Need explanation and graphical representation of ABBE'S LAW

  • Thread starter David Drue Stauffer
  • Start date
D

David Drue Stauffer

#1
ABBE'S LAW

Hi Guy's.
This may sound a bit naive, but I'm looking for an explanation and graphical representation of ABBE'S LAW. I have the definition but "a picture is worth a thousand words". While developing a metrology course (basic), it would be nice to be able to provide this information.
Can you help? Dave
[email protected]


------------------
Dave S.
 
Elsmar Forum Sponsor

Jerry Eldred

Forum Moderator
Super Moderator
#2
I am unfortunately at a disadvantage. My library is packed up for a soon-coming office move. I recommend in the interrim that if you have access to GIDEP to review some of their calibration procedures. If you could possibly post or email me with some manufacturer/model number combinations that might be calibrated using methods associated with Abbe's Law, I would be happy to check my CD-ROM library for some illustrations. I did a brief web search on Abbe's Law and found some Microscopy course info that gave me a hit on that search word. If you try a search that way, perhaps you would find something to cover your needs. Please feel free to email me directly. I'll be glad to see what I can find.

------------------
 
#3
Obtain a copy of "Fundamentals of Dimensional
Metrology" by Ted Busch Wilkie Brothers Foundation,Delmar Publishers Inc.
Includes history and pictures.
 
D

David Drue Stauffer

#4
Thanks Jerry, I tried a net search as well with MSN that resulted in no "finds".
I'll try some other browsers.
I don't have any examples of mfg/models to give, only trying to graphically represent the principle for clarification in the ppt. course I am writing for basic metrology.
I'll keep searching, but thanks for your response and tips. If anythings pops up when you think about it, drop me another e-mail.
Thanks, Dave.

------------------
Dave S.
 
D

David Drue Stauffer

#5
Sam, thank you for the lead, I did find an example of the law, the formula, and an illustration using a bench micrometer in the textbook "Fundamentals of Precision Measurement" Mitutoyo Metrology Institute.
I will check Amazon.com for the book you suggested, it would probably be a good source for my class.
Dave

------------------
Dave S.
 
Thread starter Similar threads Forum Replies Date
S Need help with analysing a survey on minitab Using Minitab Software 1
M IATF 16949 8.5.1.3 Verification of job set-ups - Do we need secondary check? IATF 16949 - Automotive Quality Systems Standard 7
P Electrosurgical Device User Need: Cord Flexibility -> Requirement Other Medical Device and Orthopedic Related Topics 4
P Do I need to get registered or have German entity to sell IVD products in Germany? CE Marking (Conformité Européene) / CB Scheme 2
J Documentation structure - Do I need Work Instructions? Document Control Systems, Procedures, Forms and Templates 23
G Need resources / tutorials about OPS (Operation) for ISO IT (Information Technology) Service Management 8
D Do non-IATF customers need to be included in audit scope? IATF 16949 - Automotive Quality Systems Standard 23
M Do you need an Applicable general safety and performance requirements Checklist? EU Medical Device Regulations 2
Y Does Solidworks (2D/3D drafting modules) need validation? Other Medical Device and Orthopedic Related Topics 5
M Do we need to create a new CER or can we just update the existing CER EU Medical Device Regulations 3
K A proposal for the model Quality Management - I need help for the project ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
B Record Management - Does the QMS need to control templates of records? Records and Data - Quality, Legal and Other Evidence 17
Q Need clarification on requirements.... Class i, gmp & 510(k) exempt Medical Device and FDA Regulations and Standards News 12
U Do we need clinical trial data for Class IIa medical device under MDR EU Medical Device Regulations 7
G Do we need to QA cert? We only plan to supply reagents Medical Device and FDA Regulations and Standards News 3
I MSA requirement for 5 Micrometers + CP changes need customer approval? IATF 16949 - Automotive Quality Systems Standard 2
R Evaluating the need for preventive action Preventive Action and Continuous Improvement 3
R Probability - Need a help to solve the below question Statistical Analysis Tools, Techniques and SPC 5
E In need of a new TGA sponsor - Small software company Other Medical Device Regulations World-Wide 4
8 Need Help - Runout - Function Gage Inspection, Prints (Drawings), Testing, Sampling and Related Topics 7
B Need For BIS Standard Mark? Imported OEM's Power supply,Li-Ion Battery Other Medical Device Regulations World-Wide 0
F How many signatures do we need on calibration certificates? ISO 17025 related Discussions 8
B We need a QMS: file-based templates or software Other Medical Device Related Standards 23
M AQL table - I need to sample 1250pcs AQL - Acceptable Quality Level 3
atitheya Need of conducting medical trials in European Union EU Medical Device Regulations 2
L Gage R&R studies for identical Devices - Need to confirm the requirement to perform them Reliability Analysis - Predictions, Testing and Standards 2
D Does every piece of equipment used in a laboratory need to have an IQ protocol written and executed? ISO 13485:2016 - Medical Device Quality Management Systems 1
I IATF16949 Audit Preparation, Need "searchable" ANPQP 3.1 or latest IATF 16949 - Automotive Quality Systems Standard 1
A Does Class 1 Medical Device need to be certified to MDSAP? Canada Medical Device Regulations 5
S New to FAIR, need help in filling it out AS9100, IAQG 9100, Nadcap and related Aerospace Standards and Requirements 8
S ISO 9001:2015 & ISO 14001:2015 - I need a format for Design & Development planning ISO 14001:2015 Specific Discussions 2
M Informational Some things the EU MDR 2017/745 does not tell you, but you may need to know to comply with it effectively – Part 1 Medical Device and FDA Regulations and Standards News 0
S NADCAP approval for Conventional Machining and Chemical processes - need assistance AS9100, IAQG 9100, Nadcap and related Aerospace Standards and Requirements 10
S Do we need to validate Software used in Drug discovery and development process? Qualification and Validation (including 21 CFR Part 11) 2
W Tying the need for Demand Planning to a section of AS9100/9110 AS9100, IAQG 9100, Nadcap and related Aerospace Standards and Requirements 4
R Do we need to treat local law as external origin documents? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 15
S Need Assistance in Visual Inspection - Tiny electronic components AS9100, IAQG 9100, Nadcap and related Aerospace Standards and Requirements 11
D Do we need normal data for gage r&r studies? Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 5
D Do I need part variation while doing Destructive Variable Gage R&R MSA study Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 19
Ashok sunder Need ISO 45001:2018 HIRA template Occupational Health & Safety Management Standards 9
QIE Electronic IFU - new project, need input Other Medical Device and Orthopedic Related Topics 0
G Defect codes and process codes need to be controlled AS9100, IAQG 9100, Nadcap and related Aerospace Standards and Requirements 4
R Pls help --- Need expert advice on Video Measurement Measurement Uncertainty (MU) 0
M Informational FDA Panel: Too early to pull textured breast implants over cancer risk, need more data Medical Device and FDA Regulations and Standards News 0
I Training records and levels - When does training NOT need a record? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 13
M Dynamic Control Plan Draft - need review FMEA and Control Plans 2
C Advice on becoming a AS9100 Auditor - Need to audit organizations that are Design Responsible AS9100, IAQG 9100, Nadcap and related Aerospace Standards and Requirements 12
I R&D prototype documents need to be controlled? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
L 510k exemption process - Do you still need to submit technical dossier? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 5
C Do we need to make a new OFI (Opportunity for Improvement) for each document/form we update? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 23
Similar threads


















































Top Bottom