SnCl2 Research Articles

Physical, morphological, and optical properties of SnS micro- and chemical route synthesized nano-particles

Comparative study of tin sulphide (SnS) in micro- and nano-form is carried out in the present study. The market purchased SnS fine powder is considered as micro-particles. The SnS nano-particles are synthesized by chemical route. In the synthesis, stannous chloride and thioacetamide are used as the source of cations (Sn2+) and anions (S2−) respectively. The micro- and synthesized nanoparticles of SnS are comprehensively characterized for elemental compositions, phase, unit cell structure, surface morphology, crystallite size, and optical properties. The characterizations are carried out employing different analytical techniques. The determined properties are analyzed with comparison to each other.

Bioassays, characterization and electronic transitions studies of organtin(IV) dithiocarbamates of p-Bromo-N methylbenzylamine dithiocarbamates

Analogs of carbamates are called dithiocarbamtes in which both oxygen atoms of carbamates are replaced by Sulfur atoms. For the preparation of ligand para substituted N-methylbenzylamine is reacted with Carbon Disulphide (CS2) in the presence of base sodium hydroxide (NaOH). The ligand was reacted with tin salts in 2:1 and 1:1 to obtain Di- and Tri-organotin (IV) complexes. Infrared, Ultraviolet–visible, and Proton nuclear magnetic resonance spectroscopic methods were used to characterize the synthesized compounds. In all chelated dithiocarbamates, a new bond appeared due to the formation of a bond between Sulfur and the tin atom absent in the ligand. Furthermore, bioassay activities were assessed using antifungal, antibacterial, and Hela cell line (cervical cancer). The Synthesized compounds showed moderate antibacterial activity against different bacterial strains while all complexes exhibited activity against fungal and anticancer activity.

Stannous fluoride protects gingival keratinocytes against infection and oxidative stress by Porphyromonas gingivalis outer membrane vesicles

ObjectiveTo determine whether outer membrane vesicles (OMVs) of the periodontal pathogen Porphyromonas gingivalis (P. gingivalis) can infect gingival keratinocytes and stimulate reactive oxygen species (ROS) production, and to assess whether stannous fluoride (SnF2), stannous chloride (SnCl2) or 0.454% SnF2 toothpaste diluents can inhibit OMV infection.MethodsOMVs were isolated from P. gingivalis culture and their morphology was characterized using scanning electron microscopy and transmission electron microscopy. OMVs were harvested, separated from parent bacteria, labeled with fluorescent probes, and added to proliferating gingival keratinocytes. Infection was monitored by measuring uptake of fluorescence. Free radicals and ROS were quantified by adding a separate CellROX fluorescent probe following 24 h incubation with OMVs, and automated fluorescence imaging was used to assess ROS generation rates. A dose response range of SnF2 and SnCl2 concentrations as well as 0.454% SnF2 toothpaste dilutions were added to OMVs to examine their potential to neutralize OMV infectivity and protect gingival keratinocytes from development of oxidative stress. The mechanism of SnF2 inhibition of OMV infection was studied by binding SnF2 with purified lipopolysaccharides (LPS) from the bacterial culture and examining the binding of stannous to LPS using mass spectrometry.ResultsLarge numbers of OMVs were formed in P. gingivalis culture medium. They were purified along with isolating soluble LPS. Fluorescence imaging revealed that OMVs infected gingival keratinocytes and promoted oxidative stress in a dose-dependent manner. SnF2, SnCl2, and SnF2 toothpaste inhibited OMV infectivity (p < 0.05) and likewise protected gingival keratinocytes from oxidative stress (p < 0.05). Stannous precipitated LPS and OMVs from solution, forming insoluble aggregates easily isolated by centrifugation. Mass spectroscopic analysis revealed that stannous was bound to LPS in a one-to-one molecular equivalent ratio.ConclusionSnF2 not only kills bacteria, but also inhibits bacterial virulence factors, such as LPS and OMVs. SnF2, SnCl2 and stannous-containing toothpastes can precipitate OMVs and LPS to in principle protect gingival keratinocyte cells from infection leading to inflammation and oxidative stress.

