scholarly journals Radiolytic synthesis and characterization of PVA/Au nanocomposites: The influence of pH values

2008 ◽  
Vol 62 (3) ◽  
pp. 101-106 ◽  
Author(s):  
Aleksandra Krkljes ◽  
Miodrag Mitric ◽  
Zorica Kacarevic-Popovic
Keyword(s):  
Particle Size ◽  
Absorption Spectra ◽  
Au Nanoparticles ◽  
Ph Value ◽  
Strong Dependence ◽  
Nanocomposite Films ◽  
Oh Groups ◽  
Ph Values ◽  
Au Colloids ◽  
Radiolytic Synthesis

Nanocomposites which consist of polymer matrix and nanoparticles of noble metal are a very important class of nanomaterials. The optical properties of these materials are strongly dependent on the nanoparticles size as well as on the synthesized procedure of nanocomposites preparation. In this work the Au nanoparticles were synthesized by the simple radiolytic procedure, using steady state gamma irradiation, under different pH values. PVA/Au nanocomposite films were obtained by solvent evaporation from Au colloids. UV-Vis absorption spectra of Au colloids show absorption in the range of 450 to 650 nm with the maximum around 520 nm, which is the typical plasmon band of Au nanoparticles. Absorption spectra of PVA/Au nanocomposites are red shifted compared to corresponding primary Au colloids. This red shift is not result of any change in particle size distribution and can be explained by the change of dielectric property of surrounding medium. IR spectra indicated anchoring the OH groups of PVA molecule at the cluster surface. This effect limits the growing of the metal clusters and confirmed that the PVA is a god matrix for in situ synthesis of Au nanoparticles. The size of Au nanoparticles is dependent on the experimental conditions. Obtained results indicated that the pH value of solution played an important role. The values of absorption maximum (?max) were not dependent on the concentration of Au cations, but show strong dependence on the pH value of the initial solution. The increase of pH value reduced the mean diameters of nanoparticles. The lowest value of ?max was obtained for colloid with pH 7, which theoretically corresponds to the nanoparticles with minimum dimension. These results are in agreement with the XRD measurement of PVA/Au nanocomposite films and theoretical calculations. According to obtained results of radiolytic synthesis of Au nanoparticles in PVA solution can be conclude that it is possible to control the particle size by tuning the pH value of solution.

scholarly journals Influence of pH and ionic strength on the aggregation behaviors of xylan rich hemicelluloses with alkaline lignins

BioResources ◽  
2021 ◽  
Vol 16 (4) ◽  
pp. 7608-7622
Author(s):  
Guichun Hu ◽  
Jinguang Hu ◽  
Honglei Chen ◽  
Shunxi Song ◽  
Fuqiang Chu
Keyword(s):  
Particle Size ◽  
Self Assembly ◽  
Main Chain ◽  
Ph Value ◽  
Low Ph ◽  
Ph Values ◽  
Wide Range ◽  
Nacl Concentration ◽  
Aggregation Behaviors ◽  
Influence Of Ph

The evolution of xylan-rich hemicelluloses (XH) aggregation behaviors in the presence of alkaline lignins (AL) under a wide range of pH values and NaCl concentration were investigated via dynamic light scattering and turbidity measurements. XH isolated from wheat straw contain a xylose backbone with arabinose side chains and a small amount of phenol groups. XH tend to aggregate in solution due to their low ratio of arabinose to xylose and hydrophobic phenol groups. AL interact with XH through the phenol groups bonded to the hemicellulose main chain to form an AL-XH complex. As the pH value decreases, the particle size and turbidity of AL, XH and their bonded complex all increase. The size of the AL-XH complex agglomerate is greater than the size of a XH at the same pH value, which indicates that the self-assembly of lignin molecules initiate the aggregation of XH. The particle size and turbidity of XH and AL-XH complexes increase as the XH concentration increase. At low pH values, e.g., 6.0, the particle size of the AL-XH complex more obviously increases compared to the XH particles. The size and turbidity of the AL, XH, and AL-XH complex agglomerates increased as the NaCl concentration increased.

Colloidal dispersion of metal nanoparticles electrosterically stabilized with Carrageenan type κ and its application as hydrogel.

