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Insight into the experiment and extraction mechanism for separating carbazole from anthracene oil with quaternary ammonium-based deep eutectic solvents
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作者 Xudong Zhang Yanhua Liu +4 位作者 Jun Shen Yugao Wang Gang Liu Yanxia Niu Qingtao Sheng 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2024年第1期188-199,共12页
Carbazole is an irreplaceable basic organic chemical raw material and intermediate in industry.The separation of carbazole from anthracene oil by environmental benign solvents is important but still a challenge in che... Carbazole is an irreplaceable basic organic chemical raw material and intermediate in industry.The separation of carbazole from anthracene oil by environmental benign solvents is important but still a challenge in chemical engineering.Deep eutectic solvents (DESs) as a sustainable green separation solvent have been proposed for the separation of carbazole from model anthracene oil.In this research,three quaternary ammonium-based DESs were prepared using ethylene glycol (EG) as hydrogen bond donor and tetrabutylammonium chloride (TBAC),tetrabutylammonium bromide or choline chloride as hydrogen bond acceptors.To explore their extraction performance of carbazole,the conductor-like screening model for real solvents (COSMO-RS) model was used to predict the activity coefficient at infinite dilution (γ^(∞)) of carbazole in DESs,and the result indicated TBAC:EG (1:2) had the stronger extraction ability for carbazole due to the higher capacity at infinite dilution (C^(∞)) value.Then,the separation performance of these three DESs was evaluated by experiments,and the experimental results were in good agreement with the COSMO-RS prediction results.The TBAC:EG (1:2) was determined as the most promising solvent.Additionally,the extraction conditions of TBAC:EG (1:2) were optimized,and the extraction efficiency,distribution coefficient and selectivity of carbazole could reach up to 85.74%,30.18 and 66.10%,respectively.Moreover,the TBAC:EG (1:2) could be recycled by using environmentally friendly water as antisolvent.In addition,the separation performance of TBAC:EG (1:2) was also evaluated by real crude anthracene,the carbazole was obtained with purity and yield of 85.32%,60.27%,respectively.Lastly,the extraction mechanism was elucidated byσ-profiles and interaction energy analysis.Theoretical calculation results showed that the main driving force for the extraction process was the hydrogen bonding ((N–H...Cl) and van der Waals interactions (C–H...O and C–H...π),which corresponding to the blue and green isosurfaces in IGMH analysis.This work presented a novel method for separating carbazole from crude anthracene oil,and will provide an important reference for the separation of other high value-added products from coal tar. 展开更多
关键词 CARBAZOLE Model anthracene oil Deep eutectic solvents COSMO-RS Extraction mechanism
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Surfactant-assisted hydrothermally synthesized MoS_2 samples with controllable morphologies and structures for anthracene hydrogenation 被引量:9
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作者 李敏 王冬娥 +5 位作者 李佳鹤 潘振栋 马怀军 姜玉霞 田志坚 陆安慧 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 北大核心 2017年第3期597-606,共10页
