Table of contents

Preface

International Symposium on Frontier of Applied Physics is organized annually by Research Center for Physics-Indonesian Institute of Sciences. The 3rd ISFAP 2017 conference is part of Indonesian Science Expo 2017 to commemorate 50^th year anniversary of Indonesian Institute of Sciences. The conference theme is "Toward Innovation and Global Collaboration".

All papers published in this volume of Journal of Physics: Conference Series have been peer reviewed through processes administered by the proceedings Editors. Reviews were conducted by expert referees to the professional and scientific standards expected of a proceedings journal published by IOP Publishing.

One of the methods to determine the macro-bending effect in a single mode fiber is by calculating its power loss coefficient. We describe an alternative method by using the equation of fractional power in the fiber core. Knowing the fiber parameters such as its core radius, refractive indexes, and operating wavelength; we can calculate the V-number and the fractional power in the core. Because the value of the fiber refractive indexes and the propagation constant are affected by bending, we can calculate the value of the fractional power in the core as a function of the bending radius. We calculate the fractional power in the core of an SMF28 and SM600 fiber and, to verify our calculation, we measure its transmission loss using an optical spectrum analyzer. Our calculations and experimental results showed that for SMF28 fiber, there is about 4% power loss due to bending at 633 nm, about 8% at 1310 nm, about 20% at 1550 nm, and about 60% at 1064 nm. For SM600 fiber, there is about 6% power loss due to bending at 633 nm, about 11% at 850 nm, and this fiber is not suitable for operating wavelength beyond 1000 nm.

The effective cut-off wavelength is one of the important parameters in single-mode optical fiber. Nevertheless, the data sheet of an optical fiber patchcord generally does not specify the exact value of the cut-off wavelength. However, for certain applications, for example, to know the value of the numerical aperture, core radius and refractive index of the fiber at a certain wavelength, the exact value of the cut-off wavelength should be known. In this paper, we report the measurement of the cut-off wavelength of several commercially-available single-mode fiber patchcords, namely, the 780HP, SMF28, SM600, and SM2000. We used the multi-mode reference method in our measurement because it is simpler than the bend reference counterpart. From our measurements, the effective cut-off wavelengths for the above-mentioned fiber patchcords are (0.731±0.006) μm, (1.225±0.005) μm, (0.485±0.010) μm, and (1.665±0.018) μm, respectively, and its comparison with catalogue values has been discussed. The usefulness of the cut-off wavelength determination for calculating other fiber parameters has also been described.

Upconversion nanoparticles (UCNPs) converts near-infrared excitation to visible emission with advantages e.g. photostable, non-blinking, and background-free probes for bioimaging and biosensor. However, low quantum yield and low efficiency (∼1%) as drawback need to be enhanced. A plasmonic gold nano-structured surface was designed and fabricated to couple with the 980 nm radiation and produce plasmonic enhancement of the upconversion luminescence. The synthesis of the UCNPs was done by thermal decomposition and SiO₂ coating prepared by the reverse microemulsion process. Here, we report a novel tunable plasmon-enhanced fluorescence by modulating the thickness and surface roughness of gold island film on Si. The localized surface plasmon resonance (LSPR) at 980 nm was obtained, matched with the native excitation of UCNPs resulting in maximum enhancement of 10-fold of green emission band at 540 nm for the Er-doped UCNPs.

Carbon dots are new type of fluorescent nanoparticle that can be synthesis easily from natural sources. We have synthesized carbon dots from ginger and galangal herbs using microwave technique and studied their optical properties. We synthesized colloidal carbon dots in water solvent by varying microwave processing time. UV-Vis absorbance, photoluminescence, time-resolved photoluminescence, and transmission electron microscope were utilized to study properties of carbon dots. We found that microwave processing time significantly affect optical properties of synthesized carbon dots. UV-Vis absorbance spectra and time-resolved photoluminescence results show that luminescent of carbon dots is dominated by recombination process from n-π^* surface energy level. With further development, these carbon dots are potential for several applications.

We have fabricated metal and oxide nanoparticles using pulse laser ablation of Au, Ag, and Cu metal targets immersed in water. While laser ablation of Au and Ag targets in water produced metal nanoparticles which were stable for a month even without any dispersant, we found CuO nanoparticles for Cu target due to rapid oxidation of Cu in water resulted in its poor stability. Au, Ag, and CuO nanoparticles production were barely identified by naked eyes for their distinctive colour of red, yellow, and dark green colloidal suspensions, respectively. It was also verified using UV-Vis spectrometer that Au, Ag, and CuO colloidal nanoparticles have their respective surface plasmon resonance at 520, 400, and 620 nm. TEM observation showed that particle sizes for all the fabricated nanoparticles were in the range of 20 – 40 nm with crystalline structures.

Detection of nanoparticles in solution has been made possible by several means; one of them is laser-induced breakdown detection (LIBD). LIBD is able to distinguish colloids of various sizes and concentrations. This technique has been used in several solubility studies. In this study, the formation of colloids in a mixed system of silver nitrate and sodium chloride was observed by acoustic LIBD. Silver chloride has low solubility limit, therefore LIBD measurement is appropriate. Silver and chloride solutions with equal concentrations, set at below and above the solubility of silver chloride as the expected solid product, were mixed and the resulting colloids were observed. The result of LIBD measurement showed that larger particles were present as more silver and chloride introduced. However, once the concentrations exceeded the solubility limit of silver chloride, the detected particle size seemed to be decreasing, hence suggested the occurrence of coprecipitation process. This phenomenon indicated that the ability of LIBD to detect even small changes in colloid amounts might be a useful tool in study on formation and stability of colloids, i.e. to confirm whether nanoparticles synthesis has been successfully performed and whether the system is stable or not.

There are many ways to measure landslide displacement using sensors such as multi-turn potentiometer, fiber optic strain sensor, GPS, geodetic measurement, ground penetrating radar, etc. The proposed way is to use an optical encoder that produces pulse signal with high stability of measurement resolution despite voltage source instability. The landslide measurement using extensometer based on optical encoder has the ability of high resolution for wide range measurement and for a long period of time. The type of incremental optical encoder provides information about the pulse and direction of a rotating shaft by producing quadrature square wave cycle per increment of shaft movement. The result of measurement using 2,000 pulses per resolution of optical encoder has been obtained. Resolution of extensometer is 36 μm with speed limit of about 3.6 cm/s. System test in hazard landslide area has been carried out with good reliability for small landslide displacement monitoring.

