JPS6310786B2 - - Google Patents

Info

Publication number
JPS6310786B2
JPS6310786B2 JP4755280A JP4755280A JPS6310786B2 JP S6310786 B2 JPS6310786 B2 JP S6310786B2 JP 4755280 A JP4755280 A JP 4755280A JP 4755280 A JP4755280 A JP 4755280A JP S6310786 B2 JPS6310786 B2 JP S6310786B2
Authority
JP
Japan
Prior art keywords
hardness
water
triethanolamine
raw water
weight
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
Application number
JP4755280A
Other languages
Japanese (ja)
Other versions
JPS56143954A (en
Inventor
Zenichi Nishi
Tomoji Terada
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
TOZAI KOGYO KK
Original Assignee
TOZAI KOGYO KK
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by TOZAI KOGYO KK filed Critical TOZAI KOGYO KK
Priority to JP4755280A priority Critical patent/JPS56143954A/en
Publication of JPS56143954A publication Critical patent/JPS56143954A/en
Publication of JPS6310786B2 publication Critical patent/JPS6310786B2/ja
Granted legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/18Water
    • G01N33/1853Hardness of water

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Food Science & Technology (AREA)
  • Medicinal Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Pathology (AREA)
  • Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)

Description

【発明の詳細な説明】 本発明は、自然水、水道水によつて製造された
軟水や、汽缶のブロー水等に対し、それが所望硬
度を有しているかどうかを判定する水の硬度判定
薬に関する。
Detailed Description of the Invention The present invention provides a water hardness determination method for determining whether or not soft water produced from natural water, tap water, blown water from steam cans, etc. has a desired hardness. Regarding medicine.

水の硬度判定において判定対象である原水中に
投入されるエリオクロムブラツクT、カルコン、
N−N指示薬等の呈色指示薬は、原水のPH値が一
定範囲内にあるときにのみ、硬度成分の有無によ
る色相変化を生じる性質があり、又、定量分析時
において呈色指示薬を投入した原水中に投入して
硬度成分と反応させるエチレンジアミンテトラア
セチツクアシツド等のキレート剤は、硬度成分だ
けでなく、原水中に含まれる鉄イオン等とも反応
し易く、呈色指示薬の色相が変化するまでキレー
ト剤を滴定し、このキレート剤の滴定量をもつて
硬度を判定する関係上、鉄イオン等がキレート剤
と反応しないようにいんぺいしておく必要があ
る。
Eriochrome Black T, Chalcon, which is added to the raw water that is the target of water hardness determination.
Color-forming indicators such as N-N indicators have the property of causing a hue change depending on the presence or absence of hardness components only when the pH value of the raw water is within a certain range. Chelating agents such as ethylenediaminetetraacetic acid that are added to raw water to react with hardness components tend to react not only with hardness components but also with iron ions contained in raw water, causing a change in the hue of the color indicator. Since the chelating agent is titrated to 100% and the hardness is determined based on the titrated amount of the chelating agent, it is necessary to ensure that iron ions and the like do not react with the chelating agent.

従つて、水の硬度判定においては、呈色指示薬
だけでなく、原水のPH値を一定範囲内に調整する
ためのPH値調整剤、鉄イオン等をいんぺいするた
めのいんぺい剤等の液体をあらかじめ原水中に投
入しておく必要がある。
Therefore, when determining the hardness of water, in addition to a coloring indicator, liquids such as a PH value adjusting agent to adjust the PH value of raw water to within a certain range, and an impregnating agent to absorb iron ions, etc., must be used in advance. It must be placed in raw water.

そして、これら呈色指示薬、PH調整剤、いんぺ
い剤は所定の配合比で原水中に投入する必要があ
るが、従来、硬度判定に際し、その都度上述薬液
を個々に配合調整しながら投入し、拡散させる為
の撹拌をした後に判定あるいは定量分析する必要
があり、各薬液の配合調整や撹拌のために多大な
手間を要する問題があつた。
These color indicators, PH adjusters, and impregnation agents must be added to the raw water at a predetermined mixing ratio, but conventionally, when determining hardness, the above-mentioned chemical solutions are added while adjusting the mix individually each time, and then dispersed. It is necessary to carry out judgment or quantitative analysis after stirring for the purpose of dispersion, which poses a problem in that it requires a great deal of time and effort to adjust the formulation of each chemical solution and to stir it.

