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KINGDOM OF CAMBODIA NATION RELIGION KING 323 POLLUTANT RELEASE ESTIMATION TECHNIQUE MANUAL FOR BEER PRODUCTION Supported by: United Nation Institute for Training and Research (UNITAR) Prepared by: PRTR Project Management Unit Department of Hazardous Substance Management General Directorate of Environmental Protection Ministry of Environment

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Page 1: BEER PRODUCTION - prtrcambodiamoe.gov.kh · 23 Zinc sulfate Production Line Brewing Process 4. Production Process 4.1. Raw Materials In general, there are 5 main raw materials in

KINGDOM OF CAMBODIA

NATION RELIGION KING

323

POLLUTANT RELEASE ESTIMATION TECHNIQUE

MANUAL

FOR

BEER PRODUCTION

Supported by:

United Nation Institute for Training and Research

(UNITAR)

Prepared by:

PRTR Project Management Unit

Department of Hazardous Substance Management

General Directorate of Environmental Protection

Ministry of Environment

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Table of Content

List of Table .............................................................................................................................................. - 1 - List of Figure ............................................................................................................................................ - 1 - List of Equation ........................................................................................................................................ - 2 - List of Abbreviation.................................................................................................................................. - 2 - 1. Introduction....................................................................................................................................... - 3 - 2. Benefits of Using PRTR System ....................................................................................................... - 3 -

2.1. Benefit to Government ............................................................................................................. - 3 - 2.2. Benefit to Industry .................................................................................................................... - 3 - 2.3. Benefit to the Public ................................................................................................................. - 4 -

3. Target of the Manual ......................................................................................................................... - 4 - 3.1. Reporting Threshold and Emission .......................................................................................... - 4 -

4. Production Process ............................................................................................................................ - 5 - 4.1. Raw Materials........................................................................................................................... - 5 - 4.2. General Process of Beer Production ......................................................................................... - 5 -

5. Emission and Transfer of Chemicals and Pollutants......................................................................... - 6 - 5.1. Emission to Air ......................................................................................................................... - 6 -

4.1.1 . Emission from Fugitive Source/Non-Point Source ................................................................ - 6 - 4.1.2 . Emission from Point Source ................................................................................................... - 6 -

5.2. Emission to Water ..................................................................................................................... - 7 - 5.3. Emission to Land ...................................................................................................................... - 8 - 5.4. Transfer in Waste ...................................................................................................................... - 8 - 5.5. Transfer to Sewage ................................................................................................................... - 8 -

6. Emission and Transfer Estimation Techniques ................................................................................. - 8 - 6.1. Direct Measurement ................................................................................................................. - 8 -

6.1.1. Sampling Data .................................................................................................................. - 8 - 6.1.2. Continuous Emission Monitoring System (CEMS) Data ................................................ - 10 -

6.2. Mass Balance .......................................................................................................................... - 12 - 6.2.1. Overall Facility Mass Balance ....................................................................................... - 12 - 6.2.2. Individual Unit Process Mass Balance .......................................................................... - 14 -

6.3. Emission Factors .................................................................................................................... - 14 - 6.3.1. Industry-Wide Emission Factors .................................................................................... - 14 - 6.3.2. Predictive Emission Monitoring (PEM) ......................................................................... - 15 -

6.4. Engineering Calculations ....................................................................................................... - 15 - 6.4.1. Fuel Analysis .................................................................................................................. - 15 -

6.5. Alternative Emission Estimation Technique for Ethanol Emissions ...................................... - 16 - 7. Reporting ........................................................................................................................................ - 16 - Reference ................................................................................................................................................ - 17 -

List of Table

Table 1: List of the potential chemicals and pollutants from beer production. ........................................ - 4 - Table 2: List of typical air pollutants from beer production .................................................................... - 6 - Table 3: List of the main wastewater pollutants from beer production. ................................................... - 7 - Table 4: Stack Sample Test ....................................................................................................................... - 8 - Table 5: CEMS data output for three periods for hypothetical furnace ................................................. - 11 - Table 6: Emission factors for ethanol emissions from beer brewing ..................................................... - 15 -

List of Figure

Figure 1: Typical process of beer production .......................................................................................... - 6 -

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List of Equation

Equation 1: Calculation of PM concentration ........................................................................................ - 9 - Equation 2: Calculation of Emission of PM ............................................................................................ - 9 - Equation 3: Calculation of emission of PM............................................................................................. - 9 - Equation 4: Calculation of moisture percentage ..................................................................................... - 9 - Equation 5: Calculation of pollutant emission ...................................................................................... - 11 - Equation 6: Calculation of annual emission ......................................................................................... - 11 - Equation 7: Calculation of emission of pollutant per tons of product ................................................... - 11 - Equation 8: Calculation of incoming material used in the process ....................................................... - 13 - Equation 9: Calculation of flow rate of component .............................................................................. - 14 - Equation 10: Calculation of emission rate of pollutant ........................................................................ - 14 - Equation 11: Calculation of emission of pollutant ................................................................................ - 15 -

