Preparation and properties of bamboo/polymer composites enhanced by in situ polymerization of furfuryl alcohol

2019 ◽  
Vol 9 (7) ◽  
pp. 712-722 ◽  
Author(s):  
Yong Wang ◽  
Layun Deng ◽  
Zhihong Xiao ◽  
Xianjun Li ◽  
Youhua Fan ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Furfuryl Alcohol ◽  
Laser Scanning ◽  
In Situ Polymerization ◽  
Decay Resistance ◽  
Laser Scanning Microscopy ◽  
Modulus Of Rupture ◽  
Confocal Laser ◽  
Infrared Spectrometry ◽  
Addition Level

The objective of this paper aimed to develop a novel method to prepare enhanced bamboo-based materials. Furfuryl alcohol (FA) was used as the modification agent with maleic anhydride (MA) as the catalyst. Different bamboo samples were prepared with different FA addition level (10 wt%, 20 wt% and 30 wt%). The furfurylated bamboo samples were characterized by confocal laser scanning microscopy (CLSM), Fourier transform infrared spectrometry (FTIR), X-ray photoelectron spectroscopy (XPS), and thermogravimetric analysis (TGA). Moreover, the physical and mechanical properties including weight percent gain (WPG), water uptake (WU), thickness swelling (TS), modulus of rupture (MOR), and modulus of elastic (MOE) were investigated in detail. Additionally, the decay resistance of pristine and furfurylated bamboo samples was also investigated. The results showed that FA resins were incorporated into bamboo and polymerized within cell walls. The WPG, WU, and TS were dependent on FA addition level. When the FA addition level reached 30 wt%, the physical properties were all improved significantly. However, due to acidic MA as the catalyst, MOR of furfurylated bamboo samples was enhanced only 2.5% while MOE was weakened. The thermal stability and decay resistance of furfurylated bamboo were all enhanced significantly compared to pristine bamboo. Especially, furfurylated bamboo treated with 30 wt% FA achieved Class I Strong Decay Resistance (<10%) with 5.3% of mass loss.

scholarly journals Investigation of Spin Coating Cerium-Doped Hydroxyapatite Thin Films with Antifungal Properties

Coatings ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 464
Author(s):  
Simona Liliana Iconaru ◽  
Mihai Valentin Predoi ◽  
Patrick Chapon ◽  
Sofia Gaiaschi ◽  
Krzysztof Rokosz ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Spin Coating ◽  
Laser Scanning ◽  
Laser Scanning Microscopy ◽  
Confocal Laser ◽  
X Ray ◽  
Antifungal Properties ◽  
Scanning Electron

In this study, the cerium-doped hydroxyapatite (Ca10−xCex(PO4)6(OH)2 with xCe = 0.1, 10Ce-HAp) coatings obtained by the spin coating method were presented for the first time. The stability of the 10Ce-HAp suspension particles used in the preparation of coatings was evaluated by ultrasonic studies, transmission electron microscopy (TEM), X-ray diffraction (XRD), and scanning electron microscopy (SEM). The surface morphology of the 10Ce-HAp coating was studied by SEM and atomic force microscopy (AFM) techniques. The obtained 10Ce-HAp coatings were uniform and without cracks or unevenness. Glow discharge optical emission spectroscopy (GDOES) and X-ray photoelectron spectroscopy (XPS) were used for the investigation of fine chemical depth profiling. The antifungal properties of the HAp and 10Ce-HAp suspensions and coatings were assessed using Candida albicans ATCC 10231 (C. albicans) fungal strain. The quantitative antifungal assays demonstrated that both 10Ce-HAp suspensions and coatings exhibited strong antifungal properties and that they successfully inhibited the development and adherence of C. albicans fungal cells for all the tested time intervals. The scanning electron microscopy (SEM) and confocal laser scanning microscopy (CLSM) visualization of the C. albicans fungal cells adherence to the 10Ce-HAp surface also demonstrated their strong inhibitory effects. In addition, the qualitative assays also suggested that the 10Ce-HAp coatings successfully stopped the biofilm formation.

scholarly journals Antimicrobial Activity Evaluation on Silver Doped Hydroxyapatite/Polydimethylsiloxane Composite Layer

2015 ◽  
Vol 2015 ◽  
pp. 1-13 ◽  
Author(s):  
C. S. Ciobanu ◽  
A. Groza ◽  
S. L. Iconaru ◽  
C. L. Popa ◽  
P. Chapon ◽  
...  
Keyword(s):  
Antimicrobial Activity ◽  
Candida Albicans ◽  
Photoelectron Spectroscopy ◽  
Laser Scanning ◽  
Composite Layer ◽  
Physicochemical Characterization ◽  
Antimicrobial Effect ◽  
Laser Scanning Microscopy ◽  
Confocal Laser ◽  
Composite Layers

