Treatment of Natural Mordenite with Alkali and the Ammonium Exchange Capacity of the Modified Zeolite

2012 ◽  
Vol 554-556 ◽  
pp. 2031-2036
Author(s):  
Yi Fei Wang

The natural mordenite was treated hydrothermally with NaOH solutions, either with or without fusion with NaOH powder as pretreatment. Zeolite Na-P and analcime were identified as the reacted products, depending on the reaction conditions. The zeolites were identified by X-raydiffraction, and their cation exchange capacity (CEC) was determined. Zeolite Na-P has higher CEC (338 meq/100g) contrasted with the mordenite (181 meq/100g). Further more, the uptakes of NH4+ onto the zeolites have also been investigated. The Na-P has faster exchange rate, higher exchange amounts and better regeneration ability. The ammonium removal efficiency for the Na-P is above 90% at the ammonium initial concentrations less than 150 mg NH4+/g. It seemed that Na-P was fit for the further treatment of waters polluted with ammonium.

Clay Minerals ◽  
1999 ◽  
Vol 34 (3) ◽  
pp. 487-497 ◽  
Author(s):  
P. Arfaioli ◽  
O. L. Pantani ◽  
M. Bosetto ◽  
G. G. Ristori

AbstractThe ability to produce humic-like polymeric compounds, with D-glucose and L-tyrosine as starting materials, was evaluated in different mineral systems: (1) Ca-, Al- and Cu(II)-saturated montmorillonite; (2) Ca-, Al- and Cu(II)-saturated kaolinite; (3) quartz in the presence of two different amounts of the same cations (according to the cation exchange capacity of the clays); and (4) untreated quartz (as control). All systems proved to be effective in the formation of humic-like compounds, particularly quartz, in the presence of cations. The effectiveness in promoting humification reactions was strictly related to the amounts of added cations. In the reaction conditions considered, the humification appears to be due more to the cations than to the type of clay minerals. The clayey systems synthesized more complex (aromatic) substances than the quartz ones.


Minerals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 252
Author(s):  
Seokju Hong ◽  
Wooyong Um

A solid phase of natural zeolite was transformed to Na-zeolite P (NaP zeolite) by a “top-down approach” hydrothermal reaction using 3 M of NaOH solution in a 96 °C oven. Time-dependent X-ray diffraction (XRD), Fourier-transform infrared (FT-IR), XRF, and scanning electron microscopy (SEM) analysis as well as kinetic, isotherm, and cation exchange capacity experiments were performed to understand the mechanism of mineral transition from natural zeolite to NaP zeolite. The XRD crystal peaks of the natural zeolite decreased (decrystallization phase) first, and then the NaP zeolite XRD crystal peaks increased gradually (recrystallization phase). From the XRF results, the dissolution rate of Si was slow in the recrystallization phase, while it was rapid in the decrystallization phase. The specific surface area measured by BET analysis was higher in NaP zeolite (95.95 m2/g) compared to that of natural zeolite (31.35 m2/g). Furthermore, pore structure analysis confirmed that NaP zeolites have more micropores than natural zeolite. In the kinetic experiment, the results showed that the natural zeolite and NaP zeolite were well matched with a pseudo-second-order kinetic model, and reached equilibrium within 24 h. The isotherm experiment results confirmed that both zeolites were well matched with the Langmuir isotherm, and the maximum removal capacity (Qmax) values of Sr and Ni were highly increased in NaP zeolite. In addition, the cation exchange capacity (CEC) experiment showed that NaP zeolite has an enhanced CEC of 310.89 cmol/kg compared to natural zeolite (CEC = 119.19 cmol/kg). In the actual batch sorption test, NaP zeolite (35.3 mg/g) still showed high Cs removal efficiency though it was slightly lower than the natural zeolite (39.0 mg/g). However, in case of Sr and Ni, NaP zeolite (27.9 and 27.8 mg/g, respectively) showed a much higher removal efficiency than natural zeolite (4.9 and 5.5 mg/g for Sr and Ni, respectively). This suggests that NaP zeolite, synthesized by a top-down desilication method, is more practical to remove mixed radionuclides from a waste solution.


