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The paper presents the results of research carried out on esters of carbonic, adipic, and sebacic acids with respect to their use as components of fully synthetic lubricating oil produced from a polyalphaolefin base. Straight dicarboxylic acid esters were synthesized in a transesterification reaction of dimethyl carbonate, dimethyl adipate, and dimethyl sebacate with 2‐ethylhexanol and 3,5,5‐trimethylhexanol.

Oligomeric esters of adipic acid and sebacic acid were synthesized using neopentyl glycol, appropriate dimethyl adipate or dimethyl sebacate and 2‐ethylhexanol as the starting material. The basic physicochemical properties of esters were determined and their compatibility with synthetic oils were defined. They were also evaluated with respect to resistance under the influence of thermo‐oxidative factors, evaporation and susceptibility to hydrolytic decomposition. The selected esters were complemented with commercial additives to make up a fully synthetic lubricating oil with a polialphaolefin base. A special attention was paid to the effect of ester compounds on the physicochemical properties of the formulated oil.

The obtained results show that straight adipates and sebacates of 2‐ethylhexanol and 3,5,5‐trimethylhexanol as well as oligomeric esters in which molecules are terminated with 2‐ethylhexyl group can be used as component of lubricating oils. The addition of these esters reduced the pour point by a few degrees in comparison with the tested base oil. The temperature fell below 40°C. The presence of esters significantly improved the viscosity index. A positive influence of esters on the lubricating properties of the formulated oil was also observed. On the contrary, dialkyl carbonates show too low boiling point, which is indicated by the high amount of volatile components, 19‐22 percent, in final product. Adipic and sebacic oligomers containing methoxyl groups in their structures proved to be immiscible with polyalphaolefins.

The achievement of this work is the synthesis of new oligomeric esters of dicarboxylic acids, which can be excellent additives for improving properties of synthetic oils. Further studies will be focused on the use of esters as components of engine oils. This requires real motor tests.

The aim of this paper is to focus on the production of mixed‐synthetic diester base oils from the waste of electrochemical production of sebacic acid (mixtures of methyl esters of dicarboxylic acids, HOOC(CH₂)nCOOH, n=4, 6, 8).

The mixtures of methyl esters of dicarboxylic acids ((CH₂)n, n=4, 6, 8) are transesterified by pure alcohols and also different mixtures of aliphatic monohydric alcohols, C6‐C10 of iso‐ and normal structure, in the presence of a new catalyst system (tetra‐n‐butyl orthotitanate, Ti(O‐n‐Bu)₄). The effects of starting materials ratios on the reaction progress and characteristic features of the obtained diester oils have been studied.

The obtained mixed diester oils showed similar thermal properties and low pour point (minimum −70°C), and improved viscosity‐temperature properties compared with commercially available dioctyl sebacate (DOS) and dioctyl adipate (DOA) diester oils.

Because of the complexity of the obtained mixture, it was impossible to study the structure and composition of the obtained products by modern techniques such as high field NMR spectroscopy.

The mixtures of methyl esters of dicarboxylic acids obtained from different batches of sebacic acid production have different molar ratios and must be analyzed before use. The process is based on transesterification reactions of methyl esters of mixture of the aliphatic dicarboxylic acids ((CH₂)n, n=4, 6, 8) by mixture of aliphatic alcohols having iso‐ and normal structure in the presence of a new transesterification catalyst (mixture of p‐toluene sulfonic acid and tetra‐n‐butyl orthotitanate). The obtained mixed diester oils showed similar thermal properties, low pour point (minimum −70°C) and improved viscosity‐temperature properties compared with commercially available DOS and DOA diester oils.

The paper illustrates a new process for the production of mixed‐synthetic diester base oils.

The aim of this study is the synthesis and characterization of motor and hydraulic oils based on complex esters of dicarboxylic acids and polyol esters. The esters have been prepared by polyesterification of adipic or sebacic acids with polyethylene glycol and by subsequent reaction with 2‐ethylhexanol using a new high active catalyst tetraoktyltitanate (TOT)‐TlCl. The synthesis of pentaerythritol esters of monocarboxylic acids has also been undertaken in the presence of the same catalyst. The catalyst reduces the time and temperature required for the reaction to produce esters with characteristics of standard motor and hydraulic oils.

