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É«Æ×·å chromatographic peak
·åµ× peak base
·å¸ß h£¬peak height
·å¿í W£¬peak width
°ë¸ß·å¿í Wh/2£¬peak width at half height
·åÃæ»ý A£¬peak area
ÍÏβ·å tailing area
ǰÉì·å leading area
¼Ù·å ghost peak
»û·å distorted peak
·´·å negative peak
¹Õµã inflection point
Ô­µã origin
°ßµã spot
Çø´ø zone
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Çø´øÍÑβ zone tailing
»ùÏß base line
»ùÏ߯¯ÒÆ baseline drift
»ùÏßÔëÉù N£¬baseline noise
ͳ¼Æ¾Ø moment
Ò»½×Ô­µã¾Ø ¦Ã1£¬first origin moment
¶þ½×ÖÐÐÄ¾Ø ¦Ì2£¬second central moment
Èý½×ÖÐÐÄ¾Ø ¦Ì3£¬third central moment
ÒºÏàÉ«Æ×·¨ liquid chromatography£¬LC
ҺҺɫÆ×·¨ liquid liquid chromatography£¬LLC
Òº¹ÌÉ«Æ×·¨ liquid solid chromatography£¬LSC
ÕýÏàÒºÏàÉ«Æ×·¨ normal phase liquid
chromatography
·´ÏàÒºÏàÉ«Æ×·¨ reversed phase liquid
chromatography£¬RPLC
ÖùÒºÏàÉ«Æ×·¨ liquid column chromatography
¸ßЧҺÏàÉ«Æ×·¨ high performance liquid
chromatography£¬HPLC
³ß´çÅųýÉ«Æ×·¨ size exclusion chromatography£¬
SEC
Äý½º¹ýÂËÉ«Æ×·¨ gel filtration chromatography
Äý½ºÉøÍ¸É«Æ×·¨ gel permeation chromatography£¬
GPC
Ç׺ÍÉ«Æ×·¨ affinity chromatography
Àë×Ó½»»»É«Æ×·¨ ion exchange chromatography£¬IEC
Àë×ÓÉ«Æ×·¨ ion chromatography
Àë×ÓÒÖÖÆÉ«Æ×·¨ ion suppression chromatography
Àë×Ó¶ÔÉ«Æ×·¨ ion pair chromatography
ÊèË®×÷ÓÃÉ«Æ×·¨ hydrophobic interaction
chromatography
ÖÆ±¸ÒºÏàÉ«Æ×·¨ preparative liquid chromatography
Æ½ÃæÉ«Æ×·¨ planar chromatography
ֽɫÆ×·¨ paper chromatography
±¡²ãÉ«Æ×·¨ thin layer chromatography£¬TLC
¸ßЧ±¡²ãÉ«Æ×·¨ high performance thin layer
chromatography£¬HPTLC
½þ×Õ±¡²ãÉ«Æ×·¨ impregnated thin layer
chromatography
Äý½º±¡²ãÉ«Æ×·¨ gel thin layer chromatography
Àë×Ó½»»»±¡²ãÉ«Æ×·¨ ion exchange thin layer
chromatography
ÖÆ±¸±¡²ãÉ«Æ×·¨ preparative thin layer
chromatography
±¡²ã°ôÉ«Æ×·¨ thin layer rod chromatography
ÒºÏàÉ«Æ×ÒÇ liquid chromatograph
ÖÆ±¸ÒºÏàÉ«Æ×ÒÇ preparative liquid chromatograph
Äý½ºÉøÍ¸É«Æ×ÒÇ gel permeation chromatograph
Í¿²¼Æ÷ spreader
µãÑùÆ÷ sample applicator
É«Æ×Öù chromatographic column
°ô×´É«Æ×Öù monolith column monolith column
΢Á£Öù microparticle column
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¿ÕÐÄÖù open tubular column
΢¾¶Öù microbore column
»ìºÏÖù mixed column
×éºÏÖù coupled column
Ô¤Öù precolumn
±£»¤Öù guard column
Ô¤±¥ºÍÖù presaturation column
ŨËõÖù concentrating column
ÒÖÖÆÖù suppression column
±¡²ã°å thin layer plate
ŨËõÇø±¡²ã°å concentrating thin layer plate
Ó«¹â±¡²ã°å fluorescence thin layer plate
·´Ïౡ²ã°å reversed phase thin layer plate
Ìݶȱ¡²ã°å gradient thin layer plate
ÉÕ½á°å sintered plate
Õ¹¿ªÊÒ development chamber
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Æø¶¯±Ã pneumatic pump
È䶯±Ã peristaltic pump
¼ì²âÆ÷ detector
΢·Ö¼ì²âÆ÷ differential detector
»ý·Ö¼ì²âÆ÷ integral detector
×ÜÌåÐÔÄܼì²âÆ÷ bulk property detector
ÈÜÖÊÐÔÄܼì²âÆ÷ solute property detector
(ʾ²î)ÕÛ¹âÂʼì²âÆ÷ [differential] refractive index
detector
Ó«¹â¼ì²âÆ÷ fluorescence detector
×ÏÍâ¿É¼û¹â¼ì²âÆ÷ ultraviolet visible detector
µç»¯Ñ§¼ì²âÆ÷ electrochemical detector
Õô·¢(¼¤¹â)¹âÉ¢Éä¼ì²âÆ÷ [laser] light scattering
detector
¹âÃÜ¶È¼Æ densitometer
±¡²ãɨÃèÒÇ thin layer scanner
Öùºó·´Ó¦Æ÷ post-column reactor
Ìå»ý±ê¼ÇÆ÷ volume marker
