Investigation of formation and structural characteristics of the adsorbed layer of organic matter on suspended mineral particles after the examples of gumat Na adsorbtion processes on clay minerals

2004 ◽  
Author(s):  
P. V. Postnikova ◽  
Anatolii D. Aponasenko ◽  
V. S. Filimonov
Clay Minerals ◽  
2018 ◽  
Vol 53 (4) ◽  
pp. 579-602 ◽  
Author(s):  
Tatiana Maison ◽  
Sébastien Potel ◽  
Pierre Malié ◽  
Rafael Ferreiro Mählmann ◽  
Frank Chanier ◽  
...  

ABSTRACTClay minerals and organic matter occur frequently in fault zones. Their structural characteristics and their textural evolution are driven by several formation processes: (1) reaction by metasomatism from circulating fluids; (2)in situevolution by diagenesis; and (3) neoformation due to deformation catalysis. Clay-mineral chemistry and precipitated solid organic matter may be used as indicators of fluid circulation in fault zones and to determine the maximum temperatures in these zones. In the present study, clay-mineral and organic-matter analyses of two major fault zones – the Adams-Tinui and Whakataki faults, Wairarapa, North Island, New Zealand – were investigated. The two faults analysed correspond to the soles of large imbricated thrust sheets formed during the onset of subduction beneath the North Island of New Zealand. The mineralogy of both fault zones is composed mainly of quartz, feldspars, calcite, chabazite and clay minerals such as illite-muscovite, kaolinite, chlorite and mixed-layer minerals such as chlorite-smectite and illite-smectite. The diagenesis and very-low-grade metamorphism of the sedimentary rock is determined by gradual changes of clay mineral ‘crystallinity’ (illite, chlorite, kaolinite), the use of a chlorite geothermometer and the reflectance of organic matter. It is concluded here that: (1) the established thermal grade is diagenesis; (2) tectonic strains affect the clay mineral ‘crystallinity’ in the fault zone; (3) there is a strong correlation between temperature determined by chlorite geothermometry and organic-matter reflectance; and (4) the duration and depth of burial as well as the pore-fluid chemistry are important factors affecting clay-mineral formation.


1984 ◽  
Vol 19 (1) ◽  
pp. 27-36 ◽  
Author(s):  
Alena Mudroch

Abstract Surface sediment samples obtained at the offshore and nearshore area of Lake Erie were separated into eight different size fractions ranging from <2 µm to 250 µm. The concentration of major elements (Si, Al, Ca, Mg, K, Na, Fe, Mn and P), metals (Zn, Cu, Cr, Ni, V, Co and Pb) and organic matter was determined together with the mineralogical composition and morphology of the particles in each size fraction. The distribution of the metals in the offshore sediment was bimodal with the majority of the metals divided between the 63 to 250 um size fraction which also contained the highest concentration of organic matter (about 20%) and the <4 µm fraction containing up to 60% of clay minerals. However, the metals in the nearshore sediment were associated mainly with the clay minerals.


2021 ◽  
Vol 213 ◽  
pp. 106235
Author(s):  
Longmeng Wei ◽  
Hongling Bu ◽  
Yanfu Wei ◽  
Honghai Wu ◽  
Gehui Wang ◽  
...  

Fuel ◽  
2014 ◽  
Vol 135 ◽  
pp. 359-373 ◽  
Author(s):  
Utpalendu Kuila ◽  
Douglas K. McCarty ◽  
Arkadiusz Derkowski ◽  
Timothy B. Fischer ◽  
Tomasz Topór ◽  
...  

2020 ◽  
Vol 49 (6) ◽  
pp. 728-731
Author(s):  
Kenta Asahina ◽  
Takeshi Nakajima ◽  
Kazuya Morimoto ◽  
Yasuaki Hanamura ◽  
Miyuki Kobayashi

Energies ◽  
2020 ◽  
Vol 13 (7) ◽  
pp. 1690
Author(s):  
Yong Han ◽  
Yanming Zhu ◽  
Yu Liu ◽  
Yang Wang ◽  
Han Zhang ◽  
...  

