Ways to improve the well-being of the population of Vietnam

The article is devoted to the welfare problem of people in Vietnam. In this study, the emphasis is laid on the economic component of population welfare. Some basic indicator of the population welfare in Vietnam are adduced and analyzed. The problems are identified and then suggest ways to improve the welfare, the level of growth and the quality of life of the population in Vietnam. The views on the socio-economic category of "well-being" transformed throughout human evolution, depending on the level of scientific and technological progress, the quantity and quality of economic goods, religious and ethical standards, consumer preferences of society. Initially, this category is viewed only through the prism of well-being, we investigated how to achieve a uniform distribution of income society. A modern interpretation of the well-being lies in the fact that the well-being - is a basic social value, which is primarily created by the state through the redistribution of national income, the rational allocation and efficient use of economic resources for the population social and 565 economic benefits, and that, as a result contributes to sustainable the development of the national economy

Влияние концентрации модификатора на структурные и функциональные свойства модифицированных нановолокон оксигидроксида алюминия

It was shown that the concentration of the modifier (manganese ions (II)) significantly affects the structural properties of the modified aluminum oxyhydroxide. In the phase composition of the samples modified and reduced content hydroxid and oxyhydroxide aluminum phases, which leads to a drop of the specific surface area from 196,16 to 10,78 m2/g. In the modified heating samples in air joint formed of aluminum oxide and manganese phase - MnAl2O4, and in the sample with the highest content of manganese oxides, manganese own found - Mn3O4, Mn2O3. The presence of manganese oxide phases making a modified aluminum oxyhydroxide promising as a catalyst for the oxidation of organic and inorganic compounds

Evaluation of the trends of secondary and tertiary hydrocarbon migration processes based on oil density–reservoir depths relationship in Hungary

Depth of reservoirs of Hungarian oil fields and related oil density data were collected from the database of the Hungarian Mineral Resource Inventory. The purpose of the investigation was to point out the correlation between oil density and reservoir depth in some of the Hungarian hydrocarbon productive regions. Oil density related to reservoir depth in a particular area is generally linked to the migration mechanism. Zala Basin trends show a different migration process regionally and locally; tertiary migration by overflow mechanism can be supposed for the latter case. In the case of the Szeged–Kiskunság region, locally and regionally, migration along carrier beds through semipermeable sediments is present, with faults playing a significant role. In the Nagykunság region, the migration processes are similar to those in Zala, but the presence of faults seems more important. At depths below 2,000 m, the Bihar region trends are similar to those of the Szeged–Kiskunság region. In the shallower zone, hydrodynamic effects are recognizable. In two studied regions, the Battonya–Pusztaföldvár High and the Hungarian Paleogene Basin, the density of crude oil data does not show any significant variability and trend. Biodegradation and water washing were recognizable in the depth sections shallower than 2,000 m below surface. In karstic reservoirs of the Zala Basin (Nagylengyel, Sávoly), alteration is presumed at greater depths due to the karst water flow. The presented results show several trends of oil migration in the explored areas, which can be used for future estimation of the hydrocarbon potential in the Hungarian part of the Pannonian Basin

Influence of palaeoweathering on trace metal concentrations and environmental proxies in black shales

