional urinary stone inhibitor. Further, since phosphonic acid and its alkyl metal salt or ammonium salt have a rust preventive action, there is no need to worry about corrosion of the drainage pipe of the washing water. Therefore, the present invention has great economic and public health significance.

Claims (2)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 ホスホン酸及び/又はホスホン酸のアル
キル金属塩及び/又は、ホスホン酸のアンモニュウム塩
を有効成分として含有する尿石防止剤。
1. A urinary stone inhibitor comprising phosphonic acid and / or an alkyl metal salt of phosphonic acid and / or an ammonium salt of phosphonic acid as an active ingredient.
【請求項2】 請求項1記載の尿石防止剤を便器内に添
加又は設置する尿石防止方法。
2. A method for preventing or preventing urine, which comprises adding or installing the urinary stone inhibitor according to claim 1 in a toilet bowl.
JP03123893A 1993-01-26 1993-01-26 Urinary stone inhibitor and method for urinary stone prevention Expired - Fee Related JP3252000B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
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Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP03123893A JP3252000B2 (en) 1993-01-26 1993-01-26 Urinary stone inhibitor and method for urinary stone prevention

Publications (2)

Publication Number Publication Date
JPH06218392A JPH06218392A (en) 1994-08-09
JP3252000B2 true JP3252000B2 (en) 2002-01-28

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Country Status (1)

Country Link
JP (1) JP3252000B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW272244B (en) 1994-08-19 1996-03-11 Toto Ltd
KR101591614B1 (en) * 2011-10-19 2016-02-18 닛뽕소다 가부시키가이샤 Protectant against urinary calculi

Also Published As

Publication number Publication date
JPH06218392A (en) 1994-08-09

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