Search results

This paper aims to investigate the influence of high-temperature thermal action on grease performance from the angle of film-forming performance.

A static thermal aging method was used to prepare high-temperature thermal grease samples after high-temperature thermal action. On the basis of optical interference technology, the film-forming characteristics of fresh grease samples and the grease samples after high-temperature thermal action under variable speed and fixed speed conditions were explored.

The decrease in the structural entanglement performance of the grease after short-term high-temperature thermal action makes its film-forming performance better. The mechanism is that the lubricating grease soap fiber entanglement is reduced. Although the continuous high-temperature thermal action can make the grease film-forming performance better, its mechanism is that the soap fiber structure caused by high-temperature thermal action is damaged and is easy to be cut off under the action of shear.

The effect of structural system change on its film formation performance was discussed in combination with the change in grease structure characteristics, and the mechanism of action was revealed.

The purpose of this research was to synthesize a novel cross-linked latex copolymerised by butyl acrylate (BA), isobornyl methacrylate (IBOMA), hydroxy propyl methacrylate (HPMA) and dodecafluoroheptyl methacrylate (DFMA). IBOMA is a very useful functional monomer. Its molecular structure not only contains bornyl acetate alkoxy but also includes a double bond, which can be copolymerised with other unsaturated monomers via free radical polymerization. The large nonpolar bicyclic alkyl in bornyl acetate alkoxy offers the polymer chain strong space steric protection, which endows the polymer with some special properties.

The semi-continuous seeded emulsion polymerisation technology was adopted to copolymerise BA, IBOMA, HPMA and DFMA in the water phase, which was initiated with potassium persulfate (KPS) and emulsified with the mixed surfactants of sodium dodecyl sulphate (SDS) and OP-10.

The particle size of the latex decreases with an increase in the amount of IBOMA. All the latexes have good mechanical stability and calcium ion stability. The latex has good film-forming property when the IBOMA amount is controlled moderately. The optimal IBOMA amount is 10.00 g. The thermal stability and water resistance of the film are improved.

The latexes can be applied as a binder of coatings and adhesions.

The effect of the amount of IBOMA and BA on the properties of the resultant latex and its film were investigated in detail. In comparison with the latexes copolymerised without IBOMA, the novel latex has better thermal stability and water resistance.

Polyesteramide resin based on the condensation of hydroxyethylamide derivatives of fatty acids of soybean {N, N′‐bis(2 hydroxyethyl)soybean amide} and various dibasic acid and anhydride were synthesized. Physico‐chemical characteristics and film forming properties of these resins were determined to prove its suitability as a vehicle for surface coatings. The study reveals that resins can be used for the baked type of finishes.

Ageing has been known to affect the performance of lubricants. However, there is a lot of debate as to whether ageing is beneficial or detrimental to the wear performance of lubricants.

The purpose of this research is to evaluate the effect of ageing on the viscosity, total acid number and Fourier-transform infrared spectroscopy information of a series of lubricants. The tribological performance (friction and wear) of the aged lubricants is also studied, followed by X-ray photoelectron spectroscopy analysis on the selected post-test samples to study the tribochemical features of the tribofilm.

The results show that ageing has a different impact on lubricants and tribological performances based on the physical and chemical properties.

These findings will be compared with the research on the role of water in lubricant ageing (Part II of this study).

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.

The flammability of poly-acrylate (PA) resin is a major disadvantage in applications that require flame resistance. Many studies, including the authors’ previous study, have proved that covalent-incorporated phosphorous-containing (P-containing) monomer onto the PA resin can exhibit better flame resistance than that by an additive approach. However, other properties such as thermal stability, coating properties are still deteriorated. To further improve the flame-retardancy and other comprehensive properties of the P-containing PA resin, in this study, melamine formaldehyde(MF) resin was used not only as a curing agent to enhance the coating properties of the PA resin, but also as a nitrogen-containing (N-containing) resin to form a P-N synergistic effect and therefore further improve its flame retardancy.

Epoxy resin phosphorous acid-modified (EPPA-modified) PA (EPPA-PA) resin was first prepared and then using MF resin as curing agent. The flame retardancy of the cured resin was tested by the limiting oxygen index (LOI) and UL 94 methods. The thermal stability of the cured resin was studied by TGA. The coating technology such as adhesion property, pencil hardness and anti-solvent properties were characterized according to methods of International Standards ISO2409-1992, ISO 15184-1998 and ISO-15184-2012, respectively. The micro-char morphology of the char residue was observed by SEM.

