ZnO With TiO2
ZnO With TiO2
Erviani Rusman, Heryanto Heryanto, Ahmad Nurul Fahri, Inayatul Mutmainna, Dahlang Tahir*
Abstract. Composite ZnO/TiO2 have been successfully synthesized by green synthesis method
with various calcination temperature 500oC, 600oC, 700oC, and 800oC (TiO2 concentrations: 2.5
g and 5 g) for photocatalyst application. In this study, Calopogonium mucunoides leaf extract
was used as reducing and stabilizing agent. The synthesized composites were characterized by
using Fourier Transform Infra-Red (FTIR), X-Ray Diffraction (XRD), and UV-Visible
spectroscopy. The XRD spectra shows the hexagonal phase with wurtzite structure of ZnO and
anatase for TiO2. The best degradation performance is 98.26% (only 10 min) for ZnO/TiO2 (5 g)
with calcination temperature is 800oC. This is due to the highest distance between two optical
phonon mode (LO-TO) and lowest attenuating and propagating constant. The composite
ZnO/TiO2 shows high potentials photodegradation of organic dyes with the high stable
recyclability up to 5 cycles (>95%) only for every 15 minutes. High potentials for applicability
with the concept environmentally friendly principles and stability for circular chemistry, and
INTRODUCTION
Hazardous contaminants in wastewater are affected by the textile industries,
agricultural industries [1-3]. Azo dye is a hazardous pollutant that contains (-N=N-)
bond and phenyl or naphthyl group [4-6]. They are producing aromatic amines during
the decomposition process and potentially cause carcinogenic and mutagenic. On the
other hand, the presence of azo dye in water causes severe effects on clean water
availability and the environment [5-8]. The type of azo dyes is a mono-azo dye
(methylene blue, methylene orange, AO7 (acid orange 7)), diazo dye (congo red, 6B
(direct lake blue)), and poly azo dyes (direct black BN) [6]. One of the most widely
used azo dye is Congo Red (CR). CR is used in processing textile, paper, cosmetic, and
pharmaceutical industries [9,10]. Those dye are difficult to degrade to be a severe issue
wastewater are interested researchers in finding the polluted water treatment method to
chemical process [12,13]. The photocatalyst is one of the most effective and simple
techniques used in water treatment because it removes organic contaminants easily [11,
not produce second contaminants [3]. This method used extracts of various plants as
reducing or stabilizing agents. Plant extract contains phytochemicals that act as bio-
reduction materials for capping agents in particular nanoparticles' synthesis process [16].
The reported materials nanoparticles have been produced by using green synthesis are:
Au, Ag, Pt, Pd, α-Fe2O3, CeO2-, ZnO, TiO2, ZrO2, and SnO2 [19-22]. TiO2 and ZnO are
chemically stable semiconductors that can produce an active charge during irradiation
by light with suitable wavelengths [12,23,24]. Zinc oxide is n-type semiconductor with
high excitation binding energy, bandgap width (3,37eV for anatase phase),
process for ZnO will create electron-hole by gain energy of electron for exciting to the
conduction band [1]. The electron at the conduction band moves easily to the valence
to control and minimize the recombination rate in ZnO consequently increase the charge
[36-41]. It is using as a photocatalytic due to its good optical properties, low cost, and
high chemical stability [40-42]. The catalyst was used for photodegradation of chemical
or organic pollutants in wastewater under visible irradiation [43,44]. Doping TiO2 with
metals or non-metal ions will increase the visible light absorbance capacity or reactivity
method for MB, R6G, OTC degradation [1], ZnO/TiO2 by using solid-state for
methylene blue [13,35], ZnO and TiO2 commercial for phenothiazine decolorization
[36], and ZnO/TiO2 thin film by using the hydrothermal method for orange G
materials that can be easily integrated into wastewater plants and reused for real
applications is crucial. The principles process of synthesized these photocatalysts
a legume and easily grow were impacting agricultural if growth uncontrolled and semi-
using this type of a legume for photocatalyst, means that contributes to the green
to produce clean water from decontaminant. In this study, a facile, suitable for mass-
friendly principles, circular chemistry, and efficiency of use the energy and chemicals
[47-49].
