A Comparison of Ethanol, Methanol and Butanol Blending with Gasoline and Relationship with Engine Performances and Emissions
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California Biobutanol Multimedia Evaluation Tier II Work Plan
California Biobutanol Multimedia Evaluation Tier II Work Plan Prepared By Butamax™ Advanced Biofuels, LLC for the California Environmental Protection Agency Multimedia Working Group July 2013 Biobutanol Multimedia Evaluation Tier II Work Plan Table of Contents Table of Contents ........................................................................... 2 Table of Tables ............................................................................... 6 Table of Figures.............................................................................. 7 1. Executive Summary ................................................................. 8 1.1. Scope ................................................................................................................. 8 1.2. Background ....................................................................................................... 8 2. Tier I Conclusions .................................................................. 10 2.1. Conclusions of the Tier I Report ..................................................................... 10 2.2. Formulation of the Tier II Work Plan ............................................................. 11 3. Impact of Biobutanol on Elastomers .................................... 12 3.1. Statement of the Knowledge Gap ................................................................... 12 3.2. Test Plan.......................................................................................................... 13 4. Impact of Biobutanol on Fiberglass Resins and Sealants -
A Study on the Emissions of Butanol Using a Spark Ignition Engine and Their Reduction Using Electrostatically Assisted Injection
A STUDY ON THE EMISSIONS OF BUTANOL USING A SPARK IGNITION ENGINE AND THEIR REDUCTION USING ELECTROSTATICALLY ASSISTED INJECTION BY BENJAMIN R. WIGG THESIS Submitted in partial fulfillment of the requirements for the degree of Master of Science in Mechanical Engineering in the Graduate College of the University of Illinois at Urbana-Champaign, 2011 Urbana, Illinois Adviser: Professor Dimitrios C. Kyritsis Abstract Butanol is a potential alternative to ethanol and offers many benefits including a much higher heating value and lower latent heat of vaporization. It also has a higher cetane number than ethanol and improved miscibility in diesel fuel. Additionally, butanol is less corrosive and less prone to water absorption than ethanol, which allows it to be transported using the existing fuel supply pipelines. However, while some previous research on the emissions of butanol-gasoline blends is available, little research exists on the emissions of neat butanol. This thesis focuses on two areas of study. The first area relates to on the comparison of UHC, NOx, and CO emissions of several butanol-gasoline and ethanol-gasoline blended fuels during combustion in an SI engine. The objective was to compare the emissions of butanol combustion to the ones of ethanol and gasoline. The second part of the study relates to the use of electrostatically assisted injection as a means of reducing the UHC emissions of butanol by decreasing the fuel droplet size using a charge electrode and extraction ring designed for a port fuel injector. Emissions measurements taken with and without a charge applied to the injector were used to determine the effect of applying a voltage to the fuel spray on engine emissions. -
Enhanced Butanol Production by Free and Immobilized Clostridium Sp