Presently, a wide range of polyurethane adhesives can be obtained using different kinds of polyols and isocyanates. However, the applied temperature of the polyurethane adhesive is not more than 80°C. The film of polyurethane adhesive will be softened and deformed when its applied temperature is more than 100°C. Thus, the mechanical property of the polyurethane adhesive is decreased clearly, which limits its further application. The purpose of the study is to improve the heat resistance of polyols, especially polyester polyols and its resultant polyurethane adhesives.

The more rigid benzene ring is introduced into the polyester polyols to improve the heat resistance of its resultant polyurethane adhesive.

The more rigid benzene ring has ben introduced into the polyester polyols and the heat resistance of its resultant polyurethane adhesive is improved.

The polyester polyols with more rigid benzene ring have been prepared successfully by the vacuum melting method when diethylene glycol, neopentyl glycol, 1,6-hexanediol, ethanediol, isophthalic acid, terephthalic acid, sebacic acid and adipic acid are used as raw materials and tetra-isopropyl titanate is adopted as the catalyst.

The purpose of this paper is synthesis of polyesteramide resin from jatropha oil and monomer from recycling of poly(ethylene terephthalate) (PET) to get the excellent benefit of individual structure. Along with the synthesis of polyesteramide resin, this research work will also help in recycling of PET waste and help for the conversion of monomer obtained from recycling of PET to value-added application.

Polyesteramide resin was synthesized by conventional method, i.e. by converting jatropha oil to corresponding fatty amide, i.e. hydroxyl ethyl jatropha oil fatty acid amide (HEJA), and treating it with dicarboxylic acid, i.e. sebacic acid but bis(2-hydroxyethyl) terepthalamide (BHETA) is added, i.e. monomer of PET, and then resin synthesis is carried out. Synthesized resin is cured with isocyanate and used for coating application. Coating is characterized for physical, mechanical, thermal and anticorrosive properties.

Coating shows excellent balance of flexibility and hardness due to structural difference in BHETA and HEJA. Aromatic structure of BHETA was helpful for increasing hardness and for retardation of degradation, and at the same time, aliphatic structure of HEJA was helpful for increasing flexibility of the coating. Amide linkage present in both help for better adhesion of coating to metal surface, which also helps to improve the mechanical properties and anticorrosive properties.

This method is the practical solution for synthesis of polyesteramide resin and then coating from PET waste and jatropha oil. Hence the method developed is simple and it helps for recycling of PET waste and conversion of recycled product to value-added material.

To the best of the authors’ knowledge, this is the first study which use jatropha oil (fatty amide of jatropha oil) and PET waste (monomer of PET waste) simultaneously for the synthesis of polyesteramide resin and then coating.

Linseed oil was employed to modify polyesteramide resin via the condensation of hydroxyethylamide derivatives of fatty acids of linseed oil, i.e. {N, N′‐bis(2 hydroxylethyl) linseed amide} and phthalic anhydride and dicarboxylic acids such as adipic acid, succinic acid and sebacic acid. The polyesteramide resins obtained were tested for their application as a vehicle/binder in the preparation of surface coatings. The resins obtained were also characterised for their physico‐chemical properties, film forming properties and chemical resistance.

The purpose of this paper is to study, analyze and present the lubricating mechanism and tribological properties of two types of oil‐based titanium complex grease containing Polytetrafluoroethylene (PTFE).

Two types of oil‐based sebacic acid/stearic acid titanium complex greases containing PTFE additive were synthesized using 3 L reaction vessel, and the base oils including neopentyl polyol ester and mixed oil of 650SN and neopentyl polyol (1:1.8). Friction‐reduction, antiwear, and load‐carrying properties of greases were evaluated using a four‐ball tester, and their dropping point and penetration were characterized using relevant ASTM standards. Morphologies of wear scar and chemical states of typical elements on worn surfaces were characterized by means of scanning electron microscope and X‐ray photoelectron spectroscopy, respectively.

Tribological results show that titanium complex grease containing PTFE had better friction‐reduction and antiwear properties than base grease. However, PTFE could not improve the load‐carrying capacity of base grease. Moreover, a synergistic effect between deposited film and adsorptive film contributes to good tribological properties of titanium complex grease.

Such a very useful lubricating material could be used in industrial applications including steel plants, power plants, packaging, and fertilizer industries.

The lubricating mechanism of titanium complex grease containing PTFE was proposed by tribochemical analysis of worn surfaces. The mechanism should become the direction of the theoretical and applied research of grease in the future.

