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Development by inspection

The second difference is that divided development is a once-in, once-out process once in A, once in B, rinse, then fix. Water bath development is meant to be a repeatable process. After immersion in the second bath, the film is returned to the A bath and the process repeated as many times as necessary to achieve the desired contrast or density. For this reason, water bath development is best used in conjunction with development by inspection. [Pg.43]

Nonetheless, there are still a few valid reasons to learn how to develop by inspection. The most important is that it allows complete and total control over every image. A second reason is that it might help save negatives when there is doubt as to the correctness of exposure. A third reason is that when developing films by the water bath method to control contrast it is often desirable to visibly monitor development (Chapter 4 Film Development Water Bath Development). The fourth, and final reason, is there may come a time when film will again be hand-coated with loose tolerances. [Pg.134]

The technique of development by inspection should be approached in the same way one would approach any new process. Start by creating practice negatives and developing them until you are confident in your ability to judge their quality. Only then should you work with important images. [Pg.134]

One final point, development by inspection is really only suited for 4X5 inches and larger sheet film. This is because development by inspection assumes that each negative will be developed to an ideal density for that particular negative. [Pg.134]

Even if a chemical desensitizer has been used, the safelight should not be turned on until at least halfway through the estimated development time. This is because film looses its sensitivity as development proceeds. If a desensitizer has been used, the safelight can be left on when the estimated halfway point has been reached (see Desensitizers, below). Without the use of a desensitizer, the safelight should only be turned on for brief intervals, 15 to 20 seconds at a time, after the estimated halfway point. Pyro developers aid in desensitizing the film by hardening the surface of the emulsion as development proceeds (see Pyro and Development by Inspection, below). [Pg.135]

Check the density increase every 1 to 3 minutes, depending on how close you estimate you are to full development. As completion gets closer, you can begin checking every 30 seconds, but remember, the film is still sensitive to light, unless a desensitizer has been used therefore, only check as often as necessary. You will find that after developing by inspection a few times you will need to check less as you will be able to estimate the progress of development without frequent inspection. [Pg.135]

The short list that you developed by inspection of the tables in Appendix 1 and the structures drawn should suggest that some additional tests may be needed to distinguish among the possibilities. For instance, one compound may be a methyl ketone, and the other may not. The iodoform test is called for to distinguish the two possibilities. The tests for the subsidiary functional groups may also be required. These tests are described in Experiments 52B and 52C. These tests should also be studied carefully there is no substitute for firsthand knowledge about these tests. [Pg.459]

The QAP system additionally was developped for inspection documentation purposes to meet the modern requirements in process documentation (ISO 9000). It is the basic system required to install a fully automated inspection by a camera system and image processing. [Pg.629]

Magnetic Particle Inspection was developed by Professor AW de Forest in 1928. De Forest and Doane started the company Magnaflux, the name of which became synonymous with MPI. [Pg.639]

The principal equipment for the ultrasonic examination is the P-scan system, PS-4, which is a computerised ultrasonic system, developed by FORCE Institute, for automatic, mechanical and manual ultrasonic examination of welds and materials. The system has documentation and storage facilities for all data related to each inspection operation, and includes visualisation of the inspection results in the form of images of the material volume examined. [Pg.872]

The use of electromagnetic acoustic transducers (EMAT) obviates the coupling problems already referred to, and has been applied successfully to the inspection of boiler tubes. Ultrasonic time of flight diffraction (TOFD), developed by the Harwell Laboratory" , is utilised to fingerprint flaws (cracks) in process plant. Subsequent examination at, say, six month intervals can indicate any growth or extension of the crack. It is claimed that changes in crack height of 0-5 mm or less be estimated. [Pg.1145]

During the course of the development of our group s alkylation/reductive decyanation strategy, a very reliable method for distinguishing between syn-and anfz-l,3-diols was discovered [17,18]. The acetonide methyl groups reliably display diagnostic C-NMR chemical shifts, allowing for stereochemistry to be determined simply by inspection (Fig. 1). Evans later extended the C-NMR chemical correlation to polypropionate chains [19,20]. [Pg.57]

While quality was formerly achieved by inspection of final products, it is accomplished now by prevention through controlling critical steps in the production processes along the agri-food chain. Hazard analysis critical control points (HACCP) represent a typical example of such a preventive approach. Although this concept was developed primarily to assure food safety, the basic principle is also applicable to assuring non-safety quality attributes such as color, flavor, and nutritional value. " This section translates the HACCP principles into a critical quality control point (CQP) concept that can be part of a system to assure food quality. [Pg.560]

Monitor the patient for symptom relief. Have the desired outcomes jointly developed by the health care team and the patient/caregiver been achieved and to what degree Inspect the daily diary completed by the patient/caregiver since the last clinic visit and quantitate the clinical response (e.g., number of micturitions, number of incontinence episodes, and pad use). If a diary has not been used, ask the patient how many incontinence pads have been used and how they have been doing in terms of accidents since the last visit. If appropriate, administer a short-form instrument used to measure symptom impact and condition-specific quality of life and compare previous result(s). [Pg.812]

Although the resulting direct product may not be reduced, it can be made so by application of the magic formula, or often by inspection. The nonvanishing of the integral is then determined by the existence of the totally symmetric representation in the resulting direct sum. This procedure will be illustrated by the development of spectroscopic selection rules in Section 12.3.3. [Pg.108]

Instrumentation for revealing the presence of bulk quantities of concealed drugs will differ from those developed to find evidence of minute quantities on surfaces. Bulk detection is concerned with amounts ranging from grams to kilograms [4], Bulk detection is done by manual inspection, X-ray, CT scans, and acoustic inspection. X-ray or CT scanners used as bulk detectors have sensitivity of 2-10 g, and suspect items are subsequently confirmed by chemical analysis. Hand-held acoustic inspection instruments such as the Acoustic Inspection Device (AID) and the Ultrasonic Pulse Echo (UPE) developed by Pacific Northwest National Laboratories/Battelle, can be used for analysis of cargo liquids in sealed containers of various sizes within seconds [5]. The acoustical velocity and attenuation of multiple echoes returned to the instrument is evaluated by software which compares the data to the shipping manifest. [Pg.790]

If no chemical steps are coupled to the ET at the electrode, the reaction mechanism is fully described by A (thermodynamics), n (stoichiometry), D (transport), as well as ks, and a (kinetics). It is characteristic to find a fully developed reverse peak in the cyclic voltammogram [49]. Qualitatively, it is important to diagnose full diffusion control (Er). Cyclic voltammetry allows this by inspection of the peak potential difference A p = E — For Er, A p is independent of v, while for Eqr an increase of v (faster timescale) causes AEp to increase (Figure 8a) [50]. [Pg.15]


See other pages where Development by inspection is mentioned: [Pg.134]    [Pg.134]    [Pg.135]    [Pg.135]    [Pg.137]    [Pg.137]    [Pg.137]    [Pg.309]    [Pg.134]    [Pg.134]    [Pg.135]    [Pg.135]    [Pg.137]    [Pg.137]    [Pg.137]    [Pg.309]    [Pg.165]    [Pg.352]    [Pg.114]    [Pg.97]    [Pg.102]    [Pg.415]    [Pg.446]    [Pg.95]    [Pg.136]    [Pg.227]    [Pg.145]    [Pg.139]    [Pg.58]    [Pg.220]    [Pg.236]    [Pg.24]   


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