Teacher Resources Overview the Father of Chemical Warfare
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Stainless Steels in Ammonia Production
Stainless Steels in Ammonia Production Committee of Stainless Steel Producers American Iron and Steel Institute Washington, D.C. CONTENTS INTRODUCTION ...................... 4 PROCESS DESCRIPTION ....... 5 CORROSIVES IN AMMONIA PROCESSES .......... 5 CONSIDERATIONS FOR SELECTING STAINLESS STEELS .................................... 6 Desulfurization of Natural Gas ................. 6 Catalytic Steam Reforming of Natural Gas ................. 6 Carbon Monoxide Shift ......... 8 Removal of Carbon Dioxide . 10 Methanation .......................... 11 Synthesis of Ammonia ......... 11 Turbine-Driven Centrifugal Compression Trains ........ 14 STAINLESS STEELS ................ 15 Metallurgical Structure ......... 16 High-Temperature Mechanical Properties ..... 16 Thermal Conductivity ........... 20 Oxidation Resistance ........... 21 Sulfidation Resistance .......... 22 REFERENCES .......................... 22 The material presented in this booklet has been prepared for the general information of the reader. It should not be used without first securing competent advice with respect to its suitability for any given application. While the material is believed to be technically correct, neither the Committee of Stainless Steel Pro- ducers nor the companies represented on the The Committee of Stainless Steel Producers acknowledges the help Committee warrant its suitability for any gen- by Gregory Kobrin, Senior Consultant, Materials Engineering, E.I. eral or particular use. DuPont de Nemours & Company in assembling data for this booklet. single-train plants came increasing demands on materials of construc- INTRODUCTION tion. The process for making am- monia is considered to be only Approximately 12 elements are es- moderately corrosive, so considera- sential to plant growth. Of these, nit- ble use is made of carbon and low- rogen is the main nutrient and is re- alloy steels for vessels and piping. quired in much larger amounts than However, numerous applications any other element. -
2020 Stainless Steels in Ammonia Production
STAINLESS STEELS IN AMMONIA PRODUCTION A DESIGNERS’ HANDBOOK SERIES NO 9013 Produced by Distributed by AMERICAN IRON NICKEL AND STEEL INSTITUTE INSTITUTE STAINLESS STEELS IN AMMONIA PRODUCTION A DESIGNERS’ HANDBOOK SERIES NO 9013 Originally, this handbook was published in 1978 by the Committee of Stainless Steel Producers, American Iron and Steel Institute. The Nickel Institute republished the handbook in 2020. Despite the age of this publication the information herein is considered to be generally valid. Material presented in the handbook has been prepared for the general information of the reader and should not be used or relied on for specific applications without first securing competent advice. The Nickel Institute, the American Iron and Steel Institute, their members, staff and consultants do not represent or warrant its suitability for any general or specific use and assume no liability or responsibility of any kind in connection with the information herein. Nickel Institute [email protected] www.nickelinstitute.org CONTENTS INTRODUCTION ............................ 4 PROCESS DESCRIPTION ............ 5 CORROSIVES IN AMMONIA PROCESSES ............... 5 CONSIDERATIONS FOR SELECTING STAINLESS STEELS .......................................... 6 Desulfurization of Natural Gas ....................... 6 Catalytic Steam Reforming of Natural Gas ....................... 6 Carbon Monoxide Shift .............. 8 Removal of Carbon Dioxide . 10 Methanation ............................. 11 Synthesis of Ammonia ............. 11 -
The Haber Process
