Crystalline Structure of Clinoptilolite Zeolite

What is CLINOMAX?

Zeolite vs. Clinoptilolite: Understanding the Difference
Understand what Clinoptilolite Zeolite means, the active ingredient in CLINOMAX.

Let us clarify what these two terms mean and the relationship between them, given that they are often cited in isolation.

The relationship is simple: Zeolite is the family, Clinoptilolite is the most distinguished member.

The term Zeolite refers to a large mineralogical group with more than 40 natural species/structures (frameworks). Although all are zeolites, not all share the same qualities or applications.

Clinoptilolite is the most abundant and commercially widely used natural zeolite. It stands out within the group for its purity, robust crystalline structure, and very high Cation Exchange Capacity (CEC). It is Clinoptilolite that delivers the expected results at industrial scale.

In summary: when you seek an efficient and safe natural zeolite, you are, technically, looking for Clinoptilolite.

Chemical Definition

Molecular composition and crystalline structure

Chemical Formula

Complete General Formula:

(Li, Na, K)α(Mg, Ca, Sr, Ba)d[Alα+2d-Sin-(α+2d)O2n]∙mH2O

Simplified Formula (most common):

(Na,K)2O·Al2O3·10SiO2·6H2O

Balancing Cations:

  • • Na⁺ (Sodium)
  • • K⁺ (Potassium)
  • • Ca²⁺ (Calcium)
  • • Mg²⁺ (Magnesium)

Tetrahedral Structure:

  • • SiO₄ (Silicon Tetrahedra)
  • • AlO₄ (Aluminum Tetrahedra)
  • Si/Al ratio: 4-5.5
  • System: Monoclinic
Crystalline Structure
Monoclinic system with a three-dimensional network of microporous channels

Parameter a

1.762 nm

Parameter b

1.791 nm

Parameter c

0.739 nm

The unit cell is based on 72 oxygen atoms (n = 36) and 24 water molecules (m = 24), with balancing cations occupying specific positions in the microporous channels.

Microporous Channel System

Three-dimensional network of interconnected channels that confers unique molecular sieve properties

Three-dimensional model of the crystalline structure of clinoptilolite (automatic rotation). Cell: Cappelletti et al., 1999.

Channel A (10-membered ring)
Main channels parallel to the c-axis, responsible for most of the ion-exchange capacity
0.31 × 0.76 nm

Occupying cations: Na⁺, Ca²⁺, Mg²⁺

B channels (8-membered ring)
Secondary channels parallel to the c-axis, complementing the porous structure
0.36 × 0.46 nm

Occupying cations: Ca²⁺, Na⁺

C-channels (8-membered ring)
Perpendicular channels (a-axis) interconnecting channels A and B, forming a three-dimensional network
0.26 × 0.47 nm

Occupying cations: K⁺

Result: Natural Molecular Sieve

The combination of these three channel types creates a three-dimensional micropore network that allows selective passage of molecules by size and charge. Molecules smaller than the channel diameters can diffuse into the structure and adsorb onto active sites, while larger molecules are excluded. This property is fundamental for applications in gas separation, water purification, and selective ion adsorption.

Geological Origin

Natural formation under specific geological conditions

Formation Process
Crystallization from volcanic ash in alkaline environments

Natural zeolites, including clinoptilolite, form through diagenetic alteration of volcanic ash rich in reactive glass (primarily silicic volcanic glass) in alkaline aqueous environments. This process occurs over millions of years under specific conditions of temperature, pressure, and pH.

Required Geological Conditions:

  • Alteration of volcanic ash rich in reactive glass.
  • Marine or lacustrine environments with alkaline pH (8–10)
  • Moderate temperature (50–200 °C) and low pressure
  • Extended geological time (millions of years)
  • Absence of contamination by other minerals

Deposits of high purity (80-100% clinoptilolite) are rare and occur in regions with exceptionally favorable geological conditions, where crystallization was complete and contamination by other minerals such as quartz, feldspar, or montmorillonite was minimal. These ideal conditions yield zeolites with superior physicochemical properties and consistent performance in industrial applications.

Physical-Chemical Properties

Characteristics that confer superior performance in industrial applications

Unique Crystalline Structure

Monoclinic framework with interconnected microporous channels of 0.4–0.7 nm, forming a highly selective natural molecular sieve.

High Cation Exchange Capacity

CEC of 150–190 meq/100g, higher than most clay minerals, enabling efficient adsorption of heavy metals and ammonia.

High Surface Area

39 m²/g, at the high end for natural zeolites (14–30 m²/g), resulting in greater adsorption capacity.

Pureza Excepcional

80–100% pure clinoptilolite vs. 50–70% in common commercial zeolites, ensuring consistent and predictable performance.

Ionic Selectivity
Adsorption preference for specific cations (Ames selectivity series, 1960)

Selectivity Order (highest → lowest):

Cs⁺ > Rb⁺ > K⁺ > NH₄⁺ > Ba²⁺ > Sr²⁺ > Na⁺ > Ca²⁺ > Fe³⁺ > Al³⁺ > Mg²⁺ > Li⁺

This selectivity is fundamental for applications in ammonia removal (NH₄⁺), heavy metal adsorption (Pb²⁺, Cd²⁺, Cu²⁺) and removal of Cs⁺ and Sr²⁺ ions from aqueous solutions.

Why CLINOMAX is Superior?

Comparison between common commercial zeolites and high-purity CLINOMAX™

ParameterCommon ZeolitesCLINOMAX™Improvement
Teor de Clinoptilolita50-70%80-100%+43% a +100%
Surface Area (BET)14-30 m²/g39 m²/g+30% a +178%
CEC (Cation Exchange Capacity)1.0-1.4 mEq/g1.5-1.9 mEq/g+7% a +90%
Heavy MetalsVariableControlled per report/CoAGuaranteed safety
80-100%
Clinoptilolite Purity

vs 50-70% in standard commercial zeolites

39 m²/g
BET Surface Area

~+77% vs the average (22 m²/g)

Laudo/CoA
Heavy Metals

Heavy metal content controlled as per analysis report/CoA

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CLINOMAX™ is a brand of Grupo BENTONISA, a trusted name for over 50 years in high-value, mineral-based industrial solutions.

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