¼Ç¼Æ÷ recorder
»ý·ÖÒÇ integrator
Áó·ÖÊÕ¼¯Æ÷ fraction collector
¹¤×÷Õ¾ work station
¹Ì¶¨Ïà stationary phase
¹Ì¶¨Òº stationary liquid
ÔØÌå support
ÖùÌî³ä¼Á column packing
»¯Ñ§¼üºÏÏàÌî³ä¼Á chemically bonded phase
packing
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¶à¿×ÐÍÌî³ä¼Á porous packing
Îü¸½¼Á adsorbent
Àë×Ó½»»»¼Á ion exchanger
»ùÌå matrix
ÔØ°å support plate
Õ³ºÏ¼Á binder
Á÷¶¯Ïà mobile phase
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Õ¹¿ª¼Á developer
µÈË®ÈݼÁ isohydric solvent
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ÏÔÉ«¼Á color [developing] agent
ËÀʱ¼ä t0£¬dead time
±£Áôʱ¼ä tR£¬retention time
µ÷Õû±£Áôʱ¼ä t'R£¬adjusted retention time
ËÀÌå»ý V0£¬dead volume
±£ÁôÌå»ý vR£¬retention volume
µ÷Õû±£ÁôÌå»ý v'R£¬adjusted retention volume
ÖùÍâÌå»ý Vext£¬extra-column volune
Á£¼äÌå»ý V0£¬interstitial volume
(¶à¿×Ìî³ä¼ÁµÄ)¿×Ìå»ý VP£¬pore volume of porous
packing
ÒºÏà×ÜÌå»ý Vtol£¬total liquid volume
Ï´ÍÑÌå»ý ve£¬elution volume
Á÷ÌåÁ¦Ñ§Ìå»ý vh£¬hydrodynamic volume
Ïà¶Ô±£ÁôÖµ ri.s£¬relative retention value
·ÖÀëÒò×Ó ¦Á£¬separation factor
Á÷¶¯ÏàÇ¨ÒÆ¾àÀë dm£¬mobile phase migration
distance
Á÷¶¯ÏàÇ°ÑØ mobile phase front
ÈÜÖÊÇ¨ÒÆ¾àÀë ds£¬solute migration distance
±ÈÒÆÖµ Rf£¬Rf value
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Ïà¶Ô±ÈÒÆÖµ Ri.s£¬relative Rf value
±£Áô³£ÊýÖµ Rm£¬Rm value
°åЧÄÜ plate efficiency
Õۺϰå¸ß hr£¬reduced plate height
·ÖÀë¶È R£¬resolution
ÒºÏàÔØºÉÁ¿ liquid phase loading
Àë×Ó½»»»ÈÝÁ¿ ion exchange capacity
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ÉøÍ¸¼«ÏÞ permeability limit
Åųý¼«ÏÞ Vh£¬max£¬exclusion limit
ÍÏβÒò×Ó T£¬tailing factor
ÖùÍâЧӦ extra-column effect
¹Ü±ÚЧӦ wall effect
¼ä¸ô±ÛЧӦ spacer arm effect
±ßԵЧӦ edge effect
°ßµã¶¨Î»·¨ localization of spot
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ÉúÎï×ÔÏÔÓ°·¨ bioautography
¹éÒ»·¨ normalization method
Äڱ귨 internal standard method
Íâ±ê·¨ external standard method
µþ¼Ó·¨ addition method
ÆÕÊÊУ׼(ÇúÏß¡¢º¯Êý) calibration function or curve
Æ×´øÀ©Õ¹(¼Ó¿í) band broadening
(·ÖÀë×÷ÓõÄ)У׼º¯Êý»òУ׼ÇúÏß universal
calibration function or curve [of separation]
¼Ó¿íУÕý broadening correction
¼Ó¿íУÕýÒò×Ó broadening correction factor
ÈܼÁÇ¿¶È²ÎÊý ¦Å0£¬solvent strength parameter
Ï´ÍÑÐòÁÐ eluotropic series
Ï´ÍÑ(ÁÜÏ´) elution
µÈ¶ÈÏ´ÍÑ gradient elution
ÌݶÈÏ´ÍÑ gradient elution
(ÔÙ)Ñ­»·Ï´ÍÑ recycling elution
ÏßÐÔÈܼÁÇ¿¶ÈÏ´ÍÑ linear solvent strength gradient
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Õ¹¿ª development
ÉÏÐÐÕ¹¿ª ascending development
ÏÂÐÐÕ¹¿ª descending development
Ë«ÏòÕ¹¿ª two dimensional development
»·ÐÎÕ¹¿ª circular development
ÀëÐÄÕ¹¿ª centrifugal development
ÏòÐÄÕ¹¿ª centripetal development
¾¶ÏòÕ¹¿ª radial development
¶à´ÎÕ¹¿ª multiple development
·Ö²½Õ¹¿ª stepwise development
Á¬ÐøÕ¹¿ª continuous development
ÌݶÈÕ¹¿ª gradient development
ÔȽ¬Ìî³ä slurry packing
Í£Á÷½øÑù stop-flow injection
·§½øÑù valve injection
ÖùÉϸ»¼¯ on-column enrichment
Á÷³öÒº eluate
ÖùÉϼì²â on-column detection
ÖùÊÙÃü column life
ÖùÁ÷ʧ column bleeding
ÏÔÆ× visualization
»î»¯ activation
·´³å back flushing
ÍÑÆø degassing
¹µÁ÷ channeling
¹ýÔØ overloading
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