Cresols Health and Safety Guide
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Degradation of Phenol and P-Cresol in Reactors Water Science and Technology
m33 18/9/00 6:35 pm Page 237 Degradation of phenol and p-cresol in reactors Water Science and Technology Herbert H. P. Fang* and Gong-Ming Zhou** * Environmental Engineering Research Centre, Department of Civil Engineering, The University of Hong Kong, Pokfulam Road, Hong Kong SAR, China ** National Engineering Research Center for Urban Pollution Control, Tongji University, Shanghai, China Abstract The effects of hydraulic retention time (HRT) and phenol concentration on the degradation of phenol and p-cresol in wastewater were investigated in two respective UASB (upflow anaerobic sludge blanket) reactors with effluent recirculation at 37 oC for over 440 days. After acclimation, nearly all the Vol 42 Nos 5–6pp 237–244 phenol and p-cresol at moderate concentrations could be degraded without carbohydrate as a co-substrate. Treating a wastewater containing 800 mg/l of phenol and 300 mg/l of p-cresol at HRT ranging 2-12 hours, the first reactor consistently removed 95% of phenol, 65% of p-cresol and 85% of COD at 8-12 hours of HRT; the efficiency, however, decreased at lower HRT. Treating wastewater containing a constant p-cresol concentration of 400 mg/l at 24 hours of HRT, the second reactor was able to remove 75-80% of COD when the phenol was 1200 and 1500 mg/l; the removal efficiency decreased as phenol concentration further increased. High levels of residual phenol and p-cresol in the effluent suppressed the activity of biogranules. The suppression of bioactivity was not permanent. Biomass was able to regain its activity fully after lowering the phenolic concentrations in the wastewater. -
Category Assessment Document For
U.S. EPA HPV Challenge Program Category Assessment Document for Acids and Caustics from Petroleum Refining Category Tar acids, cresylic, sodium salts, caustic solutions (CAS No. 68815-21-4); Neutralizing agents (petroleum), spent sodium hydroxide (CAS No. 064742- 40-1); Phenols, sodium salts, mixed with sulfur comp; gasoline alky scrubber residues (CAS No. 68988-99-8); Sludges (petroleum), acid (CAS No. 064742-24-1). Submitted by: American Petroleum Institute Petroleum HPV Testing Group American Petroleum Institute 1220 L Street NW Washington, DC 20005 Consortium Registration # 1100997 July 6, 2009 Acids and Caustics From Petroleum Refining Consortium Registration # 1100997 CATEGORY ASSESSMENT DOCUMENT Acids and Caustics from Petroleum Refining Table of Contents Tables ........................................................................................................................................... 3 Figures ......................................................................................................................................... 3 Annexes........................................................................................................................................ 3 Plain Language Summary ......................................................................................................... 4 1. Introduction ........................................................................................................................ 5 2. Category Description ........................................................................................................ -
Oxidation of Phenol and Cresol by Electrochemical Advanced Oxidation Method in Homogeneous Medium: Application to Treatment of A
Oxidation of phenol and cresol by electrochemical advanced oxidation method in homogeneous medium : application to treatment of a real effluent of aeronautical industry Marcio Pimentel To cite this version: Marcio Pimentel. Oxidation of phenol and cresol by electrochemical advanced oxidation method in homogeneous medium : application to treatment of a real effluent of aeronautical industry. Other. Université Paris-Est, 2008. English. NNT : 2008PEST0271. tel-00742470v2 HAL Id: tel-00742470 https://tel.archives-ouvertes.fr/tel-00742470v2 Submitted on 7 May 2010 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Université Paris-Est Marne-La-Vallée