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Physical & Chemical properties

Explosiveness

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Endpoint:
explosive properties of explosives
Type of information:
not specified
Adequacy of study:
other information
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
secondary literature
Remarks:
Data comes from a sheet with no reference to data sources, and therefore cannot be assigned as reliable.
Reason / purpose for cross-reference:
reference to same study
Principles of method if other than guideline:
No data.
Parameter:
other: Explosive under influence of flame
Remarks:
migrated information
Remarks on result:
positive (not further specified)
Parameter:
other: Explosive (not specified)
Remarks:
migrated information
Remarks on result:
positive (not further specified)
Remarks:
sunlight

May explode on heating, on exposure to sunlight or if subjected to shock or sparks.

Executive summary:

The ICSC provides information relating to explosive potential of the Chlorine dioxide, when heated, exposed to sunlight, or subjected to shock or sparks.

Endpoint:
explosive properties of explosives
Type of information:
not specified
Adequacy of study:
other information
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
secondary literature
Remarks:
The publication summarises observations from other references, but doesn't provide experimental details; therefore it cannot be assigned as reliable.
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to other study
Parameter:
other: Explosive (not specified)
Remarks:
migrated information
Remarks on result:
positive (not further specified)

Liquid ClO2 is extremely unstable and dangerously explosive. The slightest shock will initiate detonation and decomposition to chlorine and oxygen.

Gaseous ClO2 exhibits a very peculiar property, in that it "auto-decomposes", following an induction period. These properties have been studied extensively by many workers (ref.1,2,3,4,7,8). The induction period is related to the surface/volume ratio of the equipment, and the partial pressure of ClO2 and temperature. The force of the ensuing explosion is determined by ClO2 concentration, the presence of oxidisables, the location of the explosion, and the shape and size of the equipment containing it. (...) As the decomposition products are oxygen and chlorine, the ClO2 decomposition can initiate a second more powerful explosion if reducing agents such as methanol are present, or with standing flames, the decomposition can initiate thermite fires in metal equipment. In addition to these peculiarities, the mechanism of decomposition of chlorine dioxide is via a branched chain mechanism, so that not only is there no prior warning of an explosion, but the resulting burning velocity and detonation forces can be extremely high. It is postulated that ClO2 is the key intermediate in the burning of ammonium perchlorate (ref.5,6), and thus contributes to its high velocity and efficiency as a solid rocket fuel.

Interpretation of results:
explosive
Remarks:
Migrated information
Executive summary:

As an introduction to safety management in chlorine dioxide plants, this publication summarises observations from other references about explosive properties of the substance, in particular parameters that can influence the induction period, and the gravity of the consequences.

Endpoint:
explosive properties of explosives
Type of information:
not specified
Adequacy of study:
other information
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
secondary literature
Remarks:
Data comes from a handbook using secondary data sources, and therefore cannot be assigned as reliable. However, please note that it is a compilation of numerous information, and considered as a reference among literature on hazardous reactions
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to other study
Principles of method if other than guideline:
No data.
Parameter:
other: Explosive (not specified)
Remarks:
migrated information
Remarks on result:
positive (not further specified)

Chlorine dioxide is considerably endothermic (deltaH°f (g) +103.3 kJ/mol, 1.53 kJ/g) and of limited stability. It is a powerful oxidant and explodes violently on the slightest provocation as gas or liquid [1]. It is initiated by contact with several materials, on heating rapidly to 100°C or on sparking [2], or by impact as solid at -100°C [3]. A small sample exploded during vacuum distillation at below -50°C [4], and it was stated that decomposition by sparking begins to become hazardous at concentrations of 7–8% in air [3], and that at 10% concentration in air (0.1 bar partial pressure) explosion may occur from any source of initiation energy, such as sunlight, heat or electrostatic discharge [5]. A kinetic study of the decomposition shows that it is explosive above 45°C even in absence of light, and subject to long induction periods due to formation of intermediate dichlorine trioxide. UV irradiation greatly sensitises the dioxide to explosion [6]. The solid (a dimer) can be relatively safely handled below -40°C and the gas at pressures below 50 mbar [7]. A guide on fire and explosion hazards in industrial use of chlorine dioxide is available [8], and preparative precautions have been detailed [9]. An improved and safer method for continuous production of chlorine dioxide is claimed [10]. A thorough review has been written, detailing numerous incidents, of hazards attending industrial preparation and use of chlorine dioxide (now much used as a low chlorine bleach). Liquid ClO2 can separate from aqueous solutions >60 g/l, it is exceedingly shock sensitive. A partial pressure of 130 mbar in air is thought entirely safe, as are aqueous solutions (but not necessarily the head space above them) [11]. The safe use of chlorine dioxide and sodium chlorite has been reviewed [12].

