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Carbon quantum dots boost microbial biofilm-based hydrovoltaic electricity generation SCIE
期刊论文 | 2026 , 288 | WATER RESEARCH
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Abstract :

Microbial biofilm-based hydrovoltaic electricity generators (BioHEGs) have recently been developed as promising and readily available platforms for green energy harvesting, despite their unsatisfactory output performances and unspecified mechanisms regarding electric current production. Herein, carbon quantum dots (CQDs) were used to construct a nano-biohybrid system with Shewanella oneidensis MR-1 (S. oneidensis), through which the CQDs/S. oneidensis BioHEG achieved a maximum open-circuit voltage of ca. 0.65 V and short-circuit current density of ca. 5.23 mu A & sdot;cm-2. In addition, both the hydrovoltaic effect and electrical conductivity of CQDs/S. oneidensis nano-biohybrids were noticeably improved due to enhanced secretion of extracellular polymeric substances (EPS) and accelerated electron transfer upon CQDs implantation, thereby leading to a nearly 14-fold increase in output power density compared to the bare S. oneidensis cells. Studies aimed to elucidate the underlying mechanism indicated that the hybridization of CQDs and S. oneidensis greatly promoted the metabolic synthesis of outer membrane c-type cytochromes (OM c-Cyts) and the extracellular secretion of riboflavin (RF), which was demonstrated to be decisive in the current producing process of the CQDs/ S. oneidensis BioHEG. This work thus proposes a viable strategy to boost the hydrovoltaic electricity generation capacity of microbial biofilms and provides a new perspective on the mechanism of accelerated electron transfer pathways inside BioHEGs.

Keyword :

Carbon quantum dots Carbon quantum dots Hydrovoltaic electricity generation Hydrovoltaic electricity generation Metabolic synthesis Metabolic synthesis Shewanella oneidensis Shewanella oneidensis

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GB/T 7714 Chen, Ting-Ting , Yan, Zhi-Wu , Cai, Feng-Ying et al. Carbon quantum dots boost microbial biofilm-based hydrovoltaic electricity generation [J]. | WATER RESEARCH , 2026 , 288 .
MLA Chen, Ting-Ting et al. "Carbon quantum dots boost microbial biofilm-based hydrovoltaic electricity generation" . | WATER RESEARCH 288 (2026) .
APA Chen, Ting-Ting , Yan, Zhi-Wu , Cai, Feng-Ying , He, Qiu-Xiang , You, Han-Hui , Rensing, Christopher et al. Carbon quantum dots boost microbial biofilm-based hydrovoltaic electricity generation . | WATER RESEARCH , 2026 , 288 .
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Morphological regulation of sulfur-vacancy-rich CdS for tunable CO2 photoreduction under visible light irradiation SCIE
期刊论文 | 2025 , 12 (8) , 3110-3117 | INORGANIC CHEMISTRY FRONTIERS
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In this work, morphological control with a series of sulfur-vacancy-rich CdS photocatalysts has been achieved toward the optimization of their performances in CO2 photoreduction. Results show that sulfur-vacancy-rich CdS nano-platelets (p-CdS-Vs) exhibit the highest CO2 photoreduction activity with a CO yield of 4058.5 mu mol h-1 g-1, which is 10 and 6 times those of sulfur-vacancy-rich CdS nanowires (w-CdS-Vs, 372.8 mu mol h-1 g-1) and nanorods (r-CdS-Vs, 638.7 mu mol h-1 g-1), respectively, amongst the highest numbers for CdS-based photocatalysts reported hitherto. The superior CO2 photoreduction performance of p-CdS-Vs is attributable to its high efficiency of electron transport and suppressed recombination of photogenerated charge carriers. A mechanistic study indicates the critical role of surface sulfur vacancies that provide a microenvironment to trap unpaired electrons for the separation of photogenerated carriers so that the photocatalytic efficiency of CO2-to-CO reduction is largely improved in this current system.

