Different effects of NaCl and Na2SO4 on soil net nitrogen mineralization in coastal wetlands.

NaCl and Na2SO4 are the foremost salt compositions in coastal wetlands, while their effects on soil net nitrogen mineralization still remain unclear. Aimed at investigating the two salt compositions on soil net nitrogen mineralization, a 30-day laboratory incubation experiment was respectively conducted by adding 5‰ NaCl and Na2SO4 to incubated coastal wetland soils under aerobic conditions. Our results showed that Na2SO4 addition increased the rates of mineralization (Rmin) by an average of 33.03% and nitrification (Rnit) by 23.84% during the incubation (p < 0.05). In contrast, NaCl addition significantly reduced Rmin by 71% and Rnit by 44% at day 7 (p < 0.05). The activities of fluorescein diacetate, arylamidase and urease in Na2SO4 addition treatments were higher than those in NaCl addition treatment. These results demonstrated the ion-specific effects of salt type on nitrogen mineralization rates and enzyme activities.

The Influence of Solution pH on the Kinetics of Resorcinol Electrooxidation (Degradation) on Polycrystalline Platinum.

Electrochemical oxidation of resorcinol on a polycrystalline platinum electrode was investigated in five different solutions, namely 0.5 and 0.1 M H2SO4, 0.5 M Na2SO4, 0.5 and 0.1 M NaOH. The rates of electrochemical degradation of resorcinol were determined based on the obtained reaction parameters, such as resistance, capacitance and current-density. The electrochemical analyses (cyclic voltammetry and a.c. impedance spectroscopy) were carried-out by means of a three-compartment, Pyrex glass cell. These results showed that the electrochemical oxidation of resorcinol is strongly pH-dependent. In addition, the energy dispersive X-ray (EDX) spectroscopy technique was employed for Pt electrode surface characterization. Additionally, the quantitative determination of resorcinol removal was performed by means of instrumental high-performance liquid chromatography/mass spectrometry (HPLC/MS) methodology.

Comparative studies in electrochemical degradation of sulfamethoxazole and diclofenac in water by using various electrodes and phosphate and sulfate supporting electrolytes.

In this study, the electro-oxidation capacities of Na2SO4 and potassium phosphate buffer supporting electrolytes were tested and compared for destruction of the sulfamethoxazole (SMX) and diclofenac (DCF) on platinum (Pt) electrode and graphite carbon electrode in aqueous medium. The suitability of pharmaceutical active compounds (PhACs) for electrochemical oxidation was tested by cyclic voltammetry (CV) technique performed in the potential range -1.5 to +1.5 V versus Ag/AgCl, which confirmed the electro-activity of the selected PhACs. The degradation and mineralization were monitored by ultraviolet (UV)-Vis spectrophotometry and HPLC. 0.1 M Na2SO4 supporting electrolyte was found to be more effective for mineralization of SMX and DCF, with efficiency of 15-30% more than the 0.1 M phosphate buffer supporting electrolyte on the platinum (Pt) and carbon electrodes. The Pt electrode showed better performance in the degradation of the two PhACs while under the same conditions than the carbon electrode for both 0.1 M Na2SO4 and 0.1 M potassium phosphate buffer supporting electrolytes. The SMX and DCF degradation kinetics best fitted the second-order reaction, with rate constants ranging between 0.000389 and 0.006 mol(2) L(-2) min(-1) and correlation coefficient (R(2)) above 0.987. The second-order degradation kinetics indicated that the rate-determining step in the degradation could be a chemical process, thus suggesting the active involvement of electrolyte radical species in the degradation of SMX and DCF. Results obtained from a real field sample showed a more than 98% removal of the PhACs from the wastewater by electrochemical degradation.

Oxidized 3,3',5,5'-tetramethylbenzidine nanobelts enhance colorimetric sensing of H2O2.

