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厌氧消化，生物固体，污染，甲基苯丙胺，吸附 1

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Major applications of heat pipe and its advances coupled with sorption system: a review

Yang YU, Guoliang AN, Liwei WANG

《能源前沿（英文）》 2019年 第13卷 第1期   页码 172-184 doi: 10.1007/s11708-019-0610-6

摘要： Heat pipe utilizes continuous phase change process within a small temperature drop to achieve high thermal conductivity. For decades, heat pipes coupled with novel emerging technologies and methods (using nanofluids and self-rewetting fluids) have been highly appreciated, along with which a number of advances have taken place. In addition to some typical applications of thermal control and heat recovery, the heat pipe technology combined with the sorption technology could efficiently improve the heat and mass transfer performance of sorption systems for heating, cooling and cogeneration. However, almost all existing studies on this combination or integration have not concentrated on the principle of the sorption technology with acting as the heat pipe technology for continuous heat transfer. This paper presents an overview of the emerging working fluids, the major applications of heat pipe, and the advances in heat pipe type sorption system. Besides, the ongoing and perspectives of the solid sorption heat pipe are presented, expecting to serve as useful guides for further investigations and new research potentials.

关键词： heat pipe     sorption system     heat transfer     solid sorption heat pipe    

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Sorption mechanisms of diphenylarsinic acid on natural magnetite and siderite: Evidence from sorption

《环境科学与工程前沿（英文）》 2022年 第16卷 第9期 doi: 10.1007/s11783-022-1547-2

摘要：

• DPAA sorption followed pseudo-secondary and intra-particle diffusion models.

关键词： Diphenylarsinic acid (DPAA)     Sorption     Magnetite     Siderite     Sequential extraction     EXAFS    

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Thermodynamic study on dynamic water and organic vapor sorption on amorphous valnemulin hydrochloride

Jinbo OUYANG, Jingkang WANG, Yongli WANG, Qiuxiang YIN, Hongxun HAO

《化学科学与工程前沿（英文）》 2015年 第9卷 第1期   页码 94-104 doi: 10.1007/s11705-015-1460-3

摘要： The sorption of water and organic vapors on valnemulin hydrochloride was determined by dynamic vapor sorption at 25 °C. The adsorption-desorption behavior of water vapor and a series of organic vapors was investigated to probe the structural changes in valnemulin hydrochloride before and after sorption. The isothermal adsorption equilibrium data was evaluated using Guggenheim-Anderson-deBoer (GAB) and Brunauer-Emmett-Teller (BET) models. The BET model is applicable only at low relative pressures (0.1≤RP≤0.4) while the GAB model is applicable in the whole range of RPs (0.1≤RP≤0.9). The sorption kinetics at high RPs was determined by fitting the sorption data to the Avrami equation and the sorption content time relationship could be predicted by the Avrami equation. Finally, the possible sorption mechanism of valnemulin hydrochloride was also discussed.

关键词： valnemulin hydrochloride     water vapor     organic vapors     sorption     kinetics    

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Simulation and experiments on a solid sorption combined cooling and power system driven by the exhaust

Peng GAO, Liwei WANG, Ruzhu WANG, Yang YU

《能源前沿（英文）》 2017年 第11卷 第4期   页码 516-526 doi: 10.1007/s11708-017-0511-5

摘要： A solid sorption combined cooling and power system driven by exhaust waste heat is proposed, which consists of a MnCl sorption bed, a CaCl sorption bed, an evaporator, a condenser, an expansion valve, and a scroll expander, and ammonia is chosen as the working fluid. First, the theoretical model of the system is established, and the partitioning calculation method is proposed for sorption beds. Next, the experimental system is established, and experimental results show that the refrigerating capacity at the refrigerating temperature of –10°C and the resorption time of 30 min is 1.95 kW, and the shaft power is 109.2 W. The system can provide approximately 60% of the power for the evaporator fan and the condenser fan. Finally, the performance of the system is compared with that of the solid sorption refrigeration system. The refrigerating capacity of two systems is almost the same at the same operational condition. Therefore, the power generation process does not influence the refrigeration process. The exergy efficiency of the two systems is 0.076 and 0.047, respectively. The feasibility of the system is determined, which proves that this system is especially suitable for the exhaust waste heat recovery.

