C60-丙烯酸月桂酯共聚物的合成及其摩擦学行为

合成了一种新颖的油溶性C60-丙烯酸月桂酯共聚物,采用四球摩擦磨损试验机、扫描电子电镜研究了其作为液体石蜡润滑添加剂的摩擦学特性,结果表明,C60-丙烯酸月桂酯共聚物可提高石蜡基础液的抗磨性能,改善微观磨损状态.     

富勒烯-苯乙烯-甲基丙烯酸三元共聚物的合成及其摩擦学性能

纳米微球;富勒烯-苯乙烯-甲基丙烯酸三元共聚物的合成及其摩擦学性能     

Design of surface properties of PET films: effect of fluorinated block copolymers

This paper demonstrates that the addition of fluorinated block copolymers to PET solutions can be used to prepare PET films with controlled surface morphology, porosity and chemical composition, by exploiting the phenomenon known as breath figures (BF) formation during a spin-coating procedure. Surface features, such as number, depth and diameter of pores and chemical composition, can be tuned by varying the experimental conditions: relative humidity, solution composition and amount of the fluorinated block copolymer added to the PET solutions (in the range of 0.5-10 wt% with respect to PET). BF patterns are more evident at relatively high concentrations of PET (3 wt%) and content of fluorinated block copolymer (10 wt% with respect to PET) in the solution. According to the obtained results, the fluorinated block copolymer seems to play a role in different steps of the mechanism of BF formation. XPS measurements showed a surface composition much richer in fluorinated segments than expected from bulk composition. The combined surface roughness and surface segregation of fluorinated segments have only a limited effect on the macroscopic wettability of the surfaces.     

Tribological properties of graphene nanosheets as an additive in calcium grease

The addition of graphene nanosheets (GNSs) in lubricating grease could significantly reduce the interfacial friction and improve the load-bearing capacity of the parts. Therefore, it has been considered as having great potential as lubricant additives. In this study, we synthesized GNSs that are prepared by a modified Hummer method, and investigated the effect of GNS with different concentration (0.5%, 1%, 2%, 3%, and 4?wt%) on the tribological properties of the calcium grease. The friction and wear experiments were performed using a four-ball tribometer. Transmission electron microscopy (TEM) and scanning electron microscopy (SEM) were employed to examine the GNS and the friction mechanisms. Results indicate that the friction reduction ability and anti-wear property of the base grease can be improved with the addition of GNS. It was also found that the friction reduction decreases by 61%, and the wear scar diameter (WSD) decreases by 45%, and the extreme-pressure (EP) properties increased 60% at 3?wt% GNS. It is clear that the GNS in grease easily forms protective deposited films to prevent the rubbing surfaces from coming into direct contact, thereby improving the entire tribological behavior of the grease.     

ROD-LIKE AGGREGATES FROM POLYSTYRENE-b-POLY(4-VINYLPYRIDINE)-b-POLYSTYRENE TRIBLOCK COPOLYMER IN AQUEOUS MEDIA

INTRODUCTIONRecently, solution-state assembly of block copolymers has attracted much interest. On the one hand, theversatility of morphology control can be used for the preparation of unique nanostructured materials with variousarchitectures[1-8]. On the other hand, some self-assembled structures are biomimetic[9,10]. The balance betweenthree major forces acting on the system affects block copolymer morphologies in solutions[11,12]. These threeforces include the stretching of the core-for…     

Reverse atom transfer radical random copolymerization of styrene and methyl methacrylate in the presence of diatomite nanoplatelets

Diatomite nanoplatelets were used for in situ random copolymerization of styrene and methyl methacrylate by reverse atom transfer radical polymerization to synthesize different well‐defined nanocomposites. Inherent features of the pristine diatomite nanoplatelets were evaluated by Fourier transform infrared spectroscopy, nitrogen adsorption/desorption isotherm, scanning electron microscope, and transmission electron microscope. Gas and size exclusion chromatography was also used to determine conversion and molecular weight determinations, respectively. Considerable increment in conversion (from 81% to 97%) was achieved by adding 3 wt% diatomite nanoplatelets in the copolymer matrix. Moreover, molecular weight of random copolymer chains was increased from 12 890 to 13 960 g·mol⁻¹ by addition of 3 wt% diatomite nanoplatelets; however, polydispersity index (PDI) values increases from 1.36 to 1.59. Proton nuclear magnetic resonance spectroscopy was used to evaluate copolymers composition. Thermal gravimetric analysis results indicate that thermal stability of the nanocomposites is improved by adding diatomite nanoplatelets. Differential scanning calorimetry shows an increase in glass transition temperature from 66°C to 71°C by adding 3 wt% of diatomite nanoplatelets.     

