Determination of residual alkali in sodium hypochlorite | Autotitrator COM-A19 - JM Science

Determination of residual alkali in sodium hypochlorite | Autotitrator COM-A19

Hiranuma Aquacounter Autotitrator COM-A19

Sodium hypochlorite is produced by having sodium hydroxide absorb chlorine gas. Produced sodium hypochlorite contains sodium chloride generated by the degradation of hypochlorous acid.

This report introduces an example for the determination of residual alkali (sodium hydroxide, sodium carbonate) in the sodium hypochlorite with potentiometric titration.

Determination of available chlorine in sodium hypochlorite | Autotitrator COM-A19 - JM Science

Determination of available chlorine in sodium hypochlorite | Autotitrator COM-A19

Hiranuma Aquacounter Autotitrator COM-A19
Sodium hypochlorite is used for bleaching and sterilization of tap water because of its strong oxidizing and disinfecting properties. Sodium hypochlorite is relatively stable at the alkaline region. However, it is unstable at the acidic region and becomes hypochlorous acid (HClO). It oxidizes water and generates chlorine (Cl2). The concentration of available chlorine has to be measured regularly because sodium hypochlorite degrades slowly and generates sodium chloride.
This report introduces an example for determination of available chlorine as follows:.
1) Add potassium iodide to sodium hypochlorite to generate free iodine.
2) Titrate the free iodine generated from the reaction (1) with sodium thiosulfate to determine available chlorine (2) by redox titration.
Cl₂ +2KI → I₂ + 2KCl・・・(1)
I₂ + 2Na₂S₂O₃ → 2NaI + Na₂S₄O₆・・・(2)
Fractional determination for mixture of sodium hydroxide and sodium carbonate | Autotitrator COM-A19 - JM Science

Fractional determination for mixture of sodium hydroxide and sodium carbonate | Autotitrator COM-A19

Hiranuma Aquacounter Autotitrator COM-A19

Sodium hydroxide and sodium carbonate have important roles as alkali component chemicals, which are used in a broad range of industries. The concentration of both components have to be determined because these are sometimes used with mixed.

This report introduces an example that the mixture solution of sodium hydroxide and sodium carbonate are fractionally determined with potentiometric titration. 

Purity determination of sodium hydroxide | Autotitrator COM-A19 - JM Science

Purity determination of sodium hydroxide | Autotitrator COM-A19

Hiranuma Aquacounter Autotitrator COM-A19

Sodium hydroxide is one of the most elemental reagent in chemical industrial reagents. Its production amount is large and it is used in a broad range of fields. Sodium hydroxide absorbs carbonate gas and water in atmosphere because of its properties, the purity of sodium hydroxide is gradually reduced. Japanese Industrial Standard (JIS) K8576 defines determination method for purity of sodium hydroxide (titration with indicator). Representative impure substance in sodium hydroxide includes sodium carbonate.

This report introduces an example for the quantitative determination of sodium hydroxide purity and sodium carbonate by successive and fractional potentiometric titration.

Quantitative determination of copper ion in plating solution | Autotitrator COM-A19 - JM Science

Quantitative determination of copper ion in plating solution | Autotitrator COM-A19

Hiranuma Aquacounter Autotitrator COM-A19
The photometric titration using a photometric probe is generally applied for the determination of copper ion (Cu2+). However, the measurement of cloudy or colored sample has difficulty to analyze with the photometric titration. The measurement using copper ion-selective electrode performs the potentiometric titration which it is not affected by the suspended particle and the indicator reagent is not required for the titration.
Cu²⁺ + Na₂EDTA → Cu-EDTA + 2Na²⁺
This report introduces an example of the measurement for copper ion in plating solution with chelatometric titration using copper ion-selective electrode.
Quantitative determination of lead ion | Autotitrator COM-A19 - JM Science

Quantitative determination of lead ion | Autotitrator COM-A19

Hiranuma Aquacounter Autotitrator COM-A19

The chelatometric titration is generally used for the determination of lead ion (Pb2+). The pH region the lead ion can be directly titrated is pH 3.5 ~ 10 (stability constant = 17.88).1 However, it generates Pb(OH)2 precipitation at alkaline region. When performing titration under alkaline condition, the auxiliary complexing agent such as ethanolamine, tartaric acid, or citric acid should be added in advance to generate weak chelatometric complex and avoid the generation of lead hydroxide precipitation.

