Patent classifications
C09D133/24
Barrier coating structure
The present disclosure provides a barrier-coating structure that includes a polymer-matrix composite having a first surface and a second surface. The barrier-coating structure includes a flexible layer having a first surface and a second surface and a sol-gel layer having a first surface and a second surface. The first surface of the flexible layer contacts the second surface of the flexible layer. The barrier-coating structure includes a barrier layer having a first surface and a second surface. The sol-gel and/or the barrier layer may comprise one or more reactive substituents. The first surface of the barrier layer may be a laser-ablated surface.
Monolayer polymeric coatings for modifying metal oxide surfaces
The invention is directed to methods of modifying metal oxide or hydroxylated polymer surfaces using compositions of water soluble polymers that adsorb onto such surfaces and that contain functional groups which directly modify such surfaces without further processing. In some embodiments, compositions used in such methods include water-soluble oxide-adsorbing polymers having water solubility in an indicated temperature range, an indicated concentration in the aqueous solution, and a molecular weight range, wherein each of the water-soluble oxide-adsorbing polymers comprises a linear copolymer comprising a first monomer having at least one hydrophilic moiety and a second monomer having at least one lipophilic moiety and wherein a first monomer: second monomer molecular ratio is at least 3:1.
PLANOGRAPHIC PRINTING PLATE PRECURSOR, METHOD OF PREPARING PLANOGRAPHIC PRINTING PLATE, PLANOGRAPHIC PRINTING METHOD, AND CURABLE COMPOSITION
Provided are a planographic printing plate precursor including a support, and an image recording layer in this order, in which the image recording layer contains polymer particles containing an addition polymerization type resin, and the addition polymerization type resin contains a polymerizable group and a hydrophilic structure; a method of producing a planographic printing plate using the planographic printing plate precursor; a planographic printing method using the planographic printing plate precursor; and a curable composition containing the polymer particles.
Rapid set aqueous coating
Two-part aqueous coating compositions as well as methods of using thereof are described. The first coating component can comprise one or more polymers and the second coating component can comprise a flocculant. The first coating component and the second coating component can be provided as separate aqueous compositions. The first coating component and a second coating component that can be co-applied (e.g., simultaneously or sequentially) to a surface form a rapid set coating.
Rapid set aqueous coating
Two-part aqueous coating compositions as well as methods of using thereof are described. The first coating component can comprise one or more polymers and the second coating component can comprise a flocculant. The first coating component and the second coating component can be provided as separate aqueous compositions. The first coating component and a second coating component that can be co-applied (e.g., simultaneously or sequentially) to a surface form a rapid set coating.
Flow cell package and method for making the same
- James Tsay ,
- Anmiv Prabhu ,
- David Heiner ,
- Edwin Li ,
- Alexandre Richez ,
- John M. Beierle ,
- Kevan Samiee ,
- Kristina Munoz ,
- Leonid Malevanchik ,
- Ludovic Vincent ,
- Naiqian Zhan ,
- Peyton Shieh ,
- Robert Yang ,
- Samantha Schmitt ,
- Sang Park ,
- Scott Bailey ,
- Sean M. Ramirez ,
- Sunmin Ahn ,
- Valerie Uzzell ,
- Wei Wei ,
- Yuxiang Huang ,
- Tyler Jamison Dill
A flow cell package includes first and second surface-modified patterned wafers and a spacer layer. The first surface-modified patterned wafer includes first depressions separated by first interstitial regions, a first functionalized molecule bound to a first silane or silane derivative in at least some of the first depressions, and a first primer grafted to the first functionalized molecule in the at least some of the first depressions. The second surface-modified patterned wafer includes second depressions separated by second interstitial regions, a second functionalized molecule bound to a second silane or silane derivative in at least some of the second depressions, and a second primer grafted to the second functionalized molecule in the at least some of the second depressions. The spacer layer bonds at least some first interstitial regions to at least some second interstitial regions, and at least partially defines respective fluidic chambers of the flow cell package.
Flow cell package and method for making the same
- James Tsay ,
- Anmiv Prabhu ,
- David Heiner ,
- Edwin Li ,
- Alexandre Richez ,
- John M. Beierle ,
- Kevan Samiee ,
- Kristina Munoz ,
- Leonid Malevanchik ,
- Ludovic Vincent ,
- Naiqian Zhan ,
- Peyton Shieh ,
- Robert Yang ,
- Samantha Schmitt ,
- Sang Park ,
- Scott Bailey ,
- Sean M. Ramirez ,
- Sunmin Ahn ,
- Valerie Uzzell ,
- Wei Wei ,
- Yuxiang Huang ,
- Tyler Jamison Dill
A flow cell package includes first and second surface-modified patterned wafers and a spacer layer. The first surface-modified patterned wafer includes first depressions separated by first interstitial regions, a first functionalized molecule bound to a first silane or silane derivative in at least some of the first depressions, and a first primer grafted to the first functionalized molecule in the at least some of the first depressions. The second surface-modified patterned wafer includes second depressions separated by second interstitial regions, a second functionalized molecule bound to a second silane or silane derivative in at least some of the second depressions, and a second primer grafted to the second functionalized molecule in the at least some of the second depressions. The spacer layer bonds at least some first interstitial regions to at least some second interstitial regions, and at least partially defines respective fluidic chambers of the flow cell package.
Monomers, polymers and coating formulations that comprise at least one <i>N</i>-halamine precursor, a cationic center and a coating incorporation group
A modified surface with at least one cationic center and at least one compound. The surface can be modified by various methods. The result of these methods is that the cationic center and the compound are connected to the modified surface. The cationic center and the compound are connected to the modified surface so that both of the cationic center and the compound are available upon the modified surface to react with other chemicals or microorganisms that come into contact with or near to the modified surface. The availability of the cationic center and the compound cause the modified surface to have a functionality that it would not otherwise have. The number of molecules of the cationic center relative to the number of molecules of the at least one compound may influence the functionality of the modified surface.
Monomers, polymers and coating formulations that comprise at least one <i>N</i>-halamine precursor, a cationic center and a coating incorporation group
A modified surface with at least one cationic center and at least one compound. The surface can be modified by various methods. The result of these methods is that the cationic center and the compound are connected to the modified surface. The cationic center and the compound are connected to the modified surface so that both of the cationic center and the compound are available upon the modified surface to react with other chemicals or microorganisms that come into contact with or near to the modified surface. The availability of the cationic center and the compound cause the modified surface to have a functionality that it would not otherwise have. The number of molecules of the cationic center relative to the number of molecules of the at least one compound may influence the functionality of the modified surface.
Temperature Responsive Device for Mechanobiological Manipulation
Biocompatible, mechanically-dynamic thermoresponsive devices, methods for forming the devices, and exemplary applications for the devices are described. The devices include a series of wells therein and provide for temperature-controlled mechanostimulation of single cells or groups of cells that can be retained in the wells of a device. Mechanostimulation can be single instance of any duration, continuous, or regular or irregular cyclic mechanostimulation of single cells, cell clusters, cell spheroids, or organoids and may be utilized in any of a variety of biomedical applications including, without limitation, cellular engineering, cellular phenotyping, and drug discovery/screening.