This study focuses on the nanostructure of shale samples with type III kerogen and its effect on methane adsorption capacity. The composition, pore size distribution, and methane adsorption capacities of 12 shale samples were analyzed by using the high-pressure mercury injection experiment, low-temperature N2/CO2 adsorption experiments, and the isothermal methane adsorption experiment. The results show that the total organic carbon (TOC) content of the 12 shale samples ranges from 0.70% to ~35.84%. In shales with type III kerogen, clay minerals and organic matter tend to be deposited simultaneously. When the TOC content is higher than 10%, the clay minerals in these shale samples contribute more than 70% of the total inorganic matter. The CO2 adsorption experimental results show that micropores in shales with type III kerogen are mainly formed in organic matter. However, mesopores and macropores are significantly affected by the contents of clay minerals and quartz. The methane isothermal capacity experimental results show that the Langmuir volume, indicating the maximum methane adsorption capacity, of all the shale samples is between 0.78 cm3/g and 9.26 cm3/g. Moreover, methane is mainly adsorbed in micropores and developed in organic matter, whereas the influence of mesopores and macropores on the methane adsorption capacity of shale with type III kerogen is small. At different stages, the influencing factors of methane adsorption capacity are different. When the TOC content is <1.4% or >4.5%, the methane adsorption capacity is positively correlated with the TOC content. When the TOC content is in the range of 1.4–4.5%, clay minerals have obviously positive effects on the methane adsorption capacity.


2019 ◽  
Vol 85 (10) ◽  
Author(s):  
Tao Wang ◽  
Zhaomo Tian ◽  
Anders Tunlid ◽  
Per Persson

ABSTRACT The interactions between dissolved organic matter (DOM) and mineral particles are critical for the stabilization of soil organic matter (SOM) in terrestrial ecosystems. The processing of DOM by ectomycorrhizal fungi contributes to the formation of mineral-stabilized SOM by two contrasting pathways: the extracellular transformation of DOM (ex vivo pathway) and the secretion of mineral-surface-reactive metabolites (in vivo pathway). In this study, we examined how changes in nitrogen (N) availability affected the formation of mineral-associated carbon (C) from these two pathways. DOM was extracted from forest soils. The processing of this DOM by the ectomycorrhizal fungus Paxillus involutus was examined in laboratory-scale studies with different levels of ammonium. At low levels of ammonium (i.e., under N-limited conditions), the DOM components were slightly oxidized, and fungal C metabolites with iron-reducing activity were secreted. Ammonium amendments decreased the amount of C metabolites, and no additional oxidation of the organic matter was detected. In contrast, the hydrolytic activity and the secretion of N-containing compounds increased, particularly when high levels of ammonium were added. Under these conditions, C, but not N, limited fungal growth. Although the overall production of mineral-associated organic C was not affected by ammonium concentrations, the observed shifts in the activities of the ex vivo and in vivo pathways affected the composition of organic matter adsorbed onto the mineral particles. Such changes will affect the properties of organic matter-mineral associations and, thus, ultimately, the stabilization of SOM. IMPORTANCE Nitrogen (N) availability plays a critical role in the cycling and storage of soil organic matter (SOM). However, large uncertainties remain in predicting the net effect of N addition on soil organic carbon (C) storage due to the complex interactions between organic matter, microbial activity, and mineral particles that determine the formation of stable SOM. Here, we attempted to disentangle the effects of ammonium on these interactions in controlled microcosm experiments including the ectomycorrhizal fungus P.involutus and dissolved organic matter extracted from forest soils. Increased ammonium levels affected the fungal processing of the organic material as well as the secretion of extracellular metabolites. Although ammonium additions did not increase the net production of mineral-adsorbed C, changes in the decomposition and secretion pathways altered the composition of the adsorbed organic matter. These changes may influence the properties of the organic matter-mineral associations and, thus, the stabilization of SOM.


2020 ◽  
Vol 195 ◽  
pp. 107926
Author(s):  
Guangzhao Zhou ◽  
Zhaobin Gu ◽  
Zhiming Hu ◽  
Jin Chang ◽  
Xianggang Duan ◽  
...  

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