Adverse effects of cigarette filter silica on lungs: Comparison with natural crystalline silica particles.

As a common additive in cigarette filters, nanosilica has been implemented to reduce the release of harmful substances in cigarette smoke. However, the potential risk of occupational exposure for cigarette factory workers is unknown. We collected physical examination data from 710 cigarette factory workers to evaluate the adverse effects of cigarette filter silica exposure. We also established mouse models induced by cigarette filter silica and crystalline silica separately to compare the lung inflammation, pulmonary function, apoptosis, and fibrosis of the two models. Workers in the rolling and packing workshop exposed to cigarette filter silica had a higher rate of abnormal lung function (17.75%) than those in the cutting workshop (0.87%). Animal experiments showed that compared with the same dose of crystalline silica, cigarette filter silica resulted in higher levels of inflammatory factors in the bronchoalveolar lavage fluid (BALF) of mice at day 7, and lower levels of total lung capacity (TLC), inspiratory capacity (IC), vital capacity (VC), and forced vital capacity (FVC) in mice at day 28. Additionally, both exposed groups of mice showed increased levels of caspase 3, collagen I (Col-Ⅰ), α-smooth muscle actin (α-SMA) and hydroxyproline (HYP) in the lungs, as well as collagen accumulation and fibrous nodules at day 28, with no significant difference between the two groups. The results suggested that cigarette filter silica caused more severe early lung inflammation and late ventilation impairment than the same dose of crystalline silica. In the future, we need to pay more attention to nanosilica protection in cigarette factories to prevent pulmonary dysfunction in workers.

Impact of Respiratory Dust on Health: A Comparison Based on the Toxicity of PM2.5, Silica, and Nanosilica.

Respiratory dust of different particle sizes in the environment causes diverse health effects when entering the human body and makes acute or chronic damage through multiple systems and organs. However, the precise toxic effects and potential mechanisms induced by dust of different particle sizes have not been systematically summarized. In this study, we described the sources and characteristics of three different particle sizes of dust: PM2.5 (<2.5 µm), silica (<5 µm), and nanosilica (<100 nm). Based on their respective characteristics, we further explored the main toxicity induced by silica, PM2.5, and nanosilica in vivo and in vitro. Furthermore, we evaluated the health implications of respiratory dust on the human body, and especially proposed potential synergistic effects, considering current studies. In summary, this review summarized the health hazards and toxic mechanisms associated with respiratory dust of different particle sizes. It could provide new insights for investigating the synergistic effects of co-exposure to respiratory dust of different particle sizes in mixed environments.

Selection of Silica Type and Amount for Flowability Enhancements via Dry Coating: Contact Mechanics Based Predictive Approach.

PURPOSE: To investigate the effect of dry coating the amount and type of silica on powder flowability enhancement using a comprehensive set of 19 pharmaceutical powders having different sizes, surface roughness, morphology, and aspect ratios, as well as assess flow predictability via Bond number estimated using a mechanistic multi-asperity particle contact model. METHOD: Particle size, shape, density, surface energy and area, SEM-based morphology, and FFC were assessed for all powders. Hydrophobic (R972P) or hydrophilic (A200) nano-silica were dry coated for each powder at 25%, 50%, and 100% surface area coverage (SAC). Flow predictability was assessed via particle size and Bond number. RESULTS: Nearly maximal flow enhancement, one or more flow category, was observed for all powders at 50% SAC of either type of silica, equivalent to 1 wt% or less for both the hydrophobic R972P or hydrophilic A200, while R972P generally performed slightly better. Silica amount as SAC better helped understand the relative performance. The power-law relation between FFC and Bond number was observed. CONCLUSION: Significant flow enhancements were achieved at 50% SAC, validating previous models. Most uncoated very cohesive powders improved by two flow categories, attaining easy flow. Flowability could not be predicted for both the uncoated and dry coated powders via particle size alone. Prediction was significantly better using Bond number computed via the mechanistic multi-asperity particle contact model accounting for the particle size, surface energy, roughness, and the amount and type of silica. The widely accepted 200 nm surface roughness was not valid for most pharmaceutical powders.

