Chattanooga Intelect 225P, Intelect 230P Operator's Manual

1n
MODEL
225P/230P
ULTRASOUND
I
I
~
----~-:==----
I
mPERATmR'S
MANUAL
INSTALLATION
mPERATimN
MAINTENANCE
PARTS
P.N.
73778
REV C
table of
contents
Description
Page.
FOREWORD
...................................................................
2
WARRANTY
INFORMATION
....................................................
2
SAFETY INSTRUCTIONS
.......................................................
3
SPECIFICATIONS
..............................................................
4
ULTRASOUND
THERAPY INDICATIONS
........................................
5
ULTRASOUND
THERAPY CONTRAINDICATIONS
...............................
5
INTELECT
225P/230P
OPERATING CONTROLS
................................
6
OPERATING PROCEDURE
.....................................................
7
DESCRIPTION
OF
THE
UL
TRASDUND
FIELD
...................................
8
PLOT
OF
ULTRASOUND
FIELD SPATIAL DISTRIBUTIONS
......................
9
ABBREVIATIONS
..............................................................
9
TROUBLESHOOTING
.........................................................
1 0
MAINTENANCE
AND
SERVICE INSTRUCTIONS
...............................
11
ULTRASOUND
CALIBRATION
.................................................
12
COMPONENT
LOCATION, CIRCUIT BOARD
.......................
17,
19,
21,
23
PARTS LIST
.....................................................
18,
20, 22,
24
SCHEMATICS
............................................................
25-39
foreword
This manual
has
been
prepared
for
the
owners
and
operators
of
the
lntelect®Model
225P/230P.
It
contains
general
instructions
on
operation.
safety
practices,
maintenance
and
parts
information.
In
order
to
obtain
maximum life and
efficiency
from
your
Model
225P/230P
and
to
aid in
the
safe
operation
of
the
unit,
read and
understand
this
manual
thoroughly
and become
totally
familiar
with
the
controls
on
the
panel and
the
applicator
that
comes
with
the
unit
before
operating
it.
The
specifications
put
forth
in
this
manual
were
in
effect
at
the
time
of
publication.
However.
owing
to
Chattanooga
Corporation's
policy
of
continuous
improvement,
changes
to
these
specifications
may be made
at
any
time
without
obligation on
the
part
of
Chattanooga
Corporation.
·
full one
year
warranty
Chattanooga
Corporation
("Company")
warrants
that
lntelect®Model
225P/230P
("Product")
is
free
of
defects
in
material
and
workmanship.
This
warranty
shall remain in
effect
for
one ( 1 l
year
from
the
date
of
the
original
consumer
purchase
of
this
Product
and
extends
to
any
owner
of
the
Product
during
the
warranty
period.
If
this
Product
fails
to
function
during
the
one
year
warranty
period because
of a defect
in
material
and
workmanship,
Company
or
the
selling
dealer
will replace
or
repair
this
Product
without
charge
within a period
of
thirty
(30J days
from
the
date
on which
the
defective
Product
is
returned
to
the
Company
or
the
dealer. Company
or
the
dealer
will ship
the
replacement
or
the
repaired
Product
to
the
consumer's
residence.
THIS
WARRANTY
DOES
NOT
COVER:
1.
Replacement
parts
or
labor
furnished
by anyone
other
than
the
Company,
the
dealer
or
an
approved Company
service
agent.
2.
Defects
or
damage caused by
labor
furnished
by
someone
other
than
the
Company,
the
dealer
or
an approved Company
service
agent.
3. Any
malfunction
or
failure
in
the
Product
while
it
is in
the
possession
of
the
owner
during
the
warranty
period
if
the
malfunction
or
failure is
not
caused by a
defect
in
material
and
workmanship
or
if
the
malfunction
or
failure
is caused by unreasonable use. including
the
failure
to
provide reasonable and
necessary
maintenance.
COMPANY
SHALL
NOT
BE
LIABLE
FOR
INCIDENTAL
OR
CONSEQUENTIAL
DAMAGES
TO PROPERTY OR
BUSINESS.