The mineralogical and chemical compositions of Lower Carboniferous (Tournaisian) marine black shale from the Kowala quarry, the Holy Cross Mountains, Poland, were investigated. This study focuses on disturbances in palaeoenvironmental proxies caused by palaeoweathering, which progressively changed the major and trace element abundances. Palaeomagnetic investigations reveal that the Devonian – Carboniferous succession was weathered during the Permian-Triassic by the infiltration of oxidizing fluids related to karstification following post-Variscan exhumation. The weathering process led to vermiculitization of chlorite, partial dissolution of calcite and replacement of pyrite by hematite and goethite. Moreover, the concentrations of some trace metals, including Co, Cu, Pb, Mo, Ni, As and U, significantly decreased. Consequently, some elemental abundance ratios that are used as environmental proxies, including U/Th, Ni/Co and V/Cr, were altered. Elements that are bound to iron sulphides (e.g., Mo) appear to be especially prone to mobilization by even a lightly weathered black shale. The documented weathering, including changes in elemental concentrations, can potentially create misinterpretations of the original palaeoenvironmental conditions. In addition, the palaeoweathering of the studied samples appears to have substantially changed the carbon, oxygen, nitrogen and molybdenum stable isotope values. The nitrogen and molybdenum stable isotope ratios, in particular, appear to be most sensitive to the effects of weathering and therefore are good indicators of (palaeo)weathering processes. The major cause of these changes is the decay of organic matter and pyrite. For the organic carbon stable isotopes ratios, the main factor that controlls this process appears to be the preferential degradation of labile organic matter. A combination of the total organic carbon (TOC), total sulphur (TS) content, Mo concentration and stable isotope compositions seems to be the most useful for identify (palaeo)weathering. Our results suggest that reductions in TS and Mo in tandem with diminished Mo stable isotope values in the absence of obvious changes to the TOC content provide the most compelling evidence of (palaeo)weathering

Stream and slope weathering effects on organic-rich mudstone geochemistry and implications for hydrocarbon source rock assessment: a Bowland Shale case study

This study contributes to the exploration and quantification of the weathering of organic-rich mudstones under temperate climatic conditions. Bowland Shales, exposed by a stream and slope, were sampled in order to develop a model for the effects of weathering on the mudstone geochemistry, including major and trace element geochemistry, Rock-Eval pyrolysis and δ13Corg. Four weathering grades (I – IV) are defined using a visual classification scheme; visually fresh and unaltered (I), chemically altered (II, III) and ‘paper shale’ that typifies weathered mudstone on slopes (IV). Bedload abrasion in the stream exposes of visually fresh and geochemically unaltered mudstone. Natural fractures are conduits for oxidising meteoric waters that promote leaching at the millimetre scale and/or precipitation of iron oxide coatings along fracture surfaces. On the slope, bedding-parallel fractures formed (and may continue to form) in response to chemical and/or physical weathering processes. These fractures develop along planes of weakness, typically along laminae comprising detrital grains, and exhibit millimetre- and centimetre-scale leached layers and iron oxide coatings. Fracture surfaces are progressively exposed to physical weathering processes towards the outcrop surface, and results in disintegration of the altered material along fracture surfaces. Grade IV, ‘paper shale’ mudstone is chemically unaltered but represents a biased record driven by initial heterogeneity in the sedimentary fabric. Chemically weathered outcrop samples exhibit lower concentrations of both ‘free’ (S1) (up to 0.6 mgHC/g rock) and ‘bound’ (S2) (up to 3.2 mgHC/g rock) hydrocarbon, reduced total organic carbon content (up to 0.34 wt%), reduced hydrogen index (up to 58 mgHC/gTOC), increased oxygen index (up to 19 mgCO + CO2/gTOC) and increased Tmax (up to 11 °C) compared with unaltered samples. If analysis of chemically weathered samples is unavoidable, back-extrapolation of Rock-Eval parameters can assist in the estimation of pre-weathering organic compositions. Combining Cs/Cu with oxygen index is a proxy for identifying the weathering progression from fresh material (I) to ‘paper shale’ (IV). This study demonstrates that outcrop samples in temperate climates can provide information for assessing hydrocarbon potential of organic-rich mudstones

Geogenic and atmospheric sources for volatile organic compounds in fumarolic emissions from Mt. Etna and Vulcano Island (Sicily, Italy)