MoS_2 samples with controllable morphologies and structures were synthesized using surfactantassisted hydrothermal processes.The effects of surfactants(PEG,PVP,P123,SDS,AOT,and CTAB)on the morphologies and structure... MoS_2 samples with controllable morphologies and structures were synthesized using surfactantassisted hydrothermal processes.The effects of surfactants(PEG,PVP,P123,SDS,AOT,and CTAB)on the morphologies and structures of MoS_2 samples were investigated.The results revealed that spherical,bulk-like,and flower-like MoS_2 particles assembled by NH4~+-intercalated MoS_2 nano-sheets were synthesized.The morphologies of the MoS_2 samples and their structures(including the slab length and the number of stacked layers) of MoS_2 nano-sheets in these samples could be controlled by adjusting the surfactants.Mono-dispersed spherical MoS_2 particles could be synthesized with PEG via the creation of MoS_2 nano-sheets with slab lengths shorter than 15 nm and fewer than six stacked layers.Possible formation mechanisms of these MoS_2 samples created via surfactant-assisted hydrothermal processes are proposed.Further,the catalytic activities of MoS_2 samples for anthracene hydrogenation were evaluated in a slurry-bed reactor.The catalyst synthesized with the surfactant PEG exhibited the highest catalytic hydrogenation activity.Compared with the other catalysts,it had a smaller particle size,mono-dispersed spherical morphology,shorter slab length,and fewer stacked layers;these were all beneficial to exposing its active edges.This work provides an efficient approach to synthesize transition metal sulfides with controllable morphologies and structures. 展开更多
关键词 Molybdenum sulfide Surfactant-assisted Controllable morphology Mono-dispersed Active edges anthracene hydrogenation
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Interlayer Energy Transfer from Naphthalene to Anthracene Chromophores Organized in Langmuir-Blodgett Films 被引量:3
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作者 LiQianLI ChiMingCHE 《Chinese Chemical Letters》 SCIE CAS CSCD 2002年第1期49-52,共4页
Interlayer energy transfer between 2, 3-naphtho-10-hexadecylaza-15-crown-5 (NC16) and N-[1-(9-methoxyanthryl)]decylaza-15-crown-5 (A10C) within multilayer Langmuir-Blodgett films has been studied by steady-state fluor... Interlayer energy transfer between 2, 3-naphtho-10-hexadecylaza-15-crown-5 (NC16) and N-[1-(9-methoxyanthryl)]decylaza-15-crown-5 (A10C) within multilayer Langmuir-Blodgett films has been studied by steady-state fluorescence spectra. The donor and acceptor could be separated precisely by inserting stearic acid (SA) spacers. The efficiency of the energy transfer increases with the decrease in the donor-acceptor distance by a quadratic manner, suggesting the donor excitations are delocalized in the layer. 展开更多
关键词 Energy transfer L-B film NAPHTHALENE anthracene.
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Isolation and purification of carbazole contained in anthracene slag by extraction combined with medium pressure liquid chromatography 被引量:1
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作者 Zhihao Ma XianyongWei +5 位作者 Mingyao Zhou Guanghui Liu Fangjing Liu Zhongqiu Liu Xinyue Yu Zhimin Zong 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2019年第12期2925-2929,共5页
Ultrasonic-assisted extraction(UAE)combined with medium pressure liquid chromatography(MPLC)was designed for carbazole separation from anthracene slag(AS).The effects of liquid/solid ratio,temperature,and extraction t... Ultrasonic-assisted extraction(UAE)combined with medium pressure liquid chromatography(MPLC)was designed for carbazole separation from anthracene slag(AS).The effects of liquid/solid ratio,temperature,and extraction times on carbazole separation were investigated.When using CC14 and ethyl acetate as extraction solvents and combining with MPLC,carbazole recovery and purity are 75.1%and 95.4%,respectively.The mechanism for carbazole separation were presumed by examining intermolecular interactions such as N-H…π,π-π,and C-Cl…πinteractions.These results demonstrate that UAE/MPLC has a considerable potential as a green and promising strategy for separating and purifying carbazole and other chemicals from AS. 展开更多