List of Abbreviation

- BOD Biochemical Oxygen Demand

- CAS Chemical Abstracts Service

- CASRN Chemical Abstracts Service Registry Numbers

- CEMS Continuous Emissions Monitoring System

- CMC Carboxymethyl cellulose

- CO Carbon Monoxide

- COD Chemical Oxygen Demand

- DO Dissolve Oxygen

- EET Emission Estimation Technique

- EFR Emission Factor Rating

- g Grams

- Kg Kilograms

- m3 Cubic meters

- MoE Ministry of Environment

- NO2 Nitrogen Oxide

- oC Celsius

- PEM Predictive Emission Monitoring

- PM Particulate Matter

- PM10 Particulate Matters < 10 micrometer

- PRTR Pollutants Release and Transfer Register

- PVA Polyvinyl alcohol

- SO2 Sulfur Dioxide

- t Tons

- TN Total Nitrogen

- TP Total Phosphorous

- TSP Total Suspended Particulate

- TSS Total Suspended Solids

- VOCs Volatile Organic Coumpounds

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1. Introduction

A Pollutant Release and Transfer Register (PRTR) is a catalogue or register of potentially harmful

pollutant releases or transfers to the environment from a variety of sources. A PRTR includes information

about releases or transfers to air, water and soil as well as about wastes transported to treatment and disposal

sites. The development and implementation of a PRTR system adapted to national needs represents a means

for governments to track generation, release and the fate of various pollutants over time.

A PRTR can be an important tool in the total environment policy of a government providing

information about the pollution burden that would be otherwise difficult to obtain, encouraging reporters

to reduce pollution, and engendering broad public support for government environmental policies. Indeed,

governments may wish to set forth long-term national environmental goals to promote sustainable

development and then use PRTR as an important tool to examine objectively how well these goals are being

met.

This Emission Estimation Technique (EET) Manual aims to assist Cambodia manufacturing,

industrial and service facilities to report the emissions of listed substances from their facilities to Ministry

of Environment (MoE). Please refer to main book on “Basic Release estimation technique manual under

Pollutant release and transfer register (PRTR) system” to understand about the procedure of

determining business and substances required for notification. However, this Manual describes the

procedures and recommended approaches for estimating emissions from facilities engaged in Beer

Production manufacturing.

2. Benefits of Using PRTR System

The following are some of the possible used and benefits of implementing PRTR system from the

perspective of three main stakeholders such as: Government, Industry, and the public:

2.1. Benefit to Government

PRTR will provide comprehensive information to assist the government in addressing some issue as

following:

Identifying industries or facilities which are generating potentially harmful chemical release in

to the environment;

Providing information on pollutants being release and how much is being release and over what

time period;

Identifying geographic area of pollutants being release and how much of each substance is going

to air, water and land

Pointing out the geographic distribution of pollutant emission

Monitoring enforcement of current regulation

Providing inventory data that related to chemical substance and environmental Pollution issues

for measuring national progress toward risk reduction and pollution prevention goal and

Reducing monitoring work and government expending while large waste is decrease

PRTR system will obtain enough information regarding to chemical substances, and pollutants for

the government to identify the future workplan or determine priority action plans to prevent and reduce

pollution as well as any possible serve impact to human health and environment. In additional to this, PRTR

system will also help reduce government national budget’s expenditure on monitoring and inspecting work

as well.

2.2. Benefit to Industry

The private sector, such as factories and industries, may wrongly believe that PRTR reporting of

chemicals substance use, waste generation and emission will be a burden. The experiences from PRTR

implementing from private sector of other countries show that PRTR is the very vital tool in providing key

information for their trade implementing as below:

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Providing information regarding to efficiency level of raw material and other resources

consumption in the production such as chemical substance consumption, water consumption,

electricity, fuel, and so on.

Identifying the loss of raw materials and resources during the production process from leaking

or any utility’s error.

Identifying types and quantity of waste from the production

Identifying the types of pollutant release and emission to the environment

Monitoring production flow from raw material until the semi-final product or final product in

order to understand whether there is any technical problem or not

Providing the data regarding to the loss of raw materials or the other resource during the

production process.

In short, all participants in PRTR system from private sector including companies, and factories will

receive information regarding to management process of production, raw materials, and waste, which will

help them improve their waste management status and reduce any risk in their facility that could be able to

decrease company’s expenditure and increase their production efficiency.

2.3. Benefit to the Public

Regarding to the principle of agenda 21 stating that “communities and workers have right to access

information on chemical risks and have its origin in a straightforward notion” means that those who are

potentially exposed to risks from chemical are entitle to known about these risks so they can make informed

choices and take appropriate actions. Thus, PRTR is the significant tool for ensuring community and

workers can access information.

Moreover, PRTR data is very useful in helping public access all kinds of information, which relevant

to harmful environmental impacts like chemical or hazard waste disposal so that the public will able to

participate in making decision with government in order to reach to pollution prevention, as well as, to

reduce the harmful health effect to the human as well.

3. Target of the Manual

This manual aims to:

Provide procedures to enable users to compile emission database that meet quality criteria for

transparency, consistency, completeness

Provide estimation methods and emission factors for database compiler

3.1. Reporting Threshold and Emission

The list of all types of pollutants and chemicals released and transferred into the environment that

the production establishment oblige to report can be found in the Table 3 and Table 4 in Section 5.3 of

Basic Release Estimation Technique Manual or in the Annex 2 and Annex 3 of the Sub-Decree on

Management of Pollutant Release and Transfer Register.

Table 1: List of the potential chemicals and pollutants from beer production.

