Fast pyrolysis bio-oil production in an entrained flow reactor pilot

Bio-oil produced from biomass fast pyrolysis could constitute an alternative to fossil liquid fuels, especially to be combusted for local district heating. So far, only few studies have dealt with bio-oil production by biomass fast pyrolysis in an entrained flow reactor [1], yet it could constitute an alternative to the better-known fluidised bed pyrolysis process. In the context of the BOIL project with the CCIAG Company (Grenoble district heating), a new pilot based on an entrained flow reactor concept has been designed [2]. The pilot design has been carried out on the basis of woody biomass fast pyrolysis experiments and modeling performed in a drop tube reactor as a first step laboratory-scale study, and also CFD modeling [2-3]. The facility is composed of a biomass injection system with a hopper and a feeding screw, an electrically heated pyrolysis reactor, a cyclone to separate gas and char, 3 heat exchangers to cool the gas (at 30°C, 0°C and 0°C respectively) and condense bio-oil, and a post-combustion unit to burn the incondensable species. Gas temperature is maintained at 350°C from the reactor outlet to the entrance of the first heat exchanger in order to avoid bio-oil condensation. Several conditions were tested in 14 runs: 3 different biomass feedstocks, varying biomass feeding rates from 2 to 9 kg/h and two reactor temperatures 500°C and 550°C. 85 kg of bio-oil has been produced for combustion tests. Recovered bio-oil mass yield is on average 50%, its LHV is about 15 MJ/kg, its water content 26%w and its pH 2.15. We identified three main difficulties during the runs: about 15% of the bio-oil go through the heat exchanger, some char particles go through the cyclone which causes regular plugging of the first heat exchanger. Detailed analyses of the bio-oil produced have been done and the chemical and physical bio-oil characteristics have been compared to the European Standard recommendations [4]. With a regularly cleaning of the first heat exchanger, we successfully produce bio-oil with physical and chemical properties in agreement with the European Standard recommendations. Combustion tests of the bio-oil produced have been carried on by the CIRAD. They succeeded in obtaining a stable flame (without the use of a pilot flame) in a 50 kW burner and a 250 kW combustion chamber. However the physical and chemical characteristics of the bio-oil involve the use of specific pump and pulverization system adapted. In perspective for future projects, it would be interesting to perform pilot modifications in order to increase bio-oil yield and to minimize heat exchanger cleaning, and to test other resources like agricultural biomass or solid recovered fuels. Bibliography 1. J.A. Knight, C.W. Gorton, R.J. Kovac, Biomass 6, pp. 69-76, 1984. 2. Fast pyrolysis reactor for organic biomass materials with against flow injection of hot gases - US 20170166818 A1 3. Guizani, S.Valin, J.Billlaud, M.Peyrot, S.Salvador, Fuel, 2017, 207, pp.71-84. 4. C.Guizani, S.Valin, M.Peyrot, G.Ratel S.Salvador, Woody biomass fast pyrolysis in a drop tube reactor - Pyro2016 conference 5. Fast pyrolysis bio-oils for industrial boilers – Requirements and test methods – EN 1690

Imaging the essential role of spin-fluctuations in high-Tc superconductivity

We have used scanning tunneling spectroscopy to investigate short-length electronic correlations in three-layer Bi2Sr2Ca2Cu3O(10+d) (Bi-2223). We show that the superconducting gap and the energy Omega_dip, defined as the difference between the dip minimum and the gap, are both modulated in space following the lattice superstructure, and are locally anti-correlated. Based on fits of our data to a microscopic strong-coupling model we show that Omega_dip is an accurate measure of the collective mode energy in Bi-2223. We conclude that the collective mode responsible for the dip is a local excitation with a doping dependent energy, and is most likely the (pi,pi) spin resonance.Comment: 4 pages, 4 figure

