CO2 Company Policy and the Bloodhound
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IIIHI||||||||III US005304628A United States Patent (19) (11) Patent Number: 5,304,628 Kinoshita Et Al
IIIHI||||||||III US005304628A United States Patent (19) (11) Patent Number: 5,304,628 Kinoshita et al. (45) Date of Patent: Apr. 19, 1994 (54) RADIATION-CURING RESIN (56) References Cited COMPOSITION U.S. PATENT DOCUMENTS 3,280,078 10/1966 Hostettler et al. .................. 522/163 (75) Inventors: Masashi Kinoshita, Tokyo; Hidenobu 4,500,704 2/1985 Kruper, Jr. et al. o Ishikawa, Chiba, both of Japan 4,686,276 8/1987 Myers ................. 4,808,658 2/1989 Walz et al. ..... - . 528/49 73) Assignee: Dainippon Ink and Chemicals, Inc., 4,948,700 8/1990 Maeda et al. ...... 522A101 Tokyo, Japan 5, 100,767 3/1992 Yanagawa et al. 522/100 5,102,702 4/1992 Grundke et al........ ... 525/526 (21) Appl. No.: 924,748 5,175,231 12/1992 Rappaport et al. ................. 528/106 Primary Examiner-Susan Berman 22 Filed: Aug. 4, 1992 Attorney, Agent, or Firm-Armstrong, Westerman, 30 Foreign Application Priority Data Hattori, McLeland & Naughton (57) ABSTRACT Aug. 5, 1991 JP Japan .................................. 3-195340 A radiation-curing resin composition comprising (A) a 51) Int. Cl......................... C08F 2/50; C08G 63/52; resin having a carboxylic acid group and an unsaturated C08G 18/OO double bond and (B) a compound containing a cyclo 52 U.S.C. ...................................... 528/370; 528/44; carbonate group. The composition is excellent in stabil 528/75; 528/306; 522/16; 522/97; 522/100; ity and curing properties and provides a cured film 522/101; 522/163 excellent in water resistance, solvent resistance, chemi 58) Field of Search ..................... 522/163, 92,93, 94, cal resistance, and heat resistance. -
(12) United States Patent (10) Patent N0.: US 6,225,009 B1 Fleischer Et Al
US006225009B1 (12) United States Patent (10) Patent N0.: US 6,225,009 B1 Fleischer et al. (45) Date of Patent: *May 1, 2001 (54) ELECTROCHEMICAL CELL WITH A NON- (51) Int. Cl.7 ........................... .. H01M 4/52; H01M 4/60; LIQUID ELECTROLYTE H01M 10/40 52 US. Cl. ........................ .. 429/306; 429/213; 429/220; (75) Inventors: Niles A Fleischer; J00st Manassen, ( ) 429/221; 429/224 lgiithRzfsllfech?ggzs?ogig?lgigméylm; (58) Field Of Search ............................ ..442299//23236 320261, 221234; Marvin S. Antelman, Rehovot, all of ’ ’ (IL) (56) References Cited (73) Assignee: E.C.R. -Electr0-Chemical Research US. PATENT DOCUMENTS Ltd” Rehovot (IL) 4,366,216 * 12/1982 McGinness ........................ .. 429/213 ( * ) Notice: PawntSubject is to mendedany disclaimer, or adjusted the term under of this 35 4,847,174 * 7/1989 §$1I1l:r:1_etj1_'_Palmer et a1. ....... .. 429/112 U-S-C- 154(b) by 0 days- 5,731,105 * 3/1998 Fleischer et al. .............. .. 429/213 X This patent is subject to a terminal dis- * Cited by examiner Clalmer' Primary Examiner—Stephen Kalafut (21) APPL NO; 09/068,864 (74) Attorney, Agent, or Firm—Mark M. Friedman (22) PCT Filed: Sep. 23, 1997 (57) ABSTRACT (86) PCT NO; PCT/US97/16901 A non-liquid electrolyte containing electrochemical cell which operates ef?ciently at room temperature. The cell § 371 Datei May 19, 1998 includes (a) a non-liquid electrolyte in which protons are _ mobile, (b) an anode active material based on an organic § 102(6) Date' May 19’ 1998 com P ound which is a source of P rotons durin g cell (87) PCT Pub. -
Gas-Phase Boudouard Disproportionation Reaction Between Highly Vibrationally Excited CO Molecules
