JPH0532703B2 - - Google Patents
Info
- Publication number
- JPH0532703B2 JPH0532703B2 JP17205882A JP17205882A JPH0532703B2 JP H0532703 B2 JPH0532703 B2 JP H0532703B2 JP 17205882 A JP17205882 A JP 17205882A JP 17205882 A JP17205882 A JP 17205882A JP H0532703 B2 JPH0532703 B2 JP H0532703B2
- Authority
- JP
- Japan
- Prior art keywords
- cooling water
- deterioration
- copper ions
- color
- extract
- 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 - Lifetime
Links
- 239000003153 chemical reaction reagent Substances 0.000 claims description 26
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 claims description 22
- 229910001431 copper ion Inorganic materials 0.000 claims description 22
- 230000006866 deterioration Effects 0.000 claims description 22
- 239000000498 cooling water Substances 0.000 claims description 18
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 12
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 claims description 9
- 238000004040 coloring Methods 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 8
- 239000002202 Polyethylene glycol Substances 0.000 claims description 7
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 7
- 238000002485 combustion reaction Methods 0.000 claims description 7
- LMBWSYZSUOEYSN-UHFFFAOYSA-N diethyldithiocarbamic acid Chemical compound CCN(CC)C(S)=S LMBWSYZSUOEYSN-UHFFFAOYSA-N 0.000 claims description 7
- 229950004394 ditiocarb Drugs 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 7
- 229920001223 polyethylene glycol Polymers 0.000 claims description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims description 6
- RGCKGOZRHPZPFP-UHFFFAOYSA-N alizarin Chemical compound C1=CC=C2C(=O)C3=C(O)C(O)=CC=C3C(=O)C2=C1 RGCKGOZRHPZPFP-UHFFFAOYSA-N 0.000 claims description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 5
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 4
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 claims description 4
- 229940071106 ethylenediaminetetraacetate Drugs 0.000 claims description 4
- PHTQWCKDNZKARW-UHFFFAOYSA-N isoamylol Chemical compound CC(C)CCO PHTQWCKDNZKARW-UHFFFAOYSA-N 0.000 claims description 4
- 239000001509 sodium citrate Substances 0.000 claims description 4
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 claims description 4
- 229910052938 sodium sulfate Inorganic materials 0.000 claims description 4
- 235000011152 sodium sulphate Nutrition 0.000 claims description 4
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 claims description 4
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 claims description 3
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 claims description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 claims description 2
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Natural products CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims 1
- 238000012360 testing method Methods 0.000 description 19
- 239000000243 solution Substances 0.000 description 16
- 239000007788 liquid Substances 0.000 description 13
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 230000002528 anti-freeze Effects 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 229910000838 Al alloy Inorganic materials 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- -1 aluminum ions Chemical class 0.000 description 3
