Nuclear Magnetic Relaxation Times Research Articles

Multi-shelled hollow porous carbon nanospheres-based evaporator for highly efficient solar-driven desalination

Carbon-based materials stand out as photothermal materials for interfacial solar evaporation due to their high solar absorptance, chemical stability, adjustable structure, ease of preparation, and low cost compared to other candidate materials. Development of multifunctional carbon-based materials that can endow the fabricated evaporators with reduced energy loss and evaporation enthalpy is highly demanded to achieve extraordinary evaporation rates. Herein, high-solar-absorptivity multi-shelled hollow porous carbon nanospheres are fabricated and incorporated with an insulating hydrogel bottom layer into an integrated solar evaporator. It achieves a fast photothermal response and a remarkably high solar evaporation rate of 2.4 kg m−2 h−1 under one sun. Multiphysics simulation indicates that the porous multi-shelled hollow structure enables sufficient and effective interactions between water and the hydrophilic carbon surfaces, thus producing more intermediate water (IW) and lowering the evaporation enthalpy. The solar-driven water evaporation in the evaporator is probed by in-situ low-field nuclear magnetic resonance relaxation time measurements, based on which conversion of free water (FW) into IW during solar evaporation is proposed. The molecular dynamics simulations reveal that the evolution of FW clusters into IW is facilitated on the carbon surface, thus replenishing the evaporated IW and maintaining continuous high evaporation rates. The demonstrated solar evaporator exemplifies the effectiveness of structural and thermal management in enhancing solar-driven desalination.

Predicting the Stability of Formulations Containing Lyophilized Human Serum Albumin and Sucrose/Trehalose Using Solid-State NMR Spectroscopy.

Stabilization of proteins by disaccharides in lyophilized formulations depends on the interactions between the protein and the disaccharide (system homogeneity) and the sufficiently low mobility of the system. Human serum albumin (HSA) was lyophilized with disaccharides (sucrose and/or trehalose) in different relative concentrations. Solid-state nuclear magnetic resonance (ssNMR) spectroscopy 1H T1 and 1H T1ρ relaxation times were measured to determine the homogeneity of the lyophilized systems on 20-50 and 1-3 nm domains, respectively, with 1H T1 relaxation times also being used to determine the β-relaxation rate. HSA/sucrose systems had longer 1H T1 relaxation times and were slightly more stable than HSA/trehalose systems in almost all cases shown. HSA/sucrose/trehalose systems have 1H T1 relaxation times between the HSA/sucrose and HSA/trehalose systems and did not result in a more stable system compared with binary systems. Inhomogeneity was evident in a sample containing relative concentrations of 10% HSA and 90% trehalose, suggesting trehalose crystallization during lyophilization. Under these stability conditions and with these ssNMR acquisition parameters, a 1H T1 relaxation time below 1.5 s correlated with an unstable sample, regardless of the disaccharide(s) used.

Controlled Sublimation Rate of Guest Drug from Polymorphic Forms of a Cyclodextrin-Based Polypseudorotaxane Complex and Its Correlation with Molecular Dynamics as Probed by Solid-State NMR.

Encapsulation of active pharmaceutical ingredients (APIs) in confined spaces has been extensively explored as it dramatically alters the molecular dynamics and physical properties of the API. Herein, we explored the effect of encapsulation on the molecular dynamics and physical stability of a guest drug, salicylic acid (SA), confined in the intermolecular spaces of γ-cyclodextrin (γ-CD) and poly(ethylene glycol) (PEG)-based polypseudorotaxane (PPRX) structure. The sublimation tendency of SA encapsulated in three polymorphic forms of the γ-CD/PEG-based PPRX complex, monoclinic columnar (MC), hexagonal columnar (HC), and tetragonal columnar (TC), was investigated. The SA sublimation rate was decreased by 3.0-6.6-fold and varied in the order of MC form > HC form > TC form complex. The 13C and 1H magic-angle spinning (MAS) solid-state nuclear magnetic resonance (NMR) spectra and 13C spin-lattice relaxation time (T1) indicated that the encapsulated SA molecules existed as the monomeric form, and its molecular mobility increased in the order of MC form > HC form > TC form complex. In the complexes, a rapid chemical exchange between two dynamic states of SA (free and bound) was suggested, with varying adsorption/desorption rates accounting for its distinct molecular mobility. This adsorption/desorption process was influenced by proton exchange at the interaction site and interaction strength of SA in the complexes, as evidenced by 1H MAS spectra and temperature dependency of the 13C carbonyl chemical shift. A positive correlation between the molecular mobility of SA and its sublimation rate was established. Moreover, the molecular mobility of γ-CD and PEG in the complexes coincided with that of SA, which can be explained by fast guest-driven dynamics. This is the first report on the stability improvement of an API through complexation in polymorphic supramolecular host structures. The relationship between the molecular dynamics and physical properties of encapsulated API will aid in the rational design of drug delivery systems.

