Literature DB >> 17324391

Butadiene production process overview.

Wm Claude White1.   

Abstract

Over 95% of butadiene is produced as a by-product of ethylene production from steam crackers. The crude C4 stream isolated from the steam cracking process is fed to butadiene extraction units, where butadiene is separated from the other C4s by extractive distillation. The amount of crude C4s produced in steam cracking is dependent on the composition of the feed to the cracking unit. Heavier feeds, such as naphtha, yield higher amounts of C4s and butadiene than do lighter feeds. Crackers using light feeds typically produce low quantities of C4s and do not have butadiene extraction units. Overall butadiene capacity is determined by ethylene cracker operating rates, the type of feed being cracked, and availability of butadiene extraction capacity. Global butadiene capacity is approximately 10.5 million metric tons, and global production is approximately 9 million metric tons [Chemical Marketing Associates, Inc. (CMAI), 2005 World Butadiene Analysis, Chemical Marketing Associates, Inc. (CMAI), 2005]. Crude C4s are traded globally, with the United States being the only significant net importer. Finished butadiene is also traded globally, with the largest exporters being Canada, Western Europe, Saudi Arabia and Korea. The largest net importers are Mexico, the United States and China. The global demand for butadiene is approximately 9 million metric tons [Chemical Marketing Associates, Inc. (CMAI), 2005 World Butadiene Analysis, Chemical Marketing Associates, Inc. (CMAI), 2005]. Production of styrene-butadiene rubber and polybutadiene rubber accounts for about 54% of global butadiene demand, with tire production being the single most important end use of butadiene synthetic rubbers. Other major butadiene derivatives are acrylonitrile-butadiene-styrene (ABS) and styrene butadiene latex (about 24% of demand combined).

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Year:  2007        PMID: 17324391     DOI: 10.1016/j.cbi.2007.01.009

Source DB:  PubMed          Journal:  Chem Biol Interact        ISSN: 0009-2797            Impact factor:   5.192


  23 in total

Review 1.  Microbial production of 2,3-butanediol for industrial applications.

Authors:  Chan Woo Song; Jong Myoung Park; Sang Chul Chung; Sang Yup Lee; Hyohak Song
Journal:  J Ind Microbiol Biotechnol       Date:  2019-08-29       Impact factor: 3.346

2.  Epigenetic events determine tissue-specific toxicity of inhalational exposure to the genotoxic chemical 1,3-butadiene in male C57BL/6J mice.

Authors:  Grace Chappell; Tetyana Kobets; Bridget O'Brien; Natalia Tretyakova; Dewakar Sangaraju; Oksana Kosyk; Kenneth G Sexton; Wanda Bodnar; Igor P Pogribny; Ivan Rusyn
Journal:  Toxicol Sci       Date:  2014-09-18       Impact factor: 4.849

3.  Structure and mechanism of styrene monooxygenase reductase: new insight into the FAD-transfer reaction.

Authors:  Eliot Morrison; Auric Kantz; George T Gassner; Matthew H Sazinsky
Journal:  Biochemistry       Date:  2013-08-20       Impact factor: 3.162

4.  Persistence and repair of bifunctional DNA adducts in tissues of laboratory animals exposed to 1,3-butadiene by inhalation.

Authors:  Melissa Goggin; Dewakar Sangaraju; Vernon E Walker; Jeffrey Wickliffe; James A Swenberg; Natalia Tretyakova
Journal:  Chem Res Toxicol       Date:  2011-04-13       Impact factor: 3.739

5.  Base Excision Repair of N6-Deoxyadenosine Adducts of 1,3-Butadiene.

Authors:  Susith Wickramaratne; Douglas M Banda; Shaofei Ji; Amelia H Manlove; Bhaskar Malayappan; Nicole N Nuñez; Leona Samson; Colin Campbell; Sheila S David; Natalia Tretyakova
Journal:  Biochemistry       Date:  2016-10-21       Impact factor: 3.162

6.  Column switching HPLC-ESI(+)-MS/MS methods for quantitative analysis of exocyclic dA adducts in the DNA of laboratory animals exposed to 1,3-butadiene.

Authors:  Melissa Goggin; Uthpala Seneviratne; James A Swenberg; Vernon E Walker; Natalia Tretyakova
Journal:  Chem Res Toxicol       Date:  2010-04-19       Impact factor: 3.739

Review 7.  Response of transposable elements to environmental stressors.

Authors:  Isabelle R Miousse; Marie-Cecile G Chalbot; Annie Lumen; Alesia Ferguson; Ilias G Kavouras; Igor Koturbash
Journal:  Mutat Res Rev Mutat Res       Date:  2015-05-30       Impact factor: 5.657

8.  Molecular dosimetry of 1,2,3,4-diepoxybutane-induced DNA-DNA cross-links in B6C3F1 mice and F344 rats exposed to 1,3-butadiene by inhalation.

Authors:  Melissa Goggin; James A Swenberg; Vernon E Walker; Natalia Tretyakova
Journal:  Cancer Res       Date:  2009-03-10       Impact factor: 12.701

9.  Palladium-catalyzed 1,4-difunctionalization of butadiene to form skipped polyenes.

Authors:  Matthew S McCammant; Longyan Liao; Matthew S Sigman
Journal:  J Am Chem Soc       Date:  2013-03-12       Impact factor: 15.419

10.  Quantitative high-performance liquid chromatography-electrospray ionization-tandem mass spectrometry analysis of the adenine-guanine cross-links of 1,2,3,4-diepoxybutane in tissues of butadiene-exposed B6C3F1 mice.

Authors:  Melissa Goggin; Chris Anderson; Soobong Park; James Swenberg; Vernon Walker; Natalia Tretyakova
Journal:  Chem Res Toxicol       Date:  2008-04-29       Impact factor: 3.739

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