Systems and methods of removing coke/tar from water in a quench water recycling loop of a steam cracker quench system are disclosed. The systems include a quench water separator that has a feed calming compartment for reducing eddies in feed to the quench water separator. The feed calming compartment is defined, at least in part, by a perforated baffle in the quench water separator. The methods include the use of the quench water separator with the perforated baffle and the calming compartment to separate coke/tar from quench water in the quench water recycling loop.

Provided are a heating furnace and a graphite production method both of which allow a carbonization step and a graphitization step to be consecutively performed. The heating furnace is a heating furnace for producing graphite from a polymeric material, and includes a heating furnace body for subjecting the polymeric material to heat treatment. The heating furnace body includes a closed vessel for containing the polymeric material. A gas outlet pipe is connected to the closed vessel, the gas outlet pipe being for letting, out of the heating furnace body, a pyrolytic gas generated from the polymeric material.

A metal oxide catalyst synthesized using supercritical carbon dioxide extraction is provided, wherein the metal oxide catalyst includes an active site containing at least one type of metal oxide and a support for loading the active site and the metal oxide is an oxide of a metal selected from the group consisting of transition metals (atomic number 21 to 29, 39 to 47, 72 to 79, or 104 to 108), lanthanide (atomic number 57 to 71), post-transition metals (atomic number 13, 30 to 31, 48 to 50, 80 to 84, and 112), and metalloids (atomic number 14, 32 to 33, 51 to 52, and 85) in the periodic table, and a combination thereof.

A process for the production of a catalyst comprising the steps of: dissolving the requisite quantities of copper nitrate and nickel nitrate in de-ionised water to provide a sub-0.30 molar aqueous solution of copper nitrate and nickel nitrate together in the ratio required; providing an ammoniacal solution by adding concentrated aqueous solution of ammonia in a quantity equal to between six and ten times the quantity required to realise both a 1:6 molar ratio for Cu.sup.2+ to ammonia and a 1:6 molar ratio for Ni.sup.2+ to ammonia; loading gamma alumina with 1 to 30% w/w of copper and nickel in a weight ratio of nickel to copper of 1:5 to 2:1 by suspending the requisite quantity of gamma alumina in said ammoniacal solution to achieve the required loading of copper and nickel; stirring the resulting gamma alumina suspension for at least 4 h at room temperature; then the volatile components evaporate under ambient conditions leaving dry loaded gamma alumina, which is calcined at a temperature of at least 260° C. for at least 30 min with a constant heating up rate; a catalyst or catalyst mixture, the catalyst or each catalyst in the catalyst mixture being obtainable by the above-mentioned process; and the use of the catalyst or catalyst mixture for the conversion of exhaust gases from an internal combustion engine into carbon dioxide, water and nitrogen.

Disclosed are a phosphorus-containing high-silica molecular sieve, its preparation and application thereof, wherein the molecular sieve comprises about 86.5-99.8 wt % of silicon, about 0.1-13.5 wt % of aluminum and about 0.01-6 wt % of phosphorus, calculated as oxides and based on the dry weight of the molecular sieve, the molecular sieve has an XRD pattern with at least three diffraction peaks, the first strong peak is present at a diffraction angle of about 5.9-6.9°, the second strong peak is present at a diffraction angle of about 10.0-11.0°, and the third strong peak is present at a diffraction angle of about 15.6-16.7°. The phosphorus-containing high-silica molecular sieve shows an improved hydrocracking activity in the presence of nitrogen-containing species when used in the preparation of hydrocracking catalysts.

A catalyst comprising a microporous crystalline metallosilicate having a Constraint Index of 12, or 10, or 8, or 6 or less, a binder, a Group 1 alkali metal or a compound thereof and/or a Group 2 alkaline earth metal or a compound thereof, a Group 10 metal or a compound thereof, and, optionally, a Group 11 metal or a compound thereof; wherein the catalyst is calcined in a first calcining step before the addition of the Group 10 metal or compound thereof and optionally the Group 11 metal or compound thereof; and wherein the first calcining step includes heating the catalyst to first temperatures of greater than 500° C.; and wherein the catalyst is calcined in a second calcining step after the addition of the Group 10 metal or compound thereof and optionally the Group 11 metal or compound thereof wherein the second calcining step includes heating the catalyst to temperatures of greater than 400° C.

A horizontal pyrolysis furnace has a kiln and two barrels. The two barrels are respectively a processing barrel rotatably disposed in the kiln and a takeover barrel detachably connected with the processing barrel. Each one of the two barrels has a gate assembly and at least one spiral guiding plate. The gate assembly of the processing barrel is mounted on an end of the processing barrel, and extends out from the kiln. The two gate assemblies of the two barrels are detachably connected such that the two barrels are able to rotate synchronously. The at least one spiral guiding plate is fixed on an inner surface of one of the two barrels, and the spiral guiding plates of both barrels have an identical helical direction.

An installation for the conversion of uranium hexafluoride (UF.sub.6) to uranium dioxide (UO.sub.2) comprises a hydrolysis reactor (4) for the conversion of UF.sub.6 into uranium oxyfluoride powder (UO.sub.2F.sub.2), a pyrohydrolysis furnace (6) for converting the UO.sub.2F.sub.2 powder supplied by the reactor (4) into UO.sub.2 powder, a supply device (8) comprising reagent injection ducts (10) for the injection of UF.sub.6, water vapor or H.sub.2, and a control system (16) designed to control the supply device (8) so as to supply at least one of the reagent injection ducts (10) with a neutral gas during a shut-down or start-up phase of the conversion installation.

Process for fixed-bed reforming of a hydrocarbon-based feedstock comprising n-paraffinic, naphthenic and aromatic hydrocarbons, at a temperature of between 400 and 700° C., a pressure of between 0.1 and 4 MPa, and a mass flow of feedstock treated per unit mass of catalyst and per hour of between 0.1 and 10 h.sup.−1, by bringing said feedstock into contact with a catalyst comprising platinum, a promoter metal selected from the group consisting of rhenium and iridium, a halogen selected from the group consisting of fluorine, chlorine, bromine and iodine, and a porous alumina support in the form of an extrudate characterized by a length “l” of between 1 and 10 mm, a section comprising four lobes, the largest diameter “D” of the cross section of said extrudate being between 1 and 3 mm.

A system and related methods for the production of lime sorbent compositions from a calcium carbonate feedstock formed using flash calcination to produce the intermediate calcium oxide material.