大气中CO2体积分数升高对污染土壤中Cu、Cd形态分布及其生物活性的影响

采用OTC-1型开顶式培养箱,模拟研究了CO2体积分数升高对2种小麦的生长以及根际、非根际中Cu和Cd形态分布的影响.结果表明,CO2体积分数的升高显著提高了小麦地上部和地下部生物量,降低了小麦根际和非根际的pH值.临麦2号和宁麦8号小麦地上部干重分别增加了36.9%和25.2%,地下部干重则分别增加了55.1%和59.7%.此外,CO2体积分数升高对不同重金属形态分布的影响随小麦品种和重金属种类的不同而异.在高CO2体积分数条件下,可交换态(F1)Cu和Cd含量显著提高,其中临麦2号根际土壤可交换态Cu和Cd含量分别较对照增加10.6%和29.6%,宁麦8号根际土壤可交换态Cu和Cd分别较对照增加11.0%和20.3%;碳酸盐结合态(F2)Cu和Cd均有所降低,其中宁麦8号和临麦2号根际Cu降低均达极显著(分别降低73.6%和50.0%);铁锰氧化物结合态(F3),有机结合态(F4)和残渣态(F5)Cu和Cd在CO2体积分数升高情况下变化较小.同时CO2体积分数升高还显著增加了2种小麦地上部和地下部铜累积量,增加了临麦2号地上部和地下部镉累积量和宁麦8号地上部镉累积量,但对宁麦8号地下部镉累积量无显著影响.     

Mercury in some chemical fertilizers and the effect of calcium superphosphate on mercury uptake by corn seedlings(Zea mays L.)

Mercury (Hg) contents in ten chemical fertilizers were determined, and the effect of calcium superphosphate (CSP) on the uptake and translocation of Hg in corn seedlings was investigated by pot experiments. CSP was applied at the levels of 0, 66.7, and 133.4 mg P2O5/kg to Hg-treated (2 mg/kg) and untreated soils. CSP had the highest Hg content (5.1 mg/kg), followed by the NPK compound fertilizer 15-5-5 (15% N, 5% P2O5, 5% K2O) (1.2 mg/kg), then by nitrogen fertilizers (except for ammonia sulfate) and potassium fertilizers. Application of CSP did not obviously iuence the biomass of corn roots, but it significantly increased the biomass of corn shoots in Hg-treated soil. Application of CSP at the levels of 66.7 and 133.4 mg P2O5/kg did not obviously iuence the uptake of Hg by corn seedlings on soils without Hg treatment, but it decreased the Hg uptake of corn seedlings significantly on Hg-treated soils. The transfer coefficient of Hg in corn seedlings improved slightly on soils without Hg treatment, but decreased slightly on Hg-treated soils with the application of CSP. These results implied that CSP could ameliorate Hg toxicity to corn seedlings by inhibiting the uptake and the translocation of Hg in plants on Hg-polluted soils.     

Mercury in some chemical fertilizers and the e ect of calcium superphosphate on mercury uptake by corn seedlings (Zea mays L.)

Mercury (Hg) contents in ten chemical fertilizers were determined, and the e ect of calcium superphosphate (CSP) on the uptake and translocation of Hg in corn seedlings was investigated by pot experiments. CSP was applied at the levels of 0, 66.7, and 133.4 mg P2O5/kg to Hg-treated (2 mg/kg) and untreated soils. CSP had the highest Hg content (5.1 mg/kg), followed by the NPK compound fertilizer 15-5-5 (15% N, 5% P2O5, 5% K2O) (1.2 mg/kg), then by nitrogen fertilizers (except for ammonia sulfate) and potassium fertilizers. Application of CSP did not obviously influence the biomass of corn roots, but it significantly increased the biomass of corn shoots in Hg-treated soil. Application of CSP at the levels of 66.7 and 133.4 mg P2O5/kg did not obviously influence the uptake of Hg by corn seedlings on soils without Hg treatment, but it decreased the Hg uptake of corn seedlings significantly on Hg-treated soils. The transfer coe cient of Hg in corn seedlings improved slightly on soils without Hg treatment, but decreased slightly on Hg-treated soils with the application of CSP. These results implied that CSP could ameliorate Hg toxicity to corn seedlings by inhibiting the uptake and the translocation of Hg in plants on Hg-polluted soils.     

