Electrochemical corrosion behaviors of straight WC–Co alloys: Exclusive variation in grain sizes and aggressive media

The electrochemical corrosion behaviors of straight WC–10Co cemented carbides with grain sizes of 1.2, 2.6, 6.1 and 8.2 μm, were comparatively investigated in the solutions of NaOH (pH = 13), Na₂SO₄ (pH = 7) and H₂SO₄ (pH = 1) respectively. To insure a sole variable of WC grain sizes, specific magnetic saturation values of the alloys are adjusted to be identical. The results show a good linear dependence for R_ct (charge transfer resistance) and I_corr (corrosion current density) against the grain sizes. A high sensitivity of the grain sizes to both R_ct and I_corr are identified in NaOH and H₂SO₄. In the solutions of NaOH and Na₂SO₄, the alloys with smaller WC grain sizes exhibit better corrosion resistances, while the alloys with larger WC grain sizes exhibit better corrosion resistances in H₂SO₄. Additionally, in terms of the corrosiveness, NaOH is the weakest and H₂SO₄ is the most aggressive for all the alloys. The corrosion mechanisms were discussed in light of the SEM surface observation, X-ray photoelectron spectroscope analysis and the electrical equivalent circuits for electrochemical impedance spectroscopy.     

Effects of Ni addition and cyclic sintering on microstructure and mechanical properties of coarse grained WC–10Co cemented carbides

Coarse grained WC–10(Co, Ni) cemented carbides with different Ni contents were fabricated by sintering-HIP and cyclic sintering at 1450 °C. The effects of Ni addition and cyclic sintering on the microstructures, magnetic behavior and mechanical properties of coarse grained WC–10(Co, Ni) cemented carbides have been investigated using scanning electron microscope (SEM), magnetic performances tests and mechanical properties tests, respectively. The results showed that the mean grain size of hardmetals increases from 3.8 μm to 5.78 μm, and the shape factor Pwc decreases from 0.72 to 0.54, with the Ni content increases from 0 to 6 wt.%. Moreover, the W solubility reaches the highest value of 10.33 wt.% when the Ni content is 2 wt.%. The hardness and transverse rupture strength of WC–8Co–2Ni are 1105 HV₃₀ and 2778 MPa, respectively. The cyclic sintering is conducive to increase the WC grain size of WC–10(Co, Ni) and improves the transverse rupture strength of WC–10Co without compromising the hardness of alloys.     

Grain size effects on contact resistance of top-contact pentacene TFTs

Multiple top-contact OTFTs with various channel lengths (L_c) were successfully scaled-down to the L_c of 1.8 μm by using the membrane shadow mask and the interface between the evaporated Au and pentacene was analyzed based on the channel resistance method. For large grain pentacene (S-80) deposited at 80 °C, the parasitic resistance (R_p) at V_GS = −20 V has 1.8 ± 0.2 kΩ cm, whereas for small grain pentacene (S-20) deposited at 20 °C has 4.2 ± 0.2 kΩ cm, which means that R_p depends on the grain size of pentacene. The grain size and grain boundary trap density for pentacene can be possibly origins to determine R_p, which is critically correlated with bulk transport in pentacene. The grain boundary trap density (N_t) for S-80 and S-20 was extracted as (5.6 ± 0.5) × 10¹¹ and (1.2 ± 0.3) × 10¹² cm⁻² from the Levinson plots, respectively. In addition, activation energy of R_p for S-80 is in the range from 42 to 48 meV, whereas for S-20 is from 72 to 108 meV.     

A corrosion study of nanocrystalline copper thin films

Thin nanocrystalline, compact films, based on the copper–nitrogen system, up to 2.5 μm thickness and 3.5% nitrogen, were deposited by magnetron sputtering at different partial pressure ratios of N₂ and Ar, without formation of Cu_xN compounds, the nitrogen concentration influencing grain size (down to 30 nm) and film homogeneity. Electrochemical corrosion properties were investigated using polarization curves and electrochemical impedance spectroscopy in 0.5 M NaCl aqueous solution, and compared with pure bulk copper; morphology was examined by scanning electron microscopy. Significant variations in corrosion currents between samples were attributed to grain size and structural defects on the grain boundaries.     

