Microscopy Methods Research Articles

Temporal evolution of mechanical properties in PDMS: A comparative study of elastic modulus and relaxation time for storage in air and aqueous environment

Polydimethylsiloxane (PDMS) is a soft, biocompatible polymer extensively employed in biomedical research, notable for its tunable mechanical properties achieved through cross-linking. While many studies have assessed the mechanical properties of PDMS utilizing macroscopic and microscopic methods, these analyses are often limited to freshly prepared samples. However, the mechanical properties of PDMS can be expected to change during prolonged exposure to water or air, such as interface polymer chain loosening or surface hardening, which are critical considerations in applications like cell culture platforms or microfluidic devices. This paper presents a comprehensive 10-day investigation of the evolution of PDMS surface mechanical properties through AFM-based nano-indentation. We focused on the most commonly utilized crosslinker-to-base ratios of PDMS, 1:10 (r10) and 1:20 (r20), under conditions of air and deionized water storage. For r10 samples, a hardening process was detected, peaking at 2.12 ± 0.35 MPa within five days for those stored in air and 1.71 ± 0.16 MPa by the third day for those immersed in water. During indentation, the samples displayed multiple contact points, suggesting the formation of distinct regions with varying mechanical properties. In contrast, r20 samples exhibited better stability, with an observed elastic modulus averaging 0.62 ± 0.06 MPa for air-stored and 0.74 ± 0.06 MPa for water-stored samples. Relaxation experiments, interpreted via the General Maxwell Model featuring two distinct component responses, a relatively consistent fast response τ1 (on the order of 10−1 s), and a more variable, slower response τ2 (on the order of 10 s), throughout the study period. The identification of two distinct relaxation times suggests the involvement of two disparate material property regimes in the relaxation process, implying changes in the surface material composition at the interface with air/water. These variations in mechanical properties could significantly influence the long-term functionality of PDMS in various biomedical applications.

Using Thin Ultra-High-Molecular-Weight Polyethylene Coatings to Reduce Friction in Frost-Resistant Rubbers.

Frost-resistant rubbers retain their highly elastic properties over a wide temperature range. They are used in various friction units (e.g., seals), but their high friction coefficient and low wear resistance lead to the need for frequent replacement. In this paper, we propose applying thin (several hundred microns) UHMWPE coatings to formed rubber rings. The application technology depends on the required coating thickness. Friction tests of the coatings and pure UHMWPE were performed using the ball-on-disk (unidirectional sliding) scheme for various loads and velocities. In the experiments, the friction coefficients and temperatures near the contact area were determined. Friction tracks were studied using microscopy methods. The sliding contact of the ball and the two-layer material was modeled to obtain the dependences of the deformation component of friction on the sliding velocity for coatings of different thicknesses. UHMWPE is sensitive to frictional heating, so the thermal problem of determining the temperature in the contact area was also solved. It is shown that the minimum friction coefficient occurs for coatings with a thickness of 600 μm. At the same time, in the case of the 300 μm coating, the surface of the friction track is practically no different from the initial one. Thus, the studied combination of polymers provides antifrictional properties and wear resistance to the surface layer while maintaining the damping properties of rubber.

Block copolymer micelles stabilized Pickering emulsions in templating ultralight conducting PEDOT: PSS elastomeric aerogels

Amphiphilic copolymers poly(N-(2-methacryloylxy) ethyl pyrrolidone)-block-poly(2-(perfluorooctyl) ethyl methacrylate) (PNMPm-b-PFMAn) with similar m/n of about 10 preferred to form spherical micelles in water regardless of the molecular weight. These PNMPm-b-PFMAn micelles as Pickering emulsifiers commonly favored the formation of O/W Pickering emulsions in the cyclohexane/water systems, and the corresponding interfacial structures were characterized by the confocal laser scanning microscopy (CLSM) method. Moreover, high internal phase Pickering emulsions (HIPPEs) were formed at high volume ratio of oil/water (VO/VW), which were excellent templates in generating structurally well-defined 3D porous PEDOT:PSS aerogels with low density and high conductivity. It was noticed that the HIPPE-templated PEDOT:PSS aerogels were mainly composed of hierarchically connected nano-/micro-level fibers, which were significantly different from the randomly intertangled lamellar micro-belts of PEDOT:PSS aerogels prepared by the hydrogel method under the same conditions. In addition, the HIPPE-templated stretchable and compressible PEDOT:PSS aerogels showed wide strain-invariant resistance (SIR) range and remarkable cycling stability, which were far superior to the hydrogel ones.

