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burette µÎ¶¨¹Ü calconcarboxylic acid ¸ÆÖ¸Ê¾¼Á calibrated curve У׼ÇúÏß calibration У׼ catalyzed reaction ´ß»¯·´Ó¦ cerimetry îæÁ¿·¨ charge balance µçºÉƽºâ chelate òüºÏÎï chelate extraction òüºÏÎïÝÍÈ¡ chemical analysis »¯Ñ§·ÖÎö chemical factor »¯Ñ§ÒòËØ chemically pure »¯Ñ§´¿ chromatography É«Æ×·¨ chromophoric group ·¢É«ÍÅ coefficient of variation ±äÒìϵÊý color reagent ÏÔÉ«¼Á color transition point ÑÕɫת±äµã colorimeter ±ÈÉ«¼Æ colorimetry ±ÈÉ«·¨ column chromatography ÖùÉ«Æ× complementary color »¥²¹É« complex ÂçºÏÎï complexation ÂçºÏ·´Ó¦ complexometry complexometric titration ÂçºÏµÎ¶¨·¨ complexone °±ôÈÂçºÏ¼Á concentration constant Ũ¶È³£Êý conditional extraction constant Ìõ¼þÝÍÈ¡³£Êý conditional formation coefficient Ìõ¼þÐγɳ£Êý conditional potential Ìõ¼þµçλ conditional solubility product Ìõ¼þÈܶȻý confidence interval ÖÃÐÅÇø¼ä confidence level ÖÃÐÅˮƽ conjugate acid-base pair ¹²éîËá¼î¶Ô constant weight ºãÁ¿ contamination Õ´ÎÛ continuous extraction Á¬ÐøÝÍÈ¡ continuous spectrum Á¬Ðø¹âÆ× coprecipitation ¹²³Áµí correction УÕý correlation coefficient Ïà¹ØÏµÊý crucible ÛáÛö crystalline precipitate ¾§ÐγÁµí cumulative constant ÀÛ»ý³£Êý curdy precipitate ÄýÈé×´³Áµí degree of freedom ×ÔÓÉ¶È demasking ½â±Î derivative spectrum µ¼Êý¹âÆ× desiccant; drying agent ¸ÉÔï¼Á desiccator ±£¸ÉÆ÷ determinate error ¿É²âÎó²î deuterium lamp ë®µÆ deviation Æ«²î deviation average ƽ¾ùÆ«²î dibasic acid ¶þÔªËá dichloro fluorescein ¶þÂÈÓ«¹â»Æ dichromate titration ÖØ¸õËá¼Ø·¨ dielectric constant ½éµç³£Êý differential spectrophotometry ʾ²î¹â¶È·¨ differentiating effect Çø·ÖЧӦ dispersion ɫɢ dissociation constant Àë½â³£Êý distillation ÕôÁó distribution coefficient ·ÖÅäϵÊý distribution diagram ·Ö²¼Í¼ distribution ratio ·ÖÅä±È double beam spectrophotometer Ë«¹âÊø·Ö¹â¹â¶È¼Æ dual-pan balance Ë«ÅÌÌìÆ½ dual-wavelength spectrophotometry Ë«²¨³¤·Ö¹â¹â¶È·¨ electronic balance µç×ÓÌìÆ½ electrophoresis µçÓ¾ eluent ÁÜÏ´¼Á end point ÖÕµã end point error ÖÕµãÎó²î enrichment ¸»¼¯ eosin Êïºì equilibrium concentration ƽºâŨ¶È equimolar series method µÈĦ¶ûϵÁз¨ Erelenmeyer flask ×¶ÐÎÆ¿ eriochrome black T (EBT) ¸õºÚT error Îó²î ethylenediamine tetraacetic acid (EDTA) ÒÒ¶þ°·ËÄÒÒËá evaporation dish Õô·¢Ãó exchange capacity ½»»»ÈÝÁ¿ extent of crosslinking ½»Áª¶È extraction constant ÝÍÈ¡³£Êý extraction rate ÝÍÈ¡ÂÊ extraction spectrphotometric method ÝÍÈ¡¹â¶È·¨ Fajans method ·¨Ñî˹·¨ ferroin ÁÚ¶þµª·ÆÑÇÌúÀë×Ó filter ©¶· filter ÂË¹âÆ¬ filter