scholarly journals Antibacterial Superabsorbent Polymers from Tara Gum Grafted Poly(Acrylic acid) Embedded Silver Particles

Polymers ◽  
2018 ◽  
Vol 10 (9) ◽  
pp. 945 ◽  
Author(s):  
Mingfang Chi ◽  
Chang Liu ◽  
Jie Shen ◽  
Zhehai Dong ◽  
Zi Yang ◽  
...  
Keyword(s):  
Electron Microscope ◽  
Acrylic Acid ◽  
Photoelectron Spectroscopy ◽  
Silver Ions ◽  
Absorption Capacity ◽  
Superabsorbent Polymers ◽  
X Ray ◽  
Amorphous Nanoparticles ◽  
Silver Composite ◽  
Poly Acrylic Acid

Tara gum/silver composite superabsorbent polymers were synthesized with tara gum grafted poly(acrylic acid), using K2S2O8 (KPS) as an initiator and N,N′-methylenebisacrylamide (MBA) as a cross-linker. The products were characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), transmission electron microscope (TEM), scanning electron microscope (SEM) and X-ray photoelectron spectroscopy (XPS). The results showed that the silver ions were partially reduced to Ag0 and the amorphous nanoparticles containing Ag0 and Ag2O were around 10~50 nm in size The tara gum/silver composite superabsorbent polymers exhibited an interconnected porous structure with strong water absorption capacity. The swelling ratio of each product could reach 473 g/g in distilled water and 62 g/g in 0.9% NaCl solution. The antimicrobial activity of the samples against Staphylococcus aureus and Escherichia coli increased with the addition of AgNO3 from 0 to 125 mg. This work indicates that the developed tara gum/silver composite superabsorbent polymers can be potentially used for biomedical applications.

Gamma Irradiation Assisted Synthesis of Ag/rGO Composites and their Surface Properties

2017 ◽  
Vol 898 ◽  
pp. 2224-2230
Author(s):  
Ying Liang ◽  
Bin Fang ◽  
Fang Fang Lin ◽  
Xu Min Zhu
Keyword(s):  
Graphene Oxide ◽  
Electron Microscope ◽  
Gamma Irradiation ◽  
Surface Properties ◽  
Photoelectron Spectroscopy ◽  
Absorbed Dose ◽  
Silver Ions ◽  
Broad Absorption Band ◽  
X Ray ◽  
Transmission Electron

Ag/rGO composites were synthesized under gamma irradiation using silver nitrate and graphene oxide (GO) as the starting materials. Comparing with traditional methods, gamma irradiation is a simple and “green” technique. In the irradiation system, silver ions were reduced to silver nanoparticles (AgNPs) by the electrons generated from the radiolysis of solvent. GO nanosheets provided reactive sites for the formation of AgNPs and acted as a colloidal surfactant preventing the aggregation of AgNPs. Meanwhile, GO were partially reduced to reduced graphene oxide (rGO). X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscope, transmission electron microscope, Raman spectra and UV-Vis absorption spectra were applied for the characterization of Ag/rGO composites. The results showed that the absorbed dose (3.1 kGy, 4.7 kGy, 9.4 kGy and 27.4 kGy) plays an important role in the size distribution of AgNPs and the reduction degree of GO nanosheetes. The Ag/rGO composites exhibit a broad absorption band at visible light due to the surface plasmon resonance of AgNPs. Because of the unique surface properties, Ag/rGO composites behave enhanced performance for the adsorption of organic dye from water.

scholarly journals Antimicrobial Activity of Silver Containing Crosslinked Poly(Acrylic Acid) Fibers

Micromachines ◽  
2019 ◽  
Vol 10 (12) ◽  
pp. 829 ◽  
Author(s):  
Mohammad Mofidfar ◽  
Eun Seon Kim ◽  
Emily L. Larkin ◽  
Lisa Long ◽  
Wayne D. Jennings ◽  
...  
Keyword(s):  
Antimicrobial Activity ◽  
Acrylic Acid ◽  
Infectious Diseases ◽  
Photoelectron Spectroscopy ◽  
Food Packaging ◽  
Uv Spectroscopy ◽  
Wound Dressings ◽  
Bacterial Strains ◽  
X Ray ◽  
Poly Acrylic Acid

