Shell Phase Research Articles

Oxidation-Induced Oxide Shell Rupture and Phase Separation in Eutectic Gallium-Indium Nanoparticles.

Eutectic gallium-indium (EGaIn), a room-temperature liquid metal, has garnered significant attention for its applications in soft electronics, multifunctional materials, energy engineering and drug delivery. A key factor influencing these diverse applications is the spontaneous formation of a native passivating oxide shell that not only encapsulates the liquid metal but also alters the properties from the bulk counterpart. Using environmental scanning transmission electron microscopy, we report in situ observations of the oxidation of EGaIn nanoparticles by ambient air under high-energy electron beam irradiation. Our findings demonstrate that uneven oxide shell growth, driven by inward diffusion of adsorbed O species, creates unbalanced stresses. This compels the liquid metal to deform toward regions with slower oxide growth, resulting in shell rupture and allowing the liquid metal core to flow out. This process initiates top-down self-similar replication of the core-shell liquid metal nanoparticles, causing larger particles to break down into smaller particles. Additionally, internal oxidation triggers phase separation within the liquid core, ultimately leading to the pulverization of the liquid metal into finer solid particles rich in indium. These mechanistic insights into the oxidation behavior of the liquid metal hold practical implications for leveraging this process to reconfigure EGaIn nanoparticles for various applications.

Unlocking thermal management capacity: Optimized organic-inorganic hybrid shell phase change microcapsules with controllable structure and enhanced conductivity

Microencapsulated phase change material (MPCM) stands as a strong candidate for temperature control of thermal management systems in broad fields like building construction. A novel design strategy for hybridized shell-based MPCM (HMPCM) containing methyl methacrylate (MMA) and silica was developed by the interfacial hydrolysis-condensation method, with characteristics of controllable structure and enhancement in the interaction between the polymer and inorganic thermal conductivity additives. Two hybridized shell structures, including a homogeneous structure and another unique porous cavity structure shaped like a foam, can be obtained by adjusting for preparation conditions. The results reveal that the thermal conductivity is significantly enhanced by hybridized shells compared to pure MMA shells, with a dramatic increment of 92.16 %. Therefore, a highly satisfactory microcapsule material characterized by superior thermal conductivity and energy storage efficiency exceeding 99.9 % was fabricated. The results of thermal cycling reliability assessments underscore the favorable attributes of microcapsules, encompassing stable charging/discharging behavior, exceptional phase change reversibility, and prompt thermal responsiveness. Moreover, the feasibility of microcapsules in building thermal management applications has been verified. The temperature difference of 10.3 °C between the matrix with and without microcapsules demonstrates the capability of HMPCMs to effectively regulate the temperature of the surrounding environment. Consequently, these newly developed HMPCMs reinforced by hybridized shells are promising thermoregulation materials for thermal management systems that await further applications.

Chitosan-based bilayer shell phase change nano-capsules with excellent anti-permeability for thermal regulation dressings

Nano-encapsulated phase change materials (NEPCMs) with appropriate phase change temperature range and excellent anti-permeability have significant application value in the field of thermal regulation dressings. In this study, NEPCMs were synthesized using the microemulsion polymerization method, with eutectic fatty acids (LA-SA) as the core material and poly(methyl methacrylate) (PMMA) as the shell material. Subsequently, using the electrostatic adsorption method, chitosan (CS) was successfully coated onto the outer surface of NEPCMs, resulting in the preparation of a novel bilayer shell nano-encapsulated phase change materials (BS-NEPCMs) for thermal regulation dressings. The impact of core/shell ratio, CS acid solution concentration and cross-linking agent content on capsule properties was investigated. It was found that BS-NEPCMs exhibited excellent cyclical stability and thermal stability. In particular, the CS shell layer provided excellent interfacial impermeability effects for the capsules, achieving an anti-permeability efficiency of 96.21 %. This not only helps address the problem of high leakage rates in single wall capsules, but also ensures that the capsules maintain high phase change enthalpies of 99.32 J/g and 96.38 J/g, respectively. The dressings based on BS-NEPCMs demonstrated good thermal regulation at 33–42 °C with maximum phase change enthalpies of 39.53 J/g and 34.08 J/g, respectively. Swelling and rheological analysis showed that the dressing exhibits a gel state, with a swelling ratio of 343 %, an elastic modulus of 15 kPa and a viscous modulus of 4 kPa. This study indicated that BS-NEPCMs hold significant promise for various applications in energy storage and body thermal regulation fields.

