基本信息
- 标准SMILES
[O][Cl+][O-]- InChIKey
OSVXSBDYLRYLIG-UHFFFAOYSA-N- 分子式
- ClO2
- 平均分子量
- 67.45 g/mol
- 单同位素质量
- 66.95868192
概述
Chlorine dioxide is a yellow to reddish-yellow manufactured gas. It does not occur naturally in the environment. When added to water, chlorine dioxide forms chlorite ion, which is also a very reactive chemical. Chlorine dioxide is used as a bleaching agent at paper manufacturing plants, and in public water treatment facilities to make water safe to drink. In 2001, chlorine dioxide and chlorite were used to decontaminate a number of public buildings following the release of anthrax spores in the United States.
名称与标识
- 首选名称
- Chlorine Dioxide
- IUPAC
- Chlorosyloxidanyl
- 中文名
- 二氧化氯
- 英文名
- Chlorine dioxide
- 分子式
- ClO2
- 分子量
- 67.45
名称与别名
展开更多名称
数据库标识
- CAS
10049-04-4- PubChem CID
- 24870
- DTXSID
DTXSID5023958- ChEMBL
CHEMBL4297725- ChEBI
CHEBI:29415- EC Number
- 233-162-8
- Nikkaji
- J342.197J
性质
结构计算性质
- XLogP
- 1.4
- 极性表面积
- 18.1 Ų
- 氢键供体
- 0
- 氢键受体
- 1
- 可旋转键
- 0
- 重原子
- 3
- 形式电荷
- 0
- 复杂度
- 7.5
实验与物化性质
Chemical Classes
Toxic Gases & Vapors -> Oxidizers
Flammable agents - 4th degree
Pesticides
Pesticide -> EPA IRIS
Fungicides
Active substance -> EU Pesticides database: Not approved
Density
1.6 (Liquid at 32 °F) (NIOSH, 2024) - Denser than water; will sink
1.77 g/cu cm
Density: 1.642 at 0 °C (liq)
Relative density (water = 1): 1.6 (liquid, 0 °C)
1.6 (liquid at 32 °F)
3.09 @ 11°C
Color/Form
Yellowish-brown gas
Yellow to reddish-yellow gas at room temperature
Solid chlorine dioxide is a yellowish-red crystalline mass; liquid is reddish-brown
Yellow to red gas or a red-brown liquid (below 52 degrees F) ...
For more Color/Form (Complete) data for Chlorine dioxide (6 total), please visit the HSDB record page.
Solubility
0.3 % at 77 °F (NIOSH, 2024)
In water, 3.01 g/L at 25 °C and 34.5 mm Hg
2000 cc (gas) in 100 cc cold water
In water, 1.823X10-2 at 298.15 K
Soluble in water
Soluble in alkaline and sulfuric acid solutions
Boiling Point
52 °F at 760 mmHg (NIOSH, 2024)
11 °C
11 °C
52 °F
11 °C @760 [mm Hg]
52 °F
Decomposition
When heated to decomposition it emits toxic fumes of /chloride/.
Decomposition by sparking begins to become hazardous at concentrations of 7-8% in air.
The major chlorine dioxide /disinfectant by-products/ (DBPs) include chlorite (ClO2 -) and chlorate ions, with no direct formation of organohalogen DBPs. Unlike the other disinfectants, the major chlorine dioxide DBPs are derived from decomposition of the disinfectant as opposed to reaction with precursors.
物理化学性质
- 熔点
- -59 °C · -59°C
- 沸点
- 11 °C · 11°C
- 密度
- 3.09 g/L · 3.09g/L
- 蒸气压
- 0 · 0-22900Pa at 20-25℃
- 溶解度
- 2 O · slightly soluble in H2O
- 形态
- orange-green gas
- 颜色
- orange-green
- 水溶解性
- Soluble ºC
- 比热容
- 0.62 J/ · Cp(gas): 0.62 J/(g·K), at 25℃
- Henry's Law Constant
- 1 · 1.0×10-2 mol/(m3Pa) at 25℃, Burkholder et al. (2019)
- 介电常数
- 1.7 · 1.7(77.0℃)
- 暴露限值
- 0.1 ppm · ACGIH:TLV-CEILING 0.1 ppm (0.28 mg/m3)OSHA:PEL-TWA 0.1 ppm (0.3 mg/m3)NIOSH:REL-TWA 0.1 ppm; REL-STEL 0.3 ppm
- 稳定性
- May decompose explosively on shock, friction or concussion, or on heating rapidly. Strong oxidant - reacts violently with combustible and reducing materials, and with mercury, ammonia, sulphur and many organic compounds.
- 化妆品成分功效
- ANTIMICROBIALDEODORANT
- LogP
- -3.22 · -3.22--2.9 at 20℃
- CAS 数据库
- 10049 · 10049-04-4(CAS DataBase Reference)
- NIST化学物质信息
- Chlorine dioxide(10049-04-4)
- EPA化学物质信息
- Chlorine dioxide (10049-04-4)
化学性质
黄绿色或黄红色气味。有类似氯气和硝酸的特殊刺激臭味。液体为红褐色,固体为橙红色。 易溶于水,溶于碱溶液、硫酸。
安全与法规
GHS分类
GHS Classification
Danger
H270: May cause or intensify fire; oxidizer [Danger Oxidizing gases]
P220, P244, P260, P264, P271, P273, P280, P284, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P320, P321, P363, P370+P376, P391, P403, P403+P233, P405, and P501 (click each P-code to see the statement)
Danger
H301: Toxic if swallowed [Danger Acute toxicity, oral]
P260, P264, P270, P273, P280, P301+P316, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P321, P330, P363, P391, P405, and P501 (click each P-code to see the statement)
危害信息
Regulatory Information
Chemical: Chlorine oxide, (ClO2)
Hazard Traits - Neurotoxicity; Respiratory Toxicity
Regulation (EC) No 1331/2008
Chlorine oxide (ClO2) is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Chlorine oxide (ClO2) are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)
Status: Active Update: 15-05-2023 https://echa.europa.eu/registration-dossier/-/registered-dossier/15450
Chlorine dioxide: Does not have an individual approval but may be used as a component in a product covered by a group standard. It is not approved for use as a chemical in its own right.
Fire Hazards
Excerpt from ERG Guide 143 [Oxidizers (Unstable)]:
Not combustible but enhances combustion of other substances. Many reactions may cause fire or explosion. Risk of fire and explosion. See Chemical Dangers.
Hazards Summary
Chlorine dioxide is a yellow to reddish-yellow manufactured gas. It does not occur naturally in the environment. When added to water, chlorine dioxide forms chlorite ion, which is also a very reactive chemical. Chlorine dioxide is used as a bleaching agent at paper manufacturing plants, and in public water treatment facilities to make water safe to drink. In 2001, chlorine dioxide and chlorite were used to decontaminate a number of public buildings following the release of anthrax spores in the United States.
Corrosive--can cause serious skin burns; [ICSC] Rats exposed to 0.1 ppm for 5 hours/day for 45 days had no adverse effects while exposures to 2.5 ppm for 7 hours/day for 30 days caused severe lung inflammation; [ACGIH]
FDA Requirements
Chlorine dioxide (CAS Reg. No. 10049-04-4) may be safely used in food in accordance with the following prescribed conditions: (a)(1) The additive is generated by one of the following methods: (i) Treating an aqueous solution of sodium chlorite with either chlorine gas or a mixture of sodium hypochlorite and hydrochloric acid. (ii) Treating an aqueous solution of sodium chlorate with hydrogen peroxide in the presence of sulfuric acid. (iii) Treating an aqueous solution of sodium chlorite by electrolysis. (2) The generator effluent contains at least 90 percent (by weight) of chlorine dioxide with respect to all chlorine species as determined by Method 4500-ClO2 E in the "Standard Methods for the Examination of Water and Wastewater," 20th ed., 1998, or an equivalent method. ... (b)(1) The additive may be used as an antimicrobial agent in water used in poultry processing in an amount not to exceed 3 parts per million (ppm) residual chlorine dioxide as determined by Method 4500-ClO2 E, referenced in paragraph (a)(2) of this section, or an equivalent method. (2) The additive may be used as an antimicrobial agent in water used to wash fruits and vegetables that are not raw agricultural commodities in an amount not to exceed 3 ppm residual chlorine dioxide as determined by Method 4500-ClO2 E, referenced in paragraph (a)(2) of this section, or an equivalent method. Treatment of the fruits and vegetables with chlorine dioxide shall be followed by a potable water rinse or by blanching, cooking, or canning.
