Preparation and Characterization of PA6-PEG/Li High Performance Static Dissipation Composites

2017 ◽  
Vol 70 (6) ◽  
pp. 669
Author(s):  
Chongling Yang ◽  
Shouzai Tan ◽  
Gengen Chen ◽  
Litao Guan
Keyword(s):  
High Performance ◽  
Condensation Reaction ◽  
Polyamide 6 ◽  
Decomposition Temperature ◽  
Reaction Conditions ◽  
Comprehensive Properties ◽  
Ft Ir ◽  
Optimal Reaction ◽  
Resistivity Testing

A copolymer of PA6 (polyamide 6) and PEG (polyethylene glycol) was synthesized by a condensation reaction. The optimal reaction conditions were determined as the following: a reaction temperature of 255°C, –0.04 MPa vacuum, and a condensation time of 40 min. A series of novel PA6-PEG/Li composites were developed by melt blending the PA6-PEG copolymer (10 wt-% PEG) with three different kinds of colourless lithium salts (LiCl, C18H35LiO2, LiAc). FT-IR, NMR, thermogravimetric (TGA), electronic universal testing, and resistivity analyses were employed to investigate the comprehensive properties of the copolymers and composites. The results of FT-IR and 1H NMR analyses revealed that the PEG was copolymerized with PA6 successfully. TGA results indicated that the decomposition temperature of the PA6-PEG copolymer was above 350°C. Resistivity testing revealed that the surface resistivity (Rs) of the copolymer decreased from 1 × 1014 to 5.67 × 109 Ω square–1 with an increase of the content of PEG. The PA6-PEG/LiCl composite showed an excellent static dissipation performance of 2.71 × 108 Ω square–1.

scholarly journals Synthesis and Characterization of Graphene Oxide Derivatives via Functionalization Reaction with Hexamethylene Diisocyanate

Proceedings ◽  
2018 ◽  
Vol 3 (1) ◽  
pp. 8 ◽  
Author(s):  
José A. Luceño-Sánchez ◽  
Georgiana Maties ◽  
Camino Gonzalez-Arellano ◽  
Ana M. Díez-Pascual
Keyword(s):  
Graphene Oxide ◽  
High Performance ◽  
Organic Molecules ◽  
Hexamethylene Diisocyanate ◽  
Reaction Conditions ◽  
Ft Ir ◽  
Oxygen Groups ◽  
Functionalization Reaction ◽  
Ft Ir Spectroscopy

Graphene oxide (GO), the oxidized form of graphene, shows unique properties, such as strong mechanical strength, high thermal conductivity, amphiphilicity, and surface functionalization capability that make it very attractive in various fields, ranging from medicine to optoelectronic devices and solar cells. However, its insolubility in non-polar and polar aprotic solvents hinders some applications. To solve this issue, novel functionalization strategies are pursued. In this regard, the current study deals with the preparation and characterization of hexamethylene diisocyanate (HDI)-functionalized GO. Different reaction conditions were tested to optimize the functionalization degree (FD), and detailed characterization was conducted via Fourier-transformed infrared (FT-IR) spectroscopy to confirm the success of the functionalization reaction. The HDI-GO could further react with other organic molecules or polymers via the remaining oxygen groups, which makes them ideal candidates as nanofillers for high-performance GO-based polymer nanocomposites.

scholarly journals Synthesis and characterization of polymethylsilsesqui oxane microspheres by the two-step sol-gel method

e-Polymers ◽  
2012 ◽  
Vol 12 (1) ◽  
Author(s):  
Jiangbo Wang ◽  
Zhong Xin
Keyword(s):  
Ph Value ◽  
Condensation Reaction ◽  
Sol Gel ◽  
Average Diameter ◽  
Reaction Conditions ◽  
Gel Method ◽  
Sol Gel Method ◽  
Ft Ir ◽  
Thermal Stability Of

