# Reduction of Charges for Certain Cotton Textile Products Produced or Manufactured in the Republic of Turkey

> Briefs, arguments, decisions, and more.

URL: https://www.frixlaw.com/law-library/documents/fr%3AC1-29109

## Record

- **Collection:** Federal Register
- **Document type:** Correction
- **Published:** November 29, 2001
- **Citation:** 66 FR 59602

## Text

Lilyea

COMMITTEE FOR THE IMPLEMENTATION OF TEXTILE AGREEMENTS
Reduction of Charges for Certain Cotton Textile Products Produced or Manufactured in the Republic of Turkey
November 16, 2001.

Correction

In notice document 01-29109 appearing on page 58123 in the issue of Tuesday, November 20, 2001, make the following corrections:

(1) On page 58123, beginning in the first column, the last paragraph, the
Authority
citation, should have appeared as follows;

“Authority:

Section 204 of the Agricultural Act of 1956, as amended (7 U.S.C. 1854); Executive Order 11651 of March 3, 1972, as amended.”

(2) On the same page, in the third column, the first paragraph should have appeared as follows;

“The Committee for the Implementation of Textile Agreements has determined that this action falls within the foreign affairs exception of the rulemaking provisions of 5 U.S.C. 553(a)(1).”

[FR Doc. C1-29109 Filed 11-28-01; 8:45 am]
BILLING CODE 1505-01-D
!!!INSERT NAME HERE!!!

ENVIRONMENTAL PROTECTION AGENCY
40 CFR Part 92
Control of Air Pollution From Locomotives and Locomotive Engines; Republication

CFR Correction

Editorial Note:

On Monday, November 26, 2001, this rule document FR Doc. 01-55530 appeared on 66 FR 58953-58964. Due to additional text being inadvertently added, it is being reprinted in its entirety.

In Title 40 of the Code of Federal Regulations, Parts 87 to 99, revised as of July 1, 2001, part 92 is corrected in § 92.120 by revising equations (1) and (2) in paragraph (c)(2)(v), in § 92.121 by revising paragraphs (b)(2)(vi), (b)(2)(ix), (b)(2)(xi)(A), and (b)(4)(iv), and by revising § 92.132 to read as follows:

§ 92.120
NDIR analyzer calibration and checks.

(c)* * *

(2)* * *

(v)* * *

y = Ax
4
+ Bx
3
+ Cx
2
+ Dx + E  (1)

y = x/(Ax
4
+ Bx
3
+ Cx
2
+ Dx + E) (2)

where:

y = concentration.

x = chart deflection.

§ 92.121
Oxides of nitrogen analyzer calibration and check.

(b)* * *

(2)* * *

(vi) Turn on the NO
X
generator O
2
(or air) supply and adjust the O
2
(or air) flow rate so that the NO indicated by the analyzer is about 10 percent less than indicated in step in paragraph (b)(2)(v) of this section. Record the concentration of NO in this NO + O
2
mixture.

(ix) Switch off the NO
X
generation, but maintain gas flow through the system. The oxides of nitrogen analyzer will indicate the total NO
X
in the NO + O
2
mixture. Record this value.

(xi)* * *

(A) Percent Efficiency=(1 + (a − b)/(c − d))(100)

where:

a=concentration obtained in paragraph (b)(2)(viii) of this section.

b=concentration obtained in paragraph (b)(2)(ix) of this section.

c=concentration obtained in paragraph (b)(2)(vi) of this section.

d=concentration obtained in paragraph (b)(2)(vii) of this section.

(4)* * *

(iv) Calculate the concentration of the converter checking gas using the results from step in paragraph (b)(4)(iii) of this section and the converter efficiency from paragraph (b)(2) of this section as follows:

Concentration=(((X-Y)(100))/Efficiency) + Y

§ 92.132
Calculations.

(a)
Duty-cycle emissions.
This section describes the calculation of duty-cycle emissions, in terms of grams per brake horsepower hour (g/bhp-hr). The calculation involves the weighted summing of the product of the throttle notch mass emission rates and dividing by the weighted sum of the brake horsepower. The final reported duty-cycle emission test results are calculated as follows:

(1)(i) E
idc
=(Σ(M
ij
)(F
j
))/(Σ(BHP
j
)(F
j
))

Where:

E
idc
=Duty-cycle weighted, brake-specific mass emission rate of pollutant i (i.e., HC, CO, NO
X
or PM and, if appropriate, THCE or NMHC) in grams per brake horsepower-hour;

M
ij
=the mass emission rate pollutant i for mode j;

F
j
=the applicable weighting factor listed in Table B132-1 for mode j;

BHP
j
=the measured brake horsepower for mode j.

(ii) Table B132-1 follows:

Table B132-1—Weighting Factors for Calculating Emission Rates

Throttle notch setting
Test mode
Locomotive not equipped with multiple idle notches
Line-haul
Switch
Locomotive equipped with multiple idle notches
Line-haul
Switch

Low Idle
1a
NA
NA
0.190
0.299

Normal Idle
1
0.380
0.598
0.190
0.299

Dynamic Brake
2
0.125
0.000
0.125
0.000

Notch 1
3
0.065
0.124
0.065
0.124

Notch 2
4
0.065
0.123
0.065
0.123

Notch 3
5
0.052
0.058
0.052
0.058

Notch 4
6
0.044
0.036
0.044
0.036

Notch 5
7
0.038
0.036
0.038
0.036

Notch 6
8
0.039
0.015
0.039
0.015

Notch 7
9
0.030
0.002
0.030
0.002

Notch 8
10
0.162
0.008
0.162
0.008

(2) Example: For the line-haul cycle, for locomotives equipped with normal and low idle, and with dynamic brake, the brake-specific emission rate for HC would be calculated as:

E
HCdc
=[(M
HCla
) (0.190) + (M
HC1
) (0.190) + (M
HC2
) (0.125) + (M
HC3
) (0.065) + (M
HC4
) (0.065) + (M
HC5
) (0.052) + (M
HC6
) (0.044) + (M
HC7
) (0.038) + (M
HC8
) (0.039) + (M
HC9
) (0.030) + (M
HC10
) (0.162)]/[(BHP
1a
) (0.190) + (BHP
1
) (0.190) + (BHP
2
) (0.125) + (BHP
3
) (0.065) + (BHP
4
) (0.065) + (BHP
5
) (0.052) + (BHP
6
) (0.044) + (BHP
7
) (0.038) + (BHP
8
) (0.039) + (BHP
9
) (0.030) + (BHP
10
) (0.162)]

(3) In each mode, brake horsepower output is the power that the engine delivers as output (normally at the flywheel), as defined in § 92.2.

