scholarly journals Effect of new crystalline phase on the ionic conduction properties of sodium perchlorate salt doped carboxymethyl cellulose biopolymer electrolyte films

2021 ◽  
Vol 28 (11) ◽  
Author(s):  
Supriya K Shetty ◽  
Ismayil ◽  
I. M. Noor

AbstractDopant induced modifications in the microstructure of sodium carboxymethyl cellulose (NaCMC) were characterized by FTIR, XRD, DSC and EIS techniques. FTIR analysis exhibited a considerable microstructural modification in NaCMC upon NaClO4⋅H2O doping invoked through complex formation via Lewis acid-base interaction and hydrogen bond formation between ions and dipoles. This resulted in the modification in the orderliness/disorderliness of polymer chains as observed from XRD deconvolution. At higher salt concentrations, the complexity of the network causes the formation of new amorphous and crystalline phases as reflected in the XRD studies. DSC analysis showed an increase in Tg as the salt concentration increased, indicating a reduction in polymer chains flexibility. The contribution of free ions has masked over the enhancement in amorphous content to conductivity at a lower concentration of salt in the matrix, later on, the formation of a new crystalline phase due to transient crosslinks by Na+…ClO4−…Na+ has affected the ion transport process.

2019 ◽  
Vol 948 ◽  
pp. 175-180 ◽  
Author(s):  
Indriana Kartini ◽  
Kukuh Handaru Iskandar ◽  
Chotimah ◽  
Eko Sri Kunarti ◽  
Rochmadi

Bioplastic composites based on carboxymethyl cellulose (CMC) and urea have been successfully synthesised at various amount of zeolites. Urea inclusion into the bioplastics was supposed to result in nitrogen slow-release composites. The bioplastic composites were prepared by solvent casting the precursor gel containing 0.5 % (w/w) urea in CMC in the petri dishes. The zeolites content was varied at 0.1, 0.5, 1.0, 2.0, and 3.0 % (w/w to CMC). It showed that the addition of zeolites to the bioplastic composites up to 0.5% increased their tensile strength. More addition of zeolites decreased the strain of the bioplastic composite. It could be due to the formation of hydrogen bonds between CMC and zeolites. The amount of urea absorbed in the bioplastics increased as the amount of zeolites increases. It is possibly to be due to the strong interaction between urea and zeolites. The ammonium ions may interact with interchangeable cations in the zeolite. This interaction will also extend the time for the bioplastics to biodegrade. The presence of zeolites in the CMC polymer chains is useful to give nitrogen slow-release composites.


2005 ◽  
Vol 13 (6) ◽  
pp. 571-580 ◽  
Author(s):  
Defeng Wu ◽  
Chixing Zhou ◽  
Xie Fan ◽  
Dalian Mao ◽  
Zhang Bian

Poly(butylene terephthalate)/epoxy/montmorillonite ternary nanocomposites (PCNs) were prepared by melt intercalation. Their morphologies were investigated using XRD and TEM. The results reveal that with epoxy resin as a compatibilizer, the clay is easily intercalated and disperses well in the matrix. Therefore, the PCNs exhibited better tensile and impact properties than neat PBT, although any surplus epoxy dispersed in the PBT matrix reduces the material performance. The melt viscoelastic behaviour of the PCNs was measured by means of a parallel plate rheometer. The PCN ternary hybrids showed a stronger solid-like response in the lower frequencies than samples without epoxy, for two reasons: the enhancement of percolation network density, and the bridge-like effect of the epoxy linking the clay and the polymer chains. The compatibilizer content influenced the morphology and performance of the nanocomposites. The optimum compatibilizer dosage of 4 wt% was decided by a novel 'crossover point' rheological method.