An epitope imprinted electrochemical sensor for highly sensitive and selective determination of prostate-specific antigen.

Asimple method forhighly selective and sensitive prostate-specific antigen (PSA) detection using a molecularly imprinted electrochemical sensor ispresented. The sensor was developed through an epitope imprinted strategy combined with electrochemical measurement techniques. An epitope molecularly imprinted polymer (EMIP) film was constructed on a AuNPs-coated gold electrode surface through electropolymerization, utilizing the C-terminus epitope of PSA (KWIKDTIVANP) as the template molecular and o-phenylenediamine as the functional monomer. The characteristics of EMIP film were investigated by using a scanning electron microscope and electrochemical test methods, including electrochemical impedance spectroscopy and cyclic voltammetry. Key parameters such as electropolymerization cycles, elution and rebinding times, and the molar ratio of template molecular to functional monomer were systematically optimized. The sensor demonstrated a detection limit (LOD) of 0.31 fg/mL and exhibited an excellent linear response towards PSA concentration ranging from 1.0 fg/mL to 0.1 µg/mL. Furthermore, the EMIP sensor showed excellent selectivity against other biological macromolecules, such as bovine serum albumin, human serum albumin, alpha-fetoprotein, and carcinoembryonic antigen. With recoveriesbetween 95.89 and 106.04% for PSA detection in human serums theEMIP/AuNPs/AuE electrochemical sensor showed great potential in real sample analysis.

Structural features of skeletal muscle titin aggregates

Titin is a multidomain protein of striated and smooth muscles of vertebrates. The protein consists of repeating immunoglobulin-like (Ig) and fibronectin-like (FnIII) domains, which are β-sandwiches with a predominant β-structure, and also contains disordered regions. In this work, the methods of atomic force microscopy (AFM), X-ray diffraction and Fourier transform infrared spectroscopy were used to study the morphology and structure of aggregates of rabbit skeletal muscle titin obtained in two different solutions: 0.15 M glycine-KOH, pH 7.0 and 200 mM KCl, 10 mM imidazole, pH 7.0. According to AFM data, skeletal muscle titin formed amorphous aggregates of different morphology in the above two solutions. Amorphous aggregates of titin formed in a solution containing glycine consisted of much larger particles than aggregates of this protein formed in a solution containing KCl. The “KCl-aggregates” according to AFM data had the form of a “sponge”-like structure, while amorphous “glycine-aggregates” of titin formed “branching” structures. Spectrofluorometry revealed the ability of titin “glycine aggregates” to bind to the dye thioflavin T (TT), and X-ray diffraction revealed the presence of one of the elements of the amyloid cross β-structure, a reflection of ~4.6 Å, in these aggregates. These data indicate that the “glycine-aggregates” of titin are amyloid or amyloid-like. No similar structural features were found in titin “KCl-aggregates”; they also did not show the ability to bind to thioflavin T, indicating the non-amyloid nature of these titin aggregates. Fourier transform infrared spectroscopy revealed differences in the secondary structure of the two types of titin aggregates. The data obtained demonstrate the features of structural changes during the formation of intermolecular bonds between molecules of the giant titin protein during its aggregation. The data expand the understanding of the process of amyloid protein aggregation.

Temperature Studies of the LaMn2Si2 Intermetallide by the Raman Spectroscopy and Magnetic Force Microscopy Methods

Raman spectra of the LaMn2Si2 compound were obtained for the first time by Raman spectroscopy. The change of Raman spectral characteristics in the temperature range of 263–553 K was investigated. The high sensitivity of the Raman spectroscopy method to a change in the magnetic state caused by a temperature influence has been determined. A change in the spectral characteristics of the vibration mode of manganese atoms near the Curie and Neel temperatures has been revealed. The magnetic force microscopy technique was used to investigate the surface features of the LaMn2Si2 compound at room temperature. A change in the type of magnetic domain structure in LaMn2Si2 after cooling from 298 to 263 K has been found.

