The use of a composition including at least one acido-basic neutralising agent for decontaminating an atmosphere contaminated by a corrosive gas, the acido-basic neutralising agent having at least 2 pKa's and being characterised by: pKa 1≤pKa 2, pKa 1>2, pKa 2<12, 4<½ (pKa 1+pKa 2)<10 pKa 1, representing the smallest of the basic pKa's and pKa 2 representing the largest of the acidic pKa's. Also, a method for decontaminating an atmosphere contaminated by a corrosive gas comprising the spraying of the neutralising agent, and to a decontamination device.

A gas-liquid contacting apparatus and method are described, in which at least one rotor assembly including packing is arranged in a contacting chamber containing at least one stator assembly including at least one heat exchanger arranged to thermally modulate the gas-liquid contacting so that each stator assembly is operatively arranged with each stator assembly to provide gas-liquid contacting at temperatures effective for mass exchange between the gas and liquid. The rotor and stator assemblies may be of annular shape, or may be of disk shape in a stacked array of rotor assemblies alternating with stator assemblies. Such apparatus and method are usefully employed for CO.sub.2 capture from CO.sub.2-containing flue gases such as combustion effluents from power generation plants.

Scavenging chemicals used in mitigation treatments of hydrogen sulfide in hydrocarbon streams often continue to react and form polymers that foul the processing system. Disclosed herein are methods for determining if a scavenging chemical mitigator, or its reaction or degradation product, will polymerized during or after mitigation treatments. This information allows for the optimization of mitigation treatments that pre-emptively control or prevent polymer formation. Such pre-emption measures reduce the cost and time related to remedial actions to treat polymer-fouled equipment.

Devices and methods for controlling humidity including an aqueous saturated solution of a salt and/or a sugar in combination with an additive in which all components of the saturated solution are food grade. The device may or may not include a container, such as a flexible pouch, encasing the aqueous saturated solution and/or an absorbent pad. The pouch or other container may be made of a material which is moisture permeable and liquid impermeable, for example, and the aqueous saturated solution further comprises a thickening agent. In some embodiments, the components of the aqueous saturated salt solution are separately contained in different compartments of the device container, and a user may activate the device to mix the components together.

A method for separating gaseous carbon dioxide from a gas mixture by cyclic adsorption/desorption using a sorbent material adsorbing said gaseous carbon dioxide, wherein the method comprises the following sequential and in this sequence repeating steps: (a) an adsorption step; (b) and isolating step; (c) injecting a stream of saturated or superheated steam and thereby inducing an increase in internal pressure of the reactor unit and an increase of the temperature of the sorbent from ambient atmospheric temperature to a temperature between 60 and 110° C., starting the desorption of CO2; (d) extracting at least the desorbed gaseous carbon dioxide from the unit and separating gaseous carbon dioxide from water by condensation in or downstream of the unit, while preferably still injecting; (e) bringing the sorbent material to ambient atmospheric pressure conditions and ambient atmospheric temperature conditions

Scavenging chemicals used in mitigation treatments of hydrogen sulfide in hydrocarbon streams often continue to react and form polymers that foul the processing system. Disclosed herein are methods for determining if a scavenging chemical mitigator, or its reaction or degradation product, will polymerized during or after mitigation treatments. This information allows for the optimization of mitigation treatments that pre-emptively control or prevent polymer formation. Such pre-emption measures reduce the cost and time related to remedial actions to treat polymer-fouled equipment.

A process for removal of mercury in a gas dehydration system comprising (a) adding a complexing agent to a recirculated glycol solvent as part of the glycol solution feed prior to or at the dehydration liquid contactor and recirculating continuously with the glycol solvent, (b) selectively reacting the complexing agent with mercury in the wet natural gas to remove the mercury from the dry natural gas product, (c) and feeding the rich glycol with the complexing agent to a regenerator and continuously regenerating.

The invention relates to a process for dehumidifying a moist gas mixture. The invention further relates to an apparatus for dehumidifying a moist gas mixture and to the use of said apparatus in the process according to the invention.

A method of treating a switchable polarity material comprises introducing a first feed stream comprising a solvent and a non-polar form of the switchable polarity material to a first side of a gas diffusion membrane. A second feed stream comprising an acid gas is introduced to a second side of the gas diffusion membrane opposing the first side of the gas diffusion membrane. Molecules of the acid gas of the second feed stream are diffused across the gas diffusion membrane and into the first feed stream to form a product stream comprising a polar form of the switchable polarity material. A treatment system for a switchable polarity material, and a method of liquid treatment are also described.

The invention relates to a method for treating emergency spill or leak of halogen which is bromine or chlorine, comprising contacting an aqueous solution of quaternary ammonium halide with the halogen.