Low temperature superplasticity in a friction-stir-processed ultrafine grained Al–Zn–Mg–Sc alloy

Friction stir processing (FSP) was used to create a microstructure with ultrafine grains (0.68 μm grain size) in an as-cast Al–8.9Zn–2.6Mg–0.09Sc (wt.%) alloy. The ultrafine grained alloy exhibited superplasticity at relatively low temperatures and higher strain rates. Optimum ductility of 1165% at a strain rate of 3 × 10⁻² s⁻¹ and 310 °C was obtained. Enhanced superplasticity was also achieved at a temperature as low as 220 °C. Experimentally observed parametric dependencies and microstructural examinations indicated that the operating deformation mechanism might be the Rachinger grain boundary sliding accommodated by intragranular slip. The FSP microstructure became highly unstable at 390 °C onwards, thus, affecting ductility adversely. In situ transmission electron microscopy heating was used to understand the instability phenomenon, which has been attributed to the drop in particle pinning forces due to the dissolution of metastable precipitates and microstructural heterogeneity.     

The influence of SDS and CTAB surfactants on the surface morphology and surface topography of electroless Ni–P deposits

The effect of surfactants sodium dodecyl sulphate (SDS) and cetyltrimethyl ammonium bromide (CTAB) on the surface roughness, surface morphology and surface topography of electroless nickel (EN)–phosphorus surface protective coating obtained from an alkaline bath is presented in this paper. In this study the influence of surfactant concentrations on the surface roughness of coated samples were investigated. It was observed that the surface roughness, surface morphology and surface topography of Ni–P coating were clearly influenced by the addition of surfactants SDS and CTAB. EN deposits with addition of surfactant SDS and CTAB at a concentration of 0.6 g/l produce a smooth surface and the average roughness (R_a) value is 1.715 μm for SDS and 1.607 μm for CTAB which is less than the R_a value of EN deposit without surfactant addition (1.885 μm). The mean average roughness (R_a) value with addition of surfactant is 1.796 μm.EN deposit with addition of surfactants consists of a significant fraction of particles of nickel. In the presence of SDS, fine nickel particles have dispersed uniformly on the substrate surface resulting in smoother surface finish of the deposited layers. In the presence of CTAB, at lower concentrations (upto 0.6 g/l) coalescence of nickel particles have been deposited on the substrate surface and at the higher concentration (above 0.6 g/l) uniformly improved surface finish of the deposited layer is resulted. The complete experimental details, results obtained and their analysis are presented in this paper.     

Preparation of Fe2B boride coating on low-carbon steel surfaces and its evaluation of hardness and corrosion resistance

Fe₂B coating was prepared on low-carbon steel by surface alloying. A series of experiments were carried out to examine some surface properties of boride coating. The surface heat treatment of coated low-carbon steel was performed at 700 °C, 800 °C and 900 °C for 2 h, 4 h, 6 h and 8 h under hydrogen atmosphere. The boride coating was revealed by XRD analysis and the microstructure of the boride coating was analyzed by scanning electron microscopy (SEM). Depending on the temperature and time of the process, the hardness of the borided low-carbon steel ranged from 99 to 1100 HV. The hardness showed a maximum (about 1100 HV) at 900 °C for 8 h. The corrosion resistance of the borided samples was evaluated by the Tafel polarization and electrochemical impedance spectroscopy (EIS). Shift in the corrosion potential (E_corr) towards the noble direction was observed, together with decrease in the corrosion current density (I_corr), increase in the charge transfer resistance (R_ct) and decrease in the capacitance (C_c), which indicated an improvement in corrosion resistance with increasing temperature and time of the treatment.     

