Teflon Trough Research Articles

Langmuir–Blodgett films of magnetic nanowires

One-dimensional magnetic nanomaterials are scientifically interesting and of great importance due to their morphology-dependent properties. As a consequence of magnetic interactions between magnetic nanowires (MNWs) their bottom-up assembly remains a tough challenge. For the first time, using the Langmuir–Blodgett (LB) technique, we prepared two-dimensional (2D) large scale LB films of MNWs, which were synthesized by template directed electrodeposition method, on glass substrates. Using a plastic pipette, MNWs dispersed in chloroform were spread on the surface of the pure water subphase in a Teflon trough. After the stabilization of the monolayer, the Langmuir film was compressed and the surface pressure-area isotherm was recorded. By pulling up the substrate through the Langmuir film, mono- and bilayers of MNWs were deposited on the substrates at the target surface pressures of 10 mN/m and 15 mN/m. The surface pressure isotherm and field emission scanning electron microscope (FE-SEM) images showed that MNWs were successfully transformed onto the substrates. FESEM micrographs showed that the assembly of MNWs was different from that of metallic nanowires. Furthermore, the results showed that rotating the substrate by 90 degrees, after the deposition of the first layer, and then depositing the second layer on it does not lead to the creation of a hierarchical structure. These results open up new opportunities for the applications of magnetic nanomaterials in physical and chemical sensors, data-storage media and magnetic switching devices. Besides, this study affords fundamental insights into the formation of magnetic monolayers and multilayers.

Equilibrium of phosphatidylcholine-ergosterol in monolayers at the air-water interface

The purpose of this study was to investigate the interaction between phosphatidylcholine (PC) and ergosterol (ERG) in monolayers at the air–water interface. We measured the surface tension of pure and mixed lipid monolayers at 22 °C using the Langmuir method with a Teflon trough and Nima 9002 tensiometer. Surface tension values were used to calculate π-A isotherms and determine molecular surface areas.Interactions between PC and ERG caused significant deviation from the additivity rule. The theory described in this paper was used to determine a stability constant reflecting the area occupied by one molecule of the PC–ERG complex and the complex formation energy (Gibbs energy).

Complex formation equilibria between cholesterol and diosgenin analogues in monolayers determined by the Langmuir method.

The purpose of this study was to investigate the interaction between diosgenin analogues [DioA: diosgenin acetate (DAc) and (25R)-5α,6β-dihydroxyspirostan-3β-ol acetate (DSol)] and cholesterol (Ch) monolayers at the air/water interface. The surface tension of pure and mixed lipid monolayers at 22 °C was measured by using the Langmuir method with a Teflon trough and a Nima 9002 tensiometer. The surface tension values were used to calculate the π-A isotherms and to determine the molecular surface areas. The interactions between Ch and each DioA resulted in significant deviations from the additivity rule. The theory described in this work was used to determine the stability constants, the areas occupied by one molecule of Ch-DAc or Ch-DSol, and the complex formation energy (Gibbs free energy) values.

Para‐Xylene Ultra‐selective Zeolite MFI Membranes Fabricated from Nanosheet Monolayers at the Air–Water Interface

AbstractThe control of membrane morphology and microstructure is crucial to improve the separation performance of molecular‐sieve membranes. This can be enabled by making thin, dense, and uniform seed‐crystal coatings, which are then intergrown into continuous membranes. Herein, we show a novel and simple floating particle coating method can give closely packed monolayers of zeolite nanosheets on nonporous or porous supports. The zeolite nanosheet monolayer is formed at the air–water interface in a conical Teflon trough. As the water in the trough is drained, the monolayer is deposited on a support placed below. Membranes prepared by gel‐free secondary growth of the nanosheets deposited by this method show unprecedented ultra‐selective performance for separation of para‐ from ortho‐xylene (separation factor >10 000).

Para-Xylene Ultra-selective Zeolite MFI Membranes Fabricated from Nanosheet Monolayers at the Air-Water Interface.

The control of membrane morphology and microstructure is crucial to improve the separation performance of molecular-sieve membranes. This can be enabled by making thin, dense, and uniform seed-crystal coatings, which are then intergrown into continuous membranes. Herein, we show a novel and simple floating particle coating method can give closely packed monolayers of zeolite nanosheets on nonporous or porous supports. The zeolite nanosheet monolayer is formed at the air-water interface in a conical Teflon trough. As the water in the trough is drained, the monolayer is deposited on a support placed below. Membranes prepared by gel-free secondary growth of the nanosheets deposited by this method show unprecedented ultra-selective performance for separation of para- from ortho-xylene (separation factor >10 000).