Some
states
do
not
allow
the
exclusion
or
limitation
of
incidental
or
consequential
damages.
so
the
above
limitation
or
exclusion may
not
apply
to
you.
TO
OBTAIN
SERVICE
from
the
Company
or
the
selling
dealer
under
this
warranty,
the
1
owner
must
do
or
abide by
the
following:
1 . A
written
claim
must
be made
within
the
warranty
period
to
the
Company
or
the
selling
dealer.
If
the
claim
is
made
to
the
Company,
written
claim should be
sent
to:
P.O. Box
4287,
101
Memorial
Drive,
Chattanooga,
Tennessee
37405.
2.
The
Product
must
be
returned
to
the
Company
or
the
selling
dealer
by
the
owner.
This
warranty
gives you
specific
legal
rights,
and you may also have
other
rights
which
vary
from
state
to
state.
Company does
not
authorize
any
person
or
representative
to
create
for
it
any
other
obligation
or
liability in
connection
with
the
sale
of
this
Product.
Any
representative
or
agreement
not
contained
in
the
warranty
shall be void and
of
no
effect.
2
safety
instructions
1 . WARNING: Explosion hazard
if
used in
the
presence
of
flammable
anesthetics.
2. WARNING:
For
continued
protection
against
fire
hazard replace
fuses
only
with
ones
of
the
same
type
and rating.
3. Read,
understand
and
practice
the
safety
and operating
instructions.
Know
the
limitations
and
hazards
associated
with
the
Ultrasound.
Observe
the
safety
and operational decals placed on
the
unit.
4. Grounding-Make
certain
that
the
unit
is electrically grounded by plugging
into
an
electrical
outlet
with
a ground terminal
receptacle
CU-ground
outlet).
Follow
the
National
Electric
Code.
5. The
lntelect
Model
225P/230P
should
not
be
connected
to
any
other
device when
in
use.
6.
CAUTION: Federal law
restricts
this
device
to
sale by,
or
on
the
order
of, a physician
or
licensed
practitioner.
7. The
generator
should
be
routinely checked
before
each use
to
determine
that
all
controls
function
normally; especially
that
the
INTENSITY
control
does properly
adjust
the
intensity
of
the
ultrasonic
power
output
in a stable
manner. Also
determine
that
the
TREATMENT
TIME
control
does actually
terminate
ultrasonic
output
power
when
the
timer
reaches zero.
8.
CAUTION:-Use
of
controls
or
adjustments
or
performance
of
procedures
other
than
those
specified herein may
result
in
hazardous exposure
to
ultrasonic
energy.
3
specifications
Frequency-
1.0
MHz
± 5%
Duty
Cycle - 1
00%
(continuous
mode)
50%
± 1
0%
(pulse model
20%
± 1
0%
(pulse model
Pulse
Duration
- 5
msec ± 20%
(50%
duty
cycle
pulsed mode)
2
msec ± 20%
£20%
duty
cycle pulsed
model
Pulse
Repitition
Rate
- 1
00
Hz ±
20%
Ultrasonic
Power-
variable
from 1 watt
to
20
watts,
lntelect
230P
variable
from 1 watt
to
10
watts,
lntelect
225P
Output
Meter
Accuracy-
±
20%
(for
any
output
above 1
0%
of
maximum)
Temporal Peak/Average
Intensity
Ratio-
2:1, ± 20%
for
50%
Duty
Cycle.
5:1,
±
20%
for
20%
Duty
Cycle.
Output:
1.
Continuous-1 MHz
signal
that
is on as long as
the
timer
is running.
2.
Pulse-1 MHz
signal modulated
100%
by
the
100
Hz
rectangular
wave
with
the
selected
Duty
cycle.
Timer
Accuracy:
1 .
Less
than
0. 5
minutes
for
settings
less
than 5 minutes
2. 1 0%
for
settings
from 5 minutes
to
1 0
minutes
3. 1
minute
for
settings
greater
than
1 0
minutes
Applicator:
1.