2018 ◽  
Vol 4 (1) ◽  
Author(s):  
Mardi Wibowo

Since year 1977 until 2005, PT. ANTAM has been exploited nickel ore resources at Gebe Island – Center ofHalmahera District – North Maluku Province. Mining activity, beside give economically advantages also causedegradation of environment quality espicially land quality. Therefore, it need evaluation activity for change ofland quality at Gebe Island after mining activity.From chemical rehabilitation aspect, post mining land and rehabilitation land indacate very lack and lackfertility (base saturated 45,87 – 99,6%; cation exchange capacity 9,43 – 12,43%; Organic Carbon 1,12 –2,31%). From availability of nutrirnt element aspect, post mining land and rehabilitation land indicate verylack and lack fertility (nitrogen 0,1 – 1,19%). Base on that data, it can be concluded that land reclamationactivity not yet achieve standart condition of chemical land.Key words : land quality, post mining lan


Author(s):  
Geraldo R. Zuba Junio ◽  
Regynaldo A. Sampaio ◽  
Altina L. Nascimento ◽  
Luiz A. Fernandes ◽  
Natália N. de Lima ◽  
...  

ABSTRACTThis study aimed to evaluate the chemical attributes of an Inceptisol cultivated with castor bean (Ricinus communis L.), variety ‘BRS Energia’, fertilized with sewage sludge compost and calcium (Ca) and magnesium (Mg) silicate. The experiment was conducted at the ICA/UFMG, in a randomized block design, using a 2 x 4 factorial scheme with three replicates, and the treatments consisted of two doses of Ca-Mg silicate (0 and 1 t ha-1) and four doses of sewage sludge compost (0, 23.81, 47.62 and 71.43 t ha-1, on dry basis). Soil organic matter (OM), pH, sum of bases (SB), effective cation exchange capacity (CEC(t)), total cation exchange capacity (CEC(T)), base saturation (V%) and potential acidity (H + Al) were evaluated. There were no significant interactions between doses of sewage sludge compost and doses of Ca-Mg silicate on soil attributes, and no effect of silicate fertilization on these attributes. However, fertilization with sewage sludge compost promoted reduction in pH and increase in H + Al, OM and CEC. The dose of 71.43 t ha-1 of sewage sludge compost promoted the best soil chemical conditions.


Materials ◽  
2021 ◽  
Vol 14 (10) ◽  
pp. 2617
Author(s):  
Alicja Szatanik-Kloc ◽  
Justyna Szerement ◽  
Agnieszka Adamczuk ◽  
Grzegorz Józefaciuk

Thousands of tons of zeolitic materials are used yearly as soil conditioners and components of slow-release fertilizers. A positive influence of application of zeolites on plant growth has been frequently observed. Because zeolites have extremely large cation exchange capacity, surface area, porosity and water holding capacity, a paradigm has aroused that increasing plant growth is caused by a long-lasting improvement of soil physicochemical properties by zeolites. In the first year of our field experiment performed on a poor soil with zeolite rates from 1 to 8 t/ha and N fertilization, an increase in spring wheat yield was observed. Any effect on soil cation exchange capacity (CEC), surface area (S), pH-dependent surface charge (Qv), mesoporosity, water holding capacity and plant available water (PAW) was noted. This positive effect of zeolite on plants could be due to extra nutrients supplied by the mineral (primarily potassium—1 ton of the studied zeolite contained around 15 kg of exchangeable potassium). In the second year of the experiment (NPK treatment on previously zeolitized soil), the zeolite presence did not impact plant yield. No long-term effect of the zeolite on plants was observed in the third year after soil zeolitization, when, as in the first year, only N fertilization was applied. That there were no significant changes in the above-mentioned physicochemical properties of the field soil after the addition of zeolite was most likely due to high dilution of the mineral in the soil (8 t/ha zeolite is only ~0.35% of the soil mass in the root zone). To determine how much zeolite is needed to improve soil physicochemical properties, much higher zeolite rates than those applied in the field were studied in the laboratory. The latter studies showed that CEC and S increased proportionally to the zeolite percentage in the soil. The Qv of the zeolite was lower than that of the soil, so a decrease in soil variable charge was observed due to zeolite addition. Surprisingly, a slight increase in PAW, even at the largest zeolite dose (from 9.5% for the control soil to 13% for a mixture of 40 g zeolite and 100 g soil), was observed. It resulted from small alterations of the soil macrostructure: although the input of small zeolite pores was seen in pore size distributions, the larger pores responsible for the storage of PAW were almost not affected by the zeolite addition.


Soil Research ◽  
1981 ◽  
Vol 19 (1) ◽  
pp. 93 ◽  
Author(s):  
GP Gillman

The cation exchange capacity of six surface soils from north Queensland and Hawaii has been measured over a range of pH values (4-6) and ionic strength values (0.003-0.05). The results show that for variable charge soils, modest changes in electrolyte ionic strength are as important in their effect on caton exchange capacity as are changes in pH values.


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