No Parameter Source of Emission How it happens

1 (Particulate Matter)-

PM

Raw Material Storage,

Crushing

Raw material Preparation,

Crushing

2 Acetone Laboratory Discharge of wastewater from

the laboratory

3 Acrylamide Laboratory Discharge of wastewater from

the laboratory

4 Arsenic & compounds Boiler/Waste Storage, Water

Treatment Plant/ Wastewater

Treatment Plant

Combustion/Solid Waste

Burning, Water

Treatment/Discharge from the

production line

5 BOD5 Wastewater Treatment Plant Discharge of wastewater from

the production line/Toilet

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6 Calcium chloride Production Line Brewing Process

7 CH4 Wastewater Treatment Plant

Fermentation Stage

Fermentation of organic

8 Chloride Water Treatment Plant Discharge of wastewater from

water treatment plant

9 CO Boiler Combustion

10 CODcr Wastewater Treatment Plant Discharge of wastewater from

the production line/Toilet

11 Ethanol Fermentation stage Fermentation of organic

12 Ethyl Acetate Fermentation stage Fermentation of organic

13 Mercury & compounds Boiler/Waste Storage Combustion/Solid Waste

Burning

14 NH3 Wastewater Treatment Plant Discharge from the production

line/Toilet

15 NOx Boiler Combustion/Solid Waste

Burning

16 Oil and Grease Wastewater Treatment Plant,

Fuel Storage

Discharge of wastewater from

the production line/Toilet

17 Phosphoric Acid Water Treatment Plant/

Sanitation process

Discharge of wastewater

18 Polychlorinated

Dioxins & Furan

Boiler/Waste Storage Combustion/Solid Waste

Burning

19 SO2 Boiler Combustion/Solid Waste

Burning

20 Sodium hydroxide Wastewater Treatment Plant Waste Water Process

21 Sulfuric Acid Sanitation process/cleaning agent Discharge of wastewater

22 VOC Fermentation stage Fermentation of organic

23 Zinc sulfate Production Line Brewing Process

4. Production Process

4.1. Raw Materials

In general, there are 5 main raw materials in the beer production such as rice, malt, yeast, hop, and

water. In addition to this, there are a few other chemicals found in the other processes rather the production

as well. Those typical chemicals are Acetone, Acrylamide, Cadmium and its compounds, Ethanol,

Methanol, Nitric Acid, Phenol, Phosphoric Acid, Sulfuric Acid (H2SO4), Calcium Chloride (CaCl2),

Phosphoric Acid (H3PO4), Zinc Sulfate (ZnSO4), Calcium sulfate (CaSO4), Sodium hydroxide (NaOH).

4.2. General Process of Beer Production

In general, the beer production process for commercial purpose consists of 11 stages as following:

(1). The dirt from the malt and rice is removed during the air conveying system into crushing

process. (2). The starch (of malt and rice) from above process will be put in the Mash cupper and add more

treated water in. The temperature of the starch solution will be increased by the heat from the

boiler until it reaches boiling temperature. CaCl2 and H3PO4 will be added during the boiling

process in order to break drown the big protein and glucose molecule into the smaller pieces. (3). After the heating process, the output from that will be transferred into Mash Tun by storing it

in an exact temperature in order to turn amino acids into glucose. (4). Then it will be transferred to Mash filter in order to remove the spent grain from the solution,

and the output of this process is called “wort” (5). Wort will be carried into Wort cupper where it will be boiled by using the steam power and

adding CaCl2 and H3PO4 in order to adjust the pH and then put Hop into cupper to get the smell

and bitter taste of beer. (6). The amount of wort mixed with hop will be sent to Whirlpool tank that has a centripetal force

that cause solid particles suspended in a rotating mass of liquid to migrate to the center of the

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bottom of the vessel in a cone-shaped mass. In the stage, ZnSO4 will be added in order to make

solid protein-based particles, and hop fragment-containing sediment, called Trub. The trub must

be removed before sending to the next stage. (7). After 1 hour of boiling, the clear hot wort will be sent pass through a cooling system, and clean

air (dried, no oil, no batteries), and yeast (Saccharomyces Carlsbergbensis Var Uvarum) will be

added and keep the mixture of it into the storage tanks. (8). After 3 weeks, wort will be transferred to alcohol and CO by the yeast in the Fermentation Tank

and Storage tank. (9). After that, it will be sent to Beer Filter tanks in order remove yeast and other sediments to get

bright beers.

(10). The bright beers will be carried out to packaging lines.

(11). The bright beers will be packed into cans, bottles, and kegs to be the final beer products.

Figure 1: Typical process of beer production

5. Emission and Transfer of Chemicals and Pollutants

5.1. Emission to Air

4.1.1. Emission from Fugitive Source/Non-Point Source

Not all pollution is emitted from the factory chimney, or boiler. The emission from fugitive source

mostly releases from the production building, waste storage, and chemical storage warehouse where

possibly an incident of chemical or pollutant leak or spill out happen. The emission from this kind of source

seem to be difficult to identify the exact amount of pollutant released into the atmosphere.

4.1.2. Emission from Point Source

Unlike the pollution from fugitive source, the emission from non-point source refers to the emission

of pollutant from the specific sources such as factory chimney, boiler and so on. The main pollutants from

the beer production are following:

Table 2: List of typical air pollutants from beer production

No Parameter Source of Emission How it happens

1 Ethanol Fermentation stage Fermentation of organic

Malt and rice Crushing Dirt/waste

Water Mash Cupper

Boiler Mash TUN

Air emission Mash Filter Spent grain

Hop Wort Cupper

ZnSO4 Whirlpool Trub

Coolant Wort cooler Yeast

Coolant Ferment storage Spent yeast

Beer filterWastewater

Treatment Plant

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2 Ethyl Acetate Fermentation stage Fermentation of organic

3 VOC Fermentation stage Fermentation of organic

4 CO Boiler Combustion

5 CH4 Wastewater Treatment Plant

Fermentation Stage

Fermentation of organic

6 SO2 Boiler Combustion/Solid Waste

Burning

7 NOx Boiler Combustion/Solid Waste

Burning

8 Arsenic & compounds Boiler/Waste Storage Combustion/Solid Waste

Burning

9 Mercury & compounds Boiler/Waste Storage Combustion/Solid Waste

Burning

10 Polychlorinated Dioxins &

Furan

Boiler/Waste Storage Combustion/Solid Waste

Burning

11 (Particulate Matter)- PM Raw Material Storage,

Crushing

Raw material Preparation,

Crushing

In order to deal with this air emission, pollution control equipment need to be installed in the factory

especially at the source of emission. There are variety of pollution control devices as wet scrubber, bag

filter, Electrostatic precipitator, and so on in order work to prevent pollutants from emitting into atmosphere.

