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¡¡¡¡absolute error µ´¹ï»~®t

absorbance §l¥ú«×

absorbent §lªþ¾¯

absorption curve §l¦¬¦±½u

absorption peak §l¦¬®p

absorptivity §l¦¬¨t¼Æ

accident error °¸µM»~®t

accuracy ­ãÚÌ«×

acid-base titration »ÄÆPºw©w

acidic effective coefficient »Ä®ÄÀ³¨t¼Æ

acidic effective curve »Ä®ÄÀ³¦±½u

acidity constant »Ä«×±`¼Æ

activity ¬¡«×

activity coefficient ¬¡«×¨t¼Æ

adsorption §lªþ

adsorption indicator §lªþ«ü¥Ü¾¯

affinity ¿Ë©M¤O

aging ³¯¤Æ

amorphous precipitate µL©w§Î¨IÕà

amphiprotic solvent ¨â©Ê·»¾¯

amphoteric substance ¨â©Êª«½è

amplification reaction ©ñ¤j¤ÏÀ³

analytical balance ¤ÀªR¤Ñ¥­

analytical chemistry ¤ÀªR¤Æ¾Ç

analytical concentration ¤ÀªR¿@«×

analytical reagent (AR) ¤ÀªR¸Õ¾¯

apparent formation constant ªíÆ[§Î¦¨±`¼Æ

aqueous phase ¤ô¬Û

argentimetry »È¶qªk

ashing ¦Ç¤Æ

atomic spectrum ­ì¤l¥úÃÐ

autoprotolysis constant ½è¤l¦Û»¼±`¼Æ

auxochrome group §U¦â¹Î

back extraction ¤ÏµÑ¨ú

band spectrum ±aª¬¥úÃÐ

bandwidth ±a¼e

bathochromic shift ¬õ²¾

blank ªÅ¥Õ

blocking of indicator «ü¥Ü¾¯ªº«Ê³¬

bromometry ·Í¶qªk

buffer capacity ½w½Ä®e¶q

buffer solution ½w½Ä·»²G

burette ºw©wºÞ

calconcarboxylic acid ¶t«ü¥Ü¾¯

calibrated curve ®Õ­ã¦±½u

calibration ®Õ­ã

catalyzed reaction ¶Ê¤Æ¤ÏÀ³

cerimetry à°¶qªk

charge balance ¹q²ü¥­¿Å

chelate îg¦Xª«

chelate extraction îg¦Xª«µÑ¨ú

chemical analysis ¤Æ¾Ç¤ÀªR

chemical factor ¤Æ¾Ç¦]¯À

chemically pure ¤Æ¾Ç¯Â

chromatography ¦âÃЪk

chromophoric group µo¦â¹Î

coefficient of variation ÅÜÉݨt¼Æ

color reagent Åã¦â¾¯

color transition point ÃC¦âÂàÅÜÂI

colorimeter ¤ñ¦â­p

colorimetry ¤ñ¦âªk

column chromatography ¬W¦âÃÐ

complementary color ¤¬¸É¦â

complex µ¸¦Xª«

complexation µ¸¦X¤ÏÀ³

complexometry complexometric titration µ¸¦Xºw©wªk

complexone ®òßnµ¸¦X¾¯

concentration constant ¿@«×±`¼Æ

conditional extraction constant ±ø¥óµÑ¨ú±`¼Æ

conditional formation coefficient ±ø¥ó§Î¦¨±`¼Æ

conditional potential ±ø¥ó¹q¦ì

conditional solubility product ±ø¥ó·»«×¿n

confidence interval ¸m«H°Ï¶¡

confidence level ¸m«H¤ô¥­

conjugate acid-base pair ¦@³m»ÄÆP¹ï

constant weight ùÚ¶q

contamination ªg¦Ã

continuous extraction ³sÄòµÑ¨ú

continuous spectrum ³sÄò¥úÃÐ

coprecipitation ¦@¨IÕà

correction ®Õ¥¿

correlation coefficient ¬ÛÃö¨t¼Æ

crucible ©X³ú

crystalline precipitate ´¹§Î¨IÕà

cumulative constant ²Ö¿n±`¼Æ

curdy precipitate ¾®¨Åª¬¨IÕà

degree of freedom ¦Û¥Ñ«×

