The organic carbon (OC)-rich, black shale succession of the Middle Triassic Bravaisberget Formation in Spitsbergen contains scattered dolomite-ankerite cement in coarser-grained beds and intervals. This cement shows growth-related compositional trend from non-ferroan dolomite (0–5 mol % FeCO3) through ferroan dolomite (5–10 mol % FeCO3) to ankerite (10–20 mol % FeCO3, up to 1.7 mol % MnCO3) that is manifested by zoned nature of composite carbonate crystals. The d13C (-7.3‰ to -1.8‰ VPDB) and d18O (-9.4‰ to -6.0‰ VPDB) values are typical for burial cements originated from mixed inorganic and organic carbonate sources. The dolomite-ankerite cement formed over a range of diagenetic and burial environments, from early post-sulphidic to early catagenic. It reflects evolution of intraformational, compaction-derived marine fluids that was affected by dissolution of biogenic carbonate, clay mineral and iron oxide transformations, and thermal decomposition of organic carbon (decarboxylation of organic acids, kerogen breakdown). These processes operated during Late Triassic and post-Triassic burial history over a temperature range from approx. 40°C to more than 100°C, and contributed to the final stage of cementation of the primary pore space of siltstone and sandstone beds and intervals in the OC-rich succession.
Alkali-aggregate reactivity (AAR) is one of the major causes of damage in concrete. Potential susceptibility of aggregates to this reaction can be determined using several methods. This study compares gravel alkali reactivity results obtained from different tests conducted on coarse aggregates with complex petrography. The potential for the reactivity in the aggregates was revealed in the chemical test using treatment with sodium hydroxide. Optical microscopy, scanning electron microscopy and X-ray diffraction were used to identify the reactive constituents. The expansion measured in the mortar bars test confirmed that the aggregate was potentially capable of alkali silica reactivity with consequent deleterious effect on concrete.
The research was aimed at examining the impact of the petrographic composition of coal from the Janina mine on the gasification process and petrographic composition of the resulting char. The coal was subjected to fluidized bed gasification at a temperature below 1000°C in oxygen and CO2 atmosphere. The rank of coal is borderline subbituminous to bituminous coal. The petrographic composition is as follows: macerals from the vitrinite (61.0% vol.); liptinite (4.8% vol.) and inertinite groups (29.0% vol.). The petrofactor in coal from the Janina deposit is 6.9. The high content of macerals of the inertinite group, which can be considered inert during the gasification, naturally affects the process. The content of non-reactive macerals is around 27% vol. The petrographic analysis of char was carried out based on the classification of International Committee for Coal and Organic Petrology. Both inertoid (34.7% vol.) and crassinetwork (25.1% vol.) have a dominant share in chars resulting from the above-mentioned process. In addition, the examined char contained 3.1% vol. of mineroids and 4.3% vol. of fusinoids and solids. The calculated aromaticity factor increases from 0.75 in coal to 0.98 in char. The carbon conversion is 30.3%. Approximately 40% vol. of the low porosity components in the residues after the gasification process indicate a low degree of carbon conversion. The ash content in coal amounted to 13.8% and increased to 24.10% in char. Based on the petrographic composition of the starting coal and the degree of conversion of macerals in the char, it can be stated that the coal from the Janina deposit is moderately suitable for the gasification process.
Palaeomagnetic−petrographic−structural analyses of Proterozoic–Lower Palaeozoic metamorphosed carbonates from 12 locations within Oscar II Land (Western Spitsbergen) have been carried out to determine their usefulness in palaeogeographic reconstructions for Caledonian time. Structural analyses confirm that metacarbonates record several stages of deformation: D1, D2 ductile phases related to Caledonian metamorphism and a D3 brittle phase related to Late Cretaceous–Paleogene evolution of the West Spitsbergen Fold Belt. The latter is represented by thrust faults, localized folds with strain slip cleavages and late extensional collapse. Petrographic investigations reveal that Caledonian greenschist facies metamorphism was characterized by the high activity of H 2 O−CO 2 −rich fluids which promoted extensive recrystallization and within−rock spatial reorganization of sampled meta carbonates. Microscopic, SEM and microprobe analyses exclude the existence of any primary pre−metamorphic ferromagnetic minerals (primary−related to sedimentation and or early diagenesis) and point to metamorphic 4C superstructure (Fe 7 S 8 ) pyrrhotite as the main ferromagnetic carrier in investigated rocks. This is confirmed by the three−component isothermal remanent magnetization (IRM) procedures and the results of thermal demagnetizations. In 12 sites a total number of 72 independently oriented palaeomagnetic samples were collected from which 181 specimens were drilled and thermally demagnetized. Sampled metacarbonates are weakly magnetized (NRM <0.2mA/m). The statistically significant palaeomagnetic results were achieved only from 1 of 12 investigated sites. In one site situated in the Western overturned limb of the Holmesletfjellet Syncline intermediate unblocking temperatures – “pyrrhotite related” component WTSJ5M superimposed on the S1 Caledonian schistosity was recognized (D = 100.7 ° , I = −21.4 °a 95% = 5.5 ° , k = 58.23). Coincidence of WTSJ5M with Silurian–Devonian sector of the Baltica reference path after unfolding of the syncline by the angle of 130 ° suggests synfolding origin of this direction. Further, this suggests that Holmesletfjellet Syncline originated as an open fold and has been transformed into an overturned syncline during the Late Caledonian shortening or in the Late Cretaceous–Palaeogene time.
The aim of the paper is the petrographic characterization of coal from the Wieczorek mine and the residues after its gasification. The coal was subjected to gasification in a fluidized bed reactor at a temperature of about 900°C and in an atmosphere of oxygen and CO2. The petrographic, proximate, and ultimate analysis of coal and char was performed. The petrographic composition of bituminous coal is dominated by macerals of the vitrinite group (55% by volume); macerals of inertinite and liptinite groups account for 23% and 16.0%, respectively. In the examined char, the dominant component is inertoid (41% vol.). Mixed dense and mixed porous account for 10.9% and 13.5% vol., respectively. In addition, the examined char also contained unreacted particles such as fusinoids, solids (11.3% vol.), and mineroids (5.1% vol.). The char contains around 65% vol. of low porosity components, which indicates a low degree of carbon conversion and is associated with a low gasification temperature. The char was burned and the resulting bottom and fly ashes were subjected to petrographic analysis. Their composition was compared with the composition of ashes from the combustion of bituminous coal from the Wieczorek mine. Bottom ashes resulting from the combustion of bituminous coal and char did not differ significantly in the petrographic composition. The dominant component was mineroid, which accounted for over 80% vol. When it comes to fly ash, a larger amount of particles with high porosity is observed in fly ash from bituminous coal combustion.