Chemical Physics 330 (2006) 506–514 www.elsevier.com/locate/chemphys Gas-phase Boudouard disproportionation reaction between highly vibrationally excited CO molecules Katherine A. Essenhigh, Yurii G. Utkin, Chad Bernard, Igor V. Adamovich *, J. William Rich Nonequilibrium Thermodynamics Laboratories, Department of Mechanical Engineering, The Ohio State University, Columbus, OH 43202, USA Received 3 September 2006; accepted 21 September 2006 Available online 30 September 2006 Abstract The gas-phase Boudouard disproportionation reaction between two highly vibrationally excited CO molecules in the ground elec- tronic state has been studied in optically pumped CO. The gas temperature and the CO vibrational level populations in the reaction region, as well as the CO2 concentration in the reaction products have been measured using FTIR emission and absorption spectroscopy. The results demonstrate that CO2 formation in the optically pumped reactor is controlled by the high CO vibrational level populations, rather than by CO partial pressure or by flow temperature. The disproportionation reaction rate constant has been determined from the measured CO2 and CO concentrations using the perfectly stirred reactor (PSR) approximation. The reaction activation energy, 11.6 ± 0.3 eV (close to the CO dissociation energy of 11.09 eV), was evaluated using the statistical transition state theory, by comparing the dependence of the measured CO2 concentration and of the calculated reaction rate constant on helium partial pressure. The dispro- À18 3 portionation reaction rate constant measured at the present conditions is kf =(9±4)· 10 cm /s. The reaction rate constants obtained from the experimental measurements and from the transition state theory are in good agreement. -
Alder Reactions of [60]Fullerene with 1,2,4,5-Tetrazines and Additions to [60]Fullerene-Tetrazine Monoadducts
University of New Hampshire University of New Hampshire Scholars' Repository Doctoral Dissertations Student Scholarship Spring 2002 Diels -Alder reactions of [60]fullerene with 1,2,4,5-tetrazines and additions to [60]fullerene-tetrazine monoadducts Mark Christopher Tetreau University of New Hampshire, Durham Follow this and additional works at: https://scholars.unh.edu/dissertation Recommended Citation Tetreau, Mark Christopher, "Diels -Alder reactions of [60]fullerene with 1,2,4,5-tetrazines and additions to [60]fullerene-tetrazine monoadducts" (2002). Doctoral Dissertations. 81. https://scholars.unh.edu/dissertation/81 This Dissertation is brought to you for free and open access by the Student Scholarship at University of New Hampshire Scholars' Repository. It has been accepted for inclusion in Doctoral Dissertations by an authorized administrator of University of New Hampshire Scholars' Repository. For more information, please contact [email protected]. INFORMATION TO USERS This manuscript has been reproduced from the microfilm master. UMI films the text directly from the original or copy submitted. Thus, some thesis and dissertation copies are in typewriter face, while others may be from any type of computer printer. The quality of this reproduction is dependent upon the quality of the copy submitted. Broken or indistinct print, colored or poor quality illustrations and photographs, print bleedthrough, substandard margins, and improper alignment can adversely affect reproduction. In the unlikely event that the author did not send UMI a complete manuscript and there are missing pages, these will be noted. Also, if unauthorized copyright material had to be removed, a note will indicate the deletion. Oversize materials (e.g., maps, drawings, charts) are reproduced by sectioning the original, beginning at the upper left-hand comer and continuing from left to right in equal sections with small overlaps. -
