Patent classifications
C08J2333/26
Process for fast dissolution of powder comprising low molecular weight acrylamide-based polymer
A process for making down a powder is provided. The process comprises making down a powder comprising one or more acrylamide-based polymer(s) to form a made down powder solution, comprising blending a mixture of the powder and a solvent for no more than about 15 minutes to yield the made down powder solution, wherein the powder comprises particles having been dry-cut to a median particle size of from about 200 microns to about 10,000 microns.
Ion-exchange membrane having an imprinted non-woven substrate
The present disclosure provides an ion-exchange membrane that includes a supporting substrate impregnated with an ion-exchange material. The supporting substrate includes an imprinted non-woven layer, and the imprinting includes a plurality of deformations at a surface density of at least 16 per cm.sup.2. The supporting substrate may lack a reinforcing layer. In some examples, the supporting substrate may include only a single layer of the imprinted non-woven fabric.
Acrylamide copolymerization for sequestration and production of single-stranded nucleic acid
Provided herein, in some embodiments, are methods, compositions and kits for large-scale production of long single-stranded DNA in solution.
POLYMER GELS AND METHODS FOR MONITORING GEL INTEGRITY IN WELLBORES
A polymer gel may comprise a polymer gel base material and superparamagnetic nanoparticles. At least 25 wt. % of the superparamagnetic nanoparticles may have diameters in a first size range between a first diameter and a second diameter. At least 25 wt. % of the superparamagnetic nanoparticles may have diameters in a second size range between a third diameter and a fourth diameter. The Brownian relaxation time of the portion of the superparamagnetic nanoparticles in the first size range may be at least 5 times the Neel relaxation time of the portion of the superparamagnetic nanoparticles in the first size range. The Neel relaxation time of the portion of the superparamagnetic nanoparticles in the second size range may be at least 5 times the Brownian relaxation time of the portion of the superparamagnetic nanoparticles in the second size range. Methods for monitoring gel integrity in a wellbore are further included.
INTERPENETRATING NETWORKS WITH COVALENT AND IONIC CROSSLINKS
The invention features a composition comprising a self-healing interpenetrating network hydrogel comprising a first network and a second network. The first network comprises covalent crosslinks and the second network comprises ionic or physical crosslinks. For example, the first network comprises a polyacrylamide polymer and second network comprises an alginate polymer.
METHOD TO PREPARE POLYMER MATERIALS WITH INTERLOCKED POROUS STRUCTURES BY FREEZING AND DEMULSIFICATION OF EMULSION
The present invention provides a method to prepare polymer materials with interlocked porous structures by freezing and demulsification, which includes: (1) Preparing an emulsion containing uncrosslinked polymers and crosslinking agents. The uncrosslinked polymers are presented in the organic phase, and the crosslinking agents are presented in the organic phase or water phase. Under freezing, the demulsification is occurred which leads to the interaction between polymers and crosslinking agents, and the crosslinked materials are obtained. (2) After removing the ice crystals, polymer materials with interlocked porous structures are synthesized. The method provided by the present invention is simple to operate, and can well adjust the porous structures of obtained porous polymer materials. In addition, it is suitable for large scale manufacturing. At the same time, this process can form different functional porous polymer materials by simply changing the used monomers. Particularly, it can prepare melt-blown fabrics with antibacterial property, high-throughput vertical porous structures and high-temperature sterilizable feature, therefore, it can be used to manufacture medical products such as masks.
RHEOLOGY MODIFICATION BY POROUS GEL PARTICLES
Modification of the rheology of a liquid medium, aqueous or nonaqueous, with polymers in the form of specific particles obtained by grinding (micronizing) a porous macrogel, itself prepared by a process comprising a radical polymerization step which comprises reacting in the presence of pore formers monomers containing monomers bearing at least two ethylenic unsaturations, typically in combination with monomers bearing a single ethylenic unsaturation; a polymerization initiator; and optionally a polymerization control agent. These polymer particles keep other particles in suspension within the liquid medium, and also the stabilized suspensions are obtained.
Polymer gel with crosslinker and filler
An aqueous dispersion includes polyacrylamide, a crosslinker, and a filler. The crosslinker includes at least one of hydroquinone or hexamethylenetetramine. The filler includes at least one of a metal oxide or a nanomaterial. The metal oxide includes at least one of zirconium oxide, zirconium hydroxide, or titanium oxide. The nanomaterial includes at least one of graphene, graphene oxide, or boron nitride. In some cases, the filler is a nanocomposite of the metal oxide and the nanomaterial.
METHOD OF PROVIDING HOMOGENEOUS AQUEOUS POLYACRYLAMIDE CONCENTRATES AND USE THEREOF
Process of providing polyacrylamides to a site-of-use comprising at least the steps of mixing a polyacrylamide powder at a manufacturing site with an aqueous liquid, thereby obtaining a homogeneous aqueous polyacrylamide concentrate, transporting said concentrate in a transport unit from the manufacturing site to the site-of-use, and removing the homogeneous aqueous concentrate from the transport unit at the site-of-use. Process of treating subterranean, oil and/or gas bearing formations by injecting an aqueous treatment fluid into at least one wellbore, wherein the aqueous treatment fluid is manufactured by mixing at least an aqueous base fluid with said homogeneous aqueous polyacrylamide concentrate at the site-of-use.
Three-dimensional nanofabrication by patterning of hydrogels
The present invention enables three-dimensional nanofabrication by isotropic shrinking of patterned hydrogels. A hydrogel is first expanded, the rate of expansion being controlled by the concentration of the crosslinker. The hydrogel is then infused with a reactive group and patterned in three dimensions using a photon beam through a limited-diffraction microscope. Functional particles or materials are then deposited on the pattern. The hydrogel is then shrunk and cleaved from the pattern.