Accelerated biodegradation of nitrophenols in the rhizosphere of Spirodela polyrrhiza

We investigated the biodegradation of 2-nitrophenol (2-NP), 4-nitrophenol (4-NP), and 2,4-dinitrophenol (2,4-DNP) in the rhizosphere of Spirodela polyrrhiza plants by conducting degradation experiments with three river water samples supplemented with each nitrophenol (NP). We then isolated NP-degrading bacteria both from the S. polyrrhiza roots and from the river water. In the river water samples, removal of the three NP was accelerated in the presence of S. polyrrhiza plants. The three NPs persisted in an autoclaved solution with sterile plants suggests that NP removal was accelerated largely by bacterial NP biodegradation rather than by adsorption and uptake by the plants. We isolated 8 strains of NP-degrading bacteria: 6 strains from the S. polyrrhiza roots and 2 strains from river water without the plants. The 2-NP- and 2,4-DNP-degrading bacteria were isolated only from the S. polyrrhiza roots. The 4-NPdegrading bacteria different from those isolated from the river water samples were also found on S. polyrrhiza roots. The 2-NP- and 4-NP-degrading strains isolated from the roots utilized the corresponding NP (0.5 mmol/L) as the sole carbon and energy source. The 2,4-DNP-degrading strains isolated from the roots showed substantial 2,4-DNP-degrading activity, but the presence of other carbon and energy sources was required for their growth. The isolated NP-degrading bacteria from the roots must have contributed to the accelerated degradation of the three NPs in the rhizosphere of S. polyrrhiza. Our results suggested that rhizoremediation with S. polyrrhiza may be effective for NP-contaminated surface water.     

Effect of Ce doping of TiO2 support on NH3-SCR activity over V2O5-WO3/CeO2-TiO2 catalyst

CeO2–TiO2composite supports with different Ce/Ti molar ratios were prepared by a homogeneous precipitation method, and V2O5–WO3/CeO2–TiO2catalysts for the selective catalytic reduction（SCR） of NOx with NH3 were prepared by an incipient-wetness impregnation method. These catalysts were characterized by means of BET, XRD, UV–Vis,Raman and XPS techniques. The results showed that the catalytic activity of V2O5–WO3/TiO2 was greatly enhanced by Ce doping（molar ratio of Ce/Ti = 1/10） in the TiO2 support.The catalysts that were predominantly anatase TiO2 showed better catalytic performance than the catalysts that were predominantly fluorite CeO2. The Ce additive could enhance the surface adsorbed oxygen and accelerate the SCR reaction. The effects of O2 concentration, ratio of NH3/NO, space velocity and SO2 on the catalytic activity were also investigated. The presence of oxygen played an important role in NO reduction. The optimal ratio of NH3/NO was 1/1 and the catalyst had good resistance to SO2 poisoning.     

Efficiency of white lupin in the removal of mercury from contaminated soils： Soil and hydroponic experiments

This study examined the ability of the white lupin to remove mercury (Hg) from a hydroponic system (Hg concentrations 0, 1.25, 2.5, 5 and 10 μmol/L) and from soil in pots and lysimeters (total Hg concentration (19.2 ± 1.9) mg/kg availability 0.07%, and (28.9 ± 0.4) mg/kg availability 0.09%, respectively), and investigated the accumulation and distribution of Hg in different parts of the plant. White lupin roots efficiently took up Hg, but its translocation to the harvestable parts of the plant was low. The Hg concentration in the seeds posed no risk to human health according to the recommendations of the World Health Organization, but the shoots should not be used as fodder for livestock, at least when unmixed with other fodder crops. The accumulation of Hg in the hydroponically-grown plants was linear over the concentration range tested. The amount of Hg retained in the roots, relative to the shoots, was almost constant irrespective of Hg dose (90%). In the soil experiments, Hg accumulation increased with exposure time and was the greater in the lysimeter than in the pot experiments. Although Hg removal was the greater in the hydroponic system, revealing the potential of the white lupin to extract Hg, bioaccumulation was the greatest in the lysimeter-grown plants; the latter system more likely reflects the true behaviour of white lupin in the field when Hg availability is a factor that limits Hg removal. The present results suggest that the white lupin could be used in long-term soil reclamation strategies that include the goal of profitable land use in Hg-polluted areas.     

Uptake and accumulation of phenanthrene and pyrene in spiked soils by Ryegrass(Lolium perenne L.)

