SU587988A1 - Method of preparing a catalyst for ammonia synthesis - Google Patents
Method of preparing a catalyst for ammonia synthesisInfo
- Publication number
- SU587988A1 SU587988A1 SU762327310A SU2327310A SU587988A1 SU 587988 A1 SU587988 A1 SU 587988A1 SU 762327310 A SU762327310 A SU 762327310A SU 2327310 A SU2327310 A SU 2327310A SU 587988 A1 SU587988 A1 SU 587988A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- catalyst
- preparing
- calcined
- impregnated
- ammonia synthesis
- Prior art date
Links
Landscapes
- Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
спресссхвьтают в форме таблеток ( мм) под давлением 2,5 ат. Таблетки прокаливан при 900 С и пропитьшают 50 мл спиртового раствора, содержащего 0,12 г КОН и суишт при 100° С. Приготовленный таким образом катализтор . следуюищК химический состав (вес.%) 1,0 АГаОз, 0,5 СаО, 0,5 МоО,, 0,1 К,0, осталь нос FejOj. П р и м е р 2. По npHhfcpy 1 готоа т таблежи из 97,7 г FejOj, 1,0 г AljOs, 1,2 г СаС2О4 и 0,5 г MoOj. Таблетки сушат при 120°С, в{)опитывают 50 мл спиртового раствора , содержащего 0,35 г КСШ и суивт при 100° Приготсвлеиный таким обрт:зом катализатор {имеет спедуюнщй состав (вес.%): 1,0 AljOji 0,5 СаО, 0,5 MoOj, 0,3 KjO, остальное FejOsВ табл. 1 приведено оодержа1{ие ЫНз(об.%) в азоговсщорошгой смеси на предггагаемом катализаторе (согшсно примерам 1 и 2) по сравне1шю с осаждешшгм катализатором. Ниже приведено зтачение механической прочности на раздавлива1ше таблеток катализаторов ( мм). Услови испытаид : .ат, W 15000 Ч- Образец12 Известный Механическа прочность ш раздавлившше , кг/см 50075050 При приготовлешш катализаторов предлагаемым способом нет сточных вод, требук цих утилизации. Полученные этим методом катал торы имеют активность более высокую или равную активности осажденного катализатора. Меха1Шческа прочность катализаторов, npitfOTOBленных по предлагаемому методу, значительно превьаиает механическую .прочность осаждешюго катализатора . Таблица 1The press in the form of tablets (mm) under a pressure of 2.5 at. The tablets are calcined at 900 ° C and 50 ml of an alcohol solution containing 0.12 g of KOH and dried at 100 ° C are passed through. The catalyst thus prepared is prepared. The following chemical composition (wt.%) 1.0 AGaOz, 0.5 CaO, 0.5 MoO ,, 0.1 K, 0, the rest of the nose FejOj. EXAMPLE 2. According to npHhfcpy 1, ready-to-use tablés from 97.7 g of FejOj, 1.0 g of AljOs, 1.2 g of CaC2O4, and 0.5 g of MoOj. Tablets are dried at 120 ° С, 50 ml of an alcohol solution containing 0.35 g KSSH and suivt at 100 ° C are impregnated in a) solution: thus the catalyst {has the following composition (weight%): 1.0 AljOji 0.5 CaO, 0.5 MoOj, 0.3 KjO, the rest FejOsВ table. 1 shows the content of LNH3 (vol.%) In the nitrogen-gel mixture on the pre-catalyst of the catalyst (equivalent to examples 1 and 2) compared with the precipitating catalyst. The following shows the crush strength of the catalyst tablets (mm). Condition test: .AT, W 15000 H - Sample12 Known Mechanical strength crush, kg / cm 50075050 When preparing catalysts by the proposed method, there is no waste water, recycling requirements. The catalysts obtained by this method have activity higher or equal to the activity of the precipitated catalyst. The mechanical durability of catalysts, npitfOTOBennyh on the proposed method, significantly exceeds the mechanical strength of the precipitating catalyst. Table 1
Формула чизобретеии Chizobretenie formula
Способ приготовлешш катализатора дл свшеэа аммиака путем смешешш соединений жпеза и алюмини , до лени в смесь раствора трехокиси молибдена в аммиачной воде и соли кальци с посдедукщей сушкой каталиaatopHdi MiaccH при 100-120° С, прокаливанием, пропиткой спиртовым pacTBtqjOM гидроокиси кали и повторны сушксй, отличающ и и с тем, что, с целью исключе ш A method for preparing a catalyst for ammonia with ammonia by mixing compounds of aluminum and aluminum, into a mixture of molybdenum trioxide solution in ammonia water and calcium salt with a gradual drying of catalys aatopHdi MiaccH at 100-120 ° C, calcined, impregnated with hydrochloric acid hydroxyl hydroxide at a temperature of 100-120 ° C, calcined, impregnated with hydrochloric acid hydroxide hyacinth hydroxide at 100–120 ° C, calcined, impregnated with hydrochloric acid hydroxide hydroxides in 100–120 ° C, calcined, impregnated with hydrochloric acid hydroxide hydroxides in 100–120 ° C, calcined, impregnated with hydrochloric acid hydroxide hyacinthium hydroxide at 100–120 ° C, calcined, impregnated with hydrochloric acid hydroxide hydroxides and hydrochloric acid at a temperature of 100–120 ° C, calcined, impregnated with pacTBtqjOM hydrohydroxy hydroxy acid hydroxides, and dried hydrosaccharides. and and with the fact that, in order to exclude
сточных вод и получени катализатора, с более высокой механической прочностью, в качестве со€ дине1шй железа и алюмини берут их окислы , в качестве соли кальци - оксалат кальци и прокаливание при 900-1200° С.sewage and obtaining a catalyst with higher mechanical strength, their oxides are taken as co-dated iron and aluminum, calcium is a calcium oxalate and calcination at 900-1200 ° C as calcium salt.
