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Fluorine and silicon materials have received the keen attention of many researchers because of their water repellency and low surface free energy. The purpose this study was to prepare vinyl acetate (VAc)-vinyl ester of neodecanoic acid (VeoVa 10) copolymer latex modified with fluorine and silicone monomer, which is emulsified with the novel surfactants of disodium laureth sulfosuccinate (MES) and octylphenol polyoxyethylene ether (OP-10).

A series of modified latices containing fluorine-silicon have been prepared by semi-continuous seeded emulsion polymerisation of mixed monomers of VAc, VeoVa10, hexafluorobutylmethacrylate (HFMA) and vinyltriethoxysilane (VTES) and emulsified by novel surfactants of MES and OP-10.

The optimum conditions for preparing the modified latex is as follows: the amount of the surfactant was 4.0 Wt.% and the mass ratio of the anionic and nonionic surfactant was 3:1; the dosage of initiator was 0.4 Wt.% and the mass ratio of the main monomer was 3:1; and the amounts of VTES and HFMA were 2.0 and 6.0 Wt.%, respectively. In comparison with the conventional latex, the hydrophobicity of latex film was improved further.

The modified p (VAC-VeoVa) latex is prepared via semi-continuous seeded emulsion polymerisation, which is emulsified with the novel mixed surfactants of MES and OP-10. There are two main innovations. One is that the novel p (VAC-VeoVa) latex containing fluorine-silicon is prepared successfully. The other is that the emulsifier is composed of the novel mixed surfactants of MES and OP-10.

Silane cross-linkers have been used to strengthen the mechanical stabilities and friction resistance of plastic products. Therefore, the effect of silane cross-linkers on latex has been studied through preparing modified self-cross-linking long fluorocarbon polyacrylate latex. In this paper, nonionic surfactant alcohol ether glycoside (AEG1000) and anionic polymerizable surfactant 1-allyloxy-3-(4-nonylphenol)-2-propanol polyoxyethylene (10) ether ammonium sulfate (DNS-86) acted as mixed emulsifier and 3-(methacryloyloxy) propyltrimethoxysilane (KH-570) and bis (2-ethylhexyl) maleate (DOM) were used as functional monomers.

The modified acrylate polymer latex was synthesized through the semi-continuous seeded emulsion polymerization with methyl methacrylate (MMA), butyl acrylate (BA), dodecafluoroheptyl methacrylate (DFMA) and hydroxypropyl methacrylate (HPMA) as main monomers. Potassium persulfate (KPS) was applied to initiate polymerization reaction, nonionic surfactant AEG1000 and DNS-86 acted as emulsifier, KH-570 and DOM were used as functional monomers, respectively.

The optimum conditions of synthesizing the modified latex were the following. The mass ratio of monomers containing MMA, BA, DFMA, HPMA, KH-570 and DOM was 13.58:13.58:0.90:1.20:0.15:0.60, the usage of initiator KPS was 0.5% of the total weight of monomers and the amount of emulsifier was 7% of all monomers with AEG1000:DNS-86 = 1:1. The results indicated that the conversion of monomer was 99% and the coagulation was about 2.0%.

The resultant latex was modified silane cross-linker KH-570 and DOM, which positively affected the comprehensive properties of latex and its film. Apart from this, the novel mixed emulsifier was used to improve the size and distribution of latex particles and reduce environmental problems caused by the use of emulsifiers.

Motivated by the globally increasing concern over environmental protection, the interest of a large part of the scientific community focuses on the development of green surfactants aiming to replace traditional toxic surfactants-based alternatives. The purpose of this paper is to prepare acrylate copolymer latex modified with fluorine and silicone monomer, which is emulsified with the green surfactants of sodium rosinate and alkyl polyglycoside (APG).

A series of acrylic copolymer latexes containing fluorine–silicon have been prepared by semi-continuous seed emulsion polymerisation of mixed monomers of methyl methacrylate (MMA), butyl acrylate (BA), hexafluorobutylmethacrylate (HFMA) and vinyltriethoxysilane (VTES) and emulsified by green mixed surfactants of sodium rosinate and APG.

The optimum recipe of preparing the emulsion is as follows: the amount of emulsifiers is 6 per cent and the mass ratio of sodium rosinate to APG is 1:3. The amount of initiator is 0.4 per cent, and the amounts of the silicon monomer and fluorine monomer are 5 and 7 per cent, respectively. In comparison with the acrylate latex prepared without fluorine monomer and silicon monomer, the thermal stability and the water resistance of the film of the resultant latex clearly improved.

The acrylic copolymer latexes containing fluorine–silicon emulsified with green surfactants can be used in the coatings, adhesives, finishing agents and so on.

The acrylic copolymer latexes containing fluorine–silicon have been prepared by semi-continuous seed emulsion polymerisation. The green mixed surfactants of sodium rosinate and APG have been used as the emulsifiers to replace traditional toxic surfactants-based alternatives.

Modified styrene/butadiene (S/B) latexes from Dow Europe have been shown to give added performance in primer/sealers by offering excellent moisture vapour barrier, hydrolytic stability and high binder efficiency.

The purpose of this paper is to discuss the durability and flexibility characteristics of latex modified ferrocement in comparison with conventional ferrocement particularly when exposed to severe environmental conditions.

The research programme encompasses the laboratory investigation on the structural, the deformation behaviour and characteristic of latex modified ferrocement elements cured in air and salt‐water environments. The tests include determination of load and deflection characteristics, moments, crack widths, crack spacing, and the number of cracks when subjected to static flexure.

