Experimental investigation of chestnut shells gasification

Fossil fuels substitution with renewable energy sources is necessary for an effective decarbonization. Biomass can represent a valid alternative to fossil fuels, reducing greenhouse gas emissions. Furthermore, bioenergy generation avoids costs and problems related to biomass disposal. This study presents the energetic valorisation of chestnut shells, a byproduct of the chestnut transformation processes. Through a thermo-conversion system based on gasification, this material was considered not as a waste, but as a resource to be exploited to produce bioenergy and biochar. The fuel gas produced through the gasification process can partially replace the LPG currently used to meet the energy required for the brulage and steam peeling processes. Experimental gasification tests were carried out to evaluate this biomass by means of a laboratory scale micro-gasifier (Imbert downdraft type). Chestnut shells were pelletized with a pelletizer machine to avoid the bridging effect inside the gasifier and increase its energy density. The fuel gas obtained was sampled and analyzed to measure its composition and HHV. In addition, the gasification efficiency was calculated obtaining a value of 70%, a result in line with the ones obtained with higher quality biomasses

Experimental investigation of moisture influence on biochar and biochar-soil blends thermophysical properties

Biochar is a carbonaceous and porous material obtained through pyrolysis or gasification. It can be extremely valuable as soil amendment since it increases the organic matter content and fertility, the microbial activity, the water retention, and the crop yields. Moreover, biochar soil application has the potential for long-term carbon sequestration which makes its application to soil interesting even outside agricultural crops. In recent years, the study of the variation of the thermophysical properties of the soil induced by mixing with biochar has attracted interest. In this work, the effect of the water content on thermal conductivity of biochar was investigated by means of the guarded hot plate apparatus λ-Meter EP500e. The same procedure was applied to various mixtures of biochar and soil. Furthermore, the specific heat was measured in order to obtain the thermal diffusivity in the various conditions through a calorimeter. Solar reflectance was also measured following the ASTM C1549 using a solar spectrum reflectometer SSR-ER. The obtained thermophysical properties can be used for the evaluation of the temperature trend of soil at different depths during the seasonal variations

Airborne pathogens diffusion: A comparison between tracer gas and pigmented aerosols for indoor environment analysis

The evaluation of airborne pathogens diffusion is a crucial practice in preventing airborne diseases like COVID-19, especially in indoor environments. Through this transmission route, pathogens can be carried by droplets, droplet nuclei and aerosols and be conveyed over long distances. Therefore, understanding their diffusion is vital for prevention and curbing disease transmission. There are different techniques used for this purpose, and one of the most common is the utilization of tracer gas, however, it has limitations such as the difference in size between the gas molecules and the respiratory droplets, as well as its incapability to take into account evaporation. For this reason, a new method for evaluating the diffusion of respiratory droplets has been developed. This approach involves the use of an ultrasonic emitter to release and disperse pigmented aerosols, and a colorimeter for the following quantitative evaluation. A comparison with the tracer gas technique has been carried out, showing for the pigmented aerosols methodology a response that is dependent on different relative humidity conditions, while there is no clear difference in the dispersion of tracer gas at high or low humidity

Biochar powders coating to improve evaporative cooling in Maisotsenko-cycle systems

This work presents an experimental study on the performance of biochar powder coatings on aluminum surfaces for use in indirect evaporative coolers based on the Maisotsenko cycle. The performance of the biochar coated samples was compared to cellulose-coated aluminum samples and uncoated ones. Results showed that biochar coatings improved the performance of uncoated aluminum, with the 150 μm particle size coating offering performance comparable to cellulose. However, wetting times were longer, which has implications for spraying strategies

Influence of Alloying Elements and Solution Heat Treatment on Microstructure and Microhardness of the Ni-Nb-M System (M = Al, Ti, Cr, Fe)

Ni-based superalloys are widely used in critical components of aircraft engines and turbines and also in the petrochemical industry, for applications in highly corrosive environments. These alloys have as main characteristics their superior mechanical, corrosion and oxidation resistance at high temperatures, as well as creep resistance. The chemical composition associated with carrying out heat treatments directly influences the phases formed (such as the ordered cubic phase γ’-Ni3(Al,Ti) in the fcc γ-Ni matrix), and depending on the alloying elements and fraction, there is the possibility of an increase in mechanical strength. There is a certain gap in the literature regarding the study of ternary superalloys based on Ni-Nb, and the influence of the third alloying element on the microstructure and microhardness. In this context, the objective of the study is to characterize pseudo-eutectic alloys of the Ni-15Nb-xM and Ni-20Nb-xM systems (xM = 2Al, 4Ti, 15Fe and 15Cr, wt.%) and investigate the influence of alloy elements and solution heat treating on their microstructure and properties through X-Ray Diffraction, Optical Microscopy, Scanning Electron Microscopy and Vickers Microhardness. Microhardness and microstructures were significantly influenced by the addition of alloying elements. The addition of Cr had a significant effect on the hardness of the cast samples. All alloys showed microhardness and microstructural changes after solution heat treatment

Type-1 Collagen differentially alters β-catenin accumulation in primary Dupuytren's Disease cord and adjacent palmar fascia cells

