Inorganic Solutes Research Articles

NaCl-induced effects on photosynthesis, ion relations, and growth of Chloris gayana Kunth in the presence of two levels of KCl

Soil salinization is a widespread environmental problem that impacts agriculture. Potassium fertilization is often associated with stress mitigation. Aiming to identify the ability of Rhodes grass (Chloris gayana Kunth) to cope with high salt as well as to investigate the potential of K+ fertilization to alleviate stress symptoms, we investigated the combined effects of NaCl and KCl on photosynthesis, ion distribution, and growth of two Rhodes grass cultivars, Callide and Reclaimer. Plants were grown under different regimes (0, 200, 400, and 600 mM NaCl + 1 or 10 mM KCl). For Reclaimer, 10 mM KCl induced positive effects in photochemistry under 0 and 200 mM NaCl, as illustrated by fluorescence transients OJIP-bands and JIP-test parameters. However, such improvements did not lead to superior biomass accumulation nor net photosynthesis compared to the corresponding treatments under 1 mM KCl, which may not justify KCl application. In Callide 10 mM KCl induced deleterious effects on photochemistry of plants under low NaCl levels. High salinity (600 mM) induced stress-triggered biomass reduction of up to 70% in both cultivars, but all plants remained photosynthetically active. Exposure of both cultivars to NaCl concentrations equal to or higher than 200 mM triggered response mechanisms such as the ability to accumulate inorganic solutes accounting to osmotic potential, stomata closure, and excretion (up to 70%) of the retained Na+ onto the leaf surface irrespective of KCl. Our data reinforce that Rhodes grass is an auspicious forage crop for saline environments and, therefore, in revegetation programs for saline soils pasture in subtropical regions.

Adsorption performance with field emission scanning electron microscopy of fruit peel induced Silver Nanoparticles in C16H18ClN3S for waste water treatment

There is a growing demand for cost-effective and sustainable technologies for treating wastewater as water consumption increases and conventional technologies become more expensive. Nanoparticles have a great deal of potential for use in the treatment of waste water. Their unique surface area allows them to effectively remove toxic metal ions, pathogenic microorganisms, organic and inorganic solutes from water. This study investigated the potential of orange and banana peels as renewable nano adsorbents for removing dyes and dissolved organic compounds from textile wastewater. Orange and banana peels are an optimal selection due to their favourable chemical characteristics, namely the presence of cellulose, pectic, hemicellulose, and lignin. Their capacity to adsorb diverse anionic and cationic compounds on their surface-active sites is attributed to their unique functional group compositions. Silver nanoparticles are able to adsorb heavy metals due to their exceptionally low electrical and thermal resistance and surface plasmon resonance. The samples were thoroughly characterised using field emission scanning electron microscopy (FESEM), UV–Visible spectrometry, Fourier transform infrared spectroscopy (FTIR) and XRD. The nanoparticles were prepared (10 gm,50 gm,100 gm) and subsequently introduced to the wastewater sample. The optical density values were recorded at various time points. The optical density values demonstrate a decline over the course of the experiment, with a notable decrease observed over time. The results of this study provide valuable insights into the efficacy of these natural adsorbents and their potential for sustainable water purification technologies. For the purpose of this research, high performance instrumentation methods were performed as follows:•Field emission scanning electron microscopy for surface morphology studies.•Gas chromatography-mass spectrometry (GC–MS) for analytical technique that combines gas chromatography (GC) and mass spectrometry (MS) to identify unknown substances or contaminants.•Optical density values were measured for different timings of degradation.

