Preparation and Growth Characteristics of Mesocarbon Microbeads

2013 ◽  
Vol 750-752 ◽  
pp. 1121-1124 ◽  
Author(s):  
Zhi Wang ◽  
Chun Hong Yu

Mesocarbon microbeads (MCMBs) have been synthesized from coal tar pitch. Scanning electron microscopy (SEM) and laser particle size analyzer were used to evaluate the structure and partical size. The effect of process parameters on the growth and morphologies of MCMBs was investigated. The results show that the optimum temperature range is 410-430 °C and the growth time has a suitable range. The diameter and yield of MCMBs will increase and the spherical degree does not change with the extension of time.

2020 ◽  
Vol 7 (4) ◽  
pp. 816-824
Author(s):  
D. M. Puente-Siller ◽  
A. E. García-Castillo ◽  
J. A. López-Corpus ◽  
A. Perea-Garduño

AbstractIt has recently been reported that coal tar pitch (CTP) can be utilised as raw material for the production of graphene nanocapsules (GNCs) because it is formed by a great quantity of aromatic organic compounds (which promote the rearrangement of double bonds by a process of polymerisation). Due to the importance of graphene and the search for a non-expensive methodology to produce it, this work used CTP to synthesise GNCs using an in situ activation technique at low temperatures and evaluating the effect of the working temperature on the formation of such nanostructures. In other words, analysing the form of the particle as the temperature rises from 600 to 900 °C. As result of the experimentation, powders were obtained and analysed by the techniques of X-Ray Diffraction, Raman Spectroscopy and Microscopy, employing Field Emission Scanning Electron Microscopy by normal mode as well as by Scanning Transmission Electron Microscopy and a High-Resolution Scanning Electron Microscopy. The results show that working with temperatures between 800 and 850 °C promotes the production of GNCs, considering that their size reduces as the working temperature rises.


2018 ◽  
Vol 3 (1) ◽  
pp. 12 ◽  
Author(s):  
Zaimahwati Zaimahwati ◽  
Yuniati Yuniati ◽  
Ramzi Jalal ◽  
Syahman Zhafiri ◽  
Yuli Yetri

<p>Pada penelitian ini telah dilakukan isolasi dan karakterisasi bentonit alam menjadi nanopartikel montmorillonit. Bentonit alam yang digunakan diambil dari desa Blangdalam, Kecamatan Nisam Kabupaten Aceh Utara.  Proses isolasi meliputi proses pelarutan dengan aquades, ultrasonic dan proses sedimentasi. Untuk mengetahui karakterisasi montmorillonit dilakukan uji FT-IR, X-RD dan uji morfologi permukaan dengan Scanning Electron Microscopy (SEM). Partikel size analyzer untuk menganalisis dan menentukan ukuran nanopartikel dari isolasi bentonit alam. Dari hasil penelitian didapat ukuran nanopartikel montmorillonit hasil isolasi dari bentonit alam diperoleh berdiameter rata-rata 82,15 nm.</p><p><em>In this research we have isolated and characterized natural bentonite into montmorillonite nanoparticles. Natural bentonite used was taken from Blangdalam village, Nisam sub-district, North Aceh district. The isolation process includes dissolving process with aquades, ultrasonic and sedimentation processes.  The characterization of montmorillonite, FT-IR, X-RD and surface morphology test by Scanning Electron Microscopy (SEM). Particle size analyzer to analyze and determine the size of nanoparticles from natural bentonite insulation. From the research results obtained the size of montmorillonite nanoparticles isolated from natural bentonite obtained an average diameter of 82.15 nm.</em></p>


2005 ◽  
Vol 87 (1) ◽  
pp. 77-83 ◽  
Author(s):  
Tong-Qi Li ◽  
Cheng-Yang Wang ◽  
Xiu-Jun Liu ◽  
Jia-Ming Zheng ◽  
Hui Wang

