Charge Neutralization Research Articles

Experimental study of aerosol behavior in ambient electric and magnetic fields at low indoor relative humidity

The tendency of aerosols to carry viral particles featured significantly in public discourse during the SARS Covid-19 pandemic. In this research, the potential significance of the aerosol electric charge, especially as it relates to indoor relative humidity (RH) is considered. While electrostatic interactions may occur at any level of humidity, the level of humidity has a strong influence on these interactions. Above 55 % RH, there is sufficient moisture in the air to facilitate neutralization of the electric charges of particles and surfaces, whereas, at lower humidity levels, less moisture and higher surface resistivities enable increasingly stronger electrostatic interactions. Experiments were designed and conducted to study the behavior of electrically charged aerosols in fields emanating from capacitive touchscreens and permanent magnets. These preliminary experimental results suggest that operating indoor environments closer to the 55–60 % RH range could reduce interactions between these charged aerosols and capacitive touchscreens. This relative humidity range is within the acceptable ranges of humidity recommended by ASHRAE standard 55 which defines thermal environmental conditions for human occupancy.

In Situ Formed Organic Ion-Associate Liquid-Phase Microextraction without Centrifugation from Aqueous Solutions Using Thymol Blue and Estrogens

In this study, we present a method for ion-associated liquid phase (IALP) separation and concentration of analytes from an aqueous matrix into an IALP formed in situ by the charge neutralization reaction of organic cations and anions, without centrifugation. The effects of various factors on the extraction efficiency and other parameters are investigated, whereas no instrumental stirring, such as vortexing or ultrasonics, is required because the solvent (IALP) is formed in situ. The organic cation and anion used are ethylhexyloxypropylammonium and dodecyl sulfate, respectively. The developed in situ IALP microextraction method for phase separation without centrifugation is tested using the thymol blue dye and several endocrine disruptors. The tested endocrine disruptors (bisphenol A, 17β-estradiol, 17α-ethinylestradiol, and estrone) are analyzed via high-performance liquid chromatography/fluorescence detection, with respective detection limits of 0.02, 0.02, 0.02, and 0.4 μg L−1, and the corresponding enrichment factor ranging from 47 to 71. This IALP microextraction method can be used to separate and concentrate environmental water samples of different matrices. The employed IALP is fast and easy to use, enables an approximately 100-fold analyte concentration, and has a high affinity for estrogens, thus holding promise for the separation, concentration, and quantitation of diverse trace analytes.

Synthesis and characterization of cationic tamarind seed polysaccharide: An effective flocculating agent

A series of cationic tamarind seed polysaccharides (CTSPs) with different degrees of substitution were synthesized by etherification of tamarind seed polysaccharides (TSP) with 3-chloro-2-hydroxypropyl trimethylammonium chloride (CHPTAC). By elemental analysis, zeta potential and FTIR, the successful linking of cationic groups on the chain of TSPs were confirmed, and the substitution degrees were determined as 0.143, 0.197 and 0.346, respectively. NMR data indicated that the quaternary ammonium groups were linked to C6 of T-Gal. Subsequently, the flocculation behaviors of CTSPs in kaolin solution were investigated, and the results showed that both the degree of substitution and pH affected their flocculation properties. Charge neutralization and positional blocking effects caused flocculation to show an increasing and then decreasing trend with increasing substitution of CTSPs, whereas the lower the pH, the less flocculant was required to achieve the same flocculation effect. The presence of positive charges allowed CTSPs to effectively remove negatively charged waste water such as kaolin suspensions.

Can membrane permeability of zwitterionic compounds be predicted by the solubility-diffusion model?