Forensic Discrimination of Various Subtypes of Regenerated Cellulose Fibers in Clothing Available on the Consumer Market

The discrimination of five subtypes of regenerated cellulose fibers, i.e., viscose, bamboo, lyocell, modal, and cupro, from both men’s and women’s clothing available on the prevalent apparel market was described. The examinations were conducted using optical microscopy (in transmitted white light and polarized light), scanning electron microscopy coupled with energy dispersive X-ray spectrometry (SEM–EDX), and Fourier Transform Infrared Spectroscopy (FTIR). The microscopic methods revealed characteristic features of the morphological structure of the examined fibers, enabling the identification of differences between the subtypes. As a result, the microscopic methods were found to be the most effective for identifying and distinguishing between the types of examined fibers. Although the FTIR technique did not allow for distinguishing between the fiber subcategories, it contributed to the enlargement of the IR spectra databases for regenerated cellulose fibers. Based on the findings, a general scheme of the procedure for identifying the tested fibers was proposed.

THIN AND ULTRATHIN STRUCTURE OF ENVELOPES OF STEPHANOSTOMUM BACCATUM (TREMATODA: ACANTHOCOLPIDAE) METACERCARIAE IN YELLOWFIN SOLE, LIMANDA ASPERA.

The structure of the envelopes (capsule and cyst) surrounding metacercariae of Stephanostomum baccatum (Nicoll, 1907) in the second intermediate host, the yellowfin sole Limanda aspera (Pallas 1814), is examined with the methods of light and transmission electron microscopy. The cyst, presumably formed by secretions of the metacercarial tegument, consists of 2 layers: the outer, very thin layer of an electron-dense, finely granular substance and the inner layer composed of loose material of a moderate electron density that includes dense bodies varying in size, shape, and localization. The capsule, formed by the host's cells, is also organized into 2 distinct layers. The inner layer of the capsule is loose, consisting of evenly spaced debris of degenerated cells and lipid droplets with inclusions of intact macrophages between them. The outer layer of the capsule consists of parallel rows of cells arranged around the parasite, with fibroblasts and macrophages being dominant types and granulocytes and lymphocytes found in smaller numbers. Aggregations of collagen fibers are located in narrow spaces between the cells. The number of lipid droplets in the outer layer is significantly smaller than in the inner layer. The capsules formed around the examined trematodes have several structural features that distinguish them from those of S. baccatum and Stephanostomum sp. metacercariae recovered from other fishes of the family Pleuronectidae. The major morphological features of such capsules are the lack of epithelioid or giant multinucleated cells and the presence of numerous lipid droplets. Investigating the structural details of the envelopes surrounding metacercariae in trematodes, as well as other helminths, contributes to our scientific understanding of parasite biology, which can, in turn, have broader implications for understanding host-parasite interactions and evolutionary biology.

Estimation of local variation in Young's modulus over a gold nanocontact using microscopic nanomechanical measurement method.

Nanoscale materials tend to have a single crystal domain, leading to not only size dependence but also orientation dependence of their mechanical properties. Recently, we developed a microscopic nanomechanical measurement method (MNMM), which enabled us to obtain equivalent spring constants (force gradients) of nanocontacts while observing their atomic structures by transmission electron microscopy (TEM). Therein, we evaluated Young's modulus based on a model that a newly introduced layer at the thinnest section of a nanocontact determined the change in the measured equivalent spring constant, and discussed their size dependence. However, this model is not general for other nanomaterials that do not exhibit the introduction of a new atomic layer while stretching. In this study, using MNMM, we propose a new analytical method to directly retrieve the local Young's modulus of nanomaterials by measuring initial lattice spacing and its displacement of a local region in the TEM image during the stretching of the nanocontact. This reveals the size dependence of local Young's modulus at various positions of the nanocontact at once. As a result, our estimated Young's modulus for a gold [111] nanocontact showed a size dependence similar to the one previously reported. This indicates that this analytical method benefits in revealing the mechanical properties of not only nanomaterials but also structurally heterogeneous materials such as high-entropy alloys.&#xD.

