Crumb Infill Turf Characterization
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Research Collection
Research Collection Doctoral Thesis Some reactions in the D-ring of the steroids Author(s): Boyce, Sam Framroze Publication Date: 1958 Permanent Link: https://doi.org/10.3929/ethz-a-000089222 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 Prom. Nr. 2111 SOME REACTIONS IN THE D-RING 0! THE STEROIDS Thesis presented to The Swiss Federal Institute of Technology Zurich for the Degree of Doctor of Technical Science by SAM FRAMROZE BOYCE Indian Citizen Accepted on the recommendation of Prof. Dr. L. Ruzicka Priv. Doz. Dr. H. Heusser The Commercial Printing Press Private Ltd., Bombay 1958 TO THE MEMORY OF MY DEAR PARENTS ACKNOWLEDGEMENTS For giving me the opportunity to carry out this work, for his encouragement and keen interest during its progress, I here express my deep gratitude to Prof. L. Ruzicka. I am also indebted to Prof. L. Ruzicka and Prof. PI. A. Plattner for guidance of this work. My sincere thanks are also due to P. D. Dr. H. Heussor for his continued co-operation and helpful suggestions during the course of this work. To Prof. V. Prelog, I am obliged for the valuable discussions and critical comments. Finally, I am indebted to Prof. M. Giinthard for the infra-red spectra and to Mr. W. Manser for the micro-analysis. m CONTENTS GENERAL INTRODUCTION 1 Pabt I REARRANGEMENT OF a-HALOGENO-20-KETOSTEROIDS Theoretical Part 3 Experimental Part 10 Pabt Ha BASE CATALYSED REACTIONS WITH A16-3 jS-ACETOXY- 14,15 0-EPOXY-5-ALLOETIOCHOLENIC ACID METHYL ESTER Theoretical Part 18 Experimental Part 27 Pabt lib BASE AND ACID CATALYSED REACTIONS WITH A16-3j3- ACETOXY-14,15/3-EPOXY-20-KETO-5-ALLOPREGNENE Theoretical Part .. -
United States Patent (19) 11 Patent Number: 6,037,477 Ishii Et Al
USOO6037477A United States Patent (19) 11 Patent Number: 6,037,477 Ishii et al. (45) Date of Patent: Mar. 14, 2000 54) OXIDATION PROCESS OF ETHERS 838909 2/1996 Japan. 75 Inventors: Yasutaka Ishii, 19-21, OTHER PUBLICATIONS Besshohonmachi, Takatsuki-shi, Osaka Ishii et al., J. Org. Chem., vol. 61, pp. 4520-4526 (1996). 569-1112, Tatsuya Nakano, Himeji, Yoshino et al., J. Org. Chem., vol. 62, No. 20, pp. both of Japan 6810–6813 (Oct. 1997). Takeno et al., Aerobic Oxidation by Using N-hydroxyph 73 Assignees: Daicel Chemical Industries, Ltd.; thalimide, 67th Spring Annual Meeting of Chemical Society Yasutaka Ishii, both of Osaka, Japan of Japan, Lecture Draft II, Dec. 1994. 21 Appl. No.: 09/074,604 Primary Examiner Johann Richter ASSistant Examiner-Dominic Keating 22 Filed: May 8, 1998 Attorney, Agent, or Firm-Birch, Stewart, Kolasch & Birch, 30 Foreign Application Priority Data LLP May 13, 1997 JP Japan .................................... 9-122526 57 ABSTRACT 51) Int. Cl." .................. C07D 207/404; CO7D 207/448; An ether is oxidized with oxygen under an oxidation catalyst CO7D 487/06; CO7D 207/444 comprising an imide compound (Such as 52 U.S. Cl. .......................... 548/545; 548/548; 548/549; N-hydroxyphthalimide) or the imide compound and a 548/453 co-catalyst to produce the corresponding chain or cyclic 58 Field of Search ..................................... 548/545, 548, ester or anhydride. The co-catalyst may be a transition metal 548/549 compound. The above proceSS provides a process for oxi dizing an ether by oxygen efficiently to produce the corre 56) References Cited sponding oxide (Such as an ester, an hydride) with high conversion and Selectivity. -
Novel Approach to Introduce Alkyl Chains Into PEDOT:PSS and Its Effect on the Performance As a Flexible Electrode