In this paper, fluid source(s) and processes controlling the chemical composition of volatile organic compounds (VOCs) in gas discharges from Mt. Etna and Vulcano Island(Sicily, Italy) were investigated. The main composition of the Etnean and Volcano gas emissions is produced by mixing, to various degrees, of magmatic and hydrothermal components. VOCs are dominated by alkanes, alkenes and aromatics, with minor, though significant, concentrations of O-, S- and Cl(F)-substituted compounds. The main mechanism for the production of alkanes is likely related to pyrolysis of organic-matterbearing sediments that interact with the ascending magmatic fluids. Alkanes are then converted to alkene and aromatic compounds via catalytic reactions (dehydrogenation and dehydroaromatization, respectively). Nevertheless, an abiogenic origin for the light hydrocarbons cannot be ruled out. Oxidative processes of hydrocarbons at relatively high temperatures and oxidizing conditions, typical of these volcanic-hydrothermal fluids, may explain the production of alcohols, esters, aldehydes, as well as O- and S-bearing heterocycles. By comparing the concentrations of hydrochlorofluorocarbons (HCFCs) in the fumarolic discharges with respect to those of background air, it is possible to highlight that they have a geogenic origin likely due to halogenation of both methane and alkenes. Finally, chlorofluorocarbon (CFC) abundances appear to be consistent with background air, although the strong air contamination that affects the Mt. Etna fumaroles may mask a possible geogenic contribution for these compounds. On the other hand, no CFCs were detected in the Vulcano gases, which are characterized by low air contribution. Nevertheless, a geogenic source for these compounds cannot be excluded on the basis of the present data

Exceptional preservation of palaeozoic steroids in a diagenetic continuum

The occurrence of intact sterols has been restricted to immature Cretaceous (~125 Ma) sediments with one report from the Late Jurassic (~165 Ma). Here we report the oldest occurrence of intact sterols in a Crustacean fossil preserved for ca. 380 Ma within a Devonian concretion. The exceptional preservation of the biomass is attributed to microbially induced carbonate encapsulation, preventing full decomposition and transformation thus extending sterol occurrences in the geosphere by 250 Ma. A suite of diagenetic transformation products of sterols was also identified in the concretion, demonstrating the remarkable coexistence of biomolecules and geomolecules in the same sample. Most importantly the original biolipids were found to be the most abundant steroids in the sample. We attribute the coexistence of steroids in a diagenetic continuum-ranging from stenols to triaromatic steroids-to microbially mediated eogenetic processes

Imaging and quantification of gas hydrate and free gas at the Storegga Slide offshore Norway

Wide–angle reflection seismic experiments were performed at the Storegga slide offshore Norway in 2002 with the goal to quantify the amount of gas hydrate and free gas in the sediment. Twenty‐two stations with Ocean Bottom Hydrophones (OBH) and Seismometers (OBS) were deployed for a 2D and a 3D experiment. Kirchhoff depth migration is used to transform the seismic wide–angle data into images of the sediment layers and to obtain P wave velocity–depth functions. The gas hydrate and free gas saturations are estimated from the elastic properties of the sediment on the basis of the Frenkel–Gassmann equations. There is 5–15% gas hydrate in the pore space of the sediment in the gas hydrate stability zone (GHSZ). The free gas saturation takes the value of 0.8% for a homogeneous distribution of gas in the pore water and 7% for the model of a patchy gas distribution

Fault-controlled hydration of the upper mantle during continental rifting

Water and carbon are transferred from the ocean to the mantle in a process that alters mantle peridotite to create serpentinite and supports diverse ecosystems1. Serpentinized mantle rocks are found beneath the sea floor at slow- to ultraslow-spreading mid-ocean ridges1 and are thought to be present at about half the world’s rifted margins2, 3. Serpentinite is also inferred to exist in the downgoing plate at subduction zones4, where it may trigger arc magmatism or hydrate the deep Earth. Water is thought to reach the mantle via active faults3, 4. Here we show that serpentinization at the rifted continental margin offshore from western Spain was probably initiated when the whole crust cooled to become brittle and deformation was focused along large normal faults. We use seismic tomography to image the three-dimensional distribution of serpentinization in the mantle and find that the local volume of serpentinite beneath thinned, brittle crust is related to the amount of displacement along each fault. This implies that sea water reaches the mantle only when the faults are active. We estimate the fluid flux along the faults and find it is comparable to that inferred for mid-ocean ridge hydrothermal systems. We conclude that brittle processes in the crust may ultimately control the global flux of sea water into the Earth