Gelation that can occur when copper or aluminium bronze powder is permitted to stand in nitrocellulose lacquer can be prevented by the addition of below one percent of lauric acid. Butyl acetyl ricinoleate will impart highgloss, plasticity, pliability to nitro‐cellulose lacquers and impart permanence, and improves the ageing properties and low temperature flexibility to the product. Acrylic coatings of improved gloss and pattern control have been provided by the addition of methyl hydroxystearate. When barium α‐sulphostearate is added to interior or exterior paints it can produce films of improved hardness. Methyl linoleate can be employed to retard the hardening of Japanese film lacquer. Compositions with good heat stability and good thixotropic properties and which are suitable for use as a base for paints have been evolved by reacting hydrogenated castor oil with toluene di‐isocyanate and emulsifiable and polyethylene wax. The use of aluminium stearate in paints at elevated temperatures can result in films of high opacity, good build, sag resistance, heavy pigmented tolerance and good sealing properties. Myristic acid‐based alkyd aryl ketones have been utilised to impart lustre to wooden surfaces, and stearic acid terminated polyamide/polyimide for coatings for electrical insulators of magnetic wire have been applied to give improved lustre. Diethylene glycol esters of dilinoleic acid can be used to produce non‐drip paints, as can ethylene diamine bis hydroxystearate, and glyceryl trihydroxystearate. Hydrogenated castor oil is useable in the making of thixotropic agents applicable to paints have been prepared from the material, plus oligomers of hydroxystearic acid/ethylenediamine/sebacic acid polymers. Ethyl linoleate and ethyl linoleate have been used as penetrants in anti‐corrosive paints based upon alkyd resins. Aluminium stearate can prevent excess penetration by paints of surfaces. Bis (hydroxymethyl) propanediol oleate has found use in alkyd resins derivative coatings with butylated melamine resins‐hardening materials to give pinhole resistant coatings. Butyl stearate is a good low temperature plasticiser for paints. Butyl acetyl ricinoleate imparts good plate release and cold crack resistance to leather lacquers, and provides good handle and excellent low temperature flexibility to coated fabrics on thick unsupported sheetings.

The purpose of this paper is to prepare a new modified polybutylene terephalate (MPBT) for fused deposition modeling (FDM) to increase the variety of materials compatible with printing. And the printing materials can be used to print components with a complex structure and functional mechanical parts.

The MPBT, poly(butylene terephalate-co-isophthalate-co-sebacate) (PBTIS), was prepared for FDM by direct esterification and subsequent polycondensation using terephthalic acid (PTA), isophthalic acid (PIA), sebacic acid (SA) and 1,4-butanediol (BDO). The effects of the content of PIA (20-40 mol%) on the mechanical properties of PBTIS were investigated when the mole per cent of SA (α_SA) is zero. The effects of α_SA (0-7mol%) on the thermal, rheological and mechanical properties of PBTIS were investigated at n_PTA/n_PIA = 7/3. A desktop wire drawing and extruding machine was used to fabricate the filaments, whose printability and anisotropy were tested by three-dimensional (3D) printing experiments.

A candidate content of PIA introducing into PBT was obtained to be about 30 per cent, and the Izod notched impact strength of PBTIS increased with the increase of α_SA. The results showed that the PBTIS (n_PTA/n_PIA = 7/3, α_SA = 3-5mol%) is suitable for FDM.

New printing materials with good Izod notched impact strength were obtained by introducing PIA and SA (n_PTA/n_PIA = 7/3, α_SA = 3-5 mol%) into PBT and their anisotropy are better than that of ABS.

To evaluate the efficiency of complex esters as plasticizers in polyvinyl chloride plastisols and plasticates.

Several poly(vinyl chloride) plastisols and plasticates were prepared with standard phthalate plasticizers and complex esters and were characterised using standard and laboratory methods.

The use of mixtures of three new CE with standard phthalate plasticizers increased the physical, mechanical and electric characteristics of the resulting PVCPs and PVCPl.

The use of three new CE, obtained by esterification of dicarboxylic acids (adipic, sebacic, pelargonic), poly(ethylene glycol) and i‐octanole, as plasticizers of poly(vinyl chloride) plastisols and plasticates was investigated. The use of CE based on other organic acids could be explored.

The results confirmed the efficiency of plasticization of PVC by CE. Such a finding has significant industrial implication.

Several findings are original and are of importance to relevant industry. The new CE with high molecular weights were effective plasticizers of PVC. The efficiency of the plasticizers depended on their chemical structure. The molecular weight of the CE had no influence on the compatibility of plasticizers and other components of the PVC plastisols and plasticates.