关键词： solid sorption     exhaust waste heat     combined cooling and power system     exergy efficiency    

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Nexus between polymer support and metal oxide nanoparticles in hybrid nanosorbent materials (HNMs) for sorption

Ryan C. SMITH,Jinze LI,Surapol PADUNGTHON,Arup K. SENGUPTA

《环境科学与工程前沿（英文）》 2015年 第9卷 第5期   页码 929-938 doi: 10.1007/s11783-015-0795-9

摘要： Metal oxide nanoparticles like hydrated ferric oxide (HFO) or hydrated zirconium oxide (HZrO) are excellent sorbents for environmentally significant ligands like phosphate, arsenic, or fluoride, present at trace concentrations. Since the sorption capacity is surface dependent for HFO and HZrO, nanoscale sizes offer significant enhancement in performance. However, due to their miniscule sizes, low attrition resistance, and poor durability they are unable to be used in typical plug-flow column setups. Meanwhile ion exchange resins, which have no specific affinity toward anionic ligands, are durable and chemically stable. By impregnating metal oxide nanoparticles inside a polymer support, with or without functional groups, a hybrid nanosorbent material (HNM) can be prepared. A HNM is durable, mechanically strong, and chemically stable. The functional groups of the polymeric support will affect the overall removal efficiency of the ligands exerted by the Donnan Membrane Effect. For example, the removal of arsenic by HFO or the removal of fluoride by HZrO is enhanced by using anion exchange resins. The HNM can be precisely tuned to remove one type of contaminant over another type. Also, the physical morphology of the support material, spherical bead versus ion exchange fiber, has a significant effect on kinetics of sorption and desorption. HNMs also possess dual sorption sites and are capable of removing multiple contaminants, namely, arsenate and perchlorate, concurrently.

关键词： ion exchange     sorption     arsenic     perchlorate     fluoride    

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Diphenylarsinic acid sorption mechanisms in soils using batch experiments and EXAFS spectroscopy

Meng Zhu, Yongming Luo, Ruyi Yang, Shoubiao Zhou, Juqin Zhang, Mengyun Zhang, Peter Christie, Elizabeth L. Rylott

《环境科学与工程前沿（英文）》 2020年 第14卷 第4期 doi: 10.1007/s11783-020-1237-x

摘要： DPAA sorption data was found to fit the Freundlich equation. Kf was significantly positive correlated with oxalate-extractable Fe2O3. Ligand exchange was the main mechanism for DPAA sorption on soils. Bidentate binuclear and monodentate mononuclear DPAA bonds were identified. Diphenylarsinic acid (DPAA) is a phenyl arsenic compound derived from chemical warfare weapons. Macroscopic and microscopic work on DPAA sorption will provide useful information in predicting the partitioning and mobility of DPAA in the soil-water environment. Here, batch experiments and extended X-ray absorption fine structure (EXAFS) spectroscopy were used to investigate the sorption mechanisms of DPAA. The DPAA sorption data from 11 soil types was found to fit the Freundlich equation, and the sorption capacity, Kf, was significantly and positively correlated with oxalate-extractable Fe2O3. The Kf values of eight of the 11 untreated soils (1.51–113.04) significantly decreased upon removal of amorphous metal (hydr)oxides (0.51–13.37). When both amorphous and crystalline metal (hydr)oxides were removed from the untreated soils, the Kf values either decreased or slightly increased (0.65–3.09). Subsequent removal of soil organic matter from these amorphous and crystalline metal (hydr)oxide-depleted samples led to further decreases in Kf to 0.02–1.38, with only one exception (Sulfic Aquic-Orthic Halosols). These findings strongly suggest that ligand exchange reactions with amorphous metal (hydr)oxides contribute most to DPAA sorption on soils. EXAFS data provide further evidence that DPAA primarily formed bidentate binuclear (2C) and monodentate mononuclear (1V) coring-sharing complexes with As-Fe distances of 3.34 and 3.66 Å, respectively, on Fe (hydr)oxides. Comparison of these results with earlier studies suggests that 2C and 1V complexes of DPAA may be favored under low and high surface coverages, respectively, with the formation of 1V bonds possibly conserving the sorption sites or decreasing the steric hindrance derived from phenyl substituents.

