Professional Documents
Culture Documents
VERIFICATION STATEMENT
I hereby verify that this report was written by ______________________________________
and all information regarding this company and the projects involved are not confidential.
Name
Designation
Date
I|Page
Herewith, I endorse the project titled Statistical Process Control for Base Oil Monitoring to
be pursued under my supervision by _______________________________________. The
above-mentioned person shall adhere to all rules and safety measures as per company
regulations during his or her tenure.
Name
Designation
Date
II | P a g e
ACKNOWLEDGEMENT
First and foremost, I would like to express my gratitude to Centre of Student Internship,
Mobility and Adjunct Lectureship (CSIMAL) for giving me an opportunity to undergo a 14
weeks internship program in Petronas Lubricants International located in Tangga Batu,
Melaka. CSIMAL has done an excellent job by mapping out an elaborate internship program
which facilitates pursuance of industrial projects with specified objectives and outcomes
besides assigning supervisors to us and carrying out meetings to cater students problem
regarding internship program. Hereby, I would like to thank my UTP supervisor, Madam
Noorfidza Yub Harun who was willing to come all the way to Petronas Lubricants
International to evaluate my presentation and guided me all this while when there is any issue
in my internship period. Furthermore, I am also grateful for my department manager
Pn.Salwa for his valuable support, guidance and encouragement during my internship
training. Without her guidance, I would not be able to learn a lot and gain knowledge as
much as I can.
In addition, there are also other people that helped me a lot throughout the learning process in
Hammer Engineering. I would like to express my immense gratitude to Mr. Mohd Huzzairi,
Quality Control Executive, for being my totem of inspiration in the aspect of always being
hungry for knowledge. Also to Mr. Mustakim and Mr. Zainuddin, Lab Technicians, who
taught me the technical know-hows and performance and quality monitoring system which
has been used within the company. I also would like to thank all the staffs of Quality Control
department, notably Mr.Badrul for offering their assistance which provides me with
wonderful experience. Last but not least, I would like to give acknowledgement to all parties
who had also contributed directly and indirectly to the success of my Industrial Internship
Program.
Yours Sincerely,
Anderson J
III | P a g e
TABLE OF CONTENTS
Page
No
Index
No
II
Acknowledgements
III
Table of Contents
IV
Objectives of SIIP
VI
Chapter 3 Methodology
19
10
29
11
12
13
References
14
Appendix
IV | P a g e
V|Page
Page
No
List of Tables
No
12
29
29
30
30
31
VI | P a g e
Page
No
List of Figures
No
10
13
14
15
32
33
34
35
36
10
38
11
39
12
40
13
41
14
42
VII | P a g e
To introduce and provide a framework for process problem solving and quality
improvement of lubricants
It is also my utmost priority and responsibility to cater the companys needs in equipotence
with my desired outcomes. I have addressed the problems that are improvable under my work
function and I have decided to tackle them in this project with the help and advice of my
superiors:
To ensure the consistent achievement of Quality Dept.s target of 95% first time right
for blending products.
1|Page
The Statistical Process Control for Base Oil Monitoring project centralises within the
following scope of study:
To describe the role of variability and statistical methods in controlling and improving
process quality
To learn and perform standardised testing procedures for the CTQ parameters for the
base oils.
To learn and operate various statistical analysis softwares and produce graphical
representation of data that is easily interpreted for evaluation.
2|Page
At present, my host company, PETRONAS Lubricants already has statistical process control
as part of their quality control procedure to meet customer requirements. But in my opinion,
this practice is too far on the customer end as the quality testing procedure is performed post
production, where product variation would require a complete re-compounding for the off spec batch .This would prove costly in terms of raw material costs, equipment run-time and
down-time, and also wasted man-hours spent on blending a failed batch of lubricants. There
are cases where blended batches which turned to be off-spec had to be discarded because recompounding had little or no effect on their condition. These are severely uneconomical
situations that could be averted with necessary precaution.
The whole idea of emphasising quality at the end of process is drifting away from the
function of quality control to quality assurance, and in cases of outliers from the product
specification at this point is costly to rework on its quality. My opinion of statistical process
control is not just about its use in quality control but also its role in ensuring competitiveness
of our products in the lubricant industry. In any industry, regardless of their nature, compete
for three things: quality, delivery, and price. Quality alone cant be the single deciding factor
of the products success, but then again, with great quality, the delivery and price
performance would be competitive as well.
To deviate the cost-intensive bottlenecks in the quality control procedure, I have come up
with the notion of using Statistical Process Control for base oils viscosity that are being used
for lubricants. I must admit that this idea is leveraged from the knowledge and experience of
my supervisor, Mr Huzzairi, who is also the Quality Control executive, and Mr Mustakim,
Senior Technician in our Quality Control lab.
They have devised a plan for me to execute the project without going through much of the
organisational red-tapes or resistances and they have also helped me to access and retrieve
data for the lab test reports, batch manufacturing reports, among other remote details via their
SAP account. In addition to that, they have also granted me permission to access all the files
3|Page
and records necessary for the execution of my project provided that I would hold myself
responsible in keeping company confidentiality and product formulation secrecy at all times.
1.4 RELEVANCY
My concern on relevancy is levied on two broad spectrums. The relevancy of this project to
my field of studies and the relevancy of this project to my work function in the Quality
Department.
As far as relevancy of this project to my field of studies is concerned, Statistical Process
Control is major discipline of chemical engineering and is an endorsed training area by
Centre of Student Internship, Mobility, and Adjunct Lectureship (CSIMAL). Although I have
not taken this course earlier, I have taken proactive measures and self-taught myself in this
subject. I have enrolled in the UTP e-learning portal of Dr Bhattacharjees Statistical Process
Control class and have used his study materials extensively. Through his book suggestions, I
have acquired many good textbooks on this matter and have garnered invaluable knowledge
which is essential for this projects execution. In addition, to that I have also used study
materials on this subject matter from universities worldwide namely, Plymouth University,
Arizona State University, King Fahd University, Worcester Polytechnic Institute, and John
Hopkins University.
