An atomizing liquid gel with reversible phase transition characteristics includes: a sugar-based gelling agent, 0.1-3.0 wt %; an atomizing liquid, 97.0-99.9 wt %; a molecule of the sugar-based gelling agent is a sugar molecule introduced with an amide group and/or an aryl group, and the sugar molecule optionally further includes at least one hydrophobic structural part selected from —C.sub.xH.sub.y, —O—C.sub.xH.sub.y and ##STR00001##
and x>2 and y>2. The atomizing liquid gel has characteristics of thermal reversible phase transition and/or shear reversible phase transition, a temperature of gel-sol phase transition is 100° C.-248° C., and a critical shear stress of the gel-sol phase transition is 40-800 Pa. Under heating and/or oscillation, the atomizing liquid gel converts from the gel state to a sol state, and the atomizing agent fixed in the gel releases to form an inhalable aerosol. When the heating and/or oscillation are stopped, the atomizing liquid gel is quickly recovered from the sol state to the gel state, and the unatomized atomizing agent is refixed in the gel. The use of the atomizing liquid gel solves the problem of liquid leakage of the liquid nicotine of the atomizer caused by the smoke condensate after the smoking stops, the change of air pressure or the action of external force during transportation.

The present disclosure relates to the technical field of material and heat exchange and in particular, to a coating material applied to a heat exchanger, a method of preparing the coating material, a heat exchanger, and a method of treating the heat exchanger. The coating material of the present disclosure applied to a heat exchanger includes a hydrophobic material and a light-to-heat conversion material. Under irradiation of visible light, the light-to-heat conversion material can effectively increase the surface temperature of a coated object, which is beneficial to increasing the surface temperature of the coated object while exerting the hydrophobic performance of the hydrophobic material, thus further improving the effect in slowing down frosting.

The present disclosure relates to the technical field of material and heat exchange and in particular, to a coating material applied to a heat exchanger, a method of preparing the coating material, a heat exchanger, and a method of treating the heat exchanger. The coating material of the present disclosure applied to a heat exchanger includes a hydrophobic material and a light-to-heat conversion material. Under irradiation of visible light, the light-to-heat conversion material can effectively increase the surface temperature of a coated object, which is beneficial to increasing the surface temperature of the coated object while exerting the hydrophobic performance of the hydrophobic material, thus further improving the effect in slowing down frosting.

Described herein is the use of organic materials in methods of barocaloric cooling. The barocaloric effects may be exhibited where the organic material is near a non-isochoric phase transition, such as a non-isochoric first-order phase transition. The organic material has one or more carbon atoms and may be an organic compound or a salt thereof. In some cases that organic material is a soft matter material, such as a plastic crystal or a liquid crystal. The methods may be adapted for use of the organic material as a heating agent.

The present application pertains to liquid-liquid phase transition compositions and processes. In one embodiment a liquid-liquid phase transition process comprises first forming a composition comprising a glycol polymer and water and then phase transitioning the composition at or above the composition's cloud point temperature to form at least two liquid phases. The enthalpy of liquid-liquid phase transition may be greater than 5 kJ per kg as measured by a calorimeter and each liquid phase may have unique and advantageous properties. In another embodiment the application pertains to compositions suitable for liquid-liquid phase transition compositions.

A system for the production of molten salt. The system can have a preparation tank configured to melt raw salts, and a bubbler system in communication with the preparation tank. The bubbler can be configured to maintain vacuum conditions within the preparation tank and to remove gases from the preparation tank. A method for producing molten salt includes a step of providing a system for the production of molten salt. The system can have a preparation tank configured to melt raw salts, and a bubbler system in communication with the preparation tank. The bubbler can be configured to maintain vacuum conditions within the preparation tank and to remove gases from the preparation tank. Then, the method can include inserting raw salt into the preparation tank, and heating the raw salt to form molten salt. Then filtering the molten salt, and storing the molten salt.

A system for the production of molten salt. The system can have a preparation tank configured to melt raw salts, and a bubbler system in communication with the preparation tank. The bubbler can be configured to maintain vacuum conditions within the preparation tank and to remove gases from the preparation tank. A method for producing molten salt includes a step of providing a system for the production of molten salt. The system can have a preparation tank configured to melt raw salts, and a bubbler system in communication with the preparation tank. The bubbler can be configured to maintain vacuum conditions within the preparation tank and to remove gases from the preparation tank. Then, the method can include inserting raw salt into the preparation tank, and heating the raw salt to form molten salt. Then filtering the molten salt, and storing the molten salt.

There is provided a composition comprising a slurry of capsules, the capsules having shells comprising silica and said shells encapsulating phase change materials (PCM); and a cementitious binder. There is also provided a method for preparing said composition.

There is provided a composition comprising a slurry of capsules, the capsules having shells comprising silica and said shells encapsulating phase change materials (PCM); and a cementitious binder. There is also provided a method for preparing said composition.

The present application pertains to liquid-liquid phase transition compositions and processes. In one embodiment a liquid-liquid phase transition process comprises first forming a composition comprising a glycol polymer and water and then phase transitioning the composition at or above the composition's cloud point temperature to form at least two liquid phases. The enthalpy of liquid-liquid phase transition may be greater than 5 kJ per kg as measured by a calorimeter and each liquid phase may have unique and advantageous properties. In another embodiment the application pertains to compositions suitable for liquid-liquid phase transition compositions.