Instruction Manual Innov-X Systems Alpha Series™ X-Ray Fluorescence Spectrometers
Instruction Manual Innov-X Systems Alpha Series™ X-Ray Fluorescence Spectrometers
Instruction Manual Innov-X Systems Alpha Series™ X-Ray Fluorescence Spectrometers
INNOV-X SYSTEMS
ALPHA SERIES
X-RAY FLUORESCENCE
SPECTROMETERS
August 2005
Version 2.1
TABLE OF CONTENTS
Topic
Page
Chapter 1: INTRODUCTION
1.0 Inspecting the Analyzer
1.1 Components Included with the Analyzer
1.2 Quick Start Instructions
1.3 Introduction to XRF
1-1
1-1
1-2
1-3
2-1
2-1
2-1
2-2
2-3
2-3
2-4
2-5
3-1
3-1
3-2
3-3
3-3
3-4
3-7
3-8
3-9
3-12
3-13
3-14
3-14
4-1
4-1
4-1
4-3
4-3
4-7
4-8
4-14
5S-1
5S-1
5S-1
5S-2
5S-3
5S-6
Chapter 1 Introduction
1.0 INSPECTING YOUR INNOV-X ANALYZER
Upon receipt:
1.
2.
Locate and remove the shipping papers and documentation from under the lids foam padding.
Remove the Innov-X Analyzer and all of the components from the protective carrying case and
identify each on the enclosed shipping list.
3. Connect the battery charger to an 110V-240V AC power source. Place one Li-ion battery on the
charger and charge it for at least 2 hours. Charge the second battery.
4. Charge the HP iPAQ using the attached AC adaptor for at least hour.
5. Read and review the Quick Start section of the Users Manual. Innov-X recommends that you read
the entire manual.
6. Install the fully charged battery into the analyzer.
7. Press the ON/OFF button on the back of the analyzer and the power button on the iPAQ.
8. Select Innov-X from the start menu located in the upper left hand corner of iPAQ screen.
9. Select the desired analysis mode (i.e., Analytical, FastID, Pass/Fail or Soil). The instrument will
undergo a one minute hardware initialization period.
10. Standardize the instrument with the 316 Stainless Steel mask. Standardize the instrument every 4
hours or as directed by the display.
11. Release the software trigger lock and analyze a sample of known composition, in order to verify the
correct operation of the analyzer.
12. Analyze samples of unknown composition.
1-2
10. Release the software trigger lock by tapping the locked icon on the iPAQ screen and tapping yes
in response to the software prompt.
11. Test standard to verify instrument performance.
12. Results will display on screen. Subsequent tests may be started from either the Results or
Analysis screens.
Emitted Electron
Detector
Electron
K
Primary X-ray Photons
X-ray Tube
In XRF Spectrometry, high-energy primary X-ray photons are emitted from a source (X-ray tube) and
strike the sample. The primary photons from the X-ray tube have enough energy to knock electrons out of
the innermost, K or L, orbitals. When this occurs, the atoms become ions, which are unstable. Electrons
seek stability; therefore, an electron from an outer orbital, L or M, will move into the newly vacant space at
the inner orbital. As the electron from the outer orbital moves into the inner orbital space, it emits an
energy known as a secondary X-ray photon. This phenomenon is called fluorescence. The secondary Xray produced is characteristic of a specific element. The energy (E) of the emitted fluorescent X-ray
photon is determined by the difference in energies between the initial and final orbitals of the individual
transitions.
1-3
1400
X-ray Intensity
1200
1000
800
600
400
200
0
0
10
15
20
25
Energy (keV)
History
Wilhelm Roentgen discovered X-rays in 1895. Methods for identifying and quantifying elements using
XRF were first published by Henry Moseley in 1913. Much research and development of XRF continued
after Moseley's pioneering work, especially during WWII when rapid developments in the aircraft,
automotive, steel and other metals industries heightened the need to identify alloys quickly and reliably.
However, the first commercial XRF Spectrometers weren't available until the early 1950's. Those systems
were based on WDXRF technology and measured the characteristic wavelength of an element, one element
at a time. Although the use of these systems was critical for elemental analyses, they were large,
expensive, and required highly skilled operators to use and maintain them.
In the late 1960's, EDXRF technology, which measures the characteristic energy of an element, began to
rival the use of WDXRF due to the development of Si (Li) solid state detectors, which offered better energy
resolution of the signal. EDXRF systems offered the potential of collecting and displaying information on
all of the elements in a sample at the same time, as opposed to one at a time with typical WDXRF systems.
Many of the early EDXRF systems used radioisotopes for excitation instead of X-ray tubes, which could
require changing sources to determine all the elements of interest. Some of those early EDXRF systems
did not easily resolve multiple elements in a single analytical run.
As can be imagined, the equipment and applications of XRF Spectrometers have developed tremendously
since the 1960's. Advancements in technology, electronics, computers, software and the use and
modification of them for XRF Spectrometers by instrument manufacturers, research scientists & engineers,
and industrial users alike have led to the current state of the art in XRF Spectrometers. Now a mature
technology, XRF Spectrometry is routinely used for R&D, QC and analytical services in support of
production.
Elemental Analysis
1-4
XRF Spectrometry is the choice of many analysts for elemental analysis when compared to the other
techniques available. Wet chemistry instrument techniques for elemental analysis require destructive and
time-consuming specimen preparation, often using concentrated acids or other hazardous materials. Not
only is the sample destroyed, waste streams are generated during the analytical process that need to be
disposed of, many of which are hazardous. These wet chemistry elemental analysis techniques often take
twenty minutes to several hours for specimen preparation and analysis time. All of these factors lead to a
relatively high cost per sample. However, if PPB and lower elemental concentrations are the primary
measurement need, wet chemistry instrument elemental analysis techniques are necessary.
XRF Spectrometry easily and quickly identifies and quantifies elements over a wide dynamic concentration
range, from PPM levels up to virtually 100% by weight. XRF Spectrometry does not destroy the sample
and requires little, if any, specimen preparation. It has a very fast overall sample turnaround time. These
factors lead to a significant reduction in the per sample analytical cost when compared to other elemental
analysis techniques.
All elemental analysis techniques experience interferences, both chemical and physical in nature, and must
be corrected or compensated for in order to achieve adequate analytical results. Most wet chemistry
instrument techniques for elemental analysis suffer from interferences that are corrected for by both
extensive and complex specimen preparation techniques, instrumentation advancements, and by
mathematical corrections in the system's software. In XRF Spectrometry, the primary interference is from
other specific elements in a substance that can influence (matrix effects) the analysis of the element(s) of
interest. However, these interferences are well known and documented; and, instrumentation
advancements and mathematical corrections in the system's software easily and quickly correct for them.
In certain cases, the geometry of the sample can effect XRF analysis, but this is easily compensated for by
grinding or polishing the sample, or by pressing a pellet or making glass beads.
Quantitative analysis for XRF Spectrometry is typically performed using Empirical Methods (calibration
curves using standards similar in property to the unknown) or Fundamental Parameters (FP). FP is
frequently preferred because it allows elemental analysis to be performed with no standards or calibration
curves. This enables the analyst to use the system immediately, without having to spend additional time
setting up individual calibration curves for the various elements and materials of interest. The capabilities
of modern computers allow the use of this no-standard mathematical analysis, FP, accompanied by stored
libraries of known materials, to determine not only the elemental composition of an unknown material
quickly and easily, but even to identify the unknown material itself.