关键词 anthracene SLAG ULTRASONIC-ASSISTED EXTRACTION Medium pressure liquid chromatography INTERMOLECULAR interactions
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Fluorescence Quenching of Anthracene by N,N-Diethylaniline and Phenothiazine in Triton X-100/n-C_(10)H_(21) OH/H_2O Microemulsion 被引量:1
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作者 GUO Xia XU Hui GUO Rong 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2003年第4期484-488,共5页
The photo-induced electron transfer reactions of anthracene with N,N -diethylaniline(DEA) and phenothiazine(PTZ) occur in the membrane phase of a Triton X-100/ n -C 10 H 21 OH(1-decanol)/H 2O microemulsion. DEA and PT... The photo-induced electron transfer reactions of anthracene with N,N -diethylaniline(DEA) and phenothiazine(PTZ) occur in the membrane phase of a Triton X-100/ n -C 10 H 21 OH(1-decanol)/H 2O microemulsion. DEA and PTZ exist in the membrane phase of the microemulsion. Anthracene exists in the oil continuous phase of the W/O microemulsion and in the oil core and membrane phase of the O/W microemulsion. 展开更多
关键词 Electron transfer process Fluorescence quenching anthracene Phenothiazine N N -dieth\|ylaniline MICROEMULSION
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Effect of Anthracene on the Interaction Between Platymonas helgolandica var. tsingtaoensis and Heterosigma akashiwo in Laboratory Cultures
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作者 BI Rong WANG You +2 位作者 WANG Renjun LI Wei TANG Xuexi 《Journal of Ocean University of China》 SCIE CAS 2015年第1期105-113,共9页
Two species of marine phytoplankton, Platymonas helgolandica var. tsingtaoensis and Heterosigma akashiwo, were cul- tivated in bi-algal cultures to investigate the effect of anthracene (ANT) on the interaction betwe... Two species of marine phytoplankton, Platymonas helgolandica var. tsingtaoensis and Heterosigma akashiwo, were cul- tivated in bi-algal cultures to investigate the effect of anthracene (ANT) on the interaction between them. Without ANT, H. akashiwo out-competed P. helgolandica at low initial biomass ratios (P. helgolandica (P): H. akashiwo (H) = 1:4 and 1 : 1), but not at the highest (P:H=4:I). This observation was consistent with the description in Lotka-Volterra two species competition model. It was found that P. helgolandica was excluded at low initial biomass ratios, while the unstable equilibrium between two species was predicted at the highest. For both species, carrying capacity and maximal specific growth rate decreased in bi-algal cultures compared to those in monocultures. H. akashiwo exhibited a higher sensitivity to ANT than P helgolandica. This resulted markedly in a reduced cell den- sity of H. akashiwo but an increased cell density ofP. helgolandica. Carrying capacity ofP. helgolandica was consistently higher in bi-algal cultures with ANT than those without ANT, suggesting that ANT, through the elimination of H. akashiwo, generated the dominance of P helgolandica independently of initial biomass ratios. This study showed a density-dependent effect of harmful alga (H. akashiwo) on dietary alga (P helgolandica), and indicated that ocean pollutant ANT could induce the succession of marine phytoplankton. 展开更多
