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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2019 · IF 4.784

5-hydroxymethylfurfural-embedded poly (vinyl alcohol)/sodium alginate hybrid hydrogels accelerate wound healing

Fanhui Kong,Conghui Fan,Yulian Yang,Bae Hoon Lee,Kun Wei

Treating large acute or chronic wounds remains a challenging task because of a lack of effective methods to accelerate wound healing. Though growth factor-based wound products are found to be effective, they are costly and are potentially associated with increased cancer mortality. Effective, safe, and affordable strategies to tackle large or chronic wounds need to further be designed and developed. Here, we designed a new antioxidant-embedded hydrogel system for speeding up the wound healing process. We prepared multifunctional poly (vinyl alcohol)/sodium alginate (PVA/SA) hydrogels with the incorporation of 5-hydroxymethylfurfural (5-HMF) and silver nanoparticles (Ag-NPs), and investigated their physiochemical and biological properties in vitro and in vivo. PVA, SA, 5-HMF, and Ag-NPs were employed for good mechanical properties, good biocompatibility, anti-inflammation, and anti-bacterial activity, respectively. 5-HMF is commonly found in many food products (e.g. honey, coffee, and black garlic) and is known as an antioxidant. In our in vitro study, 5-HMF was found to effectively facilitate the proliferation and migration of human skin fibroblasts (HSF), and collagen production. Besides, 5-HMF-embedded PVA/SA hybrid hydrogels supported controlled release and good cell compatibility, and more importantly accelerated wound healing in vivo through ameliorated inflammation, enhanced angiogenesis/vascularization, increased collagen production, and promoted re-epithelialization.

✓ 已验证 产品关联 DOI PubMed 高影响因子
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DYES AND PIGMENTS · 2019 · IF 4.018

Near-infrared squaraine fluorescent probe for imaging adenosine 5′-triphosphate in live cells

Guimei Wang,Xiaoxue Jiang,Nanyan Fu

Adenosine 5′-triphosphate (ATP), as a “molecular currency” for intracellular energy transfer, not only participates in various physiological activities, but also involves in various pathological processes of living cells. Therefore, the establishment of a simple, rapid, sensitive and accurate ATP analysis method is of great significance for the study of its physiological functions. In this work, we rationally design a near-infrared phenylboronic acid group-functionalized dicyanovinyl squaraine ( SQ-PBA3 ), with which a supramolecular assembly was constructed for fluorescent imaging of ATP. In PBS buffer, SQ-PBA3 changes self-assembly when adding cetyltrimethyl ammonium bromide (CTAB) deriving fluorescence response of SQ-PBA3 to ATP with the maximum emission at 700 nm, due to the specificity of phenylboronic acid to diols and the multiple electrostatic interactions between SQ-PBA3 , ATP and CTAB molecules. Meanwhile, the probe was successfully applied to monitor intracellular ATP level in MCF-7 cells with high sensitivity and selectivity.

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SURFACE REVIEW AND LETTERS · 2019 · IF 0.748

TEXTURE AND STRUCTURE VARIATION OF PEROVSKITE LaFeO3/ZSM-5 DURING HIGH-TEMPERATURE DESULFURIZATION

DONGJING LIU,WEIGUO ZHOU,JIANG WU

Perovskite LaFeO 3 /ZSM-5 is synthesized via citrate route for H 2 S removal at high temperatures. It shows good thermal stability after heat treatment at 500–700 ∘ C with respect to slight changes in crystallographic phase and textural property. It presents the optimal desulfurization performance at 600 ∘ C with sulfur capacity of 1017 μ mol S/g and products of S, LaS 2 , and Fe 7 S 8 . Sulfidation at 500 ∘ C yields the same products as sulfidation at 600 ∘ C but displays the lowest sulfur capacity of 408 μ mol S/g. Sulfidation at 700 ∘ C produces La 2 O 2 S, Fe 3 S 4 , and unreacted LaFeO 3 . The activation energy of the sulfidation reaction over LaFeO 3 /ZSM-5 is 109.6 kJ/mol.