The ZnO/TiO2 composites for concentration of TiO2 are 2.5 g and 5 g, and various
XRD, FTIR, and UV-Vis spectroscopy. The XRD spectra used for analysis the
structural properties and FTIR spectra for the optical properties in the form of the
refractive index (n) and extinction coefficient (k) by applying Kramers Kronig (KK)
relation. The longitudinal and transversal optical phonon mode, the complex dielectric
function (real part (1) and imaginary part (2)), energy loss function (Im (-1/ 𝜀)), and
the optical absorption coefficient were determined from the n and k. The photocatalyst
EXPERIMENTAL
Calopogonium mucunoides (CM) leaves were taken from the Enrekang district,
South Sulawesi, Indonesia. Zinc acetate dihydrate (Zn(CH 3COO)2 ∙ 2H2O) (Merck),
titanium dioxide (TiO2) (Merck), and natrium hydroxide (NaOH) (Merck), and congo
The CM leaves were washed several times by distilled water to remove debris and
dirt, then dry them at room temperature for one week. The leaves were powdered using
blender and sieved the powder with 100 Mesh for uniform size. The extract was
80oC for 20 minutes. It was filtered with Whatman No.1 filter paper. The filtrate was
used for synthesis ZnO/TiO2, for more detail illustration of synthesized processes see
Figure 1.
Synthesis of ZnO/TiO2
Sol gel method was used for green synthesis ZnO/TiO2. The solution prepared
precursor. It was stirred at constant temperature 95oC and speed 500 rpm. After 15
minutes heated, TiO2 was added to the zinc oxide solution. TiO2 solution was prepared
2.5 g and 5 g TiO2 powder by added 10 ml distilled water, then homogenized for 5
minutes by constant stirring at 200 rpm using magnetic stirrer. NaOH was added
dropwise to the solution till pH 7. The paste was formed after continuous heating and
stirring for overnight. The sample paste was evaporated at 80oC for 10 hours and
continue calcined for 2 hours at the temperature 500oC, 600oC, 700oC, and 800oC to
Characterization
CuKα radiation at wavelength (λ) 1.54 Å (25o ≤ 2θ ≤ 65o, 40kV, 30 mA, scan rate 2
min-1, step size 0.02o) was used to determine the structure and crystallite size of the
groups that present and optical properties of the samples. UV-Vis spectrophotometer
activity of CR.
Photocatalytic Mechanism
powder into 100 ml of CR solution (40 mg/L). The solution was stirred and exposed to
light using 300W Osram Tungsten Halogen lamp as a light source. To analyze the CR
concentration after degradation process, the solution was carried out every 5 minutes
and filtered it. Concentration of the solution after the degradation process was
determined by:
C0 -Ct
D (%)= ( ) ×100% (1)
C0
where D (%) is the percentage of degradation, C0 is the initial concentration (at t is 0
ZnO/TiO2 (2.5 g) at temperature 500oC. The 0.04 g of ZnO/TiO2 was added into 100 ml
CR solution (40 mg/L). The solution was stirred at 150 rpm by using magnetic stirrer
and it was irradiated for 15 minutes. The solution was filtered, and the concentration
was analyzed by using UV-Vis spectrophotometer. The composite was washed with
distilled water and centrifuged at 1500 rpm within 5 minutes. These steps were applied
repeatedly for 5 times. The sediment was dried at 80 oC within 10 minutes. Dried
composite was added back into 100 ml CR solution. It was repeated for five cycles.
XRD analysis
The XRD spectra were used to identify the crystalline phase of composites
Figure 3 shows XRD diffraction patterns for composite ZnO/TiO2 (TiO2 is 2.5 g and
5.0 g) at various calcination temperature. For all samples shows several diffraction
peaks 2θ of ZnO at 31.84o, 34.48o, 36.36o, 47.68o, 56.74o, and 62.98o which correspond
to the crystal planes (100), (002), (101), (102), (110), and (103) based on JCPDS card
no: 36-1451 [50]. The presence of TiO2 in the composite ZnO/TiO2 was confirmed by
the peaks 2θ at 25.38o, 37.94o, 47.64o, and 62.96o which correspond to the crystal planes
(101), (004), (200), and (204) for structure anatase based on JCPDS card no: 21-1272
[51] as can be seen in Figure 3 (a) and for TiO2 is 5 g in Figure 3 (b).