关键词 anthracene interspecific competition PHYTOPLANKTON population growth
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Establishment and evaluation of a mouse model of skin squamous cell carcinoma induced by 7, 12-dimethyl-benzodiazepine [a] anthracene at high dose
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作者 Nan Liu Ao Wang Yan-Ping Bai 《Journal of Hainan Medical University》 2020年第2期12-16,共5页
Objective: To establish a mouse model of skin squamous cell carcinoma induced by high dose 7, 12-dimethyl-benzodiazepine [a] anthracene, and to provide experimental basis for the prevention and treatment of skin squam... Objective: To establish a mouse model of skin squamous cell carcinoma induced by high dose 7, 12-dimethyl-benzodiazepine [a] anthracene, and to provide experimental basis for the prevention and treatment of skin squamous cell carcinoma. Methods: 36 BALB/c mice were randomly divided into 3 groups, respectively is: the high dose group (group A), low dose group (group B), and blank control group (group c), recorded in the process of building body weight in mice, and skin changes back, local skin tissue for building after HE staining of PCNA immunohistochemical staining, and the expression of PCNA positive staining level as reflected in mice skin squamous cell carcinoma of the malignant indicators, using the Image Pro Plus calculation PCNA staining of integral optical density (IOD) and positive area, and the results were statistically analyzed. Results: at 12 weeks, there were statistically significant differences in tumor number and tumor volume between group A and group B (P<0.05), and the tumor bearing rate was up to 83.3% and 66.7%, and the incidence of SCC was up to 75% and 33.3%. Immunohistochemical analysis showed statistical differences in IOD and positive area of mice in groups A, B and C (P<0.01). Conclusion: compared with the mouse model of skin squamous cell carcinoma established by the traditional two-stage protocol, this model has the characteristics of shorter experimental period, higher tumor formation rate and easier operation, providing a reliable experimental basis for the study of skin squamous cell carcinoma. 展开更多
关键词 squamous cell carcinoma DMBA 7 12-dimethyl-benzodiazepine[a] anthracene Mouse model
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Electrocarboxylation of Anthrone to Anthracene-9-carboxylic Acid in the Presence of CO_2 被引量:1
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作者 ZHANG Li WANG Huan +2 位作者 ZHAO Jian-qing CHEN Bao-li LU Jia-xing 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2011年第6期1027-1030,共4页
Electrocarboxylation of anthrone in the presence of CO2 to anthrance-9-carboxylic acid directly was carried out. The electroreduction behavior of anthrone was examined by cyclic voltammetry in the absence and presence... Electrocarboxylation of anthrone in the presence of CO2 to anthrance-9-carboxylic acid directly was carried out. The electroreduction behavior of anthrone was examined by cyclic voltammetry in the absence and presence of CO2. Then the influences of the supporting electrolytes, temperature, electrode material and anthrone concentration on the carboxylation yield were investigated. Under the optimized conditions, anthrancene-9-carboxylic acid was obtained in a good yield(96.1%). 展开更多
关键词 anthracene-9-carboxylic acid ANTHRONE Carbon dioxide ELECTROCARBOXYLATION
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Charge Transport Properties of Tetrabenz[a,c,h,j]-anthracene Derivatives 被引量:3
