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Transition Metal Phosphides for the Catalytic Hydrodeoxygenation of Waste Oils Into Green Diesel
catalysts Review Transition Metal Phosphides for the Catalytic Hydrodeoxygenation of Waste Oils into Green Diesel M. Consuelo Alvarez-Galvan * , Jose M. Campos-Martin * and Jose L. G. Fierro * Energy and Sustainable Chemistry Group (EQS), Instituto de Catálisis y Petroleoquímica, CSIC, c/Marie Curie, 2 Cantoblanco, 28049 Madrid, Spain * Correspondence: [email protected] (M.C.A.-G.); [email protected] (J.M.C.-M.); jlgfi[email protected] (J.L.G.F.) Received: 28 February 2019; Accepted: 15 March 2019; Published: 22 March 2019 Abstract: Recently, catalysts based on transition metal phosphides (TMPs) have attracted increasing interest for their use in hydrodeoxygenation (HDO) processes destined to synthesize biofuels (green or renewable diesel) from waste vegetable oils and fats (known as hydrotreated vegetable oils (HVO)), or from bio-oils. This fossil-free diesel product is produced completely from renewable raw materials with exceptional quality. These efficient HDO catalysts present electronic properties similar to noble metals, are cost-efficient, and are more stable and resistant to the presence of water than other classical catalytic formulations used for hydrotreatment reactions based on transition metal sulfides, but they do not require the continuous supply of a sulfide source. TMPs develop a bifunctional character (metallic and acidic) and present tunable catalytic properties related to the metal type, phosphorous-metal ratio, support nature, texture properties, and so on. Here, the recent progress in TMP-based catalysts for HDO of waste oils is reviewed. First, the use of TMPs in catalysis is addressed; then, the general aspects of green diesel (from bio-oils or from waste vegetable oils and fats) production by HDO of nonedible oil compounds are presented; and, finally, we attempt to describe the main advances in the development of catalysts based on TMPs for HDO, with an emphasis on the influence of the nature of active phases and effects of phosphorous, promoters, and preparation methods on reactivity. -
US Schedule for Internet V2
Draft as of March 23, 2007 Subject to legal review for accuracy, clarity and consistency. Annex 3.3 - - Industrial/Textile Schedule for the United States Tariff Elimination US 8 digit Description MFN RATE Schedule 03011000 Live ornamental fish Free I 03019100 Live trout Free I 03019200 Live eels Free I 03019300 Live carp Free I 03019900 Live fish, other than trout, eel, carp or ornamental fish Free I 03021100 Trout, fresh or chilled, excluding fillets, other meat portions, livers and roes Free I Pacific, Atlantic and Danube salmon, fresh or chilled, excluding fillets, other 03021200 meat portions, livers and roes Free I Salmonidae other than trout or Pacific, Atlantic & Danube salmon, fresh or 03021900 chilled, excluding fillets, other meat portions, livers & roes Free I Halibut and Greenland turbot, fresh or chilled, excluding fillets, other meat 03022100 portions, livers and roes Free I 03022200 Plaice, fresh or chilled, excluding fillets, other meat portions, livers and roes Free I 03022300 Sole, fresh or chilled, excluding fillets, other meat portions, livers and roes 1.1 cents/kg A Flat fish, nesi, fresh or chilled, excluding fillets, other meat portions, livers 03022900 and roes Free I Albacore or longfinned tunas, fresh or chilled, excluding fillets, other meat 03023100 portions, livers and roes Free I Yellowfin tunas, fresh or chilled, excluding fillets, other meat portions, livers 03023200 and roes Free I Skipjack or stripe-bellied bonito, fresh or chilled, excluding fillets, other meat 03023300 portions, livers and roes Free -
Phosphorus and Sulfur Cosmochemistry: Implications for the Origins of Life
