RESUMO
Ammonia is one of the most widely produced chemicals worldwide, which is consumed in the fertilizer industry and is also considered an interesting alternative in energy storage. However, common ammonia production is energy-demanding and leads to high CO2 emissions. Thus, the development of alternative ammonia production methods based on available raw materials (air, for example) and renewable energy sources is highly demanding. In this work, we demonstrated the utilization of TiB2 nanostructures sandwiched between coupled plasmonic nanostructures (gold nanoparticles and gold grating) for photoelectrochemical (PEC) nitrogen reduction and selective ammonia production. The utilization of the coupled plasmon structure allows us to reach efficient sunlight capture with a subdiffraction concentration of light energy in the space, where the catalytically active TiB2 flakes were placed. As a result, PEC experiments performed at -0.2 V (vs. RHE) and simulated sunlight illumination give the 535.2 and 491.3 µg h-1 mgcat-1 ammonia yields, respectively, with the utilization of pure nitrogen and air as a nitrogen source. In addition, a number of control experiments confirm the key role of plasmon coupling in increasing the ammonia yield, the selectivity of ammonia production, and the durability of the proposed system. Finally, we have performed a series of numerical and quantum mechanical calculations to evaluate the plasmonic contribution to the activation of nitrogen on the TiB2 surface, indicating an increase in the catalytic activity under the plasmon-generated electric field.
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The determination of secondary volatile degradation products in drying oil extracts is substantial to prevent formation of undesirable metal formates in paintings and/or other artefacts. This study develops a simple, cost-effective, and reliable, high-performance liquid chromatography with diode array detector (HPLC-DAD) method to determine three secondary volatile degradation products (methanol, formaldehyde, and formic acid) in drying oils, including linseed, poppy-seed, and walnut oil. Extraction of analytes was performed using QuEChERS-based procedure followed by metal oxide-based dispersive solid-phase extraction (d-SPE) clean-up and presented a good performance for all of the volatile analytes of interest with recoveries in the range of 90-120% after application of the nanostructured cerium oxide-based (CeO2) and zirconia-based (ZrO2) sorbents prepared by favorable and ecological-friendly methods. With a new clean-up solution for samples with high-fat content, it was possible to achieve higher recoveries than with commercial Z-Sep/C18 sorbent. In all cases, relative standard deviations (RSD) of less than 10% were achieved. No significant matrix interference was observed due to the application of effective sorbents in nanostructured form. The developed method was applied to samples of drying oils, and it was found that after storage for three months, all methanol was most likely oxidized to formaldehyde and formic acid. The concentrations of formaldehyde were in the range of 260 - 304 µgâg-1, while formic acid concentrations ranged between 72 - 386 µgâg-1. The highest concentration of formaldehyde (304 µgâg-1) and formic acid (386 µgâg-1) was found in linseed oil.
Assuntos
Óleo de Semente do Linho , Metanol , Cromatografia Líquida de Alta Pressão/métodos , Formaldeído , Formiatos , Óleos , Óxidos , Extração em Fase Sólida/métodosRESUMO
Lead carboxylates are an extensive group of compounds studied for their promising industrial applications and for their risky behavior when they are formed in oil paintings as corrosion products of lead-based pigments, leading to serious deterioration of paintings. Although the processes leading to the formation of aggregates, protrusions or inclusions, affecting undesirably the appearance of paintings, are assumed to be long term, neo-formed lead carboxylates are detectable in the early stage of paint drying. To uncover the chemical changes in lead pigments during the drying of oil paint films, model systems consisting of minium (Pb3O4) and four common drying oils were studied by X-ray powder diffraction (XRPD), 13C and 207Pb solid state NMR (ssNMR) spectroscopy and Fourier-transformed infrared spectroscopy (FTIR). For the first time, a degradation mechanism of Pb3O4via the crystallization of lead formate (Pb(HCOO)2), at the end of oxidative polymerization of oil paint films, was uncovered. The formation of formic acid in oils was proved by gas chromatography-mass spectrometry (GC-MS). Vapor experiments evidenced the susceptibility of Pb3O4 to react with volatile formic acid released during the autoxidation of oils comparably to the direct pigment-binder interactions in paint films. The investigation of the local environment of lead atoms in the paint film by 207Pb WURST-CPMG NMR spectroscopy showed that Pb(ii) atoms reacted with linseed oil preferentially to form highly crystalline Pb(HCOO)2, while the local chemical environment of Pb(iv) atoms did not change. The results proved the co-existence of (i) highly crystalline Pb(HCOO)2, (ii) a highly mobile amorphous phase corresponding to free carboxylic acids or a nascent lead soap phase and (iii) the remaining Pb3O4 in the polymeric/ionomeric network. Pb(HCOO)2 is assumed to be an intermediate for the conversion of Pb3O4 to lead soaps and/or lead carbonates.