The goal of this study was the preparation, physicochemical characterization, and microbiological evaluation of novel hydroxyapatite doped with silver/polydimethylsiloxane (Ag:HAp-PDMS) composite layers. In the first stage, the deposition of polydimethylsiloxane (PDMS) polymer layer on commercially pure Si disks has been produced in atmospheric pressure corona discharges. Finally, the new silver doped hydroxyapatite/polydimethylsiloxane composite layer has been obtained by the thermal evaporation technique. The Ag:HAp-PDMS composite layers were characterized by various techniques, such as Scanning Electron Microscopy (SEM), Glow Discharge Optical Emission Spectroscopy (GDOES), and X-ray photoelectron spectroscopy (XPS). The antimicrobial activity of the Ag:HAp-PDMS composite layer was assessed againstCandida albicansATCC 10231 (ATCC—American Type Culture Collection) by culture based and confirmed by SEM and Confocal Laser Scanning Microscopy (CLSM) methods. This is the first study reporting the antimicrobial effect of the Ag:HAp-PDMS composite layer, which proved to be active againstCandida albicansbiofilm embedded cells.

Spectral characterisation of new organic fluorescent dyes with an alkoxysilane moiety and their utilisation for the labelling of layered silicates

2013 ◽  
Vol 67 (1) ◽  
Author(s):  
Martin Danko ◽  
Matej Mičušík ◽  
Mária Omastová ◽  
Juraj Bujdák ◽  
Dušan Chorvát
Keyword(s):  
Dicarboxylic Acid ◽  
Photoelectron Spectroscopy ◽  
Laser Scanning ◽  
Fluorescent Dyes ◽  
Stokes Shift ◽  
Particle Surface ◽  
Acid Anhydride ◽  
Laser Scanning Microscopy ◽  
Layered Silicates ◽  
Confocal Laser

AbstractNew fluorescence dyes with an alkoxysilane moiety were synthesised by the condensation of 3-(triethoxysilyl)-1-propanamine (3-aminopropyltriethoxysilane) with 4,10-benzothioxanthene-3,1′-dicarboxylic acid anhydride (BTXA) and N,N-dimethylaminonaphthalene-1,8-dicarboxylic acid anhydride (DMANA), which was accompanied by the formation of an imidic bridge. The compounds N-(3-(triethoxysilyl)propyl)-thioxantheno[2,1,9-dej]isoquinoline-1,3-dione (BTX-S) and 4-(N′, N′-dimethyl)-N-(triethoxysilyl)propyl-1,8-naphthalene dicarboxylic acid imide (DMAN-S) were characterised by steady-state and time-resolved fluorescence spectroscopy in chloroform and ethanol. Both conjugates (BTX-S and DMAN-S) exhibited absorption and emission bands in the same region as the un-substituted BTXA and DMANA. An important Stokes shift was observed for DMAN-S in ethanol. A high fluorescence quantum yield was observed for BTX-S in both solvents and for DMAN-S in chloroform. In addition, the newly developed fluorescent silane dyes were covalently attached to the microscopic particles of layered silicates and on the surface of SiO2 wafers as a proof of concept for fluorescence particle (surface) visualisation. The surface wafer modification was precisely characterised by X-ray photoelectron spectroscopy (XPS). Successful covalent linkage onto the particles of layered silicates was proved by confocal laser scanning microscopy technique.

scholarly journals Electrochemical and surface analytical techniques applied to microbiologically influenced corrosion investigation

2018 ◽  
Vol 36 (4) ◽  
pp. 349-363 ◽  
Author(s):  
László Trif ◽  
Abdul Shaban ◽  
Judit Telegdi
Keyword(s):  
Photoelectron Spectroscopy ◽  
Laser Scanning ◽  
Electrochemical Impedance ◽  
Electrochemical Techniques ◽  
Analytical Techniques ◽  
Laser Scanning Microscopy ◽  
Microbiologically Influenced Corrosion ◽  
Microbial Consortia ◽  
Confocal Laser ◽  
The Impact

AbstractSuitable application of techniques for detection and monitoring of microbiologically influenced corrosion (MIC) is crucial for understanding the mechanisms of the interactions and for selecting inhibition and control approaches. This paper presents a review of the application of electrochemical and surface analytical techniques in studying the MIC process of metals and their alloys. Conventional electrochemical techniques, such as corrosion potential (Ecorr), redox potential, dual-cell technique, polarization curves, electrochemical impedance spectroscopy (EIS), electrochemical noise (EN) analysis, and microelectrode techniques, are discussed, with examples of their use in various MIC studies. Electrochemical quartz crystal microbalance, which is newly used in MIC study, is also discussed. Microscopic techniques [scanning electron microscopy (SEM), environmental SEM (ESEM), atomic force microscopy (AFM), confocal laser microscopy (CLM), confocal laser scanning microscopy (CLSM), confocal Raman microscopy] and spectroscopic analytical methods [Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS)] are also highlighted. This review highlights the heterogeneous characteristics of microbial consortia and use of special techniques to study their probable effects on the metal substrata. The aim of this review is to motivate using a combination of new procedures for research and practical measurement and calculation of the impact of MIC and biofilms on metals and their alloys.