Phytoremediation has long been recognized as a cost-effective method for the removal of polycyclic aromatic hydrocarbons （PAHs） from soil. A study was conducted to investigate the uptake and accumulation of PAHs in root and shoot of Lolium perenne L. Pot experiments were conducted with series of concentrations of 3.31-378.37 mg/kg for phenanthrene and those of 4.22-365.38 mg/kg for pyrene in a greenhouse. The results showed that both ryegrass roots and shoots did take up PAHs from spiked soils, and generally increased with increasing concentrations of PAH in soil. Bioconcentration factors（BCFs） of phenanthrene by shoots and roots were 0.24- 4.25 and 0.17-2.12 for the same treatment. BCFs of pyrene by shoots were 0.20-1.5, except for 4.06 in 4.32 mg/kg treatment, much lower than BCFs of pyrene by roots （0.58-2.28）. BCFs of phenanthrene and pyrene tended to decrease with increasing concentrations of phenanthrene and pyrene in soil. Direct uptake and accumulation of these compounds by Lolium perenne L. was very low compared with the other loss pathways, which meant that plant-promoted microbial biodegradation might be the main contribution to plant-enhanced removal of phenanthrene and pyrene in soil. However, the presence of Lolium perenne L. significantly enhanced the removal of phenanthrene and pyrene in spiked soil. At the end of 60 d experiment, the extractable concentrations of phenanthrene and pyrene were lower in planted soil than in non-planted soil, about 83.24%-91.98% of phenanthrene and 68.53%-84.10% of pyrene were removed from soils, respectively. The results indicated that the removal of PAHs in contaminated soils was a feasible approach by using Lolium perenne L.     

Synthesis of novel CeO2-BiVO4/FAC composites with enhanced visible-light photocatalytic properties

To utilize visible light more effectively in photocatalytic reactions, a fly ash cenosphere （FAC）-supported CeO2-BiV04 （CeO2-BiVO4/FAC） composite photocatalyst was prepared by modified metalorganic decomposition and impregnation methods. The physical and photophysical properties of the composite have been characterized by X-ray diffraction （XRD）, scanning electron microscope （SEM） and energy dispersive X-ray spectroscopy （EDX）, X-ray photoelectron spectroscopy （XPS）, and UV-Visible diffuse reflectance spectra. The XRD patterns exhibited characteristic diffraction peaks of both BiVO4 and Ce02 crystalline phases. The XPS results showed that Ce was present as both Ce4＋ and Ce3＋ oxidation states in Ce02 and dispersed on the surface of BiV04 to constitute a p-n heterojunction composite. The absorption threshold of the CeO2-BiVO4/FAC composite shifted to a longer wavelength in the UV-Vis absorption spectrum compared to the pure Ce02 and pure BiV04. The composites exhibited enhanced photocatalytic activity for Methylene Blue （MB） degradation under visible light irradiation. It was found that the 7.5 wt.% CeO2-BiVO4/FAC composite showed the highest photocatalytic activity for MB dye wastewater treatment.     

不同磷水平下丛枝菌根真菌对纳米氧化锌生物效应的影响

纳米ZnO颗粒是应用最为广泛金属型纳米颗粒(nanoparticles,NPs)之一,对作物和土壤微生物的影响值得关注.丛枝菌根(arbuscular mycorrhizal,AM)是自然界中普遍存在的植物-真菌共生体,对各种环境胁迫具有一定的抵御能力,但菌根效应受土壤和植物磷含量的影响.分别设置0、20、50、100 mg·kg~(-1)这4个磷水平,在接种或不接种AM真菌Funneliformis mosseae、添加或不添加纳米ZnO(500 mg·kg~(-1))条件下在温室中利用玉米进行土壤盆栽试验.结果表明,纳米ZnO没有显著影响玉米生长,但不利于菌根侵染和磷素吸收,并引起锌在植物体内的积累.纳米ZnO和高磷降低玉米菌根侵染,但AM真菌在所有磷水平下均显著促进植物生长.施磷和接菌均可使土壤p H升高、降低纳米ZnO源锌的生物有效性,从而降低锌向玉米地上部分的转运和积累,体现出一定保护作用.接菌在多数情况下显示出积极的菌根效应,尤其在低磷、添加纳米ZnO条件下更为显著.结果首次表明,AM真菌、磷肥均有助于减轻纳米ZnO引起的土壤污染及其所产生的生态和健康风险.     

