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Advanced Sustainable Systems · 2022 ·Vol. 7 ·期 2 ·2200378 · IF 6.737

Integration of Photo-Fenton Reaction and Membrane Filtration using Lignin@t-FeC2O4/g-C3N4 Nanofibers Toward Accelerated Fe(III)/Fe(II) Cycling and Sustainability

Ziying Xiong,Hai Hu,Ziqi Cao,Yaxin Hu,Di Sun,Hengfei Qin,Shifei Kang

Photocatalysis water treatment without artificial energy is cost-effective, waste-free and sustainable. Coventional powder photocatalysts have tiny contact surfaces, low catalytic efficiency, and are difficult to recycle and reuse, restricting their usage. Herein, a Lignin@t-FeC 2 O 4 /g-C 3 N 4 material is developed by engineering hollow quadrangle t-FeC 2 O 4 and g-C 3 N 4 nanosheets on lignin membranes through facile impregnation coating and precipitation reaction. Fast mass transport, catalytic activity and accessibility characterize hollow tetragonal FeC 2 O 4 · 2H 2 O. TEM, SEM and FTIR show that lignin binds t-FeC 2 O 4 and g-C 3 N 4 . The g-C 3 N 4 nanosheets are uniformly wrapped on the surface of lignin fibers, and t-FeC 2 O 4 is loaded between them. This structure increases visible light absorption and active site-contaminant contact. The chain reaction produces extremely active hydroxyl radicals from hydrogen peroxide because the Lignin@t-FeC 2 O 4 /g-C 3 N 4 modules are rich inFe II , according to XPS. Transient photocurrent response curves and electrochemical impedance spectroscopy suggest a promoted charge migration and isolation at the redox reaction interface in the Lignin@t-FeC 2 O 4 /g-C 3 N 4 system. As a result, Lignin@t-FeC 2 O 4 /g-C 3 N 4 degrades 99% Rhodamine B within 40 minutes, and this performance is stable even under difficult conditions, such as low hydrogen peroxide concentration and high pH. This study combines lignin membranes with the photo-Fenton reaction, and thus provides new concept for the development and application of membranes and photocatalysis.

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ENERGY · 2022 · IF 8.857

Research on the co-pyrolysis of coal slime and lignin based on the combination of TG-FTIR, artificial neural network, and principal component analysis

Zhanshi Ni,Haobo Bi,Chunlong Jiang,Hao Sun,Wenliang Zhou,Zhicong Qiu,Liqun He,Qizhao Lin

Confronted with the shortage of fossil energy, the large inventory and the serious pollution of industrial solid waste, the development of clean and efficient industrial solid waste disposal methods have become a trend. In this study, Thermogravimetric-Fourier transform infrared spectrometry was utilized to carry out the co-pyrolysis experiment of coal slime and lignin. Pyrolysis experiments were carried out following 7 different mass mixing ratios. The initial pyrolysis temperatures of CS, S9G1, S7G3, S5G5, S3G7, S1G9, and LIG were 414.5, 373.3, 287.6, 233.3, 225.8, 218.6, and 209.6 °C, respectively. By observing the evolution of the gaseous products of the sample pyrolysis, the results showed that the gaseous products mainly include hydrocarbons, aldehydes, ethers, and alcohols. The ratio of lignin in the mixture was changed, and the interaction between the sample particles was different. The principal component analysis method provided helps to understand the mechanism of co-pyrolysis of coal slime and lignin. The relative error of the established artificial neural network prediction was less than 2.5%. This paper comprehensively analyzed the interaction and gas evolution law during the co-pyrolysis of coal slime and lignin.