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作者 陈自然 余文浩 李权 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2012年第6期851-856,共6页
Charge transport properties of F, OH, OCH3, SH and SCH3-substituted tetra- benz[a,c,h,j]- anthracene derivative molecules have been investigated theoretically at the B3LYP/6-31G** level using Marcus theory. The resu... Charge transport properties of F, OH, OCH3, SH and SCH3-substituted tetra- benz[a,c,h,j]- anthracene derivative molecules have been investigated theoretically at the B3LYP/6-31G** level using Marcus theory. The results showed that at 300 K, the hole or electron transport capability of F or SH-substituted molecules was better obviously than that of OH or OCH3-substituted molecules, The electron transport capability of SCH3-substituted and F or SH-substituted molecules was superior to their hole transport capability, respectively. F, SH or SCH3-substituted tetrabenz[a,c,h,j]-anthracene derivative molecules can be used as electron transport materials. 展开更多
关键词 tetrabenz[a c h j]-anthracene charge transport marcus theory theoretical calculation
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A Two-dimensional Anthracene-9,10-dicarboxylate Zinc(Ⅱ) Coordination Polymer Based on Binuclear [Zn_2Cl_2] Nodes: Synthesis, Characterization and Luminescent Properties 被引量:2
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作者 王军杰 张仁春 +2 位作者 张道军 常泽 章应辉 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2014年第5期695-700,共6页
A two-dimensional(2D) 44 topological ZnⅡ coordination polymer {[Zn2Cl2(L)(4bpy)2]}∞(H2L = anthracene-9,10-dicarboxylic acid, 4bpy = 4,4ˊ-bipyridine) based on binuclear [Zn2Cl2] nodes has been synthesized an... A two-dimensional(2D) 44 topological ZnⅡ coordination polymer {[Zn2Cl2(L)(4bpy)2]}∞(H2L = anthracene-9,10-dicarboxylic acid, 4bpy = 4,4ˊ-bipyridine) based on binuclear [Zn2Cl2] nodes has been synthesized and characterized by IR, elemental analysis, X-ray powder diffraction and single-crystal X-ray diffraction analysis. Moreover, the luminescent properties of the correspon- ding compound have been briefly investigated. 展开更多
关键词 zinc(Ⅱ) coordination polymer anthracene-9 10-dicarboxylic acid binuclear [Zn2Cl2] nodes luminescent properties
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ELECTRON TRANSFER AND PHOTOCHEMICAL VALENCE ISOMERIZATION IN ANTHRACENE AND NORBORNADIENE SYSTEMS
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作者 Bao Wen ZHANG Wen Yuan QIAN Qian Hong WU Yi CAO Lab.of Photochem.,Institute of Photographic Chemistry Academia Sinica,Beijing 100101. 《Chinese Chemical Letters》 SCIE CAS CSCD 1993年第8期711-714,共4页
To harvest the sun light and to promote the amount of energy stored,a new binary compound which links a sensitizer(electron donor), anthracene,and substrate(electron acceptor),norbornadiene,in a non- conjugated manner... To harvest the sun light and to promote the amount of energy stored,a new binary compound which links a sensitizer(electron donor), anthracene,and substrate(electron acceptor),norbornadiene,in a non- conjugated manner without increase in molecular weight was synthesized.The inter-and intramolecular photosensitized isomerization and the mechanism were studied. 展开更多
关键词 ELECTRON TRANSFER AND PHOTOCHEMICAL VALENCE ISOMERIZATION IN anthracene AND NORBORNADIENE SYSTEMS
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SYNTHESIS OF 1,2-ACEANTHRYLENEDIONE THROUGH ACYLATION OF ANTHRACENE WITH OXALYL CHLORIDE
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作者 ZHANG Chunyan CHEN Min +2 位作者 YU Long JIANG Deli YAN Yongsheng 《Chinese Journal of Reactive Polymers》 2007年第1期61-65,共5页
