sulfur trioxide
Conditions | Yield |
---|---|
With chlorine In neat (no solvent) at 1100 - 1150°C;; | 100% |
With chlorine In neat (no solvent) addn. of SiO2, NaCl or Na2SO4 increase reaction temp.; react. accelerated;; | |
With chlorine In neat (no solvent) in presence of charcoal strong react.; addn. of NiSO4, CuSO4, MgSO4, Fe2O3 or KCl reduced yield; no influence of overheated water vapor;; react. detected at 700 - 1150°C;; |
Conditions | Yield |
---|---|
manganese(IV) oxide 450°C; | 98% |
2Na2O*3MoO3*V2O5 440°C; | 98.4% |
two-stage catalyst contact cooled by SO2 gas, external heat exchangers, temp. in contact bed:400-411°C; | 98% |
Conditions | Yield |
---|---|
vanadia Kinetics; 437°C; | 98% |
platinum Kinetics; 415°C; | 98% |
vanadia Kinetics; 452°C; | 97% |
sulfur trioxide
Conditions | Yield |
---|---|
3-stage contact bed; | 98% |
no C content in pyrite; | 96% |
no C content in pyrite; | 96% |
Conditions | Yield |
---|---|
With catalyst: Fe compd. High Pressure; higher yield with increasing pressure, 600-630°C at 100 at; | 97% |
With catalyst: Fe compd. High Pressure; higher yield with increasing pressure, 600-630°C at 100 at; | 97% |
Kinetics; 420°C; |
Conditions | Yield |
---|---|
With hydrogenchloride; copper dichloride In neat (no solvent) Kinetics; (450°C, 1.5 s); | 95% |
With hydrogenchloride SO3 stabilized as Lewis-addukt(HCl.SO3); O2: 30l/h, HCl: 8l/h; 60min; | 40% |
Kinetics; 420°C; |
Conditions | Yield |
---|---|
With oxygen In neat (no solvent) heating in a stream of O2 at 550 - 600°C (formation of SO2 from 82 % of S and of Ag2SO4), later at 980 - 1070°C (decomposition of Ag2SO4);; | A 95% B 5% |
With O2 In neat (no solvent) heating in a stream of O2 at 550 - 600°C (formation of SO2 from 82 % of S and of Ag2SO4), later at 980 - 1070°C (decomposition of Ag2SO4);; | A 95% B 5% |
SbCl5*SO3
A
pyrosulfuryl chloride
C
antimonypentachloride
D
sulfur trioxide
Conditions | Yield |
---|---|
70°C in vac.; | A n/a B n/a C n/a D 95% |
A
pentachlorobenzene
B
sulfur trioxide
C
Bis-pentachlor-phenyl-quecksilber
Conditions | Yield |
---|---|
130-220°C; | A <1 B 80% C 64% |
Conditions | Yield |
---|---|
130-220°C; | A 78% B 80% |
Conditions | Yield |
---|---|
With pyrographite 700°C; | A n/a B 80% C n/a |
With C 700°C; | A n/a B 80% C n/a |
700°C; | A n/a B 50% C n/a |
disulfur dioxide
A
sulfur dioxide
B
sulfur trioxide
C
sulfur
Conditions | Yield |
---|---|
With oxygen In neat (no solvent) oxidn. of S2O2 with an excess of O2, min. ignition pressure at 32°C 54 Torr, at 150°C 2 Torr, mechanism discussed, sometimes react. with lightening, inhibition by SO2;; | A 10-25 B 15-30 C 80% |
A
Pentafluorobenzene
B
pentafluorobenzenesulfonic acid
C
sulfur trioxide
D
bis(pentafluorophenyl)mercury(II)
Conditions | Yield |
---|---|
130-220°C; | A 12% B 9% C 70% D 53% |
130-240°C; | |
130-240°C; |
A
(p-HC6F4)2Hg
B
1,2,4,5-Tetrafluorobenzene
C
2,3,5,6-tetrafluorobenzenesulfonic acid
D
sulfur trioxide
Conditions | Yield |
---|---|
130-230°C; | A 17% B 17% C 17% D 60% |
Conditions | Yield |
---|---|
130-220°C; | A 44% B 60% |
bis(pentafluorosulfur) peroxide
