Clarke), Britney (Nigel Clauzel) and Meat (Kerry Ellis) Lead vocals are sung by Pop (Nigel Planer), Khashoggi (Alexander Hanson), Gallileo (Tony Vincent), Scaramouche (Hannah Jane Fox), Killer Queen (Sharon D. Macraeīonus Disc 2 Track 2 produced by Brian May, mixed by Justin Shirley-Smithīonus Disc 2 Tracks 3 and 4 produced and mixed by Simon Sayer, Carlos Martos and Arturo Sorianoīonus Disc 2 Tracks 5 and 6 produced by Simon Sayer, mixed by Simon Sayer and James Loughreyīonus Disc 2 Tracks 7-11 produced by Queen, mixed by Justin Shirley-Smithīonus Disc 2 mastered by Peter Mew at Abbey Road Studios Photography by Catherine Ashmore and Dave Bennettīonus Disc 2 Track 1 produced and mixed by Joshua J. Mastered by Miles Showell at Metropolis Mastering Production tools by Kris Fredriksson and Joshua J. Macrae at Allerton Hill and Cosford Mill studios. Mixed by Justin Shirley-Smith and Joshua J. Recorded live at the Dominion Theatre, London, 12th and 13th July 2002 Produced by Justin Shirley-Smith and Brian May We Are The Champions (Queen + German Cast on 'Wetten Dass' TV programme, 2004) We Will Rock You (Queen + German Cast on 'Wetten Dass' TV programme, 2004)ġ1. Somebody To Love (German Cast on 'Wetten Dass' TV programme, 2004)ġ0. Radio Ga Ga (German Cast on 'Wetten Dass' TV programme, 2004)ĩ. Bohemian Rhapsody (Queen + London Cast, Party At The Palace 2002)Ĩ. Crazy Little Thing Called Love (Algo loco es al amor) (Spanish Cast)ħ. No-One But You (Solo Por Ti) (Queen + Eva Maria, Short Version)Ĥ. Another One Bites The Dust (Queen + Annie Crummer)Ģ. No-One But You (Only The Good Die Young)ġ. Re-released 15 October 2012 to mark the 10th anniversary, with a bonus disc.ġ1. Released 11 November 2002, and reissued in a different sleeve in May 2003.
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There was no significant difference between the average pH of the phenolphthalein indicator and the average pH of the ethanol extract of Adam's Eve Leaves, ethanol extracts of white Cambodia flowers and ethanol extracts of Telang flowers in producing color changesĮxperiment on natural acid-base indicators is usually done by extracting the natural sources with certain solvent, testing the extract with acid, base and neutral solutions, observing the color changes, making conclusion and discharging the remaining extract at the end of the experiment. Research journals on making natural indicators from ethanol extracts of various plants compared to phenolphthalein indicators so that secondary data from these journals can be processed statistically Natural indicators are needed as a substitute for synthetic indicators in determining acid-base titrations one of them is anthocyanin dye Research results and conclusions: Based on the results of statistical data processing using the t-test there was no difference in the average pH of the phenolphthalein indicator with the average pH of ethanol extracts of adam air leaves (Rheo discolor), white frangipani flowers and Clitoria teratea L., with a significance value > 0.05 and the equality test (precision) had the requirements of good equality. The research method is to collect research journals on making natural indicators from ethanol extracts of various plants compared to phenolphthalein indicators so that secondary data from these journals can be processed statistically. This study was to ensure an ethanol extract of some plants could be used as an acid-base indicator that had a pH range of color change and the value of the equality parameter was not significantly different from the phenolphthalein indicator. The extraction was carried out with ethanol because the compounds of anthocyanin were polar. Natural indicators using anthocyanin compounds can be an alternative to synthetic indicators on acid-base titration because anthocyanin is an organic compound that is unstable with changes in pH. K is a constant which will cancel in intensity ratios, c a is the concentration of the alpha component, R a is an angular dependent term which is defined in equation 12-10, m m is the absorption coefficient for the mixture,Īppendix 8 p. 408 to 409, equation 14-1),Įquation 12-1 can be simplified for comparison of two reflections which correspond to two different phases in a metal sample, such as a powder mixture of molybdenum and copper. Phase Composition for mixed phase metals (more than one crystal structure):Īs Cullity described on p. In addition, account must be made for the multiplicity of planes in a crystal, variation in thermal broadening with angle and some other factors, see The intensity from a diffractometer in reflection geometry must be corrected for the angular dependence of absorption/beam profile and for the Lorentz Polarization factor which is also angularly dependent. There are alternative approaches to determination of phase composition including density measurements, thermal analysis and spectroscopy, but XRD remains the most robust and simplest technique so it is of dominant importance. For a multi-phase metal this corresponds to a quantitative analysis of the phase composition. This means that for a