Figure 3 (c) and (d) shows enlarger XRD spectra for diffraction peak from 30 o to
37 o for various calcination temperature. It shows there are shifts toward the highest of
the diffraction angle for 2.5 gr TiO2 at 600oC and 700oC due to the lattice reduction and
for 800oC small shits backward to the lower of the diffraction angle due to the some of
the atoms are uniform arrangement and forming new cluster crystal [52-54]. For
composite with 5.0 g TiO2 shows shifts to the higher diffraction angle regularly due to
the number of atoms Ti filled the lattice of ZnO over than the capacity for the lattice
reduction or may due to the large ionic radius of Ti compared with that of Zn [55].
leaves extract for various calcination temperature (500 oC, 600oC, 700oC, 800oC) and
temperature ≤ 600oC but for > 600oC the intensity peak reduces drastically or almost
disappears may due to the phase change from TiO2 to ZnTiO3. In addition, the (102) and
(103) planes of ZnO overlap with the (200) and (204) planes of TiO 2. It shows that there
is perfect interaction occurs between the lattice of ZnO and TiO 2 to produce ZnO/TiO2
composite [56]. At the lowest temperature, there are some small peaks that occur at 2θ:
30.14o, 42.96o, 50.78o, and 60.70o correspond to the crystal plane (220), (400), (422),
and (440), respectively, identified ZnTiO3 phase based on the JCPDS card No: 39-0190
[57]. For the temperature increases from 500 oC to 600oC, the diffraction peaks intensity
of ZnTiO3 were decrease and the phase transformation occurred at the temperature
800oC clearly can be seen the intensity of ZnTiO3 decreases and Zn2TiO4 increase. It
shows that some of the ZnTiO3 phase were decomposed to forming Zn2TiO4 phase as
can be seen at the diffraction peaks 32.24 o, 34.90 o, 36.82 o, and 56.96o based on the
JCPDS: 01-073-0578 [11,14,58]. The peak intensities decrease and the width of FWHM
increase by increasing the calcination temperature from 600oC to 700oC may due to the
From the XRD spectra in Figure 3 clearly shows relationship between calcination
temperatures with the peak intensities. At low calcination temperature (500oC) the
intensity of diffraction peaks are sharp and decrease with increasing the calcination
𝐾.𝜆
Γ= 𝛽.𝐶𝑜𝑠 𝜃 (2)
where Γ is the crystallite size, θ is the Bragg diffraction angle, K is the constant about
0.9, λ is the wavelength of X-ray (for Cu is 1.5406 Å), and is full width at half-length
maximum (FWHM). The average of crystallite size, dislocation density, and strain were
FTIR analysis
Figure 4. FTIR spectra of ZnO/TiO2 synthesized from Calopogonium mucunoides
leaves extract for various calcination temperature (500 oC, 600oC, 700oC, 800oC) and
Figure 4 shows FTIR spectra at the wavenumber 350-4000 cm-1 for identified the
functional groups and vibrational bonds of composite ZnO/TiO2. The peak 446 cm-1
corresponding to the vibration bond of Zn-O [3,62]. The peak at 723 cm-1 correspond to
the O-Ti-O band [63]. The function group of C-H band at the wave number 1000-1100
cm-1 [14] and at the wavenumber 1447 cm-1 and 1665 cm-1, there are chemical bonds of
C=C-C and C=C tensile vibration, respectively [21,55]. O-H bond appears at the
wavenumber 2504 cm-1 and 3455 cm-1 corresponding to vibration band from suspension
of hydroxyl group in adsorbed water [3,64]. A weak infrared peak at 2338 cm-1
probably due to the CO2 vibration bond absorbed during calcination process. The peak
at 2968 cm-1 is mainly due to the stretching vibration of C-H bond from the absorption
Optical properties
The optical properties (refractive index (n) and extinction coefficient (k)) were
determined from the quantitative analysis of FTIR spectra by applying K-K relation
[65-67]. For the analysis optical properties, we have used only wavenumber in the range
from 860 cm-1 to 1115 cm-1 due to the C=C-C bonding which probably come from the
green synthesis methods. The FTIR spectra form the equipment is in the form of
transmittance (T(ω)), where need to be converted to the reflectance (R(ω)) [68] by the
relations:
A(ω)=2-log[T(ω)%] (3)
R(ω)=100-[T(ω)+A(ω)] (4)
following equations for determining the optical properties (refractive index for real part
1-R(ω)
n(ω)= (5)
1+R(ω)-2√R(ω)cos∅(ω)
2√R(ω)cos∅(ω)
k(ω)= (6)
1+R(ω)-2√R(ω)cos∅(ω)
(ω) is the phase change from the incident photon beam bombardment to the sample
and traveling at the surface down to few atoms at the sample and then reflected photon
ω ∞ lnR(ω' )-lnR(ω)
φ(ω)=- π ∫0 (7)
ω'2 -ω2
For easily computational of by (ω), the K-K (Kramers-Kronig) relation was used and
4ωj ln(√R(ω))
φ(ω)=- ∆ω ∑i (8)
π ω2i -ω2j
j+1.
