Bulk density of solid biofuels

Diesel exhaust fluid (DEF) is an additive used in diesel-powered vehicles to help the catalytic reduction of nitrous oxides. Thus, the use of AdBlue and other exhaustive fluids improves ambient air quality. DEF testing package according to ISO 22241:2019 includes the measurements listed below: Urea content (ISO 22241-2C), Density at 20 °C (EN ISO 12185) , Refractive index at 20 °C (ISO 22241-2C), Alkalinity as NH₃ (ISO 22241-2D), Biuret (ISO 22241-2E), Aldehydes (ISO 22241-2F), Insoluble matter (ISO 22241-2G), Phosphate (ISO 22241-2H), Determination of Al, Ca, Cr, Cu, Fe, K, Mg, Na, Ni, and Zn content (ISO 22241-2I).

Standard EN 228 outlines the testing requirements and methods for gasoline quality testing. The following tests are included in the package: Standard Parameter Requirements EN ISO 5164 RON Min. 95 EN ISO 5163 MON Min. 85 EN 237 Lead content Max. 5 mg/l EN ISO 12185 Density at 15 °C 720–775 kg/m3 EN ISO 20846 Sulfur content Max. 10 mg/kg EN 16136 Manganese content Max. 2 mg/l EN ISO 7536 Oxidation stability Min. 360 minutes EN ISO 6246 Washed gum content Max. 5 mg/100ml EN ISO 2160 Copper corrosion Class 1 ASTM D4176 Appearance Bright and clear EN ISO 22854 Hydrocarbon composition Benzene max. 1 v%, aromatics max. 35 v%, olefins max. 18 v%, oxygenates* EN 13016-1 Vapor pressure at 37.8 °C (DVPE) Depends on volatility class** EN ISO 3405 Distillation characteristics Final boiling point max. 210 °C, distillation residue max. 2 v%, evaporated volumes*** * For gasoline with max. 3.7 m% of oxygen, allowed oxygenate contents are methanol 3 v%, ethanol 10 v%, iso-propanol 12 v%, iso-butanol 15 v%, tert-butanol 15 v%, ethers with five or more carbon atoms 22 v%, and other oxygenates 15 v%. For gasoline with max. 2.7 m% of oxygen, allowed oxygenate contents are methanol 3 v% and ethanol 5 v%. ** For volatility class A: 45–60 kPa, B: 45–70 kPa, C: 50–80 kPa, D: 60–90 kPa, E: 65–95 kPa, and F: 70–100 kPa *** Percentage evaporated at 70 °C (E70): winter 22–50 v%, summer 22–48 v%, at 100 °C (E100): 46–71 v%, and at 150 °C (E150): min. 75 v%

This metal screening analysis includes the semi-quantitative determination of 70 elements. The method can be used, for example, to determine the background concentrations of metals in environmental samples or to study the elemental distribution of unknown samples. Screening is also often performed to assess which metals should be analyzed by a quantitative method. The measurement is performed using a high-resolution ICP-MS technique (ICP-SFMS), which can identify very low elemental concentrations. A semi-quantitative determination of the following elements is included: Ag, Al, As, Au, B, Ba, Be, Bi, Br, Ca, Cd, Ce, Co, Cr, Cs, Cu, Dy, Er, Eu, Fe, Ga, Gd, Ge, Hf, Hg, Ho, I, Ir, K, La, Lu, Mg, Mn, Mo, Na, Nb, Nd, Ni, Os, P, Pb, Pd, Pr, Pt, Rb, Re, Rh, Ru, S, Sb, Sc, Se, Si, Sm, Sn, Sr, Ta, Tb, Te, Th, Ti, Tl, Tm, U, V, W, Y, Yb, Zn and Zr. However, please note that some elements may not be determinable due to matrix interference. During this semi-quantitative analysis, the instrument is calibrated for about 30 elements. The rest of the analytes are quantified using sensitivity factors for calibrated elements with similar mass and first ionization potential, considering isotope abundances. Quantitative analysis is also available at an additional price. During this analysis, all elements are calibrated (excluding halogens and Os). Please ask for an offer for this service.

