Carbonaceous minerals as corrosion products on the surface of bottles

2020 ◽  
Vol 61 (6) ◽  
pp. 185-191
Author(s):  
A. Özcan ◽  
◽  
B. Arman ◽  
S. Demirli ◽  
M. Orhon
Keyword(s):  
Analytical Techniques ◽  
Test Methods ◽  
Critical Parameters ◽  
Humid Atmosphere ◽  
Silanol Groups ◽  
Annealing Conditions ◽  
Gel Layer ◽  
Colour Scale ◽  
Blue Solution ◽  
Ft Ir

During the corrosion process, as the ion exchange between the surface of the glass and the water progresses, the chemical structure of the surface changes and different structural layers are formed. These layers are characterised by various analytical techniques such as EPMA, XRD, FT-IR, TG-DTA and ICP-OES. Three carbonate mineral species namely calcite (CaCO3), shortite (Na2Ca2(CO3)3) and nyerereite (Na2Ca(CO3)2) have been identified at the outermost deposition layer. Critical parameters that affect the formation of the alkali depleted and silica enriched gel layer are investigated using some special test methods. Methylene blue solution reacts with the silanol groups of gel layer leaving a blue tint behind, the intensity of which varies with the extent of corrosion as the amount of silanol groups outcropped due to the increase of the porous structure area. A colour scale is developed to determine the level of corrosion and the results are correlated with the results of other known chemical analysis methods. The effect of annealing conditions on the chemical resistance of the surfaces and the role of the shape of the bottles on the water condensation at humid atmosphere are studied. The results of acid treatment and re-annealing of the corroded surfaces are described.

scholarly journals Chitosan hydrogel/silk fibroin/Mg(OH)2 nanobiocomposite as a novel scaffold with antimicrobial activity and improved mechanical properties

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Reza Eivazzadeh-Keihan ◽  
Fateme Radinekiyan ◽  
Hooman Aghamirza Moghim Aliabadi ◽  
Sima Sukhtezari ◽  
Behnam Tahmasebi ◽  
...  
Keyword(s):  
Antibacterial Activity ◽  
Cell Viability ◽  
Silk Fibroin ◽  
Analytical Techniques ◽  
Structural Features ◽  
Mechanical Tests ◽  
Chitosan Hydrogel ◽  
Biological Capacity ◽  
Ft Ir ◽  
Novel Scaffold

AbstractHerein, a novel nanobiocomposite scaffold based on modifying synthesized cross-linked terephthaloyl thiourea-chitosan hydrogel (CTT-CS hydrogel) substrate using the extracted silk fibroin (SF) biopolymer and prepared Mg(OH)2 nanoparticles was designed and synthesized. The biological capacity of this nanobiocomposite scaffold was evaluated by cell viability method, red blood cells hemolytic and anti-biofilm assays. According to the obtained results from 3 and 7 days, the cell viability of CTT-CS/SF/Mg(OH)2 nanobiocomposite scaffold was accompanied by a considerable increment from 62.5 to 89.6% respectively. Furthermore, its low hemolytic effect (4.5%), and as well, the high anti-biofilm activity and prevention of the P. aeruginosa biofilm formation confirmed its promising hemocompatibility and antibacterial activity. Apart from the cell viability, blood biocompatibility, and antibacterial activity of CTT-CS/SF/Mg(OH)2 nanobiocomposite scaffold, its structural features were characterized using spectral and analytical techniques (FT-IR, EDX, FE-SEM and TG). As well as, given the mechanical tests, it was indicated that the addition of SF and Mg(OH)2 nanoparticles to the CTT-CS hydrogel could improve its compressive strength from 65.42 to 649.56 kPa.

scholarly journals Multifunctional application of PVA-aided Zn–Fe–Mn coupled oxide nanocomposite

2021 ◽  
Vol 16 (1) ◽  
Author(s):  
Buzuayehu Abebe ◽  
H. C. Ananda Murthy ◽  
Enyew Amare Zereffa
Keyword(s):  
Charge Transfer ◽  
Analytical Techniques ◽  
Antibacterial Activities ◽  
Poly Vinyl Alcohol ◽  
Blue Dye ◽  
Ternary Oxide ◽  
Gram Positive Bacteria ◽  
Transfer Capability ◽  
Ft Ir ◽  
Synthesized Materials

