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Fire Technology

, Volume 51, Issue 1, pp 19–40 | Cite as

Combustion Characteristics of Flat Panel Televisions With and Without Fire Retardants in the Casing

  • Matthew BlaisEmail author
  • Karen Carpenter
Open Access
Article
First Online:

Abstract

A series of flat panel television burns were performed with incrementally increasing ignition sources in a single burning item apparatus. A comparison study was performed of like model televisions for the United States, Mexican and Brazilian markets. Heat release rate, smoke, combustion gas, TO-15 vapor, and halo-dioxin and furan generation were measured. A total of 18 televisions were ignited and their burning behavior studied to examine the impact of materials of construction and the presence of fire retardants in the casing of the televisions on fire growth. US market televisions required more than 500 W with greater than 180 s exposure to ignite and in four out of the 6 trials these televisions did not achieve sustained ignition. In the two cases where sustained ignition for the US market televisions occurred, it was not the flat panel display television itself which ignited, but the stand and mounting bracket which lead to fire growth. Mexican and Brazilian market televisions ignited easily with 60 s exposure to a 50 W flame. US market televisions did produce brominated dioxins or furans but the mass loss of these televisions was much lower.

Keywords

Flat panel televisions SBI testing Smoke toxicity Calorimetry pHHR Dioxins and furans 

1 Introduction

Modern televisions have changed dramatically in design and materials of construction from those of just 15 years ago. Flat panel designs now dominate the marketplace. Large screen flat panel display televisions, ≥30 inches, represent the vast majority of televisions sold internationally. Previous studies on televisions studied consol type and or cathode ray tube (CRT) systems with smaller screens and different materials of construction [1, 2, 3]. However data on modern FPD televisions combustion as described here has not been previously published in peer reviewed journals. Because polymeric materials are used in modern FPD televisions, these devices can contribute to fires as either the first item ignited, either by internal or external sources, or by becoming a second item ignited and adding to the overall fuel load. International markets also have different requirements for resistance to fire with the United States having the strictest standards for ignitability [4]. The statistical analysis of Hall points to the V rating from UL94 standard fire testing for the television housing as a driver for the better performance of televisions in the US market as compared to their European counterparts [5]. For these reasons a study was performed using small flame, external ignition sources applied to televisions that were procured during 2013 in Brazil, Mexico and the United States. Matching sizes and models were used to do a comparison of the response to ignition. Flame spread, heat of combustion, smoke production and toxic constituents of smoke were all measured in this study [6].

Underwriters Laboratories, UL, has released a comparative video [7] that shows fire loading from furnishings in modern household living rooms has increased dramatically compared to legacy rooms from the 1970s. Kerber’s study also does an excellent job of describing the impact of fuel growth of modern materials in residential fire [8]. The high energy content of modern rooms can lead to flashover conditions in as little as three to 4 min as compared to 29 min to 30 min in the legacy room. The use of polymeric materials in our homes is a significant contributor to this increased fire load. Most polymers decompose to low molecular weight vaporous components during pyrolysis [9] which burn with a large amount of energy release leading to rapid fire growth. For this reason, many modern polymers incorporate fire retardants (FR) that inhibit ignition while not significantly altering the mechanical and physical properties of the material [10, 11, 12].

Incorporation of FR in the cabinets of televisions has sparked controversy because of claims of potential health hazards. The proponents of the health hazard claims are pushing for the removal of the external ignition testing requirements for materials used in the construction of these televisions [13, 14]. Further, these groups are pushing manufacturers to cease the use of plastics with FR and to design the televisions so that potential ignition sources within the television are contained with inherently fire safe construction. The wisdom of eliminating ignition resistant plastics is questionable given media reports and product recalls related to incidences of plasma and LCD television fires that have breached the casing of the television and caused loss of life and many thousands of dollars in damages to homes [15, 16, 17, 18, 19].

