Enhancing your HPLC Separations using Temperature Programming

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Enhancing your HPLC Separations using Temperature Programming Brian Jones, Stephanie J. Marin, Jody Clark, and Dale Felix Selerity Technologies, Inc. 2484 W. Custer Road Salt Lake City, UT 84104 www.selerity.com

The High Temperature HPLC Advantage Speed Efficiency Selectivity Gradient elution

Faster and More Efficient Separations Speed Flatter van Deemter curves allow operation at flow rates many times optimal velocity Higher efficiency - better resolution Increased diffusion rates provide lower plate heights at higher flow rates Lower viscosity and back pressure permits higher flow rates with smaller particle size packings

Better Chromatography with Temperature Gradient Programming Change retention through temperature gradient programming Replace solvent gradients with temperature gradients Water less polar and more organic-like so less organic modifier needed

Obstacles to High Temperature HPLC Need a fully programmable easy-to-use oven capable of fast response Must eliminate thermal mismatch to reduce band-broadening Need columns stable at elevated temperatures Must correct for refractive index differences when mobile phase temperature is increased

The Selerity Series 9000 Total Temperature Controller Small footprint Sub-zero to 200 C Mobile phase preheating or precooling Precision mobile phase outlet temperature control Flammable vapor sensor Variable low voltage mobile phase preheater Integral high speed microcomputer control

Small and Versatile Temperature Programmable Column Heater/Chiller

Vapor Sensor Provides operator safety when working with flammable or toxic mobile phases at elevated temperatures Automatically cools and ventilates oven and sends a stop signal to the HPLC pump

Multiple Point Mobile Phase Temperature Monitoring Preheater (integral) Outlet temperature controller Auxiliary for optional user placement Electrically isolated thermocouples and RTD All can be internally calibrated to the column oven, which is itself calibrated with a NIST traceable reference standard

Cryo Capability with Mobile Phase Pre-Cooling Solid state Peltier electronic cooling Cryo fluid option for both mobile phase and oven (nitrogen and CO 2 )

Precision Mobile Phase Temperature Conditioning The hazards and detector instability problems of hot exiting mobile phases are eliminated

Fast Temperature Programming, Fast Cool-down Temperature gradients to +30 C/min Cool-down from 200 C in 2 minutes --High Analysis Throughput--

Solvent Pre-heater Design 6 1 22 3 5 4 (1) connection tubing from injector, (2) heater, (3) temperature sensor, (4) microprocessor controller, (5) column, (6) mobile phase flow

Mobile Phase Pre-heater Very fast response and non-invasive Low-mass and low-volume, <1 µl 0.005, 0.007 and 0.010 ID available Adds no dead volume

Axial Heat Profile

Variable Low Voltage Pre-heater Automatically steps power to the preheater in 60 mv DC increments Safe low voltage operation Typical voltage feeding the heater at 1 ml/min mobile phase flow brought to 150 C is only 6 volts

Variable Low Voltage Pre-heater Can lead, match, or lag oven temperature program for analyte focusing Automatically responds to changing mobile phase heat capacity through composition gradients or flow programming Convenient plug-in access in the front door

Why is Solvent Pre-heating so Important? No Pre-heating Flow Flow With Pre-heating

Separation of Barbiturates Mobile Phase Pre-heating Improves Chromatography 40 30 Barbital Pre-heater Off mv 20 Butabarbital Carbromal Secobarbital 10 Pre-heater On 0 2 4 6 8 10 12 14 Zirchrom PBD, 80 C Minutes

Separation of Steroids Using Water as a Mobile Phase 700 600 500 400 1 2 3 Flow Rate: Mobile Phase: Temperature: 4 6.0 ml/min Water 200 o C Testosterone Mix 1. Uracil 2. Androstadienedione 3. Androstenedione 4. Epitestosterone mv 300 200 1 Flow Rate: 3.0 ml/min Mobile Phase: 25:75 acetonitrile:water Temperature: 50 o C 100 2 3 4 0 0.0 0.2 0.4 0.6 0.8 1.0 1.2 1.4 1.6 1.8 2.0 Minutes Zirchrom PBD 100 X 4.6 mm column, UV 254 nm

Traditional Silica Columns Can t Take the Heat Water attacks siloxane bond or behind point of phase attachment Backside Attack H 2O: R Degradation of the Silica Support CH 3 Si + OH OH HO :OH O CH 3 Si O Si O Si H O + Si

The Selerity Blaze Silica Column Can Take the Heat Selerity polydentate phase protects the silanol groups Polymer attaches to backbone at several points R R R Si Si Si O OH O O Si O Si O Si O Si O

Separation of Analgesics on a Selerity Blaze C8 Using a Thermal Gradient 500 400 300 Acetaminophen Caffeine Salicylamide Aspirin Salicylic acid Ibuprofen Naproxen mv 200 100 0 0 1 2 3 4 5 6 7 8 9 Minutes Column: Selerity Blaze C8, 3 µm, 100 x 4.6 mm Mobile Phase: 40:60 acetonitrile:water with 0.1%TFA Flow Rate: 1.5 ml/min Detection: UV 220 nm Temperature Program: hold at 50 C for one minute, ramp to 100 C at 30 C/min, hold six min.