Diamagnetism above Tc in underdoped Bi2.2Sr1.8Ca2Cu3O10+d

Single crystals of ${\rm Bi}_{2+x}{\rm Sr}_{2-x}{\rm Ca}_{2}{\rm Cu}_{3}{\rm O}_{10+\delta}$(Bi2223) with $x=0.2$ were grown by a traveling solvent floating zone method in order to investigate the superconducting properties of highly underdoped Bi2223.Grown crystals were characterized by X-ray diffraction, DC susceptibility and resistivity measurements, confirming Bi2223 to be the main phase.The crystals were annealed under various oxygen partial pressures to adjust their carrier densities from optimally doped to highly underdoped.The fluctuation diamagnetic component above the superconducting transition temperature $T_{\rm c}$ extracted from the anisotropic normal state susceptibilities $\chi_{ab}(T)$ ($H\perp c$) and $\chi_{c}(T)$ ($H\parallel c$) was found to increase with underdoping, suggesting a decrease in the superconducting dimensionality and/or increase in the fluctuating vortex liquid region.Comment: 6 pages, 7 figures, corrected fig.4 and references, published in J. Phys. Soc. Jpn. 79, 114711 (2010

Pinning of stripes by local structural distortions in cuprate high-Tc superconductors

We study the spin-density wave (stripe) instability in lattices with mixed low-temperature orthorhombic (LTO) and low-temperature tetragonal (LTT) crystal symmetry. Within an explicit mean-field model it is shown how local LTT regions act as pinning centers for static stripe formation. We calculate the modulations in the local density of states near these local stripe regions and find that mainly the coherence peaks and the van Hove singularity (VHS) are spatially modulated. Lastly, we use the real-space approach to simulate recent tunneling data in the overdoped regime where the VHS has been detected by utilizing local normal state regions.Comment: Conference proceedings for Stripes1

Markers of sulfadoxine-pyrimethamine resistance in Eastern Democratic Republic of Congo; implications for malaria chemoprevention

Background Sulfadoxine–pyrimethamine (SP) is a cornerstone of malaria chemoprophylaxis and is considered for programmes in the Democratic Republic of Congo (DRC). However, SP efficacy is threatened by drug resistance, that is conferred by mutations in the dhfr and dhps genes. The World Health Organization has specified that intermittent preventive treatment for infants (IPTi) with SP should be implemented only if the prevalence of the dhps K540E mutation is under 50%. There are limited current data on the prevalence of resistance-conferring mutations available from Eastern DRC. The current study aimed to address this knowledge gap. Methods Dried blood-spot samples were collected from clinically suspected malaria patients [outpatient department (OPD)] and pregnant women attending antenatal care (ANC) in four sites in North and South Kivu, DRC. Quantitative PCR (qPCR) was performed on samples from individuals with positive and with negative rapid diagnostic test (RDT) results. Dhps K450E and A581G and dhfr I164L were assessed by nested PCR followed by allele-specific primer extension and detection by multiplex bead-based assays. Results Across populations, Plasmodium falciparum parasite prevalence was 47.9% (1160/2421) by RDT and 71.7 (1763/2421) by qPCR. Median parasite density measured by qPCR in RDT-negative qPCR-positive samples was very low with a median of 2.3 parasites/µL (IQR 0.5–25.2). Resistance genotyping was successfully performed in RDT-positive samples and RDT-negative/qPCR-positive samples with success rates of 86.2% (937/1086) and 55.5% (361/651), respectively. The presence of dhps K540E was high across sites (50.3–87.9%), with strong evidence for differences between sites (p < 0.001). Dhps A581G mutants were less prevalent (12.7–47.2%). The dhfr I164L mutation was found in one sample. Conclusions The prevalence of the SP resistance marker dhps K540E exceeds 50% in all four study sites in North and South Kivu, DRC. K540E mutations regularly co-occurred with mutations in dhps A581G but not with the dhfr I164L mutation. The current results do not support implementation of IPTi with SP in the study area

Group Space Allowance Has Little Effect on Sow Health, Productivity, or Welfare in a Free-Access Stall System