Assessment of the impact of landfills on groundwater quality in Eastern China: a comprehensive analysis of inorganic solutes

Assessment of the impact of landfills on groundwater quality in Eastern China: a comprehensive analysis of inorganic solutes

Flake size-dependent water transport through graphene oxide membranes and rejection of geosmin (GSM) and 2-methylisoborneol (MIB) from drinking water

Water transport through graphene oxide membranes (GOMs) and the rejection of inorganic and organic solutes have been extensively studied. However, the influence of the lateral size of GO flakes on membrane performance remains unclear. Here, we investigate the water permeation and separation performance of GOMs fabricated using various sizes of flakes. The membranes prepared with larger flakes showed higher water flux. Our experiment clearly shows that GOMs consist of both lamellae and void structures. Monte Carlo simulations indicate that water transport through the voids is faster than that through the lamellae in GO membranes. Moreover, the voids are more predominant for the membranes prepared with larger sizes of GO flakes and, hence, higher water flux for larger flake membranes. Additionally, the GOMs prepared with the large flakes effectively rejected more than 98 % of geosmin (GSM) and 2-methylisoborneol (MIB) with high reproducibility and a stable water flux of 1.49 LMH. Our results contribute to a better understanding of the complex structure of GOMs, where the rejection performance of membranes mainly depends on the interlayer space, but the water transport is governed by the voids. Our study also demonstrated the industrial potential of GOMs in drinking water purification technology.

Molecular dynamics simulations of betaine-based deep eutectic solvents with varying iso-alcohols chain lengths

Betaine-based (BET) deep eutectic solvents (DESs) made with isoalcohols of varying hydrocarbon chain lengths, namely triethylene glycol (TEG), 1, 2-ethanediol (ETD), 1, 3-propanediol (PPD) and 1, 4-butanediol (BTD) were modelled. Their effects on the formation of aqueous biphasic system (ABS) with 2 M dipotassium phosphate salt solution (K2HPO4) as well as the extraction of common protein molecules, bovine serum albumin (BSA), were studied using molecular dynamics simulation with Gromacs. Qualitative and quantitative data were used to analyse the simulation results, which includes visualised systems in equilibrium, root mean square deviation (RMSD), root mean square fluctuation (RMSF), radius of gyration, radial distribution function (RDF) and hydrogen bond analysis. The results and literature research validated the role of inorganic salt solute concentration on the phase forming ability as well as the possibility of protein denaturation. More investigations and experimental works are to be carried out regarding the type of inorganic salt and its concentration for aqueous biphasic systems (ABSs) with alcohol based DESs and salt solution for protein extraction purposes. This is essential to understand the salting-out effect and to isolate the effects of hydrocarbon chain length from other influencing factors. Additionally, inorganic salt concentrations, presence of ether linkage as well as hydrocarbon chain length is shown to play a role in the dynamics between molecules in the system as well as protein conformational changes. Overall, ABS incorporating PPD and BTD with hydrocarbon chain lengths not exceeding C4 demonstrated superior performance in terms of protein conformational stability and interaction, showcasing their efficacy in protein extraction process.

Oral secretions: A key molecular interface of plant-insect herbivore interactions

The oral secretions of insect herbivores are complex mixtures of organic and inorganic solutes and enzymes that are deposited onto plant tissues during the feeding process. Some specific components of insect oral secretions have been shown to confer important functions in mediating plant-insect interactions at the molecular level. In this review, we examined the biochemical studies of insect oral secretions to summarize the current knowledge of their compositions. We then moved beyond the functional studies of components of oral secretions, and focused on the literature that pinpointed specific molecular targets of these compounds. Finally, we highlighted the investigations of oral secretion components in the context of insect physiology, which shed light on the potential evolutionary trajectory of these multi-functional molecules.

Biogeochemistry of dissolved organic matter and inorganic solutes in soil profiles of tropical pasturelands

