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absorbance Îü¹â¶È
absorbent Îü¸½¼Á
absorption curve ÎüÊÕÇúÏß
absorption peak ÎüÊÕ·å
absorptivity ÎüÊÕϵÊý
accident error żȻÎó²î
accuracy ׼ȷ¶È
acid-base titration Ëá¼îµÎ¶¨
acidic effective coefficient ËáЧӦϵÊý
acidic effective curve ËáЧӦÇúÏß
acidity constant Ëá¶È³£Êý
activity »î¶È
activity coefficient »î¶ÈϵÊý
adsorption Îü¸½
adsorption indicator Îü¸½Ö¸Ê¾¼Á
affinity Ç׺ÍÁ¦
aging ³Â»¯
amorphous precipitate ÎÞ¶¨ÐγÁµí
amphiprotic solvent Á½ÐÔÈܼÁ
amphoteric substance Á½ÐÔÎïÖÊ
amplification reaction ·Å´ó·´Ó¦
analytical balance ·ÖÎöÌìÆ½
analytical chemistry ·ÖÎö»¯Ñ§
analytical concentration ·ÖÎöŨ¶È
analytical reagent (AR) ·ÖÎöÊÔ¼Á
apparent formation constant ±í¹ÛÐγɳ£Êý
aqueous phase Ë®Ïà
argentimetry ÒøÁ¿·¨
ashing »Ò»¯
atomic spectrum Ô­×Ó¹âÆ×
autoprotolysis constant ÖÊ×Ó×Եݳ£Êý
auxochrome group ÖúÉ«ÍÅ
back extraction ·´ÝÍÈ¡
band spectrum ´ø×´¹âÆ×
bandwidth ´ø¿í
bathochromic shift ºìÒÆ
blank ¿Õ°×
blocking of indicator ָʾ¼ÁµÄ·â±Õ
bromometry äåÁ¿·¨
buffer capacity »º³åÈÝÁ¿
buffer solution »º³åÈÜÒº
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 ×ÔÓɶÈ
demasking ½â±Î
derivative spectrum µ¼Êý¹âÆ×
desiccant; drying agent ¸ÉÔï¼Á
desiccator ±£¸ÉÆ÷
determinate error ¿É²âÎó²î
deuterium lamp 뮵Æ
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 ƵÂÊÃܶÈ
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 À­Æ½Ð§Ó¦
ligand ÅäλÌå
light source ¹âÔ´
line spectrum Ïß×´¹âÆ×
linear regression ÏßÐԻعé
liquid chromatography (LC) ÒºÏàÉ«Æ×
macro analysis ³£Á¿·ÖÎö
masking ÑÚ±Î
masking 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]Ŀ
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 ÖкÍ
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«ÃܶÈ
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»¯»¹Ô­Ö¸Ê¾¼Á
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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