Elucidation of Liquid Structures and Transport Properties of Highly Concentrated LiN(SO2F)2/Ethylene Carbonate Electrolytes

The Li+ conduction mechanism in highly concentrated ethylene carbonate (EC) solution of lithium bis(fluorosulfonyl)amide (LiFSA) was studied based on the measurements of thermal properties, density, viscosity, ionic conductivity, self-diffusion coefficients, Raman spectra, and proton nuclear magnetic resonance relaxation time. The compositions of EC and LiFSA were varied from dilute to concentrated states ([EC]/[LiFSA] = 9.2–0.80). For compositions of [EC]/[LiFSA] ≤ 1.5, the free solvents decrease, and contact ion pairs and aggregates become dominant, causing a significant change in the transport properties. Faster diffusion of Li+ compared with solvent (Li+ hopping conduction) was observed when the molar composition of [EC]/[LiFSA] ≤ 1.0 as in the case of sulfolane.

Evaluating Pore Structure of Shale Reservoirs through Pore Space Multifractal Characterization

Characteristics of pore structure are crucial to oil exploration and development in shale reservoirs, but practical evaluation of shale pore structure remains a longstanding challenge. In this study, based on nuclear magnetic resonance transverse relaxation time (T2) spectra under water-saturated and irreducible conditions, total pore space and moveable fluid space were skillfully determined. Meanwhile, multifractal spectra were used to characterize T2 distributions of total pore space and movable fluid space. The results show characteristic parameters of high probability measure areas of multifractal spectra (multifractal parameters) have strong negative correlations with T2 geometric mean value, and average radii of pore and throat increase with a decrease in the multifractal parameters, indicating the shale reservoirs with low values of the multifractal parameters may have good pore structure. Moreover, clay mineral content has strong positive effects on the multifractal parameters. In contrast, (quartz+feldspar) mineral content negatively influences on the multifractal parameters. Finally, new accurate models for permeability estimation in core scale and well-logging scale of shales are both proposed based on the multifractal parameters, which are also applicable for the other reservoirs. Overall, this study is important and timely for evaluating pore structure and predicting permeability in shale reservoirs.

Structural geometry and molecular dynamics of hybrid organic–inorganic [NH3(CH2)6NH3]CdCl4 crystals close to phase transition temperatures

Organic–inorganic hybrid perovskites are highly promising for application in various electrochemical devices, such as batteries and fuel cells. The physical properties of crystals of the organic–inorganic hybrid perovskite [NH3(CH2)6NH3]CdCl4 are important for their future application. Therefore, these crystals were grown and their phase transition temperatures TC1 = 337 K and TC2 = 472 K were determined using powder X-ray diffraction and differential scanning calorimetry. We observed that the crystallographic surroundings of 1H and 13C in the cation near TC1 did not show significant changes, whereas those of 113Cd in the anion changed significantly. The change in the coordination geometry of C1 around Cd near TC1 changed the N–H···Cl bond by connecting with the 1H of NH3. The nuclear magnetic resonance spin-lattice relaxation time T1ρ suggested that the 1H energy transfer processes in phases III and II were easier, whereas the 13C energy transfer processes were easier in phase III than in phase II. The results of the current study for [NH3(CH2)nNH3]CdCl4 (n = 6) were compared with those for n = 2, 3, 4, and 5 obtained from previous studies. The features of the length of CH2 and even–odd number of carbons in the diammonium chain are expected to facilitate potential applications in the future.