Role of (Pr20Nd80)60Tb15Cu15Ga10 intergranular addition on the magnetic properties of Nd-Fe-B sintered magnet

Intergranular addition using heavy rare earth (HRE) Dy/Tb containing alloys has been an effective way to modulate the microstructure and chemical distribution towards fabricating high-coercivity Nd-Fe-B sintered magnets. In this work, (Pr20Nd80)60Tb15Cu15Ga10 (at%) intergranular alloy powders were designed and introduced with dual purposes of forming Tb-rich matrix shell and antiferromagnetic RE6Fe13Ga grain boundary phase (GBP). With 3 wt% (Pr20Nd80)60Tb15Cu15Ga10 addition, the coercivity Hcj is significantly increased from 11.1 kOe to 17.9 kOe, accompanied with a high utilization efficiency of Tb (11.8 kOe/%) and a superior temperature coefficient of coercivity β(−0.531%/K). Microstructural analysis suggests that the improved wettability of grain boundary by (Pr20Nd80)60Tb15Cu15Ga10 addition is beneficial to form the Tb-rich matrix shell and antiferromagnetic RE6Fe13Ga GBP throughout the bulk magnets. Micromagnetic simulation is implemented to study the effect of formed ferromagnetic/antiferromagnetic GBP and Tb-rich matrix shell on the magnetization reversal process. Results show that the synergy of Tb-rich shell surrounding Nd/Pr-rich core and antiferromagnetic Nd/Pr-rich RE6Fe13Ga GBP is an effective way to promote the coercivity with high utilization efficiency of HRE Tb.

Enhancement of mechanical properties of NbCN-Ni cermets via WC addition

In this study, the microstructural and mechanical properties of sintered NbCN-Ni cermets with various WC contents were investigated. The density and grain size of the NbCN-Ni cermets increased with an increase in the sintering temperature from 1420 to 1510 °C, whereas after WC addition, the average grain size of NbCN decreased significantly. The added WC was initially dissolved in the binder phase and then dissolved in NbCN crystals and formed a white W-rich (Nb,W)CN shell phase and gray Nb-rich (Nb,W)CN core phase structure for WC contents up to 10 wt%. Meanwhile, the formation of the shell-core structure enabled the morphology of NbCN grains to gradually change from polygonal to spherical, which can be attributed to the high solubility of WC in the Ni binder. The hardness and transverse rupture strength (TRS) of the cermets first increased and then decreased with increasing sintering temperature and WC content. At a WC content of 10 wt% and sintering temperatures of 1480 and 1450 °C, the HV10 and TRS of the cermets reached maximum values of 1405 kg/mm2 and 1280 MPa, respectively. The friction coefficient of the NbCN-Ni cermets decreased from 0.7 to 0.55–0.6 after WC addition. Hence, the cermets exhibited excellent wear resistance because the introduction of WC decreased their friction coefficient and increased their hardness.

Construction of multifunctional interface engineering on Cu‐SSZ‐13@Ce‐MnOx/Mesoporous-silica catalyst for boosting activity, SO2 tolerance and hydrothermal stability

