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These conversations are recommended to be used both by therapists with their clients as well as for direct use by partners following the questions presented within. The topics represent a comprehensive range of relationship issues including consideration of unique issues as presented in the literature with the goal of aiding partners in successful management of their transition to a shared living space.We describe how the set of tools, practices, and social relations known as "precision agriculture" is defined, promoted, and debated. To do so, we perform a critical discourse analysis of popular and trade press websites. Promoters of precision agriculture champion how big data analytics, automated equipment, and decision-support software will optimize yields in the face of narrow margins and public concern about farming's environmental impacts. At its core, however, the idea of farmers leveraging digital infrastructure in their operations is not new, as agronomic research in this vein has existed for over 30 years. Contemporary discourse in precision ag tends to favour emerging digital technologies themselves over their embeddedness in longstanding precision management approaches. Following several strands of science and technology studies (STS) research, we explore what rhetorical emphasis on technical innovation achieves, and argue that this discourse of novelty is a reinvention of precision agriculture in the context of the growing "smart" agricultural economy. We overview six tensions that remain unresolved in this promotional rhetoric, concerning the definitions, history, goals, adoption, uses, and impacts of precision agriculture. We then synthesize these in a discussion of the extent to which digital tools are believed to displace farmer decision-making and whether digital agriculture addresses the biophysical heterogeneity of farm landscapes or land itself has become an "experimental technology"-a way to advance the general development of artificial intelligence. This discussion ultimately helps us name a larger dilemma that the smart agricultural economy is perhaps less about supporting land and its stewards than promising future tech and profits.The two-step bubble column-photobioreactor photosynthetic biogas upgrading system can enable simultaneous production of biomethane and value-added products from microalgae. However, due to the influence of a large number of variables, including downstream processes and the presence of microalgae, no unanimity has been reached regarding the performance of bubble column reactors in photosynthetic biogas upgrading. To investigate this further, the present work documents in detail, the design and commissioning of a lab-scale bubble column reactor capable of treating up to 16.3 L/h of biogas while being scalable. The performance of the bubble column was assessed at a pH of 9.35 with different algal densities of Spirulina platensis at 20 °C in the presence of light (3-5 klux or 40.5-67.5 μmol m-2 s-1). A liquid/gas flow (L/G) ratio of 0.5 allowed consistent CO2 removal of over 98% irrespective of the algal density or its photosynthetic activity. For lower concentrations of algae, the volumetric O2 concentration in the upgraded biomethane varied between 0.05 and 0.52%, thus providing grid quality biomethane. However, for higher algal concentrations, increased oxygen content in the upgraded biomethane due to both enhanced O2 stripping and the photosynthetic activity of the microalgae as well as clogging and foaming posed severe operational challenges.Solid-fuel stoves are at the heart of many homes not only in developing nations, but also in developed regions where there is significant deployment of such heating appliances. They are often operated inefficiently and in association with high emission fuels like wood. This leads to disproportionate air pollution contributions. Despite the proliferation of these appliances, an understanding of particulate matter (PM) emissions from these sources remains relatively low. Emissions from five solid fuels are quantified using a "conventional" and an Ecodesign stove. PM measurements are obtained using both "hot filter" sampling of the raw flue gas, and sampling of cooled, diluted flue gas using an Aerosol Chemical Speciation Monitor and AE33 aethalometer. PM emissions factors (EF) derived from diluted flue gas incorporate light condensable organic compounds; hence they are generally higher than those obtained with "hot filter" sampling, which do not. Overall, the PM EFs ranged from 0.2 to 108.2 g GJ-1 for solid fuels. The PM EF determined for a solid fuel depends strongly on the measurement method employed and on user behavior, and less strongly on secondary air supply and stove type. Kerosene-based firelighters were found to make a disproportionately high contribution to PM emissions. Organic aerosol dominated PM composition for all fuels, constituting 50-65% of PM from bituminous and low-smoke ovoids, and 85-95% from torrefied olive stone (TOS) briquettes, sod peat, and wood logs. Torrefied biomass and low-smoke ovoids were found to yield the lowest PM emissions. Substituting these fuels for smoky coal, peat, and wood could reduce PM2.5 emissions by approximately 63%.1D Ca3Co2-z M z O6 (M = Co z = 0, M = Mn z = 1, and M = Fe z = 0.4) were prepared and tested electrochemically. While the iron-containing phase was not found to be active, the iron- and manganese-containing phases were found to be potentially interesting as positive electrode materials for calcium metal-based high-energy battery technologies and were investigated by operando synchrotron X-ray diffraction. Results indicate that electrochemically driven calcium deintercalation from the crystal structure (ca. 0.7 mol per formula unit) takes place upon