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ÒõÀë×Ó½»»»É«Æ×·¨ anion exchange chromatography, AEC
ÒõÀë×Ó½»»»Ê÷Ö¬ anion exchange resin
Ó«¹â±¡²ã°å fluorescent thin layer plate
Ó«¹â¼ì²âÆ÷ fluorescence detector
Ó«¹âÉ«Æ×·¨ fluorescence chromatography
Ó­Í·É«Æ×·¨ frontal chromatography
Ó­Í·É«Æ×·¨ frontal method
Ó²£¨ÖÊ£©Äý½º hard gel
Ó¿ÀËЧӦ surge effect
Óлú¸Ä½ø¼Á organic modifier
ÓлúÏàÉúÎï´«¸ÐÆ÷ Organic biosensor
ÓÐЧ·åÊý effective peak number EPN
ÓÐЧÀíÂÛËþ°åÊý number of effective theoretical plates
ÓÐЧËþ°å¸ß¶È effective plate height
ÓÐЧÌÊ¶È effective mobility
ÓÔ»¯´¦Àí glazing
ÓÙ½¬Ìî³ä·¨ slurry packing method
ÓèÖù guard column
ÓèÖù pre-column
ԲͲģÐÍ cylindrical model
Ô²ÐÍֽɫÆ×·¨ circular paper chromatography
Ô²ÐÎÉ«Æ×·¨ circular chromatography
Ô²Öù×´³¬Î¢±¡²ãÉ«Æ×·¨ ultra micro TLC on a cylindrical suppor¡­
Ô²×¶Ä£ÐÍ conical model
ÔØÆø carrier gas
ÔØÆø¾»»¯Æ÷ carry gas cleanser
ÔØÆøÁ÷ËÙ flow rate
ÔØÆøÆ½¾ùÁ÷ËÙ average flow rate
ÔØÌå support
ÔØÌåµÄ¶Û»¯ deactivation of support
ÔØÌåµÄ»îÐÔ²¿Î» active site of support
ÔØÌåÍ¿²ã¿ª¿Ú¹ÜÖù support coated open tubular column£¬SCOT
ÔÙÉú¼Á regenerant
ÔÚÏßµç¶Ñ¼¯ on-line electrical stacking
ÔÚÖùµçµ¼Âʼì²â on-column electrical conductivity detection
ÔëÉù noise
ÔëÐÅ±È noise ¨Csignal ratio
ÔíĤÁ÷Á¿¼Æ soap film gas meter
ÔöÇ¿×ÏÍâ-¿É¼ûÎüÊÕ¼ì²â¼¼Êõ UV-visible absorption enhanced det¡­
Õ­Á£¶È·Ö²¼ narrow particle size distribution
Õ³¶È¼ì²âÆ÷ viscosity detector
Õ¹¿ª development
Õ¹¿ª²Û developing tank
Õ¹¿ª²Û±¥ºÍ Chamber saturation
Õ¹¿ª¼Á developer
ÕÛÉäÂʼì²âÆ÷ refractive index detector, RID
Õæ¿ÕÍÑÆø×°Öà vacuum degasser
ÕóÁÐëϸ¹ÜµçÓ¾ capillary array electrophoresis
Õô·¢¹âÉ¢Éä¼ì²âÆ÷ evaporative light-scattering detector, ELSD
ÕûÌåÐÔÖʼì²âÆ÷ integral property detector
ÕýÏà¸ßЧҺÏàÉ«Æ×·¨ normal phase high performance liquid chro¡­
ÕýÏàÀë×Ó¶ÔÉ«Æ×·¨ normal phase ion-pair chromatography
ÕýÏàëϸ¹ÜµçÉ«Æ× positive capillary electrokinetic chromatog¡­
Ö±½Ó»¯Ñ§Àë×Ó»¯ direct chemical ionization GC-MS
Ö±½Ó¼¤¹âÔÚÖùÎüÊÕ¼ì²â on-column direct laser detection
Ö¸ÊýʽÁ÷¶¯ exponential flow
ֽɫÆ×·¨ paper chromatography
Öû»É«Æ×·¨ displacement chromatography
ÖÆ±¸É«Æ× preparative chromatography
ÖÆ±¸É«Æ×ÒÇ preparative chromatograph
ÖÆ±¸Öù preparation column
ÖÇÄÜÉ«Æ× chromatography with artificial intelligence