Fire protection works best when approached from a layered perspective. Use of sprinklers, smoke detectors and inherently fire safe furnishings all increase the probability of preventing or surviving fires and minimizing property damage [20]. Human behavior is the one variable that is hardest to control. Numerous fires have started by placing ignition sources such as candles or heaters next to readily ignitable items made of plastics. Among the reasons that some claim that external flame source testing is not required is based on the assumption that all flat panel television are hung on walls and there is not an opportunity to come in contact with external small ignition sources. This ignores the fact that many of these televisions are mounted on stands sitting on entertainment centers, credenzas, tables and even carpeted floors. This is especially prevalent in apartment complexes where modification of the walls may not be permitted and hotels.

In this study, 18 televisions of three different models of similar sizes and weights were ignited using progressively larger open flame ignition sources of 50 W and 500 W. Half of the televisions studied were manufactured for the US market and the remaining for the Brazilian and Mexican markets. Televisions were ignited in a single burning item (SBI) apparatus as described in EN 13823: 2010 appendix E and the heat release rate and smoke generation were measured. Mass loss as a result of combustion, combustion gas generation, in-door air pollutant and chlorinated—and brominated—dioxins and furans were also measured.

2 Experimental

2.1 Materials

The composition and performance of the test items used in this study are summarized in Table 1. The polymer composition of the back case remained the same for the same model of televisions from the different markets excluding FR addition. Analysis of components was performed by Schoeniger Combustion (SC), Fourier Transform Infra-Red spectroscopy (FTIR), X-ray Fluorescence (XRF) and Inductively Coupled Plasma (ICP). Sections of the back casing were tested in accordance with UL-94 and the results are also reported in the table. FR-245 is tris(tribromophenoxy) triazine and FR8010 is Ethane—1,2-bis(pentabromophenyl). Analysis was performed by Mr. Brett Wallet of Albemarle, Baton Rouge, LA.
Table 1

Sample Television Composition and Characterization

TV Brand—Manu. Country

Television 1—Brazil (1B)

Television 2—Brazil (2B)

Television—Mexico (3M)

Television 1—U.S. (1US)

Television 2—U.S. (2US)

Televion 3—U.S. (3US)

SC

 Br (ppm)

612

235

1460

9.04 wt%

9.67 wt%

9.20 wt%

FTIR

 Polymer

HIPS

ABS

HIPS

HIPS

ABS

HIPS

 FR content

No FR

No FR

No FR

FR-245 (major); 8010 (minor)

FR-245

FR-245 (major); 8010 (minor)

XRF

 Br (ppm)

–

–

808

10.08 wt%

  

 Sb (ppm)

–

–

77

2.33 wt%

  

ICP

 Sb (ppm)

<11

<8.5

<260

2.39 wt%

1.67 wt%

1.97 wt%

UL-94

Fail

Fail

Fail

V-1

Fail

V-1

All televisions were mounted on the manufacturer supplied stands. Items 2B and 2US had identical bases with methyl methacrylate (MMA) and acrylonitrile–butadiene–styrene (ABS) with halogen free phosphate and aromatic brominated compounds added but were not fire test rated. The bases for 3M and 3US televisions were composed of MMA ABS containing halogen free phosphate and aromatic brominated compounds but were not fire test rated. The stand for 1US had a UL 94 V0 rated high impact polystyrene (HIPS) cover while the 1B stand cover did not have a fire rating but was also composed of HIPS.

2.2 SBI Apparatus Tests

A standard SBI test apparatus as described in EN 13823 appendix E was used for all television burns. Figure 1 shows a schematic drawing of the SBI test apparatus as used with the location of the television indicated in the drawing. Smoke density was measured via opacity in the exhaust duct. Heat release was measured as a function of oxygen consumption and carbon monoxide and carbon dioxide production. The sampling rate for the data acquisition system was 1 Hz.
Figure 1

SBI test apparatus schematic

2.3 Gas Sampling and Analysis System

An isokinetic sampling probe was positioned centroid to the SBI exhaust duct. A heated sample transfer line was attached to the duct probe. An EPA Method 23A sample train was attached to the heated line and the system was used to analyze for chlorinated and brominated dioxins and furans. Dioxin and furan analysis was performed by high resolution gas chromatography and high resolution mass spectrometry based on EPA Method 8290. A Summa Canister™ was also attached to sample for EPA method TO-15 to measure 98 standard volatile organic indoor pollutants as well as tentatively identified compounds via mass spectroscopy. The sample line was also attached to a Thermo Fischer Nicolet 6700 FTIR equipped with a 2-m gas cell, potassium bromide windows and gold reflectors to perform analysis of combustion gases in based on a partial least squares calibration of nine combustion gasses with a detection limit of 5 ppm or less. Sample gases were drawn through the gas cell at constant pressure of 756 mm Hg and a flow of approximately 1.5 SLPM which resulted in a concentration rise time of less than 30 s as verified during calibration.

