Preparation and Characterization of Activated Carbons from Palm Nut Shells: Effects of Calcination Temperature on Porosity and Chemical Properties

Activated carbons (ACs) calcined at 400˚C, 500˚C, and 600˚C (AC-400, AC-500, and AC-600) were prepared using palm nut shells from Gabon as raw material and zinc chloride (ZnCl2) as a chemical activating agent. Prepared ACs were characterized by physisorption of nitrogen (N2), determination of diode and methylene blue numbers for studies of porosity and by quantification and determination of surface functional groups and pH at point of zero charge (pHpzc) respectively, for studies of chemical properties of prepared ACs. Then, effects of calcination temperature (Tcal) on porosity and chemical properties of prepared ACs were studied. The results obtained showed that when the calcination temperature increases from 500˚C to 600˚C, the porosity and chemical properties of prepared ACs are modified. Indeed, the methylene blue and iodine numbers determined for activated carbons AC-400 (460 and 7.94 mg·g−1, respectively) and AC-500 (680 and 8.90 mg·g−1, respectively) are higher than those obtained for AC-600 (360 and 5.75 mg·g−1, respectively). Compared to the AC-500 adsorbent, specific surface areas (SBET) and microporous volume losses for AC-600 were estimated to 44.7% and 45.8%, respectively. Moreover, in our experimental conditions, the effect of Tcal on the quantities of acidic and basic functional groups on the surface of the ACs appears negligible. In addition, results of the pHpzc of prepared ACs showed that as Tcal increases, the pH of the adsorbents increases and tends towards neutrality. Indeed, a stronger acidity was determined on AC-400 (pHpzc = 5.60) compared to those on AC-500 and AC-600 (pHpzc = 6.85 and 6.70, respectively). Also according to the results of porosity and chemical characterizations, adsorption being a surface phenomenon, 500˚C appears to be the optimal calcination temperature for the preparation of activated carbons from palm nut shells in our experimental conditions.

Effect of Calcination Temperature on La-Modified Al2O3 Catalysts for Vapor Phase Hydrofluorination of Acetylene to Vinyl Fluoride

A La-modified Al2O3 catalyst was prepared with deposition-precipitation method. The effect of calcination temperature on the reactivity for vapor phase hydrofluorination of acetylene to vinyl fluoride. The catalysts calcined at different temperatures were characterized using NH3-TPD, pyridine-FTIR, X-ray diffraction, and Raman techniques. It was found that the calcination process could not only change the structure of these catalysts but also modify the amount of surface acidity on the catalysts. The catalyst calcined at 400 ℃ exhibited the highest conversion of acetylene （94.6%） and highest selectivity to vinyl fluoride （83.4%） and lower coke deposition selectivity （0.72%）. The highest activity was related to the largest amount of surface acidity on the catalyst, and the coke deposition was also related to the total amount of surface acidic sites.

Effect of Calcination Temperature on Catalytic Activity and Textual Property of Cu/HMOR Catalysts in Dimethyl Ether Carbonylation Reaction

The effect of calcination temperature on the catalytic activity for the dimethyl ether （DME） carbonylation into methyl acetate （MA） was investigated over mordenite supported copper （Cu/HMOR） prepared by ion-exchange process. The results showed that the catalytic activity was obviously affected by the calcination temperature. The maximal DME conversion of 97.2% and the MA selectivity of 97.9% were obtained over the Cu/HMOR calcined at 430 ℃ under conditions of 210 ℃, 1.5 MPa, and GSHV of 4883 h^-1. The obtained Cu/HMOR catalysts were characterized by powder X-ray diffraction, N2 absorption, NH3 temperature program desorption, CO temperature program desorption, and Raman techniques. Proper calcination temperature was effective to promote copper ions migration and diffusion, and led the support HMOR to possess more acid activity sites, which exhibited the complete decomposing of copper nitrate, large surface area and optimum micropore structure, more amount of CO adsorption site and proper amount of weak acid centers.