Synthesis of nanosized composite powders via a wet chemical process for sintering high performance W-Y2O3 alloy

With the aim of preparing high performance oxide dispersion strengthened tungsten-based alloys by powder metallurgy, the W-Y₂O₃ composite nanopowders were prepared by an improved bottom-up wet chemical method. Ultrasonic treatment and anionic surfactant sodium dodecyl sulfate (SDS) addition were innovatively introduced into this wet chemical method in order to fabricate homogeneous, ultrafine W-Y₂O₃ composite nanopowders. As a result, the average tungsten grain size of 40–50 nm was obtained for this composite nanopowders. For comparison, W-Y₂O₃ composite powders were also prepared by traditional mechanical milling. After that, spark plasma sintering (SPS) was employed to consolidate the powders prepared by either mechanical milling or wet chemical method to yield high density as well as suppress grain growth. It is found that the W-Y₂O₃ alloy prepared by wet chemical method and subsequent SPS possesses smaller grain size (0.76 ± 0.17 μm) and higher relative density (99.0%) than that prepared by mechanical milling and subsequent SPS. Moreover, the oxide nanoparticles (about 2–10 nm) are dispersed within tungsten grains and at grain boundaries more uniformly in W-Y₂O₃ alloy prepared by wet chemical method and subsequent SPS. Due to the ultrafine grains, high sintering density and homogeneously distributed oxide nanoparticles, the Vickers microhardness of yttria dispersion strengthened tungsten-based alloy prepared in our work reaches up to 598.7 ± 7.3 HV_0.2, higher than that reported in the previous studies. These results indicate that the improved bottom-up wet chemical method combined with ultrasonic treatment and anionic surfactant addition developed in our work is a promising way to fabricate high performance oxide dispersion strengthened tungsten-based alloys with ultrafine grain and high density.     

Effect of Ni content on the compression properties and abrasive wear behavior of the (TiB2–TiCxNy)/Ni composites

The (TiB₂–TiC_xN_y)/Ni composites were fabricated by the method of combustion synthesis and hot press consolidation in a Ni–Ti–B₄C–BN system. The effect of Ni content on the microstructure, hardness, compression properties and abrasive wear behavior of the composites has been investigated. The results indicate that with the increase in Ni content from 30 wt.% to 60 wt.%, the average size of the ceramic particles TiB₂ and TiC_xN_y decreases from 5 μm to ≤ 1 μm, while the hardness and the abrasive wear resistance of the composites decrease. The composite with the Ni content of 30 wt.% Ni possesses the highest hardness (1560.8 Hv) and the best abrasive wear resistance. On another hand, with the increase in the Ni content, the compression strength increases firstly, and then decreases. The composite with 50 wt.% Ni possesses the highest compression strength (3.3 GPa). The hardness and fracture strain of the composite with 50 wt.% Ni are 1251.2 Hv and 3.9%, respectively.     

Cr effects on magnetic and corrosion properties of Fe–Co–Si–B–Nb–Cr bulk glassy alloys with high glass-forming ability

Effects of the Cr addition on glass formation, magnetic and corrosion properties of {[(Fe_0.6Co_0.4)_0.75B_0.2Si_0.05]_0.96Nb_0.04}_100−xCr_x (x = 1, 2, 3, 4 at.%) alloys have been investigated. It was found that the addition of Cr element slightly decreases the glass-forming ability (GFA), but is very effective in increasing corrosion resistance and improving soft magnetic properties for this Fe–Co–B–Si–Nb bulk glassy alloy within the composition range examined. The Fe–Co–B–Si–Nb–Cr alloys exhibit high GFA. Full glassy rods with diameters up to 4 mm can be synthesized by copper mold casting. The Fe-based bulk glassy alloys (BGAs) exhibit a high saturation magnetization of 0.81–0.98 T as well as excellent soft magnetic properties, i.e., extremely low coercive force of 0.6–1.6 A/m and super-high initial permeability of 26,400–34,100. Furthermore, corrosion measurements show that corrosion rate and corrosion current density of these Fe-based BGAs in 0.5 M NaCl solution decrease from 7.0 × 10⁻¹ to 1.6 × 10⁻³ mm/year and 3.9 × 10⁻⁶ to 8.7 × 10⁻⁷ A/cm², respectively, with increasing Cr content from 0 to 4 at.%. The success of synthesizing the new Fe-based BGAs exhibiting simultaneously high GFA as well as excellent good soft magnetic properties combined with high saturation magnetization and enhanced corrosion resistance allows us to expect future progress as a new type of soft magnetic materials.     