applied sciences Article Novel Approach to Introduce Alkyl Chains into PEDOT:PSS and Its Effect on the Performance as a Flexible Electrode In-Seong Hwang 1, Chul-Woo Park 1, Hye-In Kang 1, Sung-yoon Joe 2, Na-Young Pak 3 and Dae-won Chung 1,* 1 Department of Polymer Engineering, College of Engineering, The University of Suwon, Hwaseong-si 18323, Korea; [email protected] (I.-S.H.); [email protected] (C.-W.P.); [email protected] (H.-I.K.) 2 Center of Advanced Materials Analysis, The University of Suwon, Hwaseong-si 18323, Korea; [email protected] 3 EverChemTech Co., Ltd., 38, Cheongwonsandan 7-gil, Mado-myeon, Hwaseong-si 18323, Korea; [email protected] * Correspondence: [email protected]; Tel.: +81-312-202-156 Abstract: We here report a synthetic route to introduce alky chains into poly (3,4-ethylenedioxythio- phene):poly (4-styrenesulfonate) (PEDOT:PSS) by the reaction with epoxyalkanes. The reaction was analyzed by FT-IR, TGA, and XPS studies, and the conductivities of derivatives were discussed as a function of the length of alkyl chains. PEDOT:PSS-C6, which is the product from a reaction with epoxyhexane, was well dispersed in methanol and transparent films from this dispersion were successfully prepared. PEDOT:PSS-C6 film showed an increase in hydrophobicity, resulting in enhanced water resistance compared to pristine PEDOT:PSS film, and a morphological study of the film exhibited clear phase separation similar to PEDOT:PSS doped by DMSO. We also observed an improvement in the conductivity and flexibility of PEDOT:PSS-C6 film compared to those of Citation: Hwang, I.-S.; Park, C.-W.; pristine PEDOT:PSS film. -
Act Global Crumb Rubber Safety Study
ACT GLOBAL CRUMB RUBBER SAFETY STUDY Prepared for Act Global By R. William Tilford, PhD. Published February 11, 2015 Act Global initiated crumb rubber testing from three independent laboratories. To validate and triangulate the results, Dr. R. William Tilford was engaged by Act Global for objective and professional oversight and review. Dr. Tilford has a doctorate in organic chemistry and fourteen years of experience as a research chemist, with a thorough understanding of how organic molecules react with each other and their environments. 1 Introduction Artificial turf has been used in sports fields since invented in 1962. Despite their many benefits, for years these fields suffered from one key drawback. The relatively thin layer of turf, normally installed over a hard durable surface such as concrete, did not provide sufficient shock absorption to accommodate the rigors of athletic competition. To address this issue, an intermediate cushioning layer of elastic material was implemented into the design in the 1990s. An ideal material with which to create this shock-absorbing interlayer was styrene butadiene rubber (SBR), which is often utilized for applications where it is necessary to protect bodies against repeated exposure to mechanical stress. The most notable example is in automobile tires which provide a constant elastic buffer between the road and automobile. Developments in recycling technologies enabled used automobile tires destined for landfills to instead be processed and repurposed as SBR crumb rubber infill. This source of SBR provides an efficient means of improving both the performance and safety of artificial turf systems. Act Global initiated a review of a crumb rubber supply used in their synthetic turf systems to examine the potential presence of any chemical species that would cause concern over its use as a raw material. -
(12) United States Patent (10) Patent No.: US 7.494,962 B2 Kinet Al
USOO74949.62B2 (12) United States Patent (10) Patent No.: US 7.494,962 B2 Kinet al. (45) Date of Patent: Feb. 24, 2009 (54) SOLVENTS CONTAINING CYCLOAKYL (56) References Cited ALKYLETHERS AND PROCESS FOR PRODUCTION OF THE ETHERS U.S. PATENT DOCUMENTS 3496,223 A * 2/1970 Mitchell et al. ............... 562/22 (75) Inventors: Idan Kin, Ottawa (CA); Genichi Ohta, Tokyo (JP); Kazuo Teraishi, Tokyo (JP); Kiyoshi Watanabe, Tokyo (JP) (Continued) (73) Assignee: Zeon Corporation, Tokyo (JP) FOREIGN PATENT DOCUMENTS (*) Notice: Subject to any disclaimer, the term of this EP 587434 A1 3, 1994 patent is extended or adjusted under 35 U.S.C. 154(b) by 349 days. (Continued) (21) Appl. No.: 10/481,340 OTHER PUBLICATIONS (22) PCT Filed: Jun. 27, 2002 Edited by Kagaku Daijiten Henshu Iinkai, “Kagaku Daijiten 9”. (86). PCT No.: PCT/UP02/06501 Kyoritsu Shuppan Co., Ltd., Aug. 25, 1962, p. 437, "Yozai'. (Continued) S371 (c)(1), (2), (4) Date: Sep. 24, 2004 Primary Examiner Gregory E Webb (74) Attorney, Agent, or Firm—Birch, Stewart, Kolasch & (87) PCT Pub. No.: WO03/002500 Birch, LLP PCT Pub. Date: Jan. 9, 2003 (57) ABSTRACT (65) Prior Publication Data The present inventions are (A) a solvent comprising at least US 2005/OO65060A1 Mar. 24, 2005 one cycloalkyl alkyl ether (1) represented by the general O O formula: R1-O R2 (wherein R1 is cyclopentyl or the like: (30) Foreign Application Priority Data and R2 is C1-10 alkyl or the like); (B) a method of prepara Jun. 28, 2001 (JP) ............................. 2001-196766 tions the ethers (1) characterized by reacting an alicyclic Oct. -
