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You are here: Home / Archives for TD-NMR

Register to Attend PANIC 2014 ! Deadline for Poster Submissions is December 20

December 2, 2013 by process nmr Chemistry, Chemometrics, Herbal Supplement, NMR, Process NMR, qNMR, Reaction Monitoring, TD-NMR

The 2nd Annual Practical Applications of NMR in Industry Conference (PANIC) will be held February 3-5 in Charlotte, NC. An excellent scientific agenda has been put together (see here). The Brochure is available here. Take note of the early registration (January 10, 2014) and poster submission (December 20, 2013) deadlines.

John Edwards of Process NMR Associates is on the organizing committee of PANIC and has been appointed as Treasurer of the Conference company.

John will be presenting an oral presentation in the one of the Nutraceutical Session:                NMR-Based Authentication of Nutraceuticals, Herbal Supplements, and Food Additives: Economic- and Efficacy-Driven Adulteration of Aloe Vera, Herbal Erectile Dysfunction Supplements, and Acacia Gum                                                                                                 John Edwards, Ph.D., Process NMR Associates, LLC – Biography

Multinuclear NMR spectroscopy offers an outstanding ability to perform targeted and non-targeted analysis of nutraceuticals, herbal supplements, and food additives. Economic adulteration of these materials with lower value adulterants and the addition of pharmaceuticals to herbal supplements in order to obtain the expected efficacy of a product is surprisingly common in the marketplace today. The development of official test methods utilizing NMR spectroscopy will allow the detailed unequivocal chemical fingerprinting of the NMR spectrum to be combined with qNMR methods to quantify active components and prove authenticity from either direct observation of adulterants or by non-targeted methods such a principal component analysis. We will discuss in detail a method developed on aloe vera juice and powder products to quantify the active components as well as identify the presence of whole leaf or inner gel material in the manufacturing process. The presence of preservatives, degradation products, additives, and adulterants can also be readily identified and quantified by 1H NMR. Statistical analysis can be performed to define the range of concentrations expected in naturally produced materials as well as determine the presence of adulterated material. The utilization of erectile dysfunction pharmaceuticals in herbal supplements to deliver the expected efficacy to the herbal products will described. Finally, the use of 13C NMR to define the authenticity of gum Arabic (acacia Senegal) used as an emulsifier in the beverage industry compared to chemically similar but inferior/cheaper gum products.

and in the poster session he has 3 posters being presented:

Development of an Automated Quantitative Chemical Mixture Analysis Method within Metrelab Research MNova – Internal Standard qNMR Measurements on Aloe Vera Raw Materials, Aloe Containing Products, Finished Beer and Samples from the Different Points in the Brewing Process

John C. Edwards, Adam J. Dicaprio, Process NMR Associates, Michael A. Bernstein, Mestrelab Research

Small Molecule Chemistry of Spontaneously Fermented Coolship Ales

Adam J. Dicaprio, John C. Edwards, Process NMR Associates

John will also chair a session on Online/At-Line NMR

ONLINE/AT LINE NMR – Wednesday, February 4

3:20 Session Chair’s Remarks – John Edwards, Ph.D., Process NMR Associates, LLC – Biography

3:25: A Compact, Portable 4.7 T Driven NMR System for Reaction Monitoring

Mark Zell, Ph.D., Senior Principal Scientist & Technical Leader, Structure Elucidation Group, Pfizer – Biography

We have been using a newly developed 4.7T (200 MHz 1H operating frequency) cryogen-free NMR system which utilizes a high-temperature (~14K) superconducting magnet cooled by a standard helium compressor, driven by a high stability power supply, and utilizing a new state-of-the-art single board spectrometer. The system is designed to be portable, allowing for rapid cooling and ramping of the magnet to field without the need for expensive cryogens or a trained engineer. We have been using this system, coupled with a microcoil flow probe to investigate a multitude of samples, ranging from traditional organic compounds to complex reaction mixtures. To date, primarily 1D 1H NMR data on these samples has been acquired. We are working toward utilizing more sophisticated multi-dimensional gradient-based experiments on this system to provide additional information on reaction mixtures in both a “stop-flow” and flow-through mode. This system works well for reaction monitoring, as it provides intermediate resolution between lower resolution 60 MHz spectrometers and traditional higher-field superconducting spectrometers at 400 MHz and above. This poster will provide an overview of this new technology and demonstrate the data we are able to achieve, in comparison to that obtained at both 60 and 400 MHz.

