Sustainability in Chemical Surface Technology

2021 ◽  
Vol 14 (4) ◽  
pp. 32-33
Author(s):  
Ulrich Hönig
Keyword(s):  
Chemical Surface

Chemical effects on UV irradiation absorption of fouled quartz sleeves in ultraviolet disinfection

2008 ◽  
Vol 8 (2) ◽  
pp. 217-222 ◽  
Author(s):  
Beibei Zhu Sun ◽  
Ernest Blatchley ◽  
Mike Oliver ◽  
Cheng Zheng ◽  
Kristofer Jennings
Keyword(s):  
Statistical Analysis ◽  
Uv Disinfection ◽  
Uv Absorbance ◽  
Ultraviolet Disinfection ◽  
High Chemical ◽  
Chemical Surface ◽  
Chemical Effects ◽  
Uv Transmittance ◽  
Main Effects ◽  
Iron And Manganese

The effects of foulant chemical composition on ultraviolet (UV) absorbance of fouled quartz sleeves in UV disinfection systems were studied. Statistical analysis was conducted to examine the effects of nine fouling chemicals on the UV transmittance changes of fouled quartz lamp sleeves. The results demonstrated that the main effects were attributable to surface concentrations of iron and manganese. The surface concentrations of calcium and copper had no significant effects on the UV absorbance of fouled sleeves. The interaction effects of copper with iron and magnesium with manganese were also revealed from the statistical analysis. The model is able to give reasonable predictions of the UV absorbance characteristics of foulants from other UV systems. However, several limitations of this model were identified. First, the model does not accurately predict the absorbance at relatively high chemical surface concentrations. Second, the model does not account for the possible effects of anions and organics on UV absorption of fouled quartz sleeves.

scholarly journals Silver Nanoparticles Functionalized by Fluorescein Isothiocyanate or Rhodamine B Isothiocyanate: Fluorescent and Plasmonic Materials

2021 ◽  
Vol 11 (6) ◽  
pp. 2472
Author(s):  
Ilaria Fratoddi ◽  
Chiara Battocchio ◽  
Giovanna Iucci ◽  
Daniele Catone ◽  
Antonella Cartoni ◽  
...  
Keyword(s):  
Silver Nanoparticles ◽  
Rhodamine B ◽  
Photoelectron Spectroscopy ◽  
Transient Absorption ◽  
Fluorescein Isothiocyanate ◽  
Dye Molecules ◽  
Chemical Surface ◽  
Vis Spectroscopy ◽  
Rhodamine B Isothiocyanate ◽  
Fluorescent Molecules

This paper presents the synthesis of silver nanoparticles (AgNPs) functionalized with fluorescent molecules, in particular with xanthene-based dyes, i.e., fluorescein isothiocyanate (FITC, λmax = 485 nm) and rhodamine B isothiocyanate (RITC, λmax = 555 nm). An in-depth characterization of the particle–dye systems, i.e., AgNPs–RITC and AgNPs–FITC, is presented to evaluate their chemical structure and optical properties due to the interaction between their plasmonic and absorption properties. UV–Vis spectroscopy and the dynamic light scattering (DLS) measurements confirmed the nanosize of the AgNPs–RITC and AgNPs–FITC. Synchrotron radiation X-ray photoelectron spectroscopy (SR-XPS) was used to study the chemical surface functionalization by structural characterization, confirming/examining the isothiocyanate–metal interaction. For AgNPs–RITC, in which the plasmonic and fluorescence peak are not superimposed, the transient dynamics of the dye fluorescence were also studied. Transient absorption measurements showed that by exciting the AgNPs–RITC sample at a wavelength corresponding to the AgNP plasmon resonance, it was possible to preferentially excite the RITC dye molecules attached to the surface of the NPs with respect to the free dye molecules in the solution. These results demonstrate how, by combining plasmonics and fluorescence, these AgNPs can be used as promising systems in biosensing and imaging applications.

scholarly journals Improving Surface Imprinting Effect by Reducing Nonspecific Adsorption on Non-imprinted Polymer Films for 2,4-D Herbicide Sensors