Mesoporous Silica Nanoparticles Induce Intracellular Peroxidation Damage of Phytophthora infestans: A New Type of Green Fungicide for Late Blight Control.

Nanopesticides are considered to be a promising alternative strategy for enhancing bioactivity and delaying the development of pathogen resistance to pesticides. Here, a new type of nanosilica fungicide was proposed and demonstrated to control late blight by inducing intracellular peroxidation damage to Phytophthora infestans, the pathogen associated with potato late blight. Results indicated that the structural features of different silica nanoparticles were largely responsible for their antimicrobial activities. Mesoporous silica nanoparticles (MSNs) exhibited the highest antimicrobial activity with a 98.02% inhibition rate of P. infestans, causing oxidative stress responses and cell structure damage in P. infestans. For the first time, MSNs were found to selectively induce spontaneous excess production of intracellular reactive oxygen species in pathogenic cells, including hydroxyl radicals (•OH), superoxide radicals (•O2-), and singlet oxygen (1O2), leading to peroxidation damage in P. infestans. The effectiveness of MSNs was further tested in the pot experiments as well as leaf and tuber infection, and successful control of potato late blight was achieved with high plant compatibility and safety. This work provides new insights into the antimicrobial mechanism of nanosilica and highlights the use of nanoparticles for controlling late blight with green and highly efficient nanofungicides.

Biocompatible nanoscale silica particles fabricated from aminopropyltriethoxysilane functionalized brick ash induced versatile pesticidal activity.

The present study is aimed to evaluate pesticidal activity and biocompatibility including ecotoxicity of functionalized silica nanoparticles that synthesized by simple, in vitro, green technology principles. Sol-gel method was adopted for the synthesis of silica nanoparticles and was functionalized by Aminopropyltriethoxysilane (APS), characterized and confirmed the uniform, monodispersive, highly stable particles with the size range of 10-200 nm. The synthesized Nano silica was screened against the developmental stages of Spodoptera litura. Pesticidal study revealed that the functionalized nanoparticles were effective against all the life stages of the insect by recording high mortality and the drastic reduction in the larval, pupae, adult emergence, and adult longevity stages. The ecotoxic effect of synthesized nano-silica was tested on soil parameters, growth parameters of Arachis hypogaea, and compatibility with Trichoderma viride. This study revealed there was no toxic effect on soil, growth parameters of Arachis hypogaea, and most significantly the growth of Trichoderma viride was not inhibited. A biocompatibility study was done by using Zebrafish and Rabbit model. The study divulges there was no toxic effect on all the developmental stages of the Embryo. Further, the nanoparticles did not exhibit any dermatotoxicological effect which confirmed no signs and symptoms of inflammation. Nano-silica emerges as a promising eco-friendly and non-toxic substitute for conventional insecticides. Its utilization has the potential to augment both environmental preservation and economic prosperity on a national scale. Furthermore, the integration of silica-based nanoparticles with biocidal agents demonstrates notable biocompatibility and the capacity to hinder bacterial adhesion.

Utilization of agricultural, industrial waste and nanosilica as replacement for cementitious material and natural aggregates - Mechanical, microstructural and durability characteristics assessment.

This study examines the effect of rice husk ash (RHA) and nanosilica, and ground granular blast furnace slag (GGBS) on concrete mechanical and durability properties. The cement had been partially replaced with nanosilica and RHA having substitution percentages up to 6% and 10% respectively whereas the sand had been partially replaced by GGBS at 20% for all mixes. A water-to-cementitious materials ratio of 0.38 and a sand-to-cementitious materials ratio of 2.04 were used to cast eight different concrete mixes. The nanosilica used in the present research possessed some favorable effects such as rich fineness, higher surface area and greater reactivity which signified one of the best cement replacement materials. Both the durability and strength of concrete specimens possessing nanosilica, RHA and GGBS was evaluated using in-elastic neutron scattering, SEM image, piezoresistive test, split tensile strength, flexural strength and compressive strength test. Concrete specimens were also subjected to chloride penetration and water absorption to examine the impact of replacement materials on the concrete's durability attributes. Concrete performance was increased by the ternary blending of concrete because of the active participation of nanosilica in durability and strength at early ages, both RHA and GGBS played an important role in improving packing density. It was found that as the percentage of cement replaced with nanosilica increases, the durability of concrete also significantly increases. But the optimum strength parameter was found when 4% of cement was replaced by the nanosilica effectively. The proposed ternary mix may be eco-friendly by saving cement and enhancing strength and durability effectively.

