2019
DOI: 10.1021/acs.energyfuels.8b03760
|View full text |Cite
|
Sign up to set email alerts
|

Determination of Olefin Contents in Liquid Hydrocarbons Using a Quantum Cascade Laser and a Photoacoustic Detector

Abstract: The determination of olefin contents in liquid hydrocarbons by means of laser-based infrared spectroscopy was demonstrated for the first time in this work. This new technique utilizes a commercial mid-infrared external-cavity quantum cascade laser and a photoacoustic detector to monitor characteristic olefin CC absorption bands in the ∼1640–1680 cm–1 (5.95–6.1 μm) region. It is suitable for measurements of olefin concentrations in a variety of samples, including those derived from partially upgraded bitumen. … Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

0
5
0

Year Published

2020
2020
2023
2023

Publication Types

Select...
6
1

Relationship

1
6

Authors

Journals

citations
Cited by 11 publications
(5 citation statements)
references
References 24 publications
0
5
0
Order By: Relevance
“…When replacing with 2% PA‐g‐Kaol, P═O decreased gradually after 400°C, that was the reason of the decompose of PA‐g‐Kaol. Compared with EVA/IFR/Kaol, ─CH 2 can exist until 500°C, it was proposed that the PA‐g‐Kaol can better protect the EVA matrix from degradation 38–40 …”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…When replacing with 2% PA‐g‐Kaol, P═O decreased gradually after 400°C, that was the reason of the decompose of PA‐g‐Kaol. Compared with EVA/IFR/Kaol, ─CH 2 can exist until 500°C, it was proposed that the PA‐g‐Kaol can better protect the EVA matrix from degradation 38–40 …”
Section: Resultsmentioning
confidence: 99%
“…Compared with EVA/IFR/Kaol, CH 2 can exist until 500 C, it was proposed that the PA-g-Kaol can better protect the EVA matrix from degradation. [38][39][40] GC-MS was used to study the exact composition of the degradation products and investigated the pyrolysis mechanism of EVA in 650 C in order to further demonstrate the specific composition of condensed phase at high temperature (Figure S3, Figure S4, and Table S1). According to the retention time and ion signals, it can be found that the residues belong to EVA/IFR/PA-g-Kaol in 650 C was similar with EVA/IFR/Kaol, which indicated that PA-g-Kaol mainly played an important role in the gas-phase during the early stage of combustion (<425 C).…”
Section: Proposed Mechanismmentioning
confidence: 99%
“…Analysis of an industrially produced cracked naphtha revealed that the cracked naphtha contained about 10 wt % olefins, that most of the olefins were aliphatic, and that the olefins were mainly concentrated in the C 5 –C 7 range . Using a photoacoustic detector, a different group characterized the 30–280 °C cut produced from thermal conversion of bitumen and found 6.3 wt % olefins . The main assumption that was made in proposing the olefin treatment process in Figure was that these olefins could be saturated by hydrogen transfer reactions under thermal conditions.…”
Section: Resultsmentioning
confidence: 99%
“…13,14 The commonly used methods for determination of olefin content are fluorescent indicator adsorption (FIA); 15 the bromine number test; 16 PIONA (n-paraffin, isoparaffin, olefin, naphthene, and aromatic) analysis by DHA (detailed hydrocarbon analysis); 17 supercritical-fluid chromatography; 18,19 proton nuclear magnetic resonance spectroscopy ( 1 H NMR); 20,21 gas chromatography (GC) with vacuum-ultraviolet detection (VUV); 22 high-performance liquid chromatography (HPLC), 23,24 or spectroscopy. 25 One of the most popular and well-adopted techniques for determination of conjugated diene content is the UOP-326 method, which is based on the determination of the diene value calculated from the concentration of unreacted maleic anhydride. 26 However, some of the previously mentioned methods and techniques exhibit notable limitations, such as prolonged analysis durations, the necessity for costly apparatus, extensive employment of solvents, and the dependence on high-quality gases (carrier or sweep gases).…”
Section: Introductionmentioning
confidence: 99%
“…Several studies on analytical methods for olefin and diolefin determination are available in the literature. , The commonly used methods for determination of olefin content are fluorescent indicator adsorption (FIA); the bromine number test; PIONA (n-paraffin, isoparaffin, olefin, naphthene, and aromatic) analysis by DHA (detailed hydrocarbon analysis); supercritical-fluid chromatography; , proton nuclear magnetic resonance spectroscopy ( 1 H NMR); , gas chromatography (GC) with vacuum-ultraviolet detection (VUV); high-performance liquid chromatography (HPLC), , or spectroscopy . One of the most popular and well-adopted techniques for determination of conjugated diene content is the UOP-326 method, which is based on the determination of the diene value calculated from the concentration of unreacted maleic anhydride .…”
Section: Introductionmentioning
confidence: 99%