Herein, oxidized 3,3',5,5'-tetramethylbenzidine (oxTMB) nanobelts were developed to enhance the colorimetric and paper-based sensing of H2O2. It was found that the minor component of Fe2+ in Na2SO4 reagent could catalyze the oxidization of TMB by H2O2 into positively charged oxTMB, which was further assembled into dark blue oxTMB nanobelts via electrostatic interaction with SO42-. The extinction originating from the absorption and scattering of oxTMB nanobelts was utilized to quantitatively detect H2O2 with a wide linear detection range (1.0-300 µM) and a low limit of detection (0.48 µM). In addition, no coffee-ring effect was observed in the test zone of the paper-based colorimetric array, which was beneficial to judge the color by naked eye. Finally, the colorimetric method was applied to detect H2O2 in contact lens care solution. This work not only proposed a new colorimetric sensing platform for H2O2, but also highlighted the minor component in the reagent might influence the experimental result.

Macro-characteristics and micro-mechanisms of Na2SO4 precipitation dissolved by KNO3 molten salt in a continuous supercritical water system.

This work aims to explore the ability of molten salt to solve salt deposition in supercritical water (SCW) related technologies including supercritical water oxidation and supercritical water gasification, with KNO3 and Na2SO4 as examples. In the pure KNO3 solution, the two-phase layering of high-density KNO3 molten salt (settling at the reactor bottom) and low-density saturated KNO3-SCW salt solution (flowing out at the top outlet of the reactor) was formed in a kettle-reactor with about 6.5 ratio of depth to inner diameter, thereby improving the accuracy of measured solubilities. The precipitation macro-characteristics of mixed KNO3 and Na2SO4 in SCW were investigated under different feed concentration conditions. The results showed that Na2SO4 deposition on the reactor sidewall could be reduced by more than 90 % when the mass ratio of KNO3 to Na2SO4 in the feed was only 0.167. No visible salt deposition was observed on the sidewall when the ratio was 0.374. All solid deposited salts were converted into the liquid molten salt as the ratio reached 3.341, and thus could easily flow out of the reactor, without plugging. 'Molten salt dissolution' mechanism may provide a more plausible explanation for mixed KNO3 and Na2SO4 in SCW. In addition, the precipitation micro-mechanisms of mixed KNO3 and Na2SO4, and the critical conditions of avoiding sidewall deposition and reactor plugging were proposed. This work is valuable for overcoming the salt deposition problem in SCW-related technologies.

Investigation of ion association kinetics in Na2SO4-H2O by excess Raman spectroscopy and 2D correlation Raman spectroscopy.

The ion association of salts aqueous solutions have long captivated the attention of researchers within the field of physical chemistry. In this paper, we have performed a comprehensive analysis of ion interactions in sodium sulfate (Na2SO4) aqueous solutions using a combination of high-resolution techniques, including excess (ERS) and two-dimensional correlation (2DCRS) Raman spectroscopy in conjunction with molecular dynamics (MD) calculations. The Raman spectrum shows that two inflection points in the Raman shift of the O-H vibration are observed with the increase in Na2SO4 concentration. Simultaneously, a new peak of the SO42- vibration appears at first inflection point, representing the formation of ion association. Further analysis based on ERS and 2CRS reveals that these two inflection points correspond respectively to the formation of ion pairs (CIPs) and small ion clusters. Importantly, MD simulations confirm the above experimental results. Our study provides evidence for ion association and clustering in aqueous in salt ion aqueous solutions.

Unexpected Effects of Sulfate and Sodium Chloride Application on Yield Qualitative Characteristics and Symmetry Indicators of Hard and Soft Wheat Kernels.

The heterogeneity of grain quality can lead to limited predictability of qualitative and quantitative characteristics of the wheat yield, especially with an increase in the importance of drought and salinity caused by climate change. This study was undertaken with the aim of creating basic tools for phenotyping and assessing the sensitivity of genotypes to salt effects at the level of some wheat kernel attributes. The study considers 36 variants of the experiment, including four wheat cultivars-Zolotaya, Ulyanovskaya 105, Orenburgskaya 10, Orenburgskaya 23; three treatment variants-control (without salt) and two salts exposure (NaCl at a concentration of 1.1 g L-1 and Na2SO4 at a concentration of 0.4 g L-1); as well as three options for the arrangement of kernels in a simple spikelet-left, middle, and right. It has been established that the salt exposure had a positive effect on the percentage of kernel fulfilling in the cultivars Zolotaya, Ulyanovskaya 105, and Orenburgskaya 23 compared to control. The kernels of the Orenburgskaya 10 variety matured better in the experiment with Na2SO4 exposure, while the control variant and NaCl gave the same effect. When exposed to NaCl, significantly greater values of weight, transverse section area, and transverse section perimeter of the kernel were noted in the cv Zolotaya and Ulyanovskaya 105. Cv Orenburgskaya 10 responded positively to the use of Na2SO4. This salt caused an increase in the area, length, and width of the kernel. The fluctuating asymmetry of the left, middle, and right kernels in the spikelet was calculated. In the cv Orenburgskaya 23 the salts affected only the kernel perimeter among parameters examined. The indicators of the general (fluctuating) asymmetry were lower in the experiments with the use of salts, i.e., kernels were more symmetrical than in the control variant, both for the cultivar as a whole and when compared taking into account the kernel location in spikelet. However, this result was unexpected, since salt stress inhibited a number of morphological parameters: the number and average length of embryonic, adventitious, and nodal roots, flag leaf area, plant height, dry biomass accumulation, and plant productivity indicators. The study showed that low concentrations of salts can positively affect the fulfilling of kernels (the absence of a cavity inside the kernel) and the symmetry of the left and right sides of the kernel.

