Introduction to Modern Liquid Chromatography, Third Edition part 16 pdf

As described above, and illustrated in Figure 3.11, the inlet and outlet check valves allow the pump head to alternately fill with mobile phase from the reservoir and deliver mobile phase

flow seat

(a)

(b)

(c)

seal

seat piston

spring

piston

Figure3.12 Check-valve designs (a) Simple ball and seat; (b, c) active check valves.

pump head Ceramic check valves may be used in some pumps, and sometimes a small spring is used to assist check-valve closure

Operation of the ball-type check valve is quite simple When the pressure on

the inlet side of the valve (below the ball in Fig 3.12a) is higher than that on the

outlet side, the ball will be displaced from the seat and solvent will flow through the

valve When the pressure is higher on the outlet side (above the ball in Fig 3.12a),

the ball will be pushed against the seat, which creates a seal so that no liquid passes through the valve As described above, and illustrated in Figure 3.11, the inlet and outlet check valves allow the pump head to alternately fill with mobile phase from the reservoir and deliver mobile phase to the column An alternative to the

ball-type check valve is the active check valve, shown in Figure 3.12b and described

in Section 3.5.1.3

(a)

(b)

(c)

(d )

Figure3.13 HPLC pump designs with corresponding flow and pressure profiles

(a) Single-piston reciprocating pump; (b) effect of a shaped driving cam; (c) dual-piston pump; (d) accumulator or tandem-piston design.

The single-piston pump with a constant-speed, linear drive will spend half

of the time filling and half of the time delivering solvent The resulting flow (and

pressure) profile is shown in Figure 3.13a These extreme pulses in flow and pressure

are undesirable for HPLC applications

An alternative single-piston design uses a specially shaped (e.g., elliptical) driving cam on the motor, or a variable-speed, stepper-driven motor, to move the piston With this modification, the piston speed can be varied within each pump cycle so that more than half of the time is spent in the delivery cycle and a small

fraction of the time is spent in the fill cycle (Fig 3.13b) Some pumps refine this

process further so that the pump controller remembers the pressure on the prior stroke and moves the piston forward rapidly at the beginning of the delivery stroke until the previous pressure is reached Then the piston slows to a constant speed until the end of the delivery stroke Even with variable-speed design and extensive pulse dampening, the single-piston pump does not produce a sufficiently stable flow and pressure for analytical HPLC Two refinements of the single-piston pump are

the dual-piston pump (Fig 3.13c, Section 3.5.1.1) and the accumulator-piston pump (Fig 3.13d, Section 3.5.1.2).

In addition to the pump components shown in Figure 3.11, most pumps have

a purge valve on the outlet side of the pump that directs the pump output to waste during pump priming, solvent changeover, and bubble removal Many pumps also have a fitting on the inlet side of the pump that allows for manually priming the pump with the aid of a syringe In the past, mechanical pulse dampers (e.g., Bourdon tubes) were used to compensate for pump pulsations; today, the need for mechanical pulse damping is due to low-pulse pump designs (e.g., dual-piston or accumulator-piston pumps, Sections 3.5.1.1, 3.5.1.2) Pulse dampers also add unwanted dwell volume for gradient applications (Section 3.5.3)

3.5.1.1 Dual-Piston Pumps

One way to minimize the pulsations of the single-piston pump is to use two pump heads in parallel so that, when one is filling, the other is delivering solvent This is

illustrated in Figure 3.13c with opposing pistons driven off the same cam Although

most designs use two cams driven off the same motor, the pistons are mounted in parallel beside each other for operational convenience With the use of a specially shaped driving-cam with the dual-piston pump, the pump output can be quite smooth, requiring little, if any additional pulse dampening Dual-piston pumps are one of the two most widely used pump designs for analytical HPLC today

