Sizing Particle and droplet
size are basic features that influence the properties and performance of solids, emulsions
and sprays. Conductivity, flexibility, gloss, hardness, stability, strength and taste
are some of the properties that can be influenced by particle size. Size and size
distributions are important in various areas such as: atmospheric aerosol dispersion,
ceramic and alloy properties, catalyst performance, crystal growth, contamination of soil
and liquids, wastewater management, medicine and spray effectiveness, paint performance,
emulsions stability and so on. Several light scattering and electrical techniques are
available in our laboratory, as well as more conventional methods as sedimentation and
microscopy. Disclaimer: Instrumental particle and droplet sizing techniques do not measure
the geometrical size but give an equivalent spherical diameter depending on the technique
Composition Knowledge of
the chemical composition of raw materials, semi products, process streams and final
products is essential for behavior, quality or for example health risk of each and every
product or medium. Therefore man puts huge effort in trying to determine even the most
untraceable elements. In particular for analysis of liquids and gases a wide variety of
analyzers is available. Measuring the composition of solids without destruction appeared
to be difficult. Apart from the traditional semi quantitative method of X-ray
fluorescence, currently the more accurate and more 'multi-component' Instrumental Neutron
Activation Analysis is available
Analysis Sample analysis can
be requested on this site. Please fill in the appropriate analysis request form below
and submit it to us. A copy of the form should be signed and enclosed with the samples for
dispatch. Make sure the samples are well packed to prevent damage during transport. The
postal address is given below: Delft Solids Solutions B.V. Kluyverweg 2A Innovation Centre
2629 HT Delft The Netherlands Delft Solids Solutions B.V. (not for delivery services) PO
Box 1038 2600 BA Delft The Netherlands A customs declaration is required for samples from
outside the European Union. For countries inside the European Union, a declaration is
recommended. Templates of the customs declaration are available on this site. Should there
be any questions concerning the sample dispatch or analysis, please do not hesitate to
contact us.
How to contact us Delft Solids
Solutions cooperates with partners such as the Delft University of Technology and employs
academically educated and scientific experienced specialists who earned their well
respected place in the Dutch scientific world (see our publications - item
references). visiting address postal address Delft Solids Solutions B.V. Kluyverweg 2A
Innovation Centre 2629 HT Delft The Netherlands (not for delivery services) Delft Solids
Solutions B.V. PO Box 1038 2600 BA Delft The Netherlands Phone: +31 (0) 15 26 825 16 Fax:
+31 (0) 15 26 825 30 If you have any questions about our company, analyses we provide or
any other observations, feel free to contact us. E-mail is merely meant for business to
business information exchange. For information about instruments and techniques, please
consult the manufacturers and relevant books. Appropriate contact addresses and literature
are available on our website.
light
scanning techniques
Photon
Correlation Spectroscopy In photon correlation spectroscopy (PCS) or quasi-elastic
light scattering (QELS) the Brownian motion (movement in random direction) of sub-micron
particles is measured as a function of time. A laser beam is diffracted by particles in
suspension. The diffusion of particles causes rapid fluctuations in scattering intensity
around a mean value at a certain angle (varying from 10 to 90°). These intensity
fluctuations depend on particle size. The calculated correlation function results in a
diffusion coefficient for a given temperature and viscosity which can be converted to
particle size. The technique is used for determination of average particle size in a range
between 3 and 3000 nm. The measurements are performed on a Coulter N4 or an ALV 5000. The
report consists of a table with average and mode effective hydrodynamic diameter and
polydispersity index, which is a measure for the width of the distribution.
Electrical
sensing zone In electrical sensing zone an electrolyte solution is used to disperse
particles. A tube with a narrow aperture is submerged in the solution and two electrodes
are placed on both sides of the aperture. Electrolyte and particles travel through the
aperture and the resistance proportional to the particle volume is measured. Each
individual particle is counted and categorized in the appropriate size class. The
technique is used for characterizing and counting narrow distributions within the range of
0.6 to 1200 µm. Particles in low concentration solutions, powders and biological material
can be analyzed. The measurements are performed on a Coulter Multisizer II. The report
consists of a graph showing the cumulative and differential volume or number distributions
and statistics as the mode, mean and median diameter, skew ness and kurtosis, standard
deviation etc.