2013 ◽  
Vol 1453 ◽  
Author(s):  
Jose Infante-Rivera ◽  
Victoria Campos ◽  
C.A. Guerrero-Salazar ◽  
Ubaldo Ortiz-Méndez ◽  
A. Olivas ◽  
...  
Keyword(s):  
Particle Size ◽  
Metal Nanoparticles ◽  
Ag Nanoparticles ◽  
Au Nanoparticles ◽  
Ph Value ◽  
Colloidal Dispersion ◽  
Long Period ◽  
Nanoparticles Dispersion ◽  
Vis Spectroscopy ◽  
Alkaline Conditions

ABSTRACTIn this work Carrageenan type κ was used as electrosteric stabilizer in order to prepare a biocompatible colloidal dispersion of novel metal nanoparticles. Gold and silver nanoparticles were synthesized by reducing the metal precursor using sodium borohydride in presence of Carrageenan type κ. The growth mechanism of metal nanoparticles and stabilization behavior by Carrageenan type κ was analyzed by UV-Vis spectroscopy and transmission electron microscopy. The morphology and particle size distribution were also studied as a function of reaction parameters and the particle size was dependent of the pH of the reaction media. The Ag nanoparticles with sphere-like morphology and average size of 10 nm were obtained. The morphology of Au nanoparticles was strongly affected by the pH value resulting in particles with snake-like morphology at alkaline conditions. The UV-Vis spectra showed that Ag nanoparticles were highly stable at alkaline conditions and for long period of time. Au nanoparticles dispersion showed a better stability for long period of time at acidic conditions. The nanoparticles dispersion electrosterically stabilized were used to prepare hydrogels by poured into a plastic mold and frozen with liquid nitrogen and then lyophilized. The morphology and thermal stability of resulting composites were analyzed by using scanning electronic microscopy and differential scanning calorimetry respectively. The degradation temperature of Carrageenan type κ was increased due to the presence of metal nanoparticles.

scholarly journals Effect of Chitosan/BSA Addition on the Physical Stability of Sunflower Oil Emulsions

2019 ◽  
Vol 2019 ◽  
pp. 1-8 ◽  
Author(s):  
Fengyan Zhou ◽  
Guo Li ◽  
Jianying Huang
Keyword(s):  
Particle Size ◽  
Bovine Serum Albumin ◽  
Zeta Potential ◽  
Sunflower Oil ◽  
Storage Stability ◽  
Emulsion Stability ◽  
Ph Value ◽  
Physical Stability ◽  
Ph Values ◽  
Oil Emulsions

Proteins and polysaccharides are important ingredients and additives in food field. The aim of this study was to study the effect of chitosan and bovine serum albumin (BSA) solution on the physical stability of sunflower oil emulsions at different pH values, temperatures, and BSA/chitosan ratios during 20-day storage in terms of their storage stability, zeta potential, particle size, and microstructure. The results showed that pH, protein/polysaccharide ratio, and temperature significantly influenced the physical stability of emulsions at lower pH. The emulsion stability decreased as the test temperatures increased, and the storage stability of BSA/chitosan coated oil emulsions was obtained when the ratio was from 8 : 1 to 1 : 1 under 4°C for 20-day storage when pH values were 3.0 and 4.0. Droplet flocculation happened with the increase of chitosan addition and pH value.

Characteristics of wood-silica composites influenced by the pH value of silica sols

Holzforschung ◽  
2018 ◽  
Vol 72 (4) ◽  
pp. 311-319 ◽  
Author(s):  
Jun Jiang ◽  
Jinzhen Cao ◽  
Wang Wang
Keyword(s):  
Particle Size ◽  
Zeta Potential ◽  
Dimensional Stability ◽  
Colloidal Particle ◽  
Ph Value ◽  
Surface Hardness ◽  
X Ray ◽  
Ph Values ◽  
First Case ◽  
Silica Sols

AbstractSouthern pine (Pinusspp.) sapwood samples were impregnated with silica sols with known zeta potential and particle size distribution at various pH values (3, 5, 7, 9, 11 and 13) to produce wood-silica composites (WSiCs). The morphological and chemical properties of the composites were evaluated by scanning electron microscopy-energy dispersive X-ray (SEM-EDXA) and Fourier transform infrared (FTIR) spectroscopy. The overall performance of the composites was characterized by X-ray diffraction (XRD) and thermogravimetric (TG) analysis, and dynamic wettability tests, and their dimensional stability and surface hardness were also investigated as well. The pH value of the sols had a remarkable effect on the distribution of zeta potential and colloidal particle size, and on their penetration and distribution in the wood. The composites produced at pH 5 and pH 11 show relatively better impregnability and overall properties. In the first case the compatibility with the wood pH (ca. 5) is relevant, and at these pH values are the sol’s particle sizes low. Sols with pH around 13 resulted in inferior properties, such as increased water absorption, high thermal degradation and poor dimensional stability. This could be ascribed to wood degradation under high alkaline conditions. The results were discussed in view of the colloidal particle redistribution and the interaction between silica sol and wood.