Effective
radiating
area-. 8. 5 CM2
± 1.
5CM2,
lntelect
230P
18%)
4.0
CM2 ± 1.0
CM2,
lntelect
225P
25%)
2.
Maximum
beam
non-uniformity
ratio-
6.0:1
3.
Beam
type
- collimating
Input
power
requirements:
£Domestic)
120V
± I
60
Hz 1
0%
£Export)
220V
± 1
50
Hz 1
0%
314
Amps
318
Amps
Size -
12"
wide x
5"
high x
12"
deep
(not
including handle)
Weight -11.
5 lbs.
4
indications for ultrasound therapy *
Some indications
for
the
use
of
ultrasound
include adhesive capsulitus,
bursitis
with
slight
calcification, myositis,
soft
tissue
injuries,
shortened
tendons
due
to
past
injury, healing
scar
tissue
and
plantar
warts.
Ultrasouno
is
an
efficient
modality when used
for
the
treatment
of
all
types
of
joint
contractures
resulting
from
capsular
tightness
and
scarring.
Ultrasound
is
the
modality
of
choice
to
obtain
therapeutic
levels
of
heating
within
body
structures
covered
by
thick
layers
of
soft
tissue.
Neither
shortwave
or
microwave
diathermy
is able
to
heat
these
underlying
structures
to
produce
results
comparable
to
ultrasound.
contraindications for ultrasound therapy *
Ultrasound
SHOULD
NOT BE
USED
over
the
eyes
or
the
reproductive
organs. Also
ultrasound
SHOULD
NOT BE
USED
over a pregnant
uterus.
Other
contraindications
include
acute
infection
or
septis,
deep vein
thrombosis,
or
arterial
disease, and
over
anesthetized
areas
or
conditions
that
cause
impairment
of
sensations, such as chemotherapy.
Ultrasound
IS NOT TO BE
USED
over
cancerous
lesions.
REF: Lehmann,
J.F.,
Therapeutic
Heat
and Cold;
13:367-378,
1972.
5
operating controls
OUTPUT
0
-------------------
ULTRASOUND
HEAD
I
ON
M
TEMP
2TYCY~E(O)
100%
50% 20%
CONTINUOUS PULSED
100
Hz
0 0
0
30
®-'···,5
' /
{ 0
~10
25
, '
, '
, '
'I I It\'
20
15
MINUTES
CHATTAN~.i?o~!':
1 .
TREATMENT
TIMER/
POWER SWITCH: This is a
0-29
minute
rotary
timer.
When
the
timer
is on,
the
green
LED
labeled
Ultrasound
On will be lit. When
Timer
is in
the
off
position,
power
to
the
generator
is
off.
2.
INTENSITY:
Rotating
this
control
knob
clockwise
increases
the
amount
of
ultrasound
power
being delivered.
3.
HEAD
MAX
TEMP
LED: This Red LED
comes
on when
the
temperature
of
the
ultrasound
head
(transducer)
reaches
approximately
140
degrees
F.
At
the
time
the
LED
comes
on,
the
unit
will
stop
producing
ultrasound,
the
Ultrasound
On
LED
will go out, and
the
Treatment
Timer
will
continue
to
run. When
the
transducer
cools
to
approximately
1
20
F,
the
LED
will go
off
and
the
ultrasound
power
will be
restored.
4.
ULTRASOUND
ON LED: This Green
LED
is
on
when
ultrasound
power
is being
transmitted
from
the
transducer
(sound head). This
LED
comes
on when
the
Treatment
Timer/Power
Switch
is
first
turned
on.
5.
20%
PULSED
SWITCH: By
pressing
this
switch,
the
operator
can
select
an
ultrasound
output
of
1
MHz
that
is pulsed
at 1 00
pulses
per
second. This
produces
rectangular
pulses
of
2
milliseconds
duration,
with
an
off
time
of
8 milliseconds
between
pulses.