The Equilibria of Diosgenin-Phosphatidylcholine and Diosgenin-Cholesterol in Monolayers at the Air/Water Interface.

Diosgenin (Dio) has shown many treatment properties, but the most important property is cytotoxic activity in cancer cells. In this study, we investigated monolayers of Dio, cholesterol (Ch), and phosphatidylcholine (PC) at the air/water interface. The measurements were carried with a Langmuir Teflon trough and a Nima 9000 tensiometer program. The surface tension values of pure and mixed monolayers were used to calculate π–A isotherms and determine molecular surface areas. We were able to demonstrate the formation of complexes between Dio and PC and Dio and Ch molecules also. We considered the equilibrium between individual components and the formed complexes. In addition, we established that diosgenin and the lipids formed highly stable 1:1 complexes.

Phosphatidylcholine-fatty Alcohols Equilibria in Monolayers at the Air/Water Interface.

Monolayers of phosphatidylcholine (PC), tetradecanol (TD), hexadecanol (HD), octadecanol (OD) and eicosanol (E) and their binary mixtures were investigated at the air/water interface. The surface tension values of pure and mixed monolayers were used to calculate π–A isotherms. The surface tension measurements were carried out at 22 °C using a Teflon trough and a Nima 9000 tensiometer. The interactions between phosphatidylcholine and fatty alcohols (tetradecanol, hexadecanol, octadecanol, eicosanol) result in significant deviations from the additivity rule. An equilibrium theory to describe the behavior of monolayer components at the air/water interface was developed in order to obtain the stability constants, Gibbs free energy values and areas occupied by one molecules of PC–TD, PC–HD, PC–OD and PC–E complexes. We considered the equilibrium between the individual components and the complex and established that phosphatidylcholine and fatty alcohols formed highly stable 1:1 complexes.

A Diy Langmuir trough Made with Adruino, LabVIEW, and 3D Printed Parts for Education and Research

Maker and DIY projects and resources have exploded in popularity and accessibility. We describe the development of a Langmuir trough system and accessories by undergraduates. LabVIEW provided the base user interface while Arduino micro-controllers were used as the interface electronics. We present a cost effective way to build a modular and disposable Teflon trough. We demonstrate that Arduino and LabVIEW interface effectively. Using a home built 3D computer-controlled router we are able to build barriers and other necessary elements. Additionally, students have designed and assembled several accessories including an automatic cleaning and deposition system. These engineering systems have been incorporated into both curriculum and research in the Biophysics lab at Augsburg College. The development of this system introduces students otherwise pursuing physics and mechanical engineering careers to research questions and challenges at the cutting edge of biophysics and materials science.

The Equilibria Between Monovalent Ions and Phosphatidylcholine Monolayer at the Air/Water Interface

The effect of monovalent ion (Li+, Na+, Cs+) interaction with monolayers of phosphatidylcholine (lecithin, PC) was investigated at the air/water interface. We present surface tension measurements of lipid monolayers obtained using a Langmuir method as a function of monovalent ion concentration. Measurements were carried out at 22 °C using a Teflon trough and a Nima 9000 tensiometer. Interactions between lecithin and monovalent ions result in significant deviations from the additivity rule. An equilibrium theory to describe the behavior of monolayer components at the air/water interface was developed in order to obtain the stability constants and area occupied by one molecule of PC–monovalent ion complexes (PC−Me+).

Phosphatidylcholine — Mg2+ equilibria in a monolayer at the air/water interface

Abstract Abstract The interaction between Mg2+ and a phosphatidylcholine (lecithin, L) monolayer at the air/water interface was investigated. Surface tension measurements (Langmuir method) of phosphatidylcholine monolayers as a function of Mg2+ concentration were carried out at 22°C using a Teflon trough and a Nima 9000 tensiometer. Interactions between phosphatidylcholine and Mg2+ result in significant deviations from additivity. An equilibrium theory was developed to obtain the stability constants and areas occupied by one molecule of LMg+ and L2Mg. The stability constants were K 1 = 9.95×102 m2 mol−1 and K 2 = 3.87×104 m2 mol−1. The area occupied by LMg+ is 77 Å2 molecule−1, while that occupied by L2Mg is 109 Å2 molecule−1. The Gibbs free energies of complexation for LMg+ and L2Mg are −16.91 ± 0.51 and −25.88 ± 0.76 kJ mol−1. Graphical abstract

