sample was ground into fine and uniform powder
and stored in an oven at 50 °C overnight. Using Cu
pulsed radiation with a wavelength of 0.154 nm, the
crystallization of the compound was determined by
monitoring the position, shape, and intensity of the
reflection from the distribution structure substrate.
2.2.3 Adsorption Properties and Reusability
(1) Establishment of Standard Curve A series of
concentration gradient solutions were obtained by
step dilution method, and the absorbance of copper
ions with different concentrations were measured by
flame atomic absorption photometer. This step was
repeated for three times to obtain the standard curve.
(2) Influencing Factors of Adsorption
Performance A series of Cu(NO
3
)
2
solutions (250
mL) with different concentrations were prepared.
The pH value of the solution was adjusted by 0.1
mg/L NaOH and 0.1 mg/L HCl. Different amount
(0.01 g, 0.02 g, 0.04 g, 0.06 g, 0.08 g, 0.10 g) of
Isatis Indigotica fort draff was added into the
Cu(NO
3
)
2
solutions with different pH values
(1,2,3,4,5,6) and different concentrations of copper
ions (20 mg/L, 40 mg/L, 60 mg/L, 80 mg/L, 100
mg/L, 150 mg/L). The resulting mixtures were
oscillated on the oscillator at room temperature for a
certain period of time (10 min, 20 min, 30 min, 40
min, 60 min, 75 min, 120 min). 1 mL of supernatant
was taken and diluted with pure water in a 50 ml
volumetric flask, and then the absorbance of the
solution was measured on the flame atomic
absorption analyzer after fully oscillating. The
concentration value was obtained by automatic
conversion of the instrument, and then the original
solution concentration value is obtained by
multiplying the concentration value by 50. After
calculation, the experimental adsorption capacity,
adsorption kinetic model parameters, and adsorption
isotherm parameters can be obtained.
(3) Reusability After the adsorption process is
completed, the adsorbent was separated from the
copper ion solution. After being washed, the
adsorbent is desorbed with eluent. After desorption,
the adsorbent was separated, and the next
adsorption-desorption process is cycled for a total of
four adsorptions-desorption experiment. Two sets of
parallel experiments were carried out to calculate
the average value of desorption efficiency.
3 RESULTS AND DISCUSSION
3.1 Characterization of Chemically
Modified Isatis Indigotica Fort
Draff based Biosorbent
3.1.1 SEM Analysis
The SEM images of RIR, RIR-NaOH, RIR-Na
2
CO
3
,
and RIR-CA are shown in Figure1-(a). The results
show that the structure of RIR is relatively dense,
and the surface of RIR-NaOH, RIR-Na
2
CO
3
, and
RIR-CA show signs of fiber surface fracture and
fiber disintegration, and the surface pores increase.
The increase in pores is beneficial to increase the
contact area between heavy metal ions and the
surface area of cellulose, and to adsorb more heavy
metal ions.
3.1.2 FTIR Analysis
The IR spectra of RIR, RIR-NaOH, RIR-Na
2
CO
3
,
and RIR-CA are shown in Figure1-(b). In general,
before and after the modification, the peak shape of
the IR spectrum is roughly the same, and there is no
big shift. Before modification, the peak is broad and
strong near 3417 cm-1, indicating that there were
many stretching vibration absorption peaks of O-H
and N-H on the surface of the Isatis Indigotica fort
draff -based biosorbent; the absorption peak of 2927
cm-1 comes from the stretching vibration of
saturated C-H bonds, the absorption peak of 1647
cm-1 comes from the stretching vibration of C=O of
aliphatic aldehyde, the absorption peak of 1415cm-1
is from the deformation vibration of CH
3
- and -CH
2
-
, the absorption peak of 1153 cm-1 is from the
stretching vibration of ester bond, and the
absorption peak of 1029cm-1 is from the bending
vibration of -OH. After modification, the peak
intensity of Isatis Indigotica decreased, the
amplitude decreased, and the wave peaks became
wider, indicating that the content of various groups
on the surface of the modified Isatis Indigotica were
reduced (Wei 2003).
3.1.3 TG Analysis
The thermograms of RIR, RIR-NaOH, RIR-
Na2CO3, and RIR-CA are shown in Figure1-(c).
According to the thermal decomposition of each
component of lignocellulosic biomass, Reddy et al.
(Xu 2021), Chen et al. (Yang 2016), and Braga et al.
(Yang 2020) divided the TG curves of the
Lignocellulosic biomass into three stages, namely,
Preparation and Adsorption Properties of Chemically Modified Isatis Indigotica Fort Draff based Biosorbent