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The purpose of this paper is to discuss the chemical characterization of failures and process materials for microelectronics assembly.

The analytical techniques used for chemical structures and compositions including Fourier transform infrared spectrometer (FTIR), scanning electron microscopy, and energy‐dispersive X‐ray spectroscopy are conducted.

The residues on the golden finger are identified to be the flux used in the assembly processes. Besides, the contaminants on the processed and incoming connector pins are verified to be polyamides (–CONH functional groups) from housing material's residue. Three liquid fluxes used in wave soldering are analyzed by their chemical structure. One flux showing the OH groups at 3430 cm⁻¹ indicates higher acid contents. This consists with the acidic values specified by the supplier. Also, the solder mask under study has ever appeared peeled‐off issue. The FTIR spectra results indicated 62.2 percent degree of curing while vendor's spec is above 70 percent.

The establishment of the Infrared spectra database for fluxes and process materials help determine the root cause of the contaminants to reduce re‐occurrence of similar problems and thus enhance the manufacturing capability. The infrared spectrophotometry technique can be used by professional original design manufacturing and/or electronics manufacturing service, providers to investigate board/component defects during product pilot run stage and volume production.

This study aims to identify the bioactive compounds in the Onion (Allium burdickii [A.B]) bulb using Raman and Fourier transform infrared spectroscopy (FTIR) spectroscopy. It assessed the extraction conditions of bioactive compounds from A.B. while evaluating the best extraction conditions.

The research opted for an experimental qualitative approach. It examined the extraction conditions of A.B., namely, temperature (°C), time (min) and mass-to-liquor ratio (M:R) using ultraviolet-visible spectrophotometry. Identification of bioactive compounds present in the dye was performed using Raman spectroscopy and the validation of the results was done by FTIR spectroscopy.

The study determined the best extraction conditions (time, temperature, M:R) for A.B bulb. The study confirmed the presence of bioactive compounds.

The limitation was quantification of bioactive compounds in A.B bulb.

The findings prove that the A.B. bulb can provide a sustainable source of bioactive compounds (functionalized compounds). The study provides suitable extraction conditions for A.B. and further elaborates on the techniques for identifying bioactive compounds in A.B. bulb extracts.

The study provides A.B. as a source of bioactive compounds and a clean dye for textile coloration.

To the best of the authors’ knowledge, there is no documented study on the qualitative analysis of bioactive compounds in A.B using Raman and FTIR. Therefore, the study fulfils the identified need to ascertain alternative procedures for the analysis of bioactive compounds.

To evaluate the competing reaction of isocyanate with cellulose and water which can provide direction for further studies on bonding and curing reactions of isocyanate with wood.

Two modern analytical techniques, Fourier transform infra‐red (FTIR) and X‐ray photoelectron spectroscopy (XPS), were used. The FTIR was used to identify the products of the reaction of phenyl isocyanate (PI) with alcohol, water, and cellulose; while the XPS was used to evaluate the proportions of isocyanate that reacted with water or cellulose when PI reacted with cellulose at different moisture contents (MCs), respectively.

Methods for the IR identifications of reaction results of PI with n‐propanol, water, and cellulose, in which the reactions of PI with water and PI with cellulose resulted in N,N′‐diphenylurea and carbamate, respectively, were developed. It was discovered that the extent of reaction of isocyanate and cellulose decreased with increasing cellulose MC, and 92.98 per cent isocyanate reacted with water when 9.78 per cent MC was reached. It was confirmed that the products of the PI reaction were distributed mainly on the surface of the cellulose particles.

The study only focused on the reaction of PI. However, the industrial isocyanates, e.g. methylene diphenyl diisocyanate (MDI), polymerized methylene diphenyl diisocyanate (p‐MDI) that have complexities in chemical structures and components, make analyses with FTIR and XPS impossible.

The paper provides some instructive information about the isocyanate reaction that will help understanding the characteristics of isocyanate and guiding the design of technology bonding isocyanate to fibre, wood, etc.

The application of FTIR and XPS for evaluating the reaction of isocyanate with cellulose having different MCs was novel and may be used as a reference for other relevant studies.

This paper aims to present the components' characterization and condition assessment of an important deteriorated Mamluk-illuminated paper manuscript housed in Al-Azhar Library, Egypt.

Different analytical techniques used in this study were the portable digital optical microscope, stereomicroscope, scanning electron microscope with EDX (SEM.EDX), portable X-ray fluorescence (pXRF), X-ray diffraction (XRD), pH measurement and Fourier transform infrared spectroscopy (FTIR).

