Preparation and Characterization of Styrene Acrylate Emulsion(SAE) Surface Sizing Agent with Rosin as Functional Monomer

2011 ◽  
Vol 236-238 ◽  
pp. 1457-1462
Author(s):  
Jian Feng Xu ◽  
Hui Ren Hu ◽  
Hui Cui
Keyword(s):  
Relative Viscosity ◽  
Functional Monomer ◽  
Optimum Conditions ◽  
Reaction Conditions ◽  
Ir Laser ◽  
Surface Sizing ◽  
Acrylate Emulsion ◽  
Ft Ir ◽  
Particle Sizer

A series of core-shell type cationic soap-free latex were prepared by using styrene(St), butyl acrylate(BA) and methyl methacrylate(MMA) as main materials and introducing rosin as the functional monomer. In this reaction, starch(CS-8), which has low relative viscosity , was used as the emulsifier and dispersant. The influencing factors of the reaction were especially studied and the optimum conditions were got. Then the products were characterized by using scanning electron microscope (SEM), FT-IR, laser particle sizer, particle charge detector(PCD). The results show that the excellent performance and good sizing effects of SAE are achieved when the reaction conditions are as follows: the starch amount is 8%(wt), the charge for the initiator(APS) is 0.5%, and the amount of rosin is 2%(wt). And the water-resistant performance of paper is improved significantly when the rosin is chosen as the functional monomer.

Effect of Water-Resistance Agent on the Performance and Surface Sizing Behavior of Styrene Acrylate Emulsion (SAE)

2012 ◽  
Vol 550-553 ◽  
pp. 3323-3330 ◽  
Author(s):  
Jian Feng Xu ◽  
Ling Long ◽  
Hui Ren Hu ◽  
Yan Bo
Keyword(s):  
Water Resistance ◽  
Orthogonal Experiment ◽  
Relative Viscosity ◽  
Optimum Conditions ◽  
Reaction Conditions ◽  
Surface Sizing ◽  
Cationic Monomer ◽  
Acrylate Emulsion ◽  
Better Than ◽  
Trimethoxy Silane

A series of starch-based styrene acrylate emulsion (SAE) modified with water-resistance agent were prepared by introducing rosin, organosilane(γ-amino propyl triethoxysilane (KH550), γ-(2,3-epoxypropoxy)-propytrimethoxysilane(KH560) and γ-methacryloxypropyl trimethoxy silane (KH570) as the functional monomer, respectively. In the reaction, starch(CS-8), which is low relative viscosity, was used as the emulsifier and dispersant. The optimum conditions of the reaction had especially been studied by orthogonal experiment and then the emulsion properties and surface sizing behaviors of the SAE modified with different kinds of water-resistance agents were compared. Finally, the products which had excellent properties were characterized and the sizing performance was investigated. The results showed that the excellent performance and good sizing effects of styrene acrylate emulsion (SAE) were achieved when the reaction conditions were as follows: rosin was selected as the water resistance-agent with the dosage of 2%(wt), the reaction temperature was 88°C, the mass ratio of St and BA was 9:11, the stirring speed was 130 round per minute and the dosage of initiator (APS), cationic monomer (DM) and CS-8 was 0.5%, 2%(wt) and 7%, respectively. The water-resistance properties of starch-based SAE were significantly improved by using rosin as the water-resistance agent and the surface sizing performance were better than that of the commercial AKD.

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 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 Synthesis, Structures, Electrochemistry, and Catalytic Activity towards Cyclohexanol Oxidation of Mono-, Di-, and Polynuclear Iron(III) Complexes with 3-Amino-2-Pyrazinecarboxylate

2020 ◽  
Vol 10 (8) ◽  
pp. 2692
Author(s):  
Anirban Karmakar ◽  
Luísa M.D.R.S. Martins ◽  
Yuliya Yahorava ◽  
M. Fátima C. Guedes da Silva ◽  
Armando J. L. Pombeiro
Keyword(s):  
Coordination Polymer ◽  
Heterogeneous Catalysts ◽  
Saturated Calomel Electrode ◽  
Two Dimensional ◽  
Reaction Conditions ◽  
Ability To Act ◽  
Tert Butyl Hydroperoxide ◽  
Ft Ir ◽  
Ft Ir Spectroscopy

The synthesis and characterization of a set of iron(III) complexes, viz. the mononuclear [Fe(L)3] (1) and [NHEt3][Fe(L)2(Cl)2] (2), the dinuclear methoxido-bridged [Fe(L)2(μ-OMe)]2.DMF.1.5MeOH (3), and the heteronuclear Fe(III)/Na(I) two-dimensional coordination polymer [Fe(N3)(μ-L)2(μ-O)1/2(Na)(μ-H2O)1/2]n (4), are reported. Reactions of 3-amino-2-pyrazinecarboxylic acid (HL) with iron(III) chloride under different reaction conditions were studied, and the obtained compounds were characterized by elemental analysis, Fourier Transform Infrared (FT-IR) spectroscopy, and X-ray single-crystal diffraction. Compound 1 is a neutral mononuclear complex, whereas 2 is mono-anionic with its charge being neutralized by triethylammonium cation. Compounds 3 and 4 display a di-methoxido-bridged dinuclear complex and a two-dimensional heterometallic Fe(III)/Na(I) polynuclear coordination polymer, respectively. Compounds 3 and 4 are the first examples of methoxido- and oxido-bridged iron(III) complexes, respectively, with 3-amino-2-pyrazinecarboxylate ligands. The electrochemical study of these compounds reveals a facile single-electron reversible Fe(III)-to-Fe(II) reduction at a positive potential of 0.08V vs. saturated calomel electrode (SCE), which is in line with their ability to act as efficient oxidants and heterogeneous catalysts for the solvent-free microwave-assisted peroxidative oxidation (with tert-butyl hydroperoxide) of cyclohexanol to cyclohexanone (almost quantitative yields after 1 h). Moreover, the catalysts are easily recovered and reused for five consecutive cycles, maintaining a high activity and selectivity.