Some Unusual, Astronomically Significant Organic Molecules
'lL-o Thesis titled: Some Unusual, Astronomically Significant Organic Molecules submitted for the Degree of Doctor of Philosophy (Ph,D.) by Salvatore Peppe B.Sc. (Hons.) of the Department of Ghemistty THE UNIVERSITY OF ADELAIDE AUSTRALIA CRUC E June2002 Preface Gontents Contents Abstract IV Statement of Originality V Acknowledgments vi List of Figures..... ix 1 I. Introduction 1 A. Space: An Imperfect Vacuum 1 B. Stellff Evolution, Mass Outflow and Synthesis of Molecules 5 C. Astronomical Detection of Molecules......... l D. Gas Phase Chemistry.. 9 E. Generation and Detection of Heterocumulenes in the Laboratory 13 L.2 Gas Phase Generation and Characterisation of Ions.....................................16 I. Gas Phase Generation of Ions. I6 A. Positive Ions .. I6 B. Even Electron Negative Ions 17 C. Radical Anions 2t tr. Mass Spectrometry 24 A. The VG ZAB 2}lF Mass Spectrometer 24 B. Mass-Analysed Ion Kinetic Energy Spectrometry......... 25 III. Characterisation of Ions.......... 26 A. CollisionalActivation 26 B. Charge Reversal.... 28 C. Neutralisation - Reionisation . 29 D. Neutral Reactivity. JJ rv. Fragmentation Behaviour ....... 35 A. NegativeIons.......... 35 Preface il B. Charge Inverted Ions 3l 1.3 Theoretical Methods for the Determination of Molecular Geometries and Energetics..... ....o........................................ .....39 L Molecular Orbital Theory........ 39 A. The Schrödinger Equation.... 39 B. Hartree-Fock Theory ..44 C. Electron Correlation ..46 D. Basis sets............ .51 IL Transition State Theory of Unimolecular Reactions ......... ................... 54 2. Covalently Bound Complexes of CO and COz ....... .........................58 L Introduction 58 tr. Results and Discussion........... 59 Part A: Covalently bound COz dimers (OzC-COr)? ............ 59 A. Generation of CzO¿ Anions 6I B. NeutralCzO+........ -
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The Preparation of Aromatic Esters of Malonic Acid 1 John H. Billman, R. Vincent Cash 2 and Eleanor K. Wakefield The preparations of four aromatic esters of malonic acid have been described in the literature. These are the diphenyl-, di-/3-naphthyl-, di- p-tolyl-, and di-p-nitrophenyl malonates. The preparation of diphenyl malonate by Bischoff and von Heden- strom (5) in 1902 illustrates one of the synthetic methods employed. Phenol and malonyl chloride were warmed on a water bath for a short time; hydrogen chloride was envolved and the solid ester crystallized on cooling. -* C1-C-CH.-C-C1 + 2 CeHtfOH C 6 H 5 -0-C-CH a -C-0-C 6 H 6 + 2 HC1 These workers tried without success to prepare this ester from malonic acid, phenol, and thionyl chloride. However, Auger and Billy (1) were able to synthesize diphenyl malonate from malonic acid, phenol, and phosphorus oxychloride. Guia (6) obtained di-/3-naphthnyl malonate rather than the desired counmarin-type compound when he heated /3-naphthol, malonyl chloride, and aluminum chloride in carbon disulfide. Backer and Lolkema (2) synthesized di-p-tolyl malonate and di-p-nitrophenyl malonate from malonyl chloride according to the above equation. The latter ester was also prepared by these investigators by treatment of the diphenyl malonate with nitric acid at 0°. Since carbon suboxide has been reported (7) to react with alcohols to yield dialkyl malonates, it seemed of interest to attempt to extend the reaction to phenols. -* 0=C=C=C=0 + 2 HOAr Ar-0-C-CH 2 -C-0-Ar Five phenols were successfully esterified with carbon suboxide, with sulfuric acid or p-toluenesulfonic acid present at catalyst. -