5.2. Emission to Water

Wastewater from the facility can be divided into 2 types such as rainwater, and wastewater from the

production. Mostly, the rainwater does not pose much impact on the environmental quality in the

community. In some cases, the factory operator designs a separate sewage system inside their facility to

connect into public sewage system in the region; however, in other cases, the rainwater will mix up with

wastewater from the production in the wastewater treatment plan before discharging into the public sewage

system.

However, the main concern is the large amount of wastewater from the production process, which

need to be treated before discharging into public sewage system. Wastewater treatment methods can be

different from one facility to another. It can be aerobic, non-aerobic, and mixed up system between aerobic

and anaerobic. The main wastewater pollutants from the beer production are as following:

Table 3: List of the main wastewater pollutants from beer production.

No Parameters Source of Emission How it happens

1 BOD5

Wastewater Treatment Plant Discharge of wastewater from

the production line/Toilet

2 CODcr

Wastewater Treatment Plant Discharge of wastewater from

the production line/Toilet

3 Oil and Grease

Wastewater Treatment Plant,

Fuel Storage

Discharge of wastewater from

the production line/Toilet

4 NH3

Wastewater Treatment Plant Discharge from the production

line/Toilet

5 Arsenic &

compounds

Water Treatment Plant/ Wastewater

Treatment Plant

Water Treatment/Discharge

from the production line

6 Chloride

Water Treatment Plant Discharge of wastewater from

water treatment plant

7 Acetone

Laboratory Discharge of wastewater from

the laboratory

8 Acrylamide

Laboratory Discharge of wastewater from

the laboratory

9 Phosphoric Acid

Water Treatment Plant/ Sanitation

process

Discharge of wastewater

10 Sulfuric Acid Sanitation process/cleaning agent Discharge of wastewater

11 Zinc sulfate Production Line Brewing Process

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12 Sodium hydroxide Wastewater Treatment Plant Waste Water Process

14 Zinc sulfate Production Line Brewing Process

15 Calcium chloride Production Line Brewing Process

5.3. Emission to Land

Whenever there is an improper management of the waste in the facility, pollutant emission to land

will happen. Soil quality will be polluted by the emission of pollutants in the form of solid waste, sludges,

sediments, spills, leak and so on. Even worse, if no immediate action taken place, those pollutants would

be able to get deeply into the ground, which pose impact to ground water quality as well.

5.4. Transfer in Waste

The impact of the pollutant does not end by just removing the waste from one place to another.

Displacing the waste from a contaminated site to another unpolluted site will cause the same problem as

the previous site. Therefore, the industrial facility have to track down all information/data regarding to the

waste generated from the production as well as from the facility. A few specific points about the transfer in

waste need to be reported in the PRTR system are (1) the amount of waste, (2) Type of pollutant in the

waste, (3) the treatment method and (4) the concentration of pollutants in the waste. The facility operator

need to be aware of the detail information about the movement of waste until its final disposal as well.

5.5. Transfer to Sewage

Like the transfer in waste section, pollutant from the industry facility will be transfered in the

environment beyond the facility boundary. The amount of wastewater discharged from the facility may go

into the existing public drainage system in the facility location or end up directly in a natural waterbody

like pond, river, sea, and so on. This could lead to an impact on the water quality in the area outside the

facility if the waste has not treated properly before the discharge.

6. Emission and Transfer Estimation Techniques

In general, there are 4 types of emission estimation techniques to estimate emissions from facilities

sampling. Those techniques are direct measurement, mass balance, engineering calculation, emission

factors.

6.1. Direct Measurement

6.1.1. Sampling Data

It is one of the method that the emission of pollutant was measured directly from the its sources such

as stack, exhaust pile from the boilers, and so on. The result from the direct measurement can be transcript

into a report format to government, specifically MoE. For sampling data to be adequate and able to be

used for MoE reporting purposes, it would need to be collected over a period of time representative

of operations for the whole year. The measurement from the stack should be done during the normal

operating status of the factory, where the result will be shown in the kg/hr or g/m3 (dry standard).

Some tests may require to be taken under maximum emissions rating, where emissions are likely to

be higher than when operating under normal operating conditions. An example of test results is summarized

in Table 1. The table shows the results of three different sampling runs conducted during one test event.

The source parameters measured as part of the test run include gas velocity and moisture content, which

are used to determine exhaust gas flow rates in m3/s. The filter weight gain is determined gravimetrically

and divided by the volume of gas sampled, as shown in Equation 1 to determine the PM concentration in

grams per m3.

Table 4: Stack Sample Test

Parameter Symbol Test 1 Test 2 Test 3

Total sampling time (sec)

Moisture collected (g)

Filter catch of PM (g)

Gmoist

Cf

7200

395.6

0.008511

7200

372.6

0.00449

7200

341.4

0.0625

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Average sampling rate (m3/s)

Standard metered volume (m3),dry

Volumetric flow rate (m3/s),dry

Concentration of particulate (g/m3)

Vm,STP

Qd

CPM

1.67*10-4

1.185

8.48

0.0718

1.67*10-4

1.160

8.43

0.0387

1.67*10-4

1.163

8.45

0.0537

Note that this example does not present the condensable PM emissions. Pollutant concentration is then

multiplied by the volumetric flow rate to determine the emission rate in kilograms per hour, as shown in

Equation 1 and Example 1.