6.
50%
PULSED
SWITCH: By
pressing
this
switch,
the
operator
can
select
an
ultrasound
output
of 1 MHz
that
is pulsed
at
1
00
pulses
per
second.
This
produces
rectangular
pulses
of
5
milliseconds
duration,
with
an
off
time
of
5 milliseconds
between
pulses.
7.
100%
CONTINUOUS
SWITCH: By
pressing
this
switch,
the
operator
can
select
an
ultrasound
output
that
is a
continuous
sinusodial
waveform
at a frequency
of 1 MHz
nominal.
8.
ULTRASOUND
OUTPUT
DISPLAY: This display
shows
the
amount
of
ultrasound
power
and
intensity
available
at
the
transducer
(sound head). The
upper
scale
is
calibrated
in
Watts
and
the
lower
scale in W/CM2.
Average
power
is
shown
when in
continuous
(1
00%1 mode. Peak
power
is
shown
when in pulsed £50%, 20%1 mode.
6
operating procedure
1 . Plug
the
unit
into
a properly grounded
outlet
of
the
proper
voltage and line
fre-
quency.
Refer
to
the
Nameplate on
the
rear
of
the
unit.
2.
Operator
should
adjust
the
applicator
handle
to
the
desired position. Tighten
the
thumbscrew
securely.
3.
Set
the
Treatment
Timer
at
the 0 (Qffl
position, and
the
Intensity
control
at
the
(fully
counter
clockwise position).
4.
At
this
point you may begin
the
treatment
by applying
lntelect
Ultrasound
Gel
to
the
area
of
the
patient
to
be
treated.
5.
Turn
the
Treatment
Timer knob
to
the
desired
treatment
time
by
turning
the
knob
beyond
the
desired
time
and
then
backing up
to
the
desired time.
6.
Select
the
operating mode by pressing
the
appropriate
switch.
Switch 5 for
the
20%
Pulsed Mode,
Switch 6 for
the
50%
Pulsed Mode,
or
Switch 7 for
the
100%
Continuous Mode. The
20%
Pulsed Mode is automatically
selected
upon
actuation
of
the
timer.
7.
You should
then
place
the
applicator
in
contact
with
the
patient's
body
with a firm
uniform
pressure.
You
must
keep
the
applicator
moving during
the
treatment.
Failure
to
keep
the
applicator
moving may
result
in
hazardous exposure
to
the
ultrasound
energy.
8.
Adjust
the
Ultrasound
Output
by
turning
the
Intensity
control
(2) until you reach
the
desired
output.
Use
the
Upper
scale
for
Watts
and
Lower
scale
forW/Cm2.
9.
If
you need
to
interrupt
the
treatment
for
any reason,
turn
the
Treatment
Timer
to
the
off
position (Bell will ringl. To resume
treatment
repeat
steps
4-8.
1
0.
At
the
end
of
the
treatment,
the
end
of
treatment
bell will sound and
the
unit
will
shut
off.
in~®
230P
POWER
IN
WATTS
5
10
~.
''f'tl~'f'~s
20
o
'I"'
·ii:rlpe::.t;,.2s
.1
.s
11.5224
0 - . 2.1
INTENSITY IN W/CM2
OUTPUT
0
INTENSITY TREATMENT
TIMER
ULTRASOUND HEAD I 0
OIN
MAXITE(O)MP
30,@·'···
..
,5
0 0 0 : 0
~10
,OUTY
CYCLEt
25":.
100%
10% 10%
, ,
''
CONnNUOUS
PULUO
100
Hz ' • ' , •
''
IEli~El
·~UTE;
s-c
·-
CHATTANOOGA
-
.....
~
c~,..,..
1
description of ultrasonic field
The spatial
distribution
of
the
radiated field
is
essentially a collimated beam
of
ultrasonic
energy
having a cross-sectional area
of
8.5
CM2
for
the
10
CM2
sound head when measured
at
a point 5
millimeters
from
the
transducer
face.