Phosphorus and Sulfur Cosmochemistry: Implications for the Origins of Life Item Type text; Electronic Dissertation Authors Pasek, Matthew Adam Publisher The University of Arizona. Rights Copyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author. Download date 07/10/2021 06:16:37 Link to Item http://hdl.handle.net/10150/194288 PHOSPHORUS AND SULFUR COSMOCHEMISTRY: IMPLICATIONS FOR THE ORIGINS OF LIFE by Matthew Adam Pasek ________________________ A Dissertation Submitted to the Faculty of the DEPARTMENT OF PLANETARY SCIENCE In Partial Fulfillment of the Requirements For the Degree of DOCTOR OF PHILOSOPHY In the Graduate College UNIVERSITY OF ARIZONA 2 0 0 6 2 THE UNIVERSITY OF ARIZONA GRADUATE COLLEGE As members of the Dissertation Committee, we certify that we have read the dissertation prepared by Matthew Adam Pasek entitled Phosphorus and Sulfur Cosmochemistry: Implications for the Origins of Life and recommend that it be accepted as fulfilling the dissertation requirement for the Degree of Doctor of Philosophy _______________________________________________________________________ Date: 04/11/2006 Dante Lauretta _______________________________________________________________________ Date: 04/11/2006 Timothy Swindle _______________________________________________________________________ Date: 04/11/2006 -
Study of Phosphorus Behaviour in Levitated Silicon-Iron Droplets
STUDY OF PHOSPHORUS BEHAVIOUR IN LEVITATED SILICON-IRON DROPLETS by Katherine Le A thesis submitted in conformity with the requirements for the degree of Master of Applied Science Department of Materials Science and Engineering University of Toronto © Copyright by Katherine Le 2016 ii Study of Phosphorus Behaviour in Levitated Si-Fe Droplets Katherine Le Master of Applied Science Department of Materials Science and Engineering University of Toronto 2016 Abstract While the treatment of relatively inexpensive ferrosilicon alloys is a potential refining route in order to generate solar grade silicon, phosphorus is one of the more difficult impurities to remove by conventional processing. In this project, electromagnetic levitation was used to investigate the dephosphorization of ferrosilicon alloy droplets exposed to H2-Ar gas mixtures under various experimental conditions including, refining time, temperature (1450°C-1720°C), H2-Ar gas concentrations and flow rate, iron alloying content, and initial phosphorus concentration. Reaction rates increased with higher refining times, temperatures, and H2 gas concentrations. With unknown parameters associated with the kinetics of gas phase reactions, the approach involved comparison of apparent activation energies derived for the chemical reaction and gas diffusion steps of the dephosphorization process. The phosphorus removal rate is thought to be controlled by the interfacial reaction step; further work is required to confirm this conclusion. iii Acknowledgements I would like to express my gratitude and respect to my supervisor, Prof. Alex McLean for the opportunity to work on this research. I am thankful for his guidance, wisdom and encouragement throughout the course of my studies. He is a truly inspiring person, and a great enabler of new learning opportunities. -
Binary and Ternary Transition-Metal Phosphides As Hydrodenitrogenation Catalysts
Research Collection Doctoral Thesis Binary and ternary transition-metal phosphides as hydrodenitrogenation catalysts Author(s): Stinner, Christoph Publication Date: 2001 Permanent Link: https://doi.org/10.3929/ethz-a-004378279 Rights / License: In Copyright - Non-Commercial Use Permitted This page was generated automatically upon download from the ETH Zurich Research Collection. For more information please consult the Terms of use. ETH Library Diss. ETH No. 14422 Binary and Ternary Transition-Metal Phosphides as Hydrodenitrogenation Catalysts A dissertation submitted to the Swiss Federal Institute of Technology Zurich for the degree of Doctor of Natural Sciences Presented by Christoph Stinner Dipl.-Chem. University of Bonn born February 27, 1969 in Troisdorf (NRW), Germany Accepted on the recommendation of Prof. Dr. Roel Prins, examiner Prof. Dr. Reinhard Nesper, co-examiner Dr. Thomas Weber, co-examiner Zurich 2001 I Contents Zusammenfassung V Abstract IX 1 Introduction 1 1.1 Motivation 1 1.2 Phosphides 4 1.2.1 General 4 1.2.2 Classification 4 1.2.3 Preparation 5 1.2.4 Properties 12 1.2.5 Applications and Uses 13 1.3 Scope of the Thesis 14 1.4 References 16 2 Characterization Methods 1 2.1 FT Raman Spectroscopy 21 2.2 Thermogravimetric Analysis 24 2.3 Temperature-Programmed Reduction 25 2.4 X-Ray Powder Diffractometry 26 2.5 Nitrogen Adsorption 28 2.6 Solid State Nuclear Magnetic Resonance Spectroscopy 28 2.7 Catalytic Test 33 2.8 References 36 3 Formation, Structure, and HDN Activity of Unsupported Molybdenum Phosphide 37 3.1 Introduction -
