Crystallization characteristics of Ni-W-P composite coatings reinforced by CeO_2 and SiO_2 nano-particles

Ni-W-P composite coatings reinforced by Ce O2 and Si O2 nano-particles on the surface of common carbon steels, were prepared by double pulse electrodeposition. The crystallization course was characterized by phase structures, crystallinity, grain sizes and microstructures. The results indicate that as-deposited composite coating is amorphous. Whereas it turns into the crystalline structure with 98.25% crystallinity, and Ni3 P, Ni2 P and Ni5P2 alloy phases precipitate from structures at 400 °C. Thereafter, Ni2 P and Ni5P2 metastable alloy phases turn into Ni3 P stable alloy phase at 500 °C. The crystallization course of the composite coating has finished when being heat-treated at 700 °C. The average sizes of Ni grains increase with the rise of heat treatment temperature from400 °C to 700 °C. Ce O2 and Si O2 nano-particles deposited into Ni-W-P alloys can delay the crystallization course and habit the growth of alloy phases.

Friction and Wear Characteristics of Brush Plating Ni/nano-Al2O3 Composite Coating under Sand-Containing Oil

Ni-matrix composite coating containing AI2O3 nano-particles is prepared by brush plating. The effects of the nano-particles on the microstructure, microhardness and tribological properties of the composite coating under the lubrication of a diesel oil containing sand are investigated. The results show that the microstructure of the composite coating is finer than that of the pure nickel coating due to the codeposition of the nano-particles. When the nano-particle concentration in the electroplating bath reaches 20 g/L, the microhardness, and wear resistance of the composite coating is as much as 1.6 times and 1.3-2.5 times of those of the pure nickel coating respectively. The main hardening mechanism of the composite coating is superfine crystal grain strengthening and dispersion strengthening. The composite coating is characterized by scuffing as it slides against Si3N4 under the present test conditions.

Corrosion Behavior of Electrodepositing Ni/Al_2O_3 Composite Coatings under the Presence of NaCl Deposit

The morphology and corrosion behavior of Ni/Al2O3 composite coatings prepared using double-pulsed electrodepositing technique after oxidized under 800 ℃ NaCl deposit in air environment were analyzed by scanning electrical microscope (SEM), X-ray diffraction(XRD) and energy dispersive spectrum(EDS). The results showed that the corrosion of all composite coatings was accelerated under NaCl deposits, and the corrosion products were rather porous with poor adherence to the matrix. Al2O3 particles in the coatings can refine the grain size and improve the high temperature corrosion resistance of the coatings. Within the test scope, the more Al2O3 particles in the coatings, the lower corrosion rates could be obtained, and the corrosion mechanism was also discussed.

Microstructure and Tribological Properties of Laser Clad Ni-Ag/TiC Composite Coating

Ni-Ag/TiC composite coating was prepared on the 45 steel substrates by means of laser cladding. Microstructure and wear properties of composite coatings were analyzed using optical microscopy, field emission scanning electron microscopy and wear machine. The experimental results show that defects, such as cracks and pores, do not occur in the laser-cladded Ni-Ag/TiC composite coating and 45 steel substrate, and they present good metallurgical bonding between them. Compared with Ni/TiC composite coating, micro- hardness values of the two coatings do not present evident differences. The wear experiment result shows that Ni-Ag/TiC composite coated with Ag possesses low friction coefficient and good wear resistance compared with Ni/TiC composite coating.

MICROSTRUCTURE OF ELECTRODEPOSITED Ni-W-P-SiC COMPOSITE COATINGS

ＭＩＣＲＯＳＴＲＵＣＴＵＲＥＯＦＥＬＥＣＴＲＯＤＥＰＯＳＩＴＥＤＮｉＷＰＳｉＣＣＯＭＰＯＳＩＴＥＣＯＡＴＩＮＧＳ①ＧｕｏＺｈｏｎｇｃｈｅｎｇ，ＹａｎｇＸｉａｎｗａｎ，ＬｉｕＨｏｎｇｋａｎｇＤｅｐａｒｔｍｅｎｔｏｆＭｅｔａｌｕｒｇｙ，Ｋｕｎｍｉｎ...