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A simple low-temperature water-based and one-pot synthesis was developed for the preparation of nanocrystalline CeO2 that was used for degradation of the toxic organophosphate pesticide parathion methyl. By changing the reaction temperature in the range from 5 °C to 95 °C, several properties (i.e., crystallinity, grain size and surface area) of nanoceria can be easily controlled. The catalytic decomposition of parathion methyl to its degradation product 4-nitrophenol was highly dependent on the CeO2 preparation temperature. It was demonstrated that at low temperature (i.e. 5 °C), CeO2 with very small crystallites (<2 nm) and high surface area can be obtained. For practical use, it was demonstrated that highly crystalline CeO2 can be prepared at room-temperature (30 °C) in at least 100 g batches. It was shown that precipitated nanoceria had high thermal stability and its post-synthesis annealing up to 400 °C did not significantly alter the material properties and hence the catalytic activity. Furthermore, as shown by the reusability tests, the sorbent can be reactivated by simply washing with water which demonstrated its durability.
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Surface catalyzed reactions can be a convenient way to deactivate toxic chemical warfare agents (CWAs) and remove them from the contaminated environment. In this study, pure titanium oxide, magnesium hydroxide, and their composites TiO2/Mg(OH2) were prepared by thermal decomposition and precipitation of the titanium peroxo-complex and/or magnesium nitrate in an aqueous solution. The as-prepared composites were examined by XRD, XPS, HRTEM, and nitrogen physisorption. Their decontamination ability was tested on CWA surrogates and determined by high-performance liquid chromatography (HPLC) and gas chromatography coupled with mass spectrometry (GC-MS). Dimethyl methyl phosphonate (DMMP) was used as a G simulant for the nerve agents sarin (GB) and soman (GD) while 2-chloroethyl ethyl sulfide (2-CEES) and 2-chloroethyl phenyl sulfide (2-CEPS) were used as surrogates of sulfur mustard (HD). The activity of the as-prepared composites was correlated with acid-base properties determined by potentiometric titrations and pyridine adsorption studied by in situ DRIFTS. The mixing of Ti and Mg led to an increase of the surface area and the amount of surface -OH groups (with an increasing amount of Ti) that caused improved degradation of DMMP.
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Anthracyclines are a class of pharmaceuticals used in cancer treatment have the potential to negatively impact the environment. To study the possibilities of anthracyclines (represented by pirarubicin and valrubicin) removal, chemical inactivation using NaOH (0.01 M) and NaClO (5%) as decontamination agents and adsorption to powdered nanocrystalline titanium dioxide (TiO2) were compared. The titanium dioxide (TiO2) nanoparticles were prepared via homogeneous precipitation of an aqueous solution of titanium (IV) oxy-sulfate (TiOSO4) at different amount (5-120 g) with urea. The as-prepared TiO2 samples were characterized by XRD, HRSEM and nitrogen physisorption. The adsorption process of anthracycline cytostatics was determined followed by high-performance liquid chromatography coupled with mass spectrometry (LC-MS) and an in-situ Diffuse Reflectance Infrared Fourier Transform Spectroscopy (DRIFTS) technique. It was found that NaClO decomposes anthracyclines to form various transformation products (TPs). No TPs were identified after the reaction of valrubicin with a NaOH solution as well as in the presence of TiO2 nanoparticles. The best degree of removal, 100% of pirarubicin and 85% of valrubicin, has been achieved in a sample with 120 grams of TiOSO4 (TIT120) and TiO2 with 60 grams (TIT60), respectively.