ÖÊÁ¿Á÷Á¿ mass flow rate
ÖÊÁ¿É«Æ× mass chromatography
ÖÊÁ¿Ðͼì²âÆ÷ mass detector
ÖÊÁ¿Ðͼì²âÆ÷ mass flow rate sensitive detector
ÖпÕÏËάÒÖÖÆÆ÷ hollow fiber suppressor
ÖÐѹҺÏàÉ«Æ× middle-pressure liquid chromatography
ÖØ½¨É«Æ×ͼ reconstructive chromatogram
ÖØ¾ù·Ö×ÓÁ¿ weight mean molecular weight
ÖáÏòÀ©É¢ longitudinal diffusion
ÖáÏòÎüÊÕ³Ø absorption pool of axial direction
ÖáÏòѹËõÖù axial compression column
Öù¶Ëµçµ¼Âʼì²â out-let end detection of electrical conductiv¡­
Öù¸ºÔØÄÜÁ¦ column loadability
ÖùºóÑÜÉú»¯ post-column derivatization
ÖùÀÏ»¯ column ageing
ÖùÀÏ»¯ condition (aging) of column
ÖùÁ÷³öÎï (column) effluent
ÖùÁ÷ʧ column bleeding
ÖùÄÚ¾¶ column internal diameter
ÖùǰÑÜÉú»¯ pro-column derivatization
ÖùÇл»¼¼Êõ column switching technique
ÖùÇåÏ´ column cleaning
ÖùÈÝÁ¿ column capacity
ÖùÈë¿ÚѹÁ¦ column inlet pressure
ÖùÉ«Æ×·¨ column chromatography
ÖùÉϼì²â on-line detection
ÖùÉøÍ¸ÐÔ column permeability
ÖùÊÙÃü column life
ÖùÍ·½øÑù column head sampling
ÖùÍâЧӦ extra-column effect
ÖùÎÂÏä column oven
ÖùЧ column efficiency
Öùѹ column pressure
ÖùÔÙÉú column regeneration
ÖùÖÐÑÜÉú»¯ on-column derivatization
×¢Éä±Ã syringe pump
ת»¯¶¨Á¿·¨ trans-quantitative method
×ÏÍâ-¿É¼û¹â¼ì²âÆ÷ ultraviolet visible detector, UV-Vis
×ÏÍâÎüÊÕ¼ì²âÆ÷ ultraviolet absorption detector
×Ô¶¯½øÑùÆ÷ automatic sampler
×ÔÓÉÈÜҺëϸ¹ÜµçÓ¾ free solution capillary electrophoresis
×Ü·ÖÀëЧÄÜÖ¸±ê over-all resolution efficiency
×ܽ»»»ÈÝÁ¿ total exchange capacity
×ÜÉøÍ¸Ìå»ý total osmotic volume
×ÝÏòÀ©É¢ longitudinal diffusion
×éºÏʽÒÇÆ÷ϵͳ building block instrument
×î¼ÑÁ÷ËÙ optimum flow rate
×î¼Ñʵ¼ÊÁ÷ËÙ optimum practical flow rate
×îС¼ì²âÁ¿ minimum detectable quantity
×îС¼ì²âŨ¶È minimum detectable concentration
ÝÍȡɫÆ×·¨ extraction chromatography
ë²µçÀë¼ì²âÆ÷ argon ionization detector
òüºÏÀë×Ó½»»»¼Á chelating ion exchanger
òüºÏÀë×ÓÉ«Æ×·¨ chelating ion chromatography
òüºÏÊ÷Ö¬ chelating resin
ÍÑÑõºËÌǺËËáµç»¯Ñ§´«¸ÐÆ÷ DNA sensor
Íâ±ê·¨ external standard method
ÍâÌÝ¶È outside gradient
Íø×´½á¹¹ reticular structure
Íù¸´±Ã reciprocating pump
Íù¸´Ê½¸ôĤ±Ã reciprocating diaphragm pump
΢·ÖÐͼì²âÆ÷ differential detector
΢¿×Ê÷Ö¬ micro-reticular resin
΢¿âÂØ¼ì²âÆ÷ micro coulometric detector
΢Á¿½øÑùÕë micro-syringe
΢Á¿É«Æ×·¨ micro-chromatography
΢ĤÒÖÖÆÆ÷ micro-membrane suppressor
