In general, ionospheric scintillations at low latitude are considered as signatures of equatorial plasma bubbles (depletions). However, some authors considered that scintillations may also be associated with plasma blobs (enhancements), but there was no in situ measurement hitherto to confirm it. We performed a case study on the concurrent observation of an ionospheric plasma blob with in situ measurements by ROCSAT‐1 (i.e. Formosa satellite‐1) and of GPS amplitude scintillations in the low‐latitude ionosphere on 1 June 2003. The blob measured in situ had a scale size of about 800 km in the F layer, and the ion density inside the blob was severely disturbed. Amplitude scintillation with S₄ > 0.3 was observed concurrently in the same longitude range as the blob measured. This case study provides evidence of simultaneously observed GPS amplitude scintillations and a blob in situ, and it confirms that scintillations can be associated with plasma blobs in the low‐latitude ionosphere.

Ketone compounds are oxidation products of crude oil in the in-situ combustion (ISC) process. Revealing the molecular composition of ketones can provide theoretical guidance for understanding the oxidation process of crude oil and valuable clues for studying the combustion state of crude oil in the reservoir. In this study, low-temperature oxidation (LTO) processes were simulated in thermal oxidation experiments to obtain thermally oxidized oil at different temperatures (170 °C, 220 °C, 270 °C, and 320 °C). A combination of chemical derivatization and positive-ion electrospray (ESI) Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) was used to analyze the molecular composition of different kinds of ketones (fatty ketones, naphthenic ketones, and aromatic ketones) in the oxidized oils at different temperatures. The results showed that the concentration of aliphatic ketones and aliphatic cyclic ketones in the product oils decreased with the increase in temperature, while aromatic ketones increased with the increase in temperature. At the same oxidation temperature, the content of ketones follows this order: fatty ketones < cycloalkanes < aromatic ketones. The concentrations of ketones reached their maximum value at 170 °C and decreased at high temperatures due to over-oxidation. It was also found that nitrogen-containing compounds are more easily oxidized to ketone compounds than their hydrocarbon counterparts in the LTO process.

This study conducted in situ combustion oxidation experiments on crude oil from Block D within the Liaohe Oilfield, utilizing a kettle furnace low-pressure oxidation reaction method at various temperatures. The molecular composition of oxidation products was analyzed using gas chromatography–mass spectrometry (GC–MS) and high-resolution mass spectrometry. The results reveal that the molecular composition of the products remains relatively stable up to 300 °C, exhibiting a slight increase in C₁₃-C₃₀ alkanes. The ratio of the peak area for C₂₁ to bisnorhopane is 0.082. From 300 °C to 450 °C, compounds with long alkyl chains gradually undergo thermal cracking, resulting in a significant increase in the production of alkanes within the C₁₀–C₃₀ range. The concentration of saturated hydrocarbons produced through thermal cracking reaches its maximum at a temperature of 400 °C. The most abundant peak of n-alkane is observed at C₂₁, with a quantified ratio of peak area for C₂₁ to bisnorhopane at 6.5, indicating a two-order magnitude increase compared to crude oil. From 500 °C to 600 °C, compounds undergo more profound thermal cracking and condensation processes. The predominant hydrocarbons consist of aromatic molecules containing two to six rings substituted with short side chains. The double bond equivalent (DBE) values of carbazoles and carboxylic acids are determined as 30 and 25, respectively. At 600 °C, the peak area ratio of naphthalene to biodecane is 300, indicating a remarkable increase of five orders of magnitude compared to the crude oil. The present study elucidates the correlation between the characteristics of combustion components in crude oil and the corresponding combustion temperature. Primary cracking reactions within crude oil are promoted effectively when keeping the combustion zone at 350 °C and 450 °C. This process significantly reduces the viscosity of heavy oil and enhances its fluidity.

This study investigates coke formation, structure, and combustion behaviors in paraffin-based Menggulin and naphthenic-based Xinjiang heavy oils under simulated in-situ combustion (ISC) conditions (350 °C, 450 °C), utilizing GC-MS, SEM, ¹³C ss-NMR, and TG-DSC. The results indicate that the crude oil composition determines the coking mechanisms: Xinjiang oil, rich in cyclic hydrocarbons and O/N/S heteroatoms, forms high-yield, compact, sheet- or block-like coke at 350 °C via π–π stacking. In contrast, Menggulin oil, composed primarily of long-chain alkanes, yields loose coke at 350 °C but produces dense, highly aromatized coke at 450 °C, which corresponds to the critical alkane cracking temperature, through intense cracking–polymerization. Temperature differentially regulates oxidative processes, thereby shaping the divergent functional group distributions. Correlations between coke structure and combustion properties reveal that oxygenated/aliphatic-rich cokes exhibit high reactivity, whereas aromatized cokes release more heat. These findings provide guidance for ISC optimization, suggesting that sufficient high-temperature energy is required for paraffinic oils while medium-temperature oxidation regulation is suitable for naphthenic oils. This work advances the theory of ISC coke formation and supports enhanced recovery of heavy oils.