Tropical soils play a critical role in the global biogeochemical cycles and are essential for maintaining the Earth's carbon balance. Understanding the dynamics of dissolved organic matter (DOM) is paramount due to its implications for ecosystem functioning and nutrient cycling. This study comprehensively evaluated the origin, distribution, and composition of DOM and inorganic solutes in Brazilian tropical agricultural soils. Multiple analytical techniques were utilized to assess DOM from soil profiles (0–100 cm depth) across a spectrum of land uses, including a native Atlantic Forest, a degraded pasture, as well as intensive grazing, extensive grazing, and silvopastoral systems. Inorganic elements were quantified to assess the coupling between the organic and inorganic biogeochemical cycles. The dominance of C4 carbon in topsoil layers suggested substantial contributions of organic matter from grasses to the soil organic matter pool. However, with increased depth, C3 carbon inputs became more prominent, indicating the influence of forest vegetation that existed prior to the implementation of agricultural managements. DOM concentrations decreased with soil depth due to reduced carbon inputs, sorption to minerals, or oxidation. DOM composition did not show significant changes among different land use and managements. Lignin was identified as the primary contributor to oxidized DOM with increasing soil depth. The composition of DOM exhibited a shift from more aromatic and higher molecular weight compounds in topsoil layers to smaller, more aliphatic compounds in subsoil layers. Our key findings revealed that aliphatic compounds, particularly fatty acids, tend to accumulate in deeper soil layers. This phenomenon was consistent in pastures dominated by grasses but not in soils near treed vegetation. Overseeding (from C3 plants) did not significantly impact DOM compositions, emphasizing the persistence of C4 plants in these systems. The presence of inorganic elements in soil water extracts showed minimal impact on DOM dynamics, suggesting decoupled organic and inorganic biogeochemical cycles in tropical pasturelands.

Solute contributions to osmotic adjustment in leaf segments of wheat (Triticum aestivum L.) exposed to polyethylene glycol-induced water deficit

ABSTRACT This study examined osmotic adjustment (OA) and solutes accumulated in leaf segments of wheat cultivar Hartog exposed to polyethylene glycol (PEG)-induced water deficit (WD) in laboratory experiments. Additional 10 mM K+ or Na+ added to basal solution with PEG −0.5 MPa enhanced leaf OA by up to 100%. Omission of nitrogen from the basal solution suppressed the expression of OA in leaf segments, but the addition of 10 mM NO3 – increased leaf OA by up to 81%. K+ and glycinebetaine were not accumulated in leaf segments exposed to WD under PEG −0.5 MPa during 48 h, but Na+, Cl−, proline and total soluble sugars accounted for up to 21, 20, 7 and 40% of OA, respectively. Total soluble sugars were the largest contributor to OA and may also contribute to membrane stability. Further data are needed on accumulation of leaf NO3 − and glycinebetaine in response to increasing nitrogen supply, and on which other inorganic and organic solutes may also contribute to OA under PEG-induced WD. Laboratory experiments with leaf segments exposed to WD under −0.5 MPa PEG, and with 10 mM K+, Na+ or NO3 − added to the basal solution, could provide an effective and rapid pre-screen of diverse germplasm sources for OA expression. Selected genotypes should then be validated by exposure to soil WD for agronomic evaluation, and for OA expression under field WD.

NPK fertilization modulates enzyme activity and mitigates the impacts of salinity on West Indian cherry.

Salt stress causes several physiological and biochemical disorders and impairs plant growth. However, adequate fertilization can improve the nutritional status and may reduce significantly the harmful effects caused by salt stress. From this perspective, this study aimed to evaluate the impact of different combinations of nitrogen, phosphorus and potassium fertilization on the antioxidant activity and accumulation of organic and inorganic solutes in West Indian cherry leaves, in the second year of production. The experimental design was in randomized blocks, with treatments distributed in a 10 × 2 factorial arrangement corresponding to ten fertilization combinations (FC) of NPK (FC1: 80-100-100%, FC2:100-100-100%, FC3:120-100-100%, FC4:140-100-100%, FC5:100-80-100%, FC6:100-120-100%, FC7:100-140-100%, FC8:100-100-80%, FC9:100-100-120%, and FC10:100-100-140% of the recommendation) and two levels of electrical conductivity of irrigation water (ECw) (0.6 and 4.0 dS m-1), with three replications. The multivariate analysis showed that irrigation with water of different electrical conductivities (0.6 and 4.0 dS m-1) resulted in different responses concerning the enzyme activity, production of organic compounds, and accumulation of inorganic solutes in the leaves. Under irrigation with low salinity water, there was greater accumulation of K+, soluble carbohydrates, and proline, and lower activity of antioxidative enzymes, especially SOD and APX. Under high salinity water, greater enzyme activity and higher concentrations of Na+ and Cl- were observed. The results indicate that the response of West Indian cherry to salinity was more towards redox homeostasis than osmotic homeostasis through the accumulation of compatible solutes. Fertilization combination FC5 (100-80-100% corresponding to 200, 24 and 80 g plant-1 of NPK) modulates the enzyme activity of SOD and APX attenuating the impacts of salinity, being an efficient combination to preserve redox homeostasis in West Indian cherry plants grown under salt stress.