High-Temperature Corrosion Behavior of Selected HVOF-Sprayed Super-Alloy Based Coatings in Aggressive Environment at 800 °C.

This study is focused on the high-temperature corrosion evaluation of selected thermally sprayed coatings. NiCoCrAlYHfSi, NiCoCrAlY, NiCoCrAlTaReY, and CoCrAlYTaCSi coatings were sprayed on the base material 1.4923. This material is used as a cost-efficient construction material for components of power equipment. All evaluated coatings were sprayed using HP/HVOF (High-Pressure/High-Velocity Oxygen Fuel) technology. High-temperature corrosion testing was performed in a molten salt environment typical for coal-fired boilers. All coatings were exposed to the environment of 75% Na2SO4 and 25% NaCl at the temperature of 800 °C under cyclic conditions. Each cycle consisted of 1 h heating in a silicon carbide tube furnace followed by 20 min of cooling. The weight change measurement was performed after each cycle to establish the corrosion kinetics. Optical microscopy (OM), scanning electron microscopy (SEM), and elemental analysis (EDS) were used to analyze the corrosion mechanism. The CoCrAlYTaCSi coating showed the best corrosion resistance of all the evaluated coatings, followed by NiCoCrAlTaReY and NiCoCrAlY. All the evaluated coatings performed better in this environment than the reference P91 and H800 steels.

Efficient capture of endocrine-disrupting compounds by a high-performance nanofiltration membrane for wastewater treatment.

Conventional polyamide (PA) nanofiltration (NF) membranes can readily adsorb aromatic compounds, such as endocrine disrupting compounds (EDCs). Therefore, these substances can easily be transported across the membrane by solution-diffusion, resulting in a poor EDC-rejection. In this work, a novel thin film nanocomposite (TFN) membrane was fabricated by incorporating covalent organic frameworks (COFs) into the PA layer via an interfacial polymerization reaction. COFs with functional groups can provide abundant active binding sites for highly efficient EDC-capture. The rejection of the optimal TFN-COF membrane for bisphenol A, bisphenol AF, and sodium 2-biphenylate was 98.3%, 99.1%, and 99.3%, respectively, which was much higher than of the rejection of the pristine NF-membrane (82.4%, 95.5%, and 96.4%, respectively). Additionally, the TFN-COF membrane could be regenerated fast and efficiently by washing with ethanol for some minutes. COF nanofillers with porous structures provide additional water channels, making it possible to overcome the permeability-selectivity trade-off of NF membranes. The water permeance (17.1 L m-2 h-1 bar-1) of the optimal membrane was about two times higher than for the pristine NF-membrane (8.7 L m-2 h-1 bar-1). In addition, the TFN-COF membrane with a COF-loading of 0.05% w/v had an excellent Na2SO4 rejection (95.2%) due to size exclusion and strong Donnan effect. This work combines traditional NF membranes and adsorption materials to achieve efficient capture and rapid release of EDCs without sacrificing salt rejections, which opens the door to develop fit-for-purpose adsorptive NF membranes.

Assessment of Hot Corrosion in Molten Na2SO4 and V2O5 of Inconel 625 Fabricated by Selective Laser Melting versus Conventional Technology.