Evaluation of the Toxicity on Lung Cells of By-Products Present in Naphthalene Secondary Organic Aerosols
life Article Evaluation of the Toxicity on Lung Cells of By-Products Present in Naphthalene Secondary Organic Aerosols Yuri Lima de Albuquerque 1 , Emmanuelle Berger 1, Sophie Tomaz 2, Christian George 2 and Alain Géloën 1,* 1 UMR Ecologie Microbienne, Université Claude Bernard Lyon 1, 69622 Villeurbanne, France; [email protected] (Y.L.d.A.); [email protected] (E.B.) 2 Univ Lyon, Université Claude Bernard Lyon 1, 69100 Villeurbanne, France; [email protected] (S.T.); [email protected] (C.G.) * Correspondence: [email protected] Abstract: In 2018, seven million people died prematurely due to exposure to pollution. Polycyclic aromatic hydrocarbons (PAHs) are a significant source of secondary organic aerosol (SOA) in urban areas. We investigated the toxic effects of by-products of naphthalene SOA on lung cells. These by- products were 1,4-naphthoquinone (1,4-NQ), 2-hydroxy-1,4-naphthoquinone (2-OH-NQ), phthalic acid (PA) and phthaldialdehyde (OPA). Two different assessment methodologies were used to monitor the toxic effects: real-time cell analysis (RTCA) and the Holomonitor, a quantitative phase contrast microscope. The chemicals were tested in concentrations of 12.5 to 100 µM for 1,4-NQ and 1 to 10 mM for 2-OH-NQ, PA and OPA. We found that 1,4-NQ is toxic to cells from 25 to 100 µM (EC50: 38.7 µM ± 5.2); 2-OH-NQ is toxic from 1 to 10mM (EC50: 5.3 mM ± 0.6); PA is toxic from 5 to 10 mM (EC50: 5.2 mM ± 0.3) and OPA is toxic from 2.5 to 10 mM (EC50: 4.2 mM ± 0.5). -
Syntheses and Eliminations of Cyclopentyl Derivatives David John Rausch Iowa State University
Iowa State University Capstones, Theses and Retrospective Theses and Dissertations Dissertations 1966 Syntheses and eliminations of cyclopentyl derivatives David John Rausch Iowa State University Follow this and additional works at: https://lib.dr.iastate.edu/rtd Part of the Organic Chemistry Commons Recommended Citation Rausch, David John, "Syntheses and eliminations of cyclopentyl derivatives " (1966). Retrospective Theses and Dissertations. 2875. https://lib.dr.iastate.edu/rtd/2875 This Dissertation is brought to you for free and open access by the Iowa State University Capstones, Theses and Dissertations at Iowa State University Digital Repository. It has been accepted for inclusion in Retrospective Theses and Dissertations by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. This dissertation has been microfilmed exactly as received 66—6996 RAUSCH, David John, 1940- SYNTHESES AND ELIMINATIONS OF CYCLOPENTYL DERIVATIVES. Iowa State University of Science and Technology Ph.D., 1966 Chemistry, organic University Microfilms, Inc., Ann Arbor, Michigan SYNTHESES AND ELIMINATIONS OF CYCLOPENTYL DERIVATIVES by David John Rausch A Dissertation Submitted to the Graduate Faculty in Partial Fulfillment of The Requirements for the Degree of DOCTOR OF PHILOSOPHY Major Subject: Organic Chemistry Approved : Signature was redacted for privacy. Signature was redacted for privacy. Head of Major Department Signature was redacted for privacy. Iowa State University Of Science and Technology Ames, Iowa 1966 ii TABLE OF CONTENTS VITA INTRODUCTION HISTORICAL Conformation of Cyclopentanes Elimination Reactions RESULTS AND DISCUSSION Synthetic Elimination Reactions EXPERIMENTAL Preparation and Purification of Materials Procedures and Data for Beta Elimination Reactions SUMMARY LITERATURE CITED ACKNOWLEDGEMENTS iii VITA The author was born in Aurora, Illinois, on October 24, 1940, to Mr. -
Of Grignard Reagent Formation. the Surface Nature of the Reaction
