National Pollutant Inventory

Last updated

The National Pollutant Inventory (NPI) is a database of Australian pollution emissions managed by the Australian Commonwealth, State and Territory Governments. A condensed version of the information collected is available to the public via the NPI website www.npi.gov.au.

Contents

Emissions

The NPI records and makes publicly available the emissions from industrial facilities and diffuse sources of 93 different chemical substances to air, land and water.

Objectives

The objectives of the NPI are to:

Sources of data

Australian industrial facilities that use certain amounts of the 93 NPI substances must estimate and report their emissions directly to their state or territory environment agency annually. The state and territory environment agencies review all NPI reports for accuracy and forward the data to the Australian Government. The reports are then displayed on the NPI public website

Exemptions

The following industrial activities are exempt from the NPI's mandatory reporting requirements: [1]

During a review of the NPI undertaken in 2005, it was suggested that two industries have their exemptions lifted. They were aquaculture, and crematoria. Reasons given were for their discharges of nutrient to the sea, and mercury to the atmosphere respectively. In 2007, Environment Ministers voted against the lifting of the reporting exemption for aquaculture, despite the review receiving 12 submissions supporting the recommendation, and 5 opposing it.

Aquaculture in Spencer Gulf

This omission of the aquaculture industry from mandatory reporting is significant for Spencer Gulf, South Australia. In this region, southern bluefin tuna and yellowtail kingfish sea-cage aquaculture are the two largest industrial contributors of nitrogenous nutrient pollution to the marine environment. [2] The Spencer Gulf is particularly vulnerable to impacts because its water exchange with the ocean is constrained and the waters are naturally very low in nutrients by world standards. The existing marine communities have evolved to these unique circumstances, and are therefore particularly susceptible to changes in their environment. [3] Iconic marine species of the region include the giant Australian cuttlefish and the little penguin, both of which are in decline.

Substances reported

Related Research Articles

<span class="mw-page-title-main">Ester</span> Compound derived from an acid

In chemistry, an ester is a compound derived from an acid in which the hydrogen atom (H) of at least one acidic hydroxyl group of that acid is replaced by an organyl group. Analogues derived from oxygen replaced by other chalcogens belong to the ester category as well. According to some authors, organyl derivatives of acidic hydrogen of other acids are esters as well, but not according to the IUPAC.

<span class="mw-page-title-main">Petrochemical</span> Chemical product derived from petroleum

Petrochemicals are the chemical products obtained from petroleum by refining. Some chemical compounds made from petroleum are also obtained from other fossil fuels, such as coal or natural gas, or renewable sources such as maize, palm fruit or sugar cane.

<span class="mw-page-title-main">Butanone</span> Chemical compound

Butanone, also known as methyl ethyl ketone (MEK), is an organic compound with the formula CH3C(O)CH2CH3. This colourless liquid ketone has a sharp, sweet odor reminiscent of acetone. It is produced industrially on a large scale, but occurs in nature only in trace amounts. It is partially soluble in water, and is commonly used as an industrial solvent. It is an isomer of another solvent, tetrahydrofuran.

<span class="mw-page-title-main">Acrylic acid</span> Chemical compound

Acrylic acid (IUPAC: propenoic acid) is an organic compound with the formula CH2=CHCOOH. It is the simplest unsaturated carboxylic acid, consisting of a vinyl group connected directly to a carboxylic acid terminus. This colorless liquid has a characteristic acrid or tart smell. It is miscible with water, alcohols, ethers, and chloroform. More than a million tons are produced annually.

<span class="mw-page-title-main">Ethyl acetate</span> Organic compound (CH₃CO₂CH₂CH₃)

Ethyl acetate is the organic compound with the formula CH3CO2CH2CH3, simplified to C4H8O2. This colorless liquid has a characteristic sweet smell and is used in glues, nail polish removers, and in the decaffeination process of tea and coffee. Ethyl acetate is the ester of ethanol and acetic acid; it is manufactured on a large scale for use as a solvent.

Substances, mixtures and exposure circumstances in this list have been classified by the International Agency for Research on Cancer (IARC) as group 2B: The agent (mixture) is "possibly carcinogenic to humans". The exposure circumstance entails exposures that are possibly carcinogenic to humans. This category is used for agents, mixtures and exposure circumstances for which there is limited evidence of carcinogenicity in humans and less than sufficient evidence of carcinogenicity in experimental animals. It may also be used when there is inadequate evidence of carcinogenicity in humans but there is sufficient evidence of carcinogenicity in experimental animals. In some instances, an agent, mixture or exposure circumstance for which there is inadequate evidence of carcinogenicity in humans but limited evidence of carcinogenicity in experimental animals together with supporting evidence from other relevant data may be placed in this group. Further details can be found in the preamble to the IARC Monographs.

Substances, mixtures and exposure circumstances in this list have been classified by the International Agency for Research on Cancer (IARC) as group 3: The agent is not classifiable as to its carcinogenicity to humans. This category is used most commonly for agents, mixtures and exposure circumstances for which the evidence of carcinogenicity is inadequate in humans and inadequate or limited in experimental animals. Exceptionally, agents (mixtures) for which the evidence of carcinogenicity is inadequate in humans but sufficient in experimental animals may be placed in this category when there is strong evidence that the mechanism of carcinogenicity in experimental animals does not operate in humans. Agents, mixtures and exposure circumstances that do not fall into any other group are also placed in this category.