3.5.1.2 Accumulator-Piston Pumps

An alternative design for the dual-piston pump is the accumulator-piston, or

tandem-piston design shown in Figure 3.13d In this case, one piston feeds into

the other piston at twice the flow rate For example, if a flow rate of 1 mL/min was

desired, the top piston (Fig 3.13d) would pump at 1 mL/min While the top piston

delivered solvent, the top (outlet) check valve would be open and the intermediate check valve (inlet for the top piston) would be closed Meanwhile the lower piston would fill at a rate of 2 mL/min, with its inlet check valve open Next, the lower piston would deliver solvent at 2 mL/min (while the upper piston filled), which would cause its inlet check valve to close and the intermediate check valve to open Half of this 2 mL/min flow (1 mL/min) would be used to fill the top piston and half would be pumped directly to the column

The accumulator-piston design, at least in theory, has several advantages over the dual-piston design Flow never stops to the column, so flow and pressure pul-sations should be minimized Because the check valves can be the most problematic components in the entire HPLC system, the reduction of the number of check valves from four (dual-piston) to three (accumulator-piston) can reduce check valve problems Furthermore, because solvent is always flowing to the column, the outlet check valve on the top pump is not necessary and it can be eliminated so that just

two check valves remain Although the simplicity of the accumulator-piston design makes it appear to be more reliable, many other factors go into the final pump per-formance (software, materials, assembly, mechanical tolerances, etc.) Most workers obtain comparable performance with either the dual-piston or accumulator-piston design

3.5.1.3 Active Check Valve

A final refinement in design can be applied to both the dual-piston and

accumulator-piston pump designs The ball-type check valve (Fig 3.12a) is

susceptible to leakage if a tiny bit of debris is lodged between the ball and the seat The surfaces are very hard (commonly sapphire and ruby), and even with the pressure of the pump pushing them closed, the ball-type valve can leak when particulates are present

The active check valve is an alternative design that works well as an inlet check

valve on the low-pressure side of the pump As illustrated in Figure 3.12b, the active

check valve depends on a polymeric seal and a mechanically driven piston to provide the sealing action During the fill stroke, the piston is lifted off the seal and solvent flows into the pump During the delivery stroke, the piston is pulled against the seal The increased surface area relative to the ball-type valve and the soft seal allows the active check valve to seal effectively, even when a small amount of particulate

matter is present In an alternative design of the active check valve (Fig 3.12c), a

ball-type check valve is used with a strong spring to close the check valve; a piston below the ball pushes it from the seat to open the valve

In the active check-valve system with dual-piston pumps (Fig 3.13c), only

two ball-type valves are used (the outlet check valves) With the accumulator-piston design, only one ball-type valve remains (the check valve between the upper and

lower pump chambers in Fig 3.13d; the outlet check valve is not needed) In both

cases a reduction in the number of ball-type check valves improves pump reliability

3.5.2 On-line Mixing

For isocratic methods the mobile phase can be hand-mixed; no additional mixing

is then required within the HPLC system On the other hand, most users take advantage of the convenience of on-line mixing and use the HPLC system to blend the mobile phase for isocratic methods, as well as for gradient methods where on-line mixing is required Even when on-line mixing is available, some premixing

of the mobile phase often gives quieter baselines, and in some cases, such as use with refractive index detection (Section 4.11), on-line mixing is unsuitable for good baselines at high sensitivity On-line mixing takes place by one of three techniques:

• high-pressure mixing

• low-pressure mixing

• hybrid systems

3.5.2.1 High-Pressure Mixing

With high-pressure-mixing systems (Fig 3.14), each solvent is delivered to the mixer

by a dedicated pump The ratio of solvents in the mobile phase is controlled by the

pumps

mixer

dwell-volume

to column

injector

A

B

Figure3.14 HPLC system with high-pressure mixing Dwell-volume located inside dashed line

relative flow rates of the pumps For example, if 1 mL/min of a 60/40 MeOH/water mobile phase (60%B) is selected, the MeOH pump delivers 0.6 mL/min and the water pump delivers 0.4 mL/min During gradient operation—where %B changes during the separation—the relative pump speeds change with the gradient program Because the solvents are blended under high pressure, outgassing (Section 3.3.1) is less of a problem than with low-pressure mixing, so degassing problems usually are minimal High-pressure-mixing systems are generally limited to the simultaneous use of two solvents, since another pump is required for each additional solvent Some HPLC systems have a solvent-selector valve on one or both pumps that allows the nonsimultaneous use of two or more solvents by the same pump This can be useful for method development (e.g., ACN and MeOH in separate runs) or for automated system flushing (e.g., flushing with water to remove buffer from the system) High-pressure mixing systems have an advantage over low-pressure mixing