Macroscopic Monochalcogenide van der Waals Ferroics: Growth, Domain Structures, and Curie Temperature.

Two-dimensional and layered van der Waals materials promise to overcome the limitations of conventional ferroelectrics in terms of miniaturization and material integration, but synthesis has produced only small (up to few micrometer-sized) ferroic crystals. Here, we report the realization of in-plane ferroelectric few-layer crystals of the monochalcogenides tin(II) sulfide and selenide (SnS, SnSe) whose linear dimensions exceed the current state of the art by up to 1 order of magnitude. Such large crystals allow the investigation of ferroic domain patterns that are unaffected by edges and finite-size effects. Analysis of the abundant stripe domains by electron microscopy and nanobeam electron diffraction shows two distinct domain types: twin domains separated by positively charged walls with alternating head-to-head and tail-to-tail polarization as well as not previously observed purely rotational domains connected by neutral domain walls with head-to-tail dipoles. Access to large crystals allowed the determination of the Curie temperature of few-layer SnSe van der Waals ferroelectrics, and it enables the investigation of this class of ferroelectrics by widely available methods such as polarized optical microscopy. The combination with layer transfer protocols promises uniform materials for exploring fundamentals and for implementing devices for information processing and energy conversion.

In Situ Generated 1‐Naphthylmethyl Radicals From Bis(1‐Naphthylmethyl)tin Dichlorides: Utilization For C‐C, C‐N, and C‐O Bond‐Forming Reactions

The in situ‐generated 1‐naphthylmethyl radicals from the thermolysis of bis(1‐naphthylmethyl)tin dichlorides combine with persistent organic radicals, 4‐hydroxy‐TEMPO or 4‐oxo‐TEMPO designs C−O bond forming products. Subsequently, the C‐N bond occurs when the 1‐naphthylmethyl radicals unite with nitric oxide (NO) under a nitrogen atmosphere.In contrast, the oxidation instead of the addition reaction predominantly happens in the 1‐naphthylmethyl radicals when nitrogen dioxide contains a high oxidation state nitrogen center, i.e., N(IV) used.The by‐product, dodecanuclear organotin cages, with twelve peripheral naphthyl units, could be isolated from the 4‐hydroxy‐TEMPO reaction. Besides, the synthesis of unsymmetrical diarylmethanes RArCH2 (R = 1‐naphthyl, 2,4,6‐Me3C6H2, 3‐ and 4‐MeC6H4, phenyl, 4‐ClC6H4; Ar = 4‐MeOC6H4, 3,4‐, 2,4‐ and 2,5‐Me2C6H3) in high yields and with good regioselectivity is reported. This new methodology involves the iodine‐mediated thermolysis of bis(arylmethyl)tin dichlorides (RCH2)2SnCl2 and an excess of an arene. This reaction involves homolytic cleavage of Sn–C bonds to give arylmethyl radicals that react with iodine in the presence of SnCl2 to give the corresponding cations, which undergo electrophilic attack on the arene. Functionalised diarylmethanes have wide applications in pharmaceutical, agrochemical, and materials sciences. Alternative synthetic approaches to this class of organic compounds that avoid using a transition‐metal catalyst or a strong Lewis acid are desirable.