The Efficiency of Polyester-Polysulfone Membranes, Coated with Crosslinked PVA Layers, in the Water Desalination by Pervaporation.

Composite polymer membranes were obtained using the so-called dry phase inversion and were used for desalination of diluted saline water solutions by pervaporation (PV) method. The tests used a two-layer backing, porous, ultrafiltration commercial membrane (PS20), which consisted of a supporting polyester layer and an active polysulfone layer. The active layer of PV membranes was obtained in an aqueous environment, in the presence of a surfactant, by cross-linking a 5 wt.% aqueous solution of polyvinyl alcohol (PVA)-using various amounts of cross-linking substances: 50 wt.% aqueous solutions of glutaraldehyde (GA) or citric acid (CA) or a 40 wt.% aqueous solution of glyoxal. An ethylene glycol oligomer (PEG 200) was also used to prepare active layers on PV membranes. Witch its help a chemically cross-linked hydrogel with PVA and cross-linking reagents (CA or GA) was formed and used as an active layer. The manufactured PV membranes (PVA/PSf/PES) were used in the desalination of water with a salinity of 35‱, which corresponds to the average salinity of oceans. The pervaporation method was used to examine the efficiency (productivity and selectivity) of the desalination process. The PV was carried at a temperature of 60 °C and a feed flow rate of 60 dm3/h while the membrane area was 0.005 m2. The following characteristic parameters of the membranes were determined: thickness, hydrophilicity (based on contact angle measurements), density, degree of swelling and cross-linking density and compared with the analogous properties of the initial PS20 backing membrane. The physical microstructure of the cross-section of the membranes was analyzed using scanning electron microscopy (SEM) method.

Investigation of the aggregation behavior of rubber asphalt components induced by short-term Aging: A perspective from molecular dynamic simulations and microscopic tests

The distribution characteristics of different rubber asphalt components remain a subject of debate, particularly under the influence of asphalt short-term aging. This paper leverages the visualization advantages of molecular dynamics (MD) simulation and integrates them with microscopic testing methods to observe morphological variations and property changes in the aggregation of different components induced by short-term aging. Short-term aging of rubber asphalt is simulated using a thin-film oven test (TFOT). By conducting Fluorescence microscope (FM) and scanning electron microscope (SEM) tests, the aggregation behavior of components under changes in fluorescence phase and microstructure before and after short-term aging is revealed. MD simulation is employed to analyze the degree of aggregation between different components before and after short-term aging. SEM test results indicate that the structure becomes looser and forms distinct pits as the rubber asphalt ages. FM test results reveal that the particle size of rubber powder particles in aged rubber asphalt decreases and aggregates gradually. Concurrently, the asphalt phase in rubber asphalt becomes more uniform after aging. MD simulation results demonstrate significant aggregation between asphaltene-asphaltene molecules and asphaltene-rubber powder molecules in aged rubber asphalt. A higher degree of asphaltene aggregation leads to reduce asphalt penetration and increase softening point and viscosity. Furthermore, rubber powder molecular chains can inhibit “π-π stacking,” and “offset π-π stacking” of the asphaltene molecules. Therefore, the accumulation effect in aged rubber asphalt is mitigated compared with aged base asphalt. The research outcomes provided a foundation for further studies on the aging and rejuvenation of rubber asphalt.

Coevolution of non-pharmaceutical interventions and infectious disease spreading in age-structured populations