Solvent-free selective oxidation of cyclohexane with molecular oxygen over manganese oxides:Effect of the calcination temperature

The effects of calcination temperature on the physicochemical properties of manganese oxide catalysts prepared by a precipitation method were assessed by X-ray diffraction,N2 adsorption-desorption,X-ray photoelectron spectroscopy,H2 temperature-programmed reduction,O2 temperature-programmed desorption,and thermogravimetry-differential analysis.The catalytic performance of each of these materials during the selective oxidation of cyclohexane with oxygen in a solvent-free system was subsequently examined.It was found that the MnOx-500 catalyst,calcined at 500 °C,consisted of a Mn2O3 phase in addition to Mn5O8 and Mn3O4 phases and possessed a low surface area.Unlike MnOx-500,the MnOx-400 catalyst prepared at 400 °C was composed solely of Mn3O4 and Mn5O8 and had a higher surface area.The pronounced catalytic activity of this latter material for the oxidation of cyclohexene was determined to result from numerous factors,including a higher concentration of surface adsorbed oxygen,greater quantities of the surface Mn4＋ ions that promote oxygen mobility and the extent of O2 adsorption and reducibility on the catalyst.The effects of various reaction conditions on the activity of the MnOx-400 during the oxidation of cyclohexane were also evaluated,such as the reaction temperature,reaction time,and initial oxygen pressure.Following a 4 h reaction at an initial O2 pressure of 0.5 MPa and 140 °C,an 8.0% cyclohexane conversion and 5.0% yield of cyclohexanol and cyclohexanone were achieved over the MnOx-400 catalyst.In contrast,employing MnOx-500 resulted in a 6.1% conversion of cyclohexane and 75% selectivity for cyclohexanol and cyclohexanone.After being recycled through 10 replicate uses,the catalytic activity of the MnOx-400 catalyst was unchanged,demonstrating its good stability.

Effect of Calcination Temperature on Surface Oxygen Vacancies and Catalytic Performance Towards CO Oxidation of Co3O4 Nanoparticles Supported on SiO2

Co3O4/SiO2 catalysts for CO oxidation were prepared by conventional incipient wetness impregnation followed by calcination at various temperatures. Their structures were char- acterized with X-ray diffraction （XRD）, laser Raman spectroscopy, X-ray photoelectron spectroscopy （XPS）, temperature-programmed reduction （TPR） and X-ray absorption fine structure （XAFS） spectroscopy. Both XRD and Raman spectroscopy only detect the existence of Co3O4 crystallites in all catalysts. However, XPS results indicate that excess Co2＋ ions are present on the surface of Co3O4 in Co3O4（200）/Si02 as compared with bulk Co3O4. Meanwhile, TPR results suggest the presence of surface oxygen vacancies on Co3O4 in Co3O4（200）/SiO2, and XAFS results demonstrate that Co3O4 in Co3O4（200）/SIO2 contains excess Co2＋. Increasing calcination temperature results in oxidation of excess Co2＋ and the decrease of the concentration of surface oxygen vacancies, consequently the for- mation of stoichiometric Co3O4 on supported catalysts. Among all Co3O4/SiO2 catalysts, Co3O4（200）/SiO2 exhibits the best catalytic performance towards CO oxidation, demonstrating that excess Co2＋ and surface oxygen vacancies can enhance the catalytic activity of Co3O4 towards CO oxidation. These results nicely demonstrate the effect of calcination temperature on the structure and catalytic performance towards CO oxidation of silicasupported Co3O4 catalysts and highlight the important role of surface oxygen vacancies on Co3O4.

Effect of calcination temperatures on photocatalytic H_(2)O_(2)-production activity of ZnO nanorods

Photocatalytic hydrogen peroxide(H_(2)O_(2))production from O_(2) and H2O is an ideal process for solar‐to‐chemical energy conversion.Herein,ZnO nanorods are prepared via a simple hydrothermal method for photocatalytic H_(2)O_(2) production.The ZnO nanorods exhibit varied performance with different calcination temperatures.Benefiting from calcination,the separation efficiency of photo‐induced carriers is significantly improved,leading to the superior photocatalytic activity for H_(2)O_(2) production.The H_(2)O_(2) produced by ZnO calcined at 300℃ is 285μmol L^(−1),which is over 5 times larger than that produced by untreated ZnO.This work provides an insight into photocatalytic H2O2 production mechanism by ZnO nanorods,and presents a promising strategy to H2O2 production.