Sliding Wear Behavior of Nanoclay Filled Polypropylene/Ultra High Molecular Weight Polyethylene/Carbon Short Fiber Nanocomposites

In the present investigation, authors made an attempt to study the sliding wear behavior of polypropylene/ultrahigh molecular weight polyethylene (PP/UHMWPE, 90/10) blends loaded with 30% carbon short fibers (CSF) as reinforcement and nanoclay as filler material. The nanocomposites have been prepared with varying amounts viz., 0, 1, 2 and 3 wt% of nanoclay. The composites were prepared by melt mixing at 60 rpm extruder speed and compression moulding at 180°C. From all the composites, 6 mm diameter and 25 mm length sliding wear specimens were prepared. Sliding wear loss, specific wear rate and coefficient of friction were investigated by using computerized pin-on–disc machine at normal applied loads of 20, 30 and 40 N; at a sliding velocity of 1.5 m/s and at two abrading distances viz., 200 and 300 m. The wear behavior data reveals that 3 wt% nanoclay filled composite exhibits higher wear resistance and lowest specific wear rate as compared to other nanocomposites. Also morphological study was carried out for wear out surfaces of all the composites using scanning electron microscopy (SEM).     

Synthesis of ricinoleate anion based ionic liquids and their application as green lubricating oil additives

Ricinoleate anion based ionic liquids (ILs) were synthesized from four different nitrogen containing cationic counterparts such as tetrabutylammonium, tetrapropylammonium, cetyltrimethylammonium, imidazolium. Tribological performance of synthesized ILs were evaluated using four ball tribo tester by blending with two lubricant base oils namely epoxy2-ethylhexyl esters of karanja fatty acids (EKE) and dioctyl sebacate (DOS). Antiwear behaviour was explored by varying different factors including concentration, applied load and rotation speed. It was found that the synthesized ILs in base oil significantly reduced the wear scar diameter by 17–25% at 0.8 wt% and a remarkable reduction in wear scar diameter was observed for all the tested applied load (40 to 80 kg) and rotation speed (1200 to 1742 rpm). Further, the load carrying capacity of base oil was improved by 25–43% at 1.25 wt% of IL dosage. The imidazolium cation containing IL outperform tribological performance among all the ILs being studied. The morphology of worn surface after the wear tests and deposition of elementals on the worn surface lubricated with neat base oil and IL blended base oil was studied by scanning electron microscope (SEM) and energy-dispersive X-ray spectroscopy (EDX).     

Influence of the Phase Morphology on the Viscoelastic Behaviour of Polymer Blends (PP-EPR)

Summary. Melts of polyethylene-propylene-rubber (EPR, blends of linear polyethylene, linear polypropylene, and PE-PP copolymer) show phase separation. The influence of the phase morphology on the viscoelastic behaviour is studied with the aid of the dynamical moduli. The measured moduli of the fraction of the linear homopolymer of an EPR agree with the moduli calculated from the molar mass distribution of this fraction. In contrast, the copolymer fraction shows a strong rubber-like behaviour (represented by a characteristic relaxation time spectrum). Mixtures of 80 wt% linear PP and of EPRs with low copolymer content are not rubber-like liquids. In addition, the moduli from them can be calculated from the moduli of the components with the aid of Palierne’s emulsion model. This clearly reveals that the linear PP forms the matrix in this case. Mixtures of 80 wt% linear PP and of EPRs with high copolymer content show rubber-like behaviour and Palierne’s emulsion model is not applicable on them. Obviously, the copolymer fraction forms a physical network.     