AbstractPolymethylsilsesquioxane (PMSQ) microspheres with an average diameter of 30nm to 6μm were prepared from methyltrimethoxysilane (MTMS) by a two-step sol-gel method in the presence of hexadecyl trimethyl ammonium chloride (HTAC). The reaction conditions including the concentration of HTAC, water/MTMS ratio, pH value and the temperature in condensation reaction were examined, and aggregation of the microspheres was not observed during the preparation process. Moreover, the structure and thermal stability of PMSQ microspheres were investigated by FT-IR, XRD, TGA, and so on.

scholarly journals Synthesis and Structural Characterization of (E)-4-[(2-Hydroxy-3-methoxybenzylidene)amino]butanoic Acid and Its Novel Cu(II) Complex

Molbank ◽  
10.3390/m1179 ◽  
2021 ◽  
Vol 2021 (1) ◽  
pp. M1179
Author(s):  
Eleftherios Halevas ◽  
Antonios Hatzidimitriou ◽  
Barbara Mavroidi ◽  
Marina Sagnou ◽  
Maria Pelecanou ◽  
...  
Keyword(s):  
Schiff Base ◽  
Gamma Aminobutyric Acid ◽  
X Ray Diffraction ◽  
Reaction Conditions ◽  
Polymeric Compound ◽  
Bridging Ligands ◽  
1H And 13C Nmr ◽  
One Dimensional ◽  
Ft Ir

A novel Cu(II) complex based on the Schiff base obtained by the condensation of ortho-vanillin with gamma-aminobutyric acid was synthesized. The compounds are physico-chemically characterized by elemental analysis, HR-ESI-MS, FT-IR, and UV-Vis. The complex and the Schiff base ligand are further structurally identified by single crystal X-ray diffraction and 1H and 13C-NMR, respectively. The results suggest that the Schiff base are synthesized in excellent yield under mild reaction conditions in the presence of glacial acetic acid and the crystal structure of its Cu(II) complex reflects an one-dimensional polymeric compound. The molecular structure of the complex consists of a Cu(II) ion bound to two singly deprotonated Schiff base bridging ligands that form a CuN2O4 chelation environment, and a coordination sphere with a disordered octahedral geometry.

Diffuse Reflectance FT-IR Characterization of Active Sites under Reaction Conditions: The Production of Oxygenates in the CO/H2 Reaction

1994 ◽  
Vol 48 (10) ◽  
pp. 1208-1212 ◽  
Author(s):  
J. J. Benítez ◽  
I. Carrizosa ◽  
J. A. Odriozola
Keyword(s):  
Infrared Spectra ◽  
Active Sites ◽  
Diffuse Reflectance ◽  
Reaction Conditions ◽  
In Situ Drifts ◽  
Ft Ir

The reactivity of a Lu2O3-promoted Rh/Al2O3 catalyst in the CO/H2 reaction is reported. Methane, heavier hydrocarbons, methanol, and ethanol are obtained. In situ DRIFTS has been employed to record the infrared spectra under the actual reaction conditions. The structure of the observed COads DRIFTS bands has been resolved into its components. The production of oxygenates (methanol and ethanol) has been correlated with the results of the deconvolution calculation. Specific sites for the production of methanol and ethanol in the CO/H2 reaction over a Rh,Lu2O3/Al2O3 catalyst are proposed.

Synthesis and Characterization of a Novel Linear Benzoxazine-Containing Polytriazole via Metal-Free Click Reaction and its Self-Crosslinking Behavior

2012 ◽  
Vol 557-559 ◽  
pp. 973-978
Author(s):  
Zhong Yi Xu ◽  
Lei Du ◽  
Li Qiang Wan ◽  
Fa Rong Huang
Keyword(s):  
Click Reaction ◽  
Decomposition Temperature ◽  
Linear Polymer ◽  
The Novel ◽  
Metal Free ◽  
Crosslinked Polymer ◽  
Degradation Behaviors ◽  
Ft Ir ◽  
Increasing Temperature

A novel linear benzoxazine-containing polytriazole was successfully synthesized via metal-free click reaction. Benefited from the advantages of click reaction, the synthesis procedure was easily and efficiently. The linear polymer could be transformed into crosslinked structure after ring-opening polymerization of oxazine induced by the increasing temperature. The FT-IR characterization verified the structure transformation between linear and crosslinked polymer. Moreover, the thermal properties and thermal degradation behaviors of linear polymer and the corresponding crosslinked polymer were studied by DSC and TGA. The novel polytriazole was proved to be a kind of thermal stable polymers with high thermal decomposition temperature (Td5over 300°C).