The energy
distribution
within
the
radiated field is
2.4
W/CM2 maximum, and
takes
a generally conic
shape having decreasing
intensity
at
progressively increasing distance
from
the
face
of
the
transducer. This field
distribution
applies
for
the
radiation
emitted
into
the
equivalent
of
an
infinite medium
of
distilled degassed
water
at
30
deg.
C.
and
with
line voltage variations
in
the
range
of±
1 0
percent
of
the
rated
line voltage. The
ultrasonic
field spatial
distribution
of
the
5
CM
2
sound head is essentially
the
same as
the
field
of
the
10
CM2
sound head.
PLOT
OF
ULTRASONIC FIELD SPATIAL
DISTRIBUTION
10
CM2
90°/o 80°/o 70°/o
&Oo/o
50°/o
40°/o
30°/o 20°/o
10°/o
,...
1\
I
I
,,
"
"
1~
v
v
\'
t
~
I
\j
\~
u
\
....
1
'
l
I
\
J
~
"
)
\
/'
/
\
20
10
0
10
20
100°/o
90°/o
80°/o 70°/o
60°/o
SOo/o
40°/o
30°/o 20°/o
10°/o
....
RADIAL DISTANCE FROM CENTER
OF
APPUCATOA HEAD
MIWMETEAS
8
p
E
A
c
E
N
T
0
F
p
0
w
E
A
PLOT
OF
ULTRASONIC FIELD SPATIAL DISTRIBUTION
5
CM
2
100o/o
90°/o
80°/o
70°/o
&Oo/o
50°/o
40°/o
30°/o 20°/o
10°/o
0°/o
-
~
20
I
j
I
I
I
~
10
v
~
v
'
~
~
fl"
0
.,
100°/o
90°/o
80°/o
\
'II
70°/o
1\
\
60~{:,
50°/o
40°/o
\
\
'
~
~
30°/o 20°/o 10°/o
Qo/o
10
20
RADIAL
DISTANCE FROM CENTER
OF
APPLICATOR
HEAD
MILLIMETERS
abbreviations
The following abbreviations
are
used
on
the
applicator heads
of
the
lntelect
225P/230P.
Area=
Effective
Radiating
Area Call.= Collimating BNR=
Beam Non-Uniformity Ratio
Freq.
=Frequency
9
p
E
R
c
E
N
T
0
F
p
0
w
E
R
trouble shooting
The following
problems
and
solutions
are
presented
to
assist
you in solving some
of
the
roblems
that
could possibly happen
to
your
lntelect
225P
or
230P.
Problem
No
power
to
unit
Unit
has
power
but
no
Ultrasound
output.
1
JS
output
meter
only
dicates
about
half-scale
or
less when INTENSITY is
set
at
maximum.
When
unit
is
energized
HEAD
MAX.
TEMP
LED
(Red)
lights
and
beeper
sounds.
Timer
will
not
set
Cause
Action
To Take
1)
Unit
not
plugged in. 1 J Plug in unit.
21
No
power
to
the
receptacle.
2)
Check
for
tripped
circuit
breaker
or
blown
fuse
on
the
facility
circuit.
3)
Input
fuse
blown.
41
Internal
fuse
blown.
31
Change
the
3/4
amp. £.315 ampl
slo-blo
fuse
located
in
the
power
entry
receptacle
on
the
back
of
the
unit.
(3/8
amp
for
220 V units.)
Remove
Power
cord
prior
to
changing
the
fuse.
41
Check
the
3 amp and 1
/2
amp
picofuses
on
the
power
supply board. This should be done only by a Qualified
Service
Technician.
51
Loose connection inside
unit
51
Check
internal
connections
for
proper
seating
of
plugs in
receptacles
and
for
broken
wires.
6)
Applicator
cable loose.
61
Replug cable
into
the
shield box .
7)
Applicator
cable broken.
BJ
Oscillator
detuned.
91
Crystal
damaged.