sulfur dioxide
A
thionyl tetrafluoride
B
pentafluorosulfur fluorosulfonate
C
sulfur trioxide
D
thionyl fluoride
E
sulfur(VI) hexafluoride
Conditions | Yield |
---|---|
byproducts: SiF4, sulfur; other Radiation; photochemical reaction with 253.7 nm radiation, 48 h; | A n/a B 45% C n/a D n/a E n/a |
Conditions | Yield |
---|---|
In gas mixt. of N2 and sulfur vapor; O2: 100l/h; 15min, tube system, products cooled; | A n/a B 41% |
1000-1370°C, rapid cooling to minimize SO3 formation; | |
very low SO3 content; |
Conditions | Yield |
---|---|
130-250°C; | A 15% B 10% C 40% |
Conditions | Yield |
---|---|
995 °C in N2; part of a Mg-S-I water splitting cycle; | A 30% B 30% |
In neat (no solvent) heating at 950-1050 K (effusion orifices with A/a ratios of 10-30); | |
1120-1200°C; 29,1mol% in 15min; 90mol% in 2h; | |
900°C, in air stream; |
sulfur trioxide
Conditions | Yield |
---|---|
In neat (no solvent) evolution of SO3 by heating FeSO4 in a glass tube by little admission of air; beginning at 590 °C, only 3% after heating 2h at 625 to 635 °C;; | 3% |
carbon disulfide
A
sulfur trioxide
B
methylammonium carbonate
Conditions | Yield |
---|---|
Bei der Explosion mit ueberschuessigem Sauerstoff; |
disulfuric acid carbonylamide chloride
A
isocyanate de chlorosulfonyle
B
sulfur trioxide
Conditions | Yield |
---|---|
at 160℃; |
2,3-disulfosuccinic acid
A
sulfur trioxide
B
water
C
methylammonium carbonate
hydrogenchloride
A
formaldehyd
B
sulfuric acid
C
sulfur trioxide
D
hydrazine
Conditions | Yield |
---|---|
at 155℃; beim Schmelzen; |
pyrosulfuryl chloride
hydrogen iodide
A
hydrogenchloride
B
sulfur dioxide
C
sulfur trioxide
D
iodine
Conditions | Yield |
---|---|
In neat (no solvent) violent reaction of dry HI even at temp. of a cold mixture of ice and sodium chloride;; |
fluorosulfonyl anhydride
A
fluorosulfonyl fluoride
B
sulfur trioxide
Conditions | Yield |
---|---|
500°C; | |
500°C; |
sulfur dichloride
sulfur trioxide
A
thionyl chloride
B
sulfur dioxide
Conditions | Yield |
---|---|
In neat (no solvent) below -10°C or under pressure;; | A 100% B n/a |
Conditions | Yield |
---|---|
SO3 in excess, 10-15 min, closed vessel 300°C; | 100% |
In neat (no solvent) formation on heating Li2SO4 in a SO3-atmosphere to .300°C;; | |
In neat (no solvent) formation on heating Li2SO4 in a SO3-atmosphere to .300°C;; | |
In neat (no solvent) reaction of SO3-vapour with Li2SO4 at 450°C; TGA; |
Conditions | Yield |
---|---|
SO3 in excess, 10-15 min, closed vessel 450°C; | 100% |
react. of Na2SO4 with SO3 at ambient temp.;; substance with Na2S2O7 and unchanged Na2SO4 obtained;; | |
In neat (no solvent) react. of Na2SO4 with an excess of SO3 above 150°C;; |
Conditions | Yield |
---|---|
In 1,2-dichloro-ethane dry CH2ClCH2Cl/3 h/5°C;; | 100% |
In 1,2-dichloro-ethane dry CH2ClCH2Cl/3 h/5°C;; | 100% |
Conditions | Yield |
---|---|
at 300℃; for 3h; | 100% |
strontium(II) carbonate
sulfuric acid
sulfur trioxide
boric acid
Conditions | Yield |
---|---|
at 180℃; for 24h; | 100% |
Conditions | Yield |
---|---|
995 °C in N2; part of a Mg-S-I water splitting cycle; | A 99% B 99% |
