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The metal cross-linking fluorinated polyacrylate colloid has a high cross-linking density, high transparency, high heat resistance and hydrophobicity. In this paper, the metal cross-linking fluorinated polyacrylate colloid is synthesized via the semi-continuous seeded emulsion polymerization technology, which uses the self-made magnesium acrylate, calcium acrylate and zinc acrylate as metal crosslinker and dodecafluoroheptyl methacrylate as a fluorine monomer. In this study, the ablation effect of the metal ions is weakened by the increased amount of environmentally friendly and polymerizable anion emulsifier DNS-86. The demulsification phenomenon of emulsion is successfully overcome through destroying the double layer structure of micelles or colloid particles by polyvalent metal ions. The colloidal particle size is smaller and the particle size distribution of the colloid is more uniform. Colloidal film has a good hydrophobicity and the glass transition temperature and the thermal decomposition temperature are high. [ABSTRACT FROM AUTHOR]

Modified latex is prepared via the soap-free emulsion polymerization of ethyl acetate (VAc) and vinyl versatate (VeoVa10). DFHMA is used as modified monomers. The composite surfactants of SR-10 and ANPEO-10 are used as the composite emulsifiers. The polymerization is initiated by potassium sulfate (KPS). The structure of latex film was characterized by Fourier transform infrared spectroscopy (FTIR). The latex films were tested by thermogravimetric analysis (TGA), differential scanning calorimetry (DSC) and contact angle (CA) determinator. The particle size of the latex emulsion particle size is determined by the Zetatrac dynamic light scatter. Results show that the optimum condition of preparing the modified latex can be obtained, i.e. the amount of emulsifier is 4.0%; the mass ratio of SR-10 to ANPEO-10 is 1:1; the amount of initiator is 0.5%; the mass ratio ofVAc to VeoVa10 is 1:1; the amount of DFHMA is 5.0%. The appearance of the latex is blue and translucent with a small particle size. The conversion rate is more than 98%. Compared with the conventional latex, the hydrophobicity and heat resistance of the film have been improved. Moreover, the latex has good chemical stability and mechanical stability. [ABSTRACT FROM AUTHOR]

Purpose: Fluorine materials have received the keen attention of many researchers because of their water repellency and low surface free energy. The purpose of this paper is to prepare self-crosslinking fluorocarbon polyacrylate latexes containing different fluorocarbon chain lengths by semi-continuous seeded emulsion polymerization technology. Design/methodology/approach: Methyl methacrylate (MMA), butyl acrylate (BA), hydroxypropyl methacrylate (HPMA) and fluorine-containing monomers were used as main monomers. The fluorine-containing monomers included hexafluorobutyl methacrylate (HFMA), dodecafluoroheptyl methacrylate (DFMA) and trifluorooctyl methacrylate (TFMA). Potassium persulfate (KPS) was used as thermal decomposition initiator, non-ionic surfactant alkyl alcohol polyoxyethylene (25) ether (DNS-2500) and anionic surfactant sodium dodecylbenzene sulfonate (SDBS) as mixed emulsifier. Findings: Through optimizing the reaction conditions, the uniform and stable latex is gained. The polymer of structure was characterized by Fourier transform infrared spectroscopy (FTIR). Thermogravimetric analysis (TGA), differential scanning calorimetry (DSC) and contact angle (CA) were tested on latex films. The particle size and distribution range of emulsion were tested with nano particle size analyzer. After comprehensively comparing the latexes and films prepared by HFMA, DFMA and TFMA, the performance of DFMA monomer modified is better. Originality/value: The self-crosslinking acrylic emulsion is prepared via semi-continuous seeded emulsion polymerization, which methyl methacrylate (MMA), butyl acrylate (BA), hydroxypropyl methacrylate (HPMA) and fluorine-containing monomers were used as main monomers. The fluorine-containing monomers were composed of hexafluorobutyl methacrylate (HFMA), dodecafluoroheptyl methacrylate (DFMA) and trifluorooctyl methacrylate (TFMA). Potassium persulfate (KPS) was used as thermal decomposition initiator, non-ionic surfactant alkyl alcohol polyoxyethylene (25) ether (DNS-2500) and anionic surfactant sodium dodecylbenzene sulfonate (SDBS) as mixed emulsifier. There are two main innovations. One is that the self-crosslinking acrylic emulsion is prepared successfully. The other is that the effects of monomers containing different fluorocarbon chain lengths on polyacrylate, such as monomer conversion rate, coagulation rate, mechanical stability, chemical stability, emulsion particle size and storage stability, are studied in detail. [ABSTRACT FROM AUTHOR]