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GB/T 7714 Qiu, Lu-Wen , Zhang, Wen-Ni , Wang, Lin-Ying et al. Morphological regulation of sulfur-vacancy-rich CdS for tunable CO2 photoreduction under visible light irradiation [J]. | INORGANIC CHEMISTRY FRONTIERS , 2025 , 12 (8) : 3110-3117 .
MLA Qiu, Lu-Wen et al. "Morphological regulation of sulfur-vacancy-rich CdS for tunable CO2 photoreduction under visible light irradiation" . | INORGANIC CHEMISTRY FRONTIERS 12 . 8 (2025) : 3110-3117 .
APA Qiu, Lu-Wen , Zhang, Wen-Ni , Wang, Lin-Ying , Li, Hao , Zhang, Tian-Kuan , Lin, Mi-Xin et al. Morphological regulation of sulfur-vacancy-rich CdS for tunable CO2 photoreduction under visible light irradiation . | INORGANIC CHEMISTRY FRONTIERS , 2025 , 12 (8) , 3110-3117 .
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一种环境水样检测装置 ipsunlight
专利 | 2025-03-03 | CN202510239213.8
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Abstract :

本发明公开了一种环境水样检测装置,属于水样检测技术领域,包括泵机构以及前端处理结构,前端处理结构包括后罩壳,后罩壳内部设有滤网单元,后罩壳的端部设有感知回控单元,外壳件上分别设有控制模块与可弹性伸缩的回弹模块,控制模块包括两个触发端子,且其中一个触发端子与回弹模块相连接。在水质检测的取样过程中,当前端处理结构中的滤网单元发生堵塞时,在泵机构的负压吸力作用下,发生弹性回缩的滤网单元接触回弹模块并通过回弹模块驱动两个触发端子接触时,触发闸阀结构往返活动并将堆积在滤网单元表面的杂质刮除,使得水样检测工作得以顺畅进行,保障水样检测效率的同时,也有利于提升水样检测结果的可靠性。

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GB/T 7714 付栋 , 邱璐雯 , 吕健 et al. 一种环境水样检测装置 : CN202510239213.8[P]. | 2025-03-03 .
MLA 付栋 et al. "一种环境水样检测装置" : CN202510239213.8. | 2025-03-03 .
APA 付栋 , 邱璐雯 , 吕健 , 何明鑫 , 温雅琪 . 一种环境水样检测装置 : CN202510239213.8. | 2025-03-03 .
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Oxygen and Bromine Vacancies Synergistically Induce Local Polarization Electric Field for Enhanced Photocatalytic Nitrogen Fixation on BiOBr SCIE
期刊论文 | 2025 , 15 (8) , 6334-6345 | ACS CATALYSIS
WoS CC Cited Count: 1
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Abstract :

The low efficiency of photogenerated charge separation significantly hinders the photocatalytic nitrogen (N2) fixation. Local polarization electric field (LPEF) induced by defects has been known to enhance charge separation, yet the synergistic effects and mechanisms related to different types of defects in pure phases remain poorly understood. In this study, defect-free bismuth oxybromide (BiOBr; BOB), together with single vacancy (BOB-VBr and BOB-VO) and dual vacancy (BOB-VBrO) analogues, were successfully synthesized, and the presence of these specific vacancies was comprehensively characterized. Notably, the dual vacancy BOB-VBrO exhibited the highest photocatalytic NH3 generation rate of 266 mu mol g-1 h-1 in a liquid-solid biphasic system, which was 6.1, 1.5, and 1.4 times higher than those of BOB, BOB-VBr, and BOB-VO, respectively. Furthermore, the NH3 generation capacity of BOB-VBrO reached an impressive rate of 978 mu mol g-1 h-1 in a gas-liquid-solid triphasic system. Photoelectrochemical tests revealed that BOB-VBrO demonstrated the highest light conversion efficiency, followed by BOB-VO, BOB-VBr, and BOB. The relative intensity of the internal electric field in BOB-VBrO was also significantly high, being 1.8, 2.4, and 3.9 times greater than those of BOB-VO, BOB-VBr, and BOB, respectively. The Br and O vacancies synergistically induced LPEF between the [O]/[Br] and [Bi] layers. In situ irradiation X-ray photoelectron spectroscopy indicated that O and Br vacancies of the oligomers could synergistically enhance the LPEF, thereby facilitating the transfer of photogenerated electrons from O/Br to Bi. Additionally, the practical feasibility of BOB-VBrO in photocatalytic N2 fixation was validated to produce liquid nitrogenous fertilizer for plant growth, revealing its potential application in agricultural production.