关键词： Diphenylarsinic acid     EXAFS     Fe (hydr)oxide     Soil organic matter     Sorption mechanism    

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Effects of different sediment fractions on sorption of galaxolide

Lixia JIN, Mengchang HE, Jinghuan ZHANG

《环境科学与工程前沿（英文）》 2012年 第6卷 第1期   页码 59-65 doi: 10.1007/s11783-010-0259-1

摘要： Sorption isotherms of galaxolide (HHCB) of different fractions from two sediments with different mineral and organic carbon contents were determined to compare HHCB sorption behavior and contribution to the total sorption. The HHCB sorption isotherms that used the batch equilibration method were studied on different sediments of different fractions. The sorption isotherms of 600°C heating fractions were detailed using the linear model, while the other fractions were nonlinear and fitted well with the Freundlich model. The dissolved organic carbon (DOC) removed, NaOH extracted, and 375°C heating fractions showed more nonlinear sorption than the original sediments, which suggested more heterogeneous sorption sites in these fractions. Compared to the original sediments, the 375°C heating fractions had higher carbon-normalized distribution coefficient ( ) values, indicating a higher sorption affinity for HHCB. Among the different sediment fractions, the contribution of the 600°C heating fractions to the overall sorption were the lowest (<20%), while the 375°C heating fractions were the highest (up to 85%).

关键词： galaxolide (HHCB)     sorption     organic carbon     sediment     carbon-normalized distribution coefficient (Koc)    

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Contribution of black carbon to nonlinearity of sorption and desorption of acetochlor on sediment

Jianqiu LIU, Yaobin ZHANG, Hong CHEN, Yazhi ZHAO, Xie QUAN

《环境科学与工程前沿（英文）》 2009年 第3卷 第1期   页码 69-74 doi: 10.1007/s11783-008-0076-y

摘要： In order to investigate the contribution of various black carbon (BC) contents to nonlinearity of sorption and desorption isotherms for acetochlor on sediment, equilibrium sorption and desorption isotherms were determined to measure sorption and desorption of acetochlor in sediment amended with various amounts of BC. In this paper, two types of BC referred to as BC400 and BC500 were prepared at 400°C and 500°C, respectively. Higher preparation temperature facilitated the formation of micropores on BC to enhance its sorption capacity. Increase of the BC content obviously increased the sorption amount and reduced the desorption amount for acetochlor. When the BC500 contents in total organic carbon (TOC) increased from 0 to 60%, Freundlich sorption coefficient ( ) increased from 4.07 to 35.74, and desorption hysteresis became gradually obvious. When the content of BC in TOC was lower than 23%, the sorption isotherm had a significant linear correlation ( = 0.05). In case of desorption, a significant nonlinear change could be observed when the content of BC was up to 13%. Increase of BC content in the sediment would result in shifting the sorption-desorption isotherms from linearity to nonlinearity, which indicated that contribution of BC to nonlinear adsorption fraction became gradually remarkable.

关键词： black carbon (BC)     sorption     desorption     sediment    

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Phenanthrene sorption to environmental black carbon in sediments from the Song-Liao watershed (China)

Jinghuan ZHANG, Mengchang HE, Chunye LIN, Ke SUN, Bin MEN, John L. ZHOU,

《环境科学与工程前沿（英文）》 2009年 第3卷 第4期   页码 434-442 doi: 10.1007/s11783-009-0150-0

摘要： Black carbon (BC) in ten contaminated sediments from the Song-Liao watershed, NE China, was isolated upon treatments using a combustion method at 375°C, and the isolates’ sorption isotherms for phenanthrene (Phen) were determined. All sorption isotherms were nonlinear and fitted well by the Freundlich model. A negative relation was found between Freundlich sorption nonlinearity parameter ( values) and BC/total organic carbon (TOC) content of the original sediments (=0.687, <0.01), indicating the dominance of BC in Phen sorption nonlinearity. The BC isolates from this industrialized region had values of 0.342 to 0.505 and log values of 6.02 to 6.42(μg·kg·OC)/(μg·L) for Phen. At a given , the BC had higher value than the original sediments, revealing a higher sorption capacity for BC. BC was responsible for 50.0% to 87.3% of the total sorption at =0.05 , clearly indicating the dominance of BC particles in overall sorption of Phen by sediments.