Download SCOPE Newsletter
With participation of the European Commission: DG GROW and Joint Research Centre Summary of joint European Commission – ESPP webinar th on P4 (phosphorus) Critical Raw Material, 9 July 2020 This ESPP SCOPE Newsletter summarises discussions at the expert webinar jointly organised by ESPP and the European Commission on 9th July, with participation of Contents the leading companies using phosphorus (P4) or its derivatives in Europe, with additional input from the The EU Critical Raw Materials: “Phosphate Rock” and “Phosphorus”........................................................................... 2 independent industry expert Willem Schipper. The content (Fig. i) Overview numbers: from phosphate rock to P4 / P4-derivatives below has been seen by the participants but does not and applications .................................................................................. 3 represent their position, it represents ESPP’s own How is P4 produced? the phosphorus furnace .............. 4 assessment. Photo: P4 furnace ................................................................................ 4 Schematic: P4 manufacture process (simplified) ................................. 4 This webinar aimed to provide expert input to the European Which chemicals critically depend on P4 / P4 derivatives? . 5 Commission’s MSA (Material System Analysis) of the EU dependency on P4 concerns many industry sectors . 5 specific industrial form of “Phosphorus”, P4, as a Critical (Fig. ii) Production via wet-acid or via P4 / P4 derivatives / ‘thermal’ Raw -
Catalog of Standard Reference Materials
NATL INST. OF STAND & TECH Bureau of Standards £-01 Admin. Bldg. AUG 1 8 1970 NBS SPECIAL PUBLICATION 260 NBS JULY 1970 EDITION PUBLICATIONS Catalog of 9TAMDARD "REFERENCE MATERIALS U.S. DEPARTMENT OF COMMERCE National Bureau of Standards - NATIONAL BUREAU OF STANDARDS The National Bureau of Standards 1 was established by an act of Congress March 3, 1901. Today, in addition to serving as the Nation's central measurement laboratory, the Bureau is a principal focal point in the Federal Government for assuring maximum application of the physical and engineering sciences to the advancement of technology in industry and commerce. To this end the Bureau conducts research and provides central national services in four broad program areas. These are: (1) basic measurements and standards, (2) materials measurements and standards, (3) technological measurements and standards, and (4) transfer of technology. The Bureau comprises the Institute for Basic Standards, the Institute for Materials Research, the Institute for Applied Technology, the Center for Radiation Research, the Center for Computer Sciences and Technology, and the Office for Information Programs. THE INSTITUTE FOR BASIC STANDARDS provides the central basis within the United States of a complete and consistent system of physical measurement; coordinates that system with measurement systems of other nations; and furnishes essential services leading to accurate and uniform physical measurements throughout the Nation's scientific community, industry, and com- merce. The Institute consists of an Office of Measurement Services and the following technical divisions: Applied Mathematics—Electricity—Metrology—Mechanics—Heat—Atomic and Molec- ular Physics—Radio Physics - —Radio Engineering -—Time and Frequency -—Astro- physics - —Cryogenics. -
Other Than Radioactive Ores) Answering to a Description in Heading 2844 Or 2845 Are to Be Classified in Those Headings and in No Other Heading of the Tariff Schedule
