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Research article · 2021 · Full text

International Journal of Statistics and Applied Mathematics

Design and development of intra lot group acceptance chain sampling plans with an emphasis on zero tolerance non-conformities

S. DevaarulT Santhi

Volume 6(1) · Pages 100–106

Research areasAdvanced Statistical Process MonitoringOptimal Experimental Design Methods

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Abstract

Author-written

In this article a new sampling plan to control product quality known to be Intra Lot Group Acceptance Chain Sampling Plan (ILGAChSP) is developed. Group Acceptance Sampling Plans are widely used in life testing experiments and has applications in research and development centers. In many testing fields, zero defective is expected in every groups or batches. Hence in this paper zero defective is emphasized during testing with an allowance of a non-conformity in a chain of i groups within the same batch of products. If a defective is found then the batch will be accepted only if ‘i’ consecutive chain of groups have zero defective in the current lot. Since ‘i’ chain of groups are tested in the same batch or lot it is termed as Intra Lot Group Acceptance Chain Sampling Plans.

Summary

Source-checked

Plain-language reading of the full paper, prepared with AI and checked against the text. Each point links to the authors' own words.

  1. Why it matters

    • Acceptance sampling tools are critical components of quality control in modern industrial settings. View evidence ↗

      Why it matters

      Acceptance sampling tools are critical components of quality control in modern industrial settings.

      In the paper's own words

      “In modern industries acceptance sampling tools and techniques are one of the major components in the field of quality control division.”

      Page 1

      Found in: Introduction

      Read it in the full textOpen PDF at page 1 ↗
    • Group acceptance sampling plans are beneficial because they can reduce inspection costs and testing time by testing more items simultaneously. View evidence ↗

      Why it matters

      Group acceptance sampling plans are beneficial because they can reduce inspection costs and testing time by testing more items simultaneously.

      In the paper's own words

      “The advantage of group acceptance sampling plans is it saves the testing time and reduces the cost of inspection if more items are tested in an experiment.”

      Page 1

      Found in: Introduction

      Read it in the full textOpen PDF at page 1 ↗
    • In life testing experiments, there is often a requirement for zero tolerance regarding non-conformities within each group. View evidence ↗

      Why it matters

      In life testing experiments, there is often a requirement for zero tolerance regarding non-conformities within each group.

      In the paper's own words

      “In fact during life testing experiment they need zero tolerance non conformities in each group.”

      Page 1

      Found in: Introduction

      Read it in the full textOpen PDF at page 1 ↗
  2. The question

    • The authors aim to develop a novel Intra Lot Group Acceptance Chain Sampling Plan (ILGAChSP) to address existing gaps in quality control for single lots. View evidence ↗

      The question

      The authors aim to develop a novel Intra Lot Group Acceptance Chain Sampling Plan (ILGAChSP) to address existing gaps in quality control for single lots.

      In the paper's own words

      “Hence in order fulfill the need and lacunae, a novel Intra Lot Group Acceptance Chain Sampling Plans are developed.”

      Page 1

      Found in: Introduction

      Read it in the full textOpen PDF at page 1 ↗
  3. What they did

    • The method involves drawing a random sample of size n (where n = g * r), dividing them into 'g' groups with 'r' items per group for life testing. View evidence ↗

      What they did

      The method involves drawing a random sample of size n (where n = g * r), dividing them into 'g' groups with 'r' items per group for life testing.

      In the paper's own words

      “Draw a random sample of size nj=g * r and put them into life test such that ‘g’ is the number of groups and r items are allocated to each group.”

      Page 3

      Found in: Algorithm of Ilgchsp to sentence a unique lot

      Read it in the full textOpen PDF at page 3 ↗
    • A lot is accepted immediately if zero non-conformities are found across all groups in the first sample. View evidence ↗

      What they did

      A lot is accepted immediately if zero non-conformities are found across all groups in the first sample.

      In the paper's own words

      “If each dj is zero, (i.e) D=0, accept the batch or lot.”

      Page 3

      Found in: Algorithm of Ilgchsp to sentence a unique lot

      Read it in the full textOpen PDF at page 3 ↗
    • The lot is rejected if more than one non-conformity is found in the first sample. View evidence ↗

      What they did

      The lot is rejected if more than one non-conformity is found in the first sample.

      In the paper's own words

      “If D > 1, reject the lot.”

