A system for carbon dioxide capture from a gas mixture comprises an absorber that receives a lean solvent system stream (containing a chemical solvent, physical-solvent, and water) from the stripper, a stripper that receives the rich solvent stream from the absorber and produces the product carbon dioxide and the lean solvent through the use of a reboiler in fluid communication with a lower portion of the stripper, a condenser in fluid communication with a vapor outlet of the stripper, a cross-exchanger in fluid communication with a rich solvent system outlet from the absorber and a rich solvent system inlet on the stripper, and a splitter. The splitter is configured to separate the rich solvent system stream into a first portion and second portion, where the first portion directly passes to the stripper and the second portion passes through the cross-exchanger prior to passing to the stripper.

Disclosed is a process for regenerating a hybrid solvent used to remove contaminants from a fluid stream and to provide an improved yield of purified fluid. Said process comprises a purification unit (12) and at least one regeneration unit (40) wherein make-up water (72) is added to the regenerated lean hybrid solvent (55) prior to reuse in the first purification unit and no water is recycled into the regeneration unit.

Puncture elements and methods for using the same are disclosed. The puncture elements according to the disclosed concept include a cutting edge or a sharp and are composed of a mineral loaded polymer. The minerals of the mineral loaded polymer include an active agent, such as a desiccant. Optionally, the puncture elements are used to puncture a cover (e.g., foil seal) of a package.

The present invention relates to a biocompatible task specific hybrid solvent (TSHS) composition that synergistically increases the carbon capture efficiency and utilizes less energy for CO.sub.2 desorption over the existing solutions. Further, the process of synthesizing such composition is discussed in this disclosure. Also, the present disclosure provides a process that involves a task specific hybrid solvent (TSHS) composition for selective capturing CO.sub.2 from any gaseous stream.

A process is proposed for producing pure hydrogen by steam reforming of a feed gas comprising hydrocarbons, preferably natural gas or naphtha, with a simultaneously low and preferably adjustable export steam flow rate. The process includes the steam reforming of the feed gas, for which the heat of reaction required is provided by combustion of one or more fuel gases with combustion air in a multitude of burners arranged within the reformer furnace. According to the invention, the combustion air, before being introduced into the burners, is heated by means of at least one heat exchanger in indirect heat exchange with the hot flue gas to temperatures of at least 530° C.

A fuel cell system for removing carbon dioxide from anode exhaust gas includes: a fuel cell having an anode configured to output an anode exhaust gas comprising hydrogen, carbon monoxide, carbon dioxide, and water; an anode gas oxidizer; and an absorption system configured to receive the anode exhaust gas, the absorption system including: an absorber column configured to absorb the carbon dioxide from the anode exhaust gas in a solvent and to output a resultant gas comprising hydrogen and a hydrocarbon that is at least partially recycled to the anode; and a stripper column configured to regenerate the solvent and to output a carbon dioxide-rich stream. The anode gas oxidizer is configured to receive and oxidize an anode gas oxidizer input stream and at least a portion of the carbon dioxide-rich stream. The anode gas oxidizer input stream comprises a portion of the anode exhaust gas.

The invention discloses methods and apparatus(es) for the removal and control of pollutants such as gases and suspended particulates in the air of an enclosed space or an outdoor environment by passing the air through absorbent media. The absorbent media includes any liquid, solid or combination of liquid and solid media that is capable of absorbing a material in which it comes in contact. In one aspect of the invention, formaldehyde is removed by air sparging through a liquid such as water, optionally containing additional scavenging agents.

An apparatus includes a housing that defines a first zone, a second zone, a third zone, and a fourth zone. The apparatus includes an inlet, a first outlet, a second outlet, and a conveyor belt. The inlet is configured to receive a carbon dioxide-containing fluid in the first zone. The first outlet is configured to discharge a carbon dioxide-depleted fluid from the first zone. The second outlet is configured to discharge a carbon dioxide-rich fluid from the third zone. The conveyor belt passes through each of the zones. The conveyor belt includes a carbon dioxide sorbent. Within the first zone, the carbon dioxide sorbent is configured to adsorb carbon dioxide from the carbon dioxide-containing fluid to produce the carbon dioxide-depleted fluid. Within the third zone, the carbon dioxide sorbent is configured to desorb the captured carbon dioxide to produce the carbon dioxide-rich fluid.

A process for removing hydrogen sulfide and carbon dioxide from a fluid stream comprises a) an absorption step in which the fluid stream is contacted with an absorbent comprising an aqueous solution (i) of an amine of the general formula (I) ##STR00001##
in which R.sub.1, R.sub.2 and R.sub.3 are each independently selected from C.sub.1-4-alkyl and C.sub.1-4-hydroxyalkyl; each R.sub.4 is independently selected from hydrogen, C.sub.1-4-alkyl and C.sub.1-4-hydroxyalkyl; each R.sub.5 is independently selected from hydrogen, C.sub.1-4-alkyl and C.sub.1-4-hydroxyalkyl; X is OH or NH(CR.sub.1R.sub.2R.sub.3); m is 2, 3, 4 or 5; n is 2, 3, 4 or 5; and o is 0 or 1; and optionally (ii) at least one tertiary amine, where the molar ratio of (i) to (ii) is greater than 0.05; wherein at least 90% of the hydrogen sulfide is removed from the fluid stream and selectivity for hydrogen sulfide over carbon dioxide is not greater than 8, wherein a CO.sub.2— and H.sub.2S-laden absorbent is obtained; b) a regeneration step in which at least a substream of the CO.sub.2— and H.sub.2S-laden absorbent is regenerated and a regenerated absorbent is obtained; and c) a recycling step in which at least a substream of the regenerated absorbent is recycled into the absorption step a). The process allows a high level of hydrogen sulfide removal with a simultaneously high coabsorption of carbon dioxide.

A process is proposed for producing pure hydrogen by steam reforming of a feed gas comprising hydrocarbons, preferably natural gas or naphtha, with a simultaneously low and preferably adjustable export steam flow rate. The process includes the steam reforming of the feed gas, for which the heat of reaction required is provided by combustion of one or more fuel gases with combustion air in a multitude of burners arranged within the reformer furnace. According to the invention, the combustion air, before being introduced into the burners, is heated by means of at least one heat exchanger in indirect heat exchange with the hot flue gas to temperatures of at least 530° C.