Impact of storage time and temperature of salad heads on the quality of fresh-cut Cichorium endivia

The impact of temperature and storage time of escarole salad heads on the quality of processed, fresh-cut salad was investigated. Based on temperatures recorded in a fresh-cut processing plant, salad heads were stored for four different storage times (0, 5, 9, and 12 d) at four temperatures (4, 7, 10, and 12 °C) before being processed. A range of quality criteria (technical yield, global visual aspect, pink cut surfaces, mechanical texture, aerobic microflora, respiration rate, atmosphere composition in fresh-cut salad pouches, nuclear magnetic resonance transverse relaxation time) were measured on processing day, after 7 d storage at 4 °C of the fresh-cut salad packaged in pouches, and 1 d after pouch opening. The results are presented for salads grown in southeast France and early-season harvest, validated by experimental repetitions with a late-season harvest and salads from another geographical origin. Storage of salad heads caused deterioration of all quality attributes except for total aerobic bacteria. The global visual aspect was the most sensitive to changes in storage conditions of salad heads (significant reduction in quality for 5 d over 7 °C). In contrast, mechanical texture (maximum load for the shear test) was only significantly different for the fresh-cut salad prepared from salad heads stored for 9 d at 12 °C. For all quality criteria, fresh-cut salads processed from salad heads stored for 5 d at 4 and 7 °C were not significantly different from those of non-stored salad heads. For storage time of 5 d or less, a temperature of 7 °C is likely as good as 4 °C for escarole salad-head storage intended for fresh-cut processing.

Physicochemical and Morphological Study of the Saccharomyces cerevisiae Cell-Based Microcapsules with Novel Cold-Pressed Oil Blends

Vegetable oils rich in polyunsaturated fatty acids are a valuable component of the human diet. Properly composed oil blends are characterized by a 5:1 ratio of ω6/ω3 fatty acids, which is favorable from a nutritional point of view. Unfortunately, their composition makes them difficult to use in food production, as they are susceptible to oxidation and are often characterized by a strong smell. Encapsulation in yeast cells is a possible solution to these problems. This paper is a report on the use of native and autolyzed yeast in the encapsulation of oils. The fatty acid profile, encapsulation efficiency, morphology of the capsules obtained, and thermal behavior were assessed. Fourier transform infrared analysis and low-field nuclear magnetic resonance relaxation time measurements were also performed. The process of yeast autolysis changed the structure of the yeast cell membranes and improved the loading capacity. Lower encapsulation yield was recorded for capsules made from native yeast; the autolysis process significantly increased the value of this parameter. It was observed that NY-based YBMCs are characterized by a high degree of aggregation, which may adversely affect their stability. The average size of the AY capsules for each of the three oil blends was two times smaller than the NY-based capsules. The encapsulation of oils in yeast cells, especially those subjected to the autolysis process, ensured better oxidative stability, as determined by DSC, compared to fresh blends of vegetable oils. From LF NMR analysis of the relaxation times, it was shown that the encapsulation process affects both spin-lattice T1 and spin-spin T2* relaxation times. The T1 time values of the YBMCs decreased relative to the yeast empty cells, and the T2* time was significantly extended. On the basis of the obtained results, it has been proven that highly unsaturated oils can be used as an ingredient in the preparation of functional food via protection through yeast cell encapsulation.

Effect of subfreezing storage on the qualities of dough and bread containing pea protein.

In this paper, -6, -9 and -12 °C were selected as subfreezing temperatures of dough containing pea protein based on the results of low-field nuclear magnetic relaxation time. The effect of storage at subfreezing temperatures on dough properties was then investigated and compared with sample storage at -18 °C. The pH value, springiness, resilience, cohesiveness of dough and sensory score of bread gradually decreased and the hardness and water loss rate of dough gradually increased with the extension of storage time. However, dough hardness, viscoelasticity and fermentation volume were maintained more effectively in subfreezing storage than in -18 °C storage. The subfreezing temperature could alleviate the damage of gluten network structure in frozen dough by ice crystals and was beneficial in maintaining the elasticity of gluten proteins. The network system of pea protein, gluten protein and starch granules in dough storage at -9 and -12 °C was more tightly connected and the microstructure was similar to that at -18 °C. There was no significant difference between the quality of bread made from the dough stored at subfreezing temperature and that stored at -18 °C for 1-6 weeks, and the preservation effect at -12 °C was closer to that at -18 °C. Subfreezing storage can keep the stability of dough containing pea protein close to traditional frozen storage (-18 °C), which provides a new method for storage and transportation of frozen dough. © 2022 Society of Chemical Industry.

PH-Responsive Association Behavior of Biocompatible Random Copolymers Containing Pendent Phosphorylcholine and Fatty Acid.