3:55 NMR Well Logging and Downhole Fluid Characterization

Martin Hürlimann, Ph.D., Scientific Advisor, Schlumberger-Doll Research – Biography

Over the last decade, NMR well logging has matured into a significant new commercial application of nuclear magnetic resonance. In this method, an NMR sensor is moved through a borehole to continuously measure the fluids inside the surrounding earth formation. The environmental conditions are exceptionally challenging for NMR measurements. The whole sensor and associated electronics have to fit into the borehole (with a typical diameter of 20 cm) and able to withstand high temperatures and pressures that can reach 175o C and 140 MPa. The sample is located outside the sensor and the applied magnetic fields are necessarily grossly inhomogeneous. Furthermore, the measurements have to be sufficiently robust so that they can be performed in a highly automated manner without the assistance of an NMR specialist and in a wide range of environments, from the arctic to the tropics. In this talk, I will review how these challenges can be overcome with novel hardware design and new measurement techniques. Current state-of-the-art well logging measurements enable the extraction of a wide range of important physical and chemical properties that include the porosity, the distribution of pore size, and estimate of the permeability, the identification and quantification of the different fluid phases occupying the pore space (water brine, crude oil, gas…), the fluid compositions, and the fluid viscosities. I will highlight new relaxation and diffusion measurements to determine two-dimensional relaxation-diffusion distribution functions. These techniques are well suited for other applications in fields beyond the oil field, including process control or the characterization of food products.

4:25 Characterizing a Hydrogenation Reaction: In situ NMR and Mechanistic Modeling

Jonas Buser, NMR Structural Characterization Group, Eli Lilly and Company – Biography

The development of a robust manufacturing process typically involves a joint effort between engineering, mathematical modeling, process chemistry, and analytical chemistry. This presentation describes the optimization of a hydrogenation reaction observed to have variable reaction completion times at manufacturing scale. On-line flow NMR (ReactNMR) was employed to characterize a detailed reaction mechanism and kinetics. Variables of pH and hydrogen pressure were examined to see how they affected the dynamic mechanism and kinetics of the reaction. A mathematical model was developed to gain further understanding of the process kinetics as well as mass transfer limitations. The model was used to predict experimental conditions capable of minimizing the hydrogenation time. This problem solving approach is being broadly adopted to solve complex reaction problems where traditional means don’t provide a comprehensive understanding of the process.

 

 

2nd Annual Practical Applications of NMR in Industry Conference (PANIC) Announced

April 11, 2013 by process nmr ESR, NMR, Process NMR, Reaction Monitoring, TD-NMR

Conference Details: 2nd Annual Practical Applications of NMR in Industry Conference
Organized by Cambridge Healthtech Institute
Hilton Charlotte University Place, Charlotte, NC, February 3-5, 2014

Building on the success of last years 1st Annual PANIC NMR Conference it has been decided that the 2nd Annual PANIC NMR Conference would be organized cooperatively between the original organizing committee and CHI.

Details on the conference can be found at: PANIC Conference Website

A promotional flyer for the conference can be found here: PANIC NMR Flyer

Anyone interested in industrial applications of all forms of NMR spectroscopy is encouraged to attend this practical NMR conference where the emphasis is placed on everyday utilization of the technology rather than cutting edge NMR research which is often far beyond the capabilities of the everyday user.

John Edwards of Process NMR Associates is serving on the organizing committee and chairing two technical sessions – one on On-Line/At-Line/Benchtop NMR and another on NMR of Materials.

