scholarly journals Evidence from Thermal Aging Indicating That the Synergistic Effect of Glyoxal and Sodium Sulfite Improved the Thermal Stability of Conformational Modified Xanthan Gum

Polymers ◽  
2022 ◽  
Vol 14 (2) ◽  
pp. 243
Author(s):  
Shuai Yuan ◽  
Jiayuan Liang ◽  
Yanmin Zhang ◽  
Hongyu Han ◽  
Tianyi Jiang ◽  
...  

Xanthan gum is prone to thermal oxidative degradation, which limits its applications. However, conformational changes in xanthan gum and appropriate stabilizers may improve its thermal stability. Therefore, in this study, we aimed to establish a strategy to maintain the viscosity of xanthan gum during long-term storage at high temperatures. We modified the original strain used for xanthan gum production by genetic engineering and added stabilizers during the production process. The structure and thermal stability of the resulting xanthan gum samples were then determined. Pyruvyl deficiency, combined with the addition of sodium sulfite and glyoxal during the production process, was found to significantly improve the maintenance of viscosity. The apparent viscosity of the new xanthan gum solution remained above 100 mPa·s after being stored at 90 °C for 48 days. Fourier-transform infrared spectra and scanning electron microscopy images showed that pyruvate-free xanthan gum with added stabilizers had more extensive cross-linking than natural xanthan gum. In conclusion, these findings may contribute to the use of xanthan gum in applications that require high temperatures for a long period of time.

2018 ◽  
Vol 781 ◽  
pp. 159-164
Author(s):  
Yuliya Murashkina ◽  
Dmitry Lipchansky

The epoxy composites filled with 5 and 10 mass % of sodium bicarbonate were prepared. Sodium bicarbonate at the heating decomposes into sodium carbonate, carbon dioxide and water. As a result, sodium bicarbonate is able to slow down the combustion process when it used as polymer filler. The thermal stability of the prepared samples was investigated at the heating in air using thermal analysis. The mechanical characteristics of epoxy composites were also studied. The gaseous products of thermal oxidative degradation were studied using mass spectrometric analysis. It was found that sodium bicarbonate accelerates the process of thermal oxidative degradation of the epoxy composites in the initial stage, but enhances thermal stability in the final stage. The addition of boric acid to sodium bicarbonate as filler is recommended to improve the thermal stability of the epoxy polymer.


Polymer ◽  
1985 ◽  
Vol 26 (10) ◽  
pp. 1549-1553 ◽  
Author(s):  
F. Lambert ◽  
M. Rinaudo

2008 ◽  
Vol 111 (2-3) ◽  
pp. 542-547 ◽  
Author(s):  
L. Fernández-Romero ◽  
J.M. Montero-Moreno ◽  
E. Pellicer ◽  
F. Peiró ◽  
A. Cornet ◽  
...  

1970 ◽  
Vol 12 (8) ◽  
pp. 2103-2109 ◽  
Author(s):  
V.V. Rode ◽  
N.M. Kotsoyeva ◽  
G.M. Cherkasova ◽  
D.S. Tugushi ◽  
G.M. Tseitlin ◽  
...  

2006 ◽  
Vol 249 ◽  
pp. 127-134 ◽  
Author(s):  
Dominique Mangelinck

The effect of Pt and Ge on the stability of NiSi films has been examined. The addition of a small amount of Pt (5 at%) in the Ni film increases the disilicide nucleation temperature to 900oC leading to a better stability of NiSi at high temperatures. For Ni films on Si1-xGex with x=0.29 and 0.58, no NiSi2 was found after annealing at 850°C. The increase in thermal stability of NiSi has been explained in terms of nucleation concept. Calculated ternary phase diagrams allow to understand the effect of the third element (Pt or Ge) on the driving force for nucleation. The redistribution of this element can also be explained with the ternary phase diagrams.


