Provided are apparatus and systems for performing a swing adsorption process. This swing adsorption process may involve passing streams through adsorbent bed units to treat the pipeline quality natural gas to form a stream that complies with liquefied natural gas (LNG) specifications. The process may involve a combined TSA and PSA process, which is utilized to remove contaminants from the feed stream.

Provided are apparatus and systems for performing a swing adsorption process. This swing adsorption process may involve passing streams through adsorbent bed units to treat the feed stream to form a stream that complies with nitrogen rejection specifications. The process may involve using at least a portion of the nitrogen rejection process product streams as a purge for the swing adsorption process.

An integrated temperature swing adsorption (TSA) process and gas fermentation process and device is disclosed. A heated tail gas stream from the gas fermentation process is used to heat and regenerate adsorbent in the TSA device. A portion of treated feedstock from the TSA device is used to cool the regenerated adsorbent. Integration of a tail gas stream from the gas fermentation zone used for regeneration of absorbent in the TSA eliminates the need for an inert gas regenerant and using TSA treated gas feedstock for cooling regenerated adsorbent allows for maximum recovery and use of available gas feedstock. Alternatively, when a pressure swing adsorption (PSA) process is also employed, a purge stream from the PSA may be used as regenerant in the TSA process.

Processes and apparatuses for reducing molecular weight fluctuation in a tail gas stream from a pressure swing adsorption process. Multiple PSA separation zone are synchronized such that when one of the PSA units is generating a low molecular weight tail gas, there is another PSA unit generating a high molecular weight tail gas.

According to one aspect of the present invention, a pressure swing adsorption (PSA) device includes an adsorption tower configured to introduce hydrogen gas and adsorb impurity components in the hydrogen gas by using a pressure swing adsorption (PSA) method, an adsorbent of one layer made of activated carbon or an adsorbent of two layers in which activated carbon and zeolite are stacked being disposed in the adsorption tower, the hydrogen gas containing carbon monoxide (CO) of 0.5 vol % or more and 6.0 vol % or less and methane (CH.sub.4) of 0.4 vol % or more and 10 vol % or less as the impurity components; and a densitometer configured to detect a concentration of CO in the hydrogen gas discharged from the adsorption tower, wherein the impurity components are adsorbed and removed to cause the CO concentration measured by the densitometer to fall below a threshold.

The present disclosure relates to relates to sorbent coated carbon fibers, modules containing the same, and their use in reducing carbon dioxide levels via direct air capture.

A pressure swing adsorption (PSA) device includes an adsorption tower configured to introduce hydrogen gas and adsorb impurity components in the hydrogen gas by using a pressure swing adsorption (PSA) method, an adsorbent of one layer made of activated carbon or an adsorbent of two layers in which activated carbon and zeolite are stacked being disposed in the adsorption tower, the hydrogen gas containing carbon monoxide (CO) of 0.5 vol % or more and 6.0 vol % or less and methane (CH.sub.4) of 0.4 vol % or more and 10 vol % or less as the impurity components; and a densitometer configured to detect a concentration of CO in the hydrogen gas discharged from the adsorption tower, wherein the impurity components are adsorbed and removed to cause the CO concentration measured by the densitometer to fall below a threshold.

The present invention addresses to the use of NaY zeolite with a Si/Al ratio>2.6 as a solid adsorbent in the process of removing H.sub.2S from natural gas through a PSA process. The described adsorbent has the capacity of removing H.sub.2S from natural gas from offshore exploration platforms, enabling in situ regeneration. The experimental development proved the high capacity of capturing H.sub.2S by the NaY zeolite in consecutive cycles of pressurization, adsorption, depressurization and purging. This capture capacity remains at 74.2% of the initial capacity, remaining stable in subsequent cycles. The structure of the material maintained crystallinity above 95% in use, in 15 consecutive cycles, allowing the reuse of the adsorbent for a prolonged period of operation, preventing the solid from being constantly changed, which is quite common in a non-regenerative process.

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.

An oxygen concentrator device comprising at least 2 separation vessels with a feed end and a product end, and a set of manifolds comprising at least one feed manifold attached to the feed end of the separation vessels and at least one equalization manifold attached to the product end of the separation vessels. The feed manifold comprises compression ports and valving; vacuum ports and valving; and, an upstream headspace equaling 2-6% of the total sorbent volume in the combined sieve beds. The equalization manifold comprises equalization ports and valving; and, a downstream headspace equaling 2-6% of the total sorbent volume in the combined sieve beds. The ratio of compression, vacuum, and equalization Cv to total sorbent volume is

[00001]$0.0005-0.005\left(\frac{\mathrm{gal}}{\min }\right)\left(\frac{1}{L_S}\right).$

Also, a method for concentrating oxygen, providing the set of manifolds described above and operating the oxygen concentrator without separately purging the sieve bed with an unused gas.