(i) For locomotive testing (or engine testing using a locomotive alternator/generator instead of a dynamometer), brake horsepower is calculated as:

BHP=HP
out
/A
eff
+ HP
acc

Where:

HP
out
=Measured horsepower output of the alternator/generator.

A
eff
=Efficiency of the alternator/generator.

HP
acc
=Accessory horsepower.

(ii) For engine dynamometer testing, brake horsepower is determined from the engine speed and torque.

(4) For locomotive equipped with features that shut the engine off after prolonged periods of idle, the measured mass emission rate M
i1
(and M
i1a
as applicable) shall be multiplied by a factor equal to one minus the estimated fraction reduction in idling time that will result in use from the shutdown feature. Application of this adjustment is subject to the Administrator's approval.

(b)
Throttle notch emissions.
This paragraph (b) describes the calculation of throttle notch emissions for all operating modes, including: idle (normal and low, as applicable); dynamic brake; and traction power points. The throttle notch (operating mode) emission test results, final reported values and values used in paragraph (a)(1) of this section are calculated as follows:

(1) Brake specific emissions (E
ij
) in grams per brake horsepower-hour of each species i (i.e., HC, CO, NO
X
or PM and, if appropriate, THCE or NMHC) for each mode j:

(i) E
HC mode
=HC grams/BHP-hr=M
HC mode
/Measured BHP in mode.

Where:

M
HC mode
=Mass HC emissions (grams per hour) for each test mode.

(ii) E
THCE mode
=THCE grams/BHP-hr=M
THCE mode
/Measured BHP in mode.

Where:

M
THCE mode
(Total hydrocarbon equivalent mass emissions (grams per hour) for each test mode):

=M
HCj
+ Σ (M
ij
) (MWC
p
)/MWC
i

M
ij
=the mass emission rate oxygenated pollutant i for mode j.

MWC
i
=the molecular weight of pollutant i divided by the number of carbon atoms per molecule of pollutant i.

MWC
p
=the molecular weight of a typical petroleum fuel component divided by the number of carbon atoms per molecule of a typical petroleum fuel component=13.8756.

(iii) E
NMHC mode
=NMHC grams/BHP-hr=M
NMHC mode
/Measured BHP in mode.

Where:

M
NMHC mode
=Mass NMHC emissions (grams per hour) for each test mode.

(iv) E
CO mode
=CO grams/BHP-hr=M
CO mode
/Measured BHP in mode.

Where:

M
CO mode
=Mass CO emissions (grams per hour) for each test mode.

(v) E
NOx mode
=NO
X
grams/BHP-hr=M
NOx mode
/Measured BHP in mode.

Where:

M
NOx mode
=Mass NO
X
emissions (grams per hour) for each test mode.

(vi) E
PM mode
=PM grams/BHP-hr=M
PM mode
/Measured BHP in mode.

Where:

M
PM mode
=Mass PM emissions (grams per hour) for each test mode.

(vii) E
AL mode
=Aldehydes grams/BHP-hr=M
AL mode
/Measured BHP in mode.

(vii) E
AL mode
=Aldehydes grams/BHP-hr=M
AL mode
/Measured BHP in mode.

Where:

M
AL mode
=Total aldehyde mass emissions (grams per hour) for each test mode.

(2) Mass Emissions—Raw exhaust measurements. For raw exhaust measurements mass emissions (grams per hour) of each species for each mode:

(i) General equations. (A) The mass emission rate, M
X mode
(g/hr), of each pollutant (HC, NO
X
, CO
2
, CO, CH
4
CH
3
OH, CH
3
CH
2
OH, CH
2
O, CH
3
CH
2
O) for each operating mode for raw measurements is determined based on one of the following equations:

M
X mode
=(DX/10
6
)(DVol)(MW
X
/V
m
)

M
X mode
=(WX/10
6
)(WVol)(MW
X
/V
m
)

Where:

X designates the pollutant (e.g., HC), DX is the concentration of pollutant X (ppm or ppmC) on a dry basis, MW
X
is the molecular weight of the pollutant (g/mol), DVol is the total exhaust flow rate (ft
3
/hr) on a dry basis, WX is the concentration of pollutant X (ppm or ppmC) on a wet basis, WVol is the total exhaust flow rate (ft
3
/hr) on a wet basis, V
m
is the volume of one mole of gas at standard temperature and pressure (ft
3
/mol).

(B) All measured volumes and volumetric flow rates must be corrected to standard temperature and pressure prior to calculations.

(ii) The following abbreviations and equations apply to this paragraph (b)(2):

α=Atomic hydrogen/carbon ratio of the fuel.

β=Atomic oxygen/carbon ratio of the fuel.

CMW
f
=Molecular weight of the fuel per carbon atom, or carbon molecular weight (g/moleC)=(12.011 + 1.008α + 16.000β).

DCO=CO concentration in exhaust, ppm (dry).

DCO
2
=CO
2
concentration in exhaust, percent (dry).

DHC=HC carbon concentration in exhaust, ppm C (dry).

DNOX=NO
X
concentration in exhaust, in ppm (dry).

DVol=Total exhaust flow rate (ft
3
/hr) on a dry basis; or

=(V
m
)(W
f
)/((CMW
f
) (DHC/10
6
+ DCO/10
6
+ DCO2/100)).

K=Water gas equilibrium constant=3.5.

K
w
=Wet to dry correction factor.

M
F
=Mass flow-rate of fuel used in the engine in lb/hr=W
f
/453.59.

MW
C
=Atomic weight of carbon=12.011.

MW
CO
=Molecular weight of CO=28.011.

MW
H
=Atomic weight of hydrogen=1.008.

MW
NO2
=Molecular weight of nitrogen dioxide (NO
2
)=46.008.

MW
O
=Molecular weight of atomic oxygen=16.000.

T=Temperature of inlet air ( °F).

V
m
=Volume of one mole of gas at standard temperature and pressure (ft
3
/mole).

W
f
=Mass flow-rate of fuel used in the engine, in grams/hr=(453.59)×(M
f
lbs/hr).

WCO
2
=CO
2
concentration in exhaust, percent (wet).

WHC=HC concentration in exhaust, ppm C (wet).

WVol=Total exhaust flow rate (ft
3
/hr) on a wet basis; or

=(V
m
)(W
f
)/((CMW
f
)(WHC/10
6
+ WCO/10
6
WCO2/100)).

(iii) Calculation of individual pollutant masses. Calculations for mass emission are shown here in multiple forms. One set of equations is used when sample is analyzed dry (equations where the concentrations are expressed as DX), and the other set is used when the sample is analyzed wet (equations where the concentrations are expressed as WX). When samples are analyzed for some constituents dry and for some constituents wet, the wet concentrations must be converted to dry concentrations, and the equations for dry concentrations used. Also, the equations for HC, NMHC, CO, and NO
X
have multiple forms that are algebraically equivalent: An explicit form that requires intermediate calculation of V
m
and DVol or WVol; and an implicit form that uses only the concentrations (e.g., DCO) and the mass flow rate of the fuel. For these calculations, either form may be used.