Au-Ag nanoalloys have been synthesized by laser irradiation technique. First, Au and Ag nanoparticles were prepared from Au and Ag pure metal (99.9%) ablated using an 800 nm femtosecond laser in distilled water. Using the same laser, Au and Ag nanoparticle with 1:1 ratio were subsequently mixed and irradiated with various irradiation time, i.e. 0, 5, 20, and 35 minutes. We varied the ablation time for each metal nanoparticles, i.e. 25 minutes and 1 hour to see its effect on the production of nanoalloys in the subsequent irradiation. Au-Ag nanoalloys were characterized and analyzed using transmission electron microscope and UV-Vis spectrophotometry. The result shows that Au-Ag nanoalloys were already formed in 20 minutes irradiation, either for the sample ablated for 25 minutes or 1 hour. The result of TEM shows that the size of Au-Ag nanoalloys prepared from 1 hour ablation was around 15.03 nm.

Determination of concentration of heavy metal ions in soil, such as silver, is very important to study soil pollution levels. Several techniques have been developed to determine silver ion concentration in soil. In this paper, we utilized laser-induced breakdown spectroscopy (LIBS) to study silver concentration in soil. We used four different data analysis methods to calculate silver concentration. In this case, we prepared soil samples with different silver ion concentrations from 400 ppm to 1000 ppm. Our analysis was focused on the 843.15 nm silver atomic absorption line. We found that plasma intensity increased as silver concentration increased. Our findings were based on our analysis using four different analysis methods. We believe that these analysis methods are able to calculate silver concentration in soil using LIBS.

Laser-induced breakdown spectroscopy (LIBS) can be used for quantitative and qualitative analysis. Calibration-free LIBS (CF-LIBS) is a method to quantitatively analyze concentration of elements in a sample in local thermodynamic equilibrium conditions without using available matrix-matched calibration. In this study, we apply CF-LIBS for quantitative analysis of Ti in TiO₂ sample. TiO₂ powder sample was mixed with polyvinyl alcohol and formed into pellets. An Nd:YAG pulsed laser at a wavelength of 1064 nm was focused onto the sample to generate plasma. The spectrum of plasma was recorded using spectrophotometer then compared to NIST spectral line to determine energy levels and other parameters. The value of plasma temperature obtained using Boltzmann plot is 8127.29 K and electron density from calculation is 2.49×10¹⁶ cm^-3. Finally, the concentration of Ti in TiO₂ sample from this study is 97% that is in proximity with the sample certificate.

The laser-induced breakdown spectroscopy (LIBS) technique was applied to detect the nutrient elements contained in fresh carrot. Nd:YAG laser the wavelength of 1064 nm was employed in the experiments for ablation. Employing simple set-up of LIBS and preparing the sample with less step method, we are able to detect 18 chemical elements including some fundamental element of carrot, i.e Mg, Al, Fe, Mn, Ti, Ca, and Mn. By applying normalized profiles calculation on some of the element, we are able to compare the concentration level of each element of the outer and inner part of carrot.

Paddy grains moisture content (MC) strongly correlated to the physical properties of rice after being milled. Incorrect MC will cause higher percentage of broken rice and prompts the grains to be more fragile. In general, paddy grains with 13 – 14% MC are ideal for post-harvest processing. The objective of this study is to measure the MC of intact paddy grain from CV. Bakwan by means of non-destructive evaluation using NIR spectral assessment. Paddy grains samples with identical MC were put into 30 mm tube glass and measured using NIR spectrophotometer. The electromagnetic radiation absorbance under consideration upon spectral measurement fell between 1000 and 2500 nm. The grains' actual MC was then measured by primary method, based on weight measurement i.e. oven method. In this study, the spectral data of the grains was then processed by means of Principal Component Analysis (PCA) before correlated with its MCs by Partial Least Square (PLS) method. The model calibration obtained correlation (r) of 0.983 and RMSEC of 1.684. Moreover, model validation produced correlation (r) of 0.973, RMSEP of 2.095, and bias of 0.2, indicating that the MC of paddy grains can be precisely identified by non-destructive evaluation using spectral analysis.

The availability information about realistic velocity earth model in the fault zone is crucial in order to quantify seismic hazard analysis, such as ground motion modelling, determination of earthquake locations and focal mechanism. In this report, we use teleseismic receiver function to invert the S-velocity model beneath a seismic station located in the Cimandiri fault zone using neighbourhood algorithm inversion method. The result suggests the crustal thickness beneath the station is about 32-38 km. Furthermore, low velocity layers with high Vp/Vs exists in the lower crust, which may indicate the presence of hot material ascending from the subducted slab.

In this study, we investigated sediment thickness effect to the receiver function waveform. We conducted forward modelling of receiver function using different thickness of low velocity sediment layers. We varied low velocity layer from 0 - 4 km thickness. We applied Gaussian width parameter of 1.5 and 2.5, which corresponds to low pass filter with a corner frequency of 0.75 and 1.25 Hz, respectively. In this numerical analysis, we applied halfspace model with low velocity layer near the surface representing sedimentary layer. We generated synthetic receiver function using Thomson-Haskell matrix method. From our modelling, changes occur in the first few seconds of calculated synthetic receiver functions. Such changes occur due to reverberation in the sedimentary layer near the surface. Such changes differ with different sedimentary thickness used in the model. We applied H-k stacking method to the calculated synthetic receiver functions to see the effect of sedimentary layers to the results of H-k stacking.

Earthquake signal observations around the world allow seismologists to obtain the information of internal structure of the Earth especially the Earth's crust. In this study, we used joint inversion of receiver functions and surface wave group velocities to investigate crustal structure beneath CBJI station in West Java, Indonesia. Receiver function were calculated from earthquakes with magnitude more than 5 and at distance 30°-90°. Surface wave group velocities were calculated using frequency time analysis from earthquakes at distance of 30°- 40°. We inverted shear wave velocity model beneath the station by conducting joint inversion from receiver functions and surface wave dispersions. We suggest that the crustal thickness beneath CBJI station, West Java, Indonesia is about 35 km.