CAS / MDL: 7782-61-8 10277-43-7
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Catalysts · 2018 ·Vol. 8 ·期 2 ·82 · IF 3.465

Catalytic Fast Pyrolysis of Kraft Lignin over Hierarchical HZSM-5 and Hβ Zeolites

Yadong Bi,Xiaojuan Lei,Guihua Xu,Hui Chen,Jianli Hu

The hierarchical HZSM-5 and Hβ zeolites were prepared by alkaline post-treatment methods adopting Na2CO3, TMAOH/NaOH mixture, and NaOH as desilication sources, respectively. More mesopores are produced over two kinds of zeolites, while the micropores portion is well preserved. The mesopores formed in hierarchical Hβ zeolites were directly related to the basicity of the alkaline solution, indicating that Hβ zeolite is more sensitive to the alkaline post-treatment. The hierarchical HZSM-5 and Hβ zeolites are more active than the parent one for catalytic fast pyrolysis (CFP) of Kraft lignin. Hierarchical zeolites retained the function of acid catalysis, while additionally creating larger mesopores to ensure the entry of bulkier reactant molecules. The increase of the condensable volatiles yield can be attributed to the improvement of the mass transfer performance, which correlates well with the change of mesoporous surface area. In particular, the condensable volatiles yield for the optimized hierarchical Hβ reached approximately two times that of the parent Hβ zeolites. In contrast to the parent HZSM-5, the optimized hierarchical HZSM-5 zeolite significantly reduced the selectivity of oxygenates from 27.2% to 3.3%.Keywords:catalytic fast pyrolysis;Kraft lignin;hierarchical zeolites;HZSM-5;Hβ

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CATALYSIS TODAY · 2018 · IF 4.667

Fe-ZSM-5 supported palladium nanoparticles as an efficient catalyst for toluene abatement

Yuexin Peng,Ling Zhang,Yiwen Jiang,Shichao Han,Qiuyan Zhu,Xiangju Meng,Feng-Shou Xiao

Catalytic combustion is considered as an efficient and economic technology to remove VOCs, and Al-ZSM-5 zeolite supported palladium catalysts (Pd/Al-ZSM-5) with good performances in this kind of reactions have been reported. In this work, it is found that Fe-ZSM-5 supported palladium catalyst (Pd/Fe-ZSM-5) exhibit higher catalytic activity in toluene combustion than the Pd/Al-ZSM-5, which is strongly related to more Pd 0 active species and higher concentration of absorbed oxygen species of Pd/Fe-ZSM-5 than those of Pd/Al-ZSM-5. More importantly, Pd/Fe-ZSM-5 has a good catalyst life and water-resistant ability, which should be potentially significant for practical applications in environment protection.

CAS / MDL: 78-10-4
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MATERIALS CHEMISTRY AND PHYSICS · 2017 · IF 2.084

CO2 adsorption on polyethylenimine-modified ZSM-5 zeolite synthesized from rice husk ash

Yisong Wang,Tao Du,Ziyang Qiu,Yanli Song,Shuai Che,Xin Fang

Mesoporous ZSM-5 zeolite as the adsorbent supporting material was synthesized from rice husk ash (RHA), and then impregnated with polyethylenimine (PEI) for amine functional modification. A series of adsorbents (ZSM-5-PEI-X) with different PEI loading ratios were characterized by XRD , FTIR , TGA/DTG, nitrogen adsorption-desorption, SEM and EDX techniques. The measurement of the adsorption capacity at different temperatures was indicated that ZSM-5-PEI-30 had the highest adsorption capacity at 120 °C (1.96 mmol/g). The experimental data were fitted by adsorption kinetic models and isotherm models, indicated that fractional-order model and the Dual-site langmuir model can be used to describe the adsorption mechanism and predict the adsorption performance. The high CO 2 adsorption selectivity and regeneration stability suggested that this adsorbent is a potential candidate in the adsorption and separation of CO 2 in industrial flue gas .