(A) Hydrocarbons and nonmethane hydrocarbons.

(
1
) Hydrocarbons. (
i
)
For petroleum-fueled engines:

M
HC mode

=(DHC)CMW
f
(DVol)(10
6
)/V
m

=((DHC/10
6
)(W
f
)/((DCO/10
6
) + (DCO
2
/100) + (DHC/10
6
) + (ΣDX/10
6
)))

M
HC mode

=(WHC)CMW
f
(WVol)(10
6
)/V
m

=((WHC/10
6
)(W
f
)/((WCO/10
6
) + (WCO
2
/100) + (WHC/10
6
) + (Σ(WX/10
6
)))

(
ii
)
For alcohol-fueled engines:

DHC=FID HC − Σ(r
x
)(DX)

WHC=FID HC − Σ(r
x
)(WX)

Where:

FID HC=Concentration of “hydrocarbon” plus other organics such as methanol in exhaust as measured by the FID, ppm carbon equivalent.

r
x
=FID response to oxygenated species×(methanol, ethanol, or acetaldehyde).

DX=Concentration of oxygenated species×(methanol, ethanol, or acetaldehyde) in exhaust as determined from the dry exhaust sample, ppm carbon (e.g., DCH3OH, 2(DCH3CH2OH)).

WX=Concentration of oxygenated species×(methanol, ethanol, or acetaldehyde) in exhaust as determined from the wet exhaust sample, ppm carbon.

ΣDX=The sum of concentrations DX for all oxygenated species.

ΣWX=The sum of concentrations WX for all oxygenated species.

(
2
) Nonmethane hydrocarbons:

M
NMHC mode
=(DNMHC)CMW
f
(DVol) (10
6
)/V
m

=((DNMHC/10
6
)(W
f
)/((DCO/10
6
) + (DCO
2
/100) + (DHC/10
6
)))

M
NMHC mode
=(WNMHC)CMW
f
(WVol) (10
6
)/V
m

=((WNMHC/10
6
)(W
f
)/((WCO/10
6
) + (WCO
2
/100) + (WHC/10
6
)))

Where:

DNMHC=FID HC − (r
CH4
)(DCH4)

WNMHC=FID HC − (r
CH4
)(WCH4)

FID HC=Concentration of “hydrocarbon” plus other organics such as methane in exhaust as measured by the FID, ppm carbon equivalent.

r
CH4
=FID response to methane.

DCH4=Concentration of methane in exhaust as determined from the dry exhaust sample, ppm.

WCH4=Concentration of methane in exhaust as determined from the wet exhaust sample, ppm.

(B) Carbon monoxide:

M
CO mode
=(DCO)MW
CO
(DVol)/10
6
/V
m

=((MW
CO
(DCO/10
6
)(W
f
)/((CMW
f
)(DCO/10
6
) + (DCO
2
/100) + DHC/10
6
) + (ΣDX/10
6
)))

M
CO mode
=(WCO)MW
CO
(DVol)(10
6
)/V
m

+ ((MW
CO
(WCO/10
6
)(W
f
)/((CMW
f
)(WCO/10
6
) + (WCO
2
/100) + WHC/10
6
) + (ΣWX/10
6
)))

(C) Oxides of nitrogen:

M
NOx mode
=(DNOX)MW
NO2
(DVol)(10
6
)/V
m

=((MW
NO2
(DNOX/10
6
)(W
f
)/((CMW
f
)(DCO/10
6
) + (DCO
2
/100) + (DHC/10
6
) + (ΣDX/10
6
)))

M
NOx mode
=(WNOX)MW
NO2
(DVol)(10
6
)/V
m

=((MW
NO2
(WNOX/10
6
)(W
f
)/((CMW
f
)(WCO/10
6
) + (WCO
2
/100) + (WHC/10
6
) + (ΣWX/10
6
)))

(D) Methanol:

M
CH3OH mode
=(DCH3OH/10
6
)32.042(DVol)/V
m

M
CH3OH mode
=(WCH3OH/10
6
)32.042(WVol)/V
m

Where:

DCH3OH=(V
m
)(10
6
)[(C
1
×AV
1
) + (C
2
×AV
2
)]/DVol
MS.

WCH3OH=(V
m
)(10
6
)[(C
1
×AV
1
) + (C
2
×AV
2
)]/WVol
MS.

C
i
=concentration of methanol in impinger i (1 or 2) in mol/ml.

AV
i
=Volume of absorbing reagent in impinger i (1 or 2) in ml.

DVol
MS
=Volume (standard ft
3
) of exhaust sample drawn through methanol impingers (dry).

WVol
MS
=Volume (standard ft
3
) of exhaust sample drawn through methanol impingers (wet).

(E) Ethanol:

M
CH3CH2OH mode
=(DCH3CH2OH/10
6
)23.035(DVol)/V
m

M
CH3CH2OH mode
= (WCH3CH2OH/10
6
)23.035(WVol)/V
m

Where:

DCH3CH2OH=(V
m
)(10
6
)[(C
1
×AV
1
)

+ (C
2
×AV
2
)]/DVol
ES.

WCH3CH2OH=(V
m
)(10
6
) [(C
1
×AV
1
) + (C
2
×AV
2
)]/WVol
ES.

C
i
=concentration of ethanol in impinger i (1 or 2) in mol/ml.

AV
i
=Volume of absorbing reagent in impinger i (1 or 2) in ml.

DVol
ES
=Volume (standard ft
3
) of exhaust sample drawn through ethanol impingers (dry).

WVol
ES
=Volume (standard ft
3
) of exhaust sample drawn through ethanol impingers (wet).

(F) Formaldehyde:

M
CH2O mode
=(DCH2O/10
6
)30.026(DVol)/V
m

M
CH2O mode
=(WCH2O/10
6
)30.026(WVol)/V
m

(
1
) If aldehydes are measured using impingers:

DCH2O=(V
m
)(10
6
)[(C
1
×AV
1
) + (C
2
×AV
2
)]/DVol
FS

WCH2O=(V
m
)(10
6
)[(C
1
×AV
1
) + (C
2
×AV
2
)]/WVol
FS

(
2
) If aldehydes are measured using cartridges:

DCH2O=(V
m
)(10
6
)(C
R
×AV
R
)/DVol
FS

WCH2O=(V
m
)(10
6
)(C
R
×AV
R
)/WVol
FS

(
3
) The following definitions apply to this paragraph (b)(2)(iii)(F):

AV
i
=Volume of absorbing reagent in impinger i (1 or 2) in ml.