EDXRF Spectrometers
EDXRF Spectrometer systems are mechanically very simple; essentially there are no moving parts. An
EDXRF system typically has three major components: an excitation source, a spectrometer/detector, and a
data collection/processing unit. The ease of use, rapid analysis time, lower initial purchase price and
substantially lower long-term maintenance costs of EDXRF Spectrometers have led to having more
systems in use today worldwide than WDXRF Spectrometer systems.
Sample/Specimen
Excitation
Source
Data Collection/
Processing Unit
Spectrometer/
Detector
EDXRF has been found most useful for scrap alloy sorting, forensic science, environmental analysis,
archaeometry and a myriad of other elemental field-oriented analyses.
1-5
Portable
Battery operated, rechargeable
X-ray Tube-based (Ag or W anode, 10-40kV, 10-100uA)
Si PiN diode detector.
Integrated pocket PC
Pistol-shaped design for difficult testing locations and welds
Auto-compensation for irregular or small samples
Fundamental Parameters for no-standard analyses
Stored Grade Libraries for rapid Grade ID's
Stored Fingerprint Libraries for rapid material ID's
1-6
For more information on how to utilize your Innov-X Systems Handheld EDXRF Spectrometer optimally,
please review this Instruction Manual or contact us directly.
1-7
Batteries
Battery Charger
iPAQ cradle and charger
Testing Stand Assembly (not standard with all units)
Standardization Clip or Standardization Clip/Welding mask.
Hold the instrument by the handle, upside down, so the bottom of the instrument base is pointing
upward. Please refer to Fig. 2.2.
Hold the instrument so that the nose is pointing away from the operator.
Open the battery door on the bottom of the handle. The batteries have a small tab attached for
ease of removal.
2-1
4.
5.
Pull out the existing battery, and replace with a new battery.
Insert the charged battery into the analyzer such that the connectors on the top of the battery are
facing to the right. Note that the battery slot is keyed so that the battery can only be inserted one
way.
Figure 2.2a. Instrument handle. Pull the rubber latch and lift
door. Reach into opening and remove battery.
Right light
Off
On
On
Blink
Off
Off
Status
Battery is charging
Battery is 80% charged
Battery is completely charged
Error. Remove battery and replace on charger. If error persists, call
Innov-X Systems Technical support.
No battery is on charger
Table 2.1 Battery charger status lights
2-2
3.
4.
5.
If the battery on the iPAQ is completely discharged, charge it for at least one half hour.
You will be required to follow the prompts on the iPAQ screen before you can use the iPAQ. This
procedure involves realigning the screen by tapping in several spots, and going through a quick
tutorial.
The iPAQ will reinitialize the Innov-X Systems software. A message will appear indicating that
this is going to happen. You must tap ok to initialize.
The software will open automatically; a message will appear indicating that several registries have
been restored. Tap ok to dismiss this message.
Set the clock to the current time. Note, this is very important, as your data is indexed by date. If
the date in the iPAQ is incorrect, you may not be able to locate your results. The instrument will
not allow you to take a reading until the date has been changed.
a. From the Start Menu, tap Settings.
b. Select the System tab, and tap clock.
c. Set the proper date. Further details about this procedure can be found in the HP iPAQ
users manual.
2-3
connector, then tilt the front end up enough so it clears the front holder allowing the iPAQ to be lifted out
of the instrument.
Note: Never grab the iPAQ and twist it side-to-side to remove it from the analyzer. Always move
the iPAQ retainer forward as instructed above, slide the iPAQ forward and remove from the
analyzer.
Use the welding mask only for welds that are larger than the opening in the mask;
Make solid contact between the surface of the mask and the material to test;
Use the mask only in the Analytical Mode not with the standard Fast ID library;
Consider using longer test periods to compensate for the smaller testing area especially
with more difficult separations.
If it is desirable to use the welding mask in FastID mode, a user can create a special Welding Mask
Library. Teach all relevant alloys with the welding mask is in position. Make sure these fingerprints are
2-4
saved in library that contains ONLY fingerprints taught with a welding mask. When measuring a weld,
make sure the Weld library is the only one selected. By creating a special finger print library using the
welding mask, a user can get good results in the Fast ID Mode as well.
2-5
5. Put three knobs to secure testing stand onto analyzer. The iPAQ clip can be secured with any of the
knobs. This clip grabs the base of the iPAQ cradle to hold the iPAQ securely in place.
6. Place the iPAQ in the cradle and connect it to the
Auxiliary Port on the analyzer using the serial cable
adaptor.
2-6
The power cord, plug or battery contacts for the battery charger are damaged.
3-1
Liquid has been spilled or an object has fallen onto the instrument.
The instrument has been exposed to rain or water.
The instrument has been dropped or damaged.
There are noticeable signs of overheating.
The instrument does not operate normally when you follow operating instructions.
Safety Precautions:
Use the correct external power source: Ensure that the voltage is appropriate (100V-240 V/ 50-60 Hz) for
charging the battery packs. Do not overload an electrical outlet, power strip, or convenience receptacle.
The overall load should not exceed 80% of the branch circuit rating.
Use cables and power cords properly:
Plug the battery charger into a grounded electrical outlet that is easily accessible at all times. Do not pull
on cords and cables. When unplugging the cord form the electrical outlet, grasp and pull the cord by the
plug.
Handle battery packs properly; do not: disassemble, crush, puncture, short external contacts, dispose of in
fire or water, or expose a battery pack to temperatures higher than 60 oC (140 oF).Do not attempt to open or
service a battery pack.
WARNING: Danger of explosion if battery is incorrectly substituted. Replace only with Innov-X
specified batteries. Used batteries may be returned to Innov-X Systems for disposal.
3.
4.
5.
6.
Proper Usage. Never point the instrument at another person. Never point the instrument into the air
and perform a test. Never hold a sample in your hand and test that part of the sample.
Establish Controlled Areas. The location of storage and use should be of restricted access to limit
potential exposure to ionizing radiation. In use, the target should not be hand held and the area at least
three paces beyond the target should be unoccupied.
Specific Controls. The instrument should be stored, in a locked case, or locked cabinets when not in
use. When in use, it must remain in the direct control of a factory trained, certified operator.
Time - Distance - Shielding Policies. Operators should minimize the time around the energized
instrument, maximize the distance from the instrument window, and shoot into high density materials
whenever possible. Under no circumstances should the operator point the instrument at themselves or
others.
Prevent Exposure to Ionizing Radiation. - All reasonable measures, including labeling, operator
training and certification, and the concepts of time, distance, & shielding, should be implemented to
limit radiation exposure to as low as reasonably achievable (ALARA).
Personal Monitoring. Radiation control regulations may require implementation of a radiation
monitoring program, where each instrument operator wears a film badge or TLD detector for an initial
period of 1 year to establish a baseline exposure record. Continuing radiation monitoring after this
3-2
period is recommended, but may be discontinued if accepted by radiation control regulators. Please
refer to Sect. 3.10 for a list of providers of film badges.
Software Trigger lock. Before using the trigger, the user must tap on a lock icon located in the
lower right hand corner of the iPAQ screen. The user must then confirm that they wish to unlock
the trigger. If the instrument is used continuously, the software trigger lock will remain off. If
five minutes elapse between tests, the trigger will lock automatically.