Enhanced Butanol Production by Free and Immobilized Clostridium sp. Cells Using Butyric Acid as Co-Substrate Laili Gholizadeh This thesis comprises 30 ECTS credits and is a compulsory part in the Master of Science with a Major in Chemical Engineering – Applied Biotechnology 120 ECTS credits No. 10/2009 Title: Enhanced Butanol Production by Free and Immobilized Clostridium sp. Cells using Butyric Acid as Co-Substrate. Author: Laili Gholizadeh Baroghi (e-mail: [email protected]) Master Thesis Subject Category: Biotechnology (Bioprocess Engineering – Biofuels) University College of Borås School of Engineering SE-501 90 BORÅS Telephone: (+46) 033 435 4640 Examiner: Prof. Mohammad Taherzadeh Supervisor and Thesis Advisor: Prof. Shang–Tian Yang Supervisor Address: OSU–Ohio State University 125 Koffolt Laboratories 140 West 19th Ave. Columbus, OH 43210–1185, USA Client: Ohio State University (OSU), Chemical & Biomolecular Engineering Department Prof. Shang–Tian Yang Columbus, Ohio; USA. Date: 08–12–2009 Keywords: Bio-butanol y Acetone–Butanol–Ethanol (ABE) y ABE- fermentation y Butyric acid y Clostridium y C. acetobutylicum ATCC 824 y C. beijerinckii ATCC 55025 y C. beijerinckii BA 101 y C. beijerinckii NCIMB 8052 y Fibrous-bed Bioreactor (FBB) y Batch y Suspended cell culture y Immobilized cell system. DEDICATION I would like to dedicate this M.Sc. Thesis to my beloved Family for all their love and encouragement and for always been supportive of my choices. “I am among those who think that science has great beauty. A scientist in his laboratory is not only a technician: he is also a child placed before natural phenomena, which impress him like a fairy tale.” − Marie Curie ABSTRACT Butanol production by four different Clostridium sp. -
Sion Technologies - from Short Time to Long Term
D3.6 Efficient, low-risk ramp- up of liquid biomass conver- sion technologies - from short time to long term Authors: Paraskevi Karka, Ivar Petersson, Stavros Papadokonstantakis, Filip Johnsson Organisation: Chalmers University of Technology City, Country: Gothenburg, Sweden Email: [email protected] Website: www.chalmers.se [Type here] Deliverable Information Grant Agreement Number 764799 Project Acronym ADVANCEFUEL Instrument CSA Start Date 1 September 2017 Duration 36 months Website www.ADVANCEFUEL.eu Deliverable Number D3.6 Deliverable Title Efficient, low-risk ramp-up of liquid biomass conversion technologies - from short time to long term Expected Submission M32 Actual Submission M34 Authors Paraskevi Karka, Ivar Petersson, Stavros Papadokonstantakis, Filip Johnsson Reviewers Yuri Kroyan, Popi Panoutsou, Ayla Uslu, Michal Wojcieszyk, Philipp von Bothmer Dissemination Level PU Public (PU), Restricted (PP), Confidential (CO) 2 ADVANCEFUEL at a glance ADVANCEFUEL (www.ADVANCEFUEL.eu) aims to facilitate the commercialisation of renewable transport fuels by providing market stakeholders with new knowledge, tools, standards and recommen- dations to help remove barriers to their uptake. The project will look into liquid advanced biofuels – defined as liquid fuels produced from lignocellulosic feedstocks from agriculture, forestry and waste – and liquid renewable alternative fuels produced from renewable hydrogen and CO2 streams. In order to support commercial development of these fuels, the project will firstly develop a framework to monitor the current status, and future perspectives, of renewable fuels in Europe in order to better understand how to overcome barriers to their market roll-out. Following this, it will investigate individ- ual barriers and advance new solutions for overcoming them. The project will examine the challenges of biomass availability for second-generation biofuels, looking at non-food crops and residues, and how to improve supply chains from providers to converters. -
Transcription 12.01.12
Lecture 2B • 01/12/12 We covered three different reactions for converting alcohols into leaving groups. One was to turn an alcohol into an alkyl chloride, that was using thionyl chloride. Second reaction was using tosyl chloride; the primary difference between those two reactions is one of stereochemistry. An inversion of stereochemistry does occur if you use thionyl chloride, because it does affect the carbon-oxygen bond, but because forming a tosylate does not touch the carbon-oxygen bond, only the oxygen- hydrogen bond, there’s no change in stereochemistry there. We then saw phosphorus tribromide that reacts very similarly to the thionyl chloride; you get an alkyl bromide instead, but it also has inversion of configuration. The last reaction is not a new mechanism, it is just an Sn2 reaction, it’s called the Finkelstein reaction. Really this works, in a sense, off of Le Châtelier’s principle. In