Plastic composition and FR content determination was performed by an external laboratory and is reported in the sample description of the materials section.

3 Procedures

One of each type of television mounted on the manufacturers supplied stand was put through progressively increasing ignition source intensity and duration. The ignition source was applied to the back, bottom edge of each television. A summary of the individual tests is presented in the results section. The initial ignition source was a 12 mm needle flame which is equivalent to a small candle flame as described in IEC 60695-11-5. Exposure times of 60 s and 180 s were used to try and achieve sustained ignition. The next progressive ignition source was a 50 W, 20 mm flame as described in UL 94 section 8 applied twice for 10 s intervals, then 60 s, and 180 s, The largest ignition source applied was a 500 W, 125 mm flame as described by UL 94 section 9. Successive exposures of 2 at 10 s, then 60 s and 180 s were used until sustained ignition was achieved. The data obtained from the progressive ignition source test determined the ignition sequence for the follow-on tests of the same item type. Subsequent tests used the largest ignition source with the longest duration condition required to ignite the test items of like manufacture. The data was also used to determine the collection time for the Summa™ canisters. Canisters were collected at pHRR and peak smoke generation times to determine EPA TO-15 indoor air pollutants concentrations. In the second and third tests for each television type, sampling was performed for dioxins and furans over the duration of the entire test.

4 Results

In the progressive ignition portion of the testing for test #1, the Brazilian market television 1B ignited with a 60 s exposure to the needle burner. The fire produced sooty black smoke with the first flaming drops occurring at 24 s. The television stand collapsed at 316 s with a resulting rapid increase in heat release as seen in Figure 2. The flame propagation covered the entire back surface of the television as well as the front screen and the interior components.
Figure 2

Heat release for Test 1 Television 1B

In test #2, the Mexican market television 3M was ignited with a 60 s exposure to the needle burner. The first burning droplets fell onto the stand with the result of the stand also catching fire at 102 s. The fire produced black sooty smoke with the stand collapsing at 510 s. Figure 3 shows the heat release rate for this test.
Figure 3

Heat release for Test #2, Mexican Market M3

In test #3 a 32 inch Brazilian market television 2B was ignited after exposure to the needle burner for 60 s. The first flaming droplets were noted at 111 s resulting in the stand catching fire and collapsing at 320 s. Figure 4 shows the heat release rate for test #3. The rapid increase in energy release corresponds to the base catching fire. The first flaming drips were seen between 5 min and 6 min with the subsequent rapid increase corresponds to the collapse of the TV stand.
Figure 4

Test #3 Brazilian Market television 2B, 32″ heat release rate

In test #4 the first of the US market television 1US was subjected to the needle burner for 60 s with the result of a guttering flame that extinguishes at 87 s. The needle burner was then applied for 180 s with flames extinguishing at 192 s. A 50 W flame source was then applied to the television for 2 s to 10 s intervals, a 60 s interval and a 180 s interval all with no ignition. The 500 W flame was then applied to a previously burned area for 60 s without result followed by an additional 180 s which breached the casing and resulted in a very slow fire with a peak heat release rate of 5 kW and very little overall mass loss for the television. Figure 5 shows the heat release rate for this test with the Y axis scale expanded to show more detail.
Figure 5