Zwitterions contain both positively and negatively charged functional groups, resulting in an overall net neutral charge. Nevertheless, the membrane permeability of the zwitterionic form of a compound is assumed to be much lower than the permeability of the uncharged neutral form. Although a significant proportion of pharmaceuticals are zwitterionic, it has not been clear so far whether their permeability is dominated by the permeation of the zwitterionic or the neutral form, since neutral fractions are often quite low as compared to the zwitterionic fraction. This complicates the in silico prediction of the permeability of zwitterionic compounds. In this work, we re-evaluated existing in vitro permeability data from literature measured with Caco-2/MDCK cell assays, using more strict exclusion criteria for effects like diffusion limitation by the aqueous boundary layers, paracellular transport, active transport and retention. Using this re-evaluated data set, we show that extracted intrinsic permeabilities of the neutral fraction are well predicted by the solubility-diffusion model (RMSE = 1.21; n = 18) if the permeability of the zwitterionic species is assumed negligible. Our work thus suggests that only the neutral species is relevant for the membrane permeability of zwitterionic compounds, and that membrane permeability of zwitterionic compounds is indeed predictable by the solubility-diffusion model.

Mutual-benefit modification of the coagulant solution and fly ash for enhanced sludge dewatering

Faced with the escalating volume of municipal sludge from wastewater treatment plants, urgent measures are required to enhance the sludge dewatering efficiency. This study introduces an innovative and cost-effective approach for mutual modifications of AlCl3 coagulant solution (AC) and fly ash (FA) powder as additives to significantly enhance sludge dewaterability. Unlike the traditional method that modifies agents alone, our technique achieves dual functionalities via blending FA with AC at room temperature. The modified FA (MFA) exhibits a 60 % increase in specific surface area to 2.176 m2/g and ζ-potential shift from –22.2 to +2.0 mV, meanwhile enhances the metal ions content in the modified AC (MAC) by dissolving 96.5 % of Ca, 70.3 % of Mg, 10.6 % of Fe, and 6.1 % of Al ions from FA. When sludge is treated with 5 % MAC and 10 % MFA, the water content in the filter cake is reduced from 84.9 % originally to 52.9 % through plate-frame pressure filtration (PFPF), a significant improvement over 65.4 % for that with unmodified AC and FA treatment, corresponding to the decreased specific resistance to filtration (SRF) and increased the filtration flux during the draining phase. The notable dewaterability enhancement through AC and FA modification is due to the enhanced flocculation and charge neutralization by the abundant metal ions in MAC, coupled with the MFA-facilitated water adsorption and drainage channel maintenance. This one-step, double-benefit modification not only surpasses traditional methods in dewatering efficiency but also reduces sludge treatment costs by 42.4 %, offering a sustainable solution to the increasing challenges of municipal sludge management.

ВЗАИМОДЕЙСТВИЕ ЛИПОПОЛИСАХАРИД-СВЯЗЫВАЮЩИХ БЕЛКОВ С РАЗЛИЧНЫМИ ФОРМАМИ ЛИПОПОЛИСАХАРИДОВ

Lipopolysaccharide-binding proteins from two common jellyfish species Aurellia aurita and Ropelema asamushi were isolated and purified, and the interaction of lipopolysaccharides (LPS) of various structural types with LBP was studied. By inhibiting the interaction, it was found that both proteins specifically bind to the lipid and core fragments of the LPS molecule. There are two types of binding sites in LBP with Kd = 3,28 × 10-6 M and Kd = 0,13 × 10-6 M (for the protein from A. aurita) and Kd = 3,66 × 10-6 M and Kd = 0,27 × 10-6 M (for protein from R. asamushi). It has been shown by dynamic light scattering that the binding of LBP to R-LPS leads to the dissociation of LPS micelles. The sizes of LPS aggregates decrease from 200 nm to 25–30 nm in the composition of LPS–LSB complexes. The data of electrokinetic measurements indicate the neutralization of the negative charge of Rd-LPS (-42,2 mV) in the LPS-LSB-R. asamushi complex up to -4,4 mV. S-LPS micelles from E. coli do not disaggregate upon binding to LBP, which is apparently due to the shielding of lipid A by O-specific chains in the S-LPS molecule. The binding of LPS to LBP may affect their endotoxic properties.

Universe is Ether based Single Instruction Quantum Computer his Activity Creates Matter and Life

Universe is actually gigant quantum computer (Seth Lloyd) made of ether – multi coloured, multilayered super conductor (Frank Wilczek). Ether constantly creates elementary particles (electron and proton), which are subjet of universe quantum computer macro instruction – Charge Neutralization Process –CNP. After matter creation (periodic table of elements), single cell organisms and life itself (rna and dna) emerged.