关键词： phenanthrene     sorption     black carbon     sediment     Song-Liao watershed    

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Selective sorption of perfluorooctane sulfonate on molecularly imprinted polymer adsorbents

Shubo DENG, Danmeng SHUAI, Qiang YU, Jun HUANG, Gang YU

《环境科学与工程前沿（英文）》 2009年 第3卷 第2期   页码 171-177 doi: 10.1007/s11783-009-0017-4

摘要： Perfluorooctane sulfonate (PFOS), as a potential persistent organic pollutant, has been widely detected in water environments, and has become a great concern in recent years. PFOS is very stable and difficult to decompose using conventional techniques. Sorption may be an attractive method to remove it from water. In this study, the molecularly imprinted polymer (MIP) adsorbents were prepared through the polymerization of 4-vinylpyridine under different preparation conditions in order to remove perfluorooctane sulfonate (PFOS) from water. The MIP adsorbents using perfluorooctanoic acid (PFOA) as the template had good imprinting effects and could selectively remove PFOS from aqueous solution. The sorption behaviors including sorption kinetics, isotherms, and effect of pH, salt, and competitive anions were investigated. Experimental results showed that the sorption of PFOS on the MIP adsorbents was very fast, pH-dependent, and highly selective. The achieved fast sorption equilibrium within 1 h was attributed to the surface sorption on the fine adsorbents. The sorption isotherms showed that the sorption selectivity of PFOS on the MIP adsorbents decreased at high PFOS concentrations, which may be due to the double-layer sorption and the formation of PFOS micelles on the sorbent surface. The sorption of PFOS on the MIP adsorbents was mainly dominated by the electrostatic interaction between the protonated vinylpyridine on the adsorbent surface and the anionic PFOS. The prepared MIP adsorbents can potentially be applied in water and wastewater treatment for selective removal of PFOS.

关键词： perfluorooctane sulfonate (PFOS)     molecularly imprinted polymer (MIP) adsorbents     selective sorption     electrostatic interaction    

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Multi-stage ammonia production for sorption selective catalytic reduction of NO

Chen ZHANG, Guoliang AN, Liwei WANG, Shaofei WU

《能源前沿（英文）》 2022年 第16卷 第5期   页码 840-851 doi: 10.1007/s11708-021-0797-1

摘要： Sorption selective catalytic reduction of nitrogen oxides (NOx) (sorption-SCR) has ever been proposed for replacing commercial urea selective catalytic reduction of NOx (urea-SCR), while only the single-stage sorption cycle is hitherto adopted for sorption-SCR. Herein, various multi-stage ammonia production cycles is built to solve the problem of relative high starting temperature with ammonia transfer (AT) unit and help detect the remaining ammonia in ammonia storage and delivery system (ASDS) with ammonia warning (AW) unit. Except for the single-stage ammonia production cycle with MnCl2, other sorption-SCR strategies all present overwhelming advantages over urea-SCR considering the much higher NOx conversion driven by the heat source lower than 100°C and better matching characteristics with low-temperature catalysts. Furthermore, the required mass of sorbent for each type of sorption-SCR is less than half of the mass of AdBlue for urea-SCR. Therefore, the multifunctional multi-stage sorption-SCR can realize compact and renewable ammonia storage and delivery with low thermal energy consumption and high NOx conversion, which brings a bright potential for efficient commercial de-NOx technology.

关键词： selective catalytic reduction (SCR)     nitrogen oxides (NOx)     ammonia     composite sorbent     chemisorption    

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Sorption and desorption of pymetrozine on six Chinese soils

Mingxing GAO,Yingying LI,Hong YANG,Yucheng GU

《环境科学与工程前沿（英文）》 2016年 第10卷 第1期   页码 1-10 doi: 10.1007/s11783-014-0715-4

摘要： Pymetrozine is a selective insecticide with a unique chemical structure and mode to control hemipteran and homopteran. While pymetrozine has brought great benefits to crop production by killing insects, its residues in soil may have a detrimental effect on environment. Therefore, it is of great importance to investigate its behaviors in soil. In this study, the sorption and desorption of pymetrozine on six Chinese soils were investigated using a batch equilibrium approach to understand its mobile behavior in the soils. Both sorption and desorption isotherms of pymetrozine were in good agreement with the Freundlich model. The sorption coefficient varied between 3.37 and 58.32 mL?g and the sorption isotherms were nonlinear, with 1/ ranging from 0.57 to 0.91. A regression equation was proposed to predict the sorption of pymetrozine on six different soil samples: log = 4.3708 − 4.5709 × log (pH in 0.01mol·L CaCl ) + 0.4700 × log OC% + 0.0057 × sand (%) + 0.0022 × CEC(clay), with = 0.9982. The organic carbon content of soil positively affected the sorption of pymetrozine, but soil pH had a negative effect on the sorption. Additionally, effects of CaCl concentration, soil to solution ratio and pesticide form were investigated. The sorption was promoted with an increase in soil to solution ratio and a decrease in CaCl concentration. The possible variation of the five formulated products of pymetrozine was also investigated.