CAS / MDL: 9002-98-6
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PETROLEUM SCIENCE AND TECHNOLOGY · 2017 · IF 0.655

Catalytic study for methanol aromatization over hierarchical ZSM-5 zeolite synthesized by kaolin

Lanyu Xing,Zhenhao Wei,Zhenhao Wen,Xuedong Zhu

Hierarchical and conventional ZSM-5 zeolites were synthesized through steam-assisted crystallization approach using acid-treatment kaolin clay as the silica and aluminium sources. The samples were characterized by XRD, SEM, NH3-TPD, N2-physisorption and TG techniques. The results showed that hierarchical ZSM-5 had rich mesopores and bigger specific surface. In conversion of methanol to aromatics, hierarchical and conventional ZSM-5 zeolites showed higher selectivity for aromatics compared with commercial ZSM-5. Under the conditions of 450 °C, 0.15 MPa, the synthesized hierarchical ZSM-5 showed longest lifetime of 380 h, which was 2 and 6 times than those of conventional and commercial ZSM-5, respectively.

CAS / MDL: 16415-12-6 4499-86-9
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JOURNAL OF MEMBRANE SCIENCE · 2017 · IF 6.035

Fabrication of novel hierarchical ZSM-5 zeolite membranes with tunable mesopores for ultrafiltration

Li Peng,Xiaohan Xu,Xun Yao,Hua Liu,Xuehong Gu

A series of novel hierarchical ZSM-5 zeolite membranes with tunable mesopore sizes have been prepared successfully by using amphiphilic organosilane 3-[(trimethoxysilyl) propyl]octyldimethyl-ammonium chloride (TPOAC) as the mesogenous template and part of the Si source. The effects of several synthesis parameters, such as the TPOAC/SiO 2 ratio, synthesis temperature and crystallization time, on the microstructures and rejection performance of the hierarchical ZSM-5 zeolite membranes were systematically investigated. Multiple techniques, such as XRD , SEM, N 2 adsorption techniques, TEM, IR, 13 C MAS NMR and 29 Si MAS NMR were employed for the characterizations. The filtration of dextran in water shows that the membranes have molecular weight cutoff (MWCO) ranging from 9500 to 943,000, corresponding to the molecular size in the range of 4.5–37   nm. The sharp increase in the rejection of dextran with the increase of molecular weight indicated narrow pore size distribution of the membrane. These results show that the hierarchical mesoporous ZSM-5 zeolite membranes have a great potential for ultrafiltration with high performance.

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CHEMISTRY-A EUROPEAN JOURNAL · 2017 ·Vol. 23 ·期 62 ·15721-15728 · IF 5.317

Hydrogels Based on Ag+-Modulated Assembly of 5′-Adenosine Monophosphate for Enriching Biomolecules

Yuanyuan Hu,Dong Xie,Yang Wu,Nangui Lin,Aixin Song,Jingcheng Hao

Graphical Stacking gels : Factors affecting the self-assembly of supramolecular hydrogels composed of combining 5′-adenosine monophosphate and Ag + are discussed (see figure). The gelation capability was enhanced by increasing the concentration of Ag + or decreasing the pH. The gels are very sensitive to light and have potential applications as photosensitive materials. Supramolecular hydrogels obtained by combining 5′-adenosine monophosphate (AMP) with Ag + were fabricated in this work. Their gelation capability was enhanced by increasing the concentration of Ag + or decreasing the pH. The gels are very sensitive to light, which endows them with potential applications as visible-light photosensitive materials. Coordination between the nucleobase of AMP and Ag + , as well as π–π stacking of nucleobases, are considered to be the main driving forces for self-assembly. The hydrogels successfully achieved the encapsulation and enrichment of biomolecules. Hydrogen bonding between the amino group of guest molecules and silver nanoparticles along the nanofibers drives the enrichment and is considered to be a crucial interaction.