Special Reports
USEPA/Office of Prevention, Pesticides and Toxic Substances; Reregistration Eligibility Decision Document for Chlorine Dioxide and Sodium Chlorite EPA 738-R-06-007 (August 2006). The RED summarizes the risk assessment conclusions and outlines any risk reduction measures necessary for the pesticide to continue to be registered in the USA.[Available from, as of December 13, 2017: http://www.epa.gov/pesticides/reregistration/status.htm]
HHS/ATSDR; Toxicological Profile for Chlorine dioxide and Chlorite (PB 2004-107332) (September 2004).[Available from, as of December 13, 2017: https://www.atsdr.cdc.gov/toxprofiles/index.asp#C]
WHO; Environmental Health Criteria 216: Disinfectants and Disinfectant By-Products (2000).[Available from, as of December 12, 2017: http://www.inchem.org/documents/ehc/ehc/ehc216.htm]
Calabrese EJ et al; The Health Effects of Chlorine Dioxide as A Disinfectant in Potable Water: A Literature Survey; J Environ Health 41 (1): 26-31 (1978). A review with 43 references on the health effects of chlorine dioxide as a disinfectant in potable water.
For more Special Reports (Complete) data for Chlorine dioxide (7 total), please visit the HSDB record page.
FIFRA Requirements
Residues of the following chemical substances are exempted from the requirement of a tolerance when used in accordance with good manufacturing practice as ingredients in an antimicrobial pesticide formulation, provided that the substance is applied on a semi-permanent or permanent food-contact surface (other than being applied on food packaging) with adequate draining before contact with food. ... (b) The following chemical substances when used as ingredients in an antimicrobial pesticide formulation may be applied to: Dairy processing equipment, and food-processing equipment and utensils. ... Pesticide Chemical: Oxychloro species (including chlorine dioxide) generated by acidification of an aqueous solution of sodium chlorite. Limit: When ready for use, the end-use concentration is not to exceed 200 ppm of chlorine dioxide as determined by the method titled, Iodometric Method for the Determination of Available Chlorine Dioxide (50-250 ppm available chlorine dioxide)
Residues of the following chemical substances are exempted from the requirement of a tolerance when used in accordance with good manufacturing practice as ingredients in an antimicrobial pesticide formulation, provided that the substance is applied on a semi-permanent or permanent food-contact surface (other than being applied on food packaging) with adequate draining before contact with food. ... (c) The following chemical substances when used as ingredients in an antimicrobial pesticide formulation may be applied to: Food-processing equipment and utensils. ... Pesticide Chemical: Oxychloro species (including chlorine dioxide) generated by acidification of an aqueous solution of sodium chlorite. Limit: When ready for use, the end-use concentration is not to exceed 200 ppm of chlorine dioxide as determined by the method titled, "Iodometric Method for the Determination of Available Chlorine Dioxide (50-250 ppm available chlorine dioxide)"
Residues of the following chemical substances are exempted from the requirement of a tolerance when used in accordance with good manufacturing practice as ingredients in an antimicrobial pesticide formulation, provided that the substance is applied on a semi-permanent or permanent food-contact surface (other than being applied on food packaging) with adequate draining before contact with food. ... (c) The following chemical substances when used as ingredients in an antimicrobial pesticide formulation may be applied to: Food-processing equipment and utensils. ... Pesticide Chemical: Oxychloro species (predominantly chlorite, chlorate and chlorine dioxide in an equilibrium mixture) generated either (i) by directly metering a concentrated chlorine dioxide solution prepared just prior to use, into potable water, or (ii) by acidification of an aqueous alkaline solution of oxychloro species (predominately chlorite and chlorate) followed by dilution with potable water. Limit: When ready for use, the end-use concentration is not to exceed 200 ppm of chlorine dioxide as determined by the method titled, "Iodometric Method for the Determination of Available Chlorine Dioxide (50-250 ppm available chlorine dioxide)"
The Agency has completed its assessment of the dietary, occupational, drinking water, and ecological risks associated with the use of pesticide products containing the active ingredient chlorine dioxide and sodium chlorite. Based on a review of these data and on public comments on the Agency's assessments for the active ingredient chlorine dioxide and sodium chlorite, the Agency has sufficient information on the human health and ecological effects of chlorine dioxide and sodium chlorite to make decisions as part of the tolerance reassessment process under FFDCA and reregistration process under FIFRA, as amended by FQPA. The Agency has determined that all chlorine dioxide and sodium chlorite pesticide-containing products are eligible for reregistration provided that: (i) current data gaps and confirmatory data needs are addressed; (ii) the risk mitigation measures outlined in this document are adopted; and (iii) label amendments are made to reflect these measures. ... Based on its evaluation of chlorine dioxide and sodium chlorite, the Agency has determined that chlorine dioxide and sodium chlorite products, unless labeled and used as specified in this document, would present risks inconsistent with FIFRA. Accordingly, should a registrant fail to implement any of the risk mitigation measures identified in this document, the Agency may take regulatory action to address the risk concerns from the use of chlorine dioxide and sodium chlorite. If all changes outlined in this document are incorporated into the product labels, then all current risks for chlorine dioxide and sodium chlorite will be substantially mitigated for the purposes of this determination.
As the federal pesticide law FIFRA directs, EPA is conducting a comprehensive review of older pesticides to consider their health and environmental effects and make decisions about their continued use. Under this pesticide reregistration program, EPA examines newer health and safety data for pesticide active ingredients initially registered before November 1, 1984, and determines whether the use of the pesticide does not pose unreasonable risk in accordance to newer safety standards, such as those described in the Food Quality Protection Act of 1996. Pesticides for which EPA had not issued Registration Standards prior to the effective date of FIFRA '88 were divided into three lists based upon their potential for human exposure and other factors, with List B containing pesticides of greater concern than those on List C, and with List C containing pesticides of greater concern than those on List D. Chlorine dioxide is found on List D. Case No: 4023; Pesticide type: insecticide, fungicide, herbicide, antimicrobial; Case Status: RED Approved 09/94; OPP has made a decision that some/all uses of the pesticide are eligible for reregistration, as reflected in a Reregistration Eligibility Decision (RED) document.; Active ingredient (AI): chlorine dioxide; Data Call-in (DCI) Date(s): 09/07/93; AI Status: The producers of the pesticide have made commitments to conduct the studies and pay the fees required for reregistration, and are meeting those commitments in a timely manner.
安全与防护
Fire Fighting
Excerpt from ERG Guide 143 [Oxidizers (Unstable)]:
In case of fire in the surroundings, use appropriate extinguishing media. In case of fire: keep drums, etc., cool by spraying with water. Combat fire from a sheltered position.
First Aid Measures
Fresh air, rest. Half-upright position. Refer for medical attention.
First rinse with plenty of water for at least 15 minutes, then remove contaminated clothes and rinse again. Refer for medical attention .
First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.
First Aid
Excerpt from NIOSH Pocket Guide for Chlorine dioxide:
(General first aid procedures)
Firefighting Hazards
A powerful oxidizer, this chemical will increase the intensity of a fire, and can cause fire upon contact with combustibles. ... Vapors are heavier than air and will collect in low areas. Containers may explode in fire. Storage containers and parts of containers may rocket great distances, in many directions.
Exposure Control and Personal Protection
TIH (Toxic Inhalation Hazard) - Term used to describe gases and volatile liquids that are toxic when inhaled. Some are TIH materials themselves, e.g., chlorine, and some release TIH gases when spilled in water, e.g., chlorosilanes. [ERG 2016].
0.1 [ppm]
Fire Fighting Procedures
If material on fire or involved in fire: Use water in flooding quantities as fog. Cool all affected containers with flooding quantities of water. Extinguish fire using agent suitable for type of surrounding fire. (Material itself does not burn or burns with difficulty.) /Chlorine dioxide hydrate, frozen/
If fire becomes uncontrollable, consider evacuation of one-third mile radius. /Chlorine dioxide hydrate, frozen/
Firefighting gear (including SCBA) may not provide adequate protection. If exposure occurs, remove and isolate gear immediately and thoroughly decontaminate personnel. ... Use water only. Do not use dry chemical or carbon dioxide extinguishers. Use water with caution as chlorine dioxide reacts with water, forming hydrogen chloride gas. ... If material or contaminated runoff enters waterways, notify downstream users of potentially contaminated waters. Notify local health and fire officials and pollution control agencies. From a secure, explosion-proof location, use water spray to cool exposed containers. If cooling streams are ineffective (venting sound increases in volume and pitch, tank discolors, or shows any signs of deforming), withdraw immediately to a secure position. The only respirators recommended for firefighting are self-contained breathing apparatuses that have full face-pieces and are operated in a pressure-demand or other positive-pressure mode.
