Unsaturated Polyesters with Pendant Double Bonds and Investigation of their Self Curable Activity

2014 ◽  
Vol 1052 ◽  
pp. 262-269 ◽  
Author(s):  
Hai Yan Li ◽  
Yi Yu Chen ◽  
Fang Fang Zhu ◽  
Chong Wen Li
Keyword(s):  
Raw Materials ◽  
Unsaturated Polyester ◽  
Side Chain ◽  
Cross Linking ◽  
Hydroxyl Groups ◽  
Double Bonds ◽  
Unsaturated Polyesters ◽  
H Nmr ◽  
Nucleophilic Addition Reaction ◽  
Ft Ir

In this paper, the self-curable unsaturated polyester was put forward as a new solution to air pollution problems caused by the cross-linking monomer’s volatilization in unsaturated polyesters (UP) industry. Two kinds of unsaturated polyesters with the vinyl double bonds at the side chain were synthesized with Itaconic acid (IA) or Itaconic anhydride (ITA) as raw materials. The first one was prepared with IA, isophthalic acid and propylene glycol (IPP-UP), and the second one was synthesized with glycidol (GL) and ITA (IG-UP). Investigation demonstrates that the latter UP resin could be self-cured through the nucleophilic addition reaction of hydroxyl groups with double bonds or the free-radical homopolymerization of double bonds when they were heated without cross-linking monomers. However, the former couldn’t. Factors on self-crosslinking activity and crosslinking mechamism of pendant vinyl bonds from IA or ITA were explored.1H-NMR and FT-IR were used to characterize.

Study on Synthesis and Characterization of Unsaturated Polyester by Enzyme-Catalyzed

2013 ◽  
Vol 575-576 ◽  
pp. 67-70
Author(s):  
Fen Juan Shao ◽  
Qun Yang ◽  
Lan Ying Li ◽  
Da Nian Lu
Keyword(s):  
High Temperature ◽  
Unsaturated Polyester ◽  
Soxhlet Extraction ◽  
Side Chain ◽  
Synthesis And Characterization ◽  
Cross Linking ◽  
Cross Link ◽  
H Nmr ◽  
Ft Ir

Unsaturated polyester was prepared with adipic acid (AA), fumaric acid (FA), itaconic acid (IA) and 1, 6-hexanediol (HD) by enzyme-catalyzed polmerization. The insoluble gel fraction (Qs), as the cross-linking degree of cured unsaturated polyesters which could be self-cross-linked at high temperature through C=C in it, was got by Soxhlet Extraction. The properties were investigated by FT-IR, 1H NMR, DSC, XRD and so on. The results indicated that the C=C in unsaturated diacids reduced the acitvity of N435, which affected the polmerization. With the introduction of C=C of IA or FA, the Mn of polyester reduced. The C=C could self-cross-link under high temperature for lengthy time. The higher the temperature and the longer the time, the Qs increased. As the C=C of IA was in the side chain, it could move easily. Then Qs of poly (AA-co-IA-co-HD) was higher than ploy (AA-co-FA-co-HD). With the increased content of unsaturated diacid, Qs increased. And the biodegradation of cross-linked polyesters became worse.

Preparation of Self Curable Unsaturated Polyester with Pendant Hydroxyl Groups and Investigation of its Curing Properties

2013 ◽  
Vol 699 ◽  
pp. 161-166 ◽  
Author(s):  
Jin Huan Meng ◽  
Hai Yan Li ◽  
Yi Yu Chen
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Main Chain ◽  
Polyester Resin ◽  
Addition Reaction ◽  
Unsaturated Polyester ◽  
Raw Material ◽  
Cross Linking ◽  
Hydroxyl Groups ◽  
Preparation Process ◽  
Ft Ir

Self curable unsaturated polyesters with pendant hydroxyl groups on main chain were synthesized through the polycondensation of maleic anhydride and glycidol at different raw material ratios. The preparation process and self-curing properties were studied. Investigation demonstrated that the unsaturated polyester resin could be self cured through the addition reaction of pendant hydroxyl groups with the double bonds on main chain when it was heated above 150°C without additional cross-linking monomer. This research may contribute to improve air pollution caused by volatile of cross-linking monomers. H-nuclear magnetic resonance (1H-NMR) and Fourier transform infrared spectroscopy (FT-IR) were used to characterize.

