Particle Size Analysis of Cotton Dust Using Scanning Electron Microscopy

1977 ◽  
Vol 99 (1) ◽  
pp. 56-60 ◽  
Author(s):  
R. E. Fornes ◽  
M. M. Kleinfelter ◽  
S. P. Hersh

Particle size distributions of dusts generated in a model card room and collected on filter media by a vertical elutriator having a particle size cut-off of 15 μm dia have been determined using scanning electron microscopy. Photomicrographs, usually at 3000×, were made of the samples and the particle diameters were estimated by the Martin method. It was found that the average particle size of cotton dust samples measured by this technique was smaller than that reported in the literature obtained by light microscopy. It was also found that the distribution of particle sizes does not follow a simple log-normal distribution unless the smallest particles observed in this study are omitted. A bimodal or perhaps a multimodal distribution yields a better representation of the data. It is concluded that scanning electron microscopy is a practical and accurate method for sizing cotton dust particles on filter surfaces.

1992 ◽  
Vol 82 (2) ◽  
pp. 111-115 ◽  
Author(s):  
C Abramson ◽  
J Wilton

Nail dust particles were analyzed by scanning electron microscopy for size and topography. The percentage of "fines" that could be inhaled and deposited in the alveoli and bronchioles were determined by quantitative particle size analysis. Distribution representing the largest total mass was graphed between 1 and 2 microns. The authors found that 86% of nail dust would reach the bronchioles and alveoli, and 31% could be expected to deposit in these areas.


Polymers ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1726
Author(s):  
Guoyu Tian ◽  
Xiuhong Zhong ◽  
Xuehai Wu ◽  
Zhaojiang Wang

The present work describes the preparation of nano-lignin particles from calcium lignosulfonate (CL). The nano-lignin was fabricated from colloidal lignin–polyacrylamide complexes via self-assembly. The sizes of the nano-lignin particles were examined by dynamic light scattering (DLS) and scanning electron microscopy (SEM). The results indicated that the average particle size of the prepared nano-lignin was approximately 100 nm. In addition, the obtained nano-lignin exhibited enhanced fluorescence intensity when compared with the original lignin, which might represent a potential application of this nano-particle product.


2013 ◽  
Vol 303-306 ◽  
pp. 2490-2494 ◽  
Author(s):  
Peng Lei ◽  
Jian Chen ◽  
Wei Li ◽  
Yan Jie Ren ◽  
Wei Qiu ◽  
...  

The method of preparation of Cu-Ni-Al prealloyed powders were studied in this paper. Cu, Ni, Al were smelted at 1500°C and N2 was chosen as atomizing media to produce the Cu-Ni-Al prealloyed powders. The morphology and particle size distribution of Cu-Ni-Al prealloyed powders were analysis with Scanning electron microscopy; the phase composition of Cu-Ni-Al prealloyed powders were analysis XRD. The results show that the morphology of Cu-Ni-Al prealloyed powders are almost nearly spherical, particle size distribution is very uniform and the average particle size is 39μm. The powders are composed of Cu and AlNi phase.


2011 ◽  
Vol 236-238 ◽  
pp. 1814-1817
Author(s):  
Hong Wang ◽  
Yan Jie ◽  
Hong Luo ◽  
Xue Feng

Monodisperse α-Fe2O3nanoparticles with average particle size of 110 nm were successfully prepared using olyvinylpyrrolidone (PVP) as surfactant via a novel hydrothermal route. The products were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM). The experiments results revealed that PVP and the concentration of NH4HCO3have played a crucial role in the formation of the monodisperse a-Fe2O3nanoparticles.


2012 ◽  
Vol 500 ◽  
pp. 29-33
Author(s):  
Bao Rang Li ◽  
Xin Ming Xi ◽  
Yang Bai

The nano-TiO2powders with the average particle size of about 40nm were used as starting materials. The compacted powders were firstly performed in Spark-plasma-sintering (SPS) at a high temperature and then sintered in air for hours at a relatively low temperature. The obtained samples were investigated by X-ray diffraction (XRD) and scanning electron microscopy (SEM). The results showed an obvious reduction in grain size was achieved by taking advantage of modified two step sintering (MTSS). The value of the relative grain growth d/do for the samples prepared by MTSS was less than 3.


