Off-line coupling of high-performance liquid chromatography and 1H nuclear magnetic resonance for the identification of filbertone in hazelnut oil

A new procedure is presented for off-line coupling of high-performance liquid chromatography and proton nuclear magnetic resonance spectroscopy (¹H NMR) in hazelnut oil analysis. The optimization of some parameters affecting both the liquid chromatography preseparation step and the effective multiple-solvent suppression required for the NMR study enabled us to determine the presence in a hazelnut oil of (E)-5-methyl-hept-2-en-4-one (filbertone), a marker previously proposed to detect the adulteration of olive oil with hazelnut oil. The described procedure requires the filtration of the oil prior to its introduction into the chromatographic system and combines the advantages of providing sufficient sensitivity and selectivity with simple methodology and reduced sample handling.     

1H NMR Study of Methyl Linoleate Ozonation.

Unsaturated fatty acids are essential components of vegetable oils and cellular membranes and the involved aspect of unsaturated fatty acids ozonation have been widely studied by different authors. In this paper, in vitro ozonolysis of unsaturated fatty acids with addition of water or ethanol has been studied by Proton Nuclear Magnetic Resonance (¹H NMR) at 250?MHz in order to explore the possibility of this technique for the detection of Criegee ozonides in characterizing ozone reaction with these substrates. The ozonolysis of methyl linoleate showed that signal intensities from formed ozonides were increased with ozone concentration increments. However, the signal intensities with addition of water were higher than those in ethanol addition. Signal intensities from olefinic double bonds were found to decrease with the increment in ozonide signals. Thus, a correspondence of the behavior of these signals is observed with a proportional rate reaction between the number of double bonds in the substrate molecule. Signals from aldehyde formation were poorly detected at lower ozone concentration. It was concluded that the evaluation of ozonide and olefinic double bond signals from 250?MHz ¹H NMR can be a useful tool in assessing ozone reaction with biomolecules. The reaction mechanism for the ozone reaction with unsaturated fatty acids in the presence of water or ethanol is analyzed.     

The strong interaction between poly(vinyl chloride) and a new eco-friendly plasticizer: A combined experiment and calculation study

Hydrogenation has been proved to be an efficient way to remove the toxicity of phthalate plasticizer. However, other influences of this hydrogenation are still unknown. Here we chose di-2-ethylhexyl phthalate (DOP) and di(2-ethylhexyl) cyclohexane-1,2-dicarboxylate (DEHHP) to study the influence on interaction with poly(vinyl chloride) (PVC). By combining experiment and calculation, we found the interaction was stronger in PVC/DEHHP than in PVC/DOP. Low-Field ¹H NMR results showed that PVC chains could restrict much more DEHHP molecules than DOP. FTIR results showed that the interaction exists in form of hydrogen bonding complex, and it was stronger in PVC/DEHHP than in PVC/DOP system. Combined with FTIR results, theoretical calculation results revealed the three-center hydrogen bonded structure of the complex. Both the proportion and the binding energy of pre-complex in DEHHP are much larger than in DOP. Here, the hydrogenation-induced change of interaction was elucidated systematically and could be generalized to other phthalate plasticizers.     

Quantification of soybean oil ethanolysis with <Superscript>1</Superscript>H NMR

In this study, proton NMR spectroscopy (200 MHz) was used for quantifying the content of ethyl esters in known mixtures of soybean oil and ethyl soyate (biodiesel). For this purpose, the peak areas of ester ethoxy and glycerol methylenic peaks in the region of 4.05–4.40 ppm were measured and a calibration plot of the respective peak areas vs. the known composition of the oil/ethyl ester mixtures was used. The transesterification values determined in this way were compared with viscosity and total glycerol determinations and a good correlation was obtained. Therefore, for routine analysis, the conversion (in %) of oil to ethyl esters was determined. The methodology presented in this work proved to be quicker and simpler than others reported in the literature, such as GC and/or HPLC.     