Well-defined pH-responsive biocompatible random copolymers composed of 2-(methacryloyloxy)ethyl phosphorylcholine and varying quantities of sodium 11-(acrylamido)undecanoate (AaU) (fAaU = 0-58 mol %) were synthesized via reversible addition-fragmentation chain transfer radical polymerization. The pH-responsive association and dissociation behavior of the random copolymers was studied via turbidity, 1H nuclear magnetic resonance relaxation time, dynamic light scattering, static light scattering (SLS), and fluorescence measurements. At basic pH levels, the random copolymers dissolved in water in a unimer state because the AaU units behaved in a hydrophilic manner as a result of the ionization of the pendent fatty acids. The random copolymers with fAaU < 52 mol % associated intramolecularly within a single polymer chain to form unimer micelles at pH 3 because of the protonation of the pendent fatty acids. On the other hand, the random copolymer with fAaU ≥ 52 mol % formed intermolecular aggregates composed of four polymer chains at pH 3, as established by the SLS measurements. The random copolymers displayed the ability to solubilize hydrophobic guest molecules, such as N-phenyl-1-naphthylamine, into the hydrophobic microdomain formed by the pendent dehydrated fatty acids at acidic pHs. At pH 4, 1-pyrememethanol is captured by the random copolymer with fAaU = 52 mol %, and it is released from the random copolymer above pH 9. Furthermore, the mucoadhesive properties of the random copolymer with fAaU = 9 mol % were studied using a surface plasmon resonance technique. The copolymer was adsorbed onto mucin at pH 3; however, the adsorption decreased at pH 7.4.

A laboratory study of the effect of clay, silt, and sand content on low-field nuclear magnetic resonance relaxation time distributions

We have developed a laboratory nuclear magnetic resonance (NMR) study to investigate the effect of clay, silt, and sand content on the NMR relaxation time distribution. Transverse NMR relaxation times ([Formula: see text]) are determined for water-saturated unconsolidated sediment mixtures of 1%–60% kaolinite clay, 5%–85% silt-size glass beads, and 8%–94% quartz sand by mass. Nearly all of the mixtures are characterized by a unimodal [Formula: see text] distribution. When clay is present in quantities greater than 10%, the clay content dominates the response. For these samples, the mean-log relaxation times ([Formula: see text]) range from 0.03 to 0.06 s, regardless of silt or sand content. For mixtures with [Formula: see text] clay, [Formula: see text] decreases with increasing clay content. When the clay content is kept the same, [Formula: see text] decreases with increasing silt content and increases with the increasing sand content. The strong effect of the clay content on the NMR response is due to the high specific surface area of the clay and the distribution of clay throughout the samples. These results will help improve the interpretation of NMR field data in soils and unconsolidated sediments.

A Needless but Interesting Controversy with Pedagogical Overtones

A decade ago four independent groups, using four independent methods, reported the unanticipated and still surprising result that the bending modulus KC of bilayers of DOPC, unlike other standard lipids, does not increase with addition of cholesterol. A recent paper, using neutron spin echo (NSE) and nuclear magnetic resonance relaxation times (NMRτ), reports that the bending modulus of DOPC increases three fold with increasing cholesterol concentration up to 50%. It would appear that this has become a controversial topic. This controversy is needless because NSE and NMRτ do not measure the bending modulus as it has been defined for decades. Each measures important, complementary, properties that could enrich our understanding of bilayer properties, notably membrane viscosity and location of the neutral plane employed in membrane mechanics. The resolution of this controversy rests on elucidating the difference between measurements on a system in equilibrium that lead directly to equilibrium properties like the bending modulus, and measurements on the same equilibrium system that lead to more complex results involving both static moduli and transport properties. While the difference between static and non-equilibrium quantities is well understood in the physical sciences and statistical thermodynamics, this emerging controversy seems to warrant a pedagogical reminder.

Nuclear Magnetic Relaxation Time near the Compensation Temperature in a Ferrimagnetic Insulator

The nuclear magnetic relaxation time $T_1$ in ferrimagnetic insulators is calculated by a Raman process of hyperfine interaction with a meanfield approximation. It is found that the 1/$T_1$ on one site rapidly increases near the compensation temperature $T_0$, whereas that on another site does not increase up to Curie temperature $T_c$. This is due to that the band width of soft magnon becomes comparable to $T_0$. The increasing behavior of 1/$T_1$ below $T_c$ is found also in another type ferrimagnet, which shows hump structure in the temperature dependence of magnetization instead of compensation. Also in this case, we find the rapid increase of 1/$T_1$ below $T_c$, even though the magnetization does not show the compensation. Such a coexistence of soft and hard magnons will lead to remarkable properties of ferrimagnet.

