Lamellar Phase Research Articles

Microstructure and mechanical properties of Tip/GWZ723 composites adjusted by Tip/Mg laminate structure

In this work, the spherical Tip was introduced into Mg-7Gd-2Y–3Zn (GWZ723) alloy, the Tip/Mg laminar-like configuration was constructed by hot extrusion. The layers quantity and interlayer spacing were adjusted by Tip content. The effects of Tip/Mg laminar-like structure parameters on the microstructure, mechanical properties, work hardening and fracture behavior of Tip/GWZ723 composites were investigated. The results indicate that after extrusion, the Tip elongates along the extrusion direction (ED) and form Tip/Mg laminar-like configuration with the matrix. The Tip aspect ratio increases with the Tip content increases, resulting in a pronounced Tip/Mg laminar-like configuration. The addition of Tip promotes DRX, refines the grain size and promotes the precipitation of the lamellar 14H LPSO phase. The Tip/Mg laminar-like configuration induces the accumulation of high-density dislocations at the interface, thereby contributing to hetero-deformation induced (HDI) hardening, which improves the work hardening rate and dynamic recovery rate. With increasing of Tip content, the HDI hardening effect becomes more pronounced. The Tip/Mg laminar-like configuration facilitates strain redistribution, alleviates stress concentration, impacts crack initiation and inhibits crack propagation, enhancing the plasticity of the Tip/GWZ723 composites. At a Tip content of 15 vol%, the 15 vol%Tip/GWZ723 composite exhibits YS of 439 MPa, UTS of 477 MPa and EL of 3.3 %.

First Order Alignment Transition in an Interfaced Active Nematic Fluid.

We investigate experimentally the dynamic phase transition of a two-dimensional active nematic layer interfaced with a passive liquid crystal. Under a temperature ramp that leads to the transition of the passive liquid into a highly anisotropic lamellar smectic-A phase, and in the presence of a magnetic field, the coupled active nematic reorganizes its flow and orientational patterns from the turbulent into a quasilaminar regime aligned perpendicularly to the field. Remarkably, while the phase transition of the passive fluid is known to be continuous, or second order, our observations reveal intermittent dynamics of the order parameter and the coexistence of aligned and turbulent regions in the active nematic, a signature of discontinuous, or first order, phase transitions, similar to what is known to occur in relation to flocking in dry active matter. Our results suggest that alignment transitions in active systems are intrinsically discontinuous, regardless of the symmetry and momentum-damping mechanisms.

Photoinduced bidirectional mesophase transition in vesicles containing azobenzene amphiphiles.

The functionality and efficiency of proteins within a biological membrane are highly dependent on both the membrane lipid composition and the physiochemical properties of the solution. Lipid mesophases are directly influenced by changes in temperature, pH, water content or due to individual properties of single lipids such as photoswitchability. In this work, we were able to induce light- and temperature-driven mesophase transitions in a model membrane system containing a mixture of 1,2-dipalmitoyl-phosphatidylcholine phospholipids and azobenzene amphiphiles. We observed reversible and reproducible transitions between the lamellar and Pn3m cubic phase after illuminating the sample for 5 min with light of 365 and 455 nm wavelengths, respectively, to switch between the cis and trans states of the azobenzene N=N double bond. These light-controlled mesophase transitions were found for mixed complexes with up to 20% content of the photosensitive molecule and at temperatures below the gel-to-liquid crystalline phase transition temperature of 33°C. Our results demonstrate the potential to design bespoke model systems to study the response of membrane lipids and proteins upon changes in mesophase without altering the environment and thus provide a possible basis for drug delivery systems.

Synchronized Codelivery of Combination Chemotherapies Intratumorally Using a Lipidic Lyotropic Liquid Crystal System.