The furfuryl alcohol (FA) resin distribution in the furfurylated bamboo

Holzforschung ◽  
2020 ◽  
Vol 0 (0) ◽  
Author(s):  
Wanju Li ◽  
Minghui Liu ◽  
Hankun Wang ◽  
Hongbo Zhai ◽  
Yan Yu
Keyword(s):  
Furfuryl Alcohol ◽  
Laser Scanning ◽  
Parenchymal Cell ◽  
Laser Scanning Microscopy ◽  
Confocal Laser ◽  
Sem Images ◽  
Microscopy Imaging ◽  
Resin Impregnation ◽  
Specific Distribution ◽  
Ft Ir

AbstractIt is well known the properties of resin impregnation wood is significantly influenced by the specific distribution pattern of resin in the modified wood. In this work, bamboo was furfurylated with an improved process. In addition to testing and evaluating its main physical, mechanical and durable properties, it was explored how the furfuryl alcohol (FA) resin is distributed in the furfurylated bamboo. To achieve this goal, scanning electron microscopy (SEM), confocal laser scanning microscopy (CLSM), nanoindentation, and imaging Fourier transform infrared microscopy (imaging FT-IR) were applied. SEM images demonstrates FA resin is mainly located in the parenchymal cell cavity of bamboo, however the existence of FA resin in the small cavities of the bamboo fibers is also observed by CLSM. In addition, the result of nanoindentation and imaging FT-IR both indicates that FA can penetrate and polymerize within the cell wall of the bamboo fiber. It is then concluded the heterogeneous but multi-scale distribution of FA resin should be responsible for the significant improvement of furfurylated bamboo in both dimensional stability and biological durability.

scholarly journals Characterisation of PMMA/ATH Layers Realised by Means of Atmospheric Pressure Plasma Powder Deposition

2015 ◽  
Vol 2015 ◽  
pp. 1-12 ◽  
Author(s):  
Lena M. Wallenhorst ◽  
Sebastian Dahle ◽  
Matej Vovk ◽  
Lisa Wurlitzer ◽  
Leander Loewenthal ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Atmospheric Pressure ◽  
Laser Scanning ◽  
Plasma Deposition ◽  
Deposition Process ◽  
Laser Scanning Microscopy ◽  
Raw Material ◽  
Confocal Laser ◽  
Coating Film ◽  
Water Contact

We report on the characteristics of aluminium trihydrate filled poly(methyl methacrylate) composite (PMMA/ATH) coatings realised by plasma deposition at atmospheric pressure. For this purpose, PMMA/ATH powder was fed to a plasma jet where the process and carrier gas was compressed air. The deposited coatings were investigated by X-ray photoelectron spectroscopy and water contact angle measurements. Further, the raw material was characterised before deposition. It was found that, with respect to the raw material, aluminium was uncovered in the course of the plasma deposition process which can be explained by plasma-induced etching of the PMMA matrix. As a result, the wettability of plasma-deposited PMMA/ATH was significantly increased. Even though a uniform coating film could not be realised as ascertained by confocal laser scanning microscopy, the deposited coatings feature notably enhanced characteristics which could be advantageous for further processing.

scholarly journals Porous Coatings Containing Copper and Phosphorus Obtained by Plasma Electrolytic Oxidation of Titanium

Materials ◽  
2020 ◽  
Vol 13 (4) ◽  
pp. 828 ◽  
Author(s):  
Krzysztof Rokosz ◽  
Tadeusz Hryniewicz ◽  
Wojciech Kacalak ◽  
Katarzyna Tandecka ◽  
Steinar Raaen ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Plasma Electrolytic Oxidation ◽  
Laser Scanning ◽  
Laser Scanning Microscopy ◽  
Confocal Laser ◽  
Phase Step ◽  
Porous Coatings ◽  
X Ray ◽  
Electrolytic Oxidation ◽  
Plasma Electrolytic

