Fabrication of g-C3N4/Y-TiO2 Z-scheme heterojunction photocatalysts for enhanced photocatalytic activity

2021 ◽  
Author(s):  
SongSik Pak ◽  
KwangChol Ri ◽  
Chenmin Xu ◽  
Qiuyi Ji ◽  
Dunyu Sun ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Fourier Transform ◽  
Photocatalytic Activity ◽  
Electron Microscope ◽  
Photoelectron Spectroscopy ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

The g-C3N4/Y-TiO2 Z-scheme heterojunction photocatalysts were successfully synthesized. The powder X-ray diffraction, scanning electron microscopy, high-resolution transmission electron microscope, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy were used for...

Two-Step Fabrication of Nano-PbS on Peacock Feathers Inspired by a Hair-Dyeing Method Used in Ancient Egypt

2013 ◽  
Vol 364 ◽  
pp. 737-741
Author(s):  
Xiao Wei Liu ◽  
Jia Jun Gu ◽  
Fang Yu Zhang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Electron Microscope ◽  
Ancient Egypt ◽  
X Ray Diffraction ◽  
X Ray ◽  
Whole Process ◽  
Transmission Electron ◽  
Dyeing Method ◽  
Scanning Electron

A rapid method towards nanoPbS on peacock feathers was reported and this is inspired by a hair-dyeing technology used in Ancient Egypt thousands of years ago. Original peacock feather was sulfhydrylated by 2, 3-dimercaptosuccinic acid (DMSA) dissolved in alcohol to enhance reaction sites, and then was immersed in the saturated PbO solution in calcium hydroxide and got the PbS peacock feather. The whole process is only two steps and could be completed within two hours. The morphology and structures of the sample were measured by the X-ray diffraction (XRD), Scanning electron microscopy (SEM), and transmission electron microscope (TEM) and results showed that the structure of original peacock feather was well duplicated. Compared with previous works, this method is faster and more efficient and thus has potentials to fabricate other functional sulfides.

Hydrothermal Synthesis of Tetragonal Phase CuInS2 Nanoparticles

2012 ◽  
Vol 557-559 ◽  
pp. 489-492
Author(s):  
Zhi Xin Chen ◽  
Ya Zhen Ye ◽  
Han Jie Huang ◽  
Guang Can Xiao ◽  
Yun Hui He
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Hydrothermal Synthesis ◽  
Photoelectron Spectroscopy ◽  
Tetragonal Phase ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

The tetragonal phase CuInS2 nanoparticles were synthesized by the reaction of Cu(Ac)2, InCl3·4H2O and thioacetamide by hydrothermal method at 200 °C for 6 h in pH 1. The products were characterized by X-ray diffraction, energy-dispersive X-ray spectrum, X-ray photoelectron spectroscopy, scanning electron microscopy (SEM) and transmission electron microscopy (TEM) techniques. Experimental results indicate that reaction temperature and the pH of solution are the important factors in the formation of CuInS2. The SEM and TEM results illuminated that the CuInS2 was composed of so many nanoparticles.

scholarly journals Photocatalytic Self-Cleaning Cotton Fabrics Coated by Cu2(OH)PO4 under Vis/NIR Irradiation

2018 ◽  
Author(s):  
Dawei Gao ◽  
Lili Wang ◽  
Chunxia Wang ◽  
Tan Chen
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Cotton Fabrics ◽  
X Ray Diffraction ◽  
Sunlight Irradiation ◽  
X Ray ◽  
Transmission Electron ◽  
Coated Cotton ◽  
Scanning Electron

In the present work, we designed a mild strategy to make Cu2(OH)PO4 (CHP) nanoparticles on cotton fabrics (CFs) to achieve multi-functionalities. The phytic acid (IP6) assisted method was employed to synthesize nanoparticles (CHP-IP6). Under Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray (EDX), transmission electron microscope (TEM), X-ray photoelectron spectroscopy (XPS) as well as thermogravimetric analysis (TGA), we characterized the coated cotton fabrics. The CHP-IP6 treated fabrics showed prominent photocatalytic activity, excellent photocatalytic stability and thorough discoloration of methylene blue (MB) stain under sunlight irradiation.

Production of nanocrystalline cellulose from bleached soda bagasse pulp

BioResources ◽  
2021 ◽  
Vol 16 (4) ◽  
pp. 7817-7829
Author(s):  
Sabah Ashrafi Birgani ◽  
Mohammad Talaeipour ◽  
Amir Hooman Hemmasi ◽  
Behzad Bazyar ◽  
Kambiz Larijani
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Fourier Transform ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Dialysis Bag ◽  
Bagasse Pulp ◽  
Scanning Electron

The cellulose used in this study was prepared from bleached soda bagasse obtained from the Pars paper factory. To prepare nanocellulose, the sample was subjected to alkaline pretreatment and then acid hydrolysis using 54% sulfuric acid at several temperatures (35, 50, 60, and 65 °C) and different times (30, 60, 90, and 120 min). Then, they were prepared using a centrifuge, dialysis bag, ultrasound, and freezer, respectively. The produced nanocellulose was characterized by transmission electron microscopy (TEM), field-emission scanning electron microscopy (FE-SEM), Fourier transform infrared spectroscopy (FTIR), and X-ray diffraction (XRD). According to the results, temperatures of 50 and 90 °C were selected for the preparation of nanocellulose. The crystallization index of the hydrolyzed pulp and produced nanocellulose was 53 and 61%, respectively. The produced nanocellulose had a fibrillar shape.