Although small pore Cu-SSZ-13 catalysts have been successful as commercial catalysts for controlling NOx emissions from mobile sources, the challenges of high light-off temperature, SO2 tolerance and hydrothermal stability still need to be addressed. Here, we synthesized a multifunctional core-shell catalyst with Cu-SSZ-13 as the core phase and Ce-MnOx supported Mesoporous-silica (Meso-SiO2) as the shell phase via self-assembly and impregnation. The core-shell catalyst exhibited excellent low-temperature activity, SO2 tolerance and hydrothermal stability compared to the Cu-SSZ-13. The Ce-MnOx species dispersed in the shell are found to enhance both the acidic and oxidative properties of the core-shell catalyst. More critically, these species can rapidly activate NO and oxidize it to NO2, which allows the NH3-SCR reaction on the core-shell catalyst to be initiated in the shell phase. Meanwhile, Ce-MnOx species can react preferentially with SO2 as sacrifice components, effectively avoiding the sulfur inactivation of the copper active sites. Furthermore, the hydrophobic Meso-SiO2 shell provides an important barrier for the core phase, which reduces the loss of active species, acid sites and framework Al of the aged core-shell catalyst and mitigates the collapse of the zeolite framework. This work provides a new strategy for the design of novel and efficient NH3-SCR catalysts.

Analysis on the effect of novel topological optimization fin structures considering eccentricity on the heat storage and release characteristics of shell and tube phase change heat accumulator

Shell and tube phase change accumulator (STPCA), as a common type of heat accumulator, can effectively solve the mismatching of time and space in solar thermal power generation by using phase change storage technology. However, the low thermal conductivity of phase change materials (PCMs) reduces its heat storage and release rate. To achieve a rapid latent heat energy storage and release, it needs to carefully modify the structure of STPCA. In the existing literature, insufficient attention has been given to simultaneously addressing the heat storage and release processes, while there is a scarcity of topological optimization methods employed in fin design. On one hand, it is difficult to find the optimal structure. On the other hand, the optimized structure is suitable for melting process but may not be suitable for solidification process. In this contribution, we initially integrated topological optimization and eccentricity to derive fin structures suitable for respective melting and solidification processes. Then, we compared and analyzed the effects of eccentricity and objective function on melting and solidification processes. Finally, we summarized the topology optimization process, objective function and eccentricity suitable for fast heat storage and release. The findings indicated that as the eccentricity increases, the rate of heat storage and release initially rises before subsequently declining. In this work, it is found that an eccentricity of 5 mm is the best. From the whole heat storage and release cycle, when the eccentricity is 5 mm, the objective function is the minimum temperature difference and the topological optimization fin structure calculated during solidification process shows the best heat storage and release performance. Compared with the topology optimization structure without eccentricity, the heat storage speed is increased by 36.43 %, and the heat release speed is increased by 15.53 %. The design law of the STPCA based on combined with the eccentricity influence and topology optimization method is summarized to help improve its heat storage and release performance.

Preparation of hydrated calcium silicate phase change microcapsules and its application of temperature regulation in deep-water natural gas hydrate layer cementing process

The effective hydration of cement at low temperatures is a critical factor affecting the sealing stability of the cement sheath. Effective hydration of cement slurry is typically accompanied by significant exotherm, and can cause the decomposition of natural gas hydrates, ultimately leading to gas migration and affecting cementing quality. To ensure effective hydration with low exothermic cement slurry, hydrated calcium silicate (C-S-H) shell phase change microcapsules (TDCSH) were prepared by oil-in-water emulsification with chemical precipitation. Compared with traditional phase change microcapsule with polymer shell, the rough C-S-H shell with large surface area improves the thermal conductive area of the microcapsules and their compatibility with the cement composition. Results showed that the TDCSH has a high phase change enthalpy of 169.9 J/g and 65.25% encapsulate efficiency compared to other inorganic shell materials. Furthermore, the addition of 3% TDCSH can reduce the hydration temperature of cement by 3.9°C and increase the compressive strength by 19.0% under the curing condition of 20°C. The mechanism of action of microcapsules in cement was analyzed. The results showed that the incorporation of TDCSH reduced the heat of hydration of cement while promoting the generation of more hydration products and increased the compressive strength of cement.