Association of Metal Cations with the Anti-PF4/Heparin Antibody Response in Heparin-Induced Thrombocytopenia.

Heparin-induced thrombocytopenia (HIT) is an antibody-mediated immune response against complexes of heparin and platelet factor 4 (PF4). The electrostatic interaction between heparin and PF4 is critical for the anti-PF4/heparin antibody response seen in HIT. The binding of metal cations to heparin induces conformational changes and charge neutralization of the heparin molecule, and cation-heparin binding can modulate the specificity and affinity for heparin-binding partners. However, the effects of metal cation binding to heparin in the context of anti-PF4/heparin antibody response have not been determined. Here, we utilized inductively coupled plasma mass spectrometry (ICP-MS) to quantify 16 metal cations in patient plasma and tested for correlation with anti-PF4/heparin IgG levels and platelet count after clinical suspicion of HIT in a cohort of heparin-treated patients. The average age of the cohort (n = 32) was 60.53 (SD = 14.31) years old, had a mean anti-PF4/heparin antibody optical density [OD405] of 0.93 (SD = 1.21) units and was primarily female (n = 23). Patients with positive anti-PF4/heparin antibody test results (OD405 ≥ 0.5 units) were younger, had increased weight and BMI, and were more likely to have a positive serotonin release assay (SRA) result compared to antibody negative patients. We observed statistical differences between antibody positive and negative groups for sodium and aluminum and significant correlations of anti-PF4/heparin antibody levels with sodium and silver. While differences in sodium concentrations were associated with antibody positive status and correlated with antibody levels, no replication was performed. Additional studies are warranted to confirm our observed association, including in vitro binding studies and larger observational cohorts.

“Click” amphotericin B in prodrug nanoformulations for enhanced systemic fungemia treatment

Severe nephrotoxicity and infusion-related side effects pose significant obstacles to the clinical application of Amphotericin B (AmB) in life-threatening systemic fungal infections. In pursuit of a cost-effective and safe formulation, we have introduced multiple phenylboronic acid (PBA) moieties onto a linear dendritic telodendrimer (TD) scaffold, enabling effective AmB conjugation via boronate chemistry through a rapid, high yield, catalysis-free and dialysis-free “Click” drug loading process. Optimized AmB-TD prodrugs self-assemble into monodispersed micelles characterized by small particle sizes and neutral surface charges. AmB prodrugs sustain drug release in circulation, which is accelerated in response to the acidic pH and Reactive Oxygen Species (ROS) in the infection and inflammation. Prodrugs mitigate the AmB aggregation status, reduce cytotoxicity and hemolytic activity compared to Fungizone®, and demonstrate superior antifungal activity to AmBisome®. AmB-PEG5kBA4 has a comparable maximum tolerated dose (MTD) to AmBisome®, while over 20-fold increase than Fungizone®. A single dose of AmB-PEG5kBA4 demonstrates superior efficacy to Fungizone® and AmBisome® in treating systemic fungal infections in both immunocompetent and immunocompromised mice.

A novel chitosan and polyferric sulfate composite coagulant for biogas slurry pretreatment by simultaneous flocculation and floatation: Performance and underlying mechanisms