Equation 1: Calculation of PM concentration

CPM = Cf / Vm,STP

Where:

Cpm = Concentration of PM or gram loading, g/m3

Cf = filter catch, g

Vm,STP = Metered volume of sample at STP, m3

Equation 2: Calculation of Emission of PM

EPM = CPM*Qd*3.6 [273 /(273+T)]

Where:

EPM = Hourly emission PM, kg/hr

CPM = concentration of PM or gram loading, g/m3

Qd = stack gas volumetric flow rate at actual condition, m3/s,dry

3.6 = 3600 second per hour multiplied by 0.001 kilograms per gram

T = temperature of the gas sample, 0C

Example 1: Using Stack Sampling Data

PM emissions calculated using Equation 1 and Equation 2 (above) and the stack sampling data for

Test 1 (presented in Table 4, and an exhaust gas temperature of 150 oC (423 K). This is shown below:

CPM = CF /Vm.STP

= 0.08551 / 1.185

= 0.072 g/m3

EPM = CPM * Qd *3.6* [273/(273+T)]

= 0.072 *8.48*3.6* (273/423K)

= 1.42kg/hr

The information from some stack tests may be reported in grams of particulate per cubic meter of

exhaust gas (wet). Use Equation 3 below to calculate the dry particulate emissions in kg/hr.

Equation 3: Calculation of emission of PM

EPM = Qa * CPM *3.6 (1-moistR/100) *[273/(273+T)]

Where:

EPM = hourly emission of PM in kilograms per hours, kg/hr

Qa = actual (ie.wet) cubic metres of exhaust gas per second, m3/s

CPM = concentration of PM or gram loading, g/m3

3.6 = 3600 second per hour multiplied by 0.001 kilograms per gram

moistR = moisture content, %

273 = 273K (0 oC)

T = stack gas temperature, oC

To calculate moisture content use Equation 4.

Equation 4: Calculation of moisture percentage

Moisture percentage = 100 * weight of water vapor per specific

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Volume of stack gas/total weight of the stack gas in that volume.

𝑚𝑜𝑖𝑠𝑡𝑅 =100 ∗

𝑔𝑚𝑜𝑖𝑠𝑡

1000 ∗ 𝑉𝑚.𝑆𝑇𝑃 𝑔𝑚𝑜𝑖𝑠𝑡

1000 ∗ 𝑉𝑚.𝑆𝑇𝑃+ 𝜌𝑆𝑇𝑃

Where:

moistR = moisture content, %

gmoist = moisture collected, g

Vm,STP = metered volume of sample at STP, m3

ᵖSTP = dry density of stack as sample, kg/m3 at STP

{if the density is not known a default value of 1.62 kg/m3

may be used. this assumes a dry gas composition of 50% air,50% CO2}

Example 2: Calculating Moisture Percentage

A 1.2m3 sample (at STP) of gas contain 410g of water. To calculate the moisture percentage use

Equation 4.

𝑚𝑜𝑖𝑠𝑡𝑅 =100 ∗

𝑔𝑚𝑜𝑖𝑠𝑡

1000 ∗ 𝑉𝑚.𝑆𝑇𝑃 𝑔𝑚𝑜𝑖𝑠𝑡

1000 ∗ 𝑉𝑚.𝑆𝑇𝑃+ 𝜌𝑆𝑇𝑃

𝑔𝑚𝑜𝑖𝑠𝑡

1000 ∗ 𝑉𝑚.𝑆𝑇𝑃 = 410/ (1000*1.2)

= 0.342

moistR = 100*0.342 / (0.342+1.62)

= 17.4%

6.1.2. Continuous Emission Monitoring System (CEMS) Data

Using CEMS (Continuous Emission Monitoring Systems) data to estimate emissions can be

applicable to power stations with suitable equipment installed, or for facilities that undertake medium term

monitoring that is representative of the power station operations over a year.

To monitor SO2, NOx, Total VOCs, and CO emissions using a CEMS, you use a pollutant

concentration monitor that measures concentration in parts per million by volume dry air (ppmvd). Flow

rates should be measured using a volumetric flow rate monitor. Emission rates (kg/hr) are then calculated

by multiplying the stack gas concentrations by the stack gas flow rates. While it is possible to determine

from this data the total emissions of an individual pollutant over a given time period (assuming the CEM

operates properly all year long), an accurate emission estimate can be derived by adding the hourly emission

estimates if the CEMS data is representative of typical operating conditions.

Although CEMS can report real-time hourly emissions automatically, it may be necessary to

manually estimate annual emissions from hourly concentration data. This section describes how to calculate

emissions from CEMS concentration data. The selected CEMS data should be representative of operating

conditions. When possible, data collected over longer periods should be used.

It is important to note that prior to using CEMS to estimate emissions, you should develop a protocol

for collecting and averaging the data in order that the estimate satisfies the facility’s State or Territory

environment authority as a requirement for General Directorate of Environment Protection.

To monitor SO2, NO2, VOC and CO emissions using CEMS, you use a pollutant concentration

monitor that measures the concentration in parts per million by volume dry air (ppmvd= volume of pollutant

gas/106 volumes of dry air). Flow rates should be measured using a volumetric flow rate monitor. Flow rate

estimated based on heat input using fuel factors may be inaccurate because these systems typically run with

high excess air to remove the moisture out of the kiln. Emission rates (kg/hr/ are then calculated by

multiplying the stack gas concentrations by the stack gas flow rates.