Defects in nanosilica catalytically convert CO2 to methane without any metal and ligand.

Active and stable metal-free heterogeneous catalysts for CO2 fixation are required to reduce the current high level of carbon dioxide in the atmosphere, which is driving climate change. In this work, we show that defects in nanosilica (E' centers, oxygen vacancies, and nonbridging oxygen hole centers) convert CO2 to methane with excellent productivity and selectivity. Neither metal nor complex organic ligands were required, and the defect alone acted as catalytic sites for carbon dioxide activation and hydrogen dissociation and their cooperative action converted CO2 to methane. Unlike metal catalysts, which become deactivated with time, the defect-containing nanosilica showed significantly better stability. Notably, the catalyst can be regenerated by simple heating in the air without the need for hydrogen gas. Surprisingly, the catalytic activity for methane production increased significantly after every regeneration cycle, reaching more than double the methane production rate after eight regeneration cycles. This activated catalyst remained stable for more than 200 h. Detailed understanding of the role of the various defect sites in terms of their concentrations and proximities as well as their cooperativity in activating CO2 and dissociating hydrogen to produce methane was achieved.

Zeta Potential of Nanosilica in 50% Aqueous Ethylene Glycol and in 50% Aqueous Propylene Glycol.

A sufficient amount of ionic surfactants may induce a zeta potential of silica particles dispersed in water-glycol mixtures of about 100 mV in absolute value. Nanoparticles of silica were dispersed in 50-50 ethylene glycol (EG)-water and 50-50 propylene glycol (PG)-water mixtures, and the zeta potential was studied as a function of acid, base, and surfactant concentrations. The addition of HCl had a limited effect on the zeta potential. The addition of NaOH in excess of 10-5 M induced a zeta potential of about -80 mV in 50% EG, but in 50% PG the effect of NaOH was less significant. The addition of CTMABr in excess of 10-3 M induced a zeta potential of about +100 mV in 50% EG and in 50% PG. The addition of SDS in excess of 10-3 M induced a zeta potential of about -80 mV in 50% EG and in 50% PG. Long-chained analogs of SDS were even more efficient than SDS, but their application is limited by their low solubility in aqueous glycols.

KCC-1-nPr-NH-Arg as an efficient organo-nanocatalyst for the green synthesis of 1,8-dioxo decahydroacridine derivatives.

In the present work, an innovative biocompatible heterogeneous organo-nanocatalyst is prepared based on the grafting of arginine amino acid on the channels and pores of dendritic fibrous nano silica. The designed organo-nanocatalyst (KCC-1-nPr-NH-Arg) was characterized by using field emission scanning electron microscopy, Fourier transform infrared spectroscopy, energy dispersive X-ray spectroscopy, map analysis, and adsorption/desorption instruments. The results of analysis show that the engineered catalyst has uniform fibrous spheres and dendritic structure with high surface area (104.9 m2 /g) and great pore volume (0.83 cm3  g-1 ). Because of exceptional dendritic structure of the prepared organo-nanocatalyst, the active sites are available and the difusion and adsorption capacity of the reagents and products increase in the pores and channels of the catalyst. Hence, KCC-1-nPr-NH-Arg was used as an capable heterogeneous basic nanocatalyst in the synthesis of 1,8-dioxo decahydroacridine derivatives from the one-pot four component reactions of aromatic aldehydes, dimedone, and ammonium acetate in solvent free conditions with shorter reaction times (13-35 minutes) and higher yields (94%-98%) in evaluation with other reported works. It is expected that the green organo-nanocatalyst can be used to synthesize other organic compounds.

Metformin functionalized dendritic fibrous nanosilica (KCC-1-nPr-Met) as an innovative and green nanocatalyst for the efficient synthesis of tetrahydro-4H-chromene derivatives.