in that the standard mixer can be replaced with a micro-mixer (Section 3.4.2.3) for applications, such as LC-MS (Section 4.14), that require minimum dwell-volumes Parts of the flow-stream that contribute to system dwell-volume are segregated within a dashed box in Figs 3.14 and 3.15 (see also Section 3.5.3)

injector pump

to column

dwell-volume mixer

solvent proportioning valve

controller

B A

Figure3.15 HPLC system with low-pressure mixing Dwell-volume located inside dashed line

3.5.2.2 Low-Pressure Mixing

With low-pressure-mixing systems (Fig 3.15), the mobile phase components are blended before they reach the pump Consequently these systems only require a single pump to deliver the mobile phase to the column Solvent blending takes place in a proportioning manifold that usually has a capacity for blending up to four different solvents The pump is operated at a constant flow rate, and the proportioning valve for each solvent is opened momentarily for a time (usually<1 sec) that is proportional

to its mobile-phase concentration Thus, for 1 mL/min of a 75/25 ACN/buffer mobile phase, the pump would deliver at a constant 1 mL/min, the ACN proportioning valve would be open 75% of the time, and the buffer valve 25% Gradients are formed by a continuous variation of the proportioning-valve–open-time ratios Because the solvents are mixed on the low-pressure side of the pump at atmospheric pressure, outgassing from the mixed solvent can generate bubbles that will cause pumping problems This means that mobile-phase degassing is required for all low-pressure-mixing systems It is also especially important, when low-pressure mixing is used, to make sure that the reservoir inlet-line frits and transfer tubing are not restricted A restriction in one of the frits (most common with the aqueous phase) can reduce the proportion of that solvent delivered to the mixer and create solvent proportioning errors To avoid this problem, it is wise to check the frits for free flow by use of the siphon test (Section 3.2.1) on a regular basis (e.g., monthly) 3.5.2.3 Hybrid Systems

Although high-pressure- and low-pressure-mixing systems are popular, at least two manufacturers (Thermo and Varian) produce a pumping system that relies

on a hybrid of the two In these hybrid systems the proportioning valves are mounted directly on the inlet to the pump (Fig 3.16), with an active check valve (Section 3.5.1.3) used for each solvent With solvents proportioned into the pump head one at a time in very small volumes, mixing takes place within the pump head under high pressure This way outgassing problems are minimized (any potential bubbles resulting from mixing stay in solution under pressure), and additional mixer volume is not needed By mounting the proportioning valves directly on the pump head, the extra dwell-volume normally associated with low-pressure mixing is eliminated When combined with a small piston-volume (24μL), one implementation

of this pump (Accela from Thermo) lists 65μL as the dwell-volume (Section 3.5.3), making it very attractive for use with gradient elution with small-peak-volume applications, such as fast HPLC and LC-MS

Figure3.16 Hybrid mixing system with proportioning valves for solvents A, B, and C

mounted on pump head (a) Cross-sectional view; (b) frontal view.

3.5.3 Gradient Systems

When gradient elution is used (Chapter 9), the mobile-phase composition must be changed during the gradient, so on-line mixing (Section 3.5.2) is required Both high-pressure- and low-pressure-mixing systems are used widely for gradient appli-cations The system dwell-volume is a major concern for gradient operations, one that is of little importance for isocratic separations A difference in dwell-volume between two HPLC systems can have a dramatic effect on the resulting chro-matograms (Section 9.2.2.4), and this is one of the primary reasons why gradient methods are hard to transfer (Section 9.3.8.2)

The dwell-volume comprises the system volume from the point at which the solvents are mixed until they reach the column inlet It can be seen in Figure 3.14 that the primary contributions to dwell-volume in a high-pressure-mixing sys-tem are the mixer, the autosampler (injector), and the connecting tubing For

a low-pressure-mixing system (Figure 3.15) additional connecting tubing on the low-pressure side of the pump and the pump head volume are included in the dwell-volume The dwell-volume should be measured (Section 3.10.1.2) for every gradient HPLC system In some cases the system can be modified to reduce the dwell-volume, such as by replacement of the mixer in high-pressure-mixing systems (Section 3.4.2.3)