Interpretation of results:
explosive
Remarks:
Migrated information
Executive summary:

The Bretherick's handbook compiles information on explosive potential of Chlorine dioxide, from twelve secondary references, showing evidence of high sensitivity.

Endpoint:
explosive properties of explosives
Type of information:
not specified
Adequacy of study:
other information
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
secondary literature
Remarks:
Data comes from reviews using secondary data sources, and therefore cannot be assigned as reliable.
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to other study
Principles of method if other than guideline:
No data.
Parameter:
other: Explosive under influence of flame
Remarks:
migrated information
Remarks on result:
positive (not further specified)
Parameter:
other: Explosive (not specified)
Remarks:
migrated information
Remarks on result:
positive (not further specified)
Remarks:
sunlight

Chlorine dioxide gas is explosive in concentrations in excess of 10% v/v at atmospheric pressure and will easily be detonated by sunlight or heat (Budavari et al., 1996).

It is marketed and transported as a stabilized aqueous solution generally less than 1% w/v (more concentrated forms are explosive).

Executive summary:

The international CICAD review and the OECD SIDS report provide information relating to explosive potential of the gas Chlorine dioxide, cited from the Merck Index, when heated or exposed to sunlight. Dilute aqueous solutions are stable (<1%w/v).

Endpoint:
explosive properties of explosives
Type of information:
experimental study
Adequacy of study:
other information
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
study well documented, meets generally accepted scientific principles, acceptable for assessment
Remarks:
This experimental study does not follow internationally recognised guidelines, and therefore cannot be fully reliable. It is nevertheless well documented, and acceptable under the test conditions.
Reason / purpose for cross-reference:
reference to same study
Principles of method if other than guideline:
A thermoregulated vessel, with pressure recording, is filled with chloride dioxide produced in-situ. Ignition is achieved with an AC electric arc.
Parameter:
other: Explosive (not specified)
Remarks:
migrated information
Remarks on result:
positive (not further specified)

The experiments and their results are summarized in the following tables, showing the dependence of tinit, and tPmax and f on the partial pressure of ClO2 and water.

Date

GA

Temp (°C)

Cooling

Water inj (µL)

Pressure (mbar) registered

Pressure (mbar) corrected

Ignition

Explosion times (ms)

Explosion pressures (mbar)

f

In

Surf

°C

PH2O (mbar)

ClO2

Air

H2O

Total

ClO2

Air

H2O

Total

(sec)

(J)

tinit

tPmax

Pmax

Pfinal

A

20.9

102

72.8

76.0

11

13

150

102

5

90

197

89

5

103

197

0.35

14

10

15

760

236

3.9

C

 

 

 

 

 

 

150

110

5

91

206

97

5

104

206

 

 

7

14

520

259

2.5

1

27.9

 

67.0

75.6

11

13

250

50

7

197

254

37

7

210

254

0.35

14

15

45

550

264

2.2

2

 

112

 

75.8

 

 

200

49

8

142

199

36

8

155

199

 

 

12

30

500

200

2.5

3

 

 

68.4

75.8

 

 

200

44

7

160

211

31

7

173

211

 

 

15

42

470

225

2.2

4

 

 

70.0

75.6

11

13

200

40

4

166

210

27

4

179

210

 

 

15

49

450

220

2.1

5

 

 

70.2

75.9

 

 

200

36

25

120

181

23

25

133

181

 

 

15

45

400

194

2.2

6

 

101

70.2

75.9

11

13

200

36

8

162

206

23

8

175

206

 

 

15

62

410

216

2.0

7

 

 

71.1

76.0

 

 

300

36

7

191

234

23

7

204

234

 

 

30

85

410

-

1.8

8

 

 

71.1

76.0

 

 

300

36

5

215

256

23

5

228

256

 

 

35

92

430

263

1.7

9

 

 

 

76.8

11

13

200

97

6

120

223

84

6

133

223

 

 

40

-

850

263

3.8

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

12

28.11

101

12

10

6

9

-

24

 

 

24

15

 

9

24

0.35

14

8

18

84

-

3.5

13

 

 

18

18

 

 

-

21

 

 

21

12

 

9

21

 

 

-

-

ca80

31

ca4

14

 

 

18

18

 

 

-

23

 

 

23

14

 

9

23

 

 

10

12

117

32

5.1

15

29.11

102

33

42

6

9

-

20

 