Identification of calcium oxalate crystals in dried or fixed tobacco leaf

1984 ◽  
Vol 42 ◽  
pp. 288-289
Author(s):  
Vicki L. Baliga ◽  
Mary Ellen Counts
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Calcium Oxalate ◽  
Growth And Development ◽  
Polarized Light ◽  
Calcium Oxalate Crystals ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

Calcium is an important element in the growth and development of plants and one form of calcium is calcium oxalate. Calcium oxalate has been found in leaf seed, stem material plant tissue culture, fungi and lichen using one or more of the following methods—polarized light microscopy (PLM), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and x-ray diffraction.Two methods are presented here for qualitatively estimating calcium oxalate in dried or fixed tobacco (Nicotiana) leaf from different stalk positions using PLM. SEM, coupled with energy dispersive x-ray spectrometry (EDS), and powder x-ray diffraction were used to verify that the crystals observed in the dried leaf with PLM were calcium oxalate.

PENINGKATAN LAJU DISOLUSI ACYCLOVIR DENGAN METODE SISTEM DISPERSI PADAT MENGGUNAKAN POLOXAMER 188

2016 ◽  
Vol 5 (1) ◽  
pp. 6
Author(s):  
Budi Setiawan ◽  
Erizal Zaini ◽  
Salman Umar
Keyword(s):  
Electron Microscopy ◽  
Thermal Analysis ◽  
Scanning Electron Microscopy ◽  
Fourier Transform ◽  
Differential Thermal Analysis ◽  
Fourier Transform Infrared ◽  
X Ray Diffraction ◽  
Poloxamer 188 ◽  
X Ray ◽  
Scanning Electron

Sebuah penelitian tentang sistem dispersi padat dari asiklovir dengan poloxamer 188 telah dilakukan formulasi dengan pencampuran secara fisika dengan rasio 1 : 1, 1 : 3, 1 : 5 dan dispersi padat 1 : 1, 1 : 3, 1 : 5 dan penggilingan 1:1 sebagai pembanding. Dispersi padat dibuat menggunakan metode pencairan (fusi), yang digabung dengan poloxamer 188 pada hotplate kemudian asiklovir dimasukkan ke dalam hasil poloxamer 188 lalu di kocok hingga membentuk masa homogen. Semua formula yang terbentuk termasuk asiklovir poloxamer 188 murni dianalisis karakterisasinya dengan Differential Thermal Analysis (DTA), X-ray Diffraction, Scanning Electron Microscopy (SEM), dan Fourier Transform Infrared (FTIR), kemudian pengambilan dilakukan  (penentuan kadar) mengunakan spektrofotometer UV pada panjang gelombang 257,08 nm dan uji laju disolusi dengan aquadest bebas CO2 menggunakan metode dayung. Hasil pengambilan  (penentuan kadar) menunjukkan bahwa semua formula memenuhi persyaratan farmakope Amerika edisi 30 dan farmakope Indonesia edisi 4 yaitu 95-110%. Sedangkan hasil uji laju disolusi untuk campuran fisik 1: 1, dan dispersi padat 1: 1, dan penggilingan 1: 1 menunjukkan peningkatan yang nyata dibandingkan asiklovir murni. Hal ini juga dapat dilihat dari hasil perhitungan statistik  menggunakan analisis varian satu arah  SPSS 17.

Hydrothermal Synthesis and Characterization of BiFeO3 Polyhedral Crystallites

2012 ◽  
Vol 174-177 ◽  
pp. 508-511
Author(s):  
Lin Lin Yang ◽  
Yong Gang Wang ◽  
Yu Jiang Wang ◽  
Xiao Feng Wang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
Xrd Pattern ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

BiFeO3 polyhedrons had been successfully synthesized via a hydrothermal method. The as-prepared products were characterized by power X-ray diffraction (XRD) pattern, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The possible mechanisms for the formation of BiFeO3 polyhedrons were discussed. Though comparison experiments, it was found that the kind of precursor played a key role on the morphology control of BiFeO3 crystals.