An innovative nanocatalyst (KCC-1-nPr-Met) has been prepared from the covalent attachment of metformin on the channels and the pores of n-propyl amine functionalized dendritic fibrous nanosilica (DFNS) and used towards efficient, green, and high yield synthesis of tetrahydro-4H-chromenes derivatives by one-pot three-component reaction of aromatic aldehydes, malononitrile, and dimedone in H2 O-EtOH at room temperature. The designed nanocatalyst has been characterized by energy dispersive X-ray spectroscopy (EDS), Fourier transform infrared spectroscopy (FT-IR), and adsorption/desorption analysis (BET) techniques. Also, field emission scanning electron microscopy (FE-SEM) was used to study the morphology of prepared nanocatalyst. The engineered nanocatalyst with uniform fibrous spheres has dendritic structure, high pore volume (0.35 cm3 /g), and great surface area (178 m2 /g). Hence, the specific dendritic structure of the prepared nanocatalyst not only improve the diffusion ability of the reactants and products, but also, increase the availability of dynamic sites in the pores and channels of the catalyst. According to the obtained results, a unique strategy was proposed towards the synthesis of important biologically active scaffolds in the presence of nontoxic and environmental friendly nanocatalyst and media. Milder reaction conditions (room temperature), shorter reaction times (5-30 minutes), excellent yields (92%-98%) of the products with higher purity, very simple workup procedure, and using of EtOH: H2 O as a green solvent are the advantages of the presented work.

Tunable synthesis of dendritic fibrous nano silica using 1-pentanol-water microemulsion at low oil to water ratio.

Dendritic fibrous nanosilica (DFNS) is a suitable nano-carrier for loading pesticides with radially oriented pores and a large surface area. The microemulsion method is standard method to prepare DFNS, and 1-pentanol is taken to replace cyclohexane as an oil solvent due to its high stability and nontoxic property. The results showed that the volume ratio of 1-pentanol (oil) to water (O/W) and the molar ratio of hexadecyltrimethylammonium bromide (CTAB) to tetraethylorthosilicate (TEOS) had effected on morphology and adsorption properties of DFNS in the water-CTAB-1-pentanol-ethanol-trimethylbenzene (TMB) microemulsion system. DFNS with bicontinuous concentric lamellar morphologies can be synthesized in this microemulsion at the meager O/W volume ratio (0.025-0.045). It features a tight mesoporous structure with a thin dendritic fibrous in 0.03 to 0.04 O/W volume ratio. The particle sizes, surface areas, and porosity of DFNS were positively correlated with the addition of the silica precursor TEOS. The size of DFNS increased from 123 to about 220 nm with the CTAB/TEOS molar ratio decreasing from 0.119 to 0.050. When the molar ratio of CTAB to TEOS  = 0.119, DFNS has a smaller particle size (123 nm) with a larger surface area and abundant honeycomb mesopores; the low O/W volume ratio strategy provides theoretical support for the industrialization development of DFNS and nano-pesticides, which plays a profound role in promoting the sustainable development of pesticide reduction, efficiency and green agriculture.

Biosorption optimization of lead(II) and cadmium(II) ions by two novel nanosilica-immobilized fungal mutants.

AIMS: This study aims at immobilization of fungal mutants on nanosilica (NSi)-carriers for designing efficient biosorbents as a significant new technology for decontamination practices and maximizing their heavy metal (HM) sorption proficiency through the experimental design methodology. MATERIALS AND RESULTS: Endophytic fungal mutant strains, Chaetomium globosum El26 mutant and Alternaria alternata S5 mutant were heat inactivated and then immobilized, each separately, on NSi carriers to formulate two separated nano-biosorbents. The formulated NSi-Chaetomium globosum El26 mutant (NSi-Chae El26 m) was investigated for Pb+2 uptake while, the formulated NSi-Alternaria alternata S5 mutant (NSi-Alt S5 m) was investigated for Cd+2 uptake, each through a batch equilibrium protocol. Before and after the metal sorption process, the designed nano-biosorbents were characterized via scanning electron microscopy, energy-dispersive X-ray spectroscopy, and Fourier transform infrared analysis. Sorption pH, contact time, sorbent concentration, and initial HM concentration were statistically optimized using a Box-Behnken design. Results showed that NSi-Chae El26 m was efficient in Pb+2 uptake with maximum biosorption capacities of 199.0, while NSi-Alt S5 m was efficient in Cd+2 uptake with maximum biosorption capacities of 162.0 mg g-1 . Moreover, the equilibrium data indicated that the adsorption of Pb+2 and Cd+2 by the tested nano-biosorbents fitted to the Freundlich isotherm. CONCLUSIONS: The formulated nano-biosorbents resulted in higher HM biosorption of metal ions from aqueous solution than that obtained by the free fungal biomass. The biosorption statistical modelling described the interactions between the tested sorption parameters and predicted the optimum values for maximum HM biosorption capacity by the two designed nano-biosorbents. SIGNIFICANCE AND IMPACT OF THE STUDY: These findings verify that members of the endophytic fungal genera Alternaria and Chaetomium are suitable to produce nano-biosorbents for decontamination practices after treatment by gamma mutagenesis, heat inactivation, and NSi immobilization. Moreover, statistical optimization can assist to evaluate the optimal conditions to produce such bioremediation material.