AV
R
=Volume of absorbing reagent use to rinse the cartridge in ml.

C
i
=concentration of formaldehyde in impinger i (1 or 2) in mol/ml.

C
R
=concentration of formaldehyde in solvent rinse in mol/ml.

DVol
FS
=Volume (standard ft
3
) of exhaust sample drawn through formaldehyde sampling system (dry).

WVol
FS
=Volume (standard ft
3
) of exhaust sample drawn through formaldehyde sampling system (wet).

(G) Acetaldehyde:

M
CH3CHO mode
=(DCH3CHO/10
6
)27.027(DVol)/V
m

M
CH3CHO mode
=(WCH3CHO/10
6
)27.027(WVol)/V
m

(
1
) If aldehydes are measured using impingers:

DCH3CHO=(V
m
)(10
6
)[(C
1
×AV
1
) + (C
2
× AV
2
)]/DVol
AS

WCH3CHO=(V
m
)(10
6
)[(C
1
×AV
1
) + C
2
× AV
2
)]/WVol
AS

(
2
) If aldehydes are measured using cartridges:

DCH3CHO=(V
m
)(10
6
)(C
R
×AV
R
)/DVol
AS

WCH3CHO=(V
m
)(10
6
)(C
R
×AV
R
)/WVol
AS

(
3
) The following definitions apply to this paragraph (b)(2)(iii)(G):

AV
i
=Volume of absorbing reagent in impinger i (1 or 2) in ml.

AV
R
=Volume of absorbing reagent use to rinse the cartridge in ml.

C
i
=concentration of acetaldehyde in impinger i (1 or 2) in mol/ml.

C
R
=concentration of acetaldehyde in solvent rinse in mol/ml.

DVol
AS
=Volume (standard ft
3
) of exhaust sample drawn through acetaldehyde sampling system (dry).

WVol
AS
=Volume (standard ft
3
) of exhaust sample drawn through acetaldehyde sampling system (wet).

(iv) Conversion of wet concentrations to dry concentrations. Wet concentrations are converted to dry concentrations using the following equation:

DX=K
W
WX

Where:

WX is the concentration of species X on a wet basis.

DX is the concentration of species X on a dry basis.

K
W
is a conversion factor=WVol/DVol=1 + DH2O.

(A) Iterative calculation of conversion factor. The conversion factor K
W
is calculated from the fractional volume of water in the exhaust on a dry basis (DH2O=volume of water in exhaust/dry volume of exhaust). Precise calculation of the conversion factor K
W
must be done by iteration, since it requires the dry concentration of HC, but HC emissions are measured wet.

(
1
) The conversion factor is calculated by first assuming DHC=WHC to calculate DVol:

DVol=(V
m
)(W
f
)/((CMW
f
)(DHC/10
6
+ DCO/10
6
+ DCO2/100))

(
2
) This estimate is then used in the following equations to calculate DVol
air
, then DH2O, then K
W
, which allows DHC to be determined more accurately from WHC:

ER16AP98.009

Where:

Y=Water volume concentration in intake air, volume fraction (dry).

DVol
air
=Air intake flow rate (ft
3
/hr) on a dry basis, measured, or calculated as:

ER16AP98.010

(
3
) The calculations are repeated using this estimate of DHC. If the new estimate for K
W
is not within one percent of the previous estimate, the iteration is repeated until the difference in K
W
between iterations is less than one percent.

(B) Alternate calculation of DH2O (approximation). The following approximation may be used for DH2O instead of the calculation in paragraph (b)(2)(iv)(A) of this section:

ER16AP98.011

Where:

ER16AP98.012

Y=Water volume concentration in intake air, volume fraction (dry).

(3)
Mass Emissions—Dilute exhaust measurements.
For dilute exhaust measurements mass emissions (grams per hour) of each species for each mode:

(i)
General equations.
The mass emission rate, M
x mode
(g/hr) of each pollutant (HC, NO
X
, CO2, CO, CH4 CH3OH, CH3CH2OH, CH2O, CH3CH2O) for each operating mode for bag measurements and diesel continuously heated sampling system measurements is determined from the following equation:

M
x mode
=(V
mix
)(Density
x
)(X
conc
)/(V
f
)

Where:

x designates the pollutant (e.g., HC), V
mix
is the total diluted exhaust volumetric flow rate (ft
3
/hr), Density
x
is the specified density of the pollutant in the gas phase (g/ft
3
), X
conc
is the fractional concentration of pollutant x (i.e., ppm/10
6
, ppmC/10
6
, or %/100), and V
f
is the fraction of the raw exhaust that is diluted for analysis.

(ii) The following abbreviations and equations apply to paragraphs (b)(3)(i) through (b)(3)(iii)(J) of this section:

(A) DF=Dilution factor, which is the volumetric ratio of the dilution air to the raw exhaust sample for total dilution, calculated as:

ER16AP98.013

Where:

WCO2=Carbon dioxide concentration of the raw exhaust sample, in percent (wet).

WCO2
e
=Carbon dioxide concentration of the dilute exhaust sample, in percent (wet).

WCO2
d
=Carbon dioxide concentration of the dilution air, in percent (wet).

(B) V
mix
=Diluted exhaust volumetric flow rate in cubic feet per hour corrected to standard conditions (528°R, and 760 mm Hg).

(C) V
f
=Fraction of the total raw exhaust that is diluted for analysis.

=((CO2
conc
/10
2
) + (CO
conc
/10
6
) + (HC
conc
/10
6
))(V
mix
)(CMW
f
)/V
m
/M
f

(iii) Calculation of individual pollutants.

(A) M
HC mode
=Hydrocarbon emissions, in grams per hour by mode, are calculated using the following equations:

M
HC mode
=(V
mix
)(Density
HC
)(HC
conc
/10
6
)/V
f

HC
conc
=HC
e
− (HC
d
)(1 − (1/DF))

HC
e
=FID HC
e
−
Ξ
(r
x
)(X
e
)

Where:

Density
HC
=Density of hydrocarbons=16.42 g/ft
3
(0.5800 kg/m
3
) for #l petroleum diesel fuel, 16.27 g/ft
3
(0.5746 kg/m
3
) for #2 diesel, and 16.33 g/ft
3
(0.5767 kg/m
3
) for other fuels, assuming an average carbon to hydrogen ratio of 1:1.93 for #1 petroleum diesel fuel, 1:1.80 for #2 petroleum diesel fuel, and 1:1.85 for hydrocarbons in other fuels at standard conditions.

HC
conc
=Hydrocarbon concentration of the dilute exhaust sample corrected for background, in ppm carbon equivalent (i.e., equivalent propane×3).