 

20

11

 

9

20

 

 

8

8

108

29

5.4

16

 

 

41

45

 

 

-

19

 

 

19

10

 

9

19

 

 

12

15

83

24

4.4

17

 

 

41

45

 

 

-

20

 

 

20

11

 

9

20

 

 

7

10

104

29

5.2

18

3.4

 

67.3

72.0

4

8

200

15

7

161

183

7

7

169

183

0.35

14

60

170

268

187

1.46

19

 

 

 

 

 

 

200

26

26

159

211

18

26

167

211

 

 

-

-

370

217

1.75

20

 

 

 

 

 

 

200

25

11

139

175

17

11

147

175

 

 

16

-

370

190

2.11

21

18.4

 

67.0

71.5

4

8

200

19

18

143

170

11

18

151

170

0.35

14

40

125

275

ca180

1.62

22

 

 

 

 

 

 

200

21

21

150

192

13

21

158

192

 

 

-

-

301

201

1.50

23

 

 

 

 

 

 

200

21

13

141

175

13

13

149

175

 

 

25

100

300

188

1.60

Decomposition of the ClO2 could not be avoided. Even with extremely low partial pressures (10 mbar and less), pressure increases of 50% (f ca 1.5) were registered. The pressure factor f rises with increasing partial pressure of ClO2. Time of initiation, tinit, and time for pressure increase tPmax, are strongly dependent on the ClO2 partial pressure. It can also be stated that water is a very good inhibitor for the decomposition, a fact which is also mentioned in the literature. It should be pointed out that experiments N°12-17 with only 9 mbar, all of which emerging from NaClO2 water solution, also were performed at lower temperatures and lower total pressures than the others.

As decomposition are taking place at partial pressures of ClO2 which are thought to be completely safe (based on literature), the equipment was controlled, the pressure transducers have been calibrated, no decomposition is registered on the oscilloscope with pure air in the explosion vessel. The conclusion has been that the ignition energy is too high. It is also well-known that an electric arc is producing a rather high amount of UV-light, which in the literature (McHale 1968, Crawford 1968) has been mentioned as a very potent decomposition source. According to the characteristics of the AC arc (see above), it is difficult to both calculate and regulate (decrease) the energy effectively. With an ignition time of 0.35 second, the nergy can be calculated to 2000 V x 20 mA x 0.35 sec = 14 J.

Executive summary:

Explosion trials with ClO2, conducted according to a non-standardised method, indicate that this gas is very sensitive to an (AC) electric arc as ignition source. Decomposition was recorded with only 10 mbar of ClO2 at a total of 170-180 mbar, the rest being mostly water vapour. This is far below what is normally said to be the lower explosion limit (ca 80 mbar). This was supposed to be due to the high energy and/or UV release of the ignition source.

The initiation period before explosion and the time to reach maximum pressure are longer, the lower the ClO2 pressure is. The pressure rise factor (Pmax/Pstart) decreases linearly with the ClO2 pressure. Water was confirmed to be a good inhibitor.

Endpoint:
explosive properties of explosives
Type of information:
not specified
Adequacy of study:
supporting study
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
secondary literature
Remarks:
Data comes from a book dedicated to chlorine dioxide, compiling very numerous literature references, but few experimental details are provided. Therefore it cannot be assigned as reliable.
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to other study
Principles of method if other than guideline:
No data.
Parameter:
other: Explosive (not specified)
Remarks on result:
positive (not further specified)

Aqueous ClO2

Aqueous ClO2 has no explosive properties.

Gaseous ClO2

The most commonly promoted characteristic of chlorine dioxide is that it is an explosive gas.

Much work has been done to investigate its explosive properties [Schumacher and Stieger 1930; Haller and Northgraves 1955; McHale and von Elbe 1967; Crawford and Dewitt 1968; McHale and von Elbe 1968; Gray and Ip 1972; Ip and gray 1972; Torregrossa et al. 1976; Paillard et al. 1986; Lopez et al. 1994]

When ClO2 is placed in a closed vessel, under some circumstances the gas can decompose energetically. The energy of the decomposition reaction increases with concentration of chlorine dioxide in the gaseous phase. Depending on a number of factors, there is an induction period where no temperature increase is noted, prior to explosive decomposition. Several factors influence the induction period. These include the surface/volume ratio of the container, the partial pressure of ClO2, and the temperature. The force of the ensuing decomposition is determined by the ClO2 concentration, the presence of oxidizable material, and the shape and size of the equipment containing the gaseous ClO2. The velocity of the decomposition wave is about 1 m/sec at 130 mm Hg pressure and about 3°C; at 207 mm Hg, the velocity of the wave is about 2 m/sec [Haller and Northgraves 1955]. As partial pressure increases, the violence of the reaction increases so that a detonation occurs at 300 mm Hg.

