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The purpose of this paper was to prepare a fluorinated acrylate resin, which would be synthesised via solution polymerisation of fluorinated monomer, acrylate monomers and other functional monomers. Relevant characterisation and application studies were also carried out. Fluorinated polymers are expected to be adopted in specific coatings to afford outstanding advantages, such as high chemical and photochemical resistance, low surface tension and low refractive index. At present, fluorinated cathodic electrodeposition (CED) coatings are attracting the attention that they deserve and seldom reported.

Cationic fluorinated acrylic resin was successfully prepared by solution polymerisation of dodecafluoroheptyl methacrylate, butyl acrylate, methyl methacrylate, dimethylaminoethyl methacrylate and methacrylic acid initiated by 2,2,-azo-bis-iso-butyronitrile in a solvent of butyl cellosolve. The resultant resin was neutralised with acetic acid. The CED coatings are prepared when moderate amounts of blocked isocyanate and distilled water were added into the resultant resin.

The hydrophobicity of the film is improved when the fluorinated monomer is introduced to co-polymerise with other monomers. The optimum conditions of preparing the resin are as follows: the amount of azodiisobutyronitrile is controlled with the range of 3.0 and 4.0 per cent; the amine value of the resin is 70 mg KOH/g; the hydroxyl value of resin and mole ratio of hydroxyl to isocyanate is 60 mg KOH/g and 1.0/1.0, respectively; the degree of neutralisation of the resin is within the range of 35 and 40 per cent.

The cationic fluorinated acrylic resin can be used to be the binder of CED coatings, which can be applied to electrodeposition finishing for high demand of exterior decorative and weather resistance, such as hardware, accessories, office furniture and so on.

The cationic fluorinated acrylic resin was successfully prepared by solution polymerisation. The hydrophobicity of the film is improved.

Fluorinated silicon polymers are expected to be adopted in specific coatings to afford outstanding advantages, such as high chemical and photochemical resistance, low surface tension and low refractive index. The modified acrylate resin is prepared via solution polymerization of fluorine and silicon monomers, acrylate monomers and other functional monomers. The purpose of this paper is that the fluorine and silicon monomers such as vinyltriethoxysilane (VTES) and hexafluorobutyl methacrylate (HFMA) and some cheap monomers such as styrene are used to prepare the cationic acrylic resin.

The fluorine and silicon modified cationic acrylic resin is prepared via solution polymerization technology, which uses butyl acrylate (BA), methyl methacrylate (MMA), styrene (St), HFMA, VTES, dimethylaminoethyl methacrylate (DMAEMA) and hydroxypropyl methacrylate (HPMA) as the co-polymerized monomers, propylene glycol monomethyl ether (PGME) as solvent and 2,2-Azo-bis-iso-butyronitrile (AIBN) as the initiator to create a resin to introduce the Si–O and C–F into the polymer chains. The cathodic electrodeposition (CED) coatings were prepared by mixing the synthetic resin and blocked isocyanate.

The influence of the amounts of HFMA and VETS on the resin and the resultant CED coatings is investigated in detail. The optimum amounts of HFMA and VETS are obtained, which is 7–8% and 4–5%, respectively. The hydrophobicity and the acid and alkaline resistance of the film are improved when VETS and HFMA are introduced to co-polymerize with other monomers.

The fluorine and silicon monomers such as VTES and HFMA and some cheap monomers such as styrene, which are used to prepare the cationic acrylic resin, are seldom reported in the open literature.

In this work, the authors used reversible addition-fragmentation transfer (RAFT) polymerization to develop a new cationic acrylate modified epoxy resin emulsion for water-borne inkjet which have the advantages of both polyacrylate and epoxy resin. The emulsion was successfully used in the canvas coating for inkjet printing. This paper aims to contribute to the development of novel cationic emulsions for inkjet printing industry.

