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Dino R Aimino

from Newark, NY
Age ~62

Dino Aimino Phones & Addresses

  • 3135 Tyler Rd, Newark, NY 14513 (315) 331-5302
  • Arcade, NY
  • Lake Ariel, PA
  • Ocala, FL
  • Rochester, NY
  • Green Cove Springs, FL

Work

Company: Bausch + lomb (valeant pharmaceuticals) - Rochester, NY Jan 2010 Position: Chemical process engineer ii

Education

School / High School: Nazareth College of Rochester- Rochester, NY 1980 Specialities: Bachelor of Science in Biology

Skills

Organic Chemistry • Metal Complexes • Process Improvement • Technology Transfer • Lean Manufacturing • DOE • Six Sigma Quality Tools • Data Analysis and Interpretation • Project Management

Ranks

Certificate: Lean Six Sigma Blackbelt

Interests

Art • Music • Obedience and Gun Dog Training • Outdoor Sports • Taxidermy • Owner/Trainer of First Flight Retrievers

Emails

a***o@bluefrognet.net

Industries

Chemicals

Resumes

Resumes

Dino Aimino Photo 1

Chief Process Engineer

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Location:
3135 Tyler Rd, Newark, NY 14513
Industry:
Chemicals
Work:
Bausch + Lomb 2010 - Apr 2014
Chemical Process Engineer Ii

Noble Biomaterials 2010 - Apr 2014
Chief Process Engineer

Anoplate Corporation 2006 - 2009
Senior Chemical Process Engineer

Eastman Kodak 1985 - 2006
Senior Process Development Chemist
Education:
Nazareth College 1980 - 1984
Bachelors, Biology
Rochester Institute of Technology
Skills:
Design of Experiments
R&D
Process Simulation
Validation
Six Sigma
Commercialization
Technology Transfer
Cross Functional Team Leadership
Chemistry
Polymers
Continuous Improvement
Manufacturing
Analytical Chemistry
Organic Chemistry
V&V
Quality System
Lean Manufacturing
Formulation
Root Cause Analysis
Materials Science
Coatings
Chemical Engineering
Polymer Science
Gas Chromatography
Characterization
Fda
Hplc
Capa
Uv/Vis
Thin Films
Polymer Chemistry
Chromatography
U.s. Food and Drug Administration
Interests:
Art
Music
Obedience and Gun Dog Training
Outdoor Sports
Taxidermy
Owner/Trainer of First Flight Retrievers
Certifications:
Lean Six Sigma Blackbelt
Dino Aimino Photo 2

Dino Aimino Newark, NY

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Work:
BAUSCH + LOMB (VALEANT Pharmaceuticals)
Rochester, NY
Jan 2010 to Apr 2014
Chemical Process Engineer II

ANOPLATE CORPORATION
Syracuse, NY
2006 to 2009
Sr. Chemical Process Engineer

EASTMAN KODAK COMPANY
Rochester, NY
1994 to 2006
Sr. Process Development Chemist

Education:
Nazareth College of Rochester
Rochester, NY
1980 to 1984
Bachelor of Science in Biology

Skills:
Organic Chemistry, Metal Complexes, Process Improvement, Technology Transfer, Lean Manufacturing, DOE, Six Sigma Quality Tools, Data Analysis and Interpretation, Project Management

Publications

Us Patents

2-Benzyloxy-4-Nitro-5-Substituted-Acylanilide Compounds And Method Of Using Them

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US Patent:
6482953, Nov 19, 2002
Filed:
Dec 3, 2001
Appl. No.:
10/011879
Inventors:
Chang-Kyu Kim - Pittsford NY
Dino Aimino - Newark NY
Assignee:
Eastman Kodak Company - Rochester NY
International Classification:
C07D26344
US Classification:
548226, 5483001, 5483351
Abstract:
Disclosed is a 2-benzyloxy-4-nitro-5-substituted-acylanilide compound of the general formula I: wherein R is hydrogen or an alkyl group, each R is an independently selected substituent and n is 0-5, and Y is a substituent group linked to the rest of the compound by a hetero atom. Also disclosed is a method for using the intermediates in manufacture of dye-forming couplers.

Synthesis Of Pyrazolotriazole Photographic Dye Forming Color Couplers And Intermediates

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US Patent:
59986298, Dec 7, 1999
Filed:
Dec 2, 1998
Appl. No.:
9/204444
Inventors:
Judith A. Bose - Webster NY
Ronald R. Valente - Rochester NY
Dino Aimino - Newark NY
Deborah D. DeMejo - Rochester NY
Assignee:
Eastman Kodak Company - Rochester NY
International Classification:
C07D24918
US Classification:
5482624
Abstract:
Photographic pyrazolotriazole dye forming coupler compound or coupler intermediate compounds can be readily prepared by inducing an elimination-addition reaction between certain pyrazolotriazole compounds and aromatic amines in the presence of an inorganic base or formate. Yields and purity are high, and reaction time is reduced with the specific set of conditions and reactants, and environmental impact from waste is reduced. The resulting compounds can be used themselves as photographic dye forming couplers or further reacted to prepare useful coupler compounds for photographic use.

Methods For Controlling Color During A Metallization Process And Resulting Products

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US Patent:
20210372044, Dec 2, 2021
Filed:
Aug 12, 2021
Appl. No.:
17/400999
Inventors:
- Scranton PA, US
Carl Jones - Peckville PA, US
Jodi Wallis - Carbondale PA, US
Dino Aimino - Newark NY, US
Thomas Dougal - Old Forge PA, US
Greg Gianforcaro - Clemson SC, US
David Curry - Valdese NC, US
International Classification:
D06P 5/10
D06B 3/10
D06B 21/00
D06M 11/83
Abstract:
System and methods that enables fabric to be metalized and dyed to reach final colors that were previously unobtainable. The systems and methods relate to processes for controlling the color of metalized fabrics. Specifically, for some embodiments, the systems and methods relate to methods of making metalized fabrics that are lighter in color than prior metalized fabrics. Such fabrics may be printed on or dyed using lighter colors than would be possible when using prior metalized fabrics. The systems and methods herein may include dye baths and wash baths that are hotter than prior art processes.

Metalized Fabric That Dissipates And Scatters Infrared Light And Methods Or Making And Using The Same

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US Patent:
20210246606, Aug 12, 2021
Filed:
Jan 28, 2021
Appl. No.:
17/161364
Inventors:
- Scranton PA, US
Carl Jones - Peckville PA, US
Jodi Wallis - Carbondale PA, US
Dino Aimino - Newark NY, US
Thomas Dougal - Old Forge PA, US
Greg Gianforcaro - Clemson NC, US
David Curry - Valdese NC, US
International Classification:
D06M 11/83
F41H 3/02
Abstract:
A metalized fabric and method for metallization of fabric. The fabric is formed using two threads with different affinities for metallization, but which threads are not metalized prior to forming into the fabric. The threads will typically be woven using an unbalanced weave to provide one side of the fabric with a resultant greater amount of metallization than the other but this is not required. Once the resultant fabric is metalized, it will typically be more suitable for consistent color dying than fabric which was formed from both metalized and unmetallized threads.
Dino R Aimino from Newark, NY, age ~62 Get Report