3.
Software Proximity sensor. The software requires that a sample be present in front of the
analyzing window. This prevents the accidental exposure of bystanders to an open beam. If the
analyzer detects that a sample is not present, it will abort the test and shut off x-rays two seconds
after the test is started.
3-3
3-4
Figure 3.2.
3-5
Figures 3.2.: Performing a testing for a sample lying on the surface of a table. This is a good way to test
small samples, rather than holding them in your hand.
To analyzer small sample:
Place the sample onto a flat surface.
Place the window of the analyzer onto the sample and begin the test.
Safety Precautions:
Do not test samples in this manner at a desk or table where the operator is sitting. If the desk is made of
wood or another non-metallic material, some radiation will penetrate the desk and may provide exposure to
legs or feet if the operator is sitting at the desk or table.
Analytical Precautions:
If the sample does not completely cover the window, be sure the surface used does not contain metals or
even trace levels of metals, as this may affect the accuracy of the XRF result. The XRF may report the
presence of additional metals in the surface material. For this type of testing, it is good to place the sample
onto a piece of 1100series aluminum alloy and perform the analysis. The operator should disable the
aluminum analysis capability (See Section 8.3.3 in the manual for instructions).
Method 2: Use the testing stand as described above (see also Fig. 3.2).
3-6
The analyzer also has a label just below the iPAQ indicating, as shown in Figure 3.7:
CAUTION: Radiation. This Equipment Produces Radiation When Energized.
This label is required by most regulatory agencies. The term When Energized refers to the condition
where the tube is fully energized and the shutter is open. This condition is also indicated by the red
blinking light on the probe.
3-8
Trigger
<0.1
Location A
(Top)
<0.1
Location B
(Right Side)
<0.1
Location C
(Bottom)
<0.1
Location D
(Left Side)
<0.1
<0.1
<0.1
<0.1
<0.1
<0.1
Table 3.1. Dose rates (units of mrem/hr) at various locations with a metal sample covering the window and
with no sample present. For no sample the analyzer is shooting the x-ray beam into air.
As shown in the Table 3-1, the dose to the operators hand is negligible. The radiation levels at the side
surfaces of the instrument snout (aluminum housing) are all <0.1 mrem/hour. Despite these low levels of
radiation, there is no reason for any body part to be in the locations denoted A, B, C and D!
Table 3-2 shows the radiation levels directly in the x-ray beam that is emitted from the analyzer. Radiation
levels at the exit aperture (or port) are substantial. There is no reason for the operator or any personnel to
be exposed by the direct beam. Operators should never hold samples in their fingers or cupped in their
hands, as this may generate a significant radiation exposure.
Operations should never point the analyzer at another person and start a test, as this may also provide
significant exposure to the person if they are within a few inches of the port of the instrument.
Radiation Levels in the Primary Beam Versus Distance from Port:
For Alloy Analysis, Standard Beam Conditions: 35kV, 5 uA, 2mm aluminum filtering:
Tube
Conditions
At Trigger,
or any part
of operators
body.
<0.05
At Window
4 inches
12 inches
36 inches
48 inches
35 kV, 5 uA,
28,160
2,080
186
24
14
2 mm Al
filtering
15 kV, 25
< 0.05
27,780
1,620
145
19
11
uA, thinner
filter
material
Table 3.2. Dose rates (units of mrem/hr) in the direct x-ray beam being emitted from the analyzer
3-9
For the x-ray energy emitted by portable XRF analyzers (10-60 keV region), the bone in the
fingers will absorb radiation about 3-5 times more than soft tissue, so the bone would be at an
elevated radiation risk compared to soft tissue. For this reason no person shall hold a test
specimen in front of the window with the fingers in the direct beam, or direct the beam at any part
of the human body. Reference: Health Physics 66(4):463-471;1994.
Misuse Example 1:
Operator holds samples in front
of window with fingers, such
that fingers are directly in the
primary beam. Do not do this!.
For fingers at the port, in the primary beam, the maximum dose to the
fingers is 28,160 mrem/hr. Assume an operator performs a 10 sec test
(typical). The dose to the operators fingers or hand is 28,160 x
(10/3600) = 78 mrem. If the operator did this 641 times/year they
would exceed the allowable annual dose of 50,000 mrem to an
extremity. In Canada, the maximum allowed dose is 500 mSv/year
(Canada ICRP radiation worker) or 50 mSv/year (Canada ICRP general
public).
If the test time was 30 seconds instead of 10 seconds, the operator would
receive a dose of 234 mrem for each exposure, and thus would
exceed the annual safe limit of 50,000 mrem after 213 tests.
Even though it is unlikely to make this mistake so many times in a year,
do not even do it once. Take the extra time to test a sample on a surface
or use a testing stand. Note: If the operator takes an average of
only two shortcuts per week and places his/her fingers within
the primary x-ray beam at the window, they will exceed the
annual dose rate.
3-10
Misuse Example 2:
Operator places analyzer
against body and pulls the
trigger to start a test. Analyzer
tests to preset testing time
(usually 10 seconds) unless
operator pulls trigger again to
stop test. This applies to
analyzer being in contact with
operator or with bystander.
Misuse Example 3:
Operator manages to initiate a
test for 10 seconds and exposes
a bystander that is standing 12
away from analyzer port. What
is exposure to bystander?
13.25 t
Dose = 1 mrem
x
D + 1.25 10
D = distance from port in inches
T = testing time
Example: Bystander is 3 away from port for a 30 second test. In this
case the dose is calculated as:
2
13.25 30
Dose = 1 mr
x = 0.38mrem
36 + 1.25 10
US OSHA: Maximum allowable level is 5,000 mrem assuming
bystanders torso is exposed. Thus, this misuse would have to occur
12,500 times in a year to the same bystander before that bystander
achieved his maximum allowed dose.
ICRP: 5000 times for rad worker, 250 for general public
3-11
Mammogram:
100-200 mrem
1-2 mrem.
From the above table, a single case of analyzer misuse, thus producing a one-time exposure of 70250 mrem, is comparable with single-event common medical x-ray procedures such as an annual
chest x-ray or mammogram, or 25-50 airline flights in a year, and thus is not considered harmful.
Regular misuse, such as taking safety shortcuts twice weekly, produces radiation exposure that
greatly exceeds these typical levels and should be avoided entirely.
3-12
Answer: The x-ray tube used in the Innov-X system produces between 1,000 and 10,000 times
lower power than most radiography systems (0.5-1 watt for Innov-X versus kW for radiography
systems). This is because a portable XRF is designed to perform surface analysis of alloys and
other samples, whereas radiography systems are designed to shoot x-rays entirely through metal
components in order to obtain an image on the other side of the object being bombarded with xrays. For example, many tube-based radiography systems use a 300-400 kV tube and currents in
the tens or hundreds of milliamps (mA). The Innov-X analyzer uses a tube operating at 35 kV and
5-30 micro-amps. The radiation levels produced are therefore thousands or tens of thousands
times lower with the Innov-X system.
Question: Should we use dosimeter badges with the Innov-X analyzer.