Enhanced photocatalytic degradation of organic pollutants by randomly oriented 2D SnS2 nanostructures

Abstract In this study, we present a bottom-up solvothermal technique using tin tetrachloride pentahydrate (SnCl4.5H2O) and thioacetamide as precursors to synthesize SnS2 nanostructures. Different solvents including isopropyl alcohol, ethanol (EN), and ethylene glycol were used in the reaction to enhance the photodegradation efficiency of organic pollutants, Methylene Blue (MB), and Tetracycline (TC) in an aqueous medium under simulated solar light irradiation. The SnS2 nanostructures synthesized with these solvents were characterized using various structural, morphological, and optical techniques, including x-ray diffraction, RAMAN, field emission scanning electron microscope, x-ray photoelectron spectroscopy, UV–Vis, and Brunauer–Emmett–Teller analysis. The choice of solvent was found to significantly affect the structural, morphological, and optical properties of the SnS2 nanostructures. Notably, the sample synthesized with EN as the solvent displayed a unique morphology, enhanced light-harvesting ability, efficient charge carrier separation, and a larger specific surface area, all of which contributed to its superior photocatalytic activity. This sample achieved 99.9% degradation of MB and 95% degradation of TC within 20 and 40 min, respectively. The kinetic analysis revealed maximum rate constant (k) values of 0.15242 min−1 for MB and 0.060 95 min−1 for TC, as determined by the pseudo-first-order kinetic model. We also discuss the plausible mechanism involving visible light-induced electron–hole pairs that generate reactive species, leading to the mineralization of dyes into H2O, CO2, and other gaseous products. The synthesized SnS2 nanostructures demonstrate significant potential for enhanced photocatalytic activity in organic pollutant degradation, underscoring their promise in addressing water pollution challenges.

Stannous Chloride-Modified Glass Substrates for Biomolecule Immobilization: Development of Label-Free Interferometric Sensor Chips for Highly Sensitive Detection of Aflatoxin B1 in Corn.

This study presents the development of stannous chloride (SnCl2)-modified glass substrates for biomolecule immobilization and their application in fabricating sensor chips for label-free interferometric biosensors. The glass modification process was optimized, identifying a 5% SnCl2 concentration, a 45 min reaction time, and a 150 °C drying temperature as conditions for efficient protein immobilization. Based on the SnCl2-modified glass substrates and label-free spectral-phase interferometry, a biosensor was developed for the detection of aflatoxin B1 (AFB1)-a highly toxic and carcinogenic contaminant in agricultural products. The biosensor realizes a competitive immunoassay of a remarkable detection limit as low as 26 pg/mL of AFB1, and a five-order dynamic range. The biosensor performance was validated using real corn flour samples contaminated with Aspergillus flavus. The proposed approach not only provides a powerful tool for AFB1 detection for food safety monitoring but also demonstrates the potential of SnCl2-modified substrates as a versatile platform for the development of next-generation biosensors.

Preventing dentin erosion with silver diamine fluoride and salivary pellicle: an in vitro study

ObjectivesTo investigate the preventive and discoloring effects of a single and two weekly applications of 38% silver diamine fluoride (SDF) against dentin erosion.Materials and methods180 dentin blocks were divided into four groups. Group 1 (SDF2) received two weekly applications of 38% SDF. Group 2 (SDF1) received a single application of 38% SDF. Group 3 (SNF) received a daily application of stannous chloride/amine fluoride/sodium fluoride (standard of care for dental erosion). Group 4 (DW) received a daily application of deionized water. The treated blocks were subjected to a 14-day erosive challenge. Crystal characteristics, elemental composition, surface morphology, percentage of surface microhardness loss (%SMHL), surface loss, and color change (ΔE) were investigated using X-ray diffraction (XRD), energy-dispersive spectrometry (EDS), scanning electron microscopy (SEM), hardness testing, profilometry, and digital spectrophotometry, respectively.ResultsXRD and EDS showed dentin surfaces had silver compounds in SDF2 and SDF1, and stannous chloride in SNF. SEM revealed less dentin demineralization with tubular occlusion in SDF2, SDF1, and SNF, but severe demineralization in DW. The %SMHL of SDF2, SDF1, SNF, and DW were 10.8 ± 2.1, 15.7 ± 2.1, 17.9 ± 2.1, and 28.7 ± 2.0 (SDF2 < SDF1 < SNF < DW, p < 0.05). Surface loss (µm) of SDF2, SDF1, SNF, and DW were 5.0 ± 0.6, 6.0 ± 0.6, 6.0 ± 0.7, and 9.0 ± 0.5 (SDF2 < SDF1 = SNF < DW, p < 0.001). ΔE of SDF2, SDF1, SNF, and DW were 26.0 ± 3.4, 12.1 ± 3.8, 6.9 ± 3.5, and 3.9 ± 3.6 (SDF2 > SDF1 > SNF = DW, p < 0.001).Conclusion38% SDF with two weekly applications provided better preventive effects against dentin erosion, but it might discolor dentin.Clinical relevanceThe increased 38% SDF application showed a better anti-erosive potential against dentin erosion. However, SDF caused black staining on the dentin.

