A method and apparatus are disclosed for carbon dioxide removal and sequestration from ambient air or point source emissions by integration of four self-sufficient systems including a PEO renewable energy generation system, a desalination system, a pH-swing hydration or a direct hydration system, and a bicarbonate fixed, and alkalinity enhanced dense brine sequestration system, in which, the synergy between the PEO energy generation system and other three systems including provision of all needed renewable energy for operation of other three systems, the synergy between the desalination and other systems including provision of freshwater needed for the PEO energy generation system and the pH-swing system, as well as provision of a dense brine fluid from the desalination system to the pH-swing or the direct hydration system, and in the case of available freshwater supply where the desalination system can be avoided.

An ion removal device based on electrochemical and photoelectrochemical methods, and the application of energy conversion and storage are provided. In the ion removal process based on the electrochemical and photoelectrochemical fluidization battery device, the positive active material in the flow battery is the positive pole of device, the negative active material in the fluid battery is the negative pole of the device, and the salt solution is the electrolyte in the middle stream. The positive and negative active materials include organic materials such as 4-hydroxy-piperidinol oxide, riboflavin sodium phosphate or methyl viologen, which have the advantages of low raw material cost, environmental friendliness, high sustainability, excellent electrochemical performance, high specific capacity and good cycle stability etc. The electrolyte can be separated from the positive and negative active liquid flow materials according to the fixed sequence of self-assembly of fluid battery mold.

The present invention discloses a solvent assisted cavitation process for the removal of pollutants from waste water comprising treating waste water in a batch or continuous process in a cavitation device fed with 1-10% of an immiscible solvent resulting in a reduction in concentration of ammoniacal nitrogen and/or COD in the waste water.

The present invention discloses a solvent assisted cavitation process for the removal of pollutants from waste water comprising treating waste water in a batch or continuous process in a cavitation device fed with 1-10% of an immiscible solvent resulting in a reduction in concentration of ammoniacal nitrogen and/or COD in the waste water.

Methods are provided for treating intimately dispersed mixtures of water, bitumen, and fine clay particles, such as oil sands mature fine tailings (MFT). Select methods use dissolved silicate ions and a base (alkali), optionally in combination with a biopolymer, to flocculate a slurry. A mixing regime is disclosed involving the addition to MFT of silicate ions in solution and alkali, to initiate aggregation/destabilization of clay particles. Methods are exemplified that provide distinct sediment layers in conjunction with the release of residual bitumen (for example 40-50% of the initial bitumen content). In these exemplified embodiments, a densely packed bottom layer containing ˜75 wt. % solids showed high yield stress values (3.5-5.5 kPa) and entrapped little residual bitumen (0.2-0.3 wt. %). The methods accordingly segregate a material suitable for reclamation.

Methods are provided for treating intimately dispersed mixtures of water, bitumen, and fine clay particles, such as oil sands mature fine tailings (MFT). Select methods use dissolved silicate ions and a base (alkali), optionally in combination with a biopolymer, to flocculate a slurry. A mixing regime is disclosed involving the addition to MFT of silicate ions in solution and alkali, to initiate aggregation/destabilization of clay particles. Methods are exemplified that provide distinct sediment layers in conjunction with the release of residual bitumen (for example 40-50% of the initial bitumen content). In these exemplified embodiments, a densely packed bottom layer containing ˜75 wt. % solids showed high yield stress values (3.5-5.5 kPa) and entrapped little residual bitumen (0.2-0.3 wt. %). The methods accordingly segregate a material suitable for reclamation.

A method of separating and recovering a cobalt salt and a nickel salt includes a separation step of separating, by using a nanofiltration membrane, a cobalt salt and a nickel salt from a rare metal-containing aqueous solution containing at least both the cobalt salt and the nickel salt as rare metals, in which the nanofiltration membrane has a glucose permeability of 3 times or more a sucrose permeability, the sucrose permeability of 10% or less, and an isopropyl alcohol permeability of 50% or more when a 1,000 mg/L glucose aqueous solution, a 1,000 mg/L sucrose aqueous solution, and a 1,000 mg/L isopropyl alcohol aqueous solution, each having a pH of 6.5 and a temperature of 25° C., individually permeate through the nanofiltration membrane at an operating pressure of 0.5 MPa.

A system for distilling water is disclosed. The system comprises a heat source, and a plurality of open-cycle adsorption stages, each stage comprising a plurality of beds and an evaporator and a condenser between a first bed and a second bed, wherein each bed comprises at least two vapor valves, a plurality of hollow tubes, a plurality of channels adapted for transferring water vapor to and from at least one of the condenser or the evaporator, a thermally conductive water vapor adsorbent, and wherein each vapor valve connects a bed to either the condenser or the evaporator.

The invention relates to a process for working up water containing 4,4′-dichlorodiphenyl sulfoxide and/or 4,4′-dichlorodiphenyl sulfone as impurities, comprising: (a) mixing the water containing 4,4′-dichlorodiphenyl sulfoxide and/or 4,4′-dichlorodiphenyl sulfone as impurities with an organic solvent in which 4,4′-dichlorodiphenyl sulfoxide and/or 4,4′-dichlorodiphenyl sulfone have a solubility of at least 0.5 wt % based on the amount of 4,4′-dichlorodiphenyl sulfoxide and/or 4, 4′-dichlorodiphenyl sulfone and organic solvent at 20° C., which forms a two-phase system with water and which can be stripped from water with a stripping gas and subsequently separating the obtained mixture into an aqueous phase and an organic phase, and (b) stripping the organic solvent from the aqueous phase with a stripping gas.

Liquid solution concentration methods and related systems involving osmosis units and energy recovery are generally described. In some embodiments, an osmotic system has a pump, a first reverse osmosis unit, a second reverse osmosis unit, and one or more energy recovery devices. Various embodiments are directed to features such as balancing streams, recirculation streams, and/or valving that alone or in combination may afford improved energy efficiency and/or system performance. Some embodiments may improve performance of certain types of energy recovery devices in combination with osmosis units, such as isobaric or turbine energy recovery devices.