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Pyrolysis, one of the most promising thermal conversion technologies for biomass conversion, can decompose biomass into solid bio-char, liquid bio-oil, and combustible gas to meet different energy needs. However, pyrolysis efficiency and product quality are not as good as expected when raw biomass is used owing to the properties of raw biomass (e.g., high moisture, oxygen, and alkali metal contents). Torrefaction is an emerging biomass pretreatment technology that can improve the physical and chemical properties of raw biomass, and pyrolysis efficiency and final product quality can therefore be improved by using torrefied biomass. We review several advantages of pyrolysis of torrefied biomass in terms of the conversion process and final product quality.

Researchers are devoting great effort to combine photocatalytic nanoparticles (PNPs) with biological processes to create efficient environmental purification technologies (i.e., intimately coupled photobiocatalysis). However, little information is available to illuminate the responses of multispecies microbial aggregates against PNP exposure. Periphytic biofilm, as a model multispecies microbial aggregate, was exposed to three different PNPs (CdS, TiO2, and Fe2O3) under xenon lamp irradiation. There were no obvious toxic effects of PNP exposure on periphytic biofilm as biomass, chlorophyll content, and ATPase activity were not negatively impacted. Enhanced production of extracellular polymetric substances (EPS) is the most important protection mechanism of periphytic biofilm against PNPs exposure. Although PNP exposure produced extracellular superoxide radicals and caused intracellular reactive oxygen species (ROS) accumulation in periphytic biofilm, the interaction between EPS and PNPs could mitigate production of ROS while superoxide dismutase could alleviate biotic ROS accumulation in periphytic biofilm. The periphytic biofilms changed their community composition in the presence of PNPs by increasing the relative abundance of phototrophic and high nutrient metabolic microorganisms (families Chlamydomonadaceae, Cyanobacteriacea, Sphingobacteriales, and Xanthomonadaceae). This study provides insight into the protection mechanisms of microbial aggregates against simultaneous photogenerated and nanoparticle toxicity from PNPs.

AbstractThe inclusive top quark pair ($$t\bar{t}$$ t t ¯ ) production cross-section $$\sigma _{t\bar{t}}$$ σ t t ¯ has been measured in proton–proton collisions at $$\sqrt{s}=13\,\text {TeV}$$ s = 13 TeV , using 36.1 fb$$^{-1}$$ - 1 of data collected in 2015–2016 by the ATLAS experiment at the LHC. Using events with an opposite-charge $$e\mu $$ e μ pair and b-tagged jets, the cross-section is measured to be: $$\begin{aligned} \sigma _{t\bar{t}} = 826.4 \pm 3.6\,\mathrm {(stat)}\ \pm 11.5\,\mathrm {(syst)}\ \pm 15.7\,\mathrm {(lumi)}\ \pm 1.9\,\mathrm {(beam)}\,\mathrm {pb}, \end{aligned}$$ σ t t ¯ = 826.4 ± 3.6 ( stat ) ± 11.5 ( syst ) ± 15.7 ( lumi ) ± 1.9 ( beam ) pb , where the uncertainties reflect the limited size of the data sample, experimental and theoretical systematic effects, the integrated luminosity, and the LHC beam energy, giving a total uncertainty of 2.4%. The result is consistent with theoretical QCD calculations at next-to-next-to-leading order. It is used to determine the top quark pole mass via the dependence of the predicted cross-section on $$m_t^{\mathrm{pole}}$$ m t pole , giving $$m_t^{\mathrm{pole}}=173.1^{+2.0}_{-2.1}\,\text {GeV}$$ m t pole = 173 . 1 - 2.1 + 2.0 GeV . It is also combined with measurements at $$\sqrt{s}=7\,\text {TeV}$$ s = 7 TeV and $$\sqrt{s}=8\,\text {TeV}$$ s = 8 TeV to derive ratios and double ratios of $$t\bar{t}$$ t t ¯ and Z cross-sections at different energies. The same event sample is used to measure absolute and normalised differential cross-sections as functions of single-lepton and dilepton kinematic variables, and the results are compared with predictions from various Monte Carlo event generators.