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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH · 2019 · IF 3.375

Effect of La-Modified Supporter on H2S Removal Performance of Mn/La/Al2O3 Sorbent in a Reducing Atmosphere

Haifeng Li,Sheng Su,Yan Peng,Linkang Wu,Kai Xu,Lijun Liu,Mengxia Qing,Song Hu,Yi Wang,Jun Xiang

High temperature sorbents for removing H2S comprising manganese oxide and Al2O3 support modified with La loadings were prepared with wet impregnation. The removal of H2S and the regeneration of sorbents were conducted at 850 °C to investigate the effect of the support modified with La on the desulfurization ability and durability of the Mn/La/Al2O3 sorbents. The fresh sorbent, first sulfide sorbent, and fourth regenerated sorbent were characterized by nitrogen isothermal adsorption, X-ray power diffraction, scanning electron microscopy, and H2 temperature-programmed reduction. The results showed that the highest initial breakthrough sulfur capacity (BSC) was obtained with Mn/0.78%La/Al2O3(M/0.78L), and the initial BSC decreased with increased La loadings due to the inhibiting of excessive La on the reaction between MnO and H2S. The BSC of sorbents with lower La loadings suffered more serious deactivation than MnxOy/Al2O3 during successive desulfurization–regeneration cycles, and the BSC durability of sorbents increased with an increase in La loadings and calcination temperature of La/Al2O3. Mn/4.83%La/Al2O3 with La/Al2O3 calcined at 900 °C (M/4.83H) had the best BSC durability, which was better than the BSC durability of MnxOy/Al2O3 (M) during several desulfurization–regeneration cycles. The characterization results showed that the structure of the M/4.83H sorbent was more stable than other sorbents. The M/4.83H sorbent derived the La(AlO3) phase, which could maintain the structural stability of the sorbent during several desulfurization–regeneration cycles. The formation of the LaAlO3 phase may inhibit MnxOy from dissolving into Al2O3, which was beneficial for the durability of sorbents during several successive desulfurization–regeneration cycles.

CAS / MDL: 1344-28-1
研究领域: 化学工程 · 材料科学 · 环境科学
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JOURNAL OF HAZARDOUS MATERIALS · 2019 · IF 7.65

Multiple bimetallic (Al-La or Fe-La) hydroxides embedded in cellulose/graphene hybrids for uptake of fluoride with phosphate surroundings

Yali Guo,Xu Xing,Yanan Shang,Baoyu Gao,Lei Zhang,Qinyan Yue,Li Qian,Zihang Wang

To insight into the selective adsorption mechanism of fluoride in the bimetallic system, Fe-La or Al-La composites were comparatively embedded onto the cellulose/graphene hybrids (CG hybrids) to fabricate the Fe-La@CG hybrids or Al-La@CG hybrids for fluoride uptake with existing phosphate. The results showed that Al-La@CG hybrids were mainly in the amorphous nature, while Fe-La@CG hybrids have the identical diffraction peaks as compared with those of hydrated lanthanum oxides (HLO) and hydrated iron oxides (HFO). Fluoride capture by Al-La@CG and Fe-La@CG hybrids followed the similar tendencies with the pH altering, but the adsorption performance of Al-La@CG hybrids was better than that of Fe-La@CG hybrids at the same pH levels. Adsorption of fluoride onto Al-La@CG hybrids exhibited less sensitivity and high selectivity with existing phosphate as compared with that of Fe-La@CG hybrids, which further indicated that the Al-La@CG hybrids were more preferable for fluoride adsorption. The fraction areas of La-F and Al-F accounted for 79.1 % and 20.9%, which indicated that the fluoride onto the Al-La@CG hybrids was mainly based on the La species. Similarly, La-F in exhausted Fe-La@CG hybrids accounted for 55.6%, higher than that (44.4%) of Fe-F.