Institut Francilien des Sciences Appliquées (IFSA) Laboratoire Géomatériaux et Géologie de l'Ingénieur THÈSE pour obtenir le grade de Docteur de l’Université Paris-Est Marne-la-Vallée Spécialité : Sciences et Techniques de l'Environnement présentée et soutenue publiquement par Marcio PIMENTEL le 24 septembre 2008 Etudes de l'oxydation de phénol et crésols par l'oxydation électrochimique avancée en milieu homogène. Application au traitement d'effluent de l'industrie aéronautique Phenol and cresols treatment in aqueous solution by electro-Fenton process: Application to the mineralization of aeronautic wastewater industry. Directeur de thèse : Prof. -
New Strategies for Separations Through Reactions
Sddhand, Vol. 10, Parts 1 & 2, April 1987, pp. 163-183. © Printed in India. New strategies for separations through reactions V G GAIKAR and M M SHARMA* Department of'Chemical Techno[ogy, University of Bombay, Matunga, Bombay 400 019, India Abstract. Separations through reactions can provide reliable and economically viable alternatives to established methods of separation, particularly for close boiling substances. New strategies in 'Dissociation Extraction' and "Dissociation Extractive Crystallization' for separation of close boiling acidic/basic mixtures have been highlighted. Separations with aqueous solutions of hydrotrope and aqueous micellar solutions have been brought out. Separations by membranes with facilitated transport is potentially attractive. Keywords. Separations through reactions; dissociation extraction; reactive crystallization; dissociation extractive crystallization; reactive distillation; separations with hydrotropes; micelles in separations: membrane separations; hydrometallurgical separations; separations with supercritical fluids. I. Introduction In chemical process industries separations of a variety of mixtures are frequently encountered and the cost of separation may dominate the capital investment and operational expenses. Quite often physical methods of separation, such as distillation, crystallization, solvent extraction followed by distillation and adsorp- tion, are used, which exploit the differences in physical properties like boiling points, solubility, melting points etc. However, for systems having close boiling points or which are thermally unstable, these methods are either not applicable or not economically viable. In such cases the strategy of selective reactions may prove to be attractive. There is, therefore, a clear incentive to probe newer methods of separations through reactions to achieve better selectivity and higher throughput. An ideal situation would be where separation and the desired reaction are conducted simultaneously. -
Butylated Hydroxytoluene (BHT) Crops
Butylated Hydroxytoluene (BHT) Crops 1 2 Executive Summary 3 A petition was filed with the NOSB to use butylated hydroxytoluene (BHT) as an antioxidant in a number of pheromone 4 formulations. Pheromones and BHT would be enclosed in a plastic matrix, allowing slow release of the materials into the 5 air. Due to low volatility of BHT, most of it would remain in the dispenser and direct contact with the crop would be 6 negligible. BHT is an alkylated cresol that can be synthesized several ways. The p-cresol starting material is isolated from 7 coal tar or petroleum. It is also obtained synthetically from toluene. The p-cresol is alkylated with isobutylene gas in the 8 presence of an acidic catalyst to produce BHT. It is used as an antioxidant in food, and is also used as a stabilizer in 9 pesticides, gasoline, lubricants, soaps and cosmetics, and as an antiskinning agent in paints and inks. 10 11 The material has not been reviewed by NOSB before, and because it is synthetic and on List 3, is currently prohibited for 12 use in organic production under the National Organic Program Standards. However, pheromone formulations that use 13 BHT have been widely used by organic farmers. Impacts on the environment and human health from this application 14 should be negligible. The TAP reviewers unanimously concluded that BHT should be added to the National List as an 15 allowed synthetic with the annotation: for use in organic crop production systems as an antioxidant for pheromones 16 enclosed in plastic dispensers. The reviewers were all concerned with the precedent that this set, and made it clear that 17 addition to the National List should be made only if application and use is limited. -