Synthesis and Characterization of Fluorinated Alkyl Substituted Disiloxane

2014 ◽  
Vol 529 ◽  
pp. 13-15
Author(s):  
Qing Chuan Xi ◽  
Ke Cao ◽  
Ya Wen Huang ◽  
Guan Jun Chang ◽  
Jun Xiao Yang
Keyword(s):  
High Performance ◽  
Chemical Structure ◽  
Rust Resistance ◽  
Condensation Reaction ◽  
Synthesis And Characterization ◽  
Silicon Oil ◽  
Temperature Performance ◽  
Diffusion Pump ◽  
Measurement Results

Alkyl substituted disiloxanes demonstrated promising applications as high performance hydraulic oil, diffusion pump oil, etc. In this study, fluorinated alkyl substituted disiloxane was synthesized via Grignard reaction followed by condensation reaction. Its chemical structure was verified by FTIR and NMR. Measurement results showed that this silicon oil exhibited good high temperature performance, oxidation resistance and rust resistance.

Structure and Properties of Modifier for Heat Transfer Printing on Cotton Fabric

2011 ◽  
Vol 331 ◽  
pp. 426-429
Author(s):  
Yi Mu ◽  
Lan Wang ◽  
Ming Hua Wu ◽  
Jun Xiong Lin
Keyword(s):  
Heat Transfer ◽  
Spherical Shape ◽  
Decomposition Temperature ◽  
Polymerization Process ◽  
Structure And Properties ◽  
Transfer Printing ◽  
Transmission Electron ◽  
Ft Ir ◽  
Regular Spherical Shape

Modifier for heat transfer printing on cotton fabrics was prepared by semi-continuous emulsion polymerization process with butyl acrylate (BA), styrene (St), acrylonitrile (AN) and cross-linking monomer. FT-IR characterization of modifier groups showed that individual monomer well carried out polymerization. Transmission electron microscopy (TEM) photos demonstrated that latex particles had regular spherical shape and uniform distribution. TGA curves indicated that thermal decomposition temperature of modifier was 439 oC. As for the transfer printing products had good colour fastness, high transfer rate and no formaldehyde.

PREPARATION AND CHARACTERIZATION OF GLYCYRRHETINIC ACID-MODIFIED POLOXAMER 188/CHITOSAN NANOPARTICLES

NANO ◽  
2013 ◽  
Vol 08 (04) ◽  
pp. 1350042 ◽  
Author(s):  
JING WANG ◽  
LI GUO ◽  
LI FANG MA
Keyword(s):  
High Performance ◽  
Drug Loading ◽  
Chitosan Nanoparticles ◽  
Spherical Shape ◽  
Glycyrrhetinic Acid ◽  
Poloxamer 188 ◽  
H Nmr ◽  
Ft Ir