Источники информащш, прин тые во вниMaime при экспертизе:Sources of information taken into consideration at the examination:
1.Авторское свидетельство СССР .№ 230098, М. кл. В 01 3 37/08, 1967.1. Authors certificate of the USSR .№ 230098, M. class. B 01 3 37/08, 1967.
2.Авторское свидетельство СССР № 453864, М. -кл. В 01 J 11/22, 1973.2. USSR author's certificate number 453864, M. -kl. On 01 J 11/22, 1973.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU762327310A SU587988A1 (en) | 1976-02-24 | 1976-02-24 | Method of preparing a catalyst for ammonia synthesis |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU762327310A SU587988A1 (en) | 1976-02-24 | 1976-02-24 | Method of preparing a catalyst for ammonia synthesis |
Publications (1)
Publication Number | Publication Date |
---|---|
SU587988A1 true SU587988A1 (en) | 1978-01-15 |
Family
ID=20649839
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU762327310A SU587988A1 (en) | 1976-02-24 | 1976-02-24 | Method of preparing a catalyst for ammonia synthesis |
Country Status (1)
Country | Link |
---|---|
SU (1) | SU587988A1 (en) |
-
1976
- 1976-02-24 SU SU762327310A patent/SU587988A1/en active
Similar Documents
Publication | Publication Date | Title |
---|---|---|
SU562191A3 (en) | The method of producing isoprene | |
CA1281336C (en) | Method of preparing acetal or ketal | |
BR8303437A (en) | PROCESS FOR THE PREPARATION OF DIMETHYL ETER BY CATALYTIC DEHYDRATION OF METHANOL | |
GB593849A (en) | Process for preparing catalytic material | |
US3971832A (en) | Process for producing ortho-methylphenols | |
SU587988A1 (en) | Method of preparing a catalyst for ammonia synthesis | |
SU638597A1 (en) | 4-methyl-2-propenyltetrahydropyranol-4 as fragrant substance for perfumery compositions | |
ES2015573B3 (en) | CATALYST COMPONENTS FOR ALPHA-OLEPHINE POLYMERIZATION CATALYSTS AND PROCEDURE FOR THE MANUFACTURE OF THEM. | |
SU593730A1 (en) | Catalyst for methanol synthesis | |
Matsuura et al. | Oxidative Coupling of Methane over a Li2O–BeO System Catalyst | |
JPS52131508A (en) | Continuous preparation of diisopropylether | |
JPS5714544A (en) | Orthoalkylation of phenols | |
RU2801303C2 (en) | Catalyst intended for dehydrogenation of alkylaromatic hydrocarbons and method for its production | |
AR217394A1 (en) | CATALYST CONDENSATION PROCEDURE OF IMIDA-ALCOHOL, FOR THE PREPARATION OF POLYMER POLYMER POLYMERIC COMPOUNDS | |
SU422443A1 (en) | METHOD FOR PREPARING CATALYST FOR HYDROGENING BENZENE | |
ES489506A0 (en) | PROCEDURE FOR OBTAINING C2-C5 OLEFINS. | |
SU910178A1 (en) | Catalyst for dehydrogenating cyclohexanol | |
US2853535A (en) | Catalytic process for preparing a conjugate diene containing 5 to 8 carbon atoms by dehydrating a tertiary alcohol | |
IT1167673B (en) | PROCESS PERFECTED FOR THE PREPARATION OF ALCHILATION CATALYSTS | |
JPS56122318A (en) | Preparation of ethylene | |
SU688501A1 (en) | Method of preparing m-dioxanes | |
SU593732A1 (en) | Catalyst for cracking isopropylbenzene | |
SU767098A1 (en) | Method of preparing potassium 1,2,6,6-tetramethylpiperidine-1-oxyl-4-xanthogenate | |
SU118204A1 (en) | Method for preparing 2-hydroxy-4-aminobenzoic acid | |
SU1668366A1 (en) | Method for obtaining sulfenamide m |