Removal of beta-lactam antibiotic in water environment by adsorption technique using cationic surfactant functionalized nanosilica rice husk.

This study aims to investigate the adsorption characteristics of cationic surfactant, cetyltrimethylamonium bromide (CTAB) onto negatively nanosilica rice husk surface and the application for antibiotic treatment in water environment. Adsorption of CTAB onto nanosilica increased with an increase of solution pH, due to an enhancement of the electrostatic attraction between cationic methylamomethylamonium groups and negatively charged nanosilica surface enhanced at higher pH. Adsorption of CTAB decreased with a decrease of ionic strength while a common intersection point (CIP) was observed for adsorption isotherm at different ionic strengths, suggesting that hydrophobic interactions between alkyl chains in CTAB molecules significantly induced adsorption and admicelles with bilayer formation were dominant than monolayer of hemimicelles. The CTAB functionalized nanosilica (CFNS) was applied for removal of beta-lactam amoxicillin (AMX). The best conditions for AMX treatment using CFNS were selected as pH 10, contact time 60 min and CFNS dosage 10 mg/mL. Removal efficiency of AMX using CFNS reached to 100% under optimum conditions while it was only 25.01% using nanosilica without CTAB. The maximum AMX adsorption capacity using CFNS of about 25 mg/g was much higher than other adsorbents. The effects of different organics such as humic acid, anionic surfactant, and other antibiotics on AMX removal using CFNS were also studied. A two-step model can fit CTAB uptake isotherms onto nanosilica and AMX onto CFNS well at different KCl concentrations. Based on the desorption of CTAB with AMX adsorption as well as adsorption isotherms, the change in surface charge and functional vibration groups after adsorption, we indicate that AMX adsorption onto CFNS was mainly controlled by electrostatic interaction. We reveal that CFNS is an excellent adsorbent for antibiotic treatment from aqueous solution.

Synthesis of Nanosilica for the Removal of Multicomponent Cd2+ and Cu2+ from Synthetic Water: An Experimental and Theoretical Study.

Copper and cadmium ions are among the top 120 hazardous chemicals listed by the Agency for Toxic Substances and Disease Registry (ATSDR) that can bind to organic and inorganic chemicals. Silica is one of the most abundant oxides that can limit the transport of these chemicals into water resources. Limited work has focused on assessing the applicability of nanosilica for the removal of multicomponent metal ions and studying their interaction on the surface of this adsorbent. Therefore, this study focuses on utilizing a nanosilica for the adsorption of Cd2+ and Cu2+ from water. Experimental work on the single- and multi-component adsorption of these ions was conducted and supported with theoretical interpretations. The nanosilica was characterized by its surface area, morphology, crystallinity, and functional groups. The BET surface area was 307.64 m2/g with a total pore volume of 4.95×10-3 cm3/g. The SEM showed an irregular amorphous shape with slits and cavities. Several Si-O-Si and hydroxyl groups were noticed on the surface of the silica. The single isotherm experiment showed that Cd2+ has a higher uptake (72.13 mg/g) than Cu2+ (29.28 mg/g). The multicomponent adsorption equilibrium shows an affinity for Cd2+ on the surface. This affinity decreases with increasing Cu2+ equilibrium concentration due to the higher isosteric heat from the interaction between Cd and the surface. The experimental data were modeled using isotherms for the single adsorption, with the Freundlich and the non-modified competitive Langmuir models showing the best fit. The molecular dynamics simulations support the experimental data where Cd2+ shows a multilayer surface coverage. This study provides insight into utilizing nanosilica for removing heavy metals from water.