If you are interested in presenting or sponsoring the conference please contact CHI through the website.

SMASH Posters Cover Aloe Vera NMR Test Method, Heavy Petroleum Average Molecule Characterization, and 60 MHz Permanent Magnet NMR Applications

September 13, 2012 by process nmr Herbal Supplement, NMR, PAT, Process NMR, Reaction Monitoring, TD-NMR

Quantitative 1H qNMR Method for Complex Mixture Analysis: Determination of Acetylated Polysaccharides, Glucose, Maltodextrin, Isocitrate, Preservatives, Additives and Degradation Products in Aloe Vera Leaf Juice – Raw Material and Consumer Products

Practical Applications of Compact, Cryogen-Free High-Resolution 60 MHz Permanent Magnet NMR Systems for Reaction Monitoring and Online/At-Line Process Control

Calculation of Average Molecular Descriptions of Heavy Petroleum Hydrocarbons by Combined Analysis by Quantitative 13C and DEPT-45 NMR Experiments

Process NMR Associates to Contribute Invited Talk and 3 Posters at the 1st Practical Applications of NMR in Industry Conference (PANIC), October 15-17, Schaumburg IL

August 19, 2012 by process nmr Herbal Supplement, IR-ATR, NMR, PAT, Process NMR, Reaction Monitoring, TD-NMR

News – Dr. John Edwards of Process NMR Associates will be presenting the following 3 posters and invited talk at the 1st Practical Applications of NMR in Industry Conference (PANIC), Schaumburg, IL, October 15-17, 2012

Invited Talk

On-line Applications of 60 MHz High-Resolution NMR Systems in Industry: Direct Measurements, Chemometric Correlations, and Multiple Spectroscopy Data Fusion

John C. Edwards Process NMR Associates, LLC, Danbury, CT

For the past two decades high resolution 1H NMR systems combined with chemometric analyses have been utilized in refineries and chemical plants to predict the chemical and physical properties of process streams and finished products. The ability to perform these analyses with on-line NMR instrumentation has allowed tighter control and optimization of the plant to obtain margin improvement, reduced reworking of off-specification materials, and higher yields of finished products. Examples of refinery and petrochemical applications will be given along with some examples of multinuclear NMR applications utilizing 31P and 19F NMR. The permanent magnet based 1.5 Tesla NMR instruments will be described along with a description of how these compact, cryogen-free NMR systems can be utilized on the bench-top or in the fume-hood as continuous or stop-flow chemistry sensors for reaction monitoring, mixing/dilution monitoring, or purity/conversion monitoring. Food applications will also be described such as dairy (butter, cream cheese) and edible or essential oil analysis. Finally, the ability to improve the quality of the correlations derived in the chemometric modelling by “fusing” NMR data with spectral information from other spectroscopies (NIR, Mid-IR) will be discussed.

Poster 1

1H qNMR Determination of Acetylated Polysaccharides, Glucose, Maltodextrin, Isocitrate, Degradation Products, Preservatives and Additives in Aloe Vera Leaf Juice

John C. Edwards Process NMR Associates, LLC, Danbury, CT

Aloe Vera is a botanical component that is used widely in the cosmetic, natural product, herbal supplement, and pharmaceutical industries. The widespread use of Aloe Vera has lead to the need to adequately analyze the authenticity, quality, and quantity of the various components present in this material. The 1H qNMR method described here was developed and validated by Process NMR Associates for a number of NMR service customers and the method will be included in an upcoming Monograph on Aloe Vera published by the American Herbal Pharmacopoeia. The method can be used for the detection and quantitation of the primary components of interest in Aloe Vera juice products and raw materials for compliance with IASC (International Aloe Science Council) certification requirements, specifically, for determination of the content of acetylated polysaccharides, the presence of glucose, the presence and content of maltodextrin, and the content of isocitrate. Additionally, for meeting quality control specifications beyond IASC requirements, the presence and content of the following groups of compounds can be determined: degradation products (e.g., lactic acid, pyruvic acid, succinic acid, fumaric acid, acetic acid, formic acid, and ethanol), preservatives (e.g., potassium sorbate, sodium benzoate, and citric acid/citrate), and other atypical impurities, additives, or adulterants (e.g., methanol, glycine, glycerol, sucrose, maltodextrin, flavorants (propylene glycol/ethanol)). We will describe a common internal-standard NMR methodology that does not require additional equipment or advanced automation software. The method is applicable to a number of different Aloe Vera raw materials and products, including liquid and dried juices. In aloe vera finished products the method is only applicable when the observable aloe vera constituents are present at a high enough concentration to be observed and are not obscured by additional product ingredients with signals in overlapping areas.