In this work, an injectable in situ depot-forming lipidic lyotropic liquid crystal (L3C) system is developed to codeliver a precisely synchronized combination of chemotherapeutics intratumorally. The developed L3C system is composed of amphiphilic lipids and surfactants, including monoolein, phosphatidylcholine, tocopherol acetate, and d-α-tocopherol polyethylene glycol 1000 succinate. Owing to its amphiphilic nature, the developed formulation can coaccommodate both hydrophobic and hydrophilic chemotherapeutic moieties simultaneously. The study presents a proof of concept by designing a combination chemotherapy regimen in vitro and demonstrating its in vivo translation using doxorubicin and paclitaxel as model hydrophilic and hydrophobic drug moieties, respectively. The synchronized combination of the two chemotherapeutics with maximum synergistic activity was identified, coloaded in the developed L3C system at predefined stoichiometric ratios, and evaluated for antitumor efficacy in the 4T1 breast tumor model in BALB/c mice. The drug-loaded L3C formulation is a low-viscosity injectable fluid with a lamellar phase that transforms into a hexagonal mesophase depot system upon intratumoral injection. The drug-loaded depot system locally provides sustained intratumoral delivery of the chemotherapeutics combination at their precisely synchronized ratio for over a period of one month. Results demonstrate that the exposure of the tumor to the precisely synchronized intratumoral chemotherapeutics combination via the developed L3C system resulted in significantly higher antitumor activity and reduced cardiotoxicity compared to the unsynchronized combination chemotherapy or the synchronized but uncoordinated drug delivery administered by a conventional intravenous route. These findings demonstrate the potential of the developed L3C system for achieving synchronized codelivery of the chemotherapeutics combination intratumorally and improving the efficacy of combination chemotherapy.

Numerical analysis of machinability and surface alterations in cryogenic machining of additively manufactured Ti6Al4V alloy

Metal additive manufacturing (AM) technology has been utilized in many industries including automotive, aerospace, and medical. AM Ti6Al4V (Ti64) alloy is highly noticed for production of medical instruments such as dental implants and the machining process is mostly needed during the production or post-processing of these components. Numerical model, as a powerful tool, can be efficiently used for analyzing the machining process. A customized model was employed using a user-written subroutine in this work to evaluate machinability and microstructural changes in cryogenic machining of AM Ti64 alloy. For this purpose, the microstructural changes were simulated as the new numerical outputs. The numerical results of cutting forces, temperature, nano-hardness, and alpha lamellae thickness (grain size) were successfully verified by corresponding experiments from literature. Then, the impact of tool geometry (including rake and clearance angles, cutting edge radius, and nose radius) on the machinability performance was examined. It was found that, the variation of clearance and rake angles were more effective on depth of the hardened layer compared to the other parameters. Thickness of alpha lamellae phase near the machined surface and depth of the affected layer by nano-hardness changes were changed from 0.9 to 1.58 µm, and from 18 to 40 µm, respectively. Overall, it was concluded that the variation of insert positioning made by tool holder (change in rake and clearance angles) was an effective parameter on the process outputs when machining AM Ti64 alloy.

Self-Assembly of Lamellae-in-Lamellae by Double-Tail Cationic Surfactants.

The molecular structures of surfactants play a pivotal role in influencing their self-assembly behaviors. In this work, using simulations and experiments, an unconventional hierarchically layered structure in the didodecyldimethylammonium bromide (DDAB)/water binary system: lamellae-in-lamellae is revealed, a new self-assembly structure in surfactant system. This self-assembly structure refers to a lamellar structure with a shorter periodic length (inner lamellae) embedded in a lamellar phase with a longer periodic length (outer lamellae). The normal vectors of these two lamellar regions orient perpendicularly. In addition, it is observed that this lamellar-in-lamellar phase disappears when the two tails of the cationic surfactants become longer. The formation of the lamellar-in-lamellar architecture arises from multiple interacting factors. The key element is that the short tails of the DDAB surfactants enhance hydrophilicity and rigidity, which facilitates the formation of the inner lamellae. Moreover, the lateral monolayer of the inner lamellae provides shielding from the water and prompts the formation of the outer lamellae. These findings indicate that molecular structures and flexibility can profoundly redirect the hierarchical self-assembly behaviors in amphiphilic systems. More broadly, this work presents a new strategy to deliberately program hierarchical nanomaterials by designing specific surfactant molecules to act as tunable scaffolds, reactors, andcarriers.