The table below presents example CEMS data output for three periods for hypothetical furnace. The

output includes pollutant concentrations in parts per millions dry basis (ppmvd), diluent (O2 or CO2)

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concentration in percent by volume dry basis (%v, d) and gas flow rates; and may include emission rates in

kilograms per hour (kg/hr). This data represents a snapshot of a hypothetical boiler operation. While it is

possible to determine total emissions of an individual pollutant over a given time period from this data,

assuming the adding the hourly emission estimates if the CEMS data is representative of typical operating

conditions.

Table 5: CEMS data output for three periods for hypothetical furnace

Time O2 Content Concentration (ppmvd) Gas Flow

Rate (Q)

Production Rate

of Product

(A)

% by volume SO2 NOx CO VOC m3/s tonnes/hour

1 10.3 150.9 142.9 42.9 554.2 8.52 290

2 10.1 144.0 145.7 41.8 582.9 8.48 293

3 11.8 11.8 112.7 128.4 515.1 8.85 270

Hourly emissions can be based on concentration measurement as shown in Equation 5.

Equation 5: Calculation of pollutant emission

Ei = (C * MW * Qst * 3600)/[22.4 *((T+273)/273) * 106 ]

Where:

Ei = Emissions of pollutant I,kg/hr

C = pollutant concentration, ppmv,d

MW = molecular weight of the pollutant, kg/kg-mole

Qst = actual stack gas volumetric flow rate, m3/s

3600 = conversion factor, s/hr

22.4 = volume occupied by one mole of gas at standard

Temperature and pressure (0oc and 101.3 kPa

T = temperature of gas sample oC

106 = conversion factor, pp.kg/kg

Actual annual emissions can be calculated by multiplying the emission rate in kg/hr by the number

of actual operating hours per year (OpHrs) as shown in Equation 6 for each typical time period and summing

the results.

Equation 6: Calculation of annual emission

Ekpy,i = ∑(𝐸𝑖 ∗ 𝑂𝑝𝐻𝑟𝑠)

Where:

Ekpy,I = annual emission of pollutant I, kg/yr

Ei = emissions of pollutant I, kg/hr (from Equation 5)

OpHrs = operating hours, hr/yr

Emission in kilograms of pollutant per tonne of product produced can be calculated by dividing the

emission rate in kg/hr by the activity rate (production rate (tonnes/hr) during the same period. This is shown

in Equation 7 below.

It should be noted that the emission factor calculated below assumes that the selected time period (ie.

Hourly) is representative of annual operating conditions and longer time period should be used for

reporting. Use of the calculation is shown in Example below.

Equation 7: Calculation of emission of pollutant per tons of product

Ekpt, i = 𝐸𝑖

𝐴⁄

Where:

Ekpt, I = emission of pollutant I per tonne of product produced, kg/t

Ei =` hourly emission of pollutant i, kg/hr

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A = production, t/hr

Example 3: Application of Equation 5, Equation 6, and Equation 7

This example shows how SO2 emissions can be calculated using Equation based on the CEMS data

for Time period 1 shown in the Table 5, and an exhaust gas temperature of 150 oC (423 K).

ESO2,1 = (𝐶 ∗ 𝑀𝑊 ∗ 𝑄 ∗ 3600)

[22.4 ∗ (𝑇 + 273273⁄ ) ∗ 106⁄

= (150.9 ∗ 64 ∗ 8.52 ∗ 3600)

[22.4 ∗ (423273⁄ ) ∗ 106⁄

= 296 217 90734 707 692⁄

= 8.53 kg/hr

For Time Period 2, also at 150 oC

ESO2,2 = 8.11 kg/hr

For Time Period 3, also at 150 oC

ESO2,3 = 7.23 kg/hr

Say representative operating conditions for the year are:

Period 1 = 1500 hr

Period 2 = 2000 hr

Period 3 = 1800 hr

Total emissions for the year are calculated by adding the results of the three Time Periods using

Equation 6:

ESO2,2 = ESO2,1 * OpHrs + ESO2,2 * OpHrs + ESO2,3 * OpHrs

= (8.53 * 1500) + (8.11 * 2000) + (7.23 * 1800) kg

= 42 021 kg/yr

Emissions, in terms of kg/tonne of product produced when operating in the same mode as

time period 1, can be calculated using Equation 7.

Ekpt,SO2 = 𝐸𝑆𝑂2

𝐴⁄

= 8.53290⁄

= 2.94 * 10-2 Kg SO2 emitted per tonne of product produced

When the furnace is operating as in time periods 2 or 3, similar calculation can be undertaken

for emissions per tonne

6.2. Mass Balance

A mass balance identifies the quantity of substance going in and out of an entire facility,

process, or piece of equipment. Emissions can be calculated as the difference between input and

output of each listed substance. Accumulation or depletion of the substance within the equipment

should be accounted for in your calculation.

6.2.1. Overall Facility Mass Balance

Mass balances can be used to characterize emissions from a facility providing that sufficient data is

available pertaining to the process and relevant input and output streams. Mass balances can be applied to

an entire facility. This involves the consideration of material inputs to the facility (purchases) and materials

exported from the facility in products and wastes, where the remainder is considered as a ‘loss’ (or a release

to the environment).

The mass balance calculation can be summarized by:

Total mass into process = Total mass out of process

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This equation could be written as:

Equation 8: Calculation of incoming material used in the process

Inputs = Products + Transfers + Emissions

Where:

Inputs = All incoming material used in the process.