paper ÂËÖ½ filtration ¹ýÂË fluex ÈܼÁ fluorescein Ó«¹â»Æ flusion ÈÛÈÚ formation constant Ðγɳ£Êý frequency ƵÂÊ frequency density ƵÂÊÃÜ¶È frequency distribution ƵÂÊ·Ö²¼ gas chromatography (GC) ÆøÏàÉ«Æ× grating ¹âÕ¤ gravimetric factor ÖØÁ¿ÒòËØ gravimetry ÖØÁ¿·ÖÎö guarantee reagent (GR) ±£Ö¤ÊÔ¼Á high performance liquid chromatography (HPLC) ¸ßЧҺÏàÉ«Æ× histogram Ö±·½Í¼ homogeneous precipitation ¾ùÏà³Áµí hydrogen lamp ÇâµÆ hypochromic shift ×ÏÒÆ ignition ׯÉÕ indicator ָʾ¼Á induced reaction ÓÕµ¼·´Ó¦ inert solvent ¶èÐÔÈܼÁ instability constant ²»Îȶ¨³£Êý instrumental analysis ÒÇÆ÷·ÖÎö intrinsic acidity ¹ÌÓÐËá¶È intrinsic basicity ¹ÌÓмî¶È intrinsic solubility ¹ÌÓÐÈܽâ¶È iodimetry µâµÎ¶¨·¨ iodine-tungsten lamp µâÎÙµÆ iodometry µÎ¶¨µâ·¨ ion association extraction Àë×ÓµÞºÏÎïÝÍÈ¡ ion chromatography (IC) Àë×ÓÉ«Æ× ion exchange Àë×Ó½»»» ion exchange resin Àë×Ó½»»»Ê÷Ö¬ ionic strength Àë×ÓÇ¿¶È isoabsorptive point µÈÎüÊÕµã Karl Fisher titration ¿¨¶û•·ÑЪ¶û·¨ Kjeldahl determination ¿Ê϶¨µª·¨ Lambert-Beer law Àʲ´-±È¶û¶¨ÂÉ leveling effect ÀƽЧӦ ligand ÅäλÌå light source ¹âÔ´ line spectrum Ïß×´¹âÆ× linear regression ÏßÐԻعé liquid chromatography (LC) ÒºÏàÉ«Æ× macro analysis ³£Á¿·ÖÎö masking ÑڱΠmasking index ÑÚ±ÎÖ¸Êý mass balance ÎïÁÏÆ½ºâ matallochromic indicator ½ðÊôָʾ¼Á maximum absorption ×î´óÎüÊÕ mean, average ƽ¾ùÖµ measured value ²âÁ¿Öµ measuring cylinder Á¿Í² measuring pipette ÎüÁ¿¹Ü median ÖÐλÊý mercurimetry ¹¯Á¿·¨ mercury lamp ¹¯µÆ mesh [ɸ]Ä¿ methyl orange (MO) ¼×»ù³È methyl red (MR) ¼×»ùºì micro analysis ΢Á¿·ÖÎö mixed constant »ìºÏ³£Êý mixed crystal »ì¾§ mixed indicator »ìºÏָʾ¼Á mobile phase Á÷¶¯Ïà Mohr method ζû·¨ molar absorptivity Ħ¶ûÎüÊÕϵÊý mole ratio method Ħ¶û±È·¨ molecular spectrum ·Ö×Ó¹âÆ× monoacid Ò»ÔªËá monochromatic color µ¥É«¹â monochromator µ¥É«Æ÷ neutral solvent ÖÐÐÔÈܼÁ neutralization ÖÐºÍ non-aqueous titration ·ÇË®µÎ¶¨ normal distribution Õý̬·Ö²¼ occlusion °ü²Ø organic phase ÓлúÏà ossification of indicator ָʾ¼ÁµÄ½©»¯ outlier ÀëȺֵ oven ºæÏä paper chromatography(PC) ֽɫÆ× parallel determination ƽÐвⶨ path lenth ¹â³Ì permanganate titration ¸ßÃÌËá¼Ø·¨ phase ratio Ïà±È phenolphthalein (PP) ·Ó̪ photocell ¹âµç³Ø photoelectric colorimeter ¹âµç±ÈÉ«¼Æ photometric titration ¹â¶ÈµÎ¶¨·¨ photomultiplier ¹âµç±¶Ôö¹Ü phototube ¹âµç¹Ü pipette ÒÆÒº¹Ü polar solvent ¼«ÐÔÈܼÁ polyprotic acid ¶àÔªËá population ×ÜÌå postprecipitation ºó³Áµí precipitant ³Áµí¼Á precipitation form ³ÁµíÐÎ precipitation titration ³ÁµíµÎ¶¨·¨ precision ¾«ÃÜ¶È preconcentration