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dc.contributor.authorTripathi D.-
dc.contributor.authorSingh R.K.-
dc.contributor.authorKumar K.-
dc.contributor.authorSingh, Udai Pratap-
dc.date.accessioned2022-02-22T11:41:49Z-
dc.date.available2022-02-22T11:41:49Z-
dc.date.issued2021-
dc.identifier.citationInternational Journal of Chemical Reactor Engineering-
dc.identifier.issn15426580-
dc.identifier.urihttps://doi.org/10.1515/ijcre-2021-0123-
dc.identifier.urihttp://repository.iitr.ac.in/handle/123456789/20861-
dc.description.abstractCoker kero stream is obtained from delayed coking which contains saturates with alpha olefins and PNA compounds which was physicochemical characterised. The fractions present in coker kero may be used further for value added products such as alkyl benzene and naphthalene etc. The study described potential of coker kero via aromatics and non-aromatics separation by using liquid-liquid extraction (LLE) with N-methyl pyrrolidone (NMP), acetonitrile and methanol as solvents of different polarity. Methanol imparts best colour improvement as per ASTM D-1500. Beside this, adsorption study on coker kero was performed using fuller's earth, chalk powder, red ochre and wood-stick's ash as adsorbents. The adsorption study suggested that fuller's earth not only separate aromatics and non-aromatics form coker kero, but also acts as a better adsorbent than graphitic carbon (activated charcoal) and is found suitable for colour improvement comparatively. This study inferred the separation of polar components, improvement in the colour, odour and established the stable fuel. FT-IR study suggested that N-methyl Pyrrolidone gives better results comparatively other solvents. HC22 type analysis of coker kero raffinate and extract phase confirm the sharp extraction of coker kero feed using N-Methyl pyrrolidone as it is a good solvent for extraction of aromatics. GCMS and HRMS compositional analysis successfully performed for the coker kero and it is separated aromatic and non-aromatic fractions. © 2021 Walter de Gruyter GmbH, Berlin/Boston 2021.-
dc.language.isoen_US-
dc.publisherDe Gruyter Open Ltd-
dc.relation.ispartofInternational Journal of Chemical Reactor Engineering-
dc.subjectcoker kero-
dc.subjectGCMS-
dc.subjectHC22-
dc.subjectLAB-
dc.subjectsolvent extraction-
dc.titleValue addition study on coker kero for producing alpha olefin and alkyl benzene-
dc.typeArticle-
dc.scopusid55620608000-
dc.scopusid57242460300-
dc.scopusid57225661487-
dc.scopusid57649843400-
dc.affiliationTripathi, D., Department of Chemistry, Indian Institute of Technology Roorkee, Uttarakhand, Roorkee, 247 667, India, Analytical Science Division, CSIR-Indian Institute of Petroleum, Uttarakhand, Dehradun, 248 005, India-
dc.affiliationSingh, R.K., Analytical Science Division, CSIR-Indian Institute of Petroleum, Uttarakhand, Dehradun, 248 005, India-
dc.affiliationKumar, K., Separation Process Division, CSIR-Indian Institute of Petroleum, Uttarakhand, Dehradun, 248 005, India-
dc.affiliationSingh, U.P., Department of Chemistry, Indian Institute of Technology Roorkee, Uttarakhand, Roorkee, 247 667, India-
dc.description.fundingThe dominance of extracted aromatics was also supported by FT-IR spectra . The prominent peaks observed at 1693 cm of C=O stretching, followed by bending of C–N–C at 1225 cm confirms the contamination of NMP in the extract. The peaks of CH stretching vibrations at 2955,2925 and 2855 cm regions indicate the coker kero extract also contains saturates, which is further confirmed by CH bending at 1467 and 1378 cm and support the presence of 6.2 wt% of saturates (). The absorption near 1601 cm of C=C stretching of aromatics shows the presence of a significant concentration of aromatics in the extract. The various absorption bands of bending vibrations in the 965–701 cm regions are the characteristics of various substituted aromatic structures, which are further confirmed by relative absorbance. This suggests the presence of alkyl-substituted benzenes 4.0 wt%. () in concentration in coker kero extract. The extract also contains 18.2 wt% of naphthalene; therefore, it can be used for the commercial production of naphthalene balls. −1 −1, 2 −1 2 −1 −1 −1-
dc.description.correspondingauthorTripathi, D.; Department of Chemistry, Uttarakhand, India; email: dtripathi@cy.iitr.ac.in Singh, U.P.; Department of Chemistry, Uttarakhand, India; email: u.singh@cy.iitr.ac.in-
Appears in Collections:Journal Publications [CY]

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