      Page 3

      Found in: Algorithm of Ilgchsp to sentence a unique lot

      Read it in the full textOpen PDF at page 3 ↗
  4. What they found

    • The ILGAChSP is effective at discriminating between high-quality (good) and low-quality (bad) lots. View evidence ↗

      What they found

      The ILGAChSP is effective at discriminating between high-quality (good) and low-quality (bad) lots.

      In the paper's own words

      “From figure (1), it is found that ILGAChSP well discriminate between good and bad lots.”

      Page 3

      Found in: Interpretation

      Read it in the full textOpen PDF at page 3 ↗
    • The Operating Characteristic (OC) curve exhibits a 'good shoulder effect,' providing confidence to producers that quality is being maintained. View evidence ↗

      What they found

      The Operating Characteristic (OC) curve exhibits a 'good shoulder effect,' providing confidence to producers that quality is being maintained.

      In the paper's own words

      “there is good shoulder effect on the OC curve. This gives a confidence to the producer to maintain the quality.”

      Page 3

      Found in: Interpretation

      Read it in the full textOpen PDF at page 3 ↗
    • The outgoing quality of a batch after inspection is lower than the incoming quality, which is an advantage for the consumer. View evidence ↗

      What they found

      The outgoing quality of a batch after inspection is lower than the incoming quality, which is an advantage for the consumer.

      In the paper's own words

      “The outgoing quality of the batch after the inspection is small when compared to the incoming quality of the lot.”

      Page 6

      Found in: Introduction

      Read it in the full textOpen PDF at page 6 ↗
    • Increasing the chaining index 'i' leads to a decrease in the operating ratio. View evidence ↗

      What they found

      Increasing the chaining index 'i' leads to a decrease in the operating ratio.

      In the paper's own words

      “It is found that the operating ratio decreases while increasing the chaining index i.”

      Page 6

      Found in: Introduction

      Read it in the full textOpen PDF at page 6 ↗
  5. What it means

    • The authors conclude that the developed tables enable quality control practitioners to implement the ILGAChSP in practice. View evidence ↗

      What it means

      The authors conclude that the developed tables enable quality control practitioners to implement the ILGAChSP in practice.

      In the paper's own words

      “Tables are constructed to facilitate quality control practitioners to implement the ILGAChSP plans.”

      Page 6

      Found in: Introduction

      Read it in the full textOpen PDF at page 6 ↗
    • The authors state that the probability of lot acceptance drops rapidly as product quality deteriorates. View evidence ↗

      What it means

      The authors state that the probability of lot acceptance drops rapidly as product quality deteriorates.

      In the paper's own words

      “It is found that the probability of acceptance of the batch or lot decreases rapidly if the quality deteriorates”

      Page 6

      Found in: Introduction

      Read it in the full textOpen PDF at page 6 ↗

Visual summary

3 visuals

Illustrations explain the paper; charts are replotted from the paper's own table values.

AI-generated illustration
AI-generated conceptual illustration (industrial mechanical components in a quality control setting). It explains the idea and does not show study data.↗ Enlarge
ILGAChSP Decision Flowchart
AI-generated conceptual illustration (industrial mechanical components in a quality control setting). It explains the idea and does not show study data.

AI-generated conceptual illustration (industrial mechanical components in a quality control setting). It explains the idea and does not show study data.

Open full-size image ↗

ILGAChSP Decision Flowchart

AI-generated conceptual illustration (industrial mechanical components in a quality control setting). It explains the idea and does not show study data.

View source evidence ↗
Replotted from source data
Replotted from Table 1 (page 3) of the original paper. Every bar is the paper's own table value.↗ Enlarge
0.0001: n=100 Pa1(p) vs n=50 Pa2(p) vs n=200 Pa3(p)
Replotted from Table 1 (page 3) of the original paper. Every bar is the paper's own table value.

Replotted from Table 1 (page 3) of the original paper. Every bar is the paper's own table value.

Open full-size image ↗

0.0001: n=100 Pa1(p) vs n=50 Pa2(p) vs n=200 Pa3(p)

Replotted from Table 1 (page 3) of the original paper. Every bar is the paper's own table value.

View source evidence ↗
Replotted from source data
Replotted from Table 1 (page 3) of the original paper. Every bar is the paper's own table value.↗ Enlarge
0.002: n=100 Pa1(p) vs n=50 Pa2(p) vs n=200 Pa3(p)
Replotted from Table 1 (page 3) of the original paper. Every bar is the paper's own table value.

