6 research outputs found
XRD data of raw lotus fibers and lotus fibers after being treated with hydrogen peroxide
XRD data of raw lotus fibers and lotus fibers after being treated with hydrogen peroxid
Supplementary Material for RSC Open Science 23.6.2017
Supplementary Material for RSC Open Science 23.6.201
Monodisperse Ag Nanoparticle-Decorated Bacterial Nanocellulose as Flexible Surface-Enhanced Raman Scattering Sensors for Trace Detection of Toxic Thiram
Surface-enhanced Raman spectroscopy (SERS) is becoming
an attractive
technique for applications in food safety detection, environmental
monitoring, disease diagnosis, and molecular identification. However,
SERS substrates often suffer from low sensitivity, poor signal homogeneity,
and stability. Herein, solution-processable monodisperse Ag nanoparticles
(M-AgNPs) with an average diameter of 66 nm are synthesized by a size-controllable
seeded-growth method. Furthermore, the M-AgNPs were coated on the
surface of bacterial nanocellulose (BNC) to form flexible monodisperse
Ag nanoparticles@bacterial nanocellulose (M-Ag@BNC) SERS sensors by
a simple vacuum-assisted filtration. The SERS performance of flexible
M-Ag@BNC substrates with various M-Ag loadings is systematically investigated.
Due to the highly homogeneous distribution of M-AgNPs, the optimal
M-Ag-12@BNC SERS sensor exhibits high sensitivity with a detection
sensitivity of 10–13 M for methylene blue, excellent
reproducibility (relative standard deviation (RSD) = 4.48%), and prominent
storage stability (over 20 days). Besides, the hydrophilic BNC with
good permeability and adsorption properties can absorb target molecules
in the high-density hot-spot regions to further enhance SERS performance.
Finite-difference time domain (FDTD) is also used to simulate and
verify the strong electric field distribution of a M-AgNP-based SERS
sensor. Finally, the M-Ag-12@BNC SERS sensor is successfully applied
to detect pesticide residues on irregular fruit surfaces by a simple
and feasible paste-and-read method. The sensitivity of a flexible
M-Ag@BNC SERS sensor for thiram is up to 10–8 M.
The flexible, ultrasensitive, and stable M-Ag@BNC SERS sensor exhibits
potential applications in trace identification of hazardous organic
molecules
Monodisperse Ag Nanoparticle-Decorated Bacterial Nanocellulose as Flexible Surface-Enhanced Raman Scattering Sensors for Trace Detection of Toxic Thiram
Surface-enhanced Raman spectroscopy (SERS) is becoming
an attractive
technique for applications in food safety detection, environmental
monitoring, disease diagnosis, and molecular identification. However,
SERS substrates often suffer from low sensitivity, poor signal homogeneity,
and stability. Herein, solution-processable monodisperse Ag nanoparticles
(M-AgNPs) with an average diameter of 66 nm are synthesized by a size-controllable
seeded-growth method. Furthermore, the M-AgNPs were coated on the
surface of bacterial nanocellulose (BNC) to form flexible monodisperse
Ag nanoparticles@bacterial nanocellulose (M-Ag@BNC) SERS sensors by
a simple vacuum-assisted filtration. The SERS performance of flexible
M-Ag@BNC substrates with various M-Ag loadings is systematically investigated.
Due to the highly homogeneous distribution of M-AgNPs, the optimal
M-Ag-12@BNC SERS sensor exhibits high sensitivity with a detection
sensitivity of 10–13 M for methylene blue, excellent
reproducibility (relative standard deviation (RSD) = 4.48%), and prominent
storage stability (over 20 days). Besides, the hydrophilic BNC with
good permeability and adsorption properties can absorb target molecules
in the high-density hot-spot regions to further enhance SERS performance.
Finite-difference time domain (FDTD) is also used to simulate and
verify the strong electric field distribution of a M-AgNP-based SERS
sensor. Finally, the M-Ag-12@BNC SERS sensor is successfully applied
to detect pesticide residues on irregular fruit surfaces by a simple
and feasible paste-and-read method. The sensitivity of a flexible
M-Ag@BNC SERS sensor for thiram is up to 10–8 M.
The flexible, ultrasensitive, and stable M-Ag@BNC SERS sensor exhibits
potential applications in trace identification of hazardous organic
molecules
Monodisperse Ag Nanoparticle-Decorated Bacterial Nanocellulose as Flexible Surface-Enhanced Raman Scattering Sensors for Trace Detection of Toxic Thiram
Surface-enhanced Raman spectroscopy (SERS) is becoming
an attractive
technique for applications in food safety detection, environmental
monitoring, disease diagnosis, and molecular identification. However,
SERS substrates often suffer from low sensitivity, poor signal homogeneity,
and stability. Herein, solution-processable monodisperse Ag nanoparticles
(M-AgNPs) with an average diameter of 66 nm are synthesized by a size-controllable
seeded-growth method. Furthermore, the M-AgNPs were coated on the
surface of bacterial nanocellulose (BNC) to form flexible monodisperse
Ag nanoparticles@bacterial nanocellulose (M-Ag@BNC) SERS sensors by
a simple vacuum-assisted filtration. The SERS performance of flexible
M-Ag@BNC substrates with various M-Ag loadings is systematically investigated.
Due to the highly homogeneous distribution of M-AgNPs, the optimal
M-Ag-12@BNC SERS sensor exhibits high sensitivity with a detection
sensitivity of 10–13 M for methylene blue, excellent
reproducibility (relative standard deviation (RSD) = 4.48%), and prominent
storage stability (over 20 days). Besides, the hydrophilic BNC with
good permeability and adsorption properties can absorb target molecules
in the high-density hot-spot regions to further enhance SERS performance.
Finite-difference time domain (FDTD) is also used to simulate and
verify the strong electric field distribution of a M-AgNP-based SERS
sensor. Finally, the M-Ag-12@BNC SERS sensor is successfully applied
to detect pesticide residues on irregular fruit surfaces by a simple
and feasible paste-and-read method. The sensitivity of a flexible
M-Ag@BNC SERS sensor for thiram is up to 10–8 M.
The flexible, ultrasensitive, and stable M-Ag@BNC SERS sensor exhibits
potential applications in trace identification of hazardous organic
molecules
Measurement and Correlation of Solubility of Glutathione in Four Binary Solvents from 278.15 to 318.15 K
The solubilities of glutathione in
four binary solvent
mixtures (water + acetone, water + 1,4-dioxane, water + acetonitrile,
and water + tetrahydrofuran) were measured using a dynamic laser monitoring
method at temperatures ranging from 278.15 to 318.15 K. The molar
fraction solubility of glutathione in the binary solvent increased
with increasing water content and temperature. The modified Apelblat,
CNIBS/R-K, Van’t Hoff–Jouyban–Acree, Apelblat–Jouyban–Acree,
and NRTL were applied to calculate the solubility of glutathione in
these mixtures. The relative average deviation and root-mean-square
deviation indicated a good correlation between the experimental and
model solubility data. In addition, the KAT-LSER model was used to
evaluate the solvent effect in the solvent–solvent and solvent–solute
interactions. The results showed that the nonspecific dipolarity/polarizability
interactions between the solvent and the solute were the main influencing
factors, followed by the hydrogen bonding interactions between the
solvent and the solute