2017 ◽  
Vol 6 (1) ◽  
pp. 31 ◽  
Author(s):  
Dessy Kurniasari ◽  
Sri Atun

Tujuan penelitian ini adalah untuk membuat dan mengetahui karakteristik nanopartikel dari ekstrak etanol temu kunci (Boesenbergia pandurata) dan rasio optimal variasi konsentrasi kitosan dan NaTPP dalam pembuatan nanopartikel temu kunci.            Pembuatan ekstrak temu kunci (Boesenbergia pandurata) menggunakan metode maserasi menggunakan etanol teknis 96% dilanjutkan evaporasi hingga terbentuk ekstrak kental temu kunci. Koloid nanopartikel dibuat dengan mencampurkan ekstrak temu kunci dalam etanol p.a, akuades, larutan kitosan dalam asam asetat glasial, dan larutan NaTPP. Ada 9 variasi komposisi antara larutan kitosan dan  NaTPP yakni rasio (5:1); (10:1); (15:1); (20:1); (3,33:1); (8:1); (9:1); (11:1); dan (12:1). Padatan dalam koloid nanopartikel dipisahkan dengan cara sentrifugasi. Endapan yang didapatkan disimpan dalam freezer. Koloid nanopartikel yang terbentuk dikarakterisasi menggunakan Particle Size Analyzer (PSA) dan Zeta Sizeruntuk mengetahui ukuran partikel dan nilai zeta potensial. Padatan yang didapatkan dari proses sentrifugasi selanjutnya dikarakterisasi menggunakan Scanning Electron Microscopy (SEM) untuk mengetahui kondisi morfologi padatan tersebut. Karakterisasi dengan KLT pada padatan yang didapatkan bertujuan untuk mengetahui kesamaan kandungan senyawa antara ekstrak etanol temu kunci dan ekstrak etanol temu kunci dalam sediaan berukuran nano.            Koloid nanopartikel yang telah dibuat berwarna kuning dan setelah di sentrifugasi terbentuk padatan berwarna kuning kecokelatan. Karakterisasi menggunakan PSA menunjukkan ukuran partikel pada rentang 389-877 nm sebanyak 98,1% pada rasio konsentrasi kitosan dan NaTPP = (8:1). Nilai rerata zeta potensial adalah 41,87 mV. Hasil foto SEM menunjukkan morfologi partikel yang memiliki permukaan yang tidak rata. Rf keenam sampel menunjukkan hasil bahwa senyawa yang terkandung dalam ekstrak etanol temu kunci maupun ekstrak etanol temu kunci dalam sediaan nanopartikel adalah sama. Kata Kunci : kitosan, NaTPP, ekstrak etanol temu kunci, KLT, SEM, PSA, zeta sizer


2013 ◽  
Vol 631-632 ◽  
pp. 486-489
Author(s):  
Zhi Wang

Carbon nanotube-Mesocarbon microbead composites were synthesized from coal tar pitch with carbon nanotubes (CNTs) as additive. The effect of CNTs addition and process parameters on the growth and morphologies of Mesocarbon microbeads (MCMBs) was investigated. The results show that adding CNTs enhances the nucleation and inhibits the growth and coalescence of MCMBs. Under the same thermal condensation conditions, the MCMBs made in the presence of CNTs tend to have smaller size, lower yield and more uniform size distribution, but more CNTs can lead to poor spherical degrees. Compared with the raw CNTs, the CNTs treated with blended acid can achieve better sphere and more uniform MCMBs with increasing CNTs ratio.


2019 ◽  
Vol 2019 ◽  
pp. 1-8 ◽  
Author(s):  
Xiangfeng Chu ◽  
Junsong Liu ◽  
Shiming Liang ◽  
Linshan Bai ◽  
Yongping Dong ◽  
...  

In this paper, g-C3N4-WO3 composite materials were prepared by hydrothermal processing. The composites were characterized by means of X-ray powder diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), and N2 adsorption-desorption, respectively. The gas sensing properties of the composites were investigated. The results indicated that the addition of appropriate amount of g-C3N4 to WO3 could improve the response and selectivity to acetone. The sensor based on 2 wt% g-C3N4-WO3 composite showed the best gas sensing performances. When operating at optimum temperature of 310°C, the responses to 1000 ppm and 0.5 ppm acetone were 58.2 and 1.6, respectively, and the ratio of the S1000 ppm acetone to S1000 ppm ethanol reached 3.7.


2010 ◽  
Vol 434-435 ◽  
pp. 850-852
Author(s):  
Qi Wang ◽  
Bo Yin ◽  
Zhen Wang ◽  
Gen Li Shen ◽  
Yun Fa Chen

In present work, ceria microspheres were synthesized by template hydrothermal method. Crystalline form of the as-synthesized ceria microspheres was defined by X-ray powder diffraction (XRD) and high resolution transmission electron microscopy (HRTEM). Dispersibility of ceria microspheres was comprehensively characterized using scanning electron microscope (SEM) observation and laser particle size analyzer. Furthermore, the ultraviolet light absorption performances of ceria microspheres with several different sizes were compared by ultraviolet visible spectrophotometer. The results showed that ceria microspheres presented excellent UV absorbent property and the size influence was remarkable.


2020 ◽  
Vol 21 (1) ◽  
pp. 30
Author(s):  
Dewi Mustika Rahim ◽  
Netti Herawati ◽  
Hasri Hasri