material with multiple phases, crystalline/amorphous or several crystalline phases, XRD can be used to determine the volume fraction of these phases. The integrated intensity from a diffraction peak is proportional to the volume fraction of that material in a sample. From the FCC brass structure determine the distance of closest approach and find the number fraction zinc in the brass key.Vegard's Law predicts a straight line for this plot for brass.Make a plot of closest approach distance versus number fraction zinc, at 0 this is the distance for pure copper determined above and at 1.0 this is the number determined above for copper.Determine the distance of approach for the two patterns ( for HCP this is "a", for FCC this is "a"/ √ (2).Index both crystal structures and determine the lattice parameters.Measure the diffractometer trace for copper and zinc.In the powder mixture a calculation of the relative intensity of two peaks will be used to determine the amount of BCC Moly and FCC copper in a mixture containing independent crystals of these two materials. Vegard's Law will be used to determine the zinc content by consideration of the shift in the lattice parameter for the FCC pattern. This lab will involve the analysis of composition of two samples, a brass key, composed of a substitutional solution of zinc in copper (FCC) and a physical mixture of copper (FCC) and molybdenum (BCC) powder. 139 section 4-12 and equation 4-21 for Diffractometer. 12-6, Chapter 14 (Phase Analysis), Chapter 7 (Diffractometer), pp. New Cullity and Stock: Chapter 11, Figure 11-6, Chapter 12 (PhaseĪnalysis), Chapter 6 (Diffractometer), Chapter 4 (Calculated Diffracted Intensity) Objective: To become familiar with use of the diffractometer for quantitative analysis of phases in mixtures/alloys of metals. There are twelve possible directions for zone axes as listed in Table 1, with 6 unique directions and their opposites.Lab 6: Diffractometer/Phase Analysis & CompositionĬopper Wire (oriented), Copper Plate (unoriented), Zinc Powder, Brass Key, Moly Powder, Moly/Copper Powder Such twinned structure has only one situation that can satisfy the following: both the directions from the matrix and the directions from the twin are parallel to the twinning plane ( 112) and the incident electron beam direction. The directions of both the matrix crystal and the twinned crystal are parallel to the ( 112) twinning plane and perpendicular to the paper plane, i.e., the directions from both the crystals are parallel to the incident electron beam during TEM observations. The matrix crystal and the twinned crystal are indicated in blue and orange color, respectively. In twinned martensite, a metastable hexagonal ω-Fe phase always exists in the twin boundary region of the body-centered cubic (bcc) -type twinning structure. Things are easily moved around, subordinated to other things, etc. For me, it’s a thinking program because it doesn’t force into a hierarchy, so I can dump down a bunch of concepts all connected to one think, like “unclassified” and then start figuring out the relationships, with different kinds of links. Most view it as an information storage program, but I use DT for that. It helps me see connections better than anything. They have one on their web site with around 65,000 nodes! It doesn’t look complex because you only see a small piece at a time. It’s dynamic, meaning that any note clicked on becomes the center, showing the parents (yes, multiple parents makes a note, in effect, a multiple replicant), the children and the siblings. (2) when they work well, they became too complex and collapse of their own weight. The problems with most is that (1) they usually force you into a tree structure, unable to change the root, unless they are a concept map. Also if someone could tell me how Inspiration integrates with DT I would really appreciate it And I’ll do my best to answer any questions you might have. I would love to hear any feedback others have, regarding things I may have missed with these tools or other programs I should check out. But if you’re looking for a straightforward mindmapping tool with decent DEVONthink integration, MindNode seems to be the one to get. I’m still interested in trying out Inspiration because of some of its other features. It’s also the least expensive package I evaluated, another plus. It’s good news for me because with the exception of its hotkeys (which may be configurable, I’m not sure yet) I found it the most intuitive. Its documents are natively displayable by DT, and the printed PDF is fully searchable. I’m waiting on a response from support before I can try it out.Īt this point MindNode is in the lead for me. MindManager required me to register to download the demo, and since I already had three demos on my machine I didn’t feel like it The Inspiration demo said I didn’t have permission to run it. Two other products I’ve considered but haven’t evaluated yet are MindManager and Inspiration. Print dialog has option to scale to fit to one page which made it render nicely
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