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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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