To pose relevance to my departments work function is not a hard task if exercised, but can
be easily overlooked if one has not planned thoroughly. The aim of the project is not to
actively seek to discontinue cost-intensive re-blending procedures but to reduce costly
reworks by employing strategic quality control procedures, and this is where Statistical
Process Control comes into action. Having the objectives and methodology thoughtfully
planned out and consistently performing checks to ensure if we comply with the
aforementioned aspects would ensure relevancy of this project on all stages.
4|Page
CHAPTER 2
2.1 FEASIBILITY OF PROJECT
In this particular section, we will discuss the reasons that makes this project doable and
within the reach of my competence. The two main aspects we will look into is the feasibility
of the scope within the project and if the project will reach completion in the specified
timeframe, specifically within the internship period.
The scope of study as described in the earlier chapter, is aligned with the subject Statistical
Process Control offered in final year of undergraduate study for Chemical Engineering
students of UTP, provided that they choose the major of Process Analysis and Control.
Although I have not undertaken the course yet, I have made massive effort to self-educate
myself on that topic. I must say Dr. Bhattacharjee of Chemical Engineering Department, UTP
has been a great help to my project without being directly involved. I have downloaded his
lecture materials and followed through his literature suggestions to acquire the much sought
after essential knowledge on Statistical Process Control. Thereby, it is safe to say this project
is bounded well within the scope of studies and is anticipated to cover all of it.
As far as the timeframe is concerned, I was quite hesitant to undertake this project when I
found out from the literatures, that a yearlong data is necessary for accurate, and reliable
analysis. As push came to shove, I realised that any documented data from yesteryears is as
good as the one that I would obtain myself. So I took the challenge of retrieving and
analysing from recorded data, a process that is termed retro-analysis, as it would be
described in the rest of the report. Therein, it would help me to design a solid framework for
another yearlong data acquisition and analysis, which I would hand-over to the quality
department personnel to complete, as I would be concluding my internship beforehand. Thus,
the feasibility of the project within the timeframe is upheld.
5|Page
Within one project, this probably the one time where I reviewed the most literatures for one
subject matter. Statistical Process Control (SPC) is a relatively complex statistical tool and
proportionally fruitful with reference to its complexity. Along the journey of in-depth
literature analysis, I have figured out the dire necessities of the project and have acquired the
knowledge to utilise them to produce the project deliverables. I have summarised the gist of
my learnings in this part of the project and I have carefully brought about the knowledge
from the literatures with a fair balance of detail and comprehensibility so the readers may
garner the most out of these literatures.
Along the line, I have briefly introduced our industry, petroleum lubricants and our material
of study, base oils, before we dive on to the details of SPC. I have defined the meaning of
quality as a starter to signify the need to use the tools of quality, primarily SPC. I have
detailed more on the importance of quality to our company in the methodology part of this
report as I find it more relevant to be placed there (Chapter 3).
Beginning with the control charts, I have written in depth on the selection criteria for control
charts, setting up the desired control chart, testing and interpreting a control chart, and finally
the process capability and process performance analysis.
Sulphur
content (%)
content (%)
Process
Group I
< 90
> 0.03
80 > 120
Solvent-refined
Group II
90
< 0.03
80 > 120
Hydro-treated
Group III
90
< 0.03
120
Hydro-cracked
Group IV
Group V
Chemical reaction
Commonly, quality has been perceived as the character that signifies superiority of a product
in the eyes of the customer and the manufacturer alike. But what is quality from an industrial
perspective? Below are some definitions of quality verbatim from the literatures;
The totality of features and characteristics of a product or service that bear on its
ability to satisfy stated or implied needs ~ BS 4778: Part 1: 1987 (ISO 8402: 1986)
The term quality has been articulated in many ways in literatures but only (Morris, 2010) had
categorized them efficiently into;
1) Design Quality
2) Manufacturing Quality
3) Performance Quality
Since our project focuses on a manufacturing perspective, we will probe in that a little bit
more. Another significant literature in the field of statistical process control, (Montgomery,
2009) had particularly stated that for service industries, the improvement of quality signifies a
reduction of variability of processes and products.
Thereby, it is evident that conformance to specification, and reduction of variability from the
said specification is the key to manufacturing quality. It describes the very intention of this
project, which is to monitor base oils viscosity and bring it to statistical control, thereby
reducing the variation in lubricant products from its specification.
To manufacture a product that satisfies or goes beyond customer expectations, the production
process of it should be able to operate with little inconsistency in the desired specifications of
the products quality characteristics. This is where statistical process control comes in use. As
(Montgomery, 2009) defines, Statistical process control (SPC) is a powerful range of
problem-solving tools used to achieve process stability and improving capability by reducing
variability. SPC is one of the vital scientific progresses of the twentieth century because it is
based on comprehensive core principles, is easy to use, has substantial effect, and proven
functional to any process.
8|Page
The 7 major tools of SPC has endured the test of time and has proven to be crucial in making
the most out of raw data, deriving quality from numbers. Some details about the tools as
described by (Oakland, 2003), are given below;
Control Charts
Developed by Walter Shewhart in 1920s, control chart is perhaps the most significant and
sophisticated tool among the 7 tools of quality. Shewharts postulated the notion of
assignable causes (common causes) and non-assignable causes (special causes). With the
development of control charts, he devised a rule to detect the special causes and also
accurately anticipated the range which common causes fall in the charts. This helps the users
minimise the risk of reacting to a special cause when it is in fact a common cause, and the
risk of not reacting to a special cause when one is present.