CAS / MDL: 9005-53-2
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Asian Journal of Pharmaceutical Sciences · 2022 · IF 9.273

Lignin-assisted construction of sub-10 nm supramolecular self-assembly for photothermal immunotherapy and potentiating anti-PD-1 therapy against primary and distant breast tumors

Xudong Fan,Tianxiang Yue,Aidi Liu,Xiaowei Xie,Weixiang Fang,Yinghui Wei,Hangsheng Zheng,Hongyue Zheng,Meiqi Zhou,Jigang Piao,Fanzhu Li

Photothermal therapy (PTT) has brought hope for cancer treatments, with hyperthermia-induced immunogenic cell death (ICD), which is a critical part of therapeutically induced antitumor immune responses. Limited immune stimulation response in PTT is the primary reason for incomplete tumor ablation, therefore demonstrating urgent requirements for ICD amplifier. Herein, a sub-10 nm supramolecular nanoassembly was formed by co-assembly of clinically approved aluminum adjuvant and commonly used indocyanine green (ICG) under the assistance of lignosulfonate (LS, a green and sustainable multifunctional lignin derivative) for localized photothermal-immunotherapy of breast cancer. The overall results revealed that LS-Al-ICG is capable of inducing amplified ICD, efficiently eliciting solid immune responses through dendritic cells (DCs) activation and cytotoxic T-cell responses initiation for tumor killing. Moreover, anti-PD-1 therapy blocked the PD-1 pathway and led to remarkable anti-tumor efficacy against laser-irradiated primary tumors and distant tumors by potentiating systemic tumor specific T cell immunity. The results of this study demonstrate a handy and extensible approach for engineering green natural lignin nanoparticles for cancer immunotherapy, which shows promise for delivering other therapeutics in biomedical applications.

CAS / MDL: 7446-70-0 3599-32-4
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Journal of Energy Chemistry · 2021 · IF 9.676

Regulating the nanoscale intimacy of metal and acidic sites in Ru/γ-Al2O3 for the selective conversions of lignin-derived phenols to jet fuels

Shanshuai Chen,Weichen Wang,Xue Li,Puxiang Yan,Wanying Han,Tian Sheng,Tiansheng Deng,Wanbin Zhu,Hongliang Wang

Catalytic hydrodeoxygenation (HDO) of biomass-derived oxy-compounds to advanced hydrocarbon fuels usually requires bifunctional catalysts containing metals and acidic sites. The appropriate tuning of metal and/or acidic active sites at interfaces of bifunctional catalysts can significantly improve catalyst activity and product selectivity. Here, 4-trifuoromethyl salicylic acid (TFMSA), as a hydrothermal stable organic acid, was employed to tailor the bifunctional interface of Ru/γ-Al 2 O 3 to enhance the catalytic performance on converting lignin-derived phenols to jet fuel range cycloalkanes. More than 80% phenol was converted into cyclohexane at 230 °C for 1 h over Ru/γ-Al 2 O 3 modified by TFMSA, which was about three times higher than that over unmodified Ru/γ-Al 2 O 3 . X-ray diffraction (XRD), Transmission electron microscope (TEM), H 2 chemisorption, and energy dispersive X-ray spectroscopy (EDS) elemental mapping results indicated that Ru nanoparticles and TFMSA were well distributed on γ-Al 2 O 3 , and a nanoscale intimacy between Ru and TFMSA was reached. Meanwhile, Fourier transform infrared spectroscopy after pyridine adsorption (Py-FT-IR) analysis proved that Brønsted acidic sites on the catalytic interfaces of TFMSA modified Ru/γ-Al 2 O 3 had been improved. Moreover, the kinetic and density functional theory (DFT) results suggested that the synergistic effects of adjacent Ru nanoparticles and acidic sites were crutial for promoting the rate-limiting conversion step of phenol HDO to cyclohexane.

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SEPARATION AND PURIFICATION TECHNOLOGY · 2021 · IF 7.312

Synergy effect between adsorption and heterogeneous photo-Fenton-like catalysis on LaFeO3/lignin-biochar composites for high efficiency degradation of ofloxacin under visible light

Xin Chen,Ming Zhang,Haowei Qin,Jiancheng Zhou,Quanhao Shen,Ke Wang,Wenshuai Chen,Maochang Liu,Naixu Li

