¡¡¡¡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 ®Õ㦱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
eluent ²O¬~¾¯
end point ²×ÂI
end point error ²×ÂI»~®t
enrichment ´I¶°
eosin ˮ›
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
ignition ¨`¿N
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«×
isoabsorptive point µ¥§l¦¬ÂI
Karl Fisher titration ¥dº¸¡¡¶O·²º¸ªk
Kjeldahl determination ³Í¤ó©w´áªk
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 °ò㪫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) ¼Ð㪫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 éw±`¼Æ
standard curve ¼Ð㦱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¯Åéw±`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¥
1-(2-pyridylazo)-2-naphthol (PAN) 1-(2-¡@Ôr°¸´á)-2-¡@×ô