Thin Layer Research Articles

A Comparison of the Edge Testing of Indirect Composite Layered Zirconia Crowns and Monolithic Zirconia Crowns Without Aging: An In Vitro Study.

Introduction The main reason veneered zirconia restorations fail is due to porcelain veneer chipping. This chipping usually starts from wear marks on the chewing surface. As a result, small cracks under the contact area can grow into larger ones across the veneer layer. The veneer ceramic layer is more vulnerable to fractures because it has lower toughness and slightly lower stiffness compared to the base framework material. Thus, even when there's significant chipping, the main framework material usually stays protected with a thin layer of veneer ceramic on top. The aim of this in vitro study is to compare the edge strength of Monolithic Zirconia Crowns with that of Indirect Composite Layered Zirconia Crowns without aging. Materials and methods This research involved creating 12 hand-layered all-ceramic crowns and 12 indirect composite layered zirconia crowns. The sample size was determined using a G*Power calculation (Heinrich-Heine-Universität Düsseldorf, Düsseldorf, Germany). The zirconia frameworks (Upcera HT White; UPCERA Dental America Inc., Cerritos, CA, US) were milled and sintered following the manufacturer's instructions. For the all-ceramic group, veneering porcelain (e.max Ceram; Ivoclar Vivadent, Schaan, Liechtenstein) was hand-applied. In contrast, the indirect composite group utilized Ceramage (Shofu, Kyoto, Japan). An Instron 4501 universal testing machine (Instron Corp., Canton, MA, USA) was employed for the edge chipping tests, and a Vickers indenter (Shanghai Toyo Diamond Tools Co., LTD, Shanghai, China) was used to apply the load. The mean value for edge chipping was analyzed using an unpaired t-test with IBM SPSS Statistics for Windows, Version 26 (Released 2019; IBM Corp., Armonk, NY, USA). The normality of the data was confirmed, and statistical significance was set at 0.05. Results Monolithic Zirconia Crowns (Group 1) require significantly more force (mean: 405 N) to induce an edge chip compared to Indirect Composite Layered Zirconia Crowns (Group 2) (mean: 300 N). The 95% confidence interval (83.43261 N to 109.90072 N) confirms the statistical significance of this difference. Conclusion In conclusion, when evaluating restorative materials based on both esthetic and functional criteria, monolithic zirconia stands out due to its combination of strength, esthetic potential, biocompatibility, and versatility.

Fabrication of Efficient and Simple-Structured Perovskite Solar Cells Using a Multifunctional Biocolina Surface Treatment.

The electron transport layer (ETL)-free perovskite solar cells (PSCs) have gained significant interest by simplifying the manufacture process and reducing the time/energy required for the fabrication of ETLs. Unfortunately, the performance of these ETL-free PSCs still lags behind those of the conventional counterparts due to the slow electron extraction and undesired interfacial charge recombination loss at the buried interface. In this work, a facile and multifunctional biocolina thin layer is incorporated on the bottom electrodes to regulate the interface energy level alignment by forming an interface dipole layer, resulting in a suppressed nonradiative recombination and an improved charge extraction. Furthermore, the biocolina thin layer possess the capability to passivate the surface defects within the perovskite films while simultaneously facilitate the formation of perovskite crystals. Consequently, a remarkable enhancement in photovoltaic performance is observed in the biocolina-based ETL-free PSCs with an increase from 15.96% to an outstanding 20.01%. Additionally, the biocolina extends the stability and relieves the hysteresis effect through the interface defect passivation and inhibition of interface charge accumulation. This research contributes to the development of cost-effective, simplified designs for highly efficient ETL-free PSCs by modifying the bottom electrodes.