On-machine dry electric discharge truing of diamond wheels for micro-structured surfaces grinding

Precision grinding with diamond wheels gives a promising alternative to achieve high quality micro-structured surfaces on optical molds. However, it is difficult to true these diamond wheels efficiently, because of the remarkable resistance property and the geometrical limitation of small wheel profile. In this paper, an on-machine dry-EDT method to precision shape and prepare diamond wheels with various profiles was proposed for micro-structured surface grinding. Firstly, the fundamental truing errors were analyzed based on the dry-EDT kinematics. And then the capabilities of dry-EDT truing for high abrasive concentration metal bonded diamond wheels were presented. Next, the effects of kinematic parameters variables on trued wheel profile accuracy were investigated. Finally, the micro-structured surfaces on SiC ceramic and tungsten carbide WC were ground by these trued diamond wheels. The experiments results showed that the arc-shaped diamond wheel (diameter of 200 mm) with 4 μm profile error (PV) and 1.0023 mm profile radius, and the V-shaped diamond wheel with 22.5 μm V-tip radius and 120.03° profile angle could be obtained by on-machine dry EDT. The kinematic parameters of dry-EDT have an important influence on truing profile accuracy of diamond wheels, especially for the tip of V-shaped wheel. The subsequent grinding show that the edge radius of V groove array on SiC is less than 2 μm, while the radius of included corner is around 55 μm. The PV error of ground arc groove array on WC is less than 5 μm. The surface roughness of ground micro-structured surface R_a is 142 nm and 97 nm for SiC and WC, respectively.     

Estimation of residual corrosion rates of steel under cathodic protection in soils via voltammetry

Steel coupons were buried in soil for 2 months under cathodic protection. Their residual corrosion rates were deduced from voltammetry and weight loss measurements. In aerated soils, the current density due to O₂ reduction, j_K,O2, was modelled with a mixed activation–diffusion controlled kinetic. The anodic part j_A of the current density j, computed as j_A = j − j_K,O2, obeyed Tafel law. Its extrapolation to the protection potential gave a corrosion rate (∼7 μm yr⁻¹) consistent with that obtained from weight loss measurements. With a deficient protection, corrosion rates remained at ∼80 μm yr⁻¹, a value given by both methods.     

Electrical mapping of AISI 304 stainless steel subjected to intergranular corrosion performed by means of AFM–LIS in the contact mode

The paper presents results of the AFM-based approach to local impedance spectroscopy (LIS) measurements performed in a 20 × 20 μm grid within an austenite grain–grain boundary region for sensitized AISI 304 stainless steel (SS). Maps of electrical parameters obtained on the basis of localized impedance spectra were demonstrated, presenting their changes and correlation with the sample topography. Performed research revealed significant differences in the electrical distribution of the contact resistance considered as the passive layer resistance and contact capacitance considered as the passive layer capacitance determined for austenite grain interiors and austenite grain boundaries affected by intergranular corrosion.     

