#X-ray Photoelectron Spectroscopy

[ajinkya-2012]

X-Ray Photoelectron Spectroscopy Market

[whats-in-a-sentence]

The investigators deposited atomically precise nanoribbons of graphene sheets in a chevron pattern onto a gold surface, as shown in figures 4.18a, b and used XPS to ensure that the graphene did not suffer any oxidation during this process. As shown in figure 4.18c, the carbon 1s peak has a chemical bonding environment characteristic of the absence of oxygen.

"Chemistry" 2e - Blackman, A., Bottle, S., Schmid, S., Mocerino, M., Wille, U.

[materialsscienceandengineering]

Neutralizing electronic inhomogeneity in cleaved bulk MoS₂

Molybdenum disulfide (MoS2) is a highly versatile material that can function, for example, as a gas sensor or as a photocatalyst in green hydrogen production. Although the understanding of a material usually starts from investigating its bulk crystalline form, for MoS2 much more studies have been devoted to mono and few layer nanosheets. The few studies conducted thus far show diverse and irreproducible results for the electronic properties of cleaved bulk MoS2 surfaces, highlighting the need for a more systematic study. Dr. Erika Giangrisostomi and her team at HZB carried out such a systematic study at the LowDosePES end-station of the BESSY II light source. They utilized X-ray photoelectron spectroscopy technique to map the core-level electron energies across extensive surface areas of MoS2 samples. Using this method, they were able to monitor the changes in the surface electronic properties after in-situ ultra-high-vacuum cleaving, annealing and exposure to atomic and molecular hydrogen.

Read more.

[edgetechindutries]

The difference between 3mol/5mol/8mol yttria-stabilized zirconia ceramics

Zirconium oxide is a widely used ceramic material. It has three phases with different structures, namely the monoclinic phase, tetragonal phase, and cubic phase. Different phase contents can have a greater influence on the performance of zirconia ceramic materials. At present, the most common yttrium-stabilized zirconia materials are yttrium-stabilized zirconia materials. Among them, 3Y-TZP (3% (molar fraction) Y2O3) material has the best mechanical properties. It is also the most commonly used type of zirconia ceramic material current and has broad application prospects in different industries, such as the chemical industry, machinery, etc. The performance of 3Y-TZP prepared by the different methods is quite different. To obtain zirconia ceramic materials with higher mechanical properties, the sintering temperature can be controlled, doped, etc. Adding additives can also change the grain size and phase composition of the material to a certain extent. The grain size and phase composition will have a significant effect on the physical properties of ceramic materials, so studying the influence of grain morphology and phase composition on ceramic materials is of great significance in exploring the overall improvement of the performance of zirconia materials.

1. Effect of yttrium content on relative density

The molar fraction of yttrium oxide corresponding to the maximum densification is 3%, and the relative density reaches 98.113%. Before the critical point, with the increase of yttrium oxide content, the density of the sample gradually increases and then gradually decreases after the boundary point. The relative density of the sintered body with a molar fraction of yttrium oxide of 3% is greater than that of other groups, indicating that Y2O3 can promote the densification of zirconia during sintering. This is because the radius of Y3+ (1.06A) is larger than the radius of Zr4+ (0.87A). When Y2O3 forms a substitutional solid solution with ZrO2, the lattice of the main crystal phase of ZrO2 is distorted, the defects increase, and it is convenient for the structural unit to move and promote sintering, thereby obtaining a higher density. When the yttrium oxide content exceeds the critical value, the role of Y2O3 in the zirconia matrix is ​​weakened, and excessive Y2O3 hinders the crystallization of zirconia during sintering, so the relative density gradually decreases. In addition, X-ray photoelectron spectroscopy (XPS) analysis shows that Y3+ is concentrated at the grain boundary, which will strongly hinder the movement of the grain boundary, prevent or delay the separation of pores from the grain boundary so that the densification process can continue in the later stage of sintering. When the yttrium oxide content is 3% (molar fraction), this effect is maximized. Therefore, at around 3% (molar fraction), the density of zirconia ceramic material reaches the maximum.

2. Effect of yttrium oxide content on mechanical properties of zirconia ceramics

With the increase of yttrium oxide molar fraction, the bending strength of zirconia ceramics increases rapidly, and the maximum strength value is obtained at a yttrium oxide content of 3% (molar fraction). When the yttrium oxide content is increased, the strength value no longer increases but gradually decreases.

With the increase of yttrium molar fraction, the hardness of zirconia ceramic material increases, and the hardness of the material reaches the maximum value at 3%. Then, with the increase of yttrium content, the hardness of zirconia gradually decreases.

