The Simple Non-degenerate Relativistic Gas: Statistical Properties and Brownian Motion

This paper shows a novel calculation of the mean square displacement of a classical Brownian particle in a relativistic thermal bath. The result is compared with the expressions obtained by other authors. Also, the thermodynamic properties of a non-degenerate simple relativistic gas are reviewed in terms of a treatment performed in velocity space.Comment: 6 pages, 2 figure

Catalytic hydrodechlorination as polishing step in drinking water treatment for the removal of chlorinated micropollutants

This Accepted Manuscript will be available for reuse under a CC BY-NC-ND license after 24 months of embargo periodThe presence of micropollutants in fresh waters represents an important challenge for drinking water treatment plants (DWTPs). In particular, the chlorinated ones are especially harmful given their high toxicity and strong bioaccumulation potential. The aim of this work is to evaluate the feasibility of catalytic hydrodechlorination (HDC) for the removal of a representative group of chlorinated micropollutants commonly found in the source waters of DWTPs: the antibiotic chloramphenicol (CAP), the anti-inflammatory diclofenac (DCF), the antibacterial agent triclosan (TCL) and the antidepressant sertraline (SRT). The complete degradation of the isolated micropollutants (3 mg L−1) was achieved in 1 h reaction time using a Pd/Al2O3 catalyst load of 0.25 g L−1 and a H2 flow rate of 50 N mL min−1. The experimental data were properly described by a pseudo-first order kinetic equation, obtaining degradation rate constants in the range of 0.32–1.56 L gcat−1 min−1 and activation energy values within 42–52 kJ mol−1. In all cases, the final reaction products were chlorine-free compounds and thus, HDC effluents were non-toxic (<0.1 TU). Remarkably, the catalyst showed a suitable stability upon five consecutive applications. The versatility of the process was demonstrated in the treatment of the micropollutants mixture in different aqueous matrices (mineral, surface and tap waters). Strikingly, the removal rate was not affected by the presence of co-existing substances, being the micropollutants completely removed in 15 min with 1 g L−1 catalyst concentration. Finally, the potential of HDC for the removal of trihalomethanes, by-products formed along the oxidation step by chlorination in DWTPs, was also demonstratedThis research has been supported by the Spanish MINECO thorough the project CTM2016-76454-R and by the CM through the project P2018/EMT-4341. J. Nieto-Sandoval thanks the Spanish MINECO for the FPI predoctoral grant (BES-2017- 081346). M. Munoz thanks the Spanish MINECO for the Ramón y Cajal postdoctoral contract (RYC-2016-20648

Topological Dirac states in asymmetric Pb1-xSnxTe quantum wells

The electronic structure of lead-salt (IV-VI semiconductor) topological quantum wells (T-QWs) is investigated with analytical solutions of the effective 4x4 Dimmock k & BULL; p model, which gives an accurate description of the bands around the fundamental energy gap. Specific results for three-layer Pb1-xSnxTe nanostructures with varying Sn composition are presented and the main differences between topological and normal (N) QWs highlighted. A series of new features are found in the spectrum of T-QWs, in particular in asymmetric QWs where large (Rashba spin-orbit) splittings are obtained for the topological Dirac states inside the gap

Adsorption of micropollutants onto realistic microplastics: role of microplastic nature, size, age, and NOM fouling

This work aims at evaluating the role of nature, size, age, and natural organic matter (NOM) fouling of realistic microplastics (MPs) on the adsorption of two persistent micropollutants (diclofenac (DCF) and metronidazole (MNZ)). For such goal, four representative polymer types (polystyrene (PS), polyethylene terephthalate (PET), polypropylene (PP) and high-density polyethylene (HDPE)) were tested. MPs were obtained by cryogenic milling of different commercial materials (disposable bottles, containers, and trays), and fully characterized (optical microscopic and SEM images, FTIR, elemental analysis, water contact angle and pHslurry). The micropollutants hydrophobicity determined to a high extent their removal yield from water. Regardless of the MP's nature, the adsorption capacity for DCF was considerably higher than the achieved for MNZ, which can be related to its stronger hydrophobic properties and aromatic character. In fact, aromatic MPs (PS and PET) showed the highest adsorption capacity values with DCF (~100 μg g−1). The MP size also played a key role on its adsorption capacity, which was found to increase with decreasing the particle size (20–1000 μm). MPs aging (simulated by Fenton oxidation) led also to substantial changes on their sorption behavior. Oxidized MPs exhibited acidic surface properties which led to a strong decrease on the adsorption of the hydrophobic micropollutant (DCF) but to an increase with the hydrophilic one (MNZ). NOM fouling (WWTP effluent, river water, humic acid solution) led to a dramatic decrease on the MPs sorption capacity due to sorption sites blocking. Finally, the increase of pH or salinity of the aqueous medium increased the micropollutants desorptionThis research has been supported by the Autonoma University of Madrid and Community of Madrid through the project SI1-PJI-2019-00006, and by the Spanish MINECO through the project PID2019-105079RB-I00. Muñoz and J. Nieto-Sandoval thank the Spanish MINECO for the Ramón y Cajal postdoctoral contract (RYC-2016-20648) and the FPI predoctoral grant (BES-2017-081346), respectively. D. Ortiz thanks the Spanish MIU for the FPU predoctoral grant (FPU19/04816