copper(II) oxide In gas equil. react.; | |
platinum In gas equil. react.; |
Conditions | Yield |
---|---|
In sulfuric acid aq. H2SO4; (NH42PbCl6 and oleum filled in glass tube; torch-sealed under vac.; heated up to 250°C; maintained for 24 h, slowly cooled (1.8 K/h); ppt. collected by decantation of mother liqour under inert condns.; | 99% |
Conditions | Yield |
---|---|
In liquid sulphur dioxide Ar; 20°C;; condensation of SO2; residue washed with FCCl3; elem. anal.;; | 96% |
sulfur trioxide
triethoxyantimony
ethoxyantimony bis(ethyl sulfate)
Conditions | Yield |
---|---|
In dichloromethane SO3 soln. was added to Sb compd. at -50°C (N2 or Ar); evapn., drying in vac.; elem. anal.; | 96% |
perfluoropropylene
sulfur trioxide
1,2,2-trifluoro-2-hydroxy-1-trifluoromethylethanesulfonic acid sultone
Conditions | Yield |
---|---|
150°C, 5 h; | 94% |
150°C, 5 h; | 94% |
60°C; | 92% |
Conditions | Yield |
---|---|
With sulfuric acid In water; benzene | 93% |
With phosphoric acid; sulfuric acid In water; benzene | 87% |
Conditions | Yield |
---|---|
fresh distilled SO3, 2.7 atm, below 80°C, 1 h; | 93% |
fresh distilled SO3, 2.7 atm, below 80°C, 1 h; | 93% |
fresh distilled SO3, 2.7 atm, below 80°C, 1 h; | 93% |
Conditions | Yield |
---|---|
In dichloromethane SO3 soln. was added to Sb compd. at -50°C (N2 or Ar); elem. anal.; | 93% |
((CH3)3Sn)C(C6H9)CH(Sn(CH3)3)
sulfur trioxide
(CH3)3SnSO3C(C6H9)CHSO3Sn(CH3)3
Conditions | Yield |
---|---|
In dichloromethane absence of air and moisture; 2 equiv. SO2, stirring at -78°C for 4 h; evapn., distn.; elem. anal.; | 93% |
Conditions | Yield |
---|---|
A 91% B n/a |
hexafluoro-1,3-butadiene
sulfur trioxide
buta-1,3-diene
4-trifluorovinyltrifluoro-1,2-oxathietane 2,2-dioxide
Conditions | Yield |
---|---|
In liquid sulphur dioxide dropping SO3 into a soln. of CF2=CFCF=CF2 in SO2 at -10°C followed by stripping SO2 and butadiene; distn.; | 91% |
In sulfur dioxide dropping SO3 into a soln. of CF2=CFCF=CF2 in SO2 at -10°C followed by stripping SO2 and butadiene; distn.; | 91% |
sulfur trioxide
(5,7,12,14-tetramethyldibenzo[b,i][1,4,8,11]tetraazacyclotetradecinate(2-))V(O2SO2)
Conditions | Yield |
---|---|
In dichloromethane Ar-atmosphere; slow addn. of SO3 to V-complex at 0°C, stirring atroom temp. for 2 h; ether addn., collection (filtration), washing (CH2Cl2, ether); elem. anal.; | 91% |
sulfuric acid
phthalocyaninealuminum chloride
sulfur trioxide
Conditions | Yield |
---|---|
In sulfuric acid mixt. Al complex and oleum was stirred at room temp. for 16 h.; react. mixt. was cooled to ambient temp., poured onto ice, ppt. was filtered off, washed with 1% aq. HCl, water, dried in vac. at 90°C; | 91% |
Chlorotrifluoroethylene
sulfur trioxide
3-chlorotrifluoro-1,2-oxathietane 2,2-dioxide
Conditions | Yield |
---|---|
at 70°C; | 90% |
sulfur trioxide
chlorine monofluoride
A
fluorosulfonyl fluoride
Conditions | Yield |
---|---|
byproducts: Cl2; from -196 °C to room temp., excess ClF; | A n/a B 90% |
Conditions | Yield |
---|---|
220-280 °C, 30 atm NH3, 30 min; | 90% |
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