The perovskite-type LaFeO 3 serves as a promising photo-Fenton-like catalyst, but its low adsorption ability and catalytic activity inhibit the effective removal of ofloxacin. Herein, the LaFeO 3 and lignin-biochar composites were fabricated by a facile sol–gel pyrolysis route. As compared with LaFeO 3 nanoparticles, the LaFeO 3 /lignin-biochar composites showed better adsorption and degradation ability due to the synergistic effect between LaFeO 3 nanoparticles and lignin-biochar. Compared with LaFeO 3 , the adsorption capacity of LaFeO 3 /lignin-biochar for ofloxacin increased from 0.72 to 30.4 mg·g −1 . Importantly, this catalyst exhibited the improved degradation efficiency of ofloxacin during 75 min (95.6 % for LaFeO 3 /lignin-biochar Vs 53.4 % for LaFeO 3 ) as the adsorption process was combined with the photo-Fenton-like process. Notably, the lignin-biochar in the LaFeO 3 /lignin-biochar composites decreased the bandgap of LaFeO 3 nanoparticles from 2.10 eV to 1.79 eV due to the interface interaction between LaFeO 3 and lignin-biochar, facilitating the enhanced photo-Fenton-like activity. The hydroxyl radicals that were generated in the photo-Fenton-like process effectively induced the oxidative degradation of ofloxacin, which was confirmed by free radical capture experiments and ESR characterization. Moreover, the photo-Fenton-like degradation pathway of ofloxacin was proposed according to LC-MS analyses, and the toxicity analysis of degradation intermediates was further carried out. Hence, the LaFeO 3 /lignin-biochar composite was a promising photo-Fenton-like catalyst to eliminate ofloxacin via coupling of adsorption and photo-Fenton-like processes.

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Journal of Environmental Chemical Engineering · 2021 · IF 5.909

Selective organic phase hydrodeoxygenation of typical phenolic monomers and two lignin oils over highly active Pd/Hβ catalyst for high-grade bio-fuel production

Lin Hu,Xian-Yong Wei,Mei-Ling Xu,Yu-Hong Kang,Xian-Hou Guo,Feng-Bin Zhang,Zhi-Min Zong,Hong-Cun Bai

The selective hydrodeoxygenation (HDO) of lignin-derived bio-oil still meets the great challenges due to its complex oxygenated organic component. In this research, first time, Pd-based zeolite catalysts were prepared by the modified deposition-precipitation (DP) method for the HDO conversion of guaiacol. Notably, for the same Si/Al ratio of zeolite, Pd 2% /Hβ catalyst showed the higher catalytic activity on the HDO of guaiacol than that Pd 2% /M and Pd 2% /HZSM-5 catalyst, which mainly originated from the synergetic effect between metal nanoparticles size and acid sites of catalyst. As one of typical phenolic monomers , guaiacol can be converted into high yield of hydrocarbons under the condition of 220 °C, 3 MPa H 2 , and 4 h in n -hexane over Pd 2% /Hβ (DP) catalyst. This highly active catalyst exhibited the good recyclability in the HDO conversion of guaiacol. In addition, other typical phenolic monomers can be converted into high yield of hydrocarbons over this highly active catalyst. Considering this, after HDO upgrading, real lignin oil (RLO) can be converted into high yield of hydrocarbons with the carbon number (CN) in range of C7-C15. This work highlighted that the depolymerization monomers from lignin can be further upgraded by this high active catalyst through HDO to obtain jet hydrocarbons fuel .

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FUEL · 2021 · IF 6.609

Hydrogenolysis of lignin to phenolic monomers over Ru based catalysts with different metal-support interactions: Effect of partial hydrogenation of C(sp2)-O/C

Yishuang Wu,Zixiang Lin,Xun Zhu,Xun Hu,Mortaza Gholizadeh,Hongqi Sun,Yong Huang,Shu Zhang,Hong Zhang

Catalytic hydrogenolysis of lignin to phenolic monomers has received a lot of attention, but it is still a challenge because the cleavage of the strong C(sp 2 )-O/C bonds between structural units is usually under harsh conditions, resulting in the presence of the competing reaction of hydrogenation. Herein, hydrogenolysis of an herbaceous lignin into phenolic monomers was performed over Ru supported on various (non)-functionalized graphitized carbon nanotubes (CNT, CNT-OH, CNT-COOH, and CNT-NH 2 ), which were featured by different hydrogenation performances originally from the diverse metal-support interactions. Among the investigated supports, CNT-NH 2 enables the formation of the finest Ru nanoparticles with an average size of 1.86 nm, leading to the highest yield of phenolic monomers from lignin hydrogenolysis. The best hydrogenolysis performance of Ru@CNT-NH 2 was mainly from the partial hydrogenation of C(sp 2 )-O/C bonds to C(sp 3 )-O/C bonds in lignin, thus reducing their bond dissociation energy (BDE). The intimacy between hydrogenolysis and hydrogenation was further proved by depolymerization of a lignin β-O-4 model compound.