The dimensionality and regional strike analyses of the Cimandiri Fault, West Java, Indonesia have been investigated. The Cimandiri Fault consists of six segments. They are Loji, Cidadap, Nyalindung, Cibeber, Saguling and Padalarang segments. The magnetotelluric (MT) investigation was done in the Cibeber segment. There were 42 observation points of the magnetotelluric data, which were distributed along 2 lines. The magnetotelluric phase tensor has been applied to determine the dimensionality and regional strike of the Cibeber segment, Cimandiri Fault, West Java. The result of the dimensionality analysis shows that the range values of the skew angle value which indicate the dimensionality of the study area are -5 ≤ β ≥ 5. These values indicate if we would like to generate the subsurface model of the Cibeber segment by using the magnetotelluric data, it is safe to assume that the Cibeber segment has the 2-D. While the regional strike analysis presents that the regional strike of the Cibeber segment is about N70-80°E.

Strong negative Indian Ocean Dipole (IOD) event took place in the tropical Indian Ocean during 2016. Based on the Dipole Mode Index (DMI), the event has shown two peaks: in July and September. It is shown that the second peak was stronger than the first peak. Evolution of the event has started in May, reached its first peak in July, weaken in August, but rebounded and came to its second peak in September. The event was terminated in November. Robust sea surface temperature (SST) dipole patterns were observed during both peaks. In July, the SST anomaly in the eastern (western) pole of the IOD reached +1°C (-1.5°C). Meanwhile, during the second peak of the event, the SST anomaly in the eastern (western) pole of the IOD rose (fall) to nearly +2.5°C (-1°C). As a consequence, strong convective activities were observed over the maritime continent causing heavy rainfall during the peak of the event. On the other hand, there was a significant reduce of the rainfall over the eastern Africa during the peak of the event.

In this study, we applied receiver functions analysis to determine the crustal thickness, the ratio of Vp/Vs and the S wave velocity in the southern part of the Central Java. We selected tele-seismic data with magnitude more than 6 (M>6) and epicenter distance 30°-90° recorded from 3 broadband stations: UGM, YOGI, and WOJI station, as part of Indonesia-Geophone Network (IA-GE). Inversions were performed using nonlinear Neighborhood Algorithm (NA). We observed Ps phase conversion on the receiver functions corresponding to Moho depth at around 36-39 km. We also observed strong negative phase arrivals at around 10-12 s which might be associated with Indo-Australian subducting slab underneath the stations. The inversion results show the presence of low velocity zone with high Vp/Vs ratio (>1.78) in the middle crust around the study area which could be related to the Merapi-Lawu Anomaly (MLA).

In this study, we determined the main direction of geoelectric strike in the southern part of the Wayang Windu geothermal field using magnetotellurics (MT) data. The strike direction was obtained by analyzing data using impedance polar and Zstrike rose diagram. We investigated 51 MT data at different sites of the southern part of the Wayang Windu geothermal field. Determination of geoelectric strike direction is important since the strike is the rotation references in MT data processing. Our findings had pointed out that the geoelectric strike direction in this study area is in accordance with the direction of geological structure and has a good correlation with structures delineated from 3D MT inversion model.

Ni-based superalloy is widely used for high performance components in power generation turbine due to its excellent mechanical properties. However, Ni-based superalloy has low oxidation resistantance. Therefore, surface coating is required to improve oxidation resistance at high temperatures. Al-Si as a coting material was successfully co-deposited on Ni-based substrate by pack cementation method at 900 °C for about 4 hours. The oxidation test was carried out at high temperature of 1000 °C for 100 hours. Micro structural characterization and analysis on crystal orientation were perfomed by using Field Emission Scanning Electron Microscope (FE-SEM) and Electron Back Scatter Diffraction (EBSD) technique, respectively. The results showed that the coating layer with a homogenous layer and had a thickness of 53 μm consisting of β-NiAl with cubic structure and Ni₂Al₃ with hexagonal structure. TGO layer was developed after oxidation and had a thickness of about 5 μm consisting of α-Al₂O₃ and spinel NiCr₂O₄. The phase composition map and crystal orientation acquired by EBSD technique was also discussed both in TGO and coating layers.

XANES analysis has been performed with the aim of knowing the Fe oxidation state in a synthesized LiFePO₄ and its base materials. XANES measurements were performed at SLRI on energy around Fe K-edge. An XRD analysis has also been performed with the aim of knowing the phase composition, lattice parameters and crystallite size of the LiFePO₄ as well as the base materials. From the XRD analysis, it was found that the dominating phase in the iron sand sample was Fe₃O₄ and the only phase found after calcination was LiFePO₄. The latter phase exhibited crystallite size of 100 nm and lattice parameters a = 10.169916 Å, b = 5.919674 Å, c = 4.627893 Å. Qualitative analysis of XANES data revealed that the oxidation number of Fe in the sample before calcination was greater than that after calcination and Fe in the natural iron sand, indicated by the E₀ values of 7129.2 eV, 7120.6 eV and 7124.4 eV respectively.

The characteristics of sonicated Bayah natural zeolite with and without ferric chloride hexahydrate solution using infrared method has been studied. High intensity ultrasonic waves were exposed to the samples for 40 min, 80 min and 120 min. Infra red spectra analysis was conducted to evaluate zeolite vibrational spectrum contributions, namely, the vibrations from the framework of the zeolite, from the charge-balancing cations, and from the relatively isolated groups, such as the surface OH groups and their behavior after sonication process. An addition of FeCl₃.6H₂O and sonication process on natural zeolite improved secondary building units link by forming oxygen bridges and also close relationship with duration of applied high intensity ultrasonic process. Longer ultrasonic process resulted in more increment of O-H absorbance.

The optical, electrical and structural characteristics of InGaN-based blue light-emitting diodes (LEDs) were investigated to identify the degradation of LED before and after current injection. The sample was injected by high current of 200 A/cm² for 5 and 20 minutes. It was observed that injection of current shifts light intensity and wavelength characteristics that indicated defect generation. Transmission Electron Microscopy (TEM) characterization was carried out in order to clarify the structure degradation caused by defect in active layer which consisted of 14 quantum well with thickness of about 5 nm and confined with barrier layer with thickness of about 12 nm. TEM results showed pre-existing defect in LED before injection with high current. Furthermore, discontinue and edge defect was found in dark spot region of LED after injection with high current.