On the fatigue behavior of γ-based titanium aluminides: role of small cracks

Gamma-TiAl based alloys have recently received attention for potential elevated temperature applications in gas-turbine engines. However, although expected critical crack sizes for some targeted applications (e.g. gas-turbine engine blades) may be less than ∼500 μm, most fatigue-crack growth studies to date have focused on the behavior of large (on the order of a few millimeters) through-thickness cracks. Since successful implementation of damage-tolerant life-prediction methodologies requires that the fatigue properties be understood for crack sizes representative of those seen in service conditions, the present work is focused on characterizing the initiation and growth behavior of small (a∼25–300 μm) fatigue cracks in a γ-TiAl based alloy, of composition Ti–47Al–2Nb–2Cr–0.2B (at.%), with both duplex (average grain size of ∼17 μm) and refined lamellar (average colony size of ∼145 μm) microstructures. Results are compared to the behavior of large (a>5 mm), through-thickness cracks from a previous study. Superior crack initiation resistance is observed in the duplex microstructure, with no cracks nucleating after up to 500 000 cycles at maximum stress levels (R=0.1) in excess of the monotonic yield stress, σ_y. Comparatively, in the lamellar microstructure cracks nucleated readily at applied maximum stresses below the yield stress (85% σ_y) after as few as 500 cycles. In terms of crack growth, measurements for small fatigue cracks in the duplex and lamellar microstructures showed that both microstructures have comparable intrinsic fatigue-crack growth resistance in the presence of small flaws. This observation contrasts previous comparisons of large-crack data, where the lamellar structure showed far superior fatigue-crack growth resistance than the duplex structure. Such “small-crack effects” are examined both in terms of similitude (i.e. crack tip shielding) and continuum (i.e. biased microstructural sampling) limitations of traditional linear elastic fracture mechanics.     

Nanoscaled grain boundaries and pores,microstructure and mechanical properties of translucent Yb:[LuxY(1−x)O3] ceramics

Translucent ceramics of Yb:[Lu_xY_(1?x)O₃] system doped by ZrO₂ was sintered from nanopowder synthesized by laser evaporation. The relative density of the ceramics was 99.97%, residual pores had sizes from 8 nm to 20 nm, Young modulus was 200 GPa at the applied load of 2000 mN, the microhardness was 12.8 GPa. The grains of ceramics had sizes 1–10 μm, but the thickness of grain boundaries was about 1 nm. The transcrystalline type of the crack propagation was detected in the specially broken ceramics. The results indicated high strength of grain bonds and good perfection of grain boundaries in the studied ceramics but an increased content of pores (higher than 10^?3 vol.%) and stoichiometry deviation (Lu:Y:O = 0.21:0.79:3) from the required one (Lu:Y:O = 0.25:0.75:3).     

Sintering of tungsten powder with and without tungsten carbide additive by field assisted sintering technology

Tungsten powder (0.6–0.9 μm) was sintered by field assisted sintering technology (FAST) at various processing conditions. The sample sintered with in-situ hydrogen reduction pretreatment and pulsed electric current during heating showed the lowest amount of oxygen. The maximum relative density achieved was 98.5%, which is from the sample sintered at 2000 °C, 85 MPa for 30 min. However, the corresponding sintered grain size was 22.2 μm. To minimize grain growth, nano tungsten carbide powder (0.1–0.2 μm) was used as sintering additive. By mixing 5 and 10 vol.% WC with W powder, densification was enhanced and finer grain size was obtained. Relative density above 99% with grain size around 3 μm was achieved in W–10 vol.% WC sintered at 1700 °C, 85 MPa, for 5 min.     

Sintering behavior and non-linear properties of ZnO varistors processed in microwave electric and magnetic fields at 2.45 GHz

