C01B2203/0266

METHODS FOR PROCESSING A HYDROCARBON OIL FEED STREAM UTILIZING A GASIFICATION UNIT AND STEAM ENHANCED CATALYTIC CRACKER

An integrated process for upgrading a hydrocarbon oil feed stream utilizing a gasification unit and steam enhanced catalytic cracker includes solvent deasphalting the hydrocarbon oil stream to form at least a deasphalted oil stream and heavy residual hydrocarbons, the heavy residual hydrocarbons including at least asphaltenes; processing the heavy residual hydrocarbons in a gasification unit to form syngas and gasification residue; hydrotreating the deasphalted oil stream to form a light C.sub.5+ hydrocarbon stream, and a heavy C.sub.5+ hydrocarbon stream; steam enhanced catalytically cracking the light C.sub.5+ hydrocarbon stream to form a light steam enhanced catalytically cracked product stream including olefins, benzene, toluene, xylene, naphtha, or combinations thereof; and steam enhanced catalytically cracking the heavy C.sub.5+ hydrocarbon stream to form a heavy steam enhanced catalytically cracked product including olefins, benzene, toluene, xylene, naphtha, or combinations thereof.

INTEGRATION OF HYDROGEN LIQUEFACTION WITH GAS PROCESSING UNITS
20200141637 · 2020-05-07 ·

A method of liquefying hydrogen, including dividing a hydrogen stream into at least a first fraction and a second fraction, introducing the first fraction into a refrigeration cycle of a hydrogen liquefaction unit, thereby liquefying a product hydrogen stream, withdrawing one or more warm hydrogen stream(s) from the hydrogen liquefaction unit, and returning the one or more warm hydrogen stream to the hydrogen stream, wherein the second fraction is combined with a high-pressure nitrogen stream to form an ammonia synthesis gas stream.

SYSTEMS AND PROCESSES FOR MOLTEN MEDIA PYROLYSIS

Systems and methods for molten media pyrolysis for the conversion of methane into hydrogen and carbon-containing particles are disclosed. The systems and methods include the introduction of seed particles into the molten media to facilitate the growth of larger, more manageable carbon-containing particles. Additionally or alternatively, the systems and methods can include increasing the residence time of carbon-containing particles within the molten media to facilitate the growth of larger carbon-containing particles.

SYSTEMS AND PROCESSES FOR MOLTEN MEDIA PYROLYSIS

Systems and methods for molten media pyrolysis for the conversion of methane into hydrogen and carbon-containing particles are disclosed. The systems and methods include the introduction of seed particles into the molten media to facilitate the growth of larger, more manageable carbon-containing particles. Additionally or alternatively, the systems and methods can include increasing the residence time of carbon-containing particles within the molten media to facilitate the growth of larger carbon-containing particles.

PRESSURE SWING ADSORPTION APPARATUS FOR HYDROGEN PURIFICATION FROM DECOMPOSED AMMONIA GAS AND HYDROGEN PURIFICATION METHOD USING THE SAME

The present disclosure relates to a pressure swing adsorption apparatus for hydrogen purification from decomposed ammonia gas and a hydrogen purification method using the same, and more particularly, the pressure swing adsorption apparatus of the present disclosure includes a plurality of adsorption towers including a pretreatment unit and a hydrogen purification unit wherein the adsorption towers of the pretreatment unit and the hydrogen purification unit are packed with different adsorbents, thereby achieving high purity hydrogen purification from mixed hydrogen gas produced after ammonia decomposition, making it easy to replace the adsorbent for ammonia removal, minimizing the likelihood that the lifetime of the adsorbent in the hydrogen purification unit is drastically reduced by a very small amount of ammonia, and actively responding to a large change in ammonia concentration in the raw material.