In this paper, we firstly synthesized glycyrrhetinic acid-modified double amino-terminated poloxamer 188 (GA–NH–POLO–NH–GA). The structure of the synthesized compound was confirmed by 1H-NMR and Fourier transform infrared (FT-IR) spectroscopy. Then the nanoparticles composed of GA–NH–POLO–NH–GA/chitosan (GA–NH–POLO–NH–GA/CTS) were prepared by an ionic gelation process. The characterization of the nanoparticles was measured by dynamic light scattering (DLS) and scanning electron microscope (SEM). The results showed that the nanoparticles were well dispersed with a spherical shape and the particle size was distributed between 100 nm and 300 nm. The cytotoxicity based on MTT assay against cells (QGY-7703 cells and L929 cells) showed that the nanoparticles had low toxicity and good biocompatibility. The encapsulation efficiency and drug loading of 5-fluorouracil-loaded nanoparticles (5-FU nanoparticles) were measured by high-performance liquid chromatography (HPLC) and fluorescence spectroscopy, ultraviolet-visible (UV-vis) absorbance. The encapsulation of 5-Fu-loaded CTS nanoparticles was 12.8% and the drug loading was 2.9%, while the encapsulation of 5-Fu-loaded GA–NH–POLO–NH–GA/CTS nanoparticles was 20.9% and the drug loading was 3.36%. The release profile showed that the GA–NH–POLO–NH–GA/CTS nanoparticles were available for sustained release of 5-Fu. The GA–NH–POLO–NH–GA/CTS nanoparticles have a higher affinity to the QGY-7703 cells, so indicated that the GA–NH–POLO–NH–GA/CTS nanoparticles have the capacity of liver-targeting in vitro.

Synthesis and characterization of the solid uranium(VI) dioxo-diacetohydroxamate complex

2007 ◽  
Vol 95 (8) ◽  
Author(s):  
Cynthia-May S. Gong ◽  
Frédéric Poineau ◽  
Kenneth R. Czerwinski
Keyword(s):  
Solid Phase ◽  
Uranyl Acetate ◽  
Proton Nuclear Magnetic Resonance ◽  
Acetohydroxamic Acid ◽  
Acetate Dihydrate ◽  
Reaction Conditions ◽  
X Ray ◽  
Ft Ir ◽  
X Ray Absorption

A novel dry synthesis for the uranium(VI) dioxo-diacetohydroxamate (UAHA) complex has been developed. The complex was generated in >80% yield by mechanically grinding solid uranyl acetate dihydrate (UAc) with solid acetohydroxamic acid in stoichiometric amounts. The resulting UOThe UAHA solid was extensively characterized by ultraviolet-visible (UV-vis), Fourier-transform infrared (FT-IR), and extended X-ray absorption fine structure (EXAFS) spectroscopies. The compound did not fluoresce after laser excitation. Proton nuclear magnetic resonance (NMR) spectra were obtained of the complex in DThe easy synthesis and purification of UAHA enables researchers to strictly control reaction conditions; to eliminate interfering salts and water; and to study the complex in the solid-phase.

scholarly journals Design of High-Performance Polybenzoxazines with Tunable Extended Networks Based on Resveratrol and Allyl Functional Benzoxazine

Polymers ◽  
2020 ◽  
Vol 12 (12) ◽  
pp. 2794
Author(s):  
Yunliang Xing ◽  
Xianru He ◽  
Rui Yang ◽  
Kan Zhang ◽  
Shengfu Yang
Keyword(s):  
High Performance ◽  
Condensation Reaction ◽  
Good Thermal Stability ◽  
Chemical Structures ◽  
Dsc Measurements ◽  
Mannich Condensation ◽  
Polymerization Behavior ◽  
Oxazine Ring ◽  
Nmr Techniques ◽  
Ft Ir

A novel resveratrol-based bio-benzoxazine monomer (RES-al) containing an allyl group has been synthesized using resveratrol, allylamine, and paraformaldehyde via Mannich condensation reaction, and its chemical structures have been characterized by FT-IR spectroscopy and NMR techniques. The polymerization behavior of this benzoxazine resin has been investigated using in situ FT-IR and differential scanning calorimeter (DSC) measurements, and the thermal-mechanical properties of its corresponding polybenzoxazines are evaluated by DMA and TGA. We show that by controlling the curing process of the oxazine ring, the C=C bond in resveratrol, and the allyl group in RES-al, the cross-linking network of the polybenzoxazine can be manipulated, giving rise to tunable performance of thermosets. As all curable functionalities in RES-al are polymerized, the resulted polybenzoxazine exhibits a good thermal stability with a Tg temperature of 313 °C, a Td5 value of 352 °C, and char yield of 53% at 800 °C under N2.

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