The results showed that by using MF resin as curing agent has provided the PA resin with excellent coating properties and thermal stability, but also gave a P-N synergistic effect which has greatly enhanced the flame retardancy of the cured resin. The cured resin system containing only 1.7 Wt.% P content and 5.3 Wt.% N content can reach a LOI of 26.9 per cent and pass the V-0 rating in the UL-94 test.

This resin system releases formaldehyde due to the MF resin.

It is expected that the large-scale production of this EPPA-PA resin cured by MF resin system will enable practical industrial applications.

This method for the synthesis of a P- and N-containing PA resin system is newfangled.

In this work, the blends of poly(methyl methacrylate), PMMA and poly(methyl vinyl ether-alt-maleic acid monoethyl ester), PMVEMA-ES are studied as organic coatings to evaluate the impact of intermolecular hydrogen bonding on the physical and thermal characteristics of the prepared coatings.

PMMA (Mw = 120,000 g mol-1) was chosen as our binder material. Due to the low adhesion property of PMMA on polar substrates, it was blended with PMVEMA-ES, which contains polar –COOH groups, to improve the adhesion and thermal properties of the coatings by forming intermolecular hydrogen bonds. A cross-hatch adhesion test was carried out to evaluate the adhesion strength of different ratios of PMMA/PMVEMA-ES blends as coatings. In addition, changes in the glass-transition temperature, Tg as the composition varies were studied using Differential Scanning Calorimetry, DSC. Then, glossiness and hiding power tests were also conducted to evaluate the physical properties of the prepared coatings.

Upon a closer look at the DSC results, it was found that blends consisting of 12.5, 25.0 and 87.5 wt. % PMMA were completely compatible due to the presence of only a single Tg in their thermograms. Other blend compositions showed two distinct Tgs, indicating partial compatibility. Furthermore, the addition of PMVEMA-ES caused the Tg of PMMA to shift to lower temperatures, a strong indication of intermolecular hydrogen bonding interactions between the two components. From the cross-hatch adhesion results, the addition of PMVEMA-ES improved the adhesion properties of PMMA coating, except for blends consisting of 62.5 and 75.0 wt. % PMMA possibly due to the partial incompatibility between the two components. These findings were further corroborated with the results of glossiness and hiding power measurements. The superior result was seen for the blend consisting of 12.5 wt. % PMMA with strong adhesion property, high glossiness, compatibility and high translucency.

PMVEMA-ES can potentially be used as an adhesion promoter in PMMA-based coating formulations.

This is the first report on the properties of PMMA/PMVEMA-ES blends as coatings.

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.

Lead Industries Group Ltd announce that the Antimony and Zircon activities of Associated Lead Manufacturers have been transferred to a new subsidiary company, Anzon Ltd, with effect from 1st January, 1977.

The purpose of this paper was to examine the film-forming behaviour of simple compositions of polyalphaolefin (PAO) containing an oil-soluble polyalkylene glycol (OSP) alone, a zinc dialkyl dithiophosphate (ZDDP) alone and then combinations of an OSP and ZDDP.

A Mini-Traction Machine with Spacer Layer Imaging technology was used to evaluate friction and film formation under a specific contact pressure, temperature and slide-to-roll ratio. Electrical contact resistance measurements were used to follow surface film formation.

The inclusion of an OSP to a PAO showed evidence of friction-reducing behaviour with low friction values over the rubbing cycle but no significant tribo-film build up. When a ZDDP (1 per cent) is added to the PAO, a thick tribo-film forms of about 100 nm. Addition of an OSP (10 per cent) shows this film still forms despite the OSP being a polar and surface-active additive.

The study was conducted under a narrow range of test conditions (e.g. temperature and contact pressure), and future work will focus on friction and film formation across a broader set of conditions.

Despite OSPs being polar and surface-active, they do not interfere with the ZDDP in forming an anti-wear film in a PAO and, therefore, their inherent properties of good deposit control could enhance the performance of modern lubricants.

OSPs offer promising benefits as friction reducers in PAOs. The research also suggests that OSPs do not negate the formation of ZDDP anti-wear tribo-films when in combination in a PAO.