demasking ¸Ñ½ª

derivative spectrum ¾É¼Æ¥úÃÐ

desiccant; drying agent ¤zÀ꾯

desiccator «O¤z¾¹

determinate error ¥i´ú»~®t

deuterium lamp É÷¿O

deviation °¾®t

deviation average ¥­§¡°¾®t

dibasic acid ¤G¤¸»Ä

dichloro fluorescein ¤G´âº·¥ú¶À

dichromate titration ­«»Ì»Ä¹[ªk

dielectric constant ¤¶¹q±`¼Æ

differential spectrophotometry ¥Ü®t¥ú«×ªk

differentiating effect °Ï¤À®ÄÀ³

dispersion ¦â´²

dissociation constant Öøѱ`¼Æ

distillation »]ÃH

distribution coefficient ¤À°t¨t¼Æ

distribution diagram ¤À¥¬¹Ï

distribution ratio ¤À°t¤ñ

double beam spectrophotometer Âù¥ú§ô¤À¥ú¥ú«×­p

dual-pan balance Âù½L¤Ñ¥­

dual-wavelength spectrophotometry Âùªiªø¤À¥ú¥ú«×ªk

electronic balance ¹q¤l¤Ñ¥­

electrophoresis ¹qªa

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end point ²×ÂI

end point error ²×ÂI»~®t

enrichment ´I¶°

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equilibrium concentration ¥­¿Å¿@«×

equimolar series method µ¥¼¯º¸¨t¦Cªk

Erelenmeyer flask À@§Î²~

eriochrome black T (EBT) »Ì¶ÂT

error »~®t

ethylenediamine tetraacetic acid (EDTA) ¤A¤GÓi¥|¤A»Ä

evaporation dish »]µo¥×

exchange capacity ¥æ´«®e¶q

extent of crosslinking ¥æÁp«×

extraction constant µÑ¨ú±`¼Æ

extraction rate µÑ¨ú²v

extraction spectrphotometric method µÑ¨ú¥ú«×ªk

Fajans method ªk·¨´µªk

ferroin ¾F¤G´áµá¨ÈÅKÖäl

filter º|¤æ

filter Âo¥ú¤ù

filter paper Âo¯È

filtration ¹LÂo

fluex ·»¾¯

fluorescein º·¥ú¶À

flusion º²¿Ä

formation constant §Î¦¨±`¼Æ

frequency ÀW²v

frequency density ÀW²v±K«×

frequency distribution ÀW²v¤À¥¬

gas chromatography (GC) Éa¬Û¦âÃÐ

grating ¥ú¬]

gravimetric factor ­«¶q¦]¯À

gravimetry ­«¶q¤ÀªR

guarantee reagent (GR) «Oµý¸Õ¾¯

high performance liquid chromatography (HPLC) °ª®Ä²G¬Û¦âÃÐ

histogram ª½¤è¹Ï

homogeneous precipitation §¡¬Û¨IÕà

hydrogen lamp ²B¿O

hypochromic shift µµ²¾

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indicator «ü¥Ü¾¯

induced reaction »¤¾É¤ÏÀ³

inert solvent ´k©Ê·»¾¯

instability constant ¤£Ã­©w±`¼Æ

instrumental analysis »ö¾¹¤ÀªR

intrinsic acidity ©T¦³»Ä«×

intrinsic basicity ©T¦³ÆP«×

intrinsic solubility ©T¦³·»¸Ñ«×

iodimetry ¸Kºw©wªk

iodine-tungsten lamp ¸KÂë¿O

iodometry ºw©w¸Kªk

ion association extraction Öäl½l¦Xª«µÑ¨ú

ion chromatography (IC) Öäl¦âÃÐ

ion exchange Öäl¥æ´«

ion exchange resin Öäl¥æ´«¾ð¯×

ionic strength Öäl±j«×

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Lambert-Beer law ®Ôªy-¤ñº¸©w«ß

