SIZED-CONTROLLED ZnO NANOPARTICLES, SYNTHESIS AND MORPHOLOGY

2009 ◽  
Vol 08 (03) ◽  
pp. 277-279 ◽  
Author(s):  
MOHSEN OFTADEH ◽  
MASOUD SALAVATI-NIASARI ◽  
FATEMEH DAVAR

Zinc oxide nanoparticles were successfully prepared through the decomposition of zinc acetylacetonate precursor in oleylamine in the presence of triphenylphosphine. The products were characterized by X-ray diffraction, transmission electron microscopy, and Fourier transform infrared spectroscopy.

Biomolecules ◽  
2019 ◽  
Vol 10 (1) ◽  
pp. 38 ◽  
Author(s):  
Banzeer Ahsan Abbasi ◽  
Javed Iqbal ◽  
Riaz Ahmad ◽  
Layiq Zia ◽  
Sobia Kanwal ◽  
...  

This study attempts to obtain and test the bioactivities of leaf extracts from a medicinal plant, Geranium wallichianum (GW), when conjugated with zinc oxide nanoparticles (ZnONPs). The integrity of leaf extract-conjugated ZnONPs (GW-ZnONPs) was confirmed using various techniques, including Ultraviolet–visible spectroscopy, X-Ray Diffraction, Fourier Transform Infrared Spectroscopy, energy-dispersive spectra (EDS), scanning electron microscopy, transmission electron microscopy, and Raman spectroscopy. The size of ZnONPs was approximately 18 nm, which was determined by TEM analysis. Additionally, the energy-dispersive spectra (EDS) revealed that NPs have zinc in its pure form. Bioactivities of GW-ZnONPs including antimicrobial potentials, cytotoxicity, antioxidative capacities, inhibition potentials against α-amylase, and protein kinases, as well as biocompatibility were intensively tested and confirmed. Altogether, the results revealed that GW-ZnONPs are non-toxic, biocompatible, and have considerable potential in biological applications.


Clay Minerals ◽  
2004 ◽  
Vol 39 (4) ◽  
pp. 391-404 ◽  
Author(s):  
J. E. F. C. Gardolinski ◽  
G. Lagaly ◽  
M. Czank

AbstractKaolinite and synthetic γ-Al(OH)3 (gibbsite or hydrargillite) were reacted with phenylphosphonic, phenylphosphinic and 2-nitrophenol-4-arsonic acids. The products were studied by powder X-ray diffraction, transmission electron microscopy/selected area electron diffraction/ energy dispersive X-ray/Fourier transform infrared and simultaneous thermogravimetric/differential thermal analysis. The acids were not intercalated but, instead, easily destroyed the structure of the minerals. Lamellar Al phenylphosphonate and aluminium phenylphosphinate and phenylarsonate with polymeric linear-chain structures were formed from kaolinite. The reaction between gibbsite and the same acids yielded almost identical products. No evidence of formation of grafted kaolinite derivatives after the reaction with phenylphosphonic acid was found.


2015 ◽  
Vol 19 (56) ◽  
Author(s):  
Muflihatun ◽  
Siti Shofiah ◽  
Edi Suharyadi

Nanopartikel Nikel Ferit (NiFe2O4) telah disintesis dengan metode kopresipitasi dengan memvariasi konsentrasi NaOH dan suhu sintesis. Struktur kristal, ukuran partikel, dan morfologi dari sampel dianalisa menggunakan X-ray diffraction (XRD) dan transmission electron microscopy (TEM). Ukuran butir pada konsentrasi NaOH 3, 5, dan 10 M masing-masing adalah 5,7; 4,3; dan 4,2 nm, sedangkan pada suhu 60, 80, dan 150°C berturut-turut adalah 4,2; 4,9; dan 5,5 nm. Analisa fourier transform infrared (FTIR) menunjukkan dua puncak serapan pada rentang ~400-600 cm-1 yang terkait dengan site oktahedral dan tetrahedral pada struktur NiFe2O4. Sifat magnetik NiFe2O4 hasil analisa vibrating sample magnetometer (VSM) menunjukkan bahwa sampel berperilaku ferromagnetik dengan nilai koersivitasnya pada rentang 42-47 Oe. Sampel dengan variasi konsentrasi NaOH, koersivitasnya cenderung menurun dengan menurunnya ukuran partikel. Sementara sampel dengan variasi suhu, semakin kecil ukuran partikel, koersivitasnya cenderung meningkat. Pada 15 kOe, nilai magnetisasi terbesar (6,17 emu/g) diperoleh pada sampel dengan rasio fasa α-Fe2O3 paling rendah.