The Equilibria of Sphingolipid-Cholesterol and Sphingolipid–Sphingolipid in Monolayers at the Air–Water Interface

Monolayers of sphingomyelin (SM), ceramide (Cer) and cholesterol (Ch) and binary mixtures SM–Ch, SM–Cer and Cer–Ch were investigated at the air–water interface. SM, Cer and Ch were used in the experiment. The surface tension values of pure and mixed monolayers were used to calculate π-A isotherms. Surface tension measurements were carried out at 22 °C using a Teflon trough and a Nima 9000 tensiometer. Interactions between sphingolipid and Ch as well as sphingolipid and another sphingolipid result in significant deviations from the additivity rule. An equilibrium theory to describe the behavior of monolayer components at the air–water interface was developed in order to obtain the stability constants and Gibbs free energy values of SM–Ch, SM–Cer and Cer–Ch complexes. We considered the equilibrium between the individual components and the complex and established that sphingolipid and Ch as well as sphingolipid and another sphingolipid formed highly stable 1:1 complexes.

Observation of Nanoparticle-Enhanced Marangoni Transport near a Freezing Out Front

We report observation of an unusual nanoparticle (NP)-enhanced Marangoni flow near the melting point of a dodecanethiol ligated Au NP–octadecane solution. A thermal gradient (0.74 °C/cm) is applied to a thin film of this NP–octadecane mixture in an open Teflon trough parallel to the liquid–vapor surface. Half the mixture is frozen, and the other half is liquid. Over a period of many hours, thermal and solutal Marangoni flow transports the liquid in the direction of the solidified mixture where a “mountain” of this material builds up over time at the liquid–solid boundary due to the presence of this liquid flow. Small quantities of NPs in the bulk solution (NP volume fractions of ∼10–5) enhance this Marangoni flow by upward of factors of 4 relative to pure octadecane. We believe that this effect is due to the freezing out of NPs (relative to the liquid octadecane) within a thin liquid film that flows over the solidified NP–octadecane mixture; this freezing out of NPs within the thin film creates a large NP...

The Equilibria of Lipid–K+ Ions in Monolayer at the Air/Water Interface

The effect of K+ ion interaction with monolayers of phosphatidylcholine (lecithin, PC) or cholesterol (Ch) was investigated at the air/water interface. We present surface tension measurements of lipid monolayers obtained using a Langmuir method as a function of K+ ion concentration. Measurements were carried out at 22°C using a Teflon trough and a Nima 9000 tensiometer. Interactions between lecithin and K+ ions or Ch and K+ ions result in significant deviations from the additivity rule. An equilibrium theory to describe the behavior of monolayer components at the air/water interface was developed in order to obtain the stability constants and area occupied by one molecule of lipid–K+ ion complex (LK+). The stability constants for lecithin–K+ ion (PCK+) complex, K_{{{text{PCK}}^{ + } }} = { 3}. 2 6times 10^{ 2} {text{dm}}^{ 3} ,{text{mol}}^{ - 1} , and for cholesterol–K+ ion (ChK+) complex, K_{{{text{ChK}}^{ + } }} = { 1}.00 times 10^{ 3} {text{dm}}^{ 3} ,{text{mol}}^{ - 1} , were calculated by inserting the experimental data. The value of area occupied by one PCK+ complex is 60 Å2 molecule−1, while the area occupied by one ChK+ complex is 40.9 Å2 molecule−1. The complex formation energy (Gibbs free energy) values for the PCK+ and ChK+ complexes are −14.18 ± 0.71 and −16.92 ± 0.85 kJ mol−1, respectively.

The Equilibrium of Phosphatidylcholine–Amino Acid System in Monolayer at the Air/water Interface

Monolayers of phosphatidylcholine, tyrosine, and phenylalanine and binary mixtures phosphatidylcholine-tyrosine or phosphatidylcholine-phenylalanine were investigated at the air/water interface. Phosphatidylcholine (lecithin, PC), tyrosine (Tyr), and phenylalanine (Phe) were used in the experiment. The surface tension values of pure and mixed monolayers were used to calculate π-A isotherms. The surface tension measurements were carried out at 22°C using an improved Teflon trough and a Nima 9000 tensiometer. The Teflon trough was filled with a subphase of triple-distilled water. Known amounts of lipid dissolved in 1-chloropropane were placed at the surface using a syringe. The interactions between lecithin and amino acid result in significant deviations from the additivity rule. An equilibrium theory to describe the behavior of monolayer components at the air/water interface was developed in order to obtain the stability constants of PC-Tyr as well as PC-Phe complexes. We considered the equilibrium between the individual components and the complex and established that lecithin and amino acid formed highly stable 1:1 complex.

