Zirconium octoate which functions as a deep and highly effective auxiliary drier, is the most recognized alternative to lead-based driers. When used in combination with cobalt driers in white paints, it ensures the preservation of the film's color and prevents yellowing. This combination also safeguards the film from weathering effects. Unlike lead-based driers, zirconium octoate does not generate sulfides in sulfur-polluted atmospheres, eliminating the formation of black spots on the film. In comparison to lead-based driers, films dried with zirconium octoate exhibit greater flexibility, shorter drying times, and lower hardness. However, in lower temperatures and humid conditions, this trend may be reversed.
• It is a powerful through drier
• It is the most recognized alternative to lead
• It has a high solubility, though imparts better gloss
• It prevents yellowing while is used with cobalt
• It is very efficient as a drier in waterproof paints
Synonyms: Zirconium 2-ethylhexanoate, Zirconium 2-ethylcaproate
Chemical Formula: Zr(C8H15O2)4
Molecular Weight: Approximately 663.9 g/mol
CAS Number: 22464-99-9
Properties:
• Odor: Zirconium octoate is generally odorless.
• Solubility: It is soluble in organic solvents such as alcohols, ketones, and esters.
• Melting Point: Zirconium octoate does not have a distinct melting point but may solidify at lower temperatures.
In order to determine the zirconium content in paint driers, we rely on the ASTM D3969-01 standard test method. This method provides specific guidelines and procedures for accurately measuring zirconium using the EDTA method. Here is a detailed description of how we conduct the analysis:
1. Preparation:
a. We prepare a 0.1 M ethylenediaminetetraacetic acid (EDTA) solution by dissolving the appropriate amount of EDTA in distilled water and adjusting the pH to around 10 using a sodium hydroxide solution.
b. We calibrate a spectrophotometer at a suitable wavelength (specified in the standard) using a blank solution (distilled water) and a zirconium 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 50 mL of distilled water to the beaker and stir the mixture until the sample is completely dissolved.
c. The solution is transferred quantitatively to a 250 mL volumetric flask and diluted to the mark with distilled water.
3. Titration Procedure:
a. We pipette 25 mL of the prepared sample solution into a 250 mL conical flask.
b. We add 5 mL of a suitable buffer solution to the conical flask to adjust the pH within the desired range.
c. We add a suitable indicator (specified in the standard) to the solution. The indicator will undergo a color change.
d. We titrate the solution with the prepared 0.1 M EDTA solution by slowly adding it from a burette while stirring the solution.
e. The titration is continued until the color change of the indicator reaches its endpoint, indicating the completion of the reaction.
4. Calculation:
a. The volume of the EDTA solution used for the titration is recorded.
b. The zirconium 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 zirconium concentration is calculated from the multiple titrations to obtain a more precise result.
By adhering to the ASTM D3969-01 standard test method, we can accurately determine the zirconium content in paint driers using the EDTA method.
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 zirconium octoate with different metal content.
Product / Grade | Zirconium Octoate 24 % | Zirconium Octoate 18 % | Zirconium Octoate 16 % | Zirconium Octoate 12 % |
Diluent | White Spirits | White Spirits | White Spirits | White Spirits |
Metal Content | 24 ± 0.2 % | 18 ± 0.2 % | 16 ± 0.2 % | 12 ± 0.2 % |
Appearance | Clear Liquid | Clear Liquid | Clear Liquid | Clear Liquid |
Color | Light Yellow | Light Yellow | Light Yellow | Light Yellow |
Solids Content | 65 ± 2 % | 45 ± 2 % | 38 ± 2 % | 30 ± 2 % |
Density (at 20°C) | 1.14 ± 0.01 | 1.03 ± 0.01 | 0.99 ± 0.01 | 0.92 ± 0.01 |
Viscosity (at 25°C) (Ford cup 4) | ||||
Standard Barrel Weight (Net. Kg) | 200 | 200 | 180 | 180 |