研究领域: 材料科学 · 环境科学
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Journal of Environmental Sciences · 2025 · IF 6.3

Tribridged hydroxyl groups regulated by Ni/La ratio for enhanced ozone decomposition over Ni-La bimetallic basic carbonate catalysts

Fengyu Li,Ruixing Mao,Lun Feng,Jiaqi Li,Miaomiao Xiao,Langlang Wang,Yixing Ma,Xueqian Wang

This study investigates the application of the Ni 2 La 1 bimetallic basic carbonate catalyst in ozone decomposition, which demonstrates excellent catalytic activity under both low-humidity and high-humidity conditions (90 % relative humidity). The catalyst was synthesized via a co-precipitation method, with the Ni/La molar ratio (Ni:La = 2:1) optimized to enhance its structural and functional properties. This optimization endowed the Ni 2 La 1 catalyst with a more developed layered structure, providing an increased number of surface active sites, which significantly improved its catalytic activity and stability. The results indicate that the Ni 2 La 1 catalyst achieves an ozone decomposition conversion efficiency exceeding 90 % under high-humidity conditions and maintains stable catalytic performance over a continuous operation period of 48 hours. Mechanistic studies further reveal that tribridged hydroxyl groups serve as the primary active sites and play a crucial role in the ozone decomposition reaction. Additionally, the Ni 2 La 1 catalyst exhibits a unique hydroxyl regeneration mechanism, where strong interactions with water molecules facilitate the continuous regeneration of tribridged hydroxyl groups, thereby ensuring stability and sustained catalytic activity in humid environments. This research provides a new pathway for the application of Ni-La bimetallic basic carbonate catalysts in environmental catalysis and green chemical reactions. In particular, it offers robust theoretical support and practical insights for ozone mitigation technologies under high-humidity conditions.

研究领域: 环境催化 · 绿色化学 · 材料科学 · 大气污染控制
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2024 · IF 20.2

Efficient catalytic hydrolysis of HCN by La-TiO2: La modulates the generation of surface-rich hydroxyl environment

Jiaqi Li,Mingfei Wang,Jiamin Qi,Xueqian Wang,Langlang Wang,Fei Wang,Kai Li,Yixing Ma,Ping Ning

Hydrogen cyanide (HCN), a common toxic and hazardous air pollutant in industrial exhaust, catalytic hydrolysis of HCN has been the focus of air pollution control research. In this study, a catalyst material (La-TiO 2 ) with high catalytic hydrolysis activity for HCN was obtained by loading La 2 O 3 on the TiO 2 surface, which could realize the complete conversion of HCN at 150 °C with high selectivity of NH 3 and CO 2 . The relevant characterization confirms that La 2 O 3 can be uniformly distributed on the TiO 2 , which can adjust the acid-base structure of the catalyst surface and induce the generation of multi-hydroxyl structures in TiO 2 . On this basis, the combination of in-situ technique and density functional theory (DFT) calculations confirmed that the loading of La 2 O 3 prompted the La-TiO 2 catalyst to activate H 2 O to generate surface hydroxyl groups (-OH), which further enriched the hydroxyl groups on TiO 2 and substantially improved the hydrolysis activity and NH 3 selectivity of the catalyst. And the study confirms that the hydroxyl-rich environment easy combine with the reaction intermediate (formic acid) to generate CO 2 and H 2 O, which accelerated the reaction rate, thus improving the conversion efficiency of HCN and lowering the catalytic conversion temperature. In addition, O 2 can continuously consume the remaining hydrogen atoms after the dissociation of H 2 O to generate hydroxyl groups again, thus effective enhancing catalyst stability. This study provides new theoretical support for the catalytic hydrolysis of HCN and new insights and ideas for the design and development of catalysts for the catalytic hydrolysis of HCN.

CAS / MDL: 1344-28-1
研究领域: 环境科学 · 催化化学
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FUEL · 2024 · IF 6.7

La-doped bimetallic PCN-777 (La-Zr) catalyst synthesized by oil-bath heating for efficient oxidative desulfurization of dibenzothiophene

Mingyu Liao,Miaomiao Zheng,Gexian Li,Xiaolin Pi,Yuanjie Xiao,Linfeng Zhang,Huadong Wu,Jia Guo