2016 ◽  
Vol 2016 ◽  
pp. 1-6 ◽  
Author(s):  
Muthusamy Govarthanan ◽  
Min Cho ◽  
Jung-Hee Park ◽  
Jum-Suk Jang ◽  
Young-Joo Yi ◽  
...  

Agroindustrial byproduct mediated green synthesis of silver nanoparticles was carried out using cottonseed oilcake (CSOC) extract. The aqueous silver nitrate formed stable silver nanoparticles with CSOC extract as a reducing agent for Ag+to Ag0. The synthesized nanoparticles were characterized using energy dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM), Fourier transform infrared (FTIR) spectroscopy, and X-ray diffraction (XRD) techniques. The synthesized silver nanoparticles (AgNPs) (4 mM) significantly inhibited the growth of phytopathogens,Pseudomonas syringaepv.actinidiaeandRalstonia solanacearum. Further, cytotoxicity of AgNPs was evaluated using rat splenocyte cells. The splenocyte viability was decreased according to the increasing concentration of AgNPs and 90% of cell death was observed at 100 μg/mL.


2017 ◽  
Vol 41 (19) ◽  
pp. 10880-10889 ◽  
Author(s):  
Ping Yuan ◽  
Ming Zhang ◽  
Ninglin Zhou ◽  
Cheng Chi ◽  
Xiaohong Chu ◽  
...  

In this study, a carbon dots-genipin covalent conjugate (CDs–GP) was synthesized, characterized by Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), transmission electron microscopy (TEM), and fluorescence spectroscopy (FL).


2021 ◽  
Vol 18 (4) ◽  
pp. 691-701
Author(s):  
Faruk Arodiya ◽  
Chirag Makvana ◽  
Kokila Parmar

Generally, synthesis and encapsulation process improve therapeutic value of nano encapsulated drugs. The silver nanoparticles (AgNPs) biosynthesized from Ziziphus nummularia leaves and encapsulated with polyvinyl pyrrolidone (PVP) polymer as antibacterial agents, due to its high bioavailability, better encapsulation and less toxic properties. The nanoparticles (AgNPs) biosynthesized from Ziziphus nummularia leaves and capped with polyvinyl pyrrolidone (PVP) polymer, The acquired AgNPs and polymeric functionalized AgNPs were fully characterised by the UV- Visible spectroscopy , Transmission electron microscopy (TEM), X-Ray diffraction pattern (XRD) and Fourier transform infrared spectroscopy (FTIR).The crystalline Ag NPs and Polymer Functionalized AgNPs have a face-centered cubic structure with an average size of 9.20 nm, according to X-ray Diffraction spectroscopy. Fourier Transform Infrared spectroscopy revealed that biomolecules such as proteins are incapable of reducing metal ions and the formation of an encapsulating layer in terms of metal ions. High-Resolution transmission electron microscopy revealed that Polymer functionalized AgNPs ranged in size of 10 nm. AgNPs and Polymer functionalized AgNPs showed effective antimicrobial and antioxidant activity. The biosynthesized monodisperse silver nanoparticles and encapsulated silver nanoparticles demonstrated better antimicrobial and antioxidant activity which can be used in various biomedical applications.


