Lead octoate is a secondary drier, through drier, that enhances flexibility. It is the most important drier in applications where drying at low temperatures is required (temperatures below 10 degrees Celsius). However, it should not be used in aluminum-based paints due to its tendency to cause wrinkling, nor in paints resistant to fumes and vapors. In the presence of sulfur in polluted air, lead driers produce black lead sulfide, which leads to darkening and reduced glossiness of the resulting film. Moreover, due to its lead content, this drier is toxic. Therefore, the best substitute for this product is C60 drier, which offers a safer alternative.
• It is a through drier
• It is toxic and forbidden in many applications
• It is the most important drier in low temperature
• It is suitable for using with grease
• It should not be used in aluminum-based paints
Synonyms: Lead 2-ethylhexanoate and Lead 2-ethylcaproate
Chemical Formula: Pb (C8H15O2)2
Molecular Weight: Approximately 763.7 g/mol
CAS Number: 301-08-6
EC Number: 206-108-6
Properties:
- Odor: Lead octoate may have a mild odor.
- Solubility: It is soluble in organic solvents such as alcohols, ketones, and esters.
- Melting Point: Lead octoate does not have a distinct melting point but may solidify at lower temperatures.
To accurately determine the lead content in drying catalysts such as Lead octoate, we follow the ASTM D2374-05 standard test method. This method provides clear guidelines and procedures for conducting the analysis. Here is an overview of how we perform the test:
1. Preparation:
a. We prepare a 0.01 M ethylenediaminetetraacetic acid (EDTA) solution by dissolving the appropriate amount of EDTA in distilled water. The pH is adjusted to around 10 using a sodium hydroxide solution.
b. We prepare a buffer solution by dissolving 67 grams of ammonium chloride and 570 mL of ammonium hydroxide in distilled water. The pH is adjusted to approximately 10.5 using a sodium hydroxide solution.
c. We calibrate a spectrophotometer at a wavelength of 510 nm using a blank solution (distilled water) and a lead standard solution.
2. Sample Preparation:
a. We accurately weigh around 1 gram of the paint drier sample into a 250 mL beaker.
b. We add 100 mL of distilled water to the beaker and stir the mixture until the sample is completely dissolved.
c. The solution is quantitatively transferred to a 250 mL volumetric flask and diluted to the mark with distilled water.
3. Titration Procedure:
a. We pipette 50 mL of the prepared sample solution into a 250 mL conical flask.
b. To adjust the pH, we add 10 mL of the buffer solution to the conical flask.
c. 5 drops of xylenol orange indicator are added to the solution, causing it to turn yellow.
d. The prepared 0.01 M EDTA solution is slowly added from a burette while continuously stirring the solution.
e. The titration continues until the color changes from yellow to a pinkish-red, indicating the endpoint of the titration.
4. Calculation:
a. The volume of the EDTA solution used for the titration is noted.
b. The lead concentration in the sample is calculated using the volume of EDTA solution and the concentration of the EDTA solution.
c. Any necessary corrections or adjustments specified in the ASTM standard are applied.
5. Repeat and Average:
a. The entire procedure is repeated at least two more times using fresh samples.
b. The volume of EDTA solution used for each titration is recorded.
c. The average lead concentration is calculated from the multiple titrations to obtain a more accurate result.
By following these steps outlined in the ASTM D2374-05 standard, we can reliably determine the lead content in drying catalysts like Lead octoate.
For this purpose, we use the ASTM D1644-01 standard, we follow a step-by-step procedure to determine the nonvolatile matter content of varnishes. Here is how we conduct the analysis:
1. Sample Preparation: We obtain a representative sample of the varnish to be tested. Ensure that the sample is well-mixed and free from any visible contaminants or particles.
2. Weighing: Using a precision balance, we accurately weigh a specific amount of the varnish sample. The amount is typically specified in the standard and may vary depending on the expected nonvolatile matter content.
3. Evaporation: We transfer the weighed sample into a suitable container or weighing dish. The container is then placed in an oven set at a specific temperature, as indicated in the standard. The varnish is allowed to evaporate under controlled conditions to remove the volatile components.
4. Drying: After the evaporation phase, we transfer the container with the dried residue to a desiccator to cool to room temperature. This ensures that any moisture absorbed during cooling is minimized.
5. Weighing Residue: Once the sample has cooled, we reweigh the container with the dried residue using the same precision balance. The weight of the container and residue is recorded for later calculations.