玉米根系对苯并(a)芘的吸收及苯并(a)芘在植株内的积累

在人工气候室内用Poagland营养液栽培玉米,测定了玉米根、叶、茎、粒及伤流液中BaP的本底值。表明玉米根系可以吸收BaP并向上运输,但地上部的累积在一定程度上取决于根系环境中BaP的量。 在玉米的不同生育期向培养液添加BaP的试验表明,灌浆期的添加会增加籽粒中BaP的累积,因此,避免土壤的严重污染对控制进入食物链的BaP量是有意义的。     

羽叶鬼针草对Pb的吸收特性及修复潜力

羽叶鬼针草对土壤中Pb的吸收特性和修复潜力的研究结果表明:①鬼针草对Pb有很强的吸收能力,在土壤Pb浓度为2 000mg·L^-1时,鬼针草地上部和根系中Pb含量达到最高,分别为2 164.7mg·kg^-1和1 509.3 mg·kg^-1;②鬼针草植物对Pb的吸收有很强的分异特征,植物吸收的Pb主要富集于地上部,Pb在植物体内的分布规律是叶子>茎>根系>种子;③不同生长期植物对Pb的吸收速度是不同的,植物在开花期对Pb的吸收速度最大,吸收量根系为15.81 mg·(kg·d)^-1,地上部是19.83 mg·(kg·d)^-1.羽叶鬼针草具备修复土壤Pb污染的潜力.     

Combined effects of elevated temperature and CO2 concentration on Cd and Zn accumulation dynamics in Triticum aestivum L.

A simulated climate warming experiment was conducted to evaluate the combined effects of elevated temperature and CO_2 concentration on the bioaccumulation,translocation and subcellular distributions of Cd and Zn in wheat seedlings(Triticum aestivum L.cv.Xihan 1.) at Dingxi,Gansu Province,China.The objective was to find evidence that global climate change is affecting the bioaccumulation of Cd and Zn in T.aestivum L.cv.Xihan 1.The results showed that compared to control A,elevated temperature and CO_2 increased Cd bioaccumulation in the shoots by 1.4–2.5 times,and increased that in the roots by 1.2–1.5times,but decreased Zn levels in wheat shoots by 1.4–2.0 times,while decreased that in the roots by 1.6–1.9 times.Moreover,temperature and CO_2 concentration increase also led to increased Cd concentration,and decreased Zn concentration in subcellular compartments of wheat seedlings.The largest Cd concentration increase(174.4%) was observed in the cell wall and debris fractions of shoots after they were subjected to the highest CO_2 and temperature treatment(TC3).The largest Zn concentration decrease(53.1%) was observed in the soluble(F3) fractions of shoots after they were subjected to the medium CO_2 and temperature treatment(TC2).The temperature and CO_2 increase had no significant effect on the proportional distribution of Cd and Zn in the subcellular fractions.The root-to-shoot translocation of Cd increased with the increasing temperature and CO_2 concentration.However,the Zn distributions only fluctuated within a small range.     

Preparation of FexCe1-xOy solid solution and its application in Pd-only three-way catalysts

FeO_x-CeO₂ mixed oxides with increasing Fe/(Ce+Fe) atomic ratio (1-20 mol%) were prepared by sol-gel method and characterized by X-ray powder diffraction (XRD), Brunauer-Emmett-Teller (BET) and Hydrogen temperature-programmed reduction (H₂-TPR) techniques. The dynamic oxygen storage capacity (DOSC) was investigated by mass spectrometry with CO/O₂ transient pulses. The powder XRD data following Rietveld refinement revealed that the solubility limit of iron oxides in the CeO₂ was 5 mol% based on Fe/(Ce+Fe). The lattice parameters experienced a decrease followed by an increase due to the influence of the maximum solubility limit of iron oxides in the CeO₂. TPR analysis revealed that Fe introduction into ceria strongly modified the textual and structural properties, which influenced the oxygen handling properties. DOSC results revealed that Ce-based materials containing Fe oxides with multiple valences contribute to the majority of DOSC. The kinetic analysis indicated that the calculated apparent kinetic parameters obey the compensation effect. The three-way catalytic performance for Pd-only catalysts based on the Fe doping support exhibited the redundant iron species separated out of the CeO₂ and interacted with the ceria and Pd species on the surface, which seriously influenced the catalytic properties, especially after hydrothermal aging treatment.     