Thermo and pH Dual-Responsive Micelles of N-phthaloylchitosan-g-Poly(N-isopropylacrylamide) and Poly(acrylic acid-co-tert-butyl acrylate) for Drug Delivery

A novel amphiphilic copolymer N-phthaloylchitosan graft poly(N-isopropylacrylamide) and poly(acrylic acid-co-tert-butyl acrylate) (PHCS-g-PNIPAAm&P(AA-co-tBA)) was synthesized. The graft copolymer could form micelles in aqueous medium, and the critical micelle concentration (CMC) of the copolymer was 7.5 × 10^{? 3}mg/mL. The lower critical solution temperature (LCST) of the micelles was measured to be 30°C. Transmission electron microscopy (TEM) image showed that the micelles exhibited a regular spherical shape, and the mean diameter of the micelles was 94.1 ± 0.8 nm as determined by dynamic light scattering (DLS). The potential usefulness of the micelles as drug delivery systems was investigated using anti-inflammation drug prednisone acetate as the model. The drug loading capacity of the micelles was measured to be 22.86 wt%, and the DLS results showed that the mean diameter of the drug-loaded micelles was 133.3 ± 2.4 nm. In vitro drug release studies indicated that the micelles exhibited thermo and pH dual-responsive release profiles.     

Waste marble dust-filled sustainable polymer composite selection using a multi-criteria decision-making technique

This research works with the optimal design of marble dust-filled polymer composites using a multi-criteria decision-making (MCDM) technique. Polylactic acid (PLA) and recycled polyethylene terephthalate (rPET)-based composites containing 0, 5, 10, and 20 wt% of marble dust were developed and evaluated for various physicomechanical and wear properties. The results showed that the incorporation of marble dust improved the modulus and hardness of both PLA and rPET. Moreover, a marginal improvement in flexural strength was noted while the tensile and impact strength of the matrices were deteriorating due to marble dust addition. The outcomes of wear analysis demonstrated an improvement in wear resistance up until 10 wt% filler reinforcement, after which the incidence of dust particles peeling off from the matrix was observed, thereby reducing its efficiency. The best tensile modulus of 3.23 GPa, flexural modulus of 4.39 GPa, and hardness of 83.95 Shore D were obtained for 20 wt% marble dust-filled PLA composites. The lowest density of 1.24 g/cc and the highest tensile strength of 57.94 MPa were recorded for neat PLA, while the highest impact strength of 30.94 kJ/m² was recorded for neat rPET. The lowest wear of 0.01 g was obtained for the rPET containing 5 wt% marble dust content. The experimental results revealed that for the examined criteria, the order of composite preference is not the same. Therefore, the optimal composite was identified by adopting a preference selection index-based MCDM technique. The findings demonstrated that the 10 wt% marble dust-filled PLA composite appears to be the best solution with favorable physical, mechanical, and wear properties.     

Volume shrinkage and abrasive wear properties of crosslinked Poly(ester-urethane-acrylate)/MMA copolymer: Effect of chain length

The current study deals with the preparation of novel crosslink transparent poly(ester-urethane-acrylate)/methyl methacrylate (TPEUMA) copolymers and the effect of hydroxyl terminated aromatic polyester (PEs) was also investigated. The properties of TPEUMA were investigated in terms of double bond concentration, polymerization shrinkage, abrasive wear analysis and chemical resistance. The volume shrinkage decreased due to the significant reduction in the concentration of double bonds. The first two effects reflect in lowering the abrasive wear resistance properties at room temperature, while the larger chain length between crosslink decreases the hardness. Decrease in polymerization shrinkage shows more condensed microstructure which was revealed by the abrasive wear rate of TPEUMAs due to hydrogen bonding near to crosslink point. Increase in the chain length of PEs, decreases the glass transition temperature of TPEUMA copolymer which results in loose microstructure. Worn surface were studied using scanning electron microscope to give insight on the wear mechanism of TPEUMA crosslink. It can be suggested from the present study that this copolymer can be used for a broad range of optical applications.     

Improved Adhesion of UV Treated EVA Copolymer by Adding Small Amounts of Fillers

The influence of adding small amounts of calcium carbonate or sepiolite fillers on the adhesion properties of UV surface-treated ethylene vinyl acetate copolymer (EVA) was studied. In this paper, it has been demonstrated that the addition of 3-7 wt% filler enhanced the extent of the surface modifications (wettability, surface chemistry, roughness) and increased the adhesion of EVA. These effects were more marked when 7 wt% sepiolite filler was added to EVA, likely due to its higher aspect ratio.     

