Abstract: A backrest pivoting system can have a backrest and an actuator for pivoting the backrest. The actuator is pivotably connected to the backrest by a pivot defining a first pivot axis. The backrest can pivot about a guide member which defines a second pivot axis coaxial with the first pivot axis. A backrest pivoting system can include an actuator and a resilient member mounted in series with the actuator. There is also provided an extendable user support assembly comprising a lower body support panel and a core support panel supported by a frame, the lower body support panel being translatable relative to the frame such that an opening is created between the lower body support panel and the core support panel when the lower body support panel is translated away from the core support panel. There is also provided a method for placing a bed in a vascular position.

Abstract: A device for a timepiece, comprising a support, an inertial regulating member mounted so as to rotate relative to the support by an elastic suspension connecting said regulating member to the support. The regulating member comprises a number n of rigid portions interconnected in pairs by n elastic coupling links. The elastic suspension comprises n elastic suspension links respectively connecting each rigid portion to the support.

Abstract: A process for producing magnesia can include contacting CO2-containing emissions with a magnesium-containing material to produce magnesium carbonate; subjecting the magnesium carbonate to calcination to produce a CO2 by-product and magnesia; and recycling at least a portion of the CO2 by-product for contacting the magnesium-containing material to produce the magnesium carbonate. The magnesium-containing material can include mining residues, such as phyllosilicate or chrysotile mining residue, and the magnesium carbonate produced can include precipitated nesquehonite that is subjected to calcination to produce the magnesia.

Abstract: A process for producing magnesia can include contacting CO2-containing emissions with a magnesium-containing material to produce magnesium carbonate; subjecting the magnesium carbonate to calcination to produce a CO2 by-product and magnesia; and recycling at least a portion of the CO2 by-product for contacting the magnesium-containing material to produce the magnesium carbonate. The magnesium-containing material can include mining residues, such as phyllosilicate or chrysotile mining residue, and the magnesium carbonate produced can include precipitated nesquehonite that is subjected to calcination to produce the magnesia.

Abstract: It is described an extracorporeal blood treatment apparatus (1) with a user interface (12) device capable configuring and allowing execution of one or more isolated ultrafiltration tasks during the course of a dialysis treatment. The extracorporeal blood treatment apparatus (1) is controlled in a normal mode, where dialysis fluid is fed to the blood treatment unit (2), and in an isolated ultrafiltration mode, where fresh dialysis fluid is no longer fed to the blood treatment unit (2).

Abstract: Techniques are described for chemical sequestration of carbon dioxide and production of precipitated magnesium carbonate. The process can include contacting carbon dioxide from industrial emissions with water and magnesium-containing particulate material, such as serpentinite, which is thermally pre-treated and has a particle size of at most 75 microns. The process can also include separation of the loaded aqueous stream from the solids, followed by precipitation of magnesium carbonate material that includes carbon and oxygen from industrial emissions and magnesium from serpentinite or chrysotile mining residue, for example.

Abstract: It is described an extracorporeal blood treatment apparatus (1) with a user interface (12) device capable configuring and allowing execution of one or more isolated ultrafiltration tasks during the course of a dialysis treatment. The extracorporeal blood treatment apparatus (1) is controlled in a normal mode, where dialysis fluid is fed to the blood treatment unit (2), and in an isolated ultrafiltration mode, where fresh dialysis fluid is no longer fed to the blood treatment unit (2).

Abstract: A process for producing magnesia can include contacting CO2-containing emissions with a magnesium-containing material to produce magnesium carbonate; subjecting the magnesium carbonate to calcination to produce a CO2 by-product and magnesia; and recycling at least a portion of the CO2 by-product for contacting the magnesium-containing material to produce the magnesium carbonate. The magnesium-containing material can include mining residues, such as phyllosilicate or chrysotile mining residue, and the magnesium carbonate produced can include precipitated nesquehonite that is subjected to calcination to produce the magnesia.

Abstract: It is described an extracorporeal blood treatment apparatus (1) with a user interface (12) device capable configuring and allowing execution of one or more isolated ultrafiltration tasks during the course of a dialysis treatment. The extracorporeal blood treatment apparatus (1) is controlled in a normal mode, where dialysis fluid is fed to the blood treatment unit (2), and in an isolated ultrafiltration mode, where fresh dialysis fluid is no longer fed to the blood treatment unit (2).

Abstract: Techniques are described for chemical sequestration of carbon dioxide and production of precipitated magnesium carbonate. The process can include contacting carbon dioxide from industrial emissions with water and magnesium-containing particulate material, such as serpentinite, which is thermally pre-treated and has a particle size of at most 75 microns. The process can also include separation of the loaded aqueous stream from the solids, followed by precipitation of magnesium carbonate material that includes carbon and oxygen from industrial emissions and magnesium from serpentinite or chrysotile mining residue, for example.

Abstract: Techniques are described for chemical sequestration of carbon dioxide and production of precipitated magnesium carbonate. The process can include contacting carbon dioxide from industrial emissions with water and magnesium-containing particulate material, such as serpentinite, which is thermally pre-treated and has a particle size of at most 75 microns. The process can also include separation of the loaded aqueous stream from the solids, followed by precipitation of magnesium carbonate material that includes carbon and oxygen from industrial emissions and magnesium from serpentinite or chrysotile mining residue, for example.