Corrosion resistance of electrodeposited RE-Ni-W-P-SiC composite coating

Immersion experiment results show that corrosion rate of the as deposited RE Ni W P SiC composite coating in HCl solutions increases with the rise of HCl concentration. On the contrary, the corrosion rate of the composite coating after heat treatment decreases with increasing HCl concentration. The corrosion rates of the composite coatings in as deposited state and after heat treatment in H 2SO 4 and H 3PO 4 solutions respectively decrease with the rise of H 2SO 4 and H 3PO 4 concentrations. The corrosion rate of the composite coating as deposited in FeCl 3 solutions decreases with increasing FeCl 3 concentration, while the rate of the composite coating after heat treatment increases with the rise of FeCl 3 concentration. The corrosion rate of 316L stainless steel in the corrosion media of H 2SO 4, HCl, H 3PO 4 and FeCl 3 solutions at different concentrations increases with rising concentration. In addition, the corrosion rate of 316L stainless steel in the corrosion media of H 2SO 4, HCl, H 3PO 4 and FeCl 3 solutions respectively is much greater than that of the RE Ni W P SiC composite coating as deposited and after heat treatment in the same corrosion media. [

Effects of addition of rare earth on properties and structures of Ni-W-B-SiC composite coatings

The effects of rare earth (RE) on the composition, phase structures, surface morphologies and hardness of electrodeposited RE Ni W B SiC composite coatings were discussed. The results show that W and SiC contents in the coatings increase with the increase of RE in the bath. When RE is added in the coatings, the grains are refined and the trend of formation of amorphous coatings is increased. Moreover, the thermal stability of the RE Ni W B SiC composite coatings is enhanced. The hardness of the coatings is increased with the increase of heat treatment temperature, and it reaches the peak value when heated at 400 ℃. Besides, the hardness of the RE Ni W B SiC coatings is higher than that of the Ni W B SiC coatings.

Microstructure of electrodeposited RE-Ni-W-P-SiC composite coating

The components and microstructure of the RE Ni W P SiC composite coating were analyzed by means of EPXDS, SEM and XRD. The results showed that the composite coating containing 5%～14%RE, 4%～7%SiC, 12%～15%P and 5%～6%W was obtained by use of appropriate bath composition and plating conditions. The as deposited composite coating is amorphous and it becomes mixture when the temperature is raised from 200 ℃ to 400 ℃. However, the composite coating is crystal when the temperature is over 400 ℃. Scanning electron microscopy indicates that the heat treatment temperature has no effect on the surface morphologies of the RE Ni W P SiC composite coating. This is to say that the composite coating has a better heat stability of microstructure and high temperature oxidation.

Thermodynamics of electrodeposited Ni-B-SiC composite coatings

The φ pH diagram of Ni B H 2O system was drawn, and the mechanism of electrodepositing Ni B SiC composite coatings was discussed. The results show that the deposition of Ni and B occurs prior to that of H 2 because of the over potential of H 2 evolution on the Fe substrate. Boron can not singly deposit in aqueous solution. Nickel and boron can co deposit in the form of Ni 4B 3 without evolution of hydrogen when the cathodical potential is kept to be -1.415 ～ -1.700?V.

PROPERTIES OF ELECTRODEPOSITED AMORPHOUS Ni-W-P-SiC COMPOSITE COATINGS

The Effects of heat treatment temperature on the hardness,wear resistance and structure of the amorphous Ni-W-P-SiC composite coatings have been investigated.The results show that Ni-W-P-SiC composite coatings are amorphous under 300℃, partially crystalline at 300-400℃,and crystalline when heat treatment temperature reaches 400℃,the crystals being fine Ni3P phase particles.The hardness,wear resistance and the crystallization temperature of the composite coatings increase when an additive is added into the bath.The hardness and wear resistance of the coatings increase with increasing heat treatment temperature,and they will reach their peak values when the heat treatment temperature reaches 400℃.Corrosion experiment indicates that the corrosion resistance of amorphous Ni-W-P-SiC composite coatings in various kinds of corrosive media except nitric acid is better than that of stainless steel 1Cr18Ni9Ti.Scanning electron microscopy observation shows that the additive has no effect on the surface appearance of the coatings,but the current density and the pH value have considerable effects on the surface appearance.