Poster 2

Compact, Cryogen-Free, High-Resolution 60 MHz Permanent Magnet NMR Systems for Reaction Monitoring and On-Line/At-Line Process Control Observing 1H, 19F, 31P

John C. Edwards1, Tal Cohen2, Paul J. Giammatteo1

1. Process NMR Associates, LLC Danbury, CT
2. Aspect AI, Shoham, Israel

A compact high resolution NMR system will be described that can be situated on the bench-top or in the fume hood to be used as a continuous or stop-flow detector and/or an “in-situ” reaction monitoring system. The same system can be fully integrated into on-line shelters for on-line process control or utilized by engineers and technicians in an “at-line” environment. The system uses a unique 1.5 Tesla permanent magnet that can accommodate sample tube diameters of 3-10 mm with half-height spectral resolution (water resonance) approaching 1-3 Hz depending on the sample volume size and with excellent single pulse sensitivity. These systems can be utilized in a traditional NMR methodology approach or combined with chemometric approaches that allow NMR data to predict chemical and physical properties of materials via regression analyses that establish correlations between observed spectral variability and sample-to-sample property variance [1].

1) “Process NMR Spectroscopy: Technology and On-line Applications”, John C. Edwards, and Paul J. Giammatteo, in Process Analytical Technology: Spectroscopic Tools and Implementation Strategies for the Chemical and Pharmaceutical Industries, 2nd Ed., Editor Katherine Bakeev, Blackwell-Wiley, 2010

Poster 3

Calculation of Average Molecular Descriptions of Heavy Petroleum Hydrocarbons by Combined Analysis by Quantitative 13C and DEPT-45 NMR Experiments

John Edwards Process NMR Associates, LLC, Danbury, CT

Much debate has centered around the validity and accuracy of NMR measurements to accurately describe the sample chemistry of heavy petroleum materials. Of particular issue has been the calculated size of aromatic ring systems that in general seem to be underestimated in size by NMR methods. This underestimation is principally caused by variance in chemical shift ranges used by researchers to define the aromatic carbon types observed in the 13C NMR spectrum, in particular the bridgehead aromatic carbons that can be shown to overlap strongly with the protonated aromatic carbons. The ability to discern between bridgehead aromatic carbons and protonated carbons in the 108-129.5 ppm region of the spectrum is key in the derivation of molecular parameters that describe the “molecular average” present in the sample. Utilizing methodologies developed by Pugmire and Solum for the solid-state 13C NMR analysis of coals and other carbonaceous solids we have developed a new liquid-state 13C NMR method that allows the relative quantification of overlapping protonated and bridgehead aromatic carbon signals to be determined. The NMR experiments involve the combined analysis of both quantitative 13C single pulse excitation which observes all carbons quantitatively, and a DEPT45 polarization transfer which observes only the protonated carbons in the sample. Though the DEPT45 results are not quantitative across all carbon types (CH, CH2, and CH3) due to polarization transfer differences, the technique is well enough understood that simple multiplication factors allow the relative intensities of the different carbons to be determined. The average ring system sizes derived from these NMR experiments tend to be several ring systems larger than has been calculated in previous studies. In heavy petroleum asphaltenes the average aromatic ring system is 5-7 rings in size which is in agreement with FTICR-MS and fluorescence measurements, rather than the 3-4 rings previously reported.