1
OJ
Shorted
applicator
cable
71
Replace cable only
with
the
same
type
of
cable.
81
Recalibrate.
9J Replace
transducer
head in
the
applicator
and
recalibrate.
1
OJ
Check
the
cable
with
an ·ohmmeter,
If
the
cable is
shorted,
re-pl~ce
the
cable
with
the
same
type.
11 J
Water
in
applicator
head. 11 1 Remove
the
transducer
head
and
dry
out
the
inside
of
the
applicator.
If
the
D-ring is
defective, replace
it.
Consult
the
factory.
121
Timer
kriob loose
10
121 Remove cap on
the
knob and
tigtrten
the
collet.
Rotate
the
timer
fully clock-wise and
then
lassen
the
collet
so
that
the
knob is
free.
Align
the
white
line on
the
knob
with
the
29
min.
mark
on
the
timer
scale
and
re-tighten
the
knob collet.
Perform
section 4 of
calibration
procedure.
maintenance and
service
instructions
1. To fully maintain compliance
with
Federal Regulation
Title
21 (21 CFRl
this
unit
must
be
recalibrated
annually.
It
is
recommended
that
all
Chattanooga
Corporation
Ultrasound
Products
be
returned
to
the
factory
or
an authorized servicing dealer
for
repairs
or
recalibrations.
It
is also recommended
after
the
replacement
or
repair
of
any
major
component. (See
Section
for
Calibration
Procedures.)
2.
The following
items
should be checked
at
least
monthly
to
insure
proper
operation
of
this
unit:
. 1
Power
cord
and plug. Check
to
make
sure
the
cord
is
not
frayed, kinked
or
has
torn
or
cut
insulation .
. 2
Transducer
(applicator) Cable. Check
to
make
sure
the
cable is flexible,
free
of
kinks,
not
frayed
and
that
insulation is
intact
.
. 3
Transducer
(applicator) Handle. Check
to
make
sure
that
it
is
not
cracked
or
broken .
.4
Transducer
(applicator) Face. Check
to
see
that
there
is no build-up
of
gel
of
foreign
material
on
the
stainless
steel
face
.
. 5 LED's. Check each
function
to
see
if
the
LED is
on
when you
are
using
that
function.
11
calibration
CAUTION: An
Electrical
Shock
Hazard
is
present
during several
portions
of
the
calibration
-.procedure. Calibration should be
performed
by a Qualified
Service
Technician.
1.
TEST
EQUIPMENT
REQUIRED
.1
Power
line
monitor
(expanded scale
voltmeter
for
rated
line voltage ± 1 0%),
VI~
model
WV-1208
or
equivalent
for
120VAC
line .
. 2
Autotransformer,
adjustable
from
90%
to
11
0%
of
rated
line voltage,
150
watts
or
greater
.
. 3
Ultrasound
Power
Meter,
Ohmic
Instruments
Model
UPM-30
or
equivalent .
.4
Oscilloscope, Hameg
Hm
204-2
or
equivalent .
. 5 Probe,
voltate,
X1
0, Scope,
low
capacitance
.
. 6 Probe,
current,
Textronix
P6021
AC
current
probe
or
equivalent .
. 7
Voltmeter,
Digital,,
3~
1/2
digits, Simpson Model
461
or
equivalent .
. 8 Probe,
temperature,
Fluke Model
BOT-150
or
equivalent .
. 9
Source
of
approximately
1/2
gallon
of
distilled de-oxygenated
(<5
PPMJ
water
at
30
degrees
Celsuis
for
use in
UPM-30
power
meter
(item
#3)
.
.
10
Counter,
frequency,
10
MHz,
Triplett
7000
or
equivalent .
. 11
Stopwatch,
Siliconix Model
705
or
equivalent .
.
12
Applicator
current
transformer
adapter
(see Fig. 1
J.
2.1NSTRUMENT
PREPARATION
. 1 Remove
the top
cover
of
the
unit
by removing
the
four
#6
truss
head
screws
(two
on
each side) and
lift
the
cover
off
the
cabinet
.