scholarly journals Synthesis and antioxidant properties of 2-(3-(hydroxyimino)methyl)-1H-indol-1-yl)acetamide derivatives

2020 ◽  
Vol 6 (1) ◽  
Author(s):  
Chandravadivelu Gopi ◽  
Magharla Dasaratha Dhanaraju
Keyword(s):  
Antioxidant Activity ◽  
Condensation Reaction ◽  
Antioxidant Properties ◽  
Side Chain ◽  
Antioxidant Power ◽  
H Nmr ◽  
Antioxidant Agents ◽  
Phenyl Rings ◽  
Ferric Reducing Antioxidant Power ◽  
Ft Ir

Abstract Background The main aim of this work was to synthesise a novel N-(substituted phenyl)-2-(3-(hydroxyimino) methyl)-1H-indol-1-yl) acetamide derivatives and evaluate their antioxidant activity. These compounds were prepared by a condensation reaction between 1H-indole carbaldehyde oxime and 2-chloro acetamide derivatives. The newly synthesised compound structures were characterised by FT-IR, 1H-NMR, mass spectroscopy and elemental analysis. Furthermore, the above-mentioned compounds were screened for antioxidant activity by using ferric reducing antioxidant power (FRAP) and 1,1-diphenyl-2-picrylhydrazyl (DPPH) methods. Result The antioxidant activity result reveals that most of the compounds were exhibiting considerable activity in both methods and the values are very closer to the standards. Among the synthesised compounds, compound 3j, 3a and 3k were shown remarkable activity at low concentration. Conclusion Compounds 3j, 3a and 3k were shown highest activity among the prepared analogues due to the attachment of halogens connected at the appropriate place in the phenyl ring. Hence, these substituted phenyl rings considered as a perfect side chain for the indole nucleus for the development of the new antioxidant agents.

Enhanced Thermal Stability of Esterified Lignin in Different Solvent Mediums

2018 ◽  
Vol 9 (1) ◽  
pp. 39-49 ◽  
Author(s):  
Sharifah Nurul Ain Syed Hashim ◽  
Sarani Zakaria ◽  
Chin Hua Chia ◽  
Sharifah Nabihah Syed Jaafar
Keyword(s):  
Thermal Stability ◽  
Alkaline Solution ◽  
Room Temperature ◽  
Hydroxyl Groups ◽  
Aqueous Alkaline Solution ◽  
Alkali Lignin ◽  
Weight Percentage ◽  
H Nmr ◽  
Ft Ir ◽  
Thermal Stability Of

In this study, soda alkali lignin from oil palm empty fruit bunch (EFB-AL) and kenaf core (KC-AL) are esterified with maleic anhydride under two different conditions, namely i) pyridine at temperature of 120°C for 3h and ii) aqueous alkaline solution at room temperature for 4h. As a result, the weight percentage gain (WPG) of the esterified EFB-AL (EFB-EL) and esterified KC-AL (KC-EL) in pyridine demonstrated a higher compared to aqueous alkaline solution. The FT-IR results of EFB-EL and KC-EL in both solvents exhibited some changes at the carbonyl and hydroxyl groups. Furthermore, the esterification process induced the carboxylic peak to appear in both alkali lignin samples. The outcome is confirmed by conducting H-NMR analysis, which demonstrated ester and carboxylic acid peaks within the spectral analysis. Finally, the TGA results showed both EFB-EL and KC-EL that are exposed to aqueous alkaline actually possessed better thermal stability and higher activation energy (Ea) compared to the esterified samples in pyridine.

