Abstract: Apparatuses, kits and methods useful in the storage and delivery of nutritional compositions and other fluids are described. In a general embodiment, an integrated storage and delivery system for nutritional compositions comprises a container defining a chamber, a finish, and a penetrable seal. The finish defines an opening and the penetrable seal separating the chamber from an external environment. A spike assembly is attached to the container. The spike assembly including a cap and a spike. The cap is engaged with the finish of the container and the spike defines a projection having a distal end defining a second opening. The projection is moveable between a first position in which the distal end is adjacent a first side of the penetrable seal and a second position in which the distal end is adjacent a second side of the penetrable seal.

Abstract: Methods for producing substantially single phase yttrium phosphate which exhibits the xenotime crystal structure are disclosed. The methods can be practiced without the use of high temperatures (e.g., the methods can be practiced at temperatures less than 1000° C.). The resulting yttrium phosphate can be in the form of particles which comprise interwoven strands of crystals of yttrium phosphate and/or nanoparticles prepared from such particles.

Abstract: Methods for producing substantially single phase yttrium phosphate which exhibits the xenotime crystal structure are disclosed. The methods can be practiced without the use of high temperatures (e.g., the methods can be practiced at temperatures less than 1000° C.). The resulting yttrium phosphate can be in the form of particles which comprise interwoven strands of crystals of yttrium phosphate and/or nanoparticles prepared from such particles.

Abstract: Methods and apparatus for making ceramic honeycombs by steps including compounding a plasticized ceramic batch mixture and forming the mixture into ceramic honeycombs by continuous extrusion, drying and firing, wherein one or more ceramic powders for the batch mixture are supplied by in-line homogenization as a powder feed having a median particle size D50 that varies from a maximum value to a minimum value by an amount not exceeding 15% of the maximum value during a 24-hour period of continuous extrusion.

Abstract: The present disclosure relates to aluminum titanate-containing ceramic-forming batch materials and methods using the same.

Abstract: The disclosure relates to methods for making aluminum titanate-containing ceramic bodies, and methods for predicting shrinkage and minimizing shrinkage variability of said bodies from target size.

Abstract: A method for controlling the dimensional shrinkage or growth of AT honeycomb structures during the firing process by control of the alkali metal ion content in the AT-forming batch materials extruded into an AT green body structure that is heated to form the fired AT honeycomb structure.

Abstract: Trace cross-contamination in mixtures or preforms of plasticized ceramic-forming powder mixtures, arising for example in manufacturing facilities where components of one ceramic product being manufactured can contaminate mixtures for another product to be manufactured, are controlled by one or more of: the targeted decontamination of shared production lines, rapid trace analysis of the mixtures to establish the presence and/or concentration levels of contaminants, the application of statistical models to project final product properties based on the analyzed concentrations, and decisional analysis of appropriate corrective actions based on the statistical projections.

Abstract: A method for reducing shrinkage variability of ceramic honeycombs formed from batch mixtures including inorganic materials and a pore former. X is a cumulative amount of pore former particles having a diameter less than 37 ?m. There is a maximum value of X (Xmax) and a minimum value of X (Xmin) during a production period, and ?X=Xmax?Xmin. The method fixes an amount of pore former fines such that X ranges from 25%-71% by volume, and ?X is ?23% throughout the production period.

Abstract: Methods for producing substantially single phase yttrium phosphate which exhibits the xenotime crystal structure are disclosed. The methods can be practiced without the use of high temperatures (e.g., the methods can be practiced at temperatures less than 1000° C.). The resulting yttrium phosphate can be in the form of particles which comprise interwoven strands of crystals of yttrium phosphate and/or nanoparticles prepared from such particles.