Answer: Dosimeter badges are required by some states, and optional by other states. Innov-X
recommends that operators wear badges, at least for the first year of operation, as a general
precaution to flag any misuse of the analyzer. Dosimeter badges are available for the torso
(generally worn on the belt loop or shirt pocket) and are available as ring badges. The best
single badge to obtain is a ring badge that is worn on a finger, on the opposite hand used to hold
the analyzer. This will record accidental exposure for the most likely case an operator grabbing
a small sample and holding it in one hand while analyzing it. Note: these badges generally have a
threshold of 10 mrem, and are renewed monthly. So it will take several cases of misuse even to
obtain a reading on a typical badge. When purchasing a badge, obtain the type used for x-ray and
low energy gamma ray radiation.
Keep the system in a controlled location, where only authorized users are likely to have access to
the analyzer at any given time.
Make a simple sign that is kept with the analyzer indicating that an operator must have completed
a training class provided by your company or must have attended an Innov-X training course in
order to use the analyzer. Note that when the Innov-X system is turned on, the screen displays a
message indicating that the system should only be used by authorized personnel.
Emergency Response:
Because the Innov-X system is a battery operated, x-ray tube based analyzer, the emergency response plan
is very simple. If the operator believes the analyzer is locked up in an OPEN position, they should do
two things:
1.
2.
Press the On/Off switch on the base to power the analyzer off. The green LED indicator will turn
off, indicating system power is off. At this point it is not possible for the analyzer to be producing
x-rays.
As an additional precaution, the operator may remove the battery trap door at the bottom of the
analyzer (have the nose pointing away from personnel), and pull out the battery. Even if the
operator has failed to properly power the system off in Step #1, removing the battery guarantees
that no x-rays can be produced. There is no electrical power being provided to the x-ray tube.
Note: It would be highly unusual for an operator to somehow lock up the analyzer with the x-ray tube
powered on. This would require the operator to crash the iPAQ during an analysis. If this happens the
analyzer will shut off the x-ray tube 10 seconds after the last communication with the iPAQ. However, if at
any time the operator believes the x-ray tube is on and no test is in progress, powering off the analyzer and
3-13
restarting will automatically shut down the x-ray tube and close the shutter. It will no longer be possible to
produce x-rays at this point.
AEIL
Houston, TX
713-790-9719
Purpose of device. Generally this is Analytical or Industrial. Be sure to inform the state
registration office that the device will NOT be used for radiography or for medical uses.
Radiation Safety Officer Monitors training, safe use, and controls access to the instrument.
Authorized Users Trained by Innov-X Factory Authorized Representatives in the safe and proper
use of the XRF.
Operating parameters of the analyzer 35 kV, 5-30 micro-amps.
Type of system, either fixed, mobile or portable. Generally the correct choice is Portable.
User Training Specified Indicate that only individuals receiving manufacturer training,
documented by a manufacturers training certificate will operate the instrument.
Personal Monitoring. This may be required by radiation control authorities. Many registration
forms will ask that you indicate whether or not you intend to perform dosimeter monitoring.
Copy of Registration & Manual at the Job Site
If you have any questions regarding the type of registration form or filling out the form, please contact
Innov-X Systems. Many states may confuse a portable XRF system that uses a tube with medical or
3-14
industrial radiography systems. This is because of the relative newness of portable tube-based systems. In
all likelihood, Innov-X personnel have experience providing the necessary documentation to the state in
question, and can readily assist the customer in this process.
3-15
Chapter 4 Operation
4.0 OPERATION - GENERAL
Power to the instrument is controlled by the ON/OFF button located at the rear of the analyzer. The green
LED next to this button will illuminate when the analyzer power is on. The iPAQ operates on the Microsoft
Windows CE operating system and is activated separately by the power button on the right top face, just
over the display. The trigger is locked via the software.
General tips
The Start Menu is found in the upper left corner of the iPAQ screen. This is used to launch all
applications, including the Innov-X Systems Analyzer software.
The instrument is designed as a point and shoot system that requires little, if any, entry of
information for most operations. In the event the user modifies the grade library, enters testing
information data, or performs other functions, it will be necessary to enter data via the virtual
keyboard, which can be accessed by tapping the keyboard icon in the lower right corner. The
iPAQ also includes character recognition software. This can be selected from the drop-down
menu to the right of the keyboard icon.
The File toolbar which will be used to Change Functions, Screens and Options is located at the
bottom of the screen.
It is possible to cut, copy, rename and delete files from within Windows File Explorer by selecting
the file to be modified and holding the stylus on the screen for 2 seconds.
Pressing buttons on the bottom of the iPAQ will perform various functions that are described in
the iPAQ documentation. The button on the right hand size of the analyzer is the iPAQ task
manager. Pressing this button will show all programs that are currently open. Open files can be
closed from this menu. Simply hold the stylus on the file for a few seconds. The option to close
the file will appear.
Main Menu screen: Used to select the analysis mode, open the results screen, and change the
administrator password.
Analysis Screen: Used to change settings, edit libraries, and perform tests.
Results Screen: Displays results from current reading, allows scrolling back to previous test
results. Allows recorded data to be exported to a comma delimited file which is directly
compatible with Microsoft Excel.
4-1
are available on the analyzer are shown in blue. For information on adding additional analysis modes to an
analyzer, please contact the Innov-X Sales Department at 781-938-5005.
Use the Main Menu to select the desired analysis mode.
The analysis mode can be selected by either tapping on the
name of the method (shown in blue) or by selecting the
appropriate mode from the Modes menu.
The administrative password can be changed by selecting
Options Change Password.
It is possible to go directly to the Results Screen by selecting
ViewResults. If the results screen is opened in this
manner, it is possible to view results when the iPAQ is not
connected to the analyzer.
4-2
4.4 STANDARDIZATION
4.4.1 Standardization Procedure
Before performing tests, it is necessary to standardize the instrument. This automated procedure involves
collecting a spectrum on a known standard (Alloy 316) and comparing a variety of parameters to values
stored when the instrument was calibrated at the factory. If there are any problems with the instrument,
they will be indicated by an error message.
The standardization procedure takes about 1 minute. Standardization must be done any time the analyzer
hardware is initiated or restarted and must be repeated if the instrument is operating for more than 4 hours.
4-3
It is possible to re-standardize the instrument at any point while the software is running. Standardization is
always initiated from the Analysis Screen of any Mode.
If the analyzer is restarted, you will be required to standardize the
instrument before performing any measurements. This is indicated by
the message Standardization Required. Please place a
standardization clip over the analyzer window. Then tap here to
standardize. on the analysis screen
4-4
4-5
After closing the Standardization Failed message, two additional screens will appear. The first is a picture
of the spectrum generated during the standardization. The second is a summary comparing factory set
values for resolution, count rate, and peak positions to values calculated during the standardization.
When standardization fails, verify that the standardization mask is in place, and attempt standardization
again. To restandardize after a failure, tap the grey box in the center of the display, or choose
FileStandardize. If you are using a weld collimator, make sure that the solid part of the mask is
covering the window.
If standardization fails again, exit the analysis screen and power off the instrument. Restart and
restandardize. If the standardization fails a 3rd time, you will be prompted to perform a soft reset of the
iPAQ. Selecting Yes on this screen will automatically soft reset the IPAQ. You should also power cycle the
instrument. Restart and restandardize. If the standardization fails again, replace the battery in the instrument
and attempt another standardization. If this fails, please contact the Innov-X Systems service center at 781-
938-5005.