Bacterial and fungal pathogens have caused serious problems to the human health. This is particularly true for untreatable infectious diseases and clinical situations where there is no reliable treatment for infected patients. To increase the antimicrobial activity of materials, we introduce silver nanoparticle (NP) patches in which the NPs are incorporated to the surface of smooth and uniform poly(acrylic acid) (PAA) nanofibers. The PAA nanofibers were thermally crosslinked with ethylene glycol via heat treatment through a mild method. The characterization of the resulting PAA-silver NP patches was done using scanning electron microscopy (SEM), UV spectroscopy, X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). To demonstrate the antimicrobial activity of PAA, we incorporated the patches containing the silver NPs into strains of fungi such as Candida albicans (C. albican) and bacteria such as Methicillin-resistant Staphylococcus aureus (MRSA). The PAA-silver fibers achieved zones of inhibition against C. albicans and MRSA indicating their antimicrobial activity against both fungi and bacteria. We conclude that silver NP patches exhibited multiple inhibitory actions for the interruption and blockage of activity fungal and bacterial strains, which has the potential as an antimicrobial agent in infectious diseases. Moreover, the proposed material has the potential to be used in antimicrobial textile fabrics, food packaging films, and wound dressings.

Preparation and characterization of nanocrystalline PbSe in poly(acrylic acid-co-styrene)

2001 ◽  
Vol 16 (10) ◽  
pp. 2922-2927 ◽  
Author(s):  
Yangyang Sun ◽  
Xuefeng Qian ◽  
Jie Yin ◽  
Junchao Huang ◽  
Xiaodong Ma ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Acrylic Acid ◽  
Photoelectron Spectroscopy ◽  
Ambient Pressure ◽  
Matrix Metal ◽  
X Ray ◽  
Transmission Electron ◽  
Visible Spectra ◽  
Key Factor ◽  
Poly Acrylic Acid

The in situ reduction method was used to prepare nanocrystalline PbSe in a poly(acrylic acid-co-styrene) matrix. Metal precursor-doped polymer film was treated with selenium and reducing reagent (NaBH4) in ethylenediamine, leading to the formation of assemblies of crystalline semiconductive PbSe in polymer. The preparation was done at room temperature and ambient pressure. X-ray diffraction, x-ray photoelectron spectroscopy, infrared, scanning electron microscopy, transmission electron microscopy, and ultraviolet-visible spectra were used to characterize the as-prepared materials. The key factor for successful preparation of this composite was also discussed.

scholarly journals Preparation and Characterization of Visible-Light-Activated Fe-N Co-Doped TiO2and Its Photocatalytic Inactivation Effect on Leukemia Tumors

2012 ◽  
Vol 2012 ◽  
pp. 1-9 ◽  
Author(s):  
Kangqiang Huang ◽  
Li Chen ◽  
Jianwen Xiong ◽  
Meixiang Liao
Keyword(s):  
Electron Microscope ◽  
Photoelectron Spectroscopy ◽  
Sol Gel ◽  
Light Therapy ◽  
Cell Counting ◽  
Visible Absorption ◽  
X Ray ◽  
Photocatalytic Inactivation ◽  
Inactivation Efficiency ◽  
Co Doped

The Fe-N co-doped TiO2nanocomposites were synthesized by a sol-gel method and characterized by scanning electron microscope (SEM), transmission electron microscope (TEM), X-ray diffraction (XRD), ultraviolet-visible absorption spectroscopy (UV-vis) and X-ray photoelectron spectroscopy (XPS). Then the photocatalytic inactivation of Fe-N-doped TiO2on leukemia tumors was investigated by using Cell Counting Kit-8 (CCK-8) assay. Additionally, the ultrastructural morphology and apoptotic percentage of treated cells were also studied. The experimental results showed that the growth of leukemic HL60 cells was significantly inhibited in groups treated with TiO2nanoparticles and the photocatalytic activity of Fe-N-TiO2was significantly higher than that of Fe-TiO2and N-TiO2, indicating that the photocatalytic efficiency could be effectively enhanced by the modification of Fe-N. Furthermore, when 2 wt% Fe-N-TiO2nanocomposites at a final concentration of 200 μg/mL were used, the inactivation efficiency of 78.5% was achieved after 30-minute light therapy.

Preparation of Carbon Nanofibers from Polyacrylonitrile Nanofibers by Electrospinning

2011 ◽  
Vol 415-417 ◽  
pp. 642-647
Author(s):  
En Zhong Li ◽  
Da Xiang Yang ◽  
Wei Ling Guo ◽  
Hai Dou Wang ◽  
Bin Shi Xu
Keyword(s):  
Electron Microscope ◽  
Carbon Nanofibers ◽  
Photoelectron Spectroscopy ◽  
Solution Concentration ◽  
Dimethyl Formamide ◽  
Ultrafine Fibers ◽  
X Ray ◽  
Scanning Electron ◽  
Pan Fibers