Tem- and neutron reflection studies on surfaces and interfaces with block copolymers

The behavior of block copolymers at various interfaces is studied by transmission electron microscopy and neutron reflection. A thin film of a symmetric diblock copolymer of styrene and methyl methacrylate forms layer structures when in contact with air and a random copolymer of styrene and acrylonitrile containing 35 wt% acrylonitrile. When the random copolymer has an acrylonitrile content of 25 wt%, a competition between layer formation and diffusion of disordered micelles takes place. Driving force for these processes are different interfacial tensions and a changing miscibility behavior as a function of acrylonitrile contents of the random copolymers. The ordering behavior of a symmetric diblock copolymer of deuterated styrene and isoprene in contact with poly(3,5-dimethyl phenylene ether) is studied by neutron reflection. Polystyrene-block-poly(ethene-co-but-1-ene)-block-polystyrene with cylindrical PS microdomains shows an interfacial phase transition to lamellae near to the interface with different polymers. The morphological studies are in agreement with adhesion data obtained by peel tests on different bilayer specimens.     

Mono- and Di-valent Salts as Modifiers of PEO-PPO-PEO Block Copolymer Interactions with Silica Nanoparticles in Aqueous Dispersions

Colloidal stabilization of nanoparticle dispersions is central to applications including coatings, mineral extraction, and dispersion of oil spills in oceanic environments, which often involves oil-mineral-aggregates (OMAs). We have an ongoing interest in the modulation of amphiphile micellization and adsorption behavior in aqueous colloidal dispersions in the presence of various additives. Here we evaluate the effect of added salts CaCl₂, MgCl₂, and NaCl on the micellization and adsorption behavior of the poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) triblock copolymer Pluronic P105 (EO₃₇PO₅₆EO₃₇). In 0.10 wt% silica nanoparticle (10.6 nm average diameter) dispersion, adsorbed block copolymer layer formation begins at a critical surface micelle concentration (csmc) of 0.02 wt%, well below the critical micellization concentration of Pluronic P105 in water. Dye solubilization experiments demonstrate an increase in the csmc upon addition of each salt. Each added salt reaches a level of maximum effectiveness in its ability to disfavor Pluronic P105 adsorption at the silica surface. These peak levels occur at concentrations of 0.005, 0.03, and 0.05 M for CaCl₂, MgCl₂, and NaCl, respectively, in the presence of 0.10 wt% silica nanoparticles. We explain these results in the context of an electrostatic displacer mechanism and discuss possible connections to OMA-dispersant formation.     

Influence of functional sulfonic acid groups on styrene–divinylbenzene copolymer pyrolysis

The decomposition ratio of cation exchange resin (sulfonated ST-DVB copolymer) after pyrolysis is only 50 wt%, while that of ST-DVB copolymer is 90 wt%. Fundamental experiments were performed to investigate the reason for the low decomposition ratio of the former. The cation resin consists of base polymer (ST-DVB copolymer) and functional sulfonic acid groups. Chemical analyses of the pyrolysis products showed that most of the functional groups decomposed at about 300°C and generated SO₂ gas. However, only a small amount of the base polymer was pyrolyzed even at 600°C and the total decomposition ratio was only 50 wt%. The XPS studies on the residue showed that 35% of the functional sulfonic acid groups was converted to sulfonyl and sulfur bridges between the base polymers during pyrolysis. These bridges made the base polymers, namely ST-DVB copolymer, thermally stable.     

Effect of PEO‐PPO‐PEO copolymer on the mechanical and thermal properties and morphological behavior of biodegradable poly (L‐lactic acid) (PLLA) and poly (butylene succinate‐co‐L‐lactate) (PBSL) blends

A blend of two biodegradable and semi‐crystalline polymers, poly (L‐lactic acid) (PLLA; 70 wt%) and poly (butylene succinate‐co‐L‐lactate) (PBSL; 30 wt%), was prepared in the presence of various polyethylene oxide‐polypropylene oxide‐polyethylene oxide (PEO‐PPO‐PEO) triblock copolymer contents (0.5, 1, 2 wt%). Mechanical, thermal properties, and Fourier transform infrared (FTIR) analysis of the blends were investigated. It was found that the addition of copolymer to PLLA/PBSL improved the fracture toughness of the blends as shown by mode I fracture energies. It was supported by morphological analysis where the brittle deformation behavior of PLLA changed to ductile deformation with the presence of elongated fibril structure in the blend with copolymer system. The glass transition temperature (T_g), melting temperature (T_m) of PLLA, and PBSL shift‐closed together indicated that some compatibility exists in the blends. In short, PEO‐PPO‐PEO could be used as compatibilizer to improve the toughness and compatibility of the PLLA/PBSL blends. Copyright © 2010 John Wiley & Sons, Ltd.     