When the yttrium content is 3% (molar fraction), the particle size of yttrium-stabilized zirconia is the smallest, and zirconia has a higher density. When the molar fraction of yttrium is 3%, a certain amount of elongated crystals appear in the microstructure of zirconia. The long crystals act as solidification bridges between the tiny zirconia particles and the bulk, which makes the zirconia material more tightly bonded and obtains a higher bonding strength. This is why the ceramic has a higher hardness when the yttrium content is 3%.

[realdrake]

Sustainable Biopolymer Membranes for Organic Solvent Nanofiltration: A Breakthrough in Green Technology

The increasing demand for sustainable alternatives to fossil-bas…

The increasing demand for sustainable alternatives to fossil-based polymer materials has led to the development of innovative biopolymer membranes for organic solvent nanofiltration (OSN). In a recent study, researchers have successfully fabricated interpenetrating biopolymer network (IPN) membranes from natural compounds, agarose and natural rubber latex, without the use of toxic cross-linking agents. This breakthrough technology offers a promising solution for the separation of molecular species in harsh organic media, benefiting various industries such as petrochemical, biorefining, paint, pharmaceutical, and food.

Key Features of the Biopolymer Membranes

The biopolymer membranes exhibit excellent solvent resistance and tunable molecular sieving, making them suitable for a wide range of applications. The membranes are biodegradable, ensuring an environmentally friendly end-of-life phase. The use of natural materials and water as a solvent during fabrication reduces the environmental impact of the production process. Additionally, the membranes demonstrate high mechanical strength, thermal stability, and resistance to fouling, making them suitable for long-term operation in harsh environments.

Fabrication and Characterization of the Membranes

The IPN membranes were fabricated by combining agarose and natural rubber latex through a self-assembly and self-cross-linking process. The morphology and chemical information of the membranes were characterized using various techniques, including scanning electron microscopy (SEM), atomic force microscopy (AFM), and nano-Fourier transform infrared (nano-FTIR) spectroscopy. The results revealed a textured dense microstructure with a water contact angle of 71° ± 1° and a roughness value of 138.75 nm. The membranes' surface chemistry was also analyzed using X-ray photoelectron spectroscopy (XPS), which showed a high concentration of hydroxyl and carboxyl groups, contributing to their hydrophilic nature.

Nanofiltration Performance and Biodegradability

The nanofiltration performance of the membranes was evaluated using a crossflow filtration system. The results showed a linear correlation between the pure solvent flux and the solubility parameter, indicating that the membranes can be used with optimum linear control over polar solvents. The membranes demonstrated long-term stability over 72 h of continuous crossflow nanofiltration at 20 bar. The biodegradability of the membranes was confirmed through enzymatic treatment, ensuring a sustainable end-of-life phase. The membranes' biodegradability was further evaluated using a soil burial test, which showed a significant reduction in membrane weight and molecular weight over a period of 6 months.

API Purification and Impurity Removal

The membranes were successfully used for the purification of an active pharmaceutical ingredient (API) and the removal of a carcinogenic impurity. The results showed that the membranes can effectively remove impurities below the threshold of toxicological concern, making them suitable for pharmaceutical applications. The membranes' ability to remove impurities was further evaluated using a range of analytical techniques, including high-performance liquid chromatography (HPLC) and mass spectrometry (MS).

Scalability and Industrial Applications

The scalability of the membrane fabrication process was evaluated using a pilot-scale setup. The results showed that the membranes can be fabricated on a large scale while maintaining their performance and properties. The membranes' potential for industrial applications was further evaluated through collaborations with industry partners, which showed promising results in the areas of petrochemical, biorefining, and pharmaceuticals.

The development of biopolymer membranes for OSN offers a sustainable solution for the separation of molecular species in harsh organic media. The use of natural materials, water as a solvent, and the biodegradability of the membranes reduce the environmental impact of the production process. The membranes' excellent solvent resistance, tunable molecular sieving, and long-term stability make them suitable for various industrial applications. This breakthrough technology has the potential to replace traditional fossil-based polymer materials, contributing to a more sustainable future.

[ajinkya-2012]

X-Ray Photoelectron Spectroscopy Market

[nidarsanafwr]

https://social.studentb.eu/read-blog/174753_x-ray-photoelectron-spectroscopy-market-size-overview-share-and-forecast-2031.html

X-ray photoelectron spectroscopy Market Size, Overview, Share and Forecast 2031

[dangerdust2]

Exposure to silica dust is one of the oldest known causes of pulmonary diseases, and is associated with a variety of occupations, such as construction, quarrying, and chemical industries.

While the inhalation of fine silica particles is a well-recognized risk factor for silicosis, several studies have reported an association between silica exposure and sarcoidosis or sarcoid-like granulomatous lung diseases.

According to the literature, silica exposure may also be a trigger for other conditions, including hypersensitivity pneumonitis (HP), lung cancer, tuberculosis, chronic obstructive pulmonary disease, and kidney disease.