In the face of emerging major infectious diseases, non-pharmaceutical interventions (NPIs) such as mask-wearing are the primary means of disease control in the early stages due to the lack of effective pharmaceutical interventions. Yet the current understanding of the dynamic feedback loop between NPIs and infectious disease spreading remains limited. In this study, we proposed an asymmetrically coupled dynamic model of the coevolution of mask-wearing behaviour and infectious disease spreading in an age-structured population to describe the bidirectional relationship between NPIs such as mask-wearing and infectious disease spreading. A theoretical analysis framework was developed by extending the microscopic Markov chain method. To reflect the spreading process more realistically, we conducted numerical simulations from a mesoscopic perspective through an age-contact data-driven approach. Critical transition, multi-wave epidemics, multi-transitions, and mixed-phase transitions resulting from the coevolution of mask and disease are observed. The results highlight the critical role of NPIs in controlling disease spreading. The mask-wearing can effectively reduce the daily peak infection density and prevent large-scale outbreaks within a short period. However, it will also prolong the duration of the epidemic and cause the disease to exist in the population for a long time. There is a trade-off between the two. For certain diseases with specific spreading capabilities, pharmaceutical interventions such as vaccination, which can directly reduce the disease’s infectiousness, may result in more people being infected if NPIs are not implemented as early as possible. In addition, results from Anhui indicate that people aged 42 years are at high risk of being infected because of their large population base, which suggests that priority should be given to the prevention and control of this group.

Mitochondrial Structure, Dynamics, and Physiology: Light Microscopy to Disentangle the Network.

Mitochondria serve as energetic and signaling hubs of the cell: This function results from the complex interplay between their structure, function, dynamics, interactions, and molecular organization. The ability to observe and quantify these properties often represents the puzzle piece critical for deciphering the mechanisms behind mitochondrial function and dysfunction. Fluorescence microscopy addresses this critical need and has become increasingly powerful with the advent of superresolution methods and context-sensitive fluorescent probes. In this review, we delve into advanced light microscopy methods and analyses for studying mitochondrial ultrastructure, dynamics, and physiology, and highlight notable discoveries they enabled.

Synthesis and evaluation of an environmentally friendly phosphorus-free and nitrogen-free polymer as a scale and corrosion inhibitor

Polyepoxysuccinic acid (PESA) was modified by glycidyl (Gly) to obtain a phosphate-free and nitrogen-free polymer (Gly-PESA), and its scale and corrosion inhibition properties were studied.The effects of Gly-PESA concentration, calcium ion concentration and temperature to scale inhibition performance were studied by static scale inhibition method. The corrosion inhibition performance of Gly-PESA was studied by static weight-loss method. The morphology and structure of calcium scale and steel surface were characterized by spectroscopic and microscopic methods. The scale inhibition efficiency of Gly-PESA for CaCO3 and CaSO4 was 98.06% and 92.6%, respectively. Under the same experimental conditions, the scale inhibition effect of Gly-PESA was obviously better than that of PESA. Gly-PESA could effectively inhibit the growth of CaCO3 and CaSO4 crystals and cause their crystal lattice distortion or crystal dispersion. The corrosion inhibition efficiency of Gly-PESA for carbon steel was 78.17%. The adsorption of Gly-PESA on the surface of the steel test piece followed Langmuir adsorption isotherm, and formed a protective film, which increased the corrosion resistance of the steel test piece, thus effectively protecting the steel test piece. Therefore, Gly-PESA was a green scale and corrosion inhibitor, which solved the problem of environmental pollution.

Extrinsic and intrinsic drivers of prevalence and abundance of hard-bodied ticks (Acari: Ixodidae) in one-humped camel (Camelus dromedarius)

