Effect of the crosslinking degree and the nickel salt load on the thermal decomposition of poly(2-hydroxyethyl methacrylate) hydrogels and on the metal release from them

2006 ◽  
Vol 295 (2) ◽  
pp. 393-400 ◽  
Author(s):  
César Teijón ◽  
Rosa Olmo ◽  
M. Dolores Blanco ◽  
José M. Teijón ◽  
Arturo Romero
Keyword(s):  
Thermal Decomposition ◽  
Nickel Salt ◽  
Hydroxyethyl Methacrylate ◽  
Metal Release ◽  
Crosslinking Degree ◽  
Salt Load

scholarly journals Hydrogels Obtained via γ-Irradiation Based on Poly(Acrylic Acid) and Its Copolymers with 2-Hydroxyethyl Methacrylate

2020 ◽  
Vol 10 (14) ◽  
pp. 4960 ◽  
Author(s):  
Marin Micutz ◽  
Rodica Mihaela Lungu ◽  
Viorel Circu ◽  
Monica Ilis ◽  
Teodora Staicu
Keyword(s):  
Glass Transition ◽  
Transition Temperature ◽  
Glass Transition Temperature ◽  
Acrylic Acid ◽  
Aqueous Solutions ◽  
Functional Groups ◽  
Chemical Transformations ◽  
Hydroxyethyl Methacrylate ◽  
Γ Irradiation ◽  
Crosslinking Degree

Hydrogels containing both carboxyl and hydroxyl functional groups have been prepared by γ-irradiation of either aqueous solutions of acrylic acid (AA) and mixtures of AA and 2-hydroxyethyl methacrylate (HEMA) in different ratios, or aqueous solutions of poly(AA), PAA, and poly(AA-co-HEMA) obtained via solution polymerization. A higher absorbed dose is required in order to prepare hydrogels from monomer solutions, compared with those from polymer solutions. The range for the absorbed doses was chosen so that the probability of crosslinking reactions is higher than that of degradation ones. As the radiation energy deposited in a sample increases, the equilibrium swelling degree and the average molar mass between crosslinks diminishes. Chemical transformations induced by radiation were investigated by means of FTIR spectroscopy and thermal analysis of polymers before and after irradiation. For all these systems, the formation of a three-dimensional network enhances the glass transition temperature and thermal stability, but a further increase in the crosslinking degree may have the reverse effect on the glass transition temperature. Depending on the preparation protocol and/or hydrogel composition, superabsorbent materials that can bind different compounds throughout side functional groups may be obtained.

Synthesis and Properties of Waterborne UV Polyurethane

2011 ◽  
Vol 311-313 ◽  
pp. 1087-1092 ◽  
Author(s):  
Xin Qi Zhou ◽  
You Ming Cao ◽  
Jun Ling Tian
Keyword(s):  
Thermal Decomposition ◽  
Particle Size ◽  
Infrared Spectroscopy ◽  
Raw Materials ◽  
Waterborne Polyurethane ◽  
Toluene Diisocyanate ◽  
Target Product ◽  
Hydroxyethyl Methacrylate ◽  
Uv Curable ◽  
Decomposition Properties

Toluene diisocyanate(TDI), polyethylene glycol(PEG), double-propionic acid(DMPA), hydroxyethyl methacrylate(HEMA) and other raw materials were used to synthesis UV-curable waterborne polyurethane, and the effect of the synthesis condition on the particle size of the emulsion was investigated in this paper. The structure of the polyurethane was identified by infrared spectroscopy (IR), thermal decomposition properties was measured through the thermogravimetric(TG). The results showed that, the target product is expected waterborne UV polyurethane by IR. With DMPA content increasing, the particle size decrease, stability and appearance of the emulsion turn better. With the mole ration of PEG/DMPA decreasing, adhesion and water absorption of the film increase. TG analysis indicates that the thermal decomposition performance of the Waterborne UV Polyurethane （WPUA） is excellent.

Applications of Photoelectron Microscopy

1976 ◽  
Vol 34 ◽  
pp. 506-507
Author(s):  
William J. Baxter
Keyword(s):  
Electron Microscopy ◽  
Thermal Decomposition ◽  
Chemical Composition ◽  
Ultraviolet Radiation ◽  
Thin Layer ◽  
Edge Effects ◽  
Electron Optics ◽  
Surface Layers ◽  
Crystalline Orientation ◽  
Fluorescent Screen

In this form of electron microscopy, photoelectrons emitted from a metal by ultraviolet radiation are accelerated and imaged onto a fluorescent screen by conventional electron optics. image contrast is determined by spatial variations in the intensity of the photoemission. The dominant source of contrast is due to changes in the photoelectric work function, between surfaces of different crystalline orientation, or different chemical composition. Topographical variations produce a relatively weak contrast due to shadowing and edge effects.Since the photoelectrons originate from the surface layers (e.g. ∼5-10 nm for metals), photoelectron microscopy is surface sensitive. Thus to see the microstructure of a metal the thin layer (∼3 nm) of surface oxide must be removed, either by ion bombardment or by thermal decomposition in the vacuum of the microscope.