Abstract: A process has been developed in order to recover and recycle the metals present in spent batteries, including alkaline spent batteries alone or mixed with other types of spent batteries. This method shows a good potential in terms of metals recoveries efficiencies and economic feasibility. Firstly, the spent batteries are crushed (optionally after having been frozen in the case of spent batteries of mixed types). Then, the undesirable parts (plastics, steel cases, papers, etc.) are removed by screening. The collected powder, containing the metals, is mixed with a solution of sulfuric acid in the presence of a reducing agent. The solid/liquid separation is carried out by filtration and the leachate is purified in order to selectively recover the metals.

Abstract: Techniques are described for chemical sequestration of carbon dioxide and production of precipitated magnesium carbonate. The process can include contacting carbon dioxide from industrial emissions with water and magnesium-containing particulate material, such as serpentinite, which is thermally pre-treated and has a particle size of at most 75 microns. The process can also include separation of the loaded aqueous stream from the solids, followed by precipitation of magnesium carbonate material that includes carbon and oxygen from industrial emissions and magnesium from serpentinite or chrysotile mining residue, for example.

Abstract: Processes, methods, system and uses in relation to chemical sequestration of carbon dioxide from a carbon dioxide containing gas by carbonation of an alkaline earth metal containing material. The carbon dioxide containing gas is contacted with an aqueous slurry in a carbonation unit for carbonation of at least a portion of the alkaline earth metal to produce a carbon dioxide depleted gas and a carbonate loaded slurry which is substantially exempt of precipitated alkaline earth. metal carbonates. The carbonate loaded slurry is then separated into an aqueous phase and a solid phase; and the aqueous phase is supplied to a precipitation unit for precipitating alkaline earth metal carbonates. The carbonation stage may be performed at a carbonation temperature between about 10° C. and about 40° C. and a carbonation pressure between about 1 bar and about 20 bars. The solid phase may be recycled to the carbonation stage.

Abstract: It is described an extracorporeal blood treatment apparatus (1) with a user interface (12) device capable configuring and allowing execution of one or more isolated ultrafiltration tasks during the course of a dialysis treatment. The extracorporeal blood treatment apparatus (1) is controlled in a normal mode, where dialysis fluid is fed to the blood treatment unit (2), and in an isolated ultrafiltration mode, where fresh dialysis fluid is no longer fed to the blood treatment unit (2).

Abstract: A process for decontaminating a medium polluted with metals and hydrophobic organic compounds (HOC) includes providing an acidic slurry of water, acid, chloride salt, surfactant, and the polluted medium. Flotation is preformed on the acidic slurry to form a HOC-rich froth and an HOC-depleted slurry and the froth is recovered. The slurry is separated to obtain a treated solid and a liquid effluent rich in metallic ions. Preferably, the process also includes recuperating the metals by chemical precipitation and/or electrodeposition to produce a treated solution. Also provided are a decontaminant having an acid, a chloride salt, and a surfactant as well as a chemical kit for decontaminating the polluted medium including the decontaminant in which the acid, chloride salt and surfactant can be mixed with polluted medium in the presence of water before removing at least a portion of the metals and HOC from the polluted medium.

Abstract: Processes, methods, system and uses in relation to chemical sequestration of carbon dioxide from a carbon dioxide containing gas by carbonation of an alkaline earth metal containing material. The carbon dioxide containing gas is contacted with an aqueous slurry in a carbonation unit for carbonation of at least a portion of the alkaline earth metal to produce a carbon dioxide depleted gas and a carbonate loaded slurry which is substantially exempt of precipitated alkaline earth. metal carbonates, The carbonate loaded slurry is then separated into an aqueous phase and a solid phase; and the aqueous phase is supplied to a precipitation unit for precipitating alkaline earth metal carbonates. The carbonation stage may be performed at a carbonation temperature between about 10° C. and about 40° C. and a carbonation pressure between about 1 bar and about 20 bars. The solid phase may be recycled to the carbonation stage.

Abstract: A process for decontaminating a medium polluted with metals and hydrophobic organic compounds (HOC) includes providing an acidic slurry of water, acid, chloride salt, surfactant, and the polluted medium. Flotation is preformed on the acidic slurry to form a HOC-rich froth and an HOC-depleted slurry and the froth is recovered. The slurry is separated to obtain a treated solid and a liquid effluent rich in metallic ions. Preferably, the process also includes recuperating the metals by chemical precipitation and/or electrodeposition to produce a treated solution. Also provided are a decontaminant having an acid, a chloride salt, and a surfactant as well as a chemical kit for decontaminating the polluted medium including the decontaminant in which the acid, chloride salt and surfactant can be mixed with polluted medium in the presence of water before removing at least a portion of the metals and HOC from the polluted medium.

Abstract: Described is a process for decontaminating wood treated with preservative such as chromium copper arsenate (CCA) including contacting the contaminated wood with water and inorganic acid at a concentration between 0.05 and 0.8 N at less than 100° C. to leach out the contaminants and then separate the wood from the solution. Also described is a process for extracting metals such as copper from a solution containing chromium, copper and arsenic, such as the leachate solution used to decontaminate CCA-treated wood, by precipitation using a coagulant at a pH favoring precipitation of arsenic and continued solubility of copper, or by ion exchange resins.

Abstract: A process for treating a waste material coming from aluminum production, the waste material containing contaminants polycyclic aromatic hydrocarbons (PAH) and inorganic fluoride compounds containing fluoride ions, involves flotation of a waste mixture of the waste material in the presence of a surfactant capable of producing PAH-rich micelles that are floated to produce froth containing the PAH-rich micelles; and stabilization of the waste mixture by adding a fluoride ion stabilizer to form stabilized fluoride compounds with reduced solubility in the waste mixture and in a toxicity characteristics leaching procedure test, to produce decontaminated solids containing the stabilized fluoride compounds and a leachate solution.