Fabrication of fine ceramics based on alumina, bentonite and glass bead has been carried out by powder metallurgy. The preparation of powder has been performed using High Energy Milling (HEM) with wet milling process and using toluene as medium for 2 hours. The powder milling result was dried in oven at 100 °C for 24 hours. After that, the powder was compacted into pellet by using hydraulic press with 80 kgf/cm² pressure at room temperature. Then, the pellet was sintered at 900 °C for 4 hours. Materials characterization such as physical properties (true density, bulk density, porosity, and water absorption), average particle diameter, hardness, microstructure and phase were measured by Archimedes method, Particle Size Analyzer (PSA), Hardness Vickers (HV), Scanning Electron Microscope (SEM-EDX) and X-Ray Diffraction (XRD). From the result, the optimum condition is sample D (with addition of 30 wt.% γ-Al₂O₃) with sintering temperature of 900 °C for 4 hours. At this condition, these properties were measured: average particle diameter of 4.27 μm, true density of 2.32 g/cm³, porosity of 5.57%, water absorption of 2.46%, bulk density of 2.39 g/cm³, and hardness of 632 HV. The fine ceramic has four phases with albite (Al₂NaO₈Si₃) and quartz (SiO₂) as dominant phases and corundum (Al₂O₃) and nepheline (AlNaO₄Si) as minor phases.

Nanocrystalline Ni-doped ZnO (NZO) thin films were synthesized on glass substrate using sol-gel spin coating methods. The effect of annealing on the structural and optical properties of nanocrystalline thin film was studied using X-ray diffractometer (XRD), field emission scanning electron microscopy (FESEM), UV-VIS spectrophotometry, and photoluminescence (PL). The results showed that the annealing temperature strongly influenced the physical properties of nanocrystalline NZO thin films. The photocatalytic properties of nanocrystalline NZO thin films were evaluated using an aqueous solution of Rhodamine-B. The photocatalytic activity of nanocrystalline NZO thin films increased with the increase of annealing temperature. The results indicated that the structure, morphology, and band gap energy of nanocrystalline NZO thin films played an important role in photocatalytic activity.

This paper reports a study on surface-enhanced Raman scattering (SERS) phenomenon of triangular silver nanoplate (NP) films towards bisphenol A (BPA) detection. The NP films were prepared using self-assembly technique with four different immersion times; 1 hour, 2 hours, 5 hours, and 8 hours. The SERS measurement was studied by observing the changes in Raman spectra of BPA after BPA absorbed on the NP films. It was found that the Raman intensity of BPA peaks was enhanced by using the prepared SERS substrates. This is clearly indicated that these SERS silver substrates are suitable to sense industrial chemical and potentially used as SERS detector. However, the rate of SERS enhancement is depended on the distribution of NP on the substrate surface.

Hematite microcubes with truncated edges have been successfully deposited on cotton cellulose via one-step hydrothermal process using anhydrous FeCl₃ and glycine as Fe(III) precursor and chelating agent, respectively. The amount of glycine significantly affects the morphology and yield of hematite. The addition of 0.495 g of glycine to 50 ml of 0.1 M FeCl₃ solution with 0.400 g of cotton resulted to hematite-deposited cellulose having ∼15% hematite content. The reduction of glycine to 0.247 g increased the amount of hematite on the surface of the cotton cellulose to ∼20% by weight. However, the hematite microcubes have a wide size distribution, with particle size in the range of 0.684 μm to 1.520 μm. Without glycine, hematite cannot be formed in the solution.

Tremendous industrialization in the last century has led to the generation of huge amount of waste. One of the recent hot research topics is utilizing any advance materials and methods for waste removal. Natural zeolite as an inexpensive porous material with a high abundance holds a key for efficient waste removal owing to its high surface area. However, the microporous structure of natural zeolite hinders the adsorption of waste with a bigger molecular size. In addition, the recovery of natural zeolite after waste adsorption into its pores should also be considered for continuous utilization of this material. In this study, the porosity of natural zeolite from Tasikmalaya, Indonesia, was hydrothermally-modified in a Teflon-lined autoclave filled with certain pore directing agent such as distilled water, KOH, and NH₄OH to obtain hierarchical pore structure. After proper drying process, the as-treated natural zeolite is impregnated with iron cation and heat-treated at specified temperature to get Fe-embedded zeolite structure. XRD observation is carried out to ensure the formation of magnetic phase within the zeolite pores. The analysis results show the formation of maghemite phase (γ-Fe₂O₃) within the zeolite pore structure.

Hybrid polymer latex based on combination of organic-inorganic materials, poly(methyl methacrylate-co-butyl acrylate) (PMMBA) and organo-montmorillonite (OMMT) were synthesized via miniemulsion polymerization technique. Modification of montmorillonite (MMT) through the incorporation of myristyltrimethylammonium bromide (MTAB) into the clay's interlayer spaces were investigated by Small-Angle X-ray Scattering (SAXS), Fourier Transform Infrared Spectroscopy (FTIR), Thermogravimetric Analysis (TGA) and Transmission Electron Microscopy (TEM). Barrier property and thermal stability of polymer latex film sample were investigated through its Water Vapor Transmission Rate (WVTR) and Thermogravimetric Analysis (TGA). The results indicated that addition of OMMT as filler in PMMBA increased the barrier property and thermal stability of the latex film. Addition of 8.0% (wt) OMMT increased the barrier property and thermal stability. Miniemusion polymerization process with higher addition (>8.0 wt%) of OMMT resulting in high latex viscosity, particle size, and high amount of coagulum. The utilization of this hybrid polymer could benefits paper and board industries to produce high quality barrier paper for food packaging.

In this study, porous carbon made from coffee bean waste (CBW) was carbonized at 500 °C, 600 °C, and 700 °C to find effective temperature. It is verified from the IR spectrum that carbonization process at certain temperature can effectively break cellulose bonding and make aromatics functional group while preserving its carbon structure. The TG-DTA curve shows four stages of decomposition process and confirms most effective carbonization temperature. Activation process of as-carbonized CBW was carried out using solvothermal method in KOH and NH₄OH steam environment at 200 °C with variation of 30%, 40%, and 50% solvothermal volume. Scanning electron micrographs reveals significant increase of porosity on the carbon surface and differences of structural pores between the variations. The results show the possible potential of utilizing low temperature-solvothermal method for nanoporous carbon material.