Sliding wear behaviors of electrodeposited Ni composite coatings containing micrometer and nanometer Cr particles

Micrometer and nanometer Cr particles were co-deposited with Ni by electroplating from a nickel sulfate bath containing a certain content of Cr particles. Cr microparticles are in a size range of 1-5 μm and Cr nanoparticles have an average size of 40 nm. The friction and the wear performance of the co-deposited Ni-Cr composite coatings were comparatively evaluated by sliding against Si3N4 ceramic balls under non-lubricated conditions. It is found that the incorporation of Cr particles enhances the microhardness and wear resistance of Ni coatings. The wear resistance of Ni composite coating containing Cr nanoparticles is higher than that of the Ni composite coating containing Cr microparticles with a comparable Cr particle content. The co-deposition of smaller nanometer Cr particles with Ni effectively reduces the size of Ni crystals and significantly increases the hardness of the composite coatings due to grain-refinement strengthening and dispersion-strengthening,resulting in a significant improvement of wear resistance of the Ni-Cr nanocomposite coatings.

CATHODIC PROCESS AND WEAR RESISTANCE OF ELECTRO-DEPOSITED RE-Ni-W-P-SiC COMPOSITE COATING

Cathodic deposition current density of the composite coatings increases when SiC par-ticles and rare earth (RE) were added in the bath, which is profitable for Ni- W-P alloy to deposit in the cathod, forming Ni-W-P-SiC and RE-Ni-W-P-SiC composite coatings. On the contrary, the addition of PTFE in the bath decreases cathodic deposition current density of the coatings. The current density increases a little when the amount of RE is 7-9g/l; however, the current density increases greatly when the amount of RE is increased to 11-13g/l. Bui ij the amount of RE is raised further, the current density decreases. Hardness and wear resistance of RE-Ni-W-P-SiC composite coating have been studied, and the results show that the hardness and wear resistance of RE-Ni-W-P-SiC composite coating increase with increasing heat treatment tempera-ture, which reach peak values at 400℃; while the hardness and wear resistance of the coating decrease with the rise of heat treated temperature continuously.

Parameter optimization for plasma-sprayed Al2O3p/Al composite coatings on AZ31 magnesium alloy

Al2O3p/Al composite coatings were prepared on the surface of AZ31 magnesium alloy by plasma spraying technology with mixed powders of Al and Al2O3. An orthogonal test containing six factors and five levels was carried out to acquire the optimum technical parameters. Mierostruetures and properties of the composite coatings were studied. The results show that the coatings consist of Al2O3 particulates distributed uniformly and Al matrix, and the interface between the particulate and matrix is continuous, compact and clean. With increasing the mass fraction of Al2O3 in the mixed powders, the volume fraction of Al2O3 in the coatings iacreases. The Al2O3p/Al composite coating with 14% Al2O3 volume fraction has more compact microstrueture and more satisfactory properties.

Laser Cladding Al-Si/Al_2O_3-TiO_2 Composite Coatings on AZ31B Magnesium Alloy

To improve the wear resistance and corrosion resistance of magnesium alloys, a 5 kW continuous wave CO2 laser was used to investigate the laser surface cladding on AZ31 B magnesium alloys with Al-Si/Al2O3-TiO2 composite powders. A detailed microstructure, chemical composition, and phase analysis of the composite coatings were studied by scanning electron microscopy （SEM）, energy dispersive spectroscopy （EDS）, and X-ray diffraction （XRD）. The laser cladding shows good metallurgical bonding with the substrate. The composite coatings are composed of Mgl7Al12, Al3Mg2, Mg2Si, Al2O3, and TiO2 phases. Compared to the average microhardness （50HV0.05） of the AZ3 1 B substrate, that of the composite coatings （230HV0.05） is improved significantly. The wear resistances of the surface layers were evaluated in detail. The results demonstrate that the wear resistances of the laser surface-modified samples are considerably improved compared to the substrate. It also show that the composite coatings exhibit better corrosion resistance than that of the substrate in 3.5wt% NaCI solution.

Structure and characteristics of electrodeposited RE-Ni-W-P-B_4C-PTFE composite coatings

Hardness, friction and wear characteristics of electrodeposited RE Ni W P B 4C PTFE composite coatings were studied, and the reason for these fine characteristics was explained in respect of structure. The results show that 1) the structure of RE Ni W P B 4C PTFE composite coatings experiences a transformation process from amorphous to mixture then to crystal as the heat treatment temperature rises; 2) incorporating of B 4C greatly increases the hardness of the coating; 3) the wear resistance of the coating is best with heat treatment for 1?h at 300?℃, which is greatly superior to that of the other traditional coatings.