The Infrared Absorption Spectrum of Carbon Sub Oxide
AUGUST, 1937 JOURNAL OF CHEMICAL PHVSICS VOLUME 5 The Infrared Absorption Spectrum of Carbon Suboxide R. C. LORD, JR.* AND NORMAN WRIGHT Departments of Chemistry and Physics, University of Michigan, A nn Arbor, Michigan (Received "May 24, 1937) The infrared absorption spectrum of carbon suboxide vapor has been studied under low dispersion in the region from 2).1 to 25).1. The vibrational bands observed may be satisfactorily accounted for on the basis of a linear symmetric structure for the carbon suboxide molecule, in agreement with evidence obtained from Raman spectra and from electron diffraction investigations. ECENT studies of the structure of the material was prepared by the pyrolysis of R carbon suboxide molecule by electron dif diacetyl tartaric anhydride8 and was purified by fractiont ,2 and by ultraviolet absorption and two distillations in an all-glass system. Measure 3 Raman spectra - 5 have made desirable an in ments of the vapor pressure of the suboxide over vestigation of the molecule's absorption spectrum a range of temperatures up to O°C agreed in the infrared region. The information to be satisfactorily with those in the literature. 9 The gained from such an investigation should be absorption cell was filled by distilling the middle particularly helpful since the spectroscopic and fraction of the particular sampJe at hand into electron diffraction evidence indicates that the the evacuated ce1l, the desired pressure being most probable form of the carbon suboxide obtained by surrounding the distilling vessel molecule is one possessing a symmetry center. with a bath of acetone of the proper temperature. -
Carbon Dioxide Hydrogenation to Aromatic Hydrocarbons by Using an Iron/Iron Oxide Nanocatalyst
Carbon dioxide hydrogenation to aromatic hydrocarbons by using an iron/iron oxide nanocatalyst Hongwang Wang*1, Jim Hodgson1, Tej B. Shrestha2, Prem S. Thapa3, David Moore3, Xiaorong Wu4, Myles Ikenberry5, Deryl L. Troyer2, Donghai Wang4, Keith L. Hohn5 and Stefan H. Bossmann*1 Full Research Paper Open Access Address: Beilstein J. Nanotechnol. 2014, 5, 760–769. 1Kansas State University, Department of Chemistry, 201CBC doi:10.3762/bjnano.5.88 Building, Manhattan, KS 66506, USA, 001-785-532-6817, 2Kansas State University, Department of Anatomy & Physiology, 130 Coles Received: 11 March 2014 Hall, Manhattan, KS 66506, USA, 3University of Kansas, Microscopy Accepted: 30 April 2014 and Analytical Imaging Laboratory, 1043 Haworth, Lawrence, KS Published: 02 June 2014 66045, USA, 4Kansas State University, Department of Biological and Agricultural Engineering, 150 Seaton Hall, Manhattan, KS 66506, Associate Editor: J. J. Schneider USA and 5Kansas State University, Department of Chemical Engineering, 1016 Durland Hall, Manhattan, KS 66506, USA © 2014 Wang et al; licensee Beilstein-Institut. License and terms: see end of document. Email: Hongwang Wang* - [email protected]; Stefan H. Bossmann* - [email protected] * Corresponding author Keywords: aromatic hydrocarbons; carbon dioxide reduction; heterogenous catalysis; iron/iron oxide nanocatalyst Abstract The quest for renewable and cleaner energy sources to meet the rapid population and economic growth is more urgent than ever before. Being the most abundant carbon source in the atmosphere of Earth, CO2 can be used as an inexpensive C1 building block in the synthesis of aromatic fuels for internal combustion engines. We designed a process capable of synthesizing benzene, toluene, xylenes and mesitylene from CO2 and H2 at modest temperatures (T = 380 to 540 °C) employing Fe/Fe3O4 nanoparticles as cata- lyst. -