2021 ◽  
Vol 3 (1) ◽  
Author(s):  
Jie Zhang ◽  
Chunhua Wang ◽  
Fengteng Zhang ◽  
Wei Lin

Abstract In this communication, sulfate dodecyl sodium (SDS)-induced thermodynamics and conformational changes of collagen were studied. We used ultrasensitive differential scanning calorimetry (US-DSC) to directly monitor the thermal transition of collagen in the presence of SDS. The results show that SDS affects the conformation and thermal stability of collagen very differently depending on its concentrations. At CSDS ≤ 0.05 mM, the enhanced thermal stability of collagen indicates the stabilizing effect by SDS. However, a further increase of SDS leads to the denaturation of collagen, verifying the well-known ability of SDS to unfold proteins. This striking difference in thermodynamics and conformational changes of collagen caused by SDS concentrations can be explained in terms of their interactions. With increasing SDS, the binding of SDS to collagen can be dominated by electrostatic interaction shifting to hydrophobic interaction, and the latter plays a key role in loosening and unfolding the triple-helix structure of collagen. The important finding in the present study is the stabilizing effect of SDS on collagen molecules at extreme low concentration. Graphical abstract


2021 ◽  
Author(s):  
◽  
Lucjan Sajkowski

<p>A primary goal of this thesis was to obtain kinetic data on the breakdown and isomerisation reactions of naphthalene disulfonate (NDS) and naphthalene sulfonate (NSA) compounds under geothermal conditions. A secondary aim of this study was to investigate NDS/NSA isomerisation transformations as well as to study their kinetics and identify products of thermal disproportionation. Because of their apparent thermal stability, naphthalene disulfonate solutions have been frequently injected into active geothermal reservoirs and their subsequent detection (“recovery”) in nearby wells/bore holes used as an indicator of well connectivity and local permeability. The results obtained in this thesis will enable a more insightful interpretation of field injection results and fluid flow in active geothermal reservoirs. The studies presented in this thesis were designed to determine the thermal stability of aqueous NDS and NSA at high temperatures from 100 to 400°C in pure water and different salt solutions (i.e. NaCl +/- Na2SO4 and Na2S) at saturated vapour pressure. The stabilities and isomerisation transformations of NDS and NSA were also studied in the presence of solid materials (i.e. quartz, greywacke, pumice) which may occur in the host geological environment of hydrothermal/geothermal reservoirs in the Earth’s crust. Dilute aqueous solutions of NDS and NSA were contained in sealed silica glass ampoules (purged of atmospheric oxygen) and placed in stainless steel pressure vessels and heated for varying times to the desired high temperatures. Additional experiments were also conducted in which dilute NDS and NSA solutions were pumped from a de-oxygenated reservoir container through a flow-through autoclave containing different rock and mineral phases at temperatures up 400°C. The resulting NDS and NSA isomers were then analysed using HPLC and GC-MS methodologies. The 1,5-naphthalene disulfonate isomer (1,5-NDS) was found to be the least stable at pHt = 3 - 8 and readily transformed to 1-naphthalene sulfonate (1-NSA) at t ≥ 200°C. The 2-NSA was found to be the most stable isomer but disappeared at t ≥ 300°. The experimental data indicated that the stabilities of all the NDS and NSA studied as a function of temperature, pH and salt (NaCl) concentration were in the sequence: 1,5-NDS < 1,6-NDS < 2,6-NDS ≈ 2,7-NDS < 2-NSA. The presence of dissolved salts was shown to slow down the decomposition rates. Results from flow-through autoclave experiments suggest that between 100 and 250°C, the stabilities of 2,6-NDS, 2,7-NDS, 1,5-NDS and 1,6-NDS are mainly controlled by solution pH, while at t ≥ 300°C, temperature is the main stability controlling factor. Additionally, no adsorption of NDS/NSA on the surface of minerals was observed. A new high-performance liquid chromatography (HPLC) method combined with solid-phase extraction (SPE) was developed to enable detection of NDS/NSA breakdown products at t ≥ 300°C. In hydrothermal solutions at temperatures greater than 300°C, all the naphthalene sulfonate isomers become unstable with the formation naphthalene (NAP) and the two naphthol isomers, 1-naphthol (1-NAP) and 2-naphthol (2-NAP), as confirmed by both the new HPLC/SPE method and GC-MS (gas chromatography–mass spectroscopy). In addition, 1-chloronaphthalene was also detected (using GC-MS) as a high temperature reaction product NDS/NSA disproportionation in 0.05 m NaCl solutions. The results of the experiments carried out during this thesis indicate that the stabilities the naphthalene mono- and disulfonates are a function of temperature, pH and salt concentration. The naphthalene sulfonates transform to different isomers and the kinetics of these isomerisation reactions have been determined. At temperatures ≥ 300°C, the NDS and NSA compounds disproportionate to the naphthalene “backbone” molecule as well as to the two stable naphthols and 1-chloronaphthalene (in chloride containing solutions). The application of naphthalene sulfonates to determine well connectivity and local permeabilities in active geothermal reservoirs is thus rather more complicated than previously appreciated. An understanding of the various isomer transformations and their kinetics is required. Furthermore, naphthalene sulfonates injected into high temperature geothermal reservoirs are unstable and breakdown to naphthalene, naphthols and probable halogenated naphthalene compounds, none of which have been considered in the interpretation of NDS/NSA recovery data in active geothermal reservoirs. The thermal stabilities of NAP, 1- and 2-NAP and 1-chloronaphthalene indicate that these compounds may also be employed as connectivity tracers in high temperature (t ≥ 300°C) systems.</p>