The desulfurization of fuels is a crucial step in the production of clean energy. The design of metal–organic frameworks (MOFs) with bimetallic active sites is a new way to achieve deep oxidative desulfurization (ODS). Traditional methods for synthesizing MOFs involve high temperatures and pressures, which can be hazardous. Oil bath heating provides a safer and more convenient way to synthesize catalysts at a slower heating rate with full uniform heating. In this work, a series of La-doped bimetallic PCN-777(La-Zr) catalysts were synthesized by heating in an oil bath. The microstructures of the catalysts were investigated using various techniques, such as XRD, FT-IR, Raman, BET, SEM, TEM, etc. Compared with PCN-777(H) synthesized by hydrothermal method, PCN-777(O) synthesized by oil-bath heating exhibits a higher specific surface area (2017.01 m 2 /g) and a more homogeneous pore size distribution. PCN-777(0.2La-Zr) demonstrated outstanding catalytic performance in ODS of dibenzothiophene (DBT), which could remove 100 % of DBT within 40 min at 60 ℃ and still exhibited high desulfurization efficiency after 12 cycles. The outstanding catalytic ability of PCN-777(0.2La-Zr) should be related to the synergistic effect of its homogeneous pore channels and unsaturated metal sites. The present study exhibits that bimetallic MOFs have possible application potential in the field of ODS, and offers a novel idea for promoting the catalytic ability of ODS by catalyst synthesis in an oil bath.

CAS / MDL: 13520-92-8
研究领域: 催化材料 · 能源化学 · 环境科学
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SEPARATION AND PURIFICATION TECHNOLOGY · 2023 · IF 8.6

Photothermal catalytic hydrolysis of COS with enhanced efficiency over constructed alkali-modified La-Ti catalyst: Adjusting photogenerated electron behavior through metal‐support interactions

Rui Cao,Langlang Wang,Xueqian Wang,Yibing Xie,Xiang Li,Ping Ning

The low-temperature conversion of corrosive carbonyl sulfide (COS) in steel by-product gas is essential for the clean utilization of this gas. Herein, La-Ti@K catalysts doped with La nanoparticles were shown to exhibit significant photopromoted thermocatalytic activity and stability under UV light irradiation. At a reaction temperature of 60 °C, the TOF value increased from 4.84 × 10 -4 s −1 (TiO 2 , thermal treatment) to 8.43 × 10 -4 s −1 (La-Ti@K, photothermal treatment), and the H 2 S selectivity exceeded 99%. This was because La doping increased the density of basic sites on TiO 2 , which promoted the continuous dissociation of H 2 O in the system and the regeneration of –OH under UV irradiation. Moreover, the photogenerated electrons from TiO 2 were transferred to La to maintain the metallic La nanoparticles, as well as to ensure the activation and photothermal hydrolysis of COS. The presence of a suitable electron-metal-support interaction (EMSI) between the electron-rich La nanoparticles and TiO 2 might be responsible for these phenomena. In addition, theoretical calculations revealed that light-induced electron transfer was conducive to H 2 O dissociation and COS activation, while La doping reduced the free energy of the hydrolysis reaction. This work demonstrates the effectiveness of La-Ti@K catalyst in COS photothermal hydrolysis and provides a theoretical basis for further understanding of the photothermal catalytic mechanism.

CAS / MDL: 13463-67-7
研究领域: 环境科学 · 催化化学 · 材料科学
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2021 ·Vol. 32 ·期 2 ·1941-1950 · IF 2.478

Photo-renewable electrode based on porous carbon-loaded La-TiO2 for detection of catechol and hydroquinone

Chen Jiabing,Lu Youluan,Huang Leshu,Shi Zhen,Zheng Yin,Song Xinjian,Wu Chenyi,Wu Zaikun