Chemosensors ◽  
2021 ◽  
Vol 9 (3) ◽  
pp. 43
Author(s):  
Jin Chul Yang ◽  
Suck Won Hong ◽  
Jinyoung Park
Keyword(s):  
Morphological Changes ◽  
Unit Weight ◽  
Dichlorophenoxyacetic Acid ◽  
Surface Imprinting ◽  
Imprinted Polymer ◽  
Nonspecific Adsorption ◽  
Chemical Surface ◽  
Silane Modification ◽  
Silanized Silica ◽  
2,4 Dichlorophenoxyacetic Acid

Surface imprinting used for template recognition in nanocavities can be controlled and improved by surface morphological changes. Generally, the lithographic technique is used for surface patterning concerning sensing signal amplification in molecularly imprinted polymer (MIP) thin films. In this paper, we describe the effects of silanized silica molds on sensing the properties of MIP films. Porous imprinted poly(MAA–co–EGDMA) films were lithographically fabricated using silanized or non-treated normal silica replica molds to detect 2,4-dichlorophenoxyacetic acid (2,4-D) herbicide as the standard template. The silanized mold MIP film (st-MIP) (Δf = −1021 Hz) exhibited a better sensing response than the non-treated normal MIP (n-MIP) (Δf = −978 Hz) because the imprinting effects, which occurred via functional groups on the silica surface, could be reduced through silane modification. Particularly, two non-imprinted (NIP) films (st-NIP and n-NIP) exhibited significantly different sensing responses. The st-NIP (Δfst-NIP = −332 Hz) films exhibited lower Δf values than the n-NIP film (Δfn-NIP = −610 Hz) owing to the remarkably reduced functionality against nonspecific adsorption. This phenomenon led to different imprinting factor (IF) values for the two MIP films (IFst-MIP = 3.38 and IFn-MIP = 1.86), which was calculated from the adsorbed 2,4-D mass per poly(MAA–co–EGDMA) unit weight (i.e., QMIP/QNIP). Moreover, it was found that the st-MIP film had better selectivity than the n-MIP film based on the sensing response of analogous herbicide solutions. As a result, it was revealed that the patterned molds’ chemical surface modification, which controls the surface functionality of imprinted films during photopolymerization, plays a role in fabricating enhanced sensing properties in patterned MIP films.

scholarly journals Chemical Surface Modification of Oil Palm Fibre: a Case study of developed Oil Palm Fibre-Plastic Composites

2021 ◽  
Vol 1107 (1) ◽  
pp. 012091
Author(s):  
E. Baffour-Awuah ◽  
S. A. Akinlabi ◽  
T. C. Jen ◽  
I. P. Okokpujie ◽  
S. Hassan ◽  
...  
Keyword(s):  
Surface Modification ◽  
Oil Palm ◽  
Chemical Surface ◽  
Plastic Composites ◽  
Chemical Surface Modification ◽  
Oil Palm Fibre ◽  
Palm Fibre

scholarly journals Amperometric Biosensors Based on Direct Electron Transfer Enzymes

Molecules ◽  
2021 ◽  
Vol 26 (15) ◽  
pp. 4525
Author(s):  
Franziska Schachinger ◽  
Hucheng Chang ◽  
Stefan Scheiblbrandner ◽  
Roland Ludwig
Keyword(s):  
Electron Transfer ◽  
Electrode Materials ◽  
Direct Electron Transfer ◽  
Accurate Determination ◽  
Direct Electrochemistry ◽  
Product Analysis ◽  
Amperometric Biosensors ◽  
Chemical Surface ◽  
Fusion Enzymes ◽  
Cost Efficient