<span class="mw-page-title-main">Methyl isobutyl ketone</span> Chemical compound

Methyl isobutyl ketone (MIBK) is the common name for the organic compound 4-methylpentan-2-one, condensed chemical formula (CH3)2CHCH2C(O)CH3. This colourless liquid, a ketone, is used as a solvent for gums, resins, paints, varnishes, lacquers, and nitrocellulose.

Glycol ethers are a class of chemical compounds consisting of alkyl ethers that are based on glycols such as ethylene glycol or propylene glycol. They are commonly used as solvents in paints and cleaners. They have good solvent properties while having higher boiling points than the lower-molecular-weight ethers and alcohols.

This is the list of extremely hazardous substances defined in Section 302 of the U.S. Emergency Planning and Community Right-to-Know Act. The list can be found as an appendix to 40 C.F.R. 355. Updates as of 2006 can be seen on the Federal Register, 71 FR 47121.

<span class="mw-page-title-main">2-Ethoxyethanol</span> Chemical compound

2-Ethoxyethanol, also known by the trademark Cellosolve or ethyl cellosolve, is a solvent used widely in commercial and industrial applications. It is a clear, colorless, nearly odorless liquid that is miscible with water, ethanol, diethyl ether, acetone, and ethyl acetate.

<span class="mw-page-title-main">2-Methoxyethanol</span> Chemical compound

2-Methoxyethanol, or methyl cellosolve, is an organic compound with formula C
3
H
8
O
2
that is used mainly as a solvent. It is a clear, colorless liquid with an ether-like odor. It is in a class of solvents known as glycol ethers which are notable for their ability to dissolve a variety of different types of chemical compounds and for their miscibility with water and other solvents. It can be formed by the nucleophilic attack of methanol on protonated ethylene oxide followed by proton transfer:

<span class="mw-page-title-main">Dimethyl carbonate</span> Chemical compound

Dimethyl carbonate (DMC) is an organic compound with the formula OC(OCH3)2. It is a colourless, flammable liquid. It is classified as a carbonate ester. This compound has found use as a methylating agent and more recently as a solvent that is exempt from the restrictions placed on most volatile organic compounds (VOCs) in the United States. Dimethyl carbonate is often considered to be a green reagent.

<span class="mw-page-title-main">Ethyl acrylate</span> Chemical compound

Ethyl acrylate is an organic compound with the formula CH2CHCO2CH2CH3. It is the ethyl ester of acrylic acid. It is a colourless liquid with a characteristic acrid odor. It is mainly produced for paints, textiles, and non-woven fibers. It is also a reagent in the synthesis of various pharmaceutical intermediates.

A pollutant release and transfer register (PRTR) is a system for collecting and disseminating information about environmental releases and transfers of hazardous substances from industrial and other facilities.

<span class="mw-page-title-main">Acetic acid</span> Colorless and faint organic acid found in vinegar

Acetic acid, systematically named ethanoic acid, is an acidic, colourless liquid and organic compound with the chemical formula CH3COOH. Vinegar is at least 4% acetic acid by volume, making acetic acid the main component of vinegar apart from water and other trace elements.

Radical theory is an obsolete scientific theory in chemistry describing the structure of organic compounds. The theory was pioneered by Justus von Liebig, Friedrich Wöhler and Auguste Laurent around 1830 and is not related to the modern understanding of free radicals. In this theory, organic compounds were thought to exist as combinations of radicals that could be exchanged in chemical reactions just as chemical elements could be interchanged in inorganic compounds.

<span class="mw-page-title-main">Biological oxidizer</span>

A biological oxidizer is a device that uses micro-organisms to treat wastewater and the volatile organic compounds produced by commercial and industrial operations. Biological oxidation devices convert biodegradable organic compounds into carbon dioxide and water. This is a natural occurring process which differs from traditional chemical and thermal oxidizing agents and methods. Some of the more commonly used micro-organisms are heterotrophic bacteria, which play an important role in biological degradation processes. Generally, these micro-organisms are rod shaped and facultative. Biological oxidizers provide a stable environment which allows bacteria to naturally oxidize and stabilize a large number of organics in a more efficient manner. Some of the emissions that may be treated biologically include:

2-Ethoxyethyl acetate is an organic compound with the formula CH3CH2OCH2CH2O2CCH3. It is the ester of ethoxyethanol and acetic acid. A colorless liquid, it is partially soluble in water.

References

  1. NPI data | National Pollution Inventory Australian Government, Department of Environment, Australia. Accessed 2014-03-23
  2. "Chapter 13 - Coastal Processes and Water Quality - Spencer Gulf Port Link Bulk Commodies Export Facility Environmental Impact Statement" Archived 2014-01-27 at the Wayback Machine Spencer Gulf Port Link, South Australia (2013). Accessed 2014-03-23.
  3. Draft Spencer Gulf Marine Plan. Coast and Marine Conservation Branch, Natural and Cultural Heritage, Department for Environment and Heritage, Government of South Australia, Adelaide (2006). ISBN   0 7590 1081 1