Understanding the role of d‐Allulose and soy protein addition in pectin gels

Abstractd‐Allulose (a monosaccharide and C3 epimer of fructose), one of the common rare sugars is getting attention due to its low caloric values. In this study, d‐Allulose was used as a replacement of sucrose at different ratios (d‐Allulose/Sucrose: 35/0, 20/15, 10/25, 0/35) to formulate pectin‐based soft confectionery gels. Soy protein isolate was also added to increase the protein content. Physical properties, such as hardness, moisture content, pH, and color, were measured for the gels. Higher hardness values were obtained for the soy protein containing gels due to pectin–soy protein interaction (p &lt; 0.05). Also, higher moisture content was observed in soy protein containing gels (p &lt; 0.05). In addition, nuclear magnetic resonance T2 relaxation times were measured at low field (~0.5 T) to determine how the water distribution in the samples changed and to observe how d‐Allulose affected the polymer–water interactions. The study also showed that the presence of d‐Allulose increased the crystallization tendency (% crystallinity of 7.9) of the pectin gels. X‐ray diffraction results showed the d‐allulose peaks at 33.76 and 48.68oθ. Morphologies of the gels were also examined by scanning electron microscope. Sugar type and soy protein isolate addition were found to have significant impact on the gel formulations.

Structure and Role of BCOR PUFD in Noncanonical PRC1 Assembly and Disease.

Polycomb repression complex 1 (PRC1) is a multiprotein assembly that regulates transcription. The Polycomb group ring finger 1 protein (PCGF1) is central in the assembly of the noncanonical PRC1 variant called PRC1.1 through its direct interaction with BCOR (BCL-6-interacting corepressor) or its paralog, BCOR-like 1 (BCORL1). Previous structural studies revealed that the C-terminal PUFD domain of BCORL1 is necessary and sufficient to heterodimerize with the RAWUL domain of PCGF1 and, together, form a new protein-protein binding interface that associates with the histone demethylase KDM2B. Here, we show that the PUFD of BCOR and BCORL1 differ in their abilities to assemble with KDM2B. Unlike BCORL1, the PUFD of BCOR alone does not stably assemble with KDM2B. Rather, additional residues N-terminal to the BCOR PUFD are necessary for stable association. Nuclear magnetic resonance (NMR) structure determination and 15N T2 relaxation time measurements of the BCOR PUFD alone indicate that the termini of the BCOR PUFD, which are critical for binding PCGF1 and KDM2B, are disordered. This suggests a hierarchical mode of assembly whereby BCOR PUFD termini become structurally ordered upon binding PCGF1, which then allows stable association with KDM2B. Notably, BCOR internal tandem duplications (ITDs) leading to pediatric kidney and brain tumors map to the PUFD termini. Binding studies with the BCOR ITD indicate the ITD would disrupt PRC1.1 assembly, suggesting loss of the ability to assemble PRC1.1 is a critical molecular event driving tumorigenesis.

Programmable Nuclear-Spin Dynamics in Ti(IV) Coordination Complexes.

Interstitial patterning of nuclear spins is a nascent design principle for controlling electron spin superposition lifetimes in open-shell complexes and solid-state defects. Herein we report the first test of the impact of the patterning principle on ligand-based nuclear spin dynamics. We test how substitutional patterning of 1H and 79/81Br nuclear spins on ligands modulates proton nuclear spin dynamics in the ligand shell of metal complexes. To do so, we studied the 1H nuclear magnetic resonance relaxation times (T1 and T2) of a series of eight polybrominated catechol ligands and six complexes formed by coordination of the ligands to a Ti(IV) ion. These studies reveal that 1H T1 values can be enhanced in the individual ligands by a factor of 4 (from 10.8(3) to 43(5) s) as a function of substitution pattern, reaching the maximum value for 3,4,6-tribromocatechol. The T2 for 1H is also enhanced by a factor of 4, varying by ∼14 s across the series. When complexed, the impact of the patterning design strategy on nuclear spin dynamics is amplified and 1H T1 and T2 values vary by over an order of magnitude. Importantly, the general trends observed in the ligands also match those when complexed. Hence, these results demonstrate a new design principle to control 1H spin dynamics in metal complexes through pattern-based design strategies in the ligand shell.