Synthesis of Eco-friendly Nano-Structured Biosurfactants from Vegetable Oil Sources and Characterization of Their Interfacial Properties for Cosmetic Applications

MRS Advances ◽  
2018 ◽  
Vol 4 (07) ◽  
pp. 377-384 ◽  
Author(s):  
DaNan Yea ◽  
SeonHui Jo ◽  
JongChoo Lim
Keyword(s):  
Raw Materials ◽  
Coconut Oil ◽  
Interfacial Properties ◽  
Interfacial Property ◽  
Solution Stability ◽  
H Nmr ◽  
Wetting Property ◽  
Potential Applicability ◽  
Ft Ir

ABSTRACTIn this study, 3 types of zwitterionic phospholipid biosurfactants LDP(S), CDP(S) and CTDP(S) were prepared from 3 different raw materials such as rapeseed oil, coconut oil and cottonseed oil respectively. The structure of the resulting phospholipid biosurfactants was elucidated by FT-IR, 1H NMR and 13C NMR spectroscopies and their interfacial properties have been examined such as CMC, static surface tension, wetting property, solution stability, and foam property. Interfacial property measurement and prescription test in cosmetic formulation prepared with the newly synthesized biosurfactants revealed that CDP(S) biosurfactant possesses excellent mildness and superior interfacial properties, indicating the potential applicability in cosmetic product formulations.

Side Chain Influence on Main Chain Orientation of PPV-Type Oligomers

1999 ◽  
Vol 598 ◽  
Author(s):  
Ruth Müllner ◽  
Laurence Noirez ◽  
Egbert Zojer ◽  
Franz Stelzer ◽  
Günther Leising
Keyword(s):  
Magnetic Field ◽  
Neutron Diffraction ◽  
Main Chain ◽  
Side Chain ◽  
Phenylene Vinylene ◽  
Spectroscopic Methods ◽  
Polarized Optical Microscopy ◽  
Chain Orientation ◽  
H Nmr ◽  
Ft Ir

ABSTRACTOligo (p-phenylene vinylene)s OPV were synthesized having cyanobiphenyloxy-groups bonded to the vinylene double bonds via alkylene spacers. A Pd(0)-reaction was used to synthesize the oligomers starting with the dibromo-substituted benzene and the alkenyloxy-biphenyl-nitrile. The orientation of the mesogens by a magnetic field and their influence on the orientation of the main chain was investigated by means of neutron diffraction ND. Data on the photophysics of the oligomers were gained using several spectroscopic methods such as UV/VIS, polarized optical microscopy POM, SEC, 1H-NMR, FT-IR.

Synthesis and Characterization of an Alendronate-Chitosan Conjugate

2011 ◽  
Vol 140 ◽  
pp. 53-57 ◽  
Author(s):  
Xiao Hong Shao ◽  
Ji Qing Xu ◽  
Yan Peng Jiao ◽  
Chang Ren Zhou
Keyword(s):  
Drug Delivery ◽  
Drug Delivery System ◽  
Synthesis And Characterization ◽  
Hydroxyl Groups ◽  
Amino Groups ◽  
H Nmr ◽  
Ft Ir ◽  
Novel Drug Delivery System ◽  
Novel Drug

The biomineral-binding alendronate-chitosan conjugate (Scheme 1) was developed as a novel drug delivery system. Alendronate was conjugated to the hydroxyl groups of chitosan, thereby maintaining the amino groups of chitosan intact. By means of FT-IR and 1H NMR, the characterization was conducted to confirm the successful synthesis of alendronate-chitosan conjugate.

scholarly journals Synthesis of Fluorinated Amphiphilic Block Copolymers Based on PEGMA, HEMA, and MMA via ATRP and CuAAC Click Chemistry

2014 ◽  
Vol 2014 ◽  
pp. 1-11 ◽  
Author(s):  
Fatime Eren Erol ◽  
Deniz Sinirlioglu ◽  
Sedat Cosgun ◽  
Ali Ekrem Muftuoglu
Keyword(s):  
Block Copolymer ◽  
Block Copolymers ◽  
Amphiphilic Block Copolymers ◽  
Random Copolymers ◽  
Side Chain ◽  
Dipolar Cycloaddition ◽  
Controlled Synthesis ◽  
H Nmr ◽  
Ft Ir ◽  
Click Coupling