CAS / MDL: 14898-67-0
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BIORESOURCE TECHNOLOGY · 2020 · IF 7.539

Volatile–char interactions during biomass pyrolysis: Cleavage of C–C bond in a β–5 lignin model dimer by amino-modified graphitized carbon nanotube

Yong Huang,Shasha Liu,Jie Zhang,Syed Shatir A. Syed-Hassan,Xun Hu,Hongqi Sun,Xun Zhu,Jianbin Zhou,Shu Zhang,Hong Zhang

This study investigated the interactions between volatile and char during biomass pyrolysis at 400 °C, employing a β–5 lignin dimer and amino-modified graphitized carbon nanotube (CNT–NH 2 ) as their models, respectively. The results demonstrated that both –NH 2 and its carrier (CNT) facilitated the conversion of the β–5 dimer, which significantly increased from 9.7% (blank run), to 61.6% (with CNT), and to 96.6% (with CNT–NH 2 ). CNT mainly favored the breakage of C–O bond in the feedstock to produce dimers with a yield of 55.5%, while CNT–NH 2 promoted the cleavage of both C–O and C–C bonds to yield monomers with a yield up to 63.4%. Such significant changes in the pyrolysis behaviors of the β–5 lignin dimer after the introduction of CNT–NH 2 were considered to be mainly caused by hydrogen-bond formations between –NH 2 and the dimeric feedstock/products, in addition to the π–π stacking between CNT and aromatic rings.

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DYES AND PIGMENTS · 2020 · IF 4.613

Comparison of N-doped carbon dots synthesized from the main components of plants including cellulose, lignin, and xylose: Characterized, fluorescence mechanism, and potential applications

Xiufen Liao,Congjin Chen,Ruxia Zhou,Quanlong Huang,Qinglong Liang,Zuqiang Huang,Yanjuan Zhang,Huayu Hu,Yanglin Liang

In this study, N-doped carbon dots (N-CDs) synthesized from the main components of plants, including cellulose (N-cCDs), lignin (N-lCDs), and xylose (N-xCDs), were compared. TEM, XRD , FT-IR, and XPS were carried out to characterize their morphology and chemical composition. Results show that the three obtained N-CDs contained N-doped sp 2 and sp 3 hybrid carbon core, which was surrounded by oxygen- and nitrogen-containing functional groups. The three N-CDs exhibited a novel double excitation-one emission phenomenon, and their fluorescence were significantly enhanced by N-doping. Moreover, this study indicated that high lignin-containing biomass is not appropriate for producing CDs by hydrothermal method . Cellulose is conducive to produce CDs, while it needs a relatively high temperature and a long time. Low-molecular carbohydrate-rich biomass and nitrogen-containing biomass is the better carbon source to produce the CDs. Also, this study revealed that N-cCDs and N-xCDs are excellent candidates for fluorescent ink, fabrics identifying, temperature sensing, and Hg 2+ sensing. Due to its poor fluorescence property, N-lCDs is not suitable for fluorescent ink and fabrics identification.

CAS / MDL: 6119-70-6
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FUEL PROCESSING TECHNOLOGY · 2019 · IF 4.507

Assessing the chemical composition of heavy components in bio-oils from the pyrolysis of cellulose, hemicellulose and lignin at slow and fast heating rates

Zhe Xiong,Junhao Guo,Weerawut Chaiwat,Wei Deng,Xun Hu,Hengda Han,Yuanjing Chen,Kai Xu,Sheng Su,Song Hu,Yi Wang,Jun Xiang