Process NMR Associates to Present 3 Posters at SMASH NMR Conference, September 9-12, 2012

August 19, 2012 by process nmr Herbal Supplement, IR-ATR, NMR, PAT, Process NMR, Reaction Monitoring, TD-NMR

News – John Edwards of Process NMR Associates will be presenting the following 3 posters at SMASH NMR Conference, Providence RI, September 9-12, 2012. Process NMR Associates will also have a vendor table where John will be available to discuss the exciting range of high and low resolution permanent magnet NMR products available through the company and it’s partners Aspect AI and Cosa-Xentaur.

Poster 1
Quantitative Proton Nuclear Magnetic Resonance Spectrometry (1H-NMR) for Determination of Acetylated Polysaccharides, Glucose, Maltodextrin, and Isocitrate in Aloe Vera Leaf Juice

John C. Edwards, Process NMR Associates, Danbury, Connecticut

Aloe Vera is a botanical component that is used widely in the cosmetic, natural product, herbal supplement, and pharmaceutical industries. The widespread use of Aloe Vera has lead to the need to adequately analyze the authenticity, quality, and quantity of the various components present in this material. The qNMR method described here was developed and validated by Process NMR Associates (Danbury, CT) and is similar to an independently validated method developed by Jiao et al [1]. The method described is to be included in an upcoming Monograph on Aloe Vera published by the American Herbal Pharmacopoeia. The method can be used for the detection and quantitation of the primary components of interest in Aloe Vera juice products and raw materials for compliance with IASC (International Aloe Science Council) certification requirements, specifically, for determination of the content of acetylated polysaccharides, the presence of glucose, the presence and content of maltodextrin, and the content of isocitrate. Additionally, for meeting quality control specifications beyond IASC requirements, the presence and content of the following groups of compounds can be determined: degradation products (e.g., lactic acid, pyruvic acid, succinic acid, fumaric acid, acetic acid, formic acid, and ethanol), preservatives (e.g., potassium sorbate, sodium benzoate, and citric acid/citrate), and other atypical impurities, additives, or adulterants (e.g., methanol, glycine, glycerol, sucrose, maltodextrin, flavorants (propylene glycol/ethanol)). We will describe a common internal-standard NMR methodology that does not require additional equipment or advanced automation software. The method is applicable to a number of different Aloe Vera raw materials and products, including liquid and dried juices. In aloe vera finished products the method is only applicable when the observable aloe vera constituents are present at a high enough concentration to be observed and are not obscured by additional product ingredients with signals in overlapping areas.

1. “Quantitative 1H-NMR spectrometry method for quality control of Aloe vera products”, Jiao, P., Jia, Q., Randel, G., Diehl, B., Weaver, S., Milligan, G., J AOAC Int., 93(3), 842-848, 2010

Poster 2
Practical Applications of Compact, Cryogen-Free High-Resolution 60 MHz Permanent Magnet NMR Systems for Reaction Monitoring and Online/At-Line Process Control

John C. Edwards, Process NMR Associates, LLC, 87A Sand Pit Road, Danbury, CT 06810 USA

For the past two decades high resolution 1H NMR at 60 MHz has been utilized to monitor the chemical physical properties of refinery and petrochemical feedstreams and products1. These approaches involve the use of partial least squares regression modelling to correlate NMR spectral variability with ASTM and other official test methods, allowing the NMR to predict results of physical property tests or GC analysis. The analysis is performed in a stop flow environment where solenoid valves are closed at the beginning of the NMR experiment. This approach allows up to 5 or 6 different sample streams to be sent to the sample in order to maximize the impact of the instrument. The current work with these permanent magnet NMR systems is to utilize them as chemistry detectors for bench-top reaction monitoring, mixing monitoring, dilution monitoring, or conversion monitoring. In the past use of NMR for these applications has been limited by the need to bring the “reaction” to the typical “superconducting” NMR lab. A compact high resolution NMR system will be described that can be situated on the bench-top or in the fume hood to be used as a continuous or stop-flow detector and/or an “in-situ” reaction monitoring system. The system uses a unique 1.5 Tesla permanent magnet that can accommodate sample diameters of 3-10 mm with half-height resolution approaching 1-3 Hz (depending on the sample size) and excellent single pulse sensitivity. Reaction monitoring can be performed using a simple flow cell analyzing total system volumes of 2 to 5 mL depending on the length and diameter of the transfer tubing. Further, detection limits of analytes in the 200+ ppm range are possible without the use of typical deuterated NMR solvents. Analysis times of 5 to 20 seconds are also possible at flow rates of 5 to 20+ ml/minute. Reaction monitoring directly in standard 5-10 mm NMR tubes using conventional (non-deuterated) reactants, solvents and analytes will also be described. Examples of 1H, 19F and 31P analyses will be described.