HC
e
=Hydrocarbon concentration of the dilute exhaust bag sample, or for diesel continuous heated sampling systems, average hydrocarbon concentration of the dilute exhaust sample as determined from the integrated HC traces, in ppm carbon equivalent. For petroleum-fueled engines, HC
e
is the FID measurement. For methanol-fueled and ethanol-fueled engines:

FID HC
e
=Concentration of hydrocarbon plus methanol, ethanol and acetaldehyde in dilute exhaust as measured by the FID, ppm carbon equivalent.

r
x
=FID response to oxygenated species x (methanol, ethanol or acetaldehyde).

X
e
=Concentration of species x (methanol, ethanol or acetaldehyde) in dilute exhaust as determined from the dilute exhaust sample, ppm carbon.

HC
d
=Hydrocarbon concentration of the dilution air as measured, in ppm carbon equivalent.

(B) M
NOx mode
= Oxides of nitrogen emissions, in grams per hour by mode, are calculated using the following equations:

M
NOx mode
=(V
mix
) (Density
NO2
) (NOx
conc
/10
6
) /V
f

NOx
conc
=(NOx
e
− NOx
d
(1 − (1/DF)))

Where:

Density
NO2
=Density of oxides of nitrogen is 54.16 g/ft
3
(1.913 kg/m
3
), assuming they are in the form of nitrogen dioxide, at standard conditions.

NOx
conc
=Oxides of nitrogen concentration of the dilute exhaust sample corrected for background, in ppm.

NOx
e
=Oxides of nitrogen concentration of the dilute exhaust bag sample as measured, in ppm.

NOx
d
=Oxides of nitrogen concentration of the dilution air as measured, in ppm.

(C) M
CO2 mode
=Carbon dioxide emissions, in grams per hour by mode, are calculated using the following equations:

M
CO2 mode
=(V
mix
) (Density
CO2
) (CO
2conc
/10
2
) /V
f

CO
2conc
=CO
2e
− CO
2d
(1 − (1/DF))

Where:

Density CO
2
=Density of carbon dioxide is 51.81 g/ft
3
(1.830 kg/m
3
), at standard conditions.

CO
2conc
=Carbon dioxide concentration of the dilute exhaust sample corrected for background, in percent.

CO
2e
=Carbon dioxide concentration of the dilute exhaust bag sample, in percent.

CO
2d
=Carbon dioxide concentration of the dilution air as measured, in percent.

(D)(
1
) M
CO mode
=Carbon monoxide emissions, in grams per hour by mode, are calculated using the following equations:

M
CO mode
=(V
mix
)(Density
CO
)(CO
conc
/10
6
)/V
f

CO
conc
=CO
e
− CO
d
(1 − (1/DF))

CO
d
=(1 − 0.000323R)CO
dm

Where:

Density
CO
=Density of carbon monoxide is 32.97 g/ft
3
(1.164 kg/m
3
), at standard conditions.

CO
conc
=Carbon monoxide concentration of the dilute exhaust sample corrected for background, water vapor, and CO
2
extraction, ppm.

CO
e
=Carbon monoxide concentration of the dilute exhaust sample volume corrected for water vapor and carbon dioxide extraction, in ppm.

CO
e
=(1 − (0.01 + 0.005/α)CO
2e
− 0.000323RH)CO
em
, where α is the hydrogen to carbon ratio as measured for the fuel used.

CO
em
=Carbon monoxide concentration of the dilute exhaust sample as measured, in ppm.

RH = Relative humidity of the dilution air, percent.

CO
d
=Carbon monoxide concentration of the dilution air corrected for water vapor extraction, in ppm.

CO
dm
=Carbon monoxide concentration of the dilution air sample as measured, in ppm.

(
2
) If a CO instrument which meets the criteria specified in § 86.1311 of this chapter is used and the conditioning column has been deleted, CO
em
must be substituted directly for CO
e
, and CO
dm
must be substituted directly for CO
d.

(E) M
CH4 mode
=Methane emissions corrected for background, in gram per hour by mode, are calculated using the following equations:

M
CH4 mode
=(V
mix
) (Density
CH4
) (CH
4conc
/10
6
) /V
f

CH
4conc
=C
CH4e
− C
CH4d
(1 − (1/DF))

Where:

Density
CH4
=Density of methane is 18.89 g/ft
3
at 68 °F (20 °C) and 760 mm Hg (101.3kPa) pressure.

CH
4conc
=Methane concentration of the dilute exhaust corrected for background, in ppm.

C
CH4e
=Methane concentration in the dilute exhaust, in ppm.

C
CH4d
=Methane concentration in the dilution air, in ppm.

(F) M
CH3OH mode
=Methanol emissions corrected for background, in gram per hour by mode, are calculated using the following equations:

M
CH3OH mode
=(V
mix
)(Density
CH3OH
) (CH
3
OH
conc
/10
6
)/V
f

CH3OH
conc
=C
CH3OHe
− C
CH3OHd
(1 − (1/DF))

C
CH3OHe
=((3.817)(10
− 2
)(T
EM
) (((C
S1
)(AV
S1
)) + (C
S2
) (AV
S2
)))/((P
B
)(V
EM
))

C
CH3OHd
=((3.817)(10
-2
)(T
DM
)(((C
D1
) (AV
D1
)) + (C
D2
) (AV
D2
)))/((P
B
)(V
DM
))

Where:

Density
CH3OH
=Density of methanol is 37.71 g/ft
3
(1.332 kg/m
3
), at 68 °F (20 °C) and 760 mm Hg (101.3kPa) pressure.

CH3OH
conc
=Methanol concentration of the dilute exhaust corrected for background, in ppm.

C
CH3OHe
=Methanol concentration in the dilute exhaust, in ppm.

C
CH3OHd
=Methanol concentration in the dilution air, in ppm.

T
EM
=Temperature of methanol sample withdrawn from dilute exhaust, °R.

T
DM
=Temperature of methanol sample withdrawn from dilution air, °R.

P
B
=Barometric pressure during test, mm Hg.

V
EM
=Volume of methanol sample withdrawn from dilute exhaust, ft
3
.

V
DM
=Volume of methanol sample withdrawn from dilution air, ft
3
.

C
S
=GC concentration of aqueous sample drawn from dilute exhaust, μg/ml.

C
D
=GC concentration of aqueous sample drawn from dilution air, μg/ml.

A
VS
=Volume of absorbing reagent (deionized water) in impinger through which methanol sample from dilute exhaust is drawn, ml.

A
VD
=Volume of absorbing reagent (deionized water) in impinger through which methanol sample from dilution air is drawn, ml.

1
=first impinger.

2
=second impinger.

