scholarly journals Chitosan and Carboxymethyl Chitosan from Fish Scales of Labeo rohita

2013 ◽  
Vol 61 (1) ◽  
pp. 145-148 ◽  
Author(s):  
Tanvir Muslim ◽  
Mohammad Habibur Rahman ◽  
HOsne Ara Begum ◽  
Md. Azizur Rahman

Chitin was extracted from the fish scales of Labeo rohita and chitosan was successfully prepared from it by deacetylation reaction. The prepared chtiosan was characterized by FT-IR spectral analysis and degree of decetylation was determined by pH-metric titration. The molecular weight of chitosan was estimated by viscometric method. Chitosan was converted into its carboxymethyl derivative using alkali and monochloroacetic acid. The prepared carboxymethyl chitosan was characterized by FT-IR spectral analysis and degree of substitution was estimated. Dhaka Univ. J. Sci. 61(1): 145-148, 2013 (January) DOI: http://dx.doi.org/10.3329/dujs.v61i1.15116

2012 ◽  
Vol 506 ◽  
pp. 158-161 ◽  
Author(s):  
A. Jaidee ◽  
Pornchai Rachtanapun ◽  
S. Luangkamin

N,O-Carboxymethyl chitosans were synthesized by the reaction between shrimp, crab and squid chitosans with monochloroacetic acid under basic conditions at 50°C. The mole ratio of reactants was obtained from various reaction conditions of shrimp chitosan polymer and oligomer types. The mole ratio 1:12:6 of chitosan:sodium hydroxide:monochloroacetic acid was used for preparing carboxymethyl of chitosan polymer types while carboxymethyl of chitosan oligomer types were used the mole ratio 1:6:3 of chitosan:sodium hydroxide:monochloroacetic acid. The chemical structure was analyzed by fourier transformed infrared spectroscopy (FT-IR) and proton nuclear magnatic resonance spectroscopy (1H-NMR). The FT-IR was used for confirm the insertion of carboxymethyl group on chitosan molecules. The 1H-NMR was used for determining the degree of substitution (DS) of carboxymethylation at hydroxyl and amino sites of chitosans. Carboxymethyl chitosan samples had the total DS of carboxymethylation ranging from 1.0-2.2. The highest of DS of carboxymethylation was from shrimp chitosan oligomer type.


2019 ◽  
Vol 31 (9) ◽  
pp. 2029-2036
Author(s):  
Vandana Suryavanshi ◽  
Alekha Kumar Sutar ◽  
Tungabidya Maharana

In this work, the chitosan flake was converted to carboxymethyl chitosan (CMCS) by carboxymethylation process using monochloroacetic acid in alkaline condition. The structure of carboxymethyl chitosan was confirmed by NMR, FT-IR, XRD, TGA and SEM techniques. The average molecular weight of carboxymethyl chitosan was obtained by viscometry method. The carboxymethylation reaction of chitosan was optimized for the reaction time, reaction temperature, amount of chitosan, amount of monochloroacetic acid. Response surface methodology (RSM) was used to analyze degree of substitution, degree of acetylation and yield with respect to reaction conditions. At the optimization reaction condition the degree of substitution, degree of acetylation (%) and yield (%) values are 0.56, 33.99 and 78.2, respectively.


1995 ◽  
Vol 74 (06) ◽  
pp. 1452-1456 ◽  
Author(s):  
Johannes Treib ◽  
Anton Haass ◽  
Gerhard Pindur ◽  
Ulrich T Seyfert ◽  
Wolfgang Treib ◽  
...  