Effects of Calcination Temperature on the Acidity and Catalytic Performances of HZSM-5 Zeolite Catalysts for the Catalytic Cracking of n-Butane

The acidic modulations of a series of HZSM-5 catalysts were successfully made by calcination at different treatment temperatures, i.e. 500, 600, 650, 700 and 800 ℃, respectively. The results indicated that the total acid amounts, their density and the amount of B-type acid of HZSM-5 catalysts rapidly decreased, while the amounts of L-type acid had almost no change and thus the ratio of L/B was obviously enhanced with the increase of calcination temperature （excluding 800 ℃）. The catalytic performances of modified HZSM-5 catalysts for the cracking of n-butane were also investigated. The main properties of these catalysts were characterized by means of XRD, N2 adsorption at low temperature, NH3-TPD, FTIR of pyridine adsorption and BET surface area measurements. The results showed that HZSM-5 zeolite pretreated at 800 ℃ had very low catalytic activity for n-butane cracking. In the calcination temperature range of 500-700 ℃, the total selectivity to olefins, propylene and butene were increased with the increase of calcination temperature, while, the selectivity for arene decreased with the calcination temperature. The HZSM-5 zeolite calcined at 700 ℃ produced light olefins with high yield, at the reaction temperature of 650 ℃ the yields of total olefins and ethylene were 52.8% and 29.4%, respectively. Besides, the more important role is that high calcination temperature treatment improved the duration stability of HZSM-5 zeolites. The effect of calcination temperature on the physico-chemical properties and catalytic performance of HZSM-5 for cracking of n-butane was explored. It was found that the calcination temperature had large effects on the surface area, crystallinity and acid properties of HZSM-5 catalyst, which further affected the catalytic performance for n-butane cracking.

CO oxidation over Co_3O_4/SiO_2 catalysts:Effects of porous structure of silica and catalyst calcination temperature

The catalytic performances of Co3O4/SiO2 catalysts prepared by incipient wetness impregnation for CO oxidation were investigated using three kinds of silica as carriers with different pore sizes of 7.7,14.0 and 27.0 nm.The effects of calcination temperature on the catalyst surface and micro structure properties as well as catalytic performance for the oxidation of carbon monoxide were also studied.All catalysts were characterized by N2 adsorption-desorption,XRD,XPS,FTIR,H2-TPR and O2-TPD.It was found that the properties and crystal size of cobalt-containing species strongly depended on the pore size of silica carrier.While the silica pore size increased from 7.7 to 27.0 nm,the Co3O4 crystal size increased from 8.5 to 13.5 nm.Moreover,it was demonstrated that if the spinel crystal structure of Co3O4 was obtained at a calcination temperature as low as 150℃,the catalyst sample would have a high Co3O4 surface dispersion and an increase of surface active species,and thus exhibit a high activity for the oxidation of carbon monoxide.

Deoxygenation of methyl laurate to hydrocarbons on silica-supported Ni-Mo phosphides: Effect of calcination temperatures of precursor

SiO2-supported Ni-Mo bimetallic phosphides were prepared by temperature-programmed reduction （TPR） method from the phosphate precur- sors calcined at different temperatures. Their properties were characterized by means of ultraviolet-visible diffuse reflectance spectroscopy （UV-Vis DRS）, H2 temperature-programmed reduction （H2-TPR）, X-ray diffraction （XRD）, transmission electron microscopy （TEM）, CO chemisorption, H2 and NH3 temperature-programmed desorptions （H2-TPD and NH3-TPD）. Their catalytic performances for the deoxygena- tion of methyl laurate were tested in a fixed-bed reactor. When the precursors were calcined at 400 and 500 ℃, respectively, NiMoP2 phase could be formed apart from Ni2P and MoP phases in the prepared C400 and C500 catalysts. However, when the precursors were calcined at 600, 700 and 800 ℃, respectively, only Ni2P and MoP phases could be detected in the prepared C600, C700 and C800 catalysts. Also, in C400, C500 and C600 catalysts, Mo atoms were found to be entered in the lattice of Ni2P phase, but the entering extent became less with the increase of calcination temperature. As the calcination temperature of the precursor increased, the interaction between Ni and Mo in the prepared catalysts decreased, and the phosphide crystallite size tended to increase, subsequently leading to the decrease in the surface metal site density and the acid amount. C600 catalyst showed the highest activity among the tested ones for the deoxygenation of methyl laurate. As the calcination temperature of the precursor increased, the selectivity to C12 hydrocarbons decreased while the selectivity to C11 hydrocarbons tended to increase. This can be mainly attributed to the decreased Ni-Mo interaction and the increased phosphide particle size. In sum, the structure and performance of Ni-Mo bimetallic phosphide catalyst can be tuned by the calcination temperature of precursor.