- 239000002826 coolant Substances 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 230000003449 preventive effect Effects 0.000 description 3
- 239000012085 test solution Substances 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- PTFCDOFLOPIGGS-UHFFFAOYSA-N Zinc dication Chemical compound [Zn+2] PTFCDOFLOPIGGS-UHFFFAOYSA-N 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000008235 industrial water Substances 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000005749 Copper compound Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 239000013522 chelant Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000012809 cooling fluid Substances 0.000 description 1
- 150000001880 copper compounds Chemical class 0.000 description 1
- 229910000365 copper sulfate Inorganic materials 0.000 description 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01P—COOLING OF MACHINES OR ENGINES IN GENERAL; COOLING OF INTERNAL-COMBUSTION ENGINES
- F01P11/00—Component parts, details, or accessories not provided for in, or of interest apart from, groups F01P1/00 - F01P9/00
- F01P11/14—Indicating devices; Other safety devices
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01P—COOLING OF MACHINES OR ENGINES IN GENERAL; COOLING OF INTERNAL-COMBUSTION ENGINES
- F01P11/00—Component parts, details, or accessories not provided for in, or of interest apart from, groups F01P1/00 - F01P9/00
- F01P11/06—Cleaning; Combating corrosion
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N31/00—Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroup; Apparatus specially adapted for such methods
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01P—COOLING OF MACHINES OR ENGINES IN GENERAL; COOLING OF INTERNAL-COMBUSTION ENGINES
- F01P2025/00—Measuring
- F01P2025/80—Concentration anti-freeze
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Combustion & Propulsion (AREA)
- Mechanical Engineering (AREA)
- General Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Physics & Mathematics (AREA)
- Molecular Biology (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
この発明は、冷却水等中の銅イオンの量を、色
濃度の相違として検出し、これを基準の色見本と
対比すること等により、容易に銅イオンの量を測
定し冷却水の劣化程度を判定する方法に関するも
のである。
この発明は、殊に内燃機関用冷却水の劣化状態
を簡単に試験するために開発されたもので、同様
に他の用途に供せられる種々の冷却液の劣化程度
の判定に適用できる。
現在内燃機関用冷却水の劣化程度の判定は分析
機器により溶存金属量の測定、防錆剤含有量の測
定によつておこなわれ、また、濃度管理として比
重、屈折率の測定が行なわれている。
しかるに、分析機器による溶存金属量の判定及
び防錆剤含有量の測定は、正確であり、冷却水の
劣化程度を判定するのに適しているが、しかし、
これらの方法では高価な分析機器と多くの工数を
必要とし、現場で簡単に冷却水の劣化を判定する
ことは出来ない。
一方、比重、または屈折率の測定では、冷却水
に使用されるエチレングリコールを主材とする不
凍液等の濃度測定は可能であるが、5%位の低い
濃度で使用される冷却水用防錆剤の濃度測定は不
可能である。さらに、これらの濃度測定では、冷
却水に含まれている防錆剤の量を測定することが
できず、防錆剤の劣化によるトラブルを防止する
ことは不可能である。
ところで、最近の自動車エンジンは、エンジン
の高速回転化、車体の軽量化、省エネルギーとい
う時代の要請を受けてアルミニウム合金化、スリ
ム化あるいはラジエータ機構の容量逓減化等が活
発に行なわれている。
また、自動車エンジン冷却用のラジエータ溶液
は、不凍液、防錆剤等を始めとして種々の添加剤
が水とともに用いられて、次第に品質が向上して
きているのが現状である。
このラジエータ溶液の品質向上は、長期に亙る
使用に堪え、交換という面倒な作業を省いた点
で、使用者に取つては極めて便利となつている
が、前述したようにエンジン自体の構造の小型
化、アルミニウム合金化あるいはラジエータ機構
の容量逓減化に伴うラジエータ溶液の強力ポンプ
による循環作用の高速化等によつてラジエータ溶
液は苛酷な環境下におかれることとなり、どうし
ても配合添加物の機能低下すなわちラジエータ溶
液の急速な劣化進行は避けえない。
したがつて従来のように不交換のまま長期に亙
つてラジエータ溶液を継続して使用するときは、
エンジンそのものを悪化させ重大な事故を派生す
る危険さえ生じかねない。
そこでラジエータ溶液の劣化を簡単に判定する
ことが出来る技術の開発が望まれるのであるが、
未だ、満足すべき判定技術が開発されるに至つて
いないことは前述の通りである。
この発明の発明者は上述のごとき事情におい
て、ラジエータ溶液の機能劣化に大きく作用する
金属イオン、銅イオンであることに着目し、この
銅イオンを簡単に検出でき、しかも色濃度変化に
よつてラジエータ溶液の劣化程度を判定できるこ
とを見出してこの発明を完成した。
なお、ラジエータ溶液中には銅イオンの他にア
ルミニウムイオン、鉄イオン、鉛イオン、亜鉛イ
オンが存在する可能性があるが、イオン化傾向の
最も小さい銅イオンが他の金属への影響が最も強