Making ammonia - the Haber process Background During the last century, the populations of Europe and America rose very rapidly. More food and more crops were needed to feed more and more people. So farmers began to use nitrogen compounds as fertilisers. The main source of nitrogen compounds for fertilisers was sodium nitrate from Chile. By 1900 supplies of this were running out. Another supply of nitrogen had to be found or many people would starve. The obvious source of nitrogen was the air (about 78% of the air is nitrogen). Unfortunately, nitrogen is not very reactive. This made it difficult to convert it into ammonium salts and nitrates for use as fertilisers. A German chemist called Fritz Haber solved the problem. In 1904, Haber began studying the reaction between nitrogen and hydrogen. By 1908 he had found the conditions needed to make ammonia (NH3). Eventually, the Haber process became the most important method of manufacturing ammonia. 1. Why did farmers start to use nitrogen compounds as fertilisers? 2. What problem did farmers face in 1900? 3. How long did it take Fritz Haber to work out the conditions needed to make nitrogen and hydrogen react together? 4. What does the Haber process make? 5. Haber was an apprentice plumber before studying to become a chemist. How was Haber’s background useful to him as a chemist? The Haber process The raw materials for the Haber process are Natural gas, air and water. In the first stage, Natural gas (which is mostly methane) is reacted with steam to produce carbon dioxide and hydrogen. -
THEODORE WILLIAM RICHARDS January 31, 1868-April 2, 1928
NATIONAL ACADEMY OF SCIENCES T H E O D O R E W I L L I A M R ICHARDS 1868—1928 A Biographical Memoir by JAMES BRYANT CONANT Any opinions expressed in this memoir are those of the author(s) and do not necessarily reflect the views of the National Academy of Sciences. Biographical Memoir COPYRIGHT 1974 NATIONAL ACADEMY OF SCIENCES WASHINGTON D.C. THEODORE WILLIAM RICHARDS January 31, 1868-April 2, 1928 BY JAMES BRYANT CONANT HEODORE WILLIAM RICHARDS was a precocious son of distin- Tguished parents. He was born in Philadelphia on January 31, 1868, the third son and fifth child of William Trost Richards and Anna Matlack Richards, who had been married on June 30, 1856. As strict members of the Society of Friends, the Matlack family looked askance at a young man who earned his living painting pictures. Anna was "read out of meeting." The Quaker marriage ceremony took place in the house of a friend. The first months of the honeymoon were devoted to the com- position and illustration of a manuscript volume of poems for the lady who had first brought the young couple together. A mutual interest in Browning and Tennyson had started an acquaintanceship which rapidly became a romance. An old friend and fellow artist of Philadelphia reminiscing long after W. T. Richards had established his reputation as a landscape painter said, "He amazed me by getting married and resigning his position as designer [in a local firm manufacturing gas fixtures] in order to devote himself entirely to his art. -
From Physical Chemistry to Chemical Physics, 1913-1941
International Workshop on the History of Chemistry 2015 Tokyo From Physical Chemistry to Chemical Physics, 1913-1941 Jeremiah James Ludwig-Maximillian University, Munich, Germany There has never been one unique name for the intersection of chemistry and physics. Nor has it ever been defined by a single, stable set of methods. Nevertheless, it is possible and arguably rewarding to distinguish changes in the constellation of terms and techniques that have defined the intersection over the years. I will speak today about one such change, the advent and ascendancy of chemical physics in the interwar period. When the young Friedrich Wilhelm Ostwald first began to formulate his campaign for “physical chemistry” in 1877, he used the term almost interchangeably with two others, “general chemistry” and “theoretical chemistry.” According to his vision of what would soon become a new chemical discipline, physical chemistry would investigate and formulate the general principles that underlie all chemical reactions and phenomena. The primary strategy that he and his allies used to generate these principles was to formulate mathematical “laws” or “rules” generalizing the results of numerous experiments, often performed using measuring apparatus borrowed from physics. Their main fields of inquiry were thermochemistry and solution theory, and they avoided and often openly maligned speculations regarding structures or mechanisms that might underlie the macroscopic regularities embodied in their laws.1 In the first decades of the 20th-century, the modern atomic theory was firmly established, and with only a slight delay, the methods of 19th-century physical chemistry lost a considerable proportion of their audience. Theories relying upon atomistic thinking began to reshape the disciplinary intersections of chemistry and physics, and by the end of the 1930s, cutting-edge research into the general principles of chemistry looked quite different than it had at the turn of the century. -