Synthesis of fluorinated amphiphilic block copolymers via atom transfer radical polymerization (ATRP) and Cu(I) catalyzed Huisgen 1,3-dipolar cycloaddition (CuAAC) was demonstrated. First, a PEGMA and MMA based block copolymer carrying multiple side-chain acetylene moieties on the hydrophobic segment for postfunctionalization was carried out. This involves the synthesis of a series of P(HEMA-co-MMA) random copolymers to be employed as macroinitiators in the controlled synthesis of P(HEMA-co-MMA)-block-PPEGMA block copolymers by using ATRP, followed by a modification step on the hydroxyl side groups of HEMA via Steglich esterification to afford propargyl side-functional polymer, alkyne-P(HEMA-co-MMA)-block-PPEGMA. Finally, click coupling between side-chain acetylene functionalities and 2,3,4,5,6-pentafluorobenzyl azide yielded fluorinated amphiphilic block copolymers. The obtained polymers were structurally characterized by1H-NMR,19F-NMR, FT-IR, and GPC. Their thermal characterizations were performed using DSC and TGA.

Synthesis and Application of Glyoxalted Polyacrylamide Paper Strengthening Agent

2011 ◽  
Vol 236-238 ◽  
pp. 1385-1390 ◽  
Author(s):  
Zhao Yang Yuan ◽  
Hui Ren Hu ◽  
Yang Bing Wen
Keyword(s):  
Ph Value ◽  
Raw Materials ◽  
Strength Properties ◽  
Synthesis Conditions ◽  
Paper Making ◽  
H Nmr ◽  
Dimethyl Ammonium ◽  
Ft Ir ◽  
Radical Solution ◽  
Diallyl Dimethyl Ammonium Chloride

The glyoxalted polyacrylamide(GPAM) resins were obtained by cross-linking reaction between glyoxal and cationic polyacrylamide(CPAM) through aqueous solution copolymerization. The based CPAM was synthesized with acrylamide(AM) and diallyl dimethyl ammonium chloride(DADMAC) as raw materials by living free radical solution polymerization. Various synthesis conditions were discussed and the optimum conditions for copolymer’s synthesis were as follows: the amount of DADMAC 20%(wt), the charge of the initiator 0.5%(wt), the dosage of chain transfer agent(2-mercaptoethanol) 1.0%(wt), and the charge of crosslinking monomer 9.0%, the dosage of glyoxal 25%(wt), the pH value of the tertiary reaction 7.5-8.0 and the tertiary temperature about 65°C. The structure of the resulting product was characterized by FT-IR, 1H-NMR. Then the GPAM resins were used in the process of paper-making as wet-end additive, the results showed that the paper sheets can get a significant increase in strength properties from the added novel product.

Modification of styrene polymer by attaching suitable groups as side chain

e-Polymers ◽  
2009 ◽  
Vol 9 (1) ◽  
Author(s):  
Mehrdad Mahkam ◽  
Bakhshali Massoumi ◽  
Hossien Mirfatahi
Keyword(s):  
Thermogravimetric Analysis ◽  
Cycloaddition Reaction ◽  
Side Chain ◽  
H Nmr ◽  
Azide Ion ◽  
Ft Ir ◽  
Commercial Polymers ◽  
Polymerization Method ◽  
Thermal Stability Of ◽  
Dimethyl Acetylene Dicarboxylate

AbstractChemical modification of inexpensive commercial polymers, such as styrene, is a safe methodology to obtain new copolymers. The 4-chloromethyl styrene (CMS) was copolymerized with styrene (in various mole ratios) by free radical polymerization method at 70 ºC using α,α-azobis(isobutyronitrile) (AIBN) as an initiator. The azide ion was covalently attached to the obtained copolymers with replacement of all the chlorine atoms in CMS units. The 1,3-dipolar click cycloaddition reaction between azido polymers and dimethyl acetylene dicarboxylate (DMAD) yielded polymers with 1,2,3-triazoles in side chain. The polymers, obtained in quantitative yields, were characterized by FT-IR and 1H NMR spectroscopy; thermogravimetric analysis (TGA) and GPC studies. The thermogravimetric analysis (TGA) indicated that the thermal stability of copolymers increases with incorporation of 1,2,3-triazole groups in side chains of copolymers.

Sign in / Sign up

Export Citation Format

Share Document