Page 1
Appendix
See Tables A.1, A.2, A.3, A.4, A.5.
© Metallurgical Industry Press, Beijing and Springer Science+Business Media Singapore 2016D. Wang, Flotation Reagents: Applied Surface Chemistry on Minerals Flotationand Energy Resources Beneficiation, DOI 10.1007/978-981-10-2027-8
173
Page 5
Tab
leA.1
(con
tinued)
Reagent
(maincomponent)
Codename
State
Dosage
(g/t)
Dilu
tion
concentration
Addinglocatio
nCom
mon
sulfide
ores
Noble
metal
Heavy
nonferrous
metal
Metallic
and
nonm
etallic
oxides
Grinding
Stirring
Flotation
PbZn
Cu
FeCo,
Ni
12
34
56
78
910
1112
1314
1516
Alcohols
Frother
65Liquid
5–90
Undilu
ted
××
××
××
××
Branchedethanol
70Liquid
15–90
Undilu
ted
××
××
××
××
Pentanol,hexylalcohol
cyclopentanol,cyclohexanol
71A
Liquid
15–90
Undilu
ted
××
××
××
××
Alcohols
73Liquid
23–230
Undilu
ted
××
××
××
××
Linearalcoholswith
4–8C
77A
Liquid
13–90
Undilu
ted
××
××
××
×
Pine
oil
Liquid
13–90
Undilu
ted
××
××
××
××
××
×
Cresylic
acid
Liquid
23–90
Undilu
ted
××
××
××
××
×
Eucalyptusoil
Liquid
23–90
Undilu
ted
××
××
××
××
Polyglycol
Dow
frother
200
Liquid
5–90
××
××
××
××
××
×
Polypropyleneglycol
ethers
250
Liquid
5–90
Undilu
ted
××
××
××
××
××
×
Appendix 177
Page 10
Tab
leA.2
(con
tinued)
Reagent
Com
ponent
Characteristic
Preparation
App
lication
АзолягА
Dialkylbenzenesodium
sulfon
ate
R1=C10–C12,R2-C5–C7
Activecontent:45
%Na 2SO
4:10–15
%Unsulfonatedmatter:5%
Prepared
bybenzene
sulfon
ationof
prod
uctsfrom
fossiloil
0.5–
10%
solutio
n
Некаль
1,2,3-tributyl
naph
thalenesulfonicacid
solutio
n
Activematter:16–20
%NaC
l:<0
.7%
Prepared
bysulfon
atingof
alky
lnaph
thalene
1–10
%aqueou
ssolutio
n
Emulgator
Mixturesof
naph
thenic
acid,
hydrocarby
lsulfon
ate,
and
petroleum
hydrocarbo
n
Prod
uctsby
petroleum
hydrocarbo
nof
fossiloil
3–10
%em
ulsion
Isoo
ctylph
osph
ate
Mixturesof
phosph
oric
acid
mon
oester
sodium
salt,
and
phosph
oric
acid
diester
sodium
salt
Phosph
oric
acid
mon
oester
sodium
salt:
30%,
di-iso-octylph
osph
ate:
70%
Prod
uctsof
reactio
nof
P 2O5
andalcoho
l1–
10%
solutio
n
ИМ-50
R–CO–NHOH,
C7–C9:ИМ-50,
ИМ-51,ИМ-52else
Moisturecontent:7–9%
Activeconstituent:>7
5%
Prod
uctsof
carbox
ymethy
ldealtwith
hydrox
ylam
ine
sulfate
1–10
%solutio
nheated
to40
–50
°C,
10–50
%hy
drocarbo
noilsolutio
n
Dith
iocarbon
ate
ROCSS
Me
Class
1:87
%,class2:
83%
Isop
ropy
l:80
%,amyl:8
7,85
,76%
,C6–C8 9:ИМ-68dithiocarbon
ate,
C7–C9:ИМ-79dithiocarbon
ate
Alcoh
oldialky
lpho
spho
rodithioic
acid
anddithiocarbon
ithioic
acid:
60–90
%
Alcoh
oldialky
lpho
spho
rodithioic
acid
(RO) 2PS
SMe
Isop
ropy
l,ethy
lcontent:>6
0%,
alcoho
ldialky
lpho
spho
rodithioic
acid
andethy
ldialky
lpho
spho
rodithioic
acid
Prod
uctsof
neutralizationof
theprod
uctsof
heatingP 2S 5
andalcoho
lwith
Na 2CO3,
NH3and(N
H4)2C
O3
5–10
%solutio
n,C6–C89,C7–C9:5–
10%
emulsion
with
alcoho
ldithioph
osph
ate (con
tinued)
182 Appendix