The certain challenge for the utilization of bio-oil is to investigate the nature and formation of reactive large molecular (heavy) components (>200 Da) in bio-oil. In order to investigate the chemical composition of the heavy components in the bio-oils from the pyrolysis of cellulose , hemicellulose and lignin, the molecular formulas of the heavy compounds and the large aromatic structures were obtained based on the results from the Fourier transform ion cyclotron resonance mass spectrometer (FT-ICR MS) and the ultraviolet fluorescence (UV-F) spectrometer. The results indicated that both the oxygen content and yield of the heavy components showed the highest in the cellulose-oil and the lowest in the lignin-oil. The large molecular compounds were formed mainly via the recombination of the O-containing species, which could be changed at different temperatures and heating rates. Large amount of heavy saccharide and phenolic species existed in cellulose-oil and hemicellulose-oil, while almost no saccharide species and little phenolic species were detected in the lignin-oil. The main heavy components in the lignin-oil were lipids rather than the phenolic species. The heavy components in the bio-oil from the biomass should be mainly derived from the pyrolysis of the cellulose individually or the interactions among the three components.

CAS / MDL: 9014-63-5
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Journal of Cleaner Production · 2023 · IF 11.1

Sustainable and efficient extraction of lignin from wood meal using a deep eutectic system and adsorption of neutral red dye with the extraction residue

Simin Wang,Min Liu,Wuxia Ge,Can Jin,Wentao Bi

In this study, the efficient extraction of lignin from wood meal using a deep eutectic system (DESys) was explored, and the obtained lignin was characterized. The impact of various factors, such as the type of DESys components, extraction time, temperature, water content, and solid-liquid ratio, on the lignin extraction process was systematically investigated. The results indicated that a DESys with a carboxylic acid as the HBD provided the highest lignin extraction efficiency. The obtained lignin was characterized in terms of its molecular weight distribution, elemental composition , functional groups, crystalline structure, and thermal stability. The results showed that the lignin obtained by DESys-based extraction had similar properties to lignin extracted using traditional method. Additionally, the study examined the utilization of the residue left after lignin extraction for the adsorption of cationic pollutants, such as the cationic dye neutral red (NR). The residue was found to contain carboxyl groups , which enabled it to adsorb NR efficiently. The kinetic and thermodynamic models suggested that the adsorption was a chemisorption process. Furthermore, the residue showed selective adsorption for cationic dye over anionic dye. This selectivity was attributed to interactions between the residue's functional groups and the cationic dye molecule. Overall, this study provided a sustainable and comprehensive approach to lignin extraction from lignocellulosic biomass using DESys. It also demonstrated the potential of using the residue from the extraction process for the removal of cationic pollutants from wastewater, showcasing a multi-faceted approach to the valorization of lignocellulosic materials .

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INDUSTRIAL CROPS AND PRODUCTS · 2023 · IF 5.9

Preparation of lignin-based personal multifunctional protective mask interlayer with antibacterial, anti-UV and iodine trapping effects and exploration of its iodine trapping mechanism

Jingyu Xu,Weiming Liu,Jinghui Zhou,Yue Kong,Mingzhu Gong,Masod Almajarsh,Xiaozhou Zhao,Xing Wang

Personal multifunctional protective mask is becoming an effective and convenient device for maintaining human health. When used in a normal environment, it can prevent the spread of respiratory viruses and bacteria, and absorb UV rays. When used in extreme environments full of iodine vapor, it can effectively absorb iodine vapor. Herein, an eco-friendly multifunctional nanofiber membrane with rapid sterilization ability, ultraviolet absorption and iodine vapor trapping capacity was prepared using lignin and polyvinylpyrrolidone as raw materials through electrostatic spinning technology. The results showed that PVP-WSL and PVP-IL have bactericidal rates of 21.86% and 34.08% for E. coli , 30.27% and 52.64% for S. aureus , respectively. These mask barriers have good UV resistance performance (the UV transmittance was lower than 0.015%) and effective trapping capacity of iodine vapor (the iodine maximum trapping capacity of the PVP-WSL and PVP-IL nanofiber membranes were equally determined to be 294 mg/g and 225 mg/g, respectively). In addition, these membranes have strong thermal stability (initial thermal decomposition temperature was higher than 350 °C) and mechanical properties (tensile strength higher than 1.07 MPa). This work fully meets the requirements of public health protection for degradable and high-performance media and is ideal for multifunctional personal protective equipment.

CAS / MDL: 25249-54-1 9003-39-8
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