Исследование сорбционных и термодинамических характеристик поверхностно-активного вещества сульфонола

The statics of process of dehydration and property of synthetic surface-active substance of sulfonol as object of drying is investigated. Are experimentally received and isotherms of sorbtion of sulfonol are mathematical described. As a result of the analysis of curves of sorbtion conclusions are drawn on change of the form of communication of a moisture with a material, recommendations for choice final humidity of a dried up product are made. The analysis of thermodynamics internal mass exchange is carried out at interaction of sulfonol with water.Исследована статика процесса обезвоживания и свойства синтетического поверхностно-активного вещества сульфонола как объекта сушки. Экспериментально получены и математически описаны изотермы сорбции сульфонола. В результате анализа кривых сорбции сделаны выводы об изменении формы связи влаги с материалом, даны рекомендации по выбору конечной влажности высушиваемого продукта. Проведен анализ термодинамики внутреннего массопереноса при взаимодействии сульфонола с водой

Characteristics of insulin therapy of diabetes mellitus type 1 in children and adolescents receiving glucocorticoids

BACKGROUND: In coexistence of diabetes mellitus type 1 (DM1) with severe autoimmune and inflammatory diseases some patients need simultaneous administration of insulin and glucocorticoids (GC). GC therapy in patients with DM1 can worsen glycemic control. AIM: To determine characteristics of insulin therapy of DM1 in children and adolescents receiving GC. DESCRIPTION OF CLINICAL CASES: We observed 5 patients with DM1 receiving GC for juvenile idiopathic arthritis (JIA), juvenile systemic sclerosis (JSS), juvenile dermatomyositis (JDM), ulcerative colitis (UC), and reactive arthritis (RA). Intra-articular administration of GC did not significantly influence glycemic control. In case of GC pulse therapy hyperglycemia and increased insulin requirements were recognized in 3–6 hours after GC receipt, persisted from few hours up to 3 days after each administration. While therapy with oral GC in high doses the worst glycemic control was registered in daylight hours. To overcome insulin resistance change of time of injection and 10%-increase of long-acting insulin analogue, additional injections of ultrashort-acting insulin analogues, temporal prescription of short-acting human insulin were used. While GC therapy insulin daily dose was individual and could reach 2.0 U/kg. After transition to maintaining doses of GC or discontinuation of GC therapy patients returned to standard or relatively low insulin requirements. Levels of glycosylated hemoglobin differed significantly among patients at different stages of treatment, were maximal while long-term therapy with high doses of oral GC, but mostly depended on patient’s compliance. CONCLUSION: Bettering of glycemic control while receiving GC can be reached by timely dose correction of insulin therapy, selection of individual schemes, taking into account time of receipt and pharmacokinetic characteristics of GC. Adherence of the patient and his family to treatment of DM1 plays an important role in glycemic control

Measurements of KL Branching Fractions and the CP Violation Parameter |eta+-|

We present new measurements of the six largest branching fractions of the KL using data collected in 1997 by the KTeV experiment (E832) at Fermilab. The results are B(KL -> pi e nu) = 0.4067 +- 0.0011 B(KL -> pi mu nu) = 0.2701 +- 0.0009 B(KL -> pi+ pi- pi0) = 0.1252 +- 0.0007 B(KL -> pi0 pi0 pi0) = 0.1945 +- 0.0018 B(KL -> pi+ pi-) = (1.975 +- 0.012)E-3, and B(KL -> pi0 pi0) = (0.865 +- 0.010)E-3, where statistical and systematic errors have been summed in quadrature. We also determine the CP violation parameter |eta+-| to be (2.228 +- 0.010)E-3. Several of these results are not in good agreement with averages of previous measurements.Comment: Submitted to Phys. Rev. D; 20 pages, 22 figure

Reading tea leaves worldwide: Decoupled drivers of initial litter decomposition mass‐loss rate and stabilization