(G) M
C2H5OH mode
=Ethanol emissions corrected for background, in gram per hour by mode, are calculated using the following equations:

M
CH3CH2OH mode
=(V
mix
)(Density
CH3CH2OH
) ((CH
3
CH
2
OH
conc
/10
6
))/V
f

CH
3
CH
2
OH
conc
=C
CH3CH2OHe
− C
CH3CH2OHd
(1 − (1/DF))

C
CH3CH2OHd
=((2.654)(10
− 2
)(T
DM
)(((C
D1
)(AV
D1
)) + (C
D2
)(AV
D2
)))/((P
B
)(V
DM
))

C
CH3CH2OHe
=((2.654)(10
−

2
)(T
EM
)(((C
S1
)(AV
S1
)) + (C
S2
)(AV
S2
)))/((P
B
)(V
EM
))

Where:

Density
C2H5OH
=Density of ethanol is 54.23 g/ft
3
(1.915 kg/m
3
), at 68 °F (20 °C) and 760 mm Hg (101.3kPa) pressure.

CH
3
CH
2
OH
conc
=Ethanol concentration of the dilute exhaust corrected for background, in ppm.

C
CH3CH2OHe
=Ethanol concentration in the dilute exhaust, in ppm.

C
CH3CH2OHd
=Ethanol concentration in the dilution air, in ppm.

T
EM
= Temperature of ethanol sample withdrawn from dilute exhaust, °R.

T
DM
=Temperature of ethanol sample withdrawn from dilution air, °R.

P
B
=Barometric pressure during test, mm Hg.

V
EM
=Volume of ethanol sample withdrawn from dilute exhaust, ft
3
.

V
DM
=Volume of ethanol sample withdrawn from dilution air, ft
3
.

C
S
=GC concentration of aqueous sample drawn from dilute exhaust, μg/ml.

C
D
=GC concentration of aqueous sample drawn from dilution air, μg/ml.

A
VS
= Volume of absorbing reagent (deionized water) in impinger through which ethanol sample from dilute exhaust is drawn, ml.

A
VD
=Volume of absorbing reagent (deionized water) in impinger through which ethanol sample from dilution air is drawn, ml.

1
=first impinger.

2
=second impinger.

(H) M
CH2O mode
=Formaldehyde emissions corrected for background, in gram per hour by mode, are calculated using the following equations:

M
CH2O mode
=(V
mix
)(Density
CH2O
) ((CH
2
O
conc
/10
6
)/V
f

CH2O
conc
=C
CH2Oe
− C
CH2Od
(1 − (1/DF))

C
CH2Oe
=((4.069)(10
−2
)(C
FDE
)(V
AE
) (Q)(T
EF
))/((V
SE
)(P
B
)

C
CH2Od
=((4.069)(10
− 2
)(C
FDA
)(V
AA
)(Q)(T
DF
))/(V
SA
)(P
B
)

Where:

Density
CH2O
=Density of formaldehyde is 35.36 g/ft
3
(1.249 kg/m
3
), at 68 °F (20 °C) and 760 mmHg (101.3 kPa) pressure.

CH2O
conc
=Formaldehyde concentration of the dilute exhaust corrected for background, ppm.

C
CH2Oe
=Formaldehyde concentration in dilute exhaust, ppm.

C
CH2Od
=Formaldehyde concentration in dilution air, ppm.

C
FDE
=Concentration of DNPH derivative of formaldehyde from dilute exhaust sample in sampling solution, μg/ml.

V
AE
=Volume of sampling solution for dilute exhaust formaldehyde sample, ml.

Q = Ratio of molecular weights of formaldehyde to its DNPH derivative = 0.1429.

T
EF
=Temperature of formaldehyde sample withdrawn from dilute exhaust, °R.

V
SE
=Volume of formaldehyde sample withdrawn from dilute exhaust, ft
3.

P
B
=Barometric pressure during test, mm Hg.

C
FDA
=Concentration of DNPH derivative of formaldehyde from dilution air sample in sampling solution, μg/ml.

V
AA
=Volume of sampling solution for dilution air formaldehyde sample, ml.

T
DF
=Temperature of formaldehyde sample withdrawn from dilution air, °R.

V
SA
=Volume of formaldehyde sample withdrawn from dilution air, ft
3.

(I) M
CH3CHO mode
=Acetaldehyde emissions corrected for background, in grams per hour by mode, are calculated using the following equations:

M
CH3CHO mode
= (V
mix
)(Density
CH3CHO
)((CH
3
CHO
conc
/10
6
)/V
f

CH3CHO
conc
=C
CH3CHOe
− C
CH3CHOd
(1—(1/DF))

C
CH3CHOe
=((2.774)(10
− 2
) (C
ADE
)(V
AE
)(Q)(T
EF
))/((V
SE
)(P
B
)

C
CH3CHOd
=((2.774)(10
− 2
) (C
ADA
)(V
AA
)(Q)(T
DF
))/(V
SA
)(P
B
)

Where:

Density
CH3CHO
=Density of acetaldehyde is 51.88 g/ft
3
(1.833 kg/m
3
), at 68 °F (20 °C) and 760 mmHg (101.3 kPa) pressure.

CH3CHO
conc
=Acetaldehyde concentration of the dilute exhaust corrected for background, ppm.

C
CH3CHOe
=Acetaldehyde concentration in dilute exhaust, ppm.

C
CH3CHOd
=Acetaldehyde concentration in dilution air, ppm.

C
ADE
=Concentration of DNPH derivative of acetaldehyde from dilute exhaust sample in sampling solution, μg/ml.

V
AE
=Volume of sampling solution for dilute exhaust acetaldehyde sample, ml.

Q=Ratio of molecular weights of acetaldehyde to its DNPH derivative

=0.182

T
EF
=Temperature of acetaldehyde sample withdrawn from dilute exhaust, °R.

V
SE
=Volume of acetaldehyde sample withdrawn from dilute exhaust, ft
3.

P
B
=Barometric pressure during test, mm Hg.

C
ADA
Concentration of DNPH derivative of acetaldehyde from dilution air sample in sampling solution, μg/ml.

V
AA
=Volume of sampling solution for dilution air acetaldehyde sample, ml.

T
DF
=Temperature of acetaldehyde sample withdrawn from dilution air, °R.

V
SA
=Volume of acetaldehyde sample withdrawn from dilution air, ft
3.

(J) M
NMHC mode
=Nonmethane hydrocarbon emissions, in grams per hour by mode.