The fouling and passivation of the electrodes tend to reduce the sensitivity and lifetime of the electrodes. In this work, the mesoporous carbon-doped La-TiO 2 modified electrode not only has a good detection signal for catechol and hydroquinone, but also can achieve the purpose of electrode regeneration under illumination. A series of porous carbon materials LTOF-T (La-Ti Organic Frameworks-Temperature, LTOF-T) were prepared by hydrothermal method and pyrolysis method using La(NO 3 ) 3 ⋅6H 2 O, p -tricarboxylic acid, citric acid monohydrate, and tetra- n -butyl titanate as raw materials. The materials were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), N 2 adsorption–desorption, and Raman spectroscopy. The electrochemical behaviors of catechol (CA) and hydroquinone (HQ) on different electrodes were investigated by cyclic voltammetry (CV) and differential pulse voltammetry (DPV). Under the optimal conditions, HQ and CA concentrations were linear in the range of 0.4–20 μmol/L, and the detection limits were 0.039 μmol/L (HQ) and 0.034 μmol/L (CA) at the signal noise ratio of 3. The electrode can be regenerated under visible light irradiation within 60 min.

研究领域: 分析化学 · 材料科学 · 环境科学
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APPLIED PHYSICS A-MATERIALS SCIENCE & PROCESSING · 2020 ·Vol. 126 ·期 4 ·1-10 · IF 1.81

High-sensitivity and high-selectivity detection of methanol based on La-doped SnO2 sensor

Chen Yu,Dong Zegang,Xue Xinxin,Chen Song,Natan Avi,Lv Yu,Chen Cheng,Yang Yinye,Cen Weifu,Yang Yang

Pure SnO 2 and La-doped SnO 2 nanocomposite were prepared through hydrothermal method, and their gas sensing performances were studied. Results indicate that the sensing response of the 5 wt% La-doped SnO 2 nanocomposite reached 29.5 when exposed to 75 ppm methanol at the optimal operating temperature of 220 °C, which was over seven times larger than that of pure SnO 2 nanoparticles. In addition, the response and recovery time were shortened to 12 s and 7 s, respectively. Moreover, the 5 wt% La-doped SnO 2 nanocomposite presents a good selectivity toward methanol among methanal, methanol, ammonia, acetone and benzene gases. The improvement in the gas sensing properties of the 5 wt% La-doped SnO 2 nanocomposite toward methanol can be attributed to the smaller crystallite size, larger surface area and the modified chemical nature of nanocomposite surface.

CAS / MDL: 10277-43-7 10025-69-1
研究领域: 材料科学 · 传感器技术
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2023 · IF 9.9

Fabrication of CdLa2S4@La(OH)3@Co3S4 Z-scheme heterojunctions with dense La, S-dual defects for robust photothermal assisted photocatalytic performance

Houfeng Zhang,Bojing Sun,Junjie Wang,Qian Zhu,Dongfang Hou,Chen Li,Xiu-qing Qiao,Dong-sheng Li

Optimize the separation and transport mechanism of photogenerated carriers in heterojunction composites, and make full use of the active sites of each material are key factors to enhance photocatalytic activity. Herein, we successfully synthesize defective CdLa 2 S 4 @La(OH) 3 @Co 3 S 4 (CLS@LOH@CS) Z-scheme heterojunction photocatalysts through a facile solvothermal method, which show broad-spectrum absorption and excellent photocatalytic activity. La(OH) 3 nanosheets not only greatly increase the specific surface area of photocatalyst, but also can be coupled with CdLa 2 S 4 (CLS) and form Z-scheme heterojunction by converting irradiation light. In addition, Co 3 S 4 with photothermal properties is obtained by in-situ sulfurization method, which can release heat to improve the mobility of photogenerated carriers, and also be used as a cocatalyst for hydrogen production. Most importantly, the formation of Co 3 S 4 leads to a large number of sulfur vacancy defects in CLS, and thus improving the separation efficiency of photogenerated electrons and holes, and increasing the catalytic active sites. Consequently, the maximum hydrogen production rate of CLS@LOH@CS heterojunctions can reach 26.4 mmol g -1 h −1 , which is 293 times than pristine CLS (0.09 mmol g -1 h −1 ). This work will provide a new horizon for synthesizing high efficiency heterojunction photocatalysts through switching the separation and transport modes of photogenerated carrier.