Small fire: Use water. Do not use dry chemicals or foams. CO2 or Halon may provide limited control. Large fire: Flood fire area with water from a distance. Do not move cargo or vehicle if cargo has been exposed to heat. Move containers from fire area if you can do it without risk. Do not get water inside containers: a violent reaction may occur. Fire involving tanks or car/trailer loads: Cool containers with flooding quantities of water until well after fire is out. Dike fire-control water for later disposal. ALWAYS stay away from tanks engulfed in fire. For massive fire, use unmanned hose holders or monitor nozzles; if this is impossible, withdraw from area and let fire burn.
Storage Conditions
Store separately from all other flammable materials. Prior to working with chlorine dioxide you should be trained on its proper handling and storage. This chemical is a powerful oxidizer, and is shock-, light- and heat sensitive. It is violently explosive in air at concentrations over 10%. Keep frozen when not in use. Store in tightly closed containers in a cool, dark, well-ventilated area at temperatures well below 130 °C. Gas explosions may occur above 130 °C. Use only nonsparking tools and equipment, especially when opening and closing containers of this chemical. Sources of ignition, such as smoking and open flames, are prohibited where this chemical is used, handled, or stored in a manner that could create a potential fire or explosion hazard. Use explosion-proof electrical equipment and fittings in storage area.
Cleanup Methods
Evacuate and restrict persons not wearing protective equipment from area of spill or leak until cleanup is complete. Remove all ignition sources. Ventilate area of leak or spill. If the gas is leaked, stop the flow of gas if it can be done safely. If the source of the leak is a cylinder and the leak cannot be stopped in place, remove the leaking cylinder to a safe place in the open air and repair the leak or alow the cylinder to empty. If the leak can be stopped in place, bubble chlorine dioxide through a solution made up of reducing agent sodium bisulfide and sodium bicarbonate with a trap in the line. For liquid spills, allow chlorine dioxide to evaporate with all available ventilation. Keep chlorine dioxide out of a confined space, such as a sewer, because of the possibility of an explosion, unless the sewer is designed to prevent the buildup of explosive concentrations. It may be necessary to contain and dispose of this chemical as a hazardous waste. If material or contaminated runoff enters waterways, notify downstream users of potentially contaminated waters.
Chlorine dioxide, hydrate, frozen, when spilled in water. Small spills (from a small package or a small leak from a large package): First: Isolate in all directions 100 ft/30 m. Then: Protect persons downwind: Day 0.1 mi/0.2 km, Night 0.1 mi/0.2 km. Large spills (from a large package or many small packages): First: Isolate in all directions 100 ft/30 m. Then: Protect persons downwind: Day 0.2 mi/0.3 km, Night 0.4 mi/0.6 km. /Chlorine dioxide, hydrate, frozen/
1) Remove all ignition sources. 2) Ventilate area of spill or leak. 3) If in gaseous form, stop flow of gas. If source of leak is a cylinder and leak cannot be stopped in place, remove leaking cylinder to safe place in open air, and repair leak or allow cylinder to empty. 4) If in liquid form, evacuate persons not wearing protective equipment. ... Allow ... to evaporate while providing all available ventilation.
Disposal Methods
SRP: Recycle any unused portion of the material for its approved use or return it to the manufacturer or supplier. Ultimate disposal of the chemical must consider: the material's impact on air quality; potential migration in air, soil or water; effects on animal, aquatic and plant life; and conformance with environmental and public health regulations. If it is possible or reasonable use an alternative chemical product with less inherent propensity for occupational harm/injury/toxicity or environmental contamination.
SRP: Wastewater from contaminant suppression, cleaning of protective clothing/equipment, or contaminated sites should be contained and evaluated for subject chemical or decomposition product concentrations. Concentrations shall be lower than applicable environmental discharge or disposal criteria. Alternatively, pretreatment and/or discharge to a permitted wastewater treatment facility is acceptable only after review by the governing authority and assurance that "pass through" violations will not occur. Due consideration shall be given to remediation worker exposure (inhalation, dermal and ingestion) as well as fate during treatment, transfer and disposal. If it is not practicable to manage the chemical in this fashion, it must be evaluated in accordance with EPA 40 CFR Part 261, specifically Subpart B, in order to determine the appropriate local, state and federal requirements for disposal.
Use large volume of concentrated solution of ferrous salt or bisulfite solution as reducing agent. Then neutralize and flush to sewer with abundant water.
毒理信息
Target Organs
Developmental (effects while organs are developing), Gastrointestinal (Stomach and Intestines, part of the digestive system), Respiratory (From the Nose to the Lungs)
Cardiovascular
Eyes, respiratory system
Ecotoxicity Values
LC50; Species: Pimephales promelas (Fathead minnow) juvenile; Conditions: flow through; Concentration: 0.02 mg/L for 96 hr
LC50; Species: Pimephales promelas (Fathead minnow) adult- 1 yr old; Conditions: flow through; Concentration: 0.17 mg/L for 96 hr
LC50; Species: Lepomis macrochirus (Bluegill) young of the year; Conditions: flow through; Concentration: 0.15 mg/L for 96 hr
LC50; Species: Carcinus maenas (Green or Europeon shore crab); Conditions: renewal; Concentration: 500 mg/L for 48 hr /technical product/
For more Ecotoxicity Values (Complete) data for Chlorine dioxide (16 total), please visit the HSDB record page.
Environmental Fate
Hydrogen peroxide (H2O2), chlorite, chlorate, Cl2O3, oxygen (O2), and chlorine have all been reported as intermediates or products /of chlorine dioxide breakdown/. Presumably chlorine dioxide will not persist in open basins or reservoirs, although it can remain for days in clean distribution systems.
It is generally accepted that the predominant reaction product of chlorine dioxide in water treatment is chlorite and that chlorate and other ions are produced in minor amounts ... an approximately 50% conversion of chlorine dioxide to chlorite was reported ... /in/ water containing natural humic acids.
Chlorine dioxide does not cause formation of trihalomethanes, does not react with ammonia, and does not cause formation of chloramines. It can ... disproportionate to chlorate and chlorite ... by raising pH to 11 or 12 ... this is not believed to be an important reaction in water undergoing treatment.
/Products formed during oxidative treatment of water/: both oxygenated and chlorinated products may be formed, the latter being found most prominently in connection with reactions of phenolic substances. Other products that might affect health are quinones and 1,2-epoxy compounds.
Exposure Routes
The substance can be absorbed into the body by inhalation.
inhalation, ingestion (liquid), skin and/or eye contact
Toxicity Summary
IDENTIFICATION AND USE: Chlorine dioxide is a yellowish-brown gas with unpleasant odor similar to chlorine and nitric acid. Its uses include bleaching cellulose, paper-pulp, flour, leather, fats and oils, textiles, and beeswax. It is also used for purification of water, taste and odor control of water, cleaning and detanning leather, in the manufacture of chloride salts, and as an oxidizing agent, bactericide, antiseptic and deodorizer. Chlorine dioxide was found to be highly effective against various microorganisms tested at very low concentrations in a minimum contact time of 30 to 60 seconds. HUMAN STUDIES: Potential symptoms of overexposure are irritation of eyes, nose, and throat, as well as coughing, wheezing, bronchitis, and pulmonary edema. Workers industrially exposed to low concentrations of the gas in air have been noted occasionally to suffer from irritation of the eyes and to see haloes about lights, but these effects have been minor compared to respiratory irritation. Bronchoscopy and biopsy revealed slight chronic bronchitis in 7 of 12 workers. Only two workers who had been exposed just prior to examination showed physical signs of respiratory effects. Workers acutely exposed to chlorine dioxide developed both reactive airways dysfunction syndrome (RADS), a form of occupational asthma, and an upper airways reactive disorder that was called reactive upper airways disfunction syndrome (RUDS). A positive association was found between exposure of the mother to chlorine dioxide-treated water during pregnancy and prematurity of the newborn. Children born of mothers who drank disinfected water treated with either chlorine dioxide or hypochlorite were noted to have an increased incidence of small cranial circumference, small body length, and neonatal jaundice. Chlorine dioxide was found to be weakly genotoxic in human leukocytes. ANIMAL STUDIES: Chlorine dioxide is very toxic by inhalation in rats. Clinical signs of toxicity included respiratory distress. Macroscopically, pulmonary edema and emphysema were seen in all groups of chlorine dioxide-exposed animals, with the incidence increasing in a dose-related manner. Chlorine dioxide is toxic when administered in solution by the oral route to rats. Two males and two females receiving 80 mg chlorine dioxide/kg body weight died, and a further two males at 40 mg/kg body weight also died within 48 hr of administration. There were no deaths at 20 mg/kg body weight. A developmental study in rats did not demonstrate any impairment of reproductive function, and there were no signs of developmental effects among rats receiving up to 10 mg aqueous chlorine dioxide/kg body weight per day. A negative result was obtained for micronucleus formation, and there were no increases in the number of structural or numerical chromosome aberrations in mice treated with chlorine dioxide. However, chlorine dioxide increased water genotoxicity in assays with E. coli and with S. cerevisiae. In Chinese hamster ovary cells at 2.5-15 ug/mL, there was a marked dose-related, statistically significant increase in the number of metaphases with chromosome aberrations. In the presence of metabolic activation, cell toxicity and an absence of mitotic cells were observed at 75 ug/mL. An increase in the number of metaphases with chromosome aberrations was noted at 50 ug/mL. ECOTOXICITY STUDIES: Developmental abnormalities in the sea urchin were evident at exposure to the chlorine dioxide concentration 250 mg/L. Compared with the control, pre-hatch malformations were 6% higher; retarded development, 2%; post-hatch malformations, 20%; skeletal malformations, 21%; and gut malformations, 11%. Survival of larval kelp bass was not significantly affected by chlorine dioxide. In Fathead minnows (Pimephales promelas) chlorine dioxide exposure produced dose-dependent gill pathology including epithelial lifting, hypertrophy, hyperplasia, lamellar fusion, and necrosis. Complete recovery, even in fish with severe hypertrophy and lamellar fusion, was achieved within 4 days. Chlorine dioxide concentrations ranging from 0.1 to 0.5 mg/L induced micronuclei in Vicia faba at acid pH, while 1-2 mg/L chlorine dioxide gave positive responses at neutral pH. Chlorine dioxide produced positive responses in the Tradescantia micronucleus test.