いので、銅イオンの定量測定でラジエータ溶液の
劣化判定には充分であることが分かつている。
以下、この発明の詳細を一実施例を示す図面に
ついて説明する。
第1図及び第2図に示すように、この発明の内
燃機関用冷却水等の簡易劣化判定方法では、試薬
と抽出液、及び色見本基準チヤートを準備する必
要がある。すなわち、試薬1は瓶2に入れて試験
管3、色見本基準チヤート4と共に例えばケース
5に収納して準備しておく。抽出液6も瓶7に入
れて備えさせる。試薬1は冷却水中の銅イオンと
反応して発色化合物を生成できる物質を含むもの
で、その様な物質としては、ジエチルジチオカル
バミン酸ナトリウム、無水硫酸ナトリウム、硫酸
ナトリウム、トリエタノールアミンと平均分子量
200のポリエチレングリコール200S(商品名、三
洋化成工業株式会社製)とエチレンジアミンテト
ラアセテート4Naとクエン酸ナトリウム及びアリ
ザリンシアニンブルーで構成された物質を使用す
る。
抽出液は試薬と被試験溶液を反応させて生成す
る発色銅化合物を溶解液として分離抽出できるも
ので、その様な抽出液としては、酢酸エチル、酢
酸ブチル、イソアミルアルコール、クロロホル
ム、四塩化炭素、メチルエチルケトン、ベンゼン
の溶剤を使用する。
色見本基準チヤート4は第2図に示すように、
銅イオンの量に応じて段階的に異なる多数の色濃
度を表したものである。
次ぎに試験に際しては、被試験溶液(ラジエー
タ溶液)を抜取つて試験管3に入れ、これに発色
化合物を生成できる試薬を投入し、生成した発色
化合物を抽出液で抽出し、前記銅イオンの濃度に
よつて色濃度を異にする色見本基準チヤートと比
較検討対比して被試験液の劣化程度を判定する。
次ぎに予め作成する基準色見本チヤートの例と
して3種の基準色見本チヤート[A][B]及び
[C]を示す。ここで使用する試薬及び試料は以
下の通りである。
試薬(1)
ジエチルジチオカルバミン酸ナトリウム 2.0g
無水硫酸ナトリウム 50.0
トリエタノールアミン 10.0
ポリエチレングリコール200S 40.0
を加熱溶解させ、ペースト状にしたもの。ただ
し、ホリエチレングリコール200Sを加えずに、
水に溶解してもよい。
試薬(2)
ジエチルジチオカルバミン酸ナトリウム 2.0g
エチレンジアミンテトラアセテート4Na 2.0
クエン酸ナトリウム 2.0
無水硫酸ナトリウム 50.0
トリエタノールアミン 10.0
ポリエチレングリコール200S 33.9
及び
アリザリンシアニンブルー 0.1
の加熱溶解させ、ペースト状とする。ただし、ポ
リエチレングリコール200Sを加えずに、水に溶
解してもよい。
試薬(3)
ジエチルジチオカルバミン酸ナトリウム 20.0g
硫酸ナトリウム(Na2SO4・10H2O) 250
トリエタノールアミン 100
を水に溶解して1とする。
試料(4)
硫酸銅(CuSO4・5H2O)39.2gを水に溶解し
1とする。
試料(5)
エチレングリコール 30.0g
水 67.0
89%リン酸 0.5
トリエタノールアミン 1.5
安息香酸ナトリウム 1.0
This invention detects the amount of copper ions in cooling water, etc. as a difference in color density, and compares this with a standard color sample to easily measure the amount of copper ions and determine the degree of deterioration of the cooling water. This relates to a method for determining. This invention was developed specifically to easily test the deterioration state of cooling water for internal combustion engines, and can similarly be applied to determining the degree of deterioration of various cooling fluids used for other purposes. Currently, the degree of deterioration of cooling water for internal combustion engines is determined by measuring the amount of dissolved metals and rust inhibitor content using analytical equipment, and the specific gravity and refractive index are also measured to control the concentration. . However, although the determination of dissolved metal content and the measurement of rust inhibitor content using analytical instruments are accurate and suitable for determining the degree of deterioration of cooling water,
These methods require expensive analytical equipment and a lot of man-hours, and it is not possible to easily determine the deterioration of cooling water on site. On the other hand, when measuring specific gravity or refractive index, it is possible to measure the concentration of antifreeze, etc., which is mainly composed of ethylene glycol, used in cooling water, but it is possible to measure the concentration of antifreeze, etc., which is used in cooling water at a low concentration of about 5%. Measuring the concentration of the agent is not possible. Furthermore, with these concentration measurements, it is not possible to measure the amount of rust preventive agent contained in the cooling water, and it is impossible to prevent troubles due to deterioration of the rust preventive agent. Nowadays, in response to the demands of the times for higher engine speeds, lighter vehicle bodies, and energy savings, modern automobile engines