Safe Handling of Cresols, Xylenols & Cresylic Acids
Safe Handling of Cresols, Xylenols & Cresylic Acids I. Introduction Cresols, xylenols and cresylic acids are hazardous substances and dangerous both to people and the environment if handled improperly. Cresols, xylenols and cresylic acid products produced by Sasol Chemicals (USA) LLC are highly versatile materials and are used as intermediates in the manufacture of a wide variety of industrial products such as resins, flame retardants, antioxidants, and coatings. In these and other applications, cresylic acids can be stored, transferred, processed and disposed of safely when proper procedures and safeguards are used. “Cresol” refers to any of the three isomers of methylphenol (C7H8O) or combinations thereof. “Cresols” commonly refer to a mixture which is predominantly methylphenol but may also contain lesser amounts of other alkylphenols. “Xylenol” is a common name for any of the six isomers of dimethylphenol (C8H10O) or their various combinations. Material which is predominantly dimethylphenol but which also contains ethylphenols and other alkylphenols may be referred to as “Xylenols”. “Cresylic acid” is a generic term referring to various combinations of cresols, xylenols, phenol or other alkylphenols (ethylphenols, propylphenols, trimethylphenols, etc.). See Table A for specific information on individual isomers. Purpose & Scope The purpose of this document is to provide information gathered through Sasol’s long experience in the safe handling of cresylic acids. It focuses on basic and practical information about working safely with these substances. Additional references are provided and it is strongly recommended that these and others be consulted prior to working with cresylic acids. Please do not hesitate to contact your regional Sasol office if we can be of assistance in the safe storage, handling, processing and disposal of our products. -
Rhodotomla Cresolica Sp. Nov., a Cresol-Assimilating Yeast Species Isolated from Soil
INTERNATIONAL JOURNALOF SYSTEMATIC BACTERIOLOGY, Apr. 1997, p. 324-327 Vol. 47, No. 2 0020-7713/97/$04,00+0 Copyright 0 1997, International Union of Microbiological Societies Rhodotomla cresolica sp. nov., a Cresol-Assimilating Yeast Species Isolated from Soil WOUTER J. MIDDELHOVEN1* AND FRANS SPAAIJ' La boratorium voor Microbiologie, Wageningen Agricultural University, 6700 EJ Wageningen, The Netherlands, and Labor fur Schimmelpilze und Hefen, 72076 Tubingen, Germany2 A cresol-assimilating yeast strain of a previously undescribed species belonging to the genus Rhodotorula was isolated from soil. The new strain differs from the previously described species of the genus in its pattern of assimilation of carbon and nitrogen compounds, G+C content, and low levels of DNA-DNA-homology. The new species Rhodotorula cresolica is described. The type strain is CBS 7998. Several yeast species are able to assimilate a great variety of Gilford Response UV-VIS spectrophotometer and thermal programming soft- benzene compounds as sole sources of carbon and energy. ware heating at a rate of O.l"C/min. The G+C content was calculated by the following formula: G+C content = (2.08 X T,) - 106.4, where T,,, is the thermal Strains displaying this property have been found in culture denaturation temperature. A standard preparation of Candida parapsilosis CBS collections (5) and in several natural habitats (7, 12 . In a 604 DNA (T,, 70.6"C) was included as a control in every determination. The previous publication, the isolation of yeast strain G36.2 (T = value reported below is the mean 2 standard deviation from three determina- type strain) from soil polluted with ortho-cresol was reported tions. -
M-Cresol Crl
