A 1.5D model of a complex geometry laboratory scale fuidized bed clc equipment

The awareness of the climate changes has resulted in the development of new technologies allowing to increase the effectiveness and to lower the costs of CO2 separation from the flue gas. One of the most promised combustion technology of fossil fuels is Chemical Looping Combustion (CLC). The technology is considered to be one of the cheapest techniques for CO2 capture (1). Since it is still an emerging technology and the complexity of processes are still not sufficiently recognized, the development of a simple model of CLC equipment is of practical significance. The paper presents a 1.5D model of the laboratory-scale fluidized bed CLC equipment for Innovative Idea for Combustion of Solid Fuels via Chemical Looping Technology – NewLoop. The idea combines two technologies making them complementary: Chemical looping with Oxygen Uncoupling (CLOU) and In-situ Gasification Chemical Looping (iG-CLC). Experimental studies, calculations and model validation were performed for the CLC unit (Fig. 1). The unit constitutes two cycles: the main cycle and internal cycle with Air Reactor (AR) and Fuel Reactor (FR). Smooth glass microspheres with the Sauter mean diameter of particles of 141 µm and the density of 2450 kg/m3 were used during the investigation. Since the model is in the development stage the study was conducted for the cold tests at which the unit operated stably and smoothly. The model is performed by the use of Comprehensive Simulator of Fluidized and Moving Bed equipment (CeSFaMB). The CeSFaMB has its first successful version completed in 1987. Since then, various versions have been developed and validated for a wide range of cases (2). The first operational results with this CLC unit, i.e. fluidization dynamics are discussed, since the geometry of the system is rather complex. Pressure drops, void fractions, bubble diameter and rising velocity are determined. The results show good agreement between calculated and experimental parameters. On the matter of fluidization dynamics, CeSFaMB produces the parameters as function of vertical coordinate. As an example, the void fractions as well as bubble diameter and rising velocity in the dense region of the Air Reactor are illustrated in Fig 2. Please click Additional Files below to see the full abstract

Distribution of the DAZ gene transcripts in human testis.

Involvement of variety of genes, especially located on Y chromosome, is critical for the regulation of spermatogenesis. In particular, fertility candidate genes such as deleted in azoospermia (DAZ) are believed to have important function in sperm production, since DAZ is frequently deleted in azoospermic and severy oligozoospermic men. The role of the DAZ gene is supported by its exclusive expression in the testis and by its deletion in about 10% of azoospermic and severely oligozoospermic patients. The distribution of DAZ transcripts in seminiferous epithelium of human testis is reported in the present study. The use of Adobe Photoshop and Scion Image softwares allowed for semi-quantitative analysis of in situ RT-PCR (ISRT-PCR) results. The intensity of ISRT-PCR product's fluorescence was different within individual seminiferous tubules. It was clearly shown by using the pseudocolour scale and transforming the intensity of the fluorescence into levels of greyscale images. The more intense fluorescence characterised single spermatogonia and those organized in small groups inside separate tubules. The most intense accumulation of DAZ mRNA was observed in spermatogonia

Joint genomic and proteomic analysis identifies meta-trait characteristics of virulent and non-virulent Staphylococcus aureus strains

Staphylococcus aureus is an opportunistic pathogen of humans and warm-blooded animals and presents a growing threat in terms of multi-drug resistance. Despite numerous studies, the basis of staphylococcal virulence and switching between commensal and pathogenic phenotypes is not fully understood. Using genomics, we show here that S. aureus strains exhibiting virulent (VIR) and non-virulent (NVIR) phenotypes in a chicken embryo infection model genetically fall into two separate groups, with the VIR group being much more cohesive than the NVIR group. Significantly, the genes encoding known staphylococcal virulence factors, such as clumping factors, are either found in different allelic variants in the genomes of NVIR strains (compared to VIR strains) or are inactive pseudogenes. Moreover, the pyruvate carboxylase and gamma-aminobutyrate permease genes, which were previously linked with virulence, are pseudogenized in NVIR strain ch22. Further, we use comprehensive proteomics tools to characterize strains that show opposing phenotypes in a chicken embryo virulence model. VIR strain CH21 had an elevated level of diapolycopene oxygenase involved in staphyloxanthin production (protection against free radicals) and expressed a higher level of immunoglobulin-binding protein Sbi on its surface compared to NVIR strain ch22. Furthermore, joint genomic and proteomic approaches linked the elevated production of superoxide dismutase and DNA-binding protein by NVIR strain ch22 with gene duplications