Reclamation of impacted urban phreatic water through nanofiltration technology: Insight on natural organic matter removal by fluorescence spectroscopy

Nanofiltration (NF) is a promising technology called to play a relevant role in water reclamation, which lies in the core of circular economy in the water sector. The aim of this study was to assess two aromatic polyamide-based NF membranes (the looser NF270 and the tighter NF90 ones) for the treatment of urban impacted phreatic water. The focus was centred on the removal of dissolved inorganic and organic solutes and on the differences observed between solutes. Membrane ions rejection was modelled by the Solution-Electro-Diffusion Film Model (SEDFM). DOC was tracked by Fluorescence Excitation-Emission Matrices (FEEM) coupled to Parallel Factor Analysis (PARAFAC) to get insight into the character of DOC rejected by or permeated through the membranes. Results showed that the NF90 membrane systematically achieved upper values in the rejection of ions than the looser NF270 one. Variations between ions could be interpreted by the mechanisms ruling their rejection, i.e. Donnan and dielectric exclusion phenomena. Experimental rejections were also satisfactorily fit by the SEDFM, indicating that that the presence of DOC in the phreatic water did affect modelling of ions transport through the membranes. DOC was rejected at very high percentages (>90%) by both membranes, but FEEM-PARAFAC analysis revealed that humic- and tryptophan- like components were more rejected (>90% for both membranes) than tyrosine-like compounds (45% for NF270 and 57% for NF90). The finding is of relevance from a point of view of disinfection practices, as it has been observed that humic-like substances are strongly correlated with DBPs formation.

Three-compartment membrane electrolyzer combining simultaneous desalination and oxidative degradation in treating nanofiltration concentrate

The complex organic and inorganic solutes present in nanofiltration's purification by-product (NF concentrate, NFC) pose challenges to the water processing procedure. To address this, a three-compartment membrane electrolyzer was proposed that facilitates electro-driven ion migration for crystallization alongside synchronous anodic oxidation for organic degradation. With a hydraulic retention time (HRT) of 5 min and a current exceeding 50 mA, the system effectively separated over 25 % of inorganic salts and accomplished reclamation through crystallization in the concentration compartment. Simultaneously, it achieved oxidation of pollutants by more than 35 % based on the total nitrogen index and removed upwards of 15 % of organic carbon. Notably, the efficiency of pollutant removal correlated strongly with the intensity of the current. Furthermore, this study uncovered two issues encountered during the electrochemical process: membrane fouling and electrode fouling. During concentration, metal cations readily formed organic pollution by complexing with organic pollutants, while the crystallization of inorganics on the surface of anion exchange membranes emerged as a pivotal factor hindering current enhancement, similar to the formation of deposited salt in a solution. Long HRT can lead to electrode contamination and corrosion which subsequently affect current efficiency. Energy consumption verified the feasibility of the electrolyzer for NFC processing. Based on our findings, a current intensity of 100 mA (equivalent to a density of 8 mA/cm2) was deemed optimal, striking a balance between pollutant removal and various limiting factors associated with each pollutant. Consequently, this innovative advancement in membrane electrolyzers helps in overcoming limitations in synergistic desalination, ion recovery, and organic removal, establishing a fundamental component of the abbreviated flow process for future NFC treatment.