Identification of phytoconstituents from Houttuynia cordata Thunb. as dipeptidyl peptidase-IV and sodium glucose cotransporter 2 inhibitors guided by molecular docking

PurposeHouttuynia cordata Thunb. is an edible medicinal herb belonging to the Saururaceae family. Although the effects of the plant extracts on several diabetic-related parameters have been documented in the past, there is no documentation of the effects of this plant on sodium/glucose cotransporter 2 or dipeptidyl peptidase-IV- key drug targets for type 2 diabetes. The present study identified and screened phytoconstituents present in H. cordata Thunb. and characterized their ADME/Tox properties. The compounds present in aqueous and hydroalcoholic extracts of H. cordata Thunb. were identified using High-Performance Thin Layer Chromatography, and Gas Chromatography tandem mass spectrometry. Compounds obeying the Lipinski's Rule of 5 and having high gastrointestinal absorption were then selected and docked with dipeptidyl peptidase-IV and sodium/glucose cotransporter 2. ResultsChromatographic analysis showed the presence of several compounds by matching their recorded spectra with the data bank mass spectra from the NIST library. ADME/Tox properties and docking of the identified compounds indicate the potentiality of the compounds as antidiabetic drug candidates. ConclusionsThe compounds from Houttuynia cordata have good binding affinities to peptidase-IV and sodium/glucose cotransporter 2 and can therefore be used as their inhibitors. However, isolation of these phytoconstituents and their in vivo activity will help give a better insight and will open a new area of investigation of individual components and their pharmacological potency.

Imaging ultra-weak UV light below 100 pW cm-2 using a 4H-SiC photodetector with an Al2O3 interfacial layer.

Weak light detection is crucial in various practical applications such as night vision systems, flame monitoring, and underwater operations. Decreasing the dark current of a photodetector can effectively mitigate noises, consequently enhancing the signal-to-noise ratio and overall weak light detection performance. Herein, we demonstrate a 4H-SiC UV photodetector capable of detecting extremely weak UV light. This device comprises a photosensitive layer of 4H-SiC, two TiN electrodes and an atomically thin Al2O3 interfacial layer between TiN and the C surface of 4H-SiC. Under 360 nm UV light illumination, the proposed Al2O3 device demonstrates an ultra-low dark current of 18 fA, possibly benefiting from the effective passivation of interfacial carriers, and a boosted photo-to-dark current ratio of 6.7 × 107. Consequently, it achieves a weak-light detection limit as low as 31.8 pW cm-2, significantly outperforming the control device lacking Al2O3. When compared to previously reported SiC photodetectors, our Al2O3 device boasts an exceptional large linear dynamic range of 172 dB. Leveraging this, we construct a photodetector array capable of clearly imaging an object under ultra-weak light illumination below the 100 pW cm-2 level. The proposed photodetector represents a significant advancement in the development of highly sensitive image sensors for weak light detection.

Transformation of the diamond surface with a thin iron coating during annealing and transport properties of the formed conductive layer

In our study, we annealed polycrystalline diamond films with nanometer-thick iron coatings. Based on analysis of X-ray photoelectron spectroscopy data the presence of two catalytic processes was suggested. One is the continuous absorption of sp3 carbon by iron nanoparticles with subsequent extrusion of the sp2 phase from the formed iron carbide, which leads to the creation of deep tracks into the diamond bulk that are filled with graphite stacks. The other process involves a thin layer of iron carbide on the surface and results in the creation of sp2 layers, which are made up of fused graphene-like patches and are oriented mainly along the surface of the diamond film. For the sample annealed at 800 °C for 1 h, the sp2 layers formed exhibit semi-metallic conductivity with quantum corrections caused by disorders. At the same time, no evidence of iron contribution in conductivity of the annealed Fe-coated film was detected, implying that upon transforming the diamond, iron moved quite deep into the bulk. In addition, the formed conductive layer on the diamond surface shows mechanical stability, ensuring the reproducibility of conductivity measurements even after six months of storage in air. The study has revealed the potential for targeted metal-assisted formation of sp2 carbon-based conducting pathways on diamond surfaces for electronic devices.

Impact of Buried Interface Texture on Compositional Stratification and Ion Migration in Perovskite Solar Cells

AbstractDespite the striking increase in the power conversion efficiency (PCE) of lead‐based perovskite solar cells (PSCs), their poor operational stability impedes their commercialization. Among the various factors that influence device stability, ion migration has been identified as a key driver of degradation. In this work, the focus is on studying ion migration‐induced degradation in inverted architecture PSCs, which employ either a thin polymer layer or a self‐assembled monolayer (SAM) for hole extraction. It is demonstrated that the difference in texture imposed by the use of these hole transport layers (HTL) is an important and thus far inconspicuous factor that impacts ion migration, and consequently device stability. By investigating the buried interface in detail, it is revealed that its texture has a strong impact on the vertical compositional stratification in the perovskite active layer. By monitoring bias‐induced ion migration in devices with different hole extraction layers, it is demonstrated that the smooth polymer‐based HTL results in a higher degree of ion migration than the rough SAM HTL, corresponding to a stronger degradation in the former. These results further indicate that the use of SAMs for hole extraction is a promising strategy to suppress ion migration and improve device efficiency.