AbstractZinc oxide (ZnO) is a fascinating semiconductor material with many applications such as adsorption, photocatalysis, sensor, and antibacterial activities. By using a poly (vinyl alcohol) (PVA) polymer as a capping agent and metal oxides (iron and manganese) as a couple, the porous PVA-aided Zn/Fe/Mn ternary oxide nanocomposite material (PTMO-NCM) was synthesized. The thermal, optical, crystallinity, chemical bonding, porosity, morphological, charge transfer properties of the synthesized materials were confirmed by DTG/DSC, UV–Vis-DRS, XRD, FT-IR, BET, SEM-EDAX/TEM-HRTEM-SAED, and CV/EIS/amperometric analytical techniques, respectively. The PTMO-NCM showed an enhanced surface area and charge transfer capability, compared to ZnO. Using the XRD pattern and TEM image analysis, the crystalline size of the materials was confirmed to be in the nanometer range. The porosity and superior charge transfer capabilities of the PTMO-NCM were confirmed from the BET, HRTEM (IFFT)/SAED, and CV/EIS analysis. The adsorption kinetics (adsorption reaction/adsorption diffusion) and adsorption isotherm test confirmed the presence of a chemisorption type of adsorbate/methylene blue dye-adsorbent/PTMO-NCM interaction. The photocatalytic performance was tested on the Congo red and Acid Orange-8 dyes. The superior ascorbic acid sensing capability of the material was understood from CV and amperometric analysis. The noble antibacterial activities of the material were also confirmed on both gram-negative and gram-positive bacteria.

The Effect of Support Pretreatment with Ammonia on Pd/SiO2 Catalyst

2018 ◽  
Vol 922 ◽  
pp. 125-129
Author(s):  
Ji Soo Kwon ◽  
Jae Ho Baek ◽  
Hak Sung Lee ◽  
Man Sig Lee
Keyword(s):  
Silanol Group ◽  
N2 Adsorption ◽  
Ammonia Water ◽  
Co Chemisorption ◽  
Silanol Groups ◽  
Pd Dispersion ◽  
Highly Dispersed ◽  
High Metal ◽  
Ft Ir ◽  
Effect Of Support

We have reported the effect of support pretreatment with ammonia on Pd/SiO2 catalyst in this study. SiO2 was pretreated with ammonia water to increase the Pd dispersion before the preparation of Pd/SiO2 catalysts. The effect of support pretreatment with ammonia on Pd/SiO2 catalyst was investigated by XRD, FT-IR, N2-adsorption and FE-TEM. The Pd supported on pretreated SiO2 were characterized by XRD, CO-chemisorption and FE-TEM. The pretreatment of SiO2 with ammonia water lead to decrease of silanol groups (Si-OH) up to temperature 200 °C. This decline of silanol groups on the SiO2 affects highly dispersed Pd/SiO2 as 6.52 %. The result showed that the decrease of silanol group on the SiO2 was favorable for the Pd dispersion. It is reason that absence of the silanol groups contribute to the high metal reducibility.

scholarly journals Green synthesis of cuprous oxide (Cu2O) nano particles using aloe vera plant

2021 ◽  
Vol 10 (2) ◽  
pp. 54-58
Author(s):  
Giang Nguyen Thi Le ◽  
Tu Nguyen Cong ◽  
Thang Pham Van ◽  
Mai Nguyen Thi Tuyet ◽  
Lan Nguyen Thi ◽  
...  
Keyword(s):  
Green Synthesis ◽  
Aqueous Extract ◽  
Cuprous Oxide ◽  
Aloe Vera ◽  
Analytical Techniques ◽  
Nano Particles ◽  
Oxide Nanoparticles ◽  
Characterization Techniques ◽  
Cuprous Oxide Nanoparticles ◽  
Ft Ir

In the present work,  a green synthesis of  cuprous oxide nanoparticles  was demonstrated using the freshly prepared aqueous extract of the aloe vera plant and the cupper oxide nanoparticles  were characterized by the analytical techniques such as UV-Vis, FT-IR, XRD, and EDX. Characterization techniques confirmed that the biomolecules involved  in the formation of cupper oxide nanoparticles and also they stabilized the nanoparticles.

scholarly journals Less Reactive Thiol Ligands: Key towards Highly Mucoadhesive Drug Delivery Systems

Polymers ◽  
2020 ◽  
Vol 12 (6) ◽  
pp. 1259 ◽  
Author(s):  
Iram Shahzadi ◽  
Andrea Fürst ◽  
Zeynep Burcu Akkus-Dagdeviren ◽  
Shumaila Arshad ◽  
Markus Kurpiers ◽  
...  
Keyword(s):  
Intestinal Mucosa ◽  
Polyacrylic Acid ◽  
Drug Delivery Systems ◽  
Bond Formation ◽  
Work Of Adhesion ◽  
Gel Layer ◽  
Thiol Ligands ◽  
Mucus Gel ◽  
Ft Ir ◽  
Acetyl Cysteine