Test #4, US market television 1US

In test #5, a US market television 3US was also subjected to the progressive ignition regime with very similar results as obtained in Test # 4. The needle burner was applied for 60 s with the result of a guttering flame that extinguishes at 96 s. Flaming drops were noted at 81 s that extinguished on impact with the floor. The needle burner was then applied for 180 s with flames extinguishing upon removal of the burner. The casing material melted during this process and retreated from the flame. A 50 W flame source was then applied to a different area of the television for 2 s to 10 s intervals, a 60 s interval and a 180 s interval all with no ignition. The 500 W flame was then applied to a previously burned area for 60 s without result followed by an additional 180 s but melting drops extinguished the burner at 105 s. The Burner was relit and the exposure continued for the remaining time. At 150 s into the exposure flaming drops were produced. A 180 s exposure was then performed on a previously tested part of the surface which produced a breach in the case and produced a slow fire that produced flaming drops. The fire self extinguished at 14 min 30 s. A pHRR of 2 kW was obtained as shown in Figure 6.
Figure 6

Test #5 Heat Release rate US Market television 3US

The last of the progressive ignition tests was planned to be test #6 however the ignition source was applied to the stand mounting bracket instead of the television case. The stands were determined to be a different material and were not UL-94 fire test rated. Test #17 using US market television 2US was the final progressive ignition experiment and was determined to be very similar to test 4 and 5. The television was subjected to the needle flame for 60 s with the result of immediately extinguishment on removal of ignition source. The needle flame was then applied for 180 s with flames extinguishing at 180 s. A 50 W flame source was then applied to the television for 60 s with the flame extinguishing in 62 s. It was then was then applied for 180 s with flames extinguishing at 180 s. The 500 W flame ignition source was then applied for 10 s without ignition followed by a 60 s exposure which breached the casing and resulted in a very slow fire over a period of 46 min with a peak heat release rate of 110 kW. Figure 7 shows the heat release rate for test #17.
Figure 7

Test #17, Heat release for US market television 2US

In all subsequent tests, a 500 W ignition source was applied for 180 s to the back of each television. A total of two of each type of television was challenged under this technique. In all of the non-US market televisions this resulted in higher peak heat release rates in much shorter times. Comparing the 1B and 1US television, same model, gives the greatest contrast as shown in Figures 8 and 9. The Brazilian version reaches 295 kW in as little as 365 s while US versions fails to achieve sustained ignition. It is important to note that the red line in Figure 8, test 1, represents ignition with a needle flame while tests 7 and 8 used the 500 W burner. The minor differences in the tests 7 and 8 are more a function of the normal variability in flame spread on the surface.
Figure 8

Combined Heat Release Rate Plots for 3 Brazilian Market Model 1B Televisions

Figure 9

Combined Heat Release Rate Plots for 3 US Market Model 1US Televisions

The 3M and 3US televisions show the same trend but not as dramatically and there is more variability in the performance for both the US and Mexican market televisions as shown in Figures 10 and 11. This is primarily due to the design and composition of the television stands of this model. None of the stands were rated for fire and were significantly involved in the early stages of the fire in tests 9 (2 min), 10 (2 min), 15 (3 min) and 16 (4 min). The major difference between tests 15 and 16 is that the front face of the television becomes involved in the fire early in test 16 and not at all in test 15. In test 5 the stand was not involved in the fire and this television failed to achieve sustained ignition and test number 2 used the smaller, needle flame ignition source.
Figure 10

Combined Heat Release Rate Plots for 3 Mexican Market Model 3M Televisions

Figure 11

Combined Heat Release Rate Plots for 3 US Market Model 3US Televisions

The 2B and 2US televisions were smaller in size than the other televisions tested in this program being a 32 inch model however the mass of plastics in the rear casing was actually higher than the 40 inch models. All of the tests for the 2B and 2US televisions can be found in Figures 12 and 13. The Brazilian televisions burned faster and with greater peak heat release rate than those comparable to the US market using the same ignition source. Test 3 and 6 were ignited with the needle flame. In test 6, the needle flame came in direct contact with the stand which ignited and resulted in near complete combustion of the television. It did require an extended time to achieve a rapid combustion, approximately 10 min. In the 500 W ignition source fires the non-FR televisions reached pHRR of near 280 kW at between 3 and 6 min. In test 17, the stand for the television was not involved in the fire, by selective location of the ignition source, and this television required approximately 30 min to achieve free burning with a steep rise in heat release rate as shown in Figure 13.
Figure 12