Replotted from Table 1 (page 3) of the original paper. Every bar is the paper's own table value.

Open full-size image ↗

0.002: n=100 Pa1(p) vs n=50 Pa2(p) vs n=200 Pa3(p)

Replotted from Table 1 (page 3) of the original paper. Every bar is the paper's own table value.

View source evidence ↗

Figures & tables

From the original paper
OC Function values for known fraction defectives with i=1,g=1Table 1Page 3Comparison OF OC CurveFigure 1Page 3Computation of AOQ valuesTable 2Page 4Values of np tabulated against i and g for the given values of Pa(p) for IGChSPTable 3Page 4Values of p2/p1 tabulated against i and g values of α and β and values for IGChSPTable 4Page 4AOQ CURVEFigure 2Page 4Parametric values for IGChSP indexed through AOQLTable 5Page 5Parametric values for IGChSP indexed through AOQLTable 5Page 5Values of np* and h*values for IGChSP @ 1-α = 0.95Table 6Page 5Relative slope for acceptable and limiting quality levels for IGChSPTable 7Page 5
FULL TEXT Original article · reflowed for reading

Introduction

In modern industries acceptance sampling tools and techniques are one of the major components in the field of quality control division. These techniques are employed for incoming or receiving lots of the quality of the product manufactured in the industries. The advantage of group acceptance sampling plans is it saves the testing time and reduces the cost of inspection if more items are tested in an experiment. Dodge (1955) [9] has found that zero acceptance numbers in certain sampling plans does not discriminate between good and bad lots. Hence he suggested an allowance of one defective in the current lot and with zero defective in the preceding i lots. But in modern industries quality control practitioners insist that when the sampling plan is administered then the first lot should be capable of meeting the consumer requirement. In fact during life testing experiment they need zero tolerance non conformities in each group. If a defective is found then the same experiment is to be conducted for i such groups in the same lot and the lot should be accepted if all the successive chain of groups have zero defective during testing. Hence in order fulfill the need and lacunae, a novel Intra Lot Group Acceptance Chain Sampling Plans are developed. The efficiency measures Operating Characteristic Function, ASN, ATI, AOQ are developed. Designing through standard quality levels leads to the determination of parameters. The motto of this article is to improve the efficiency of sampling algorithm of the Group Acceptance Sampling with Chain sampling procedure for a single lot. Srinivasa Rao G, et al. (2020), have developed Group Acceptance Sampling Plans for Resubmitted Lots under Type II Generalized Half Logistic Distribution. "Resubmitted sampling plan consists of repeat sampling process, once the consumer is not accepted a production lot based on a single acceptance sampling plan then take the second sample of same size for testing; and build a decision removing the first sample results under the provisions of the statutes or contract". Muhammad Aslam and Chi-Hyuck Jun (2009) [15] , have contributed to GASP for truncated life tests based on the inverse Rayleigh and Log-Logistic distributions. They have compared the results for the two distributions, the inverse Rayleigh and loglogistic distributions when the consumer's risk and the other plan parameters are specified. The minimum number of groups required is determined by considering the consumer's risk when the true mean equals the specified life (μ = μ 0 ). Srinivasa Rao G (2009) [32] , has studied GASP for generalized exponential distribution. The number of groups g required for in the case of the generalized exponential distribution is determined. Muhammad Aslam, et al., (2017) [15] , have developed Group SkSP-R sampling plan for accelerated life tests with an assumption of Weibull model. They have determined the parameters using non-linear optimization technique. Aiman Fikri Jamaludin, Zakiyah Zain and Nazrina Aziz (2016) [1] , have modified Group Chain Sampling Plans for Lifetimes with a Rayleigh Distribution. Optimal number of groups and operating characteristic values are determined for the known consumer's risk, test termination time and mean ratio. Srinivasa Rao Gadde (2019) [30] , have studied Group acceptance sampling plans for resubmitted lots under exponentiated Fréchet distribution. Muhammad Aslam et al. (2010) [17] , have developed Group Acceptance Sampling Plan of Lifetime Data for Generalized Pareto Distribution. They have compared GASP with the existing sampling plan and found that the mew sampling plan performs better in terms of minimum sample size to reach the decision. Muhammad Aslam et al. (2012) [19] have developed Two-Stage Improved Group Plans for Burr Type XII Distributions. The authors have constructed tables for Burr type XII distribution and log-logistic distribution. Srinivasa Rao B, CH. Srinivas Kumar and K. Rosaiah (2014) [27] , have studied Group Acceptance Sampling Plans for Life Tests Based on Half Normal Distribution. They have observed that the minimum number of groups required decreases as the test termination time multiplier increases. Sudamani Ramaswamy and Sutharani (2013) [35] , have designed GASP for a Weibull and Gamma Models by minimizing the angle on the OC curve. Muhammad Aslam, Muhammad Shoaib and Hina Khan (2011) [16] , have developed Improved Group Acceptance Sampling Plan for Dagum Distribution under Percentiles Lifetime. They found that if the subgroup size r = 1, then the sampling plan becomes the ordinary single sampling plan.Subba Rao R, A. Naga Durgamamba and R.R.L. Kantam (2014) [33] , have developed Hybrid Group Acceptance Sampling Plan Based on Size Biased Lomax Model. The HGASP is as follows: Select the number of testers, r and assign the r items to each predefined groups, g, the required sample size for a lot is n = rg. Pre-fix the acceptance number, c for each group and the experiment time t 0 . Accept the lot if at most c failures occurs in each of all groups. Terminate the experiment if more than c failures occur in any group and reject the lot. Muhammad Aslam & Chi-Hyuck Jun (2009), have developed A group acceptance sampling plan for truncated life test having Weibull distribution. Srinivasa Rao B, M. Ch. Priya, and R. R. L. Kantam (2014) [33] , have developed sampling plans for linear failure rate distribution. Harsh Tripathi, Sanku Dey and Mahendra Saha (2020) [11] , have developed Double and group acceptance sampling plan for truncated life test based on inverse log-logistic distribution. Balakrishnan N. et al. (2006) [3] , have contributed to Sampling plans based on Generalized Birnbaum -Saunders distribution. G. Srinivasa Rao, K. Rosaiah, M. Sridhar Babu (2016) [27] , have studied GASP using Exponentiated Frhet Model. Muhammad Aslam, P. Jeyadurga, Saminathan Balamurali, and Ali Hussein AL-Marshadi (2019) [18] , have studied Time-Truncated Group Plan under a Weibull Distribution based on Neutrosophic Statistics. Neutrosophic statistics fuzzy statistics, in which set values are considered rather than crisp values. Whenever the data may be imprecise, incomplete, and unknown, and exact computation is not possible then the neutrosophic statistics can be used. Aiman Fikri Jamaludin, Zakiyah Zain and Nazrina Aziz (2016) [2] , have Modified Group Chain Sampling Plans for Lifetimes Following a Rayleigh Distribution. "Accept the lot if no defective items are found in the current under inspection sample provided the preceding i samples also contain no defective items. Also accept the lot if no defective items are found in the current under inspection sample provided any one of i preceding samples contains at most one defective item and the rest (i-1) samples have no defective items. Otherwise, reject the lot". The OC function is as follows:

