Methods for treating hematological malignancies and ewing's sarcoma
US-2023026872-A1 · Jan 26, 2023 · US
US12351530B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12351530-B2 |
| Application number | US-202017070069-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 14, 2020 |
| Priority date | Oct 18, 2019 |
| Publication date | Jul 8, 2025 |
| Grant date | Jul 8, 2025 |
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A method of making a fiber reinforced composite includes: infiltrating a preform having a perimeter with an electrophoretic gel; adding nanoparticles to wells located in the electrophoretic gel outside the preform perimeter; introducing the nanoparticles to the preform using gel electrophoresis; removing the electrophoretic gel to result in a preform having embedded nanoparticles; and infiltrating the preform having embedded nanoparticles with a matrix material or a matrix material precursor.
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What is claimed is: 1. A method of making a fiber reinforced composite comprising: infiltrating a preform with an electrophoretic gel, the preform having a perimeter and comprising a fiber structure, the preform in a tank of the electrophoretic gel; adding particles to wells located in the tank outside the preform perimeter; wherein the particles comprise nanoparticles having a size that is less than the diameter of the fibers used to make a tow; and wherein an initial coating of a matrix material is disposed onto the preform prior to infiltrating the preform with the electrophoretic gel and preforming electrophoresis; introducing the particles to the preform using gel electrophoresis, wherein a voltage is applied from multiple sides of the preform during the gel electrophoresis and the voltage is applied simultaneously or sequentially; removing the electrophoretic gel to result in a preform having embedded particles; and infiltrating the preform having embedded particles with the matrix material or a matrix material precursor, wherein 1) The preform comprises carbon fiber, SiC fiber, Al 2 O 3 —SiO 2 fiber, silicon dioxide (SiO 2 ) fiber, aluminum silicate fiber, aluminum oxide (Al 2 O 3 ) fiber, titanium oxide (TiO 2 ) fiber, zirconium silicate fiber, silicon nitride fiber, boron nitride (BN) fiber, and combinations thereof, 2) The particles comprise carbon (C), silicon oxide (SiO 2 ), boron nitride (BN), boron carbide (B 4 C), aluminum oxide (Al 2 O 3 ), zirconium oxide (ZrO 2 ), zirconium boride (ZrB 2 ), zinc oxide (ZnO 2 ), molybdenum disulfide (MoS 2 ), silicon nitride (Si 3 N 4 ), and combinations thereof, and/or 3) The matrix material comprises carbon (C), silicon carbide (SiC), silicon oxide (SiO 2 ), boron nitride (BN), boron carbide (B 4 C), aluminum oxide (Al 2 O 3 ), zirconium oxide (ZrO 2 ), zirconium boride (ZrB 2 ), zinc oxide (ZnO 2 ), molybdenum disulfide (MoS 2 ), silicon nitride (Si 3 N 4 ), and combinations thereof. 2. The method of claim 1 , wherein introducing the particles to the preform using gel electrophoresis results in the particles being introduced and deposited in a controlled size gradient. 3. The method of claim 1 , wherein the preform comprises uniaxial fiber layup, a 2D woven fabric layup, 3D weave or a combination thereof. 4. The method of claim 1 , wherein the preform comprises carbon fiber, Al 2 O 3 —SiO 2 fiber, SiC fiber, silicon dioxide (SiO 2 ) fiber, aluminum silicate fiber, aluminum oxide (Al 2 O 3 ) fiber, titanium oxide (TiO 2 ) fiber, zirconium silicate fiber, silicon nitride fiber, boron nitride (BN) fiber, and combinations thereof. 5. The method of claim 1 , wherein the particles comprise carbon (C), silicon carbide (SiC), silicon oxide (SiO 2 ), boron nitride (BN), boron carbide (B 4 C), aluminum oxide (Al 2 O 3 ), zirconium oxide (ZrO 2 ), zirconium boride (ZrB 2 ), zinc oxide (ZnO 2 ), molybdenum disulfide (MoS 2 ), silicon nitride (Si 3 N 4 ), and combinations thereof. 6. The method of claim 1 , wherein the electrophoretic gel comprises agarose, polyacrylamide, starch or a combination thereof. 7. The method of claim 1 , wherein the matrix material comprises carbon (C), silicon carbide (SiC), silicon oxide (SiO 2 ), boron nitride (BN), boron carbide (B 4 C), aluminum oxide (Al 2 O 3 ), zirconium oxide (ZrO 2 ), zirconium boride (ZrB 2 ), zinc oxide (ZnO 2 ), molybdenum disulfide (MoS 2 ), Silicon nitride (Si 3 N 4 ), and combinations thereof. 8. The method of claim 1 , wherein the particles further have sizes of 0.1 to 100 micrometers (μm). 9. The method of claim 1 , wherein the particles are present in an amount of 1 to 20 wt % based on the weight of the preform. 10. The method of claim 1 , further comprising densifying the preform having an infiltrated matrix material and embedded particles to form a fiber reinforced composite having a porosity less than 15%. 11. The method of claim 1 , wherein the particles have functional groups grafted onto a surface or are coated in a surfactant to provide functional groups. 12. The method of claim 2 , wherein the controlled size gradient has a particle size gradient ranging from smallest on a first size of the fiber reinforced composite to largest on a second side of the fiber reinforced composite.
Gas infiltration of green bodies or pre-forms · CPC title
submicron sized, i.e. from 0,1 to 1 micron · CPC title
micrometer sized, i.e. from 1 to 100 micron · CPC title
Two-dimensional, e.g. woven structures · CPC title
Carbon, e.g. graphite · CPC title
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