Keyword :

BiOBr BiOBr local polarizationelectric field local polarizationelectric field photocatalytic nitrogen fixation photocatalytic nitrogen fixation synergy mechanism synergy mechanism vacancies vacancies

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GB/T 7714 Zhong, Zhou , Zhang, Heng-Jian , Yang, Ya-Ying et al. Oxygen and Bromine Vacancies Synergistically Induce Local Polarization Electric Field for Enhanced Photocatalytic Nitrogen Fixation on BiOBr [J]. | ACS CATALYSIS , 2025 , 15 (8) : 6334-6345 .
MLA Zhong, Zhou et al. "Oxygen and Bromine Vacancies Synergistically Induce Local Polarization Electric Field for Enhanced Photocatalytic Nitrogen Fixation on BiOBr" . | ACS CATALYSIS 15 . 8 (2025) : 6334-6345 .
APA Zhong, Zhou , Zhang, Heng-Jian , Yang, Ya-Ying , Zhang, Tian-Kuan , Qu, Xing-Hua , Ma, Li et al. Oxygen and Bromine Vacancies Synergistically Induce Local Polarization Electric Field for Enhanced Photocatalytic Nitrogen Fixation on BiOBr . | ACS CATALYSIS , 2025 , 15 (8) , 6334-6345 .
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Unique heterostructures of ZnCdS nanoplates with Bi2S3−terminated edges for optimal CO2−to−CO photoconversion EI
期刊论文 | 2025 | Nano Materials Science
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Photocatalytic conversion of chemical fuels has emerged as a most challenging subject in photocatalysis which is considered as one of the sustainable solutions for environmental issues related to the energy shortage and anthropogenic carbon emissions. Herein, unique heterostructures of ZnCdS nanoplates with Bi2S3−terminated edges were prepared through a facile cation exchange pathway, by which the controlled photocatalytic CO2 conversion was achieved. The optimized BZCS–NS−5 photocatalyst exhibited an excellent capacity of CO2 photoreduction with a CO production rate of ca. 513.2 ± 5.1 μmol g−1 h−1 and a selectivity of ca. 91.0%, which were among the highest activities for sulfide photocatalysts documented in the literature. The outstanding photocatalytic performance was attributable to the formation of Z−scheme heterostrucutres between Bi2S3 and ZnCdS, in a way the separation and migration of photocarriers were accelerated. This work thus provides a feasible strategy for the construction of heterostructures to enhance the activity and selectivity of CO2−to−CO conversion via delicate design and controlled synthesis of photocatalysts. © 2022 Chongqing University

Keyword :

Bismuth compounds Bismuth compounds Carbon dioxide Carbon dioxide Heterojunctions Heterojunctions Layered semiconductors Layered semiconductors Nanostructures Nanostructures Photocatalysis Photocatalysis Semiconductor alloys Semiconductor alloys Sulfur compounds Sulfur compounds

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GB/T 7714 Zou, Zhi−Wei , Zhang, Hui−Ying , Lan, Jing−Yu et al. Unique heterostructures of ZnCdS nanoplates with Bi2S3−terminated edges for optimal CO2−to−CO photoconversion [J]. | Nano Materials Science , 2025 .
MLA Zou, Zhi−Wei et al. "Unique heterostructures of ZnCdS nanoplates with Bi2S3−terminated edges for optimal CO2−to−CO photoconversion" . | Nano Materials Science (2025) .
APA Zou, Zhi−Wei , Zhang, Hui−Ying , Lan, Jing−Yu , Luo, Jia−Hui , Xie, Yi−Chao , Li, Ya−Feng et al. Unique heterostructures of ZnCdS nanoplates with Bi2S3−terminated edges for optimal CO2−to−CO photoconversion . | Nano Materials Science , 2025 .
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Chitosan hydrogel catalyst shifts PMS activation towards a singlet oxygen-dominated non-radical pathway for efficient pollutant degradation SCIE
期刊论文 | 2025 , 525 | CHEMICAL ENGINEERING JOURNAL
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The viability and sustainability of advanced oxidation processes (AOPs) for the removal of organic pollutants are critically dependent on the catalytic efficiency, environmental compatibility, and reusability of catalysts employed. In this study, we presented a novel recyclable cobalt-incorporated MoS2 chitosan hydrogel composite (CM@CS) as an efficient AOP catalyst for the degradation of atrazine (ATZ) activated by peroxymonosulfate (PMS). The CM@CS composite demonstrated exceptional catalytic performances, particularly at low ATZ concentrations (0.1 mg/L). The degradation rate achieved nearly 100 % with 10 mg CM@CS and 0.01 mM PMS, showing superior catalytic efficacy compared to that of the Co-MoS2 (CM) powder. Besides, the CM@CS composite primarily activated PMS through a non-radical pathway dominated by singlet oxygen (1O2), distinguishing from the radical-driven mechanisms by CM catalysts. This non-radical behavior is attributed to structural and electronic modifications induced by the hydrogel matrix, including enhanced carbonyl functionality and improved charge transfer efficiency. The CM@CS composites exhibited high degradation efficiency across various water matrices due to the reliability of the non-radical pathway, minimal metal ion leaching benefited from the confinement and fixation of active sites in hydrogels, and excellent recyclability. These findings highlight CM@CS as a promising catalyst for advancing non-radical PMS activation mechanisms for applications in practical water remediation.