Dynamically cured natural rubber/EVA blends: influence of NR‐g‐poly(dimethyl (methacryloyloxymethyl)phosphonate) compatibilizer

Graft copolymer of natural rubber and poly(dimethyl(methacryloyloxymethyl)phosphonate) (NR‐g‐PDMMMP) was prepared in latex medium via photopolymerization. It was then used to promote the blend compatibility of dynamically cured 40/60 natural rubber (NR)/ethylene vinylacetate copolymer (EVA) blends using various loading levels at 1, 3, 5, 7, 9, 12, and 15 wt%. It was found that the increasing loading levels of NR‐g‐PDMMMP in the blends caused the increasing elastic modulus and complex viscosity until reaching the maximum values at a loading level of 9 wt%. The properties thereafter decreased with the increasing loading levels of NR‐g‐PDMMMP higher than 9 wt%. The smallest vulcanized rubber particles dispersed in the EVA matrix with the lowest tan δ value was also observed at a loading level of 9 wt%. Furthermore, the highest tensile strength and elongation at break (i.e., 17.06 MPa and 660%) as well as the lowest tension set value (i.e., 27%) were also observed in the blend using this loading level of the compatibilizer. Addition of NR‐g‐PDMMMP in the dynamically cured NR/EVA blends also improved the thermal stability of the blend. That is, the decomposition temperature increased with the addition of the graft copolymer. However, the addition of NR‐g‐PDMMMP in the blends caused the decreasing degree of crystallinity of the EVA phase in the blend. However, the strength properties of the blend are still high because of the compatibilizing effect. Copyright © 2009 John Wiley & Sons, Ltd.     

Effect of water content on the size and membrane thickness of polystyrene-block-poly(ethylene oxide) vesicles

The asymmetric amphiphilic block copolymer polystyrene962-block-poly(ethylene oxide)227(PS962-b-PEO227) canforms micelles with N, N-dimethylformamide(DMF) as co-solvent and water as selected solvent, and when the water content of the mixed solvent is higher than 4.5 wt%, the vesicle will be dominated. This work finds that once vesicles are formed in the DMF-water mixed solvent, the vesicle size and membrane thickness can be tuned by further increasing water content. As the water fraction elevated from 4.8 wt% to 13.0 wt%, the vesicle size dercreases from 246 nm to 150 nm, while the membrane thickness increases from 28 nm to 42 nm. In addition, the block copolymer packing and the free energy are analyzed as the vesicle size becomes small and the membrane becomes thick.     

Preparation of ABA triblock copolymer assemblies through “one-pot” RAFT PISA

Poly(N,N-dimethyl acrylamide)-block-poly(styrene)-block-poly(N,N-dimethyl acrylamide)(PDMAc-bPSt-b-PDMAc) amphiphilic triblock copolymer micro/nano-objects were synthesized through reversible addition-fragmentation chain transfer(RAFT) dispersion polymerization of St mediated with poly(N,Ndimethyl acrylamide) trithiocarbonate(PDMAc-TTC-PDMAc) bi-functional macromolecular RAFT agent.It is found that the morphology of the PDMAc-b-PSt-b-PDMAc copolymer micro/nano-objects like spheres,vesicles and vesicle with hexagonally packed hollow hoops(HHHs) wall can be tuned by changing the solvent composition.In addition,vesicles with two sizes(600 nm,264 nm) and vesicles with HHHs features were also synthesized in high solid content systems(30 wt% and 40 wt%,respectively).Besides,as compared with typical AB diblock copolymers(A is the solvophilic,stabilizer block,and B is the solvophobic block),ABA triblock copolymers tend to form higher order morphologies,such as vesicles,under similar conditions.The finding of this study provides a new and robust approach to prepare block copolymer vesicles and other higher order micelles with special structure via PISA.