are increasingly being made of aluminum alloy, slimmer, or have a radiator mechanism with a lower capacity. Furthermore, the quality of radiator solutions for cooling automobile engines is gradually improving as various additives, including antifreeze and rust preventive agents, are used together with water. The improved quality of this radiator solution has made it extremely convenient for users in that it can withstand long-term use and eliminates the troublesome work of replacing it.However, as mentioned above, the small structure of the engine itself The radiator solution is placed in a harsh environment due to the use of aluminum alloys, aluminum alloys, or faster circulation of the radiator solution by powerful pumps due to the gradual decrease in the capacity of the radiator mechanism, which inevitably leads to a decline in the functionality of the additives. Rapid deterioration of the radiator solution is unavoidable. Therefore, when using the radiator solution continuously for a long period of time without replacing it as in the past,
This may even cause the engine itself to deteriorate and cause a serious accident. Therefore, it is desired to develop a technology that can easily determine the deterioration of radiator solution.
As mentioned above, a satisfactory determination technique has not yet been developed. In view of the above-mentioned circumstances, the inventor of this invention focused on copper ions, which are metal ions that greatly affect the functional deterioration of radiator solutions. This invention was completed by discovering that the degree of deterioration of a solution can be determined. Note that in addition to copper ions, aluminum ions, iron ions, lead ions, and zinc ions may exist in the radiator solution, but copper ions, which have the least tendency to ionize, have the strongest influence on other metals. It has been found that quantitative measurement of copper ions is sufficient for determining the deterioration of radiator solutions. Hereinafter, details of the present invention will be explained with reference to the drawings showing one embodiment. As shown in FIGS. 1 and 2, in the simple method for determining deterioration of cooling water for internal combustion engines, etc. of the present invention, it is necessary to prepare a reagent, an extract, and a color sample reference chart. That is, the reagent 1 is placed in a bottle 2 and stored together with a test tube 3 and a color sample standard chart 4 in a case 5 for example. The extract 6 is also placed in the bottle 7 and prepared. Reagent 1 contains a substance that can react with copper ions in the cooling water to produce a color-forming compound; such substances include sodium diethyldithiocarbamate, anhydrous sodium sulfate, sodium sulfate, triethanolamine, and
A substance composed of 200 polyethylene glycol 200S (trade name, manufactured by Sanyo Chemical Industries, Ltd.), ethylenediaminetetraacetate 4Na, sodium citrate, and alizarin cyanine blue is used. The extract liquid can be separated and extracted by dissolving the colored copper compound produced by reacting the reagent and the test solution. Examples of such extract liquids include ethyl acetate, butyl acetate, isoamyl alcohol, chloroform, carbon tetrachloride, Use methyl ethyl ketone, benzene solvent. The color sample reference chart 4 is as shown in FIG.