A review on group acceptance sampling plans

Nazrina Aziz et al. (2020) [22] , have compared Group Chain Sampling Plan and Modified Group Chain Sampling Plan Based on Mean Product Lifetime for Rayleigh Distribution. Muhammad Farouk, Nazrina Aziz, Zakiyah Zain (2019) [21] , have studied The Two-sided Group Chain Sampling Plan for Pareto Distribution of the second Kind. Rosaiaha K, G S Raob, S V Prasad (2016) [26] , have studied Group Acceptance Sampling Plans Based on Truncated Life Tests for Type-II Generalized Log-Logistic Distribution. Radhakrishnan, R and Alagirisamy, K (2011) [23] , have constructed group acceptance sampling plan using weighted binomial distribution. Radhakrishnan R and K. Alagirisamy (2012) [24] have given tables for group acceptance sampling plan indexed through indifference quality level and inverse Rayleigh distribution Sudamani Ramaswamy AR and Priyah Anburajan (2012) [32] , have studied GASP Using Inverse Rayleigh and Log-logistic models. Sudamani Ramaswamy AR and S. Jayasri (2014) [36] , have studied Time Truncated Group Sampling Plan using Weighted Binomial for Various Distributions. Muhammad Azam et al. (2015), have developed two stage group acceptance sampling plan for half normal percentiles. Dodge HF (1955) [9] has developed chain sampling inspection plans. Clark CR (1960) [5] has developed OC curves for Chain sampling plans. Frishman and Fred (1960) [10] have developed an extended Chain sampling plan. Dodge H. F and Stephens K. S (1964) [10] have given a general family of Chain sampling inspection plans. Dodge HF and Stephens KS (1964) have developed some new chain sampling inspection plans. Soundrarajan V (1978) has given procedure and tables for construction and selection of chain sampling plans. Govindaraju. K and Subramani. K (1992) have designed chain sampling plans for given AQL and LQL. Govindaraju and Lai (1998) have developed modified chain sampling plans for costly or destructive items. Suresh and Devaarul (2002) have developed mixed sampling plans with Chain sampling attribute plan. Radhakrishnan and Sampathkumar (2006) have constructed chain sampling plans using various parameter for ChSP, It is found that there is a research gap to sentence a lot by applying GAS and Chain Sampling Protocol for a single lot. Hence a novel algorithm is developed and the necessary measures of the new plan are derived.