)&f1y3X SECTION VI PRODUCTS OF THE CHEMICAL OR ALLIED INDUSTRIES VI-1 Notes 1. (a) Goods (other than radioactive ores) answering to a description in heading 2844 or 2845 are to be classified in those headings and in no other heading of the tariff schedule. (b) Subject to paragraph (a) above, goods answering to a description in heading 2843 or 2846 are to be classified in those headings and in no other heading of this section. 2. Subject to note 1 above, goods classifiable in heading 3004, 3005, 3006, 3212, 3303, 3304, 3305, 3306, 3307, 3506, 3707 or 3808 by reason of being put up in measured doses or for retail sale are to be classified in those headings and in no other heading of the tariff schedule. 3. Goods put up in sets consisting of two or more separate constituents, some or all of which fall in this section and are intended to be mixed together to obtain a product of section VI or VII, are to be classified in the heading appropriate to that product, provided that the constituents are: (a) Having regard to the manner in which they are put up, clearly identifiable as being intended to be used together without first being repacked; (b) Entered together; and (c) Identifiable, whether by their nature or by the relative proportions in which they are present, as being complementary one to another. Additional U.S. Notes 1. In determining the amount of duty applicable to a solution of a single compound in water subject to duty in this section at a specific rate, an allowance in weight or volume, as the case may be, shall be made for the water in excess of any water of crystallization which may be present in the undissolved compound. -
Minerals, Critical Minerals
MINERALS, CRITICAL MINERALS, AND THE U.S. ECONOMY Prepublication Version THIS PREPUBLICATION VERSION OF MINERALS, CRITICAL MINERALS, AND THE U.S. ECONOMY has been provided to the public to facilitate timely access to the committee’s findings. Although the substance of the report is final, editorial changes may be made throughout the text, and citations will be checked prior to publication. The final report will be available through the National Academies Press in the December/January timeframe. MINERALS, CRITICAL MINERALS, AND THE U.S. ECONOMY Committee on Critical Mineral Impacts on the U.S. Economy Committee on Earth Resources Board on Earth Sciences and Resources Division on Earth and Life Studies THE NATIONAL ACADEMIES PRESS Washington, D.C. www.nap.edu Prepublication Version – Subject to Further Editorial Revision THE NATIONAL ACADEMIES PRESS • 500 Fifth Street, N.W. • Washington, DC 20001 NOTICE: The project that is the subject of this report was approved by the Governing Board of the National Research Council, whose members are drawn from the councils of the National Academy of Sciences, the National Academy of Engineering, and the Institute of Medicine. The members of the committee responsible for the report were chosen for their special competences and with regard for appropriate balance. This study was supported by the Department of the Interior / U.S. Geological Survey, under Award No. 06HQGR0204, and by the National Mining Association. The opinions, findings, and conclusions or recommendations contained in this document are those of the authors and do not necessarily reflect the views of the organizations or agencies that provided support for the project. -
Tribochemistry of Phosphorus Additives: Experiments and First-Principles Calculations
RSC Advances View Article Online PAPER View Journal | View Issue Tribochemistry of phosphorus additives: experiments and first-principles calculations† Cite this: RSC Adv.,2015,5,49270 M. I. De Barros-Bouchet,*a M. C. Righi,*b D. Philippon,a S. Mambingo-Doumbe,c T. Le-Mogne,a J. M. Martina and A. Bouffetc Organophosphorus compounds are common additives included in liquid lubricants for many applications, in particular automotive applications. Typically, organic phosphites function as friction-modifiers whereas phosphates as anti-wear additives. While the antiwear action of phosphates is now well understood, the mechanism by which phosphites reduce friction is still not clear. Here we study the tribochemistry of both phosphites and phosphates using gas phase lubrication (GPL) and elucidate the microscopic mechanisms that lead to the better frictional properties of phosphites. In particular, by in situ spectroscopic analysis we show that the friction reduction is connected to the presence of iron phosphide, which is formed by tribochemical reactions involving phosphites. The functionality of elemental phosphorus in reducing the friction of iron-based interfaces is elucidated by first principle Received 13th January 2015 calculations. In particular, we