4-6
In order to continue testing, replace the battery immediately, and then tap
OK. The analysis screen will remain open, and the instrument will
reinitialize. This process will take 1 minute. It is not necessary to restandardize, provided that less than 4 hours has elapsed since the last
standardization and the battery swap is completed within 10 minutes.
After re-initialization is completed, testing can continue.
If the battery is not replaced, and cancel is selected, the Analysis screen
will close. When the software is restarted, the instrument will go through
a complete 1 minute initialization and will require standardization.
4-7
4-8
Select Direct Edit for a text field which will accept data
from the virtual keyboard, or a bar code scanner.
Select Unused to eliminate the field from the Test Info screen.
To add an entry from a drop-down list, tap the +/- symbol next to
appropriate field, and select Add. Type the new info into the blank
text box that appears. Select OK and the entry will be added to the
drop-down menu.
4-9
All modifications to trees are made from the menu shown on the right.
It is possible to add, edit, delete or rename trees. Select the
appropriate choice from the menu to perform any of these functions.
When you have finished creating/editing your tree, highlight it and
select Done.
4-10
Enter the Name of the Tree in the text box and select OK.
4-11
Once the tree is started, continue to Tap Add Item to add a top level
menu item, or select an item and tap Add SubItem to link a
subcategory to the item. Continue until all items have been added.
In this example, the part numbers for pipes and valves are separated
into categories. The pipes are further subdivided by material type.
1.
4-12
2.
3.
4.
5.
6.
4-13
You will then be presented with the same test information screen described in Section 4.5.2: Entering Test
Information.
4-14
6.
7.
You will be prompted to Select Synchronization Settings. Select Files only. It is important
to make sure that Files is the only item checked. Otherwise, the files such as address books and
emails will be copied from the desktop computer to the iPAQ.
8.
9.
A folder will automatically be created on the PCs desktop with the name of the device entered in
step 8 above. Results files saved on the iPAQ will automatically be synched and will be stored in
this folder. Opening this folder and clicking on the name of the file will open the file in Excel.
10. After ActiveSync is set up correctly, copying results to a desktop computer will consist of
4-15
a.
b.
c.
4-16
After choosing which readings to export, you may choose to export all
data, or just data from a specific mode. Selecting the arrow to the
right of the mode to export will open a drop-down menu. Select the
mode for which you want to export data.
All standardization data are stored as results files. These data are
automatically included in exported results files when the selected
Mode to export is All. Additionally, it is possible to export only the
standardization data by selecting Standardization as the Mode to
export.
When the proper selections have been made, select OK. A Save As
box will appear. Select the folder in which you want to save the data,
and name the file. The file Type will always be Comma Separated
Values. The recommended Location is Main memory and Folder is
None. This will export files into the My Documents folder in the
main Memory of the iPAQ.
If you select a File Name which already exists, you will be asked if
you want to replace the existing file. If you do, select Yes. Otherwise
select No and choose another file name.
4-17
A status bar will indicate the progress of the export. It may take
several minutes to export many readings. Daily downloading and
weekly erasing of data simplifies and shortens this procedure.
When all readings are exported, a message will appear confirming the
export. Tap ok to acknowledge and clear the reading.
4-18
Two columns appear on the screen; the column on the left lists fields
which will NOT be exported, and the right-hand column lists fields
which will be exported.
Fields can be moved from one column to another via the >> and <<
buttons located in the center of the screen
Exported field order can be changed by using the Up/Down buttons.
Select a field and move it up or down as desired
Once all changes have been made, choose Specify Chemistry if
changes need to be made to the list of exported elements.
In chemistry is not edited, select Save Changes to keep the modified
settings, or Discard Changes to ignore any changes.
When all changes have been made, tap Save Changes or Discard
changes, depending on whether the changes should be saved.
4-19
Choose the File name, and make sure that Comma Separated Values
and Main Memory are selected. This will save the spectrum to the
My Documents folder in the Main Memory of the iPAQ.
4-20
4-21
4-22
Chapter 5
Soil Analysis
The Innov-X analyzer can be used to analyze in situ (directly on the ground), bagged or prepared soil
samples. A guide to Soil analysis using field portable X-ray fluorescence is found in the appendix. This
document summarizes EPA Method 6200 which is the standard protocol for field screening. It also
provides information on prepared sample testing.
5S-1
5S-2
The standard soil chemistry display can be modified by using the View Menu. As with all Innov-X
analytical modes, it is possible to view spectra and Test Information.
5S-3
The minimum testing time is the required time that must elapse before results can be calculated. Live
Update results will not be displayed on the screen until the minimum has elapsed, likewise a test must
complete the minimum time before any test end condition can be used. If a test is stopped before the
minimum testing time has elapsed, the test will be aborted, and no results will be calculated.
Maximum testing time is relevant only if Maximum Testing Time is selected from Set Test End
Condition. This will automatically end the test at a preset testing time. Typically, the maximum testing
time will be in excess of 30 seconds, and may be 1 or 2 minutes, depending on detection limits and desired
precision.
It should be noted, that all testing times in this section refer to Real Time, the time the measurement takes
when timed on a normal clock. The time stored with each analytical result (accessible by selecting
ViewTest Information from the Results screen), refers to the tests Live Time. This is the amount of
time that the analyzer hardware was collecting spectra. Since there is some detector dead time associated
with a measurement, the live time of a test will be slightly shorter than the preset Real time.
5S-4
specified relative standard deviation of the reading. Additionally, you can set up an action level for a single
element. As soon as the measuring statistics are good enough to ensure that that the reading is above,
below or at the action level, the test will end automatically. This allows for very rapid tests for elements
that are well above or below an action level.
In all modes, pressing Stop, or pulling the trigger will end the test. If the minimum testing time has
elapsed, results will be calculated. Otherwise the test will be aborted without calculating results.
Changes to the test end condition are made by selecting OptionsSet
Test End Condition
The currently selected end condition will be displayed at the bottom
of the screen above the Start button on the Ready To Test screen.
Manual: This option allows you to look at the results which are
being continually updated on the screen and determine when the
results look satisfactory. The test will continue until the trigger is
pulled, or Stop is tapped on the iPAQ screen. Results will be
calculated if the testing time has exceeded the Minimum Test time
which is set up in OptionsSet Testing Times. In order to preserve
battery life, the software will stop if the testing time exceeds 300
seconds, since there is little to no advantage to continuing a test
beyond 300 seconds.
To use Manual Test End Condition, simply choose OptionsSet Test
End Condition and select Manual. Press OK to return to the analysis
screen.
5S-5
Action Level: System ends test when result for target analyte
including chosen precision level is above or below pre-set action
level.
To choose to end a test based on an Action Level, select OptionsSet
Test End Condition and select Action Level. Select a target analyte,
specify an action level in ppm, and a confidence level. This
confidence level refers to the number of sigma required for the
precision. This should typically be set to 2. Tap OK to save your
selections.
5S-6
Standard Test Only: The analyzer will provide analysis for the standard suite of elements.