Free-access stalls allow sows to choose the protection of a stall or use of a shared group space. This study investigated the effect of group space width, 0.91 (SS), 2.13 (IS), and 3.05 (LS) m, on the health, production, behavior, and welfare of gestating sows. Nine replications of 21 (N = 189) gestating sows were used. At gestational d 35.4 ± 2.3, the pregnant sows were distributed into 3 pens of 7 sows, where they remained until 104.6 ± 3.5 d. Each treatment pen had 7 free-access stalls and a group space that together provided 1.93 (SS), 2.68 (IS), or 3.24 (LS) m2/sow. Baseline measurements were obtained before mixing. Back fat depth, BW, BCS, and lameness were measured monthly, and skin lesions were scored weekly. Blood was collected monthly for hematological, immunological, and cortisol analyses. Sow behavior was video recorded continuously during the initial 4 d of treatment and 24 h every other week thereafter. Behavior was analyzed for location, posture, pen investigation, social contact, and aggression. Skin response to the mitogen concanavalin A (Con A) was tested at mean gestational d 106. Litter characteristics including size and weight were collected at birth and weaning. The data were analyzed using a mixed model. Multiple comparisons were adjusted with the Tukey-Kramer and Bejamini-Hochberg methods. Group space allowance had no effect on any measure of sow health, physiology, or production (P ≥ 0.10). Sows in the SS, IS, and LS pens spent 77.88% ± 3.88%, 66.02% ± 3.87%, and 63.64% ± 3.91%, respectively, of their time in the free-access stalls (P = 0.12). However, SS sows used the group space less than IS and LS sows (P = 0.01). Overall, pen investigatory behavior was not affected by group space allowance (P = 0.91). Sows in the LS pens spent more time in a social group than SS sows (P = 0.02), whereas sows in IS pens were intermediate to, but not different from, the other treatments (P ≥ 0.10). The size of the social groups was also affected by the group space allowance (P = 0.03), with SS sows forming smaller groups than LS sows; again, IS sows were intermediate to, but not different from, the other treatments. Although the group space allowance had no measurable impact on the health, physiology, or productivity of the sows, the lower group space use and social contact of the SS sows reduced the behavioral diversity benefits of group housing and may indicate an avoidance of social stressors or a lack of physical comfort in the smallest pens

Suppression of circulating IgD+CD27+ memory B cells in infants living in a malaria-endemic region of Kenya

Background: Plasmodium falciparum infection leads to alterations in B cell subset distribution. During infancy, development of peripheral B cell subsets is also occurring. However, it is unknown if infants living a malaria endemic region have alterations in B cell subsets that is independent of an age effect. Methods: To evaluate the impact of exposure to P. falciparum on B cell development in infants, flow cytometry was used to analyse the distribution and phenotypic characteristic of B cell subsets in infant cohorts prospectively followed at 12, 18 and 24 months from two geographically proximate regions in western Kenya with divergent malaria exposure i.e. Kisumu (malaria-endemic, n = 24) and Nandi (unstable malaria transmission, n = 21). Results: There was significantly higher frequency and absolute cell numbers of CD19+ B cells in Kisumu relative to Nandi at 12(p = 0.0440), 18(p = 0.0210) and 24 months (p = 0.0493). No differences were observed between the infants from the two sites in frequencies of naïve B cells (IgD+CD27-) or classical memory B cells (IgD-CD27+). However, immature transitional B cells (CD19+CD10+CD34-) were higher in Kisumu relative to Nandi at all three ages. In contrast, the levels of non-class switched memory B cells (CD19+IgD+CD27+) were significantly lower overall in Kisumu relative to Nandi at significantly at 12 (p = 0.0144), 18 (p = 0.0013) and 24 months (p = 0.0129). Conclusions: These data suggest that infants living in malaria endemic regions have altered B cell subset distribution. Further studies are needed to understand the functional significance of these changes and long-term impact on ability of these infants to develop antibody responses to P. falciparum and heterologous infections

Cellular and Molecular Mechanisms Underlying the Strong Neonatal IL-12 Response of Lamb Mesenteric Lymph Node Cells to R-848

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