Algorithm of Ilgchsp to sentence a unique lot

Step 1: Let the size of the batches be large and life experiment is conducted with type I censoring with a specified minimum time t 0 .

Step 2: Draw a random sample of size n j =g * r and put them into life test such that 'g' is the number of groups and r items are allocated to each group. Let it be the first sample, j=1.

Step 3: count the number of non-conformities in the first sample comprising of group of items.

Let it be d 1 +d 2 +….+d g =∑ 𝑑=D.

Step 3: If each d j is zero, (i.e) D=0, accept the batch or lot.

Step 4: If D > 1, reject the lot.

Step 5: If D =1, draw 'i' consecutive samples as in step 2 such that group testing is conducted for the chain of groups in the current lot.

Step 6: Accept the batch provided succeeding 'i' consecutive samples from the same lot have zero defective in the batch.

Otherwise reject it. The OC function of Intra Lot Group Acceptance Chain sampling plan is P a (p) = (P 0.r ) g + P 1,n (P 0,r ) ig Where, P 0,r = Probability of getting exactly 0 defective in a sample of r units. Such that n=g*r P 1,r = Probability of getting exactly 1 defective in a sample of r units. i = Chaining index of groups in the same lot. The OC function of Intra Group Chain sampling plan with type B probabilities is, P a (p) = (𝑒 -𝑛𝑝 ) 𝑔 + (𝑛𝑝𝑒 -𝑛𝑝 ) 𝑔 (𝑒 -𝑛𝑝 ) 𝑖𝑔 i.e P a (p) = (𝑒 -𝑟𝑔𝑝 ) 𝑔 + (𝑟𝑔𝑝𝑒 -𝑟𝑔𝑝 ) 𝑔 (𝑒 -𝑟𝑔𝑝 ) 𝑖𝑔

Interpretation

From figure (1), it is found that ILGAChSP well discriminate between good and bad lots. Upto a process average of 0.005, there is good shoulder effect on the OC curve. This gives a confidence to the producer to maintain the quality.

Figures and tables from the paper

Table 1. OC Function values for known fraction defectives with i=1,g=1
pn=100 Pa1(p)n=50 Pa2(p)n=200 Pa3(p)
0.00010.9997036630.9999254580.998829
0.0020.9078178590.9735975980.722588
0.0030.8198609110.9444549280.532211
0.0040.7225877770.9078178590.373133
0.0050.6248434220.8657064010.253225
0.0060.5322113410.8198609110.168146
0.0070.4478328940.7717498560.110045
0.0080.3731330540.7225877770.071351
0.0090.3084010260.6733589190.046002
0.010.2532250590.6248434220.029572
0.0110.2068017080.5776439390.018993
0.0120.1681457230.5322113410.012203
0.0130.1362255420.4888686730.007853
0.0140.1100454910.4478328940.005064
0.0150.088691250.4092342230.003275
0.0160.0713509810.3731330540.002123
0.0170.0573210180.3395345440.001381
0.0180.0460023520.3084010260.000901
0.0190.036892070.279662450.000589
0.020.0295724980.2532250590.000386

Table text extracted from the original PDF; superscript letters are shown inline. The original table image is below.