6. Calculation: We calculate the nonvolatile matter content of the varnish by subtracting the weight of the container from the weight of the container with the residue. The difference represents the weight of the nonvolatile matter in the varnish sample.
By following the ASTM D1644-01 standard, we ensure a standardized and reliable approach to determine the nonvolatile matter content of varnishes. This analysis helps assess the film-forming properties and quality of varnish coatings.
For this purpose, we use the ASTM D1200-10 standard, we follow a step-by-step procedure to determine the viscosity of liquids using the Ford Viscosity Cup. Here is how we conduct the analysis:
1. Cup Selection: We select the appropriate Ford viscosity cup based on the expected viscosity range of the liquid to be tested. The Ford viscosity cups are available in different sizes, denoted by a numerical value.
2. Cup Preparation: We ensure that the Ford viscosity cup is clean and free from any contaminants or residue. If necessary, we clean the cup thoroughly and dry it before proceeding with the analysis.
3. Sample Preparation: We obtain a representative sample of the liquid to be tested. Ensure that the sample is well-mixed and free from any visible particles or contaminants.
4. Cup Filling: We pour a sufficient amount of the liquid sample into the Ford viscosity cup. The cup should be filled to a predetermined level specified in the standard, typically near the top orifice of the cup.
5. Timing: Using a stopwatch or timer, we measure the time it takes for the liquid to completely flow out through the orifice of the Ford viscosity cup. The timing starts as the cup is inverted to allow the liquid to flow.
6. Recording: We record the time it takes for the liquid to flow out completely, typically expressed in seconds. This time is known as the Ford viscosity cup efflux time.
7. Calculation: We use the recorded efflux time to calculate the viscosity of the liquid using a specific formula provided in the ASTM D1200-10 standard. The formula incorporates the cup's calibration constant, which is specific to each cup size.
By following the ASTM D1200-10 standard, we ensure a standardized and reliable approach to determine the viscosity of liquids using the Ford Viscosity Cup. This method is commonly used in industries such as coatings, paints, and adhesives to evaluate the flow properties and consistency of liquid materials.
For this purpose, we use the ASTM D1544-04 standard test method. we follow a step-by-step procedure to determine the color of transparent liquids using the Gardner Color Scale. Here is how we conduct the analysis:
1. Sample Preparation: We obtain a representative sample of the transparent liquid to be tested. Ensure that the sample is properly homogenized and free from any visible particles or contaminants.
2. Apparatus Setup: We set up the spectrophotometer that is calibrated according to the standard's specifications. This instrument is capable of measuring color based on the Gardner Color Scale.
3. Calibration: We calibrate the spectrophotometer using appropriate reference standards provided by the standard or as specified in the procedure. Calibration ensures accurate color measurement and comparison.
4. Sample Placement: We pour a sufficient amount of the sample into a suitable transparent container, ensuring an adequate depth for measurement. The container should be clean and free from any residue that may affect color evaluation.
5. Measurement: We place the container with the sample in the spectrophotometer and follow the instrument's instructions to measure the color. The device quantifies the color based on the Gardner Color Scale, which ranges from a pale yellow (Gardner Color 1) to a dark brown (Gardner Color 18).
6. Data Collection: We record the color measurement obtained from the instrument, typically expressed as a Gardner Color number. This number corresponds to a specific color shade on the Gardner Color Scale.
7. Comparison: We compare the measured Gardner Color number of the sample to the reference values or standards provided in the ASTM D1544-04 standard. This allows us to evaluate the color of the sample and determine its compliance with the specified requirements or industry standards.
By following the ASTM D1544-04 standard, we ensure a standardized and reliable approach to determine the color of transparent liquids using the Gardner Color Scale.
In this table you can find the technical properties of lead octoate with different metal content.
Product / Grade | Lead Octoate 36 % | Lead Octoate 32 % | Lead Octoate 24 % |
Diluent | White Spirits | White Spirits | White Spirits |
Metal Content | 36 ± 0.2 % | 32 ± 0.2 % | 24 ± 0.2 % |
Appearance | Clear Liquid | Clear Liquid | Clear Liquid |
Color | Light Yellow | Light Yellow | Light Yellow |
Solids Content | 71 ± 2 % | 66 ± 2 % | 45 ± 2 % |
Density (at 20°C) | 1.35 ± 0.01 | 1.26 ± 0.01 | 1.09 ± 0.01 |
Viscosity (at 25°C) (Ford cup 4) | |||
Standard Barrel Weight (Net. Kg) | 275 | 220 | 200 |