Acylation of anthracene and oxalyl chloride in the presence of anhydrous AlCl3 was investigated. Pure 1,2-aceanthrylenedione, which is used as new functional macromolecule, was prepared by extraction and recrystallati... Acylation of anthracene and oxalyl chloride in the presence of anhydrous AlCl3 was investigated. Pure 1,2-aceanthrylenedione, which is used as new functional macromolecule, was prepared by extraction and recrystallation. The structure of 1,2-aceanthrylenedione was identified by measure of melting point, GC/MS, FTIR and 1HNMR analyses. The influences of various parameters, such as solvent, dosage of catalyst, molar ratio of anthracene to oxalyl chloride, reaction temperature, and reaction time were studied. The anhydrous AlCl3 was found to catalyze the reaction with high yeild and good selectivity. When the reaction temperature is 303K, reaction time is 5h and molar ratio of anthracene to oxalyl chloride is 1:2, the yield and selectivity of 1,2-aceanthrylenedione is 83.8 % and 92.3% respectively. 展开更多
关键词 Functional macromolecule intermediate 1 2-aeanthrylenedione anthracene ACYLATION Anhydrous AlCl3.
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EPR Study of the Thermal Decomposition of Transannular Peroxide of Anthracene
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作者 Lubomir Lapcik Jr. Barbora Lapcikova Andrej Stasko 《International Journal of Organic Chemistry》 2011年第2期37-40,共4页
Thermal decomposition of transannular peroxide of anthracene (POA) (or 9,10-epidioxido anthracene) was studied by means of electron paramagnetic resonance spectroscopy (EPR) in the solid as well as in the liquid phase... Thermal decomposition of transannular peroxide of anthracene (POA) (or 9,10-epidioxido anthracene) was studied by means of electron paramagnetic resonance spectroscopy (EPR) in the solid as well as in the liquid phases. Decomposition process proceeds via cleavage of the O-O bridge of the POA molecule, generating thus an alcoxy intermediate radical. Its concentration increases to a certain equilibrium stage during the time scale of the experiment. EPR spectra in the solid state were of the singlet type at the temperatures over 350 K, a doublet like anisotropic spectra were measured at the room temperature, both having g-value 2.0033. EPR spectrum from POA decomposed in benzene indicates four protons with higher (2aH = 0.305 mT, 2aH = 0.335 mT) and four protons with a lower (2aH = 0.075 mT, 2aH = 0.105 mT) splitting constants, corresponding well the radical expected after cleavage of O-O bridge. 展开更多
关键词 ENDOPEROXIDE anthracene Free Radicals EPR DECOMPOSITION KINETICS
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A Novel Palladium(Ⅱ)Complex Self-assembled from Anthracene-9-carboxylic Acid:Synthesis,Crystal Structure and Spectroscopic Properties
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作者 代爽 蒋选丰 +1 位作者 童金 于澍燕 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2013年第10期1530-1536,共7页
A novel palladium(II) complex [(TMEDA)Pd(anca)2].2DMSO (1, TMEDA = N,N,N',N'-tetramethylethylethylenediamine, anca = anthracene-9-carboxylic acid) was synthesized and characterized by single-crystal X-ray di... A novel palladium(II) complex [(TMEDA)Pd(anca)2].2DMSO (1, TMEDA = N,N,N',N'-tetramethylethylethylenediamine, anca = anthracene-9-carboxylic acid) was synthesized and characterized by single-crystal X-ray diffraction, 1H NMR, UV-Vis and fluorescence spectroscopy. The cell belongs to orthorhombic Aba2 space group with a = 19.698(7), b = 21.045(7) c = 9.062(3) A, Z = 