Test result indicates a significant improvement in reducing and bridging micro cracks, especially in the pre‐peak load region. Fracture toughness and deformability increased significantly. However, the post peak behaviour was quite similar to conventional ferrocement.

The results show that latex modification has improved the mechanical properties of cement mortars, particularly their flexural strength.

There are three double bonds in the chemical structure of diallyl maleate. The purpose of this study is that the acrylate is modified with diallyl maleic anhydride to make the propionate resin present a spatial network structure, thereby improving the performance of the acrylate resin.

Methyl methacrylate (MMA) and butyl acrylate(BA) were used as were used as main monomers. Diallyl maleate (DAM) was used as crosslinking monomer and dodecafluoroheptyl methacrylate (DFMA) was used as fluoromonomer. Potassium persulfate (KPS) was used as thermal decomposition initiator, sodium lauryl sulfate (AS) and sodium dodecyl sulfonate (SDS) were used as anionic emulsifiers, and EFS-470 (Alkyl alcohol polyether type nonionic emulsifier) was a non-ionic emulsifier.

Through optimizing the reaction conditions, the uniform and stable latex is obtained. The polymer of structure was characterized by Fourier transform infrared spectroscopy (FTIR). Thermogravimetric analysis (TGA) and contact angle (CA) were tested on latex films. The particle size and distribution range of emulsion were tested with nano particle size analyzer.

The experimental results showed that the thermal decomposition temperature of the acrylic coating film increased by 20.56°C after modification. In addition, the effect of cross-linking density on the water contact angle of the fluorocarbon groups in DFMA when they migrate to the surface of the latex film during drying has been explored. The experimental results show that a higher degree of cross-linking will hinder the migration of fluorocarbon groups to the surface of the resin film.

The purpose of the study is to show an improvement in resistance (permeability) and durability (residual strength) of modified wood compared to natural wood.

A relevance way to increase the durability and resistance of wood is processing with polymers. Novosibirsk State Technical University, Novosibirsk State University of Architecture and Civil Engineering (Sibstrin) and the Norilsk State Industrial Institute researched the resistance of elements of mine treatment plants made of wood modified with synthetic polymers. The study was carried out according to V.A. Kucherenko. Modification of such species as birch and pine can significantly increase wood resources by extending its service life and improving its physical and mechanical properties. Latex-organosilicon modifier was used as a modifier.

Latex clogs the capillaries of wood, preventing the penetration of aggressive solutions into it, and potassium methyl silicate interacts with hydrophilic OH groups, increasing the water-repellent properties of the surface of cells and wood capillaries.

The results of long-term and predictive tests of modified wood in aggressive environments of treatment facilities are presented. As a result, diffusion of aggressive media into the wood becomes more difficult and its resistance and durability increase.

The purpose of this paper is to develop a high-performance composite emulsion cement waterproof coating. The coating has excellent durability and is effective in protecting cement mortar substrates from harmful ions.

The polymer cement waterproof coatings with different emulsion compounding ratios were tested for mechanical properties and water resistance after alkali immersion, water immersion, thermal aging and UV aging, and the coatings were analyzed by infrared spectroscopy after aging to evaluate its durability. Meanwhile, the coating that presents favorable durability was applied to cement mortar test blocks. The protective effect of the coating on the test blocks was tested by immersion method, and X-ray diffraction analysis was performed on the eroded test blocks.

The coating with neoprene latex/acrylate latex weight ratio of 90/10 presents favorable durability and has superior overall performance. Besides, when it is applied to cement mortar blocks, the coatings effectively reduced the erosive effect of harmful ions on cement mortar blocks, resulting in much lower mass change ratios and less internal structural damage of the blocks significantly.

The obtained coating will be of great application potential for use in building waterproofing construction. Moreover, the coating can practically prevent chloride ions and sulfate ions from penetrating cement-based materials.

The purpose of this paper is to prepare a kind of novel multi‐layer core‐shell latex, and to evaluate the effect of the preparation methodology.

Core‐shell poly(siloxane)/polystyrene/polymethyl methacrylate (PSi/PSt/PMMA) latex particles were prepared by seeded‐emulsion polymerisation with three stages. The core of cured PSi was prepared with octamethyl cyclotetrasiloxane (D4) and tetraethoxysilane (TEOS) by co‐condensation. Using vinyltriethoxysilane (VTEOS) as coupling agent, functional PSi particles with vinyl groups on surfaces were prepared by hydrolysis and condensation of VTEOS in core formation stage. Then, the functional PSi particles were used as seeds to copolymerise with styrene and methyl methacrylate sequentially in shell stage I and stage II to form PSi/PSt/PMMA latex particles.

FTIR, TEM, DSC and XPS showed that the PSi/PSt/PMMA latex particles had multi‐layer core‐shell structure with cured PSi as core, PSt as shell I and PMMA as shell II.

In the present work, PSi/PSt/PMMA latex particles having multi‐layer core‐shell structure with cured PSi as core, PSt as shell I and PMMA as shell II were prepared. This methodology can be employed to prepare new functional materials for various applications.

Multi‐layer core‐shell particles offer a new area of material science that has wide applications in coatings or modified polymer materials production.

The method developed in the study reported in this paper provides a new strategy to develop new types of core‐shell materials with multi‐layer structure.