Uncontaminated gaseous ClO2 only explodes above a temperature of 88°C; below that temperature, only an exotherm is observed [Gilmont 1968]. Water has a strong inhibiting effect on the decomposition of gaseous ClO2 up to 90°C [Crawford and Dewitt 1968].

Due to its sensitivity to temperature, pressure and shock, it is impossible to store or ship as a pure liquid or a compressed gas.

Liquid ClO2

Above melting temperature (-59°C), ClO2 forms a red, unstable liquid which is very explosive at temperatures above -40°C. Liquid ClO2 will also separate from aqueous concentrated solutions (for example above 60 g/L at normal temperatures). Pure liquid ClO2 is sensitive to shock and light, and decomposes with about 1/3 of the force of TNT [Sattelberger et al. 2002].

Executive summary:

The Simpson's book, dedicated to chlorine dioxide, summarizes several studies on its explosive properties.

Gaseous ClO2 can decompose explosively as a function of temperature and pressure. The decomposition can be triggered by a spark. The induction time can be substantially decreased by the presence of impurities, which include gaseous organics, or oxidizable materials, which include rubber, cork, or sulfur. At a constant temperature, as the partial pressure of ClO2 increases, the violence of the reaction increases.

Aqueous ClO2 has no explosive properties.

Endpoint:
explosive properties of explosives
Data waiving:
study scientifically not necessary / other information available
Justification for data waiving:
other:
Justification for type of information:
In accordance with column 2 of REACh Annex VII, the study does not need to be conducted if, for mixtures of inorganic oxidising substances (UN Division 5.1) with organic materials, the concentration of the inorganic oxidising substance is less than 15% by mass, if assigned to UN Packaging Group I (high hasard) or II (medium hasard).
Note also that Simpson (2005) reports that aqueous ClO2 has no explosive properties.
Finally, no physical hazard is established in the harmonised entry and according the above observations. However, based on the potential hazard if off-gassing, the EUH018 phrase is proposed.
Endpoint:
explosiveness
Type of information:
not specified
Adequacy of study:
other information
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
secondary literature
Remarks:
Data comes from an online compilation using secondary data sources, and therefore cannot be assigned as reliable. However, please note that the endpoint is cited in the database as peer reviewed.
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to other study
Principles of method if other than guideline:
No data.
Parameter:
other: Explosive under influence of flame
Remarks:
migrated information
Remarks on result:
positive (not further specified)
Parameter:
other: Explosive (not specified)
Remarks:
migrated information
Remarks on result:
positive (not further specified)
Remarks:
sunlight

Explodes when heated or by reaction with organics. [1]

In concentrations in excess of 10%, 1 atm, easily detonated by sunlight, heat, contact with mercury or carbon monoxide. [2]

Explosive decomposition at 100 deg C. Explosive hazard by heating, exposing to sunlight, contacting mercury or carbon monoxide. [3]

Executive summary:

The HSDB database provides information, from several sources, relating to explosive potential of the substance Chlorine dioxide, when heated or exposed to sunlight.

Description of key information

Solution of chlorine dioxine generated in-situ at less than 2% in water (as registered): not considered to be explosive, but potential hazard if off-gassing.

Key value for chemical safety assessment

Explosiveness:
non explosive

Additional information

The properties of gaseous chlorine dioxide are discussed because, although the substance as registered is in-situ generated aqueous solution, under certain conditions off-gassing may occur. Thus, the properties of gaseous chlorine dioxide, as well as the properties of the aqueous solution are important.


An experimental, non-standard, study is available, as well as numerous literature data regarding explosive properties of chlorine dioxide gas and safe management. The gas is well-known to be sensitive to various sources of ignition (heat, light, shock, and in particular sparks), and is characterised by an induction period.


Water was shown to be a good inhibitor, and diluted aqueous solutions are considered to be stable. Partial pressure of ClO2 over the solution, and therefore potential hazard, is a function of concentration and temperature (please refer to points 4.6 and 4.13).

Justification for classification or non-classification

The gas has a Harmonised Classification as Oxidising, therefore it does not need to be classified in any other hazard class.

For chlorine dioxide in aqueous solution, no physical hazard is established in the harmonised entry. However, based on the potential hazard if off-gassing, the EUH018 phrase will be proposed.