Effect of α-Tocopherol During In Vitro Ozonation of Methyl Linoleate: Its Implication in Ozone Therapy

Systemic ozone therapy is widely used as an oxidant therapy to treat many conditions and diseases. It is known that ozone therapy acts through a transient oxidative stress produced by lipid ozonation products. The convenience of supporting patients with antioxidants during systemic ozone therapy applications is now under discussion. We studied the reaction of linoleate (one of the main constituents of cellular membranes and plasma phospholipids) with ozone in presence or absence of α-tocopherol, in order to explore whether the combination of ozone and antioxidant has some effect on fatty acid ozonation products. Proton nuclear magnetic resonance spectroscopy (¹H NMR) was used for following the reaction between 4.8mol mmol of methyl linoleate and 2.08 or 4.32mmol of ozone, with addition of different amounts of α-tocopherol (0.10, 0.18, and 0.26μmol). Ozonide (δ=5.15ppm) and aldehydes (δ=9.63ppm and δ=9.74ppm) intensities from ¹H NMR signals markedly decreased with α-tocopherol addition. When αtocopherol is absent, the intensities from olefinic proton signals diminished with ozone concentration increment; however, with αtocopherol in the mixture a smaller decrement was achieved. No detectable signals were found with the ozonation of α-tocopherol without methyl linoleate in the reaction mixture. These results suggest that α-tocopherol reacts with those products released from the reaction of ozone with methyl linoleate. This fact points out that antioxidant supplementation during systemic ozone therapy (major and minor autohemotherapy, rectal insufflation, and so forth) can be detrimental toward achieving the needed transient oxidative stress responsible for biological activities.     

A PLS regression model using NIR spectroscopy for on-line monitoring of the biodiesel production reaction

In this work, a Partial Least Squares (PLS) regression model using Near-Infrared (NIR) spectroscopy was developed to monitor the progress of the catalyzed transesterification reactions of soybean oil that produce biodiesel. The NIR spectra were collected during the transesterification reaction with a lab made spectrophotometric flow cell. Proton Nuclear Magnetic Resonance (¹H NMR) spectroscopy was employed for determining the conversion percentage of glycerides to methyl esters during the transesterification reaction and used as reference to build the PLS calibration model employing NIR spectroscopy data. The model, constructed with selected spectral range has not been tried before and allows the monitoring of the transesterification reaction in terms of conversion ratio for different temperatures. The model was validated and the values of Root Mean Square Error of Prediction (RMSEP) found for two different temperatures were 0.74% and 1.27% (of conversion) for reactions carried out at 20 ± 0.2 °C and 55 ± 0.2 °C, respectively.     

Rapid determination of iodine value by 1H nuclear magnetic resonance spectroscopy

High-resolution ¹H nuclear magnetic resonance (¹H NMR) has been found to be an effective tool for the direct, rapid, and automated determination of the iodine value (IV) of vegetable oils, including hydrogenated oils (IV=45.9–140.2). The total time required to obtain the ¹H NMR data is about 3 min per sample. The IV is calculated from the number of double-bonded protons and the average molecular weight derived directly from the spectrum. The average of olefinic protons and allylic plus divinyl protons area was used to calculate the absolute number of double-bonded protons. The ¹H NMR results were compared with those obtained by the traditional Wijs-cyclohexane methods. The correlation coefficient between traditional IV and the novel ¹H NMR method was r ²=0.9994 for the regression equation Y=0.9885X + 2.8084, where X was the result given by the traditional method. With the proposed regression equation, IV calculated by the ¹H NMR method was within an error of ± 1 unit of the result obtained by the traditional method. The proposed method is practically viable if one can afford to have the NMR system.     

Reinforcement of model filled elastomers: characterization of the cross-linking density at the filler-elastomer interface by H NMR measurements

The cross-linking density at the filler-elastomer interface is analyzed by ¹H NMR measurements in model reinforced elastomers composed by grafted nanosilica particles and cross-linked ethylacrylate chains. We have focused our attention on the effect of introducing fillers on the relaxation of the bulk polymer matrix which is observed at long times (t>100 μs). Measurements performed at high temperature (T>T_g+120 K) have revealed that its relaxation is affected by the topological constraints existing at the particle surface. We deduce that the effect of particles in the bulk matrix can be interpreted as that of an homogeneous additional constraint density which increases proportionally to the surface area introduced in the matrix.     

FTIR spectroscopic and1 H MAS NMR studies of the influence of lattice chemistry and structure on Brønsted acidity in zeolites

The influence of the Si/Al ratio, of the nature of the T-atom and of the pore size on the acidic strength of Brønsted sites in zeolites has been investigated using changes of the vibrational properties of Brønsted OH(OD) groups and a shift change of Brønsted protons in nuclear magnetic resonance upon adsorption of weak bases. Deuterated acetonitrile and trichloro-acetonitrile have been chosen to probe the acidic strengths of ZSM-5, FeZSM-5, mordenite and zeolite Y, which are often used as catalysts. From the results of the FTIR and 1 H MAS NMR studies it can be concluded that the chemical composition of the lattice dominates the acidic strength of the Brønsted sites in zeolites. Differences in structure or pore size play a much smaller role.     