The results obtained by different microscopes showed that the gilding in the surface of illuminated paper sheets was performed with gold leaves. Additionally, these microscopes revealed that the illuminated paper manuscript has different aspects of deterioration such as adhered dirt, staining, some micro-cracks, cracks and detachment of some parts in some illuminated areas. The results of elemental analysis by EDX, portable XRF and XRD analysis showed that the orange red pigment is red lead (Pb₃O₄), blue pigment is azurite (2CuCo₃.Cu (OH)₂), and the gold layer is has consisted of brass alloy (Cu-Zn) with a small amount of gold element (Au). The pH measurement stated that the historical paper in the acidity level. The ATR-FTIR analysis also revealed the oxidation of cellulose. Moreover, it was found from ATR-FTIR that Arabic gum was used as a binder for the pigments.

This study presents the important results of analytical methods used for condition assessment and identification of the components of an important Mamluk-illuminated paper manuscript, where these results referred that the studied paper manuscript had different aspects of deterioration. The conservation steps either conservation treatment or preventive conservation are urgently needed in future studies.

Three common glob top encapsulant materials, two epoxy‐based, and one silicone‐based, were characterized prior to temperature cycling using differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), dynamic mechanical spectroscopy (DMS), gas chromatograph‐mass spectrometry (GC‐MS), and Fourier transform infrared spectroscopy (FTIR). After cycling between ‐55 to +125°C, for 1,000 cycles, the same samples were again analysed using DMS and FTIR. For the epoxy‐based samples, the DMS results indicated that temperature cycling in a humid environment can seriously affect the physical and mechanical properties of these samples. FTIR data also indicated that the molecular changes in the epoxy‐based samples appeared quite extensive after cycling, indicating a high level of degradation on the molecular scale. On the other hand, the silicon‐based glob top appeared to have survived the temperature cycling quite well.

Gourd fibres (GF) are a natural biodegradable fibre material with excellent mechanical properties and high tensile strength. The use of natural fibres in composite materials has gained popularity in recent years due to their various advantages, including renewability, low cost, low density and biodegradability. Gourd fibre is one such natural fibre that has been identified as a potential reinforcement material for composites. However, it has low surface energy and hydrophobic nature, which makes it difficult to bond with matrix materials such as polyester. To overcome this problem, chemically adapted gourd fibre has been proposed as a solution. Chemical treatment is one of the most widely used methods to improve the properties of natural fibres. This research evaluates the feasibility and effectiveness of incorporating chemically adapted gourd fibre into polyester composites for industrial fabrication. The purpose of this study is to examine the application of chemically modified GF in the production of polyester composite engineering materials.

This work aims to evaluate the effectiveness of chemically adapted gourd fibre in improving the adhesion of gourd fibre with polyester resin in composite fabrication by varying the GF from 5 to 20 wt.%. The study involves the preparation of chemically treated gourd fibre through surface modification using sodium hydroxide (NaOH), permanganate (KMnO₄) and acetic acid (CH₃COOH) coupling agents. The mechanical properties of the modified fibre and composites were investigated. It was then characterized using scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR) to determine the changes in surface morphology and functional groups.

FTIR characterization showed that NaOH treatment caused cellulose depolymerization and caused a significant increase in the hydroxyl and carboxyl groups, showing improved surface functional groups; KMnO₄ treatment oxidized the fibre surface and caused the formation of surface oxide groups; and acetic acid treatment induced changes that primarily affected the ester and hydroxyl groups. SEM study showed that NaOH treatment changed the surface morphology of the gourd fibre, introduced voids and reduced hydrophilic tendencies. The tensile strength of the modified gourd fibres increased progressively as the concentration of the modification chemicals increased compared to the untreated fibres.

This work presents the designed composite with density, mechanical properties and microstructure, showing remarkable improvements in the engineering properties. An 181.5% improvement in tensile strength and a 56.63% increase in flexural strength were got over that of the unreinforced polyester. The findings from this work will contribute to the understanding of the potential of chemically adapted gourd fibre as a reinforcement material for composites and provide insights into the development of sustainable composite materials.

The purpose of this paper is to investigate the effect of thermal‐oxidative aging at 150°C on the mechanical properties of carbon fibre reinforced bismaleimide composites.

Composites specimens after thermo‐oxidative aging at 150°C for various times (up to 1,000 h) were investigated by scanning electron microscopy (SEM) for fracture morphology, Fourier transform infrared (FTIR) spectroscopy for chemical structures, and flexural strength test and inter‐laminar shear strength (ILSS) test for mechanical properties.

The results indicated that the mechanical properties of carbon fibre/BMI composites were affected significantly by testing temperature rather than by aging time. SEM results showed that the good adhesion of fibre and matrix resulted in the better mechanical properties. The composites showed lower flexural strength and ILSS at 150°C due to the viscoelastic behaviour of matrix resin. The FTIR spectra confirmed the decomposition of crosslinked maleimide occurred just on the surface of composites during various aging times.