Other Columns That Can Take the Heat Columns stable at high temperatures Hamilton PRP-1 columns Thermo Hypersil-Keystone Hypercarb ZirChrom TM stationary phases Other columns under evaluation

Blank Thermal Gradients 50:50 Acetonitrile:Water at 254 nm 1400 1200 1000 Thermo Hypersil-Keystone Hypercarb Selerity Blaze C8 Hamilton PRP-1 Zirchrom Diamondbond Zirchrom CARB Zirchrom PBD 40 to 200 C at 15 /min hold 5 min 40 to 100 C at 15 /min hold 5 min 40 to 150 C at 15 /min hold 5 min 40 to 200 C at 15 /min hold 5 min 40 to 200 C at 15 /min hold 5 min 40 to 150 C at 15 /min hold 5 min mv 800 600 400 200 0 0.0 2.5 5.0 7.5 10.0 12.5 15.0 17.5 20.0 22.5 25.0 27.5 30.0 Minutes

Separation of Analgesics using a Hypercarb Column and a Thermal Gradient mv 175 150 125 100 75 (1)Caffeine (2)Aspirin (3)Salicylic Acid (4)Ibuprofen (5)Phenacetin (6)Acetaminophen (7)Naproxen 50 25 0 0 1 2 3 4 5 6 7 Minutes Column: Thermo Hypersil-Keystone Hypercarb, 7 µm, 100 x 4.6 mm Mobile Phase: 35:65 acetonitrile:water with 0.1% TFA Flow Rate: 4.0 ml/min Detection: UV 220 nm Temperature Program: thermal gradient from 125 to 200 C at 30 /min, hold five min.

Separation of Narcotics on Hypercarb Column Using a Thermal Gradient 300 mv 250 200 150 Morphine Hydromorphone Codeine Methadone Hydrocodone Oxycodone Diacetylmorphine 100 50 0 0 1 2 3 4 5 6 7 8 9 Minutes Column: Thermo Hypersil-Keystone Hypercarb, 7 µm, 100 x 4.6 mm Mobile Phase: 50:50 acetonitrile:50 mm ammonium acetate ph 9.0 Flow Rate: 1.0 ml/min Detection: UV 220 nm Temperature Program: hold at 50 C for two minutes, ramp to 150 C at 30 /min, hold ten min.

Aromatic Hydrocarbons at Three 800 60 Temperatures Uracil Benzene Toluene Ethylbenzene Naphthalene Biphenyl Tetrahydronaphthalene Anthracene Phenanthrene Chrysene mv 400 150 o C 20 100 o C 0 50 o C Chrysene elutes at 22 min 0 1 2 3 4 5 6 7 8 9 10 Minutes ZirChrom PBD 100 x 4.6 mm, UV 254 nm, 35:65 Acetonitrile:Water, 2.0 ml/min

Aromatic Hydrocarbons on PBD Column Using a Temperature Gradient 150 10 Uracil Benzene Toluene Ethylbenzene Naphthalene Biphenyl Tetrahydronaphthalene Anthracene Phenanthrene Chrysene (+impurity) mv 5 -baseline corrected- 0 0 1 2 3 4 5 6 7 Minutes Column: Zirchrom PBD 100 x 4.6 mm Mobile Phase: 35:65 Acetonitrile:Water Flow Rate: 2.0 ml/min Detection: UV 254 nm Temperature Program: 50 C to 150 C at 20 /min

Conclusions Temperature programming can be used successfully with 4.6 mm ID columns Independent mobile phase pre-heater control allows for improvement in peak efficiency The benefits of elevated temperature HPLC are now available for routine use

Future Work Explore the new capability of precision mobile phase temperature matching in subambient HPLC Determine optimal preheater program profiles as a function of column dimensions and oven ramp rates

Acknowledgements Thermo Hypersil-Keystone Hamilton Company ZirChrom Separations

Turn up the Heat Bring on the Cold Selerity Technologies Inc. 2484 W. Custer Rd. Salt Lake City, UT 84121 801-978-2295 hotlc@selerity.com www.selerity.com Patent applications have been filed relative to the new technologies presented in this work.