ГОСТ 34895-2022 (ISO 14532:2014) Газ природный. Качество. Термины и определения (с Поправкой)

AAS method

3.2.2.21

absorber

3.3.3.7

absorption-spectroscopic method

3.2.2.11

addition of odours

3.9.9

adjustment of measuring instrument

3.5.1.2

alkyl disulfide

3.6.3.3

alkyl mercaptan

3.6.3.1

alkyl sulfide

3.6.3.2

analysis function

3.6.4.6

atomic absorption spectrometry method

3.2.2.21

automatic dew point hygrometer

3.11.3

automatic hydrocarbon dew point analyzer

3.11.6

automatic Karl Fischer titrator

3.11.8

auxiliary gases

3.4.5

back-pressure regulator

3.3.3.4

bomb calorimeter

3.11.10

bracketing

3.5.1.10

bridge component

3.6.2.7

bubbler

3.3.3.6

bubbling type heavy hydrocarbons absorber

3.3.3.6

calibration

3.5.1.1

calibration function

3.6.4.5

calibration interval

3.5.1.6

caloric property

3.10.3

calorimetric method

3.2.2.9

carbonyl sulfide

3.6.3.4

carrier gas

3.4.4

CD

3.4.6

certified reference gas mixtures

3.6.6.3

certified reference material

3.6.6.2

chemiluminescence detector

3.4.6

chromatographic resolution

3.6.5.4

CNG

3.1.5

component composition

3.6.1.5

composite sample

3.3.1.9

compressed natural gas

3.1.5

compression factor

3.7.2.3

condenser

3.3.3.1

continuous sampling of liquefied natural gas

3.3.1.6

conventional normalization

3.6.5.1

corrected value of molar fraction

3.6.1.9

correction

3.5.1.4

correction factor

3.5.1.5

CRM

3.6.6.2

cyclic sulphide

3.6.3.5

density

3.7.2.4

detection threshold

3.9.11

dew point hygrometer

3.11.1

dew point method

3.2.2.10

dielcometric method

3.2.2.12

direct measurement

3.2.1.1

direct measurement of components

3.6.1.6

direct sampling

3.3.1.2

ED

3.4.7

electrochemical detector

3.4.7

electrochemical method

3.2.2.20

electrolytic method

3.2.2.14

energy

3.7.3.4

equation of state

3.10.4

extended working range

3.5.1.8

fast loop

3.3.2.12

FID

3.4.8

flame ionization detector

3.4.8

flame photometric detector

3.4.10

flash back

3.8.7

floating piston cylinder

3.3.2.5

flow proportional incremental sampler

3.3.2.7

flow proportional incremental sampling

3.3.1.5

flow type heavy hydrocarbon absorber

3.3.3.7

FPD

3.4.10

fugacity

3.10.6

fugacity coefficient

3.10.7

gas chromatograph

3.4.3

gas family

3.8.2

gas quality

3.1.8

glycols

3.6.3.9

gross calorific value

3.7.3.1

group of components

3.6.2.4

3.6.3.6

HCDP

3.7.4.2

heating device

3.3.3.5

hot loop

3.3.2.10

hydrocarbon dew point

3.7.4.2

hydrocarbon dew point analyzer

3.11.4

hydrogen sulphide

3.6.3.6

ideal gas

3.7.2.1

incremental sampler

3.3.2.6

incremental sampling

3.3.1.4

indirect measurement

3.2.1.2

indirect measurement of components

3.6.1.7

indirect sampling

3.3.1.3

initial value of molar fraction

3.6.1.8

in-line instrument

3.3.1.13

interchangeability

3.8.1

interferometric method

3.2.2.13

intermittent sampling of liquefied natural gas

3.3.1.7

introduction unit

3.4.2

iodometric method

3.2.2.4

ISO standard reference conditions

3.7.1.4

Karl Fischer coulometric method

3.2.2.18

Karl Fischer method

3.2.2.16

Karl Fischer titration method

3.2.2.17

Karl Fischer titrator

3.11.7

laboratory instrument

3.3.1.16

lifting

3.8.8

limit gas

3.8.4

liquefied natural gas

3.1.6

liquefied natural gas regasification

3.1.7

liquid separator

3.3.3.2

LNG

3.1.6

lower range value

3.2.1.3

main component

3.6.2.1

masking of odour

3.9.10

mass concentration

3.6.1.4

mass concentration of water vapours

3.7.4.3

mass fraction

3.6.1.2

mass-spectrometric method

3.2.2.8

mean normalization

3.6.5.2

measuring system

3.4.1

mercaptan sulfur

3.6.3.7

methane number

3.7.5.1

methanol

3.6.3.10

minor component

3.6.2.2

molar fraction

3.6.1.1

multi-point calibration

3.5.1.11

natural gas

3.1.1

natural gas for domestic applications

3.1.4

natural gas for industrial applications

3.1.3

natural gas, prepared for transportation by main gas pipelines

3.1.2

net calorific value

3.7.3.2

normal pressure

3.8.5

normal reference conditions

3.7.1.3

odorant

3.9.1

odorimeter

3.11.9

odorization

3.9.2

odour character

3.9.4

odour intensity

3.9.5

odour perception

3.9.3

on-line instrument

3.3.1.14

other components

3.6.2.5

oxidative microcoulometry method

3.2.2.7

PHLC

3.7.4.5

photocolorimetric method

3.2.2.5

piezoelectric method

3.2.2.15

portable instrument

3.3.1.15

potential hydrocarbon liquid content

3.7.4.5

potentiometric method

3.2.2.2

potentiometric titration

3.2.2.3

pressure reducer

3.3.3.3

purging time

3.3.4.2

pycnometer

3.11.11

pycnometric method

3.2.2.19

quality attribute

3.1.9

real gas

3.7.2.2

reference component

3.6.2.6

reference gas

3.8.3

reference material

3.6.6.1

reference measuring system

3.6.6.4

relative density

3.7.2.5

relative response factor

3.6.4.3

representative sample

3.3.1.8

residence time

3.3.4.1

residual property

3.10.5

response

3.6.4.1

response factor

3.6.4.2

response function

3.6.4.4

retrograde phenomena

3.7.4.4

RM

3.6.6.1

run-by-run normalization

3.6.5.3

sample conditioning system

3.3.2.9

sample container

3.3.2.4

sample line

3.3.2.8

sample probe

3.3.2.3

sampling

3.3.1.1

sampling device

3.3.2.2

sampling place

3.3.1.12

sampling point

3.3.1.11

sampling system

3.3.2.1

sensory fatigue

3.9.8

sensory rating

3.9.6

single-point calibration

3.5.1.9

span

3.2.1.5

spot sample

3.3.1.10

standard reference combustion conditions

3.7.1.2

standard reference conditions for determination

3.7.1.1

TCD

3.4.9

terminal threshold

3.9.7

test pressure

3.8.6

thermal conductivity detector

3.4.9

thermal property

3.10.2

thermodynamic property

3.10.1

thioether

3.6.3.5

total sulfur

3.6.3.8

trace components

3.6.2.3

ultraviolet fluorescence method

3.2.2.6

upper range value

3.2.1.4

vent line

3.3.2.11

visual dew point hygrometer

3.11.2

visual hydrocarbon dew point analyzer

3.77.5

volume fraction

3.6.7.3

volumetric conversion

3.5.7.3

water dew point

3.7.4.7

Wobbe index

3.7.3.3

working range

3.5.1.7

working standard

3.6.6.5

yellow tipping

3.8.9