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The ASTM D2606-94 standard outlines a procedure for determining the solubility of pentachlorophenol (PCP) wood preservative in heavy hydrocarbon solvents. This test is essential for verifying that a given solvent possesses sufficient carrying capacity to keep the preservative in solution throughout the treatment process and during its service life in treated wood.
The procedure is straightforward: a specific mass of pentachlorophenol is combined with a defined amount of the hydrocarbon solvent at an elevated temperature. The presence of any undissolved solids is visually assessed, and if necessary, quantitatively confirmed through chloride analysis as specified in Test Method D 2085.
The test procedure involves a primary screening and, if required, a secondary quantitative phase:
Standard Procedure: A mixture of 10 g (±0.1 g) of pentachlorophenol and 90 g (±1.0 g) of the hydrocarbon solvent is maintained at 150°F (65.5°C) with constant stirring for 30 minutes. If undissolved PCP is visually observed, the solvent is immediately deemed nonconforming.
Quantitative Confirmation: If no solids are observed, or if there is doubt, the solution is cooled to 75°F (24°C) and held for 4 hours. During the first 2 hours, it is stirred every 15 minutes. It is then left undisturbed for the remaining 2 hours (or centrifuged for 10 minutes). A sample of the supernatant liquid is then analyzed using Test Method D 2085.
Testing for Type A Solvents (AWPA P9): When evaluating Hydrocarbon Solvent Type A, the test mixture consists of 6 g (±0.1 g) of technical PCP (AWPA P8) with the fraction of the solvent that is undistilled above 500°F from a 100 mL D 86 distillation. This mixture is also stirred at 150°F for 30 minutes.
Maximum Solvency Determination: To find the exact maximum solvency, a gradient series of PCP solutions is prepared in 1% concentration intervals. Once the approximate solvency is found, a finer series in 0.1% intervals is prepared and tested to pinpoint the precise limit.
The following tables summarize the critical test conditions and procedures defined in the standard.
| 🟦 Parameter | 📏 Requirement | 🎯 Tolerance |
|---|---|---|
| Pentachlorophenol (Initial Mix) | 10 g | ± 0.1 g |
| Hydrocarbon Solvent (Initial Mix) | 90 g | ± 1.0 g |
| Heating & Mixing Temperature | 150°F (65.5°C) | Maintain continuously |
| Initial Mixing Duration | 30 minutes | Constant stirring |
| Secondary Cooling Temperature | 75°F (24°C) | Hold for 4 hours |
| Post-Treatment Analysis | Test Method D 2085 | Supernatant liquid |
| 📏 Solvency Testing Phase | 📐 Concentration Intervals | ⚡ Purpose |
|---|---|---|
| Initial Estimation | 1.0 % increments | Identify the approximate solvency range |
| Fine Determination | 0.1 % increments | Determine exact solvency to nearest 0.1% |
It determines whether a heavy hydrocarbon solvent can adequately dissolve pentachlorophenol to ensure the preservative remains in solution during wood treatment and subsequent use.
If undissolved pentachlorophenol is visually observed after the 30-minute heating and stirring period at 150°F, the solvent is classified as nonconforming.
The solution is cooled to 75°F for 4 hours. The supernatant liquid is then analyzed using ASTM D2085 to confirm the precise amount of pentachlorophenol in solution.
For Type A solvents, the test uses 6 g of technical PCP combined with the undistilled fraction of the solvent (boiling above 500°F) obtained from a 100 mL D 86 distillation.