To fabricate porous copper coatings on titanium, we used the process of plasma electrolytic oxidation (PEO) with voltage control. For all experiments, the three-phase step-up transformer with six-diode Graetz bridge was used. The voltage and the amount of salt used in the electrolyte were determined so as to obtain porous coatings. Within the framework of this study, the PEO process was carried out at a voltage of 450 VRMS in four electrolytes containing the salt as copper(II) nitrate(V) trihydrate. Moreover, we showed that the content of salt in the electrolyte needed to obtain a porous PEO coating was in the range 300–600 g/dm3. After exceeding this amount of salts in the electrolyte, some inclusions on the sample surface were observed. It is worth noting that this limitation of the amount of salts in the electrolyte was not connected with the maximum solubility of copper(II) nitrate(V) trihydrate in the concentrated (85%) orthophosphoric acid. To characterize the obtained coatings, numerous techniques were used. In this work, we used scanning electron microscopy (SEM) coupled with electron-dispersive X-ray spectroscopy (EDS), conducted surface analysis using confocal laser scanning microscopy (CLSM), and studied the surface layer chemical composition of the obtained coatings by X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), glow discharge of optical emission spectroscopy (GDOES), and biological tests. It was found that the higher the concentration of Cu(NO3)2∙3H2O in the electrolyte, the higher the roughness of the coatings, which may be described by 3D roughness parameters, such as Sa (1.17–1.90 μm) and Sp (7.62–13.91 μm). The thicknesses of PEO coatings obtained in the electrolyte with 300–600 g/dm3 Cu(NO3) 2∙3H2O were in the range 7.8 to 10 μm. The Cu/P ratio of the whole volume of coating measured by EDS was in the range 0.05–0.12, while the range for the top layer (measured using XPS) was 0.17–0.24. The atomic concentration of copper (0.54–0.72 at%) resulted in antibacterial and fungicidal properties in the fabricated coatings, which can be dedicated to biocompatible applications.

Synthesis of dual functional procaine-derived carbon dots for bioimaging and anticancer therapy

Nanomedicine ◽  
2020 ◽  
Vol 15 (7) ◽  
pp. 677-689 ◽  
Author(s):  
Xiaoming Zhao ◽  
Tianyang Qi ◽  
Mingxi Yang ◽  
Wenjing Zhang ◽  
Chenfei Kong ◽  
...  
Keyword(s):  
Anticancer Activity ◽  
Photoelectron Spectroscopy ◽  
Carbon Dots ◽  
Laser Scanning ◽  
Underlying Mechanism ◽  
Laser Scanning Microscopy ◽  
Confocal Laser ◽  
Dual Function ◽  
Dual Functional

Aim: Procaine-derived carbon dots, termed P-dots, expectedly offer both fluorescent biomarker function and anticancer activity. Materials & methods: P-dots were synthesized by condensing procaine, citric acid and ethylenediamine via hydrothermal synthesis and characterized by transmission electron microscopy, Fourier transform infrared spectroscopy and x-ray photoelectron spectroscopy. The cellular uptake behavior and the bioimaging performance of P-dots were assessed by confocal laser scanning microscopy. Their antitumor activity was evaluated using the CCK-8 assays and in vivo antitumor experiments, and the underlying mechanism was evaluated by flow cytometry and western blotting. Results: P-dots exhibited excellent luminescence properties suitable for bioimaging and considerable anticancer activity associated with caspase-3-related cell apoptosis. Conclusion: The synthesized procaine-derived carbon dots presented a dual function consisting of bioimaging and anticancer activity, which may enable their implementation as safe and effective clinical nanotherapeutics.

Fabrication of highly stable and durable furfurylated wood materials. Part II: the multi-scale distribution of furfuryl alcohol (FA) resin in wood

Holzforschung ◽  
2020 ◽  
Vol 74 (12) ◽  
pp. 1147-1155
Author(s):  
Wanju Li ◽  
Minghui Liu ◽  
Hankun Wang ◽  
Yan Yu
Keyword(s):  
Cell Wall ◽  
Furfuryl Alcohol ◽  
Laser Scanning ◽  
Chinese Fir ◽  
Laser Scanning Microscopy ◽  
Confocal Laser ◽  
Microscopy Imaging ◽  
Multi Scale ◽  
Ray Cells ◽  
Ft Ir

AbstractThe aim of this investigation was mainly to evaluate the multi-scale distribution of furfuryl alcohol (FA) resin in modified Chinese fir and poplar wood. 13C CP/MAS NMR, Scanning Electron Microscopy (SEM), Confocal Laser Scanning Microscopy (CLSM), Nanoindentation and Imaging Fourier transform infrared microscopy (Imaging FT-IR) were applied to describe the FA resin distribution in wood from bulk to cell wall scale. The results showed that FA resin were mainly located in the cell cavity of Chinese fir tracheids. For poplar, FA resin was mostly deposited in the cavity of fibers and ray cells, while little was found in the adjacent vessels. Lots of pits of wood cells were covered with FA resin which implied a higher risk of drying after wood furfurlation in practical production. Nanoindentation demonstrated that FA resin could easily infiltrate into the wood cell wall because both reduced modulus and hardness of the modified wood cell walls were significantly improved. This conclusion was further supported by the results of imaging FT-IR.

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