SummaryThe plasma clearance of hydroxyethyl starch (HES) depends on the initial molecular weight and the degree of substitution. So far, little attention has been paid to the clinical relevance of the C2/C6 substitution ratio of hydroxyethyl starch.10 patients with cerebrovascular circulatory disturbance received hemodilution therapy for 10 days, consisting of 10% HES 200/0.5 (mean molecular weight 200 kD, degree of substitution 0.5) with a C2/C6 ratio of 13.4. A second group of 10 patients received a starch solution with identical initial molecular weight and degree of substitution but with a C2/C6 ratio of 5.7.After the administration of a single dose, no significant differences between the two groups were observed. After repeated administration, significant differences could be detected in hemorheology, coagulation and elimination (p<0.01). The larger C2/C6 ratio led to a higher intravascular mean molecular weight (95 vs. 84 kD), which in turn led to a higher increase in serum concentration during the therapy (14.7 vs.8.6 mg/ml). Hematocrit was lowered more (-30,5 vs. -23,5%) and plasma viscosity was increased more. There was also a more pronounced increase in partial thromboplastin time (+30% vs. +13%) and a factor of 2 larger decrease of factor VIII/von Willebrand factor-complex (p <0.01), which exceeded the dilution effect.The higher C2/C6 ratio of HES 200/0.5/13.4 slows down enzymatic degradation. After repeated administration of this starch, large molecules accumulate which are inefficiently degraded. The same effect has been observed after therapy with highly-substituted HES. This accumulation of large molecules leads to a beneficial longer lasting volume effect. The disadvantages include an increase in plasma viscosity and coagulation disturbances, which cannot be explained with the respective dilution effect alone. For these reasons, the C2/C6 ratio is of clinical relevance and should be included in the product labeling in the future.


Author(s):  
Joshua O. Ighalo ◽  
Ibrahim O. Tijani ◽  
Oluwaseun J. Ajala ◽  
Fisayo O. Ayandele ◽  
Omodele A. Eletta ◽  
...  

Background: Modified bio-based adsorbents from plant sources can be used for pollution remediation by adsorption due to their low cost and availability in large quantities. Objective: In this study, the competitive biosorption of Pb(II) and Cu(II) by Micropogonias undulates functionalised fish scales (FFS) was conducted. The functionalisation was done by wet impregnation with Fe2+. Method: The biosorbent was characterised by Fourier Transform Infrared Spectroscopy (FT-IR), Scanning Electron Microscopy with Energy-Dispersive X-ray Spectroscopy (SEM-EDS) and Branueur–Emmett–Teller (BET) analyses. Results: The major constituents in the FFS were calcium and phosphorus from the collagen and apatite on the scales. Optimum removal efficiency for both metals was >99% at 10 g/l dosage. It was observed that the Langmuir isotherm model and the pseudo second order kinetics model were the best fit for the experimental data. The monolayer adsorption capacity of FFS for Pb(II) and Cu(II) was observed to be 96.15 mg/g and 100 mg/g respectively. Conclusion: The study revealed that the competitive biosorption of heavy metals can be achieved (at a good adsorption capacity) using functionalised Micropogonias undulates fish scales.


Drug Research ◽  
2021 ◽  
Author(s):  
Anuroop Kumar ◽  
Netrapal Singh ◽  
Mordhwaj Kumar ◽  
Uma Agarwal

AbstractThis article reports an amide based Chemosensor used for selective detection of divalent Cu+2 and Ni+2 ions via Fluorescence turn off. The selective sensing ability of Chemosensor was investigated in presence of different metal ions Mg2+, Ag+, Fe2+, K+, Cu2+, Ni2+, Hg2+, Pb2+, Mn2+, Pd2+, Cd2+ and Mn3+ as competitive ions. The receptor i. e. Chemosensor formed complexes with metal ions in 1:1 stoichiometric ratio. The detection limit and binding constant calculated as 1.92×10–4 and 1.4×10–4 M and 2.16×103 M−1 and 3.09×103 M−1 for Cu2+ and Ni2+ions respectively. The complexes were characterized by UV/visible, FT-IR, 13C NMR and 1H NMR spectroscopy. Further the structure and Crystallinity were calculated by P-XRD spectral analysis. The crystallinity found to be 65.27 and 67.87% respectively


Author(s):  
C. Meganathan ◽  
S. Sebastian ◽  
I. Sivanesan ◽  
Keun Woo Lee ◽  
Byoung Ryong Jeong ◽  
...  
Keyword(s):  
Ft Ir ◽  

2012 ◽  
Vol 584 ◽  
pp. 136-140 ◽  
Author(s):  
S. Janarthanan ◽  
Y.C. Rajan ◽  
R. Sugaraj Samuel ◽  
S. Pandi