View original table image
OC Function values for known fraction defectives with i=1,g=1↗ Enlarge
Table 1
OC Function values for known fraction defectives with i=1,g=1

OC Function values for known fraction defectives with i=1,g=1

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Original paper tableSource PDF · page 3 ↗
Figure 1. Comparison OF OC Curve
Comparison OF OC Curve↗ Enlarge
Figure 1
Comparison OF OC Curve

Comparison OF OC Curve

Open full-size image ↗
Original paper figureSource PDF · page 3 ↗
Table 2. Computation of AOQ values
PPa(p)AOQ
0.00010.9988290.000079906
0.0020.7225880.001156141
0.0030.5322110.001277306
0.0040.3731330.001194026
0.0050.2532250.0010129
0.0060.1681460.000807101
0.0070.1100450.000616252
0.0080.0713510.000456646
0.0090.0460020.000331214
0.010.0295720.000236576

Table text extracted from the original PDF; superscript letters are shown inline. The original table image is below.

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Computation of AOQ values↗ Enlarge
Table 2
Computation of AOQ values

Computation of AOQ values

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Original paper tableSource PDF · page 4 ↗
Table 3. Values of np tabulated against i and g for the given values of Pa(p) for IGChSP
iG0.990.950.750.500.250.100.050.01
110.08600.20660.56641.00641.66062.49023.12444.6487
120.06000.14150.37220.63691.00641.44451.76222.4902
130.04860.11390.29400.49470.76681.08001.30171.7959
140.04200.09780.24960.41570.63690.88711.06171.4445
150.03740.08700.22030.36420.55360.76500.91131.2283
210.06700.16220.45590.83871.46192.32463.00314.6056
220.04660.11060.29540.51530.83871.24911.56412.3246
230.03780.08880.23210.39600.62670.90561.11211.5984
240.03260.07620.19650.33090.51530.73210.73210.8889
250.02910.06770.17300.28890.28890.62520.75351.1498
310.05690.13890.40140.76711.40682.30492.99614.6052
320.03950.09430.25610.45640.76711.18461.51392.3049
330.03200.07560.20000.34660.56120.83371.04321.5498
340.02760.06480.16880.28780.45640.66250.81701.1846
350.02460.05750.14830.25030.39140.55980.68340.9723
410.05050.12410.36870.73161.39162.30282.99584.6052
420.03500.08390.23160.42170.73161.16241.50162.3028
430.02830.06720.17990.31650.52450.79961.01591.5383
440.02440.05750.15130.26120.42170.62560.78261.1624
450.02180.05100.13270.22620.35920.52310.64670.9425

Table text extracted from the original PDF; superscript letters are shown inline. The original table image is below.

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Values of np tabulated against i and g for the given values of Pa(p) for IGChSP↗ Enlarge
Table 3
Values of np tabulated against i and g for the given values of Pa(p) for IGChSP

Values of np tabulated against i and g for the given values of Pa(p) for IGChSP

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Original paper tableSource PDF · page 4 ↗
Table 4. Values of p2/p1 tabulated against i and g values of α and β and values for IGChSP
igp2/p1 for——np1 for α=0.05p2/p1 for——np1 for α =0.10
α=0.05 β =0.10α=0.05 β =0.05α=0.05 β =0.01α=0.01 β = 0.10α=0.01 β= 0.05α=0.01 β = 0.01
10126.436534.394752.87300.087167.862088.2906135.72410.0339
9125.415533.066450.83110.090664.810384.3202129.62070.0355
8124.305731.622548.61150.094761.561080.0927123.12200.0374
7123.091030.042046.18190.099758.078175.5613116.15620.0396
6121.749628.296843.49910.105954.313170.6629108.62620.0424
5120.251326.347240.50210.113750.198565.3091100.39590.0459
10220.027326.055940.05420.057549.338364.190098.67570.0233
9219.182724.956538.36420.060047.060461.225194.11780.0245
4118.552424.134937.10100.124145.636559.368991.26390.0505
8218.276723.776236.54970.063044.645058.079089.28100.0258

Table text extracted from the original PDF; superscript letters are shown inline. The original table image is below.

