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.

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.

Polymerization of Silicone Modified Acrylate Emulsion and Preparation of Self-Cleaning Exterior Wall Paint

2010 ◽  
Vol 168-170 ◽  
pp. 2055-2059 ◽  
Author(s):  
Bo Quan Jiang ◽  
Shu Fen Hu ◽  
Yu De Liu ◽  
Min Wei Wang
Keyword(s):  
Silicone Oil ◽  
National Standards ◽  
Chinese Government ◽  
Exterior Wall ◽  
Optimum Conditions ◽  
Acrylic Emulsion ◽  
Operation Conditions ◽  
Acrylate Emulsion ◽  
Optimum Formula ◽  
Better Than

Vinyl triethoxyl silicane, hydrogen silicone oil and microcrystal wax were separately used to modify the acrylic emulsion, wollastonite and synthesize the silicone wax emulsion for preparing exterior wall paint. The optimum conditions for the modifications and synthesis were experimentally presented. Under the optimum formula and operation conditions the silicone-modified acrylic emulsion exhibited good quality and all the property indexes of the exterior wall paint with a contact angle of about 140° were better than those regulated in the national standards issued by Chinese government. The structure of the modified acrylate emulsion, measured by infrared spectroscopy, was proved to be a real silicate-acrylate copolymerization emulsion.

Lipase-Catalyzed Acyl-L-Carnitines Synthesis in [Bmim]PF6 Ionic Liquid

2009 ◽  
Vol 5 (1) ◽  
Author(s):  
Jin-qiang Tian ◽  
Qiang Wang ◽  
Zhong-yuan Zhang
Keyword(s):  
Ionic Liquid ◽  
Lipase Activity ◽  
Molecular Sieves ◽  
Reaction Medium ◽  
Molar Ratio ◽  
Reaction Conditions ◽  
Optimal Reaction ◽  
Better Than

In order to significantly improve the biosynthesis of acyl-L-carnitines catalyzed by lipase, there must be an efficient and suitable reaction medium that is not only polar but also hydrophobic. [Bmim]PF6, which satisfies the above two requirements, was applied as the medium. The optimal reaction conditions were: for isovaleryl-L-carnitine, 0.22aW, 200mg molecular sieves, 60ºC, 4:1 of molar ratio (fatty acid:L-carnitine), 150rpm and 60h; for octanoyl-L-carnitine and palmitoyl-L-carnitine, 0.22aW, 250 mg molecular sieves, 5:1 of molar ratio (fatty acid:L-carnitine), 200rpm, 48h, 60ºC (octanoyl-L-carnitine) and 65ºC (palmitoyl-L-carnitine). Their overall yields could reach 59.14%, 90.79% and 98.03%, respectively. The yields of isovaleryl-L-carnitine, octanoyl-L-carnitine and palmitoyl-L-carnitine in [Bmim]PF6 were 16.21%, 73.67% and 44.22 % more than those in acetonitrile, respectively. [Bmim]PF6 as the medium was better than acetonitrile. It could not only enhance the yields of acyl-L-carnitines, but also protect the lipase activity.

Synthesis and Structural Characterization of a Novel Composite Modified Starch

2011 ◽  
Vol 396-398 ◽  
pp. 1180-1183
Author(s):  
He Ping Li ◽  
Hu Qiang Lv ◽  
Yao Zhang ◽  
Yong Zhe Yang
Keyword(s):  
Structural Characterization ◽  
Orthogonal Experiment ◽  
Acid Catalyst ◽  
Chloroacetic Acid ◽  
Normal Pressure ◽  
Modified Starch ◽  
Optimum Conditions ◽  
X Ray Diffraction ◽  
Mass Fractions

In the normal pressure and presence of catalyst, a novel composite modified starch or functional surfactant was synthesized by using the cassava starch as the main feedstock through the alkalization, etherification and oxidation etc.. The degree of substitution was up to 1.21. Based on the orthogonal experiment and computer-aid methods, the optimum conditions were resulted as follows: the mass fractions(vs. dry starch) of chloroacetic acid, catalyst and oxidant were 32%, 0.01% and 1.14% respectively, and the reaction temperature of etherification was at 50°C for 4.1h. The structural characterization of the composite modified starch was determined by IR and X-ray diffraction.

scholarly journals Synthesis of NdAlO3 Nanoparticles and Evaluation of the Catalytic Capacity for Biodiesel Synthesis

Nanomaterials ◽  
2019 ◽  
Vol 9 (11) ◽  
pp. 1545 ◽  
Author(s):  
Dionicio-Navarrete ◽  
Arrieta-Gonzalez ◽  
Quinto-Hernandez ◽  
Casales-Diaz ◽  
Zuñiga-Diaz ◽  
...  
Keyword(s):  
Mass Ratio ◽  
Reaction Products ◽  
Optimum Conditions ◽  
Reaction Conditions ◽  
Catalyst Synthesis ◽  
Synthesis Of Nanoparticles ◽  
Biodiesel Synthesis ◽  
Dta Analysis ◽  
Optimum Reaction ◽  
Catalytic Capacity