Biogas slurry from anaerobic digestion is rich in nutrients but has not been fully utilized due to a high content of suspended solids (SS) causing clogging during agricultural irrigation. This study aimed to evaluate the performance of a novel chitosan and polyferric sulfate (CTS-PFS) composite coagulant for simultaneous flocculation and floatation to enhance SS removal while preserving nutrients in biogas slurry. Orthogonal method was used for experimental design to determine the optimal synthesis and operational conditions of CTS-PFS. Results show that CTS-PFS outperformed individual CTS and PFS coagulant in terms of SS removal and nutrient (nitrogen, phosphorus, and potassium) preservation. Compared to individual CTS and PFS coagulation, the combination of CTS and PFS at the mass ratio of 1:6 showed significantly higher performance by 41.5 % increase in SS removal and 5.2 % reduction in nutrient loss. The improved performance of CTS-PFS was attributed to its formation of polynuclear hydroxyl complexes with ferric oxide groups (e.g. Fe-OH, Fe-O-Fe, Fe-OH-Fe and COO-Fe) to strengthen charge neutralization and adsorption bridging. Data from this study further confirm that CTS-PFS enhanced the removal of small suspended particles and dissolved organic matter in the molecular weight range of 0.4–2.0 kDa and preserved ammonia and potassium better in biogas slurry. Bubbles were generated as hydrogen ions from coagulant hydrolysis interacted with bicarbonate and carbonate in biogas slurry for removing the produced flocs by floatation. Floc flotation was more effective in CTS-PFS coagulation due to the significant production of uniform bubbles, evidenced by the reduction in the viscosity of biogas slurry.

Understanding arsenic-ulexite interactions in evaporite environments: Evidence from XRPD, micro-XRF, micro-FT-IR, and XPS studies

World-class borate deposits often form from As-rich waters, this study addresses the understudied association of arsenic (As) species with evaporite borates, focusing on the Puna region's borate deposits (Central Andes of Argentina). The research aims to characterize the association between borate minerals and high As concentrations in brines and thermal waters. To achieve this, five borate samples were collected from the Olaroz salt flat nucleus and thermal springs, alongside associated water samples. Comprehensive analytical techniques, including ICP-MS, ICP-OES, synchrotron-based micro-XRF, XRPD, Rietveld analysis, micro-FT-IR, and XPS, were employed to determine bulk and surface chemical compositions, mineral identification, and solid speciation of As and boron. The study reveals that under oxidizing conditions and in absence of organic matter, aqueous arsenic species interact with ulexite through a stepwise process involving charge neutralization, cationic bridge formation, and surface complex formation with polyborate and As(V) oxyanions. However, in environments associated with microbial mats or organic-rich sediments, the dissolved As(V) is reduced to As(III), which forms complexes with functional groups of organic matter. The coexistence of As(III) and As(V) in specific layers suggests potential remediation strategies targeting organic matter for the removal of the more toxic As(III) in similar geological settings.

Anisotropic tribology and electrification properties of sliding-mode triboelectric nanogenerator with groove textures

Sliding-mode triboelectric nanogenerator (S-TENG) is based on the coupling of triboelectrification and electrostatic induction, converting electrical energy from sliding motion. Introducing micro-textures into the sliding surface, and adjusting the angle between the texture and sliding direction (direction angle) may achieve performance anisotropy, which provides novel ideas for optimizing the tribology and electrification performance of S-TENG. To guide the performance optimization based on the anisotropy, in this paper, groove micro-textures were fabricated on the surface of S-TENG, and anisotropic tribology and electrification performance were obtained through changing the direction angle. Based on the surface analysis and after-cleaning tests, the mechanism of the anisotropy was explained. It is shown that the anisotropy of friction coefficient can be attributed to the changes of texture edge induced resistance and groove captured wear debris, while the voltage anisotropy is due to the variations of debris accumulated on the sliding interface and the resulting charge neutralization. Among the selected 0°–90° direction angles, S-TENG at angle of 90° exhibits relatively small stable friction coefficient and high open-circuit voltage, and thus it is recommended for the performance optimization. The open-circuit voltage is not directly associated with the friction coefficient, but closely related to the wear debris accumulated on the sliding interface. This study presents a simple and convenient method to optimize the performance of S-TENG, and help understand the correlation between its tribology and electrical performance.

Efficient porphyrin integrated UiO-66 probes for ratiometric fluorescence sensing of antibiotic residues in milk.