Inconel 625 samples, obtained by Selective Laser Melting (SLM) and conventional technology, were tested for hot corrosion resistance against a molten mixture of Na2SO4 and V2O5. The assessments were performed in air, at 900 °C with exposure time of up to 96 h, and at 1000 °C for 8 h. Weight gain was higher for samples obtained by SLM, with 37.4% after 8 h, 3.98% after 24 h, 4.46% after 48 h, and 5.8% after 96 h at 900 °C (22.6% at 1000 °C, 8 h). Three stages of corrosion were observed, the first and last with a high corrosion rate, while the second one showed a slower corrosion rate. Corrosion behaviour depends on the morphology of the grain boundary, which can influence the infiltration of corrosive salts, and on the formation of Cr2NiO4 compound, which acts as a temporary barrier.

Na2SO4 and NaCl salts differentially modulate the antioxidant systems in the highly stress tolerant halophyte Prosopis strombulifera.

Prosopis strombulifera (Lam.) Benth. is a halophytic shrub abundant in high-salinity areas in central Argentina, with high tolerance against NaCl but strong growth inhibition by Na2SO4. In the present study, the modulation of the antioxidant systems (enzymatic and non-enzymatic components) was analyzed under different salt treatments (NaCl, Na2SO4 and the iso-osmotic mixture) in hydroponic cultivation. Na2SO4-treated plants showed strong indications of oxidative stress (H2O2 and O2-• increase). Modifications in antioxidant enzymes activities were observed mainly under Na2SO4 treatment, where CAT seems to play an important role in early detoxification of H2O2 in roots, whereas SOD and APX have a predominant role in leaves. As part of the non-enzymatic system, 21 compounds were identified in leaves, being polyphenols the most abundant. Control plants contained the major variety of detected phytochemicals (14). Na2SO4-treated plants contained 10 compounds and NaCl-treated plants nine compounds, but with a different profile. NaCl-treated plants showed the highest antioxidant capacity. Our findings confirm that different types of salt treatments provoke a differential modulation of the antioxidant systems. Polyphenols and other ROS-detoxifying compounds, in a joint action with the enzymatic antioxidant system, are proposed to have a fundamental role in the cellular protection of P. strombulifera plants under severe oxidative stress. Our findings also highlight the potential of this halophyte as a valuable source of bioactive compounds with high antioxidant activity and health benefits.

Corrosion Behavior of Steel-Reinforced Green Concrete Containing Recycled Coarse Aggregate Additions in Sulfate Media.

Novel green concrete (GC) admixtures containing 50% and 100% recycled coarse aggregate (RCA) were manufactured according to the ACI 211.1 standard. The GC samples were reinforced with AISI 1080 carbon steel and AISI 304 stainless steel. Concrete samples were exposed to 3.5 wt.% Na2SO4 and control (DI-water) solutions. Electrochemical testing was assessed by corrosion potential (Ecorr) according to the ASTM C-876-15 standard and a linear polarization resistance (LPR) technique following ASTM G59-14. The compressive strength of the fully substituted GC decreased 51.5% compared to the control sample. Improved corrosion behavior was found for the specimens reinforced with AISI 304 SS; the corrosion current density (icorr) values of the fully substituted GC were found to be 0.01894 µA/cm2 after Day 364, a value associated with negligible corrosion. The 50% RCA specimen shows good corrosion behavior as well as a reduction in environmental impact. Although having lower mechanical properties, a less dense concrete matrix and high permeability, RCA green concrete presents an improved corrosion behavior thus being a promising approach to the higher pollutant conventional aggregates.

Differential effects of NaCl and Na2SO4 on the halophyte Prosopis strombulifera are explained by different responses of photosynthesis and metabolism.

Prosopis strombulifera (Lam.) Benth. is a halophytic shrub found in highly saline soils in Argentina, with high tolerance against NaCl but strong growth inhibition by Na2SO4. In the present study, the differences in the physiological responses caused by these salts and an iso-osmotic combination thereof on photosynthesis, mineral composition and metabolism were analyzed. Na2SO4 treated plants were the most affected by salinity, showing a significant decrease in several photosynthetic parameters. Proline and cysteine accumulated significantly in the plants in response to salt stress. These results show by the first time that the SO42- anion is triggering damage in the photosynthetic apparatus and consequently affecting the photosynthetic process, which may explain the strong growth inhibition in these plants at high salinity. Moreover, the SO42- anion provoke challenges in the incorporation of nutrients, decreasing the levels of K, Ca, P and Mg, and inducing a strong antioxidant activity in P. strombulifera.

