Simultaneous Experimental Analysis of Oil Content And Molecular Composition of Shale Fractions

The important research content and basis of exploration and development is to evaluate the reservoir property, oil bearing property, fluidity and compressibility of shale reservoir.The key of exploration and development is to evaluate the oil-bearing and fluidity of shale reservoir.In this paper, the "shale oil content and fine components synchronous experimental analysis device" is used. Five temperature ranges of 30 ℃-90 ℃, 90 ℃-150 ℃, 100 ℃- 200 ℃, 150 ℃-250 ℃ and 250 ℃-300 ℃ were adopted. The heating rate of each temperature segment was 25 ℃ / min, and the final temperature was kept constant for 5 min. The oil content of shale (pyrolysis S1) was cut into five fractions.Simultaneous determination of oil content and molecular composition of shale fractions,and the external standard method was used to evaluate the oil content and fluidity.The results show that the five fractions of shale are mainly composed of nC1-nC9 gas, nC10-nC15 gasoline, nC12-nC20 kerosene, nC15-nC22 diesel oil and nC18-nC26 heavy oil of the first member of Qingshangkou formation in Songliao basin.There are differences in the fractionation and oil content characteristics of samples with different maturity in different wells.The parent material, properties and quality of crude oil are reflected in shale. The higher the maturity of shale oil is, the more light components are, the larger the light / heavy ratio parameter value of (gasoline + kerosene + diesel) and heavy oil is, the better the fluidity is, and the easier to exploit effectively.

The Impact of Agricultural Use of Retisols on the Molecular Structure of Humic Substances

Agricultural soil use does not only affect the amount of soil organic matter, but also the molecular composition of humic (HAs) and fulvic acids (FAs). Changed hydrothermal conditions and composition of the incoming plant residues are reflected in the rate of humification and its products. The objective of this study was to compare the molecular composition of HAs and FAs isolated from Eutric Albic Stagnic Histic Retisol (Loamic), two Eutric Albic Retisols (Loamic)—mature and arable. Plots of mature Retisols are located at a middle taiga (Komi Republic, Russia) in a bilberry-green-moss birch-spruce forest. The plot of Retisols arable is located in the fields of the Syktyvkar state farm, which is 3.3 km northeast of mature Retisol plots. The development period is about 40 years, it is sowed with a pea-oat mixture. The results obtained indicate that soil reclamation essentially increases the proportion of aromatic components and decreases the content of carboxyl and ester groups in the humic substance (HS) structure. An increased extent of hydromorphism of Retisols leads to the enrichment of HS with aliphatic fragments.

Investigation of the Effect of Nanocrystalline Calcium Carbonate-Substituted Hydroxyapatite and L-Lysine and L-Arginine Surface Interactions on the Molecular Properties of Dental Biomimetic Composites

Differences in the surface interactions of non-stoichiometric nanocrystalline B-type carbonate-substituted hydroxyapatite (n-cHAp) with the amino acids L-Lysine hydrochloride (L-LysHCl) and L-Arginine hydrochloride (L-ArgHCl) in acidic and alkaline media were determined using structural and spectroscopic analysis methods. The obtained data confirm that hydroxyapatite synthesized using our technique, which was used to develop the n-cHAp/L-LysHCl and n-cHAp/L-ArgHCl composites, is nanocrystalline. Studies of molecular composition of the samples by Fourier transform infrared spectroscopy under the change in the charge state of L-Lysine in environments with different alkalinity are consistent with the results of X-ray diffraction analysis, as evidenced by the redistribution of the modes’ intensities in the spectra that is correlated with the side chains, i.e., amide and carboxyl groups, of the amino acid. During the formation of a biomimetic composite containing L-Lysine hydrochloride and n-cHAp, the interaction occurred through bonding of the L-Lysine side chain and the hydroxyl groups of hydroxyapatite, which created an anionic form of L-Lysine at pH ≤ 5. In contrast, in biocomposites based on L-Arginine and n-cHAp, the interaction only slightly depends on pH value, and it proceeds by molecular orientation mechanisms. The X-ray diffraction and infrared spectroscopy results confirm that changes in the molecular composition of n-cHAp/L-ArgHCl biomimetic composites are caused by the electrostatic interaction between the L-ArgHCl molecule and the carbonate-substituted calcium hydroxyapatite. In this case, the bond formation was detected by Fourier transform infrared (FTIR) spectroscopy; the vibrational modes attributed to the main carbon chain and the guanidine group of L-Arginine are shifted during the interaction. The discovered interaction mechanisms between nanocrystalline carbonate-substituted hydroxyapatite that has physicochemical properties characteristic of the apatite in human dental enamel and specific amino acids are important for selecting the formation conditions of biomimetic composites and their integration with the natural dental tissue.

The study of molecular composition in biomimetic interface of biocomposite/dentin

The aim of the study is the problem of formation of the biomimetic interface between the dental product and dentin of the human tooth as well as the investigations of molecular-chemical features in biointerface with the use of molecular multivariate IR-visualization. The data on synchrotron IR-mapping made enabled to differentiate the regions of sound dentin tissue and biomimetic transition layer and also to determine molecular groups responsible for the process of integration.