A study of the densification behavior and grain growth mechanisms of ZnO-based varistors composed of 98 mol.% ZnO–2 mol.% (Bi₂O₃, Sb₂O₃, Co₃O₄, MnO₂) has been carried out. The pressed samples were sintered in microwave electric (E) and magnetic (H) fields using a single-mode cavity of 2.45 GHz. The effect of the sintering temperature (900–1200 °C), holding time (5–120 min) and sintering mode (E, H) on the microstructure and electrical properties of the sintered varistor samples were investigated. The grain growth kinetics was studied using the simplified phenomenological equation Gⁿ = kte^(?Q/RT). The grain growth exponent (n) and apparent activation energy (Q) values were estimated for both electric and magnetic heating modes and were found to be n = 3.06–3.27, Q = 206–214 kJ mol^?1, respectively. The lower value of n estimated in the E field was attributed to a volume diffusion mechanism, whereas the higher n value in the H field sintering was correlated mainly to a combined effect of volume and surface diffusion processes. Samples sintered in the H and E fields showed high final densities. Moreover, the ones sintered in the H field presented slightly higher density values and bigger grains for all sintering temperatures than E field heated ones. The optimal sintering conditions were achieved at 1100 °C for a 5 min soaking time for both H and E field processed samples, where respectively densities of 99.2 ± 0.5% theoretical density (TD) and 98.3 ± 0.5% TD along with grain size values of G = 7.2 ± 0.36 μm and G = 6.6 ± 0.33 μm were obtained. Regarding the electrical properties, breakdown voltage values as high as 500–570 V mm^?1 were obtained, together with high non-linear coefficients α = 29–39 and low leakage currents (J_l ≈ 5 × 10^?3 mA cm^?2), respectively, for E and H field sintered varistor samples. Moreover, samples sintered in an H field systematically exhibited higher breakdown voltage values compared to the ones sintered in the E field. This was attributed to an improved coupling between the H field and the present dopants within the ZnO matrix, this latter being mostly semiconductive, thus leading to an enhanced reactivity and improved properties of the electrostatic barrier.     

Effect of annealing on microstructure and properties of Cu–30Ni alloy tube

The microstructure, mechanical properties and seawater corrosion resistance of annealed Cu–30Ni alloy tube were investigated using mechanical test, optical microscope, scanning electronic microscope and electrochemical measurement system, respectively. The recrystallizations gradually increased with the increase of annealing temperature and holding time. The hardness and tensile strength, which maintained invariability with annealing temperature at 680–720 °C, dramatically decreased with annealing temperature at 720–770 °C. As annealing temperature and holding time increase, corrosion potential (E_C) increased while corrosion rate (i_C) decreased at the beginning of seawater immersion. But after 15 days’ seawater immersion, as annealing temperature and holding time increase, E_C firstly increased and then decreased, on the contrary, i_C firstly decreased and then increased. The Ni-rich surface film and the Ni-rich sub-grains were responsible for the initial and extended immersion, respectively. It was found that the Cu–30Ni alloy tube annealed at 720 °C for 30 min exhibited favorable comprehensive mechanical properties and seawater corrosion resistance.     

In situ measurement of bond resistance varying with process parameters during ultrasonic wedge bonding

Interconnection joints are the signal and power carriers for chip-to-package, and their electrical property determines the whole component/device performances. With the process parameters (P, F and t) varying, the bond resistance was in situ measured during ultrasonic bonding. The influence of the process parameters on the bond resistance was obvious. The measured bond resistance changed in the range from 64.5 mΩ to 72.5 mΩ with the ultrasonic power (P) increasing. The maximum change of the single bond resistance was about 4 mΩ. The causation was analyzed in two aspects, evolution of the bond interface and deformation of the bond wire. Interfacial resistance (R_I) and deformation resistance (R_D) were two primary parts of the variance value.     

Grinding characteristics of micro-abrasive pellet tools fabricated by a LIGA-like process

The purpose of this paper was to investigate the wearing and grinding characteristics of the micro-abrasive pellet tools with 4–6 μm diamond particles fabricated by a LIGA-like process that has micro-lithography with photoresist mold and nickel/diamond composite electroforming. The results showed that when the micro-pellet tool containing partial resist joint with a root on the substrate was designed and fabricated, the tool against alumina sandpaper in wear test showed lesser amount of micro-pulled-out pellets than the tools with flat joint type, which displayed the tool to have better adhesion strength. In addition, when the micro-diamond tools were used to grind silicon wafers, the surface appearance of wafers showed ductile behavior. The surface roughness of wafers ground with increased pellet tool rotation speed became better and R_a=0.05 μm was achieved.