Determining effect of partial substitution of paramagnetic Mn2+ ions in perovskite (MA)2Zn1-xMnxCl4 mixed crystals through MAS NMR relaxation times

This study discusses the effects of the partial replacement of Zn2+ ions with paramagnetic Mn2+ ions (x = 0.1, 0.3, 0.5, and 0.7) in ecofriendly (MA)2Zn1-xMnxCl4 lead-free perovskite crystals through magic angle spinning nuclear magnetic resonance relaxation times. These crystals are grown and their structures are measured through X-ray diffraction experiments. Further, the spin-lattice relaxation time, T1ρ, in the rotating frame is measured for 1H and 13C nuclei of (MA)+ cations to understand the local environments with respect to the Mn2+ ion content. The structures and chemical shifts for CH3 and NH3 with x = 0.1 and 0.3 were highly similar to those with x = 0, whereas those for CH3 and NH3 with x = 0.5 and 0.7 were highly similar to those with x = 1. Nonetheless, the 1H T1ρ depending on the paramagnetic ion content became shorter because (MA)+ cations were bound to the paramagnetic Mn2+ layer through N–H⋯Cl bonds. The main effects were the differences in the metal Zn2+ and Mn2+ ions.

1H-NMR-relaxation and colorimetry for evaluating nanopolymeric dispersions as stone protective coatings

• New nano-latexes were tested as stone protective agents. • 1 H NMR relaxometry provides pore size distribution in stone samples. • Changes in pore size distribution and moisture content reflect treatments’ efficacy. • Non-destructive techniques allowed the selection of experimental nano-products. Non-destructive and non-invasive assessment of new nanopolymeric dispersions for protecting stone materials was accomplished; the effectiveness of five formulations was tested regarding commercial products widely used in conservation on Lecce, Montescaglioso and Matera stones. We observed the specimens’ wettability during capillary water absorption up to saturation by nuclear magnetic transverse relaxation time measurements, using a surface and portable probe. The comparison between treated and the untreated ones, concerning their specific hydration behavior, allowed establishing the effects of the polymer films. Finally, color evaluations were performed to inspect differences induced by treatments. The data analysis enabled to select the most satisfactory protective coating for each lithotype.

New Approach to Analyze 2D Map T1–T2

Based on the method of two-dimensional (2D) nuclear magnetic resonance (NMR) relaxometry, a technique was developed for determining the joint distribution of the correlation time $$ \tau_{c} $$ and the Van Vleck second moments $$ \Delta \omega^{2} $$. The field of application is the study of slow molecular motions corresponding to the condition of the ratio of nuclear magnetic relaxation times T1/T2 > 1.05 (the relation of spin–lattice relaxation time T1 to spin–spin relaxation time T2). The technique is based on the use of a priori information about the mechanism of nuclear magnetic relaxation in a system. The technique has used this information in the regularization solution of an inverse problem. In contrast to the known method for calculating 2D maps of the joint distribution P2 (T1, T2), the proposed method for constructing a 2D map of the joint distribution $$ Q_{2} \left( {\tau_{c} ,\Delta \omega^{2} } \right) $$ does not depend on the main characteristic of the NMR relaxometer—the resonance frequency $$ \omega_{0} $$. The technique was used to analyze the characteristics of sorbed water in clay rocks–argillite.

Experiment on determination of ethanol chemical shift and concentration of ethanol solution based on nuclear magnetic resonance instrument

In this designing experiment, a nuclear magnetic resonance instrument was used to study the chemical shift properties of ethanol based on the principle of magnetic shielding effect. At the same time, the nuclear magnetic resonance method was used to study the transverse relaxation time and signal strength of ethanol aqueous solution in the range of 5%to 40%. The relationship between different mass fraction of ethanol-aqueous solution and nuclear magnetic resonance signal intensity, relaxation time and solution concentration were analysed. According to the results, due to the limitation of experimental instruments, no regular changes were observed. The results show that the addition of copper sulphate can increase the ethanol content and the effect of the ethanol content on the lateral relaxation time: the ethanol content varies between 5% and 40%, and the lateral relaxation time changes from 8.42ms to 40.35ms.According to the experimental results, the empirical formulas of the concentration and lateral relaxation time of ethanol aqueous solution with fixed amount of copper sulphate were fitted. Using this relationship, the NMR measurement of the concentration of ethanol-water solution can be achieved, which provides a new method for the convenient and accurate measurement of the concentration of ethanol solution.