即ち、上述薬液を予め所定の配合比で調整し、
これを溶液としての水又はアルコールに混合して
保存しておき、硬度判定時にこの配合調整された
溶液を原水中に投入するようにすれば、上述の問
題を解決できるのであるが、呈色指示薬としての
エリオクロムブラツクT、カルコン、N−N指示
薬等の水溶液、アルコール溶液は共に不安定で長
期間保存できない欠点があり、上述のようにこれ
ら薬液を予め水溶液又はアルコール溶液として長
期に亘つて保存できないからである。
That is, the above-mentioned chemical solution is adjusted in advance at a predetermined mixing ratio,
The above problem can be solved by mixing this with water or alcohol as a solution and storing it, and then adding this mixed solution into the raw water when determining hardness. Both aqueous and alcoholic solutions of Eriochrome Black T, chalcone, N-N indicators, etc., are unstable and cannot be stored for long periods of time. Because you can't.

そこで、溶媒としてトリエタノールアミンを使
用すれば長期に亘つて保存できることが知られて
いるが(例えば上野景平著「キレート商定法」南
江堂参照)、トリエタノールアミンは気温が低く
なると粘度が高くなり、原水への投入操作が煩わ
しく、原水中への拡散性も悪いので入念に撹拌す
る必要がある等の取扱いにくい問題がある。
Therefore, it is known that triethanolamine can be stored for a long period of time if used as a solvent (for example, see Keihei Ueno's "Chelate Commercial Law" Nankodo), but triethanolamine becomes more viscous when the temperature drops. However, there are problems in that it is difficult to handle, such as the operation of adding it to raw water is troublesome, and the dispersibility into raw water is poor, so it is necessary to carefully stir it.

又、呈色指示薬としてエリオクロムブラツクT
を使用した場合、溶媒として多価アルコール特に
ポリグリコールを使用すると、直射日光及び空気
中に曝露しても著しい安定性を示すことも知られ
ているが(例えば、特公昭40−6832号公報参照)、
この多価アルコールを用いた溶液も、前述のトリ
エタノールアミンを用いた溶液と同様粘度が高
く、取扱いにくい問題がある上、多価アルコール
自体は単に呈色指示薬の安定性を保つ溶媒として
の機能があるに過ぎず、硬度判定時において何ら
有用な機能を発揮し得るものではないので、溶媒
としての水に比べて製造コストが上昇する要因と
なる。
In addition, Eriochrome Black T is used as a color indicator.
It is also known that when a polyhydric alcohol, particularly a polyglycol, is used as a solvent, it exhibits remarkable stability even when exposed to direct sunlight and air (see, for example, Japanese Patent Publication No. 6832/1983). ),
A solution using this polyhydric alcohol has a high viscosity and is difficult to handle, just like the solution using triethanolamine mentioned above, and the polyhydric alcohol itself simply functions as a solvent to maintain the stability of the color indicator. However, since it cannot exhibit any useful function in determining hardness, it becomes a factor that increases the manufacturing cost compared to water as a solvent.

更に、上述のような呈色指示薬の溶液とした場
合に生じる不都合を避けるために、各薬剤を粉末
にして予め配合調整しておき、硬度判定の都度原
水中に投入して撹拌溶解するようにしたものもあ
るが、粉末の薬剤を原水中に溶解させるために更
に十分な撹拌が必要となり、手間的に何ら有用な
ものにできなかつた。
Furthermore, in order to avoid the inconveniences that would occur if a color indicator solution was used as described above, each drug should be prepared in powder form beforehand, and then added to the raw water and stirred and dissolved each time the hardness was determined. However, in order to dissolve the powdered drug in the raw water, sufficient stirring was required, and the process was time-consuming and could not be of any use.

本発明は、上記の点に鑑み、合理的な配合によ
り判定薬を水溶液にして拡散性が良好で撹拌が簡
単に行えるようにすると共に、長期に亘つて安定
した呈色が行えるようにし、水の硬度判定を容易
確実に、かつ、迅速に行えるものを提供する事を
目的とする。
In view of the above points, the present invention has been developed to make a determination drug into an aqueous solution through a rational formulation, which has good diffusivity and can be easily stirred, and also enables stable coloring over a long period of time. The purpose of the present invention is to provide a device that allows easy, reliable, and quick hardness determination.