Before we get all technical on the calculations, lets get along with the types of control charts
present. The flowchart below summarises the types of control charts with much ease of
understanding.
9|Page
In the field of SPC in manufacturing, the most common chart is the Xbar- R chart as it is the
most sensitive chart in terms of process variation, especially with sample sizes more than
4.This is in line with the justification of (Oakland, 2003)the larger the sample size, the
closer the mean control chart limits to the process mean. But for our specific application,
for batch manufacturing, an Individual-Moving Range (I-MR) chart would be more
pragmatic as multiple samples from the same tank of base oil will only yield identical results.
Moreover, its simplicity and ease of interpretation would prove useful for my lab mates
(technicians, chemist and others) as the goal here is to produce base oil monitoring system
with repeatability and accessibility. Much alike the Xbar-R chart, the I-MR chart is good at
indicating changes in mean level (accuracy/ central tendency) and variation (precision/
spread) with much dependability. The only downside is the reduced sensitivity due lack of
subgroups unlike the Xbar - R Chart but with continuous observation and monitoring that can
be accounted for. Thus, I-MR chart will be control chart of choice for our project purpose.
10 | P a g e
At least 100 data points are needed for a control chart to labelled perfect. If you have
less than 100, consider it a preliminary study and re-assess the process after you get
100 data points.
Data must be tested for normality. Normality tests will be discussed later in the Tests
and Interpretation.
Centreline
The centreline shall signify the process mean, and shall be labelled as thus .The centreline
(CL) will typically be positioned at:
Centre of specification
11 | P a g e
Refer the constants used in the design of control charts for range for the values of D. Table
below highlights the value for n = 2 only. n = 2 is used because the value for moving range is
observed from two successive observations.
.001
.999
.025
.975
(Oakland, 2003)
12 | P a g e
The standard deviation, can be calculated from a previous data from a stable process or can
be calculated from the mean moving range. The d2 is known as the Hartleys Constant with
the value of 1.128 for n = 2.
Control limits:
Warning limits:
or
[3 ]
or
[2 ]
(Montgomery, 2009)
13 | P a g e
Normality Tests
As our chart requires our data to have an assumption of normality we are obliged to put our
data to a normality test. Upon going through a handful of normality tests such as the
probability plot, Anderson- Darling test, Ryan- Joiner test and the Kolmogorov- Smirnov test,
I have found the Anderson Darling test to be the most compatible with our application. The
Anderson- Darling test relates the empirical cumulative distribution function of your sample
data with the distribution projected if the data was normal. If this measured difference is
adequately large, the test will reject the null hypothesis of population normality (Minitab
Assistant, 2015).
In case your data is not normal, you can apply a function of transformation to enable your
data to be approximately normal for your analysis. For our case, since we have all positive
integers we are best apt at using a Box- Cox transformation. (Minitab Assistant, 2015)
Variability tests
There are a total of eight tests for the Shewhart control charts test for special causes as
described (Nelson, 1984). But as for general ease of use and predictability Test 1 and Test 2
have been apparent in the quality control area.
(Nelson, 1984)
14 | P a g e
. .
=
6
The difference between Upper Specification Limit (USL) and Lower Specification Limit
(LSL) is termed as Engineering Tolerance whilst the Natural Tolerance is derived from the
range where assignable or common causes fall into, 3 (from +3 to -3, hence 6 range) .
15 | P a g e
The reason to use Process Capability and Process Performance Analysis is mainly because
the synergistic enhancement it provides to the control charts. To understand this, Dr. Hans
(Bajaria, 2011) has claimed that these three questions could identify three unique sets of
causes.
1. Is the process stable?
Method to know: Control Chart
2.
Thus, this is an opportunity for us to further refine our results to a greater precision while
gaining knowledge about yet another powerful statistical tool. The fine line of difference
between Process Capability and Process Performance is distinguished from the value for
standard deviation used. Process performance are computed just like the Process capability
apart from the fact that Process performance uses overall standard deviation for the time
period, overall instead of the one that is used for short-term which is the standard deviation
(within) the particular data set, within.
Ppk for process centring capability and process centring performance respectively. This index
is the spread of the process average to the closest specification limit divided by half the
natural tolerance. (Morris, 2010)
Pp and Ppk should ideally be used to check against Cp and Cpk and to gauge and enable
improvement over time.
17 | P a g e
Bibliography
Bajaria, D. H. (2011, December 14). American Society of Quality. Retrieved from American Society of
Quality: http://asq.org/learn-about-quality/overview.html
Minitab Assistant. (2015, November 2). Retrieved from Minitab Statistical Software :
http://support.minitab.com
Montgomery, D. (2009). Introduction to Statistical Quality Control (6th edition). Jefferson City: John
Wiley & Sons Inc.
Morris, R. (2010). The Book of Statistical Process Control (2nd edition). Cincinnati: The Zontec Press.
Mortier, R., Fox, M., & Orszulik, S. (2010). Chemistry and Technology of Lubricants (3rd edition). New
York: Springer Science+Business Media B.V.
Nelson, L. (1984). The Shewhart Control Chart--Tests for Special Causes. Journal of Quality
Technology Vol.16, 237-239.
Oakland, J. (2003). Statistical Process Control (5th edition). Oxford: Butterworth Heinemann.
18 | P a g e
CHAPTER 3
3.0 METHODOLOGY
CASE STUDY
Here, I will explain the problem statement briefly to understand the process problem as a
whole part. When I first presented the notion of improvising the current SPC system, my
supervisor and lab technician werent in agreement as I proposed to revise the SPC of the
product line which was advised by consultants hired by the company to liaise on quality
issues and improvement considerations.