4, V= 3757(2) A3, C40H46N206PdS2, Mr = 821.31, D, = 1.452 g/cm3, F(000) = 1704, the final R = 0.0272, wR = 0.0667 and GOOF = 0.999. Complex 1 exhibits an interesting distorted clip-shaped molecular configuration which is stabilized by intramolecular C-H...O hydrogen bonds. The cells are packed into a 3D supramolecular structure based on the intermolecular C-H...zr interactions which further construct the tubular channels serving as guest molecular channels to include the DMSO solvent molecules inside. Furthermore, the spectroscopic properties of 1 were also investigated. 展开更多
关键词 palladium(II) complex anthracene-9-carboxylic acid SELF-ASSEMBLY crystal structure spectroscopic property
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吉西他滨联合顺铂方案治疗复发性三阴性乳腺癌的疗效观察 被引量:1
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作者 申鹏 刘正义 +2 位作者 闫园 于博凡 于洋 《中国合理用药探索》 CAS 2024年第2期62-68,共7页
目的:探究吉西他滨联合顺铂方案在蒽环、紫杉类药物治疗后复发性三阴性乳腺癌(TNBC)患者中的应用效果。方法:选取2019年1月~2021年1月期间某院收治的81例蒽环、紫杉类药物治疗后复发性TNBC患者作为研究对象,采用随机、单盲试验研究方法... 目的:探究吉西他滨联合顺铂方案在蒽环、紫杉类药物治疗后复发性三阴性乳腺癌(TNBC)患者中的应用效果。方法:选取2019年1月~2021年1月期间某院收治的81例蒽环、紫杉类药物治疗后复发性TNBC患者作为研究对象,采用随机、单盲试验研究方法,依据随机数字表法分为A组(n=40)和B组(n=41)。A组患者给予注射用盐酸吉西他滨联合卡培他滨片治疗,B组患者给予注射用盐酸吉西他滨联合注射用顺铂治疗。比较两组临床疗效、血清肿瘤标志物[癌胚抗原(CEA)、糖类抗原153(CA153)、糖类抗原125(CA125)]水平变化、生活质量情况[欧洲癌症研究与治疗组织生命质量量表(EORTC QLQ-C30)]、不良反应发生情况及治疗后2年内患者的预后情况。结果:治疗后,B组治疗总有效率(82.93%)高于A组(60.00%,P<0.05)。两组血清CEA、CA153、CA125水平均降低(P<0.05),且B组低于A组(P<0.05)。两组EORTC QLQ-C30评分在疲劳、失眠方面均降低(P<0.05),且B组低于A组(P<0.05);两组EORTC QLQ-C30评分在总体健康方面均升高(P<0.05),且B组高于A组(P<0.05);两组EORTC QLQ-C30评分在恶心呕吐、食欲丧失、便秘方面比较无统计学差异(P>0.05)。两组患者治疗期间不良反应总发生率比较无统计学差异(P>0.05)。B组患者2年内复发率(14.63%)低于A组(40.00%,P<0.05),中位无进展生存期[(6.65±1.45)个月]长于A组[(4.26±1.23)个月,P<0.05],稳定病例数(58.54%)高于A组(30.00%,P<0.05)。结论:与吉西他滨联合卡培他滨相比,吉西他滨联合顺铂治疗方案在蒽环、紫杉类药物治疗后复发性TNBC患者中临床疗效更佳,可有效降低患者血清肿瘤标志物水平,提高生活质量,改善预后。 展开更多
关键词 吉西他滨 顺铂 蒽环 紫杉类药物 三阴性乳腺癌 复发
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基于蒽核深蓝光材料的合成及电致发光性能
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作者 张越华 邢龙江 +7 位作者 聂飞 陈文铖 穆英啸 彭少洪 何念 孙宇曦 曾庆明 霍延平 《发光学报》 EI CAS CSCD 北大核心 2024年第2期269-279,共11页
以蒽作为三线态‐三线态湮灭(TTA)型蓝光材料的基元,通过在蒽的9和10位分别引入弱给电子基团二苯并噻吩和弱吸电子基团苯氰,设计合成了两个给体‐受体型深蓝光TTA材料4‐(10‐(二苯并[b,d]噻吩‐4‐基)蒽‐9‐基)苯腈(2)和4‐(10‐(二苯... 以蒽作为三线态‐三线态湮灭(TTA)型蓝光材料的基元,通过在蒽的9和10位分别引入弱给电子基团二苯并噻吩和弱吸电子基团苯氰,设计合成了两个给体‐受体型深蓝光TTA材料4‐(10‐(二苯并[b,d]噻吩‐4‐基)蒽‐9‐基)苯腈(2)和4‐(10‐(二苯并[b,d]噻吩‐2‐基)蒽‐9‐基)苯腈(3),并对它们的热稳定性、电化学性质、光物理性质及电致发光性质进行了系统表征。在纯膜状态下,两个化合物的光致发光峰分别位于445 nm和451 nm处,光致发光量子产率分别为40.2%和57.9%。基于化合物2和3的非掺杂器件的电致发光峰分别位于448 nm和458 nm处,实现了深蓝光发射。两个器件获得了较好的发光效率,其最大电流效率分别为4.2 cd·A^(-1)和6.9 cd·A^(-1),最大功率效率分别为2.3 lm·W^(-1)和3.6 lm·W^(-1),最大外量子效率分别为3.8%和5.6%。即使在1 000 cd·m^(-2)亮度下,两个器件的外量子效率依然保持在3.7%和5.4%,表现出极低的效率滚降。 展开更多
关键词 二苯并噻吩 苯氰 深蓝光TTA材料
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二氧化铅电极改性及电催化降解焦化废水中蒽
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作者 章丽萍 袁合霞 +4 位作者 安逸云 王晶 段梦楠 雷文波 王丽芳 《矿业科学学报》 CSCD 北大核心 2024年第2期286-294,共9页
为了研究电催化对焦化废水中污染物的降解效果,采用电沉积法制备了Ti/PbO_(2)、Ti/PANI/PbO_(2)和Ti/PANI/PbO_(2)-Ce三种电极,对电极进行扫描电镜和X射线衍射表征、电化学性能测试、产羟基自由基(·OH)能力测试和加速寿命测试。结... 为了研究电催化对焦化废水中污染物的降解效果,采用电沉积法制备了Ti/PbO_(2)、Ti/PANI/PbO_(2)和Ti/PANI/PbO_(2)-Ce三种电极,对电极进行扫描电镜和X射线衍射表征、电化学性能测试、产羟基自由基(·OH)能力测试和加速寿命测试。结果表明,经聚苯胺(PANI)和铈(Ce)改性的Ti/PANI/PbO_(2)-Ce电极具有更好的表面形貌和更高的催化活性,能产生更多的·OH,析氧电位为1.83 V,加速寿命时间为720 min。采用Ti/PANI/PbO_(2)-Ce电极降解焦化废水中的蒽,考察了主要因素对降解效果的影响,得到蒽的最佳降解条件为电压14 V,板间距1.0 cm,电解质浓度0.35 mol/L,反应时间120 min,pH值10。Ti/PANI/PbO_(2)-Ce电极显示了良好的电催化性能。 展开更多
关键词 电催化氧化 聚苯胺 羟基自由基 焦化废水
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二十烷、蒽和对二丁基环己烷在氧化钙中的吸附和扩散特性
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作者 孙立鹏 鲁家荣 +8 位作者 姜海英 赵德明 李国梁 岳远宁 李金明 辛德兴 闫昊 陈小博 刘熠斌 《石油炼制与化工》 CAS CSCD 北大核心 2024年第10期32-40,共9页