Figure 5. The optical properties (refractive index (n) and extinction coefficient (k))
determined from the FTIR spectra in Figure 4, from the optical properties the dielectric
function, the energy loss function Im (−1/ε1(ω)) are determined for various calcination
and intersection point at the lower wavenumber indicated by TO and the values are
presented in Table 2. Figure 5(a) depicts the transverse optical (TO) of ZnO/TiO2 (2.5
g) shifts to the lower wavenumber by increase the calcination temperature up to 700 oC,
but for 800oC the TO shifts to the higher wavenumber may due to the effect of the weak
strain in the crystal structure. Figure 5(b) shows TO was decreased with increasing the
temperature. In this study, the highest distance between the two optical phonon
vibration mode ((LO-TO)) for ZnO/TiO2 (5 g) at 800oC may due to some H2O loses in
the lattice consequently increase optical bandgap [64,69]. The (LO-TO) was increased
with the increasing the TiO2 concentration at the same calcination temperature but not
for 700oC may due to the number of defect (dislocation density) increase consequently
the atomic bonding unstable and rearrange to form new atomic cluster in the lattice
structure [70,71].
Table 2. Transverse optical (TO) phonon mode, longitudinal optical (LO) phonon
The real part (ε1 ) and imaginary part (ε2 ) of dielectric function functions were
ε2 (ω)=2n(ω)k(ω) (10)
The main peak position of the imaginary part (ε2 ) and the energy loss function Im
(-1/1(ω)) were used for confirmation of the TO and LO phonon vibration modes from
the intersection point between n and k, respectively. These finding shows consistency
result as can be seen in the Figure 5, indicated that the effectiveness of the FTIR spectra
for determining optical properties and for identification optical phonon modes. The
energy loss function also identified as a plasma frequency as reported in Ref. [65,66,72]
important parameters to identified stability of the covalent bond and the lattice match in
𝜇0 𝜀0 𝜀1(𝜔) 2
𝜀 (𝜔)
𝛼 = 𝜔√ [√1 + ( 2 ) − 1] (11)
2 𝜀 (𝜔)
1
𝜇0𝜀0 𝜀1(𝜔) 2
𝜀 (𝜔)
𝛽 = 𝜔√ [√1 + ( 2 ) + 1] (12)
2 𝜀 (𝜔)
1
where µ0 is a constant related to the permeability and ε0 is also constant for permittivity
in a free space.
Figure 6. Attenuation constant (α) (first and third rows) and propagation constant (β)
(second and fourth rows) as a function of the wavenumber for calcination temperature
from 500oC (left) to 800oC (right). First and second rows for 2.5 gr of TiO 2 in ZnO/TiO2
composite and the third and fourth rows for 5 gr of TiO 2 in ZnO/TiO2 composite.
For 2.5 gr of TiO2 in ZnO/TiO2 composite shows the attenuation and propagation
constant increase with increasing the calcination temperature from 500oC (left) to 800oC
(right) and opposite trend for 5 gr of TiO2 in ZnO/TiO2 composite as can be seen in
Figure 6. The best composite for photocatalyst is for low attenuating and propagating
constant, means that the structure will easily suppressing recombination of the charge
particle due to the higher strain between the atoms [52, 54]. In this study shows 5 gr of
TiO2 in ZnO/TiO2 composite high potentials compared than that of 2.5 gr TiO2 in
extract for various calcination temperature (500oC, 600oC, 700oC, 800oC) and TiO2
spectra in Figure 7. Band gap values were obtained by using Touch Plot method and
the corresponding results are presented in Table 4, which determined by the relation as
follows:
m=1/2 for the direct allowed transition, and E g is band gap energy.
The calcination temperature from 500oC to 700oC, the band gap of composite
ZnO/TiO2 for 5 g TiO2 is same but for composite with 2.5 g TiO2 is fluctuates due to the
effect of cohesion force between the atoms of Zn and Ti. For calcination temperature
from 700oC to 800oC, the sample for the different concentration of TiO2 shows
increases the band gap may due to the effect of particle size and crystal phase in the
CR with ZnO/TiO2 during irradiation, for the solution can be identified visually or by
the absorbance spectra at the wavelength 400-600 nm. The time for every sample to
hydroxyl and superoxide radical which play the important roles in photodegradation.