leveling effect ©Ô¥­®ÄÀ³

ligand °t¦ìÊ^

light source ¥ú·½

line spectrum ½uª¬¥úÃÐ

linear regression ½u©Ê¦^Âk

liquid chromatography (LC) ²G¬Û¦âÃÐ

macro analysis ±`¶q¤ÀªR

masking 񯫦

masking index ±»½ª«ü¼Æ

mass balance ª«®Æ¥­¿Å

matallochromic indicator ª÷ÄÝ«ü¥Ü¾¯

maximum absorption ³Ì¤j§l¦¬

mean, average ¥­§¡­È

measured value ´ú¶q­È

measuring cylinder ¶qµ©

measuring pipette §l¶qºÞ

median ¤¤¦ì¼Æ

mercurimetry ¨E¶qªk

mercury lamp ¨E¿O

mesh [¿z]¥Ø

methyl orange (MO) ¥Ò°ò¾í

methyl red (MR) ¥Ò°ò¬õ

micro analysis ·L¶q¤ÀªR

mixed constant ²V¦X±`¼Æ

mixed crystal ²V´¹

mixed indicator ²V¦X«ü¥Ü¾¯

mobile phase ¬y°Ê¬Û

Mohr method ²öº¸ªk

molar absorptivity ¼¯º¸§l¦¬¨t¼Æ

mole ratio method ¼¯º¸¤ñªk

molecular spectrum ¤À¤l¥úÃÐ

monoacid ¤@¤¸»Ä

monochromatic color ³æ¦â¥ú

monochromator ³æ¦â¾¹

neutral solvent ¤¤©Ê·»¾¯

neutralization ¤¤©M

non-aqueous titration «D¤ôºw©w

normal distribution ¥¿ºA¤À¥¬

occlusion ¥]ÂÃ

organic phase ¦³Éó¬Û

ossification of indicator «ü¥Ü¾¯ªº»ø¤Æ

outlier Öøs­È

oven ¯M½c

paper chromatography(PC) ¯È¦âÃÐ

parallel determination ¥­¦æ´ú©w

path lenth ¥úµ{

permanganate titration °ª¿ø»Ä¹[ªk

phase ratio ¬Û¤ñ

phenolphthalein (PP) ×ô¡@

photocell ¥ú¹q¦À

photoelectric colorimeter ¥ú¹q¤ñ¦â­p

photometric titration ¥ú«×ºw©wªk

photomultiplier ¥ú¹q­¿¼WºÞ

phototube ¥ú¹qºÞ

pipette ²¾²GºÞ

polar solvent Ìå©Ê·»¾¯

polyprotic acid ¦h¤¸»Ä

population Á`Ê^

postprecipitation ¦Z¨IÕà

precipitant ¨IÕྯ

precipitation form ¨IÕà§Î

precipitation titration ¨IÕàºw©wªk

precision ºë±K«×

preconcentration ¹w´I¶°

predominance-area diagram ɬ¶Õ°Ï°ì¹Ï

primary standard °ò­ãª«½è

prism Ù±Ãè

probability ·§²v

proton ½è¤l

proton condition ½è¤l±ø¥ó

protonation ½è¤l¤Æ

protonation constant ½è¤l¤Æ±`¼Æ

purity ¯Â«×

qualitative analysis ©w©Ê¤ÀªR

quantitative analysis ©w¶q¤ÀªR

quartering ¥|¤Àªk

random error ÀHÉó»~®t

range ¥þ¶Z(Ìå®t)