A 44-year-old woman was admitted to hospital with end-stage renal failure, productive cough, and decreased exercise tolerance. She had owned nine cats, which resulted in long-term exposure (18 years) to silica-containing bentonite cat litter. 

X-ray photoelectron spectroscopy revealed the presence of silicon in the lung biopsy specimen, as well as in the patient’s cat litter.

The pulmonary condition was suggestive of sarcoid-like lung disease, rather than silicosis, sarcoidosis, or hypersensitivity pneumonitis, according to the clinicopathological findings.

Renal failure appeared to be a result of chronic hypercalcemia due to extrarenal calcitriol overproduction in activated alveolar macrophages.

Ultimately, the patient was diagnosed with sarcoid-like lung disease complicated by end-stage renal failure from exposure to bentonite cat litter.

We believe that our patient’s disease was a result of the chronic inhalation of bentonite dust, as we excluded other possible causes and observed a significant improvement after the causative agent had been removed.

[carbon-black-deri]

How is carbon black measured?

Carbon black is a versatile material used in a variety of industries, including rubber, plastics, coatings, inks, and more. To ensure its quality and suitability for specific applications, carbon black is measured using various parameters and techniques. In this article, we will take an in-depth look at the different methods used for carbon black measurement and provide a comprehensive guide to understanding this important aspect of carbon black analysis.

Particle size distribution:

One of the key measurements of carbon black is its particle size distribution. Particle size affects the performance and behavior of materials in different applications. There are various techniques for measuring particle size, such as laser diffraction, sedimentation, and microscopy. Laser diffraction is a popular method that uses scattered light to determine size distribution, while sedimentation involves measuring the sedimentation rate of particles. Microscopy allows detailed examination at the level of individual particles.

Specific surface area:

The surface area of carbon black significantly affects its properties, such as its ability to adsorb species, interact with other materials, and provide reinforcement. Traditionally, the BET (Brunauer-Emmett-Teller) method is used to measure specific surface area. The technique involves the adsorption of gas molecules onto the surface of carbon black and determining the amount of gas adsorbed. The higher the specific surface area, the more effective the carbon black is in many applications.

Structural and surface chemistry:

The structure and surface chemistry of carbon black play a crucial role in determining its performance. Morphological characteristics, such as aggregate size, shape and porosity, affect the dispersion and reinforcing capabilities of carbon black. Techniques such as transmission electron microscopy (TEM) and scanning electron microscopy (SEM) provide valuable insights into the structure and morphology of carbon black particles. Surface chemistry can be analyzed by techniques such as X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FTIR), which help identify the functional groups and surface features of carbon black.

Tint Strength and Chroma:

Tinting strength refers to the ability of carbon black to impart color or hue to a material. It is an important parameter for the ink, plastics and coatings industries. Tinting intensity can be measured by comparing the color intensity of a sample mixed with a standard reference material. Colorimetry is a precise method that uses color parameters such as Lab* values or CIE (International Commission on Illumination) color space coordinates to quantify the color properties of carbon black. These measurements are critical to maintaining consistency and meeting color specifications for various applications.

Rheological properties:

The rheological properties of carbon black, such as viscosity and flow behavior, are critical to its processing properties in the rubber and polymer industries. The Mooney viscosity test is commonly used to measure the viscosity of rubber compounds filled with carbon black. In addition, dynamic mechanical analysis (DMA) and rotational viscometry help determine the effect of carbon black on the viscoelastic behavior of the material.

Accurate measurement and characterization of carbon black is critical to ensuring its quality, performance and suitability for specific applications. Particle size distribution, specific surface area, structure and surface chemistry, tinting strength and rheological properties are key parameters used to measure and analyze carbon black. These measurements enable manufacturers and end users to select the appropriate carbon black grade based on their desired results.

If you want to know about high-quality carbon black products, please contact DERY for more information!

[josephscott2504]

The market is driven by factors such as rise in government initiatives to create awareness pertaining to contamination level in drugs & formulations coupled with R&D analysis is expected propel the market growth. Rise in government regulations and certifications emphasizing drug safety for various raw materials and formulation are expected to contribute to the X-Ray photoelectron spectroscopy industry in the forthcoming period. However, significant costs of set up for new market entrants are likely to create hindrances in the market growth in the forecast period up to 2025.

X-Ray photoelectron spectroscopy also termed as electron spectroscopy for chemical investigation is widely used to investigate chemical proportion of surfaces. The proliferated use of XPS in investigative laboratories across the globe acts as a problem solving capability of the technique. The capacity to discover the initial atomic layers to assign chemical states to the discovered atoms renders X-Ray photoelectron spectroscopy to be an optimal addition to any analytical theory.