Items | Specifications | Results |
Appearance | White Powder | Qualified |
Melting Point | 190-220 | 212.5-212.6 |
Loss in Drying(80℃) | ＜0.5% | 0.4% |
Phosphorus Content | 16-18% | 16.6% |
Conclusion | Up to standard of our company. |
Pentaerythritol octahydrogen tetraphosphate is an organophosphorus compound. In simpler terms, it's a molecule with a carbon backbone (from pentaerythritol) attached to chains of phosphates (phosphorus and oxygen).
Its primary commercial importance is as a reactive flame retardant.
Detailed Breakdown of the Name
The name describes the structure of the molecule perfectly. Let's dissect it:
Pentaerythritol:
This is the central "core" or "backbone" of the molecule.
It's an organic compound with the formula C(CH₂OH)₄.
Imagine a central carbon atom connected to four identical -CH₂OH arms. This tetrahedral structure makes it very sturdy and allows it to connect to multiple other groups.
Octahydrogen:
"Octa-" means eight, and "hydrogen" means hydrogen atoms.
This tells us there are eight hydrogen atoms associated with the acidic parts of the phosphate groups.
Tetraphosphate:
"Tetra-" means four, and "phosphate" refers to a unit containing phosphorus and oxygen (a PO₄ group).
This means there are four phosphate groups attached to the pentaerythritol core.
Structure and Formula
Chemical Formula: C(CH₂OPO₃H₂)₄ or more commonly written as C₅H₁₈O₁₆P₄
Abbreviation: It is often abbreviated as PETP or, more accurately, as the acid form of PEPA (Pentaerythritol Phosphate).
How it's built: Each of the four -OH groups on the pentaerythritol core is esterified with a phosphoric acid (H₃PO₄) group. However, it's not fully neutralized, so it retains its acidic hydrogen atoms.
A simplified way to visualize the structure:
You have a central C atom with four arms: -CH₂-O-P(=O)(OH)-OH
This same unit repeats on all four arms.
Key Properties
Appearance: Typically a white, crystalline powder.
Acidity: It is a polyprotic acid, meaning it can donate multiple protons (H⁺ ions) due to its several acidic -OH groups on the phosphate units.
High Phosphorus Content: It has a very high percentage of phosphorus by weight, which is crucial for its function as a flame retardant.
Primary Use: Flame Retardant
This is the most important application of this compound. It is used as a reactive (or chemical) flame retardant primarily in polyester resins and polyurethane foams.
How it works as a Flame Retardant:
Condensed Phase Action: When the plastic it's in catches fire, PETP decomposes.
Char Formation: It promotes the formation of a thick, stable, carbonaceous layer (char) on the surface of the burning material. This char acts as a protective barrier.
Barrier Function: This barrier insulates the underlying plastic from the heat of the flame and prevents the escape of flammable gases (fuel) that would otherwise feed the fire.
Gas Phase Action (Secondary): It also releases phosphorus-containing radicals that can scavenge high-energy H⁺ and OH⁻ radicals in the flame, helping to extinguish it.
Why is it "reactive"?
Unlike "additive" flame retardants that are just mixed in physically, PETP is designed to chemically react during the polymerization process. It becomes an integral part of the polymer chain itself. This has a major advantage: it doesn't leach or migrate out of the plastic over time, making it a more permanent and environmentally stable solution.
Comparison with Glycerol
To connect it to your previous question, you can think of it as a more complex and specialized cousin of glycerol:
Glycerol has three -OH groups and is used for moisture, sweetness, and as a backbone for fats.
Pentaerythritol has four -OH groups, making it stiffer and more symmetrical.
When you attach phosphate groups to these alcohols, you get molecules with very different, more industrial properties (like flame retardancy) instead of the food/cosmetic properties of glycerol.
Summary
In essence, pentaerythritol octahydrogen tetraphosphate is a specialized, high-phosphorus chemical primarily used to make plastics and foams fire-resistant by building itself directly into the polymer's molecular structure, promoting the formation of a protective char layer when exposed to flame.
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