1.“Process NMR Spectroscopy: Technology and On-line Applications” John C. Edwards, and Paul J. Giammatteo, in Process Analytical Technology: Spectroscopic Tools and Implementation Strategies for the Chemical and Pharmaceutical Industries, 2nd Ed., Editor Katherine Bakeev, Blackwell-Wiley, 2010

Poster 3
Calculation of Average Molecular Descriptions of Heavy Petroleum Hydrocarbons by Combined Analysis by Quantitative 13C and DEPT-45 NMR Experiments

John C. Edwards

Process NMR Associates, LLC, 87A Sand Pit Rd, Danbury, CT 06810 USA

Over the years much debate has centered around the validity and accuracy of NMR measurements to accurately describe the sample chemistry of heavy petroleum materials. Of particular issue has been the calculated size of aromatic ring systems that in general seem to be underestimated in size by NMR methods. This underestimation is principally caused by variance in chemical shift ranges used by researchers to define the aromatic carbon types observed in the 13C NMR spectrum, in particular the bridgehead aromatic carbons that can be shown to overlap strongly with the protonated aromatic carbons. The ability to discern between bridgehead aromatic carbons and protonated carbons in the 108-129.5 ppm region of the spectrum is key in the derivation of molecular parameters that properly describe the “molecular average” present in the sample. Utilizing methodologies developed by Pugmire and Solum [1] for the solid-state 13C NMR analysis of coals and other carbonaceous solids we have developed a new liquid-state 13C NMR method that allows the relative quantification of overlapping protonated and bridgehead aromatic carbon signals to be determined [2]. The NMR experiments involve the combined analysis of both quantitative 13C single pulse excitation which observes “all carbons in the sample” and DEPT45 polarization transfer which observes only the protonated carbons in the sample. Though the DEPT45 results are not quantitative across all carbon types (CH, CH2, and CH3) due to polarization transfer differences, the technique is well enough understood that simple multiplication factors allow the relative intensities of the different carbons to be determined. An additional aspect of the experiments is the addition of a standard material (PEG polymer) that allows the calculation of the absolute percentage of the carbons observed by the NMR technique. This allows the relative amount of bridgehead carbon to be calculated by direct comparison of the aromatic region with the standard signal intensity. The average ring system sizes derived from these NMR experiments tend to be several ring systems larger than has been calculated in previous studies. In asphaltenes for example the ring systems are 5-7 rings in size rather than the 3-4 rings reported previously. The ring sizes determined by this new combined NMR method are in agreement with FTICR-MS and fluorescence measurements.

1) “Carbon-13 Solid-State NMR of Argonne Premium Coals”, Mark S. Solum, R.J. Pugmire, David M. Grant, Energy Fuels, 1989, 3(2), pp 187-193

2)” Comparison of Coal-Derived and Petroleum Asphaltenes by 13C Nuclear Magnetic Resonance, DEPT, and XRS”, A. Ballard Andrews, John C. Edwards, Andrew E. Pomerantz, Oliver C. Mullins, Dennis Nordlund, and Koyo Norinaga, Energy Fuels, 2011, 25 (7), pp 3068–3076

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