在823.15~923.15 K的温度范围内,采用蒙特卡洛方法和分子动力学方法研究了二十烷(C_(20)H_(42))、蒽(C_(14)H_(10))和对二丁基环己烷(C_(14)H_(28))在氧化钙5 nm的孔道中的吸附和扩散性能,分析了3种分子在氧化钙孔道中的吸附等温线、分... 在823.15~923.15 K的温度范围内,采用蒙特卡洛方法和分子动力学方法研究了二十烷(C_(20)H_(42))、蒽(C_(14)H_(10))和对二丁基环己烷(C_(14)H_(28))在氧化钙5 nm的孔道中的吸附和扩散性能,分析了3种分子在氧化钙孔道中的吸附等温线、分子扩散动力学、概率密度分布和径向分布函数。吸附等温线的分析结果表明:C_(14)H_(10)在氧化钙孔道内的吸附量最大,923.15 K时C_(14)H_(28)吸附量最小,823.15 K时C_(20)H_(42)吸附量最小;C_(20)H_(42)和C_(14)H_(10)为多层吸附,C_(14)H_(28)为单层吸附。分子扩散动力学分析结果表明:C_(20)H_(42)的扩散系数最大,C_(14)H_(28)次之,C_(14)H_(10)最小;扩散性能主要受温度和分子构型影响,根据扩散活化能可知,C_(14)H_(10)的扩散受温度影响最大,C_(14)H_(28)次之,C_(20)H_(42)最小。概率密度分布和径向分布函数分析结果表明:C_(14)H_(10)在距离孔道表面0.4,0.7,1.1 nm附近存在3个吸附层;C_(20)H_(42)和C_(14)H_(28)的吸附层在距离孔道表面0.5 nm附近的空间中。 展开更多
关键词 二十烷 对二丁基环己烷 氧化钙 吸附 扩散 分子模拟
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一株蒽降解菌的分离筛选及降解特性初析
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作者 朱倬漪 姜昕 +2 位作者 马鸣超 曹凤明 王佳馨 《中国土壤与肥料》 CAS CSCD 北大核心 2024年第3期198-208,共11页
多环芳烃(PAHs)是土壤中最常见的典型持久性有机污染物,蒽作为其典型代表,常被用作降解PAHs的模型化合物和检测PAHs污染的指示物。采集北京郊区受污染土样,通过驯化和富集,分离出185株具有蒽降解潜力的菌株,采用高效液相色谱法定量测定... 多环芳烃(PAHs)是土壤中最常见的典型持久性有机污染物,蒽作为其典型代表,常被用作降解PAHs的模型化合物和检测PAHs污染的指示物。采集北京郊区受污染土样,通过驯化和富集,分离出185株具有蒽降解潜力的菌株,采用高效液相色谱法定量测定菌株的蒽降解效率,筛选获得一株可高效降解蒽的菌株R4004-2。经菌落形态观察、16S rRNA和gyrB基因系统发育分析、基因组框架图ANI、DDH和dDDH值分析,确定R4004-2为施氏假单胞菌(Pseudomonas stutzeri)。菌株R4004-2以蒽为唯一碳源,对蒽的降解率可达82.3%,在肉汤培养基中的生长速度最快。在蒽含量为0.25 mg/kg的污染土壤中,施氏假单胞菌R4004-2可以有效定殖,具有修复污染土壤的潜力。基于转录组以及代谢组结果,施氏假单胞菌R4004-2通过双加氧酶进行对蒽的第一步氧化,后续分别通过蒽醌的氧化以及1-羟基-2-萘甲酸酯的分解两个途径完成对蒽的降解,初步解析了其降解机制。 展开更多
关键词 降解菌 降解机制 组学分析
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Pilot Test of Preparing 2-Alkylanthraquinone Using Alkylation-Oxidation Technology
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作者 Zheng Bo Qian Jianguo +6 位作者 Shi Peng Pan Zhiyong Qie Siyuan Zhang Yueqin Fei Jianqi Qiao Liang Zong Baoning 《China Petroleum Processing & Petrochemical Technology》 SCIE CAS CSCD 2024年第1期88-97,共10页
To expedite the development of industrial technology for producing 2-alkylanthraquinone,a novel pilot test of alkylation-oxidation technology was conducted.The process mainly included anthracene alkylation,separation ... To expedite the development of industrial technology for producing 2-alkylanthraquinone,a novel pilot test of alkylation-oxidation technology was conducted.The process mainly included anthracene alkylation,separation of anthracene and 2-alkylanthracene,oxidation of 2-alkylanthracene,and product purification.Optimal alkylation conditions yielded a 91.1%conversion of anthracene and a 71.73%selectivity for 2-alkylanthracene.To address the separation problem of anthracene and 2-alkylanthracene,solvent-assisted distillation technology was developed,resulting in a 98.9%purity of 2-alkylanthracene and a 91.82%separation yield.When the molar ratio of H2O_(2) to 2-alkylanthracene was 7:1,a 98.96%conversion of 2-alkylanthracene and a 99.94%selectivity for 2-alkylanthraquinone were achieved.A novel composition of 2-alkylanthraquinone,including 2-tert-butylanthraquinone,2-tert-amylanthraquinone,and 2-hexylanthraquinone,was developed.This composition could be effectively separated and purified through a combination of crystallization and washing processes.The elemental composition of the product met the existing standards,and its hydrogenation performance closely matched that of commercially available 2-tert-amylanthraquinone products. 展开更多
关键词 anthracene 2-alkylanthracene 2-alkylanthraquinone ALKYLATION OXIDATION hydrogen peroxide
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