Antibacterial Properties of V-doped Titanium-bearing Blast Furnace Slag Prepared at Different Calcination Temperatures

Perovskite-type V-doped titanium-bearing blast furnace slag (VTBBFS) photocatalyst was prepared by high-temperature solid phase method.The influence of calcination temperature on the photocatalytic and antibacterial properties of VTBBFS was studied in details.Its composition and microstructure were evaluated by X-ray diffractometer,ultraviolet-visible absorption spectrometer,Fourier transform infrared spectrometer and scanning electron microscope.The antibacterial properties of VTBBFS to Candida albicans were investigated by flask oscillation method.The results showed that the optical absorption and antibacterial properties of VTBBFS were the best with 10%(ω) doping of vanadium,prepared at 800℃ for 2 h,and its sterilization rate was close to 100% to Candida albicans (ATCC10231).The minimum inhibitory and minimum bactericidal concentrations were 25 and 50 mg/mL.When the concentration was 0.2 μg/mL,the catalyst had the least toxic toxicity.

Effects of Calcination Temperature of Boron-Containing Magnesium Oxide Raw Materials on Properties of Magnesium Phosphate Cement as a Biomaterial

A new magnesium phosphate bone cement （MPBC） was prepared as a byproduct of boroncontaining magnesium oxide （B-MgO） after extracting Li2CO3 from salt lakes. We analyzed the elementary composition of the B-MgO raw materials and the effects of calcination temperature on the performance of MPBC. The phase composition and microstructure of the B-MgO raw materials and the hydration products （KMgPO4.6H2O） of MPBC were analyzed by X-ray diffraction and scanning electron microscopy. The results showed that ionic impurities and the levels of toxic elements were sufficiently low in B-MgO raw materials to meet the medical requirements for MgO （Chinese Pharmacopeia, 2O10 Edition） and for hydroxyapatite surgical implants （GB23101.1-2O08）. The temperature of B-MgO calcination had a marked influence on the hydration and hardening of MPBC pastes. Increasing calcination temperature prolonged the time required for the MPBC slurry to set, significantly decreased the hydration temperature, and prolonged the time required to reach the highest hydration temperature. However, the compressive strength of hardened MPBC did not increase with higher calcination temperatures. In the 900-1 000 ~C temperature range, the hardened MPBC had a higher compressive strength. Imaging analysis suggested that the setting time and the highest hydration temperature of MPBC pastes were dependent on the size and crystal morphology of the B-MgO materials. The production and microstructure compactness of KMgPOa＇6H2O, the main hydration product, determined the compressive strength.

Effect of calcination temperature on the pozzolanic activity of maize straw stem ash treated with portlandite solution

The effect of calcination temperature on the pozzolanic activity of maize straw stem ash(MSSA)was evaluated.The MSSA samples calcined at temperature values of 500,700,and 850℃ were dissolved in portlandite solution for 6 h,thereby obtaining residual samples.The MSSA and MSSA residual samples were analyzed using Fourier transform infrared spectroscopy,X-ray powder diffraction scanning electron microscopy,and X-ray photoelectron spectroscopy to determine vibration bonds,minerals,microstructures,and Si 2p transformation behavior.The conductivity,pH value,and loss of conductivity with dissolving time of the MSSA-portlandite mixed solution were also determined.The main oxide composition of MSSA was silica and potassium oxide.The dissolution of the Si^(4+) content of MSSA at 500℃ was higher than those of the other calcination temperatures.The conductivity and loss of conductivity of MSSA at 700℃ were higher than those of the other calcination temperatures at a particular dissolving time due to the higher KCl content in MSSA at 700℃.C-S-H was easily identified in MSSA samples using X-ray powder diffraction,and small cubic and nearly spherical particles of C-S-H were found in the MSSA residual samples.In conclusion,the optimum calcination temperature of MSSA having the best pozzolanic activity is 500℃,but excessive agglomeration must be prevented.

Influence of Calcination Temperature on TiO_2 Nanotubes’Catalysis for TiO_2/UV/O_3 in Landfill Leachate Solution