Fe2AlB2@FeAl layered double hydroxides with core-shell heterostructures for electromagnetic wave absorption

The rapid development of high-performance materials has garnered considerable attention in addressing electromagnetic pollution. The construction of core-shell heterostructures is an effective approach for regulating the electromagnetic parameters of absorbers. However, these heterostructures usually lack a direct channel for charge transport between the core phase and the adhesive shell phase. Herein, Fe2AlB2@FeAl-layered double hydroxides with core-shell heterostructures were prepared using a top-down approach. The tightly connected FeAl-LDHs nanosheets to the Fe2AlB2 parent phase improved electronic transport. Compared with raw Fe2AlB2, the spherical absorber with an embroidered structure demonstrated stronger reflection loss (-15.6 dB for Fe2AlB2, −58.6 dB for Fe2AlB2@FeAl-LDHs) and a broader effective absorption bandwidth (2.2 GHz for Fe2AlB2, 3.6 GHz for Fe2AlB2@FeAl-LDHs) due to the enhanced dielectric and magnetic losses. This study presents a practical method for designing new controllable core-shell heterostructures for electromagnetic wave-absorbing materials.

Fabrication of core-shell polyacrylate latex pressure sensitive adhesives modified by fluorinated monomer and film properties

In this work, a series of fluorinated core-shell polyacrylate latex pressure sensitive adhesives (PSAs) were successfully synthesized through monomer-starved seeded semi-continuous emulsion polymerization. Specifically, (meth)acrylate monomers were employed as the main materials, with dodecafluoroheptyl methacrylate (DFMA) were used as modified monomer. The impact of fluorine monomer DFMA on the resulting core-shell latex and PSA properties was thoroughly examined. FTIR analysis confirmed the successful incorporation of DFMA into the latex copolymer through emulsion polymerization. TEM images illustrated that the morphology of latex particles exhibit a distinct core-shell structure. The results also showed that with the addition of DFMA, the water absorption and water whitening of the latex films decreased, while the water contact angle and thermal stability are improved. Interestingly, the latex films with DFMA added to the shell phase exhibit a larger WCA value when compared to those with DFMA in the core phase, further confirmed by XPS results. Finally, the adhesive properties of the fluorinated core-shell acrylate PSA were evaluated. The results of shear strength and gel content demonstrate that the prepared PSA exhibits excellent cohesive properties. Thus, this work could present a feasible strategy for optimizing the comprehensive properties of acrylate latex PSAs.

Hierarchical nanoengineered emulsion with robust adhesion enables superior self-cleaning cotton fabrics

Self-cleaning treatment is of vital importance for the practical application of functional cotton fabrics. However, developing highly efficient, eco-friendly, and durable hydrophobic and oleophobic treatment agents still remains a great challenge. Herein, inspired by the design of the inorganic–organic nanonetwork, we successfully synthesized a novel core–shell structured emulsion of nano-SiO2/fluorine-silicon polyacrylate through semi-continuous emulsion polymerization. The introduction of long-chain alkyl methacrylate octadecyl ester within the shell phase results in a more organized arrangement of fluorine atoms on the surface of cotton fabrics, leading to a rapid reduction in the surface free energy of latex film. The sample is optimized with 20 wt% dodecafluoroheptyl methacrylate and 1 wt% SiO2. The nanoengineered emulsion exhibits strong adhesion and effectively transforms the hydrophilic cotton fabrics into hydrophobic (143.2°) and oleophobic (121.6°) materials. Besides, the self-cleaning characteristic can withstand 25 laundering cycles and 800 abrasion cycles with enhanced robustness. This work opens up a pathway to develop effective, green but long-lasting amphiphobic agents for functional fabrics and sustainable textiles.

Controlled construction of Co3S4@CoMoS yolk-shell sphere for efficient hydrodesulfurization promoted by hydrogen spillover effect

A yolk-shell structured Co3S4@CoMoS catalyst was prepared through Oswald ripening method and subsequently used for hydrodesulfurization (HDS) reaction. The shells, constructed from Co-promoted MoS2 nanosheets, possess abundant active sites and facilitate the adsorption of reactants through the development of pore channels. The MoS2 sheets are arranged in a staggered and convoluted manner, creating numerous defect sites. The shorter MoS2 slabs provide a wide distribution of reactive sites, ensuring efficient reactions. The Co3S4 species within the inner core acts as an auxiliary active phase, inducing the hydrogen spillover effect in the HDS system. This facilitates the transfer of active hydrogen species to the CoMoS shell, where both CoMoS and Co3S4 phases synergistically enhance the HDS reaction. The Co3S4@CoMoS catalyst achieved up to 99.2% dibenzothiophene (DBT) conversion and 94.9% 4,6-dimethyldibenzothiophene conversion at the lower dosage (30 mg). The structure-activity relationships between active phase and HDS activity were investigated via in-situ infrared spectroscopy and other characterizations as well as density functional theory calculations.