Effect of combining aminomethacrylate and fluoride against erosive and abrasive challenges on enamel and dentin.

This study evaluated the effect of solutions containing aminomethacrylate copolymer (AA) and sodium fluoride (F; 225ppm F-) or fluoride plus stannous chloride (FSn; 225ppm F-, 800ppm Sn2+) against enamel and dentin erosion/abrasion. Solutions F, FSn, AA, F+AA, FSn+AA, and deionized water as negative control were tested. Bovine enamel and dentin specimens (n=13/solution/substrate) underwent a set of erosion-abrasion cycles (0.3% citric acid [5min, 4×/day], human saliva [1h, 4×/day], brushing [15 s, 2×/day], and treatments [2min, 2×/day]) for each of five days. Initial enamel erosion was evaluated using Knoop microhardness after the first and second acid challenge on day 1, and surface loss with profilometry after day 5. KOH-soluble fluoride was assessed. Data were analyzed with ANOVA/Tukey tests. The combination of fluoride and AA resulted in higher protection against enamel erosion, whereas this was not the case for the combination of AA and FSn. All treatments protected against enamel and dentin loss. The lowest surface loss values were observed with F+AA and FSn+AA. The polymer did not significantly influence the KOH-soluble fluoride formation on enamel/dentin specimens. The aminomethacrylate copolymer effectively enhanced the efficacy of sodium fluoride against initial erosion and improved the control of enamel and dentin wear of F and FSn solutions.

Radiolabeling and preclinical evaluation of technetium-99m labeled colistin

IntroductionAntibiotic resistance is a burden on the healthcare system. In present study, we have labeled an antibiotic named Colistimethate sodium (CMS) with technetium-99m (99mTc) to develop a SPECT based imaging tracer. MethodsWe standardised the labeling using 0.5–2 mg of CMS (in water) using stannous chloride dihydrate as a reducing agent followed by addition of 370 ± 74 MBq of 99mTc. A group of mice were injected intravenously (in tail vein) with 4–6 MBq of [99mTc]Tc-CMS diluted with saline and euthanized at various time intervals. microSPECT Imaging (ϒ-eye) was acquired to study the biodistribution in the healthy mice. ResultsWe standardised the labeling using 0.5 mg of colistin in 0.5 ml of saline with addition of 30 μg stannous chloride dihydrate. The retention factor value was 0.1–0.3 as compared to 0.9–1.0 for free 99mTc by TLC and retention time was found to be 14.2 ± 1.3 min as evaluated by HPLC. The biodistribution data showed uptake in lungs, spleen, and liver at 30 min but the uptake decreased in lung at 60 min. The imaging data corroborated with the biodistribution data. ConclusionsWe could successfully label [99mTc]Tc-CMS 99mTc and we could study its biodistribution in healthy mice.