solution, in theory, sodium iodide can displace bromide, but sodium bromide can displace iodide, so you can have an Sn2 reaction that goes back and forth and back and forth and back and forth. Except, sodium iodide is somewhat soluble in acetone, while sodium chloride and sodium bromide are not. So, in fact, one of the things that we get out of this as a by-product is sodium bromide, which, again, is not soluble in acetone and therefore precipitates out and is no longer part of the reaction mixture, so there’s no reverse reaction possible. Because of this solubility trick, it allows this reaction to be pulled forward, which means you can get the alkyl iodide. -
Aldehydes and Ketones
Organic Lecture Series Aldehydes And Ketones Chap 16 111 Organic Lecture Series IUPAC names • the parent alkane is the longest chain that contains the carbonyl group • for ketones, change the suffix -e to -one • number the chain to give C=O the smaller number • the IUPAC retains the common names acetone, acetophenone, and benzophenone O O O O Propanone Acetophenone Benzophenone 1-Phenyl-1-pentanone (Acetone) Commit to memory 222 Organic Lecture Series Common Names – for an aldehyde , the common name is derived from the common name of the corresponding carboxylic acid O O O O HCH HCOH CH3 CH CH3 COH Formaldehyde Formic acid Acetaldehyde Acetic acid – for a ketone , name the two alkyl or aryl groups bonded to the carbonyl carbon and add the word ketone O O O Ethyl isopropyl ketone Diethyl ketone Dicyclohexyl ketone 333 Organic Lecture Series Drawing Mechanisms • Use double-barbed arrows to indicate the flow of pairs of e - • Draw the arrow from higher e - density to lower e - density i.e. from the nucleophile to the electrophile • Removing e - density from an atom will create a formal + charge • Adding e - density to an atom will create a formal - charge • Proton transfer is fast (kinetics) and usually reversible 444 Organic Lecture Series Reaction Themes One of the most common reaction themes of a carbonyl group is addition of a nucleophile to form a tetrahedral carbonyl addition compound (intermediate). - R O Nu - + C O Nu C R R R Tetrahedral carbonyl addition compound 555 Reaction Themes Organic Lecture Series A second common theme is -
N-BUTYL ALCOHOL
Right to Know Hazardous Substance Fact Sheet Common Name: n-BUTYL ALCOHOL Synonyms: Propyl Carbinol; n-Butanol CAS Number: 71-36-3 Chemical Name: 1-Butanol RTK Substance Number: 1330 Date: November 1998 Revision: January 2008 DOT Number: UN 1120 Description and Use EMERGENCY RESPONDERS >>>> SEE BACK PAGE n-Butyl Alcohol is a colorless liquid with a strong, sweet Hazard Summary alcohol odor. It is used as a solvent for fats, waxes, shellacs, Hazard Rating NJDOH NFPA resins, gums, and varnish, in making hydraulic fluids, and in HEALTH - 2 medications for animals. FLAMMABILITY - 3 REACTIVITY - 0 f ODOR THRESHOLD = 1 to 15 ppm FLAMMABLE f Odor thresholds vary greatly. Do not rely on odor alone to POISONOUS GASES ARE PRODUCED IN FIRE determine potentially hazardous exposures. CONTAINERS MAY EXPLODE IN FIRE Hazard Rating Key: 0=minimal; 1=slight; 2=moderate; 3=serious; Reasons for Citation 4=severe f n-Butyl Alcohol is on the Right to Know Hazardous f n-Butyl Alcohol can affect you when inhaled and by Substance List because it is cited by OSHA, ACGIH, DOT, passing through the skin. NIOSH, DEP, IRIS, NFPA and EPA. f Contact can irritate and burn the skin. f This chemical is on the Special Health Hazard Substance f n-Butyl Alcohol can irritate and burn the eyes with possible List. eye damage. f Inhaling n-Butyl Alcohol can irritate the nose, throat and lungs. f Exposure to n-Butyl Alcohol can cause headache, dizziness, nausea and vomiting. SEE GLOSSARY ON PAGE 5. f n-Butyl Alcohol can damage the liver, kidneys, hearing, and sense of balance. -
N-Butanol As Biofuel: Characteristics and Evaluation of Its Application in Internal Combustion Engines Through 1D Simulation