Preparation and Thermal Performance Enhancement of Low Temperature Eutectic Composite Phase Change Materials Based on Na2SO4·10H2O.

In this paper, a series of Na2SO4·10H2O⁻KCl eutectic mixtures were prepared by adding different mass fractions of KCl (1 wt.%, 3 wt.%, 5 wt.%, or 7 wt.%) to Na2SO4·10H2O. Polyacrylamide (PAM) was proposed as the thickener, sodium tetraborate decahydrate (STD) was proposed as the nucleating agent, and expanded graphite (EG) was proposed as the high thermal conductivity medium for Na2SO4·10H2O⁻5 wt.% KCl eutectics. The results showed that in Na2SO4·10H2O⁻5 wt.% KCl eutectics with 5 wt.% PAM and 5 wt.% STD, almost no phase separation occurred, and the degree of supercooling was reduced to 0.4 °C. The thermal performance of Na2SO4·10H2O⁻5 wt.% KCl composite phase change materials (CPCMs) with varying contents of EG was explored. The results showed that EG could improve the thermal conductivity effectively and that the mass fraction of EG should be no more than 3%, otherwise the crystallization value and supercooling would deteriorate. The thermal reliability of the Na2SO4·10H2O⁻5 wt.% KCl eutectic CPCMs containing 5 wt.% PAM, 5 wt.% STD, and 3 wt.% EG was investigated, mainly through the ambient temperature, thermal cycling test, and TGA analysis. The results demonstrated that these CPCMs showed perfect thermal reliability.

Characteristics of activated carbon remove sulfur particles against smog.

Sulfur particles, which could cause diseases, were the main powder of smog. And activated carbon had the very adsorption characteristics. Therefore, five sulfur particles were adsorbed by activated carbon and were analyzed by FT-IR. The optimal adsorption time were 120 min of Na2SO3, 120 min of Na2S2O8, 120 min of Na2SO4, 120 min of Fe2(SO4)3 and 120 min of S. FT-IR spectra showed that activated carbon had the eight characteristic absorption of S-S stretch, H2O stretch, O-H stretch, -C-H stretch, conjugated C[bond, double bond]O stretch or C[bond, double bond]C stretch, CH2 bend, C-O stretch and acetylenic C-H bend vibrations at 3850 cm-1, 3740 cm-1, 3430 cm-1, 2920 cm-1, 1630 cm-1, 1390 cm-1, 1110 cm-1 and 600 cm-1, respectively. For Na2SO3, the peaks at 2920 cm-1, 1630 cm-1, 1390 cm-1 and 1110 cm-1 achieved the maximum at 20 min. For Na2S2O8, the peaks at 3850 cm-1, 3740 cm-1 and 2920 cm-1 achieved the maximum at 60 min. The peaks at 1390 cm-1, 1110 cm-1 and 600 cm-1 achieved the maximum at 40 min. For Na2SO4, the peaks at 3430 cm-1, 2920 cm-1, 1630 cm-1, 1390 cm-1, 1110 cm-1 and 600 cm-1 achieved the maximum at 60 min. For Fe2(SO4)3, the peaks at 1390 cm-1, 1110 cm-1 and 600 cm-1 achieved the maximum at 20 min. For S, the peaks at 1630 cm-1, 1390 cm-1 and 600 cm-1 achieved the maximum at 120 min. It provided that activated carbon could remove sulfur particles from smog air to restrain many anaphylactic diseases.

Adsorption characteristics of sulfur powder by bamboo charcoal to restrain sulfur allergies.