The divinyl silane modified self-crosslinking polyacrylate latex was successfully prepared by semicontinuous seeded emulsion polymerization. Methyl methacrylate (MMA) and butyl acrylate (BA) were used as main monomers and the reaction was initiated by potassium persulfate (KPS). The modified monomer 1, 3-divinyltetramethyldisiloxane (DVMS) and crosslinked monomer hydroxyethyl acrylate (HEA) were introduced into the basic dispersion. Sodium dodecyl sulfonate (SDS) anionic surfactant and alkyl polyglycoside (APG) nonionic emulsifier were utilized as composite emulsifiers. The structure of latex film was characterized by Fourier transform infrared spectroscopy (FTIR). The latex films were tested by thermogravimetric analysis (TGA), differential scanning calorimetry (DSC) and contact angle (CA) and apparent crosslinking percentage. The particle size of the emulsion was measured by Zetatrac dynamic light scattering instrument. The optimum conditions are as follows: the amount of composite emulsifier is 5.0%, the mass ratio of SDS to APG is 1:1, the amount of initiator is 0.5%, the amount of DVMS is 5.0%, and the amount of HEA is 1.0%. The emulsion has good mechanical stability and chemical stability, and the storage stability is ideal. The dispersion is blue and translucent, with a small particle size. The apparent crosslinking percentage of the latex film is above 89%, and the highest contact angle was more than 98°. The polyacrylate colloidal film prepared in this paper has outstanding thermal stability and hydrophobicity. [ABSTRACT FROM AUTHOR]

Purpose: Fluorine materials have received the keen attention of many researchers because of their water repellency and low surface free energy. The purpose of this paper is to prepare fluorine-containing soap-free acrylic emulsion, which sodium allyoxypropyl hydroxypropyl sulfonate (COPS-1) and anionic emulsifier sodium a-alkenyl sulfonate (a-AOS) were combined as polymerizable emulsifier, and undecylenic acid (UA) and dodecafluoroheptyl methacrylate(DFMA) were introduced as functional monomer. Design/methodology/approach: The fluorinated polyacrylate emulsion was successfully prepared by semi-continuous seed emulsion polymerization, wherein the main monomers were methyl methacrylate (MMA) and butyl methacrylate (BA), and the initiator was potassium persulfate (KPS). Sodium alloxypropyl sulfonate (COPS-1) and an anionic emulsifier sodium a-alkenyl sulfonate (a-AOS) were compounded as a polymerizable emulsifier. Besides, undecylenic acid (UA) and dodecafluoroheptyl methacrylate (DFMA) were introduced as the functional monomers. Findings: The optimum recipe of preparing the modified latex is as follows: the amount of emulsifier was 4%, the ratio of emulsifier (COPS-1: AOS) was 3: 1, and the content of initiator was 0.6%. In this case, the conversion rate of acrylic polymer emulsion was high and the polymerization stability was good. When the amount of monomer UA was 2% and the amount of DFMA was 4%, the overall performance of the emulsion was the best. Originality/value: The fluorine-containing soap-free acrylic emulsion is prepared via semi-continuous seeded emulsion polymerisation, which sodium allyoxypropyl hydroxypropyl sulfonate (COPS-1) and anionic emulsifier sodium a-alkenyl sulfonate (a-AOS) were combined as polymerizable emulsifier, and undecylenic acid (UA) and dodecafluoroheptyl methacrylate (DFMA) were introduced as functional monomer. There are two main innovations. One is that the fluorine-containing soap-free acrylic emulsion is prepared successfully. The other is that the undecylenic acid is introduced as functional monomer. [ABSTRACT FROM AUTHOR]