关键词： desorption     pymetrozine     sorption     soil    

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Effects of phosphorus concentration on Cr(VI) sorption onto phosphorus-rich sludge biochar

DING Wenchuan,PENG Wenlong,ZENG Xiaolan,TIAN Xiumei

《环境科学与工程前沿（英文）》 2014年 第8卷 第3期   页码 379-385 doi: 10.1007/s11783-013-0606-0

摘要： To investigate effects of phosphorus content on Cr(VI) sorption onto phosphorus-rich biochar, sewage sludge of different phosphorus concentrations from 4 to 60 mg·g by dry weight were prepared and carbonized to make biochar for batch sorption experiments. Test results revealed that different phosphorous concentration of raw sludge had respective impacts on surface area, pore surface area, average pore diameter and pH value of derived biochar. The adsorption kinetics of phosphorus-rich biochar could be described by the pseudo-second-order model. The sorption isotherm data followed Langmiur model better than Freundlich model. Biochar produced from sludge with phosphorus concentration of 20 mg·g gave the largest chromium sorption capacity, which could be attributed to its largest surface area and pores surface area comparing with those of biochars from sludge with other phosphorus concentrations. The chromium loaded biochar was analyzed using Fourier Transform Infrared Spectroscopy and X-ray Diffraction measurement. The results indicated that chemical functional groups hydroxyl and methyl on surface of biochar were involved in Cr(VI) binding and its reducing to Cr(III). Then, a portion of Cr(III) in form of various phosphate precipitates was bound onto biochar surface and the rest was released into the solution. The experimental results suggested that phosphorus played an important role in pore and surface area development of sludge biochar during pyrolytic process. It also could react with Cr(III) on the biochar surface that impacted on capacity of Cr(VI) removal from solution by sludge biochar. Therefore, phosphorus concentration in sludge should be considered when sludge pyrolytic residue would be reused for heavy metals sorbing.

关键词： phosphorus     biochar     sewage sludge     hexavalent chromium     adsorption    

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Sorption of tetracycline to sediments and soils: assessing the roles of pH, the presence of cadmium and

Guixiang ZHANG, Xitao LIU, Ke SUN, Ye ZHAO, Chunye LIN

《环境科学与工程前沿（英文）》 2010年 第4卷 第4期   页码 421-429 doi: 10.1007/s11783-010-0265-3

摘要： Batch sorption experiments were conducted to evaluate the sorption behavior of tetracycline (TC, H L) on sediments and soils in the presence and absence of cadmium (Cd), as affected by pH and properties of sediments and soils. The results indicated stronger nonlinearity and higher capacity of TC sorption on sediments than on soils. Sorption of TC also strongly depended on environmental factors and sediment/soil properties. Lower pH facilitated TC sorption through a cation exchange mechanism, which also took place at pH values above 5.5, where TC existed as a zwitterion (H L ) or anions (HL and L ). When pH was above 7, however, ligand-promoted dissolution of TC might occur due to TC weakening the Al-O bond of aluminum oxide and the Fe-O bond of iron oxide. Natural organic matter (NOM) plays a more important role in TC sorption than cation exchange capacity (CEC) and clay contents. The presence of Cd (II) increased TC sorption on both sediments and soils, which resulted from the decrease of equilibrium solution pH caused by Cd exchange with H ions of sediment/soil surfaces. The increase of TC sorption was also related to the formation of TC-Cd complexes, where Cd acted as a bridge between the sediment/soil and TC.