Ecotoxicity Excerpts
/AQUATIC SPECIES/ Antifouling biocides are commonly used in coastal electric power stations to prevent biofouling in their condenser cooling systems. However, the environmental impact of the chemical biocides is less understood than the thermal stress effects caused by the condenser effluents. In this study, Chaetoceros lorenzianus, a representative marine diatom, was used to analyze the toxicity of two antifouling biocides, chlorine and chlorine dioxide. The diatom cells were subjected to a range of concentrations of the biocides (from 0.05 to 2 mg/L, as total residual oxidants, TRO) for contact time of 30min. They were analyzed for viability, genotoxicity, chlorophyll a and cell density endpoints. The cells were affected at all concentrations of the biocides (0.05-2 mg/L), showing dose-dependent decrease in viability and increase in DNA damage. The treated cells were later incubated in filtered seawater devoid of biocide to check for recovery. The cells were able to recover in terms of overall viability and DNA damage, when they had been initially treated with low concentrations of the biocides (0.5 mg/L of Cl2 or 0.2 mg/L of ClO2). Chlorophyll a analysis showed irreparable damage at all concentrations, while cell density showed increasing trend of reduction, if treated above 0.5 mg/L of Cl2 and 0.2 mg/L of ClO2. The data indicated that in C. lorenzianus, cumulative toxic effects and recovery potential of ClO2 up to 0.2 mg/L were comparable with those of Cl2, up to 0.5 mg/L concentration in terms of the studied endpoints. The results indicate that at the biocide levels currently being used at power stations, recovery of the organism is feasible upon return to ambient environment. Similar studies should be carried out on other planktonic and benthic organisms, which will be helpful in the formulation of future guidelines for discharge of upcoming antifouling biocides such as chlorine dioxide.
/AQUATIC SPECIES/ Environmental effect evaluation of disinfection of combined sewer overflow events with alternative chemical disinfectants requires that the environmental toxicity of the disinfectants and the main by-products of their use are known. Many disinfectants degrade quickly in water which should be included in the evaluation of both their toxicity as determined in standardized tests and their possible negative effect in the water environment. Here we evaluated according to the standardized ISO 8692 test the toxicity towards the green microalgae, Pseudokirchneriella subcapitata, of three disinfectants: performic acid (PFA), peracetic acid (PAA) and chlorine dioxide (ClO2) as well as two by-products of their use: hydrogen peroxide (H2O2) and chlorite. All of the five chemicals investigated showed clear toxicity to the algae with well-defined dose response curves. The EC50 values ranged from 0.16 to 2.9 mg/L based on nominal concentrations leading to the labeling of the chemicals as either toxic or very toxic. The five investigated chemicals decreased in toxicity in the order chlorine dioxide, performic acid, peracetic acid, chlorite and hydrogen peroxide. The stability of the chemicals increased in the same order as the toxicity decrease. This indicates that even though ClO2 has the highest environmental hazard potential, it may still be suitable as an alternative disinfectant due to its rapid degradation in water.
/AQUATIC SPECIES/ Whether the implementation of additional treatments for the removal of estrogens from wastewater treatment works (WwTWs) effluents will eliminate their feminizing effects in exposed wildlife has yet to be established, and this information is crucial for future decisions on investment into WwTWs. Here, granular activated carbon (GAC), ozone (O(3)), and chlorine dioxide (ClO(2)) were investigated for their effectiveness in reducing steroidal estrogen levels in a WwTW effluent and assessments made on the associated estrogenic and reproductive responses in fathead minnows (Pimephales promelas) exposed for 21 days. All treatments reduced the estrogenicity of the standard-treated (STD) effluent, but with different efficacies; ranging between 70-100% for total estrogenicity and 53-100% for individual steroid estrogens. In fish exposed to the GAC- and ClO(2)- (but not O(3)-) treated effluents, there was no induction of plasma vitellogenin (VTG) or reduction in the weight of the fatpad, a secondary sex character in males, as occurred for fish exposed to STD effluent. This finding suggests likely benefits of employing these treatment processes for the reproductive health in wild fish populations living in rivers receiving WwTW discharges. Exposure of pair-breeding minnows to the GAC-treated effluent, however, resulted in a similar inhibition of egg production to that occurring for exposure to the STD effluent (34-40%). These data, together with a lack of effect on egg production of the estrogen, ethinylestradiol (10 ng/L), alone, suggest that chemical/physical properties of the effluents rather than their estrogenicity were responsible for the reproductive effect and that these factor(s) were not remediated for through GAC treatment. Collectively, our findings illustrate the importance of assessing integrative biological responses, rather than biomarkers alone, in the assessment and improvement of WwTW technologies for the protection of wild fish populations.
/AQUATIC SPECIES/ Epidemiological evidence suggests a link between consumption of chlorinated drinking water and various cancers. Chlorination of water rich in organic chemicals produces carcinogenic organochlorine by-products (OBPs) such as trihalomethanes and haloacetic acids. Since the discovery of the first OBP in the 1970s, there have been several investigations designed to determine the biological effects of single chemicals or small artificial OBP combinations. However, there is still insufficient information regarding the general biological response to these compounds, and further studies are still needed to evaluate their potential genotoxic effects. In the current study, we evaluated the effect of three drinking water disinfectants on the activity of cytochrome P450 (CYP)-linked metabolizing enzymes and on the generation of oxidative stress in the livers of male and female Cyprinus carpio fish (carp). The fish were exposed in situ for up 20 days to surface water obtained from the Trasmene lake in Italy. The water was treated with 1-2 mg/L of either sodium hypochlorite (NaClO) or chlorine dioxide (ClO2) as traditional disinfectants or with a relatively new disinfectant product, peracetic acid (PAA). Micronucleus (MN) frequencies in circulating erythrocytes from the fish were also analyzed as a biomarker of genotoxic effect. In the CYP-linked enzyme assays, a significant induction (up to a 57-fold increase in the deethylation of ethoxyresorufin with PAA treatment) and a notable inactivation (up to almost a 90% loss in hydroxylation of p-nitrophenol with all disinfectants, and of testosterone 2beta-hydroxylation with NaClO) was observed in subcellular liver preparations from exposed fish. Using the electron paramagnetic resonance (EPR) spectroscopy radical-probe technique, we also observed that CYP-modulation was associated with the production of reactive oxygen species (ROS). In addition, we found a significant increase in MN frequency in circulating erythrocytes after 10 days of exposure of fish to water treated with ClO2, while a non-significant six-fold increase in MN frequency was observed with NaClO, but not with PAA. Our data suggest that the use of ClO2 and NaClO to disinfect drinking water could generate harmful OBP mixtures that are able to perturb CYP-mediated reactions, generate oxidative stress and induce genetic damage. These data may provide a mechanistic explanation for epidemiological studies linking consumption of chlorinated drinking water to increased risk of urinary, gastrointestinal and bladder cancers.