Dual-emissive fluorescence probes were designedby integrating porphyrin into the frameworks of UiO-66 for ratiometric fluorescence sensing of amoxicillin (AMX). Porphyrin integrated UiO-66 showed dual emission in the blue and red region. AMX resulted in the quenching of blue fluorescence component, attributable to the charge neutralization and hydrogen bonds induced energy transfer. AMX was detected using (F438/F654) as output signals. Two linear relationships were observed (from 10 to 1000nM and 1 to 100µM), with a limit of detection of 27nM. The porphyrin integrated UiO-66 probe was used to detect AMX in practical samples. This work widens the road for the development of dual/multiple emissive fluorescence sensors for analytical applications, providing materials and theoretical supporting for food, environmental, and human safety.

Catalytic promiscuity, cytotoxicity and protein cleavage mediated by mononuclear copper(II) complexes: oxidative and hydrolytic activities

In this work, we describe the synthesis and structural and spectroscopic characterizations of two copper(II) complexes, [(Cu)(L1)(Cl2)].4H2O (1), where L1 is 2-(pyridin-2-yl)-1,3-bis(pyridin-2-ylmethyl)-hexahydropyrimidine, and [Cu(L2)](ClO4)2 (2), where L2 is N1,N1,N3-tris(pyridin-2-ylmethyl)propane-1,3-diamine. The crystalline structure analysis indicates that both complexes are mononuclear and pentacoordinated compounds. In the case of complex 1, it bears a neutral charge, with the ligand coordinating to the Cu(II) center in a tridentate manner, utilizing N-donor atoms. Additionally, two cis-chlorido ligands completing the coordination sphere. On the other hand, complex 2 is a cationic complex, with the ligand coordinated in a pentadentate manner, with only N-donor atoms for coordination around the Cu(II). Complex 1 showed catalytic promiscuity, displaying hydrolytic and oxidative activity. The hydrolytic activity was investigated using bis(2,4-dinitrophenyl) phosphate (2,4-BDNPP) as a phosphodiester substrate and applying the Michaelis–Menten approach, obtaining the following kinetic parameters: kcat = 1.21 × 10-4 s−1; KM = 3.35 × 10-3 molL-1. Complex 1 also accelerates the oxidation of the 3,5-di-tert-butylcatechol (3,5-DTBC) substrate with catalytic efficiency equal to 6.11 L mol-1s-1. Interestingly, we demonstrated that this Cu(II) complex 1 can also cleave the very stable peptide bonds from BSA (bovine serum albumin) through an oxidative mechanism using ascorbate as a reducing agent. Complexes 1 and 2 show good cytotoxic activity against two cancer cell lines: A431 from human squamous cell carcinoma and K562 from chronic myeloid leukemia. This study showed that complexes 1 and 2 are selective towards cancer cells.

Charge-Switchable nanoparticles to enhance tumor penetration and accumulation

Nanoparticle-based drug delivery systems hold potential in chemotherapy, but their limited accumulation in tumor tissues hinders effective drug concentration for combating tumor growth. Hence, altering the physicochemical properties of nanoparticles, particularly their surface charge, can enhance their performance. This study utilized a computational model to explore a nanoparticle drug delivery system capable of dynamically adjusting its surface charge. In the model, nanoparticles in the bloodstream were assigned a neutral or positive charge, which, upon reaching the tumor microenvironment, switched to a neutral or negative charge, and releasing chemotherapy drugs into the extracellular space. Results revealed that circulating nanoparticles with a positive surface charge, despite having a shorter circulation and high clearance rate compared to their neutral counterparts, could accumulate significantly in the tissue due to their high transvascular rate. After extravasation, neutralized surface-charged nanoparticles tended to accumulate only near blood microvessels due to their low diffusion rate, resulting in substantial released drug drainage back into the bloodstream. On the other hand, nanoparticles with a negative surface charge in the tumor’s extracellular space, due to the reduction of nano-bio interactions, were able to penetrate deeper into the tumor, and increasing drug bioavailability by reducing the volume of drained drugs. Furthermore, the analysis suggested that burst drug release yields a higher drug concentration than sustained drug release, however their creation of bioavailability dependent on nanoparticle accumulation in the tissue. The study’s findings demonstrate the potential of this delivery system and offer valuable insights for future research in this area.