The novel fluoro-silicone polyacrylate latex was successfully synthesized in the presence of a novel green mixed emulsifier of β -cyclodextrin (β -CD) and sodium lauroyl glutamate (SLG) by semi-continuous seeded emulsion polymerization, which was initiated with potassium persulphate. Methyl methacrylate (MMA) and butyl acrylate (BA) were used as the main monomers, while hexafluorobutyl methacrylate (HFMA) and vinyltriethoxysilane (VTES) were used as the functional monomers. The resultant latex and its film were characterized by Fourier transform infrared spectroscopy, thermogravimetric analysis, differential scanning calorimetry and contact angle determinator, respectively. The optimum conditions of preparing the fluoro-silicone polyacrylate latex are as follows: the amount of compound emulsifiers are 7.0%; β -CD: SLG = 1:2; the amount of initiator is 0.7%; the appropriate proportion of main monomer of MMA: BA = 1:1; and the amounts of HFMA and VTES are 6.0% and 4.0%, respectively. In this case, the resultant latex has high conversion rate, low gel rate and good stability. Results showed that both thermal stability and hydrophobic property of the latex are improved with the incorporation of a small amount of HFMA and VTES. [ABSTRACT FROM AUTHOR]

Abstract: The novel modified acrylate colloid was synthesized by semi‐continuous seeded emulsion polymerization which was initiated with potassium persulfate (KPS), and octylphenol polyoxyethylene ether (OP‐10) and sodium dodecyl benzene sulfonate (SDBS) were used as surfactants. Butyl acrylate (BA) and methyl methacrylate (MMA) were used as the main monomers and hexafluorobutyl methacrylate (HFMA, C8H8F6O2), and benzyl methacrylate (BZMA, C11H12O2) were used as functional monomers. Factors such as the amount of initiator, mass ratio of SDBD to OP‐10 and monomers, which have an influence on particle size and morphology of the resultant colloid, are studied. Chemical composition of the modified acrylate colloid was evaluated by Fourier transform infrared spectrometry (FTIR). The thermal performances were characterized by differential scanning calorimetry (DSC) and thermogravimetry (TG). Furthermore, surface hydrophobicity of the latex film was examined by measurement of water absorption and water contact angle. Results indicate that the modified acrylate colloid has highest monomer conversion rate and lowest coagulation percentage when the mass fraction of emulsifier was 4% and mass ratio of SDBS to OP‐10 was 1:2, mass fraction of initiator was 0.3%, mass percent of HFMA was 6%, and the amount of BZMA was 2%. Benzene ring‐containing monomer is effectively participated in the reaction and has improved the thermal performance and surface properties of copolymer colloid. The resultant colloid has excellent hydrophobicity and low surface energy. Solid content of the resultant colloid was about 30% (wt %). [ABSTRACT FROM AUTHOR]

The polyacrylate latex containing fluorine and silicon were successfully synthesized by semi-continuous seeded emulsion polymerization in the presence of the mixed emulsifier of novel sodium lauroyl glutamate (SLG) anion surfactant and BCE-10 nonionic surfactant, which methyl methacrylate (MMA) and butyl acrylate (BA) were used as main monomers and hexafluorobutyl methacrylate (HFMA) and vinyltriethoxysilane (VTES) were used as the functional monomers. Potassium persulfate (KPS) was used as the initiator. The structural groups of the latex films were evaluated by Fourier transform infrared spectroscopy (FTIR). Thermal performance of the film was evaluated by differential scanning calorimetry (DSC) and thermogravimetric analysis. The latex particle size and its distribution were measured by the dynamic light scattering detector. Furthermore, surface hydrophobicity of the latex film was examined by measurement of water contact angle (WCA). WCA and thermal stability of the film are increased with the increased amount of HFMA and VTES. Factors, which have an influence on the properties of the resultant latex and its film, are investigated in detail. Results show that the optimal condition of synthesizing the emulsion is as follows: the amount of emulsifiers is 7.0%; mass ratio of SLG to BCE-10 is 1:1; the amount of initiator is 0.8%; the mass ratio of MMA to BA is 1:1; the content of the fluorine monomer and silicon monomer is 6.0%. [ABSTRACT FROM AUTHOR]