For more Ecotoxicity Excerpts (Complete) data for Chlorine dioxide (14 total), please visit the HSDB record page.
Signs and Symptoms
Cough. Headache. Laboured breathing. Nausea. Shortness of breath. Sore throat. Symptoms may be delayed.
Redness. Pain.
Redness. Pain.
irritation eyes, nose, throat; cough, wheezing, bronchitis, pulmonary edema; chronic bronchitis
EPA IRIS Information
Chlorine dioxide
Cardiovascular
3 x 10 ^-2 mg/kg-day
2 x 10 ^-4 mg/m^3
Human Toxicity Excerpts
/HUMAN EXPOSURE STUDIES/ An assessment of the safety of chronically administered chlorine water disinfectants in man was conducted in 3 phases. Phase I, a rising dose tolerance investigation, examined the effects of single dose incr concn admin of disinfectants to normal healthy adult male volunteers. Phase II considered the impact on normal subjects of 12 wk daily ingestion of the disinfectants at a concn of 5 mg/L. In phase III, chlorite, at a concn of 5 mg/L, was administered daily to glucose 6-phosphate dehydrogenase (G-6-PD)-deficient subjects. The study affirmed the relative safety and tolerance of normal healthy adult males and normal healthy adult male G-6-PD-deficient individuals to daily 12 wk ingestion of 500 mL of chlorine disinfectants at a concentration of 5 mg/L. /Disinfection byproducts/
/HUMAN EXPOSURE STUDIES/ In a series of extensive human volunteer studies on water disinfectants, groups of 10 males received aqueous chlorine dioxide in drinking-water by a range of different protocols (a sequence of rising concentrations of up to around 0.34 mg/kg body weight over a 16-day period, approximately 0.035 mg/kg body weight on every third day for 12 weeks, or approximately 3.6 x 10-5 mg aqueous chlorine dioxide/kg body weight per day daily for 12 weeks). Observations included physical examination (blood pressure, respiration rate, pulse, oral temperature, and electrocardiography), extensive blood biochemistry, hematology, and urinalysis, and the subjective recording of taste. There were no significant adverse effects recorded for any of the parameters measured.
/SIGNS AND SYMPTOMS/ Potential symptoms of overexposure are irritation of eyes, nose, and throat; coughing, wheezing, bronchitis, pulmonary edema; chronic bronchitis.
/SIGNS AND SYMPTOMS/ ... A 5 ppm concentration of chlorine dioxide was definitely irritating and ... 19 ppm of the gas inside a bleach tank was more than sufficient to cause the death of one worker (time of exposure not specified) ... . Based on these findings, /investigators/ suggested in 1950 a maximal acceptable concentration of 1 ppm.
For more Human Toxicity Excerpts (Complete) data for Chlorine dioxide (26 total), please visit the HSDB record page.
法规信息
FDA Requirements
Chlorine dioxide (CAS Reg. No. 10049-04-4) may be safely used in food in accordance with the following prescribed conditions: (a)(1) The additive is generated by one of the following methods: (i) Treating an aqueous solution of sodium chlorite with either chlorine gas or a mixture of sodium hypochlorite and hydrochloric acid. (ii) Treating an aqueous solution of sodium chlorate with hydrogen peroxide in the presence of sulfuric acid. (iii) Treating an aqueous solution of sodium chlorite by electrolysis. (2) The generator effluent contains at least 90 percent (by weight) of chlorine dioxide with respect to all chlorine species as determined by Method 4500-ClO2 E in the "Standard Methods for the Examination of Water and Wastewater," 20th ed., 1998, or an equivalent method. ... (b)(1) The additive may be used as an antimicrobial agent in water used in poultry processing in an amount not to exceed 3 parts per million (ppm) residual chlorine dioxide as determined by Method 4500-ClO2 E, referenced in paragraph (a)(2) of this section, or an equivalent method. (2) The additive may be used as an antimicrobial agent in water used to wash fruits and vegetables that are not raw agricultural commodities in an amount not to exceed 3 ppm residual chlorine dioxide as determined by Method 4500-ClO2 E, referenced in paragraph (a)(2) of this section, or an equivalent method. Treatment of the fruits and vegetables with chlorine dioxide shall be followed by a potable water rinse or by blanching, cooking, or canning.
FIFRA Requirements
Residues of the following chemical substances are exempted from the requirement of a tolerance when used in accordance with good manufacturing practice as ingredients in an antimicrobial pesticide formulation, provided that the substance is applied on a semi-permanent or permanent food-contact surface (other than being applied on food packaging) with adequate draining before contact with food. ... (b) The following chemical substances when used as ingredients in an antimicrobial pesticide formulation may be applied to: Dairy processing equipment, and food-processing equipment and utensils. ... Pesticide Chemical: Oxychloro species (including chlorine dioxide) generated by acidification of an aqueous solution of sodium chlorite. Limit: When ready for use, the end-use concentration is not to exceed 200 ppm of chlorine dioxide as determined by the method titled, Iodometric Method for the Determination of Available Chlorine Dioxide (50-250 ppm available chlorine dioxide)
Residues of the following chemical substances are exempted from the requirement of a tolerance when used in accordance with good manufacturing practice as ingredients in an antimicrobial pesticide formulation, provided that the substance is applied on a semi-permanent or permanent food-contact surface (other than being applied on food packaging) with adequate draining before contact with food. ... (c) The following chemical substances when used as ingredients in an antimicrobial pesticide formulation may be applied to: Food-processing equipment and utensils. ... Pesticide Chemical: Oxychloro species (including chlorine dioxide) generated by acidification of an aqueous solution of sodium chlorite. Limit: When ready for use, the end-use concentration is not to exceed 200 ppm of chlorine dioxide as determined by the method titled, "Iodometric Method for the Determination of Available Chlorine Dioxide (50-250 ppm available chlorine dioxide)"
Residues of the following chemical substances are exempted from the requirement of a tolerance when used in accordance with good manufacturing practice as ingredients in an antimicrobial pesticide formulation, provided that the substance is applied on a semi-permanent or permanent food-contact surface (other than being applied on food packaging) with adequate draining before contact with food. ... (c) The following chemical substances when used as ingredients in an antimicrobial pesticide formulation may be applied to: Food-processing equipment and utensils. ... Pesticide Chemical: Oxychloro species (predominantly chlorite, chlorate and chlorine dioxide in an equilibrium mixture) generated either (i) by directly metering a concentrated chlorine dioxide solution prepared just prior to use, into potable water, or (ii) by acidification of an aqueous alkaline solution of oxychloro species (predominately chlorite and chlorate) followed by dilution with potable water. Limit: When ready for use, the end-use concentration is not to exceed 200 ppm of chlorine dioxide as determined by the method titled, "Iodometric Method for the Determination of Available Chlorine Dioxide (50-250 ppm available chlorine dioxide)"
The Agency has completed its assessment of the dietary, occupational, drinking water, and ecological risks associated with the use of pesticide products containing the active ingredient chlorine dioxide and sodium chlorite. Based on a review of these data and on public comments on the Agency's assessments for the active ingredient chlorine dioxide and sodium chlorite, the Agency has sufficient information on the human health and ecological effects of chlorine dioxide and sodium chlorite to make decisions as part of the tolerance reassessment process under FFDCA and reregistration process under FIFRA, as amended by FQPA. The Agency has determined that all chlorine dioxide and sodium chlorite pesticide-containing products are eligible for reregistration provided that: (i) current data gaps and confirmatory data needs are addressed; (ii) the risk mitigation measures outlined in this document are adopted; and (iii) label amendments are made to reflect these measures. ... Based on its evaluation of chlorine dioxide and sodium chlorite, the Agency has determined that chlorine dioxide and sodium chlorite products, unless labeled and used as specified in this document, would present risks inconsistent with FIFRA. Accordingly, should a registrant fail to implement any of the risk mitigation measures identified in this document, the Agency may take regulatory action to address the risk concerns from the use of chlorine dioxide and sodium chlorite. If all changes outlined in this document are incorporated into the product labels, then all current risks for chlorine dioxide and sodium chlorite will be substantially mitigated for the purposes of this determination.