After much brainstorming and going through documented quality records from the past, we
agreed that if theres a room for improvement it should be on one of our departments Key
Performance Index (KPI), which is First Time Right for products. The target for the
aforementioned KPI is 95% which is achieved most of the time, but variability and
inconsistency of which has not been satisfactory. As I type this case, we had just underwent
quality audit for ISO TS 16494, for which the above problem have been highlighted.
Thereby, Mr.Huzzairi, being the quality executive and chemist for our lab, has conducted the
Root Cause Analysis (RCA) of this particular matter and discovered the root causes of the
said problem. The documents of which I will be unable to provide as they are not meant to be
disclosed but the causes are described briefly as follows:
Effect: - Re-blending / Unable to achieve First Time Right target.
Cause(s): - Technical difficulties in the DCS (Distributary Control System)
-
Ergo, Mr. Huzzairi explained to me that there lies the potential for improvisation in our
current Base Oil Monitoring system. Mr. Mustakim, the lab technician had provided me the
details and records of the current Base Oil Monitoring system. Upon going through the files, I
had developed confidence to develop a statistical monitoring system for Base Oils and hence
it gave rise to this project, Statistical Process Control of Base Oil Monitoring System.
19 | P a g e
As stated in the case study, I have decided that ultimately I will be developing a framework
for statistical process control of base oil monitoring system. But in order to come up with an
effective system, I need to analyse the existing condition of the base oil monitoring system.
As stated in the feasibility study, it is impractical for me to gather enough data to observe
significant trends/ pattern that produces meaningful statistical information about the process
in the duration of 14 weeks of my internship. Hence, I have prioritised myself to these two
project deliverables:
I.
Collect a year-long data from Base Oil Monitoring System and retro-analyse them
using SPC tools, producing graphical representation of my findings, together with my
interpretation of it.
II.
20 | P a g e
Herewith, I will detail in on the methodologies I have employed in the execution of the
project deliverables mentioned above.
Methodologies for Project Deliverable I:
1. Find the base oil types which are in use and has been on production from last year to
this year. Negate any types of base oil deemed obsolete.
2. Trace back all the documented records of the types of base oils selected for the study.
Use the SAP/ERP software or manually refer the hardcopies of the records from the
files in the filing cabinet.
3. Record the data in Microsoft Excel for future use. Return all the files to their
respective places.
4. Refer to the existing SPC system for the lubricant products developed by consultant.
Analyse the SPC tools being used and find out how relevant and appropriate they are
to our specific application. Refer back to the related literatures and look for
improvisation prospects.
5. Compare and contrast between the Statistical Process Control tools that are available
with the one that is currently being used. At the end of reviewing literatures, you
should arrive at the most accurate SPC tool(s) suited for our specific application.
6. Scout and try out different statistical analysis softwares. Select the most appropriate
software for our specific application. Do pay attention to the functionalities and
standards of it, not forsaking its cost/benefit ratio or overall cost efficiency for that
matter.
7. Using the desired statistical software, analyse the collected data by the selected
Statistical Process Control method(s)/tool(s).
8. Produce graphical representations of the data and interpret them with statistical
significance. Record the findings in the results section of the project report.
21 | P a g e
1. Critically review the findings of project deliverable I. Identify the problems (special
cause variations/ outliers/ instability/ abnormality/ etc.) and address them. This will
help us improvise the existing monitoring system.
2. The problems are from a retro-analysed data. The causes of which must be known to
the person-in-charge (Mr. Huzzairi/ Mr. Mustakim). Liaise with them and identify the
nature of the problems.
3. Record all findings in a file, in both hard copy and soft copy. Make sure the time of
occurrence for the variations/abnormality/instability tallies with the retro-analysed
data. Documentation of these findings is important as a precaution in the future and
also to come up with a mitigation plan in case it should occur.
4. Based on the findings and knowledge of pre-existing base oil monitoring system,
outline the procedures to monitor the base oil to be used in accordance with the
statistical process control tool(s) selected earlier.
5. Ensure the reproducibility of methods/ documents/charts of the new framework for
base oils monitoring system.
6. Present the findings to the supervisor, Mr. Huzzairi and ensure the rectification of
earlier limitations from the existing base oils monitoring system.
7. Thank and acknowledge team for invaluable support and sharing of knowledge.
22 | P a g e
ASTM D 7042: Test Method for Dynamic Viscosity and Density of Liquid by
Stabinger Viscometer, and the calculation of Kinematic Viscosity.
II)
ASTM D 4052: Test method by Anton Parr densitometer for Density, Relative
Density and API gravity of liquids.
23 | P a g e
24 | P a g e
Data Collection
Identifying
Improvement
Opportunities
Selection of SPC
tool(s)
Data Analysis
Data Identification
and
Documentation
Reporting the
findings
Selection of Case
Study
25 | P a g e
No
Activities
Category
Week
1
1.
2.
3.
4.
5.
Data collection
6.
7.
8.
9.
Prepare report
10.
11.
Planning
Executing
10
11
12
13
14
/
/
/
/
Reporting
26 | P a g e
Softwares
1. Microsoft Excel Microsoft Excels spread sheeting functions are not unheard of. Its
use in that particular scope is unparalleled. I have used Microsoft Excel for tabulating
collected data for base oils. I have noted that currently we are using Microsoft Excel
for Statistical Process Control in our premises. However, I was keen on creating more
detail and clarity in the graphical representation of my data, hence a more subtle
software was chosen, particularly one whose function is statistical analysis.
2. Minitab Statistical Software Minitab is a statistical software that fulfils the need
for charting and analyses almost exclusively for quality control field. It performs
27 | P a g e
almost all types of statistical analyses imaginable, or at least the ones that I have come
across so far in every literature that I analysed. The control charts and process
capability and performance analyses I have performed were generated using this
software. This software has a vital role in putting the clarity of graphical
representation of data in this project which I believe would certainly be of great value
for this project.