UNIVERSIDADE ESTADUAL DE CAMPINAS Faculdade de Engenharia Mecânica WAGNER ROBERTO DA SILVA TRINDADE n-Butanol as biofuel: characteristics and evaluation of its application in internal combustion engines through 1D simulation n-Butanol como biocombustível: características e avaliação de sua aplicação em motores de combustão interna através de simulação 1D CAMPINAS 2016 Agência(s) de fomento e nº(s) de processo(s): Não se aplica. Ficha catalográfica Universidade Estadual de Campinas Biblioteca da Área de Engenharia e Arquitetura Luciana Pietrosanto Milla - CRB 8/8129 Trindade, Wagner Roberto da Silva, 1975- T736n N-Butanol as biofuel: characteristics and evaluation of its application in internal combustion engines through 1D simulation / Wagner Roberto da Silva Trindade. – Campinas, SP: [s.n.], 2016. Orientador: Rogério Gonçalves dos Santos. Dissertação (mestrado) – Universidade Estadual de Campinas, Faculdade de Engenharia Mecânica. 1. Butanol. 2. Biofuel. 3. Internal combustion engines. 4. Simulation. I. Santos, Rogério Gonçalves dos, 1978-. II. Universidade Estadual Campinas. Faculdade de Engenharia Mecânica. III. Título. Informações para Biblioteca Digital Título em outro idioma: N-butanol como biocombustível : características e avaliação de sua aplicação em motores de combustão interna através de simulação 1D Palavras-chave em português: Butanol Biocombustível Motores de combustão interna Simulação Área de concentração: Térmica e Fluídos Titulação: Mestre em Engenharia Mecânica Banca examinadora: Rogério Gonçalves dos Santos [Orientador] Waldyr Luiz Ribeiro Gallo Guenther Carlos Krieger Filho Data de defesa: 12-12-2016 Programa de Pós-Graduação: Engenharia Mecânica Dedicatória À Andrea, Beatriz e Helena: minha força, minha alegria e minha luz. Agradecimentos À Andrea, Beatriz e Helena – esposa e filhas queridas – que sempre estiveram ao meu lado, me apoiando e motivando e que não me deixaram desitir nos momentos mais difíceis. -
Alcoholsalcohols
AlcoholsAlcohols Chapter 10 1 Structure of Alcohols • The functional group of an alcohol is H an -OH group bonded to an sp3 O 108.9° hybridized carbon. C H – Bond angles about the hydroxyl oxygen H H atom are approximately 109.5°. • Oxygen is sp3 hybridized. –Two sp3 hybrid orbitals form sigma bonds to a carbon and a hydrogen. – The remaining two sp3 hybrid orbitals each contain an unshared pair of electrons. 2 Nomenclature of Alcohols • IUPAC names – The parent chain is the longest chain that contains the OH group. – Number the parent chain to give the OH group the lowest possible number. – Change the suffix -etoe -ol.ol • Common names – Name the alkyl group bonded to oxygen followed by the word alcohol.alcohol 3 Nomenclature of Alcohols OH o o 1o OH 1 2 OH 1-Propanol 2-Propan ol 1-Bu tanol (Pro py l alco ho l) (Isoprop yl alcoh ol) (Bu tyl alcoh ol) OH 2o OH 1o OH 3o 2-Butanol 2-M eth yl-1-p ropan ol 2-M eth yl-2-p ropan ol (sec-Butyl alcohol) (Isobutyl alcohol) (tert -Butyl alcohol) 4 Nomenclature of Alcohols • Compounds containing more than one OH group are named diols, triols, etc. CH2 CH2 CH3 CHCH2 CH2 CHCH2 OH OH HO OH HO HO OH 1,2-Ethanediol 1,2-Propanediol 1,2,3-Propanetriol (Ethylene glycol) (Propylene glycol) (Glycerol, Glycerine) 5 Physical Properties • Alcohols are polar compounds. – They interact with themselves and with other polar compounds by dipole-dipole interactions. • Dipole-dipole interaction: The attraction between the positive end of one dipole and the negative end of another. -
Strategies to Introduce N-Butanol in Gasoline Blends
sustainability Article Strategies to Introduce n-Butanol in Gasoline Blends Magín Lapuerta *, Rosario Ballesteros and Javier Barba Escuela Técnica Superior de Ingenieros Industriales, University of Castilla-La Mancha, Av. Camilo José Cela s/n, 13071 Ciudad Real, Spain; [email protected] (R.B.); [email protected] (J.B.) * Correspondence: [email protected] Academic Editors: Gilles Lefebvre and Francisco J. Sáez-Martínez Received: 13 February 2017; Accepted: 7 April 2017; Published: 12 April 2017 Abstract: The use of oxygenated fuels in spark ignition engines (SIEs) has gained increasing attention in the last few years, especially when coming from renewable sources, due to the shortage of fossil fuels and global warming concern. Currently, the main substitute of gasoline is ethanol, which helps to reduce CO and HC emissions but presents a series of drawbacks such as a low heating value and a high hygroscopic tendency, which cause higher fuel consumption