show that the work of separation and shear strength of iron dramatically Accepted 21st May 2015 decrease by increasing the phosphorus concentration at the interface. These results suggest that the DOI: 10.1039/c5ra00721f functionality of phosphites as friction modifiers may be related to the amount of elemental phosphorus www.rsc.org/advances that they can release at the tribological interface. I. Introduction a previous publication,19 Philippon et al. evidenced clearly the formation of iron phosphide species from trimethyl-phosphite Organophosphorus compounds are important extreme pres- (TMPi) molecules and they detailed the reaction mechanism of sure (EP) and anti-wear (AW) additives used in different TMPi on an iron surface. -
Hughes, Matt (2014) Silica Supported Transition Metal Phosphides- Alternative Materials for the Water-Gas Shift Reaction
Hughes, Matt (2014) Silica supported transition metal phosphides- Alternative materials for the water-gas shift reaction. PhD thesis. https://theses.gla.ac.uk/5548/ Copyright and moral rights for this work are retained by the author A copy can be downloaded for personal non-commercial research or study, without prior permission or charge This work cannot be reproduced or quoted extensively from without first obtaining permission in writing from the author The content must not be changed in any way or sold commercially in any format or medium without the formal permission of the author When referring to this work, full bibliographic details including the author, title, awarding institution and date of the thesis must be given Enlighten: Theses https://theses.gla.ac.uk/ [email protected] Silica supported transition metal phosphides- Alternative materials for the water-gas shift reaction Matt Hughes School of Chemistry University of Glasgow Thesis presented for fulfilment of the degree Doctor of philosophy June 2014 Abstract Transition metal phosphides remain relatively unexplored as water-gas shift catalysts; however the little that has been done has produced promising results in terms of performance due to the presence of oxygen rich phases. They can be produced through a number of approaches, the most common being reduction of the phosphate precursor using hydrogen. Bimetallic phosphides have also generated interest recently, e.g. with the addition of cerium there are improvements to the phosphides‟ activity and with the addition of palladium a decrease in reduction temperature is evident in the precursor material. Nickel phosphide and a range of bimetallic derivatives on a silica support were investigated for their activity in both high and low temperature water-gas shift reactions. -
(CDR) by CASRN Or Accession Number
List of Chemicals Reported for the 2012 Chemical Data Reporting (CDR) by CASRN or Accession Number For the 2012 CDR, 7,674 unique chemicals were reported by manufacturers (including importers). Chemicals are listed by CAS Registry Number (for non-confidential chemicals) or by TSCA Accession Number (for chemicals listed on the confidential portion of the TSCA Inventory). CASRN or CASRN or ACCESSION ACCESSION NUMBER CA INDEX NAME or GENERIC NAME NUMBER CA INDEX NAME or GENERIC NAME 100016 Benzenamine, 4-nitro- 10042769 Nitric acid, strontium salt (2:1) 10006287 Silicic acid (H2SiO3), potassium salt (1:2) 10043013 Sulfuric acid, aluminum salt (3:2) 1000824 Urea, N-(hydroxymethyl)- 10043115 Boron nitride (BN) 100107 Benzaldehyde, 4-(dimethylamino)- 10043353 Boric acid (H3BO3) 1001354728 4-Octanol, 3-amino- 10043524 Calcium chloride (CaCl2) 100174 Benzene, 1-methoxy-4-nitro- 100436 Pyridine, 4-ethenyl- 10017568 Ethanol, 2,2',2''-nitrilotris-, phosphate (1:?) 10043842 Phosphinic acid, manganese(2+) salt (2:1) 2,7-Anthracenedisulfonic acid, 9,10-dihydro- 100447 Benzene, (chloromethyl)- 10017591 9,10-dioxo-, sodium salt (1:?) 10045951 Nitric acid, neodymium(3+) salt (3:1) 100185 Benzene, 1,4-bis(1-methylethyl)- 100469 Benzenemethanamine 100209 1,4-Benzenedicarbonyl dichloride 100470 Benzonitrile 100210 1,4-Benzenedicarboxylic acid 100481 4-Pyridinecarbonitrile 10022318 Nitric acid, barium salt (2:1) 10048983 Phosphoric acid, barium salt (1:1) 9-Octadecenoic acid (9Z)-, 2-methylpropyl 10049044 Chlorine oxide (ClO2) 10024472 ester Phosphoric acid,