Fritz Arndt and His Chemistry Books in the Turkish Language
42 Bull. Hist. Chem., VOLUME 28, Number 1 (2003) FRITZ ARNDT AND HIS CHEMISTRY BOOKS IN THE TURKISH LANGUAGE Lâle Aka Burk, Smith College Fritz Georg Arndt (1885-1969) possibly is best recog- his “other great love, and Brahms unquestionably his nized for his contributions to synthetic methodology. favorite composer (5).” The Arndt-Eistert synthesis, a well-known reaction in After graduating from the Matthias-Claudius Gym- organic chemistry included in many textbooks has been nasium in Wansbek in greater Hamburg, Arndt began used over the years by numerous chemists to prepare his university education in 1903 at the University of carboxylic acids from their lower homologues (1). Per- Geneva, where he studied chemistry and French. Fol- haps less well recognized is Arndt’s pioneering work in lowing the practice at the time of attending several in- the development of resonance theory (2). Arndt also stitutions, he went from Geneva to Freiburg, where he contributed greatly to chemistry in Turkey, where he studied with Ludwig Gattermann and completed his played a leadership role in the modernization of the sci- doctoral examinations. He spent a semester in Berlin ence (3). A detailed commemorative article by W. Walter attending lectures by Emil Fischer and Walther Nernst, and B. Eistert on Arndt’s life and works was published then returned to Freiburg and worked with Johann in German in 1975 (4). Other sources in English on Howitz and received his doctorate, summa cum laude, Fritz Arndt and his contributions to chemistry, specifi- in 1908. Arndt remained for a time in Freiburg as a cally discussions of his work in Turkey, are limited. -
Book Review Tuxedo Park, by Jennet Conant (Simon & Schuster, 2002), 330 Pp., ISBN 0684872870, $26.00
Book Review Tuxedo Park, by Jennet Conant (Simon & Schuster, 2002), 330 pp., ISBN 0684872870, $26.00 Reviewed by Jane A. Roman Department of Chemistry, Regis College, Weston, MA In the early chapters of this book, Jennet Conant, granddaughter of James Conant former President of Harvard and esteemed scientist, describes brilliantly the life of Alfred Lee Loomis, philanthropist, scientist and Wall Street tycoon. Prompted by the mysterious circumstances surrounding the suicide of her granduncle, William Richards, son of Nobel laureate Theodore William Richards, Jennet using her granduncles’ notes and letters, wrote this biography, which is a small but significant chapter in the history of American science. Her accounts of Loomis depict his relationships with many Nobel Laureates in science and also detail an illicit love affair Loomis had with Manette Hobart, the wife of Garrett A. Hobart III, his protégé and secretary at Tuxedo Park. The setting for most of the book is the region of Tuxedo Park in Orange County, New York where Loomis established a research laboratory, funded solely by his personal fortune. Very important discoveries in radar detection, atomic fission, and other wartime inventions that led the allies to victory over the Germans were made there. Because the circumstances surrounding her granduncle’s death and the hush-up carried out by her family were indicative of the gentry at that time, Ms. Conant was prompted to reveal in her novel the relationship her granduncle had with Loomis in Tuxedo Park. From his papers and letters, she describes how Richards and his friend at Princeton, George Kistiakowsky, came to work at Tuxedo Park, often referring to it as a private scientific playground in the Ramapo Mountains. -
Nitrogenase; Nitrogen Fixation Vs Haber-Bosch Process
Nitrogenase; Nitrogen Fixation vs Haber-Bosch Process Anna Balinski, Jacob Watson Texas A&M University, College Station, TX 77843 Abstract Comparison of Processes Haber-Bosch Process Overview:The Nitrogen Cycle is a chemical cycle which recycles nitrogen into usable forms, such as ammonium, nitrates, and nitrites. Nitrogen and nitrogen compounds are important Haber-Bosch Reaction because they make up our atmosphere as well as our earthly environments. Nitrogen can be recycled into ammonium naturally via nitrogen fixing bacteria, or synthetically using the + - Discovered by Fritz Haber, process scaled up by Haber-Bosch process. Nitrogen fixation in bacteria follows the reaction N2 + 8 H + 8 e 2 • Carl Bosch