Abstract 2096: Role Of Divalent Cations In The Enzymatic Activation Of Coagulation Factor XII By Lipopolysaccharides

Background: Lipopolysaccharide (LPS) is the primary pathogenic factor in Gram-negative sepsis. LPS is a polyanionic molecule that may act as a site of initiation of coagulation by activating factor (F)XII. While the physicochemical properties of LPS are known to be sensitive to interactions with divalent cations, it is unknown whether divalent cations modulate the activation of FXII by LPS. Aims: To determine whether divalent cations regulate the kinetics of FXII activation by select LPS chemotypes from E. coli . Methods: Aggregates of E. Coli LPS chemotypes O26:B6 and Rd2 were prepared in ultrapure water in the presence or absence of calcium (Ca 2+ ). The biophysical characterization of LPS chemotypes were determined by dynamic light scattering (DLS) and measurement of zeta potential (ZP). Chromogenic substrate assays were used to study the effects of LPS on FXII activation. Results: The LPS O26:B6 and Rd2 in the absence of Ca 2+ produced aggregates in form of micelles with hydrodynamic diameters of 190±10 and 200±7 nm and ZP of -25±0.8 and -60±2 mV, respectively. The presence of Ca 2+ produced aggregates in the form of vesicles with hydrodynamic diameters of 400±15 and 1300±60 nm and ZP of –11±2 and –3±0.5 mV, respectively. FXII was incubated in HEPES buffer with the distinct LPS morphologies in varying salt concentrations. We found maximal autoactivation of FXII by O26:B6 and Rd2 chemotypes at lower NaCl concentrations. The presence of Ca 2+ , however, selectively reduced the ability of O26:B6 to activate FXII. Strikingly, the neutralization of the surface net charge of the LPS chemotype Rd2 by Ca 2+ ions abrogated the amidolytic activity of Rd2. Conclusions: The presence of calcium ions induces changes in the physicochemical properties of LPS that result in distinct effects on FXII activation in vitro . We are currently studying whether this phenomena is conserved for other divalent cations including Zn, Mg, Cu, and Mn.

Biocompatible nanoparticles for metals removal from fresh water with potential for rare earth extraction applications

Freshwater contamination by metals can come from a variety of sources and be damaging to wildlife, alter landscapes, and impact human health. Metals removal is desirable not only for improving water quality and preventing adverse effects but also for metals collection and recycling. Nanoadsorption of metals is economically feasible and nanoscale materials exhibit a high surface-area-to-volume ratio that is promising for high adsorption and reactivity. However, the extraordinarily small dimensions of these materials allow them to maneuver biological systems, and combined with high reactivity, this translocation can result in toxicity. In this work, nanoparticles (NPs) composed of a magnetite core coated in hydroxyapatite (HA) and functionalized for adsorption with titanium dioxide (TiHAMNPs) were synthesized. The magnetic core enabled NP retrieval, while HA enhanced adsorption and minimized toxicity. Here, synthesis and characterization are presented, revealing a stable NP structure exhibiting a near neutral surface charge. Results of adsorption studies showed that as compared to silica-coated magnetite nanoparticles (SiMNPs), traditionally used for this application, TiHAMNPs exhibited significantly higher adsorption (43.28% more Cu removal) after 24 h. The equilibrium rate constant for the adsorption of Cu by TiHAMNPs was 0.0003 g/(min*mg) and TiHAMNP adsorption data indicated that TiHAMNPs adsorb metals in a monolayer at the particle surface with a maximum capacity of 2.8 mmol/g. Metabolic and toxicity assays showed TiHAMNPs were highly biocompatible as compared to SiMNPs. This work also explores rare earth element (REE) separation applications of TiHAMNPs, finding that TiHAMNPs may provide a promising alternative for REE retrieval and/or separation.

