The present invention provides a beverage and a dermatological composition comprising water molecules, the water molecules having oxygen atoms of different isotopes, the beverage being enriched in at least one of the oxygen isotopes, the enrichment being in reference to (i) the amount of that oxygen isotope in the water used to produce the beverage or (ii) the amount of that oxygen isotope in ground water, or (iii) Vienna Standard Mean Ocean Water. The water molecules may be derived from a plant source, such as a juice, a sap or a tree water.

The present invention is generally directed to a reactor for the production of low-carbon syngas from captured carbon dioxide and renewable hydrogen. The hydrogen is generated from water using an electrolyzer powered by renewable electricity or from any other method of low-carbon hydrogen production. The improved catalytic reactor is energy efficient and robust when operating at temperatures up to 1800° F. Carbon dioxide conversion efficiencies are greater than 75% with carbon monoxide selectivity of greater than 98%. The catalytic reactor is constructed of materials that are physically and chemically robust up to 1800° F. As a result, these materials are not reactive with the mixture of hydrogen and carbon dioxide or the carbon monoxide and steam products. The reactor materials do not have catalytic activity or modify the physical and chemical composition of the conversion catalyst. Electrical resistive heating elements are integrated into the catalytic bed of the reactor so that the internal temperature decreases by no more than 100° F. from the entrance at any point within the reactor. The catalytic process exhibits a reduction in performance of less than 0.5% per 1000 operational hours.

The present invention is generally directed to a reactor for the production of low-carbon syngas from captured carbon dioxide and renewable hydrogen. The hydrogen is generated from water using an electrolyzer powered by renewable electricity or from any other method of low-carbon hydrogen production. The improved catalytic reactor is energy efficient and robust when operating at temperatures up to 1800° F. Carbon dioxide conversion efficiencies are greater than 75% with carbon monoxide selectivity of greater than 98%. The catalytic reactor is constructed of materials that are physically and chemically robust up to 1800° F. As a result, these materials are not reactive with the mixture of hydrogen and carbon dioxide or the carbon monoxide and steam products. The reactor materials do not have catalytic activity or modify the physical and chemical composition of the conversion catalyst. Electrical resistive heating elements are integrated into the catalytic bed of the reactor so that the internal temperature decreases by no more than 100° F. from the entrance at any point within the reactor. The catalytic process exhibits a reduction in performance of less than 0.5% per 1000 operational hours.

The freezing point of a liquid in a chilled liquid containment system is decreased by the addition of a mixture of sodium nitrite and sodium nitrate. Solutions of nitrite/nitrate in a ratio of 1.0:1 to 3.0:1 at a concentration of at least 25% lowers the freezing point of water to as low as −33° C. or lower, permitting water to remain liquid well below its ambient freezing point and preventing pipes containing the nitrite/nitrate solution from bursting when exposed to subzero temperatures. This allows liquids to remain liquid at much lower temperatures than normal, allowing the circulation of the liquids at lower temperatures and protecting their containment systems from the damage that could occur when the liquids freeze into their solid state while within the containment systems.

The freezing point of a liquid in a chilled liquid containment system is decreased by the addition of a mixture of sodium nitrite and sodium nitrate. Solutions of nitrite/nitrate in a ratio of 1.0:1 to 3.0:1 at a concentration of at least 25% lowers the freezing point of water to as low as −33° C. or lower, permitting water to remain liquid well below its ambient freezing point and preventing pipes containing the nitrite/nitrate solution from bursting when exposed to subzero temperatures. This allows liquids to remain liquid at much lower temperatures than normal, allowing the circulation of the liquids at lower temperatures and protecting their containment systems from the damage that could occur when the liquids freeze into their solid state while within the containment systems.

Provided are a structured catalyst for CO shift or reverse shift that can realize a long life time by suppressing the decline in function, a method for producing the same, a CO shift or reverse shift reactor, a method for producing carbon dioxide and hydrogen, and a method for producing carbon monoxide and water. The structured catalyst for CO shift or reverse shift (1) includes a support (10) of a porous structure composed of a zeolite-type compound, and at least one CO shift or reverse shift catalytic substance (20) present in the support (10), the support (10) has channels (11) connecting with each other, and the CO shift or reverse shift catalytic substance (20) is present at least in the channels (11) of the support (10).

Provided are a structured catalyst for CO shift or reverse shift that can realize a long life time by suppressing the decline in function, a method for producing the same, a CO shift or reverse shift reactor, a method for producing carbon dioxide and hydrogen, and a method for producing carbon monoxide and water. The structured catalyst for CO shift or reverse shift (1) includes a support (10) of a porous structure composed of a zeolite-type compound, and at least one CO shift or reverse shift catalytic substance (20) present in the support (10), the support (10) has channels (11) connecting with each other, and the CO shift or reverse shift catalytic substance (20) is present at least in the channels (11) of the support (10).

The invention relates to a process for producing synthesis gas (5) in which hydrocarbon (2) is decomposed thermally in, a first reaction zone (11) to hydrogen and carbon, and hydrogen formed is passed from the first reaction zone (Z1) into a second action zone (Z2) in order to be reacted therein with carbon dioxide (4) to give water and carbon monoxide. The characteristic feature here is that energy required for the thermal decomposition of the hydrocarbon is supplied to the first reaction zone (Z1) from the second reaction zone (Z2).

The invention relates to a process for producing synthesis gas (5) in which hydrocarbon (2) is decomposed thermally in, a first reaction zone (11) to hydrogen and carbon, and hydrogen formed is passed from the first reaction zone (Z1) into a second action zone (Z2) in order to be reacted therein with carbon dioxide (4) to give water and carbon monoxide. The characteristic feature here is that energy required for the thermal decomposition of the hydrocarbon is supplied to the first reaction zone (Z1) from the second reaction zone (Z2).

The invention relates to a system for generating superheated steam using hydrogen peroxide, formed by: a container for storing hydrogen peroxide, which stores a solution of peroxide that is used during the reaction to generate superheated steam; a hydrogen peroxide discharge pump connected to a first connecting duct, said discharge pump being used to pump the hydrogen peroxide solution to a reaction container via a second connecting duct; and a steam generating reaction container or reactor, in which the reaction takes place and the superheated steam is generated, said reaction container or reactor receiving the hydrogen peroxide solution in order for the reaction to take place and the superheated steam to be generated and subsequently conveyed through a nozzle and an outlet duct towards installations that are to undergo cleaning and/or stimulation.