In this work, the epoxy acrylate was synthesized from RAFT agent and epoxy resin firstly. Cationic macromolecular emulsifier was prepared by RAFT polymerization, using 2,2’-Azobisisobutyronitrile as initiator, 2-(dimethylamino)ethyl methacrylate and styrene as monomer, which was directly used to prepare the emulsion. The influences of the amount of 2-(dimethylamino)ethyl methacrylate on particle size, zeta potential and water contact angle were studied. Finally, the cationic emulsion was used to print images by inkjet printing.

The emulsion has the smallest particle size, the highest potential and the highest water contact angle when the DM content is 13 Wt.%. The transmission electron microscopy analysis reveals the latex particles is core-shell sphere with the diameters in the range 120–200 nm. The emulsion was successfully used in the canvas coating for inkjet printing. This work will contribute to the development of novel cationic emulsions for inkjet printing industry.

The emulsion was successfully used in the canvas coating for inkjet printing. This work will contribute to the development of novel cationic emulsions for inkjet printing industry.

At present, the conventional method of preparing cationic fluorinated acrylic latex is to emulsify copolymerised monomers with cationic surfactants. However, there has been a wide concern about using Gemini surfactants to prepare cationic polymer latex to improve its properties. The purpose of this paper was to focus on the synthesis of novel self-crosslinked cationic fluorinated acrylic latex (SCFAL), during which the copolymerised monomers were initiated with a water soluble azo initiator and emulsified with mixed surfactants of Gemini emulsifier and alkyl polyglycoside (APG).

The novel SCFAL was prepared successfully by the semi-continuous seeded emulsion polymerisation of butyl acrylate, methyl methacrylate, hexafluorobutyl methacrylate (HFMA) and hydroxy propyl methacrylate (HPMA) in aqueous medium.

The conversion is the maximum and the coagulation percentage the minimum when the amounts of emulsifier and initiator are 8 and 0.6 per cent, respectively. The average particle size of the latex is significantly reduced with the increase of the amount of emulsifiers used. However, the average particle size of the latex is increased with the increase of the amount of HPMA. The particle size of the latex is of a unimodal distribution, which means that the particle size was reasonably uniform. Contact angle is increased with the increase of the amount of the HFMA.

The novel SCFAL can be widely used as significant components in the field of coatings, leather, textile, paper, adhesives and so on.

SCFAL, which was emulsified with novel mixed surfactants of Gemini surfactant and APG, has been prepared successfully. Influences of amount of initiator, emulsifier, HPMA and HFMA on emulsion polymerisation and/or properties of novel latex are investigated in detail.

The color painting of ancient buildings has high historical and artistic value but is prone to aging due to long-term outdoor exposure. The purpose of this study is to develop a new type of sealing coating to mitigate the impact of ultraviolet (UV) light on color painting.

The new coating was subjected to a 500-h UV-aging test. Compared with the existing acrylic resin Primal AC33, the UV aging behavior of the new coating, such as color difference and gloss, was studied with aging time. The Fourier infrared spectra of the coatings were analyzed after the UV-aging test.

Compared with AC33, the antiaging performance of SF8 was substantially improved. SF8 has a lower color difference value and better light retention and hydrophobicity. The Fourier transform infrared spectroscopy results showed that the C-F bond and Si-O bonds in the resin of the optimized sealing coating protected the main chain C-C structure from degradation during the aging process; thus, the resin maintained good stability. The hindered amine light stabilizer TN292 added to the coating inhibited the antiaging process by trapping active free radicals.

To address the problem of UV aging of oil-decorated colored paintings, a new type of sealing coating with excellent antiaging properties was developed, laying the foundation for its demonstration application on the surface of ancient buildings.

Stimulated by emphasis on non‐pollution in industrial painting processes, electrocoating becomes continually more attractive. By 1975 it is predicted that at least half of the output of the entire U.S. automobile industry will be primed by electro‐coating. Maleinised oils, epoxy esters and acrylics comprise the most important electrocoating vehicles. A great deal of work is underway with polyesters and with epoxy‐acrylic compositions.