Conclusively, I have utilised the least of resources to achieve and garner most benefits as I
planned. This is inspired from the Paretos principle of 80/20. Pareto proposed that 80 percent
of effects originates from 20 percent of causes. Akin to that, out of five softwares I tried out
for SPC purposes, Statit, Qi Macros, Dell Statistica, Excel and Minitab, only Minitab fits our
specific application.
28 | P a g e
CHAPTER 4
4.0 RESULTS AND DISCUSSION
4.1 FINDINGS
The findings from data collection is tabulated as follows. The following conditions applies
for all the following data sets:
1. Some data sets are naturally larger due to difference in production demand
2. Dates are omitted as sampling date differs for each type of base oil.
3. Data sets are ordered chronologically.
Sample,n
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
KV@100C KV@40C
cSt
cSt
3.194
12.745
2.862
11.176
2.69
10.12
2.81
10.55
2.9135
11.237
2.954
11.296
3.082
11.31
2.96
11.2
2.883
11.28
3.13
12.19
3.067
11.75
3.0245
11.767
3.051
11.64
2.989
11.51
2.55
9.18
2.72
10.12
2.919
11.16
2.929
11.516
2.75
10.321
2.807
10.599
2.82
10.561
2.77
10.545
2.672
9.9371
2.776
10.412
2.768
10.399
2.788
10.503
@15
g/cm3
0.8345
0.8382
0.8326
0.8358
0.8343
0.8341
0.8340
0.8337
0.8333
0.8317
0.8299
0.8294
0.8297
0.8311
0.8298
0.8293
0.8310
0.8303
0.8336
0.8332
0.8319
0.8331
0.8332
0.8331
0.8330
0.8320
Sample,n
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
KV@100C KV@40C
cSt
cSt
6.06
32.94
6.08
33.74
6.08
33.74
6.11
33.62
6.11
34.12
6.15
34.34
6.19
34.82
6.38
34.42
6.11
34.42
6.15
34.55
6.12
33.92
6.12
33.94
6.11
33.44
6.26
35.24
6.05
33.22
6.03
33.06
6.23
34.75
6.22
34.72
6.10
33.71
6.09
33.75
6.10
33.67
6.16
34.44
6.18
34.06
6.13
33.69
6.11
33.45
@15
g/cm3
0.8480
0.8465
0.8472
0.8454
0.8472
0.8496
0.8480
0.8483
0.8483
0.8486
0.8462
0.8462
0.8444
0.8478
0.8462
0.8460
0.8477
0.8478
0.8469
0.8469
0.8473
0.8482
0.8481
0.8465
0.8470
29 | P a g e
Sample,n
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
49
KV@100C KV@40C
cSt
cSt
31.30
471.68
30.76
448.26
31.27
473.16
31.44
472.80
30.70
455.90
33.50
515.50
33.43
517.92
33.51
519.76
33.59
515.24
33.10
514.43
33.14
514.50
33.52
515.65
33.49
515.30
33.38
514.40
33.41
516.52
31.04
460.04
30.98
462.37
30.66
461.80
30.54
449.12
30.92
451.86
30.97
460.48
30.98
446.23
30.97
463.58
33.07
510.52
30.95
462.57
30.94
459.83
30.35
462.22
30.37
454.78
30.05
461.65
30.38
448.69
32.99
504.97
30.73
461.12
30.21
476.92
32.77
506.68
32.64
488.04
31.76
483.05
31.76
484.68
31.92
488.54
32.11
490.71
31.71
485.10
31.66
486.86
32.72
508.74
31.92
488.54
31.65
483.07
31.94
488.10
31.10
471.43
31.50
474.80
30.84
460.02
31.23
459.00
@15
g/cm3
0.9002
0.9001
0.9020
0.9012
0.8966
0.9013
0.9014
0.9110
0.9009
0.8998
0.9001
0.9011
0.9013
0.9011
0.9011
0.8975
0.8969
0.8969
0.8969
0.8968
0.8966
0.8970
0.8968
0.9016
0.8967
0.8970
0.8969
0.8970
0.8970
0.8929
0.9028
0.8962
0.9016
0.9028
0.9041
0.9033
0.9028
0.9016
0.9028
0.9027
0.9032
0.9027
0.9016
0.9018
0.9018
0.9048
0.9049
0.9005
0.9006
Sample,n
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
KV@100C KV@40C
cSt
cSt
4.20
19.03
4.17
19.40
4.24
19.13
4.19
18.94
4.19
19.12
4.19
18.93
4.24
19.20
4.20
19.02
4.20
18.84
4.27
19.35
4.23
19.17
4.31
19.69
4.17
18.65
4.20
18.84
4.16
18.57
4.25
19.00
4.26
18.65
4.24
18.70
4.24
18.89
4.22
18.89
4.23
18.91
4.33
19.63
4.27
19.33
4.28
19.19
4.28
19.30
4.32
19.20
4.29
19.36
4.20
18.72
4.25
19.04
4.26
19.03
4.30
19.06
4.29
19.05
4.28
19.25
@15
g/cm3
0.8351
0.8353
0.8351
0.8345
0.8342
0.8344
0.8344
0.8342
0.8340
0.8345
0.8343
0.8348
0.8322
0.8333
0.8334
0.8339
0.8337
0.8345
0.8343
0.8341
0.8342
0.8357
0.8353
0.8353
0.8352
0.8361
0.8357
0.8350
0.8355
0.8358
0.8357
0.8357
0.8358
30 | P a g e
Sample,n
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
KV@100C KV@40C
cSt
cSt
10.52
79.77
10.62
79.38
10.61
79.33
10.43
77.98
10.46
78.19
10.45
78.98
10.57
78.96
10.53
79.33
10.39
76.73
10.34
77.08
10.29
76.50
10.32
76.50
10.82
83.22
10.80
82.83
10.80
82.80
10.44
78.89
10.41
78.79
10.43
78.94
10.30
78.03
10.54
80.38
10.53
80.37
10.40
78.65
10.58
79.93
10.59
80.69
10.24
76.41
10.62
80.45
10.32
77.68
10.41
79.16
@15
g/cm3
0.8638
0.8625
0.8625
0.8625
0.8626
0.8641
0.8642
0.8641
0.8625
0.8625
0.8624
0.8626
0.8654
0.8654
0.8654
0.8657
0.8658
0.8655
0.8663
0.8661
0.8661
0.8658
0.8662
0.8662
0.8658
0.8672
0.8656
0.8665
31 | P a g e
Moving Range
Individual Value
I-MR Chart
Confirm that the process is stable.