The Effects of Aminium and Ammonium Cations on the Ice Nucleation Activity of K‐Feldspar

AbstractMineral dust is one of the most abundant types of ice nucleating particles in the atmosphere. During atmospheric transport, mineral dust particles can become coated with inorganic and organic solutes, which can impact their ice nucleation activity. Aminium cations formed from amines are one type of organic solute that can coat mineral dust particles in the atmosphere, but their effects on the ice nucleation activity of mineral dust have not been studied. We investigated the effects of primary, secondary, and tertiary aminium cations with methyl and ethyl groups, as well as ammonium cations, on the ice nucleation activity of K‐feldspar, an important type of mineral dust, in the immersion freezing mode at low cation concentrations (0.2–20 mM) using a droplet‐freezing apparatus. Ammonium cations substantially increased the ice nucleation activity of K‐feldspar, consistent with previous studies. In contrast, primary aminium cations significantly reduced K‐feldspar ice nucleation activity, and secondary and tertiary aminium cations had no significant effect (the effect was less than the uncertainty of our measurements). Our combined results are consistent with the following mechanisms: ammonium cations undergo ion exchange with K‐feldspar, providing exposed N–H groups for hydrogen bonding with ice; primary aminium cations undergo ion exchange with K‐feldspar, exposing a hydrophobic tail that is not effective at nucleating ice; secondary and tertiary aminium cations do not undergo ion exchange with K‐feldspar due to steric effects caused by the multiple hydrophobic groups on the cation.

Salinity and exogenous H2 O2 improve gas exchange, osmoregulation, and antioxidant metabolism in quinoa under drought stress.

Climate change-induced concurrent drought and salinity stresses significantly threaten global crop yields, yet the physio-biochemical responses to combined stress in quinoa remain elusive. This study evaluated quinoa responses under four growth conditions: well-watered, drought stress, salt stress, and drought + salt stress with (15 mM) or without (0 mM) exogenous hydrogen peroxide (H2 O2 ) application. All examined stresses (alone or in combination) reduce quinoa growth and net photosynthesis, although salt stress was found to be less destructive than drought and combined stress. Strikingly, superoxide dismutase (SOD), peroxidase (POD), catalase (CAT), stomatal conductance (gs ), photosynthetic rate (PN ), K+ uptake, shoot height, shoot fresh, and dry weight were increased by 46.1%, 22.2%, 101.6%, 12.9%, 12.1%, 22.4%, 7.1%, 14%, and 16.4%, respectively, under combined stress compared to drought alone. In addition, exogenous H2 O2 effectively improved gaseous exchange, osmolytes' accumulation, and antioxidant activity, resulting in reduced lipid peroxidation, which eventually led to higher plant growth under all coercive conditions. The principle component analysis (PCA) indicated a strong positive correlation between antioxidant enzymes and inorganic ions, which contributed efficiently to osmotic adjustment, particularly under conditions of salinity followed by combined stress. In short, in combination, salt stress has the potential to mitigate drought-induced injuries by promoting the absorption of inorganic solutes for osmoregulation in quinoa plants. Furthermore, exogenous application of H2 O2 could be opted to enhance quinoa performance to increase its tolerance mechanism against drought and salinity, even under combined stress.

Dynamic relationship between membrane fouling and reverse diffusion of inorganic draw solutes in forward osmosis

Both membrane fouling and reverse diffusion limit the application of forward osmosis (FO), and the combined effects further decrease water generation. Herein, the effects of typical inorganic draw solutes (DSs) were investigated on the dynamic relationship between membrane fouling from two organic pollutants and reverse diffusion. The formation of a membrane fouling layer decreased the amount of Ca2+ ions reverse-diffusing from a CaCl2 DS and increased the amount of NH4+ ions reverse-diffusing from a NH4Cl DS. When sodium alginate was used as the feed solute, reverse-diffused ions from the CaCl2/NH4Cl DS resulted in the formation of a three-dimensional network structure, further exacerbating membrane fouling. Moreover, greater reverse diffusion of NH4+ from the NH4Cl DS resulted in more membrane fouling in comparison with the CaCl2 DS (i.e., water recovery of 246.4 ± 4.7 g), resulting in a lower water recovery value of 151.4 ± 10.6 g. During the filtration of humic acid, the membrane fouling layer caused by the CaCl2 DS led to the formation of a cake filtration layer that was more severe than that formed when the NH4Cl DS was used. This study provides a reliable basis for draw solute optimization to extend the application of FO systems.

Optical manipulation and fusion of aqueous droplets containing inorganic and organic solutes in air using the dual-beam laser trapping technique.