The accurate determination of analyte concentrations with selective, fast, and robust methods is the key for process control, product analysis, environmental compliance, and medical applications. Enzyme-based biosensors meet these requirements to a high degree and can be operated with simple, cost efficient, and easy to use devices. This review focuses on enzymes capable of direct electron transfer (DET) to electrodes and also the electrode materials which can enable or enhance the DET type bioelectrocatalysis. It presents amperometric biosensors for the quantification of important medical, technical, and environmental analytes and it carves out the requirements for enzymes and electrode materials in DET-based third generation biosensors. This review critically surveys enzymes and biosensors for which DET has been reported. Single- or multi-cofactor enzymes featuring copper centers, hemes, FAD, FMN, or PQQ as prosthetic groups as well as fusion enzymes are presented. Nanomaterials, nanostructured electrodes, chemical surface modifications, and protein immobilization strategies are reviewed for their ability to support direct electrochemistry of enzymes. The combination of both biosensor elements—enzymes and electrodes—is evaluated by comparison of substrate specificity, current density, sensitivity, and the range of detection.

scholarly journals Crystallization of TiO2-MoS2 Hybrid Material under Hydrothermal Treatment and Its Electrochemical Performance

Materials ◽  
2020 ◽  
Vol 13 (12) ◽  
pp. 2706
Author(s):  
Katarzyna Siwińska-Ciesielczyk ◽  
Beata Kurc ◽  
Dominika Rymarowicz ◽  
Adam Kubiak ◽  
Adam Piasecki ◽  
...  
Keyword(s):  
Hydrothermal Treatment ◽  
Surface Composition ◽  
Specific Capacity ◽  
Diffraction Method ◽  
Lithium Ion ◽  
Surface Concentration ◽  
Molar Ratio ◽  
Storage Device ◽  
X Ray ◽  
Chemical Surface

Hydrothermal crystallization was used to synthesize an advanced hybrid system containing titania and molybdenum disulfide (with a TiO2:MoS2 molar ratio of 1:1). The way in which the conditions of hydrothermal treatment (180 and 200 °C) and thermal treatment (500 °C) affect the physicochemical properties of the products was determined. A physicochemical analysis of the fabricated materials included the determination of the microstructure and morphology (scanning and transmission electron microscopy—SEM and TEM), crystalline structure (X-ray diffraction method—XRD), chemical surface composition (energy dispersive X-ray spectroscopy—EDS) and parameters of the porous structure (low-temperature N2 sorption), as well as the chemical surface concentration (X-ray photoelectron spectroscop—XPS). It is well known that lithium-ion batteries (LIBs) represent a renewable energy source and a type of energy storage device. The increased demand for energy means that new materials with higher energy and power densities continue to be the subject of investigation. The objective of this research was to obtain a new electrode (anode) component characterized by high work efficiency and good electrochemical properties. The synthesized TiO2-MoS2 material exhibited much better electrochemical stability than pure MoS2 (commercial), but with a specific capacity ca. 630 mAh/g at a current density of 100 mA/g.

scholarly journals DFT Study of the Electronic Structure of Cubic-SiC Nanopores with a C-Terminated Surface

2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
M. Calvino ◽  
A. Trejo ◽  
M. I. Iturrios ◽  
M. C. Crisóstomo ◽  
Eliel Carvajal ◽  
...  
Keyword(s):  
Electronic Structure ◽  
Band Gap ◽  
Density Functional ◽  
Surface Passivation ◽  
Phase Changes ◽  
Surface Relaxation ◽  
Oh Radicals ◽  
Functional Theory ◽  
Band Gap Engineering ◽  
Chemical Surface

A study of the dependence of the electronic structure and energetic stability on the chemical surface passivation of cubic porous silicon carbide (pSiC) was performed using density functional theory (DFT) and the supercell technique. The pores were modeled by removing atoms in the [001] direction to produce a surface chemistry composed of only carbon atoms (C-phase). Changes in the electronic states of the porous structures were studied by using different passivation schemes: one with hydrogen (H) atoms and the others gradually replacing pairs of H atoms with oxygen (O) atoms, fluorine (F) atoms, and hydroxide (OH) radicals. The results indicate that the band gap behavior of the C-phase pSiC depends on the number of passivation agents (other than H) per supercell. The band gap decreased with an increasing number of F, O, or OH radical groups. Furthermore, the influence of the passivation of the pSiC on its surface relaxation and the differences in such parameters as bond lengths, bond angles, and cell volume are compared between all surfaces. The results indicate the possibility of nanostructure band gap engineering based on SiC via surface passivation agents.

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