Wo 2007/095255 A2
(12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (43) International Publication Date (10) International Publication Number 23 August 2007 (23.08.2007) PCT WO 2007/095255 A2 (51) International Patent Classification: (71) Applicant (for all designatedStates except US):DUPONT A23B 7/154 (2006.01) TATE & LYLE BIO PRODUCTS COMPANY, LLC [US/US]; 4417 Lancaster Pike, Wilmington, DE 19805 (21) International Application Number: PCT/US2007/003841 (US). (22) International Filing Date: (72) Inventors; and 12 February 2007 (12.02.2007) (75) Inventors/Applicants (for US only): WEHNER, Ann (25) Filing Language: English [US/US]; 1 Pickering Trail, Hockessin, DE 19707 (US). FENYVESI, Gyorgyi [US/US]; 224 Oakwood Road, (26) Publication Language: English Wilmington, DE 19803 (US). MUSKA, Carl, F. [US/US]; (30) Priority Data: 5400 Turkey Point Road, Northeast, MD 21901 (US). 60/772,194 10 February 2006 (10.02.2006) US DESALVO, Joseph, W. [US/US]; 486 South Apple Tree 60/772,193 10 February 2006 (10.02.2006) US Lane, Lafayette Hill, PA (US). JOERGER, Melissa 60/772,120 10 February 2006 (10.02.2006) US [US/US]; 155 Woodland Road, Newark, DE 19702 (US). 60/772,471 10 February 2006 (10.02.2006) US MILLER, Robert [US/US]; 1410 Delaware Avenue, Apt. 60/772,1 11 10 February 2006 (10.02.2006) US Al, Wilmington, DE 19806 (US). PALEFSKY,Irwin, A. 60/772,110 10 February 2006 (10.02.2006) US [US/US]; 600 Harbor Blvd., Weehawken, NJ 07086 (US). 60/772,1 12 10 February 2006 (10.02.2006) US POLADI, Raja, Hari, Prasad [IN/US]; 8 Meghan Lane, 60/846,948 25 September 2006 (25.09.2006) US Bear, DE 19701 (US). -
Wildland Fire Emission Factors in North America: Synthesis of Existing Data, Measurement Needs and Management Applications
CSIRO PUBLISHING International Journal of Wildland Fire 2020, 29, 132–147 https://doi.org/10.1071/WF19066 Wildland fire emission factors in North America: synthesis of existing data, measurement needs and management applications Susan J. PrichardA,E, Susan M. O’NeillB, Paige EagleA, Anne G. AndreuA, Brian DryeA, Joel DubowyA, Shawn UrbanskiC and Tara M. StrandD AUniversity of Washington School of Environmental and Forest Sciences, Box 352100, Seattle, WA 98195-2100, USA. BPacific Wildland Fire Sciences Laboratory, US Forest Service Pacific Northwest Research Station, 400 N. 34th Street, Seattle, WA 98103, USA. CMissoula Fire Sciences Laboratory, US Forest Service Rocky Mountain Research Station, 5775 W Broadway Street, Missoula, MT 59808, USA. DScion Research, Te Papa Tipu Innovation Park, 49 Sala Street, Rotorua 3010, Private Bag 3020, Rotorua 3046, New Zealand. ECorresponding author. Email: [email protected] Abstract. Field and laboratory emission factors (EFs) of wildland fire emissions for 276 known air pollutants sampled across Canada and the US were compiled. An online database, the Smoke Emissions Repository Application (SERA), was created to enable analysis and summaries of existing EFs to be used in smoke management and emissions inventories. We evaluated how EFs of select pollutants (CO, CO2,CH4,NOx, total particulate matter (PM), PM2.5 and SO2) are influenced by combustion phase, burn type and fuel type. Of the 12 533 records in the database, over a third (n ¼ 5637) are represented by 23 air pollutants, most designated as US Environmental Protection Agency criteria air pollutants, greenhouse gases, hazardous air pollutants or known air toxins. Among all pollutants in the database, including the most common pollutants PM, CO, CO2 and CH4, records are unevenly distributed with a bias towards flaming combustion, prescribed burning and laboratory measurements. -