It is titrated at pH around 4 ~ 5 when performing under acidic condition. This report introduces an example that the lead ion in sample solution adjusted to pH 5 by hexamine solution is determined with using XO indicator (red purple →yellow).
Pb²+ + Na₂EDTA  →  Pb-EDTA + 2Na+

Quantitative determination of manganese ion | Autotitrator COM-A19 - JM Science

Quantitative determination of manganese ion | Autotitrator COM-A19

Hiranuma Aquacounter Autotitrator COM-A19
Manganese ion can be determined by chelatometric titration. The stability constant of Mn (II)-EDTA complex is relatively large (13.81),¹ but the suitable pH range for the reaction between manganese ion and EDTA is confined from 7 to 11. Since manganese ion is oxidized with air in alkaline solution, ascorbic acid or hydroxylamine is added for the titration to avoid the oxidation. The report introduces an example of the titration performed at alkaline condition (pH 10) adjusted by ammonia.
Mn²+ + Na₂EDTA  →  Mn-EDTA + 2Na+
Determination of ferrous and ferric ion in steel cleaning solution | Autotitrator COM-A19 - JM Science

Determination of ferrous and ferric ion in steel cleaning solution | Autotitrator COM-A19

Hiranuma Aquacounter Autotitrator COM-A19
A wide variety of the determination methods for each component in acidic solution containing ferrous ion (Fe2+) and ferric ion (Fe3+) has been developed. This report introduces an example of the successive determination for ferric and ferrous ions in the steel cleaning solution. First, Fe3+ ions are determined by chelatometric titration with EDTA at acidic pH using salicylic acid as the indicator (purple →yellow). The all Fe2+ ions are continuously oxidized to Fe3+ ion with ammonium peroxodisulfate. Finally, the Fe3+ ion oxidized from Fe2+ is determined by chelatometric titration with EDTA titrant as well as the above description.
Fe³+ +  Na₂EDTA  →  FeEDTA + 2Na+
Fe²+ →   Fe³+  +  e-
Determination of trace chloride ion in copper sulfate solution | Autotitrator COM-A19 - JM Science

Determination of trace chloride ion in copper sulfate solution | Autotitrator COM-A19

Hiranuma Aquacounter Autotitrator COM-A19

This report introduces an example of the determination of trace chloride ion in the solution containing highly concentrated copper sulfate.

The precipitation titration with silver nitrate standard solution is generally used for the determination of chloride ion in copper sulfate solution. The endpoint of the titration is detected with indicator method or the potentiometric method. The potentiometric method is used for this sample because the color change of indicator reagent is obscure in this sample containing highly concentrated copper sulfate. However, it tends to show the difficulty to detect the endpoint because of the less sensitivity of electrode under highly concentrated copper sulfate. Therefore the potentiometric titration is performed with the specially treated silver electrode that the silver chloride is coated.
Cl- + AgNO₃ → AgCl + NO₃-

Quantitative determination of zinc ion | Autotitrator COM-A19 - JM Science

Quantitative determination of zinc ion | Autotitrator COM-A19

Hiranuma Aquacounter Autotitrator COM-A19
Zinc ion can be readily determined by chelatometric titration. The titration with EDTA can be performed at the wide pH region (pH 4.5 ~ 10). The stability constant of Zn-EDTA complex is relatively large,1 there are a lot of highly sensitive indicator reagents for this titration. The report introduces an example that the sample adjusted to pH around 5.3 is photometrically titrated with EDTA titrant using XO indicator (red purple →yellow).
Zn²⁺ + Na₂EDTA → Zn-EDTA + 2Na⁺
Determination of alkaline component in photoresist remover solution (Determination of carbonates with barium chloride addition method) | Autotitrator COM-A19 - JM Science

Determination of alkaline component in photoresist remover solution (Determination of carbonates with barium chloride addition method) | Autotitrator COM-A19

Electric & Electronics

Strong alkaline solution is used as remover for residual photoresist on the substrate after the development of the substrate for liquid crystal display instrument etc. The composition depends on the intended use but sodium hydroxide, potassium hydroxide, and tetramethylammonium hydroxide (TMAH) are used as remover.

TMAH can be determined by potentiometric titration with hydrochloric acid standard solution. TMAH could absorb carbon dioxide gas and generate carbonates, it indicates another inflection point at pH around 4 on the titration with hydrochloric acid standard solution. This report introduces an example of fractional determination for TMAH and carbonates.

Determination of alkaline component in photoresist remover solution | Autotitrator COM-A19 - JM Science

Determination of alkaline component in photoresist remover solution | Autotitrator COM-A19

Electric & Electronics

Strong alkaline solution is used as remover for residual photoresist on the substrate after the development of the substrate for liquid crystal display instrument etc. The composition depends on the intended use but sodium hydroxide, potassium hydroxide, and tetramethylammonium hydroxide (TMAH) are used as remover.

TMAH can be determined by potentiometric titration with hydrochloric acid standard solution. TMAH could absorb carbon dioxide gas and generate carbonates, it indicates another inflection point at pH around 4 on the titration with hydrochloric acid standard solution. This report introduces an example of fractional determination for TMAH and carbonates.

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