The significant increase of waste due to vast development of human civilization and industrialization has plunged humanity into various environmental issues. Nowadays, the concern on waste handling and conversion into more valuable material has become one of hot research topics. Biomass waste has great abundance with various types that can be utilized for many applications such as landfill, recycled-material, adsorbent, separation, catalysis, and so on. In this study, coffee bean waste (CBW) was used as a source to produce hydrophobic layer. The CBW was converted into amorphous carbon using simple carbonization method at 500 °C, dispersed in acetic acid and then mixed with polyvinyl alcohol (PVA) at low temperature heating. In order to investigate effects of composition on hydrophobicity properties, ratio of carbon and PVA was varied. In addition, acetic acid was used to evaluate effect of dispersant on hydrophobic properties. SEM analysis reveals unique morphology of carbon layer. The measurement of contact angle demonstrates that this unique morphology possesses comparable hydrophobicity with that of some well-known materials. Fourier transform infrared spectroscopy (FTIR) analysis confirms the effect of PVA bonding and carbon layer on its hydrophobicity.

Hybrid materials Nano-ZnO/polyurethane film was prepared with different zinc oxide (ZnO) content in polyurethane as a matrix. The film was deposited on low carbon steel plate using high volume low pressure (HVLP) method. To observe thermal behaviour of the film, the sample was investigated using thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). Fourier transform infrared spectroscopy (FTIR) was used to see whether any chemical reaction of ZnO in polyurethane occured. TGA and FTIR results showed that the decomposition temperature shifted to a higher point and the chemical reaction of zinc oxide in polyurethane occurred. The surface morphology changed and the corrosion resistance increased with an increase of ZnO content

This paper reports the characterization of dross from galvanizing process and its recovery using acidic leaching method. The diffraction profile of dross showed identical peaks with that of ZnO. The X-ray Fluorescence (XRF) analysis identified the content of following metals: Zn, Fe, Mn, Ga, Co, and W. The thermal behaviour examination revealed the existence of some volatiles within the initial sample. The acidic leaching at various concentrations of sulphuric acid was conducted to determine the optimum concentration for zinc recovery and the highest yield of zinc sulphate. It is concluded that the optimum concentration of H₂SO₄ for this kind of dross is 4 M with 71.9% yield of ZnSO₄. The result of leaching process was confirmed by infrared spectrum, where various absorptions corresponding to SO₄^2- and Zn-O bands were observed.

We have studied ferroelectric behaviour of barium titanate (BaTiO₃) thin films prepared with sol-gel method. BaTiO₃ solutions were deposited onto silicon substrates with different numbers of layers via spin coating method. The obtained samples were sintered at 700 °C and 800 °C. Structure and ferroelectric properties of the samples were investigated using X-ray diffraction (XRD) and Sawyer–Tower circuit. As observed from XRD patterns, number of layers affected the films structure. Results also showed that crystallographic system of BaTiO₃ thin films was characterized by a tetragonal structure. Maximum polarization increased with an increase in layer number. Spontaneous polarization was also observed increasing with an increase in temperature.

Organoclay/polyurethane film composite was prepared by adding organoclay with different content (1, 3, and 5 wt.%) in polyurethane as a matrix. TGA and DSC showed decomposition temperature shifted to a lower point as organoclay content change. FT-IR spectra showed chemical bonding of organoclay and polyurethane as a matrix, which means that the bonding between filler and matrix occured and the composite was stronger but less bonding occur in composite with 5 wt.% organoclay. The corrosion resistance overall increased with the increasing organoclay content. Composite with 5 wt.% organoclay had more thermal stability and corrosion resistance may probably due to exfoliation of organoclay.

Durability of Thermal Barrier Coating or TBC can be optimized by inducing Self-Healing capabilities with intermetallic materials MoSi₂. Nevertheless, high temperature operation causes the self-healing materials to become oxidized and lose its healing capabilities. Therefore, a method to introduce ceramic encapsulation for MoSi₂ is needed to protect it from early oxidation. The encapsulation process is synthesized through a simple precipitation method with colloidal aluminum hydroxide as precursor and variations on calcination process. Semi-quantitative analysis on the synthesized sample is done by using X-ray diffraction (XRD) method. Meanwhile, qualitative analysis on the morphology of the encapsulation was carried out by using Scanning Electron Microscope (SEM) and Field Emission Scanning Electron Microscope (FESEM) equipped with dual Focus Ion Beam (FIB). The result of the experiment shows that calcination process significantly affects the final characteristic of encapsulation. The optimum encapsulation process was synthesized by colloidal aluminum hydroxide as a precursor, with a double step calcination process in low pressure until 900 °C.

Hybrid materials organoclay/epoxy resin films were prepared by varying organoclay content in epoxy resin as a matrix. The film were investigated by thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), and thermal conductivity. TGA and FT-IR results confirmed that the melting temperature shifted to a lower point. The thermal conductivity and corrosion resistant generally increase with increasing organoclay content. The changes on these properties may due to cross link between organoclay and epoxy.

MoSi₂ is well known as a material for high temperature application because it has high oxidation and corrosion resistance. The aim of this research is to develop MoSi₂ coating with Al doping on Stainless Steel 316 (SS316) substrate using High-Energy Milling method. Aluminium is added to the coating as a dopant to increase formation of MoSi₂ coating layer on the substrate. The variations used here based on the concentrations of doping Al (at.%) and duration of milling. Results show that the MoSi₂ coatings with variations of 30 and 50 at.% of Al doping and 3 and 6 hours of milling times were successfully coated on the surface of SS 316 using the high-energy milling method. The most optimum coating result after oxidation test at 1100 °C for 100 hours is shown by MoSi₂-30%Al with 3 hours of milling times. From the oxidation results, the Al doping into MoSi2 coating was able to increase the oxidation resistance of the SS 316 substrate.