STUDY ON PROPERTIES OF PULSE ELECTRODEPOSITED RE-Ni-W-P-SiC COMPOSITE COATINGS

The effects of pulse frequency f and duty cycle r on the deposition rate, composition, morphology, and hardness of pulse electrodeposited RE （rare earth）-Ni-W-P-SiC composite coatings have been studied. The results indicate that pulse current can improve the deposition rate of RE-Ni-W-P-SiC composite coatings; W, P, and SiC contents in the coating decrease with the increase of pulse frequency and reach the lowest value at f = 33Hz, whereas the RE content in the composite coatings increases with the increase of pulse frequency. SiC content decreases with the increase of duty cycle, W content reaches the lowest value, and P content reaches the highest value at r = 0.4; pulse current and RE can lead to smaller size of the crystalline grains; however, the effects of different pulse frequency and duty cycle on the morphologies of RE-Ni-W-P-SiC composite coatings are not obvious. The hardness of RE-Ni-W-P-SiC composite coatings is the highest when the duty cycle is at 0.6 and 0.8 and pulse frequency is at 50Hz. At the same pulse frequency, the hardness of RE-Ni-W-P-SiC composite coatings at r= 0.8 is higher than that at r= 0.6.

Oxidation resistance of co-deposited Ni-SiC nanocomposite coating

Ni-6.0%SiC (mass fraction) nanocomposite coating was prepared from a nickel sulfate bath by co-electrodeposition of Ni and SiC nanoparticles in an average size of 30 nm. The oxidation at 1 000 ℃ shows that the Ni-6.0%SiC nanocomposite coating has a superior oxidation resistance compared with the pure Ni film due to the formation of SiO2 oxide particles along grain boundaries, blocking the outward diffusion of Ni and changing the oxidation growth mechanism. The effect of SiC nanoparticles on the oxidation progress was discussed in detail.

Effect of Al_2O_3on Structure and Wearability of Composite Coating

The composite coating was prepared by thermal spray welding after making composite powder,which is composed of Ni-based self-melted alloy and AlOceramic powder including nano,sub-micron and micron powders.The influences of contents and sizes of AlOon the structure and wearability were investigated.The results show that the wear resistance of the coating would be increased greatly by adding AlO,but the spray weldability decreases with increasing AlOcontent.So there is an optimal content of AlOpowder.The composite coating with AlOnano or sub-micron powder of 0.5% has the best abrasive resistance,while the optimal content of AlOmicron powder is 1 %.

ELECTROPLATED Zn-Ni-SiO_2 COMPOSITE COATINGS TREATED WITH A SILANE COUPLING AGENT TO REPLACE CHROMATING

The fixing of a silane coupling agent to Zn-Ni-silica (SiO2) composite coatings was studied for the purpose of developing a coating process as an alternative to chromating. The corrosion resistance of Zn-Ni-silica composite coatings was rem arkably improved by the silica nanoparticles in the composite, which were disper sed in the surface of this film. The silane coupling agent formed chemical bonds with the inorganic silica particles during the silane coupling treatment on the se composite coatings. The treatment suppressed the formation of white corrosion products to the same extent as chromating, as measured in salt spray tests. It is concluded that treating Zn-Ni-silica composite coatings with silane coupling agents is a viable alternative technique to chromating.

MICROSTRUCTURAL STUDY OF Fe-Cr-Al/Al COMPOSITE COATINGS DURING OXIDATION AND SULFIDATION AT 900℃

The microstructure of a composite coating system, which was composed of an inner layer of Fe-Cr-Al and an outer layer of aluminum, was studied after it was respectively oxidized and sulfurdized at elevated temperatures. Apart from the Al2O3 scale formed on the surface, the microstructure of the composite coatings exposed at 900℃ in air for 4h was a three-layer structure. The first layer consisted of a solid solution of Cr and Fe in α aluminum and an intermetallic compound FeAl3 while the second layer was a single phase of the aluminide and the third layer still remained the same appearance as the original Fe-Cr-Al coating. The microstructural observation of the specimen tested at 850-900℃ at low oxygen pressure and high sulfur pressure for 576h revealed that the surface coatings of the specimen had transformed into a duplex structure containing an outer layer and a thicker aluminide layer beneath. X-ray diffraction results showed that the out layer was composed of Al2S3 and Al2O3 and that AlCrFee was the main phase composition of the aluminide layer, with a few of Al2S3 and Al2O3 accompanied.