3.00
2.75
2.50
0.4
0.2
0.0
1
10
13
16
19
Normality Plot
The points should be close to the line.
22
25
Normality Test
(Anderson-Darling)
Results
P-value
Pass
0.893
The E3-type base oil is the least used base oil among all the other types in this study. The
data collection for E3-type had to be taken from late 2014 to obtain a yearlong data with
regular interval. The reason behind this is because it has been diminishingly reduced in use
for blending as of this year.
1. General Pattern: The I-MR chart exhibits a global trend. The abnormality of point 15
(below lower control limit) and point 13, 14 being 9th, 10th consecutive points on one
side of the control limit may indicate a shift in mean.
2. Variations/ Abnormalities: Test 1 - Point 1, Point 15
Test 2 - Point 13, Point 14
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3. Presence of special cause(s): No. Highly Unlikely. Normality Test suggests that the
process is following its expected natural distribution, hence the outliers can be
regarded as common cause variation.
4. Process Mean Stability: Unstable. 4 points (15.4%) of the data is out of control limits.
For the process mean to be considered stable, % of out-of-control points should be
less than 5%.
E4-TYPE Base Oil
Capability Analysis for E4-Type
Diagnostic Report
Moving Range
Individual Value
I-MR Chart
Confirm that the process is stable.
4.32
4.24
4.16
0.10
0.05
0.00
1
10
13
16
19
22
Normality Plot
The points should be close to the line.
25
28
31
Normality Test
(Anderson-Darling)
Results
P-value
Pass
0.502
1. General Pattern: The I-MR chart shows an oscillating trend in the first half and
progresses into a global trend towards the end. Theres little hiccups at point 9, 9th
consecutive point on one side of the control limit, and point 13, an outlier.
Nevertheless, its a somewhat safe and stable process.
2. Variations/ Abnormalities: Test 1 - Point 13
Test 2 - Point 9
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3. Presence of special cause(s): No. Highly Unlikely. Normality Test suggests that the
process is following its expected natural distribution, hence the outliers can be
regarded as common cause variation.
4. Process Mean Stability: Very stable. 1 point (3.0%) of the data is out of control limits.
For the process mean to be considered stable, % of out-of-control points should be
less than 5%.
E6-TYPE Base Oil
Capability Analysis for E6-Type
Diagnostic Report
Moving Range
Individual Value
I-MR Chart
Confirm that the process is stable.
6.2
6.1
6.0
0.2
0.1
0.0
1
11
13
15
17
Normality Plot
The points should be close to the line.
19
21
23
25
Normality Test
(Anderson-Darling)
Results
P-value
Pass
0.188
1. General Pattern: The I-MR chart was very stable and was varying randomly within
the central line until point 15 went out-of-control above the upper control limit and
the process seemed oscillatory. Causative data was tracked, and the value (6.20) was
well within the specification (6.00 - 6.50). As the point out of control is too few
(4.0%) compared to the bulk of the data, a mean shift is unlikely and the outlier is
deemed as a common-cause variation.
2. Variations/ Abnormalities: Test 1 - Point 14
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3. Presence of special cause(s): No. Highly Unlikely. There is only one out of control
point on the I-MR chart. Besides, Normality Test also confirms that the process is
following its expected natural distribution, hence the outliers can be regarded as
common cause variation.
4. Process Mean Stability: Very stable. 1 point (4.0%) of the data is out of control limits.
For the process mean to be considered stable, % of out-of-control points should be
less than 5%.
Moving Range
Individual Value
I-MR Chart
Confirm that the process is stable.
34
32
30
2
1
0
1
11
16
21
26
31
Normality Plot
The points should be close to the line.
36
41
46
Normality Test
(Anderson-Darling)
Results
P-value
Fail
< 0.005
1. General Pattern: The I-MR chart has serious case of out-of-control points most
evidently on the first half of the chart. Heavily one-sided data point also indicates a
shift in mean. The abnormalities indicates a special-cause variation exists in this data
set. The frequently alarming points in the MR-chart shows suggestive evidence that
the process is excessively out of control.
35 | P a g e
Moving Range
Individual Value
I-MR Chart
Confirm that the process is stable.
10.8
10.5
10.2
0.4
0.2
0.0
1
10
13
16
19
Normality Plot
The points should be close to the line.
22
25
28
Normality Test
(Anderson-Darling)
Results
P-value
Pass
0.248
1. General Pattern: The I-MR chart is very steadily showing pattern of global trend,
though it may not be called ideal at this nature. Nevertheless, the process obeys to the
control limits very well and there are little reason to investigate the random shifts in
moving range which are not strongly suggesting any unassignable variation.
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1. Reliability of study: Reliable. The total number of observation satisfies the Total N
needed for the study. From earlier test for normality (Anderson Darling test), the
data has displayed normal behaviour. Hence, no reason for false or inaccurate
capability and performance analysis.