上記目的を達成する為の本発明による水の硬度
判定薬の特徴構成は、1−(1−ハイドロキシ−
4−メチル−2−フエノールアゾ)−2−ナフト
ール−4−スルホン酸を0.01〜1.0重量%含む水
溶液中に、トリエタノールアミン5〜50重量%
と、水中において無色で、かつ、硬度成分と不溶
性の塩を作らない酸又はその塩0.05〜20重量%を
配合してPH9.1〜11.4の水溶液にしてある点にあ
り、かかる構成から次の作用効果を奏する。
The characteristic constitution of the water hardness determining agent according to the present invention for achieving the above object is 1-(1-hydroxy-
5-50% by weight of triethanolamine in an aqueous solution containing 0.01-1.0% by weight of 4-methyl-2-phenolazo)-2-naphthol-4-sulfonic acid.
and 0.05 to 20% by weight of an acid or its salt that is colorless in water and does not form salts insoluble with the hardness component to form an aqueous solution with a pH of 9.1 to 11.4. It has an effect.

即ち、本発明者は、呈色指示薬としての1−
(1−ハイドロキシ−4−メチル−2−フエノー
ルアゾ)−2−ナフトール−4−スルホン酸(以
下カルマガイドと略称する。)が水に対して比較
的安定であること、並びに、溶媒の一成分として
トリエタノールアミンを用いるとカルマガイドを
安定化できるだけではなく、原水中に含まれる鉄
イオン等をいんぺいする作用があることに着目
し、カルマガイドの溶媒として単にトリエタノー
ルアミンのみを用いるのではなく、カルマガイド
を水溶液とし、この水溶液にトリエタノールアミ
ンを配合するものであるから、トリエタノールア
ミンを単独で溶媒とするものに比べて粘性が少な
く、原水中への投入が簡単で、かつ、原水中での
拡散性も向上し撹拌操作が簡単に行える等取扱い
を極めて容易にすることができた。
That is, the present inventor has discovered that 1-
(1-Hydroxy-4-methyl-2-phenolazo)-2-naphthol-4-sulfonic acid (hereinafter abbreviated as Karmagide) is relatively stable in water, and as a component of the solvent. Focusing on the fact that using triethanolamine not only stabilizes Karma Guide, but also has the effect of destroying iron ions contained in raw water, we did not simply use triethanolamine as the solvent for Karma Guide. Since Karma Guide is made into an aqueous solution and triethanolamine is blended into this aqueous solution, it has less viscosity than a solution that uses triethanolamine alone as a solvent, and can be easily added to raw water. The dispersibility was also improved, and the stirring operation was made easier, making handling extremely easy.

又、トリエタノールアミン自体は単にカルマガ
イドを安定化する機能を有しているだけでなく、
原水中の鉄イオン等をいんぺいする機能があるこ
とから、例えば多価アルコールを溶媒とするとき
に必須の配合剤であるいんぺい剤の量を削減ある
いは皆無にすることができることと、溶媒として
その全量をトリエタノールアミンを用いるのでは
なく、水を配合する構成とから、全体として材料
の無駄が少なく、製造コストを下げることができ
る。
In addition, triethanolamine itself not only has the function of stabilizing Karma Guide, but also has the function of stabilizing Karma Guide.
Because it has the ability to absorb iron ions, etc. in raw water, it is possible to reduce or eliminate the amount of impregnating agent, which is an essential compounding agent when using polyhydric alcohol as a solvent, and the total amount of it as a solvent. Since water is added instead of using triethanolamine, overall there is less wasted material and manufacturing costs can be lowered.

従つて、呈色指示薬としてのカルマガイドの水
溶液と、いんぺい剤並びに配合液安定性保持用の
薬剤としてのトリエタノールアミンと、PH調整剤
としての硬度成分と不溶性の塩を作らない酸又は
その塩とを合理的に配合することによつて、呈色
指示薬としてのカルマガイドの安定化を長期に亘
つて図り得るものでありながら、取扱いが極めて
容易で、かつ、薬剤の配合自体に無駄が少なく、
従つて安価に製造できる水の硬度判定薬を提供で
きるに至つた。
Therefore, an aqueous solution of Karma Guide as a coloring indicator, triethanolamine as an anti-inflammatory agent and agent for maintaining the stability of the compounded solution, a hardness component as a pH adjuster, and an acid or its salt that does not form an insoluble salt. By rationally combining these, it is possible to stabilize KarmaGuide as a color indicator over a long period of time, while it is extremely easy to handle and there is little waste in the drug formulation itself. ,
Therefore, it has now become possible to provide a water hardness determining agent that can be manufactured at low cost.