Light Element Analysis Only: The analyzer will provide analysis for elements in the LEAP suite
(Typically Ti, Ba and Cr)
Sequential Testing: When sequential testing is selected, all tests will start with an analysis of elements in
the standard suite. If that test ends due to reaching the selected end condition of Maximum Test Time,
Action Level, or RSD, then the analyzer will immediately begin a second test analyzing the LEAP suite of
elements. At the conclusion of this test, the Results screen will open with two new entries. The first
summarizes the standard test results, while the second summarizes the LEAP results. For safety reasons,
the second test will not begin if the test ends due to user intervention (pulling the trigger or hitting Stop). In
this case, the Results screen will open with only one reading.
If Light Element Analysis Only is
activated, the words Light
Element Analysis Mode will
appear above the currently
selected End Condition.
Instrument operation in this mode
is identical to Standard (NonLEAP) analysis. Tests can be
started or stopped either by
pulling the trigger, or by tapping
the Start/Stop button on the iPAQ
screen. The results screen for a
test will show results for all
elements analyzed with the LEAP
mode.
Test in progress screen, LEAP
Only, Live Updates on
5S-7
As with standard tests, the minimum testing time is the required time that must elapse before results can be
calculated. Live Update results will not be displayed on the screen until the minimum has elapsed, likewise
a test must complete the minimum time before any test end condition can be used. If a test is stopped
before the minimum testing time has elapsed, the test will be aborted, and no results will be calculated.
5S-8
Possible Solutions
Soil Appendix 1
Soil Appendix 2
Soil Appendix 3
Appendix 2:
A guideline to using portable XRF according to EPA Method 6200, basic overview
of the technique of x-ray fluorescence (XRF), appropriate data quality assurance
protocols and sample preparation steps for operators analyzing prepared soil
samples.
Prepared by:
Innov-X Systems, Inc.
January, 2003
Innov-X Systems
300 Wildwood Ave, Suite 210
Woburn, MA 01801
781-938-5005
781-938-0128 (fax)
info@innov-xsys.com
www.innov-xsys.com
Soil Appendix 4
Soil Appendix 5
In-situ soil testing: The XRF is placed directly onto the ground for soil testing.
Operators remove any plant growth and foreign objects so that the analyzer probe is
flush to the soil.
Bagged soil sample testing. A soil sample is collected in a thin plastic bag (i.e. a
Baggie) and testing directly through the Baggie. Except for a few elements
namely Cr, V and Ba testing through the thin plastic used for a plastic bag has little
effect on the test result. Results for Cr, V and Ba will be lower by 20-30%.
Prepared soil sample testing. Prepared sample testing assures the operator of the
maximum possible accuracy. Prepared sample tests require a sample to be collected,
dried if necessary, sieved and ground into a powder. The prepared sample is then
placed into a baggie or XRF cup for analysis. A complete Soil Preparation Guide
is provided in Appendix 1.
All analytical methods require a uniform, homogenous sample for the best results. XRF is no
different! The methods described in EPA Method 6200, namely In-situ and bagged sample
testing, are considered field-screening methods. Although a field-screening method, in-situ
testing is a valuable technique because it generates a great deal of data very quickly. Prepared
soil samples generally offer the best accuracy, albeit with several minutes of sample preparation
required per sample.
Soil Appendix 6
In-situ testing usually provides only screening-level data quality. This is because analytical
testing always requires a uniform, homogeneous sample matrix. A laboratory achieves this by
digesting the sample into a hot acid before analysis. Testing directly on the ground does not
ensure uniformity is met. Preparing a sample provides a uniform sample and likely better
analytical data quality, although several minutes of testing time is required.
Most portable XRF operators use a mixture of in-situ and prepared sample testing. Several
examples are described below. The exact mixture of in-situ and prepared sample testing depends
upon the goals of the soil testing. The examples below serve as guidelines. Please contact InnovX (1-866-4 Innov-X or 866-446-6689) to discuss your specific testing requirements.
Example 1: Initial site investigation to provide detailed contamination data with efficient
use of laboratory analysis costs.
Problem: Site needs to be assessed for metals contamination. Little information is available about
what metals are present, likely contamination levels or geographic profile of contamination.
The goal of testing is to determine what metals are present at what levels, both in area and in
depth into soil. Additionally, testing will locate possible contamination plumes and/or possible
sources of contamination.
Recommended Testing Plan: This example uses predominately in-situ testing. The analyst will
perform in-situ testing, and gather samples into plastic bags for XRF analysis. A testing grid
should be established in two or three dimensions, every several feet. XRF tests can be taken at
each location or bagged samples can be collected from each location for later analysis. The insitu data for each element analyzed may be plotted in a 2-dimensional grid (X, Y coordinates
versus elemental concentration) to profile a site. These concentration profiles are ideal for
showing contamination patterns, boundaries and plumes. Combining this data with historical use
data from the site often allows the operator to deduce sources of contamination. Obtaining this
level of geographic data with purely laboratory analysis would produce excessive analytical costs.
Prepared sample analysis should also be done to confirm the regions where in-situ data indicates
low or non-detected levels of metal contaminant. There is little need to prepare areas where insitu testing indicates high concentration levels. Innov-X recommends the same procedure as EPA
Method 6200. For locations where in-situ tested indicate low or non-detected concentrations,
calculate the total number of in-situ tests, collect 5% of this number of tests from the various
locations, and prepare these samples according to Appendix 1. Use these prepared samples to
confirm the findings of the in-situ testing. Send a subset of these prepared samples to a
laboratory for confirmatory results.
Cost Justification. To adequately characterize a site may require 100-200 samples/acre to be sure
the contaminated areas are firmly established. This work may be done with in-situ testing to
generate laboratory savings of $5,000 - $10,000/acre depending upon the number of elements
being analyzed. The cost reduction in off-site analysis often justifies the price of the XRF.
Example 2: Monitor remediation efforts and assure site meets clearance levels before
contractors leave the site.
Goal: Minimize remediation costs by only treating contaminated soil, and obtain immediate
verification that various site locations meet clearance objectives.
Soil Appendix 7
Recommended Testing Plan: This type of project uses a lot of both in-situ and prepared sample
testing. Use in-situ testing to thoroughly delineate contamination regions in both area and depth.
To determine depth profiles, test surface soil, remove at least 1-2 inches, and retest. Repeat this
step as necessary to profile contamination depth to guide remediation activities. (XRF is a
surface technique and only analysis the first few mm of soil sample). As part of clearance, collect
several samples from cleared area. Prepare samples according to Appendix 1 and test with
portable XRF.
If XRF indicates that concentration levels are in excess of clearance requirements, then continue
remediation efforts.
If XRF indicates that concentration levels are below clearance requirements, then discontinue
remediation efforts, and send a subset of the samples to an analytical laboratory to confirm
results. Most operators safely assume that the cleanup requirements have been met for the
elements in question, but await final analysis from the laboratory.
If XRF lists concentration levels as non-detected, but the detection level reported exceeds
clearance requirements, send samples to a laboratory for final results.
Cost Justification: In-situ results are used to guide remediation efforts, in order to obtain
maximum efficiency. Efficiency is produced because contamination boundaries are firmly
established, thus avoiding remediation efforts with clean soil. Prepared sample testing is used
to assure that clearance requirements are met on-site in near real-time (pending laboratory
confirmation). Costs savings are generated by avoiding clearance failures. The contractors can
leave the site earlier and will not be called back to the site for additional cleanup.