2. Process Performance: The process is marginally under-performing. Ppk of 1.11
obeys the 3 standard (Ppk = 1.00), but it is still below our customer requirement of
4 standard of Ppk = 1.33.
3. Process Capability: The process has the potential capability of going beyond 5
standards of Cpk = 1.67 if the process is well centred and the variations are removed.
38 | P a g e
1. Reliability of study: Reliable. The total number of observation satisfies the Total N
needed for the study. From earlier test for normality (Anderson Darling test), the
data has displayed normal behaviour. Hence, no reason for false or inaccurate
capability and performance analysis.
2. Process Performance: The process is severely under-performing. Ppk of 0.67
indicates the 2 standard (Ppk = 0.67). There is much work to be done to hike up two
sigma levels to meet our customer requirement of 4 standard of Ppk = 1.33.
3. Process Capability: With a Cpk of 0.89, the process is not capable of meeting
customers desired quality requirement even if the process is well centred and the
variations are removed from the current data set. The process has to be investigated
for special cause variation, and the said variation must be removed from the data set,
before the process is re-evaluated. Upon re-evaluation, if the process fails capability
analysis again, there is a serious need for intervention.
39 | P a g e
1. Reliability of study: Reliable. The total number of observation satisfies the Total N
needed for the study. From earlier test for normality (Anderson Darling test), the
data has displayed normal behaviour. Hence, no reason for false or inaccurate
capability and performance analysis.
2. Process Performance: The process is severely under-performing. Ppk of 0.77
indicates the 2 standard (Ppk = 0.67). There is much work to be done to hike up two
sigma levels to meet our customer requirement of 4 standard of Ppk = 1.33.
3. Process Capability: With a Cpk of 0.99, the process is not capable of meeting
customers desired quality requirement even if the process is well centred and the
variations are removed from the current data set. The process has to be investigated
for special cause variation, and the said variation must be removed from the data set,
before the process is re-evaluated. Upon re-evaluation, if the process fails capability
analysis again, there is a serious need for intervention.
40 | P a g e
1. Reliability of study: Unreliable. The total number of observation satisfies the Total N
needed for the study. However, from earlier test for normality (Anderson Darling
test), the data has displayed non-normal behaviour. Thereby, it is highly likely that we
encounter false alarms and inaccurate results.
2. Process Performance: The process is severely under-performing. Ppk of 0.53 means
the process has the lowest sigma standard of 1 (Ppk = 0.67). Needless to say, this
process has overall inconsistency in its performance even if its capability index
suggests otherwise.
3. Process Capability: With a Cpk of 1.08, the process is not capable of meeting
customers desired quality requirement. The process has to be investigated for special
cause variation, and the said variation must be removed from the data set, before the
41 | P a g e
1. Reliability of study: Reliable. The total number of observation satisfies the Total N
needed for the study. From earlier test for normality (Anderson Darling test), the
data has displayed normal behaviour. Hence, no reason for false or inaccurate
capability and performance analysis.
2. Process Performance: The process is performing well. Ppk of 1.06 indicates the 3
standard (Ppk = 1.00). With sufficient effort, we can go one sigma level up to meet
our customer requirement of 4 standard of Ppk = 1.33.
3. Process Capability: With a Cpk of 1.42, the process is capable of meeting customers
desired quality requirement even if the process is well centred and the variations are
removed from the current data set.
42 | P a g e
oils (though DCS failure is another reason, it is not within our scope of study). The additional
use of additives is also cost intensive. As I type, I had just been informed of 60tons of lube
blend going to waste due to use of 40kgs of faulty additive. I suppose that is enough to
signify the magnitude and seriousness of the matter at hand. In a business perspective,
continuously running on additional costs to adhere to quality standards and requirements is
going to cause serious implications on our competitiveness. Soon, our price-cost ratio is
going tip-off and show our poor performance in the use of resources in achieving the
production plan.
Sources of Unassignable Errors
Special Cause Variations
When I brought these problems to the lab technician, Mr Mustakim, as I expected he had the
answers for me. The source of variation is known and has been addressed by the quality
department and that explains the chart for BS-Type returning to normal on the later end of the
time series in the control chart. Mr. Mustakim had shared with me that the management took
a cost cutting initiative on the base oils and the resultant management decision was a
proposed change of supplier. Since our supplier was from Singapore, we had suffered in
terms of pricing, due to transactions being processed in a foreign currency Secondly, time for
transportation and the man-hours spent for loading was also considered as our shipments
arrives in vessels and has to be transported via long-distance pipelines to our tanks. Therein,
decision was made to procure the goods from a Malaysian base oil manufacturer and
supplier, and the realization of the decision commenced.
Sadly though, the cost-cutting step has proven costly as it turned out to be quality-cutting
as well. A significant reduction in first time right for blended product was logged on May
2014. Mitigation action was pursued to avoid further losses and threats to quality. We
resumed procurement of base oils from our Singapore supplier the following month and we
have continued to do so until now.
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CHAPTER 5
5.0 CONCLUSION AND RECOMMENDATIONS
5.1 IMPACT
Surprisingly, much of my work has gathered attention not just during the commencement but
throughout the data collection up till the development of results everybody in the lab was
keen on knowing and they were keeping themselves updated with my work and it had me
driven on delivering the end results to them for them to reap the benefits.
The other two interns who were placed together with me in the lab even helped me to
troubleshoot my framework every time I am stuck at a bottleneck. With the advantage of
having their attention, it only made it easier for me to brief the lab personnel on the Statistical
Process Control for Base Oil Monitoring methods and know-hows.
