The present invention pertains to a process for refining of crude tall oil (CTO). The process comprises fractionation under vacuum of a refined CTO into at least one stream of refined tall diesel (RTD) or tall oil fatty acids (TOFA), the RTD or TOFA comprises from 2-30% by volume of resin acids and from 20-90% by volume of fatty acids, and at least one stream of resin acid(s) (RA) comprising less than 5% by volume of fatty acids. The stream of RTD or TOFA is deoxygenated forming hydrocarbon compounds in a subsequent step. This invention also relates to a refined tall diesel. Furthermore, a process for the production of a refined tall diesel (RTD) composition, wherein crude sulphate turpentine(s) (CST) is added to the refined tall diesel (RTD) composition, is described.

The present invention relates to a method for producing a hydrocarbon, including a step (Y) of converting a reaction product of at least one sulfur compound selected from the group consisting of hydrogen sulfide and a compound containing a —SH group which are contained in a hydrocarbon with an α,β-unsaturated aldehyde compound into a water-soluble compound in the presence of water, and a step (Z) of separating oil and water.

A system including biogas purification and provides biogas as feedstock to a solid oxide fuel cell. The biogas purification treatment process provides a polished biogas that is substantially free of carbonyl sulfides and hydrogen sulfide. The system uses a biogas treatment apparatus, that includes apparatus such as a packed columns, comprising copper oxide or potassium permanganate packing material, and an activated carbon component configured to treat the biogas by polishing it to remove carbonyl sulfides and deleterious trace residues, such as hydrogen sulfide, that were not removed by any prior bulk H2S removal steps. In addition, an oil removal device is used to remove any entrained fine oil droplets in the biogas. A polished biogas having in the range of 60% methane is charged to the fuel cell. Electricity generated may be fed into a grid or used directly as energy to charge electrical-powered vehicles, for example. Energy credits are tracked in real time and are appropriately assigned.

A process and a plant for purifying a crude gas stream containing sulfur components and hydrocarbons by gas scrubbing using a scrubbing medium which is selective for sulfur components in an absorption column. Heavy hydrocarbons and heavy mercaptans are removed from the crude gas in a lower section of the absorption column and the resulting, loaded scrubbing medium stream is fed separately from the other loaded scrubbing medium streams to a hot regeneration column. A vapor stream enriched in water, hydrocarbons and sulfur components is obtained as overhead product from the hot regeneration column and this stream is cooled to below its dew point and is separated in a gas-liquid-liquid phase separation apparatus. The resulting, organic liquid phase contains heavy hydrocarbons and heavy mercaptans and can thus be discharged from the process or the plant, as a result of which accumulation thereof in the scrubbing medium is prevented.

Compressed rich natural gas is divided into a cooling gas stream and a fuel gas stream. The cooling gas stream is depressurized. The cooling gas and the fuel gas are then heat exchanged to provide a first cooling step to the fuel gas. The cooled fuel gas continues into a second cooling step in a second heat exchanger, and then flows into a separator vessel where liquids are removed from the bottom of the separator and conditioned fuel gas exits the top of the separator. The conditioned fuel gas from the separator and produced from its influent is depressurized and heat exchanged to provide the second cooling fluid for the second heat exchanger.

The present invention relates to a composition for scavenging hydrogen sulphide and/or mercaptans in hydrocarbon streams, the composition comprising an oxazolidine compound and a synergistic additive.

A process and method for removing hydrogen sulfide from a gas and regenerating ferric ions consumed in the hydrogen sulfide scrubbing process at low pH. A two-scrubber regenerative chemical scrubbing system for removing hydrogen sulfide from a gas that provides an economical system for removing hydrogen sulfide from a gas at low pH without the need for chelating agents. An oxide of manganese is used as a catalyst to enhance the regeneration of ferric ions in an aqueous solution under acidic conditions in the presence of oxygen. The process may further include contacting the aqueous solution with a second gas comprising air to replenish the dissolved oxygen in the aqueous solution. The regenerated solution comprising ferric ions can be reused to treat additional hydrogen sulfide containing gases.

An absorbent for selective removal of hydrogen sulfide over carbon dioxide from a fluid stream comprises an aqueous solution of a) a tertiary amine, b) a sterically hindered secondary amine of the general formula (I) ##STR00001##
in which R.sub.1 and R.sub.2 are each independently selected from C.sub.1-4-alkyl and C.sub.1-4-hydroxyalkyl; R.sub.3, R.sub.4, R.sub.5 and R.sub.6 are each independently selected from hydrogen, C.sub.1-4-alkyl and C.sub.1-4-hydroxyalkyl, with the proviso that at least one R.sub.4 and/or R.sub.5 radical on the carbon atom bonded directly to the nitrogen atom is C.sub.1-4-alkyl or C.sub.1-4-hydroxyalkyl when R.sub.3 is hydrogen; x and y are integers from 2 to 4 and z is an integer from 1 to 4; where the molar ratio of b) to a) is in the range from 0.05 to 1.0, and c) an acid in an amount, calculated as neutralization equivalent relative to the protonatable nitrogen atoms in a) and b), of 0.05 to 15.0%. One preferred amine of the formula I is 2-(2-tert-butylaminoethoxy)ethanol. The absorbent allows a defined H.sub.2S selectivity to be set at pressures of the kind typical in natural gas processing.

A method for improved operation of a natural gas liquids stabilizer column, particularly a small-scale, is provided. The method can include the steps of: introducing a first feed stream comprising heavy hydrocarbons and natural gas to a stabilizer column to produce a top gas and a bottoms liquid, wherein the top gas has a higher concentration of natural gas as compared to the first feed stream, and the bottoms liquid has a higher concentration of heavy hydrocarbons as compared to the first feed stream; introducing a second feed stream into the stabilizer column, wherein the second feed stream has a higher concentration of natural gas as compared to the first feed stream, wherein the second feed stream is at a warmer temperature than the first feed stream when introduced into the stabilizer column, wherein the second feed stream is a gaseous stream; withdrawing the top gas from a top portion of the stabilizer column; withdrawing the bottoms liquid from a bottom portion of the stabilizer column; and sending at least a portion of the bottoms liquid to a liquid storage tank.

The invention relates to a process and a plant for removing thiols from synthesis gas. Thiols and optionally thiophene and carbon disulfide are absorbed in a dedicated absorption stage with methanol as physical absorption medium. Methanol laden with at least thiols is freed of thiols in a stripping stage with methanol vapours as stripping gas and the methanol vapours-containing thiols are freed of methanol in a scrubbing stage. The process according to the invention minimizes methanol losses and the amounts of coolant required for the process.