Biodiesel synthesis was carried out via heterogeneous catalysis of canola oil with nanoparticles of a mixed oxide based on rare earths. The catalyst synthesis (NdAlO3) was carried out based on the method proposed by Pechini for the synthesis of nanoparticles. Thermogravimetric analysis-differential thermal analysis (TGA-DTA) analysis was performed on the nanoparticle precursor gel in order to establish the optimum conditions for its calcination, with these being of 800 °C over 24 h. A pure NdAlO3 compound with an approximate size of 100 nm was obtained. The products of the transesterification reaction were analyzed using gas chromatography, FTIR, and NMR. The optimum reaction conditions were determined, namely, the temperature effect, reaction time, methanol:oil mass ratio, and recyclability of the catalyst. These studies showed the following optimal conditions: 200 °C, 5 h, methanol:oil mass ratio of 6:1, and a constant decrease in the catalytic activity of the catalyst was observed for up to six reuses, which later remained constant at around a 50% conversion rate. The maximum biodiesel yield obtained with the optimum conditions was around 75%. Analysis of the reaction products showed that the residual oil showed a chemical composition different from that of the source oil, and that both the biodiesel and glycerol obtained were of high purity.

Catalytic Synthesis of Isoamyl Acetate by Ion Exchange Resin-Supported (NH4)6[MnMo9O32] • 8H2O with Waugh Structure

2013 ◽  
Vol 750-752 ◽  
pp. 1231-1234 ◽  
Author(s):  
Li Xia Wang ◽  
Shu Heng Liu ◽  
Hua Yuan ◽  
Lin Lin Guo
Keyword(s):  
Ion Exchange ◽  
Exchange Resin ◽  
Orthogonal Experiment ◽  
Catalytic Efficiency ◽  
Ion Exchange Resin ◽  
Isoamyl Acetate ◽  
Molar Ratio ◽  
Solid Catalyst ◽  
Reaction Conditions ◽  
Optimal Reaction

Ion exchange resin-supported (NH4)6[MnMo9O32]8H2O with Waugh structure is used to prepare supported solid catalyst. Performance of this catalyst is researched by means of synthesis of isoamyl acetate. Optimal reaction conditions determined by orthogonal experiment are as follows: acid-alcohol molar ratio is 2.5:1, reaction time is 120 min, catalyst dosage is 0.8 g, dosage of water-carrying agent is 2.5 ml, esterification yield reaches 95.1%. This catalyst is characterized by high catalytic efficiency, easy separation and recovery, absence of environmental pollution and being reusable, etc.

Synthesis and characterization of non-ionic and anionic two-component aromatic waterborne polyurethane

2018 ◽  
Vol 47 (4) ◽  
pp. 290-299 ◽  
Author(s):  
Sainan Zhang ◽  
Xiankai Jiang
Keyword(s):  
Thermal Stability ◽  
Water Resistance ◽  
Soft Segment ◽  
Aqueous Dispersion ◽  
Waterborne Polyurethane ◽  
Content Type ◽  
Hydrophilic Modification ◽  
Two Component ◽  
Better Than

Purpose The purpose of this paper is to synthesize and characterize a series of two-component aromatic waterborne polyurethane (2K-WPU) which is composed of non-ionic and anionic polyisocyanate aqueous dispersion and polyurethane polyol aqueous dispersion. Design/methodology/approach The polyisocyanate aqueous dispersion was synthesized through non-ionic and anionic hydrophilic modification procedures. The values of the hydrogen bonding index (HBI) and molecule structures of WPU were obtained by Fourier transform infrared (FTIR). The thermal, mechanical and water resistance properties of 2K-WPU films were investigated. Findings The appearance of non-ionic polyisocyanate aqueous dispersion and anionic polyisocyanate aqueous dispersion was colorless translucent pan blue and yellow opaque emulsions, respectively. FTIR not only showed that 2K-WPU was obtained from the polymerization of polyisocyanate component and polyhydroxy component by polymerization but also showed that the content of hydrogen bondings of anionic 2K-WPU (WPU 2) was higher than non-ionic 2K-WPU (WPU 1). The glass-transition temperature (Tg), storage modulus and water resistance of WPU 2 were higher than WPU1, whereas the thermal stability of WPU1 was better than WPU 2. Practical implications The investigation established a method to prepare a series of 2K-WPU which was composed of non-ionic or anionic polyisocyanate aqueous dispersion and polyurethane polyol aqueous dispersion. The prepared 2K-WPU film could be applied as substrate resin material in the field of waterborne coating. Originality/value The paper established a method to synthesize a series of 2K-WPU. The effect of HBI value and the molecule structure of soft segment on the thermal stability, mechanical and water resistance properties of 2K-WPU films were studied.