΢ÈéÒºµç¶¯É«Æ× microemulsion electrokinetic chromatography
΢ÉúÎï´«¸ÐÆ÷ Microbial sensor
΢ÉúÎïÏÔÓ° bioautography
΢Ìî³äÖù micro-packed column
΢Îü¸½¼ì²âÆ÷ micro adsorption detector
΢ÐÍÖù micro-column
β´µÆø make-up gas
ζ¾õ´«¸ÐÆ÷ taste sensor
ÎÐÁ÷À©É¢ eddy diffusion
ÎÞ·ÅÉäÔ´µç×Ó·ý»ñ¼ì²âÆ÷ non-radioactive electron capture dete¡­
ÎÞ»úÀë×Ó½»»»¼Á inorganic ion exchanger
ÎÞ½ºÉ¸·Öëϸ¹ÜµçÓ¾ non-gel capillary electrophoresis
ÎÞ¿×µ¥·ÖÉ¢ÌîÁÏ non-porous monodisperse packing
ÎÞÂö¶¯É«Æ×±Ã pulse-free chromatographic pump
ÎïÀí¶Û»¯·¨ physical deactivation
Îü¸½µÈÎÂÏß adsorption isotherm
Îü¸½¼Á adsorbing material
Îü¸½¼Á»îÐÔ adsorbent activity
Îü¸½Æ½ºâ³£Êý adsorption equilibrium constant
Îü¸½ÈܼÁÇ¿¶È²ÎÊý adsorption solvent strength parameter
Îü¸½É«Æ×·¨ adsorption chromatography
Îü¸½ÐÍPLOTÖù adsorption type porous-layer open tubular colum¡­
Îü¸½Öù adsorption column
Îü¹â¶È±ÈÖµ·¨ absorbance ratio method
Ï´ÍÑÇ¿¶È eluting power
ÏÂÐÐÕ¹¿ª·¨ descending development method
ÏÔÉ«Æ÷ color-developing sprayer
ÏÞÖÆÀ©É¢ÀíÂÛ theory of restricted diffusion
ÏßËÙ¶È linear velocity
ÏßÐÔÌÝ¶È linear gradient
Ïà±ÈÂÊ phase ratio
Ïà¶Ô±£ÁôÖµ relative retention value
Ïà¶Ô±ÈÒÆÖµ relative Rf value
Ïà¶Ô»Ó·¢¶È relative volatility
Ïà¶ÔÁéÃô¶È relative sensitivity
Ïà¶Ô̼£¨ÖØÁ¿£©ÏìÓ¦Òò×Ó relative carbon response factor
Ïà¶ÔÏìÓ¦Öµ relative response
Ïà¶ÔУÕýÒò×Ó relative correction factor
Ïà½»Êø¼¤¹âÓÕµ¼µÄÈÈ͸¾µ²âÁ¿ heat lens detection of intersect ¡­
ÏàËÆÏàÈÜÔ­Ôò rule of similarity
ÏìӦʱ¼ä response time
ÏìÓ¦Öµ response
С½Ç¼¤¹âÉ¢Éä¹â¶È¼Æ low-angle laser light scattering photomet¡­
СÄÚ¾¶Ã«Ï¸¹ÜÖù Microbore column
УÕý±£ÁôÌå»ý corrected retention volume
УÕýÇúÏß·¨ calibration curve method
УÕýÒò×Ó correction factor
оƬµçÓ¾ microchip electrophoresis
Ðýת±¡²ã·¨ rotating thin layer chromatography
ÐýתСÊÒÄæÁ÷É«Æ× rotational little-chamber counter-current c¡­
Ñ¡ÔñÐÔ¼ì²âÆ÷ selective detector
Ñ­»·É«Æ×·¨ recycling chromatography
ѹµç¾§Ìå piezoelectric crystal
ѹµçÃâÒß´«¸ÐÆ÷ Piezoelectric Immunosensor
ѹµçת»»Æ÷ piezoelectric transducer
ѹÁ¦±£»¤ pressure protect
ѹÁ¦ÉÏÏÞ pressure high limit
ѹÁ¦ÌݶÈУÕýÒò×Ó pressure gradient correction factor
ѹÁ¦ÏÂÏÞ pressure low limit
ÑÎÎöÉ«Æ×·¨ salting-out chromatography
ÑÎÎöֽɫÆ×·¨ salting-out paper chromatography
ÑÜÉú»¯·¨ derivatization method
ÑÜÉú»¯ÊÔ¼Á derivatization reagent