Enhancing the coagulation process for the removal of microplastics from water by anionic polyacrylamide and natural-based Moringaoleifera

The existence of microplastics (MPs) in water is a significant global concern since they have the potential to pose a threat to human health. Therefore, there is a need to develop a sustainable treatment technology for MPs removal, as the conventional methods are inadequate to address this problem. Coagulation is a typical process in treatment plants that can capture MPs before releasing them into the environment. In this work, the removal behaviors of polyamide (PA), polystyrene (PS), and polyethylene (PE) MPs were systematically investigated through coagulation processes using aluminum sulfate (Al2(SO4)3) and Moringa oleifera (MO) seeds extract. Subsequently, the coagulation performance of Al2(SO4)3 was improved by the separate addition of anionic polyacrylamide (APAM) and naturally derived MO. Results showed that Al2(SO4)3 in combination with APAM had better performance than Al2(SO4)3 or MO alone. In the Al2(SO4)3+APAM system, the removal efficiencies were 93.47%, 81.25%, and 29.48% for PA, PS, and PE MPs, respectively. Furthermore, the effectiveness of the Al2(SO4)3 and MO blended system was approximately similar to the Al2(SO4)3+APAM system. However, the required amount of Al2(SO4)3 was decreased to 50% in the Al2(SO4)3+MO system compared to the optimal dosage in the Al2(SO4)3 system alone. The combination of 40 mg/L of Al2(SO4)3 and 60 mg/L of MO resulted in removal efficiencies of 92.99%, 80.48%, and 28.94% for PA, PS, and PE MPs, respectively. The high efficacy of these enhanced methods was due to the synergic effects of charge neutralization and agglomeration adsorption, which were validated through zeta potential assessments and visual analysis using scanning electron microscopy (SEM) images. In the case of experimental conditions, initial pH had little impact on removal efficiency, while NaCl salinity and stirring speed directly affected MPs removal. Consequently, this research took a step toward finding a green strategy to remove MPs from water systems.

Design of the beam transport optics of TRIUMF’s new 300 keV H− ion source terminal

An ion beam transport system has been designed to transport a highly intense and bright beam extracted from the H− ion source. This new system will be installed at the new injection terminal for the TRIUMF’s 500 MeV H− cyclotron. The low energy part of the transport section (25 keV) in the injection terminal has been designed with magnetic optical elements in order to maintain space charge neutralization. The injection terminal includes a permanent magnet lens, magnetic steerers, a pulser, a beam dump, and a 300 kV acceleration column with electron and positive ion suppressor rings. Beam optics calculations have been performed, including space charge effects up to 1 mA. The simulation results of the beam optics design are presented in this paper.

Lanthanum-modified pyroaurite as a geoengineering tool to simultaneously sink Microcystis cyanobacteria and immobilize phosphorus in eutrophic water

Excessive phosphorus (P) in eutrophic water induces cyanobacterial blooms that aggravate the burden of in-situ remediation measures. In order to ensure better ecological recovery, Flock & Lock technique has been developed to simultaneously sink cyanobacteria and immobilize P but requires a combination of flocculent and P inactivation agent. Here we synthesized a novel lanthanum-modified pyroaurite (LMP), as an alternative for Flock & Lock of cyanobacteria and phosphorus at the background of rich humic acid and suspended solids. LMP shows a P adsorption capacity of 36.0 mg/g and nearly 100 % removal of chlorophyll-a (Chl-a), turbidity, UV254 and P at a dosage (0.3 g/L) much lower than the commercial analogue (0.5 g/L). The resultant sediment (98.2 % as immobile P) exhibits sound stability without observable release of P or re-growth of cyanobacteria over a 50-day incubation period. The use of LMP also constrains the release of toxic microcystins to 1.4 μg/L from the sunk cyanobacterial cells, outperforming the commonly used polyaluminum chloride (PAC). Similar Flock & Lock efficiency could also be achieved in real eutrophic water. The outstanding Flock & Lock performance of LMP is attributable to the designed La modification. During LMP treatment, La acts as not only a P binder by formation of LaPO4, but also a coagulant to create a synergistic effect with pyroaurite. The controlled hydrolysis of surface La(III) over pyroaurite aided the possible formation of La(III)-pyroaurite networking structure, which significantly enhanced the Flock & Lock process through adsorption, charge neutralization, sweep flocculation and entrapment. In the end, the preliminary economic analysis is performed. The results demonstrate that LMP is a versatile and cost-effective agent for in-situ remediation of eutrophic waters.