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Values of p2/p1 tabulated against i and g values of α and β and values for IGChSP↗ Enlarge
Table 4
Values of p2/p1 tabulated against i and g values of α and β and values for IGChSP

Values of p2/p1 tabulated against i and g values of α and β and values for IGChSP

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Original paper tableSource PDF · page 4 ↗
Figure 2. AOQ CURVE
AOQ CURVE↗ Enlarge
Figure 2
AOQ CURVE

AOQ CURVE

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Original paper figureSource PDF · page 4 ↗
Table 5. Parametric values for IGChSP indexed through AOQL
7217.299422.500634.58800.066642.070554.719384.11450.0274
10316.845221.906933.67480.045640.793653.051681.54950.0188
3116.592621.568833.15230.138940.494252.638480.90810.0569
6216.240521.111032.44870.071039.314051.104278.54990.0293
9316.119220.953332.20640.047738.909050.577877.74080.0197
8315.350919.936330.63680.050136.930747.962073.70470.0208
5215.091319.584330.08940.076536.358247.182772.49160.0318

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Parametric values for IGChSP indexed through AOQL↗ Enlarge
Table 5
Parametric values for IGChSP indexed through AOQL

Parametric values for IGChSP indexed through AOQL

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Original paper tableSource PDF · page 5 ↗
Table 5. Parametric values for IGChSP indexed through AOQL
ignpmnAOQLnp0.50h0AOQL/p1 for 0.05np1 for 0.05
610.98700.10491.00640.73640.99110.1059
150.32840.18370.63691.17902.11320.0870
140.37800.20940.49471.15962.14130.0978
250.26360.14540.41571.14982.14730.0677
240.30540.16630.36421.12642.18210.0762
130.45540.24870.83873.30432.18350.1139
350.23160.12570.51531.11982.18480.0575
450.21250.11340.39601.09112.22330.0510
340.27030.14430.33091.09232.22730.0648
230.37180.19860.28891.09322.23540.0888
120.59920.31930.76711.09082.25680.1415
550.20000.10490.45641.06412.26250.0464
440.25000.13080.34661.05982.27450.0575
330.33330.17350.28781.05302.29410.0756
650.19150.09870.25031.03872.30240.0429
540.23740.12150.73161.02942.32310.0523
220.50000.25780.42171.04022.33180.1106
750.18560.09390.31651.01482.34290.0401

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Parametric values for IGChSP indexed through AOQL↗ Enlarge
Table 5
Parametric values for IGChSP indexed through AOQL

Parametric values for IGChSP indexed through AOQL

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Table 6. Values of np* and h*values for IGChSP @ 1-α = 0.95
ignp*h*
1010.26242.0000
910.28682.0000
810.31612.0000
710.35201.9998
610.39701.9991
510.45501.9955
410.53261.9779
310.64261.9021
111.11781.8552
210.81211.7420
120.77881.0939
1020.22700.9977
920.24500.9950
820.26610.9890
720.29150.9762
620.32240.9507
220.58720.9177
520.36110.9079
420.41170.8653

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Values of np* and h*values for IGChSP @ 1-α = 0.95↗ Enlarge
Table 6
Values of np* and h*values for IGChSP @ 1-α = 0.95

Values of np* and h*values for IGChSP @ 1-α = 0.95

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Table 7. Relative slope for acceptable and limiting quality levels for IGChSP
ignp0.50h0np0.95h1np0.10h2h2/h1h2/h0h0/h1
111.00641.00810.20660.09252.49022.745229.68122.723110.8998
120.63691.09080.14150.09521.44453.114932.73062.855511.4622
130.49473.30430.11390.09641.08003.304334.26931.000034.2693
140.41571.15960.09780.09720.88713.427335.26402.955511.9316
150.36421.17900.08700.09770.76503.516835.98692.982912.0645
210.83870.93050.16220.09132.32462.404026.34472.583510.1972
220.51531.04020.11060.09431.24912.777329.44682.669811.0295
230.39601.09320.08880.09570.90563.030531.65602.772111.4193
240.33091.12640.07620.09660.73213.197133.09672.838411.6603
250.28891.14980.06770.09720.62523.316334.11942.884311.8294
310.76710.86000.13890.09002.30492.318425.76542.69599.5573
320.45640.98960.09430.09341.18462.536727.14822.563510.5903
330.34661.05300.07560.09500.83372.789129.35082.648811.0808
340.28781.09230.06480.09600.66252.978931.03372.727311.3791
350.25031.11980.05750.09670.55983.120232.28122.786411.5854

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Relative slope for acceptable and limiting quality levels for IGChSP↗ Enlarge
Table 7
Relative slope for acceptable and limiting quality levels for IGChSP

Relative slope for acceptable and limiting quality levels for IGChSP

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