Ultrafine fibers were electrospun from polyacrylonitrile (PAN)/N,N-dimethyl formamide (DMF) solution as a precursor of carbon nanofibers. The effects of solution concentration, applied voltage and flow rate on preparation and morphologies of electrospun PAN fibers were investigated. Morphologies of the green fibers, stabilized fibers and carbonized fibers were compared by scanning electron microscope (SEM). The diameter of PAN nanofibers is about 450nm and the distribution of diameter is well-proportioned. Characterization of the elements changes of fibers were performed by X-ray photoelectron spectroscopy (XPS).

scholarly journals Effective Enhancement of Water Absorbency of Itaconic Acid Based-Superabsorbent Polymer via Tunable Surface—Crosslinking

Polymers ◽  
2021 ◽  
Vol 13 (16) ◽  
pp. 2782
Author(s):  
Yong-Rok Kwon ◽  
Jung-Soo Kim ◽  
Dong-Hyun Kim
Keyword(s):  
Itaconic Acid ◽  
Photoelectron Spectroscopy ◽  
Crosslinking Agent ◽  
Absorption Capacity ◽  
Gel Strength ◽  
Superabsorbent Polymer ◽  
Optimal Conditions ◽  
Retention Capacity ◽  
X Ray ◽  
Crosslinking Reactions

A superabsorbent polymer (SAP) was synthesized by copolymerizing itaconic acid and vinyl sulfonic acid. The typically low absorbency of itaconic acid-based SAPs under mechanical loads was improved by introducing surface crosslinking. Fourier-transform infrared spectroscopy and X-ray photoelectron spectroscopy were used to characterize the synthesis and surface-crosslinking reactions in the SAP. Various conditions for surface-crosslinking reactions, such as the surface-crosslinking solution, content of surface-crosslinking agent, and reaction temperature, were explored and correlated with the gel strength and absorption characteristics of the resulting SAP particles. The distilled water content in the surface-crosslinking solution strongly influenced the absorption capacity of the SAP, but this sensitivity decreased when acetone was used as a co-solvent. Itaconic acid-based SAP that was crosslinked under optimal conditions exhibited centrifuge retention capacity and absorbency under a load of 31.1 and 20.2, respectively.

scholarly journals Photocatalytic Degradation of Estriol Using Iron-Doped TiO2 under High and Low UV-Irradiation

2018 ◽  
Author(s):  
Irwing M. Ramírez-Sánchez ◽  
Erick R. Bandala
Keyword(s):  
Photocatalytic Activity ◽  
Electron Microscope ◽  
Uv Irradiation ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
Bet Surface Area ◽  
Doped Tio2 ◽  
X Ray ◽  
Transmission Electron ◽  
Iron Doped

Iron Doped TiO2 nanoparticles (Fe-TiO2) were synthesized and photocatalitically investigated under high and low fluence values of UV-radiation. The Fe-TiO2 physical characterization was performed using X-ray Powder Diffraction (XRD), Brunauer-Emmett-Teller (BET) surface area analysis, Transmission Electron Microscope (TEM), Scanning Electron Microscope (SEM), Diffuse Reflectance Spectroscopy (DRS), and X-Ray Photoelectron Spectroscopy (XPS) technique. The XPS evidenced that ferric ion (Fe3+) was in the lattice of TiO2 and co-dopants no intentionally added were also present due to the precursors of the synthetic method. The Fe3+ concentration played a key role in the photocatalytic generation of hydroxyl radical (•OH) and estriol (E3) degradation. Fe-TiO2 materials accomplished E3 degradation, and it was found that the catalyst with 0.3 at. % content of Fe (0.3 Fe-TiO2) enhanced the photocatalytic activity under low UV-irradiation compared with no intentionally Fe-added TiO2 (zero-iron TiO2) and Aeroxide® TiO2 P25. Furthermore, the enhanced photocatalytic activity of 0.3 Fe-TiO2 under low UV-irradiation may have applications when radiation intensity must be controlled, as in medical applications, or when strong UV absorbing species are present in water.

scholarly journals Fenton Degradation of Ofloxacin Using a Montmorillonite-Fe3O4 Composite

2020 ◽  
Vol 2 (1) ◽  
pp. 32
Author(s):  
Alamri Rahmah Dhahawi Ahmad ◽  
Saifullahi Shehu Imam ◽  
Wen Da Oh ◽  
Rohana Adnan
Keyword(s):  
Electron Microscope ◽  
Photoelectron Spectroscopy ◽  
High Efficiency ◽  
Solar Irradiation ◽  
Precipitation Process ◽  
Wastewater Remediation ◽  
Solution Ph ◽  
X Ray ◽  
Subsequent Degradation ◽  
Co Precipitation