ABSTRACT Organic single crystal of Phthalic Anhydride (PA) was successfully grown by slow evaporation method. The structure of the grown crystal was confirmed by X-ray diffraction analysis. FT-IR, and FT-Raman spectral analysis of the crystalline samples reveal that the crystalline sample consists of all functional groups. The placement of protons was identified from H1-NMR spectral analysis. UV-Visible and photoluminescence spectral analyses were carried out for the grown crystals. The thermal behavior was studied with TGA-DTA analyses. The existence of second harmonic generation (SHG) signal was observed using Nd:YAG laser with a fundamental wavelength of 1064 nm. Keywords: Organic crystals, NLO crystals


2003 ◽  
Vol 774 ◽  
Author(s):  
Lucy Vojtova ◽  
Nicholas J. Turro ◽  
Jeffrey T. Koberstein

AbstractSynthesis of α,ω-allyl-terminated telechelic macromonomers based on poly(tert-butyl methacrylate) (poly(t-BMA)) and poly(methacrylic acid) (poly(MAA)) was studied with the aim of preparing end-linked gels and hydrogels. Low molecular weight α-allyl-terminated poly(t-BMA) macromonomers with narrow polydispersities (Mw/Mn = 1.16) were synthesized via controlled atom transfer radical polymerization (ATRP) using a Cu(I)Br/N,N,N',N',N',N'-hexamethyltriethylenetetraamine catalyst system in conjunction with an allyl-2-bromoisobutyrate as the functional initiator. The polymerizations exhibited a linear increase of molecular weight in direct proportion to the monomer conversion and first-order kinetics with respect to monomer concentration. No significant difference was found between using polar or non-polar solvents (tetrahydrofuran or benzene, respectively). Optimization of reaction conditions to obtain the highest degree of active terminal bromine is discussed. Quenching the ATRP reaction with allyltributyltin yielded α,ω-allyl-terminated poly(t-BMA) macromonomers by replacing the terminal bromine with ω-allyl functional group. Poly(MAA) macromonomers were prepared by deprotection of the tert-butyl group from α,ω-allyl-terminated poly(t-BMA) macromonomers using concentrated trifluoroacetic acid at room temperature. Successful synthetic steps were confirmed by 1H NMR, FT-IR and MALDI-TOF MS analyses. The α,ω-allyl-terminated macromonomers were proven to be candidates for further polymerization by forming end-linked, non-soluble gels.


2011 ◽  
Vol 197-198 ◽  
pp. 1294-1298
Author(s):  
Ping Lu ◽  
Wei Bo Huang ◽  
Xue Qiang Ma ◽  
Xu Dong Liu

New polyaspartic ester (PAE) chain extender named PAE-f was prepared via two steps of Michael addition reactions:(1) Michael addition reaction between 4,4’-methylenebis(2-methyl cyclohexyl amine) (Laromin C260) and excessive dialkyl maleates(DEF); (2) The Michael addition reaction of the residual dialkyl maleates of step (1) with polyester polyamine Jeffamine D230. The two-steps method proposed could reduce the reaction time in comparison with the current one step Michael addition reaction method, thus satisfying the industrialized production. New PAE based polyureas were synthesized by reacting the PAE-f chain extender with aliphatic polyisocyanates 4,4’-diisocyanato dicyclohexylmethane (H12MDI) / polyester polyamine Jeffamine D2000 prepolymer at room temperature. FT-IR and GPC were employed to characterize the new PAE prepared, and the morphology, molecular weight distribution and mechanical properties of the prepared PAE based polyureas were investigated by means of FT-IR and GPC. The FT-IR results indicated that the hydrogen bonding degree of amidogen groups in hard segments of the prepared polyureas were high, the length of hydrogen bonding were 0.305nm~0.306nm. The GPC experimental results show that the weight average molecular weight of the PAE-f based polyureas were 4.95×104~6.05×104,Mw/Mn were 1.65~1.97, the molecular weight distribution were relatively narrow. The mechanical properties demonstrated that the tensile strength were 14.7~22.5MPa, Elongation at break were 306~511%, Yang’s modulus were 67~127MPa, Shore A hardness were 64~83. The mechanical properties confirmed that the polyureas based on PAE-f were kinds of elastomeric materials with satisfied flexibility, strength, module and hardness.


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