次の本発明の実施例について詳述する。 The following embodiments of the present invention will be described in detail.

1−(1−ハイドロキシ−4−メチル−2−フ
エノールアゾ)−2−ナフトール−4−スルホン
酸を0.01〜1.0重量%含む水溶液中に、妨害イオ
ンに対するいんぺい、及び、配合液の粘度調整を
行うと共に判定のための呈色を長期間安定させる
ための薬剤としてトリエタノールアミン5〜50重
量%と、PH調整剤として硬度成分と不溶性の塩を
作らないホウ酸又はその塩0.05〜20重量%を配合
してPH9.1〜11.4の水溶液にして水の硬度判定薬
を製造する。
In an aqueous solution containing 0.01 to 1.0% by weight of 1-(1-hydroxy-4-methyl-2-phenolazo)-2-naphthol-4-sulfonic acid, impede against interfering ions and adjust the viscosity of the blended liquid. Contains 5-50% by weight of triethanolamine as a drug to stabilize the coloration for long-term determination, and 0.05-20% by weight of boric acid or its salt, which does not form salts that are insoluble with hardness components, as a pH adjuster. Then, it is made into an aqueous solution with a pH of 9.1 to 11.4 to produce a water hardness determining agent.

上記判定薬では、自然水や水道水により製造さ
れた、例えばPH4〜12の軟水とか汽缶のブロー水
等すべての水に対して適用し、所望硬度の場合に
は青色に、それ以外の場合には赤色に呈色させて
硬度を判定するものである。
The above determination agent is applied to all types of water produced from natural water or tap water, such as soft water with a pH of 4 to 12 or blown water from steam cans, and is colored blue if it has the desired hardness, and blue in other cases. The hardness is determined by coloring red.

尚、上述PH調整剤としてのホウ酸としては、硬
度成分と水中で不溶性の塩を作らず、かつ、水中
において無色となる特性を有するものであり、そ
れら特性を有する例えば塩酸や酢酸等の酸又はそ
の塩をホウ酸に代えて適用する事も可能である。
In addition, the boric acid used as the above-mentioned PH adjuster has the property of not forming an insoluble salt in water with the hardness component, and being colorless in water. Alternatively, it is also possible to apply a salt thereof in place of boric acid.

又、判定薬を製造するに、硫化ナトリウム0.1
〜10重量%を配合しても良く、そうすれば、判定
対象水中に妨害イオンとして銅や亜鉛が存在して
もより高いいんぺい効果を上げる事ができる利点
を有する。
In addition, when manufacturing the determination drug, sodium sulfide 0.1
Up to 10% by weight may be added, which has the advantage that even if copper and zinc exist as interfering ions in the water to be evaluated, a higher effectiveness can be achieved.

従来の硬度判定として、呈色指示薬としてエリ
オクロムブラツクTを使用して実験したところ、
呈色後10分間前後しか安定した呈色が行われず、
他方、本発明硬度判定膜を使用した場合、数時間
から数日間にわたつて安定した呈色が行われ、呈
色安定性において本発明が極めてすぐれている事
が明白であつた。
In an experiment using Eriochrome Black T as a coloring indicator for conventional hardness determination,
Stable coloring occurs only for about 10 minutes after coloring,
On the other hand, when the hardness determination film of the present invention was used, stable coloring was achieved over several hours to several days, and it was clear that the present invention was extremely superior in terms of coloring stability.

図面は本発明の硬度判定薬を収容する点滴瓶で
あり、合成樹脂製の容器本体1のロ部2に先細り
形状の注入口3を形成した口部材4を嵌着すると
共に、前記容器本体1のロ部2に形成したネジ部
5に蓋6を着脱するべく構成してあり、硬度判定
に際し、前記容器本体1を圧縮し、判定対象水に
容易に定量づつ滴下していけるように構成してあ
る。
The drawing shows an infusion bottle containing the hardness determining drug of the present invention, in which a mouth member 4 having a tapered injection port 3 is fitted into the bottom 2 of a container body 1 made of synthetic resin, and the container body 1 is A lid 6 is attached to and detached from a screw part 5 formed in the bottom part 2 of the container, and the container body 1 is compressed and a fixed amount can be easily dripped into the water to be evaluated during hardness determination. There is.