1982 ◽  
Vol 22 (02) ◽  
pp. 171-180 ◽  
Author(s):  
David C. Thomas

Abstract Starch- and cellulose-based polymers have been used to control water loss for many years. Thermal degradation of the polymers is the most important problem with their use. Representative starch and cellulose fluid loss reducers were tested for their thermal stability in mud systems. The thermal decomposition was found to be dependent on both exposure time and temperature. The rate of decomposition can be predicted using first-order reaction rate kinetics and the decomposition activation energy estimated for both polymer types. This technique allows the calculation of a polymer's usable lifetime at a given temperature. A table of half-lives (time for fluid loss to double) vs. exposure temperature is presented for both starch- and cellulose-based polymers. This paper discusses the results of the calculations and the method used to obtain the data. The method is generally applicable to any material used in drilling fluids that is subject to thermal degradation. Introduction Starch, carboxymethyl cellulose (CMC), and their derivatives frequently are used in drilling fluids as viscosifiers and fluid-loss reducers. Their general properties are well known because they have been used for properties are well known because they have been used for many years. One important area that has been neglected somewhat is the effect of exposure to various temperatures for varying lengths of time on fluid-loss reduction. Vendor literature quotes maximum temperature limits for starch from 200 to 250 degrees F (93 to 121 degrees C). This information is useful but is not sufficient for precise work. The length of exposure to a certain temperature bears strongly on a polymer's stability. For example, a standard pregelatinized starch might have an API fluid loss of 20 cm3 after exposure at 250 degrees F (121 degrees C) for 4 hours, while after 24 hours its fluid loss is greater than 80 cm3 and after 48 hours is 240 cm3. Some data may show that starch gave an acceptable high-temperature high-pressure (HTHP) fluid loss at 275 or 300 degrees F (135 or 149 degrees C). These data can be misleading because a HTHP fluid-loss test can be completed in an hour, while long-term aging at the same temperature will destroy the polymer. Similar comments can be made about cellulosic polymers except that the temperatures stated are about 50 degrees F (28 degrees C) higher.Starch- and cellulose-based polymers degrade thermally by the same mechanism. The polymer chains are broken, and the glucopyranose units are converted to other compounds. The decomposition rate can be determined by use of chemical kinetics methods. This paper describes experiments that determined the stability of these polymers at various temperatures using kinetic methods. Starch Chemistry Starch, as used in drilling fluids, is a powder that disperses readily in water to give a low-viscosity fluid that can be used to seal microfractures and prevent fluid loss. This starch has been processed after separation from corn, wheat, rice, or potatoes. "Pregelatinization" is a cooking process that ruptures the starch granules to release the constituent starch polymer molecules. Cooking at 140 to 212 degrees F (60 to 100 degrees C) destroys the outer structure of the granule, yielding a thick slurry, much like thickened gravy. This slurry is dried and milled, giving the product used in drilling fluids. This gelatinization process was done at the rig in early applications of starch to drilling fluids. Cooking of starch at the rig ended in the late 1930's to early 1940's with the availability of pregelatinized starches. There has been some recent interest in ungelatinized starches to provide a "time-release" source of starch for fluid-loss control. Such materials would be limited to relatively hot wells [about 200 degrees F (93 degrees C)] because the march granules must be broken down to release the starch molecule for fluid-loss control. SPEJ P. 171


2016 ◽  
Vol 186 ◽  
pp. 31-43 ◽  
Author(s):  
Ren Zhang ◽  
Bongjoon Lee ◽  
Michael R. Bockstaller ◽  
Abdullah M. Al-Enizi ◽  
Ahmed Elzatahry ◽  
...  

Application of shear stress has been shown to unidirectionally orient the microstructures of block copolymers and polymer blends. In the present work, we study the phase separation of a novel nanoparticle (NP)–polymer blend thin film system under shear using a soft-shear dynamic zone annealing (DZA-SS) method. The nanoparticles are densely grafted with polymer chains of chemically dissimilar composition from the matrix polymer, which induces phase separation upon thermal annealing into concentrated nanoparticle domains. We systematically examine the influence of DZA-SS translation speed and thus the effective shear rate on nanoparticle domain elongation and compare this with the counterpart binary polymer blend behavior. Unidirectionally aligned nanoparticle string-domains are fabricated in the presence of soft-shear in confined thin film geometry. We expect this DZA-SS method to be applicable to various NP–polymer blends towards unidirectionally aligned nanoparticle structures, which are important to functional nanoparticle structure fabrication.


1971 ◽  
Vol 55 (3) ◽  
pp. 775-795
Author(s):  
JOHN M. GOSLINE

1. The mechanical properties of the mesogloea of the sea anemone Metridium senile were investigated. An amorphous polymer network in the matrix was found to play a major role in determining the mechanical properties of the tissue. 2. The matrix network provides an elastic mechanism based on ‘rubber elasticity’ of the folded matrix molecules. The properties of the matrix network alone account for the extensibility and elasticity of mesogloea. 3. The collagen acts as a reinforcing filler providing short-term rigidity to the flimsy polymer network. 4. The collagen fibres are not directly cross-linked to one another but are tied together through the amorphous matrix. 5. The extensibility and elasticity of the tissue appear to be dependent on a very low degree of cross-linking in the mesogloeal system. Inorganic ions mask ionized groups on the collagen and matrix polymer chains and block electrostatic interactions which could cross-link the system.


Polymers ◽  
2020 ◽  
Vol 12 (11) ◽  
pp. 2487
Author(s):  
Mohd Ibnu Haikal Ahmad Sohaimy ◽  
Mohd Ikmar Nizam Mohamad Isa

Green and safer materials in energy storage technology are important right now due to increased consumption. In this study, a biopolymer electrolyte inspired from natural materials was developed by using carboxymethyl cellulose (CMC) as the core material and doped with varied ammonium carbonate (AC) composition. X-ray diffraction (XRD) shows the prepared CMC-AC electrolyte films exhibited low crystallinity content, Xc (~30%) for sample AC7. A specific wavenumber range between 900–1200 cm−1 and 1500–1800 cm−1 was emphasized in Fourier transform infrared (FTIR) testing, as this is the most probable interaction to occur. The highest ionic conductivity, σ of the electrolyte system achieved was 7.71 × 10−6 Scm−1 and appeared greatly dependent on ionic mobility, µ and diffusion coefficient, D. The number of mobile ions, η, increased up to the highest conducting sample (AC7) but it became less prominent at higher AC composition. The transference measurement, tion showed that the electrolyte system was predominantly ionic with sample AC7 having the highest value (tion = 0.98). Further assessment also proved that the H+ ion was the main conducting species in the CMC-AC electrolyte system, which presumably was due to protonation of ammonium salt onto the complexes site and contributed to the overall ionic conductivity enhancement.


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