Combined Heat Release Rate Plots for 3 Brazilian Market model 2B televisions

Figure 13

Combined Heat Release Rate for 3 US Market model 2US televisions

The summary of the heat release and smoke generation data is presented in Table 2. Events with multiple ignition attempts have an asterisk adjacent to pHRR time. Comparing the non-FR television from Brazil and Mexico to the US market televisions shows that the non-FR televisions were easily ignited on their back cases with a small candle flame and that they reach their pHRR in between 6.67 and 13 min. The US market television required much larger ignition sources of longer duration to achieve ignition. Using the larger ignition source on the Brazilian and Mexican television to provide a direct comparison of identical conditions to the US televisions shows that the pHRR for the Brazilian and Mexican televisions nearly doubles and/or the time required to reach pHRR decreased significantly. For Tests 7 through 16 and test 18, all performed under identical condition, the US market televisions either failed to sustain ignition or burned very slowly. All of the US market televisions were proven to be compliant with UL 60065 except the 2US televisions which were a marginal fail.
Table 2

SBI Heat Release and Smoke Data for All Tests

Test number

Test item

Final ignition source and duration

pHRR (kW)

Time to pHRR (s)

Total heat released (MJ)

Max smoke release rate (m2/s)

Time to max smoke (s)

Mass loss (kg)

1

1B

50 W

154

653

98

5.10

653

6.12

60 s

2

3M

50 W

164

764

81

3.89

764

3.63

60 s

3

2B

50 W

182

403

73

4.55

421

3.49

60 s

4

1USa

500 W

5

748a

3

0.36

280

0.14

180 s

5

3USa

500 W

2

105a

1

0.26

112

0.05

180 s

6

2US

50 W

172

795

69

7.84

846

3.81

60 s

7

1B

500 W

261

439

75

10.15

420

4.26

180 s

8

1B

500 W

295

365

74

7.89

421

6.12

180 s

9

3M

500 W

306

442

87

10.80

447

4.58

180 s

10

3M

500 W

168

553

84

4.73

404

4.26

180 s

11

2B

500 W

282

339

77

7.44

363

3.81

180 s

12

2B

500 W

271

348

78

7.30

311

3.81

180 s

13

1US

500 W

2

413

0

0.23

530

0.64

180 s

14

1US

500 W

0.9

30

0

0.16

2,083

0.14

180 s

15

3US

500 W

92

1,354

56

6.23

1,327

4.17

180 s

16

3US

500 W

138

843

81

19.15

604

4.35

180 s

17

2USa

500 W

110

2,224a

41

7.01

2,172

2.99

60 s

18

2US

500 W

91

560

45

6.4

856

3.08

180 s

aMultiple ignition events

The US market televisions did produce more brominated dioxins and furans than the ones produced for Mexico or Brazil. Table 3 presents the data obtained for tests 7–18 for brominated dibenzo dioxins and furans (BDD and BDF). The total mass of BDD and BDF was calculated by multiplying the found total mass in the collectors by the dilution factor of the duct being sampled. The flow in the duct was 0.60 m3/s and the sampler flow was 1.38 × 10−4 m3/s giving a dilution factor of 4320. The numbers obtained for the US Market televisions are rational based on the structures of the FRs normally used in HIPS and ABS plastics [21]. In addition, the samples collected in each trial were also analyzed for chloro dioxins and furans. OCDD, 3268-87-9, was detected at just above background levels in all of the TVs except those made for the Mexican market. Also, 1,2,3,4,6,7,8,-HpCDD was detected at near background levels in Test #8 and #16.
Table 3

Brominated Dioxin and Furan Data for All Tests

Test no.

