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Polypropylene (PP), also known as polypropene, is a thermoplastic polymer used in a wide variety of applications. It is produced via chain-growth polymerization from the monomer propylene . Polypropylene belongs to the group of polyolefins and is partially crystalline and non-polar .
Polypropylene glycol is produced by ring-opening polymerization of propylene oxide.The initiator is an alcohol and the catalyst a base, usually potassium hydroxide.When the initiator is ethylene glycol or water the polymer is linear.
Triphenylphosphine (IUPAC name: triphenylphosphane) is a common organophosphorus compound with the formula P(C 6 H 5) 3 and often abbreviated to P Ph 3 or Ph 3 P. It is versatile compound that is widely used as a reagent in organic synthesis and as a ligand for transition metal complexes, including ones that serve as catalysts in organometallic chemistry.
The difference is quite significant when dealing with gases, and it is very important to specify which quantity is being used. For example, the conversion factor between a mass fraction of 1 ppb and a mole fraction of 1 ppb is about 4.7 for the greenhouse gas CFC-11 in air (Molar mass of CFC-11 / Mean molar mass of air = 137.368 / 28.97 = 4.74).
An alpha-olefin (or α-olefin) is an alkene where the carbon-carbon double bond starts at the α-carbon atom, i.e. the double bond is between the #1 and #2 carbons in the molecule. Alpha-olefins such as 1-hexene may be used as co-monomers to give an alkyl branched polymer (see chemical structure below), although 1-decene is most commonly used ...
Vaska's complex, trans-IrCl(CO)(PPh 3) 2, is also historically significant; it was used to establish the scope of oxidative addition reactions. This early work provided the insights that led to the flowering of the area of homogeneous catalysis. NiCl 2 (PPh 3) 2 is a tetrahedral (spin triplet) complex of Ni(II). In contrast PdCl 2 (PPh 3) 2 is ...
With respect to volatilities, p-derivatives have the lowest volatilities, and the o-derivatives have the highest volatilities. The opposite is true for flash points and fire points. Spontaneous ignition temperatures of polyphenyl ethers lie between 550 and 595 °C (1,022 and 1,103 °F), alkyl substitution reduces this value by ~50 °C (122 °F).
The polypropylene-lined drum prevents any contact between the acid and metal equipment. [ 3 ] ' Sodium hypochlorite and potassium permanganate ' : These often are used in the processing of reptile skins, bleaching the material and preparing it for further processing.