Effects of Pressure and Particle Size on the Carbonization of a Packed Bed of Biomass
Effects of Pressure and Particle Size on the Carbonization of a Packed Bed of Biomass A THESIS SUBMITTED TO THE GRADUATE DIVISION OF THE UNIVERSITY OF HAWAIʻI AT MĀNOA IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF MASTER OF SCIENCE IN MECHANICAL ENGINEERING May 2014 By Gregory Patrick Specht Thesis Committee: Michael J. Antal Jr., Chairperson Weilin Qu Beei-Huan Chao i We certify that we have read this thesis and that, in our opinion it is satisfactory in scope and quality as a dissertation for a degree of Master of Science in Mechanical Engeineering. THESIS COMMITTEE Chairperson ii © Copyright 2014 By Gregory Patrick Specht All Rights Reserved iii Abstract A relatively new technique for charcoal production has been developed called Flash CarbonizationTM and has proven to be efficient and most importantly fast. The technique begins with a packed bed of biomass pressurized at 1-2 MPa. A fire is ignited at the bottom of the bed while air is introduced through the top. The flame travels up the bed converting the biomass to bio carbon otherwise known as charcoal. One of the most important metrics a charcoal has is its Fixed Carbon Yield (yfc) or the percentage of carbon left in it after it is carbonized. Many factors affect the yfc of charcoal three in particular were investigated in this thesis; feedstock, pressure, and particle size. Each feedstock that was used in the FC process and analyzed in this thesis was sent out to a lab to discover its elemental composition. Using this data calculations were performed to discover the highest theoretical yfc each feedstock could produce. -
Plasmachemical Synthesis of Carbon Suboxide
PLASMACHEMICAL SYNTHESIS OF CARBON SUBOXIDE A Thesis by ROBERT PAUL GEIGER Submitted to the Office of Graduate Studies of Texas A&M University in partial fulfillment of the requirement for the degree of MASTER OF SCIENCE Approved by: Chair of Committee, David Staack Committee Members, Nicole Zacharia Sergio Capareda Head of Department, Jerry Caton May 2013 Major Subject: Mechanical Engineering © 2013 Robert Paul Geiger ABSTRACT A nonthermal carbon monoxide plasma is known to produce a solid deposition which is thought to be a polymer of carbon suboxide (C3O2); however there are very few investigations of this deposition in the literature. This thesis contains an analysis of the theoretical thermodynamics and kinetics of carbon suboxide formation as well as experimental results. The theoretical analysis suggests that carbon suboxide may be an equilibrium product even at ambient conditions but favors lower temperatures; furthermore if solid carbon is considered to be kinetically limited, and therefore not a product, then carbon suboxide is more likely to be a product under these pseudo-equilibrium conditions. Experimentally, solid films were produced in a dielectric barrier discharge (DBD) containing pure carbon monoxide. Optical emission spectroscopy was used to analyze the plasma and models of the emission spectra were created to determine the plasma temperatures. Deposition rates were determined to be on the order of 0.2 mg/min at a power of about 10W; it is expected however that these conditions are not optimized. The overall kinetics of carbon suboxide was analyzed and optimal conditions for operation can be estimated. Characterization of the solid depositions were carried out using Solid State Nuclear Magnetic Resonance (NMR), Fourier Transform Infrared Spectroscopy (FTIR), Electrospray Ionization Mass Spectroscopy (ESI-MS), and Matrix-assisted Laser Desorption Ionization Mass Spectroscopy (MALDI-MS).