. 2 Remove
the
two
#6
truss
head
screws
between
the
handle
latches
and
the
bezel
Cone
screw
on
each sidel. The
Front
Panel can
now
be
tilted
forward
for
easy
access
to
the
adjustments
on
the
control
board .
. 3
Insert a RF
current
probe
adaptor
between
the
ultrasound
applicator
cable and
the
RF
phono
receptacle
on
the
shield box
located
on
the
rear
panel. The
adaptor
construction
is
shown
in Fig. 1.
r---~----16AWGSOUD
BUS WIRE
l
1/2"
RF
PHONO PLUG
RF
PHONO RECEPTACLE
FIGURE 1
12
CONNECT
TO
120 V 60HZ
1220 V 50
HZJ
POWER SOURCE
108-131
VAC
,--------.
(198-242
VACJ
J:
N
UT
co
ls----1
·(i)
J):
O:IJ
...
AUTOTRANSFORMER
LINE
IN-225P/230P
UPM-30
ULTRASOUND
POWER
METER
VOLTAGE
MONITOR
FIGURE 2
3.
TEST
SET-UP
. 1
Connect
the
test
set-up
as
shown
in Fig. 2 .
. 2
Set
AC
input
voltage
with
the
autotransformer
to 1 20
C220J
V AC line
monitor
.
. 3 See
OHMIC
INSTRUMENTS
clinical engineering
notes
AN-330
for
opera-
tion
of
the
UPM-30
US.
Power
Meter.
4.TIMER
TEST
AND
ADJUSTMENT
.1
Using a
stopwatch,
check
the
accuracy
of
the
timer
with
time
settings
of
1
min
..
5 min.,
10
min.,
20
min., and
29
min
..
See
specifications
on page 4
for
required
timer
accuracy
.
. 2
If
the
timer
accuracy
is
out
of
specification,
rotate
the
timer
knob fully
clockwise
and
adjust
the
collet
on
the
knob so
that
the
white
line
on
the
knob
is aligned
with
the
29
minute
mark
on
the
timer
scale .
. 3
Repeat
steps
4.
1 and check also
that
the
white
line on
the
knob is aligned
with
the
"0"
position
on
the
scale
after
the
timer
times
out.
5.
CHECK
POWER
SUPPLY
. 1
Rotate
INTENSITY
knob fully
counterclockwise
and
the
timer
to
its
fully
clockwise
position
.
. 2
Connect
the
DC digital
voltmeter
to
the
pins 1 ( + J and 2
(-Jon
connector
P2
which
connects
to
the
control
board and
measure
the
12VDC
output.
It
should be
between
11.5
VDC
and
12.5
VDC.
6.
ADJUST
THE
DUTY
CYCLE
AND
CHECK
PULSE
FREQUENCY
.
. 1
Select
20%
DUTY
CYCLE and
connect
the
oscilloscope
voltage
probe
to
pin
#3
(signaiJ and ground clip
to
pin
#2
(com. J .
. 2
Adjust
the
time
base
of
the
oscilloscope
to 1 msec/div
and
measure
the
period
of
the
1OOHz signal.
It
should be
between
8.0
msec
and
12
msec.
13
. 3
Adjust
the
scope
time
base
for
1 0 divisions
of
one cycle
of
the
sign.,al.
On
the
control
board.
adjust
RS
for
a pulse
width
of
7. 9 divisions .
. 4
Select
50%
DUTY
CYCLE and
adjust
R4
on
the
control
board
for
a pulse
width
of
4.
7 divisions .
. 5
Select 1 00%
DUTY
CYCLE and observe
that
the
signal is a DC level less
than
.5V.
7.CHECK
AND
ADJUST
THE R.F. OSCILLATOR
. 1 Connect
the
scope
current
probe around
the
center
conductor
of
the
cur-
rent
probe
adaptor
and
connect
the
voltage
probe
to
the
outside
conductor
.