The relation between the percentages of degradation with irradiation times are
shown in Figure 9 and the corresponding results of percentage degradation for all
sample with various calcination temperature and various TiO2 concentration were
Calopogonium mucunoides leaves extract is higher than 94%. The highest efficiency is
98,26% that obtained by ZnO/TiO2 (5 g) with calcination temperature is 800oC. It
indicates the synthesis composites ZnO/TiO2 have a great potential for photocatalytic
materials.
material, crystallite size, and agglomeration level. It means that, the photodegradation
process may related to the different competing factors [14]. Based on the previous
reported which published by Selvi et.al, a diminution of the crystallite size led to an
increase in the specific surface area that could enhance the active reaction of the
Table 3. The degradation ability of samples ZnO/TiO2 to degrade CR with the different
catalysts
Percentage Degradation
Sample Temperature (oC)
degradation (%) time (min)
500 97.17 30
600 96.31 15
ZnO/TiO2 (2.5 g)
700 94.81 10
800 95.39 15
500 96.63 30
600 95.29 15
ZnO/TiO2 (5 g)
700 96.56 10
800 98.26 10
Figure 9 shows the kinetic model photocatalytic degradation of composites
ZnO/TiO2 for CR solution under light irradiation. Based on the kinetic model,
ZnO/TiO2 (5 g) at 800oC shows the best material for photocatalyst with the highest
Figure 10. Photocatalytic performance and kinetic model of composites (a-b) ZnO/TiO2
Figure 10(b) and 10(d) shows the photodegradation rate kinetic curves of CR for
(kr) in the photocatalytic reaction was calculated by the following equation [60,64]:
C
ln C0 =kr .t (14)
t
where C0 is the initial concentration and Ct is the concentration at the time t and
corresponding results for kr and R2 for composite ZnO/TiO2 are shown in Table 4. The
kr and R2 were increased with increasing the calcination temperature for ZnO/TiO 2 (5 g)
compared to ZnO/TiO2 (2.5 g) and the highest rate constant is for composite ZnO/TiO2
Table 4. Rate constants (kr), correlation coefficient values (R2), and band gap of
Photocatalytic activity
of pollutant targets with final molecules are CO2, H2O, and N2 [29]. During irradiation
processes, there is interaction between photon with the charge particle in composite
ZnO/TiO2 at the valence band and produce electron which having energy for moving by
excitation to the conduction band and remaining hole in the valence band. The
heterojunction band offset link between ZnO and TiO2 used for transfer electrons from
conduction band of ZnO to conduction band of TiO2 and transfer holes from the valence
band of TiO2 to the valence band of ZnO [1]. By this process, the number of electrons in
the conduction band of TiO2 and the number of holes in the valence band of ZnO are
increased and suppressing the recombination process. The lifetime of carrier also
increases which consequently the degradation process is faster [1,29]. The schematic of
degradation process of CR from the incoming photon, transfer charge (electron and hole)
Figure 11. Schematic degradation process of CR from the incoming photon, transfer
charge (electron and hole), produce radicals to break the bond of CR, and the final
surface of oxygen and it will increase superoxide radicals as products. Hole in valence
band reacted with H2O that absorbed in surface of semiconductor and the result of the
reaction were hydroxyl radicals (∙OH). Species of radical active such as ∙OH and ∙O2 -
were used to mineralize the organic and inorganic contaminants in wastewater [1,21].
Figure 12 shows the active radicals degraded CR dye start by the breaking the bond of
photodegradation process
Recycle
In this work, five cycles successfully show the ability of composite ZnO/TiO2 as a
friendly principles and circular chemistry, minimizing wastewater and efficiency of use
the energy, water, and chemicals. Figure 13 shows the excellent performance > 95.02%
degradation of CR dye with high stability up to 5 times for every 15 min irradiation.
five times
To show the novelty in this study, we have compared the performance of green
synthesized composite ZnO/TiO2 in this study with the previous reported references as
shown in Table 5. The treatment time and the degradation performance in this study
shows high potentially with faster and high stability. It’s indicated that the high
principles and stability for circular chemistry, minimizing wastewater and efficiency of
light sources, treatment time, and degradation performance. Clearly in this study shows faster (10 min up to30 min) with high stability (5
cycle).