As the federal pesticide law FIFRA directs, EPA is conducting a comprehensive review of older pesticides to consider their health and environmental effects and make decisions about their continued use. Under this pesticide reregistration program, EPA examines newer health and safety data for pesticide active ingredients initially registered before November 1, 1984, and determines whether the use of the pesticide does not pose unreasonable risk in accordance to newer safety standards, such as those described in the Food Quality Protection Act of 1996. Pesticides for which EPA had not issued Registration Standards prior to the effective date of FIFRA '88 were divided into three lists based upon their potential for human exposure and other factors, with List B containing pesticides of greater concern than those on List C, and with List C containing pesticides of greater concern than those on List D. Chlorine dioxide is found on List D. Case No: 4023; Pesticide type: insecticide, fungicide, herbicide, antimicrobial; Case Status: RED Approved 09/94; OPP has made a decision that some/all uses of the pesticide are eligible for reregistration, as reflected in a Reregistration Eligibility Decision (RED) document.; Active ingredient (AI): chlorine dioxide; Data Call-in (DCI) Date(s): 09/07/93; AI Status: The producers of the pesticide have made commitments to conduct the studies and pay the fees required for reregistration, and are meeting those commitments in a timely manner.
DHS Chemicals of Interest (COI)
Chlorine dioxide
1
1000
A Commercial Grade
A Placarded Amount
Toxic chemical that can be released at a facility.
安全数据
- tsca
- TSCA listed
- 安全说明
- 23-26-28-36/37/39-38-45-61
- 危险品标志
- O,T+,N
- 危险类别码
- 6-8-26-34-50
- 毒害物质数据
- 10049-04-4(Hazardous Substances Data)
- 职业暴露等级
- C
- 职业暴露限值
- TWA: 0.1 ppm (0.3 mg/m3), STEL: 0.3 ppm (0.9 mg/m3)
- 危险品运输编号
- UN 9191
- 立即威胁生命和健康浓度
- 5 ppm
毒性防护
毒性二氧化氯对人体有害,其毒性与氯气相似,能侵蚀眼睛和呼吸器官。在浓度含量高的情况下,侵人中枢神经使人致死。在空气中容许浓度为0.3 mg/m3。如已吸入时,立即移送到清净的空气中。如不慎溅人眼睛中,用水充分冲洗干净。工作前必须穿戴工作服、橡皮围裙、乳胶手套、个人专用的保护面具。在工作时,要求生产设备密闭,通风良好。下班后,务必淋浴。
急性毒性口服-大鼠 LD50: 292 毫克/公斤; 吸入-大鼠 LCL0: 500 PPM/15分
刺激数据眼睛-兔 100 毫克 轻度
职业标准TWA 0.28 毫克/立方米; STEL 0.84 毫克/立方米
包装储运
爆炸物危险特性火星, 冲撞, 阳光, 100℃以上高温灵敏爆炸; 与CO, 烃类, 氟胺类混合爆炸
可燃性危险特性与水, 或水蒸汽反应生成有毒腐蚀性氯化氢气体; 与非金属, 如磷, 硫等, 燃烧; 热分解有毒氯化物烟雾
储运特性库房低温通风干燥; 防火, 防高温, 轻搬轻放, 与氧化剂, 食品原料分开存放
灭火剂二氧化碳, 泡沫, 干粉
化学与工业
药理信息
Biological Half-Life
After oral administration of Alcide (sodium chlorite and lactic acid) in rats, the peak plasma level was obtained in 8 hr. The half-life for (36)Cl absorption from plasma was 8.03 hr, while the half life for (36)Cl elimination from plasma was 48.02 hr.
Following single gavage dosing of rats with (36)ClO2 ... peak plasma levels of (36)Cl were reached within 2 hours following dosing ... the absorption rate constant and half-time were 0.198/hour and 3.5 hours, respectively.
Metabolism/Metabolites
Both chlorine dioxide and chlorite are primarily metabolized to chloride ion. At 72 hours following single oral (gavage) administration of radiolabeled chlorine dioxide in rats, chloride ion accounted for approximately 87% of the radioactivity that had been collected in the urine and 80% of the radioactivity in a plasma sample. Chlorite was the other major metabolite, accounting for approximately 11 and 21% of the radioactivity in the urine and plasma samples, respectively. Chlorate was a minor component of the radioactivity in the urine. Similarly, chloride ion accounted for approximately 85% of the radioactivity in the 72-hour urine collection of rats that had been orally administered radiolabeled chlorite; the remainder in the form of chlorite.
Absorption, Distribution and Excretion
The distribution and chemical fate of (36)Cl-ClO2 gas subsequent to fumigation of tomatoes or cantaloupe was investigated as were major factors that affect the formation of chloroxyanion byproducts. Approximately 22% of the generated (36)Cl-ClO2 was present on fumigated tomatoes after a 2 hr exposure to approximately 5 mg of (36)Cl-ClO2. A water rinse removed 14% of the radiochlorine while tomato homogenate contained approximately 63% of the tomato radioactivity; 24% of the radiochlorine was present in the tomato stem scar area. Radioactivity in tomato homogenate consisted of (36)Cl-chloride (>/= 80%), (36)Cl-chlorate (5 to 19%), and perchlorate (0.5 to 1.4%). In cantaloupe, 55% of the generated (36)Cl-ClO2 was present on melons fumigated with 100 mg of (36)Cl-ClO2 for a 2 hr period. Edible cantaloupe flesh contained no detectable radioactive residue (LOQ = 0.3 to 0.4 ug/g); >99.9% of radioactivity associated with cantaloupe was on the inedible rind, with <0.1% associated with the seed bed. Rind radioactivity was present as (36)Cl-chloride (approximately 86%), chlorate (approximately 13%), and perchlorate (approximately 0.6%). Absent from tomatoes and cantaloupe were (36)Cl-chlorite residues. Follow-up studies have shown that chlorate and perchlorate formation can be completely eliminated by protecting fumigation chambers from light sources.
After oral administration of Alcide (sodium chlorite and lactic acid) in rats, the peak plasma level was obtained in 8 hr. At 144 hr, radioactivity was highest in plasma followed by lung, kidney, skin, bone marrow, stomach, ovary, duodenum, ileum, spleen, fat, brain, liver, and carcass. Subcellular distribution revealed that 85% of the activity in the liver homogenate resided in the cytosol. 70% of total activity in plasma was located in the trichloroacetic acid supernatant, with 30% bound to the precipitated protein fraction. Urinary excretion accounted for most of the (36)chlorine eliminated.
One study shows that "chlorine" (chemical form not characterized) derived from aqueous chlorine dioxide is absorbed by the oral route, with a wide distribution and rapid and extensive elimination. In this study, groups of four rats received a single oral gavage dose of approximately 1.5 or 4.5 mg 36ClO2/kg body weight. Blood samples were collected for up to 48 hr post-administration, and at 72 hr, animals were killed, with samples taken from kidneys, lungs, small intestine, liver, spleen, thymus, bone marrow, and testes. 36Cl was found in all tissues except testes, skin, and the remaining carcass, although levels in these tissues each accounted for less than 1% of the administered dose.
About 40% of /a single dose of/ 36Cl was recovered in urine, expired air, and feces, although the urine accounted for most (about 30%).
For more Absorption, Distribution and Excretion (Complete) data for Chlorine dioxide (6 total), please visit the HSDB record page.
用途与制造
Uses
Used in bleaching wood pulp (95% of use); Also used in bleaching textiles; disinfecting hospital equipment; disinfecting fruits, vegetables, and meats; and treating municipal water; [ACGIH]
Pulp and Paper Processing [Category: Industry]
For chlorine dioxide (USEPA/OPP Pesticide Code: 020503) ACTIVE products with label matches. /SRP: Registered for use in the U.S. but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses./
Bleaching cellulose, paper-pulp, flour, leather, fats and oils, textiles, beeswax; purification of water; taste and odor control of water; cleaning and detanning leather; manufacture of chloride salts; oxidizing agent; bactericide, antiseptic and deodorizer.
The agricultural premises and equipment uses include the disinfection of hard surfaces and equipment (such as hatching facilities and mushroom houses) and water systems (such as chiller water and humidification water in poultry houses).
Commercial, industrial, and medical uses include disinfection of ventilation systems, hard surfaces (e.g., floors, walls, and laboratory equipment), water systems, pulp/paper mills, and food rinses.
U.S. Production
2023: 850,000,000 - <1,000,000,000 lb
(1970) 79x10+3 metric tons
(1975) 81x10+3 metric tons
(1980) 146x10+3 metric tons
(1985) 226x10+3 metric tons
For more U.S. Production (Complete) data for Chlorine dioxide (9 total), please visit the HSDB record page.
Methods of Manufacturing
... From chlorine and sodium chlorite; ... From potassium chlorate and sulfuric acid; ... By passing nitrogen dioxide through a column of sodium chlorate.
