2004 to 2000 Senior Systems Engineer/Systems ArchitectEastern Bank
2012 to 2012 Implemented System Center Virtual Machine ManagerCompass Bank for Savings New Bedford, MA 1999 to 2004 Network Analyst/Microsoft Network Administrator
Education:
Microsoft System Center Suite 2000 to 2012 MDS in Technology
Name / Title
Company / Classification
Phones & Addresses
Matthew Colburn President
FIVE BLUE STARS FOUNDATION, INC
1 Beacon St, Boston, MA 02108 1730 16 St NW #7, Washington, DC 20009
Us Patents
Aromatic Substituted Ethane-Core Monomers And Polymers Thereof For Volume Bragg Gratings
- Menlo Park CA, US Austin LANE - Bellevue WA, US Matthew E. COLBURN - Woodinville WA, US
International Classification:
C07C 271/54 G03H 1/02
Abstract:
The disclosure provides recording materials including aromatic substituted ethane-core derivatized monomers and polymers for use in volume Bragg gratings, including, but not limited to, volume Bragg gratings for holography applications. Several structures are disclosed for monomers and polymers for use in Bragg gratings applications, leading to materials with higher refractive index, low birefringence, and high transparency. The disclosed derivatized monomers and polymers thereof can be used in any volume Bragg gratings materials, including two-stage polymer materials where a matrix is cured in a first step, and then the volume Bragg grating is written by way of a second curing step of a monomer.
Aromatic Substituted Methane-Core Monomers And Polymers Thereof For Volume Bragg Gratings
The disclosure provides recording materials including aromatic substituted methane-core derivatized monomers and polymers for use in volume Bragg gratings, including, but not limited to, volume Bragg gratings for holography applications. Several structures are disclosed for monomers and polymers for use in Bragg gratings applications leading to materials with higher refractive index, low birefringence, and high transparency. The disclosed derivatized monomers and polymers thereof can be used in any volume Bragg gratings materials, including two-stage polymer materials where a matrix is cured in a first step, and then the volume Bragg grating is written by way of a second curing step of a monomer.
Anthraquinone Derivatized Monomers And Polymers For Volume Bragg Gratings
The disclosure provides recording materials including anthraquinone derivatized monomers and polymers for use in volume Bragg gratings, including, but not limited to, volume Bragg gratings for holography applications. Several structures are disclosed for anthraquinone derivatized monomers and polymers for use in Bragg gratings applications, leading to materials with higher refractive index, low birefringence, and high transparency. The disclosed anthraquinone derivatized monomers and polymers thereof can be used in any volume Bragg gratings materials, including two-stage polymer materials where a matrix is cured in a first step, and then the volume Bragg grating is written by way of a second curing step of a monomer.
Aromatic Substituted Alkane-Core Monomers And Polymers Thereof For Volume Bragg Gratings
The disclosure provides recording materials including aromatic substituted alkane-core derivatized monomers and polymers for use in volume Bragg gratings, including, but not limited to, volume Bragg gratings for holography applications. Several structures are disclosed, including Formula I. When used in Bragg gratings applications, the monomers and polymers disclosed lead to materials with higher refractive index, low birefringence, and high transparency. The disclosed derivatized monomers and polymers can be used in any volume Bragg gratings materials, including two-stage polymer materials where a matrix is cured in a first step, and then the volume Bragg grating is written by way of a second curing step of a monomer.
Transparent Illumination Layer With Transparent Waveguide Structure
- Menlo Park CA, US Qi Zhang - Kirkland WA, US Andrew John Ouderkirk - Redmond WA, US Matthew E Colburn - Woodinville WA, US
International Classification:
F21V 8/00 G02B 27/01
Abstract:
An optical element includes a transparent layer, outcoupling elements, and a waveguide structure. The outcoupling elements are positioned across the transparent layer. The waveguide structure provides non-visible light to the outcoupling elements and the outcoupling elements outcouple the non-visible light as non-visible illumination light to illuminate an eye region.
Curable Formulation With High Refractive Index And Its Application In Surface Relief Grating Using Nanoimprinting Lithography
- Menlo Park CA, US Ankit VORA - Bothell WA, US Austin LANE - Bellevue WA, US Giuseppe CALAFIORE - Redmond WA, US Matthew E. COLBURN - Woodinville WA, US
Disclosed herein are materials for nanoimprinting lithography (NIL) and devices molded from the materials using NIL processes. According to certain aspects, an NIL material includes a mixture including a light-sensitive base resin and nanoparticles. The light-sensitive base resin is characterized by a first refractive index ranging from 1.58 to 1.77. The nanoparticles are characterized by a second refractive index greater than the first refractive index of the light-sensitive base resin. The mixture is curable to form a cured material characterized by a third refractive index greater than 1.78. The nanoparticles include from 45 wt. % to 90 wt. % of the cured material.
Curable Formulation With High Refractive Index And Its Application In Surface Relief Grating Using Nanoimprinting Lithography
- Menlo Park CA, US Zachary PERLMUTTER - Ballard WA, US Ankit VORA - Bothell WA, US Austin LANE - Bellevue WA, US Giuseppe CALAFIORE - Redmond WA, US Matthew E. COLBURN - Woodinville WA, US
International Classification:
G03F 7/00 C08L 63/00 C09D 11/101 B82Y 40/00
Abstract:
Disclosed herein is a nanoimprint lithography (ML) precursor material comprising a base resin component having a first refractive index ranging from 1.45 to 1.80, and a nanoparticles component having a second refractive index greater than the first refractive index of the base resin component. According to certain embodiments, further disclosed herein are a cured NIL material made by curing the NIL precursor material, a NIL grating comprising the cured NIL material, an optical component comprising the NIL grating, and methods for forming the NIL grating and the optical component using a NIL process.
Matthew Colburn (2000-2004), Amanda Cook (1995-1999), Howard Hill (1981-1991), Beth Oberon (1987-1996), Randy Helsley (1993-1993), Priscilla Grantham (1995-1999)