Nano-Silica Modified with Diamine for Capturing Azo Dye from Aqueous Solutions.

Nano-silica particles decorated with amine groups (S-DA) were prepared via a simple, one-pot method, and under very mild conditions in an attempt to improve the affinity of the silica nanoparticles toward capturing anionic organic dye, namely, methyl orange (MO). The prepared sample was characterized by different techniques such as XRD for crystallinity, SEM for morphological structure, TGA for thermal stability, BET surface area, and FTIR for surface functional groups. The prepared sample was tested for the removal of MO under different conditions including the mass of adsorbent, pH, initial concentration, and time. Results showed that the adsorption of MO was very fast with equilibrium achieved in less than 30 min and a maximum removal efficiency of 100% for a mass to volume ratio of 10 g/3 L, a pH of 2.5, initial concentration of 10 mgL-1, and under stagnant conditions. These results were compared with a bare nano-silica, which was not able to adsorb more than 3% after 24 h, indicating the important effect of amine groups. Furthermore, recycling the adsorbent was achieved by rinsing the MO-loaded adsorbent with a dilute solution of KOH. The adsorbent maintained 50% of its initial removal efficiency after four adsorption-desorption cycles.

Multifunctional Role of Silica in Pharmaceutical Formulations.

Due to the high surface area, adjustable surface and pore structures, and excellent biocompatibility, nano- and micro-sized silica have certainly attracted the attention of many researchers in the medical fields. This review focuses on the multifunctional roles of silica in different pharmaceutical formulations including solid preparations, liquid drugs, and advanced drug delivery systems. For traditional solid preparations, it can improve compactibility and flowability, promote disintegration, adjust hygroscopicity, and prevent excessive adhesion. As for liquid drugs and preparations, like volatile oil, ethers, vitamins, and self-emulsifying drug delivery systems, silica with adjustable pore structures is a good adsorbent for solidification. Also, silica with various particle sizes, surface characteristics, pore structure, and surface modification controlled by different synthesis methods has gained wide attention owing to its unparalleled advantages for drug delivery and disease diagnosis. We also collate the latest pharmaceutical applications of silica sorted out by formulations. Finally, we point out the thorny issues for application and survey future trends pertaining to silica in an effort to provide a comprehensive overview of its future development in the medical fields. Graphical Abstract.

Specific monitoring of aflatoxin M1 in real samples using aptamer binding to DNFS based on turn-on method: A novel biosensor.

In the present work, a novel biocompatible scaffold was fabricated for the DNA aptamer immobilization. For the first time, amino-functionalized dendritic fibrous nanosilica (KCC-1-nPr-NH2 ) and gold nanoparticle supported by chitosan (AuNPs-CS) were synthesized and electrodeposited successfully on the surface of the glassy carbon electrode by chronoamperometry technique. Unique oligonucleotide of aflatoxin M1 (5'-ATC CGT CAC ACC TGC TCT GAC GCT GGG GTC GAC CCG GAG AAA TGC ATT CCC CTG TGG TGT TGG CTC CCG TAT) labeled by toluidine blue was immobilization on the prepared interface. Hence, a novel aptamer-based bioassay was formed for highly sensitive quantitation of AFM1 using cyclic voltammetry and differential plus voltammetry. The structure and morphology of GQDs-CS/KCC-1-nPr-NH2 were investigated by Fourier-transform infrared spectroscopy, X-ray diffraction, atomic force, scanning electron microscopy, and energy-dispersive X-ray spectroscopy. The achieved low limit of quantification of apta-assay for detection of AFM1 was 10fM. Also, calibration curve was linear from 0.1µM to 10fM in real samples. The proposed apta-assay has acceptable long-term stability. Designed aptasensor has a lot of remarkable advantages including excellent selectivity, sensitivity, and stability that could be used as facile bio-device for the determination of AFM1 in milk samples.