Assuntos
Citostáticos/química , Doxorrubicina/análogos & derivados , Nanoestruturas/química , Titânio/química , Poluentes Químicos da Água/química , Adsorção , Cristalização , Citostáticos/isolamento & purificação , Descontaminação/métodos , Doxorrubicina/química , Doxorrubicina/isolamento & purificação , Hidrólise , Tamanho da Partícula , Hidróxido de Sódio/química , Hipoclorito de Sódio/química , Propriedades de Superfície , Poluentes Químicos da Água/isolamento & purificaçãoRESUMO
Cerium oxide nanoparticles were prepared by calcination of basic cerous carbonate (as a precursor) obtained by precipitation from an aqueous solution. Prepared samples were characterized by X-ray diffraction (XRD), infrared spectroscopy (FTIR), high resolution scanning electron microscopy (HRSEM), BET (Brunauer-Emmett-Teller) surface area and porosity measurement. Prepared cerium oxide was applied as a destructive sorbent for the fast and safe degradation of organophosphorus flame retardant triphenyl phosphate (TPP). It was shown that cerium dioxide was effective in the decomposition of TPP by cleavage of the P-O-aryl bond in the flame retardant molecule. A degradation mechanism for TPP on the ceria surface was proposed. The degradation is governed by conversion of TPP via diphenyl phosphate (DPP) to the final product identified as phenol (Ph). The key parameter increasing the degradation efficiency of CeO2 is the temperature of calcination. At optimum calcination temperature (500 °C), the produced ceria retains a sufficiently high surface area and attains an optimum degree of crystallinity (related to a number of crystal defects, and thus potential reactive sites). The fast and efficient degradation of organophosphorus flame retardant TPP was observed in a polar aprotic solvent (acetonitrile) that is miscible with water.
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INTRODUCTION: Macrocrystalline oxides of alkaline earth metals (Mg and Ca) or light metals (Al and Ti) can respond to standard warfare agents such as sulfur mustard, soman, or agent VX. In this paper, we compared the decontamination ability of sodium hydroxide (NaOH) and sodium hypochlorite (NaClO) for nitrogen mustards (cyclophosphamide [CP] and ifosfamide [IFOS]) with a new procedure using a destructive sorbent based on nanocrystalline and nanodispersive titanium dioxide (TiO2) as a new efficient and cheap material for complete decontamination of surfaces. METHODS: Titanium (IV) dioxide nanoparticles were prepared by the homogeneous hydrolysis of titanium(IV) oxysulfate (TiOSO4) with urea. The as-prepared TiO2 nanoparticles were used for the fast and safe decontamination of cytostatics from the nitrogen mustard family (CP and IFOS) in water. The adsorption-degradation process of cytostatics in the presence of TiO2 was compared with decontamination agents (0.01 M solution of sodium hydroxide and 5% solution of sodium hypochlorite). The mechanism of the decontamination process and the degradation efficiency were determined by high-performance liquid chromatography with mass spectrometry. RESULTS: It was demonstrated that a 0.01 M solution of sodium hydroxide (NaOH) decomposes CP to 3-((amino(bis(2-chloroethyl)amino)phosphoryl)oxy)propanoic acid and sodium hypochlorite formed two reaction products, namely, IFOS and 4-hydroxy-cyclophosphamide. IFOS is cytotoxic, and 4-hydroxy-cyclophosphamide is a known metabolite of CP after its partial metabolism by CYP/CYP450. IFOS degrades in the pres¬ence of NaOH to toxic IFOS mustard. Titanium(IV) dioxide nanoparticles adsorbed on its surface CP after 5 minutes and on IFOS after 10 minutes. The adsorption-degradation process of CP in water and in the presence of TiO2 led to 4-hydroxy-cyclophosphamide and IFOS, respectively, which decayed to oxidation product 4-hydroxy-ifosfamide. CONCLUSION: Nanodispersive TiO2 is an effective degradation agent for decontamination of surfaces from cytostatics in medical facilities.
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Antineoplásicos Alquilantes/química , Ciclofosfamida/química , Citostáticos/química , Descontaminação/métodos , Ifosfamida/química , Nanopartículas/química , Titânio/química , Antineoplásicos Alquilantes/metabolismo , Ciclofosfamida/metabolismo , Citostáticos/metabolismo , Humanos , Ifosfamida/metabolismoRESUMO
Nanostructured titanium(IV) oxide was used for the destructive adsorption and photocatalytic degradation of mitoxantrone (MTX), a cytostatic drug from the group of anthracycline antibiotics. During adsorption on a titania dioxide surface, four degradation products of MTX, mitoxantrone dicarboxylic acid, 1,4-dihydroxy-5-((2-((2-hydroxyethyl)amino)ethyl)amino)-8-((2-(methylamino)ethyl)amino)anthracene-9,10-dione, 1,4-dihydroxy-5,8-diiminoanthracene-9,10(5H,8H)-dione and 1,4-dihydroxy-5-imino-8-(methyleneamino)anthracene-9,10(5H,8H)-dione, were identified. In the case of photocatalytic degradation, only one degradation product after 15 min at m/z 472 was identified. This degradation product corresponded to mitoxantrone dicarboxylic acid, and complete mineralization was attained in one hour. Destructive adsorbent manganese(IV) oxide, MnO2, was used only for the destructive adsorption of MTX. Destructive adsorption occurred only for one degradation product, mitoxantrone dicarboxylic acid, against anatase TiO2.