The equilibria of phosphatidylcholine–fatty acid and phosphatidylcholine–amine in monolayers at the air/water interface

Monolayers of phosphatidylcholine, fatty acid and amine and binary mixtures phosphatidylcholine–fatty acid or phosphatidylcholine–amine were investigated at the air/water interface. Phosphatidylcholine (lecithin, PC), stearic acid (SA), palmitic acid (PA), decanoic acid (DA) and decylamine (DE) were used to the experiment. The surface tension values of pure and mixed monolayers were used to calculate π– A isotherms. The surface tension measurements were carried out at 22 °C using an improved Teflon trough and a Nima 9000 tensiometer. The Teflon trough was filled with a subphase of triple-distilled water. Known amounts of lipid dissolved in 1-chloropropane were placed at the surface using a syringe. The interactions between lecithin and fatty acid as well as phosphatidylcholine and amine result in significant deviations from the additivity rule. An equilibrium theory to describe the behaviour of monolayer components at the air/water interface was developed in order to obtain the stability constants of PC–SA, PC–PA, PC–DA and PC–DE complexes. We considered the equilibrium between the individual components and the complex and established that lecithin and fatty acid as well as phosphatidylcholine and amine formed highly stable 1:1 complexes.

Equilibria of Phosphatidylcholine − Ca2+Ions in Monolayer at the Air/Water Interface

The effect of Ca(2+) ion interaction with monolayers of phosphatidylcholine (lecithin, L) was investigated at the air/water interface. We present surface tension measurements of lecithin monolayers obtained using a Langmuir method as a function of Ca(2+) ion concentration. The measurements were carried out at 22 degrees C using a Teflon trough and a Nima 9000 tensiometer. The interactions between lecithin and Ca(2+) ions result in significant deviations from the additivity rule. An equilibrium theory to describe the behavior of monolayer components at the air/water interface was developed in order to obtain the stability constants and area occupied by one molecule of LCa(+) and L(2)Ca complexes. The stability constants, K(1) = 1.92 x 10(3) m(2) mol(-1) and K(2) = 5.35 x 10(5) m(2) mol(-1) were calculated by inserting the experimental data. The value of area occupied by one LCa(+) complex is 65 A(2) molecule(-1), while the area occupied by an L(2)Ca complex is 117 A(2) molecule(-1).

The Equilibria of Phosphatidylethanolamine-Cholesterol and Phosphatidylcholine–Phosphatidylethanolamine in Monolayers at the Air/Water Interface

Monolayers of phosphatidylethanolamine (PE), cholesterol (Ch), phosphatidylcholine (PC), and binary mixtures (PC-PE or PE-Ch) were investigated at the air/water interface. The surface tension values of pure and mixed monolayers were used to calculate π -A isotherms. The surface tension measurements were carried out at 20°C using an improved Teflon trough and a Nima 9000 tensiometer. The Teflon trough was filled with a subphase of triple-distilled water. Known amounts of lipid dissolved in 1-chloropropane were placed at the surface using a syringe. The interactions between phosphatidylethanolamine and cholesterol as well as phosphatidylcholine and phosphatidylethanolamine result in significant deviations from the additivity rule. An equilibrium theory to describe the behavior of monolayer components at the air/water interface was developed in order to obtain the stability constants of PC-PE and PE-Ch complexes. We considered the equilibrium between the individual components and the complex and established that phosphatidylethanolamine and cholesterol as well as phosphatidylcholine and phosphatidylethanolamine formed highly stable 1:1 complexes.