scholarly journals Heterogeneous Fenton-Like Catalytic Degradation of 2,4-Dichlorophenoxyacetic Acid by Nano-Scale Zero-Valent Iron Assembled on Magnetite Nanoparticles

Water ◽  
2020 ◽  
Vol 12 (10) ◽  
pp. 2909 ◽  
Author(s):  
Xiaofan Lv ◽  
Yiyang Ma ◽  
Yangyang Li ◽  
Qi Yang
Keyword(s):  
Hydrogen Peroxide ◽  
Synergistic Effects ◽  
Degradation Process ◽  
Zero Valent Iron ◽  
Dichlorophenoxyacetic Acid ◽  
Heterogeneous Fenton ◽  
Reaction Conditions ◽  
Nano Zero Valent Iron ◽  
2,4 Dichlorophenoxyacetic Acid ◽  
Better Than

Fe0@Fe3O4 nanoparticles with dispersibility and stability better than single nano zero-valent iron (nZVI) were synthesized and combined with hydrogen peroxide to constitute a heterogeneous Fenton-like system, which was creatively applied in the degradation of 2,4-dichlorophenoxyacetic acid (2,4-D). The effects of different reaction conditions like pH, hydrogen peroxide concentration, temperature, and catalyst dosage on the removal of 2,4-D were evaluated. The target pollutant was completely removed in 90min; nearly 66% of them could be mineralized, and the main intermediate product was 2,4-dichlorophenol. Synergistic effects between nZVI and Fe3O4 made the 2,4-D degradation efficiency in the Fe0@Fe3O4/H2O2 system greater than in either of them alone. More than a supporter, Fe3O4 could facilitate the degradation process by releasing ferrous and ferric ions from the inner structure. The reduction of 2,4-D was mainly attributed to hydroxyl radicals including surface-bound ∙OH and free ∙OH in solution and was dominated by the former. The possible mechanism of this Fe0@Fe3O4 activated Fenton-like system was proposed.

Preparation of starch-based styrene acrylate emulsion used as surface-treatment agent for decorative base paper

2013 ◽  
Vol 33 (4) ◽  
pp. 323-330 ◽  
Author(s):  
Jianfeng Xu ◽  
Ling Long ◽  
Huiren Hu
Keyword(s):  
Particle Size ◽  
Surface Treatment ◽  
Relative Viscosity ◽  
Particle Size Analysis ◽  
Size Analysis ◽  
Optimal Conditions ◽  
Cationic Starch ◽  
Acrylate Monomer ◽  
Base Paper ◽  
Acrylate Emulsion

Abstract A series of cationic starch (CS-8)-based styrene (St) acrylate latex preparations was prepared by the core-shell emulsion polymerization method. The latex was used in the surface-treatment of decorative base papers, for good printability and absorbability. CS-8, which has a low relative viscosity, was used as the emulsifier and dispersant. The influencing factors (dosage of CS-8 as well as the kinds and dosages of functional monomers) were studied and the optimal conditions were achieved. Then, the products were characterized by scanning electron microscopy (SEM), Fourier-transform infrared (FT-IR), laser particle size analysis and particle charge detection. The results showed that the excellent performance and good surface-treatment effects of the St acrylate emulsion (SAE) were achieved when the reaction conditions were as follows: 10 wt% starch, 2 wt% methacryloyloxyethyltrimethyl ammonium chloride (DMC) as the cationic monomer and 20 wt% ethyl acrylate (EA) as the acrylate monomer. Under the optimal conditions, the latex particle size was around 160 nm, the latex viscosity was 10 mPa·s and the latex charge density was 0.60 mmol·l-1. The printability of the decorative base paper was significantly improved and the absorbability of the paper sheet was maintained. The surface-treatment effect of the cationic starch-based SAE was superior to that of commercial polyurethane (PU).

Synthesis and Property of Siloxane and other Modifier Modified Melamine Resin

2013 ◽  
Vol 448-453 ◽  
pp. 111-114
Author(s):  
Xiao Bin Li ◽  
Lu Qi
Keyword(s):  
Infrared Spectroscopy ◽  
Polyethylene Glycol ◽  
Thermogravimetric Analysis ◽  
Polyvinyl Alcohol ◽  
Melamine Resin ◽  
Structure And Properties ◽  
Reaction Conditions ◽  
And Performance ◽  
Better Than

This work reports melamine resin was modified with siloxane, Polyvinyl alcohol (PVA) and polyethylene glycol (PEG) to improve its structure and properties, and accomplished a wide research and study on the effect of different reaction conditions, including temperature, PH and solid contents. Using infrared spectroscopy (FTIR), thermogravimetric analysis (TG) and DSC to analyzed the samples and study their composition and performance. The results showed that siloxane, Polyvinyl alcohol and polyethylene glycol (PEG) modifier can make the performance of the melamine better than unmodified ones.

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