The comparative evaluation of two aerosol droplets of different chemical compositions using the dual-beam laser trapping technique can be employed for highly sensitive and accurate measurements of the water activities of such droplets. However, it is technically difficult to load droplets of different chemical compositions into adjacent optical traps that are only a few tens of micrometers apart. To overcome this challenge, a chamber with an overhanging roof was created. This roof prevented the initially trapped droplets from being contaminated by aerosol droplets that were subsequently introduced into the chamber. Herein, we report the simultaneous laser trapping of an aqueous ammonium sulfate (AS) droplet and an aqueous succinic acid (SA) droplet in air using the dual-beam laser trapping technique. Two droplets were successfully fused through optical manipulation to form a mixed inorganic/organic droplet in air. This experimental approach is advantageous because it forms mixed inorganic/organic droplets under constant relative humidity (RH) conditions. However, in previous studies, it was necessary to compensate for changes in RH prior to and after droplet fusion. To assess the validity of theoretical predictions of the water activity of droplets containing AS and SA, the equilibrium radii of the droplet were compared with those calculated using certain theoretical models.

Concentration‐Discharge Patterns Reveal Catchment Controls Over the Stoichiometry of Carbon and Nutrient Supply to Boreal Streams

AbstractCarbon (C), nitrogen (N), and phosphorus (P) export from catchments is strongly regulated by interactions between hydrological flowpaths and their terrestrial use/storage. While concentration‐discharge (c‐Q) relationships have been widely used to understand this interplay for C, N, and P individually, how flow regulates the relative supply of these resources across spatial and temporal scales is not well documented. Here, we analyze c‐Q relationships from 12 years of data to test how seasonal flow regulates the concentrations of inorganic N (Dissolved inorganic nitrogen [DIN]) and P (Dissolved inorganic phosphorus [DIP]), dissolved organic N (DON) and C (dissolved organic carbon [DOC]) and their respective ratios across 12 streams in a boreal landscape. We observed opposing c‐Q relationships between organic and inorganic solutes. DOC and DON tended toward transport limitation with little year‐to‐year change, whereas ammonium (NH4) and DIP were increasingly source limited over time. These different c‐Q relationships translated into large (up to three‐fold) shifts in resource ratios (e.g., DOC:DIN) in response to changes in flow. Our results also highlight strong influences of catchment structure on c‐Q patterns, regardless of solute, season, and longer‐term directional changes. Here, the organic solute c‐Q responses became less transport limited over time; while inorganic solute responses became less source limited with increasing mire/decreasing forest cover. Overall, differences in timing of catchment exports for C, N, and P, create dynamic variation in solute concentrations in streams with subsequent impacts on resource stoichiometry that is central to aquatic ecological processes.

Accelerated Sulfur Oxidation by Ozone on Surfaces of Single Optically Trapped Aerosol Particles

The sulfur oxidation in mixed sodium thiosulfate/sucrose/aqueous microdroplets by gaseous ozone is studied in this work via aerosol optical tweezers coupled with Raman spectroscopy, which can simultaneously determine various physicochemical properties and the heterogeneous reaction kinetics of single optically trapped microdroplets, allowing for elucidating their complicated interplay. According to the kinetics measurement results at different relative humidities, ozone concentrations, and stoichiometries of inorganic and organic solutes, this work finds that a high aerosol ionic strength can accelerate the ozone oxidation of thiosulfate at air–water interfaces, while a high aerosol viscosity prolongs the reaction time scales due to diffusion-limited kinetics. The kinetic multilayer model of aerosol surface and bulk chemistry (KM-SUB) is utilized to investigate the observed heterogeneous kinetics results and to retrieve the surface reaction rate coefficients. The KM-SUB model fit results indicate that the observed kinetics of sulfur oxidation in binary sodium thiosulfate aqueous microdroplets with high ionic strengths is dominated by interfacial reactions, and the fitted surface reaction rate coefficients increase 1 order of magnitude when the droplet ionic strength increases around 40 M. This work further utilizes the kinetics measurements of ozone dependence to discuss the coupling among properties of ozone gas-interface-bulk partitioning and surface reaction rate in the kinetics model. Finally, this work also exploits the surface reaction of thiosulfate with ozone to retrieve the aerosol viscosity of microdroplets containing ternary aqueous sodium thiosulfate and sucrose mixtures, demonstrating the feasibility of pinning down aerosol viscosities via reaction kinetics.