Synergistic synthesis and computational analysis of novel indazole-2-Pyrone hybrids: Toxicity, Hirshfeld surface insights, and antiviral potential against HIV-1 and Coronaviruses

A novel category of hybrids, termed (Z)-6-methyl-3-(1-((1-(prop‑2-yn-1-yl)-1H-indazol-6-yl)amino)ethylidene)-2H-pyran-2,4(3H)‑dione, was synthesized by reductive coupling of N-alkyl-6-nitroindazoles and 2-pyrone using indium or stannous chloride in tetrahydrofuran (THF) with acetic acid. This process yielded (Z)-2H-pyran-2,4(3H)-diones in satisfactory yields. Each synthesized molecule underwent comprehensive characterization through NMR analysis and X-ray diffraction. Additionally, our investigation incorporates quantum chemical modeling via density functional theory (DFT) at the B3LYP/6–311G(d,p) level, along with molecular docking analysis. An analysis of the Hirshfeld molecular surface was undertaken to characterize the type of intermolecular connections. The percentage contributions, shown in the footprint plot, indicate that H…H interactions (33.0 %) are particularly significant in the constitution of the crystal. The favorable pharmacological properties of compounds 5a and 6a, such as good bioavailability, ability to penetrate the blood-brain barrier, and adherence to the Lipinski rule, make them excellent candidates for therapeutic development.

The impact of BBr3/TiCl4 ratios on the microstructural and mechanical characteristics of TiBN coatings deposited using a pulsed-PACVD technique

This study aimed to investigate the impact of precursor ratios on both the microstructural and tribological characteristics of TiBN coatings. Using the PACVD process, TiN, TiB2, and three variations of TiBN coatings with adjusted BBr3/TiCl4 ratios were applied onto H13 substrates. The coatings were characterized using XRD, FESEM, TEM, AFM, nanoindentation, and nanoscratch methods to analyze their microstructural properties, surface morphology, and mechanical behavior. The findings revealed that the TiBN coatings possessed a nanocomposite structure with TiN crystals dispersed within the BN matrix, which is amorphous. Moreover, the augmentation of the BBr3/TiCl4 ratio from 0 to 1/3 resulted in a significant rise in the hardness value, from 13.4 GPa to 25.7 GPa. However, a further increase in the ratio from 1/3 to 3/3 resulted in a decrease in hardness to 14.4 GPa because cracks were formed in the deposited coating. In comparison, the TiB2 coating exhibited a higher hardness of 19.7 GPa due to strong TiB bonds within the coating. The TiBN coating, applied with a BBr3/TiCl4 ratio of 1/3, demonstrated the lowest wear volume of 0.10 × 10−18 m3, attributed to its higher hardness and smoother surface texture.

Selective Extraction of Valuable and Critical Metals in Cassiterite Concentrate by Dry Chlorination, Part I: Thermodynamic and Modelling Perspective.

The chlorination of oxides of major concern in cassiterite concentrate with various chlorinating agents is investigated in light of their thermodynamic feasibilities to extract and recover their valuable metal components. Mechanisms responsible for the processes and their Gibbs free energy changes as a function of temperature to selectively separate and/or recover the metal(s) of interest and unwanted ones as their metallic chlorides are identified. Attention is given to gaseous (Cl2 and Cl2 + CO mixture) and solid (CaCl2 and MgCl2) chlorine sources, from which Cl2 + CO shows no reaction selectivity for any of the oxides but a feasible metal chloride formation for all. Chlorine gas (Cl2), on the other hand, could selectively form chlorides with metals of +2 oxidation state in their oxides, leaving those of high oxidation state unreacted. MgCl2, unlike CaCl2, is found capable of producing calcium, ferrous, and stannic chloride from their metallic oxides with enhanced reaction tendencies in the presence of silicon dioxide (SiO2). An overall study of the thermodynamic feasibility of all chlorine sources looked at alongside operational and environmental viabilities suitably suggests MgCl2 for a selective extraction of the valuable metal components in a cassiterite concentrate, in which case, moderate temperatures seem promising.