Scanning
electron microscopy In scanning electron microscopy (SEM) a source of electrons is
focused into a fine probe that is rastered over the surface of the specimen. The sample is
coated with a thin gold layer and bombarded with electrons to visualize the surface, which
is constantly scanned and reconstructed. A detector collects a part of the emitted
electrons and an image is built by signal modulation and amplification which looks just
like the object. Magnifications up to 20.000 times can be used. The technique is often
used when visualization of a sample is required in order to detect size and shape effects
or to create a better understanding of the material behavior. The measurements are
performed on a Philips SEM XL20; the report consists of pictures and a brief evaluation of
the analysis.
Gravitational
sedimentation In gravitational sedimentation (originally the pipette method) the
settling rate of particles in liquid is measured and related to the mass by use of the
Stokes law. Nowadays the settling rate is determined by measuring x-ray transmission in
the liquid at specific heights and time intervals and a size distribution based on
difference in mass is calculated. The technique is suitable for any material containing
elements with Z > 12 and is popular for determination of clay fractions in soil
samples. The sizing range, determined by laminar flow, is from 1 to 300 µm. The
measurements are performed on a Micromeritics Sedigraph 5100 and the report consists of a
graph showing the cumulative and differential mass distribution and statistics as the
mode, mean and median diameter, standard deviation etc.
Phase
Doppler Velocimetry In laser Doppler velocimetry particles are radiated by two laser
beams and the phase shift of the scattered light signals is measured. Two laser beams are
split into four beams of equal intensity. The beams are focused and made to intersect. The
scattered light from particles passing through the beams at their intersection is mixed at
the photo detector surface and gives a difference signal. Since the rays enter
the particle at different angles, the optical paths to a common arbitrary point on the
detector differ; the light waves are shifted relatively to each other. Two detectors allow
determination of particle size. The technique is used for determination of droplet size
and velocity distribution in sprays and nozzles from 0.5 to 90 µm. The measurements are
performed on a TSI Phase Doppler Particle Analyzer and the report consists of size and
velocity distribution results.
Laser diffraction In
laser diffraction (static light scattering) the scattering pattern, obtained from
illumination of dispersed particles with a laser beam, contains information about particle
size. The interaction between particles and light is mainly dependent on particle size,
shape, surface roughness and refractive indices of material and dispersing medium. For a
specific material, the scattering pattern of a particle is unique for its size.
Deconvolution of the sample scattering pattern with an optical model such as Mie or
Fraunhofer results in the particle size distribution. The technique is especially
applicable to samples with a broad or bimodal distribution and for information on size
trends in series of samples. Materials can be characterized in the range of 0.04 to 2000
µm and dispersion can be made in water, organic liquid as well as air. The measurements
are performed on a Malvern Mastersizer, Coulter LS 230 or a Cilas 1064. The report
consists of a graph showing the cumulative and differential volume distributions and
statistics as the mode, mean and median diameter, skewness and kurtosis, standard
deviation etc.
Sieve analysis In
sieve analysis a powder is separated into specified size fractions. Both mechanical
sieving and sonic sieving are available. The separation range is from 37 µm to 10 mm. The
measurements are performed on ATM, Retsch or Stork Veco sieves. The results are given in
sieve fractions and cumulative mass distribution.
http://www.solids-solutions.com/porosity.html
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http://www.solids-solutions.com/references.html
particle characterization, pore size distribution, porosity measurement, adsorption
isotherm, BET surface area, particle size distribution, particle size analysis, surface
characterization, chemical analysis, chemical composition, neutron activation analysis,
dynamic light scattering, lab test, droplet size, elemental analysis, chemical laboratory.