Additionally, a hydrogen purification method using the pressure swing adsorption apparatus of the present disclosure physically adsorbs and removes impurities such as moisture (H.sub.2O), ammonia (NH.sub.3) and nitrogen (N.sub.2) included in mixed hydrogen gas produced after ammonia decomposition below extremely small amounts, thereby achieving high purity hydrogen purification with improved selective adsorption of moisture, ammonia and nitrogen and maximized hydrogen recovery rate and productivity. In addition, since the temperature swing adsorption process is not introduced, there is no need for a heat source for regeneration, thereby reducing the driving cost.

Fuel endothermic reaction to cool a load

Various embodiments that pertain to fuel processing are described. A fuel processor can produce an endothermic reaction that cools a substance and produces a processed fuel from a raw fuel. A generator can employ the processed fuel to produce an electricity. The generator can supply the electricity to a load that uses the electricity to function. The load can become hot due to its functioning and can benefit from being cooled. The substance cooled by the fuel processor can cool load and in the process the substance can rise in temperature. This warmer substance can be transferred to the fuel processor to be cooled again and this cycle can continue. Further, the fuel processor can use the warmer substance to achieve the endothermic reaction.

HYDROGEN PRODUCTION SYSTEM AND HYDROGEN PRODUCTION METHOD USING BIOCHAR OVEN

Disclosed is a hydrogen production system using a biochar oven, the system including: a vertical pyrolysis furnace into which a pyrolysis target including at least one of waste plastic and fossil fuel is supplied in a free fall scheme by its own weight; a plate-shaped flameless heater configured to heat the vertical pyrolysis furnace such that a high-temperature atmosphere of 800 to 1300? C. is generated therein; a solid-gas separator installed under a bottom of the vertical pyrolysis furnace and configured to receive a biochar-gas mixture produced from the vertical pyrolysis furnace and to separate the biochar-gas mixture into the BOG and the biochar and to discharge the BOG and the biochar; and a BOG purification unit configured to receive therein the biochar separated using the solid-gas separator therefrom, and use the received biochar as an adsorbent, wherein the BOG separated using the solid-gas separator passes through the received biochar in the BOG purification unit such that impurities contained in the BOG are removed therefrom.

Apparatuses For Gasifying Glycerol Using Solar Energy, Systems Including The Apparatuses, and Methods of Using The Apparatuses

Apparatuses for gasifying glycerol using solar energy, system including the apparatuses, and methods of using the apparatuses are provided. The apparatuses may include a concentrated solar dish comprising an opening and a gasifying reactor comprising a chamber. An entrance of the chamber may be aligned to the opening. The apparatuses may also include a thermal insulator disposed on outer surfaces of the concentrated solar dish and the gasifying reactor and a pipe in the thermal insulator. The pipe may be configured to deliver glycerol into the chamber of the gasifying reactor in the form of atomized mist. The glycerol may be delivered to a portion of the chamber adjacent the opening.

COFFEE AS A CARBON SOURCE IN THE PREPARATION OF IRON AND FERRO-ALLOYS
20240175100 · 2024-05-30 ·

The present disclosure broadly relates to processes for preparing iron and ferro-alloys using coffee as a source of carbon.

METHODS AND SYSTEMS FOR ADJUSTING INPUTS TO A PYROLYSIS REACTOR TO IMPROVE PERFORMANCE

Methods and systems are disclosed that monitor the carbon and hydrogen production of a pyrolysis reactor system and adjust one or more inputs to the reactor system to improve performance when one or both of the monitored carbon and hydrogen production falls outside of a target performance specification. In particular, the ratio of fuel to oxidant (fuel/oxidant ratio) supplied to a combustion chamber of the reactor system is adjusted to below a fuel/oxidant equivalence ratio range, defined as 0.9-1.1, when both carbon and hydrogen production falls below a target carbon and hydrogen specification, and adjusted above the fuel/oxidant equivalence ratio range when only the carbon production falls below a target carbon specification. The target specification can include a number of parameters including production rate, morphology (of carbon), and operating temperature.