Emissions = Releases to air, water, and land

(Emissions include both routine and accidental releases as well as spills)

Transfers = Transfers include substances discharged to sewer, substances deposited into

landfill and substances removed from a facility for destruction, treatment,

recycling, reprocessing, recovery, or purification.

Products = Products and materials (eg. by-products) exported from the facility.

Applying this to an individual substance (substance ‘i’), the equation may be written as:

Input of substance ‘i’ = amount of substance ‘i’ in product

amounts of substance ‘i’ in waste

amount of substance ‘i’ transformed or consumed in process

emission of substance ‘i’.

Example 4: Overall Facility Mass Balance

A chemical facility receives 1000 tons of a solvent product per annum, that is stored on-site. It is

known that this solvent product contains 2 percent water that settles during storage and is drained to sewer.

The solubility of the solvent in water is 100 g/kg (ie. 0.1 weight fraction). It is known that 975 tons of

solvent per annum is utilized in the process, based on actual addition rate data. During the year, it was

recorded that 1 ton of solvent was lost due to spillage, of which 500 kg was recovered and sent for

appropriate disposal, with the rest washed to sewer. What quantity of the substance is required to be

reported? Considering the water content of the solvent and the solubility of solvent in water the following

data can be derived:

Quantity of water received in the solvent annually:

Water = 1000 tons * (2/100) = 20 tons of water (containing 100 g/kg solvent)

The solubility of solvent in this water is 100 g/kg:

Therefore, solvent in water = 20 * (0.1) = 2 tons of solvent

Excluding the water component, the quantity of solvent received annually is:

Total solvent (excluding water) = 1000 * 0.98 = 980 tons

Incorporating the solvent contained within the water component:

Total solvent received at facility (including solvent in water) = 980 + 2 = 982 tons solvent

Once the above quantities have been ascertained, the quantity of solvent released to the environment

can be determined as follows:

Solvent to sewer = drainage from solvent tank + uncaptured spillage

= 2000 kg + 500 kg

= 2500 kg

Captured spillage = 500 kg

As no solvent was spilled on unsealed ground, there are no emissions to land. Therefore, the emission

of solvent to air is derived as follows:

Air Emission = Total solvent received - sewer release - captured spillage - solvent

utilized in the process

= 982 - 2.5 - 0.5 - 975

= 4 tons

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Therefore, 4 tons of solvent is lost to the atmosphere each year from storage and handling operations.

For MoE reporting, it would then be necessary to determine the quantity of substances present in the solvent

and to determine the quantities of each of these substances emitted to atmosphere. It is important to note

that any emission controls must be taken into account when determining your emissions (eg. the solvent

released to air may be routed through an incinerator before being released to the atmosphere).

6.2.2. Individual Unit Process Mass Balance

The general mass balance approach described above can also be applied to individual unit processes.

This requires that information is available on the inputs (ie. flow rates, concentrations, densities) and

outputs of the unit process. The following general equation can be used (note that scm is an abbreviation

for standard cubic metres):

Equation 9: Calculation of flow rate of component

Ei = ΣQiWfiρi - ΣQoWoiρo

Where:

Ei = flow rate of component i in unknown stream (kg/hr)

Qi = volumetric flow rate of inlet stream, i (scm/hr)

Qo = volumetric flow rate of outlet stream, o (scm/hr)

Wfi = weight fraction of component i in inlet stream i

Woi = weight fraction of component i in outlet stream o

ρi, ρo = density of streams i and o respectively (kg/scm)

Information on process stream input and output concentrations is generally known as this information

is required for process control. The loss Ex will be determined through analysis of the process. It should be

noted that it is then necessary to identify the environmental medium (or media) to which releases occur.

6.3. Emission Factors

An emission factor is a tool that is used to estimate emissions to the environment.

In this Manual, it relates the quantity of substances emitted from a source to some common activity

associated with those emissions. Emission factors are obtained from US, European, and Australian sources

and are usually expressed as the weight of a substance emitted divided by the unit weight, volume,

distance, or duration of the activity emitting the substance (eg. grams of ethanol emitted per kiloliter of beer

produced).Emission factors are used to estimate a facility’s emissions by the general equation:

Equation 10: Calculation of emission rate of pollutant

Ei = [A * OpHrs] EFi * [1 - (CEi/100)]

Where:

Ei = emission rate of pollutant I, kg/yr

A = Activity rate, t/hr

OpHrs = Operating hours, hr/yr

EFi = uncontrolled emission factor of pollutant i, kg/t

CEi = overall control efficiency of pollutant i, %

Emission factors developed from measurements for a specific process may sometimes be used to

estimate emissions at other sites. Should a company have several processes of similar operation and size,

and emissions were measured from one process source, an emission factor could be developed and applied

to similar sources. As previously mentioned, it is advisable to have the emission factor reviewed and

approved by MoE prior to its use for estimations.

6.3.1. Industry-Wide Emission Factors

Presently, the only emission factors available are for ethanol.