Why Perovskite Thermal Stress is Unaffected by Thin Contact Layers

AbstractMetal halide perovskite photovoltaics have emerged as a high efficiency, low‐cost alternative that can potentially rival or enhance conventional silicon technology. Despite exceptional initial power conversion efficiencies, achieving compliance with international standards and widespread adoption requires further enhancements to their operational stability. Notably, addressing mechanical strain and stress in brittle perovskites has emerged as a pivotal approach to mitigate chemical degradation and improve reliability during thermal cycling. In this study, a popularized strain engineering strategy is investigated in which a high coefficient of thermal expansion (CTE) hole transport layer (i.e., PDCBT) is cast onto inorganic perovskite (CsPbI2Br) at 100 °C. Contrary to previously published results, the X‐ray diffraction (XRD):Sin2ψ and substrate curvature measurement techniques show that the hole transport layer has no discernible impact on perovskite strain. The accuracy of the XRD:Sin2ψ method for measuring strain is highlighted in contrast to an analysis based on shifts of single XRD peaks which can be influenced by multiple artifacts. The findings in this study are in accordance with mechanics theory: thin layers are unable to induce significant strain changes in perovskite thin films as the force they apply is negligible compared to that applied by a thick and stiff substrate.

The Effect of Different Ethanol Concentrations as The Extraction Solvent on Total Flavonoid Content of White Mulberry Leaves Extracts (Morus alba L.)

White mulberry leaves (Morus alba L.) contain flavonoid which empirically have many health benefits, such as reducing fever, relieving headaches and throats, coughs, dysentery, digestive disorders, flu, and according to research it has antioxidant activity. Many factors effect the total flavonoid content, one of which is the concentration of the extraction solvent. The purpose of the research was to determine the effect of different ethanol concentrations as the extraction solvent on total flavonoid content of white mulberry (Morus alba L.) leaves extract. White mulberry leaves (Morus alba L.) were extracted using the maceration method, the extract was tested for phytochemical screening and thin layer chromatography using chloroform: ethyl acetate (6: 4) as the eluent. The resulting spots were observed visually and with λ 254 nm and λ 366 nm UV light. Determination of flavonoid content by UV-Vis spectrophotometry using the AlCl3 colorimetric method at a maximum wavelength of 415 nm. The research results showed that the yield of 50% and 96% ethanol extract of white mulberry leaves (Morus alba L.) was 17.42 % and 11.04 %. Phytochemical screening showed that both extracts positively contained flavonoids. The presence of flavonoids was confirmed using a thin layer chromatography test, resulting in an average Rf value for 50% and 96% ethanol extracts are 0.71 and 0.70, close to quercetin Rf standard is 0,73 as comparison. The total flavonoid content obtained from the 50% ethanol extract was 36.0902 mgQE/g and the 96% ethanol extract was 56.4699 mgQE/g. The conclusions are the concentration of the extraction solvent effect the yield and total flavonoid content.

Cathode|Electrolyte Interface Engineering by a Hydrogel Polymer Electrolyte for a 3D Porous High-Voltage Cathode Material in a Quasi-Solid-State Zinc Metal Battery by In Situ Polymerization.

This work highlights the development of a superior cathode|electrolyte interface for the quasi solid-state rechargeable zinc metal battery (QSS-RZMB) by a novel hydrogel polymer electrolyte using an ultraviolet (UV) light-assisted in situ polymerization strategy. By integrating the cathode with a thin layer of the hydrogel polymer electrolyte, this technique produces an integrated interface that ensures quick Zn2+ ion conduction. The coexistence of nanowires for direct electron routes and the enhanced electrolyte ion infiltration and diffusion by the 3D porous flower structure with a wide open surface of the Zn-MnO electrode complements the interface formation during the in situ polymerization process. The QSS-RZMB configured with an integrated cathode (i-Zn-MnO) and the hydrogel polymer electrolyte (PHPZ-30) as the separator yields a comparable specific energy density of 214.14Whkg-1 with that of its liquid counterpart (240.38Whkg-1, 0.5MZn(CF3SO3)2 aqueous electrolyte). Other noteworthy features of the presented QSS-RZMB system include its superior cycle life of over 1000 charge-discharge cycles and 85% capacity retention with 99% coulombic efficiency at the current density of 1.0Ag-1, compared to only 60% capacity retention over 500 charge-discharge cycles displayed by the liquid-state system under the same operating conditions.