The microstructure formed on the bond coat affects the oxidation resistance, particularly the formation of a protective oxide layer. The adhesion of bond coat and TGO increased significantly by addition of reactive element. In the present work, the effect of yttrium and yttrium silicon as reactive element (RE) on NiCrAl coating was investigated. The NiCrAl (without RE) and NiCrAlX (X:Y or YSi) bond coating were deposited on Hastelloy C-276 substrate by High Velocity Oxygen Fuel (HVOF) method. Isothermal oxidation was carried out at 1000 °C for 100 hours. The results showed that the addition of RE could prevent the breakaway oxidation. Therefore, the coating with reactive element were more protective against high temperature oxidation. Furthermore, the oxidation rate of NiCrAlY coating was lower than NiCrAlYSi coating with the total mass change was ±2.394 mg/cm² after 100 hours of oxidation. The thickness of oxide scale was approximately 1.18 μm consisting of duplex oxide scale of spinel NiCr₂O₄ in outer scale and protective α-Al₂O₃ in inner scale.

In this work, Fe-Cr alloys were coated via Aluminum (Al) pack cementation, followed by Nickel (Ni) electrodeposition. The process of pack cementation was done with mixing powders of Al, Al₂0₃ and NH₄Cl with weight percentage of 15%, 85%, and 5% respectively. To control successful Al diffusion to the substrate, pack cementation was conducted for 7 hours with two holding temperatures treatment at 400 °C for 4 hours, and 800 ° C hours for 2 hours. Subsequently, the electrodeposition of Ni was applied with the solution consisting of NiSO₄, H₃BO₃, and NiCl₂. The samples were placed in the cathode, and then dipped in the solutions, while Ni plate used as anode. Successfully the samples were coated by dual Al-Ni layers, the samples were slowly heat treated at 900 °C for 10 hours. The inter-diffusion of Al and Ni were characterized with SEM/EDX to investigate the distribution of the elements. Mechanical properties of the coated substrates were analyzed with Hardness Vickers (HV). It was found the hardness of the substrate increased significantly, from originally 255 HV to the 1177 HV after pack cementation. The hardness of the substrates has decreased to 641 HV after Ni plating, but subsequent heat treatment has been able to increase the hardness to 842 HV. This phenomenon can be correlated to the inward Al diffusion, and outward Fe, Cr diffusion. The formation of intermetallic compounds due to Al inward and Fe, Cr outward diffusion were discussed in details.

Highly corrosion resistant of carbon steel coated NiCoCr was applied in corrosive of marine environtment. Carbon steel coated NiCoCr was prepared by a two step technique of NiCo electro-deposition and Cr pack cementation. The samples were exposed to 5 wt.% NaCl for 48 and 168 hours. The microstructure and corrosion product were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), and transmission electron microscopy (TEM). The corrosion resistance of carbon steel coated NiCoCr was found to be better than that of carbon steel substrate without coating. The results showed the microstructure of 48 h corroded sample has duplex layer composed of inner α-(Ni,Co), α-Cr and outer Cr₂O₃, while a quite thin and continues protective oxide of Cr₂O₃ was observed in outer layer of 168 h corroded sample. The formation of oxide scale rich in Cr₂O₃ has contributed for the better corrosion resistance of carbon steel coated NiCoCr, whereas the formation of non protective oxide of iron might caused low corrosion resistance of carbon steel substrate.

In present work, Cr-Al coatings containing 0, 1, 2, 3, and 5% W have been prepared on the surface of low carbon steel by mechanical alloying technique. The composition of each powder was milled for 2 hour in a stainless steel crucible with a ball to powder ratio of 10:1. Afterward, the Cr-Al-W powder and substrate were mechanically alloyed in air for 1 hour. The heat treatment of coated samples was carried out at 800 °C in a vacuum furnace for 2 hour. In order to characterize the phase composition and microstructure of the coating before and after heat treatment, XRD and SEM-EDX were used. The analysis results reveal that the ball milling process induces the formation of homogeneous Cr-Al-W coating structure with a thickness of about 80 μm. The phase observation shows individual peaks of each starting elements, along with the occurrence of powder refinement and solid solution formation. After heat treatment, AlCr₂ and Al₈Cr₅ phases were formed. The addition of W accelerates the formation of AlCr₂, but inhibits the formation of Al₈Cr₅. The detail of the results was presented in this paper.

Research of fabricated bonded magnets NdFeB made from NdFeB flakes with variation of external magnetic field has been done. The materials preparation process begins with milling NdFeB flakes using High Energy Milling (HEM) for 60 minutes and mixing it with 5 wt % celuna binder and performing compaction to form pellet with a pressure of 40 Kgf/cm² and then applying external magnetic field (0, 2000, 5000, 8000 and 11000 Gauss). The pellet samples were then dried using vacuum dryer with temperature of 100 °C for 1 hour. Characterization includes bulk density, measurement of magnetic properties with gauss meter, and Vibrating Sample Magnetometer (VSM). From the characterization results the best value was obtained on the external magnetic field orientation of 8000 to 11000 Gauss with a density value of 5.38 g/cm³, flux magnetic value of 465.9 – 467.1 Gauss, remanence value of 2.63–2.776 kGauss, and coercivity value of 1.905–1.925 kOe.

In this paper, the effect of Fe-Mn alloy addition on microstructures and magnetic properties of NdFeB magnetic powders was investigated. Varied Fe-Mn compositions of 1, 5, and 10 wt% were mixed with commercial NdFeB type MQA powders for 15 minutes using shaker mill. The characterizations were performed by powder density, PSA, XRD, SEM, and VSM. The Fe-Mn addition increased the powder density of NdFeB/Fe-Mn powders. On the other side, particle size distribution slightly decreased as the Fe-Mn composition increases. Magnetic properties of NdFeB/Fe-Mn powders changed with the increasing of Fe-Mn content. SEM analysis showed the particle size of NdFeB/Fe-Mn powder was smaller as the Fe-Mn composition increases. It showed that NdFeB/Fe-Mn particles have different size and shape for NdFeB and Fe-Mn particles separately. The optimum magnetic properties of NdFeB/Fe-Mn powder was achieved on the 5 wt% Fe-Mn composition with remanence M_r = 49.45 emu/g, coercivity H_c = 2.201 kOe, and energy product, BH_max = 2.15 MGOe.

The spinel based on transition-metal oxides has a typical composition of AB₂O₄. In this study, the ZnMn₂O₄ spinel was synthesized using a powder metallurgy technique. The Zn and Mn metallic powders with an atomic ratio of 1:2 were mechanically alloyed for 3 hours in aqueous solution. The mixed powder was then calcined in a muffle furnace at elevated temperature of 400, 500 and 600 °C. The X-ray Diffractometer (XRD) was used to evaluate the formation of a ZnMn₂O₄ spinel structure. The magnetic properties of the sample at varying calcination temperatures were characterized by a Vibrating Sample Magnetometer (VSM). The results show that the fraction of ZnMn₂O₄ spinel formation increases with the increase of calcination temperature. The calcination temperature also affects the magnetic properties of the samples.