<p>Abstract</p> <p>Background</p> <p>Dupuytren's Disease (DD) is a debilitating contractile fibrosis of the palmar fascia characterised by excess collagen deposition, contractile myofibroblast development, increased Transforming Growth Factor-β levels and β-catenin accumulation. The aim of this study was to determine if a collagen-enriched environment, similar to <it>in vivo </it>conditions, altered β-catenin accumulation by primary DD cells in the presence or absence of Transforming Growth Factor-β.</p> <p>Methods</p> <p>Primary DD and patient matched, phenotypically normal palmar fascia (PF) cells were cultured in the presence or absence of type-1 collagen and Transforming Growth Factor-β1. β-catenin and α-smooth muscle actin levels were assessed by western immunoblotting and immunofluorescence microscopy.</p> <p>Results</p> <p>DD cells display a rapid depletion of cellular β-catenin not evident in patient-matched PF cells. This effect was not evident in either cell type when cultured in the absence of type-1 collagen. Exogenous addition of Transforming Growth Factor-β1 to DD cells in collagen culture negates the loss of β-catenin accumulation. Transforming Growth Factor-β1-induced α-smooth muscle actin, a marker of myofibroblast differentiation, is attenuated by the inclusion of type-1 collagen in cultures of DD and PF cells.</p> <p>Conclusion</p> <p>Our findings implicate type-1 collagen as a previously unrecognized regulator of β-catenin accumulation and a modifier of TGF-β1 signaling specifically in primary DD cells. These data have implications for current treatment modalities as well as the design of <it>in vitro </it>models for research into the molecular mechanisms of DD.</p

TRPV1 in Brain Is Involved in Acetaminophen-Induced Antinociception

Background: Acetaminophen, the major active metabolite of acetanilide in man, has become one of the most popular overthe- counter analgesic and antipyretic agents, consumed by millions of people daily. However, its mechanism of action is still a matter of debate. We have previously shown that acetaminophen is further metabolized to N-(4-hydroxyphenyl)-5Z,8Z,11Z,14Z-eicosatetraenamide (AM404) by fatty acid amide hydrolase (FAAH) in the rat and mouse brain and that this metabolite is a potent activator of transient receptor potential vanilloid 1 (TRPV1) in vitro. Pharmacological activation of TRPV1 in the midbrain periaqueductal gray elicits antinociception in rats. It is therefore possible that activation of TRPV1 in the brain contributes to the analgesic effect of acetaminophen. Methodology/Principal Findings: Here we show that the antinociceptive effect of acetaminophen at an oral dose lacking hypolocomotor activity is absent in FAAH and TRPV1 knockout mice in the formalin, tail immersion and von Frey tests. This dose of acetaminophen did not affect the global brain contents of prostaglandin E-2 (PGE(2)) and endocannabinoids. Intracerebroventricular injection of AM404 produced a TRPV1-mediated antinociceptive effect in the mouse formalin test. Pharmacological inhibition of TRPV1 in the brain by intracerebroventricular capsazepine injection abolished the antinociceptive effect of oral acetaminophen in the same test. Conclusions: This study shows that TRPV1 in brain is involved in the antinociceptive action of acetaminophen and provides a strategy for developing central nervous system active oral analgesics based on the coexpression of FAAH and TRPV1 in the brain

Combined analgesics in (headache) pain therapy: shotgun approach or precise multi-target therapeutics?

<p>Abstract</p> <p>Background</p> <p>Pain in general and headache in particular are characterized by a change in activity in brain areas involved in pain processing. The therapeutic challenge is to identify drugs with molecular targets that restore the healthy state, resulting in meaningful pain relief or even freedom from pain. Different aspects of pain perception, i.e. sensory and affective components, also explain why there is not just one single target structure for therapeutic approaches to pain. A network of brain areas ("pain matrix") are involved in pain perception and pain control. This diversification of the pain system explains why a wide range of molecularly different substances can be used in the treatment of different pain states and why in recent years more and more studies have described a superior efficacy of a precise multi-target combination therapy compared to therapy with monotherapeutics.</p> <p>Discussion</p> <p>In this article, we discuss the available literature on the effects of several fixed-dose combinations in the treatment of headaches and discuss the evidence in support of the role of combination therapy in the pharmacotherapy of pain, particularly of headaches. The scientific rationale behind multi-target combinations is the therapeutic benefit that could not be achieved by the individual constituents and that the single substances of the combinations act together additively or even multiplicatively and cooperate to achieve a completeness of the desired therapeutic effect.</p> <p>As an example the fixesd-dose combination of acetylsalicylic acid (ASA), paracetamol (acetaminophen) and caffeine is reviewed in detail. The major advantage of using such a fixed combination is that the active ingredients act on different but distinct molecular targets and thus are able to act on more signalling cascades involved in pain than most single analgesics without adding more side effects to the therapy.</p> <p>Summary</p> <p>Multitarget therapeutics like combined analgesics broaden the array of therapeutic options, enable the completeness of the therapeutic effect, and allow doctors (and, in self-medication with OTC medications, the patients themselves) to customize treatment to the patient's specific needs. There is substantial clinical evidence that such a multi-component therapy is more effective than mono-component therapies.</p