3D Domain Arrangement in van der Waals Ferroelectric α‐In2Se3

AbstractOne of the exceptional features of the van der Waals (vdW) ferroelectrics is the existence of stable polarization at a level of atomically thin monolayers. This ability to withstand a detrimental effect of the depolarization fields gives rise to complex domain configurations characterized, among others, by the presence of layered “antipolar” head‐to‐head (H‐H) or tail‐to‐tail (T‐T) dipole arrangements. In this study, tomographic piezoresponse force microscopy (TPFM) is employed to study the 3D polarization arrangement in vdW ferroelectric α‐In2Se3. Sequential removal of thin layers from the polar surface using the PFM tip reveals a complex 3D profile of the domain walls in the α‐In2Se3 crystals. Antiparallel domain layers stacked along the polar direction are also observed by PFM imaging of the non‐polar surfaces showing that H‐H and T‐T domain boundaries are commonly present in α‐In2Se3. Application of TPFM to the electrically written domains allows evaluation of their geometrical lateral‐to‐vertical size aspect ratio, which shows a strong prevalence for the sidewise expansion in comparison to the forward growth. Local I–V measurements reveal a strong polarization direction dependence of conductivity due to the modulation of the energy barrier height as corroborated by theoretical modeling.

Surface Reconstruction of La2CuO4 during the Electrochemical Reduction of Carbon Dioxide to Ethylene and Its Benefits for Enhanced Performance.

Electrochemical reduction (ECR) of CO2 to C2H4 has a potential key role in realizing the carbon neutral future, which ultimately relies on the availability of an efficient electrocatalyst that can exhibit a high Faradaic efficiency (FE) for C2H4 production and robust, long-term operational stability. Here, for the first time, we report that upon applying reductive potential and electrolyte to the benchmark La2CuO4 catalyst, surface reconstruction occurred, i.e., the appearance of a distinctive phase evolution process over time, which was successfully monitored using ex situ powder XRD and operando Mott-Schottky (M-S) measurements of La2CuO4 samples that were soaked into the electrolyte and subjected to CO2-ECR for different durations. At the end of such a reconstruction process, an outermost layer consisting of lanthanum carbonate, a thin outer layer made of an amorphous Cu+ material formed over the core bulk La2CuO4, as confirmed by various characterization techniques, which resulted in the redistribution of interfacial electrons and subsequent formation of electron-rich and electron-deficient interfaces. This contributed to the enhancement in FE for C2H4, reaching as much as 58.7%. Such surface reconstruction-induced electronic structure tuning gives new explanations for the superior catalytic performance of La2CuO4 perovskite and also provides a new pathway to advance CO2-ECR technology.

Direct shear behaviors of excavated clay reinforced with geocomposite drainage layer encapsulated in thin sand layers.

The objective of this study is to assess the effectiveness of a novel structure comprising a geocomposite drainage layer and a thin sand layer (GDL + sand) in mitigating the rapid dumping of excavated clay and its associated issues, such as landslides. Two sets of direct shear tests were conducted to investigate the influence of sand layer thickness and compaction degree on the interface shear behavior of the GDL + sand structure. As the sand layer thickness increased, both the interface shear strength and friction angle gradually increased, first more sharply and then at a slower rate toward stability, while the interface cohesion decreased gradually. The optimal sand layer thickness for achieving the most effective reinforcement in stabilizing the clay was identified as 10 mm. A higher sand layer compaction degree was found to result in increased interface shear strength, interface friction angle, and interface cohesion. Building on these findings, the reinforcing efficiency of the GDL + sand structure was investigated through mechanism analysis in comparison to that of a geogrid + sand structure and GDL structure as per the interface friction coefficient. The ranking of interface friction coefficients among the three structures emerged as: geogrid + sand > GDL + sand > GDL. These results suggests that the GDL + sand structure exhibits superior reinforcement efficiency compared to the GDL structure and offers better drainage efficiency than the geogrid + sand structure.