Important Note: Never clear a site based solely on in-situ testing. Always use well-prepared
samples to make a clearance decision.
Soil Appendix 8
These procedures are taken from EPA Method 6200 and updated to be specific to the Innov-X
analyzer. Quality assurance here consists of testing known standards to verify calibration, as well
as testing blank standards to determine limits of detection and to check for sample crosscontamination or instrument contamination. EPA Method 6200 provides a detailed procedure,
which is provided here in abbreviated form.
Components of instrument QC:
1.
2.
3.
4.
5.
6.
Energy Calibration Check: The Innov-X analyzer performs this automatically; this is the
purpose of the standardization check when the analyzer is started. The software does not allow
the analyzer to be used if the standardization is not completed.
Instrument Blank: The operator should use the SiO2 (silicon dioxide) blank provided with the
analyzer. The purpose of this test is to verify there is no contamination on the analyzer window or
other component that is seen by the x-rays. Method 6200 recommends an instrument blank at
least once per day, preferably every 20 samples. For either in-situ or prepared-sample testing, the
operator should just test the SiO2 blank to be sure there are no reported contaminant metals.
Method Blank: The purpose of the method blank is to verify that cross-contamination is not
introduced into samples during the sample preparation process. Method 6200 recommends
following the sample preparation procedures with clean SiO2 once very 20 prepared samples.
This QC step is not required if the operator is not preparing samples.
Calibration Verification: Innov-X provides NIST standard reference samples for calibration
check by operator. The operator should perform a 2-minute test on a NIST standard. The
difference between the XRF result for an element and the value of the standard should be 20% or
less. Calibration Verification should be performed upon instrument startup and periodically
during testing. Note: Innov-X recommends a calibration check every 4 hours. EPA Method 6200
recommends a calibration check every 20 samples NIST reference standards are generally
applicable for Pb, As, Cr, Cu, Zn. Innov-X provides additional reference standards for other
RCRA or Priority Pollutant metals including Cd, Se, Ag, Hg, Ag, Ba, Sn, Sb, and Ni.
Soil Appendix 9
Precision Verification: Quoting from EPA A minimum of one precision sample should be run
per day by conducting from 7 to 10 replicate measurements of the sample. The precision is
assessed by calculating a relative standard deviation (RSD) of the replicate measurements for the
analyte. The RSD values should be less than 20 percent for most analytes, except chromium, for
which the value should be less than 30 percent.
Confirmatory Sample: It is recommended that one confirmatory sample is run for every 10
samples collected. According to EPA Method 6200: Confirmatory samples are collected from
the same sample material that is analyzed on site, but are sent to an off-site laboratory for formal
analysis. The purpose of a confirmatory sample is to judge the accuracy of the data obtained by
analysis on site and to allow corrections, if necessary.
Important Notes about confirmatory samples:
Innov-X always recommends that customers compare prepared-sample results to laboratory
results. To do this, collect and prepare a sample following the protocols of Appendix 1. Take a
subsample and submit to the laboratory for analysis. The single largest error in XRF analysis is
lack of sample preparation. For the best comparison, always use prepared samples.
Soil Appendix 10
7. If this result differs by more than 20% from the sample sieved through 2 mm, then
particle size effects are still affecting the XRF result. In this case samples should be
sieved through 125 m to assure data quality at the quantitative level.
wi =
ki
Ii
M (Z , i)
Soil Appendix 11
The factory calibration determines the value of the calibration constants ki for each element, and a
typical value M(Z,I). The calibration method either CN, fundamental parameters, or empirical
performs the necessary corrections to the value M(Z,I) that are important for the site-specific soil
chemistry. The XRF analyzer uses the measured intensity of each elements fluorescence from
the sample, and the calibration data, to produce elemental concentrations.
Compton Normalization:
The Compton Normalization method calibration consists of the analysis of a single, wellcharacterized standard, such as an SRM or SSCS. The standard data are normalized to the
Compton peak. The Compton peak is produced from incoherent backscattering of X-ray radiation
from the excitation source and is present in the spectrum of every sample. The matrix affects the
way in which source radiation is scattered off the samples. This scatter is directly related to the
intensity of the Compton peak. For that reason, normalizing to the Compton peak can reduce
problems with matrix effects that vary among samples. Compton normalization is similar to the
use of internal standards in analysis for organic analytes.
Fundamental Parameters Calibration:
The fundamental parameters (FP) calibration is a "standardless" calibration. Rather than
establishing a unit's calibration curve by measuring its response to standards that contain analytes
of known concentrations, FP calibration relies on the known physics of the spectrometer's
response to pure elements to set the calibration. Built-in mathematical algorithms are used to
adjust the calibration for analysis of soil samples and to compensate for the effects of the soil
matrix. The FP calibration is performed by the manufacturer, but the analyst can adjust the
calibration curves (slope and y-intercept) on the bases of results of analyses of check samples,
such as SRMs which are analyzed in the field.
Empirical Calibration:
The empirical calibration method requires that a number of site-specific calibration standards
(SSCS) are used to establish calibration parameters. The instrument response to known analytes
is measured and used to create calibration curves. Empirical calibration is effective because the
samples used closely match the sample matrix. SSCSs are well-prepared samples collected from
the site of interest in which the concentrations of analytes have been determined by inductively
coupled plasma (ICP), atomic absorption (AA), or other methods approved by the US
Environmental Protection Agency (EPA). The standards should contain all the analytes of interest
and interfering analytes. Manufacturers recommend that 10 to 20 calibration samples be used to
generate a calibration curve. The empirical method is the least desirable calibration method as it
requires that new standards and curves are generated for each site that is analyzed.
It alters the soil chemistry, since water is another chemical compound that comprises the
soil matrix.
Moisture impedes the ability to properly prepare samples.
Soil Appendix 12
Soil Appendix 13
2. Take a sub-sample (5-10 grams) of the fully-prepared sample, place it into an XRF cup
and perform at least a one-minute test on that sample.
3. Send the same sample to the laboratory for wet chemistry analysis.
4. Require the laboratory to use a total-digestion method. If the laboratory does not use a
total digestion method, they may not extract all of the elemental metal from the sample.
In this case, the lab result will be lower than the XRF result. Incomplete sample
digestion is one of the most commons sources of laboratory error, thus it is very
important to request a total digestion method.
Example of Error: The operator collects a bag of sample, performs XRF analysis on one part of the bag,
and sends the bag, or part of the bag of sample to a laboratory for analysis. The laboratory reports a very
different value than the operator obtained with the XRF.
Problem: Since the sample is very non-homogeneous, the operator did not obtain a result that was
representative of the entire bag of sample. The lab analyzed a different part of the sample and obtained a
very different result due to the non-uniformity of the sample. The solution to this problem is, at a
minimum, to test several locations in the bag of sample and report the average value. Also note the
differences between the tests, as this is indicative of the non-uniformity of the sample. Operator should
send entire bag of sample to the lab, and instruct lab to prepare the sample before removing sub-sample for
lab analysis.
Best Practice: The operator should homogenize and prepare the entire bag of sample, and then
collect a sub sample for XRF testing. After testing, the same sample should be sent to the lab.