Optical and molecular features of negatively curved surfaces created by POPE lipids: A crucial role of the initial conditions

Membrane fusion is closely related to plasma membrane domains rich in cone-shaped phosphatidylethanolamine (PE) lipids that can reverse membrane curvature under certain conditions. The phase transition of PE-based lipid membranes from the lamellar fluid phase (Lα) to the inverse hexagonal phase (HII) is commonly taken as a general model in reconstructing the membrane fusion pathway, and whose structural features have been mostly described so far using structural and microscopic techniques. The aim of this paper is to decipher the optical and molecular features of Lβ → Lα and especially of Lα → HII transition of 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphoethanolamine (POPE) lipids at pH = 7.0 when they are initially prepared in the form of both multi- and unilamellar liposomes (MLVs and LUVs). The distinction between optical properties of MLS- and LUVs-derived HII phase, provided from turbidity-sensitive temperature-dependent UV–Vis spectra, was attributed to different formation mechanisms of HII phase. Most importantly, from FTIR spectroscopic data of POPE lipids in Lβ (15 °C), Lα (50 °C) and HII (85 °C) phases we identified the changes in molecular features of POPE lipids during phase transitions. Among the latter, by far the most significant is different hydration pattern of POPE lipids in MLVs- and LUVs-derived HII phase which extends from the polar-apolar interface all the way to the terminal amino group of the POPE lipid, along with the changes in the conformation of glycerol backbone as evidenced by the signature of α-methylene groups. Molecular dynamics simulations confirmed higher water penetration in HII phase and provided insight into hydrogen bonding patterns.

Impact of surfactant polydispersity on the phase and flow behavior in water: the case of Sodium Lauryl Ether Sulfate

This study delves into the impact of molecular polydispersity on the phase behavior of Sodium Lauryl Ether Sulfate (SLES) surfactant, aiming to deepen understanding of its implications for fundamental science and industrial applications. SLE3S is utilized as a model compound: a comprehensive characterization of molecular polydispersity is conducted using Gas Chromatography–Mass Spectrometry and Nuclear Magnetic Resonance spectroscopy, juxtaposing the findings with those for SLE1S.Our comprehensive investigative approach entails: (i) employing Time-Lapse dissolution experiments in microchannel geometries to observe the dissolution and phase transitions; (ii) utilizing polarized light microscopy, confocal microscopy, and Small Angle X-ray Scattering for microstructure identification assessments; (iii) conducting rheological evaluations at various concentrations and temperatures to determine their effects on the surfactant properties.The findings reveal that SLE3S, being more polydisperse, demonstrates complex phase behavior not observed in the less polydisperse SLE1S. Notably, SLE3S exhibits a unique concentration domain, corresponding to a concentration of about 60 %wt, where hexagonal (H), cubic, and lamellar (Lα) phases coexist, resulting in highly viscoelastic heterogeneous mixtures. This behavior is attributed to the local segregation of surfactant components with varying polarity, underscoring the crucial role of molecular polydispersity in the phase behavior of SLES surfactants.

The effects of substitution of yttrium for Ce-rich mischmetal on the mechanical properties and thermal conductivity of Mg–4Al–4Zn–4RE alloy

Mechanical properties and thermal conductivity are the key parameters for Mg alloys used as the structural components for heat dissipation, balancing good mechanical properties and high thermal conductivity is still a long-term challenge. Here, we investigated the influence of Y contents on the microstructure and mechanical properties of the as-cast Mg–4Al–4Zn–(4–x)RE–xY (x: 0, 1, 2, 3, 4 wt%), where RE was the Ce-rich misch metal. Compared with Mg–4Al–4Zn–4RE alloy, the strength and ductility were significantly enhanced due to the well-optimized microstructure by the suitable substitution of Y for Ce-rich RE. Especially, the ultimate tensile strength and elongation were significantly improved from 201 MPa to 244 MPa and 8.0% to 16.8%, respectively, when the Y content was increased from 0 to 3.0 wt%. Meanwhile, the thermal conductivity still kept a high level within the range of 84.2–89.6 W(m·K)−1. The significantly improved elongation was mainly attributed to the reduction and refinement of coarse lamellar Al11RE3 intermetallic phases with increasing Y contents. The as-cast Mg–4Al–4Zn–1RE–3Y alloy exhibited high performance with a combination of high tensile properties and good thermal conductivity.