Test item

1,2,3,4,6,7,8 HpBDD 110999-47-8 (□g)

2,3,4,7,8 PeBDF 131166-92-2 (□g)

1,2,3,4,7,8 HxBDF 129880-08-6 (□g)

1,2,3,4,6,7,8 HpBDF 107555-95-3 (□g)

OBDF 103582-29-2 (□g)

7

1B

0.144

1.85

5.01

9.03

4.54

8

1B

0.109

0.408

0.346

1.24

0.570

9

3M

–

0.229

0.242

0.886

0.693

10

3M

0.527

26.4

27.2

74.7

35.4

11

2B

–

0.161

0.0786

0.264

0.171

12

2B

–

0.134

0.0683

0.292

0.127

13

1US

–

5.92

87.7

337

246

14

1US

–

0.475

1.35

4.58

2.87

15

3US

56.2

1,000

1,980

3,720

2,590

16

3US

6.91

782

1,550

2,740

1,670

17

2US

–

1.24

1.25

5.18

3.09

18

2US

–

0.626

0.566

1.74

0.842

Test no.

Test item

2,3,7,8 TeBDD 50585-41-6 (□g)

1,2,3,7,8 PeBDD 109333-34-8 (□g)

1,2,3,4,7,8 & 1,2,3,6,7,8 HxBDD 110999-44-5 & -45-6 (□g)

1,2,3,7,8,9 HxBDD 110999-46-7 (□g)

OBDD 2107-45-8 (□g)

7

1B

–

–

–

–

–

8

1B

–

–

–

–

–

9

3M

–

–

–

–

–

10

3M

–

–

0.158

–

0.449

11

2B

–

–

–

–

–

12

2B

–

–

–

–

–

13

1US

–

–

0.137

–

0.821

14

1US

–

–

–

–

–

15

3US

–

21.8

3.91

2.79

20.2

16

3US

–

17.8

2.74

1.50

7.30

17

2US

–

–

–

–

–

18

2US

–

–

–

–

–

Combustion gases were also analyzed for the gases listed in ASTM E-800 for tests 7–18. The data indicates that all of the gases of concern were below detection limit except carbon monoxide (CO) and carbon dioxide (CO2). The CO concentration exceeds 1,000 ppm for five out of six of the television for the non-US markets and 2 of those exceed the IDLH value, 1,500 ppm. Only one of the six US televisions exceeded the 1,000 ppm and it did not exceed the IDLH value; the stand was a major contributor to the fire growth in this test. Table 4 presents the data on the peak concentration of the combustion gases for this series of tests.
Table 4

Combustion Gas Analysis for Tests 7–18

Test number

Test item

CO (ppm)

CO2 (ppm)

7

1B

1,100

20,000

8

1B

1,690

21,900

9

3M

1,730

21,800

10

3M

949

15,800

11

2B

1,150

19,500

12

2B

1,200

20,300

13

1US

30

108

14

1US

22

61

15

3US

292

2,980

16

3US

1,490

14,500

17

2US

26

1,170

18

2US

856

8,390

Each test also had two intervals where Summa™ canisters were collected to determine other toxic indoor pollutants that were produced during combustion. The first value listed in Table 5 and Table 6 for each test represents the time of the pHRR and the second was collected at peak smoke. For situations where the pHRR and the peak smoke were concurrent, samples were collected in sequence without a time gap.
Table 5

TO-15 Indoor Air Pollutants

Test no.

Propene (ppb)

Bromo methane (ppb)

1,3-Butadiene (ppb)

Acrolein (ppb)

Dichloro-methane (ppb)

Vinyl acetate (ppb)

Benzene (ppb)

#7-1

909

130

177

672

39.7

56

6,750

#7-2

3,890

1,010

491

3,340

 

199

41,900

#8-1

3,740

251

654

1,750

454

 

9,900

#8-2

6,820

525

1,850

2,260

516

249

35,800

#9-1

810

93

693

351

213

 

5,990

#9-2

4,540

265

1,530

3,240

175

648

39,800

#10-1

378

51

298

125

84

20

2,770

#10-2

1,210

155

478

461

  

13,400

#11-1

604

 

89

427

44

40

3,490

#11-2

2,110

288

 

1,450

 

224

19,200

#12-1

961

50

 

732

519

52

7,600

#12-2

1,690

206

 

1,400

428

307

15,700

#13-1

27

 

16

 

826

 

115

#13-2

233

100

119

39

443

 

988

#14-1

36

   

202

 

93

#14-2

44

   

183

 

157

#15-1

33

   

194

 

390

#15-2

484

 

416

145

219

 

3,980

#16-1

105

 

97

 

154

 

716

#16-2

3,010

563

1,350

498

136

 

12,100

#17-1

374

32

279

 

154

 

1,350

#17-2

176

48

127

42

68

 

657

#18-1

2,060

440

782

321

656

 

9,600

#18-2

1,980

841

329

544

 

142

18,000

Test No.