M-CRESOL CRL CAUTIONARY RESPONSE INFORMATION 4. FIRE HAZARDS 7. SHIPPING INFORMATION 4.1 Flash Point: 202°F C.C. 7.1 Grades of Purity: 60 to 98% containing other Common Synonyms Liquid Colorless Sweet tarry odor 4.2 Flammable Limits in Air: 1.06%-1.35% cresols and xylenols. 3-Cresol 302°F. 7.2 Storage Temperature: Ambient m-Cresylic acid 4.3 Fire Extinguishing Agents: CO2, dry 3-Hydroxytoluene Sinks and mixes slowly with water. 7.3 Inert Atmosphere: No requirement chemical, foam, water spray. m-Methylphenol 7.4 Venting: Open 4.4 Fire Extinguishing Agents Not to Be Used: Not pertinent 7.5 IMO Pollution Category: A Keep people away. Avoid contact with liquid. 7.6 Ship Type: 2 Avoid inhalation. 4.5 Special Hazards of Combustion Wear goggles, self-contained breathing apparatus, and rubber overclothing (including gloves). Products: Emits highly toxic fumes. 7.7 Barge Hull Type: 3 Shut off ignition sources and call fire department. 4.6 Behavior in Fire: Vapor may form Notify local health and pollution control agencies. explosive mixture with air. 8. HAZARD CLASSIFICATIONS Protect water intakes. 4.7 Auto Ignition Temperature: 1038°F. 8.1 49 CFR Category: Poison 4.8 Electrical Hazards: Not pertinent COMBUSTIBLE. 8.2 49 CFR Class: 6.1 Fire 4.9 Burning Rate: Currently not available POISONOUS FLAMMABLE GASES MAY BE PRODUCED IN FIRE. 8.3 49 CFR Package Group: II Wear goggles and self-contained breathing apparatus. 4.10 Adiabatic Flame Temperature: Currently Extinguish with water, dry chemical, foam or carbon dioxide. not available 8.4 Marine Pollutant: Yes Cool exposed containers with water. -
Benzyl Chloride)
Screening Assessment for the Challenge Benzene, (chloromethyl)- (Benzyl chloride) Chemical Abstracts Service Registry Number 100-44-7 Environment Canada Health Canada November 2009 Screening Assessment CAS RN 100-44-7 Synopsis Pursuant to section 74 of the Canadian Environmental Protection Act, 1999 (CEPA 1999), the Ministers of the Environment and of Health have conducted a screening assessment of benzene, (chloromethyl)-, also known as benzyl chloride, Chemical Abstracts Service Registry Number 100-44-7. This substance was identified in the categorization of the Domestic Substances List (DSL) as a high priority for action under the Challenge. Benzyl chloride was identified as presenting greatest potential for exposure of individuals in Canada and had been classified by other agencies on the basis of carcinogenicity and genotoxicity. Although the substance met the categorization criteria for persistence, it did not meet the criteria for bioaccumulation potential or inherent toxicity to aquatic organisms; therefore, the focus of this assessment relates primarily to human health aspects. According to data submitted in response to a Notice issued under section 71 of the Act, no persons in Canada reported manufacturing benzyl chloride in a quantity greater than or equal to the reporting threshold of 100 kg for the 2006 calendar year. However, it was reported that 100 000–1 000 000 kg were imported into Canada in that year. The response to the section 71 notice indicated that benzyl chloride is mainly used in Canada as a chemical intermediate for the synthesis of quaternary ammonium compounds, which are used primarily as hard surface sanitizers, corrosion inhibitors, fungicides in industrial cleaners and bactericides in surfactants in household and personal care products. -
NMS Labs Demo Report
NMS Labs CONFIDENTIAL 200 Welsh Road, Horsham, PA 19044-2208 Phone: (215) 657-4900 Fax: (215) 657-2972 e-mail: [email protected] Robert A. Middleberg, PhD, F-ABFT, DABCC-TC, Laboratory Director Demo Report Patient Name 2416U-POS Report Issued 03/14/2019 11:04 Patient ID 2416U-POS Last Report Issued 03/14/2019 11:04 Chain 19000451 Age Not Given DOB Not Given 88888 Gender Not Given Clinical Example Report Attn: Example Reports Workorder 19000451 200 Welsh Road Horsham, PA 19044 Received 03/14/2019 10:51 Sample ID 19000451-001 Collect Dt/Tm Not Given Matrix Urine Source Not Given Patient Name 2416U-POS Patient ID 2416U-POS Container Type Clear vial Approx Vol/Weight Not Given Receipt Notes None Entered Reporting Analysis and Comments Result Units Limit Notes 2416U Inhalants Metabolites Panel, Urine Analysis by Gas Chromatography (GC) o-Cresol 20 mg/L 0.50 ELEVATED Synonym(s): Toluene Metabolite The mean concentration in the urine of the general population