Synthesis of silica and carbon nanoparticles from rice husks for latent fingermarks application
Research into latent fingermark developing techniques has taken many paths over the years as researchers and practitioners explore numerous methods to enhance existing powders and reagents. Currently, copious research is being dedicated to investigating the transformational improvements that coul...
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| Format: | Thesis |
| Language: | English |
| Published: |
2018
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| Subjects: | |
| Online Access: | http://eprints.usm.my/47852/1/Dr.%20Revathi%20AP%20Rajan-24%20pages.pdf |
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| Summary: | Research into latent fingermark developing techniques has taken many paths
over the years as researchers and practitioners explore numerous methods to enhance
existing powders and reagents. Currently, copious research is being dedicated to
investigating the transformational improvements that could be provided by nanosized
compounds to expand the sensitivity and selectivity of fingermark dusting powders to
develop fingermarks with high clarity and better contrast. Nonetheless, such a
technique has inherent drawbacks of limited field applicability, cost and energy
intensive, incurs health hazard to the users in the long run as well as prepared using
synthetic precursors. In this research novel synthesis techniques of silica nanoparticle
(SiNP) and carbon nanoparticle (CNP) from a sustainable eco-friendly source, rice
husk (RH) was developed. Acid digestion process was conducted to remove trace
metal impurities from RH. The filtrand was ashed to extract silica, while the filtrate
was aged to form CNP, a novel CNP synthesis technique pioneered in this research.
Sodium silicate was formed by dissolving highly pure rice husk ash, obtained from the
stepwise purification of RH, in alkali solution. Precipitation of SiNP using acetic acid
and acetone is introduced in this research to form minimally agglomerated, well
dispersed spherical SiNP with a mean particle size of 270 nm, verified using imaging
techniques. Silica chemical composition and amorphous nature were confirmed by
using spectroscopic analysis. Freeze-drying produced mesoporous pore volume (0.167
cm3/g) silica powders with a 4.2 nm average pore size (0.9 to 57.9 nm pore sizedistribution) and very high specific surface (162.00 m2/g (Brunauer-Emmett Teller,
(BET) and 238.60 m2/g Barrett-Joyner-Halenda (BJH)). Ageing of the filtrate from
acid digestion produced amorphous CNP that exhibited non-smooth, slightly irregular
spherical particles with a higher degree of agglomeration in comparison to SiNP.
Particle size distribution fell in the range of 100 to 500 nm with mean particle size of
300 nm. Molecular bonding and chemical composition of the CNP was confirmed
using spectroscopic techniques. CNP powder possessed microporous pore volume
(0.009 cm3/g) with a 61.75 nm average pore size (0.89 to 81.90 nm pore size
distribution) and low surface area value (0.558 m2/g BET and 4.816 m2/g BJH).
Spherical SiNP obtained was formulated into three derivative products namely white
nanoparticle powder, nanoparticle reagent (NPR) and multicoloured nanoparticle
powder, while the CNP powder was used as the black nanoparticle powder. A
methodological approach was conducted to compare the efficiency of the nanoparticle
products against commercial products by developing fresh and aged fingermarks of
various stages. Standard scoring system was applied to evaluate the results and
statistical analysis was employed to summarise the data. Findings revealed that the
nanoparticle powders and reagent performed on par with the existing commercial
powders while exhibiting higher selectivity. Nanoparticle synthesis from low cost
precursor in this research did not require special equipment, addition of
resins/adhesives or surface passivation. Additionally, utilisation of RH may boost
farmer’s income and incorporate non-toxic green nanotechnology into routine
investigative procedures. In conclusion, the low cost products developed exhibited
promising quality and superiority to the existing products in the market. |
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