BackgroundTicks are ectoparasites and can be vectors of a wide range of pathogens, posing significant health risks to livestock. In the Sahara Desert of Algeria, particularly among one-humped camels (Camelus dromedarius), there is a need to better understand the factors influencing tick infestation patterns to improve livestock management and health outcomes. ObjectivesThis study aimed to investigate the prevalence, intensity, and abundance of hard-bodied ticks (Acari: Ixodidae) among dromedaries, examining both intrinsic factors (sex, age, coat color) and extrinsic variables (farming systems, vegetation types, climate zones, and elevation) that might influence tick infestation in this region. MethodsTicks were collected from 286 dromedaries across nine sites in the pre-Saharan regions of Algeria, with elevations ranging from 736 m to 980 m. The sampled camels, which ranged in age from 6 days to 21 years, were examined for tick infestations. The ticks were identified through macroscopic and microscopic methods, and their abundance was analyzed in relation to the camels' characteristics and environmental factors. Three breeding systems were recognized: extensive, intensive, and mixed. ResultsA total of 980 ticks were collected, with Hyalomma dromedarii Koch, 1844 being the most abundant species (553 specimens), followed by Hyalomma impeltatum Schulze & Schlottke, 1930 (393 specimens), and Hyalomma excavatum Koch, 1844 (34 specimens). H. dromedarii showed a preference for parasitizing brown-coated dromedaries and exhibited significantly higher infestation levels during spring (p < 0.001). No significant association was observed between tick infestation and the camels' age or sex (p > 0.05). However, the farming system had a significant impact on tick abundance, with extensive and mixed systems showing higher tick burdens compared to intensive systems (p < 0.01). Additionally, the vegetation type, climate zone, and foraging habitat elevation were found to significantly influence tick densities and prevalence. ConclusionThis study provides essential insights into the tick infestation dynamics in dromedaries in drylands of Algeria. It highlights the influence of coat color, seasonality, and farming practices on tick burden, with brown-coated camels being more susceptible during the spring. The findings underline the importance of considering both intrinsic and extrinsic factors when developing effective tick control strategies, especially for camels raised in extensive or mixed farming systems in diverse arid rangelands. Future research should expand the scope to cover other arid regions in North Africa for a comprehensive understanding of tick-host dynamics.

Towards atom counting from first moment STEM images: methodology and possibilities

Through a simulation-based study we develop a statistical model-based quantification method for atomic resolution first moment scanning transmission electron microscopy (STEM) images. This method uses the uniformly weighted least squares estimator to determine the unknown structure parameters of the images and to isolate contributions from individual atomic columns. In this way, a quantification of the projected potential per atomic column is achieved. Since the integrated projected potential of an atomic column scales linearly with the number of atoms it contains, it can serve as a basis for atom counting. The performance of atom counting from first moment STEM imaging is compared to that from traditional HAADF STEM in the presence of noise. Through this comparison, we demonstrate the advantage of first moment STEM images to attain more precise atom counts. Finally, we compare the integrated potential extracted from first-moment images of a wedge-shaped sample to those values from the bulk crystal. The excellent agreement found between these values proves the robustness of using bulk crystal simulations as a reference library. This enables atom counting for samples with different shapes by comparison with these library values.

POLCAM: instant molecular orientation microscopy for the life sciences

Current methods for single-molecule orientation localization microscopy (SMOLM) require optical setups and algorithms that can be prohibitively slow and complex, limiting widespread adoption for biological applications. We present POLCAM, a simplified SMOLM method based on polarized detection using a polarization camera, which can be easily implemented on any wide-field fluorescence microscope. To make polarization cameras compatible with single-molecule detection, we developed theory to minimize field-of-view errors, used simulations to optimize experimental design and developed a fast algorithm based on Stokes parameter estimation that can operate over 1,000-fold faster than the state of the art, enabling near-instant determination of molecular anisotropy. To aid in the adoption of POLCAM, we developed open-source image analysis software and a website detailing hardware installation and software use. To illustrate the potential of POLCAM in the life sciences, we applied our method to study α-synuclein fibrils, the actin cytoskeleton of mammalian cells, fibroblast-like cells and the plasma membrane of live human T cells.

Dysprosium-containing Cobalt Sulfide Nanoparticles as Anticancer Drug Carriers.