ABSTRAK Telah dilakukan penelitian tentang sintesis nanopartikel perak menggunakan bioreduktor ekstrak daun teh hijau (Camellia Sinensis) dengan iradiasi microwave. yang untuk mengetahui pengaruh waktu sintesis dan pengaruh pH stabilizer terhadap sintesis nanopartikel perak ekstrak daun teh hijau dengan iradiasi microwave serta karakterisasinya. Larutan AgNO3 3 mM direduksi menggunakan ekstrak daun teh hijau dan di iradiasi microwave pada variasi waktu sintesis 1-5 menit. Penentuan waktu sintesis optimal menggunakan spektrofotometer UV-Vis diukur setiap 1 menit. Nanopartikel dengan waktu sistesis 4 menit, pH stabilizer menggunakan asam sitrat dan NaOH dengan pH 6-9. Karakterisasi nanopartikel menggunakan instrumen SEM-EDS (Scanning Electron Microscopy-Energy Dispersive X-Ray Spectroscopy) dan PSA (Particle Size Analyzer). Hasil penelitian menunjukkan bahwa waktu sintesis optimal adalah 4 menit. Morfologi nanopatikel perak yang dikarakterisasi menggunakan SEM (Scanning Electron Microscopy) yang dihasilkan cenderung beragregasi. Adanya kecenderungan nanopartikel untuk beragregasi menyebabkan ukuran atau diameter nanopartikel tidak seragam. Ukuran dan distribusi ukuran nanopartikel perak dikarakterisasi menggunakan PSA(Particle Size Analyzer) dihasilkan pada pH 6 antara 31,01 – 402,44 nm dengan rata-rata ukuran sebesar 91 nm, pH 7 antara 35,03 – 740,899 nm dengan rata-rata ukuran sebesar 106,3 nm, pH 8 antara 39,58 – 193,48 nm dengan rata-rata ukuran 71,7, dan pH 9 antara 35,03 – 171,25 nm dengan rata-rata ukuran sebesar 64,4 nm. Disimpulkan bahwa hasil sintesis nanopartikel perak terkecil diperoleh pada pH 9 dan waktu sintesis 4 menit. Kata kunci: Ekstrak Daun Teh Hijau, Nanopartikel Perak, Iradiasi Microwave ABSTRACT Research has been carried out on the synthesis of silver nanoparticles using a bioreductor of green tea leaf extract (Camellia Sinensis) by irradiation microwave.This research aimed to determine the effect of synthesis time and pH stabilizer on the synthesis of silver nanoparticles of green tea leaf extract by microwave irradiation and it’s characterization. The 3 mM AgNO3 solution was reduced using green tea leaf extract and microwave irradiated in a variation of the synthesis time 1-5 minutes. The determining optimum of sythesis time was done by analysis of UV-Vis spectrum for every minutes. Nanoparticles with a synthesis time of 4 minutes, the stabilizer of silver nanoparticles used citric acid and NaOH with a pH of 6-9. Characterization of nanoparticles using SEM-EDS instrument (Scanning Electron Microscopy-Energy Dispersive X-Ray Spectroscopy) and PSA (Particle Size Analyzer). The results showed that the optimal synthesis time was 4 minutes. The morphology of silver nanopaticles characterized using SEM produced tends to aggregate. The tendency of nanoparticles to aggregate causes size or diameter of nanoparticles was random. The size and distribution of size silver nanoparticles characterized using PSA were produced at pH 6 between 31.01 - 402.44 nm with an average size of 91 nm, pH 7 between 35.03 - 740,899 nm with an average size amounting to 106.3 nm, pH 8 between 39.58 - 193.48 nm with an average size of 71.7, and pH 9 between 35.03 - 171.25 nm with an average size of 64.4 nm. It was concluded that the synthesis of the smallest silver nanoparticles was obtained at pH 9 and synthesis time of 4 minutes. Keywords: Green Tea Leaf Extract, Silver Nanoparticles, Microwave Irradiation


2019 ◽  
Vol 6 (4) ◽  
pp. 633-642 ◽  
Author(s):  
Bingfeng Yan ◽  
Guangyao Wang

Abstract DCLR-P was prepared by direct coal liquefaction residue (DCLR) with ash removal. In the present experiments, mesocarbon microbeads (MCMBs) were prepared by co-carbonization of coal tar pitch (CTP) and DCLR-P. With the increase of DCLR-P content, the yield of MCMBs increased from 47.8% to 56.8%. At the same time, the particle sizes distribution of MCMBs was narrowed, resulting in the decrease of D90/D10 ratio from 154.88 to 6.53. The results showed that DCLR-P had a positive effect on the preparation of MCMBs. 1H-NMR, FTIR, SEM and XRD were used to analyze the mechanisms and characteristics of MCMBs prepared by co-carbonization of CTP and DCLR-P. The results showed that the Proton Donor Quality Index (PDQI) of DCLR-P was 13.32, significantly higher than that of CTP (0.83). This indicated that DCLR-P had more naphthenic structure than CTP, which leads to hydrogen transferring in polycondensation reaction. The aliphatic structure of DCLR-P can improve the solubility and fusibility of mesophase, thereby making the structure of MCMBs more structured. The microstructure of the graphitized MCMBs had a substantially parallel carbon layer useful for its electrical performance. The performance of graphitized MCMBs as a negative electrode material for Li-ion batteries was tested. The particle sizes, tap density, specific surface area and initial charge–discharge efficiency of graphitized MCMBs met the requirements of CMB-I in GB/T-24533-2009. However, the initial discharge capacity of graphitized MCMB was only 296.3 mA h g−1 due to the low degree of graphitization of MCMBs.


Sign in / Sign up

Export Citation Format

Share Document