Observations and impact of char layer formation and loss for engineered timber

The char layer plays a critical role in the fire behaviour of engineered timber. Several chemical and physical processes can reduce char layer thickness and integrity. A series of experiments studied 12 cross-laminated timber (CLT) columns (130 × 790 × 125 mm WxHxD) exposed to combined thermal (20 kW/m2 or 50 kW/m2) and mechanical loading (39 kN, eccentric). Char loss from the surface lamella was observed and the impact of this on the thermal response of the timber studied. In all cases, unprotected CLT exhibited fall-off of charred pieces. Cracking, shrinkage and movement of char contributed significantly to the exposure of underlying timber sections to external heating. There was no direct correlation between char fall-off and the measured glue line temperature in this configuration. To enable comparison between CLT with and without char fall-off, a thin layer of glass fibre-reinforced polymer was added to the exposed surface of six samples which prevented all char fall-off. Retention of the char layer significantly decreased temperatures beneath the char layer, loss of section and burning duration compared to samples with char fall-off.

Solvent extraction of astatine by DIPE and attempt to identify the extracted species by thin layer chromatography

Solvent extraction of astatine by DIPE and attempt to identify the extracted species by thin layer chromatography

Pengaruh pemberian sampah organik terhadap pertumbuhan dan kandungan astaxanthin pada pupa black soldier fly (Hermetia illucens (Linnaeus))

Black soldier flies (Hermetia illucens (Linnaeus)) or BSF are insects that process organic waste, with larvae rich in nutrients and potential as an alternative protein source for food and feed. Astaxanthin, an antioxidant found in plants, algae, and crustaceans, is also assumed to be present in insects like BSF. This study examined the impact of feeding different organic wastes on BSF larval growth and astaxanthin content in its pupae. The experimental design involved four treatments: fruit and vegetable scraps (BS), tofu pulp (AT), rice leftovers (N), and a mix of fruit and vegetable scraps, tofu pulp and rice left-over (C), with animal feed T51 as control. Each treatment was repeated three times. Growth parameters of BSF such as weight, length, and larval characteristics, along with the chemical content of pupae, including astaxanthin, were measured. Pupae were extracted using a triphasic maceration method with n-heptane, ethyl acetate, acetonitrile, butanol-l, and distilled water. Compound identification was done using terpenoid qualitative tests, thin layer chromatography (TLC), and liquid chromatography-mass spectrometry (LC-MS). The findings revealed that fruit and vegetable scraps (BS) significantly increased larval body size, with a weight of 0.09 ± 0.04 grams/larvae and a length of 1.49 ± 0.31 cm/larvae. LC-MS analysis detected lutein derivatives, anisodamine, resveratrol derivatives, dehydroarginine, and astaxanthin derivatives with a molecular mass of 597.23 m/z in BSF larvae fed on fruit and vegetable scraps.

Maculopapillary Bundle Degeneration in Optic Neuropathies.

