The boiler (1) has side tubed walls (2) enclosing an inner space (3) and a device for selective non catalytic reduction (7). The device for selective non catalytic reduction (7) has a lance (8) carrying a hose (9) having at least a nozzle (10) and a hose drive mechanism (11) for driving the hose within the lance. The lance (8) protrudes into the inner space (3) from a side tubed wall (2) of the boiler (1).

A method for preparing a molecular sieve SCR (selective catalytic reduction) catalyst and a prepared catalyst therethrough. In the method, several molecular sieves are mixed and modified by transition metal or rare-earth metal via ion exchange, then loaded Fe by equivalent-volume impregnation, and loaded Cu by one or more liquid ion exchange. This present invention, combined with several techniques, such as modification of stable molecular sieve by transition and rare-earth metal, Fe loading by equivalent-volume impregnation and Cu loading by one or more liquid ion exchange, and after through stable and effective modification and loading control, the obtained catalyst material is coated on a carrier substrate via size mixing and coating process to be prepared into an integral catalyst.

Disclosed herein are base metal catalyst devices for removing ozone, volatile organic compounds, and other pollutants from an air flow stream. A catalyst device includes a housing, a solid substrate disposed within the housing, and a catalyst layer disposed on the substrate. The catalyst layer includes a first base metal catalyst at a first mass percent, a second base metal catalyst at a second mass percent, and a support material impregnated with at least one of the first base metal catalyst or the second base metal catalyst. The preferred catalyst composition is a combination of manganese oxide and copper oxide.

Method of treating gas and gas treatment device, the gas treatment device comprising: a first chamber, comprising a first inlet, a first outlet and a first energy supply system, allowing the gas to enter the first chamber through the first inlet; a second chamber comprising a second outlet and a second energy supply system; a third chamber comprising a third inlet in communication with the first outlet and the second outlet; and a fourth chamber comprising a fourth inlet and a scrubbing system containing a solvent comprising water molecules (H.sub.2O), wherein the third outlet of the third chamber is in communication with the fourth inlet of the fourth chamber.

Systems, devices and methods for submarine CO.sub.2 scrubbing are disclosed. The system may comprise an assembly including a sorbent, a scrubbing inlet configured to receive a first airflow during an adsorption mode. The first airflow may comprise air received from a cabin of a submarine. The assembly may be configured to flow the first airflow over and/or through the sorbent during the adsorption mode such that the sorbent removes a portion of CO.sub.2 entrained in the first airflow. The system may also include a scrubbing outlet configured to expel the scrubbed first airflow from the assembly into the cabin. The system may include an outside air inlet configured to receive a second airflow comprising outside air during a regeneration mode. The system may include a regeneration air outlet in configured to expel the second airflow after the second airflow has flowed over and/or through the sorbent during the regeneration mode.

Disclosed are metal organic frameworks (MOFs) for adsorbing guest species, methods for the separation of gases using the MOFs, and systems comprising the MOFs. The MOFs comprise a plurality of secondary building units (SBUs), each SBU comprising a repeating unit of one metal cation connected to another metal cation via a first moiety of an organic linker; a layer of connected adjacent SBUs in which a second moiety of the linker in a first SBU is connected to a metal cation of an adjacent SBU, and wherein adjacent layers are connected to each other via linker-to-linker bonding interactions

The present invention provides a catalyst for the decomposition of nitrous oxide, said catalyst comprising oxides of cobalt, zinc and aluminum and an alkali metal promoter.

A process for the removal of nitrous oxide from a gas stream having a contaminating concentration of nitrous oxide to provide a gas stream with a significantly reduced concentration of nitrous oxide is described. The process includes the use of a process system having multiple N.sub.2O decomposition reactors each of which contain a nitrous oxide decomposition catalyst and heat transfer units each of which contain a heat sink media that are operatively connected in a particular order and arrangement for use in the process. The gas stream is passed to the process system that is operated for a period of time in a specific operating mode followed by the stopping of such operation and reversal of the process flow. These steps may be repeatedly taken in order to provide for an enhanced energy recovery efficiency for a given nitrous oxide destruction removal efficiency.

A process for the removal of nitrous oxide from a gas stream having a contaminating concentration of nitrous oxide to provide a gas stream with a significantly reduced concentration of nitrous oxide is described. The process includes the use of a process system having multiple N.sub.2O decomposition reactors each of which contain a nitrous oxide decomposition catalyst and heat transfer units each of which contain a heat sink media that are operatively connected in a particular order and arrangement for use in the process. The gas stream is passed to the process system that is operated for a period of time in a specific operating mode followed by the stopping of such operation and reversal of the process flow. These steps may be repeatedly taken in order to provide for an enhanced energy recovery efficiency for a given nitrous oxide destruction removal efficiency.

The invention relates to a process and apparatus for preparing nitric acid by catalytic oxidation of NH.sub.3 by means of oxygen and subsequent reaction of the NO.sub.x formed with an absorption medium in an absorption tower, which comprises a catalyst bed for N.sub.2O decomposition arranged in the process gas downstream of the catalytic NH.sub.3 oxidation and upstream of the absorption tower in the flow direction and a catalyst bed for NO.sub.x reduction and effecting a further decrease in the amount of N.sub.2O arranged in the tailgas downstream of the absorption tower in the flow direction, wherein the amount of N.sub.2O removed in the catalyst bed for N.sub.2O removal arranged in the process gas is not more than that which results in an N.sub.2O content of >100 ppmv and a molar N.sub.2O/NO.sub.x ratio of >0.25 before entry of the tailgas into the catalyst bed for NO.sub.x reduction and the catalyst bed for NO.sub.x reduction and effecting a further decrease in the amount of N.sub.2O arranged in the tailgas contains at least one iron-loaded zeolite catalyst and NH.sub.3 is added to the tailgas before entry into the catalyst bed in such an amount that an NO.sub.x concentration of <40 ppmv results at the outlet from the catalyst bed and the operating parameters are selected in such a way that an N.sub.2O concentration of <200 ppmv results.