. 2
Rotate
the
INTENSITY
control
clockwise as you observe
the
voltage and
current
waveforms
on
the
dual channel scope. The
waveforms
should be
within 5 degrees
of
being in phase and oscillation should be
stable
.
. 3 Repeat
step
7. 2
with
50%
duty
cycle and
then
with
20%
duty
cycle
selected
.
.4
Adjust
C4
through
the
access
hole
on
the
rear
panel (see fig. 3
for
location.
remove hole capsJ
for
phase
correction
and C7
through
its
rear
panel
access
hole
for
oscillation
stability
in
the
pulse modes £20% and
50%)
.
. 6 Replace
stainless
hole caps
on
rear
panel.
D
D
0
E@j
C-4
c-7
CJ
0
D
FIGURE 3
14
\
\,
;
'
\
'
....
... ~ ...............
0
....
,_
,.
.
;
'
-~
......
~
.,_
(
8.
CHECK
AND
ADJUST
MODULATED
RF
DUTY
CYCLE
.1
Select
20%
DUTY
CYCLE and observe
the
duty
cycle
of
the
100Hz
modulated
RF
waveform.
Re-adjust
R6
as
necessary
to
obtain
21%
duty
cycle .
. 2
Select
50%
DUTY
CYCLE and again observe
the
modulated
RF
waveform.
Re-
adjust
R4
as
necessary
to
obtain
53%
duty
cycle.
9.
OUTPUT
METER
CALIBRATION
.1
With
electrical
power
removed,
adjust
the
mechanical
zero
adjustment,
located
on
the
front
panel
under
the
meter,
to
align
the
meter
pointer
with
0 on
the
meter
dial.
. 2 Re-apply
electrical
power
to
the
unit
and
select 1 00%
duty
cycle .
. 3
Adjust
the
INTENSITY
control
on
the
front
panel
to
obtain
the
rated
output
power
on
the
UPM-30
for
the
model being used .
Model 1-225 P Model
I-230P
10.0
Watts
20.0
Watts
.4
Adjust
the
meter
calibration
potentiometer,
R18,
for
an
indication
of
the
rated
output
for
this
model on
the
front
panel
output
meter
.
. 5 Check
the
accuracy
of
the
output
meter
by comparing
its
indication
to
the
power
indicated
on
the
UPM-30
at
the
power
levels
listed
for
each model.
I-225P
Meter
UPM-30
Indication
1.0
w
2.0W
5.0
w
7.0W
10.0
w
I-230PI
Meter
Minimum
.86W
1.72
w
4.3
w
6.0
w
8.6
w
Maximum
1.14
w
2.28
w
5.7
w
8.0
w
11.4
w
UPM-30
Indication
Minimum Maximum
2.0
w
-1.72
w
2.28
w
5.0
w
4.3
w 5. 7 w
10.0
w
8.6
w 11
.4
w
15.0
w
12.9
w
17.1
w
20.0
w
17.2
w
22.8
w
.6
Vary
the
line voltage
from
108
VAC
(198VACJ
t:::>
132
VAC
C242VACJ and check
that
the
output
power
remains
within
the
limits
listed
above .
. 7
Select
50%
DUTY
CYCLE and check
the
peak
output
meter
accuracy
by comparing
its
indication
to
the
average
power
indication on
the
UPM-30.
POWER avg = (%
Duty
Cycle)
(Power
peak)
1-225P
Meter
UPM-30
Indication
Peak
Power
Average
Power
1.0
w
2.0W
5:o
w
7.0W
10.0
w
1-230P
Meter
Peak
Power
2.0W
5.0W
10.0
w
15.0
w
20.0W
Minimum Maximum
.43
w
.57
w
.86
w
1.14
w
2.15
w
2.85
w
3.0
w
4.0
w
4.3
w
5.7
w
UPM-30
Indication
Average
Power
Minimum Maximum
.86
w
1.14
w
2.15
w
2.85
w
4.3
w
5.7
w
6.5
w
8.5
w
8.6
w
11.4
w
15
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