Usually made at point of consumption from sodium chlorate, sulfuric acid, and methanol or from sodium chlorate and sulfur dioxide. Concentration of gas is limited to 10% to reduce explosion hazard.
Its industrial production is based on the reduction of chlorate. Undesirable byproducts are chlorine and chloride. ... The basic reaction mechanism of chlorine dioxide formation is the same for all known processes. All processes use chlorate as the raw material; in all processes chlorine dioxide formation takes place in strong acidic solutions; and byproduct chloride is found in all generator solutions
Reaction of sodium chlorate and sulfuric acid with sulfur dioxide or reaction of chloric acid with methanol
Formulations/Preparations
Soluble concentrates and ready-to-use liquid solutions.
Grade: Sold as hydrate in frozen form.
Alcide is a germicidal prepn which has been shown to kill a wide range of common pathogenic bacteria as well as fungi, in vitro. It contains sodium chlorite and lactic acid as the active ingredients. The 2 parts are combined in equal vol immediately prior to application resulting in the formation of chlorine dioxide.
AFCO QX (Alex C. Fergusson LLC): Active ingredient: chlorine dioxide 0.2%; alkyl* dimethyl benzyl ammonium chloride *(50%C14, 40%C12, 10%C16) 0.099%; 1-decanaminium, N-decyl-N,N-dimethyl-, chloride 0.045%; 1-decanaminium, N,N-dimethyl-N-octyl-, chloride 0.074%; and 1-octanaminium, N,N-dimethyl-N-octyl-, chloride 0.03%.
For more Formulations/Preparations (Complete) data for Chlorine dioxide (24 total), please visit the HSDB record page.
Use Classification
Food Additives -> FLOUR_TREATMENT_AGENT -> JECFA Functional Classes
Food Additives -> FLOUR_TREATMENT_AGENT -> JECFA Functional Classes
Food Additives -> FLOUR_TREATMENT_AGENT -> JECFA Functional Classes
General Manufacturing Information
Agriculture, Forestry, Fishing and Hunting
Chlorine oxide (ClO2): ACTIVE
The major chlorine dioxide by-products of concern are chlorite and chlorate. Chlorine dioxide reacts generally as an electron acceptor, and hydrogen atoms present in activated organic C-H or N-H structures are thereby not substituted by chlorine. Moreover, in contrast to chlorine, chlorine dioxide's efficiency for disinfection does not vary with pH or in the presence of ammonia, and it does not oxidize bromide. As opposed to chlorine, which reacts via oxidation and electrophilic substitution, chlorine dioxide reacts only by oxidation; this explains why it does not produce organochlorine compounds. In addition to this, chlorine dioxide is more selective in typical water treatment applications, as evidenced by its somewhat lower disinfectant demand as compared with chlorine.
Because of its nature, chlorine dioxide must be produced at the place of use, for which several different technologies exist, each having special features.
应用领域
简介稳定性二氧化氯CLO2是一种广谱、高效、无毒的新型杀菌消毒剂,在诸多领域中已得到广泛应用。与氯相比,其杀生能力要高3~5倍,并且其杀生效果基本不受pH值的影响,具有持续的抑菌效果。它安全、无毒,对人体无副作用,处理过的水无异味,不含致癌物,是国际上公认的氯系消毒剂的最理想的替代产品。
用途二氧化氯作杀菌剂,可用于鱼类的加工过程,用量为0.05g/kg(水溶液);在蔬、果的保鲜中用量为0.01%。
用途用于工业水处理,作杀菌消毒剂。亦可作纸浆和纤维的漂白,面粉、油脂、食糖的精练,皮革的脱毛等。
用途稳定性二氧化氯是新型消毒剂,用于循环水系统,能杀灭水中的微生物、原虫和藻类,并能清除水中的亚硝酸根。用于珍珠养殖业的消毒杀菌。用含20×10-6稳定性二氧化氯的冰块处理对虾,使对虾不会变黑,保鲜效果好。生菜、黄泥螺经其浸泡消毒处理,达到无菌。可用于餐具消毒,冰箱除臭,隐形眼镜片消毒,米糠油净化,汽车除臭消毒。在食品饮料,医院和医药工业中有广泛应用。国外利用载体将稳定性二氧化氯液体制成固体、胶体、颗粒、微胶囊化粉体和缓释型固体,再配以其他辅料。日本已开发了二氧化氯杀菌洗涤剂。
用途用于石油化工厂、合成氨厂和炼油厂等的循环冷却水、宾馆空调冷却水系统的杀菌、灭藻及粘泥剥离
制备方法
生产方法稳定性二氧化氯的生产,由于生产工艺和选用原料不同,有许多方法。大体上都是首先制备较高纯度的二氧化氯,然后把二氧化氯吸收到含稳定剂的水溶液中,生成稳定性二氧化氯水溶液。近年来,美国和日本等相继开发了固体二氧化氯。硫酸-氯酸钠法将氯酸钠和氯化钠的摩尔比为1:1.05的混合水溶液加入反应器,再加入98%硫酸,于35℃下进行反应,生成的二氧化氯和氯气,由通入空气驱出。把反应生成的二氧化氯和氯气的混合气体送入二氧化氯吸收塔,用含稳定剂的水溶液对流吸收,生成稳定性二氧化氯水溶液。其NaC1O3+NaCl+H2SO4→C1O2+0.5C12+Na2SO4+H2O未溶的氯气则进入氯气吸收塔,用碱液吸收生成次氯酸钠。盐酸一亚氯酸钠法将亚氯酸钠溶解于水中配成适当浓度的溶液加入反应器中,把盐酸按适当配料比在搅拌下加入反应器中进行反应,生成的二氧化氯气体,由通入空气驱出。把生成的二氧化氯气体送人二氧化氯吸收塔,用含稳定剂的水溶液对流吸收,生成稳定性二氧化氯水溶液。其NaC1O2+HCl→C1O2+NaC1+0.5H2吸附法用硅酸钙、分子筛、硅胶等多孔性物质作为吸附剂,吸附溶液中的二氧化氯后变成固体二氧化氯。