reagent blank ¸Õ¾¯ªÅ¥Õ

Reagent bottle ¸Õ¾¯²~

recording spectrophotometer ¦Û°Ê°O¿ý¦¡¤À¥ú¥ú«×­p

recovery ¦^¦¬²v

redox indicator ®ñ¤ÆÁÙ­ì«ü¥Ü¾¯

redox titration ®ñ¤ÆÁÙ­ìºw©w

referee analysis ¥òµô¤ÀªR

reference level °Ñ¦Ò¤ô¥­

reference material (RM) ¼Ð­ãª«½è

reference solution °Ñ¤ñ·»²G

relative error ¬Û¹ï»~®t

resolution ¤À¿ë¤O

rider ´å½X

routine analysis ±`³W¤ÀªR

sample ¼Ë¥»,¼Ë«~

sampling ¨ú¼Ë

self indicator ¦Û¨­«ü¥Ü¾¯

semimicro analysis ¥b·L¶q¤ÀªR

separation ¤ÀÖÃ

separation factor ¤ÀÖæ]¼Æ

side reaction coefficient °Æ¤ÏÀ³¨t¼Æ

significance test ÅãµÛ©ÊÀËÅç

significant figure ¦³®Ä¼Æ¦r

simultaneous determination of multiponents ¦h²Õ¤À¦P®É´ú©w

single beam spectrophotometer ³æ¥ú§ô¤À¥ú¥ú«×­p

single-pan balance ³æ½L¤Ñ¥­

slit ¯UÁ_

sodium diphenylamine sulfonate ¤G­fÓiÁD»Ä¶u

solubility product ·»«×¿n

solvent extraction ·»¾¯µÑ¨ú

species «¬Ê^(ª«Ïú)

specific extinction coefficient ¤ñ®ø¥ú¨t¼Æ

spectral analysis ¥úÃФÀªR

spectrophotometer ¤À¥ú¥ú«×­p

spectrophotometry ¤À¥ú¥ú«×ªk

stability constant í©w±`¼Æ

standard curve ¼Ð­ã¦±½u

standard deviation ¼Ð­ã°¾®t

standard potential ¼Ð­ã¹q¦ì

standard series method ¼Ð­ã¨t¦Cªk

standard solution ¼Ð­ã·»²G

standardization ¼Ð©w

starch Õ௻

stationary phase ©T©w¬Û

steam bath »]Éa¯D

stepwise stability constant ³v¯Åí©w±`¼Æ

stoichiometric point ¤Æ¾Ç­p¶qÂI

structure analysis µ²ÌÛ¤ÀªR

supersaturation ¹L¹¡©M

systematic error ¨t²Î»~®t

test solution ¸Õ²G

thermodynamic constant ¼ö¤O¾Ç±`¼Æ

thin layer chromatography (TLC) Á¡¼h¦âÃÐ

titrand ³Qºwª«

titrant ºw©w¾¯

titration ºw©w

titration constant ºw©w±`¼Æ

titration curve ºw©w¦±½u

titration error ºw©w»~®t

titration index ºw©w«ü¼Æ

titration jump ºw©w¬ðÅD

titrimetry ºw©w¤ÀªR

trace analysis ²ª¶q¤ÀªR

transition interval Åܦⶡ¹j

transmittance ³z®g¤ñ

tri acid ¤T¤¸»Ä

true value ¯u­È

tungsten lamp Âë¿O

ultratrace analysis ¶W²ª¶q¤ÀªR

UV-VIS spectrophotometry µµ¥~-¥i¨£¤À¥ú¥ú«×ªk

volatilization ´§µo

Volhard method ºÖº¸«¢¼wªk

volumetric flask ®e¶q²~

volumetry ®e¶q¤ÀªR

Wash bottle ¬~²~

washings ¬~²G

water bath ¤ô¯D

weighing bottle ºÙ¶q²~

weighting form ºÙ¶q§Î

weights ¯|½X

working curve ¤u§@¦±½u

xylenol orange (XO) ¤G¥Ò×ô¾í

zero level ¹s¤ô¥­

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