2010 ◽  
Vol 14 (06) ◽  
pp. 540-546 ◽  
Author(s):  
Lingling Zhang ◽  
Yongtao Lu ◽  
Yukou Du ◽  
Ping Yang ◽  
Xiaomei Wang

Meso-tetrakis(p-sulfonatophenyl)porphyrin (TPPS4) functionalized platinum nanocomposites were synthesized and characterized using ultraviolet-visible absorption spectroscopy (UV-vis), fluorescence spectroscopy (FL), Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), and X-ray diffraction (XRD) methods. The postulated configuration of TPPS4 functionalized platinum nanocomposite may be described as an antenna system containing a photoreceptive TPPS4 shell and a nanosize platinum core. Fluorescence and photoelectrochemistry studies of both TPPS4 and the platinum nanocomposites showed that efficient electron/energy transfer occurred from the TPPS4 donor to the metallic nanocore acceptor. TPPS4 functionalized platinum nanocomposites are photocatalytic active for water reduction to produce hydrogen. The turnover numbers (TONPt and TONTPPS4) and quantum yield of hydrogen (ϕH2) for the photocatalyst (nPt:nTPPS4= 250) were 44, 11056, and 1.8%, respectively, calculated on the basis of the total amount of H2 evolution for 12 h irradiation.


2014 ◽  
Vol 17 (51) ◽  
Author(s):  
Seveny Nuzully ◽  
Takeshi Kato ◽  
Edi Suharyadi

Nanopartikel magnetit (Fe3O4) telah berhasil disintesis menggunakan metode kopresipitasi dengan penambahan Polyethylene Glycol (PEG-4000) sebagai coating. Distribusi ukuran partikel dan sifat magnetik dari nanopartikel ini diteliti berdasarkan perbandingan massa Fe3O4 dan PEG, yaitu 1:1, 2:1, 3:1, 4:1, 1:2, dan 1:3. Distribusi ukuran partikel dikarakteristik dengan Transmission Electron Microscopy (TEM) sedangkan pengujian awal untuk mengetahui struktur kristal yang terkandung dalam sampel hasil sintesis dikarakteristik dengan X-Ray Diffraction (XRD), kemudian untuk mengetahui keberhasilan coating PEG dapat dikarakterisasi dengan menggunakan Fourier Transform Infra Red (FTIR) serta sifat magnetiknya dapat dikarakterisasi menggunakan Vibrating Sample Magnetometer (VSM). Sampel 1:1, 2:1, 3:1, 4:1, 1:2, 1:3 berturut-turut meiliki nilai Ms 37,2; 49,7; 55,2; 61,7; 27,7; 33,7 dan nilai Mr 4,8; 6,4; 6,6; 8,0; 3,3; 4,7. Hasil karakterisasi menunjukkan bahwa penambahan konsentrasi PEG mengakibatkan nilai saturation magnetic (Ms) dan remanence magnetic (Mr) turun, kecuali pada sampel dengan perbandingan 1:3.


2014 ◽  
Vol 17 (51) ◽  
Author(s):  
Seveny Nuzully ◽  
Takeshi Kato ◽  
Edi Suharyadi

Nanopartikel magnetit (Fe3O4) telah berhasil disintesis menggunakan metode kopresipitasi dengan penambahan Polyethylene Glycol (PEG-4000) sebagai coating. Distribusi ukuran partikel dan sifat magnetik dari nanopartikel ini diteliti berdasarkan perbandingan massa Fe3O4 dan PEG, yaitu 1:1, 2:1, 3:1, 4:1, 1:2, dan 1:3. Distribusi ukuran partikel dikarakteristik dengan Transmission Electron Microscopy (TEM) sedangkan pengujian awal untuk mengetahui struktur kristal yang terkandung dalam sampel hasil sintesis dikarakteristik dengan X-Ray Diffraction (XRD), kemudian untuk mengetahui keberhasilan coating PEG dapat dikarakterisasi dengan menggunakan Fourier Transform Infra Red (FTIR) serta sifat magnetiknya dapat dikarakterisasi menggunakan Vibrating Sample Magnetometer (VSM). Sampel 1:1, 2:1, 3:1, 4:1, 1:2, 1:3 berturut-turut meiliki nilai Ms 37,2; 49,7; 55,2; 61,7; 27,7; 33,7 dan nilai Mr 4,8; 6,4; 6,6; 8,0; 3,3; 4,7. Hasil karakterisasi menunjukkan bahwa penambahan konsentrasi PEG mengakibatkan nilai saturation magnetic (Ms) dan remanence magnetic (Mr) turun, kecuali pada sampel dengan perbandingan 1:3.


Sign in / Sign up

Export Citation Format

Share Document