Magnetic materials of magnesium ferrite (MgFe₂O₄) based on natural iron sand has been successfully prepared as an adsorbent of Pb ions. This material was synthesized by co-precipitation method with natural iron and Mg(CH₃COO)₂.4H₂O as precursor powders which were mixed with 2.0 M NH₄OH at a synthesis temperature of 50, 70 and 90 °C. The material characterizations were carried out using X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM), and Vibrating Sample Magnetometer (VSM). The XRD pattern showed that MgFe₂O₄ has single phase and its crystallite size increased and the powder density decreased as the temperature increased. The optimum temperature for the synthesis of MgFe₂O₄ was found at 50 °C, when the saturation magnetization and coercivity were at the highest values of 51.73 emu/g and 308 Oe, respectively. The result also showed that MgFe₂O₄ as an adsorbent of Pb ions has adsorption capacity of 143.07mg/g and removal efficiency of 97.3%.

The composite magnet NdFeB has been made using magnetic powder MQP-B and polyvinyl alcohol (PVA) as the binder. The mixing compositions of raw materials used are: 95 wt% NdFeB - 5 wt% PVA, 92.5 wt% NdFeB - 7.5 wt% PVA, 90 wt.% NdFeB - 10 wt% PVA, and 87.5 wt% NdFeB - 12.5 wt% PVA. Both raw materials are weighed according to the composition, and then mixed until homogeneous. Furthermore, pellet forming was made using dry pressing at 50 kgf/cm² pressures and continued with drying at 100 °C and 10 mmbar for 4 hours. The characterization includes bulk density, hardness, compressive strength measurements, and magnetic properties testing. The characterization results show that the optimal composition of binder PVA is achieved at 5–7.5 wt% NdFeB composite magnet with following properties: bulk density = 5.21–5.25 g/cm³, hardness = 302.17 - 304.32 Hv, compressive strength = 25.17–3.17 kgf/cm², magnetic flux = 1150-1170 Gauss, remanence = 70.90–74.97 emu/g or 4.7–5.0 kGauss, coercivity = 8.68–8.76 kOe, and energy product = 2.89–3.04 MgOe.

The utilization of iron oxide waste of grinding process as raw materials for making barium hexaferrite has been completed by powder metallurgy method. The iron oxide waste was purified by roasting at 800 °C temperature for 3 hours. The method used varying calcination temperature at 1000, 1100, 1200, and 1250 °C for 3 hours. The starting iron oxide waste (Fe₂O₃) and barium carbonate (BaCO₃) were prepared by mol ratio of Fe₂O₃:BaCO₃ from the formula BaO₃.98Fe₂O₃. Some additives such as calcium oxide (CaO), silicon dioxide (SiO₂), and polyvinyl alcohol (PVA) were added after calcination process. The samples were formed at the pressure of 2 ton/cm² and sintered at the temperature of 1250 °C for 1 hour. The formation of barium hexaferrite compounds after calcination is determined by X-Ray diffraction. The magnetic properties were observed by Permagraph-Magnet Physik with the optimum characteristic at calcination temperature of 1250 °C with the induction of remanence (Br) = 1.38 kG, coercivity (HcJ) = 4.533 kOe, product energy maximum (BHmax) = 1.086 MGOe, and density = 4.33 g/cm³.

Characterization of the composite membrane of LiBOB electrolyte polymers made from poly (vinylidene fluoride co-hexafluororopylene) (PVdF-HFP) as the polymer, LiBOB or LiB(C₂O₄)₂ as electrolyte salt and titanium dioxide (TiO₂) as ceramic filler of three different concentrations have been done. Sample of membrane was prepared using solution casting technique. Microstructural study by SEM shows non-uniform distribution of pore over the surface of the sample. X-ray structural analysis, impedance spectroscopy, and cyclic voltammetry (CV) studies were carried out. Membrane composite polymer of LiBOB electrolyte without additional ceramic filler with composition of 70% polymer, 30% LiBOB, and 0% TiO₂ has the greatest conductivity for forming amorphous phase and is compatible with material membrane composite. Meanwhile, sample with 70% polymer composition, 28% LiBOB and 2% TiO₂ shows oxidation reaction at the most perfect discharge despite very slow current speed.

Bipolar plates (BPP) is a vital component of proton exchange membrane fuel cells (PEMFC), which supplies fuel and oxidant to reactive sites, remove reaction products, collects produced current and provide mechanical support for the cells in the stack. This work concerns the utilization of mill scale, a by-product of iron and steel formed during the hot rolling of steel, as a potential material for use as BPP in PEMFC. On the other hand, mill scale is considered a very rich in iron source having characteristic required such as for current collector in BPP and would significantly contribute to lower the overall cost of PEMFC based fuel cell systems. In this study, the iron reach source of mill scale powder, after sieving of 150 mesh, was mechanically alloyed with the carbon source containing 5, 10, and 15 wt.% graphite using a shaker mill for 3 h. The mixed powders were then pressed at 300 MPa and sintered at 900 °C for 1 h under inert gas atmosphere. The structural changes of powder particles during mechanical alloying and after sintering were studied by X-ray diffractometry, optical microscopy, scanning electron microscopy, and microhardness measurement. The details of the presence of iron, carbon, and iron carbide (Fe-C) as the products of reactions as well as sufficient mechanical strength of the sintered materials were presented in this report.

Polyvinylidene fluoride (PVdF) is a semi-crystalline thermoplastic material with remarkably high piezoelectric coefficient and an attractive polymer matrix for micro-composite with superior mechanical and electrical properties. The conductive filler is obtained from Graphite Electrode Waste (GEW) and Natural Carbon Black (NCB). The variation of composite content (%) of PVdF/NCB/GEW were 100/0/0, 95/5/0, 95/0/5, 95/2.5/2.5. This experiment employed dry dispersion method for material mixing. The materials were then moulded using hot press machine with compression parameters of P = 5.5 MPa, T = 150 °C, t = 60 minutes, A = 5×5×(0.2 - 0.4) cm³. The electrical conductivity properties of pure PVdF, as well as PVdF/GEW, PVdF/NCB, and PVdF/NCB/GEW composites were investigated in a frequency range of 100 to 100000 Hz. The PVdF/GEW sample obtained the highest electrical conductivity. It is concluded that GEW and NCB can be incorporated into PVdF as a conductive filler to increase the conductivity of conductive material composite without solvent.