As less reactive s-protected thiomers can likely interpenetrate the mucus gel layer to a higher extent before getting immobilized via disulfide bond formation with mucins, it was the aim of this study to develop a novel type of s-protected thiomer based on the less reactive substructure cysteine-N-acetyl cysteine (Cys-NAC) in order to obtain improved mucoadhesive properties. For this purpose, two types of s-protected thiomers, polyacrylic acid-cysteine-mercaptonicotinic acid (PAA-Cys-MNA) and polyacrylic acid-cysteine-N-acetyl cysteine (PAA-Cys-NAC), were synthesized and characterized by Fourier-transform infrared spectroscopy (FT-IR) and the quantification of attached disulfide ligands. The viscosity of both products was measured in the presence of NAC and mucus. Both thiomers were also evaluated regarding swelling behavior, tensile studies and retention time on the porcine intestinal mucosa. The FT-IR spectra confirmed the successful attachment of Cys-MNA and Cys-NAC ligands to PAA. The number of attached sulfhydryl groups was in the range of 660–683 µmol/g. The viscosity of both s-protected thiomers increased due to the addition of increasing amounts of NAC. The viscosity of the mucus increased in the presence of 1% PAA-Cys-MNA and PAA-Cys-NAC 5.6- and 10.9-fold, respectively, in comparison to only 1% PAA. Both s-protected thiomers showed higher water uptake than unmodified PAA. The maximum detachment force (MDF) and the total work of adhesion (TWA) increased in the case of PAA-Cys-MNA up to 1.4- and 1.6-fold and up to 2.4- and 2.8-fold in the case of PAA-Cys-NAC. The retention of PAA, PAA-Cys-MNA, and PAA-Cys-NAC on porcine intestinal mucosa was 25%, 49%, and 76% within 3 h, respectively. The results of this study provide evidence that less reactive s-protected thiomers exhibit higher mucoadhesive properties than highly reactive s-protected thiomers.

scholarly journals Quantitative determination of tolfenamic acid and its pharmaceutical formulation using FTIR and UV spectrometry

2013 ◽  
Vol 11 (9) ◽  
pp. 1533-1541 ◽  
Author(s):  
Sofia Ahmed ◽  
Muhammad Sheraz ◽  
Ceyla Yorucu ◽  
Ihtesham Rehman
Keyword(s):  
Uv Spectroscopy ◽  
Peak Height ◽  
Test Methods ◽  
Tolfenamic Acid ◽  
Test Procedures ◽  
Titration Method ◽  
Uv Spectrometry ◽  
Analytical Wavelength ◽  
Ft Ir ◽  
Tablet Dosage

AbstractAbstract The quantitative analysis of Tolfenamic Acid (TA) both as a pure compound and in tablet dosage form has been carried out using FT-IR and UV spectroscopy. In the FT-IR method, a number of characteristic absorption peaks were examined that could be used for analytical purpose. The analysis was carried out by preparing calibration curves of peak height/area versus TA content using two points baseline correction with fixed location, and the data was also analyzed through PLS regression model. In the UV method, ethanolic solutions of the drug were analyzed at 288 nm (λmax) using 480 as the value of A (1%, 1 cm) at the analytical wavelength. The results have been compared statistically for recovery, precision, accuracy and linearity with the British Pharmacopoeial titration method that showed good validity of both test procedures. The two test methods exhibited good recovery of TA with an accuracy of 99.75–100.83% and 99.53–100.11% by FTIR spectrometry for peak height and area respectively and 100.21% for UV method. However, UV spectrometry was found to be more accurate and precise on the basis of statistical evaluation and hence can be employed in the quality control of TA in pharmaceuticals as an alternative to the titration method. Graphical abstract

Magnetic Nanoparticle Supported Ionic Liquid Phase Catalyst for Oxidation of Alcohols

2020 ◽  
Vol 73 (11) ◽  
pp. 1088
Author(s):  
Altafhusen Naikwade ◽  
Megha Jagadale ◽  
Dolly Kale ◽  
Gajanan Rashinkar
Keyword(s):  
Ionic Liquid ◽  
Liquid Phase ◽  
Photoelectron Spectroscopy ◽  
Magnetic Nanoparticle ◽  
Analytical Techniques ◽  
X Ray ◽  
Supported Ionic Liquid ◽  
Transmission Electron ◽  
Oxidation Of Alcohols ◽  
Ft Ir