Example CASE 1: Lead and arsenic. Most XRFs are calibrated for lead and arsenic. Lead
interferes with arsenic (not vice-versa though). The net effect is a worsened detection limit for
arsenic, and poorer precision. The XRF handles the correction automatically, but the precision is
affected. The loss of precision is also reported by the XRF. (Please refer to Innov-X
Applications Sheet: In-field Analysis of Lead and Arsenic in Soil Using Portable XRF for more
detail).
Example CASE 2: Bromine in the sample, but XRF is not calibrated for bromine. Bromine, as a
fire retardant, is being seen more and more in soil and other sample types. For this reason, InnovX analyzers include Br in the calibration data. If Br is not calibrated, but is present in the sample,
the analyzer will report highly elevated levels of Pb, Hg and As. The levels will depend upon the
concentration of Br in the sample.
Soil Appendix 14
Interferences between elements can be broadly categorized into a) Z, Z-1, Z+1 interferences, and
b) K/L interferences. Interference type a occurs when high levels of an element of atomic
number Z are present. This can cause elevated levels of elements with atomic number Z-1 or
Z+1. Generally, portable XRFs have good correction methods, so this interference only causes
problems with very high levels of the element in question. Example: High concentrations of Fe
(Z=26) in excess of 10% may cause elevated levels of Mn or Co (Z=25 or Z=27 respectively).
The type b interference occurs when the L-shell line of one element overlaps with the K-shell spectral
line of another element. The most common example is the lead/arsenic interference where the L-alpha line
of lead is in nearly the exact same location as the K-alpha line of arsenic.
Soil Appendix 15
If results change by
<20% from Test 1 to
Test 2 then only sieve
thru 2mm mesh.
2.
Annual fee ranging from $25 to $100, depending upon the state.
3.
Soil Appendix 17
General Appendix 1
Technical Specifications
Description:
Innov-X Systems analyzers are hand-held, battery operated energy dispersive x-ray
fluorescence analyzers. They are utilized for the detection and quantification of
elements ranging from phosphorus (atomic number 15) though uranium (atomic number
92). Measurable concentrations of elements range from ppm to 100%.
Weight:
Excitation Source:
Detector:
Power:
Battery Life:
Display:
Data Storage:
Computer:
Optional Accessories:
2.625 lbs (Base wt.) 3.375 lbs (1.6 kg) with batteries
X-ray tube, Ag or W anode, 10-40 kV, 5-50 uA, 5 filter positions
Si PiN diode, thermoelectrically cooled, resolution < 280 eV.
Li-ion batteries, or AC power with Testing Stand
4-8 hours, depending on duty cycle.
Color, high-resolution touch screen with variable backlighting on
analyzer. Software available for PC/laptop operation also.
10,000 tests with spectra minimum, expandable to 100,000+ with 1 Gb
flash card.
HP iPAQ with Intel processor, 64 Mb minimum memory, Windows CE
operating system (unless operated from PC).
Bluetooth wireless printing and data transfer, integrated bar-code reader,
wireless LAN, other standard PDA accessories.
Operating Conditions
Temp 0 40 C
Humidity 10 90 % RH, no condensation
Altitude rating 2000 meters
Innov-X does not warrant that the operation of this analyzer will be uninterrupted
or error-free. Innov-X is not responsible for damage that occurs as a result of
your failure to follow the instructions that came with the Innov-X analyzer.
This Limited Warranty does not apply to expendable parts. This Limited Warranty
does not extend to any analyzer from which the serial number has been removed
or that has been damaged or rendered defective (A) as a result of accident,
misuse, abuse, or other external causes; (b) by operation outside the usage
parameters stated in user documentation that shipped with the product; (c) by
modification or service by anyone other than (i) Innov-X, or(ii) a Innov-X
authorized service provider, (d) installation of software not approved by Innov-X.
These terms and conditions constitute the complete and exclusive warranty
agreement between you and Innov-X regarding the Innov-X analyzer you have
purchased or leased. These terms and conditions supersede any prior
agreements or representations --- including representations made in Innov-X
sales literature or advice given to you by Innov-X or any agent or employee of
Innov-X --- that may have been made in connection with your purchase or lease
of the Innov-X analyzer. No change to the conditions of this Limited Warranty is
valid unless it is made in writing and signed by an authorized representative of
Innov-X.
Limitation of Liability
IF YOUR INNOV-X ANALYZER FAILS TO WORK AS WARRANTED ABOVE,
YOUR SOLE AND EXCLUSIVE REMEDY SHALL BE REPAIR OR
REPLACEMENT. INNOV-XS MAXIMUM LIABILITY UNDER THIS LIMITED
WARRANTY IS EXPRESSLY LIMITED TO THE LESSER OF THE PRICE YOU
HAVE PAID FOR THE ANALYZER OR THE COST OF REPAIR OR
REPLACEMENT OF ANY COMPONENTS THAT MALFUNCTION IN
CONDITION OF NORMAL USE.
INNOV-X IS NOT LIABLE FOR ANY DAMAGE CAUSED BY THE PRODUCT
OR THE FAILURE OF THE PRODUCT TO PERFORM INCLUDING ANY LOST
PROFITS OR SAVINGS OR SPECIAL, INCIDENTAL, OR CONSEQUENTIAL
DAMAGES. INNOV-X IS NOT LIABLE FOR ANY CLAIM MADE BY A THIRD
PARTY OR MADE BY YOU FOR A THIRD PARTY.
THIS LIMITATION OF LIABILITY APPLIES WHETHER DAMAGE ARE
SOUGHT, OR A CLAIM MADE, UNDER THIS LIMITED WARRATNY OR AS A
TORT CLAIM (INCLUDING NEGLIGENCE AND STRICT PRODUCT LIABILITY),
A CONTRACT CLAIM, OR ANY OTHER CLAIM. THIS LIMITATION OF
LIABILITY CANNOT BE WAIVED OR AMENDED BY ANY PERSON. THIS
LIMITATION OF LIABILITY WILL BE EFFECTIVE EVEN IF YOU HAVE
ADVISED INNOV-X OR AN AUTHORIZED REPRESENTATIVE OF INNOV-X
OF THE POSSIBILITY OF ANY SUCH DAMAGES.
Software
This Limited Warranty does not warrant software products. The Innov-X software
installed on your analyzer is covered by the Innov-X Software License.
Warranty Period
The warranty period for a Model XT-245 or Model XT-260 Innov-X analyzer is
two years or four thousand hours of use, whichever occurs first. The warranty for
all other analyzers is one year or two thousands hours of use whichever occurs
first. This warranty does not extend to expendable parts. Extended warranties
are available from Innov-X.
Warranty Returns
A Return Material Authorization (RMA) Number must be obtained from the
INNOV-X Service Department before any items can be shipped to the factory.
Returned goods will not be accepted without an RMA Number. Customer will
bear all shipping charges for warranty repairs. All goods returned to the factory
for warranty repair should be properly packed to avoid damage and clearly
marked with the RMA Number.
Warranty Repairs
Warranty repairs will be done either at the customer's site or at the INNOV-X
plant, at our option. All service rendered by INNOV-X will be performed in a
professional manner by qualified personnel.
Contacting Innov-X
Be sure to have the following information available before you call Innov-X:
Methods of Contact
Phone:
781-635-5005
Fax
781-938-0128
Email
service@Innov-Xsys.com
Mail & Shipping Address: Innov-X Systems, Inc. 10 Gill Street,
Suite Q. Woburn MA 01801