286 Ace. Chem. Res. 1990,23, 286-293 Mechanism of Grignard Reagent Formation. The Surface Nature of the Reaction H. M. WALBORSKY Dittmer Laboratory of Chemistry, Florida State University, Tallahassee, Florida 32306 Received February 23, 1990 (Revised Manuscript Received May 7, 1990) The reaction of organic halides (Br, C1, I) with mag- Scheme I nesium metal to yield what is referred to today as a Kharasch-Reinmuth Mechanism for Grignard Reagent Grignard reagent has been known since the turn of the Formation century,' The name derives from its discoverer, Nobel (1)(Mg0)AMg*)2y + RX 4 [(M~'~(MQ')~~-,('MQX)+ R.] + laureate Victor Grignard. How this reagent is formed, (Mgo)x-2(MQ')2~MgX)(MgR) that is, how a magnesium atom is inserted into a car- bon-halogen bond, is the subject of this Account. ('4 (Ms0),-*(M9')2~MgX)(MgR) + + (Mg0)x-dMg*)2y+2 + 2RMgX RX + Mg - RMgX Kharasch and Reinmuth,, persuaded by the work of late under the same conditions gave Itl = 6.2 X s-l. Another system that meets the above criterion is the Gomberg and Bachmad as well as by product analyses of many Grignard formation reactions that existed in vinyl system. The lack of reactivity of vinyl halides toward SN1reactions is well-known and is exemplified the literature prior to 1954,speculated that the reaction involved radicals and that the radical reactions might by the low solvolysis rate of 2-propenyl triflate5 in 80% involve "surface adherent radicals, at least in part". The ethanol at 25 OC, kl being 9.8 X s-l. -
Methoxyethane, Physical Properties, Safety, MSDS, Enthalpy, Gas Liquid
(c) Bürkle GmbH 2021 Important Important information The tables “Chemical resistance of plastics”, “Plastics and their properties” and “Viscosity of liquids" as well as the information about chemical resistance given in the particular product descriptions have been drawn up based on information provided by various raw material manufacturers. These values are based solely on laboratory tests with raw materials. Plastic components produced from these raw materials are frequently subject to influences that cannot be recognized in laboratory tests (temperature, pressure, material stress, effects of chemicals, construction features, etc.). For this reason the values given are only to be regarded as being guidelines. In critical cases it is essential that a test is carried out first. No legal claims can be derived from this information; nor do we accept any liability for it. A knowledge of the chemical and mechanical resistance alone is not sufficient for the evaluation of the usability of a product. For example, the regulations concerning flammable liquids (explosion prevention) must also be taken into consideration. Copyright This table has been published and updated by Bürkle GmbH, D-79415 Bad Bellingen as a work of reference. This Copyright clause must not be removed. The table may be freely passed on and copied, provided that the information about the publisher is retained. Extensions, additions and translations If your own experiences with materials and media could be used to extend this table then we would be pleased to receive any additional information. Please send an E-Mail to [email protected]. We would also like to receive translations into other languages. -
Preparative Method of Novel Phthalocyanines from 3- Nitro
Available online a t www.derpharmachemica.com Scholars Research Library Der Pharma Chemica, 2012, 4(4):1397-1403 (http://derpharmachemica.com/archive.html) ISSN 0975-413X CODEN (USA): PCHHAX Preparative Method of Novel Phthalocyanines from 3- Nitro Phthalic Anhydride, Cobalt salt and Urea with Chloromethylpolyestyrene as a Heterogenous, Reusable and Efficient Catalyst Mohammad Ali Zolfigol 2, Ali Reza Pourali 1, Sami Sajjadifar 3,4 and Shohreh Farahmand 1,2,4 1Faculty of Chemistry, Bu-Ali Sina University, Hamedan, P.O. Box 6517838683, Iran 2School of Chemistry, Damghan University, Damghan, Iran 3Department of Chemistry, Faculty of Science, Ilam University, P.O. Box 69315516, Ilam, Iran 4Department of Chemistry, Payame Noor University, Tehran, P.O. Box 19395-4697, Iran _____________________________________________________________________________________________ ABSTRACT 3-Nitrophthalic anhydride was reacted with urea and cobalt salt in nitrobenzene under N 2 at 185°C and cobalt- tetraanitrophthalocyanine (CoTNP) was produced. Cobalt-tetraaminophthalocyanine (CoTAP) was produced by reduction of CoTNP caused by Sodium borohydride under N 2(g). CoTAP and chloromethylpolystyrene was refluxed in nitrobenzene or DMF at 180 oC for 12h. The mixture was cooled down to reach the room temperature and then solvent removed and the resulting precipitate was washed with water to remove excess CoTAP, and dried it to get a light green solid (CoTAP-linked-polymer). Kaywords Phthalocyanines, Cobaltetraminophthalocyanine, CoTAP ,Phthalocyanines linked polymer. _____________________________________________________________________________________________ INTRODUCTION Phthalocyanines are of interest not only as model compounds for the biologically important porphyrins but also because the intensely colored metal complexes are of commercial importance as dyes and pigments [1], the copper derivatives being an important blue pigment [2]. -
(12) United States Patent (10) Patent No.: US 9.285,681 B2 Hsieh (45) Date of Patent: Mar
USOO9285681 B2 (12) United States Patent (10) Patent No.: US 9.285,681 B2 Hsieh (45) Date of Patent: Mar. 15, 2016 (54) PHOTOSENSITIVE RESIN COMPOSITION WO WO-2009,133843 A1 * 11, 2009 AND USES THEREOF WO WO 2012, 176694 A1 * 12/2012 WO WO 2013/O12035 A1 * 1, 2013 (71) Applicant: CHI MEI CORPORATION, Tainan OTHER PUBLICATIONS (TW) "Aliphatic compounds” IUPAC Compendium of Chemical Terminol ogy one page from PAC, 1995, 67. 1307 (GLossary of class names of (72) Inventor: Li-Ting Hsieh, Tainan (TW) organic compounds and reactivity intermediates base on structure (IUPAC Recommendations 1995)) onpage 1313, obtained online (73) Assignee: CHI MEI CORPORATION, Tainan from IUPAC gold book.* (TW) CAS Registry No. 215806-04-5, one page obtained from SciFinder database on Mar. 31, 2015 idenying O 1382 as a trade name of this (*) Notice: Subject to any disclaimer, the term of this compound, American Chemical Society copyright. patent is extended or adjusted under 35 English translation of WO 2009 133843 A1 published Nov. 5, 2009, Translation from ProQuest Dialog online done Mar. 30, 2015, 75 U.S.C. 154(b) by 0 days. pages. SciFinder database entry for WO2009 133843 and the list of sub (21) Appl. No.: 14/281,715 stances identified therewith down loaged Apr. 1, 2013, 10 pages.* Derwent-ACC-No. 2009-R51511, English abstract of WO (22) Filed: May 19, 2014 2009 133843 A1 publication dated Nov. 5, 2009 (in same family as TW 201005019 A cited by applicants), Derwent Week: 201265, 6 (65) Prior Publication Data pages down loaded Apr. 1, 2015.* CAS Registry No. -
University Microfilms, Inc., Ann Arbor, Michigan ADRENOCORTICAL STEROID PROFILE IN
This dissertation has been Mic 61-2820 microfilmed exactly as received BESCH, Paige Keith. ADRENOCORTICAL STEROID PROFILE IN THE HYPERTENSIVE DOG. The Ohio State University, Ph.D., 1961 Chemistry, biological University Microfilms, Inc., Ann Arbor, Michigan ADRENOCORTICAL STEROID PROFILE IN THE HYPERTENSIVE DOG DISSERTATION Presented in Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy in the Graduate School of the Ohio State University By Paige Keith Besch, B. S., M. S. The Ohio State University 1961 Approved by Katharine A. Brownell Department of Physiology DEDICATION This work is dedicated to my wife, Dr. Norma F. Besch. After having completed her graduate training, she was once again subjected to almost social isolation by the number of hours I spent away from home. It is with sincerest appreciation for her continual encouragement that I dedi cate this to her. ACKNOWLEDGMENTS I wish to acknowledge the assistance and encourage ment of my Professor, Doctor Katharine A. Brownell. Equally important to the development of this project are the experience and information obtained through the association with Doctor Frank A. Hartman, who over the years has, along with Doctor Brownell, devoted his life to the development of many of the techniques used in this study. It is also with extreme sincerity that I wish to ac knowledge the assistance of Mr. David J. Watson. He has never complained when asked to work long hours at night or weekends. Our association has been a fruitful one. I also wish to acknowledge the encouragement of my former Professor, employer and good friend, Doctor Joseph W.