Tailoring the properties of SnS thin films deposited at room temperature by varying the amount of complexing agent for enhanced photocatalytic activity

This work examines how the characteristics and photocatalytic efficacy of modified SILAR-deposited SnS thin films are affected by the addition of a complexing agent. Stannous chloride dihydrate and sodium sulphate were used as tin and sulphur sources, respectively, while triethanolamine (TEA) served as a complexing agent in film deposition. The modified SILAR method facilitated the formation of well-adhesive thin films on the glass substrate at room temperature. The formation of SnS was demonstrated using EDAX and XPS analysis. XRD analysis proved that all the films are polycrystalline in nature with an orthorhombic crystal structure. The presence of chlorine as an involuntary dopant was observed in all the films prepared with TEA. Optical studies employing UV–visible spectroscopy found that all of the films have good visible absorption, with bandgap values ranging from 1.58 eV to 2.2 eV. Even though the films were deposited at room temperature, all films exhibited good thermal stability as per TGA analysis. The introduction of TEA caused improvements in the adhesion of the film to the substrate, a decrease in the band gap, a change in the morphology and composition, and an increase in the crystallinity and crystallite size. Due to their suitable bandgap corresponding to the visible region, SnS thin films exhibited good photocatalytic efficiency in degrading various types of dyes. The SnS thin film catalyst reduced 97% of methylene blue in 90 min at room temperature without using any reducing agent. The LCMS analysis validated the photocatalytic degradation of dye, whereas the UV–visible spectroscopic analysis gave a quantitative measure of the degradation efficiency. The reduction in photodegradation efficiency in the presence of OH radical scavengers confirmed the role of OH radicals in the degradation process. The terephthalic acid test further demonstrated the generation of OH radicals during the dye degradation process. The observed increase in photocatalytic activity of SnS thin films with TEA addition could be due to TEA-induced bandgap reduction, crystallinity increase, and crystallite size increase. The catalyst was reusable, stable, easy to recover after use, and effective against various kinds of dyes. The study emphasizes the use of complexing agents as a useful tool for modifying the characteristics and, consequently, the photocatalytic efficiency of modified SILAR-deposited SnS thin films.

Experimental toothpastes containing β-TCP nanoparticles functionalized with fluoride and tin to prevent Erosive Tooth Wear

ObjectivesThe present study aimed to synthesize toothpastes containing Beta- TriCalcium Phosphate (β-TCP) nanoparticles, functionalized with fluoride and tin, and test their ability to reduce erosive tooth wear (ETW). MethodsToothpastes were synthesized with the following active ingredients: 1100 ppm of fluoride (as sodium fluoride, F−), 3500 ppm of tin (as stannous chloride, Sn2+), and 800 ppm of β-TCP (Sizes a – 20 nm; and b – 100 nm). Enamel specimens were randomly assigned into the following groups (n = 10): 1. Commercial toothpaste; 2. Placebo; 3 F−; 4. F− + β-TCPa; 5. F− + β-TCPb; 6. F− + Sn2+; 7. F− + Sn2+ + β-TCPa and 8. F− + Sn2+ + β-TCPb. Specimens were subjected to erosion-abrasion cycling. Surface loss (in µm) was measured by optical profilometry. Toothpastes pH and available F− were also assessed. ResultsBrushing with placebo toothpaste resulted in higher surface loss than brushing with F− (p = 0.005) and F− + β-TCPb (p = 0.007); however, there was no difference between F− and F− + β-TCPb (p = 1.00). Commercial toothpaste showed no difference from Placebo (p = 0.279). The groups F−, F− + β-TCPa, F− + β-TCPb, F− + Sn2+, F− + Sn2+ + β-TCPa and F− + Sn2+ + β-TCPb were not different from the commercial toothpaste (p > 0.05). Overall, the addition of β-TCP reduced the amount of available fluoride in the experimental toothpastes. The pH of toothpastes ranged from 4.97 to 6.49. ConclusionsAlthough toothpaste containing β-TCP nanoparticles protected enamel against dental erosion-abrasion, this effect was not superior to the standard fluoride toothpaste (commercial). In addition, the functionalization of β-TCP nanoparticles with fluoride and tin did not enhance their protective effect. Clinical SignificanceAlthough β-TCP nanoparticles have some potential to control Erosive Tooth Wear, their incorporation into an experimental toothpaste appears to have a protective effect that is similar to a commercial fluoride toothpaste.

