Abstract:
A method for removing sulfur from insulating oil. The oil is exposed to at least one sulfur scavenging material and at least one polar sorbent.
Abstract:
The invention provides an iron sulfide characterized in that it comprises FeS2, Fe1−XS, Fe3O4 and FeSO4, and that the secondary particles thereof, have a 50% volume-cumulative particle diameter of from 20 to 300 &mgr;m. The invention also provides a process for producing an iron sulfide comprising the steps of introducing (a) ferrous sulfate monohydrate having a d50 of from 20 to 300 &mgr;m and (b) not less than stoichiometric amount of at least one sulfur compound selected from elemental sulfur and hydrogen sulfide into the fluidized bed of a furnace and then fluidizing, burning, and reacting the ingredients at a temperature of from 350 to less than 630° C., a superficial velocity of 0.1 m/sec or higher, and a pressure of 1 atm or higher using air as a fluidizing gas. The present invention is useful, for example, in a process of coal liquefaction or heavy-oil hydrocracking.
Abstract:
A highly efficient sulfide catalyst for reducing sulfur dioxide to elemental sulfur, which maximizes the selectivity of elemental sulfur over byproducts and has a high conversion efficiency. Various feed stream contaminants, such as water vapor are well tolerated. Additionally, hydrogen, carbon monoxide, or hydrogen sulfides can be employed as the reducing gases while maintaining high conversion efficiency. This allows a much wider range of uses and higher level of feed stream contaminants than prior art catalysts.
Abstract:
A composition is presented for a catalyst useful in the selective hydrogenation of unconjugated diolefinic hydrocarbons to monoolefinic hydrocarbons. The catalyst comprises nickel and sulfur deposited on the surface of an alumina support. The preferred catalyst does not contain halogens, noble metals, alkaline earth metals, or alkali metals and is characterized by having only a very low percentage of the total pore volume being provided by pores having an average pore diameter less than 150 angstroms. The great majority of the pore volume is present in the form of macropores having diameters of 500 to 1500 angstroms.
Abstract:
A process for the selective oxidation of olefins comprises the steps of forming a suspension of semiconductor powder in a solvent media, adding an olefin to the solvent media in the presence of an oxidant to form a mixture and, photochemically activating the mixture with illumination having an energy at least equal to the band gap of the semiconductor powder wherein the selectivity is controlled by the selection of A, of the solvent and of the oxidant. The process is one carried out at about ambient temperature and with gentle agitation. The semiconductor powder has the general formula A.sub.x B.sub.y C.sub.z where A is selected from Bi, Sn, Pt, Pd, Cu, Fe, W, V, Sb, Mo, Ru or Ag and mixtures thereof; B is Te, Sb, Ti, Cd, Mo, V or W and mixtures thereof; C is O or S; x equals 0 to 5; y equals 1 to 3; and z is a number necessary to satisfy the other elements, and is optionally metallized by an element selected from Pt, Pd, Cu or Ag.
Abstract:
C.sub.4 compounds including n-butanol and n-butanal are produced by reacting methanol, hydrogen, and carbon monoxide, in the presence of a cobalt catalyst selected from the group consisting of (a) a cobalt carbonyl, (b) a hydrido cobalt carbonyl and (c) a cobalt-containing material convertible to a cobalt carbonyl or a hydrido cobalt carbonyl, an iodine promotor and an organic sulfide having the formula:R.sub.1 --S--R.sub.2wherein R.sub.1 and R.sub.2 can be the same or different members selected from the group consisting of saturated or unsaturated, straight or branched chain alkyl radicals having from one to 24 carbon atoms, cycloalkyl radicals having from three to 40 carbon atoms, aryl radicals having from six to 20 carbon atoms, aralkyl and alkaryl radicals having from six to 40 carbon atoms and halogen substituted derivatives thereof. A high degree of selectivity towards the formation of butanol and butanal is provided by using the cobalt entity and the organic sulfide in a molar ratio in the range of about 2:1 to about 1:10, based on elemental cobalt and sulfur. The reaction is conducted at elevated temperature and pressure conditions for a time sufficient to convert methanol to n-butanol and n-butanal.
Abstract:
A process is provided for dimerization of light olefins comprising from 2 to 4 carbon atoms which comprises contacting same at a weight hourly space velocity of from about 0.1 to about 10, a temperature of from about 32.degree.F to about 350.degree.F and a pressure of from about 200 psig to about 1000 psig with a catalyst of alumina having intimately combined therewith from about 2 to about 5 weight percent nickel and from about 1 to about 3 weight percent sulfur as a result of impregnation with nickel sulfate, said alumina being gamma, eta or a mixture thereof and said catalyst having been calcined at a temperature of from 750.degree.F to about 1150.degree.F in an inert oxygen-free, non-reducing atmosphere.
Abstract:
The present invention relates generally to gas phase processes for producing carboxylic acids or alkyl esters. In one embodiment, a gas phase process for producing a carboxylic acid or an alkyl ester comprises (a) providing a catalyst support comprising deposits of cobalt thiocyanate on at least a portion of the catalyst support; (b) heating the catalyst support to convert the cobalt thiocyanate on the support to cobalt sulfide to form a supported cobalt sulfide catalyst; and (c) reacting alkene gas, steam or an alkanol gas, and a carbon-containing gas in the presence of the supported cobalt sulfide catalyst in a reactor to form a product stream, wherein the carbon-containing gas comprises carbon monoxide or a mixture of carbon monoxide and carbon dioxide, wherein when steam is used as a reactant, the product stream comprises a carboxylic acid, and wherein when alkanol gas is used as a reactant, the product stream comprises an alkyl ester.
Abstract:
Methods and systems for hydroprocessing heavy oil feedstocks to form an upgraded material involve the use of a colloidal or molecular catalyst dispersed within a heavy oil feedstock, a pre-coking hydrocracking reactor, a separator, and a coking reactor. The colloidal or molecular catalyst promotes upgrading reactions that reduce the quantity of asphaltenes or other coke forming precursors in the feedstock, increase hydrogen to carbon ratio in the upgraded material, and decrease boiling points of hydrocarbons in the upgraded material. The methods and systems can be used to upgrade vacuum tower bottoms and other low grade heavy oil feedstocks. The result is one or more of increased conversion level and yield, improved quality of upgraded hydrocarbons, reduced coke formation, reduced equipment fouling, processing of a wider range of lower quality feedstocks, and more efficient use of supported catalyst if used in combination with the colloidal or molecular catalyst, as compared to a conventional hydrocracking process or a conventional thermal coking process.