oxidation in both cases. The oxidized phases have incommensurate modulated crystal structures with the space group R 3m(00γ)0s and a = 9.127(1) Å, c 1 = 2.4226(3) Å and c 2 = 4.1857(3) Å, and γ = 0.579 (M = Co) and a = 9.217(1) Å, c 1 = 4.9076(4) Å and c 2 = 4.3387(4) Å, and γ = 1.139 (M = Mn), which exhibit differences due to the presence of manganese and Mn/Co ordering. The degree of calcium re-intercalation within the structure was found to be extremely limited, if any. Complementary experiments carried out in lithium cells did not show any reversibility either, thus pointing at intrinsic structural/migration constraints in the oxidized phase rather than slow kinetics of high desolvation energies associated with divalent ion charge carriers.Lithium-metal batteries employing concentrated glyme-based electrolytes and two different cathode chemistries are herein evaluated in view of a safe use of the highly energetic alkali-metal anode. Indeed, diethylene-glycol dimethyl-ether (DEGDME) and triethylene-glycol dimethyl-ether (TREGDME) dissolving lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) and lithium nitrate (LiNO3) in concentration approaching the solvents saturation limit are used in lithium batteries employing either a conversion sulfur-tin composite (SSn 8020 w/w) or a Li+ (de)insertion LiFePO4 cathode. Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) clearly show the suitability of the concentrated electrolytes in terms of process reversibility and low interphase resistance, particularly upon a favorable activation. Galvanostatic measurements performed on lithium-sulfur (Li/S) batteries reveal promising capacities at room temperature (25 °C) and a value as high as 1300 mAh gS -1 for the cell exploiting the DEGDME-based electrolyte at 35 °C. On the other hand, the lithium-LiFePO4 (Li/LFP) cells exhibit satisfactory cycling behavior, in particular when employing an additional reduction step at low voltage cutoff (i.e., 1.2 V) during the first discharge to consolidate the solid electrolyte interphase (SEI). This procedure allows a Coulombic efficiency near 100%, a capacity approaching 160 mAh g-1, and relevant retention particularly for the cell using the TREGDME-based electrolyte. Therefore, this work suggests the use of concentrated glyme-based electrolytes, the fine-tuning of the operative conditions, and the careful selection of active materials chemistry as significant steps to achieve practical and safe lithium-metal batteries.Fluctuations in the fuel flow rate may occur in practical combustion systems and result in flame destabilization. This is particularly problematic in lean and ultralean modes of burner operation. In this study, the response of a ceramic porous burner to fluctuations in the flow rate of different blends of methane and hydrogen is investigated experimentally. Prior to injection into the porous burner, the fuel blend is premixed with air at equivalence ratios below 0.275. The fuel streams are measured and controlled separately by programmable mass flow controllers, which impose sinusoidal fluctuations on the flow rates. To replicate realistic fluctuations in the fuel flow rate, the period of oscillations is chosen to be on the order of minutes. The temperature inside the ceramic foam is measured using five thermocouples located at the center of the working section of the burner. Proteasome inhibitor The flame embedded in porous media is imaged while the fuel flow is modulated. Analysis of the flame pictures and temperature traces shows that the forced oscillation of the fuel mixture leads to flame movement within the burner. This movement is found to act in accordance with the fluctuations in methane and hydrogen flows for both CH4(90%)-H2(10%) and CH4(70%)-H2(30%) mixtures. However, both fuel mixtures are noted to be rather insensitive to hydrogen flow fluctuation with a modulation amplitude below 30% of the steady flow. For the CH4(70%)-H2(30%) mixture, the flame in the porous medium can be modulated by fluctuations between 0 and 30% of steady methane flow without any noticeable flame destabilization.The term "globalization" doesn't refer to a current epoch of world history, but to an undulated process interrupted by harsh setbacks. Its phases of upswing are characterized by exponential growth. They end when tipping points arrive. For globalization inevitably has its winners and losers, these phases are paralleled by processes of fragmentation in other countries, macro-regions and societies. The article provides a sketch of both types of processes, illustrated by examples from world history. It thereby shows that they must not be considered mere byproducts of technological development in transport and communication, but also depend on institutions that guarantee "International Public Goods" (IPGs), above all safety, stability and connectivity. Only great powers can provide this type of goods, for only they have the resources to do so, then again for only they are confronted with a volunteer's dilemma. Moreover globalization depends on a grand narrative that marginalizes competing schools of thought. Crises emerge either when transactions driving the process reach a tipping point, or when great powers decline and are no longer ready or able to provide IPGs. Now critical discourses emerge and become hegemonic in the face of successive crises undermining the grand narrative. This results in social division between cosmopolitans and populists. Both "big players" currently face different dilemmas conditioned by their positions as hegemonic power (USA) and freerider (China), in each case causing them to act neo-isolationist. The result IPGs are no longer guaranteed, globalization is in crisis. This development has been catalysed by the Corona-pandemic.

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