Study on preparation and activation enhancement effect of cold bonded multi-solid waste wrap-shell lightweight aggregates (SWSLAs) with low cement content

Cement production consumes large amounts of depleted resources and energy, and causes environmental pollution. In order to reduce cement consumption and realize the closed-loop recycling of solid waste, cold bonded solid waste wrap-shell lightweight aggregates (SWSLAs) with a sextuplet blended system composed of dredged sediments, mineral powder, steel slag, phosphogypsum, fly ash, and a minimal amount of cement were prepared. Through the single-factor experiment, the influences of the types and dosages of solid wastes in the nuclear phase of SWSLAs (SWSLAs-NP) and shell phase of SWSLAs (SWSLAs-SP) on the strength and water resistance were explored, and the optimum ratio was obtained. On this basis, the influence of the types and amounts of activators incorporated in SWSLAs on the physical properties of aggregates was studied, and the primary microstructure of the aggregate was characterized. Our results showed that the optimal ratio of solid waste in the SWSLAs-NP was: 40 wt% of dredged sediments, 24 wt% of mineral powder, 18 wt% of steel slag, and 18 wt% of phosphogypsum. The optimal weight ratio of cement and solid waste in the SWSLAs-SP was 5:95. The resulting aggregate had a bearing capacity of single grain of 73.83 N and a water-resistance coefficient of 0.67. After the above aggregates were treated with Na2SO4 (activator) at 2%, the bearing capacity and water-resistance coefficient of the aggregates increased by 47.00% and 11.94%, respectively. The performances were even better than that of the aggregate composed of100w cement in the shell phase. Microstructural observations demonstrated that the structure of the raw material was reconstructed under the action of Na2SO4, and the raw materials reacted with each other, and thus the densification of the aggregate and its core-shell interface structure was enhanced, which improved the comprehensive performance of the aggregate. This study represents a step toward efficient utilization of industrial solid wastes.

Thermal Storage Performance of a Shell and Tube Phase Change Heat Storage Unit with Different Thermophysical Parameters of the Phase Change Material

The thermal storage performance of shell and tube phase change heat storage units is greatly influenced by the thermophysical parameters of the phase change material (PCM). Therefore, we use numerical simulations to examine how the thermal storage capability of shell and tube phase change heat storage units is affected by thermophysical parameters such as specific heat capacity, thermal conductivity, and latent heat of phase change. The findings indicate that while the rate of temperature increase and the rate of the PCM melting both slow down as specific heat capacity increases, the overall heat storage increases. Within the specified range of parameters, the average rate of heat storage increases by approximately 4% for every 50% increase in specific heat capacity. The PCM’s rate of temperature rise slows down and its overall heat storage capacity rises throughout the middle stage of the phase change heat storage process as the latent heat of phase change grows. The average heat storage rate increases by approximately 6% and 22% for every 50% increase in latent heat and thermal conductivity, respectively. Notably, when the thermal conductivity is enhanced by a factor of 1.5, the average heat storage rate experiences an almost 50% increase. The thermal conductivity of the PCM has a negligible impact on total heat storage. The choice and use of the PCM in shell and tube phase change heat storage heat exchangers has a theoretical and empirical foundation thanks to this work.

Probing the magnetic domain interaction and magnetocapacitance in PVDF – (nickel–cobalt–manganese ferrite)@barium titanate core–shell flexible nanocomposites

In this paper, we report a facile method to synthesize Ni0.93Co0.02Mn0.05Fe1.95O4−δ (NCMF)@BaTiO3 (BT) core–shell nanoparticles, analysed the impact of the BT shell phase on the magnetic domain distribution and its interaction on the final properties of the composites.