Delft Solids Solutions is located in Delft and is a testing laboratory for measurement
and analysis and characterization of porosity, pore size, pore size distribution, specific
surface area, pore volume, particle size, particle size distribution, sprays, and chemical
composition and chemical analysis of solid materials (solids), liquids and gases. The
analysis of the texture of solid materials and porosity of solid samples is determined by
different surface science techniques and surface characterization techniques, as physical
gas adsorption, chemical gas adsorption, mercury intrusion porosimetry and helium
pycnometry. Surface characterization is an important tool to predict the behaviour of
catalysts and adsorbents and medicines. Porosity of powders and porous solids can be
measured by different techniques based on adsorption of inert gases. The porosity in
powder and the porosity in porous solids are analyzed in the same way as porosity
measurement in porous materials. Instruments:
The following instruments are at our disposal: Surface Area and Porosity
of Solids Quantachrome Autosorb-6B analyzers (2) / N2 adsorption Quantachrome Autosorb-1C
analyzers (2) / CO or H2 chemisorption Quantachrome PentaPycnometer / He density
Quantachrome NOVA 1200 analyzers (2) / CO2 adsorption Quantachrome Autosorb degassers (3)
/ vacuum pre-treatment Quantachrome NOVA flow degasser / Flow pre-treatment Micromeritics
ASAP 2010 analyzers (2) / Low-pressure Ar adsorption or Kr Qsurf M3 / N2 adsorption flow
CE Instruments Pascal 140 porosimeter / Low-pressure mercury intrusion CE Instruments
Pascal 440 porosimeter / High-pressure mercury intrusion Particle Size of Solids Coulter
LS230 / Forward light scattering + PIDS Malvern Mastersizer S / Forward light scattering
Cilas 1064 / Forward light scattering Malvern 2600 / Forward light scattering Coulter N4 /
Dynamic light scattering (PCS) ALV 5000/ Static and dynamic light scattering (PCS) Coulter
Counter / Electrical sensing zone Micromeritics Sedigraph / Sedimentation PCO ccd imaging
/ Image Analysis Philips XL 20 / Scanning electron microscopy Particle Size of Sprays and
Aerosols TSI PDPA / Phase Doppler velocimetry
..and more coming soon Chemical
composition of gases VG Prima 600 / Mass Spectrometry Siemens SESAM 1 / FTIR Siemens MIPAN
/ Microwave spectrometry Chemical composition of solids Philips PW 1400 spectrometer /
X-Ray Fluorescence HOR / Instrumental Neutron Activation Analysis PerkinElmer DSC7 /
Differential Scanning Calorimetry PerkinElmer TGA7 / Thermogravimetry Porosity N2 Physical
Gas Adsorption at 77 K (Flow Technique) Single point BET (0.30 p/p0) Multi-point BET
(0.05-0.10-0.15-0.20-0.25 p/p0) Total pore volume (0.99 p/p0) 100 150 125 N2 Physical Gas
Adsorption at 77 K (Volumetric Technique) Single point BET (0.30 p/p0) Multi-point BET
(0.05-0.10-0.15-0.20-0.25 p/p0) Multi-point BET + pore volume (0.99 p/p0) 150 200 250
Adsorption isotherm, multi-point BET, total pore volume, BJH adsorption pore size
distribution (2-200 nm) 375 Adsorption and desorption isotherm, multi-point BET, total
pore volume, BJH desorption pore size distribution (2-200 nm) 400 Ar Low Pressure Physical
Gas Adsorption at 87 K (Volumetric Technique) Adsorption isotherm (10-6 0.3 p/p0), SF
micropore size distribution 0.5 2 nm 550 CO2 Physical Gas Adsorption (Volumetric
Technique) Adsorption and desorption isotherm, micropore surface area and micropore volume
(Dubinin-Radushkevic) 400 Kr Physical Gas Adsorption (Volumetric Technique) Multi-point
BET (0.05-0.10-0.15-0.20-0.25 p/p0) 300 H2 or CO Chemical Gas Adsorption (Volumetric
Technique) Dual adsorption isotherm (1-100 kPa), metal surface area, metal dispersion and
average crystallite size 425 Mercury Intrusion Porosimetry Intrusion curve 0.1 400 MPa,
porosity, apparent density, pore size distribution 4 nm 17 µm 275 Intrusion curve vacuum
0.1 MPa, porosity, apparent density, pore size distribution 17µm 120 µm 200 Intrusion
curve vacuum 400 MPa, porosity, apparent density, pore size distribution 4 nm 120 µm 375
He Pycnometry Skeletal density 125 Sizing Laserdiffraction (dry, aqueous or organic fluid
dispersion) Forward light scattering, size distribution 0.5 µm 2000 µm 275 Forward light
scattering incl. backscattering information, size distribution 0.04 µm 2000 µm 300
Photon Correlation Spectroscopy (PCS) Particle size distribution 3 nm 3 µm 225 Phase
Doppler Velocimetry Spray droplet velocity and size distribution 0.5 µm 90 µm p.o.a.