Electron g factor anisotropy in asymmetric III-V semiconductor quantum wells

The electron effective g factor tensor in asymmetric III-V semiconductor quantum wells (AQWs) and its tuning with the structure parameters and composition are investigated with envelope-function theory and the 8 x 8k . p Kane model. The spin-dependent terms in the electron effective Hamiltonian in the presence of an external magnetic field are treated as a perturbation and the g factors g(perpendicular to)* and g(parallel to)*, for the magnetic field in the QW plane and along the growth direction, are obtained analytically as a function of the well width L. The effects of the structure inversion asymmetry (SIA) on the electron g factor are analyzed. For the g-factor main anisotropy Delta g = g(perpendicular to)*-g(parallel to)*. in AQWs, a sign change is predicted in the narrow well limit due to SIA, which can explain recent measurements and be useful in spintronic applications. Specific results for narrow-gap AlSb/InAs/GaSb and AlxGa1-xAsGaAs/AlyGa1-yAs AQWs are presented and discussed with the available experimental data; in particular InAs QWs are shown to not only present much larger g factors but also a larger g-factor anisotropy, and with the opposite sign with respect to GaAs QWs

Degradation of widespread cyanotoxins with high impact in drinking water (microcystins, cylindrospermopsin, anatoxin-a and saxitoxin) by CWPO

This Accepted Manuscript will be available for reuse under a CC BY-NC-ND license after 24 months of embargo periodThe occurrence of harmful cyanobacterial blooms has unabated increased over the last few decades, posing a significant risk for public health. In this work, we investigate the feasibility of catalytic wet peroxide oxidation (CWPO) promoted by modified natural magnetite (Fe3O4-R400/H2O2), as an inexpensive, simple-operation and environmentally-friendly process for the removal of the cyanotoxins that show the major impact on drinking water: microcystins (MC-LR and MC-RR), cylindrospermopsin (CYN), anatoxin-a (ATX) and saxitoxin (STX). The performance of the system was evaluated under ambient conditions and circumneutral pH (pH0 = 5) using relevant cyanotoxin concentrations (100–500 μg L−1). The nature of the cyanotoxins determined their reactivity towards CWPO, which decreased in the following order: MC-RR > CYN > MC-LR ≫ ATX > STX. In this sense, microcystins and CYN were completely removed in short reaction times (1–1.5 h) with a low catalyst concentration (0.2 g L−1) and the stoichiometric amount of H2O2 (2–2.6 mg L−1), while only 60–80% conversion was achieved with ATX and STX in 5 h. In these cases, an intensification of the operating conditions (1 g L−1 catalyst and up to 30 mg H2O2 L−1) was required to remove both toxins in 1 h. The impact of the main components of freshwaters i.e. natural organic matter (NOM) and several inorganic ions (HCO3−, HPO42-, SO42-) on the performance of the process was also investigated. Although the former led to a partial inhibition of the reaction due to HO· scavenging and catalyst coating, the latter did not show any remarkably effect, and the versatility of the process was finally confirmed in a real surface water. To further demonstrate the effectiveness of the catalytic system, the toxicity of both the initial cyanotoxins and the resulting CWPO effluents was measured with the brine shrimp Artemia salina. Remarkably, all CWPO effluents were non-toxic at the end of the treatment.This research has been supported by the Spanish MINECO through the project CTM-2016-76454-R and by the CM through the project P2018/EMT-4341. M. Munoz thanks the Spanish MINECO for the Ramón y Cajal postdoctoral contract (RYC-2016-20648). J. Nieto-Sandoval thanks the Spanish MINECO for the FPI predoctoral grant (BES-2017-081346