Efficient thermal energy conversion and storage enabled by hybrid graphite nanoparticles/silica-encapsulated phase-change microcapsules

A novel graphite nanoparticles-decorated hybrid shell phase change microcapsule was developed, which exhibits enhanced thermophysical properties and efficient photothermal conversion performance, indicating great potential for application in DASCs.

Hydrodynamic characteristics of core/shell microdroplets formation: Map of the flow patterns in double-T microchannel

Liquid-liquid–liquid (L/L/L) flows in microchannels involving three-phase interactions are important in various chemical applications that entail liquid–liquid–liquid reactions. This work comprehensively investigates core (silicone oil)/shell (Polycaprolactone) microdroplet formation using a continuous third phase (distilled water) in a double T-junction microchannel with a diameter of 600 µm, employing Volume-of-Fluid (VOF) simulations and high-speed imaging experimental observation. Due to the satisfactory agreement between computational and experimental techniques, the theoretical flow patterns were identified and categorized into three distinct categories at various flow rates of three phases: core/shell dripping, core/shell slug, and core/shell jetting. The shell thickness increases as the ratio of shell to core phase velocity (ushell:ucore) increases. Based on the continuous phase Capillary number (Cac) and core and shell phases Weber number (Wecore,shell), a flow pattern map was generated that segregates the distinct flow patterns into different regions. When the flow of the core and shell phases fails to form a droplet due to the inertia of the continuous phase, a core/shell dripping/slug pattern is observed. The channel walls encompass the droplets that form in the slug pattern (2×10-5≤Cac≤5×10-4, 0<Weshell≤1.5×10-3, and 0<Wecore≤5×10-5) because the continuous phase has less inertia, whereas, in the dripping pattern (5.5×10-5≤Cac≤9×10-4, 7×10-5≤Weshell≤2.5×10-4, and 1×10-5≤Wecore≤7×10-5), the shell phase fluid is enclosed by the continuous phase. The transition from dripping to jetting (Cac≥0.5, 0<Weshell≤0.15, and 1×10-2≤Wecore≤8×10-2) occurs as the flow rate of a continuous fluid or shell fluid increases. A dimensionless correlation for shell thickness estimation with a 12 % tolerance was proposed with a core/shell/continuous phase's physical properties, surface tensions, and microdroplet size, using Buckingham's theory based on 200 CFD simulations. Additionally, the flow rate and viscosity substantially impact the internal fluid velocity and vorticity of core/shell microdroplets, whereas the influence of interfacial tension can be disregarded. This research lays the groundwork for future studies on mass transfer and reaction behaviors in liquid–liquid–liquid three-phase flow in double T-junction microchannels by exploring various hydrodynamic characteristics under different operating conditions for core/shell microdroplet formation.

Low-frequency magnetic fields potentiate plasma-modified magneto-electric nanoparticle drug loading for anticancer activity in vitro and in vivo

A multiferroic nanostructure of manganese ferrite barium-titanate called magneto-electric nanoparticles (MENs) was synthesized by a co-precipitation method. FTIR, Raman spectroscopy, TEM, and X-ray diffraction confirmed the presence of spinel core and perovskite shell phases with average crystallite sizes of 70–90 nm. Magnetic, optical, and magnetoelectrical properties of MENs were investigated using VSM, UV-Vis spectrophotometry, DLS, and EIS spectroscopy techniques. After pre-activation by low-pressure argon (Ar) plasma, the MENs were functionalized by a highly hydrophilic acrylic acid and Oxygen (AAc+O2) mixture to produce COOH and C=O-rich surfaces. The loading and release of doxorubicin hydrochloride (DOX) on MENs were investigated using UV-vis and fluorescence spectrophotometry under alternating low-frequency magnetic fields. Plasma treatment enabled drug-loading control by changing the particles’ roughness as physical adsorption and creating functional groups for chemical absorption. This led to reduced metabolic activity and cell adherences associated with elevated expression of pro-apoptotic genes (BCL-2, caspase 3) in 4T1 breast cancer cells in vitro exposed to alternating current magnetic field (ACMF) compared to MENs-DOX without field exposure. ACMF-potentiated anticancer effects of MENs were validated in vivo in tumor-bearing Balb/C mice. Altogether, our results suggest potentiated drug loading of MENs showing superior anticancer activity in vitro and in vivo when combined with ACMF.