NH3 + H2 and is powered by the hydrolysis of 16 ATP equivalents. The Haber-Bosch process Response to Germany’s need for ammonia for follows the reaction scheme of N2 + 3 H2 2 NH3 and is powered by using high pressures, • temperatures, and catalysts. Using the Haber-Bosch process an optimum yield of 97% explosive during WWI ammonium can be obtained. These reactions both use diatomic nitrogen as well as Nitrogen Fixation Reaction • Prolonged WWI when Germany was able to hydrogen, but differ in their final products as bacterial nitrogen fixation releases hydrogen produce fertilizer and explosives gas as a byproduct. Bacteria in the soil use nitrogen to create energy to grow and reproduce Fritz Haber Carl Bosch as well as to introduce nitrogen for use by other species. The Haber-Bosch process produces ammonium which can be used for a range of activities such as the production of fertilizers, or even explosives. -
Open-Circuit Voltage Comes from Non-Equilibrium Thermodynamics
J. Non-Equilib. Thermodyn. 2021; 46(1): 91–108 Research Article Diego del Olmo*, Michal Pavelka, and Juraj Kosek Open-Circuit Voltage Comes from Non-Equilibrium Thermodynamics https://doi.org/10.1515/jnet-2020-0070 Received June 25, 2020; revised August 14, 2020; accepted September 22, 2020 Abstract: Originally derived by Walther Nernst more than a century ago, the Nernst equation for the open- circuit voltage is a cornerstone in the analysis of electrochemical systems. Unfortunately, the assumptions behind its derivation are often overlooked in the literature, leading to incorrect forms of the equation when applied to complex systems (for example, those with ion-exchange membranes or involving mixed poten- tials). Such faws can be avoided by applying a correct thermodynamic derivation independently of the form in which the electrochemical reactions are written. The proper derivation of the Nernst equation becomes important, for instance, in modeling of vanadium redox fow batteries or zinc-air batteries. The rigorous path towards the Nernst equation derivation starts in non-equilibrium thermodynamics. Keywords: redox fow batteries, open-circuit voltage, non-equilibrium thermodynamics, Zn-air battery 1 Introduction “Thermodynamics is a funny subject. The frst time you go through it, you don’t understand it at all. The second time you go through it, you think you understand it, except for one or two points. The third time you go through it, you know you don’t understand it, but by that time you are so used to the subject, it doesn’t bother you anymore.” (Arnold Sommerfeld) The open-circuit voltage (OCV) is generally defned as the voltage between the terminals of an electrochem- ical cell when no current fows through the cell. -
Pilgrimage Through the History of German Natural Science, University City Göttingen II Kaoru Harada Email:[email protected]
Pilgrimage through the History of German Natural Science, University City Göttingen II Kaoru Harada Email:[email protected] Scientists in the same generation as F. Wohlelr (Fig. 89-96). We have seen several pictures of scientists worked in the University of Göttingen. Additional portraits of chemist outside the University have also collected in the Museum. Some of the chemists are Jöns Jacob Berzelius (1779-1848, Fig. 89), Eilhardt Mitscherlich (1794-1863), (Fig. 90), Justus Leibig (1803-1873, Fig. 91), Michel Eugene Chevreul (1786-1889), (Fig. 92, 93), F. W. Sertürner (1783-1841), (Fig. 94) and Ernst Otto Beckmann (1853-1923), (Fig. 95, 96). J. J. Berzelius (Fig. 89) was a famous Swedish chemist. He contributed much to the development of modern chemistry on the following subjects : [Discovery of elements, nomenclature of Fig. 90 Photograph of Eilhardt Mitscherlich (1794-1863). elements, elemental signs, atomic weights of elements, allotrope, J. Liebig (Fig. 91) was a great German chemist, and his young concept of catalyst and isomer]. The accurate measurements of day’s life was dynamic. He was a self taught chemist and he atomic weight based on the R. Boyl’s atomic theory were his studied at Paris for two years and he polished up his chemistry. great contribution to chemistry in the first half of the 19th century. He made human relations with L. J. Gay-Lussac (1778-1850) and A. Humboldt (1769-1859) because of J. Libig’s (1803-1873) interest on Arsenal. He got a position at Giessen University in the age 21 by the recommendation of A. -