ÑôÀë×Ó½»»»¼Á cation exchanger
ÑôÀë×Ó½»»»É«Æ×·¨ cation exchange chromatography, CEC
Ñõ»¯ÂÁÉ«Æ×·¨ alumina chromatography
ÑùÆ·»· sample loop
ÑùÆ·Ô¤´¦Àí sample pretreatment
Òº-Òº·ÖÅäÉ«Æ×·¨ liquid-liquid partition chromatography
Òº-ҺɫÆ×·¨ liquid-liquid chromatography
ÒºµÎÄæÁ÷É«Æ× drop counter-current chromatography
Òº¹ÌÉ«Æ× liquid-solid chromatography
Òº¾§¹Ì¶¨Ïà liquid crystal stationary phase
Һ̬Àë×Ó½»»»¼Á liquid ion exchanger
ÒºÏà´«ÖÊ×èÁ¦ resistance of liquid mass transfer
ÒºÏàÉ«Æ×-¸µÀïÒ¶±ä»»ºìÍâ¹âÆ×ÁªÓà liquid chromatography-FTIR
ÒºÏàÉ«Æ×-ÖÊÆ×·ÖÎö·¨ liquid chromatography-mass spectrometry
ÒºÏàÉ«Æ×-ÖÊÆ×ÒÇ liquid chromatography-mass spectrometer
ÒºÏàÉ«Æ×·¨ liquid chromatography
ÒºÏàÔØºÉÁ¿ liquid phase loading
Ò»µÎÒºÏàÉ«Æ×·¨ one drop liquid chromatography
ÒÖÖÆÆ÷ suppressor
ÒÖÖÆÐ͵絼¼ì²â suppressed conductance detection
ÒÖÖÆÐÍÀë×ÓÉ«Æ×·¨ suppressed ion chromatography, SIC
ÒÖÖÆÖù suppressed column
ÒçÁ÷Çø flooded zonevvv
Èܽâ¶È²ÎÊý solubility parameter
ÈÜÒºÐÔÄܼì²âÆ÷ solution property detector
ÈÜÕÍ swelling
ÈÜÖÊÐÔÖʼì²âÆ÷ solute property detector
ÈÝÁ¿Òò×Ó capacity factor
ÈÞë´ÙÐÔÏÙ´«¸ÐÆ÷ Human chorionic gonadotropin sensor
È齺¸½¾ÛÐÍÀë×Ó½»»»¼Á latex-agglomerated ion exchanger
Èí£¨ÖÊ£©Äý½º soft gel
Èõ¼îÐÔÒõÀë×Ó½»»»¼Á weak-base anion exchanger
ÈõËáÐÔÑôÀë×Ó½»»»¼Á weakly acidic cation exchanger
ÈûʽÁ÷ plug flow
ÈûʽÁ÷¶¯ plug flow
É«Æ×·¨ chromatography
É«Æ×·å chromatographic peak
É«Æ×·åÇøÓò¿í¶È peak width
É«Æ×¸»¼¯¹ýÑù samt injection of chromatography
É«Æ×¹¤×÷Õ¾ chromatographic working station
É«Æ×ͼ chromatogram
É«Æ×ÒÇ chromatograph
É«Æ×Ö½ chromatographic paper
É«Æ×Öù chromatographic column
É«Æ×Öù column
É«Æ×ÖùÇл»¼¼Êõ switching column technique
ɸ·Ö½éÖÊsieving medium
ÉÏÐÐÕ¹¿ª·¨ ascending development method
ÉßÁý£¨×´£©Ê÷Ö¬ snake cage resin
É䯵·Åµç¼ì²âÆ÷ radiofrequency discharge detector
ÉøÍ¸¼«ÏÞ·Ö×ÓÁ¿ permeation limit molecular weight
ÉúÎïºÄÑõ´«¸ÐÆ÷ Biological oxygen-consumption sensor
ÉúÎïÀûÓÃ¶È bioavailability
ÉúÎïĤµç¼« Biomembrane electrode
ÉúÎïÇ׺ÍÐÍ´«¸ÐÆ÷ Biological affinity sensor
ÉúÎïÉ«Æ× biological chromatography
ÉúÎïÌØÒìÐÔÖù biospecific column
ÉúÎï×ÔÏÔÓ°·¨ bioautography
ÉýÎÂËÙÂÊ temperature rate
ʪ·¨ÖùÌî³ä wet column packing
Ê®°ËÍé»ù¼üºÏ¹è½º octadecyl silane
ʯī»¯Ì¼ºÚ graphitized carbon black
ʵÐÄÔØÌå solid support