Geldanamycin and its derivatives as Hsp90 inhibitors

The Hsp90 molecule, one of the most abundant heat shock proteins in mammalian cells, maintains homeostasis and prevents stress-induced cellular damage. Hsp90 is expressed under normal conditions at a level of about 1-2 Percent of total proteins, while its expression increases 2-10 fold in cancer cells. The two main constitutively expressed isoforms of Hsp90 are known as Hsp90-alpha and Hsp90-beta, and their upregulation is associated with tumor progression, invasion and formation of metastases, as well as development of drug resistance. The Hsp90 is a key target for many newly established, potent anticancer agents containing Hsp90 N-terminal ATP binding inhibitors, such as geldanamycin, and its analogues 17AAG and 17DMAG. The therapeutic usage of geldanamycin has been limited due to its poor water solubility and severe hepatotoxicity. Therefore, its analogues, including 17AAG, 17DMAG, Tanespimycin and Retaspimycin hydrochloride, with improved pharmacokinetic profiles, have been developed

Differential requirement for P2X7R function in IL-17 dependent vs. IL-17 independent cellular immune responses

IL17-dependent autoimmunity to collagen type V (Col V) has been associated with lung transplant obliterative bronchiolitis. Unlike the T helper 1 (Th1)-dependent immune responses to Tetanus Toxoid (TT), the Th17 response to Col V in lung transplant patients and its Th1/17 variant observed in coronary artery disease patients requires IL-1β, tumor necrosis factor α and CD14(+) cells. Given the involvement of the P2X7 receptor (P2X7R) in monocyte IL-1β responses, we investigated its role in Th17-, Th1/17- and Th1-mediated proinflammatory responses. Transfer of antigen-pulsed peripheral blood mononucleated cells (PBMCs) from Col V-reactive patients into SCID mouse footpads along with P2X7R antagonists revealed a selective inhibition of Col V-, but not TT-specific swelling responses. P2X7R inhibitors blocked IL-1β induction from monocytes, including both Col V-α1 peptide-induced (T-dependent), as well as native Col V-induced (T-independent) responses. Significantly higher P2X7R expression was found on CXCR3(neg) CCR4(+)/6(+) CD4(+) [Th17] versus CXCR3(+)CCR4/6(neg) CD4(+) [Th1] subsets in PBMCs, suggesting that the paradigm of selective dependence on P2X7R might extend beyond Col V autoimmunity. Indeed, P2X7R inhibitors suppressed not only anti-Col V, but also Th1/17-mediated alloimmunity, in a heart transplant patient without affecting anti-viral Epstein-Barr virus responses. These results suggest that agents targeting the P2X7R might effectively treat Th17-related transplant pathologies, while maintaining Th1-immunity to infection

Hypercapnic Chemosensitivity in Patients with Heart Failure: Relation to Shifts in Type-1 Insulin-Like Growth Factor and Sex Hormone-Binding Globulin Levels