Plant coexistence can enhance phytoextraction of cadmium by tobacco （Nicotiana tabacum L.） in contaminated soil

A mesocosm experiment was conducted to investigate whether plant coexistence affects cadmium (Cd) uptake by plant in contaminated soil.Tobacco (Nicotiana tabacum L.var.K326) and Japanese clover (Kummerowia striata (Thunb.) Schindl.) were used.Cadmium was applied as 3CdSO 4 ·8H 2 O in solution at three levels (0,1,and 3 mg/kg soil) to simulate an unpolluted soil and soils that were slightly and moderately polluted with Cd.Tobacco (crop),Japanese clover (non-crop),and their combination were grown under each C...     

Co-adsorption of gaseous benzene, toluene, ethylbenzene, m-xylene (BTEX) and SO2 on recyclable Fe3O4 nanoparticles at 0-101% relative humidities

We herein used Fe3O4 nanoparticles(NPs) as an adsorption interface for the concurrent removal of gaseous benzene, toluene, ethylbenzene and m-xylene(BTEX) and sulfur dioxide(SO2), at different relative humidities(RH). X-ray diffraction, Brunauer–Emmett–Teller, and transmission electron microscopy were deployed for nanoparticle surface characterization.Mono-dispersed Fe3O4(Fe2O3·Fe O) NPs synthesized with oleic acid(OA) as surfactant, and uncoated poly-dispersed Fe3O4 NPs demonstrated comparable removal efficiencies.Adsorption experiments of BTEX on NPs were measured using gas chromatography equipped with flame ionization detection, which indicated high removal efficiencies(up to(95 ± 2)%) under dry conditions. The humidity effect and competitive adsorption were investigated using toluene as a model compound. It was observed that the removal efficiencies decreased as a function of the increase in RH, yet, under our experimental conditions, we observed(40 ± 4)% toluene removal at supersaturation for Fe3O4 NPs, and toluene removal of(83 ± 4)% to(59 ± 6)%, for OA-Fe3O4 NPs. In the presence of SO2, the toluene uptake was reduced under dry conditions to(89 ± 2)% and(75 ± 1)% for the uncoated and coated NPs, respectively, depicting competitive adsorption. At RH 100%,competitive adsorption reduced the removal efficiency to(27 ± 1)% for uncoated NPs whereas OA-Fe3O4 NPs exhibited moderate efficiency loss of(55 ± 2)% at supersaturation.Results point to heterogeneous water coverage on the NP surface. The magnetic property of magnetite facilitated the recovery of both types of NPs, without the loss in efficiency when recycled and reused.     

水稻光合碳在植株-土壤系统中分配与稳定对施磷的响应

为探究稻田土壤光合碳的输入及分配对施磷的响应特征,本研究选用籼性常规水稻品种（中早39）,在两个施磷（0 mg·kg^-1和80 mg·kg^-1;分别记为P₀和P₈₀）条件下进行盆栽试验,同时采用¹³CO₂连续标记技术量化光合碳在水稻-土壤系统中的分配.结果表明,施磷显著增加光合碳在水稻地上部的分配,降低其在根际土的分配（P<0.05）;施磷使拔节期水稻的光合碳含量增加了70%,根系干重降低了31%.与不施磷相比,施磷显著提高了水稻地上部全碳含量0.31 g·pot^-1（P<0.05）,显著降低了水稻根冠比;施磷使进入非根际土壤微生物量的光合碳（¹³C-MBC）显著增加了0.03 mg·kg^-1,但降低其在根际土壤的分配;光合碳在非根际土壤颗粒态有机碳（POC）和矿物结合态有机碳（MOC）的分配对施磷的响应不显著,但在根际土壤施磷处理显著降低了其在POC中的含量.因此,施磷增加了光合碳在水稻-土壤系统的分配,但降低了光合碳在土壤中的积累.本研究探讨施磷对水稻光合碳在水稻-土壤系统的分配及其稳定的影响,为缺磷土壤的合理施用磷肥及其对土壤有机碳积累的影响提供理论基础和数据支撑;对理解稻田土壤光合碳的传输与分配特征及其固碳潜力具有重要意义.     