关键词： sorption     tetracycline (TC)     pH     cadmium (Cd)     antibiotic    

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Efficient elimination of environmental pollutants through sorption-reduction and photocatalytic degradation

Njud S. Alharbi, Baowei Hu, Tasawar Hayat, Samar Omar Rabah, Ahmed Alsaedi, Li Zhuang, Xiangke Wang

《化学科学与工程前沿（英文）》 2020年 第14卷 第6期   页码 1124-1135 doi: 10.1007/s11705-020-1923-z

摘要： With the rapid development of industrial, large amounts of different inorganic and organic pollutants are released into the natural environments. The efficient elimination of environmental pollutants, i.e., photocatalytic degradation of persistent organic pollutants into nontoxic organic/inorganic chemicals, solidification or sorption-reduction of heavy metal ions, is crucial to protect the environment. Nanomaterials with large surface area, active sites and abundant functional groups could form strong surface complexes with different kinds of pollutants and thereby could efficiently eliminate the pollutants from the aqueous solutions. In this review, we mainly focused on the recent works about the synthesis of nanomaterials and their applications in the efficient elimination of different organic and inorganic pollutants from wastewater and discussed the interaction mechanism from batch experimental results, the advanced spectroscopy techniques and theoretical calculations. The adsorption and the photocatalytic reduction of organic pollutants and the sorption/reduction of heavy metal ions are generally considered as the main methods to decrease the concentration of pollutants in the natural environment. This review highlights a new way for the real applications of novel nanomaterials in environmental pollution management, especially for the undergraduate students to understand the recent works in the elimination of different kinds of inorganic and organic chemicals in the natural environmental pollution management.

关键词： nanomaterials     sorption-reduction     photocatalytic degradation     organic pollutants     heavy metal ions    

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标题 作者 时间 类型 操作

Major applications of heat pipe and its advances coupled with sorption system: a review

Yang YU, Guoliang AN, Liwei WANG

期刊论文

Sorption mechanisms of diphenylarsinic acid on natural magnetite and siderite: Evidence from sorption

期刊论文

Thermodynamic study on dynamic water and organic vapor sorption on amorphous valnemulin hydrochloride

Jinbo OUYANG, Jingkang WANG, Yongli WANG, Qiuxiang YIN, Hongxun HAO

期刊论文

Simulation and experiments on a solid sorption combined cooling and power system driven by the exhaust

Peng GAO, Liwei WANG, Ruzhu WANG, Yang YU

期刊论文

Nexus between polymer support and metal oxide nanoparticles in hybrid nanosorbent materials (HNMs) for sorption

Ryan C. SMITH,Jinze LI,Surapol PADUNGTHON,Arup K. SENGUPTA

期刊论文

Diphenylarsinic acid sorption mechanisms in soils using batch experiments and EXAFS spectroscopy

Meng Zhu, Yongming Luo, Ruyi Yang, Shoubiao Zhou, Juqin Zhang, Mengyun Zhang, Peter Christie, Elizabeth L. Rylott

期刊论文

Effects of different sediment fractions on sorption of galaxolide

Lixia JIN, Mengchang HE, Jinghuan ZHANG

期刊论文

Contribution of black carbon to nonlinearity of sorption and desorption of acetochlor on sediment

Jianqiu LIU, Yaobin ZHANG, Hong CHEN, Yazhi ZHAO, Xie QUAN

期刊论文

Phenanthrene sorption to environmental black carbon in sediments from the Song-Liao watershed (China)

Jinghuan ZHANG, Mengchang HE, Chunye LIN, Ke SUN, Bin MEN, John L. ZHOU,

期刊论文

Selective sorption of perfluorooctane sulfonate on molecularly imprinted polymer adsorbents

Shubo DENG, Danmeng SHUAI, Qiang YU, Jun HUANG, Gang YU

期刊论文

Multi-stage ammonia production for sorption selective catalytic reduction of NO

Chen ZHANG, Guoliang AN, Liwei WANG, Shaofei WU

期刊论文

Sorption and desorption of pymetrozine on six Chinese soils

Mingxing GAO,Yingying LI,Hong YANG,Yucheng GU

期刊论文

Effects of phosphorus concentration on Cr(VI) sorption onto phosphorus-rich sludge biochar

DING Wenchuan,PENG Wenlong,ZENG Xiaolan,TIAN Xiumei

期刊论文

Sorption of tetracycline to sediments and soils: assessing the roles of pH, the presence of cadmium and

Guixiang ZHANG, Xitao LIU, Ke SUN, Ye ZHAO, Chunye LIN

期刊论文

Efficient elimination of environmental pollutants through sorption-reduction and photocatalytic degradation

Njud S. Alharbi, Baowei Hu, Tasawar Hayat, Samar Omar Rabah, Ahmed Alsaedi, Li Zhuang, Xiangke Wang

期刊论文