尚、本発明の硬度判定薬は、EDTA滴定法に
よる全硬度定量分析とか自動比色による硬度判定
にも適用できるものである。
The hardness determination agent of the present invention can also be applied to total hardness quantitative analysis by EDTA titration and hardness determination by automatic colorimetry.

【図面の簡単な説明】[Brief explanation of the drawing]

図面は本発明に係る硬度判定薬を収容するため
の点滴瓶の断面図である。
The drawing is a sectional view of a drip bottle for accommodating a hardness determining drug according to the present invention.

Claims (1)

【特許請求の範囲】[Claims] 1 1−(1−ハイドロキシ−4−メチル−2−
フエノールアゾ)−2−ナフトール−4−スルホ
ン酸を0.01〜1.0重量%含む水溶液中に、トリエ
タノールアミン5〜50重量%と、水中において無
色で、かつ、硬度成分と不溶性の塩を作らない酸
又はその塩0.05〜20重量%を配合してPH9.1〜11.4
の水溶液にしてある水の硬度判定薬。
1 1-(1-hydroxy-4-methyl-2-
In an aqueous solution containing 0.01 to 1.0% by weight of triethanolamine (phenolazo)-2-naphthol-4-sulfonic acid, add 5 to 50% by weight of triethanolamine and an acid that is colorless in water and does not form a salt insoluble with the hardness component. PH9.1-11.4 by blending 0.05-20% by weight of the salt
A water hardness determination drug that is made into an aqueous solution.
JP4755280A 1980-04-09 1980-04-09 Hardness determining chemical agent for water Granted JPS56143954A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4755280A JPS56143954A (en) 1980-04-09 1980-04-09 Hardness determining chemical agent for water

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4755280A JPS56143954A (en) 1980-04-09 1980-04-09 Hardness determining chemical agent for water

Publications (2)

Publication Number Publication Date
JPS56143954A JPS56143954A (en) 1981-11-10
JPS6310786B2 true JPS6310786B2 (en) 1988-03-09

Family

ID=12778319

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4755280A Granted JPS56143954A (en) 1980-04-09 1980-04-09 Hardness determining chemical agent for water

Country Status (1)

Country Link
JP (1) JPS56143954A (en)

Also Published As

Publication number Publication date
JPS56143954A (en) 1981-11-10

Similar Documents

Publication Publication Date Title
ATE10157T1 (en) DRY STABILIZED SUPPLEMENT CONTAINING CURCUMIN COLORING.
OA10140A (en) Hair relaxer compositions
CA2511918A1 (en) Temporary visual indicators for paint and other compositions
King et al. The biochemistry of silicic acid: Micro-determination of silica
EP0204372A1 (en) Method for the preparation of photographic bath concentrates in paste form, method for processing such concentrates to give ready-for-use photographic processing baths, an apparatus suitable for such processing and a pump arrangement appertaining to this apparatus
US5287967A (en) Bag containing three component biocidal composition
JPS6310786B2 (en)
US4690902A (en) Method, reagent and kit for the determination of nitrate ions
Lugg Sullivan's reaction for the quantitative determination of cysteine and cystine
US3051661A (en) ph indicator units in tablet form
CA2221419C (en) Method for determining dissolved oxygen in water
US6176917B1 (en) Boron-containing aqueous solution particularly for addition to amyloid glue
EP0968005B1 (en) Use of isothiazolone reduction of emissions of hcn
US4818703A (en) Stabilized alkaline picrate reagent for jaffe creatinine determination
US3245819A (en) Stabilization of calcium carbonate slurries
US1937365A (en) Preparation for coloring hair
JPH0377791B2 (en)
US2265189A (en) Fuel treating agent
US20070240782A1 (en) System and method for preparing a flowable mixture for a battery
GB1572509A (en) Stabilised hemotological reagent solution
Smirk The Micro-estimation of Chlorine in whole Blood, Serum or Corpuscles
US169727A (en) Improvement in reagents for testing the strength of vinegar
Přibil et al. Complexometric determination of molybdenum (VI)
CA2153089C (en) Method of stabilizing the color of the disodium salt of 5,5'-indigotin disulfonic acid
US2378248A (en) Photographic art