Anionic lipids activate group IVA cytosolic phospholipase A2 via distinct and separate mechanisms

Previously, ceramide-1-phosphate (C1P) and phosphatidylinositol-4,5-bisphosphate [PI(4,5)P2] were demonstrated to be potent and specific activators of group IVA cytosolic phospholipase A2 (cPLA2alpha). In this study, we hypothesized that these anionic lipids functionally activated the enzyme by distinctly different mechanisms. Indeed, surface plasmon resonance and surface dilution kinetics demonstrated that C1P was a more potent effector than PI(4,5)P2 in decreasing the dissociation constant of the cPLA2alpha-phosphatidylcholine (PC) interaction and increasing the residence time of the enzyme on the vesicles/micelles. PI(4,5)P2, in contrast to C1P, decreased the Michaelis-Menten constant, increasing the catalytic efficiency of the enzyme. Furthermore, PI(4,5)P2 activated cPLA2alpha with a stoichiometry of 1:1 versus C1P at 2.4:1. Lastly, PI(4,5)P2, but not C1P, increased the penetration ability of cPLA2alpha into PC-rich membranes. Therefore, this study demonstrates two distinct mechanisms for the activation of cPLA2alpha by anionic lipids. First, C1P activates cPLA2alpha by increasing the residence time of the enzyme on membranes. Second, PI(4,5)P2 activates the enzyme by increasing catalytic efficiency through increased membrane penetration.

Brewster Angle Microscope – An Excellent Tool for Nanoscience Researchers

An indigenous development of Brewster Angle Microscope (BAM) is completed at National Chemical Laboratory (NCL), India that is real time imaging instrument capable of imaging the monolayer while compressing the barrier trough simultaneously. The instrument will be useful for the basic research in the area of nanoscience. BAM has proven to be an excellent tool for the characterization of the morphology of insoluble monolayers of the surfactant molecules at air‐water interface, which are known as Langmuir films. BAM technique that was developed more than a decade ago globally, is well‐known optical method for visualizing extremely thin films. BAM can reveal inhomoginities, particularly phase domains in ultra thin layer, without the use of special probes. The reflected light is the basis of the Brewster Angle Microscopy of the ultra‐thin films. Imaging of these monolayers yield to many morphological/phase transition based study of these monolayers. The development set up consist of p‐polarized light, designed optics, frame grabber card, CCD camera as detector and teflon trough with barrier mechanism. Movement of a teflon barrier is controlled with stepper motor. An intelligent module based on single chip microcontroller 89C51 is developed for controlled barrier movement. With BAM, the real time image of a monolayer can be viewed on PC monitor. Stored images can be analyzed further through software package developed under VC++. In house software development has been completed at NCL, for instrument control, image acquisition, and image analysis. Standard APIs available with frame grabber cards can not be made applicable for this real time application. A special algorithm has been developed for finding out the area of the interested domain marked by the user. Other analysis software function includes file management, magnification of the image, contrast and brightness control, etc. A standard monolayer of Stearic acid is used for testing purpose. The instrumentation performance has been tested with an amount of 50 microliter of concentration 1 mg/ml Stearic acid spread on the subphase and found satisfactory. Sub phase used was high purity water (Millipore Milli‐ Q) contained in Teflon trough. The monolayer is compressed using teflon barrier. Simultaneously real time imaging was done to record the first order phase behavior of the monolayer. The instrument testing was done with the help of Nanoscience group at NCL. Recently instrument automation has been updated using LabVIEW platform. With LabVIEW addition, simultaneous viewing of compressed monolayer image and barrier movement control is possible beside other functions.

Interaction of long-chain nicotinates with dipalmitoylphosphatidylcholine

The interaction of four long-chain nicotinates, compounds that are of interest as potential chemopreventive agents, with dipalmitoylphosphatidylcholine (DPPC) was investigated in monolayers at the air-water interface and in fully hydrated bilayers. For the monolayer studies, the compression isotherms of mixtures of the respective nicotinate with DPPC were recorded at various compositions on a hydrochloric acid subphase (pH 1.9-2.1, 37 +/- 2 degrees C). The headgroup of the nicotinates (24-29 A2/molecule) is larger than that of the hydrophobic tail (20 A2/molecule). The pure nicotinates exhibit a temperature- and chain length-dependent transition from an expanded to a condensed phase. Analysis of the concentration dependence of the average molecular area at constant film pressure and the concentration dependence of the breakpoint of the phase transition from the expanded to the condensed state suggests that all four DPPC-nicotinate mixtures are partially miscible at the air-water interface. Although a complex phase behavior with several phase transitions was observed, differential scanning calorimetry studies of the four mixtures are also indicative of the partial miscibility of DPPC and the respective nicotinate. Overall, the complex phase behavior most likely results from the head-tail mismatch of the nicotinates and the geometric packing constraints in the two-component lipid bilayer.