Natural oil polyols, also known as NOPs or biopolyols, are polyols derived from vegetable oils by several different techniques. The primary use for these materials is in the production of polyurethanes. Most NOPs qualify as biobased products, as defined by the United States Secretary of Agriculture in the Farm Security and Rural Investment Act of 2002. NOPs all have similar sources and applications, but the materials themselves can be quite different, depending on how they are made. All are clear liquids, ranging from colorless to medium yellow. Their viscosity is also variable and is usually a function of the molecular weight and the average number of hydroxyl groups per molecule (higher mw and higher hydroxyl content both giving higher viscosity.) Odor is a significant property which is different from NOP to NOP. Most NOPs are still quite similar chemically to their parent vegetable oils and as such are prone to becoming rancid. This involves autoxidation of fatty acid chains containing carbon-carbon double bonds and ultimately the formation of odoriferous, low molecular weight aldehydes, ketones and carboxylic acids. Odor is undesirable in the NOPs themselves, but more importantly, in the materials made from them. There are a limited number of naturally occurring vegetable oils (triglycerides) which contain the unreacted hydroxyl groups that account for both the name and important reactivity of these polyols. Castor oil is the only commercially available natural oil polyol that is produced directly from a plant source: all other NOPs require chemical modification of the oils directly available from plants. The hope is that using renewable resources as feedstocks for chemical processes will reduce the environmental footprint by reducing the demand on non-renewable fossil fuels currently used in the chemical industry and reduce the overall production of carbon dioxide, the most notable greenhouse gas. One NOP producer, Cargill, estimates that its BiOH(TM)polyol manufacturing process produces 36% less global warming emissions (carbon dioxide), a 61% reduction in non-renewable energy use (burning fossil fuels), and a 23% reduction in the total energy demand, all relative to polyols produced from petrochemicals.
Sources of natural oil polyols Ninety percent of the fatty acids that make up castor oil is ricinoleic acid, which has a hydroxyl group on C-12 and a carbon-carbon double bond. The structure below shows the major component of castor oil which is composed of the tri-ester of rincinoleic acid and glycerin:
Other vegetable oils - such as soy bean oil, peanut oil, and canola oil - contain carbon-carbon double bonds, but no hydroxyl groups. There are several processes used to introduce hydroxyl groups onto the carbon chain of the fatty acids, and most of these involve oxidation of the C-C double bond. Treatment of the vegetal oils with ozone cleaves the double bond, and esters or alcohols can be made, depending on the conditions used to process the ozonolysis product. The example below shows the reaction of triolein with ozone and ethylene glycol.
Air oxidation, (autoxidation), the chemistry involved in the "drying" of drying oils, gives increased molecular weight and introduces hydroxyl groups. The radical reactions involved in autoxidation can produce a complex mixture of crosslinked and oxidized triglycerides. Treatment of vegetable oils with peroxy acids gives epoxides which can be reacted with nucleophiles to give hydroxyl groups. This can be done as a one-step process. Note that in the example shown below only one of the three fatty acid chains is drawn fully, the other part of the molecule is represented by "R1" and the nucleophile is unspecified. Earlier examples also include acid catalyzed ring opening of epoxidized soybean oil to make oleochemical polyols for polyurethane foams and acid catalyzed ring opening of soy fatty acid methyl esters with multifunctional polyols to form new polyols for casting resins.
Triglycerides of unsaturated (containing carbon-carbon double bonds) fatty acids or methyl esters of these acids, can be treated with carbon monoxide and hydrogen in the presence of a metal catalyst to add a -CHO (formyl) groups to the chain (hydroformylation reaction) followed by hydrogenation to give the needed hydroxyl groups. In this case R1 can be the rest of the triglyceride, or a smaller group such as methyl (in which case the substrate would be similar to biodiesel). If R=Me then additional reactions like transesterification are needed to build up a polyol.
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