NMR investigation of the miscibility of new antiplasticizers in densely cross-linked epoxy-amine resins

The behaviour of antiplasticized epoxy-amine networks was investigated by variable-temperature determinations of ¹H NMR free induction decays. Up to 50 °C, all antiplasticized resins exhibited a solid-like behaviour. At higher temperatures, resins containing the less polar additives were shown to be phase-separated, in contrast to systems containing polar additives. The temperature dependence of the phase composition of the resins, as detected by NMR, supports the conclusions previously deduced from the dynamic mechanical analysis (DMA) study: non- or slightly-polar antiplasticizer molecules are sharply phase-separated in highly cross-linked epoxy-amine networks cured extensively. The resulting morphology mainly consists in nano-scale aggregates of additives entrapped within the polymer matrix.     

1HNMR and FTIR Spectroscopic Studies on the Blends of Polychloroprene with Polyethylene Vinylacetate

Abstract

The ratio of different protons obtained from the integrated peak areas of solution ¹HNMR signals tallies with the calculated values obtained from macroblend composition. ¹HNMR results indicate that the blends of polychloroprene (CR) with polyethylene vinylacetate (EVAc) shows homogenity in mixing throughout their entire compositions. The increase in absorption frequency for C-O-C asymmetric stretching with increased contents of CR in the EVAc/CR blends indicates dipolar interactions between polar vinylacetate and chloride groups.     

Effect of time on the hydration and temperature-induced phase separation in aqueous polymer solutions. H NMR study

Dehydration during temperature-induced phase separation in D₂O solutions of poly(vinyl methyl ether) (PVME), poly(N-isopropylmethacrylamide) (PIPMAm) and poly(N-isopropylacrylamide) (PIPAAm) was followed from time dependences of NMR spin-spin relaxation times T₂ of HDO. Both the time characterizing the exclusion of the water from mesoglobules (manifested by the increase in T₂ values) and the induction period which precedes the increase in T₂ values, increased in the order PVME < PIPMAm < PIPAAm. For D₂O solutions of PIPMAm/PVME (or PIPMAm/PIPAAm) mixtures a direct connection between the state of the mesoglobules (hydrated or dehydrated) formed by the component with lower LCST (PVME, PIPAAm) and the temperatures of the phase transition of the PIPMAm component was established by NMR spectroscopy.     

Study on relationship between the concentration of hydrocarbon groups in heavy oils and their structural parameter from H NMR spectra

More than 60 heavy oils samples, belonging to the hydrogen adding tail oil, catalytic oil slurry, catalytic heavy oil slurry and catalytic heavy tar waxy oil, which taken from different processing units in Nanjing Refinery, are analysed by ¹H NMR and column chromatography. The analytical data of the heavy oils by two methods are compared and correlated, while good relationships between the specific area proton's percentage in ¹H NMR spectra and the contents of paraffinic and alicyclic hydrocarbons ((P+N)%), aromatic hydrocarbons (A%) are found. Our ¹H NMR method in calculating the amount of (P+N) and A in heavy oils proved fast, convenient and reliable.     

A novel analytical method to detect adulteration of virgin olive oil by other oils

The present study focuses on the olefinic region of the ¹³C nuclear magnetic resonance (¹³C NMR) spectrum of virgin olive oil which shows 12 peaks resonating between 127.5 and 130 ppm. These peaks are assigned to the most abundant unsaturated fatty acid moieties of the olive oil, oleic and linoleic acids, which are present in α and β positions of the glycerol backbone. With the use of an internal reference pyrazine, the 12 peaks were integrated and their areas were expressed in mmol/g of virgin olive oil. The intensities of the 12 observed peaks were affected when an authentic virgin olive oil was mixed with a seed oil. This observation was used to develop a semiquantitative method to detect adulteration of virgin olive oil by other oils based on ¹³C NMR spectroscopy.     

Solid-state characterization of polyethylene reactor powders and their structural changes upon annealing

Polyethylene reactor powders prepared under different conditions were characterized using transmission electron microscopy, ¹H nuclear magnetic resonance and X-ray diffraction techniques. The molecular weight of the polyethylene reactor powders was around 1 × 10⁵. A unique domain morphology, quite different from the usual melt- or solution-crystallized lamellar structure, was observed, independent of polymerization temperature (T_poly). Annealing of reactor powders caused the aggregation of these crystalline domains, due to the significant molecular motion of the amorphous chains, before melting. The critical temperature was 20 °C higher than each T_poly, and corresponded to the temperature at the active catalyst site producing the chain growth. The morphologies of powders prepared at the lower T_poly contained smaller crystals that exhibited a constrained monoclinic form. In contrast, only usual orthorhombic crystals of larger size were found within the powder prepared at the higher T_poly. These results suggest that the competitive processes of chain propagation and crystal growth upon polymerization may lead to unique variations of the crystalline and amorphous phases, but with similar intermediate components in the phase that connects them.     