Dye-sensitized solar sub-module has been prepared as a practical application of DSSC. TiO₂ paste was deposited onto the 3.3 cm × 5 cm FTO glass by screen printing method consisting of two active cells with a dimension of 1 cm × 5 cm for each cell. The sub-module was assembled using two parts (part A and part B) hermetic sealing compound as a sealant. The performance of the sub-module was then observed using two independent measurements in the span of six days using sun simulator. Photovoltaic effect was properly occurred as indicated by the I-V curve for both of sub-module. First test showed that the sub-module with hermetic sealant has good performance with the highest efficiency of 2.9%. Meanwhile, the second test showed significant decrease of the sub-module performance with the highest efficiency of 1.43%.

Phosphoric acid is one agents used in membrane fuel cell to modify ionic conductivity. Therefore, its distribution in membrane is a key parameter to gain expected conductivity. Efforts have been made to distribute phosphoric acid in a supramolecular-structured membrane prepared with a matrix. To achieve even distribution across bulk of the membrane, the inclusion of the polyacid is carried out under pressurized chamber. Image of scanning electron microscopy (SEM) shows better phosphoric acid distribution for one prepared in pressurized state. It also leads in better performing in ionic conductivity. Moreover, data from differential scanning calorimetry (DSC) indicate that the addition of phosphoric acid is prominent in the change of membrane structure, while morphological changes are captured in SEM images.

LiMn₂O₄ as a cathode material has been synthesized via solid state reaction. The synthesis has been done by varying lithium sources such as LiOH.H₂O and Li₂CO₃ while MnO₂ was used as Mn sources. All raw materials were mixed stoichiometrically to be the precursors of LiMn₂O₄. The precursors were sintered using high temperature furnace at 800 °C for 4 hours in atmospheric condition to form final product. The final products were sieved to separate the finer and smoother particles from the coarse ones. The products were characterized by X-Ray Diffractometer (XRD) to identify phases and crystal structure. The peak wave number was also determined using Fourier Transform Infra Red (FTIR) to find functional group. LiMn₂O₄ sheets were prepared by mixing active material with polyvinylidene fluoride (PVdF) and acetylene black (AB) in mass ratio of 85:10:5 wt.% in N,N-Dimethylacetamide (DMAc) solvents to form slurry. The slurry was then coated onto Al foil with thickness of about 0.15 mm and dried in an oven. LiMn₂O₄ sheet was cut into circular discs and arranged with separator, metallic lithium, and electrolyte in a coin cell. Automatic battery cycler was used to measure electrochemical performance and specific capacity of the cell. XRD analysis showed that sample synthesized with Li₂CO₃ has higher crystallinity and more pristine than sample synthesized with LiOH.H₂O. FTIR analysis revealed that both of samples have identical functional group but sample with Li₂CO₃ source tend to degrade. Cyclic voltammetry data gave information that sample with LiOH.H₂O source has better electrochemical performance. It showed double oxidation/reduction peaks more clearly but sample with Li₂CO₃ source has higher specific capacity (64.78 mAh/g) than sample with LiOH.H₂O (50 mAh/g).

Dye-sensitized solar cell (DSSC) have been extensively studied due to its low production cost and simple production process. In this research, DSSC with improved performance is acquired by modification of TiO₂ layer through hydrothermal post-treatment with different hydrochloric acid (HCl) concentrations to obtain various particles and pore sizes. Qualitative and quantitative characterizations of the TiO₂ film were conducted using thickness measurement, scanning electron microscope (SEM), and X-ray diffraction (XRD), while the solar cell performances were characterized using current-voltage (I-V) measurement under 0.5 Sun. When hydrothermally treated with 1 mol/L HCl at 180 °C for 3 h, the DSSC showed the most optimum photo-electricity conversion performance of 3.60%, which improved the efficiency of the non-treated DSSC by a factor of 1.2. As the HCl concentration increased, the treated TiO₂ film became thinner with smaller particle size and denser structure. It was suspected that the modification in the TiO2 film morphology has led to better light absorption, which consequently resulted in the improvement of DSSC performance.

Fixed-bed reactors are commonly used as bioreactors for various applications, including chemicals production and organic wastewater treatment. Bioreactors are fixed with packing materials for attaching microorganisms. Packing materials should have high surface area and enable sufficient fluid flow in the reactor. Natural materials e.g. rocks and fibres are often used as packing materials. Commercially, packing materials are also produced from polymer with the advantage of customizable shapes. The objective of this research was to study the mixing pattern in a packed-bed reactor using bamboo as packing material. Bamboo was selected for its pipe-like and porous form, as well as its abundant availability in Indonesia. The cut bamboo sticks were installed in a reactor in different configurations namely vertical, horizontal, and random. Textile dye was used as a tracer. Our results show that the vertical configuration gave the least liquid resistant flow. Yet, the random configuration was the best configuration during mixing process.

Platinum nanoparticles on multiwall carbon nanotubes (Pt/MWCNT) play an important role in fuel cell to convert the chemical energy from a fuel into electricity. In this study, Pt/MWCNT electrocatalysts were prepared by chemical reduction of the metal salts in chitosan as the support. Firstly, commercial MWCNTs were functionalized by oxidative process using a mixture of nitric acid and sulfuric acid. Then, functionalized MWCNTs were mixed with chitosan-acetic acid solution to conduct grafting reaction with NH₂ groups in chitosan by solution polymerization method. Platinum nanoparticles were loaded onto the surface of the MWCNTs after hexachloroplatinic acid was reduced by sodium hydroxide solution. The result showed that Pt was attached on MWCNT based on analysis from EDS, XRD, and UV Vis Spectroscopy. UV Vis analysis indicates the plasmon absorbance band of Pt nanoparticles in Pt/MWCNT, while XRD analysis confirmed the size of Pt particle in nanometer. This elucidates the potential procedure to synthesize Pt/MWCNT using chitosan.