In patients suffering from heart failure (HF), autonomic imbalance develops even at early stages along with derangements of cardiopulmonary reflex control and abnormalities in metabolism of several hormones. In 34 men with stable systolic HF, we investigated hypercapnic chemosensitivity (HCS, liter/min·mm Hg) measured using the rebreathing method and defined as the slope of the regression line relating minute ventilation (VE, liter/min) to end­tidal carbon dioxide concentration (PETCO₂ , mm Hg). Serum levels of testosterone, dehydroepiandrosterone sulfate, type­1 insulin­like growth factor (IGF­1), sex hormonebinding globulin (SHBG), estradiol, and cortisol were measured using immunoassays. We found that there were no associations between HCS and clinical variables, applied therapy, and co­morbidities (all P > 0.2). Augmented HCS was accompanied by increased serum SHBG (when expressed in nM, r = 0.43, P < 0.05; when expressed as percentage of the agematched reference values, r = 0.62, P < 0.001) and the reduced serum IGF­1 (when expressed in ng/ml and as percentage of the above­mentioned values, r = –0.49, P < 0.05, and r = = –0.47, P = 0.007, respectively). The HCS was not related to serum levels of all the remaining analyzed hormones (all P > 0.2). Thus, it may be suggested that the hormone stimuli can noticeably modify the reflex mechanisms in cardiorespiratory control in the clinical setting of cardiovascular pathology.У пацієнтів із серцевою недостатністю (СН) навіть на ранніх стадіях захворювання розвивається автономний дисбаланс паралельно з розладами контролю серцево­судинної системи та відхиленнями метаболізму деяких гормонів від норми. Ми досліджували хемочутливість до гіперкапнії (HCS) у 34 чоловіків із СН, використовуючи метод зворотного дихання. Така чутливість визначалась як нахил лінії регресії при співставленні хвилинного об’єму вентиляції (л/хв) та кінцевої концентрації двооксиду вуглецю (мм рт. ст.). Рівні тестостерону, дигідроепіандростерону сульфату, інсулінподібного фактора росту типу 1 (IGF­1), глобуліну, що зв’язує статеві гормони (SHBG), естрадіолу та кортизолу визначали в сироватці крові, використовуючи імунологічні методики. Як виявилося, зв’язки між рівнем HCS, з одного боку, та клінічними показниками, застосованою терапією та супутніми захворюваннями – з другого, були відсутніми (в усіх випадках P > 0.2). Підвищена HCS супроводжувалася підвищеними рівнями SHBG (для концентрацій у наномолях на 1 л r = 0.43, P < 0.05, а для нормованих значень, наведених щодо певної вікової групи, r = 0.62, P < 0.001) та низькими рівнями IGF­1 (для концентрацій у нанограмах на 1 мл та для наведених нормованих значень r = –0.49, P < 0.05 та r = –0.47, P = 0.007 відповідно). Значення HCS не виявляли будь­яких зв’язків з рівнями всіх досліджених гормонів у сироватці. Це дозволяє думати, що гормональні стимули можуть помітно модифікувати рефлекторні механізми контролю серцево­судинної системи у клінічних випадках її патологій

Presynaptic actions of 4-Aminopyridine and γ-aminobutyric acid on rat sympathetic ganglia in vitro

Responses to bath-applications of 4-aminopyridine (4-AP) and -aminobutyric acid (GABA) were recorded intracellularly from neurones in the rat isolated superior cervical ganglion. 4-aminopyridine (0.1–1.0 mmol/l) usually induced spontaneous action potentials and excitatory postsynaptic potentials (EPSPs), which were blocked by hexamethonium. Membrane potential was unchanged; spike duration was slightly increased. Vagus nerve B-and C-fibre potentials were prolonged. In 4-AP solution (0.1–0.3 mmol/l), GABA (0.1 mmol/l), 3-aminopropanesulphonic acid or muscimol evoked bursts of spikes and EPSPs in addition to a neuronal depolarization. These bursts, which were not elicited by glycine, glutamate, taurine or (±)-baclofen, were completely antagonised by hexamethonium, tetrodotoxin or bicuculline methochloride. It is concluded that: (a) 4-AP has a potent presynaptic action on sympathetic ganglia; (b) presynaptic actions of GABA can be recorded postsynaptically in the presence of 4-AP; and (c) the presynaptic GABA-receptors revealed in this condition are similar to those on the postsynaptic membrane