CAS / MDL: 10026-22-9 10277-43-7
研究领域: 材料科学 · 化学 · 光催化 · 纳米技术
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Journal of Environmental Chemical Engineering · 2025 · IF 7.2

An efficient Mo20/SiO2-La transesterification catalyst: The promoting role of La on anti-carbon deposition

Zuhang Jin,Yiwei Zhao,Cheng Tao,Chao Zhang

Biodiesel production via solid acid catalysis route is one of the most promising and environmentally friendly ways to converting waste cooking oil (WCO) into green fuels. Mo 20 /SiO 2 -La solid acid catalyst shows satisfactory catalytic performance for the transesterification reaction. 91.0 % biodiesel yield can be obtained over the optimized catalyst at 155 ℃ with oil-to-alcohol molar ratio of 1:10 when using soybean oil as the reactant, and 87.1 % yield was obtained by using waste cooking oil. Mo 20 /SiO 2 -La has good reusability and can be regenerated by calcination and reused for at least 5 times. The catalyst was investigated by XPS, NH 3 -TPD, TGA, XRD, TPO, etc., and the promoting role of La (lanthanum) on the stability was discussed. The stability of Mo (molybdenum) active sites and the anti-carbon deposition capability of the catalyst was greatly enhanced by the introduction of La species. The LaO x species close to the Mo acidic sites effectively suppressed the deposition of free fatty acid and thus contributed to the good performance.

研究领域: 化学工程 · 可再生能源 · 催化科学
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Materials Research Express · 2021 ·Vol. 8 ·期 10 ·105002 · IF 1.62

Luminescent property of La(OH)3: Eu3+ nanorod and its decomposed compounds of LaOOH and La2O3

Wenchang Xi,Pan Jian,Xisong Mao,Deyang Ning,Xuewen Xia,Guohua Liu,Dongyang Shi,Yuanpei Lan

In this work, aiming to evaluate and compare the luminescent property of Eu3+ doped La(OH)3 nanorods and its decomposed compounds of LaOOH and La2O3, La(OH)3: Eu3+ nanorods were synthesized and the decomposition behaviors in air and hydrogen were revealed. Then the luminescent property of 0%–8% Eu3+ doped La(OH)3 nanorods and the 300 °C–800 °C calcined La(OH)3: Eu3+- 4% were studied. Results show that LaOOH is intermediate product during the degradation of La(OH)3 in air or H2, which can be formed at a temperature range in 372.3 °C–592.9 °C in air. Intensity of emission spectra of La(OH)3: Eu3+ nanorods increases with the rising of Eu3+ dopant concentration, and the emission property of Eu3+ doped LaOOH and La2O3 is varied and strengthened with that of La(OH)3: Eu3+. Luminescent matrixes of LaOOH and La2O3 show similar emission spectrum and intensity, and the transitions of the D0 → 7F1 and D0 → 7F2 of Eu3+ each bifurcate into two peaks for both europium (III) doped La2O3 and LaOOH. The revealed results suggest that LaOOH is a relative thermal-stable compound and should be an appropriate matrix as similar as La2O3 for luminescent applications.

研究领域: 材料科学 · 光学
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JOURNAL OF RARE EARTHS · 2012 · IF 0.901

Viscosities of ternary systems Y(NO3)3+La(NO3)3+H2O, La(NO3)3+Ce(NO3)3+H2O, La(NO3)3+Nd(NO3)3+H2O and their binary subsystems at different temperatures

Xiaoming PENG,Yufeng HU,Chuanwei JIN,Zhixin WANG,Chao MIAO,Zheyu LI

Viscosities were measured for the ternary systems Y(NO 3 ) 3 +La(NO 3 ) 3 +H 2 O, La(NO 3 ) 3 +Ce(NO 3 ) 3 +H 2 O, and La(NO 3 ) 3 +Nd(NO 3 ) 3 + H 2 O and their binary subsystems Y(NO 3 ) 3 +H 2 O, La(NO 3 ) 3 +H 2 O, Ce(NO 3 ) 3 +H 2 O, and Nd(NO 3 ) 3 +H 2 O at 293.15, 298.15 and 308.15 K. The results were used to test the applicability of simple equations for the viscosity of the mixed solutions. The predictions agreed well with measured values, implying that the viscosities of the examined electrolyte solutions could be related to those of their constituent binary solutions using these simple equations.

研究领域: 物理化学 · 材料科学
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