and corrosion problems, respectively. This paper shows the most relevant properties when replacing ethanol by renewable n-butanol, which presents a higher heating value and a lower hygroscopic tendency compared to the former. The test matrix carried out for this experimental study includes, on the one hand, ethanol substitution by n-butanol in commercial blends and, on the other hand, either ethanol or gasoline substitution by n-butanol in E85 blends (85% ethanol-15% gasoline by volume). The results show that the substitution of n-butanol by ethanol presents a series of benefits such as a higher heating value and a greater interchangeability with gasoline compared to ethanol, which makes n-butanol a promising fuel for SIEs in commercial blends. -
Abstract Process Economics Program Report 264 BIOBUTANOL (December 2008)
Abstract Process Economics Program Report 264 BIOBUTANOL (December 2008) World production of biofuels has experienced phenomenal growth. Various drivers for this phenomenon include high fuel prices, concerns about the environment, energy security and rural development. The majority of the growth in biofuels has been in the production of ethanol. However there are other biofuels, so-called second-generation biofuels that may offer some advantages over ethanol. Second-generation biofuels include cellulosic ethanol, covered in the PEP Report 263 Cellulosic Ethanol and the subject of this report biobutanol. Biobutanol has a number of advantages over ethanol, has a higher heating value, it is more hydrophobic than ethanol and can be transported via pipeline integrated in the existing petroleum-based fuels infrastructure and it can be added to gasoline at higher levels without engine modification. Biobutanol has garnered the interest not only in early stage companies such as Tetravitae and Gevo, whose technologies are covered in this report, but also major oil and chemical companies. BP and DuPont have formed a JV to develop biobutanol as a gasoline additive. This report covers the technological and economic aspects of the production of biobutanol via two processes. The first one is a modification of the established acetone-butanol-ethanol (ABE) fermentation developed by the University of Illinois and a licensed to Tetravitae. It incorporates an improved microorganism (Clostridium beijerincki BA101) and a gas stripping system for in situ product removal (ISPR) originally covered in PEP Review 2007-1. The second process is based on a combination of patents from GEVO and DuPont. It incorporates a novel pathway for the production of isobutanol by a solvent-tolerant microorganism developed by Gevo and a recovery process based on a DuPont patent application. -
Alcohols I 1400
ALCOHOLS I 1400 Table 1 MW: Table 1 CAS: Table 2 RTECS: Table 2 METHOD: 1400, Issue 2 EVALUATION: PARTIAL Issue 1: 15 February 1984 Issue 2: 15 August 1994 OSHA : Table 2 PROPERTIES: Table 1 NIOSH: Table 2 ACGIH: Table 2 COMPOUNDS AND SYNONYMS: (1) ethanol: ethyl alcohol. (2) isopropyl alcohol: 2-propanol. (3) tert-butyl alcohol: 2-methyl-2-propanol. SAMPLING MEASUREMENT SAMPLER: SOLID SORBENT TUBE TECHNIQUE: GAS CHROMATOGRAPHY, FID (coconut shell charcoal, 100 mg/50 mg) ANALYTE: compounds above FLOW RATE: 0.01 to 0.2 L/min (£0.05 L/min for ethyl alcohol) DESORPTION: 1 mL 1% 2-butanol in CS 2 (1) (2) (3) INJECTION VOL-MIN: 0.1 L 0.3 L 1.0 L VOLUME: 5 µL -MAX: 1 L 3 L 10 L TEMPERATURE-INJECTION: 200 °C SHIPMENT: cooled -DETECTOR: 250-300 °C -COLUMN: 65-70 °C SAMPLE STABILITY: unknown, store in freezer CARRIER GAS: N2 or He, 30 mL/min BLANKS: 2 to 10 field blanks per set COLUMN: glass, 2 m x 4-mm ID, 0.2% Carbowax 1500 on 60/80 Carbopack C or equivalent ACCURACY CALIBRATION: solutions of analyte in eluent (internal standard optional) RANGE STUDIED: see EVALUATION OF METHOD RANGE AND BIAS: not significant [1] PRECISION: see EVALUATION OF METHOD OVERALL PRECISION (S ˆ ): see EVALUATION OF METHOD rT ESTIMATED LOD: 0.01 mg per sample [2] ACCURACY: ± 14% APPLICABILITY: The working ranges are 16 to 1000 ppm ethanol (30 to 1900 mg/m 3) for a 1-L air sample; 4 to 400 ppm isopropyl alcohol (10 to 1000 mg/m 3) for a 3-L air sample; and 1 to 100 ppm t-butyl alcohol (3 to 300 mg/m 3) for a 10-L air sample.