M
NMHC mode
=(V
mix
)(Density
NMHC
) ((NMHCE
conc
/10
6
))/V
f

NMHC
conc
=NMHC
e
—(NMHC
d
)(1 − (1/DF))

NMHC
e
=FID HC
e
− (r
m
)(C
CH4e
)

NMHC
d
=FID HC
d
− (r
m
)(C
CH4d
)

Where:

Density
NMHC
=Density of nonmethane hydrocarbons=16.42 g/ft
3
(0.5800 kg/m
3
) for # 1 petroleum diesel fuel, 16.27 g/ft
3
(0.5746 kg/m
3
) for #2 diesel, and 16.33 for other fuels, assuming an average carbon to hydrogen ratio of 1:1.93 for #1 petroleum diesel fuel, 1:1.80 for #2 petroleum diesel fuel, and 1:1.85 for nonmethane hydrocarbons in other fuels at standard conditions.

NMHC
conc
=Nonmethane hydrocarbon concentration of the dilute exhaust sample corrected for background, in ppm carbon equivalent (i.e., equivalent propane × 3).

NMHC
e
=Nonmethane hydrocarbon concentration of the dilute exhaust bag sample:

FID HC
e
=Concentration of hydrocarbons in dilute exhaust as measured by the FID, ppm carbon equivalent.

rm=FID response to methane.

C
CH4e
=Concentration of methane in dilute exhaust as determined from the dilute exhaust sample.

NMHC
d
=Nonmethane hydrocarbon concentration of the dilution air:

FID HC
d
=Concentration of hydrocarbons in dilute exhaust as measured by the FID, ppm carbon equivalent.

r
m
=FID response to methane.

C
CH4d
=Concentration of methane in dilute exhaust as determined from the dilute exhaust sample, ppm.

(4)
Particulate exhaust emissions.
The mass of particulate for a test mode determined from the following equations when a heat exchanger is used (i.e., no flow compensation), and when background filters are used to correct for background particulate levels:

M
PM mode
=Particulate emissions, grams per hour by mode.

M
PM mode
=(WVol)(PM
conc
)(1 + DF)=(V
mix
)(PM
conc
)/V
f

PM
conc
=PM
e
− PM
d
(1 − (1/DF))

PM
e
=M
PMe
/V
sampe
/10
3

PM
d
=M
PMd
/V
sampd
/10
3

Where:

PM
conc
=Particulate concentration of the diluted exhaust sample corrected for background, in g/ft
3

M
PMe
=Measured mass of particulate for the exhaust sample, in mg, which is the difference in filter mass before and after the test.

M
PMd
=Measured mass of particulate for the dilution air sample, in mg, which is the difference in filter mass before and after the test.

V
sampe
=Total wet volume of sample removed from the dilution tunnel for the exhaust particulate measurement, cubic feet at standard conditions.

V
sampd
=Total wet volume of sample removed from the dilution tunnel for the dilution air particulate measurement, cubic feet at standard conditions.

DF=Dilution factor, which is the volumetric ratio of the dilution air to the raw exhaust sample, calculated as:

ER16AP98.014

(c)
Humidity calculations.
(1) The following abbreviations (and units) apply to paragraph (b) of this section:

BARO=barometric pressure (Pa).

H=specific humidity, (g H
2
O/g of dry air).

K
H
=conversion factor=0.6220 g H
2
O/g dry air.

M
air
=Molecular weight of air=28.9645.

M
H2O
=Molecular weight of water=18.01534.

P
DB
=Saturation vapor pressure of water at the dry bulb temperature (Pa).

P
DP
=Saturation vapor pressure of water at the dewpoint temperature (Pa).

P
v
=Partial pressure of water vapor (Pa).

P
WB
=Saturation vapor pressure of water at the wet bulb temperature (Pa).

T
DB
=Dry bulb temperature (Kelvin).

T
WB
=Wet bulb temperature (Kelvin).

Y=Water-vapor volume concentration.

(2) The specific humidity on a dry basis of the intake air (H) is defined as:

H=((K
H
) (P
v
)/(BARO − P
v
))

(3) The partial pressure of water vapor may be determined using a dew point device. In that case:

P
v
=P
DP

(4) The percent of relative humidity (RH) is defined as:

RH=(P
v
/P
DB
)100

(5) The water-vapor volume concentration on a dry basis of the engine intake air (Y) is defined as:

Y=((H)(M
air
)/(M
H2O
)=P
v
/(BARO − P
v
)

(d)
NO
X

correction factor.
(1) NO
X
emission rates (M
NOx mode
) shall be adjusted to account for the effects of humidity and temperature by multiplying each emission rate by K
NOx
, which is calculated from the following equations:

K
NOx
=(K)(1 + (0.25(logK)
2
)
1/2
)

K=(K
H
)(K
T
)

K
H
=[C
1
+ C
2
(exp(( − 0.0143)(10.714))]/[C
1
+ C
2
(exp(( − 0.0143)(1000H))]

C
1
= − 8.7 + 164.5exp( − 0.0218(A/F)
wet
)

C
2
=130.7 + 3941exp( − 0.0248(A/F)
wet
)

Where:

(A/F)
wet
=Mass of moist air intake divided by mass of fuel intake.

K
T
=1/[1-0.017(T
30
-T
A
)] for tests conducted at ambient temperatures below 30 °C.

K
T
=1.00 for tests conducted at ambient temperatures at or above 30 °C.

T
30
=The measured intake manifold air temperature in the locomotive when operated at 30 °C (or 100 °C, where intake manifold air temperature is not available).

T
A
=The measured intake manifold air temperature in the locomotive as tested (or the ambient temperature ( °C), where intake manifold air temperature is not available).

(e)
Other calculations.
Calculations other than those specified in this section may be used with the advance approval of the Administrator.

[FR Doc. 01-55530 Filed 11-23-01; 8:45 am]

Editorial Note:

On Monday, November 26, 2001, this rule document FR Doc. 01-55530 appeared on 66 FR 58953-58964. Due to additional text being inadvertently added, it is being reprinted in its entirety.

[FR Doc. R1-55530 Filed 11-28-01; 8:45 am]
BILLING CODE 1505-01-D
!!!Jenn!!!

FEDERAL RESERVE SYSTEM
[Docket No. R-1115]
Federal Reserve Bank Services

Correction

In notice document 01-27779 beginning on page 56310 in the issue of Wednesday, November 7, 2001, make the following corrections:

1. On page 56310, in Table 1, the title should have appeared as follows:

Table 1.—Pro Forma Cost and Revenue Performance
a

2. On page 56315, in Table 5, in the fourth column, the column title, “Estimated growth 2001 (percent)” should read, “Estimated 2001 growth (percent)”.

