The present invention generally relates to microfluidic droplets and, in particular, to multiple emulsion microfluidic droplets. In certain aspects, particles such as gel particles can be prepared in an aqueous carrier from aqueous droplets (or a non-aqueous carrier from non-aqueous droplets). For example, in some embodiments, double-emulsion droplets of a first fluid, surrounded by a second fluid, contained in a carrier fluid may be prepared, where the first fluid forms a gel and the second fluid is removed. For instance, the second fluid may be dissolved in the carrier fluid, or the second fluid may be hardened, then removed, for example, due to a change in pH. Other embodiments of the present invention are generally directed to kits containing such microfluidic droplets, microfluidic devices for making such microfluidic droplets, or the like.

A method for preparing a hydrogel includes forming a pre-gel comprising polymer and metal salt particles, unidirectionally-shrinking and dehydrating the pre-gel, and impregnating the unidirectionally shrunk and dehydrated pre-gel with an ion solution to crosslink and rehydrate the unidirectionally shrunk and dehydrated pre-gel to produce the hydrogel.

Method for producing a gel having a desired strength, by performing a step of removing a part or all of a solvent. Method for producing a gel containing a water-soluble organic polymer (A), a silicate salt (B), and a dispersant (C) for the silicate salt, including a desolvation step of removing a part or all of one or more solvents selected from the group consisting of water and a water-soluble organic solvent in the gel, or gelling a gel-forming composition containing the water-soluble organic polymer (A), the silicate salt (B), the dispersant (C) for the silicate salt, and one or more solvents selected from the group consisting of water and a water-soluble organic solvent and removing a part or all of the solvent in the composition.

The present invention concerns a method for producing a hydrogel comprising the following steps in succession: a first step (i) of providing at least one powder of an anionic polymer (A) and at least one chitosan powder (B) comprising amine functions (NH.sub.2); a second step (ii) consisting in dry mixing at least the powders (A) and (B) from the first step in order to form a mixture of powders; a third step (iii) of suspending the mixture of powders obtained from the second step in an aqueous medium having a pH that can enable the anionic polymer (A) to be dissolved without dissolving the chitosan (B); a fourth step (iv) of adding an acid to the suspension obtained from the third step in order to form the hydrogel; or the third (iii) and fourth (iv) steps are replaced by a mixing fifth step (v), comprising mixing an acidified aqueous medium including at least one compound (C) comprising at least one unit of a hexose or a unit derived from a hexose, and/or at least one phosphate of said compound (C), with said mixture comprising at least the powders (A) and (B) obtained from the second step (ii).

It is an object of the invention to provide an economically viable process for the production of hydrophobized aerogels which works both inexpensively and in a resource-conserving manner. 2.2. This object is achieved by the provision of a process for producing organically modified aerogels by producing a sol containing [SiO.sub.4/2] units and [R.sub.xSiO.sub.(4X)/2] a units, where x may be the same or different and is 1, 2 or 3, and R may be the same or different and is hydrogen or an organic substituted or unsubstituted radical, using the sol to form a gel, surface-modifying the gel obtained in the presence of more than 0.1% by weight of a phase modifier in a mixture comprising organosiloxane and initiator, wherein the mixture contains at least 20% by weight of organosiloxane and wherein the initiator consists of acid or organosiloxane or mixtures thereof and the gels obtained are dried. 2.3. The aerogels provided can be used as insulating materials, especially in thermal insulation.

Polyvinyl alcohol (PVA) gel and polyurethane (PU)ZPVA gel and gel beads, methods for making gel and gel beads with immobilized substances such as microorganisms, cells, enzymes, and/or other materials, methods for using gel and gel beads in various applications (e.g., wastewater treatment), and apparatus for manufacturing such gel and gel beads, are described.

Zeolites, improved methods for their synthesis, and catalysts, systems, and methods of using these zeolites as catalysts are described. The method of synthesis of the zeolites includes forming a mixture including a zeolitic precursor material and a structure directing agent and subjecting the mixture to high shear processing conditions.

In some examples, systems and methods are disclosed for enhancing a gel to sol transition of a polymer that includes disposing the polymer on a host material, exposing the polymer and the host material to an exposure temperature that causes the polymer to form a gel, and cooling the polymer and the host material to a cooling temperature that causes the gel to transition to a sol.

A process and system for recovering gel-mass from a gel-mass-containing waste material. The process comprises retrieving the gel-mass-containing waste material from an encapsulation process; melting the retrieved waste material to provide an oil phase and a non-oil phase; retrieving the non-oil phase to produce a recovered gel-mass; and recycling the recovered gel-mass for combination with fresh encapsulating material to provide a combined encapsulating material for use in encapsulating a same lot of the same product which was being encapsulated in the step that produced the gel-mass-containing waste material from which the gel-mass was obtained. The system comprises a heated accumulator for receiving and melting the gel-mass-containing waste material to provide an oil phase and a non-oil phase; a pumping system; an optional mixer; and a control system.

Provided is a pharmaceutical composition excellent in capability of an accelerated penetration into an affected area. The pharmaceutical composition capable of accelerated penetration into the affected area is formed by dispersing nano-bubbles, which are negatively charged and are given high internal pressures due to their surface tension, in the pharmaceutical composition in a form of a liquid or a gel including a predetermined drug.