Ô¤¸»¼¯ predominance-area diagram ÓÅÊÆÇøÓòͼ primary standard »ù×¼ÎïÖÊ prism Àâ¾µ probability ¸ÅÂÊ proton ÖÊ×Ó proton condition ÖÊ×ÓÌõ¼þ protonation ÖÊ×Ó»¯ protonation constant ÖÊ×Ó»¯³£Êý purity ´¿¶È qualitative analysis ¶¨ÐÔ·ÖÎö quantitative analysis ¶¨Á¿·ÖÎö quartering ËÄ·Ö·¨ random error Ëæ»úÎó²î range È«¾à(¼«²î) reagent blank ÊÔ¼Á¿Õ°× Reagent bottle ÊÔ¼ÁÆ¿ recording spectrophotometer ×Ô¶¯¼Ç¼ʽ·Ö¹â¹â¶È¼Æ recovery »ØÊÕÂÊ redox indicator Ñõ»¯»¹Ôָʾ¼Á redox titration Ñõ»¯»¹ÔµÎ¶¨ referee analysis Öٲ÷ÖÎö reference level ²Î¿¼Ë®Æ½ reference material (RM) ±ê×¼ÎïÖÊ reference solution ²Î±ÈÈÜÒº relative error Ïà¶ÔÎó²î resolution ·Ö±æÁ¦ rider ÓÎÂë routine analysis ³£¹æ·ÖÎö sample Ñù±¾,ÑùÆ· sampling È¡Ñù self indicator ×ÔÉíָʾ¼Á semimicro analysis °ë΢Á¿·ÖÎö separation ·ÖÀë separation factor ·ÖÀëÒòÊý side reaction coefficient ¸±·´Ó¦ÏµÊý significance test ÏÔÖøÐÔ¼ìÑé significant figure ÓÐЧÊý×Ö simultaneous determination of multiponents ¶à×é·Öͬʱ²â¶¨ single beam spectrophotometer µ¥¹âÊø·Ö¹â¹â¶È¼Æ single-pan balance µ¥ÅÌÌìÆ½ slit ÏÁ·ì sodium diphenylamine sulfonate ¶þ±½°·»ÇËáÄÆ solubility product ÈܶȻý solvent extraction ÈܼÁÝÍÈ¡ species ÐÍÌå(ÎïÖÖ) specific extinction coefficient ±ÈÏû¹âϵÊý spectral analysis ¹âÆ×·ÖÎö spectrophotometer ·Ö¹â¹â¶È¼Æ spectrophotometry ·Ö¹â¹â¶È·¨ stability constant Îȶ¨³£Êý standard curve ±ê×¼ÇúÏß standard deviation ±ê׼ƫ²î standard potential ±ê×¼µçλ standard series method ±ê׼ϵÁз¨ standard solution ±ê×¼ÈÜÒº standardization ±ê¶¨ starch µí·Û stationary phase ¹Ì¶¨Ïà steam bath ÕôÆøÔ¡ stepwise stability constant Öð¼¶Îȶ¨³£Êý stoichiometric point »¯Ñ§¼ÆÁ¿µã structure analysis ½á¹¹·ÖÎö supersaturation ¹ý±¥ºÍ systematic error ϵͳÎó²î test solution ÊÔÒº thermodynamic constant ÈÈÁ¦Ñ§³£Êý thin layer chromatography (TLC) ±¡²ãÉ«Æ× titrand ±»µÎÎï titrant µÎ¶¨¼Á titration µÎ¶¨ titration constant µÎ¶¨³£Êý titration curve µÎ¶¨ÇúÏß titration error µÎ¶¨Îó²î titration index µÎ¶¨Ö¸Êý titration jump µÎ¶¨Í»Ô¾ titrimetry µÎ¶¨·ÖÎö trace analysis ºÛÁ¿·ÖÎö transition interval ±äÉ«¼ä¸ô transmittance ͸Éä±È tri acid ÈýÔªËá true value ÕæÖµ tungsten lamp ÎÙµÆ ultratrace analysis ³¬ºÛÁ¿·ÖÎö UV-VIS spectrophotometry ×ÏÍâ-¿É¼û·Ö¹â¹â¶È·¨ volatilization »Ó·¢ Volhard method ¸£¶û¹þµÂ·¨ volumetric flask ÈÝÁ¿Æ¿ volumetry ÈÝÁ¿·ÖÎö Wash bottle Ï´Æ¿ washings Ï´Òº water bath ˮԡ weighing bottle ³ÆÁ¿Æ¿ weighting form ³ÆÁ¿ÐÎ weights íÀÂë working curve ¹¤×÷ÇúÏß xylenol orange (XO) ¶þ¼×·Ó³È zero level Áãˮƽ |
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