Fluoro-silicone modified polyacrylate latex was successfully prepared by semi-continuous seeded emulsion polymerization in the presence of a green mixed emulsifier consisting of cashew phenol polyoxyethylene ether sulfonate (BCE-10B) anionic surfactant and alkyl polyglycoside (APG) nonionic surfactant, in which the mixed monomers were initiated with potassium persulfate (KPS). The structure and properties were characterized by Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA) and contact angle (CA), respectively. Results show that the optimal conditions of synthesizing the novel emulsion are as follows: the total concentration of mixed emulsifiers is 5.0%; the optimum mass ratio of APG to BCE-10B is 2:1; the amount of initiator is 0.6%; the composition of main monomers of MMA:BA = 1:1; and the concentrations of HFMA and VTES are 4.0 and 6%, respectively. In this case, the resultant emulsion showed good thermal stability and hydrophobicity. [ABSTRACT FROM AUTHOR]

The fluorinated polyacrylate latex were successfully prepared with semi- continuous seeded emulsion polymerization of butyl acrylate (BA), methyl methacrylate (MMA) and hexafluorobutyl methacrylate (HFMA) which was initiated with potassium persulfate (KPS) initiator and emulsified with the novel mixed surfactants of sodium lauryl glutamate (SLG) and alkylphenol ethoxylates (OP-10). The structure of the resultant latex was confirmed by Fourier transform infrared spectroscopy (FTIR). The particle size of the latex was measured by Zetatrac dynamic light scattering detector. The film of latex was tested by differential scanning calorimetry (DSC), thermogravimetric analysis (TGA) and contact angle (CA). The optimum conditions of preparing the novel fluorinated polyacrylate latex are optimized and the results are as follows: the amount of emulsifiers is 4.0%; mass ratio of SLG to OP-10 is 1:1, the amount of the initiator is 0.6%. The mass ratio of MMA to BA is 1:1 and the amount of HFMA is 7.0%. In this case, the conversion is high and the polymerization stability is good. In addition, the water resistance and thermal properties of the latex films were improved significantly in comparison with the film of the latex prepared without the fluorinated monomer. [ABSTRACT FROM AUTHOR]

The acrylate latex was a kind of production of emulsion polymerization of acrylate or methyl acrylate and other vinyl ester monomers. Starch was a biomaterial which found multiple applications in various branches. Novel approach to acrylate latex manufacture implied usage of composites e.g. the acrylate latex was being doped with starch to improve its properties and create biofriendly, naturally degrading material, and diminishing negative effect of polymeric waste production. In this paper, two methods that acrylate latex modifed with starch are reviewed and summarized. The aim of the review is that provides the reference for use of the starch in modifying the acrylate latex. [ABSTRACT FROM AUTHOR]

The novel cationic polyacrylate latex containing fluorine silicon was successfully prepared via soap-free emulsion polymerization of butyl acrylate, methyl methacrylate, vinyltriethoxysilane and hexafluorobutylmethacrylate in water phase, which were initiated with water soluble azo initiator and emulsified with the mixed surfactants polymerizable emulsifier and OP-10. The films of the resultant latex were characterized by Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC) and contact angle (CA) determinator, respectively. In comparison with the conventional polyacrylate latex, the thermal stability and water resistance of novel latex film are improved. The conditions of preparing the novel cationic acrylate latexes were optimized. The optimum conditions of preparing the novel latex are as follows: the amount of emulsifiers and the initiator are 6.0% and0.3%, respectively; both the amount of VETS and amount of HFMA are 6.0%. In this case, the conversion is high and the polymerization stability is good. [ABSTRACT FROM PUBLISHER]

The novel acrylate emulsion containing phosphorus and silicon was prepared successfully via semi-continuous seeded emulsion polymerization. The conditions of synthesizing the novel emulsion were optimized. The films of the resultant emulsion were characterized by Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC) and contact angle (CA) determinator, respectively. Results show that the optimal condition synthesizing the novel emulsion was that the amount of PAM-200 is 2.00 g and the suitable way of adding KH-570 was to add KH-570 into the reaction after all other monomers were added and the optimal amount was 3.00%. Both FTIR and DSC confirm that the novel emulsion has been prepared successfully. CA indicates that the water resistance of emulsion film is improved clearly. [ABSTRACT FROM AUTHOR]