The Dispersion of SiC Nanopowders in Ethanol

2012 ◽  
Vol 512-515 ◽  
pp. 779-784 ◽  
Author(s):  
Yang Hou ◽  
Ping Hu ◽  
Wen Bo Han
Keyword(s):  
Particle Size ◽  
Test Particle ◽  
Ph Value ◽  
Ethanol Solution ◽  
Size Measurement ◽  
Tem Analysis ◽  
Particle Size Measurement ◽  
Ph Values ◽  
Isoelectric Points ◽  
The Stability

The dispersion of SiC nanopowders in ethanol solution was studied by sedimentation test, particle size measurement and TEM analysis. The dispersion behavior of SiC nanopowders in ethanol solution was strongly dependent on the pH values, types and amounts of dispersant. PEI was found to be effective for the dispersion of SiC nanopowders in ethanol solution. With the addition of PEI, the isoelectric points of SiC nanopowders in ethanol solution were at pH 9.5, and shift to pH 12.3. The stability of SiC suspension increased with the dispersant content increasing until reached 2.5 wt% PEI. The suitable pH value for the dispersion of SiC nanopowders should lower than 10.

Evaluation of Hydroxyl Groups on Hydroxyapatite and Calcium Metaphosphate by Grafting TEOS and APTES

2007 ◽  
Vol 342-343 ◽  
pp. 677-680 ◽  
Author(s):  
Chang Kuk You ◽  
Sung Min Kim ◽  
Myun Whan Ahn ◽  
Seong Yong Kim ◽  
Suk Young Kim
Keyword(s):  
Aqueous Solution ◽  
Ph Value ◽  
Ethanol Solution ◽  
Hydroxyl Groups ◽  
Acidic Media ◽  
Ph Change ◽  
Oh Groups ◽  
Ph Values ◽  
Phosphate Ions ◽  
Ph Increase

OH groups on hydroxyapatite (HA) and calcium metaphosphate (CMP) were evaluated by grafting tetraethyl orthosilicate (TEOS) and 3-aminopropyltriethyloxysilane (3-APTES) which can bond covalently with OH group of ceramic biomaterials. The prepared HA and CMP disks were soaked in pH 2 and 5 of acidic water and ethanol solution respectively, where pH change of each solution was measured during soaking of samples. After grafting TEOS and 3-APTES on HA and CMP disks, samples were ultrasonically cleaned in distilled water and soaked in pH 5 of ethanol solution, and pH measurement was carried out in the same manner. The pH value of HA and CMP in aqueous solution at pH 2 increased with time continuously, resulting from dissolution of HA and CMP by acidic condition on surface. At pH 5 in aqueous solution, it was the same though the pH increase was smaller. In case of ethanol at pH 5 with HA, though pH value went up slightly, the curve became saturated with time, while there was no change in pH with CMP. After grafting TEOS and 3-APTES, pH values were stabilized with few changes, indicating that there was no direct chemical reaction between the acidic media and the surface of samples due to covalently grafted TEOS and 3-APTES layer. In conclusion, it was confirmed that OH group on the surface of HA was crystallographic and chemical one rather than physically adsorbed one by grafting TEOS or 3-APTES and it will serve an effective binding site for calcium and phosphate ions, or minerals.

Storage Problems of Poplar Chips from Short Rotation Plantations with Special Emphasis on Fungal Development

2012 ◽  
Vol 8 (1) ◽  
pp. 123-132 ◽  
Author(s):  
Zsuzsanna Horváth ◽  
Béla Marosvölgyi ◽  
Christine Idler ◽  
Ralf Pecenka ◽  
Hannes Lenz
Keyword(s):  
Particle Size ◽  
Health Risk ◽  
Dry Matter ◽  
Ph Value ◽  
Wood Chips ◽  
Raw Material ◽  
Special Focus ◽  
Fungal Development ◽  
Short Rotation ◽  
Fungal Particles

Abstract - There are several problems in storing wood chips freshly harvested from short rotation plantations, which result in quality losses as well as in dry matter and energy losses. The factors influencing the degradation of raw material are examined in this paper with special focus on fungal development. An excessive growth of fungi is connected to dry matter losses and also to an increased health risk during raw material handling. The following factors were measured during 6 months storage of poplar wood chips depending on particle size: box temperature, moisture content, pH-value, appearance of fungi in the storage and the concentration of fungal particles in the air. The results show a close connection between particle size, temperature and attack of fungi. During the storage mesophilic and termophilic species of the genera Alternaria, Aspergillus, Cladosporium, Mucor and Penicillium appeared. The concentration of fungal particles is the highest for fine chips and decreases in bigger particles. There was a special focus on the investigation of the properties of coarse chips (G 50), which represent a good compromise between handling, storage losses and health risk due to fungal development.