It shows a large number of color densities that vary in stages depending on the amount of copper ions. Next, during the test, the solution to be tested (radiator solution) is taken out and put into test tube 3, a reagent capable of producing a coloring compound is added thereto, the produced coloring compound is extracted with an extract solution, and the concentration of the copper ions is determined. The degree of deterioration of the test liquid is determined by comparing and contrasting it with color sample standard charts with different color densities. Next, three types of standard color sample charts [A], [B], and [C] are shown as examples of standard color sample charts that are prepared in advance. The reagents and samples used here are as follows. Reagent (1) Sodium diethyldithiocarbamate 2.0g Anhydrous sodium sulfate 50.0 Triethanolamine 10.0 Polyethylene glycol 200S 40.0 Dissolved by heating to form a paste. However, without adding polyethylene glycol 200S,
May be dissolved in water. Reagent (2) Sodium diethyldithiocarbamate 2.0g 4Na ethylenediaminetetraacetate 2.0 Sodium citrate 2.0 Anhydrous sodium sulfate 50.0 Triethanolamine 10.0 Polyethylene glycol 200S 33.9 and Alizarin cyanine blue 0.1 are heated and dissolved to form a paste. However, it may be dissolved in water without adding polyethylene glycol 200S. Reagent (3) Sodium diethyldithiocarbamate 20.0g Sodium sulfate (Na 2 SO 4・10H 2 O) 250 Triethanolamine Dissolve 100 in water to make 1. Sample (4) Dissolve 39.2g of copper sulfate (CuSO 4.5H 2 O) in water to make 1. Sample (5) Ethylene glycol 30.0g Water 67.0 89% phosphoric acid 0.5 Triethanolamine 1.5 Sodium benzoate 1.0
【表】【table】
【表】【table】
【表】
試薬(1)、(2)、(3)については、ジエチルジチオカ
ルバミン酸ナトリウムの他に、前記の銅イオント
反応して発色化合物を生成する試薬も同様に使用
する。
無水硫酸ナトリウム、硫酸ナトリウムは被試験
液と抽出液とを分離を容易にするためのものであ
り、乳化破壊に働く。
トリエタノールアミンは被試験液をアルカリ性
に保持するためのものであり、発色状態の明瞭化
安定化等反応性において改善される。
ポリエチレングリコール200Sは試薬類をペー
スト状にするためのものであり、試薬と加熱溶融
または混合撹拌して使用する。試薬の固形化とそ
れによる取扱性の向上を実現化することができ
る。
エチレンジアミンテトラアセテート4Na及びク
エン酸ナトリウムは鉄イオン、亜鉛イオン、鉛イ
オンをマスキングするためのものであり、必要に
応じて使用することもできる。
以上の色見本基準チヤートから、銅イオンの量
と発色濃度が相関関係を持つことがわかる。
次ぎに実車のラジエータ液(実車液)の劣化判
定に適用した結果の例を示す。被試験液は自動車
のラジエータから抜取つたものを使用し、その組
成は次ぎの通りである。[Table] Regarding reagents (1), (2), and (3), in addition to sodium diethyldithiocarbamate, the above-mentioned reagents that react with copper ions to produce color-forming compounds are also used. Anhydrous sodium sulfate and sodium sulfate are used to facilitate separation of the test liquid and extract liquid, and work to destroy emulsification. Triethanolamine is used to keep the test solution alkaline, and improves reactivity such as clarifying and stabilizing the color development state. Polyethylene glycol 200S is used to make reagents into a paste, and is used by heating and melting or mixing and stirring with the reagents. It is possible to solidify the reagent and thereby improve ease of handling. Ethylenediaminetetraacetate 4Na and sodium citrate are for masking iron ions, zinc ions, and lead ions, and can be used as necessary. From the above color sample standard chart, it can be seen that there is a correlation between the amount of copper ions and the color density. Next, we will show an example of the results when applied to the deterioration determination of radiator fluid (actual vehicle fluid) in an actual vehicle. The liquid to be tested was taken from an automobile radiator, and its composition was as follows.
【表】【table】
【表】
25ml目盛試験管に被試験液をそれぞれ10mlづつ
採取し、試薬(1)を0.2gづつ投入し、約5分間強
く振とうし、試薬(1)を完全に溶解させた。次ぎに
酢酸エチルをそれぞれ10mlづつ入れ、10秒間強く
振とうし、約5分間静置したら、被試験と抽出液
(酢酸エチル)が完全に分離し、抽出液が上層と
なつた。この抽出液の着色程度を色見本チヤート
A,B,Cと比較した。この結果銅イオンの量が
多いものほど濃色となり、ほぼ色見本基準チヤー
トA,B,Cと一致した。[Table] 10 ml of each test solution was taken into 25 ml graduated test tubes, and 0.2 g of reagent (1) was added to each tube, followed by vigorous shaking for about 5 minutes to completely dissolve reagent (1). Next, 10 ml of ethyl acetate was added to each, shaken vigorously for 10 seconds, and left to stand for about 5 minutes. The test sample and the extract (ethyl acetate) were completely separated, and the extract formed the upper layer. The degree of coloring of this extract was compared with color sample charts A, B, and C. As a result, the larger the amount of copper ions, the darker the color, which almost matched the color sample standards charts A, B, and C.
