Lecture 17- Glass Flashcards

1
Q

what was the first type of glass made from

A

melted sand

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2
Q

why can glass be a good source of trace evidence

A

it is fragile so likely to break and transfer

it is also able to persist for a long time enough to be recoverable

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3
Q

how is the flatness of glass controlled in the manufacturing of it

A

production of float glass - molten glass floats on a molten tin bath to become flat

can be controlled thickness, flat, smooth surfaces

gives identifiable features through surface analysis

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4
Q

how is float glass normally identified

A

the side that was in contact with the tin shows a luminescence at 254nm and can have a anisotropic gradient in the refractive index

but in the manufacturing this luminescence can be removed

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5
Q

how does the composition of glass vary

A

depending on the manufacturer the mixture and ratio of components changes

this addition of things for colour and strengthening

the order and amount of things added is likely to be different

presence of coatings

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6
Q

what is added to glass to improve heat durability and where is this often seen

A

boron oxide (B2O3)

seen in cookware, glasses and car headlamps

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7
Q

what is added glass to absorb radiation and where is this often seen

A

silver (Ag) in sunglasses

strontium in TV screens

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8
Q

what are the 3 properties of glass associated with the possibility of it breaking

A

flexibility
strength
nature of the impacting object (force and shape)

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9
Q

how can a side impact on glass be determined

A

by hackle or rib marks

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10
Q

what shape is often seen when a projectile impacts glass

A

a percussive cone

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11
Q

when is glass transfer often seen in crime scenes

A

during hit and runs and ram-raids

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12
Q

do the smaller or larger fragments of glass tend to be transferred to clothing and found in investigations

A

smaller ones

more likely to see if a big chunk of glass is on your clothing

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13
Q

what are the three ways normally used to recover glass shards

A

scraping
taping
forceps

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14
Q

what is the analytical workflow for glass evidence

A
  1. gross examination recovery and collection
  2. prelim evaluation of physical characteristics
  3. physical fit assessment
  4. microscopic analysis - refractive index
  5. density measurements (often not included now)
  6. elemental analysis with SEM, XRF (non destructive)
  7. mass spec elemental analysis (destructive)
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15
Q

why is physical fit assessment matches very unlikely with glass evidence

therefore what type of information is heavily relied on from glass evidence

A

harder with smaller pieces of glass
glass can chage shape slightly - upon heat

rely on elemental analysis

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16
Q

what defined the analytical scheme employed in the analysis of glass

A

the size of the recovered fragment

large vs small

17
Q

what is analysed for larger glass fragments

A

thickness - take an average and standard deviation

colour - can be subjective though

matching edges - physical fit

density

RI measurement

18
Q

what is analysed for smaller glass fragments

A

confirm it’s glass

examine surface for distinguishing features

19
Q

how can the analysis of colour be made less subjective

A

by using MSP - microspectrophotometry

20
Q

what can be looked at to see if the sample is glass or a type of quartz/mineral

A

the birefringence

21
Q

what can be looked at to see if the sample is glass or a type of plastic

A

see if it compresses under pressure if breaks = glass, if compresses = plastic

22
Q

how is the density of a piece of glass measured

A

using a density gradient column - vary the density of the liquid and see when the glass fragment remains even - doesn’t sink or float

not most accurate but get a rough idea

combine with RI measurement to be more discriminative

23
Q

when measuring the RI of glass what method is normally used and why

A

the Single or double variation method as it is more precise than the Becke Line test

24
Q

how is the single variation method carried out

how does the double variation method differ from this

A
  1. mount sample in a medium with higher RI
  2. fix light at a certain wavelength e.g 589nm
  3. slowly heat sample on a hot stage
  4. the medium’s RI will change quicker than the samples when heating
  5. temp of lowest contrast between sample and media is recorded computationally
  6. compare to a table of known RI values

double variation method varies temp and wavelength of light = even more precise

25
is a sample from the outer edge of glass or from the main bulk likely to have a lower RI
sample in bulk likely to be lower
26
why is elemental analysis done on glass samples normally
very little discrimination is often found comparing the RI of them
27
give 3 advantages of using SEM-EDX for glass analysis
minimally destructive can analysis very small fragments (<100 micrometre)
28
what level does secondary electron mode reach of samples in SEM-EDX
surface
29
what level does back scatter electron mode reach of samples in SEM-EDX
just below the surface
30
SEM-EDX is good for the elemental analysis of glass but what technique is preferred and why
micro XRF is preferred SEM-EDX is limited by its sensitivity to some of the major components in glass also it has poor precision due to the variation in fragments orientation, shape and thickness
31
how does micro XRF differ from SEM-EDX
the detection method is the same but XRF uses X-Rays as the excitation source so is able to penetrate deeper into glass rather than the use of electrons in SEM (backscatter and secondary electron modes) this can analyse the bulk of the glass and is less affected by the fragments shape can measure smaller fragments and has a better detection limit - this is element dependent though
32
what is plasma emission spectroscopy
sample pumped into a plasma torch also known as ICP (inductively couple plasma) spark ionises argon gas and resultant ions gain energy from an induced magnetic field can achieve very high temps sample aspirated by a flow of gas
33
why is plasma emission spectroscopy good for the trace analysis of glass
higher temps reached so greater sensitivity - can be couple with mass spec more sensitive than AAS and AES background emission is low in the observed region no oxide formations = minimal chemical interference low risk of self absorption good detection limits multi element determination reproducible ionisation chance = high
34
what is two disadvantage of ICP analysis of glass how can this be overcome
sample prep can take a long time as sample is needed in a solution destructive overcome this issue is to do LDESI or MALDI mass spec instead as don't need sample in solution
35
What are two methods of sample preparation that can be used for glass analysis that speeds up the process
LIBS = laser induced breakdown LA = laser ablation laser hits and ionises sample very quickly - no need for solution = LA-ICP-MS
36
what is LA-ICP-MS
laser ablation - inductively coupled plasma - mass spectrometry allows fast elemental analysis of glass samples detection limits in ppb range very small amount of sample can be used
37
order these methods in how the provide discriminative value in the analysis of glass evidence ICP-MS, micro XRF with RI and RI alone
RI alone = very low value micro XRF and RI = 97.5% value ICP-MS = high value