Abstract: A novel method to prepare high-enthalpy biofuels has been developed based on a new chemical pattern which has never been used before in the synthesis of renewable fuels. These biofuels are based on natural oleaginous feedstock, rendering low viscosity liquids with broad liquid range and enthalpy levels much superior to those found in common biodiesel, meaning ethyl or methyl fatty esters. As in the case of biodiesel, these new biofuels contain zero sulfur, causing none of the major pollution associated with commercial diesel. High enthalpy biofuels are aliphatic nitrile compounds, containing a single nitrogen substituent, are chemically aprotic, even though their high degree of polarity is reflected in its high cetane index and solubility parameter. The present invention includes fuels associated with diesel, as well as other high-enthalpy fractions, which according to their boiling point, correspond to naphtha in the lower scale, and bunker in the upper scale.

Abstract: A catalyst system and a method for preparing polymers using the catalyst system is provided. The catalyst system includes a complex represented by the formula: [MLy(HSR)ñ]n, wherein M is a transition metal cation preferably in a lower oxidation state, L is a ligand, Y is a whole number between 0 and 5, ñ is a whole number between 1 and 6, n is the charge of the complex (preferably between −4 to 3), H is Hydrogen, S is sulphur and R is an organic group or hydrogen. The catalyst system advantageously has high hydrolytic stability which allows it to be used in a variety of polymerization systems including mass, solution, suspension and emulsion. In many cases only a small amount of the catalyst is required to promote polymerization.

Abstract: Disclosed are novel crosslinked polymers derived from methylol phenols and maleic acid species, and methods of synthesizing these macromolecules. Polyesters and chromandicarboxylic groups are the dominant linkages in the structure of general formula: ##STR1## R is H or a spacing group between aromatics, R.sub.1 is an aldehyde substituent, R.sub.2 a spacing group belonging to multihidric alcohols, a maleyl grouping, and n a whole number either 0 or 1.