Electrical Sensing Zone Coulter Counter narrow size distribution 0.6 µm 1200 µm 325
Scanning Electron Microscopy Surface and size scan incl. photographs 200 Image Analysis
Distribution and size scan incl. photographs 200 Gravitational Sedimentation Sedigraph
size distribution 1 µm 300 µm 200 Sieve Analysis Dry sieving, range 37 µm 1700 µm 150
Composition Microwave Spectrometry Gas sample analysis of 0.2 up to 2000 ppmv NH3 150 FTIR
Spectroscopy Gas sample analysis of NO, NO2, H2O, NH3, SO2, SO3, p.o.a. Mass Spectrometry
Mass spectrum from m/e 4 300 for identification Gas sample analysis on C3H6 150 150
Instrumental Neutron Activation Analysis (INAA) Package A: F, Se
140 Package B: Al, Ba, Ca, Cl, Cu, Dy, Er, Ga, K, I, In, Mg, Mn, Na, Rh, Si, Ti, V 140
Package C: As, Au, Ba, Br, Ca, Cd, Ce, Cr, Fe, Ga, K, La, Mo, Na, Pd, Pt, Re, Sb, Sc, Sm,
U, W, Yb, Zn 140 Package D: Ag, Ba, Ca, Ce, Cr, Co, Cs, Eu, Fe, Hf, Hg, Ir, Lu, Nd, Ni,
Os, Rb, Sb, Sc, Se, Sn, Sr, Ta, Tb, Te, Th, Yb, Zn, Zr 140 Package E: As, Ba, Br, Cd, Co,
Cr, Hg, Mo, Ni, Sb, Se, Sn, Zn 140 X-Ray Fluorescence (XRF) 72 components in
solids 130 Thermogravimetric analysis (TGA) TGA analysis 300 Differential Scanning
Calorimetry (DSC) DSC analysis 300 p.o.a.="price" on application Priority
Service: 40% surcharge Consultancy: 90,00 per hour Publications J.C.
Groen and L.A.A. Peffer, "Influence of dead space measurement on adsorption
characteristics of microporous zeolites", The MicroReport, 3rd quarter 1997, Vol. 8,
No. 3, p.8. J.C. Groen, M.C. Doorn, L.A.A. Peffer, in D.D. Do (Eds.), "MCM-41 and the
BdB corrected Kelvin equation for accurate mesopore size distributions from gas adsorption
data", Adsorpti. Sci. Technol., Proc. 2nd Pacific Basin Conference, Brisbane,
Australia (2000) p. 229. J.C. Groen, J. Pérez-Ramírez, L.A.A. Peffer, "Different
chemisorption methods applied to zeolite supported Pt-catalysts", in: A. Galarneau,
F. Di Renzo, F. Fajula, J. Vedrine (Eds.), Zeolites and Mesoporous Materials at the Dawn
of the 21st Century, Studies in Surface Science and Catalysis, Vol. 135, Elsevier,
Amsterdam, 2001, 2862. J.C. Groen, J. Pérez-Ramírez, and L.A.A. Peffer, "Formation
of uniform mesopores in zeolite ZSM-5 upon alkaline post-treatment?" Chem. Lett. 2002
94. J.C. Groen, J. Pérez-Ramírez, and L.A.A. Peffer, Comments on "Vanadium- and
chromium-containing mesoporous MCM-41 molecular sieves with hierarchical structure",
Micropor. Mesopor. Mater. 51 (2002) 75
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