Alfred E. Mann Institute an the University of Southern California
Mar 2013 to 2000 Research AssistantUniversity Bookstore Los Angeles, CA Dec 2012 to Mar 2013 CashierEast China University of Science and Technology
Sep 2010 to Jun 2012 Research Assistant
Education:
University of Southern California Los Angeles, CA 2012 to 2014 Master of Science in Materials ScienceEast China University of Science and Technology Sep 2008 to Jun 2012 Bachelor of Engineering in Polymer Science and Engineering
Jul 2008 to Present Office AssistantMoldex Metric Inc Culver City, CA Aug 2007 to Feb 2008 QA Document AdministratorPR and AP
May 2006 to Dec 2006Huazangsi Temple San Francisco, CA Oct 2005 to May 2006 Translator/InterpreterCal State LA University Auxiliary Service, Inc Los Angeles, CA Apr 2005 to Oct 2005 Office ClerkAmerican-De Rosa Lamparts Commerce, CA Feb 2004 to Apr 2005 Assistant BuyerGibson Overseas Inc Commerce, CA Jun 2000 to Jul 2003 Assistant to the Director of Inventory ControlLa Monde Ltd. / Wild Flavors, Inc Placentia, CA Mar 1997 to May 1999 Lab Technician
Education:
California Institute of Customer Engineering Van Nuys, CA 1999 Certificate of Medical Billing & CodingBeijing University of International Business and Economics 1993 to 1994 Certificate of Business EnglishJiangsu Institute of Petrochemical Engineering and Technology 1987 to 1991 Petroleum
Name / Title
Company / Classification
Phones & Addresses
Nan Chen Director
NAN CHEN CONSULTING, INC
29342 Chelsea Xing, Farmington, MI 48331
Nan Chen
Accident Attorney Carson
22195 Nicolle Ave, Carson, CA 90745 3109561078
Nan Chen
Chen Nan Shaolin Kung Fu Academy Fitness Center · Fitness Trainer
1158 Saratoga Ave, San Jose, CA 95129 4087405066
Nan Chen Vice-President
Marfred Industries Commercial Art/Graphic Design
810 Lawrence Dr, Thousand Oaks, CA 91320 8052140999
Nan Chen President
APEXWING TECHNOLOGY INC Business Services · Computer Related Services
5806 Cloverly Ave UNIT D, Temple City, CA 91780
Us Patents
Method For Predicting Sediment Content Of A Hydroprocessed Hydrocarbon Product
Estrella Rogel - Orinda CA, US Cesar Ovalles - Walnut Creek CA, US Pak Leung - San Ramon CA, US Nan Chen - San Ramon CA, US
Assignee:
Chevron U.S.A. INC - San Ramon CA
International Classification:
G01N 30/02 G06F 19/00
US Classification:
702 25, 73 6152
Abstract:
Disclosed herein is a method of predicting sediment content of a hydroprocessed hydrocarbon product. The method involves: (a) precipitating an amount of asphaltenes from a liquid sample of a first hydrocarbon-containing feedstock having solvated asphaltenes therein with one or more first solvents; (b) determining one or more solubility characteristics of the precipitated asphaltenes; (c) analyzing the one or more solubility characteristics; (d) determining asphaltene content of the liquid sample from the results of analyzing the one or more solubility characteristics; (e) determining one or more asphaltene stability parameters of the liquid sample from the results of analyzing the one or more solubility characteristics; and (f) correlating the asphaltene content and one of the asphaltene stability parameters of the liquid sample with at least two operation conditions associated with a refinery to predict sediment content.
Method For Estimating Sediment Content Of A Hydroprocessed Hydrocarbon-Containing Feedstock
Estrella Rogel - Orinda CA, US Cesar Ovalles - Walnut Creek CA, US Pak Leung - San Ramon CA, US Nan Chen - San Ramon CA, US
Assignee:
CHEVRON U.S.A. INC. - San Ramon CA
International Classification:
G01N 30/04 G06F 19/00 G01N 1/28
US Classification:
702 25, 73 6159, 73 6155
Abstract:
Disclosed herein is a method of estimating sediment content of a hydroprocessed hydrocarbon-containing feedstock. The method involves the steps of: (a) precipitating an amount of asphaltenes from a liquid sample of a first hydroprocessed hydrocarbon-containing feedstock having solvated asphaltenes therein with one or more first solvents in a column; (b) determining one or more solubility characteristics of the precipitated asphaltenes; (c) analyzing the one or more solubility characteristics of the precipitated asphaltenes; (d) determining asphaltene content of the liquid sample from the results of analyzing the one or more solubility characteristics of the precipitated asphaltenes; (e) determining one or more asphaltene stability parameters of the liquid sample from the results of analyzing the one or more solubility characteristics of the precipitated asphaltenes; and (f) correlating the asphaltene content and one of the asphaltene stability parameters of the liquid sample to estimate sediment content of the liquid sample.
- Los Angeles CA, US Nan Chen - Los Angeles CA, US Nichole Escamilla - Los Angeles CA, US Cesar Blanco - Los Angeles CA, US Mark Edward Thompson - Los Angeles CA, US
Adhesives, particularly reversible adhesives, reversible adhesive hydrogel meshes and polymer formulations that may be used in preparation of the reversible adhesive hydrogel meshes are disclosed. The polymer formulations may comprise a reversible monomer of a reversible adhesive polymer, acrylic acid (AA), an acrylate cross-linker, a photo-initiator for free radical polymerization, and a solvent. The disclosure also relates to a wound dressing comprising the reversible adhesive hydrogel meshes. Such wound dressings are particularly suitable for treatment of damaged sensitive tissue, for example, wounds formed on a fragile skin.