3.5.4 Special Applications

Conventional pumping systems that can generate gradients at flow rates of 0.1 to

10 mL/min and pressures up to 6000 psi are sufficient for the majority of HPLC applications There are three application areas in which conventional HPLC systems may fall short of the analytical requirements:

• low flow

• high flow

• high pressure

These areas, particularly the first two, are sufficiently specialized to support books of their own, and are described only briefly here

3.5.4.1 Low-Flow (Micro and Nano) Applications

Separations in the proteomics and other ‘‘omics’’ fields often operate on a scale that is an order of magnitude or more smaller than conventional HPLC separations (for reviews of these applications see [9–10]) Roughly classified by column internal

diameter, such separations often are called micro-LC (100– 1000 μm i.d.) and

nano-LC (75–300μm), with no clear distinction between the two Such applications require flow rates that are well below the lower limit of≈0.1 mL/min that is available

from the pumps described earlier Specially designed pumps are capable of delivering flow rates as small as 1μL/min directly—or 50 nL/min with split flow at pressures

to 6000 psi (and higher for some instruments designed for high-pressure use, Section 3.5.4.3) Obviously tubing, fittings, autosamplers, and detectors must be scaled accordingly, or extra-column effects will be unacceptable Special capillary cells for UV detectors or direct introduction of the column effluent into an MS or MS/MS detector are common

3.5.4.2 High-Flow (Prep) Applications

Preparative applications of HPLC use larger columns and require higher flow rates than conventional HPLC pumps can provide (Section 15.2) For semi-prep applications the flow rates of 10 mL/min that are available from most HPLC pumps may be sufficient Several manufacturers offer modifications of their conventional pumps that increase the maximum flow rate from≈10 mL/min to between 20 and

50 mL/min Pressures often are below those encountered for analytical applications,

so pressure limits generally are not a concern Pumping systems that deliver 300

to 2000 mL/min at pressures up to 1800 psi are available Since many preparative applications are isocratic and flow-rate control is not as critical, pneumatically amplified (constant pressure) pumps can be used for some high-flow applications Because of the large volumes of solvent used, solvent recycling or recovery systems often are necessary with high-flow applications

3.5.4.3 High-Pressure Applications

With the current availability of columns packed with sub-2-μm particles (Section 5.2.1.2), the pressure limits of conventional HPLC systems (typically≤6000 psi) may restrict taking full advantage of these small particles (e.g., very fast sep-arations; Sections 2.5.3.1, 9.3.9.2) Several manufacturers offer HPLC systems capable of operation at>6000 psi High-pressure applications often emphasize high

sample-throughput, so run time can be reduced by the use of higher flow rates and shorter columns (typically 50- or 100-mm long) To help increase sensitivity (peak height), small-diameter columns (e.g., 1.0- or 2.1-mm i.d.) are used as well These separation characteristics reduce peak volumes, and often require modification of HPLC pumps, fittings, and other system components to minimize extra-column volume Most high-pressure equipment is based on the same design as conventional HPLC equipment, but with added high-pressure and low-volume capabilities, which may limit the range of some system settings For example, one system (Waters’ Acuity UPLC) specifies a maximum flow rate of 2 mL/min at pressures<9000 psi,

and 1 mL/min at higher pressures (up to 15,000 psi maximum); however, with small-diameter columns (e.g., 1–2.1-mm i.d.), these flow rates are adequate

3.6 AUTOSAMPLERS

The introduction of the sample into the column requires that a measured quantity of sample must be added to the flowing, pressurized mobile phase For open-column, stopped-flow, or some preparative separations, manual sample injection may be satisfactory But for automated, unattended analysis, which often involves hundreds

of samples per day, sample injection must be precise, accurate, and automatic For such applications, an autosampler is used Manual injection, popular in the past,

is seldom used today except during operator training or in very low throughput environments Descriptions of the sample-injection process and equipment are presented here in terms of autosamplers, but the same principles apply for manual injection

inlet

waste

Load

to column

pump

Filled-Loop Injection

c

p

s

w

sample mobile phase

Inject

Figure3.17 Six-port sample injection valve operated in filled-loop mode (a) Load position; (b) inject position Arrow shows direction of flow; s, sample inlet; w, to waste; p, mobile phase from pump; c, to column.