ʾ²îÕÛ¹â¼ì²âÆ÷ differential refraction detector
ÊÔ¼ÁÏÔÉ«·¨ reagent color-developing method
ÊÖ¶¯½øÑùÆ÷ manual injector
ÊÖÐÔ°±»ùËáÑÜÉúÎïGC¹Ì¶¨Ïà chiral amino acid derivatives stat¡­
ÊÖÐÔ²ð·ÖÊÔ¼Á chiral selectors
ÊÖÐԹ̶¨Ïà chiral stationary phase
ÊÖÐԹ̶¨Ïà²ð·Ö·¨ chiral solid phase separation
ÊÖÐÔ»·ºý¾«ÑÜÉúÎïGC¹Ì¶¨Ïà chiral cyclodextrin der GC
ÊÖÐÔ½ðÊôÂçºÏÎïGC¹Ì¶¨Ïà chirametal stationary phase in GC
ÊÖÐÔÁ÷¶¯Ïà chiral mobile phase
ÊÖÐÔÁ÷¶¯Ïà²ð·Ö·¨ chiral mobile phase separation
ÊÖÐÔÆøÏàÉ«Æ×·¨ chiral gas chromatography
ÊÖÐÔÉ«Æ×chiral chromatography
ÊÖÐÔÊÔ¼Á chiral reagent
ÊÖÐÔÑÜÉú»¯·¨ chiral derivation method
ÊèÈܼÁÀíÂÛ solvophobic theory
ÊèÈܼÁÉ«Æ×·¨ solvophobic chromatography
ÊèÈܼÁ×÷ÓÃÀíÂÛ solvophobic interaction principle
ÊèË®×÷ÓÃÉ«Æ× hydrophobic interaction chromatography
Ê÷Ö¬½»»»ÈÝÁ¿ exchange capacity of resin
Êý¾ù·Ö×ÓÁ¿ number mean molecular weight
Ë«±£Áô»úÀí dual reservation mechanism
Ë«µç²ã electrical double layer
Ë«»îÈûÍù¸´±Ã two-piston reciprocating pump
Ë«Êø²î·Ö¼ì²âÆ÷ detector of dual-beam difference
Ë«ÏòÕ¹¿ª·¨ two-dimensional development method
Ë«Öù¶¨ÐÔ·¨ double-column qualitative method
Ë«ÖùÀë×ÓÉ«Æ×·¨ dual column ion chromatography
Ë«ÖùÉ«Æ×·¨ dual column chromatography
Ë®Äý½º hydragel
ˮϵÄý½ºÉ«Æ×Öù aqua-system gel column
˲¼äÀë×Ó»ùÌåЧӦ moment ion matrix effect
ËÀÇøÓò dead zone
ËÀÌå»ý dead volume
ËÜÁϱà plastic pump
ËáÏ´·¨ acid wash
ËáÐÔȾÁϱÈÉ«·¨ acid dye colorimetry
Ëþ°åÀíÂÛ·½³Ì plate theory equation
̼·Ö×Óɸ carbon molecular sieve
ÌÆÄÏÅųâ Donnan exclusion
ÌØÊâÑ¡Ôñ¹Ì¶¨Òº selective stationary phase
ÌݶÈÏ´ÍÑ gradient elution
ÌݶÈÏ´ÍÑ×°Öà gradient elution device
ÌݶÈÒºÏàÉ«Æ× gradient liquid chromatography
Ìå»ýÅųâÀíÂÛ size exclusion theory
Ìå»ýÅųâÉ«Æ×size exclusion chromatography
Ìå»ýÉ«Æ×·¨ volumetric chromatography
Ìî³äëϸ¹ÜÖù packed capillary column
Ìî³äÖù packed column
ÌîÁÏ packing material
Í£Á÷½øÑù stop-flow injection
ͨÓÃÐͼì²âÆ÷ common detector
Í¿±Úëϸ¹ÜÖù wall coated open tubular column£¬WCOT
Í¿²¼Æ÷ spreader
Í¿²ãëϸ¹Ü coated capillary
Í¿×Õ coat
Í¿×ÕЧÂÊ coating efficiency
ÍÏβ·å tailing peak
ÍÏβÒò×Ó tailing factor
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helen8087

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8Â¥2008-11-26 14:56:38
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