In this work, FeM composites consisting of montmorillonite and variable amounts of Fe3O4 were successfully synthesized via a facile co-precipitation process. They were characterized using X-ray photoelectron spectroscopy (XPS), field emission scanning electron microscope (FESEM), energy dispersive X-ray spectroscopy (EDX), transmission electron microscope (TEM), N2 adsorption-desorption, and Fourier transform infrared spectroscopy (FT-IR) techniques to explain the effect of Fe3O4 content on the physicochemical properties of the Fe3O4-montmorillonite (FeM) composites. The FeM composites were subsequently used as heterogeneous Fenton catalysts to activate green oxidant (H2O2) for the subsequent degradation of ofloxacin (OFL) antibiotic. The efficiency of the FeM composites was studied by varying various parameters of Fe3O4 loading on montmorillonite, catalyst dosage, initial solution pH, initial OFL concentration, different oxidants, H2O2 dosage, reaction temperature, inorganic salts, and solar irradiation. Under the conditions of 0.75 g/L FeM-10, 5 mL/L H2O2, and natural pH, almost 81% of 50 mg/L of OFL was removed within 120 min in the dark, while total organic carbon (TOC) reduction was about 56%. Moreover, the FeM-10 composite maintained high efficiency and was stable even after four continuous cycles, making it a promising candidate in real wastewater remediation.

scholarly journals Preparation and structure of SiOCN fibres derived from cyclic silazane/poly-acrylic acid hybrid precursor

2019 ◽  
Vol 6 (10) ◽  
pp. 190690
Author(s):  
Zhongkan Ren ◽  
Christel Gervais ◽  
Gurpreet Singh
Keyword(s):  
Acrylic Acid ◽  
Photoelectron Spectroscopy ◽  
Thermo Gravimetric Analysis ◽  
Ceramic Matrix Composite ◽  
Linear Structure ◽  
Cost Effective ◽  
Gravimetric Analysis ◽  
Low Viscosity ◽  
Hybrid Precursor ◽  
Poly Acrylic Acid

Ceramic matrix composite (CMC) materials have been considered a desired solution for lightweight and high-temperature applications. Simultaneously, among all different CMC reinforcements, polymer-derived ceramic (PDC) fibres have gained attention for the intrinsic thermal stability and mechanical strength with simple and cost-effective synthesis techniques. Here, carbon-rich SiOCN fibres were synthesized via hand-drawing and polymer pyrolysis of a hybrid precursor of 1,3,5,7-tetramethyl-1,3,5,7-tetravinylcyclotetrasilazane (TTCSZ) and poly-acrylic acid (PAA). The type of silazane reported in this work is considered as a major precursor for SiCN; however, it is unspinnable, due to its unfavourable physical properties (low viscosity) and chemical structure (cyclic rather than linear structure). The introduction of PAA to TTCSZ to create a hybrid precursor remarkably improved the spinnability of the silazane and should be widely applicable to other unspinnable PDC pre-ceramic polymers. Investigations on the structural and compositional development of the fibres were mainly conducted via Raman spectroscopy, Fourier-transform infrared spectroscopy, scanning electron microscopy, X-ray photoelectron spectroscopy, nuclear magnetic resonance and thermo-gravimetric analysis to determine spinnability, free carbon content, cross-linking and pyrolysis behaviour of the fibres, respectively.

ZnFe2O4 Modified by Fe(NO3)3 for the Synthesis of Ionic Ferrofluids

2010 ◽  
Vol 177 ◽  
pp. 32-36 ◽  
Author(s):  
An Rong Wang ◽  
Jian Li ◽  
Qing Mei Zhang ◽  
Hua Miao
Keyword(s):  
Particle Size ◽  
Magnetic Properties ◽  
Electron Microscope ◽  
Transmission Electron Microscope ◽  
Photoelectron Spectroscopy ◽  
Vibrating Sample Magnetometer ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Znfe2o4 Nanoparticles

Weak magnetic ZnFe2O4 nanoparticles were prepared by coprecipitation and treated with different concentrations of Fe(NO3)3 solution. Untreated and treated particles were studied using a vibrating sample magnetometer, transmission electron microscope, by X-ray diffraction, X-ray energy dispersive spectroscopy and X photoelectron spectroscopy. The results showed that, after treatment, the ZnFe2O4/γ-Fe2O3 forms disphase nanoparticles, with enlarged size, enhanced magnetic properties and with a surface parceled with Fe(NO3)3. The size of the particles and their magnetic properties are related to the concentration of the treatment solution. The particle size and magnetic properties could be controlled by controlling the concentration of treating solution, therefore nanoparticles can be more widely used.

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