The nanometre fluorinated acrylate latex was prepared via semi-continuous seeded emulsion polymerisation of butyl acrylate, methyl methacrylate and hexafluorobutyl acrylate in water phase when gemini surfactant and 2,2′-azobis[2-(2-imidazolin-2-yl)propane] dihydrochloride are used to be emulsifier and initiator, respectively. The resultant latex is characterised by Fourier transform infrared (FTIR) spectrometry, contact angle measurements, dynamic light scattering and differential scanning calorimetry (DSC). FTIR spectrum identifies the formation of terpolymer. DSC confirms that the latex is a kind of random terpolymer and the consistency among the chain segment is fairly good. The average particle size of latex is decreased with the increase of the amount of gemini surfactant. The particle size of resultant latex is 22.4 nm and is further confirmed by transmission electron microscope when the amount of gemini surfactant is 3%. However, the viscosity of latex is increased with the increase of the amount of gemini surfactant. In comparison with the nanometre fluorinated acrylate latex, the hydrophobic property of the resultant latex is improved. [ABSTRACT FROM AUTHOR]

Abstract: A series of acrylic polymer colloids were prepared via semi-continuous seeded emulsion polymerization of BA and MMA in water phase when OP-10 and AIBI is used to be emulsifier and initiator, respectively. FTIR spectrum identifies the formation of copolymers of P (MMA-co-BA). DSC confirms that the colloid is a kind of random copolymer and the consistency among the chain segment is fairly good. The emulsion polymerization conditions of preparing acrylic polymer colloid are optimized. Results show that the conversion rate is high and the coagulum is low and the particle size of the acrylic polymer colloids is small when the amount of AIBI is 0.75g. The polymerization temperature is 70°C, which is lower than the one that the emulsion polymerization is initiated with the persulfate. [Copyright &y& Elsevier]

BA-MMA-POMA copolymer latex was successfully prepared by soap-free emulsion polymerization of 2-(perfluoro-(1,1-bisisopropyl)-2-propenyl)oxyethyl methacrylate(POMA) with butyl acrylate(BA), methyl methacrylate (MMA) initiated by K [ABSTRACT FROM AUTHOR]

The new fluorinated acrylate emulsion was synthesized by using the intermediate perfluorous nonene and 2-hydroxyethyl methacrylate as the staring reactants via semi-continuous seeded emulsion polymerization. The structures, glass transition temperature, thermal property and water repellency of the fluorinated acrylate emulsion were characterized with FTIR, differential scanning calorimetry, thermal analysis, and contact angle meter. Influences of many factors such as the theoretical solid content, the temperature of the emulsion polymerization on the stability of the emulsion polymerization, the added amount of emulsifiers and the added amount of the initiator were studied. Results show that the stability of the emulsion polymerization is fairly good when the theoretical solid content is below 30% and the reaction temperature is 80°C and the added amount of emulsifiers and the initiator are 6.0-8.0% and 2.0% respectively. In comparison with the acylate emulsion, the thermal stability of the fluorinated acrylate emulsion is decreased but the water repellency of the fluorinated acrylate emulsion is greatly increased. [ABSTRACT FROM AUTHOR]

Abstract: Double fluorinated acrylate latex (DFAL) has been successfully prepared by macromolecule reaction between m-trifluoromethylphenylamine (m-TFMPA) and the single fluorinated acrylate latex (SFAL), which is prepared by semi-continuous seeded emulsion polymerization of butyl acrylate (BA), methyl methacrylate (MMA) 2-(perfluoro-(1,1-bis-isopropyl)-2-propenyl)oxyethyl methacrylate (POMA) and glycidyl methacrylate (GMA). The resultant DFAL is characterized by Fourier transform infrared (FTIR) spectrometry, contact angle determinator, dynamic light scattering detector and thermo-gravimetric analysis (TGA). Results show that the contact angle of DFAL film is improved in comparison with that of SFAL film. The surface properties especially the contact angle of the film with annealing have been improved greatly because more fluorine atom is introduced into the molecule of acrylate latex and moves to the surface of the film. However, the thermal stability of the DFAL film is not improved. [ABSTRACT FROM AUTHOR]