scholarly journals Synthesis and characterization of novel mono, bis and tris heteroaryl chalcone derivatives of 1,3,5-trimethoxybenzene

2021 ◽  
Vol 14 (1) ◽  
pp. 39-47
Author(s):  
M. Fatih Polat ◽  
Derya Aktaş Anı
Keyword(s):  
Elemental Analysis ◽  
High Purity ◽  
Synthesis And Characterization ◽  
Spectroscopic Techniques ◽  
Reaction Conditions ◽  
Chalcone Derivatives ◽  
Ft Ir ◽  
Derivatives Of

In this study, a new series consisting of 12 heteroaryl chalcone derivatives of 1,3,5-trimethoxybenzene were synthesised. Chalcones were synthesised in high purity and efficiency, via condensation of mono, bis and tris 2,4,6-trimethoxy acetophenones with hetero-2-carbaldehyde derivatives based on Claisen Schdmit condensation. The reactions feature a good scope for the all products, mild reaction conditions and good yields. The synthesized compounds were characterized by using FT-IR, NMR and elemental analysis spectroscopic techniques.

scholarly journals Synthesis of poly(γ-tert-butyl L-glutamate): influence of polymerization conditions

2019 ◽  
Vol 16 (3) ◽  
pp. 25
Author(s):  
Phung Thi Thuy Dung ◽  
Nguyen Thi Le Thu
Keyword(s):  
Ring Opening ◽  
Gel Permeation Chromatography ◽  
Attenuated Total Reflection ◽  
Resonance Spectroscopy ◽  
Reaction Conditions ◽  
Tert Butyl ◽  
Ft Ir ◽  
Hydrolysis Of ◽  
Polymerization Conditions

This work presents the synthesis and characterization of poly(γ-tert-butyl L-glutamate) (PtBuLG) via a living ring-opening polymerization procedure of γ-tert-butyl L-glutamate N-carboxyanhydride (tBuLG-NCA). The reaction conditions were investigated to optimize the polymerization yield and molecular weight polydispersity. The synthesized PtBuLG was characterized using nuclear magnetic resonance spectroscopy (NMR), gel permeation chromatography (GPC) and attenuated total reflection-Fourier transform infrared (ATR FT-IR. Finally, hydrolysis of PtBuLG resulted in poly(L-glutamic acid) (PLGA).

Synthesis and Characterization of Reactive Graft Copolymers of Poly(butyl Acrylate) and Cellulose

2005 ◽  
Vol 13 (5) ◽  
pp. 467-478
Author(s):  
Ghanshyam S. Chauhan ◽  
Baljit Singh ◽  
Suresh Kumar ◽  
Anupama Chinkara
Keyword(s):  
Butyl Acrylate ◽  
Metal Ion ◽  
Graft Copolymerization ◽  
Graft Copolymers ◽  
Optimum Conditions ◽  
Ion Sorption ◽  
Graft Yield ◽  
Ft Ir ◽  
Structural Aspects

Butyl acrylate was graft copolymerized onto cellulose extracted from pine needles by a simultaneous gamma radiation initiation method. Optimum conditions for the maximum graft yield were established. Polymerization and grafting parameters such as %grafting (Pg), % grafting efficiency (%GE), rates of polymerization (Rp), homopolymerization (Rh) and graft copolymerization (Rg) were also determined. Grafted cellulose was further functionalized to produce poly(acryloyl hydroxylamine) [Cell-g-poly(CONHOH)] so as to generate active (-CONHOH) groups on the cellulose backbone. Graft copolymers were characterized by elemental analysis, by FT-IR and by a swelling study. An attempt was also made to study the sorption of Fe+2 and Cu+2 as model metal ions onto the candidate copolymers, in order to investigate their selectivity in metal ion sorption and to determine the effect on metal ion sorption of the structural aspects of the hydrogels and other functionalized graft copolymers, so as to identify their end-uses.

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.

Preparation and Characterization of Stearic Acid-Modified Iron-Doped TiO2 Nanoparticles

2013 ◽  
Vol 777 ◽  
pp. 47-51 ◽  
Author(s):  
Jin Long Zuo ◽  
Han Qiang Tang ◽  
Qian Nie ◽  
Biao Li ◽  
Zhi Wei Liu
Keyword(s):  
Surface Modification ◽  
Stearic Acid ◽  
Optimum Conditions ◽  
Iron Ion ◽  
Emulsion Method ◽  
Iron Doped ◽  
Micro Emulsion ◽  
Ft Ir ◽  
Initial Exploration

In this study, TiO2 nanoparticles composites were prepared by the micro emulsion method, above of all samples were characterized by FT-IR, XRD. Photo activities of Fe-TiO2, TiO2 were evaluated by degradation of oil-bearing wastewater. The results show that the photo activity of Fe-TiO2 was more than that of TiO2; the best presence of iron ion dopants in TiO2 was 0.04%. Used stearic acids as the surface modification agent, Fe-TiO2 were modified by situ surface modification. The results showed that the optimum conditions of stearic acid-Fe - TiO2 :Temperature (20°C), the modified time (45 min), the ratio modifier dosage tomagnetitemass (4%). Then we did the initial exploration of Fe-TiO2 Powder that was modified by stearic acid.

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