Intramolecularly O,N,O-Coordinated Tin(II) Salts: Syntheses, Structures, Cyclization, and Transition Metal Complexation.

We report the syntheses of tin(II) salts of the types [L1SnX]SnX3 [L1=2,6-{(i-PrO)2(O)P}2C5H3N: 1, X=Cl; 2, X=Br], [L2SnCl]SnCl3 [L2=2-{(i-PrO)Ph(O)P}-6-{(i-PrO)2(O)P}C5H3N: 3], [L3SnX]SnX3 [L3=2,6-{MeO(O)C}2C5H3N: 4, X=Cl; 5, X=Br], [L4SnX]SnX3 [L4=2,6-{Et2N(O)C}2C5H3N: 6, X=Cl; 7, X=Br]. These compounds were obtained by addition of SnX2 to the corresponding ligand inducing autoionization of the respective tin(II) halide. The thermal stability of 1, 3, and 4 was elucidated, giving, under ester cleavage and cyclisation, the tin(II) derivatives 8-12. The reaction of [L1SnCl]SnCl3 (1) with W(CO)4(thf)2 afforded the tungsten tetracarbonyl complex [{L1SnCl}{SnCl3}W(CO)4] (13), representing the first example in which a tin(II) stannate anion and a tin(II) stannylium cation simultaneously coordinate to a transition metal centre. The compounds were characterized by single crystal X-ray diffraction analyses and in part by elemental analyses, IR and NMR spectroscopy, electrospray ionization mass spectrometry. DFT calculations accompany the experimental work.

Morphological Characterization of Sb-Doped SnO2 Thin Films Developed by Spray Pyrolysis

In the present work, we have successfully deposited Sb antimony doped tin dioxide (SnO2) thin films with different concentrations (0 at%, 1 at%, 3 at% and 5 at%) from a stannous (II) chloride dihydrate solution (SnCl2.2H2O), by the pyrolysis chemical spray deposition technique on ordinary microscope glass substrates preheated to a fixed temperature of 350 °C. After deposition, the films were annealed at temperatures 400 °C for 4h. The aim of this work is on the one hand to study the morphological properties of pure and doped tin dioxide thin films and to determine the different morphological parameters such as: the roughness Ra, Rq and on the other hand to study the effect of Sb doping on the morphological properties of SnO2 thin films. To achieve this purpose, the thickness of all the films was estimated by profilometer with standard scan type. The morphology of the films was examined by atomic force microscope (AFM) in contact mode at room temperature to visualize the surface of our samples (the structure, size and morphology of crystallites ... etc). The 2D and 3D AFM images confirm the formation of nanostructures on the surface, with shapes and dimensions influenced by the amount of antimony doping. All the samples show a polycrystalline morphology, and the grain size progressively decreases with the increase of the Sb concentration (1% and 3%). On the other hand, for high antimony doping (5% Sb) the grains are larger than those observed at 3% doping. The root mean square (RMS) surface roughness values for samples with Sb concentrations (5%) were found to be 8.334 nm.