Relationship between heavy metal concentrations of herbaceous plants and soils at four Pb-Zn mining sites in Yunnan, China

This paper studied the relationship between heavy metal concentrations of herbaceous plants and soils at four Pb-Zn mining sites in Yunnan, China. 50 herbaceous plant samples of 9 plant species from 4 families and 50 soil samples were collected and then ana1yzed for the tota1 concentrations of Pb, Cd, and Zn. The results showed that the average concentrations of Pb, Cd, and Zn in soil samples were 3772.83, 168.81, and 5385.65 mg/kg, respectively. The average concentrations of Pb, Cd, and Zn were 395.68, 28.14, and 1664.20 mg/kg in the shoots, and 924.12, 57.25, and 1778.75 mg/kg in the roots, respectively. Heterospecific plants at the same site and conspecific plants at various sites had different average levels of Pb, Cd, and Zn, both in the shoots and the roots. Enrichment coefficients of Pb, Cd, and Zn were greater than 1 in 2, 3, and 9 herbaceous plant samples, respectively. Translocation factors of Pb, Cd, and Zn were greater than 1 in 10, 17, and 25 herbaceous plant samples, respectively. In all 50 samples, the concentrations of Pb, Cd, and Zn between the shoots and the roots, the shoots, and the soils, and the roots and the soils had significant positive relationships.     

镉超富集植物球果菜对镉-砷复合污染的反应及其吸收积累特征

采用室外盆栽模拟方法,比较和分析了镉（Cd）-砷（As）复合污染处理对球果菜（Rorippa globosa,十字花科焊菜属,1种从农田杂草中新发现的镉超富集植物）的生长及其对Cd、As吸收和积累特征的影响.结果表明,在低浓度Cd-As复合污染条件下,由于Cd、As的拮抗作用,从而促进植物的生长发育,同时也促进地上部对Cd的吸收和积累.在Cd-As复合污染处理浓度为10 mg/kg和50 mg/kg时,株高和地上部干重达到最大（分别为35.9 cm和2.2 g/盆）,叶片中Cd积累量高于同浓度单一Cd处理.Cd-As复合污染高浓度处理表现出对球果菜生长以及Cd的吸收和积累有协同的抑制作用.同时,球果菜根部对As的吸收能力大于其地上部,相应的富集系数≤0.3,转移系数≤0.6,说明球果菜对As有一定的排斥作用.这些结果表明,球果菜有很强的忍耐Cd-As复合污染的能力,对修复Cd-As复合污染土壤具有一定的潜力.     

Atrazine accumulation and toxic responses in maize Zea mays

Atrazine accumulation, oxidative stress, and defense response in maize seedlings exposed to extraneous atrazine were studied. Accumulation of atrazine in maize increased with increasing exposure concentration. The abscisic acid (ABA) content was positively correlated with the atrazine concentrations in maize roots and shoots (p < 0.05). Hydroxyl radical (·OH) in maize was determined in vivo with electron paramagnetic resonance spectroscopy. Its intensity was positively correlated with atrazine concentration in roots and shoots (p < 0.05), and higher level of ·OH generated in roots than in shoots corresponded to the major accumulation of atrazine in roots. Superoxide dismutase, peroxidase and catalase in roots were up-regulated by atrazine exposure at 1 mg/L compared to the control and malondialdehyde content in roots was enhanced when atrazine exposure concentration reached 10 mg/L. These results suggested the exposure and accumulation of atrazine caused oxidative toxicity and antioxidant response in maize.     

Cu-Mn-Ce ternary mixed-oxide catalysts for catalytic combustion of toluene

Cu–Mn, Cu–Mn–Ce, and Cu–Ce mixed-oxide catalysts were prepared by a citric acid sol–gel method and then characterized by XRD, BET, H_2-TPR and XPS analyses. Their catalytic properties were investigated in the toluene combustion reaction. Results showed that the Cu–Mn–Ce ternary mixed-oxide catalyst with 1:2:4 mole ratios had the highest catalytic activity, and 99% toluene conversion was achieved at temperatures below 220°C. In the Cu–Mn–Ce catalyst, a portion of Cu and Mn species entered into the Ce O_2 fluorite lattice, which led to the formation of a ceria-based solid solution. Excess Cu and Mn oxides existed on the surface of the ceria-based solid solution. The coexistence of Cu–Mn mixed oxides and the ceria-based solid solution resulted in a better synergetic interaction than the Cu–Mn and Cu–Ce catalysts, which promoted catalyst reducibility, increased oxygen mobility, and enhanced the formation of abundant active oxygen species.