Gels ◽  
2021 ◽  
Vol 7 (4) ◽  
pp. 179
Author(s):  
Youjie Sheng ◽  
Canbin Yan ◽  
Yang Li ◽  
Yunchuan Peng ◽  
Li Ma ◽  
...  

The foams stabilized by nanoparticles (NPs), water-soluble polymers, and surfactants have potential application prospects in the development of new, environmentally friendly firefighting foams. In the present study, a gel foam containing a water-soluble polymer (xanthan gum, XG), hydrophilic silica NPs, hydrocarbon surfactant (SDS), and fluorocarbon surfactant (FS-50) were prepared. The surface activity, conductivity, viscosity, and foaming ability of foam dispersions were characterized. The gel foam stability under a radiation heat source and temperature distribution in the vertical foam layer were evaluated systematically. The results show that the addition of NPs and XG has a significant effect on the foaming ability, viscosity and foam thermal stability, but has a very subtle effect on the conductivity and surface activity. The foaming ability of the FS-50/SDS solution was enhanced by the addition of NPs, but decreased with increasing the XG concentration. The thermal stability of the foams stabilized by SDS/FS-50/NPs/XG increased with the addition of NPs and increasing XG concentration. Foam drainage and coarsening were significantly decelerated by the addition of NPs and XG. The slower foam drainage and coarsening are the main reason for the intensified foam thermal stability. The results obtained from this study can provide guidance for developing new firefighting foams.


Metals ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 402 ◽  
Author(s):  
Mario J. Kriegel ◽  
Martin Rudolph ◽  
Askar Kilmametov ◽  
Boris B. Straumal ◽  
Julia Ivanisenko ◽  
...  

In this work, the formation and thermal stability of the ω-Ti(Fe) phase that were produced by the high-pressure torsion (HPT) were studied in two-phase α-Ti + TiFe alloys containing 2 wt.%, 4 wt.% and 10 wt.% iron. The two-phase microstructure was achieved by annealing the alloys at 470 °C for 4000 h and then quenching them in water. Scanning electron microscopy (SEM) and X-ray diffraction (XRD) were utilized to characterize the samples. The thermal stability of the ω-Ti(Fe) phase was investigated using differential scanning calorimetry (DSC) and in situ high-temperature XRD. In the HPT process, the high-pressure ω-Ti(Fe) phase mainly formed from α-Ti. It started to decompose by a cascade of exothermic reactions already at temperatures of 130 °C. The decomposition was finished above ~320 °C. Upon further heating, the phase transformation proceeded via the formation of a supersaturated α-Ti(Fe) phase. Finally, the equilibrium phase assemblage was established at high temperatures. The eutectoid temperature and the phase transition temperatures measured in deformed and heat-treated samples are compared for the samples with different iron concentrations and for samples with different phase compositions prior to the HPT process. Thermodynamic calculations were carried out to predict stable and metastable phase assemblages after heat-treatments at low (α-Ti + TiFe) and high temperatures (α-Ti + β-(Ti,Fe), β-(Ti,Fe)).


Sign in / Sign up

Export Citation Format

Share Document