生产方法新马蒂逊法 将氯酸钠溶液(600 g/L)与硫酸(95%~98%)连续定量地从液面下送入反应器。经空气稀释后的5%~8%二氯化硫气体通过气体分布板进入反应器。为了提高收率,一般用两个反应器,第一个反应器温度30~40℃,氯酸钠含量20~22g/L,硫酸9.0mol/L,氯化钠5~6/L,第二个反应器温度40~45℃,氯酸钠含量2g/L,硫酸9.3mol/L,氯化钠7g/L。反应器产生的气体进入洗气器,用氯酸钠液洗去气体中夹带的硫酸、盐酸及未反应的二氧化硫后,进入吸收塔用冷水吸收,制成6~8g/L的二氧化氯水溶液。 将氯酸钠和氯化钠的混合水溶液按1︰1.05的摩尔比送入反应器,加硫酸(98%)在35~55℃下进行还原反应,
生产方法以氨酸盐为原料,在酸性介质中还原制得二氧化氯,由于还原剂的不同,又可分为:二氧化硫法,其中有新马蒂逊法,新大曹法;盐酸法,其中有开斯汀法;食盐法,其中有R2法、R3(SVP法)。目前工业生产应用较多的方法有新马蒂逊法,R2法、R3法、开斯汀法。R8法是80年代中期开发的新方法。1.新马蒂逊法 将600g/L氯酸钠溶液与95%~98%硫酸连续定量地送入反应器,经空气稀释的5%~8%二氧化硫气体通过气体分布板进入反应器。反应器有两个,第一反应器于30~40℃进行反应,而反应大部分在此完成,使用第二反应器可提高氯酸钠的利用率。反应器产生的气体送到洗气器中,二氧化氯气体送入吸收塔用冷水吸收,制成6~8g/L二氧化氯水溶液。第二反应器溢流出的废液进入气提塔,从塔底通入少量空气,以提出溶解在溶液中的二氧化氯,气体通过洗气塔进入二氧化氯吸收塔,用冷水吸收,制成二氧化氯水溶液。从气提塔排出废液可回收利用。其反应式如下: 2Na2ClO3+SO2+H2SO4 → 2ClO2+2Na2SO4十H22.开斯汀法 用盐酸还原氯酸钠制得二氧化氯和氯化钠,把氯化钠再电解制成氯酸钠。从电解槽出来的溶液含氯酸钠360~400g/L,氯化钠8O~100g/L,与32%盐酸同时加入第一反应器,溢流通过至第六反应器,反应器温度分别为20、40、60、80、100、103℃,使盐酸与氯酸钠充分反应。从最后第三个反应器通入空气,搅拌反应溶液,并稀释反应生成的二氧化氯气体,经二氧化氯吸收塔用冷水吸收生成二氧化氯水溶液。未被吸收的氯气用碱液吸收,制成次氯酸钠溶液。其反应式如下: NaC1O3+2HC1→ClO2+0.5Cl2+NaCl+H2O3.R2法 将氯酸钠和氧化销的摩尔比为1:1.05的混合水溶液加入反应器,再加入98%硫酸,于35~55℃进行反应,生成的二氧化氯和氢气由通入空气驱出。把反应生成的二氧化氯和氢气的混合气体进入二氧化氯吸收塔,用水对流吸收,生成二氧化氯水溶液,而来溶的氯气则进入氯气吸收塔,用碱液吸收生成次氯酸钠。其反应式如下: NaC1O3十NaCl十H2SO4 → ClO2十0.5Cl2十Na2SO4十H2O气提塔排出的废液,含有芒硝和硫酸,可供牛皮纸浆生产之用。4.R3法 该法生产二氧化氯的反应与R2法基本相同。其关键是独特的二氧化氯发生器,它在减压时可得到浓度为36%的产品。在普通常压法中这样的浓度会爆炸。把发生器底部流出的反应生成液中的硫酸钠晶体淤浆与氯酸钠和氯化钠混合进料,再煮沸,与硫酸进一步混合,从顶部进入发生器。反应产生的二氧化氯和氯气被少量空气稀释后,一起流入冷凝器,经冷却后进入吸收塔。生成二氧化氯溶液含ClO2 8g/L。其反应式如下: NaC1O3十NaCl十H2SO4 → ClO2十0.5Cl2十Na2SO4十H2O为了防止爆炸,整个系统压力维持在26.66~39.99kPa的低压,这样就保持混合物的稳定性。5.R8法 该法与R3法基本相同,使用甲醇作为还原剂生产二氧化氯,副产的芒硝产量比法R3要少。把原料工业氯酸钠。发烟硫酸、甲醇和氯化钠在特制容器(反应——蒸发——结晶为一体的单元反应器)二氧化氯发生器中,当系统温度(70+4)℃,在13.32kPa减压下,反应介质酸度控制4~5mol,氯酸钠与甲醇摩尔比约4:1时,反应产生的二氧化氯,流入冷凝器,经冷却后进入二氧化氯吸收塔,生成二氧化氯溶液含ClO2 8~10g/L。其反应式如下: 4NaCl+4H2SO4+CH3OH → 4ClO2+4NaHSO4+HCOOH+3H2O消耗定额(t/t) 新马蒂逊法 开斯汀法 R2法 R3法 R8法氯酸钠(NaCIO398.5%) 1.65~1.7 1.63 1.17 1.57~1.66 1.64硫酸(H2SO498%) 1.38~2.5 - 4.8~5.5 1.6~1.7 1盐酸(HCl 100%计) - 1.5 - - -二氧化硫(SO299.7%) 0.54~0.64 - - - -氯化钠(NaCl 90%) 0.09~0.34 - 0.95 0.95 -甲醇(HCOOH) - - - - 0.19
生产方法ClO2的生产方法很多,这里仅介绍硫酸法。即在硫酸介质中用SO2还原氯酸钠可生成二氧化氯气体:2NaClO3+SO2→2ClO2+Na2SO4将氯酸钠溶液(600g/L)与硫酸(95%~98%)连续定量地从液面下加入第一反应器,经空气稀释后的5%~8%的SO2气体分别通人第一和第二反应器。反应大部分在第一反应器内进行,温度30~40℃,氯酸钠浓度20~22g/L,硫酸9.0g/L,氯化钠5~6g/L。第一反应器溢流出的反应尚含有少量的氯酸钠,在第二反应器内与SO2充分反应,温度40~45℃,氯酸钠浓度2g/L,硫酸9.3g/L,氯化钠7g/L。第二反应器溢流出的废液进入气提塔,用少量空气气提回收溶解在废液中的二氧化氯。废液可回收硫酸钠等副产物。气提气体返回第二反应器,第二反应器生成的二氧化氯和未反应的SO2返回第一反应器。第一反应器产生的气体进入洗气塔,氯酸钠溶液从洗气塔上部,除去二氧化氯气体中夹带的硫酸、盐酸和未反应的SO2后进入第一反应器。二氧化氯气体送吸收塔用冷水吸收,制成6~8g/L的二氧化氯溶液。
生产方法以氯酸盐为原料,在酸性介质中还原制得二氧化氯,由于还原剂的不同,又可分为:1.二氧化硫法,其中有新马蒂逊法、新大曹法;2.盐酸法,其中有开斯汀法;3.食盐法,其中有R2法、R3法(SVP法)。目前工业生产应用较多的方法有新马蒂逊法,R2法、R3法、开斯汀法。R8法是80年代中期开发的新方法。新马蒂逊法 将含600 g/L氯酸钠溶液与95%~98%硫酸连续定量地送入反应器,经空气稀释的5%~8%二氧化硫气体通过气体分布板进入反应器。反应器有两个,第一反应器于30~40℃进行反应,而反应大部分在此完成,使用第二反应器可以提高氯酸钠的利用率。反应器产生的气体送到洗气器中,二氧化氯气体送入吸收塔用冷水吸收,制成6~8 g/L二氧化氯水溶液。第二反应器溢流出的废液进入气提塔,从塔底通入少量空气,以提出溶解在溶液中的二氧化氯,气体通过洗气塔进入二氧化氯吸收塔,用冷水吸收,制成二氧化氯水溶液。从气提塔排出废液可回收利用。其2Na2C1O3+SO2+H2SO4→2C1O2+2Na2SO4+H2开斯汀法用盐酸还原氯酸钠制得二氧化氯和氯化钠,把氯化钠再电解制成氯酸钠。从电解槽出来的溶液含氯酸钠360~400g/L,氯化钠80~100 g/L,与32%盐酸同时加入第一反应器,溢流通过至第六反应器,反应器温度分别为20、40、60、80、100、103℃,使盐酸与氯酸钠充分反应。从最后第三个反应器通人空气,搅拌反应溶液,并稀释反应生成的二氧化氯气体,经二氧化氯吸收塔用冷水吸收生成二氧化氯水溶液。未被吸收的氯气用碱液吸收,制成次氯酸钠溶液。其NaC1O3+2HCl→C1O2+0.5C12+NaCl+H2OR2法将氯酸钠和氯化钠的摩尔比为1:1.05的混合水溶液加入反应器,再加入98%硫酸,于35~55℃进行反应,生成的二氧化氯和氯气由通入空气驱出。把反应生成的二氧化氯和氯气的混合气体进入二氧化氯吸收塔,用水对流吸收,生成二氧化氯水溶液,而未溶的氯气则进入氯气吸收塔,用碱液吸收生成次氯酸钠。其NaClO3+NaCl+H2SO4→C1O2+0.5C12+Na2SO4+H2O气提塔排出的废液,含有芒硝和硫酸,可供牛皮纸浆生产之用。R3法本法生产二氧化氯的反应与R2法基本相同。其关键是独特的二氧化氯发生器,它在减压时可得到浓度为36%的产品。在普通常压法中这样的浓度会爆炸。把发生器底部流出的反应生成液中的硫酸钠晶体淤浆与氯酸钠和氯化钠混合进料,再煮沸,与硫酸进一步混合,从顶部送入发生器。反应产生的二氧化氯和氯气被少量空气稀释后,一起流入冷凝器,经冷却后进人吸收塔。生成二氧化氯溶液含C1O2 8g/L。其NaC1O3+NaCl+H2SO4→C1O2+0.5C12+Na2SO4+H2O为了防止爆炸,整个系统压力维持在26.66~39.99 kPa的低压,这样就保持混合物的稳定性。R8法本法与R3法基本相同,使用甲醇作为还原剂生产二氧化氯,副产的芒硝产量比R3法要少。把原料工业氯酸钠、发烟硫酸、甲醇和氯化钠在特制容器(反应——蒸发——结晶为一体的单元反应器)二氧化氯发生器中,当系统温度(70±4)℃,在13.32 kPa减压下,反应介质酸度控制4~5 mol,氯酸钠与甲醇摩尔比约4:l时,反应产生的二氧化氯,流人冷凝器,经冷却后进入二氧化氯吸收塔,生成二氧化氯溶液含C1O2 8~10 g/L。其4NaC1O3+4H2SO4+CH3OH→4C1O2+4NaHSO4+HCOOH+3H2O
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