Keyword :

Advanced oxidation processes Advanced oxidation processes Environmental sustainability Environmental sustainability Hydrogel Hydrogel Non-radical pathway Non-radical pathway PMS PMS

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GB/T 7714 Chen, Saili , Huang, Jiajia , Fang, Han-Liang et al. Chitosan hydrogel catalyst shifts PMS activation towards a singlet oxygen-dominated non-radical pathway for efficient pollutant degradation [J]. | CHEMICAL ENGINEERING JOURNAL , 2025 , 525 .
MLA Chen, Saili et al. "Chitosan hydrogel catalyst shifts PMS activation towards a singlet oxygen-dominated non-radical pathway for efficient pollutant degradation" . | CHEMICAL ENGINEERING JOURNAL 525 (2025) .
APA Chen, Saili , Huang, Jiajia , Fang, Han-Liang , Chen, Ting-Ting , Pan, Xiaohong , Yan, Zhi-Wu et al. Chitosan hydrogel catalyst shifts PMS activation towards a singlet oxygen-dominated non-radical pathway for efficient pollutant degradation . | CHEMICAL ENGINEERING JOURNAL , 2025 , 525 .
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Bi_2WO_6/BiOI光催化降解水中四环素的性能与机理
期刊论文 | 2024 , 44 (02) , 83-92 | 环境科学学报
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采用溶剂热法合成Bi_2WO_6/BiOI(BWO/BOI)复合光催化剂,并将其应用于可见光降解四环素(Tetracycline,TC).结果表明,BWO/BOI复合光催化剂与单一的Bi_2WO_6相比具有更好的光催化降解TC的性能.其中,结构优化后的BWO/BOI-4在60 min内光催化降解TC的效率达85.8%,其反应速率常数为Bi_2WO_6的1.7倍、BiOI的7.8倍.且BWO/BOI催化剂可在宽泛的pH范围(2.0~12.0)内保持优异的降解效率.能带结构分析表明,BWO/BOI构成Ⅱ型异质结,更有利于e~-和h~+的有效分离.通过自由基猝灭实验和电子顺磁共振(EPR)测试发现,在光催化体系中超氧自由基(·O_2~-)是反应的主要活性物种.

Keyword :