Preparation and characterisation of vanadium pentoxide supported rhodium catalyst

1988 ◽  
Vol 46 ◽  
pp. 946-947
Author(s):  
A. Legrouri
Keyword(s):  
Aqueous Solution ◽  
Thermal Decomposition ◽  
Physicochemical Properties ◽  
Surface Area ◽  
Vanadium Pentoxide ◽  
High Purity ◽  
Gas Adsorption ◽  
Rhodium Catalyst ◽  
Optical Methods ◽  
Reducible Oxides

The industrial importance of metal catalysts supported on reducible oxides has stimulated considerable interest during the last few years. This presentation reports on the study of the physicochemical properties of metallic rhodium supported on vanadium pentoxide (Rh/V2O5). Electron optical methods, in conjunction with other techniques, were used to characterise the catalyst before its use in the hydrogenolysis of butane; a reaction for which Rh metal is known to be among the most active catalysts.V2O5 powder was prepared by thermal decomposition of high purity ammonium metavanadate in air at 400 °C for 2 hours. Previous studies of the microstructure of this compound, by HREM, SEM and gas adsorption, showed it to be non— porous with a very low surface area of 6m2/g3. The metal loading of the catalyst used was lwt%Rh on V2Q5. It was prepared by wet impregnating the support with an aqueous solution of RhCI3.3H2O.

Observations of the Thermal Decomposition of Brucite

1968 ◽  
Vol 26 ◽  
pp. 446-447
Author(s):  
P. L. Burnett ◽  
W. R. Mitchell ◽  
C. L. Houck
Keyword(s):  
Thermal Decomposition ◽  
Magnesium Oxide ◽  
Basal Plane ◽  
Magnesium Ions ◽  
A Value ◽  
Reaction Proceeds

Natural Brucite (Mg(OH)2) decomposes on heating to form magnesium oxide (MgO) having its cubic ﹛110﹜ and ﹛111﹜ planes respectively parallel to the prism and basal planes of the hexagonal brucite lattice. Although the crystal-lographic relation between the parent brucite crystal and the resulting mag-nesium oxide crystallites is well known, the exact mechanism by which the reaction proceeds is still a matter of controversy. Goodman described the decomposition as an initial shrinkage in the brucite basal plane allowing magnesium ions to shift their original sites to the required magnesium oxide positions followed by a collapse of the planes along the original <0001> direction of the brucite crystal. He noted that the (110) diffraction spots of brucite immediately shifted to the positions required for the (220) reflections of magnesium oxide. Gordon observed separate diffraction spots for the (110) brucite and (220) magnesium oxide planes. The positions of the (110) and (100) brucite never changed but only diminished in intensity while the (220) planes of magnesium shifted from a value larger than the listed ASTM d spacing to the predicted value as the decomposition progressed.

A magnetic super lattice

1987 ◽  
Vol 45 ◽  
pp. 360-361 ◽  
Author(s):  
M.D. Bentzon ◽  
J. v. Wonterghem ◽  
A. Thölén
Keyword(s):  
Thermal Decomposition ◽  
Oleic Acid ◽  
Magnetic Fluid ◽  
Magnetic Particles ◽  
Carbon Film ◽  
Thick Layer ◽  
Amorphous Iron ◽  
Super Lattice ◽  
Carrier Liquid ◽  
Median Diameter

We report on the oxidation of a magnetic fluid. The oxidation results in magnetic super lattice crystals. The “atoms” are hematite (α-Fe2O3) particles with a diameter ø = 6.9 nm and they are covered with a 1-2 nm thick layer of surfactant molecules.Magnetic fluids are homogeneous suspensions of small magnetic particles in a carrier liquid. To prevent agglomeration, the particles are coated with surfactant molecules. The magnetic fluid studied in this work was produced by thermal decomposition of Fe(CO)5 in Declin (carrier liquid) in the presence of oleic acid (surfactant). The magnetic particles consist of an amorphous iron-carbon alloy. For TEM investigation a droplet of the fluid was added to benzine and a carbon film on a copper net was immersed. When exposed to air the sample starts burning. The oxidation and electron irradiation transform the magnetic particles into hematite (α-Fe2O3) particles with a median diameter ø = 6.9 nm.

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