3.6.1 Six-Port Injection Valves

The sample-injection valve, originally designed for manual use, is the core component

of an autosampler Although other designs exist, the six-port, rotary valve is the most commonly used A block of stainless steel comprises the valve body, as shown schematically in Figure 3.17; connections for the sample inlet (s), waste outlet (w), sample loop, pump (p), and column (c) are shown for two positions of the valve:

load and inject In the load position (Fig 3.17a), the sample and waste ports are

connected to opposite ends of the loop, and the pump is connected to the column

To inject, the rotor is moved to the inject position (3.17b), and the contents of the

loop are swept onto the column; simultaneously, the sample inlet is connected to the waste outlet for flushing, if desired

A polymeric rotor seal serves to connect three pairs of the connections (see also Fig 17.3) Valve rotor-seals are usually made of a fluoropolymer or PEEK, and include additional materials to enhance structural integrity The PEEK used in rotor seals is a different blend than that used for extruded PEEK tubing, so solvent compatibility with tetrahydrofuran and chlorinated solvents does not appear to be

a problem [11]

3.6.1.1 Filled-Loop Injection

In the filled-loop injection mode, the volume of sample injected is controlled by the

volume of the sample loop For example, when a 20-μL sample loop is used, sample

is introduced in the inject position until excess sample exits the waste port When the valve is moved to the inject position, the 20-μL volume of sample trapped in the loop is pumped onto the column

Filled-loop injection can be very precise and accurate if the sample loop is

calibrated and overfilled It is inconvenient to change sample loops, so if the injection volume must be changed regularly, filled-loop injection generally is not used

inlet

waste

Load

to column

pump

Partial-Loop Injection

c

p

s

w

sample mobile phase

Inject

Figure3.18 Six-port sample injection valve operated in partially filled loop mode (a) Load position; (b) inject position Arrow shows direction of flow; s, sample inlet; w, to waste; p, mobile phase from pump; c, to column.

3.6.1.2 Partial-Loop Injection

An alternative to the use of the injection valve in the filled-loop mode is to partially fill

the injection loop, often referred to as partial-loop injection Operation is identical to

filled-loop injection, except that the loop volume is larger than the injection volume and a measured amount of sample must be placed in the loop For example, a 100-μL loop might be mounted on the valve, and a 20-μL sample would be measured with a

calibrated syringe and pushed into the loop in the load position (Fig 3.18a) (Usually

the remainder of the loop contains mobile phase.) The valve-rotor is then moved to

the inject position (Fig 3.18b), and the loop contents are pumped onto the column.

Note that the plumbing connections are such that the flow direction through the sam-ple loop is reversed in the load and injection positions This helps ensure the integrity

of the injected plug of sample—if the sample were to flow through a large volume of sample loop prior to entering the column, unwanted peak broadening would result

Partial-loop injection can be precise and accurate if the sample aspiration and

loop filling are precise and accurate, and if less than half of the loop volume is used

One potential problem related to injection accuracy is illustrated in Figure 3.19a

[12] In this case, a 20-μL loop was mounted on the injection valve and different volumes of sample were injected When less than 10 μL or more than 40 μL were dispensed into the loop, the detector response accurately reflected the injected volume However, in the region of 10 to 40μL, the detector response was less than

the expected amount This problem is related to laminar flow (Fig 3.19b) prior to

and in the sample loop When fluids pass through tubing, the molecules at the walls

of the tubing are slowed due to friction, resulting in a bullet-shaped flow profile characteristic of laminar flow The molecules at the center of the stream travel at approximately twice the velocity of those near the walls Thus it can be seen that

if 20μL of sample is introduced into a 20-μL loop (volume defined by the dashed

lines in Fig 3.19b), some of the sample at the beginning of the injection plug will

exit the loop to waste, whereas some of the sample at the end might not have entered the loop yet The result is an injection volume smaller than intended This