2010 ◽  
Vol 5 (3) ◽  
pp. 155892501000500 ◽  
Author(s):  
D.P. Chattopadhyay ◽  
B.H. Patel

This research deals with the synthesis of nanosized copper as colloidal solution and its application to cotton fabric. Copper nano colloids were prepared by chemical reduction of copper salt using sodium borohydride as reducing agent in presence of tri-sodium citrate. The size and size distribution of the particles were examined by particle size analyzer and the morphology of the synthesized particles was examined by SEM and AFM techniques. X-ray fluorescence spectroscopy detected the presence of copper in the treated fabric. The results of particle size analysis showed that the average particle size varied from 60 nm to 100 nm. The nano copper treated cotton was subjected to soil burial test for the assessment of its resistance towards microbial attack. SEM images of treated fabric indicate copper nano particles are well dispersed on the surface of the specimens. The treatments of nano copper colloidal solution on cotton not only improve its antimicrobial efficiency but also influenced the tensile strength of the fabric sample positively. The treatment was found to enhance the color depth and fastness properties of direct dyed cotton fabric samples.


Author(s):  
SOBITHARANI P ◽  
ANANDAM S ◽  
MOHAN VARMA M ◽  
VIJAYA RATNA J ◽  
SHAILAJA P

Objective: The main objective of this study was to investigate the release pattern of a poorly water-soluble drug quercetin (QU) by fabricating its cyclodextrin nanosponges. Methods: Characterization of the original QU powder and QU-loaded nanosponges was carried out by the Fourier-transformed infrared (FTIR) spectroscopy, transmission electron microscopy (TEM), and dissolution tester. The drug release pattern was subjected to various kinetic models. Results: FTIR studies confirmed the formation of inclusion complex of drug. The particle size analysis revealed that the average particle size measured by laser light scattering method is around 400–420 nm with low polydispersity index. The particle size distribution is unimodal and having a narrow range. A sufficiently high zeta potential indicates that the complexes would be stable and the tendency to agglomerate would be miniscule. TEM image revealed the porous nature of nanosponges. The dissolution of the QU nanosponges was significantly higher compared with the pure drug. Conclusion: From the kinetic study, it is apparent that the regression coefficient value closer to unity in case of Korsmeyer-Peppas model indicates that the drug release exponentially to the elapsed time. n value obtained from the Korsmeyer-Peppas plots, i.e., 0.9911 indicating non-Fickian (anomalous) transport ; thus, it projected that delivered its active ingredient by coupled diffusion and erosion.


2011 ◽  
Vol 311-313 ◽  
pp. 96-100
Author(s):  
Jian Li Cheng ◽  
Cun Zhou ◽  
Hao Peng ◽  
Huan Wang ◽  
Yu Sun

Two kind of polyimide/silica nanocomposites which were recorded poly(amic acid)/ silica(PAA/SiO2) and SiO2in poly(amic acid) ammonium salt(PAS/SiO2) respectively, have been prepared for different methods. The size of SiO2in PAA/SiO2and PAS/SiO2are measured by Particle size analysis and the average particle size are 377nm and 53.7nm. Transmission electron microscopy(TEM) images of PAS/ SiO2confirm that the size of particles are ranged from 40 to 80nm. The stuctures of samples have been characterized by FT-IR spectra. The thermal stability of PAA/SiO2and PAS/SiO2are studied by thermogravimetric analysis (TGA) and the thermal behaviors were investigated by differential scanning calorimetry (DSC) in this paper. It is shown that PAA/SiO2have slightly better thermal properties than that of PAS/SiO2. The results obtained from Instron universal strength tester present the water-solube PAS/SiO2own the excellent mechanical prperties as same as PAA/SiO2.


Author(s):  
Rajani Indrakanti ◽  
V Brahmaji Rao ◽  
C Udaya Kiran

This article (a sequel to part-I that appeared earlier in the same journal) presents synthesis and characterisation details of conducting PPY-nanocomposite obtained from gallium nitride–doped ferrite and polypyrrole. The GaN-doped ferrite is synthesised by sol–gel method. GaNFe2O3f-PPY composites are prepared by impregnation technique. Using the SciFinder software we could not trace any report in the literature for this synthesised Ga(2x + 2)NFe2(49 − x)O3-PPY nanocomposites. The doped nanoferrite is combined with polypyrrole, an intrinsic conducting polymer, in three proportions by percentage (70%:30%), (90%:10%) and (97%:3%), to obtain two series each of three compositions for the conducting PPY-nanocomposite. The synthesised polymer composites are characterised by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, selected area electron diffraction, energy dispersive X-ray analysis and Fourier transform infrared spectroscopy. From our studies, it has been observed that the crystallite size of nanocomposites is decreased when compared to crystallite size of GaNFe2O3. The average particle size from histogram is in good agreement with Debye–Scherrer formula calculations. The scanning electron microscopy and transmission electron microscopy micrograms reveal that the particles are varying with the values of X and the percentage of PPY. The shapes observed are Globules,Tetrahedron,Nanorods of short and long lengths. The GaNFe2O3-PPY composites’ spectra revealed the shift in the band in comparison with the PPY spectra. Also, the wavelength is decreased, and vibrational frequency is increased.


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