Exposures to particulate matter with a diameter of 2.5 µm or less (PM2.5) may influence the risk of birth defects and make you allergic, which causes serious harm to human health. Bamboo charcoal can adsorb harmful substances,that was of benefitto people's health. In order to figure out the optimal adsorbtion condition and the intrinsic change of bamboo charcoal, five chemicals were adsorbed by bamboo charcoal and were analyzed by FT-IR. The optimal blast time was 80 min of Na2SO3, 100 min of Na2S2O8, 20 min of Na2SO4, 120 min of Fe2(SO4)3 and 60 min or 100 min of S. FT-IR spectra showed that bamboo charcoal had five characteristic peaks of S-S stretch, H2O stretch, O-H stretch, C[bond, double bond]O stretch or C[bond, double bond]C stretch, and NO2 stretch at 3850 cm-1, 3740 cm-1, 3430 cm-1, 1630 cm-1 and 1530 cm-1, respectively. For Na2SO3, the peaks at 3850 cm-1, 3740 cm-1, 3430 cm-1, 1630 cm-1 and 1530 cm-1 achieved the maximum at 20 min. For Na2S2O8, the peaks at 3850 cm-1, 3740 cm-1, 3430 cm-1 and 1530 cm-1 achieved the maximum at 40 min. For Na2SO4, the peaks at 3850 cm-1, 3740 cm-1 and 1530 cm-1 achieved the maximum at 40 min. For Fe2(SO4)3, the peaks at 3850 cm-1, 3740 cm-1, 1630 cm-1 and 1530 cm-1 achieved the maximum at 120 min. For S, the peaks at 3850 cm-1 and 3740 cm-1 achieved the maximum at 40 min, the peaks at 1630 cm-1 and 1530 cm-1 achieved the maximum at 40 min. It proved that bamboo charcoal could remove sulfur powder from air to restrain sulfur allergies.

Desulphurization characteristics of bamboo charcoal from sulfur solution.

Sulfur powder and sulfur dioxide (SO2) often floated in air, produced acid rain and algal blooms, and could cause diseases. Bamboo charcoal could have adsorption and filtration properties. In order to figure out the optimal adsorption condition and the intrinsic change of the bamboo charcoal, five chemicals were adsorbed by bamboo charcoal and were analyzed by FT-IR. Fe2(SO4)3's, Na2SO4's, Na2S2O8's, S's, and Na2SO3's optimal adsorption condition was the concentration of 19 g/1000 g and stir time of 20 min, 21 g/1000 g and stir time of 60 min, 7 g/1000 g and stir time of 120 min, 11 g/1000 g and stir time of 120 min, 21 g/1000 g and stir time of 60 min, respectively. FT-IR spectra showed that for FT-IR spectra of Fe2(SO4)3, the transmissivity of the peaks at 3435 cm-1 and 2925 cm-1 achieved the maximum for 60 min and the concentration was 19 g/1000 g, the transmissivity of the peaks at 1630 cm-1, 1060 cm-1 and 660 cm-1 achieved the maximum for 60 min and the concentration was 7 g/1000 g. For FT-IR spectra of Na2SO4, the transmissivity of the peaks at 1630 cm-1, 1060 cm-1 and 660 cm-1 achieved the maximum for 20 min and the concentration was 13 g/1000 g. For FT-IR spectra of Na2S2O8, the transmissivity of the peaks at 3435 cm-1, 2925 cm-1, 1630 cm-1 and 1060 cm-1 achieved the maximum for 120 min and the concentration was 19 g/1000 g. For FT-IR spectra of S, the transmissivity of the peaks at 3435 cm-1, 2925 cm-1, 1630 cm-1 and 1060 cm-1 achieved the maximum for 20 min and the concentration was 11 g/1000 g, 17 g/1000 g and 21 g/1000 g. For FT-IR spectra of Na2SO3, the transmissivity of the peaks at 3435 cm-1 achieved the maximum for 120 min and the concentration was 5 g/1000 g, the transmissivity of the peaks at 2925 cm-1, 1630 cm-1 and 1060 cm-1 achieved the maximum for 120 min and the concentration was 11 g/1000 g. In these states, the number of the transmissivity of the maximum peaks is the largest.

Metabolomic profiling of the halophyte Prosopis strombulifera shows sodium salt- specific response.