Synthesis of folic acid functionalized terbium-doped dendritic fibrous nano-silica and Interaction with HEK 293 normal, MDA breast cancer and HT 29 colon cancer cells.

A novel folic acid functionalized terbium-doped dendritic fibrous nanoparticle (Tb@KCC-1-NH2 -FA) with high surface area was synthesized using a novel hydrothermal protocol. In the present work, we report the fluorescent Tb-doted nanomaterial with emission wavelength at 497 nm which confirms the formation of Tb@KCC-1-NH2 -FA. Synthesized nanoparticles were investigated through transmission electron microscope, field emission scanning electron Microscopy, Fourier transform infrared spectra, Brunauer-Emmett-Teller, energy dispersive X-ray, Zeta potential and particle size distribution values and AFM (Atomic force microscopy) techniques. Specially, our desired nanomaterial which has FA moieties on the surface of Tb@KCC-1-NH2-FA where interact with folate receptor (FR) which there is on the surface of the various cancer cells. For this purpose, fluorescence microscopy images were used to prove the uptake of FA based nanomaterial with FR-positive MDA breast cancer and HT 29 colon cancer cells. Also HEK 293 normal cells as FR-negative cells verified the specificity of our desired nanomaterial toward the FR-positive cells. The cytotoxicity survey of Tb@KCC-1-NH2 -FA was examined by MTT assays against MDA breast cancer, HT 29 colon cancer and HEK 293 Normal cell lines which confirmed their biocompatible nature with any significant cytotoxic effects even for concentration higher than 900 µg/mL which could be used as a non-toxic catalyst or carrier in biological ambient. Hence, Tb@KCC-1-NH2 -FA were synthesized using green and hydrothermal method; the process was simple with good productivity and desired nanocomposite was non-toxic.

Long-term stabilization of Cd in agricultural soil using mercapto-functionalized nano-silica (MPTS/nano-silica): A three-year field study.

Cadmium (Cd) contamination in agricultural soil is a worldwide environmental problem. In situ stabilization has been considered an effective approach for the remediation of Cd-contaminated agricultural soil. However, information about the long-term effects of amendment on soil properties and stabilization efficiency remains limited. In the present study, mercapto-functionalized nano-silica (MPTS/nano-silica) was used to stabilize Cd in contaminated agricultural soil under field conditions for three years (with application rates of 0%, 0.2%, 0.4%, 0.6%, 0.8% and 1.0%). The application of MPTS/nano-silica reduced the soil aggregate stability (PDA0.25) (14.8%) and available K (24.9%) and significantly increased the soil dehydrogenase (DHA) (43.4%), yield of wheat grains (33.5%) and Si content in wheat tissues (55.2% in leaf, 50.4% in stem, and 37.7% in husk) (p < 0.05). More importantly, MPTS/nano-silica decreased the leachability (36.0%) and bioavailability (54.3%) of Cd in the soil and transformed Cd into a more stable fraction. The content of Cd in wheat grains decreased by 53.9%, 61.9% and 54.1% in 2017, 2018 and 2019, respectively, in comparison with the control. These results indicated that MPTS/nano-silica has long-term stabilization effects on Cd in agricultural soil and is a potential amendment for the remediation of Cd-contaminated agricultural soils.

The Contribution of Elastic Wave NDT to the Characterization of Modern Cementitious Media.

To mitigate autogenous shrinkage in cementitious materials and simultaneously preserve the material's mechanical performance, superabsorbent polymers and nanosilica are included in the mixture design. The use of the specific additives influences both the hydration process and the hardened microstructure, while autogenous healing of cracks can be stimulated. These three stages are monitored by means of non-destructive testing, showing the sensitivity of elastic waves to the occurring phenomena. Whereas the action of the superabsorbent polymers was evidenced by acoustic emission, the use of ultrasound revealed the differences in the developed microstructure and the self-healing of cracks by a comparison with more commonly performed mechanical tests. The ability of NDT to determine these various features renders it a promising measuring method for future characterization of innovative cementitious materials.