Insights on the removal of the azole pesticides included in the EU Watch List by Catalytic Wet Peroxide Oxidation

The aim of this work is to evaluate the feasibility of the Catalytic Wet Peroxide Oxidation (CWPO) process using the inexpensive and environmentally friendly Fe3O4-R400 catalyst for the removal from water of a representative group of azole pesticides recently listed in the European Union (EU) Watch Lists (penconazole (PEN), prochloraz (PCZ), tebuconazole (TEB), tetraconazole (TET), metconazole (MET)). The complete removal of these pollutants (1000 μg L−1) was achieved in <1 h reaction time under ambient conditions using a catalyst concentration of 0.5 g L−1 and the stoichiometric dose of H2O2 (3 – 5 mg L−1) at a slightly acidic pH (pH0 = 5.0). To further demonstrate the effectiveness of the process, the ecotoxicity abatement was also considered. The initial toxicity of the pesticides and the CWPO effluents were evaluated with the brine shrimp Artemia salina and the bacterium Vibrio fischeri. Remarkably, the effluents were non-toxic for V. fischeri and a decrease of more than 80% in mortality was achieved for A. salina. Furthermore, the versatility of the system was proved in real water matrices (surface water and WWTP effluent), although a slight decrease on the oxidation rate was found due to the occurrence of organic matter and inorganic salts. The reactivity of the azole pesticides was finally compared with the achieved for other groups of pollutants included in the EU Watch Lists (pharmaceuticals, hormones, and neonicotinoid pesticides). Clearly, azole compounds showed the least reactivity to oxidation, suggesting that they can be used as general indicators of the overall efficiency of the proposed catalytic system for the removal of EU Watch Lists micropollutantsThis research has been supported by the Spanish AEI through the project PID2019-105079RB-100 and by the CM, Spain through the project P2018/EMT-4341. M. Munoz, N. Lopez-Arago and J. Nieto-Sandoval thanks the Spanish AEI for the Ramón y Cajal postdoctoral contract (RYC-2016-20648), the FPI predoctoral, Spain grant (PRE2020-09452) and the FPI postdoctoral, Spain grant (BES-2017-081346), respectivel

Increasing Engineering Students’ Involvement in Circular Economy Practices.

The circular economyhas become a topic of intense interest for policymakers, scholars and business managers because it has proven to bea new paradigm to achieve the sustainability of our society. However, the main efforts made in thecircular economy cannot be limited tothe actions ofprofessional or experts. We believe that if we intend to meet current needs without compromising the ability of future generations to meet their own needs, we mustteach present generations the principles for achievingeconomic, social and environmentalsustainability in the short, mediumand long-term. This paper highlights the use of participatory guided activitiesinstead of traditional coursesto teach and engage engineering students with circular economy practices

B-Function Expression in the Flower Center Underlies the Homeotic Phenotype of Lacandonia schismatica (Triuridaceae)

Spontaneous homeotic transformations have been described in natural populations of both plants and animals, but little is known about the molecular-genetic mechanisms underlying these processes in plants. In the ABC model of floral organ identity in Arabidopsis thaliana, the B- and C-functions are necessary for stamen morphogenesis, and C alone is required for carpel identity. We provide ABC model-based molecular-genetic evidence that explains the unique inside-out homeotic floral organ arrangement of the monocotyledonous mycoheterotroph species Lacandonia schismatica (Triuridaceae) from Mexico. Whereas a quarter million flowering plant species bear central carpels surrounded by stamens, L. schismatica stamens occur in the center of the flower and are surrounded by carpels. The simplest explanation for this is that the B-function is displaced toward the flower center. Our analyses of the spatio-temporal pattern of B- and C-function gene expression are consistent with this hypothesis. The hypothesis is further supported by conservation between the B-function genes of L. schismatica and Arabidopsis, as the former are able to rescue stamens in Arabidopsis transgenic complementation lines, and Ls-AP3 and Ls-PI are able to interact with each other and with the corresponding Arabidopsis B-function proteins in yeast. Thus, relatively simple molecular modifications may underlie important morphological shifts in natural populations of extant plant taxa