The influence of calcination temperature on TiO2 nanotubes＇ catalysis for TiO2/UV/03 was investigated. TiO2 nanotubes （TNTs） were prepared via the sol-gel method and calcined at 300--700 ℃, which were labeled as TNTs-300, TNTs-400, TNTs-500, TNTs-600 and TNTs-700, respectively. TNTs were characterized by transmission electron microscopy （TEM） and X-ray diffraction （XRD）. It is found that TNTs calcined at 400 ℃ showed the best thermal stability. When the calcination temperature increased from 400 ℃ to 700 ℃, the special structure of tubes was destroyed and gradually converted into nanorods and/or particles. The transformation from anatase to rutile occurred at 600 ℃, and the rutile phase was enhanced when the calcination temperature was increased to over 600 ℃. The calcina- tion temperature＇s influence on TNTs＇ adsorption activity for for TiO2/UV/O3 was investigated in landfill leachate solution chemical oxygen demand （COD） and catalytic activity In landfill leachate solution, the adsorption activity of COD decreased in the reduced order of TNTs-300, TNTs-400, TNTs-500, TNTs-600 and TNTs-700. In photocatalytic ozonation, TNTs-400 showed the best catalytic activity while TNTs-700 exhibited the worst. In other three processes, the COD removal of TNTs-300/UV/O3 was higher than those of TNTs-500/UV/O3 and TNTs-600/UV/O3 in the first 20 rain, and then became close to those of the latter two in the following 40 rain. Compared with TNTs-300 and TNTs- 400, TNTs-600 had the best anti-fouling activity, while TNTs-500 and TNTs-700 had lower anti-fouling activity than the former three. In photocatalytic ozonation, the calcination temperature of 400 ℃ was appropriate when TNTs were obtained at the synthesis temperature of 105 ℃.

Effect of pH value and calcination temperature on synthesis and characteristics of Cu-Ni nano-alloys

Cu?Ni nano-alloys were prepared using precursors synthesized by the citrate-gel method. The effects of initial solution pH value and calcination temperature on the composition, crystalline structure, purity, morphology, homogeneity and grain size of Cu?Ni nanoparticles were investigated. Both the parameters significantly affect the crystalline structure, composition and grain size. Cu?Ni alloys prepared at pH value of 1 do not contain impurities, and their compositions are Cu0.42Ni0.58, Cu0.45Ni0.55 and Cu0.52Ni0.48 reduced at 300, 400 and 500 °C, respectively. The grain size grows with the increase of calcination temperature for the precursor prepared at pH values of 1.6 and 3. The Ni content of the alloys gradually increases with the increase of calcination temperature at pH value of 3.

Effect of the support calcination temperature on selective hydrodesulfurization of TiO_2 nanotubes supported CoMo catalysts

TiOz nanotubes （TiO2-NTs） were synthesized by the hydrothermal method. Co and Mo active components were supported on a series of the as-prepared TiO2-NTs samples which were calcined at different temperatures. The effects of support calcination temperature of CoMo/TiOz- NTs catalysts on their catalytic performance were investigated for selective hydrodesulfurization （HDS）. The samples were characterized by means of the scanning electron microscopy （SEM）, the transmission electron microscopy （TEM）, N2 adsorption-desorption, X-ray diffraction （XRD）, Raman spectroscopy and H2 temperature-programmed reduction （Hz-TPR）. The experimental results revealed that TiOz-NTs support calcined under 500℃ can maintain the nanotubular structure with higher surface area and pore volume. Meanwhile, the obtained supported CoMo/TiO2-NTs catalysts exhibited weak metal-support interaction, more octahedral Mo6＋ species and high catalytic performance in selective HDS.

Structural,electrochemical and cycling properties of Nb^(5+)doped LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2)cathode materials at different calcination temperatures for lithium-ion batteries

LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2)cathode material is prepared by sol-gel method and the effects of Nb^(5+)doping and different calcination temperatures on cathode materials were deeply investigated.Structural and morphological characterizations revealed that the optimal content of 1 mol%Nb^(5+)can stabilize layered structures,mitigate Ni^(2+)migration to Li layers,improve lithium diffusion capacity,and reduce lattice expansion/shrinkage while cycling.And calcination temperature at 800℃can not only ensure good morphology,but also suppress the mixed discharge of lithium and nickel in the internal structure.Electrochemical performance evaluation revealed that Nb^(5+)doping improves the discharge-specific capacity of the material,which is conducive to ameliorating its rate capability and cycle performance.And the material at 800℃exhibits the highest discharge specific capacity,the best magnification performance,low polarizability,and the best cycle reversibility.

Influence of calcination temperature on selective catalytic reduction of NO_x with NH_3 over CeO_2-ZrO_2-WO_3 catalyst

A series of CeO2-ZrO2-WO3 catalysts for the selective catalytic reduction （SCR） of NO with NH3 were prepared by hydrothermal method. The influence of calcination temperature on the catalytic activity, microstructure, surface acidity and redox behavior of CeO2-ZrO2-WO3 catalyst was investigated using various characterization methods. It was found that the CeO2-ZrO2-WO3 catalyst calcined at 600 ℃ showed the best catalytic performance and excellent N2 selectivity, and yielded more than 90% NO conversion in a wide temperature range of 250-500 ℃ with a space velocity （GHSV） of 60000 131. As the calcination temperature was increased from 400 to 600 ℃, the NO conversion obviously increased, but decreased at higher calcination temperature. The results implied that the higher surface area, the strongest synergistic interaction, the superior redox property and the highly dispersed or amorphous WO3 species contributed to the excellent SCR activity of the CeO2-ZrO2-WO3 catalyst calcined at 600℃.