Phospholipid Membrane Interactions of Model Ac-WL-X-LL-OH Peptides Investigated by Solid-State Nuclear Magnetic Resonance.

The role of aromatic amino acids in peripheral protein membrane binding has been reported to involve cation-π interactions with choline lipids. In this study, we have investigated the interactions of the model pentapeptide Ac-WL-X-LL-OH (where X = L, Y, F, or W) with the phospholipid membrane using solid-state NMR. The effect of guest residue X on the peptide-lipid interactome was complementary to the seminal report on the interfacial hydrophobicity scale by Wimley and White. We found that the phospholipids retained a lamellar phase in the presence of each of the peptides with an aromatic X residue, whereas the Leu peptide perturbed the bilayer to an extent where an additional isotropic phase was observed. The solid-state NMR 13C and 31P data provide additional information on the influence of these short peptides on the membrane that has not been previously reported. The magnitude of membrane perturbation was in the order of guest residue X = L > Y~F > W, which is consistent with the relative amino acid interfacial affinity reported by Wimley and White. Further work is, however, required to uncover the behavior of the peptide and localization in the membrane domain due to ambiguity of the 13C NMR data. We have launched efforts in this regard for the objective of better understanding the role of aromatic amino acids in peripheral membrane protein binding.

Electrochemical characteristic and microstructure of Ti-6Al-7Nb alloy by centrifugal casting for orthopedic implant based on ageing time variations

The alternative Ti-6Al-7Nb alloy has gained extensive progression due to its ability to eliminate the cytotoxicity of vanadium (V) in Ti-6Al-4V alloy for orthopedic implants. The production of titanium alloys by centrifugal casting shows significant potential to reduce costs. Heat treatment and aging can tailor the microstructure and improve the corrosion resistance of titanium alloys. This study examines the effects of various ageing times on the microstructure and corrosion resistance of a centrifugal cast Ti-6Al-7Nb alloy that has previously been heated and treated at a temperature of 1050 °C, and subsequently cooled to room temperature in argon atmosphere gas. Ageing was carried out at a temperature of 550 °C with variable times of 0, 4, 6, and 8 hours. The surface morphology, metal phase changes, and electrochemical characterization were tested using an optical microscope (OM), X-ray diffraction (XRD), potentiodynamic polarization (PDP), and electrochemical impedance spectroscopy (EIS). The basket-weave microstructure is formed where globularization occurs in some phases as ageing time increases. Increasing the FWHM α value is correlated with increasing the amount of α' martensite phase. As an ageing time enhances, the temperature might offer a greater driving constrain for the nucleation and expansion of the lamellar phase (α). Ageing of 8 hours has the lowest corrosion rate, 0.0023 mpy and highest corrosion resistance, 90457 Ω∙cm2, due to the partially bimodal structure and grain refinement with a smallest grain size of 327.87 µm. Tafel polarization results show that all passivated samples are stable in the Solution Body Fluid (SBF). This work can be used as a starting point for developing microstructural evolution in titanium alloys

Pressure-induced structural modifications of imogolite nanotubes and of their methylated analogues