scholarly journals Bonding of Selected Hardwoods with PVAc Adhesive

2020 ◽  
Vol 11 (1) ◽  
pp. 67
Author(s):  
Ján Iždinský ◽  
Ladislav Reinprecht ◽  
Ján Sedliačik ◽  
Jozef Kúdela ◽  
Viera Kučerová
Keyword(s):  
Adhesion Strength ◽  
Cold Water ◽  
Ph Value ◽  
Water Extract ◽  
Solid Wood ◽  
Contact Angles ◽  
Water Contact ◽  
Ph Values ◽  
Positive Tendency ◽  
The Impact

The bonding of wood with assembly adhesives is crucial for manufacturing wood composites, such as solid wood panels, glulam, furniture parts, and sport and musical instruments. This work investigates 13 hardwoods—bangkirai, beech, black locust, bubinga, ipé, iroko, maçaranduba, meranti, oak, palisander, sapelli, wengé and zebrano—and analyzes the impact of their selected structural and physical characteristics (e.g., the density, cold water extract, pH value, roughness, and wettability) on the adhesion strength with the polyvinyl acetate (PVAc) adhesive Multibond SK8. The adhesion strength of the bonded hardwoods, determined by the standard EN 205, ranged in the dry state from 9.5 MPa to 17.2 MPa, from 0.6 MPa to 2.6 MPa in the wet state, and from 8.5 MPa to 19.2 MPa in the reconditioned state. The adhesion strength in the dry state of the bonded hardwoods was not influenced by their cold water extracts, pH values, or roughness parallel with the grain. On the contrary, the adhesion strength was significantly with positive tendency influenced by their higher densities, lower roughness parameters perpendicular to the grain, and lower water contact angles.

scholarly journals Microstructure and Properties of Self-Assembly Graphene Microcapsules: Effect of the pH Value

Nanomaterials ◽  
2019 ◽  
Vol 9 (4) ◽  
pp. 587 ◽  
Author(s):  
Yan-Dong Guo ◽  
Jun-Feng Su ◽  
Ru Mu ◽  
Xin-Yu Wang ◽  
Xiao-Long Zhang ◽  
...  
Keyword(s):  
Electron Microscope ◽  
Photoelectron Spectroscopy ◽  
Self Assembly ◽  
Chemical Engineering ◽  
Ph Value ◽  
Liquid Paraffin ◽  
Energy Dispersive Spectrometer ◽  
Core Material ◽  
Microstructure And Properties ◽  
Ph Values

Graphene has attracted attention in the material field of functional microcapsules because of its excellent characteristics. The content and state of graphene in shells are critical for the properties of microcapsules, which are greatly affected by the charge adsorption equilibrium. The aim of this work was to investigate the effect of pH value on the microstructure and properties of self-assembly graphene microcapsules in regard to chemical engineering. Microcapsule samples were prepared containing liquid paraffin by a self-assembly polymerization method with graphene/organic hybrid shells. The morphology, average size and shell thickness parameters were investigated for five microcapsule samples fabricated under pH values of 3, 4, 5, 6 and 7. The existence and state of graphene in dry microcapsule samples were analyzed by using methods of scanning electron microscope (SEM), transmission electron microscope (TEM) and X-ray photoelectron spectroscopy (XPS). Fourier Transform Infrared Spectoscopy (FT-IR) and Energy Dispersive Spectrometer (EDS) were applied to analyze the graphene content in shells. These results proved that graphene had existed in shells and the pH values greatly influenced the graphene deposition on shells. It was found that the microcapsule sample fabricated under pH = 5 experienced the largest graphene deposited on shells with the help of macromolecules entanglement and electrostatic adherence. This microcapsules sample had enhanced thermal stability and larger thermal conductivity because of additional graphene in shells. Nanoindentation tests showed this sample had the capability of deforming resistance under pressure coming from the composite structure of graphene/polymer structure. Moreover, more graphene decreased the penetrability of core material out of microcapsule shells.

Study on Influence of Silicate Morphology Based on pH Value

2012 ◽  
Vol 454 ◽  
pp. 324-328
Author(s):  
Yan He ◽  
Ya Jing Liu ◽  
Yong Lin Cao ◽  
Li Xia Zhou
Keyword(s):  
Silicic Acid ◽  
Ph Value ◽  
Colorimetric Method ◽  
Absorption Spectrometry ◽  
Degree Of Polymerization ◽  
Raw Material ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ph Values ◽  
The Stability

Infra-red absorption spectrometry, X-ray diffraction observations and characterization tests based on silicon molybdenum colorimetric method were used to investigate the optimal pH value controlling the stability of the silicic acid form. The experiment process was done by using sodium silicate as raw material. The results showed that the solution of silicate influenced the polymerization. The active silicic acid solution with a certain degree of polymerization was obtained by controlling the pH values.

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