光催化 光催化 四环素 四环素 异质结 异质结 碘氧化铋 碘氧化铋 钨酸铋 钨酸铋

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GB/T 7714 邱璐雯 , 魏璐英 , 陈锦琳 et al. Bi_2WO_6/BiOI光催化降解水中四环素的性能与机理 [J]. | 环境科学学报 , 2024 , 44 (02) : 83-92 .
MLA 邱璐雯 et al. "Bi_2WO_6/BiOI光催化降解水中四环素的性能与机理" . | 环境科学学报 44 . 02 (2024) : 83-92 .
APA 邱璐雯 , 魏璐英 , 陈锦琳 , 郑雪 , 张宇晴 , 吕健 . Bi_2WO_6/BiOI光催化降解水中四环素的性能与机理 . | 环境科学学报 , 2024 , 44 (02) , 83-92 .
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Performance and mechanism of photocatalytic tetracycline degradation by Bi2WO6/MIL-101in water. EI
期刊论文 | 2024 , 44 (8) , 4652-4660 | China Environmental Science
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The Bi2WO6/MIL-101composite photocatalysts were synthesized via a hydrothermal method to facilitate the degradation of tetracycline (TC) under visible light. Research findings demonstrated that the TC degradation efficiency of Bi2WO6 under visible light was significantly enhanced following the dense growth of BWO nanosheets on the surface of MIL-101. Furthermore, the structurally optimized BWO/MIL-101-40exhibited a TC degradation efficiency of 85.9% within 60minutes, with a reaction rate constant approximately 1.4 times that of Bi2WO6 and 3.1times that of MIL-101. Additionally, BWO/MIL-101 displayed consistent and robust photocatalytic performance in neutral and alkaline conditions. Band structure analysis revealed the formation of type II heterojunctions between Bi2WO6 and MIL-101, contributing to effective photoelectron-hole separation. Quenching experiments and electron paramagnetic resonance (EPR) tests indicated superoxide radical (•O2–) and holes (h+) as the primary active species in this particular photocatalytic system. © 2024 Chinese Society for Environmental Sciences. All rights reserved.

Keyword :

Bioremediation Bioremediation Bismuth compounds Bismuth compounds Catalytic cracking Catalytic cracking Electron spin resonance spectroscopy Electron spin resonance spectroscopy Free radical reactions Free radical reactions Laser beams Laser beams Metal-Organic Frameworks Metal-Organic Frameworks Paramagnetic resonance Paramagnetic resonance Photocatalytic activity Photocatalytic activity Photodegradation Photodegradation Rate constants Rate constants Tungsten compounds Tungsten compounds

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GB/T 7714 Cai, Feng-Ying , Xu, Yu-Hang , Long, Hao-Ran et al. Performance and mechanism of photocatalytic tetracycline degradation by Bi2WO6/MIL-101in water. [J]. | China Environmental Science , 2024 , 44 (8) : 4652-4660 .
MLA Cai, Feng-Ying et al. "Performance and mechanism of photocatalytic tetracycline degradation by Bi2WO6/MIL-101in water." . | China Environmental Science 44 . 8 (2024) : 4652-4660 .
APA Cai, Feng-Ying , Xu, Yu-Hang , Long, Hao-Ran , Yuan, Yu-Xin , Zhang, Yu-Qing , He, Qiu-Xiang et al. Performance and mechanism of photocatalytic tetracycline degradation by Bi2WO6/MIL-101in water. . | China Environmental Science , 2024 , 44 (8) , 4652-4660 .
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Highly efficient degradation and detoxification of antibiotics over C-Dots/ siderite heteroaggregates in photo-Fenton systems: The crucial role of C-Dots SCIE
期刊论文 | 2024 , 349 | SEPARATION AND PURIFICATION TECHNOLOGY
WoS CC Cited Count: 2
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The substantial presence of antibiotics in aquatic environments remains as a critical environmental issue that needs to be urgently addressed. In this study, mimetics of C-Dots/siderite heteroaggregates (CSI) were studied in a visible-light-responsive Fenton system as a platform for the degradation of antibiotics in contaminated water. By virtue of the excellent electron transfer of C-Dots, the sustained conversion cycles of Fe(II) -* Fe(III) -* Fe(II) in CSI were greatly accelerated, and meanwhile the H2O2 utilization was enhanced. The optimized CSI-3 nanocomposite displayed a prominent degradation efficiency towards a series of tetracycline analogs at ppb levels. Density functional theory (DFT) calculations indicated the excellent photo-Fenton catalytic performance of CSI originated from the increased d-band center and electron density, which considerably improves the utilization of H2O2. Both experimental and theoretical studies revealed that the correlated toxicity of degradation intermediates was significantly decreased. Additionally, a continuous flow device integrating the CSI photoFenton system maintained a high degradation efficiency after long-term treatment of simulated chlortetracycline wastewater. The presented work thereby confirms a spontaneous remediation process for the decontamination and detoxification of persistent organic pollutants under the action of heteroaggregates formed by engineered nanoparticles and natural minerals.