Effects of calcination temperature on physicochemical property and activity of CuSO4/TiO2 ammonia-selective catalytic reduction catalysts

CuSO4/TiO2 catalysts with high catalytic activity and excellent resistant to SO2 and H2 O,were thought to be promising catalysts used in Selective catalytic reduction of nitrogen oxides by NH3.The performance of catalysts is largely affected by calcination temperature.Here,effects of calcination temperature on physicochemical property and catalytic activity of CuSO4/TiO2 catalysts were investigated in depth.Catalyst samples calcined at different temperatures were prepared first and then physicochemical properties of the catalyst were characterized by N2 adsorption-desorption,X-ray diffraction,thermogravimetric analysis,Raman spectra,Fourier-transform infrared spectroscopy,X-ray photoelectron spectroscopy,temperature-pro grammed desorption of NH3,temperature-programmed reduction of H2 and in situ diffuse reflectance infrared Fourier transform spectroscopy.Results revealed that high calcination temperature had three main effects on the catalyst.First,sintering and anatase transform into rutile with increase of calcination temperature,causing a decrement of specific surface area.Second,decomposition of CuSO4 under higher calcination temperature,resulting in disappears of Br(?)nsted acid sites(S-OH),which had an adverse effect on surface acidity.Third,CuO from the decomposition of CuSO4 changed surface reducibility of the catalyst and favored the process of NH3 oxidation to nitrogen oxides(NOx).Thus,catalytic activity of the catalyst calcined under high temperatures(≥600℃)decreased largely.

Novel synthesis of Z-schemeα-Bi2O_(3)/g-C_(3)N_(4) composite photocatalyst and its enhanced visible light photocatalytic performance:Influence of calcination temperature

In this study,α-Bi2O_(3)/g-C_(3)N_(4) nanocomposite with direct Z-scheme was successfully prepared through calcination of BiOCOOH/g-C_(3)N_(4) precursor at different temperature.Meanwhile,the effect of calcination temperature on the physicochemical properties ofα-Bi2O_(3)/g-C_(3)N_(4) was studied.All results confirmed that calcination tempe rature greatly influences structural,morphology,surface states,photoelectrochemical property and photocatalytic(PC)perfo rmance ofα-Bi2O_(3)/g-C_(3)N_(4) composite.Furthermore,theα-Bi2O_(3)/gC_(3)N_(4) composite was applied as photocatalyst to degrade amido black 10 B dye under visible light irradiation.It was found that the composite synthesized at 400℃exhibited the highest PC performance due to the intense visible light absorbance and high separation efficiency of electron and hole pairs.Besides,the possible PC mechanism was proposed that the photo-generated charge carrier migration inα-Bi2O_(3)/g-C_(3)N_(4) photocatalyst followed a Z-scheme structure.Finally,the stability test also manifest that theα-Bi2O_(3)/g-C_(3)N_(4) composite photocatalyst has good stability and reusability,which was a promising candidate for wastewater treatment.

Effects of Calcination Temperature on the Structure and Adsorption Performance of Ce-Mn/AC Materials

Activated carbon-supported bimetallic cerium-man- ganese （Ce-Mn/AC） materials were prepared by impregnation method to study the effect of calcination temperature on the structure and adsorption performance of absorbents. The obtained materials were characterized by using X-ray diffraction （XRD）, scanning electron microscope （SEM）, N2 adsorption-desorption iso- therm, Fourier transformed infrared （FT-IR）, and X-ray photoelectron spectroscopy （XPS）. As the results showed, the diffraction peaks of CeO2 decreased and even disappeared; Mn species were transformed from Mn3O4 to Mn2O3 on the surface of Ce-Mn/AC; the BET specific surface area increased first and then decreased on the elevating calcination temperature; the number of acid functions of AC was reduced after being modified by cerium and manganese All these changes were directly attributed to the synergistic effects between MnOx and CeO2. AC800 exhibited the best phenol adsorption capacity. The adsorption mechanism of phenol on Ce-Mn/AC was discussed with hydrophilic （hydrophobic） interaction and hard and soft acid-base theory.