A method of manufacture of high-solids hydroxide slurries from caustic calcined carbonate powder is described, whereby the properties of the slurry are its low resistance to shear thinning to facilitate transport, a high stability for transport and storage, ease of reconstitution after long periods of storage, and, as required, a high concentration of chemically reactive species at the particle surface. The method achieves these specifications by mixing caustic calcined carbonate or hydroxide powder with water in an insulated reactor vessel, and agitating the slurry sufficiently such that the hydration reaction causes the water to spontaneously boil, such that the remaining hydration proceeds spontaneously under the fixed conditions of boiling through the water loss. The mixing process is preferably carried out by a shear pump. A viscosity modifier, such as acetic acid, is used to thin the slurry to enable the mixing system to maintain uniform mixing. The reaction is terminated when the boiling has spontaneously ceased and the temperature has spontaneously dropped to a set point though the reactor heat losses, where the processing time is sufficiently long that the slurry meets the desired specifications.

A solution polymerization process uses a reactor system in which a first stage is operated in a non adiabatic (cooled) manner and is connected to a second stage containing a downstream reactor that is operated adiabatically. In an embodiment, the first reactor stage includes at least one loop reactor and the second stage includes a tubular reactor. In an embodiment, the first stage is operated with a single site catalyst and at least one downstream reactor uses a Ziegler Natta catalyst.

A method of manufacture of high-solids hydroxide slurries from caustic calcined carbonate powder is described, whereby the properties of the slurry are its low resistance to shear thinning to facilitate transport, a high stability for transport and storage, ease of reconstitution after long periods of storage, and, as required, a high concentration of chemically reactive species at the particle surface. The method achieves these specifications by mixing caustic calcined carbonate or hydroxide powder with water in an insulated reactor vessel, and agitating the slurry sufficiently such that the hydration reaction causes the water to spontaneously boil, such that the remaining hydration proceeds spontaneously under the fixed conditions of boiling through the water loss. The mixing process is preferably carried out by a shear pump. A viscosity modifier, such as acetic acid, is used to thin the slurry to enable the mixing system to maintain uniform mixing. The reaction is terminated when the boiling has spontaneously ceased and the temperature has spontaneously dropped to a set point though the reactor heat losses, where the processing time is sufficiently long that the slurry meets the desired specifications.

Methods and systems for temperature-controlled, on-site generation of peracids, namely peroxycarboxylic acids and peroxycarboxylic acid forming compositions are disclosed. In particular, methods for using an adjustable biocide formulator or generator system overcome the limitations of temperature on the kinetics of the peracid generation and/or peracid decomposition inside an adjustable biocide formulator or generator system. The methods include the controlling of the temperature of at least one raw starting material, namely water, to improve upon methods of on-site generation of peracids. The methods allow for the generation of user-selected chemistry without regard to the ambient temperatures of the raw starting materials and/or the biocide formulator or generator system.

A method for carrying out a chemical reaction includes using a reactor arrangement in which reaction tubes arranged in a reactor vessel are heated to a reaction tube temperature level between 400? C. and 1,500? C. during a reaction period using radiant heat provided by means of one or more electric heating elements arranged in the reactor vessel. In at least a part of the reactor vessel in which the heating elements are provided, a gas atmosphere is provided during the reaction period, which gas atmosphere has a defined volume fraction of oxygen.

Methods and systems for on-site, continuous generation of peracid chemistry, namely peroxycarboxylic acids and peroxycarboxylic acid forming compositions, are disclosed. In particular, an adjustable biocide formulator or generator system is designed for on-site generation of peroxycarboxylic acids and peroxycarboxylic acid forming compositions from sugar esters. Methods of using the in situ generated peroxycarboxylic acids and peroxycarboxylic acid forming compositions are also disclosed.

The present invention provides a method for extracting Tremella polysaccharides by using buffer solution, which comprises the following steps: leaching Tremella powder in a buffer solution with heating to obtain the leachate; subjecting the said leachate to solid-liquid separation and obtaining the liquid component which contains Tremella polysaccharides; subjecting the said liquid component to alcohol precipitation, and the precipitate obtained is Tremella polysaccharides. According to the method of the invention, various buffer solutions can achieve the extraction rates of Tremella polysaccharides up to 33:12%, which is 3 to 4 times of that of the traditional water extraction method, and greatly improve the extraction yields of Tremella polysaccharides.

A method for separating a dissolved product from a liquid is disclosed. A carrier liquid is cooled in a direct-contact exchanger, the direct-contact exchanger using a liquid coolant to cool the carrier liquid. The carrier liquid comprises a dissolved product. The carrier liquid and the liquid coolant are substantially immiscible. A portion of the dissolved product is condensed, frozen, deposited, desublimated, or a combination thereof out of the carrier liquid as a solid product at a liquid-liquid interface between the liquid coolant and the carrier liquid. The solid product is entrained in the carrier liquid, the liquid coolant, or a combination thereof. The solid product is separated from the carrier liquid, the liquid coolant, or a combination thereof.

Methods and systems for temperature-controlled, on-site generation of peracids, namely peroxycarboxylic acids and peroxycarboxylic acid forming compositions are disclosed. In particular, methods for using an adjustable biocide formulator or generator system overcome the limitations of temperature on the kinetics of the peracid generation and/or peracid decomposition inside an adjustable biocide formulator or generator system. The methods include the controlling of the temperature of at least one raw starting material, namely water, to improve upon methods of on-site generation of peracids. The methods allow for the generation of user-selected chemistry without regard to the ambient temperatures of the raw starting materials and/or the biocide formulator or generator system.

A method of charging and/or discharging energy in reusable fuel workpieces or particles includes a solar furnace with counter-flowing workpieces and gas, to exchange heat therebetween, with the exiting gas and workpieces being at about ambient temperature. A further aspect employs a production plant including a reduction reactor configured to use excess electrical energy generated by renewable power generators to charge and/or discharge solid-state thermochemical fuel. Another aspect includes a fuel flow control valve using air pulses. An oxygen-deprived and reusable fuel, such as magnesium manganese oxide, or magnesium iron oxide, is also provided. In another aspect, an apparatus for producing a solid-state fuel includes a reduction reactor including a reactor chamber configured to receive concentrated solar energy, and a reactor tube having a recuperation zone, a reduction zone, and a quenching zone, wherein the reduction zone passes through the reactor chamber. A discharged solid-state fuel is configured to be fed down the reactor tube and a low-oxygen gas is configured to flow up the reactor tube.