【表】
25ml目盛り試験管に被試験液をそれぞれ10mlづ
つ採取し、試薬(2)を0.2mlづつ投入し、実施例1
と同じ操作を行つた結果、銅イオンの量が多いも
の程濃色となり、ほぼ色見本基準チヤートA,
B,Cと一致した。なお銅イオンの量が多い被試
験液(No.7、8、9、10)では実施例1の色見本
チヤートA,B,Cに近い着色を示した。[Table] Collect 10 ml of each test liquid into 25 ml graduated test tubes, add 0.2 ml of reagent (2) to each test tube, and use Example 1.
As a result of performing the same operation as above, the higher the amount of copper ions, the darker the color, which is almost the color sample standard chart A,
Matched B and C. The test liquids (Nos. 7, 8, 9, and 10) containing a large amount of copper ions exhibited coloration similar to that of color sample charts A, B, and C of Example 1.
【表】
25ml目盛り試験管に被試験液をそれぞれ10mlづ
つ採取し、試薬(3)を0.2mlづつ投入し、実施例1
と同じ操作を行なつた結果、銅イオンの量が多い
もの程濃色となり、実施例1とほぼ同じ色見本基
準チヤートA,B,Cの区分を示した。
この発明は、叙上のように、銅イオンの溶出量
の多寡を銅イオンの試薬との反応によつて生じる
キレート化合物の色の濃淡によつて検知できるの
で、内燃機関用冷却液の劣化状態を始めとして、
各種の工業用水の劣化判定が極めて簡単であつ
て、熟練を要せず、何人も正確に実施できる。
また、試薬は取扱いが簡単であり、各種工業溶
液の試験定量方法、殊に内燃機関用冷却水の銅イ
オン定量による劣化判定に有効である。さらに試
薬、薬品、器具等が説明書とともに一体的に一つ
のケースに組込まれて商品化でき、内燃機関用冷
却液その他の工業用水中の銅イオン定量による劣
化判定を各現場で簡単に実施できる効果を有す
る。
以上の説明から明らかな通りこの発明によれ
ば、冷却液中の銅イオンの量を発色濃度の相違と
して検出し、これを色見本基準チヤートと対比す
ることによつて容易に冷却液の劣化を判定するこ
とができる内燃機関冷却水の劣化判定方法を得る
ことができる。
特に発色用試薬については不凍液の添加剤組成
物やエチレングリコール等の基剤並びに濃度等に
よりジエチルジチオカルバミン酸ナトリウム単独
では、発色状態の明瞭化、被試験液の分離化等が
ほとんど行なわれないが、本願発明の構成材から
なる発色用試薬によつて、発色状態の明瞭化、被
試験液の分離化等が良好に行われる。[Table] Collect 10 ml of each test liquid into 25 ml graduated test tubes, add 0.2 ml of reagent (3) to each test tube, and apply Example 1.
As a result of performing the same operation as above, the larger the amount of copper ions, the darker the color, and the color sample standard charts A, B, and C were classified almost the same as in Example 1. As described above, this invention enables detection of the amount of eluted copper ions based on the shade of color of the chelate compound produced by the reaction of copper ions with a reagent. Starting with,
Deterioration determination of various types of industrial water is extremely simple, does not require any skill, and can be performed accurately by any person. Furthermore, the reagent is easy to handle and is effective for testing and quantifying various industrial solutions, particularly for determining deterioration by quantifying copper ions in cooling water for internal combustion engines. Furthermore, reagents, chemicals, instruments, etc. can be integrated into a single case along with instructions for commercialization, making it easy to determine deterioration at each site by quantifying copper ions in coolant for internal combustion engines and other industrial water. have an effect. As is clear from the above description, according to the present invention, the amount of copper ions in the coolant is detected as a difference in color density, and by comparing this with a color sample standard chart, it is possible to easily detect the deterioration of the coolant. A method for determining deterioration of internal combustion engine cooling water can be obtained. In particular, regarding coloring reagents, sodium diethyldithiocarbamate alone hardly clarifies the coloring state or separates the test liquid, depending on the additive composition of the antifreeze solution, the base material such as ethylene glycol, and the concentration. With the coloring reagent made of the constituent materials of the present invention, the state of coloring can be clarified, the test liquid can be separated, etc. satisfactorily.