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Table 6: Emission factors for ethanol emissions from beer brewing

Process Emission Source Emission Factor Emission Factor Rating

Code

Bottle Filling Line 65.8 g/kl of beer packaged E

Bottle Soaker and Cleaner 90.7 g/1000 cases of bottles

washed

D

Can Crusher with

Pneumatic Conveyor

10.5 g/l beer recovered D

Can Filling Line 54.2 g/kl of beer packaged E

Fermenter Venting

(Closed Fermenter)

7.73 g/kl of beer packaged E

Keg Filling Line 2.67 g/kl of beer packaged D

Sterilized Bottle Filling Line 155 g/kl of beer packaged D

Sterilized Can Filling Line 135 g/kl of beer packaged D

a USEPA AP-42 Section 9.12.1, 1996

*See Section 4

Example 5: Using Emission Factors

Table 6 shows that for the bottle filling line, 65.8 g/kL of ethanol is emitted for every 1000 litres

of beer bottled. It is assumed that the brewery bottles 200 ML of beer per year. Emission reduction

efficiency for ethanol is effectively zero, with all ethanol produced emitted to air. (Therefore, CE = 0)

Emission Factor (EF ethanol) = 65.8 g/kL Beer Bottled (A)

= 200ML

Eethanol = A * EFethanol * [1 - (CE/100)]

Ethanol emission = Beer bottled/year * EFethanol = 200 ML/year * 65.8g/kL = 200 000 kL * 65.8 g/kL * kg/1000g

= 13160.0 = 13160.0 kg/year of ethanol emitted.

6.3.2. Predictive Emission Monitoring (PEM)

Predictive emission monitoring is based on developing a correlation between pollutant emission rates

and process parameters. A PEM allows facilities to develop site-specific emission factors, or emission

factors more relevant to their particular process.

Based on test data, a mathematical correlation can be developed which predicts emissions

using various parameters.

6.4. Engineering Calculations

An engineering calculation is an estimation method based on physical/chemical properties

(eg. vapor pressure) of the substance, and mathematical relationships (eg. ideal gas law).

6.4.1. Fuel Analysis

Fuel analysis is an example of an engineering calculation and can be used to predict SO2, metals,

and other emissions based on application of conservation laws, if fuel rate is measured. The presence of

certain elements in fuels may be used to predict their presence in emission streams. This includes elements

such as sulfur which may be converted into other compounds during the combustion process.

The basic equation used in fuel analysis emission calculations is the following:

Equation 11: Calculation of emission of pollutant

Ei = Qf * pollutant concentration in fuel i ( MWp÷ EWf )

Where:

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Ei = emissions of pollutant i

Qf = fuel use (kg/hr)

MW p = molecular weight of pollutant emitted (kg/kg-mole)

EW f = elemental weight of pollutant in fuel (kg/kg-mole)

Pollutant concentration by weight

For instance, SO2 emissions from coal combustion can be calculated based on the concentration of

sulfur in the coal. This approach assumes complete conversion of sulfur to SO2. Therefore, for every

kilogram of sulfur (EW = 32) burned, two kilograms of SO2 (MW = 64) are emitted. The application of this

EET is shown in Example 6.

Example 6: Using Fuel Analysis

This example shows how SO2 emissions can be calculated from coal combustion based on fuel

analysis results and the fuel flow information. The facility is assumed to operate 1500 hours per year.

E SO2 = may be calculated using Equation

Fuel flow = 2,000 kg/h

Weight percent sulfur in fuel = 0.5

ESO2 = Qf * pollutant concentration in fuel i ( MWp÷EWf )

= (2 000) * (0.5 ÷100) * (64÷32)

= 20kg/hr * 1,500 hr/yr

= 30,000 kg/yr

6.5. Alternative Emission Estimation Technique for Ethanol Emissions

The main source of ethanol emissions from the brewing process, aside from the evolution of CO2

from fermentation, is the loss of ethanol through processing and packaging operations. Ethanol (contained

in the beer) lost during production of beer flows to trade waste, or to on-site treatment. However, emissions

of ethanol from beer loss also occur through evaporation prior to reaching the trade waste or treatment

system. If the brewery has an on-site treatment facility, further emissions of ethanol and other VOCs will

need to be considered for calculation.

Emission of ethanol to air, prior to trade waste transfer or treatment, may be estimated using the

following parameters:

Volume of beer lost;

Average alcohol content of the beer;

Average temperature of the beer; and

Average time before the lost beer is transferred to trade waste or other treatment.

On-site experimentation utilizing the above parameters, under controlled conditions, is an alternative

method of estimating emissions of ethanol to the air from spilt beer. For example:

Step 1: Measure the initial alcohol content of a known quantity of beer.

Step 2: Spill the beer onto a surface and leave it for a known period of time.

Step 3: Collect the beer and measure the alcohol content.

It may be assumed that for the given volume of beer, the amount of alcohol lost during the experiment

is the loss of ethanol to the air. The results may be used to estimate ethanol emissions from spills, or in the

event of overfilling.

7. Reporting

The facility need to report the type and amount of chemicals and pollutants emission to environment

and transfer to waste and sewage. The procedure of reporting could be found in the “Basic Release

Estimation Technique Manual under Pollutant Release and Transfer Register (PRTR) system” on Section 5

about “the procedure of determining business and substances requiring notification”.

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Reference

Australia Environment. (1999). National Pollutant Inventory: Emission Estimation Techniques for Soft Drink

Manufacture. Australia.

Australia Environment. (1999). National Pollutant Inventory: Emission Estimation Techniques Manual

for Beer Manufacturing. Australia.

E&A Consultant Co., L. (2016). Initial EIA report on the Establishment of Beer Product for Daun Penh

Food & Beverage Co.ltd. Phnom Penh.

E&A Consultant Co., L. (2017). Full EIA report on the Extension of Beer Production and the

Establishment of Brewery Production for Khmer Brewery Limited. Phnom Penh.

Ministry of Economy Trade and Industry, Ministry of Environment. (2004). Manual for Calculating the

Quantity of Released Pollutant under the PRTR (Pollutant Release and Transfer Register)

system . Japan.

SBK Research and Development co., L. (2016). Initial ESIA on the Establishment of Beer Product,

Brewery Product and Dairy Product for Cambodia Beverage Company Limited. Phnom Penh.