Risks of stannous chloride without filtration for hexavalent chromium treatment

AbstractWith increasing interest in using stannous chloride without filtration to achieve hexavalent chromium maximum contaminant level compliance in California, there is new urgency to quantify its effects on water quality and risks to public health manifested in distribution and premise plumbing systems. Accordingly, a 12‐week groundwater pilot study was completed using ubiquitous premise plumbing materials under flowing (to waste) and stagnating conditions of hexavalent chromium‐containing groundwater following stannous chloride addition without filtration. Results quantified the accumulation and release of chromium and tin, with total chromium concentrations exceeding regulatory or acceptable levels under stagnating conditions. Sediment with elevated chromium, tin, arsenic, and manganese concentrations was also observed. Given these observations would likely occur and worsen over time in distribution systems that cumulatively serve large populations, the use of stannous chloride without filtration represents an unacceptable risk to public health compared to other, more well‐established, best available technologies.

Stannous fluoride forms aggregates between outer and inner membranes leading to membrane rupture of Porphyromonas gingivalis and Prevotella pallens.

Stannous has been shown to bind to free lipopolysaccharides, thus preventing them from binding to TLR receptors. This study was undertaken to determine the histomorphological mechanism of stannous binding to anaerobic bacteria. Two bacteria associated with gingivitis and advanced periodontal disease, Porphyromonas gingivalis (P. gingivalis) and Prevotella pallens (P. pallens), were cultured in 25-1,000 μM of stannous fluoride and stannous chloride for 48 h. The growth rate was estimated using absorbance OD600. Bacterial cells were then fixed and processed for transmission electron microscopy (TEM) analysis. Stannous fluoride inhibited proliferation of both P. gingivalis and P. pallens in a dose-dependent manner. There was a statistically significant suppression of the growth curve starting at 100 μM for P. pallens (P = 0.050) and 200 μM for P. gingivalis (P = 0.039). TEM analysis revealed a thick layer of polysaccharides (19.8 nm) in P. gingivalis. The outer and inner membranes were clearly visible with low electron densities in both bacteria. Stannous diffused into bacterial membranes and formed precipitates in the areas spanning outer and inner membranes and below inner membranes. Precipitates varied in size ranging from 46.4 to 84.5 nm in length, and 18.4 to 35.9 nm in width. The membranes were disintegrated in the region where stannous formed precipitates. Cytosolic contents were leaked out, and in several cases, small vesicles were formed. Stannous precipitates were more abundant in numbers and larger in size in bacteria treated with high concentrations (100-300 μM) than in low concentrations (25-50 μM) of stannous fluoride. Furthermore, most of the bacteria were disintegrated in the groups treated with 100-300 μM stannous fluoride. At low concentrations (25 μM), stannous fluoride formed complexes primarily around outer membranes, to which lipopolysaccharides are anchored. Stannous chloride results showed similar trends, but it was less potent than stannous fluoride. Stannous fluoride can penetrate bacteria, bind to the constituents of the membrane and form precipitates between outer and inner membranes and beneath inner membranes. These large precipitates damaged the integrity of membranes and allowed cytosolic contents to be leaked out. Stannous complexes formed at the outer membranes, even at low concentrations (25 μM).

Tuning of power factor in bismuth selenide through Sn/Te co doping for low temperature thermoelectric applications

The physical parameters of solid-state produced tin and tellurium co-doped bismuth selenide polycrystalline crystals were described. Powder X-ray diffraction revealed the hexagonal structure in the samples’ phase domination. A field emission scanning electron microscope was used to analyze the surface microstructure. Thermoelectric properties such as Seebeck coefficient, electrical resistivity, and thermal conductivity were analyzed in the temperature range 10–350 K. The electrical resistivity of (Bi0.96Sn0.04)2Se2.7Te0.3 was found to be four times lower than that of pure Bi2Se3. Due to donor-like effects and antisite defects, the Seebeck coefficient demonstrates a p- to n-type semiconducting transition. When compared to pure Bi2Se3, power factor and thermoelectric figure of merit of (Bi0.96Sn0.04)2Se2.7Te0.3 is found to increase by 15 and 9 times respectively. Tellurium excess boosts tin vacancies, promoting the p to n-type transition in (Bi0.96Sn0.04)2Se2.7Te0.3, making it a good option for low temperature thermoelectric and sensor applications.