Methyl-methacrylate (ppb)

Toluene (ppb)

Ethyl-benzene (ppb)

Styrene (ppb)

Chloro-methane (ppb)

Naphthalene (ppb)

#7-1

120

1,550

155

2,830

82

1,680

#7-2

 

3,710

462

1,650

726

13,300

#8-1

250

1,120

380

664

353

2,880

#8-2

470

3,410

1,300

1,560

558

14,200

#9-1

24

1,630

204

6,810

 

1,440

#9-2

 

4,920

430

3,710

1,080

11,700

#10-1

17

920

132

4,250

 

384

#10-2

 

2,060

196

2,180

293

4,060

#11-1

144

916

121

1,360

18

562

#11-2

 

2,160

191

486

604

5,380

#12-1

163

1,790

175

672

130

1,050

#12-2

 

1,890

141

845

829

5,120

#13-1

 

92

25

533

 

39

#13-2

 

456

96

2,200

 

284

#14-1

 

134

36

498

  

#14-2

 

146

27

645

 

36

#15-1

 

265

79

1,380

 

157

#15-2

 

1,120

572

1,550

 

901

#16-1

 

451

128

2,110

 

116

#16-2

 

3,150

1,500

3,790

 

1,450

#17-1

 

1,290

343

4,230

 

178

#17-2

 

514

143

1,890

 

281

#18-1

934

2,630

811

2,370

 

3,550

#18-2

546

3,520

286

1,390

129

7,280

Table 6

Tentatively Identified Compounds

Test number

2-Propenenitrile (ppb)

Benzaldehyde (ppb)

Benzonitrile (ppb)

Benzofuran (ppb)

Phenylethyne (ppb)

Indene (ppb)

Alpha methylstyrene (ppb)

#7-1

 

931

126

120

 

74

 

#7-2

 

3,910

 

644

   

#8-1

 

1,560

  

923

  

#8-2

 

3,960

 

715

 

992

 

#9-1

 

199

   

366

194

#9-2

 

2,860

 

628

 

2,260

446

#10-1

 

126

 

55

 

274

214

#10-2

 

1,170

  

1,540

778

219

#11-1

622

652

153

44

   

#11-2

2,160

 

686

 

1,570

  

#12-1

1,000

755

199

54

   

#12-2

1,270

1,210

604

 

1,070

  

#13-1

      

23

#13-2

    

138

 

86

#14-1

    

14

 

20

#14-2

      

27

#15-1

    

89

 

49

#15-2

    

732

217

487

#16-1

    

121

 

92

#16-2

 

567

  

1,800

 

731

#17-1

457

   

202

53

207

#17-2

233

 

39

 

137

54

148

#18-1

2,390

876

527

 

2,060

361

535

#18-2

2,670

2,380

1,080

 

2,760

  

The TO-15 gases and the TICs shown in Tables 5 and 6 respectively were dependent on the materials of composition of the plastic case and possibly interior components of the televisions. Many of the monomers like styrene and butadiene are present in fairly high concentration in the smoke. The faster the plastics burned the more products of incomplete combustion were produced. Bromomethane was produced in roughly the same amounts whether or not the case contained brominated FRs. The Brazilian and Mexican market televisions produced significantly greater concentrations of acrolein in most cases.