Degeneration of the maculopapillary bundle (MPB) is a prominent feature in a spectrum of optic neuropathies. MPB-selective degeneration is seen in specific conditions, such as nutritional and toxic optic neuropathies, Leber hereditary optic neuropathy (LHON), and dominant optic atrophy (DOA). Despite their distinct etiologies and clinical presentations, which encompass variations in age of incidence and monocular or binocular onset, these disorders share a core molecular mechanism: compromised mitochondrial homeostasis. This disruption is characterized by dysfunctions in mitochondrial metabolism, biogenesis, and protein synthesis. This article provides a comprehensive understanding of the MPB's role in optic neuropathies, emphasizing the importance of mitochondrial mechanisms in the pathogenesis of these conditions. Optical coherence tomography studies have characterized the retinal nerve fiber layer changes accompanying mitochondrial-affiliated optic neuropathies. Selective thinning of the temporal optic nerve head is preceded by thickening in early stages of these disorders which correlates with reductions in macular ganglion cell layer thinning and vascular atrophy. A recently proposed mechanism underpinning the selective atrophy of the MPB involves the positive feedback of reactive oxygen species generation as a common consequence of mitochondrial dysfunction. Additionally, new research has revealed that the MPB can undergo degeneration in the early stages of glaucoma, challenging the historically held belief that this area was not involved in this common optic neuropathy. A variety of anatomical risk factors influence the propensity of glaucomatous MPB degeneration, and cases present distinct patterns of ganglion cell degeneration that are distinct from those observed in mitochondria-associated diseases. This review synthesizes clinical and molecular research on primary MPB disorders, highlighting the commonalities and differences in their pathogenesis. 1.Temporal degeneration of optic nerve fibers accompanied by cecocentral scotoma is a hallmark of maculopapillary bundle (MPB) degeneration. 2.Mechanisms of MPB degeneration commonly implicate mitochondrial dysfunction. 3.Recent research challenges the traditional belief that the MPB is uninvolved in glaucoma by showing degeneration in the early stages of this common optic neuropathy, yet with features distinct from other MPB-selective neuropathies. 4.Reactive oxygen species generation is a mechanism linking mitochondrial mechanisms of MPB-selective optic neuropathies, but in-vivo and in-vitro studies are needed to validate this hypothesis.

Conjugated Microporous Polymers-Based Catalytic Membranes with Hierarchical Channels for High-Throughput Removal of Micropollutants.

Engineering a catalytic membrane capable of efficiently removing emerging organic microcontaminants under ultrahigh flux conditions is of significance for water purification. Herein, drawing inspiration from the functional attributes of lymphatic vessels involved in immunosurveillance and fluid transport with minimal energy consumption, a novel hierarchical porous catalytic membrane is engineered. This membrane, based on an innovative nitrogen-rich conjugated microporous polymer (polytripheneamine, PTPA), is synthesized using an electrospinning coupled in situ polymerization approach. The resulting bioinspired membrane with hierarchical channels comprises a thin layer (≈1.7µm) of crosslinked PTPA nanoparticles covering the interconnected electrospun nanofibers. This unique design creates an intrinsic microporous angstrom-confined system capable of activating peroxymonosulfate (PMS) to generate 98.7% singlet oxygen (1O2), enabling durable and highly efficient degradation of microcontaminants. Additionally, the presence of a thin layer of mesoporous structure between PTPA nanoparticles and macroporous channels within the interwoven nanofibers enhances mass transfer efficiency and facilitates high flux rates. Notably, the prepared hierarchical porous organic catalytic membrane demonstrates enduring high-efficiency degradation performance with a superior permeance (>95% and >2500 L m-2 h-1 bar-1) sustained over 100 h. This work introduces an innovative pathway for the design of high-performance catalytic membranes for the removal of emerging organic microcontaminants.

UV aging assessment of asphalt binder: influence of duration, zinc oxide, and aging condition

ABSTRACT Ultraviolet radiation penetrates the atmosphere resulting in photo-oxidative aging of asphalt. The conventional long-term aging method, such as pressure-aging vessel, ages the asphalt considering thermo-oxidative principle. However, asphalt undergoes predominantly photo-oxidative aging (POA) in field. Giving due importance to UV aging method will result in resilient asphalt, which can negate the impact of climate change on asphalt pavements to a certain extent. In this study, asphalt was aged using UV rays, considering different aging durations; 7, 14, and 21 days, aging temperature (room temperature and 60°C), and modification with zinc oxide nanoparticles (ZnO) as experimental factors. Further, thin asphalt layers were also subjected to natural aging by exposing them to atmosphere to develop equivalencies between laboratory and natural aging. The rheological studies indicated significant aging occurred in the laboratory in the first 7 days, followed by a decreased rate. The naturally-aged specimens depicted significant cracks after 1-, 3-, and 6-months of aging, which was relatively less in specimens with ZnO indicating its anti-POA properties. The carbonyl index was reduced by 30–75% with ZnO compared to binders without ZnO. Zero shear viscosity (ZSV) indicated that one-month naturally-aged asphalt with ZnO resulted in similar ZSV as PAV-aged binder with ZnO.