Primary and secondary metabolite profiles were analyzed in roots and leaves of the halophytic shrub Prosopis strombulifera in response to control plants (no salt added in the growing media) and to lowering the osmotic potential to -1.0, -1.9, and -2.6 MPa generated by NaCl, Na2SO4, and the iso-osmotic combination of them at 24 h after reaching such potential. A rapid production of metabolites in response to sodium salt was found, which was correlated with modifications in growth parameters. Analysis of polar metabolite profiles by GC-MS rendered a total of 108 significantly altered compounds including 18 amino acids, 19 secondary metabolites, 23 carbohydrates, 13 organic acids, 4 indole acids, among others. Primary metabolites showed a differential response under the salt treatments, which was dependent on salt type and concentration, organ and age of plants. Most of identified compounds showed the strongest accumulation at the highest salt concentration assayed for Na2SO4-treated plants, which was correlated with damaging effects of sulfate anion on plant growth. Roots of NaCl-treated plants showed a higher number of altered metabolites (analyzed by UPLC-ESI-QqTOF-MS) compared to other treatments, while leaves of Na2SO4-treated plants showed the highest number of altered signals. A low degree of overlapping between secondary metabolites altered in roots and leaves of NaCl and Na2SO4-treated plants was found. However, when both NaCl and Na2SO4 salts were present plants always showed a lower number of altered metabolites. Three compounds were tentatively identified: tryptophan, lysophosphatidylcoline and 13-hydroxyoctadecadienoic acid. Increasing knowledge on P. strombulifera metabolism will contribute to unravel the underlying biochemical mechanism of salt tolerance.

Physiological responses of a halophytic shrub to salt stress by Na2SO4 and NaCl: oxidative damage and the role of polyphenols in antioxidant protection.

Salt stress conditions lead to increased production of reactive oxygen species (ROS) in plant cells. Halophytes have the ability to reduce these toxic ROS by means of a powerful antioxidant system that includes enzymatic and non-enzymatic components. In this research, we used the halophytic shrub Prosopis strombulifera to investigate whether the ability of this species to grow under increasing salt concentrations and mixtures was related to the synthesis of polyphenolic compounds and to the maintenance of leaf pigment contents for an adequate photosynthetic activity. Seedlings of P. strombulifera were grown hydroponically in Hoagland's solution, gradually adding Na2SO4 and NaCl separately or in mixtures until reaching final osmotic potentials of -1, -1.9 and -2.6 MPa. Control plants were allowed to develop in Hoagland's solution without salt. Oxidative damage in tissues was determined by H2O2 and malondialdehyde content. Leaf pigment analysis was performed by high-performance liquid chromatography with ultraviolet, and total phenols, total flavonoids, total flavan-3-ols, condensed tannins, tartaric acid esters and flavonols were spectrophotometrically assayed. Treatment with Na2SO4 increased H2O2 production and lipid peroxidation in tissues and induced a sharp increase in flavonoid compounds (mainly flavan-3-ols) and consequently in the antioxidant activity. Also, Na2SO4 treatment induced an increased carotenoid/chlorophyll ratio, which may represent a strategy to protect photosystems against photooxidation. NaCl treatment, however, did not affect H2O2 content, lipid peroxidation, pigments or polyphenols synthesis. The significant accumulation of flavonoids in tissues under Na2SO4 treatment and their powerful antioxidant activity indicates a role for these compounds in counteracting the oxidative damage induced by severe salt stress, particularly, ionic stress. We demonstrate that ionic interactions between different salts in salinized soils modify the biochemical and morpho-physiological responses of P. strombulifera plants to salinity.

The Corrosion Behavior of Pure Iron under Solid Na2SO4 Deposit in Wet Oxygen Flow at 500 °C.

The corrosion behavior of pure Fe under a Na2SO4 deposit in an atmosphere of O2 + H2O was investigated at 500 °C by thermo gravimetric, and electrochemical measurements, viz. potentiodynamic polarization, electrochemical impedance spectroscopy (EIS), and surface characterization methods viz. X-ray diffraction (XRD), and scanning electron microscope (SEM)/energy dispersive spectroscopy(EDS). The results showed that a synergistic effect occurred between Na2SO4 and O2 + H2O, which significantly accelerated the corrosion rate of the pure Fe. Briefly, NaFeO2 was formed in addition to the customary Fe oxides; at the same time, H2SO4 gas was produced by introduction of water vapor. Subsequently, an electrochemical corrosion reaction occurred due to the existence of Na2SO4, NaFeO2, and H2O. When this coupled to the chemical corrosion reaction, the progress of the chemical corrosion reaction was promoted and eventually resulted in the acceleration of the corrosion of the pure Fe.