Methods And Apparatuses For Forming Metal Oxide Nanostructures
- Los Angeles CA, US Bharat Kumar MENON - Los Angeles CA, US Nan CHEN - Los Angeles CA, US Heather Michelle GRANDIN - Los Angeles CA, US Harald NUHN - Los Angeles CA, US Jenna Brynne LUBET - Los Angeles CA, US
International Classification:
C25D 11/26 A61L 31/08 A61L 31/02 C25D 11/00
Abstract:
Embodiments of methods and apparatuses for forming the metal oxide nanostructure on surfaces are disclosed. In certain embodiments, the nanostructures can be formed on a substrate made of a nickel titanium alloy, resulting in a nanostructure that can include both titanium oxide and nickel oxide. The nanostructure can be formed on the surface(s) of an implantable medical device, such as a stent.
- Los Angeles CA, US Nan Chen - Temple City CA, US Bharat Kumar Menon - Los Angeles CA, US Heather Michelle Grandin - San Diego CA, US Cesar Escobar Blanco - Los Angeles CA, US
International Classification:
C25D 11/26 C25D 11/34
Abstract:
Embodiments of nanostructures comprising metal oxide and methods for forming the nanostructure on surfaces are disclosed. In certain embodiments, the nanostructures can be formed on a substrate made of a nickel titanium alloy, resulting in a nanostructure containing both titanium oxide and nickel oxide. The nanostructure can include a lattice layer disposed on top of a nanotube layer. The distal surface of the lattice layer can have a titanium oxide to nickel oxide ratio of greater than 10:1, or about 17:1, resulting in a nanostructure that promotes human endothelial cell migration and proliferation at the interface between the lattice layer and human cells or tissue. The nanostructure may be formed on the outer surface of an implantable medical device, such a stent or an orthopedic implant (e.g. knee implant, bone screw, or bone staple).
A supported catalyst useful in processes for chemically refining hydrocarbon feedstocks is prepared, the catalyst comprising a metal from Group 6 of the Periodic Table, a metal from Groups 8, 9 or 10 and optionally phosphorous, wherein the metals, and phosphorous when present, are carried on a foraminous carrier or support, the carrier or support, preferably comprises porous alumina having a total pore volume (TPV) of about 0.6 cc/g to about 1.1 cc/g and comprising: (a) equal to or greater than about 78% to about 95% of TPV in pores having a diameter of less than about 200 Angstroms (Å); (b) greater than about 2% to less than about 19% of the TPV in pores having a diameter of about 200 (Å) to less than about 1000 Å; (c) equal to or greater than 3% to less than 12% of the TPV in pores having a diameter equal to or greater than about 1000 Å; and (d) a pore mode equal to or greater than about 90 Å and less than about 160 Å. Preferably the support exhibits a d50 greater than about 100 Å and less than about 150 Å.
Adjusting Source Voltage Based On Operating Voltage Response
- San Diego CA, US Yuan-cheng PAN - Saratoga CA, US Junmou ZHANG - San Diego CA, US Nan CHEN - San Diego CA, US Mohamed Waleed ALLAM - San Diego CA, US
International Classification:
H02M 1/14 H02M 3/156 H02M 1/08
Abstract:
An apparatus and a method to adjust a source voltage based on an operating voltage response are provided. The apparatus includes a circuit configured to change state from a first state to a second state comprising receiving an operating voltage from a power source through a power distribution network. The apparatus further includes a sensor configured to measure an operating voltage response to the circuit changing state to receiving the operating voltage. The apparatus further includes a control circuit configured to adjust a source voltage at the power source based on the operating voltage response measured by the sensor. The method includes changing a state to receiving an operating voltage from a power source through a power distribution network, measuring an operating voltage response to the changing state to receiving the operating voltage, and adjusting the source voltage at the power source based on the measured operating voltage response.
- Columbia MD, US Nan Chen - Berkeley CA, US Matthew P. Woods - Pasadena MD, US Bruno Nesci - Oak Lawn IL, US
International Classification:
C10G 65/00 C10G 47/12 C10G 45/08
Abstract:
A supported catalyst useful in processes for chemically refining hydrocarbon feedstocks is prepared, the catalyst comprising a metal from Group 6 of the Periodic Table, a metal from Groups 8, 9 or 10 and optionally phosphorous, wherein the metals, and phosphorous when present, are carried on a foraminous carrier or support, the carrier or support, preferably comprises porous alumina having a total pore volume (TPV) of about 0.6 cc/g to about 1.1 cc/g and comprising: (a) equal to or greater than about 78% to about 95% of TPV in pores having a diameter of less than about 200 Angstroms (Å); (b) greater than about 2% to less than about 19% of the TPV in pores having a diameter of about 200 (Å) to less than about 1000 Å; (c) equal to or greater than 3% to less than 12% of the TPV in pores having a diameter equal to or greater than about 1000 Å; and (d) a pore mode equal to or greater than about 90 Å and less than about 160 Å. Preferably the support exhibits a d50 greater than about 100 Å and less than about 150 Å.