is approximately 0.1 mg o-Cresol/L o-Cresol (Creatinine corrected) 4.0 mg/g Creat 0.10 ELEVATED Synonym(s): Toluene Metabolite Biological Exposure Index (ACGIH) for monitoring exposure to Toluene: 0.3 mg o-Cresol/g Creatinine measured in an end of shift urine specimen. Phenol - Total 20 mg/L 1.0 Less than 10 mg/L in unexposed individuals. Less than 30 mg/L when chronically exposed to 0.5 to 4.0 ppm Benzene in air. Average 200 mg/L during chronic exposure to 25 ppm Benzene in air. Phenol - Total (Creatinine corrected) 4.0 mg/g Creat 0.20 Results for sample 19000451-001 are continued on next page Page 1 of 3 NMS v.39.0 NMS Labs CONFIDENTIAL 200 Welsh Road, Horsham, PA 19044-2208 Phone: (215) 657-4900 Fax: (215) 657-2972 e-mail: [email protected] Robert A. -
Α-Chlorinated Toluenes and Benzoyl Chloride
α-CHLORINATED TOLUENES AND BENZOYL CHLORIDE Data were last reviewed in IARC (1982) and the compounds were classified in IARC Monographs Supplement 7 (1987a). 1. Exposure Data Benzyl chloride 1.1 Chemical and physical data 1.1.1 Nomenclature Chem. Abstr. Serv. Reg. No.: 100-44-7 Chem. Abstr. Name: (Chloromethyl)benzene IUPAC Systematic Name: α-Chlorotoluene Synonyms: Chloromethyl benzene; chlorophenylmethane; α-tolyl chloride 1.1.2 Structural and molecular formulae and relative molecular mass CH2Cl C7H7Cl Relative molecular mass: 126.6 1.1.3 Chemical and physical properties of the pure substance From Lide (1997), unless otherwise specified (a) Description: Colourless liquid with a pungent odour (Lewis, 1993) (b) Boiling-point: 179°C (c) Melting-point: –45°C 20 (d) Density: d10 1.10 (e) Solubility: Insoluble in water; slightly soluble in carbon tetrachloride; miscible with chloroform, diethyl ether and ethanol (Budavari, 1996) (f) Vapour pressure: 133 Pa at 22°C; relative vapour density (air = 1), 4.36 (Ver- schueren, 1996) (g) Stability: Decomposes in hot water to benzyl alcohol (United States Environ- mental Protection Agency, 1980); decomposes rapidly when heated in the pre- sence of iron (Budavari, 1996); combustible (Lewis, 1993) (h) Reactivity: Undergoes reactions both at the side-chain containing the chlorine and at the aromatic ring (Gelfand, 1979) –453– 454 IARC MONOGRAPHS VOLUME 71 (i) Flash-point: 67°C (closed cup); 74°C (open cup) (Lin & Bieron, 1993) (j) Explosive limit: Lower, 1.1% by volume of air (Lin & Bieron, 1993) (k) Octanol/water partition coefficient (P): log P, 2.30 (Verschueren, 1996) (l) Conversion factor: mg/m3 = 5.18 × ppm 1.2 Production and use The chemical processes associated with the manufacture of chlorinated toluenes are summarized in Figure 1. -
Synthesis and Selectivity of Schmidt Reactions Of
SYNTHESIS AND SELECTIVITY OF SCHMIDT REACTIONS OF DISUBSTITUTED lEREPHTHALIC AND ISOPHTHALIC ACIDS Dissertation Presented in Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy By DERRY LEE FI8HEL, B. A. ***** The Ohio S tate U n iv ersity 1959 Approved by A dviser ACKNOWLEDGMENTS The author -wishes to thank his adviser. Dr. Harold Sheohter for suggesting this research problem and for his invaluable help and criticism during the preparation of this dissertation. Thanks are also due fellow graduate students and professors in the Department of Chemistry at Ohio State University for unselfish donation of time and materials throughout the course of the investigation. A -very real debt is owed the author's wife, Jean H. Fishel, for sacrifices that only a graduate student's wife can appreciate. This work is dedicated to the author's sons, David Ward and Paul Jonathon^and to the future they deserve. i i COHTENTS Page INTRODUCTION ........................................................................................................... 1 HISTORICAL................................................................................................................ 3 The Sohmidt Réaction of Carboxylio Aoids. « ............................. 3 Selectivity of Sohmidt Reactions of Substituted Aromatic Aoids .................................................................................... 9 Kinetics and Mechanism of Schmidt Reactions of Substituted Benzoic Acids ........................................................ • 16 THE