As this had been an uprising issue before the audit, everybody had acknowledged the
importance of this issue and the impactful benefit that this system may provide. Continuous
monitoring of base oil shall ideally keep the CTQ (Critical to Quality) parameters in a stable,
ideal control. A significant reduction in the need for reblending procedures is expected from
the said action. Needless to say, this will bring us closer to the goal of achieving 95% first
time right for blended product, every time.
I have gone through a multitude of statistical analysis tools and have found the
ideal ones for our batch manufacturing process to be the I-MR chart and process
48 | P a g e
Much of the information on this framework of base oil monitoring was provided
to me by the lab technicians so I had little hurdle in introducing it to them. But I
admit it was challenging to select the right SPC tools that is suited to solve our
process problem whilst maintaining user friendliness and ease of access for
reproducibility. Fulfilling these criteria while providing this to them was my
biggest achievement as far as our objective is concerned.
I must admit this objective was not just tied to this project alone. Needless to say,
much of my knowledge that I gained at Petronas Lubricants International, be it
technical or non-technical, was mostly from sharing sessions with my supervisor
and the lab technicians. The knowledge I gained on my own is only theoretical
and sometimes impractical but it is the leverage of their experience that led me to
yield pragmatic solutions for this project.
the near future the Quality Department of Petronas Lubricants International will
consider using multivariate analysis as the SPC tool of choice.
2. Monitoring the Additives Monitoring the base oil was just the first step, to create a
systematic monitoring for the tanks in the tank farm. If a monitoring system for
additives is created in the near future, we would have a complete analysis system for
every tank in the tank farm. And if our resources allow, we can incorporate real time
monitoring similar to those of engineering process control via Distributary Control
System (DCS).
3. In the meantime, whilst expecting an aggressive growth of reliance in SPC tools, it is
necessary to maintain and upkeep the current system. My suggestion on this area is
just a piece of borrowed wisdom from the literatures (Minitab Assistant, 2015), which
is to re-assess the process regularly using SPC tools after you get 100 data points in a
specified time period.
50 | P a g e
CHAPTER 6
6.0 SAFETY TRAINING AND THE VALUE OF PRACTICAL EXPERIENCE
6.1 LESSONS LEARNT AND EXPERIENCE GAINED
I believe with the Student Industrial Internship Project coming to a conclusion, there is much
left for me to learn and practice in a boundlessly complex engineering world ahead of me.
Adhering to the SIIP objectives set by the university and the project objectives laid out by
myself, I have an ultimately superior objective that had been motivating me to pursue all of
the other objectives with great enthusiasm. The pursuit of increasing my employability by
enhancing my practical skills is what has been my driving force ever since I commenced the
internship program 8 months ago.
By continuously putting myself on the grind, I have acquired the invaluable wealth of
knowledge this industry has to offer me, and I humbly admit that I am not yet done learning,
and what I have learnt is just a grain of sand in the sea of knowledge. I have briefly described
my understandings and experiences during the period of my SIIP at Petronas Lubricants
International Sdn Bhd.
Safety Training
The safety training here was conducted by Mr. Ikhwan Razak, our safety coordinator in the
first day of reporting in to Petronas Lubricants itself. Since I have the OGSP (Oil and Gas
Safety Passport) from my previous host company, I have better understanding of the terms
explained in the safety training. Here, I will explain briefly the about the safety regulations in
Petronas Lubricants.
LOTO - Lock Out and Tag Out before servicing, repairing, cleaning, or retooling any
equipment or machinery.
UAUC Unsafe Acts and Unsafe Conditions: Unsafe Acts are the ones which arises
from human factor, and Unsafe Conditions are the safety failures in the system or the
management.
ZeTo Zero Tolerance (ZeTo) rules were devised by Petronas to be used in all of its
operating units.
51 | P a g e
Much of my leadership skills were put to the test when I have to proactively seek out
for answers regarding the status quo of the base oil monitoring system and the
problems faced by it. I also had to consistently seek out field operators and engage
them to get the base oil samples for me week in, week out.
Team Work
Individual Activities
Most of individual time spent on working out this project was largely allotted on
reviewing literatures, as I believe a good plan will always outwork a good execution.
In my case, both the planning span and the execution of the project went easier than
expected as my supervisor has provided me necessary literatures to get me started on
my knowledge gathering habit on the first day itself. The hunger for knowledge has
not subsided and I am continuing to cater my search for knowledge, with great
enthusiasm.
52 | P a g e
Productivity: The rate of work or output that is achieved without sacrificing quality.
Efficiency: Dictates how well we use our resources to achieve our goals
Ethics
Integrity: To be truthful to our work and to be able to keep promises that we have
made to our work
Result Orientation: To understand the goals set for self and the organization and take
ownership of goals.
Management Skills
Communication Skills
Collaborative Skills
Finance Skills
To budget, forecast, understand cash flow, financial statements and business metrics
To plan and manage projects, manage risks and time, decision making and workflow
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References
Bajaria, D. H. (2011, December 14). American Society of Quality. Retrieved from American Society of
Quality: http://asq.org/learn-about-quality/overview.html
Minitab Assistant. (2015, November 2). Retrieved from Minitab Statistical Software :
http://support.minitab.com
Montgomery, D. (2009). Introduction to Statistical Quality Control (6th edition). Jefferson City: John
Wiley & Sons Inc.
Morris, R. (2010). The Book of Statistical Process Control (2nd edition). Cincinnati: The Zontec Press.
Mortier, R., Fox, M., & Orszulik, S. (2010). Chemistry and Technology of Lubricants (3rd edition). New
York: Springer Science+Business Media B.V.
Nelson, L. (1984). The Shewhart Control Chart--Tests for Special Causes. Journal of Quality
Technology Vol.16, 237-239.
Oakland, J. (2003). Statistical Process Control (5th edition). Oxford: Butterworth Heinemann.
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