Corning Incorporated

Huayun Deng

Qiang Fu

John Christopher Mauro

Ye Fang

Weijun Niu

Mingqian He

Michael Joshua Snyder

Richard Allen Hayes

Theresa Chang

Lina Ma

Ying Wei

Govindarajan Natarajan

Yuhui Jin

Fei Li

Lei Zhang

David L Weidman

Yue Zhou

Aize Li

Kevin Robert McCarthy

Arthur Lawrence Wallace

Ying Zhang

Frederic Christian Wagner

Michael S Pambianchi

Hongxiang Wang

Therese Francoise Arliguie

Shu Yuan

Melanie Lian Geiger

Brian Paul Usiak

Dana Lynne Widmer-Quiel

Benjamin Leonard Linchuck

Johnathan David Jr Culpepper

Deqiu Fan

Methods of cleaning glass comprise mixing the glass with a peroxide-containing aqueous solution and heating the glass at a temperature of about 100° C. or more. In aspects, 50 wt % of the peroxide-containing aqueous solution based on an amount of the glass is mixed with the glass. The peroxide-containing aqueous solution can be removed from the glass before the heating. Alternatively, in aspects, from 10 wt % to 50 wt % of the peroxide-containing aqueous solution based on an amount of the glass can be mixed with the glass.

Methods of cleaning glass

Cross-linked shear-thinning fluids of pectic acid demonstrating increased viscosity with decreasing shear, as well as methods of producing and using the same. A shear-thinning fluid includes an aqueous solution of pectic acid cross-linked by a divalent cation is disclosed. The pectic acid may be present in an amount ranging from about 0.5 to about 3.0% (w/v), the divalent cation may be present at a concentration of from about 0.5 mM to about 7.0 mM, and the viscosity of the shear-thinning fluid increases with decreasing shear. These cross-linked shear-thinning fluids of pectic acid can be utilized for controlled release formulations, cell encapsulation, and 3D printing, and provide for an improved balance between structure fidelity/mechanical stability and cell viability.

Cross-linked shear thinning fluid with tunable rheology for 3D bioprinting and drug delivery

Glass-based substrates are described herein that may be processed by methods including applying a cover article onto a glass-based substrate, submerging the glass-based substrate in an etchant, and maintaining the submersion of the glass-based substrate in the etchant. The glass-based substrate may include a covered surface portion and an exposed surface portion. At least a portion of the covered surface portion may be in direct contact with the cover article. The covered surface portion may not be in contact with the etchant and the exposed surface portion may be in direct contact with the etchant. The etchant may contact the exposed surface portion and the cover article fora time sufficient to etch the exposed surface portion. The cover article may provide a barrier between the etchant and the covered surface portion for the entirety of the submerging.

Methods for etching glass-based substrates

Biocidal compositions including a carrier, a copper(I) salt, and a copper-assisting additive different from the carrier are provided, which in some aspects have improved antimicrobial efficacy and/or total color difference. Also provided are biocidal compositions or UV curable films thereof that exhibit high transmittance that is similar to the transmittance of an otherwise identical composition or film thereof without either the copper(I) salt or the copper-assisting additive. Also provided are biocidal additive formulations in which a copper(I) salt has a molarity of at least 20 mM.

Antimicrobial compositions including copper(I) salts and additives

A cross-bred organic semiconductor (OSC) polymer, includes a diketopyrrolopyrrole (DPP)-fused thiophene polymeric material, such that: the DPP-fused thiophene polymeric material comprises a first linear alkyl-substituted DPP portion and a second branched alkyl-substituted DPP portion, the cross-bred OSC polymer comprises a repeat unit having both the first linear alkyl-substituted DPP portion and the second branched alkyl-substituted DPP portion, and the fused thiophene is beta-substituted.

UV patternable polymer blends for organic thin-film transistors

Methods of making a bioactive glass fiber include forming a melt of a glass composition including: 50 to 70% SiO; 0.1 to 10% AlO, 5 to 30% NaO, 0.1 to 15% KO, 0.1 to 15% MgO, 0.1 to 20% CaO, and 5 to 10% PO, based on a 100 wt % of the glass composition. The melt has a viscosity of from 200 Poise to 2,000 Poise. Methods include drawing the melt into a drawn glass fiber. Bioactive glass compositions include: 60 to 70% SiO; 15 to 30% NaO, 5 to 15% KO, 1 to 10% CaO, and 5 to 10% PO, based on a 100 wt % of the glass composition.

High liquidus viscosity bioactive glass

A bioactive glass-ceramic composition as defined herein. Also disclosed are methods of making and using the disclosed compositions.

Lithium disilicate glass-ceramic compositions and methods thereof

The present disclosure is directed to pharmaceutical packages that include a coating that comprises polysilazane, and methods for the production of such. In one or more embodiments of the present disclosure, a pharmaceutical package may include a glass container comprising a first surface and a second surface opposite the first surface. The first surface may be an outer surface of the glass container. The pharmaceutical package may further include a coating positioned over at least a portion of the first surface of the glass container. The coating may include polysilazane.

Pharmaceutical packages with coatings comprising polysilazane

A chemically strengthened bioactive glass-ceramic composition as defined herein. Also disclosed are methods of making and using the disclosed compositions.

Chemically strengthened bioactive glass-ceramics

A bioactive glass composition including: 50 to 70% SiO; 0.1 to 10% AlO, 5 to 30% NaO, 0.1 to 15% KO, 0.1 to 15% MgO, 0.1 to 20% CaO, and 5 to 10% PO, based on a 100 wt % of the composition. Also disclosed is a method of making the bioactive glass composition.

A dental formulation including: a bioactive glass composition as defined herein, in an effective amount; and a suitable carrier as defined herein, in an effective amount. Also disclosed is a method of making and using the dental formulation to treat, for example, dentin sensitivities.

Bioactive glass compositions and dentin hypersensitivity remediation

A bioactive borate glass composition including, for example: 30 to 60% BO; 0.5 to 20% ZrO; 3 to 30% NaO; 0.1 to 15% KO; 0.1 to 15% MgO; 5 to 30% CaO; and 1 to 5% POin mole percents based on 100 mol % of the total composition. Also disclosed is a method of making and method of using the compositions and the bioactive borate glass dentin treatment formulations.

Bioactive borate glass and methods thereof

An aluminoborate composition, an alumino-borosilicate glass composition, or a mixture thereof, and solid or hollow microspheres thereof, as defined herein. Also disclosed are methods of making and using the disclosed compositions, for example, forming microspheres for use in bioactive applications, and composition extracts for use in treating or healing wounds.

Bioactive glass microspheres

A borophosphate glass composition including BO, PO, and CaO, and optionally a source additive selected from: LiO, NaO, KO, AlO, ZnO, MgO, FeO/FeO, CuO/CuO, and mixtures thereof, as defined herein. Also disclosed are bioactive compositions or substrates including the disclosed borophosphate glass composition, and at least one live cell. Also disclosed are methods of inhibiting or increasing the relative amount of species containing boron, phosphorous, or both, being released into an aqueous solution from aborophosphate glass composition defined herein. Also disclosed is a method of proliferating cells on a bioactive substrate as defined herein. Also disclosed are related glass compositions that exclude one of BO, PO, and CaO.

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Painted Post, NY, United States of America

Huayun Deng