Photocatalyst Syntesized Photocatalyst Dye type Light Treatment Degradation Kinetic Ref.
method dosage source time (min) (%) rate
(min-1)
ZnO–TiO2 Hydrothermal 0.5 g/L MB Solar light 6 (MB) 98.40 0.65172 [1]
nanohybrids MO (862 W) 8 (OTC) 90.30 0.27400
OTC 30 (R6G) 81.30 0.06116
(60 mg/L)
ZnO/TiO2 Sol gel 0.5 g/L Methylene UV light 360 82.00 0.2925 [14]
composite blue
(2 mmol/L)
2-D fern-like Green synthesis 0.12 g/L Methylene Tungsten 135 98.00 0.99429 [21]
ZnO/TiO2 blue lamp
(0.2 mg/L) (500W)
ZnO/TiO2 Solid state 2.5 g/L Quinoline UV light 240 92.00 0.00560 [29]
(100 mg/L)
TiO2/ZnO Solvothermal 0.2 g/L Rhodamine Xenon 80 Not available 0.01400 [32]
composite sphere B lamp
(20 µmol/L) (300 W)
ZnO/TiO2 Pulsed laser 0.5 g/L Methyl Xenon 60 98.00 0.11420 [56]
nanocomposite ablation orange lamp
(500 W)
ZnO/TiO2 Chemical 0.5 g/L Bentazon UV light 120 84.20 0.01540 [62]
nanocomposite method (20 mg/L)
ZnO/TiO2 thin DC reactive Thin film Methyl UV light 150 91.00 Not [77]
film magnetron orange available
sputtering (10 mg/L)
technique
ZnO/TiO2 Mechanical 0.5 g/L Rhodamine Mercury 30 ~45.00 Not [78]
heterojunction mixing B lamp available
(80 mg/L) (UV light)
ZnO/TiO2 Hydrothermal Not available MB Sun light 60 (MB) Not available 0.06100 [79]
composite MO 60 (MO) 0.04700
(0.02 mM)
ZnO/TiO2 Sol gel and 0.5 g/L Methyl UV light 360 99.5 0.01760 [80]
precipitation orange (40W)
(10−5 mol/L)
ZnO/TiO2 Sol gel Thin film Methylene LED 160 Not available 0.00700 [81]
core/shell deposition blue (140 mW,
(10 mM) monochro
matic light
of 400
nm)
ZnO/TiO2 Hydrothermal A piece of Methyl Xe lamp 210 ~100 Not [82]
nanocomposite composite on orange (300 W) available
Ti fabric (20 mg/L)
(1 cm×1 cm)/
100 mL
ZnO/TiO2 Electrostatically 0.6 g/L Methyl UV light 360 Not available 0.01270 [83]
modified orange
electrospinning (3 mg/L)
ZnO/TiO2 (2.5 g)
500oC Green synthesis 0.2 g/L Congo red Tungsten 30 97.17 0.11883 Present
(40 mg/L) lamp
(300W)
600 oC Green synthesis 0.2 g/L Congo red Tungsten 15 96.31 0.21997 Present
(40 mg/L) lamp
(300W)
700 oC Green synthesis 0.2 g/L Congo red Tungsten 10 94.81 0.28380 Present
(40 mg/L) lamp
(300W)
800 oC Green synthesis 0.2 g/L Congo red Tungsten 15 95.39 0.20506 Present
(40 mg/L) lamp
(300W)
ZnO/TiO2 (5 g)
500 oC Green synthesis 0.2 g/L Congo red Tungsten 30 96.63 0.50827 Present
(40 mg/L) lamp
(300W)
600 oC Green synthesis 0.2 g/L Congo red Tungsten 15 95.29 0.62944 Present
(40 mg/L) lamp
(300W)
700 oC Green synthesis 0.2 g/L Congo red Tungsten 10 96.56 0.64080 Present
(40 mg/L) lamp
(300W)
800 oC Green synthesis 0.2 g/L Congo red Tungsten 10 98.26 0.79886 Present
(40 mg/L) lamp
(300W)
Conclusion
extract by using green synthesis method. The composites were prepared for various
calcination temperature (500oC, 600oC, 700oC, and 800oC) and different concentration
of TiO2 (2.5 g and 5 g). From XRD analysis, the crystallite size of composites was
synthesis. FTIR spectra observed the Zn-O band at the peak 446 cm-1 and O-Ti-O band
at the peak 723 cm-1. The optical properties were analyzed by using K-K relation from
the infra-red spectra, it shows the highest energy loss function and distance between
800oC. It indicates the stable and strong bonding formation and the lattice match in the
degradation efficiency for composite ZnO/TiO2 (5 g) at 800oC. In this study shows high
potentially with faster and high stability, indicated that high applicability concept for
holistically integrates with environmentally friendly principles and high stability for
Acknowledge
This work was supported by the PT (Penelitian Terapan) funded by the Indonesia
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