5 Conclusions

For the televisions tested in this study, US market televisions contain significantly greater amounts of bromine and antimony in the plastics comprising the cases than corresponding televisions purchased in Mexico or Brazil indicating the US televisions were designed to be resistant to external ignition. This design characteristic was confirmed as US market televisions also showed much greater resistance to ignition of the casing to an external open flame. It required more than ten times the energy with extended exposure to cause these televisions to ignite and in four out of the six trials the televisions did not achieve sustained ignition. In the two cases where sustained ignition for the US market televisions occurred, it was not the FPD television itself which ignited, but the stand and mounting bracket leading to fire growth. The stands ignited early and provided a larger ignition source for an extended period resulting in the larger fire. These televisions had cases that were resistant to a candle sized flame ignition. Even with the ignition of these televisions the fire growth was slower and had lower pHRR than the Mexican and Brazilian market televisions. The television of the 2US design did not pass the UL-94 test but did contain 9.7% tris(tribromophenoxy) triazine and 1.67% antimony which delayed combustion compared to the 2B models. The 2B model did not contain detectable levels of antimony or bromine.

Under more severe ignition conditions the television cases protected with FRs can be ignited but tended to burn more slowly with lower pHRR release than unprotected (non-FR) cases. Not surprising, once forced to ignite, the brominated FR containing cases produced significantly greater amounts of BDD and BDF than did the corresponding non-FR FPD televisions. The levels detected for these chemicals is of the same magnitude as those detected by Blomqvist et al. [22]. This same reference compares the toxicity of the larger production of poly aromatic hydrocarbons produced in fast burning, non-flame retardant styrenic plastics, to the halo-dioxin and furans production. The trade off of BDD and BDF for PAH does not result in a decrease in overall toxicity. All of the FPD televisions which burned generated smoke and combustion products which are always toxic. This reinforces the fact that it is important to minimize the amount of combustion products generated by improving fire performance. This is particularly relevant to the practice of open pit burning of waste E&E, where extensive emissions of smoke and combustion products result. It is, therefore recommended that open pit burning of waste E&E products be prohibited.

Combustion gases for the faster burning televisions contain more carbon monoxide, acrolein, and benzene than the slower burning US market televisions. The greater the mass of FPD television consumed in fire the higher the production of these toxic chemicals. Also detected were the monomers and their degradents of the plastics used in the manufacture of the FPD televisions. As seen in test# 13 and 14 where ignition was suppressed, only small amounts of toxic chemicals were produced to include BDD and BDF, see Tables 3, 4, 5 and 6.

One very important and unexpected finding was uncovered during this study. The stands sold with US Market televisions in this study were not resistant to a needle flame ignition source and had not been listed as meeting UL-94 V0. This applies to all components of the stand including the mounting bracket for the television which is in direct contact with the television case. As noted in the results section, once the stand was ignited the fire was sufficiently intense and of long enough duration to cause US Market televisions to ignite and be consumed. It is recommended that the ignition resistance requirement in applicable standards for the case be extended to the accessories attached to the television especially wall mounting brackets and table stands.

The 5 min to 10 min of HRR above 100 kW is more than sufficient to ignite nearby combustible materials from direct flame impingement (piloted ignition) and radiant pyrolysis and could lead to rapid fire growth in a structure fire. This was noted in all of the non-FR FPD televisions tested while only two of the nine FR televisions tested in this program achieved this level of HRR. The two FR FPD televisions that produced HRR at this level involved the non-FR stands. In addition, burning droplets were noted in several cases where pool fires resulted under the televisions and this could also lead to rapid fire growth where other combustible materials are present in the cabinets, tables, stands or carpets where the televisions may be located.

The televisions tested in this program were all in the 32 inch to 40 inch range. These are relatively small for today’s market where 50 inch and 60 inch models are relatively common. The increased mass of plastics in the larger cases and the larger surface areas would result in larger total heat content as well as increased pHRR. Therefore, the values presented here are on the low end for expected values found in modern homes.

Notes

Acknowledgments

This work was funded by the North American Fire Retardant Association and the American Chemistry Council.

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Copyright information

© The Author(s) 2014

Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.

Authors and Affiliations

  1. 1.Fire Technology DepartmentSouthwest Research InstituteSan AntonioUSA
  2. 2.Fire Technology DepartmentSouthwest Research InstituteSan AntonioUSA

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