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Fractionation of Asphaltene by Adsorption onto Silica and Chemical Characterization by Atmospheric Pressure Photoionization Fourier Transform Ion Cyclotron Resonance Mass Spectrometry, Fourier Transform Infrared Spectroscopy Coupled to Attenuated Total Reflectance, and Proton Nuclear Magnetic Resonance

2016· article· en· W2432538881 on OpenAlexfundno aff
Priscila T. H. Nascimento, Alexandre F. Santos, Carlos Itsuo Yamamoto, Lílian V. Tose, Eliane V. Barros, Gustavo R. Gonçalves, Jair C. C. Freitas, Boniek G. Vaz, Wanderson Romão, Agnes de Paula Scheer

Bibliographic record

VenueEnergy & Fuels · 2016
Typearticle
Languageen
FieldChemistry
TopicPetroleum Processing and Analysis
Canadian institutionsnot available
FundersTotalNorges ForskningsrådStatoilPetrobrasConselho Nacional de Desenvolvimento Científico e TecnológicoAkzoNobelCoordenação de Aperfeiçoamento de Pessoal de Nível SuperiorNatural Resources CanadaBP
KeywordsFourier transform ion cyclotron resonanceAsphalteneChemistryAttenuated total reflectionFourier transform infrared spectroscopyAnalytical Chemistry (journal)Mass spectrometryAdsorptionPhotoionizationInfrared spectroscopyOrganic chemistryChromatographyIonChemical engineeringIonization

Abstract

fetched live from OpenAlex

Asphaltenes are defined as the petroleum fraction insoluble in n -alkanes and soluble in aromatic solvents, such as toluene. Such definition implies that asphaltenes are not a homogeneous material but a mixture of fractions. Asphaltenes represent one of the major contributors to several problematic issues for the petroleum industry. Destabilized asphaltenes can cause arterial clogging within pipelines and wellbores, corrosion and fouling of production equipment, reduction of catalyst activity in refining processes, and other problems. This work describes an investigation of the separation of asphaltenes into three different fractions by adsorption onto silica particles. These fractions (two adsorbed and one non-adsorbed onto silica) were characterized by elemental analysis (C, H, and N), Fourier transform infrared spectroscopy coupled to attenuated total reflectance (ATR–FTIR), proton nuclear magnetic resonance ( 1 H NMR) spectroscopy, and atmospheric pressure photoionization Fourier transform ion cyclotron resonance mass spectrometry (APPI–FT-ICR MS). APPI–FT-ICR MS and ATR–FTIR accessed chemical information on a molecular level [molecular formula, carbon number (CN) and double bond equivalent (DBE) distributions, and organic groups], whereas 1 H NMR and elemental analysis provided the aromaticity degree and C/H atomic ratio of the samples, respectively. The C/H atomic ratio decreases in the following the order: non-adsorbed > whole asphaltene > adsorbed > irreversibly adsorbed. The irreversible fraction adsorbed had the lowest percentage of aromatic hydrogen compared to other fractions by 1 H NMR. There was a good correlation between the results of NMR and elemental analysis. The efficiency of fractionation on silica particles was proven to be successful by the low concentration of polyaromatic hydrocabons observed for two samples adsorbed onto silica and the increasing of the aromaticity degree and C/H ratio for the non-adsorbed fraction. N 2, N 2 O, and NO compound classes were selectively separated from whole asphaltene and concentrated in polar fractions (adsorbed fractions onto silica), with their CN and DBE distributions reported. Therefore, this work demonstrated the selectivity of the fractionation method onto silica to retain highly polar compounds and, moreover, extends to the study of the adsorbent surface and how the molecules of the asphaltenes will behave against this change.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesMeta-epidemiology (narrow)
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.052
Threshold uncertainty score1.000

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.001
Science and technology studies0.0000.000
Scholarly communication0.0000.001
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.003
GPT teacher head0.199
Teacher spread0.196 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations45
Published2016
Admission routes1
Has abstractyes

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