Cationic resin is widely used in decolouring of textile wastewaters. Tonnes of resin are used in sector, and disposal of resin is being a second waste problem. The purpose of this paper is to investigate the adsorption behaviour of the methylene blue cationic dye from aqueous solution on the cation exchanger Lewatit CNP80 to understand the regenerability of cation exchanger resin from textile wastewaters.

Cationic resin was used as an alternative low-cost adsorbent for removing methylene blue dye from textile wastewaters. The adsorption study was carried out in the batch mode. Batch adsorption studies were carried out to examine the effect of parameters such as methylene blue concentration, temperature, pH, resin dose, shaking speed and contact time.

It was observed that dye-removal capacity of resin was reached from 17 mgg⁻¹ to 19.4 mgg⁻¹ at 25 °C temperature, pH 5 in 15 min. At the appropriate range of parameters, it was observed that more than 98% removal efficiency was achieved for methylene blue dye, and also, this study was focussed on whether the resin regenerates. In regeneration studies, our purpose was to recover of non-regenerable exhausted cationic resin by NaOCl. Regeneration of Lewatit CNP80 was performed in five cycles. After regeneration, the authors tried to determine whether the adsorption capacity was affected by regeneration.

In this study, the authors focussed on regeneration studies. The aim is to find easy, low-cost regeneration agent. In conclusion, the authors found that NaOCl is eligible for regeneration studies. The exhausted resin was recovered by NaOCl, and the authors also tested 5th regeneration cycles. Sodium hypochlorite is not a common regeneration agent for adsorption studies. Generally, resin is regenerated by HCl or other regeneration agent products. As a result of that, operational cost was reduced, and the other thing that the authors want to emphasise is textile industry wastewater based high temperature; therefore, this regeneration study can easily work with textile industries.

The degradation of coatings is, of course, a major area of interest for paint chemists. One of the coatings that degrades, much to the consumer's despair, is automotive coatings. The degradation of an acrylic‐melamine, cross‐linked coating containing finely dispersed pigment, metallic flake, and other additives was studied by English and Spinelli (Organic Coatings and Applied Polymer Science Proceedings, preprints of papers presented by the Division of Organic Coatings and Plastics Chemistry at the American Chemical Society, 185th National Meeting, Seattle, Washington, March 20–25, 1983, p. 733) using diffuse reflectance infra‐red spectroscopy. They found that the degradation is facilitated near the surface by ultra‐violet light and that there is a cleavage of the nitrogen‐carbon bond on the methoxymethylamino moities. Much of the degradation appears to take place at the surface level and degradation of bonds does not lead to significant self‐condensation of the degraded materials. The authors indicate that they are currently using MMR techniques to identify the products of degradation.

The conventional curing of oxirane containing molecules such as cycloaliphatic epoxies with organic acid anhydrides, organic acids, Lewis acids and blocked Lewis acids is widely practised in the industry and the reaction mechanisms are well documented and described in epoxy resin related books

An important development in the urethane coating area is the use of polyisocyanates, in combination with hydroxylated acrylic resins, to provide room‐temperature‐curing coatings. These new formulations, according to Klein and Elms [Journal of Paint Technology, 43, November (1971) p. 68], demonstrate lightfastness, good outdoor durability and solvent resistance when the acrylic resin is coreacted with an aliphatic polyisocyanate. The acrylic resins are copolymers which contain either the hydroxypropyl or hydroxybutyl ester of acrylic or methacrylic acid as one component. Hydroxypropyl acrylate acetoacetate extends the potlife of this two‐component coating. The authors describe work in which glass transition temperature is used as a means for selecting the correct hydroxylated acrylic resins for use in the system. If the glass transition temperature is between 22 and 54°C, a flexible coating with good impact resistance results, but the system requires baking. At a glass transition temperature of 54° and a hydroxyl value of 26, a composition results which dries rapidly at ambient temperatures and which provides good hardness and mar resistance. The coreactant in this instance is an aliphatic diisocyanate composition based on hexamethylene diisocyanate.