Structural modifications of single-walled aluminosilicate clay nanotubes have been studied under hydrostatic pressure by in situ synchrotron X-ray scattering. Imogolite nanotubes (INT) of nominal composition (OH)3Al2O3SiOH, and methyl-modified imogolite nanotubes (m-INT), (OH)3Al2O3SiCH3, have hydrophilic and hydrophobic internal cavities, respectively. Nanotube chiralities also differ, with zigzag (INT) and armchair (m-INT) chirality. In this work, pressure-induced changes in nanotube morphology and atomic structure are studied as a function of chirality, affinity of the inner cavity, and the pressure-transmitting medium used. Radial deformation and collapse of nanotubes are evidenced below 3 GPa, followed by the formation of a lamellar phase at higher pressures. In the case of INT, the collapse pressure value depends on the pressure transmitting medium chosen. Axial compressibility is measured, and a pseudo Young's modulus Y is determined to be equal to ∼265 GPa for INT and below 80 GPa for m-INT, underpinning the role of nanotube chirality in mechanical properties.

The molecular arrangement of ceramides in the unit cell of the long periodicity phase of stratum corneum models shows a high adaptability to different ceramide head group structures

The stratum corneum (SC) lipid matrix, composed primarily of ceramides (CERs), cholesterol and free fatty acids (FFA), has an important role for the skin barrier function. The presence of the long periodicity phase (LPP), a unique lamellar phase, is characteristic for the SC. Insight into the lipid molecular arrangement within the LPP unit cell is imperative for understanding the relationship between the lipid subclasses and the skin barrier function. In this study, the impact of the CER head group structure on the lipid arrangement and barrier functionality was investigated using lipid models forming the LPP. The results demonstrate that the positions of CER N-(tetracosanoyl)-sphingosine (CER NS) and CER N-(tetracosanoyl)-phytosphingosine (CER NP), two essentials CER subclasses, are not influenced by the addition of another CER subclass (N-(tetracosanoyl)-dihydrosphingosine (CER NdS), N-(2R-hydroxy-tetracosanoyl)-sphingosine (CER AS) or D-(2R-hydroxy-tetracosanoyl)-phytosphingosine (CER AP)). However, differences are observed in the lipid organization and the hydrogen bonding network of the three different models. A similar localization of CER NP and CER NS is also observed in a more complex lipid model, with the CER subclass composition mimicking that of human SC. These studies show the adaptability and insensitivity of the LPP unit cell structure to changes in the lipid head group structures of the CER subclasses.

Phase Behavior and Rheological Properties of AES/CAPB/H2O Ternary System

Cleaning products are often formulated as mixtures of surfactants because the properties of surfactant mixtures are easier to adjust than those of a single surfactant. Therefore, it is of great significance to study the phase diagram of surfactant mixtures. In this paper, the phase behavior of the alkyl ethoxysulfate (AES)/cocamidopropyl betaine (CAPB)/H2O ternary system was investigated at room temperature using polarizing optical microscopy (POM) and small angle X-ray scattering (SAXS), and the identified phases of the samples with various compositions were used to construct the ternary phase diagram of the AES/CAPB/H2O system which contains normal micellar phase (L1), normal hexagonal phase (H1), lamella phase (Lα), and one transition region (L1 → H1). The viscosity distribution of the AES/CAPB/H2O system was determined by a Brookfield DV2T touch screen viscometer. In addition, the effects of the weight percentage of CAPB and salts on the viscosity and rheological properties of the AES/CAPB/H2O system were also investigated. This work not only enriches the phase diagram of surfactant systems, but also has important guiding significance for the design and development of cleaning products.

The influence of microstructural evolutions on electrochemical corrosion and passive behavior in precipitation-strengthened high-entropy alloys

Effects of microstructural evolutions on electrochemical corrosion properties and passive film characteristics of precipitation-strengthened (Ni2Co2FeCr)92Al4Nb4 high-entropy alloys (HEAs) were investigated in a saline environment. Compared with single-phase FCC alloys, the appearance of nano-sized L12 particles increases the metastable pitting activities and slightly reduces the pitting potential, while the lamellar D019 phase further deteriorates the localized corrosion resistance. The chemical composition and oxide state of passive films are closely related to the different precipitation scenarios. The corrosion morphologies of the single-phase and L12-strengthened alloys are dominated by pitting, whereas the intergranular corrosion (IGC) and intragranular dealloying-like corrosion occur in the D019-strengthened alloy.