Among various materials designed for anticancer drug transport, sulfide nanoparticles are uniquely intriguing owing to their spectral characteristics. Exploration of newer nanoscale copper sulfide particles with dysprosium doping is reported herein. It leads to a change in the physicochemical properties of the sulfide nanoparticles and hence the difference in drug release and cytotoxicity. We intend to purport the suitably engineered cobalt sulfide and dysprosium-doped cobalt sulfide nanoparticles that are magnetic and NIR-absorbing, as drug delivery vehicles. The drug loading and release are based on the supramolecular drug complex formation on the surface of the nanoparticles. The nanomaterials are synthesized employing hydrothermal procedures, coated with a biocompatible poly-β-cyclodextrin, and characterized using the methods of diffractometry, microscopy, spectroscopy, thermogravimetry and magnetometry. The sustained drug release is investigated in vitro. 5-Fluorouracil is loaded in the nanocarriers. The empty and 5-fluorouracil-loaded nanocarriers are screened for their anti-breast cancer activity in vitro on MCF-7 cells. The size of the nanoparticles is below 10 nm. They show soft ferromagnetic characteristics. Further, they show broad NIR absorption bands extending up to 1200 nm, with the dysprosium-doped material displaying greater absorbance. The drug 5-fluorouracil is encapsulated in the nanocarriers and released sustainably, with the expulsion duration extending over 10 days. The IC50 of the blank and the drug-loaded cobalt sulfide are 16.24 ± 3.6 and 12.2 ± 2.6 μg mL-1, respectively. For the drug-loaded, dysprosium-doped nanocarrier, the IC50 value is 9.7 ± 0.3 μg mL-1. The ultrasmall nanoparticles possess a size suitable for drug delivery and are dispersed well in the aqueous medium. The release of the loaded 5-fluorouracil is slow and sustained. The anticancer activity of the drug-loaded nanocarrier shows an increase in efficacy, and the cytotoxicity is appreciable due to the controlled release. The nanocarriers show multi-functional characteristics, i.e., magnetic and NIR-absorbing, and are promising drug delivery agents.

Effects of heat input on microstructure evolution and corrosion resistance of underwater laser cladding high-strength low-alloy steel coating

The effects of heat input on the microstructure evolution and corrosion resistance of the high-strength low-alloy (HSLA) steel coating obtained by wire-feed underwater laser cladding were studied. Optical digital microscope, scanning electron microscope (SEM), energy dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD), transmission electron microscope (TEM), electron back-scattered diffraction (EBSD), electrochemical tests, laser microscope and other characterization methods were used. As the heat input increased, the smoothness of the underwater cladding coating improved, with little changes in elemental distribution and phase composition. However, the content of acicular ferrite increased, while the amounts of lath bainite, lath martensite, and granular bainite decreased. As the heat input increased from 0.4 to 0.55 kJ/mm, the grain size increased from 25.3 to 55.9 μm, the proportion of low-angle grain boundaries rose from 61.3 % to 69.1 %, and the texture intensity of the (110) crystal plane increased from 16.22 to 23.83. Meanwhile, the dislocation density decreased from 4.9 × 1014 to 4.1 × 1014 m−2. These changes enhanced the corrosion resistance of underwater coating. As the heat input increased from 0.4 to 0.55 kJ/mm, the corrosion current density decreased from 2.13 × 10−5 to 3.35 × 10−6 A/cm2, and the corrosion potential increased from −0.823 to −0.529 V. Additionally, the depth-to-width ratio of the corrosion pits decreased from 0.255 to 0.053. This study laid the foundation for high-quality in-situ underwater repairs of ships and submarines made of high-strength steel.

Studies on the pyrolysis and potential flame retardancy of low-substituted starch phosphates

Investigations on the pyrolysis and potential flame retardancy imparted by solvent-free and semi-dry phosphorylation of different starches using sodium orthophosphates were conducted. The samples – low-substituted starch phosphates (SP) with degrees of substitution DSP < 0.5 - were subjected to differential scanning calorimetry, thermogravimetry coupled with evolved gas analysis and pyrolysis – gas chromatography – mass spectrometry. The data obtained as well as features of charring residues examined using microscopic and spectroscopic methods were related to structural aspects of SP – analysed by means of various spectroscopic techniques - and compared with those of native starches. It was found that charring and polyphosphate formation and the thermal resistance of the solid SP residues increased significantly if the DSP was at least 0.1. Accordingly, the exothermal decomposition, the temperature-induced loss of mass and the decomposition rates of SP decreased distinctly compared to native starch. The activation temperatures of SP and the formation of low-molecular pyrolysis products including aliphatic, cyclic, and aromatic aldehydes and ketones as well as anhydrosugars decreased markedly, even at DSP < 0.1. The results confirm the potential flame-retardancy of SP achieved by flame-inhibiting effects, despite low phosphorylation degrees, in both the gas and condensed phases.