Preparation of Borosilicate Xerogel and Research on its Mineralization

2012 ◽  
Vol 476-478 ◽  
pp. 2059-2062
Author(s):  
Chen Wang ◽  
Ya Dong Li ◽  
Gu Qiao Ding
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Fourier Transform ◽  
Infrared Spectroscopy ◽  
Ph Value ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
X Ray ◽  
Compositional Changes ◽  
Scanning Electron

Tributyl borate was first adopted for the introduction of boron in the preparation of bioactive borosilicate xerogel by sol-gel method. The xerogel reacted continuously in 0.25M K2HPO4 solution with a starting pH value of 7.0 at 37 °C for 1day. The structural, morphologies and compositional changes resulting from the conversion were characterized using X-ray diffraction, scanning electron microscopy and Fourier transform infrared spectroscopy. The results indicated that speed of formation of HA was cut way back on the time with the addition of boron and the induction period for the HA nucleation on the surface of the borosilicate xerogel was short than 1 days. The conversion mechanism of the borosilicate xerogels to hydroxyapaptite was also discussed.

Influence of Salt Aid on Combustion Synthesis of Nanocrystalline CeO2 Powders

2011 ◽  
Vol 412 ◽  
pp. 5-8 ◽  
Author(s):  
Ying Zhang ◽  
Ai Chen ◽  
Hai Rong Wang ◽  
Ze Song Li ◽  
Ying Ping Shen
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Combustion Process ◽  
X Ray Diffraction ◽  
X Ray ◽  
Particle Characteristics ◽  
Transmission Electron ◽  
Nanocrystalline Ceria ◽  
Scanning Electron

The present article reports the results of studies related to the synthesis of nanocrystalline ceria powder by combustion process using salt combustion aid. Cerium nitrate as oxidant and urea as fuel were used as reagents, Sodium Chloride was compared as combustion aid. The phase analysis and particle size were compared. The product was characterized by X-ray diffraction, Scanning electron microscopy and Transmission electron microscopy. The results showed that employment of starting fuel with combustion aid resulted in synthesizing nanocrystalline ceria powder with fine agglomerates. By using combustion aid, the energetics of the combustion reaction and particle characteristics have been changed.

scholarly journals The Characteristics of Padamarang Magnesite under Calcination and Hydrothermal Treatment

2019 ◽  
Vol 29 (2) ◽  
Author(s):  
Mutia Dewi Yuniati ◽  
Feronika Cinthya Mawarni Putri Wawuru ◽  
Anggoro Tri Mursito ◽  
Iwan Setiawan ◽  
Lediyantje Lintjewas
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Fourier Transform ◽  
Infrared Spectroscopy ◽  
Fourier Transform Infrared Spectroscopy ◽  
Hydrothermal Treatment ◽  
Energy Dispersive ◽  
X Ray Diffraction ◽  
X Ray ◽  
Scanning Electron

Magnesite (MgCO3) is the main source for production of magnesium and its compound. In Indonesia, magnesite is quite rare and can be only found in limited amount in Padamarang Island, Southeast Sulawesi Provence. Thus the properties of magnesite and the reactivity degree of the obtained product are of technological importance. The aim of this work was to analyze the characteristics of Padamarang magnesite under calcination and hydrothermal treatment processes. The processes were carried out at various temperatures with range of 150-900°C for 30 minutes. The solids were characterized with respect to their chemical and physical properties by using scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDX), Fourier-transform infrared spectroscopy (FTIR), and X-ray diffraction (XRD). SEM image indicates that magnesite was formed from thin and flat hexagon sheets. The FTIR and XRD analysis disclose that MgO formed at temperature above 300°C, where as the magnesite sample also lost its mass around 50%. These results demonstrate that Padamarang magnesite decomposes to magnesium oxide and carbon dioxide at high temperature.Magnesit (MgCO3) merupakan sumber utama untuk produksi magnesium dan senyawa-senyawanya. Di Indonesia, magnesit cukup jarang dan hanya dapat ditemukan dalam jumlah yang terbatas di Pulau Padamarang, Propinsi Sulawesi Tenggara. Oleh karena itu sifat magnesit dan derajat reaktivitas dari produk-produk magnesit penting untuk diketahui. Penelitian ini bertujuan untuk menganalisis karakteristik magnesit Padamarang dengan perlakuan kalsinasi dan hidrothermal.  Proses dilakukan pada temperatur yang bervariasi dari 150-900°C selama 30 menit. Sifat kimia dan fisika dari magnesit dikarakterisasi dengan menggunakan scanning electron microscopy dengan energy-dispersive X-ray spectroscopy (SEM-EDX), Fourier-transform infrared spectroscopy (FTIR), dan X-ray diffraction (XRD). Gambar dari analisis SEM menunjukkan bahwa magnesit terbentuk dari lembaran-lembaran heksagonal yang tipis dan datar. Hasil analisis dengan FTIR dan XRD menunjukkan bahwa MgO terbentuk pada temperatur diatas 300°C, dimana sampel magnesit juga kehilangan massanya sekitar 50% pada suhu tersebut. Hal ini menunjukkan bahwa Magnesit Padamarang terdekomposisi menjadi magnesium oksida dan karbon dioksida pada temperatur tinggi.

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