Determination of unsaturated fatty acid composition by high-resolution nuclear magnetic resonance spectroscopy

High-resolution nuclear magnetic resonance (NMR) spectroscopy provides useful data for analyzing fatty acid compositions of edible vegetable oils. Quantitation of each fatty acid was carried out by evaluation of particular peaks. According to the ¹H NMR method, terminal methyl protons, divinyl protons, and allyl protons are useful to calculate linolenic acid, linoleic acid, and oleic acid, respectively. The ω-2 carbon, divinyl carbon, and allylic carbons were used for calculation of these acids by the ¹³C NMR method. Compositional results obtained by NMR coincided well with those of the conventional gas chromatography (GC) method. Results from ¹³C NMR were in better agreement with those from GC than were the results obtained by the ¹H NMR method.     

Determination of unsaturated fatty acid composition by high-resolution nuclear magnetic resonance spectroscopy

High-resolution nuclear magnetic resonance (NMR) spectroscopy provides useful data for analyzing fatty acid compositions of edible vegetable oils. Quantitation of each fatty acid was carried out by evaluation of particular peaks. According to the ¹H NMR method, terminal methyl protons, divinyl protons, and allyl protons are useful to calculate linolenic acid, linoleic acid, and oleic acid, respectively. The ω-2 carbon, divinyl carbon, and allylic carbons were used for calculation of these acids by the ¹³C NMR method. Compositional results obtained by NMR coincided well with those of the conventional gas chromatography (GC) method. Results from ¹³C NMR were in better agreement with those from GC than were the results obtained by the ¹H NMR method.     

Solid-state nuclear magnetic resonance (NMR): Application to precursors of ceramics—Polycarbosilane

The chemical structures of oxidation- and electron irradiation-cured polycarbosilane fibers has been studied by IR and chemical analysis, but its structure has not been identified in detail. In this work, the chemical structure and curing mechanism was examined by solid-state high-resolution NMR spectroscopy. From the analysis of NMR spectra, it is explained that (i) in oxidation curing of PCS fibers, oxygen attacks first the SiC₃H bond and forms the SiC₃O bond and, next, the SiC₄ backbone bond and forms the SiC₂O₂ units; (ii) in electron irradiation curing, the signal intensity of SiC₃H units decreases with the increase in dose, the increase in the signal being due to the formation of SiC₄ units; (iii) solid-state²⁹Si high-resolution (CP/MAS) NMR spectroscopy is a powerful tool for investigating the chemical structure and curing mechanism of PCS fibers complementing infrared and solid-state¹³C high-resolution NMR spectroscopy; and (iv)¹H CRAMPS NMR spectroscopy is very useful for investigating the chemical structure and curing mechanism of PCS fibers.     

Use of 13C nuclear magnetic resonance distortionless enhancement by polarization transfer pulse sequence and multivariate analysis to discriminate olive oil cultivars

Distortionless enhancement by polarization transfer (DEPT) pulse sequence was used to set up a quantitative high-resolution ¹³C nuclear magnetic resonance (NMR) method to discriminate olive oils by cultivars and geographical origin. DEPT pulse sequence enhances the intensity of NMR signals from nuclei of low magnetogyric ratio. The nuclear spin polarization is transferred from spins with large Boltzmann population differences (usually protons) to nuclear species characterized by low Boltzmann factors, e.g., ¹³C. The signal enhancement of ¹³C spectra ensures the accuracy of resonance integration, which is a major task when the resonance intensities of different spectra must be compared. The resonances of triglyceride acyl chains C _n:0, C_18:1, C_18:2, and C_18:3, were also assigned. Multivariate analysis was carried out on the 35 carbon signals obtained. By using variable reduction techniques, coupled with standard statistical methods—partial least squares and principal components analysis—it was largely possible to separate the samples according to their variety and region of origin. With one problem variety removed, 100% prediction of the three remaining varieties was achieved. Similarly, by using the three regions with greatest representation in the data, all but one of a test set of 34 samples were correctly predicted. Thus, the composition of olive oils from different cultivars and of different geographical origin were compared and successfully studied by multivariate analysis. These considerations in conjunction with the structural elucidations of triglyceride molecules demonstrated that ¹³C NMR is among the most powerful techniques yet described for analysis of olive oils.