The breakdown of plant material fuels soil functioning and biodiversity. Currently, process understanding of global decomposition patterns and the drivers of such patterns are hampered by the lack of coherent large-scale datasets. We buried 36,000 individual litterbags (tea bags) worldwide and found an overall negative correlation between initial mass-loss rates and stabilization factors of plant-derived carbon, using the Tea Bag Index (TBI). The stabilization factor quantifies the degree to which easy-to-degrade components accumulate during early-stage decomposition (e.g. by environmental limitations). However, agriculture and an interaction between moisture and temperature led to a decoupling between initial mass-loss rates and stabilization, notably in colder locations. Using TBI improved mass-loss estimates of natural litter compared to models that ignored stabilization. Ignoring the transformation of dead plant material to more recalcitrant substances during early-stage decomposition, and the environmental control of this transformation, could overestimate carbon losses during early decomposition in carbon cycle models

Reading tea leaves worldwide: decoupled drivers of initial litter decomposition mass-loss rate and stabilisation

The breakdown of plant material fuels soil functioning and biodiversity. Currently, process understanding of global decomposition patterns and the drivers of such patterns are hampered by the lack of coherent large-scale datasets. We buried 36,000 individual litterbags (tea bags) worldwide and found an overall negative correlation between initial mass-loss rates and stabilization factors of plant-derived carbon, using the Tea Bag Index (TBI). The stabilization factor quantifies the degree to which easy-to-degrade components accumulate during early-stage decomposition (e.g. by environmental limitations). However, agriculture and an interaction between moisture and temperature led to a decoupling between initial mass-loss rates and stabilization, notably in colder locations. Using TBI improved mass-loss estimates of natural litter compared to models that ignored stabilization. Ignoring the transformation of dead plant material to more recalcitrant substances during early-stage decomposition, and the environmental control of this transformation, could overestimate carbon losses during early decomposition in carbon cycle models

Research sorption and thermodynamic characteristics of surface-active substance of sulfonol

The statics of process of dehydration and property of synthetic surface-active substance of sulfonol as object of drying is investigated. Are experimentally received and isotherms of sorbtion of sulfonol are mathematical described. As a result of the analysis of curves of sorbtion conclusions are drawn on change of the form of communication of a moisture with a material, recommendations for choice final humidity of a dried up product are made. The analysis of thermodynamics internal mass exchange is carried out at interaction of sulfonol with water

HYGROSCOPIC CHARACTERISTICS AND THERMODYNAMICS INTERNAL CARRYING OVER OF WEIGHTS AT INTERACTION LACTOBACTERIA AND WATER

Researches of hygroscopic properties of a biomass lactobacteria Lactobacillus plantarum. Research of process of drying of a bacterium of containing products In the field of a hygroscopic condition, curves were for this purpose applied sorbtsii -desorption on which the kind and energy of communication of a moisture with a material have defined

Use of Asphaltene Stabilizers for the Production of Very Low Sulphur Fuel Oil

Marine fuel oil stability has always been an issue for bunkering companies and ship owners all around the world and the problem has become even more apparent with the introduction of the Global Sulphur Gap by the International Maritime Organization (IMO) in 2020. In this article, the historical background and the technical reasons why marine fuel oils lose their stability, as well as methods for preventing such instability from occurring, are presented. While it is possible to make fuel compositions stable by adjusting their composition in such a way that the components of the fuel are compatible, considering that marine fuel oils are often comprised of the least value-added products, the method of adding special fuel oil stabilizers (also known as “asphaltene dispersants”) is usually preferred. An overview of such stabilizers is presented; their chemical composition, based on the information provided by the manufacturers and/or inventors is studied. In addition, the experimental research of the produced marine fuel oil and its components is carried out. The results of the model composition studies show that adding even as little as 10% of residual asphaltene-rich components can make a composition with a high stability reserve unstable. It was also shown that the content of the asphaltene-rich component in a stable fuel can be increased from 3% to 10% by introducing stabilizers in low amounts (up to 2000 ppm), thus lowering the amount of higher value-added, mostly naphthene-paraffinic-based components. Different methods of fuel stability evaluation were studied and tested, most of them being in correlation with one another. Several types of stability enhancers were tried out on unstable fuel, with stabilizers based on alkylphenol formaldehyde resin showing the best results