3. On the same page, Table 7 should have appeared as follows:

Table 7.—Selected Check Fees

2001 Current price ranges
2002 price ranges

Items:
(per item)
(per item)

Forward-processed

City
$0.001 to 0.079
$0.001 to 0.079

RCPC
$0.003 to 0.200

$0.003 to
0.300

Forward fine-sort

City
$0.003 to 0.021
$0.003 to 0.021

RCPC
$0.003 to 0.036

$0.004
to 0.036

Qualified returned checks

City
$0.08 to 0.85
$0.08 to 0.85

RCPC
$0.10 to 1.15
$0.10 to 1.15

Raw returned checks

City
$1.05 to 5.00
$1.05 to 5.00

RCPC
$1.05 to 5.00
$1.05 to 5.00

Cash letters:
(per cash letter)
(per cash letter)

Forward-processed
a

$2.00 to 32.00

$2.25 to 36.00

Forward fine-sort
$3.00 to 14.00

$3.50 to 14.00

Returned checks: raw/qualified
$2.00 to 14.00

$2.00 to
14.50

Payor bank services:
(Fixed) (per item)
(Fixed) (per item)

MICR information
$2-15 $0.0020-0.0070

$2-15
$0.0030-0.0110

Electronic presentment
$1-11 $0.0005-0.0100

$1-
12
$0.0005-0.0100

Truncation
$2-7 $0.0020-0.0180

$2-7
$0.0040-
0.0180

Image capture
$2-15 $0.0020-0.02
$2-15 $0.002-0.02

Image delivery

Varies
b
$0.001-0.008

Varies
b

$0.002
-0.008

Image archive
N/A $0.001-0.01
N/A $0.001-0.01

Image retrieval
N/A $0.3-5
N/A $0.3-5

Note:
Bold indicates change from 2001 prices.

a
Cash letter fees for forward-processed items transported on Check Relay for 2001 and 2002 include a fifty-cent surcharge due to higher fuel costs.

b
Fixed fee varies by media type.

4. On page 56319, in Table 10, the line below the title, “In millions of dollars” should read, “[In millions of dollars]”.

5. On page 56321, in the second column, in the footnote, in the second to the last line, “shore” should read, “short”.

6. On page 56323, Table 13 should have appeared as follows:

Table 13.—Comparison of Pro Forma Balance Sheets for Federal Reserve Priced Services
[Millions of dollars—average for year]

2002
2001

Short-term assets:

Imputed reserve requirement on clearing balances
27

$ 678.5
$ 742.4

Investment in marketable securities
27

5,473.0
6,681.9

Receivables
81.7
77.3

Materials and supplies
3.8
3.6

Prepaid expenses
27.8
23.4

Items in process of collection
28

4,102.8
3,606.7

Total short-term assets
10,367.6
11,135.3

Long-term assets:

Premises
29

431.1
417.5

Furniture and equipment
177.7
185.5

Leasehold improvements and long-term prepayments
70.4
73.9

Prepaid pension costs
800.1
718.5

Total long-term assets
1,479.3
1,395.4

Total assets
$11,846.9
$12,530.7

Short-term liabilities:

Clearing balances and balances arising from early credit of uncollected items
$ 7,377.5
$ 7,424.3

Deferred credit items
28

3,509.8
3,606.7

Short-term debt
30

0.0
18.9

Short-term payables
103.9
85.4

Total short-term liabilities
10,991.2
11,135.3

Long-term liabilities:

Postemployment/retirement benefits
263.4
251.9

Long-term debt
30

0.0
479.1

Total long-term liabilities
263.4
731.0

Total liabilities
11,254.6
11,866.3

Equity
592.3
664.4

Total liabilities and equity
$11,846.9
$12,530.7

27
Funded with clearing balances.

28
Represents float costs that are directly estimated at the service level.

29
Includes allocations of Board of Governors' assets to priced services of $1.1 million for 2002 and $0.7 million for 2001.

30
No debt is imputed in 2002 because clearing balances are used as an available funding source.

7. On page 56324, Table 14 should have appeared as follows:

Table 14.—Portion of clearing balances used to fund priced services assets in 2002

[Dollar amounts in millions]

A. Short-term asset funding:

Short-term assets to be funded:

Receivables
$81.7

Materials and supplies
3.8

Prepaid expenses
27.8

Total short-term assets to be funded

113.3

Short-term funding sources:

Short-term payables

103.9

Portion of short-term assets funded with imputed short-term debt or non-core clearing balances
31

9.4

B. Long-term asset funding:

Long-term assets to be funded:

Premises
$431.1

Furniture and equipment
177.7

Leasehold improvements and long-term prepayments
70.4

Prepaid pension cost
800.1

Total long-term assets to be funded

$1,479.3

Long-term funding sources:

Postemployment/retirement benefits liability
263.4

Imputed equity
32

592.3

855.7

Portion of long-term assets funded with imputed long-term debt or core clearing balances
31

623.6

C. Total clearing balances used for funding priced-services assets

$633.0

31
Clearing balances shown on table 13 are available for funding priced-services assets. Using these balances reduces the amount available for investment in Treasury bills for the net income on clearing balances calculation. Short-term assets are funded with non-core clearing balances. Long-term assets are funded with core clearing balances; a total of $4 billion in balances is available for this purpose. No short- or long-term debt is imputed.

32
See table 16 for calculation of required imputed equity amount.

8. On page 56325, in Table 15, under the Total column, in the first entry, “$78.5” should read, “$678.5”.

9. On the same page, in Table 16, the title should have appeared as follows:

Table 16.—Derivation of the 2002 and 2001 PSAF
[Dollar amounts in millions]

10. On page 56326, in the continued Table 16, in the first entry, omit “Total equity”.

11. On the same page, in Table 17, in the Weighted assests column, in the first entry, “0.0” should read, “$0.0”.

12. On page 56328, in the “Noncash Collection Fee Schedule—Continued” table, in the fees column, “
52
40.00” should read, “40.00
52
”.

13. On page 56329, the table title should appear as follows:

Test and Contingency Options
61

[FR Doc. C1-27779 Filed 11-28-01; 8:45 am]
BILLING CODE 1505-01-D
!!!Michele

DEPARTMENT OF TRANSPORTATION
Federal Aviation Administration
14 CFR Part 121
[Docket No. FAA-2001-10770;SFAR 92-2]
RIN 2120-AH54
Flightcrew Compartment Access and Door Designs

Correction

In rule document 01-29280 beginning on page 58650 in the issue of Wednesday, November 21, 2001, make the following correction:

SFAR 92-2 [Corrected]
On page 58653, in the third column, in paragraph 4, in the 10th line, after “the” should read, “flightcrew compartment shall be available to any crewmember during flight, except for”.

[FR Doc. C1-29280 Filed 11-28-01; 8:45 am]
BILLING CODE 1505-01-D

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Source: Frix Law Library, https://www.frixlaw.com/law-library/documents/fr%3AC1-29109. Public record. Not legal advice.