Results indicated that carbon fibre/BMI composites had excellent heat resistance and aging resistance.

Due to their excellent thermal and mechanical properties, the carbon fibre/BMI composites show greater potential for their applications in some extreme fields such as aerospace and machine.

The paper investigates the relationships of the fracture morphologies of composites and chemical structures of matrix resin to the mechanical properties after thermo‐oxidative aging.

The mechanisms of the deblocking reaction of the polyurethane with blocking agent were investigated in detail relatively using thermogravimetric analysis (TGA), Fourier transform infrared spectrometry (FTIR) and X-ray photoelectron spectroscopy (XPS). This kind of method for polyurethane as the application of wood adhesives can provide the conditions of application and the main theoretical basis.

The blocking rate and latex particle size distribution were determined using the titrimetric analysis and the laser particle analysis, respectively. TGA, FTIR, XPS and differential scanning calorimetry were used to investigate the deblocking temperature and time of the blocked isocyanate in detail.

The results indicated that the blocking rate was approximately 97 per cent and the average particle size was 360 nm. The results of laser particle analysis have confirmed that the dispersivity of the blocked polyurethane emulsion was good. XPS results showed that the amount of –O = C-N-benzyl groups increased with an increasing deblocking temperature and subsequently reached equilibrium. In summary, the blocked isocyanate was deblocked at temperatures ranging from 50 to 90°C.

An important approach in future wood adhesive work would be to gain access to man-made board application data.

The paper provided some useful information about deblocking mechanisms of blocked polyurethane that would be helpful to guide applied practical applications as wood adhesive.

To promote China’s wood processing technology progress and solve the problem of shortage of the natural quality of wood is of important practical significance.

The paper is the first to use the XPS characterisation method to characterise deblocking polyurethane solution.

The purpose of this study is to extract and characterize a novel natural dye from the leaves of Lannea coromandelica and the extraction with finding ways of dyeing cotton fabric using three mordants.

The colouring agents were extracted from the leaves of Lannea coromandelica using an aqueous extraction method. The extract was characterized using analysis methods of pH, gas chromatography-mass spectrometry (GC-MS), Fourier transform infrared (FTIR), ultraviolet-visible (UV-vis) and cyclic voltammetry measurement. The extract was applied to cotton fabric samples using a non-mordant and three mordants under the two mordanting methods. The dyeing performance of the extracted colouring agent was evaluated using colour fastness properties, colour strength (K/S) and colour space (CIE Lab).

The aqueous dye extract showed reddish-brown colour, and its pH was 5.94. The GC-MS analysis revealed that the dye extract from the leaves of Lannea coromandelica contained active chemical compounds. The UV-vis and FTIR analyses found that groups influenced the reddish-brown colour of the dye extraction. The cyclic voltammetry measurements discovered the electrochemical properties of the dye extraction. The mordanted fabric samples showed better colour fastness properties than the non-mordanted fabric sample. The K/S and CIE Lab results indicate that the cotton fabric samples dyed with mordants showed more significant dye affinities than non-mordanted fabric samples.

Researchers have never discovered that the Lannea coromandelica leaf extract is a natural dye for cotton fabric dyeing. The findings of this study showed that natural dyes extracted from Lannea coromandelica leaf could be an efficient colouring agent for use in cotton fabric.

The purpose of this paper is to investigate the effects of the components of whey‐protein based aqueous polymer‐isocyanate (API) adhesives on the bond strength.

The bond test (according to the JIS K6806‐2003 standard), Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM) were used to characterise the whey‐protein based API adhesives with various formulations and processing technologies.

The good bond strength of the optimised whey‐protein based API adhesive was attributed to the formation of strong chemical bonds in the bondline and to the additions of polyisocyanate, polyvinyl alcohol (PVA) and nano‐CaCO₃ powder that improved adhesive cohesive strength by either chemical crosslinks or mechanical interlocking. The blending procedures of whey protein, PVA, polyvinyl acetate (PVAc) and p‐p‐MDI had great impacts on the performances of the whey‐protein based API adhesives.

SEM micrographs showed that the effects of blending processes on the bond strength, pot life and colour might be attributed to the particle size of hydrophobic p‐MDI droplet and p‐MDI distribution in the protein‐PVA matrix.

The study lays the foundations of the formulation design and the processing technology for preparing whey‐protein based API adhesives.

The effects of the components of whey‐protein based API adhesives and the effects of blending processes on the bond strength were investigated by means bond strength evaluation, FTIR and SEM analyses; whey protein is utilised successfully to prepare novel API adhesives for structural uses.