Deformation mode and strengthening mechanism of Mg-Gd-Er-Zn-Zr alloy with different LPSO morphology

Figuring out the effects of LPSO morphology on the deformation mode and strengthening mechanism of Mg-RE alloys is helpful to improve their formability and mechanical properties. In this work, the Mg-8Gd-1Er-1Zn-0.6Zr (GEZ811) alloys with monolithic block LPSO (B-alloy) and lamellar LPSO (L-alloy) phase were respectively prepared by different heat treatment route. The effects of the monolithic LPSO morphology on deformation mode and strengthening mechanisms during high strain rate multidirectional forging (HSMDF) were analyzed. Results showed at the initial stage of HSMDF, twinning was the dominant deformation mode for B-alloy while non-basal slip was for L-alloy. With increasing forging pass, kink band of grains became primary for B-alloy, whereas kinking and breaking of the lamellar LPSO phase was dominant for L-alloy. The optimal UTS, YS and EL of the HSMDFed B-alloy and L-alloy at 12 P were 381.6 MPa, 324.1 MPa, and 8.8 %, and 358.4 MPa, 295.0 MPa, and 5.5 %, respectively. The difference in strength between B-alloy and L-alloy resulted primarily from the contribution of grain boundary strengthening and stacking fault strengthening, while the better plasticity of B-alloy was attributed to its lower deformation activation energy and the formed kink band of grains. Retaining the block LPSO phase as much as possible in the alloy before deformation is beneficial to enhancing the mechanical performance of Mg-RE alloys.

Microstructure evolution and properties of Mg-9Gd-0.8Al alloy with lamellar phase during extrusion at different temperatures

To clarify the evolution of lamellar phases in the initial microstructure of the Mg-9Gd-0.8Al alloy during the extrusion process and the effect of lamellar phases on the dynamic recrystallization of the extruded Mg alloy, the solid solution treated Mg-9Gd-0.8Al (SS10) alloy, was extruded at different temperatures (380, 400, and 450 °C). With the extrusion temperature increasing, the average size of dynamically recrystallized (DRXed) grains and the second phases decreases firstly and then increases. However, the volume fraction of DRXed grains shows an opposite trend, while the amount of the second phases consistently decreases. The as-extruded SS10 alloy demonstrates superior mechanical properties when extruded at 400 °C, with a yield strength (YS) of 240 MPa, ultimate tensile strength (UTS) of 298 MPa, and elongation (EL) of 19.3%. The alloy achieves enhanced strength through grain boundary strengthening, dislocation strengthening, and Orowan strengthening. Moreover, the presence of DRXed grains with a weak texture plays a significant role in the improvement of the ductility of the alloy.

Processing effects on bilayer structures formation and rheological behavior of softeners using cationic di(hydrogenated tallow)dimethylammonium chloride aqueous dispersions

AbstractThe use of softeners is essential for enhancing laundered fabrics and hair textures after washing. For these, products based on double‐tailed cationic surfactants are used to reduce friction and static electricity, resulting in softer and smoother fibers. These surfactants form lamellar phases in water, which can be turned into vesicles and other bilayer aggregates upon shearing, greatly impacting on the rheological properties of these formulations. This study aims at elucidating how some parameters of the formulation process impact bilayer structures formation and the product rheology, using di(hydrogenated tallow)dimethylammonium chloride (DHTDMAC) aqueous dispersions as model system. Small angle X‐ray scattering (SAXS) analyses revealed lamellar phases starting from 3% DHTDMAC, with a bilayer thickness of 1.90 ± 0.03 nm, indicating significant carbon chain interdigitation. At this concentration (3%), bilayers exhibited a repetition distance of 69 nm, unveiling a behavior close to the one predicted for infinite swelling, in which lamellar structures persisted even at high dilution. Temperature plays a significant role in the rheological behavior, with elevated temperatures favoring vesicle formation, resulting in reduced apparent viscosity due to lower resistance of vesicles to flow. Upon heating, differential scanning calorimetry (DSC) analyses revealed a transition from Lβ (gel) to Lα (fluid) structures between 28 and 41°C, which was further confirmed by X‐ray diffraction (XRD). Both structural and thermotropic features observed were discussed and compared to information reported for a high‐purity grade homologue of DHTDMAC, dioctadecyldimethylammonium chloride (DODAC) mixed with water. These findings deepen the understanding of fabric softener formulation and the impact of bilayer structures formation on their properties, and should be used to optimize new formulations, enhancing their overall performance and sensorial quality.