A new magnetic nanoparticle supported ionic liquid phase (SILP) catalyst containing perruthenate anions was prepared by a multistep procedure. The various analytical techniques such as FT-IR spectroscopy, X-ray photoelectron spectroscopy, transmission electron microscopy, thermogravimetric analysis, energy dispersive X-ray analysis, and vibrating sample magnetometer analysis ascertained the successful formation of catalyst. The performance of a magnetically retrievable SILP catalyst was evaluated in the selective oxidation of alcohols. The split test and leaching studies of the SILP catalyst confirmed its heterogeneous nature. In addition, the reusability potential of SILP catalyst was also investigated which revealed its robust activity up to six consecutive cycles.

scholarly journals Functional Aromatic Poly(1,3,4-Oxadiazole-Ether)s with Benzimidazole Pendants: Synthesis, Thermal and Dielectric Studies

2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
Shimoga D. Ganesh ◽  
Vasantakumar K. Pai ◽  
Mahadevappa Y. Kariduraganavar ◽  
Madhu B. Jayanna
Keyword(s):  
Carboxylic Acid ◽  
Average Molecular Weight ◽  
Analytical Techniques ◽  
Gel Permeation Chromatography ◽  
Electrical Contacts ◽  
Dielectric Studies ◽  
Weight Average Molecular Weight ◽  
Nucleophilic Displacement ◽  
Ft Ir

Poly(1,3,4-oxadiazole-ether) with reactive carboxylic acid pendants was synthesized from solution polymerization via nucleophilic displacement polycondensation among 2,5-bis(4-fluorophenyl)-1,3,4-oxadiazole (BFPOx) and 4,4′-bis(4-hydroxyphenyl) valeric acid (BHPA). Without altering the polymeric segments, benzimidazole modified poly(1,3,4-oxadiazole-ether)s were prepared by varying stoichiometric ratios of 1,2-phenylenediamine. The molecular structural characterization of these polymers was achieved by, FT-IR, NMR, TGA, elemental analysis, and analytical techniques. The weight-average molecular weight of virgin polymer with carboxylic acid functionality was determined by gel permeation chromatography (GPC) and was found to be 22400 (Mw/Mn=2.07). All the synthesized polyethers were compressed into pellets and electrical contacts were established to perform dielectric properties.

In-Situ FT-IR Monitoring of a Solar Flux Induced Chemical Process

1997 ◽  
Vol 119 (3) ◽  
pp. 219-224 ◽  
Author(s):  
J. R. Markham ◽  
J. E. Cosgrove ◽  
C. M. Nelson ◽  
A. S. Bonanno ◽  
R. E. Schlief ◽  
...  
Keyword(s):  
Flow Reactor ◽  
Hydrogen Bromide ◽  
Solar Flux ◽  
Solar Furnace ◽  
Critical Parameters ◽  
Steam Temperature ◽  
Photochemical Process ◽  
Ft Ir ◽  
Formed Hydrogen

The capability to perform in-situ, on-line monitoring of processes induced by concentrated solar flux will enhance the development and utilization of solar technologies. Temperature measurements and chemical concentration measurements provide an understanding of the ongoing chemistry, process limits, and process reproducibility. A Fourier transform infrared (FT-IR) spectrometer was optically coupled to a quartz flow reactor at the High Flux Solar Furnace of the National Renewable Energy Laboratory in Golden, CO. In-situ emission/transmission spectroscopy was utilized to simultaneously monitor steam temperature and the concentration of formed hydrogen bromide during the solar flux induced reaction of steam and bromine. The photochemical process is being investigated for the production of industrial quantities of hydrogen and oxygen, where downstream electrolysis of the formed hydrogen bromide provides the hydrogen and regenerates bromine. Steam temperature was measured to increase upon the addition of bromine to the reactor. Gas temperature increases of 200°C to 400°C were observed. Hydrogen bromide concentrations up to ten percent of the reactor gas volume were measured. The FT-IR system provided quantitative information of two critical parameters of the measured process and serves to accelerate this technology area.

scholarly journals Construction of a crossed-layer-structure MoS2/g-C3N4 heterojunction with enhanced photocatalytic performance

RSC Advances ◽  
2017 ◽  
Vol 7 (10) ◽  
pp. 6131-6139 ◽  
Author(s):  
Youzhi Cao ◽  
Qiao Li ◽  
Wei Wang
Keyword(s):  
Ir Spectra ◽  
Carbon Nitride ◽  
Photocatalytic Performance ◽  
Layer Structure ◽  
Analytical Techniques ◽  
Graphitic Carbon Nitride ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ft Ir ◽  
Diffraction Patterns

A novel crossed-layer-structure MoS2/g-C3N4 (graphitic carbon nitride) was synthesized by a facile method, and was characterized by a collection of analytical techniques: X-ray diffraction patterns, FT-IR spectra, SEM, TEM, and XPS.

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