第1図はこの発明の判定方法において使用する
器材セツトの一例を示す説明図、及び第2図は色
見本基準チヤートを示す説明図である。
1……試薬、試薬瓶、3……試験管、4……色
見本基準チヤート、5……ケース、6……抽出
液、7……抽出液瓶。
FIG. 1 is an explanatory diagram showing an example of a set of equipment used in the determination method of the present invention, and FIG. 2 is an explanatory diagram showing a color sample reference chart. 1... Reagent, reagent bottle, 3... Test tube, 4... Color sample reference chart, 5... Case, 6... Extract liquid, 7... Extract liquid bottle.
Claims (1)
生成できるジエチルジチオカルバミン酸ナトリウ
ムと無水硫酸ナトリウムと硫酸ナトリウムとトリ
エタノールアミンと平均分子量が200であるポリ
エチレングリコールとエチレンジアミンテトラア
セテート4Naとクエン酸ナトリウム及びアリザリ
ンシアニンブルーで構成される発色用試薬を冷却
水に添加し、生成した発色化合物を酢酸エチル、
酢酸ブチル、イソアミルアルコール、クロロホル
ム、四塩化炭素、メチルエチルケトン、ベンゼン
の中の少なくともいずれか一つで構成される抽出
液により冷却水から分離抽出し、抽出された発色
化合物の色濃度の大きさにより、銅イオンの量を
測定して冷却水の劣化程度を判定することを特徴
とする内燃機関用冷却水等の簡易劣化判定方法。1 Sodium diethyldithiocarbamate, anhydrous sodium sulfate, sodium sulfate, triethanolamine, polyethylene glycol with an average molecular weight of 200, 4Na ethylenediaminetetraacetate, sodium citrate, and alizarin, which can react with copper ions in cooling water to produce color-forming compounds. A coloring reagent consisting of cyanine blue is added to cooling water, and the resulting coloring compound is mixed with ethyl acetate,
Separate and extract from cooling water with an extract consisting of at least one of butyl acetate, isoamyl alcohol, chloroform, carbon tetrachloride, methyl ethyl ketone, and benzene, and depending on the color density of the extracted color compound, A simple method for determining the deterioration of cooling water for an internal combustion engine, which comprises determining the degree of deterioration of the cooling water by measuring the amount of copper ions.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17205882A JPS5960356A (en) | 1982-09-30 | 1982-09-30 | Simple deterioration deciding method of cooling water or the like for internal combustion engine |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17205882A JPS5960356A (en) | 1982-09-30 | 1982-09-30 | Simple deterioration deciding method of cooling water or the like for internal combustion engine |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5960356A JPS5960356A (en) | 1984-04-06 |
| JPH0532703B2 true JPH0532703B2 (en) | 1993-05-17 |
Family
ID=15934749
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP17205882A Granted JPS5960356A (en) | 1982-09-30 | 1982-09-30 | Simple deterioration deciding method of cooling water or the like for internal combustion engine |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5960356A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2785392B1 (en) * | 1998-10-28 | 2000-12-01 | Elf Antar France | DEVICE FOR MONITORING THE CHARACTERISTICS OF A COOLING LIQUID AND METHOD FOR IMPLEMENTING IT |
| JP4669830B2 (en) * | 2006-11-17 | 2011-04-13 | ムラキ株式会社 | Coolant inspection tool and coolant inspection method |
-
1982
- 1982-09-30 JP JP17205882A patent/JPS5960356A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5960356A (en) | 1984-04-06 |
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