Keyword :

Carbon quantum dot Carbon quantum dot Catalytic degradation Catalytic degradation Siderite Siderite Tetracycline Tetracycline

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GB/T 7714 Xu, Yu-Hang , Long, Hao-Ran , Fang, Han-Liang et al. Highly efficient degradation and detoxification of antibiotics over C-Dots/ siderite heteroaggregates in photo-Fenton systems: The crucial role of C-Dots [J]. | SEPARATION AND PURIFICATION TECHNOLOGY , 2024 , 349 .
MLA Xu, Yu-Hang et al. "Highly efficient degradation and detoxification of antibiotics over C-Dots/ siderite heteroaggregates in photo-Fenton systems: The crucial role of C-Dots" . | SEPARATION AND PURIFICATION TECHNOLOGY 349 (2024) .
APA Xu, Yu-Hang , Long, Hao-Ran , Fang, Han-Liang , Wei, Lu-Ying , Cai, Feng-Ying , Rensing, Christopher et al. Highly efficient degradation and detoxification of antibiotics over C-Dots/ siderite heteroaggregates in photo-Fenton systems: The crucial role of C-Dots . | SEPARATION AND PURIFICATION TECHNOLOGY , 2024 , 349 .
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蝇蛆预处理及辅料添加对鸡粪堆肥氨挥发和温室气体排放的影响
期刊论文 | 2024 , 43 (05) , 1151-1162 | 农业环境科学学报
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为明确蝇蛆预处理及辅料添加对鸡粪堆肥过程中NH_3挥发及温室气体排放的影响,本研究分别将风化褐煤、厨余垃圾、蘑菇渣与鸡粪混合,在进行蝇蛆预处理后堆肥,研究试验过程中NH_3挥发和温室气体的排放规律。试验设置8个处理,分别为对照组(无蝇蛆预处理):纯鸡粪(CK1)、30%风化褐煤+70%鸡粪(CK2)、30%厨余垃圾+70%鸡粪(CK3)、30%蘑菇渣+70%鸡粪(CK4);试验组(蝇蛆预处理):纯鸡粪(T1)、30%风化褐煤+70%鸡粪(T2)、30%厨余垃圾+70%鸡粪(T3)、30%蘑菇渣+70%鸡粪(T4)。结果表明:蝇蛆预处理能够延长堆肥高温期,≥50℃天数均达到10 d以上,相比CK1增加5~9 d;在整个试验期间试验组NH_3挥发集中在堆肥第2天,试验组NH_3累积排放量显著低于对照组,降幅达到42.7%~61.1%,菇渣添加处理的NH_3累积排放量在对照组中最低;风化褐煤的添加能够显著降低N_2O排放,T2相比于T1降低84.2%,CK2相比于CK1降低51.7%。蝇蛆预处理能够显著降低CO_2排放当量,相比CK1降低32.1%~73.2%,其中,T4的CO_2排放当量最低。研究表明,蝇蛆预处理能够提高堆肥温度、延长堆肥高温期、显著降低NH_3排放和CO_2排放当量,若从堆肥温度及CO_2排放当量方面考虑蝇蛆预处理和菇渣组合为最优处理。

Keyword :

厨余垃圾 厨余垃圾 好氧堆肥 好氧堆肥 氨挥发 氨挥发 温室气体减排 温室气体减排 蝇蛆预处理 蝇蛆预处理

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GB/T 7714 刘尚斌 , 郑祥洲 , 王煌平 et al. 蝇蛆预处理及辅料添加对鸡粪堆肥氨挥发和温室气体排放的影响 [J]. | 农业环境科学学报 , 2024 , 43 (05) : 1151-1162 .
MLA 刘尚斌 et al. "蝇蛆预处理及辅料添加对鸡粪堆肥氨挥发和温室气体排放的影响" . | 农业环境科学学报 43 . 05 (2024) : 1151-1162 .
APA 刘尚斌 , 郑祥洲 , 王煌平 , 吴一群 , 吕健 , 张玉树 . 蝇蛆预处理及辅料添加对鸡粪堆肥氨挥发和温室气体排放的影响 . | 农业环境科学学报 , 2024 , 43 (05) , 1151-1162 .
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