Pore flow and solute rejection in pilot-scale air-gap membrane distillation

Membrane distillation (MD) is a desalination technology with promising applications in treating brines generated by reverse osmosis. Theoretically, MD can achieve 100% rejection of non-volatile contaminants such as organic and inorganic solutes and pathogens because only the vapor phase permeates through the membrane. However, polymeric membranes are subject to a wide distribution of pore sizes that may result in pore flow or liquid flux through even a new membrane resulting in poor contaminant rejection. In pilot-scale MD systems, a larger membrane area increases the hydraulic pressure in the flow channel and the transmembrane hydraulic pressure difference, thus increasing the probability of pore flow of non-volatile contaminants through the membrane and providing enhanced resolution of contaminant detection. This work reports membrane rejection of organic and inorganic non-volatile solutes in a pilot-scale air-gap MD (AGMD) element and quantifies, for the first time, transport of non-volatile solutes through the membrane because of pore flow. Pathogen rejection in the pilot-scale MD system was also measured using enteric virus surrogates MS2 and PhiX174 as tracers. Organic and inorganic solutes and both viruses were detected in the distillate, suggesting the presence of pore flow. No difference between organic and inorganic solute rejection was observed, and both decreased (from 2.5-log10 to 1.5-log10) with an increase in air-gap vacuum (from 50 to 500 mbar). At 50 mbar and low evaporator inlet temperature (40 °C), virus rejection (2.4 -log10) was higher than organic and inorganic solute rejection (1.7-log10).

Factors Impacting Rhizobium-legume Symbiotic Nitrogen Fixation with the Physiological and Genetic Responses to Overcome the Adverse Conditions: A Review

Symbiotic N2 fixation is essential for the plant’s growth because it can fix reactive nitrogen compounds in soil. However, all steps of this process can be hampered by several biotic and abiotic environmental factors. This study mainly focused on discussing the impacts of 12 major factors on this process by reviewing the significant numbers of research works. According to the information from these works, we found some significant physiological and genetic impacts caused by these factors like plasmid deletion, genomic mismanagement, abnormal molecular signals, toxicity, deficiency of minerals, deformation of rhizobial cells, protein denaturation, nucleic acid damage, acetylene reduction and nod factors limitation. Furthermore, expression of heat or acid shock proteins, internal buffering, genes spanning, extracellular immobilization, periplasmic allocation, change of lipopolysaccharides composition, intracellular accumulation of inorganic and organic solutes (Osmolyte) and activation of hydrogenase expression are shown by both micro and macro symbionts as a natural response to adapt to these stress conditions. Though the stress-tolerant strains like HR-3, HR-6, HR-10, HR-12, acta, actP, exoR, lpiA, actR, actS and phrR can be used to sense the external environment and make signals to change gene transcription during the adverse condition, the application of genetic engineering should be expanded more to promote the commercial inoculation by the production of novel stress-tolerant strains or modified genes of rhizobia and legumes.

Modeling and Experimental Validation for the Preparation of Concentrated Tea Extract Using a Forward Osmosis Process Using a Food-Grade Inorganic Draw Solute

In this study, a one-dimensional mathematical model was developed for the concentration of tea extract using a forward osmosis (FO) process. The membrane transport parameters were estimated by minimizing the error between the model output and the experimental results. The model equations were solved to predict the FO performance within allowable error limits. Further, a series of process flow sheet simulation studies were performed to investigate the effect of different operating conditions on the overall FO performance. Based on the simulation results, a multicriteria optimization was developed to attain the maximum permeate and minimum specific reverse solute flux (SRSF). Using the best-performing process flow sheet model, the feasibility of seawater and high-concentration reject brine as a draw solution was also investigated for the concentration of tea extract. The high-concentration reject brine (105.17 g L–1) can result in rapid dewatering with minimal SRSF (0.14 g L–1) along with simultaneous seawater dilution (81.38 g L–1).