Stable and unstable tiling patterns formed by ABC miktoarm star triblock terpolymers of symmetric interactions

Several discrepancies exist among previous self-consistent field calculations of symmetrically interacting ABC miktoarm star triblock terpolymer melts. Here we address this issue by including all known tiling patterns, as well as several lamellar-type phases known to bound the regions in the parameter space occupied by these patterns. After carefully studying the effect of numerical parameters on the free-energy accuracy, the central region of the phase diagram is constructed in detail; both the (3.4.6.4) pattern and the three-dimensional phase of hierarchical-hexagonal lamellae are found to be stable for the first time. The energetic and entropic contributions to the free-energy density of several phases are analyzed and compared in detail to reveal their stability mechanisms, including the important (32.4.3.4) pattern. Comparisons to previous studies of the same model system are present throughout, with our results resolving the aforementioned discrepancies and providing a sound basis for future work to build upon. Published by the American Physical Society 2024

Crystallization behavior of monoglyceride oleogels: A comparison between a fully hydrogenated palm oil and a fully hydrogenated rapeseed oil based monoglycerides

AbstractFat polymorphism plays a crucial role in many fat‐rich food products (e.g., margarine, chocolate). Due to this, polymorphism of triglycerides is widely investigated. During the previous years, the interest of using monoglyceride oleogels to replace margarine is increasing due to its structure, reduced amount of saturated fatty acids, stability and application potential. However, polymorphism of monoglyceride oleogels is less investigated. This research shows the effect of the composition (C18:0 or C18:0 and C16:0), temperature (25°C–20°C–10°C) and production process (static or lab‐scale scraped surface heat exchanger) on the crystallization behavior of monoglyceride oleogels (MO) by using differential scanning calorimetry, (synchrotron) X‐ray scattering and polarized light microscopy. Based on time‐resolved synchrotron WAXS, it was found that the rapeseed oil based MO (MO‐C18) occurred in four different polymorphs. During crystallization, transitions from an inverse lamellar phase (Lα) toward sub‐α1 and sub‐α2 could be established. Upon storage, a polymorphic transition toward β occurred. For the palm oil based MO (MO‐C18/C16), only two polymorphs were found during crystallization (Lα, sub‐α), followed by a polymorphic transition to β upon storage. By applying high shear and cooling rates during the production of MO‐C18 (dynamic production), the polymorphic transition from sub‐α2 to β occurred much faster compared to the static production method. When comparing the dynamically produced MO‐C18 and MO‐C18/C16, the thickness of 1 lamella, the crystal nanoplatelet and the fat crystals were smaller for MO‐C18/C16. This research clearly illustrates that the composition and the applied crystallization conditions have an impact on the properties from nano‐ to microscale.Practical Application: This research illustrates the importance of engineering monoglycerides oleogels to obtain food products with an improved nutritional balance. Hereby, the manuscript focuses on the crystallization behavior of monoglyceride oleogels by changing the composition and the crystallization procedure. The acquired insights go beyond the state of the art. It was found that applying high cooling rates and high shear rates by using a lab‐scale scraped surface heat exchanger affected the crystallization behavior of monoglyceride oleogels. These are crucial experiments to verify the application potential of monoglyceride oleogels in the food industry. Moreover, different polymorphic transitions occurred for the two types of monoglycerides. This is the starting point to investigate the effect of polymorphism on a final food product in order to improve the nutritional balance in fat‐rich food products.