Enhancing microscale additive manufacturing: Electrolyte-column localized electrochemical deposition for microwire and microdevice substrate connection

Electrochemical deposition is a microscale additive manufacturing technology. Due to the excellent performance of electrodeposited coating layers which exhibit no thermal stress, low porosity, and minimal microcracks, electrodeposition has been used in the connections of microdevices to solve the problems of shrinkage and deformation of microparts caused by thermal stress generated by conventional connections. Due to the low efficiency of Meniscus-Confined electrodeposition, a novel connection process for microwires and microdevice substrate using electrolyte-column localized electrochemical deposition (ECL-ECD) is proposed. The connecting mechanism is determined through simulation and experimentation. Simulation results indicated that the current density in the connection area exhibited a Gaussian distribution and the deposition layer preferentially grew at the interface between the microwire and the substrate. A high-speed camera was used to observe the liquid beam throughout the experiment, the results indicated that the microwires didn’t affect the stability of the liquid beam, and the ECL-ECD had excellent domain fixation. Smooth and dense surfaces on the connection area of the microwire and substrate were obtained at a current density of 50–60 A/dm2. Performance testing results showed that the connection point has excellent corrosion resistance and electrical properties. When the deposition time was short, the microwire was detached from the deposition area due to relatively thin deposition layer thickness and the tensile strength was only 133.82 MPa during the tensile testing. When the appropriate deposition process parameters were chosen, the fracture occurred on the microwire under tensile load and the fracture strength was 198.84 MPa, which equals the tensile strength of the microwire and indicated that the connection point can provide sufficient strength. The experimental results demonstrated that ECL-ECD can provide an effective and reliable connection process for the microwires interconnection.

Extraction and Purification of Squalene from Virgin Olive Oil via Catalytic Transesterification and Molecular Distillation

Squalene, a highly valuable compound abundant in various natural sources, shows great potential in pharmaceutical, cosmetic, and nutraceutical applications. This research article outlines a comprehensive methodology for extracting and purifying squalene from virgin olive oil, a rich source of the compound. The extraction process begins with degumming, which involves heating the olive oil to 60-70°C to reduce viscosity, followed by the addition of 2-3% warm water to hydrate phospholipids. Food-grade phosphoric acid is then added to react with the phospholipids, forming precipitates. The mixture is stirred for 20-30 minutes and allowed to rest for an additional 20-30 minutes, enabling impurities to settle. The upper layer of degummed oil is separated via decantation or centrifugation and washed with warm water for pH adjustment. Next, transesterification is performed by mixing 100 ml of virgin olive oil with 25% methanol (w/w) and a catalyst (0.5% sodium methoxide or PTSA), and heating the mixture to 80-90°C under reflux for 1-2 hours. Following transesterification, the solvent and acetone are distilled out, and acetone precipitation is repeated 2-3 times to remove unsaponified matter, which is then filtered and evaporated. The concentrated oil undergoes molecular distillation at 180°C and 0.0033 bar pressure for 1 hour, yielding the distillate and residue for further analysis. Qualitative analysis using Thin Layer Chromatography (TLC) involves Merck TLC plates with silica gel 60 F254 and a hexane: chloroform (9:1) mobile phase. Spots are developed with a 10% HCl solution, confirming the presence of squalene with an RF value of 0.93. Quantitative analysis via High-Performance Thin-Layer Chromatography (HPTLC) employs Merck TLC plates with cyclohexane as the mobile phase and CAMAG at 254 nm and 366 nm wavelengths, revealing a squalene purity of 67% and a recovery rate of 69.8%. The initial purification through transesterification facilitated the conversion of ester groups, yielding squalene-rich fractions, while acetone precipitation effectively removed saponified matter. Molecular distillation further enhanced squalene purity. TLC analysis confirmed the qualitative presence of squalene, and HPTLC provided precise quantitative measurements. The obtained squalene purity of 67% significantly enriches the initial content in virgin olive oil, though further optimization could enhance purity and yield. Complementary techniques like GC-MS or HPLC could validate the purification process. This study presents an efficient, replicable procedure for extracting and purifying squalene from virgin olive oil, with significant implications for pharmaceutical, cosmetic, and nutraceutical industries. The findings support a sustainable and ethical shift towards vegetable-derived squalene, meeting market demands while ensuring high-quality production.