✓ 已验证 产品关联 DOI PubMed 高影响因子
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INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES · 2024 ·Vol. 25 ·期 18 ·10188 · IF 4.9

Components in SLPE Alleviate AD Model Nematodes by Up-Regulating Gene gst-5

Peng Zhao,Zifu Wang,Shimei Liao,Yangxin Liao,Shijun Hu,Jianchun Qin,Donghua Zhang,Xiaohui Yan

Salvia leucanthais a perennial herb of the genusSalviain the family Labiatae, which has a wide range of biological activities, mainly including inhibition of acetylcholinesterase, antibacterial, and anti-inflammatory activity. To explore the protective effects and mechanism of action ofS. leucanthaon Alzheimer’s disease (AD), the anti-AD activity of SLE (extracts ofS. leucantha) was determined by using a transgenicCaenorhabditis elegans(C. elegans) model (CL4176). Analyses included paralysis assay, phenotypic experiments, transcriptome sequencing, RNA interference (RNAi), heat shock assays, and gas chromatography-mass spectrometry (GC-MS). SLPE (S. leucanthapetroleum ether extract) could significantly delay CL4176 paralysis and extend the longevity ofC. elegansN2 without harmful effects. A total of 927 genes were significantly changed by SLPE treatment inC. elegans,mainly involving longevity regulatory pathways—nematodes, drug metabolism—cytochrome P450, and glutathione metabolic pathways. RNAi showed that SLPE exerted its anti-AD activity through up-regulation of the genegst-5; the most abundant compound in SLPE analyzed by GC-MS was 2,4-Di-tert-butylphenol (2,4-DTBP), and the compound delayed nematode paralysis. The present study suggests that active components inS. leucanthamay serve as new-type anti-AD candidates and provide some insights into their biological functions.

CAS / MDL: 96-76-4
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Molbank · 2024 ·Vol. 2024 ·期 2 ·M1818 · IF 0.6

(E)-1-(5-(Hydroxymethyl) furan-2-yl)-4,4-dimethylpent-1-en-3-one

Zhongwei Wang,Luxiao Zhou,Peng He,Yukun Qin

This study presents a novel approach in the realm of catalytic organic synthesis by integrating biomass catalytic conversion with organic synthesis techniques. UtilizingN-acetylglucosamine as the primary feedstock, the first phase of the research involves its catalytic transformation into 5-hydroxymethylfurfural (HMF). The subsequent phase employs a condensation reaction between HMF and 3,3-Dimethyl-2-butanone to synthesize a new compound, (E)-1-(5-(hydroxymethyl) furan-2-yl)-4,4-dimethylpent-1-en-3-one. This two-step process not only demonstrates the feasibility of converting biomass into valuable chemical precursors but also exemplifies the synthesis of novel compounds through green chemistry principles. The successful execution of this methodology offers fresh insights and opens new avenues for advancements in catalytic organic synthesis, emphasizing sustainability and efficiency.

CAS / MDL: 75-97-8
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RSC Advances · 2017 ·Vol. 7 ·期 27 ·16311-16318 · IF 3.108

Selective hydrodeoxygenation of 5-hydroxymethylfurfural to 2,5-dimethylfuran on Ru–MoOx/C catalysts

Yue Yang,Qiying Liu,Dan Li,Jin Tan,Qi Zhang,Chenguang Wang,Longlong Ma

Selective hydrogenation of 5-hydroxymethylfurfural (HMF) has potential application in high quality biofuels. Herein, the catalytic hydrodeoxygenation (HDO) of HMF to 2,5-dimethylfuran (DMF) was investigated using bi-functional Ru–MoOx/C catalyst prepared by initial wetness impregnation. The high dispersion and electronic transfer between Ru and MoOx were demonstrated by a series of characterization techniques. During this HDO process, the synergy effect between metallic Ru and acidic MoOx species in the Ru–MoOx/C catalyst plays an essential role in obtaining maximized target product DMF (79.4%) via effective aldehyde group hydrogenation by Ru followed by dehydration over MoOx. This work also elucidated that DMF production proceeded through two distinct pathways: the 2,5-hydroxymethyl furan intermediate was preferable by the aldehyde group hydrogenation of HMF over the Ru–MoOx/C catalyst. Over MoOx/C catalyst, comparatively, 5-methyl furfural was the key intermediate by direct hydrogenolysis of the hydroxyl group in HMF. This kind of catalyst is stable for the first two runs by maintaining the target product yield. After the third run, the catalyst showed deactivation gradually but could be almost completely recovered after regeneration by H2 reduction.

CAS / MDL: 68-12-2 14898-67-0
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