Disclosed is a carbonation device including: a storage tank storing a carbonation subject solution; a droplet spray unit spraying the carbonation subject solution from the storage tank as droplets; a carbonation reaction tank disposed with the droplet spray unit and filled with a carbonation gas under a predetermined pressure to provide a slurry by a carbonation reaction of the droplet-sprayed carbonation subject solution with the filled carbonation gas; a carbonation gas supply unit supplying the carbonation gas into the carbonation reaction tank to maintain the carbonation gas in the carbonation reaction tank under the predetermined pressure; and a slurry outlet unit ejecting the slurry from the carbonation reaction tank to maintain the slurry formed in the carbonation reaction tank within a predetermined level, and a method of carbonation using the same.

A reagent delivery method includes placing a reagent delivery column including a plurality of reagent storage elements therein in a centrifugal device, coupling a breaching element to the housing, and rotating the centrifugal device to force the reagent storage elements toward the breaching element, breaching of the reagent storage elements releasing reagent therein and communicating the same to an external environment. A reagent delivery system includes a column having a housing, a plurality of reagent storage element sheets positioned in the housing or forming a stack, a plurality of breaching elements, and a microplate having a plurality of wells, the microplate coupled to the housing where each well corresponds or aligns with a breaching element and a reagent storage element. The system can be rotated in a centrifugal device to force the reagent storage element stacks toward the breaching elements.

A MEG stream having a first pH level is contacted with a CO.sub.2-rich gas stream to yield a MEG product having a second different and lower pH level. The system and method can be readily incorporated into a slipstream MEG recovery package, with a source of the MEG stream being a MEG regeneration section of the package. The CO.sub.2-rich gas could be a vented CO.sub.2 stream from the MEG reclamation section of the package. Unlike hydrochloric and acetic acid overdosing, CO.sub.2 overdosing of the lean MEG stream does not lead to rapid acidification of the MEG product to be stored or injected.

The disclosed embodiments relate to the manufacture of a precursor co-precipitate material for a cathode active material composition. During manufacture of the precursor co-precipitate material, an aqueous solution containing at least one of a manganese sulfate and a cobalt sulfate is formed. Next, a NH.sub.4OH solution is added to the aqueous solution to form a particulate solution comprising irregular secondary particles of the precursor co-precipitate material. A constant pH in the range of 10-12 is also maintained in the particulate solution by adding a basic solution to the particulate solution.

Provided are methods and/or systems to convert sulfide intermediates to sulfilimines using a series of continuous loop reactors instead of a batch reactor. The advantages of the methods and systems provided include improved total yield, improved heat management, improved phase mixing, and/or improved volume management.

Provided are various methods and systems for producing peroxycarboxylic acid compositions, and in particular, nonequilibrium compositions of peracetic acid. The methods and systems control flow rates and proportions of feedstocks/reactants, perform the required sequence of reaction steps to produce high yield peroxycarboxcylic acid solutions in a continuous manner, and provide optimal reaction time and reactant mixing for continuous and safe on-site production.

A method of treatment of plasma with a physiologically compatible spray dry stable acidic substance (SDSAS) prior to or contemporaneously with spray drying of the plasma that results in greater recovery and greater long-term stabilization of the dried plasma proteins as compared to spray dried plasma that has not be subject to the formulation method of the present invention, as well as compostions related to plasma dried by the methods of the present invention.

Related to is a system for preparing xylose liquid by continuously hydrolyzing hemicellulose, including a neutralizing unit, an acid-adjusting unit, a feeding unit, a liquefaction ejecting unit, a feed and discharge heat-exchanging unit and a discharge controlling unit. The neutralizing unit includes a raw material tank, a neutralizing concentrated sulfuric acid pump and a neutralizing pipeline mixer, the acid-adjusting unit includes an acid-adjusting concentrated sulfuric acid pump, an acid-adjusting pipeline mixer and an acid-adjusting tank, the feeding unit includes a feed tank, the liquefaction ejecting unit includes a liquefaction ejector and a liquefaction maintainer, the feed and discharge heat-exchanging unit includes a plate-type teed and discharge heat exchanger and a first discharge temperature sensor, and the discharge controlling unit includes a discharge valve and a reflux valve. The obtained xylose liquid exchanges heat with the hemicellulose liquid in the plate-type feed and discharge heat exchanger to decrease a temperature of the xylose liquid, whereas a temperature of the hemicellulose liquid is increased. Further disclosed is a method using the system. The simultaneous feed and discharge heat exchanges greatly reduce energy consumption, and feed and exchange are continuously run, thereby improving the production efficiency and simplifying manual operations.

An appliance for producing a personal care product. The appliance includes a reaction chamber configured to receive one or more ingredients of the personal care product. The reaction chamber includes a mechanism for mixing ingredients and an extruding mechanism. The appliance also includes a sensor configured to determine one or more conditions in the reaction chamber, the one or more conditions includes at least a pH of the personal care product. The appliance further includes a cartridge, where the cartridge holds at least one of the one or more ingredients of the personal care product. The appliance additionally includes an output port configured to allow removal of the personal care product from the reaction chamber.

The disclosed embodiments relate to the manufacture of a precursor co-precipitate material for a cathode active material composition. During manufacture of the precursor co-precipitate material, an aqueous solution containing at least one of a manganese sulfate and a cobalt sulfate is formed. Next, a NH.sub.4OH solution is added to the aqueous solution to form a particulate solution comprising irregular secondary particles of the precursor co-precipitate material. A constant pH in the range of 10-12 is also maintained in the particulate solution by adding a basic solution to the particulate solution.