The historical active episodes of the disks around γ Cassiopeiae (B0.5 IVe) and 59 Cygni (B1 IVe) revisited

The observations of all known major activity phases of the disks around the classical Be stars γ Cas and 59 Cyg with low-mass companions are comprehensively reviewed and purely qualitatively evaluated again, though taking advantage of new insights gained over the past 25 yr into the physics of Be disks. Both stars have exhibited activity cycles in the violet-to-red (V/R) flux ratio of emission lines with two peaks. This activity is indistinguishable from those of the vast majority of Be stars and so probably were caused by one-armed (m= 1) disk oscillations. The anomalous high-activity phases from 1932 to 1942 in γ Cas and between 1972 and 1976 in 59 Cyg were distinguished fromm= 1 density waves by large variations in the separations of pairs of emission peaks. In two consecutive cycles, shell phases during which the emission peaks were maximally separated alternated with single (blended) emission peaks. The amplitude in peak separation of more than a factor of two implies a high-amplitude variation in the disk aspect angle. When the peaks were blended and the disk was viewed closest to face-on, local maxima in visual brightness probably occurred inγCas, and the visibility of the stellar absorption lines was reduced, as is expected from increased free-bound emission into the line of sight (there is no time-resolved photometry for 59 Cyg from the event in the 1970s). In y Cas, the pre-event V/R variability (pre-event observations of 59 Cyg do not exist) was practically identical tom= 1 variability. In spite of the subsequent rapid rise in amplitude (up to ~4), the V/R variations connected smoothly in phase but may require an explanation involving the 3D structure of the disk. The phasing of single-peak and shell stages relative to the V/R activity was the same in both cycles ofγCas, whereas this is not clear for 59 Cyg. During both high-activity cycles ofγCas, but at different phases, transient additional pairs of emission lines appeared inγCas that were much sharper than the main ones and they also had different peak separations and V/R ratios. In the second instance, their velocities were up to ~+500 km s−1. The extremely rapid excitation of the activity phases and their short duration of only two cycles in both stars may indicate a resonant behavior of an unidentified nature. In both stars, the line emission was strongly developed at the onset of the high-activity phases but it basically disappeared at the end of them, and the disks may have been dynamically destroyed. The atypical disk variations were presumably triggered by enhanced interactions between a disk and companion star. In both systems, there seems to be less evidence for a mass-loss outburst than for a reduced mass-injection rate into the disk. The resulting lower viscous coupling between a disk and star would have facilitated the tilting of the disk.

Five‐Level Structural Hierarchy: Microfluidically Supported Synthesis of Core–Shell Microparticles Containing Nested Set of Dispersed Metal and Polymer Micro and Nanoparticles

AbstractThis study presents the development of a hierarchical design concept for the synthesis of multi‐scale polymer particles with up to five levels of organization. The synthesis of core–shell microparticles containing nested sets of dispersed metal and polymer micro‐ and nanoparticles is achieved through in situ photopolymerization using a double co‐axial capillaries microfluidic device. The flow rates of the carrier, shell, and core phases are optimized to control particle size and result in stable core–shell particles with well‐dispersed three‐level composites in the shell matrix. The robustness and reversibility of these core–shell particles are demonstrated through five cycles of drying and re‐swelling, showing that the size and structure of core–shell particles remain unchanged. Additionally, the permeability and mobility of dye molecules within the shell matrix are tested and showed that different molecular weight dyes have different penetration times. This study highlights the potential of microfluidics as a powerful tool for the controlled and precise synthesis of complex structured materials and demonstrates the versatility and potential of these core–shell particles for sensing applications as particle‐based surface‐enhanced Raman scattering (SERS).