The molar mass distribution of biomass samples soluble in pure water or organic solvents (DMF, DMSO, and THF) is measured with size exclusion chromatography (SEC) with a refractive index detector (SEC-RID). The system is calibrated with polystyrene and dextran standards. A Pullulan standard is also available upon request. In the case of lignin samples, molar mass distribution is analyzed using SEC coupled with a Ultraviolet detector at 256 nm wavelength. The lignin is dissolved in a suitable solvent before analysis. The SEC system is calibrated with a polystyrene sulfonate standard. A borate buffer is used to set the pH for the eluent. The weight-average molecular weight and number-average molecular weight are reported. For absolute molecular weight, GPC system coupled with MALS detector can be used. The mobile phase for this system is THF. An additional cost applies to this method.

Determination of the total organic fluorine (TOF) content in combustible materials using combustion ion chromatography (CIC). By default, TOF is analyzed as total fluorine (TF). If required, total inorganic fluorine (TIF) can be measured as well, and TOF calculated as the difference between TF and TIF. TOF analysis gives information about the total amount of organic fluorinated compounds. It can also be used to evaluate the presence of per- and polyfluoroalkyl substances (PFAS) in the material, even though individual PFAS compounds can't be analyzed with this method. The analysis is suitable for many different materials. Please describe the sample in detail when requesting an offer to help us prepare a quote quickly.

Determination of carbon, hydrogen, nitrogen, sulfur, and oxygen content of an organic sample. CHNS analysis (”LECO analysis”) is performed using a flash combustion method, where the sample is combusted under 25 kPa of O2 at an elevated temperature (1,000 °C), followed by gas chromatography separation and detection using a thermal conductivity detector. Oxygen is analyzed by reduction on granulated carbon at 1480 °C, utilizing high-temperature thermal decomposition and conversion of oxygen into carbon monoxide before gas chromatography separation and detection with a thermal conductivity detector. The sample can be either solid or liquid, but water in the sample affects the results. In the case of aqueous samples, it is possible to dry the sample before analysis. The displayed price includes the full CHNOS package with two parallel measurements and applies to conventional organic samples. The results are reported as wt-% of the initial sample. The addition of ash, drying, and dry loss measurements will increase the minimum required sample material to 300 mg. The analysis gives the total carbon, hydrogen, nitrogen, sulfur, and oxygen content of the material, but it does not identify any chemical structures. The measurement can be combined with other methods, such as GC-MS, 1H, and 13C NMR, to perform substance structure identification. Analysis can be split into the following packages: CHN, O, and S.

This analysis provides quantitative information about the crystalline and amorphous phases within your sample using high-resolution synchrotron X-ray diffraction (XRD). A standard analysis includes: Quantification of crystalline phases as weight percentages, Quantification of the total amorphous content, High-resolution powder diffraction data and the resulting diffractogram, A comprehensive test report detailing the findings. For more advanced needs, we also offer total scattering/pair distribution function (PDF) analysis to reveal the local atomic structure in amorphous or nano-structured materials. Do not hesitate to ask for a quote.

Our δ13C stable isotope analysis determines the ratio of 13C to 12C in a given sample material by a continuous flow isotope ratio mass spectrometer (IRMS). Results are expressed in per mille (‰) as the deviation of the isotope ratio from a standard reference material. We have more than 30 IAEA, USGS, and in-house isotopic standards available to accommodate a wide range of expected ratios. The price and turnaround time displayed apply to conventional sample matrices. The analysis is suitable for a wide range of sample materials, including, but not limited to, those listed in the table below. All of our stable isotope analyses are conducted at ISO 17025-accredited facilities. Please contact us using the form below to arrange testing on your samples.

Determination of hydroxyl group (-OH) content in lignin samples by 31P NMR. The method is suitable for lignin that has or might have free hydroxyl groups. The lignin is dissolved in a deuterated solvent (typically CDCl3:Pyridine), and an internal standard is added to the sample. Then, the hydroxyl groups in the sample + internal standard are phosphorylated, and the mixture is analyzed using 31P NMR. The number of free hydroxyl groups can be determined from the NMR spectra by comparing the phosphorus signal of the internal standard to the phosphorus signals of the phosphorylated sample material. The following OH-groups can be quantified (in mmol/g): Aliphatic OH, Phenolic OH, Carboxylic acid , Syringyl OH, Guaiacyl OH, Catechols, p-hydroxyphenyl OH, Total OH. The price can depend on whether your samples require specialized deuterated solvents or preparation conditions (i.e., high temperature or long dissolution time).

Measurement of the refractive index of powder samples with the Becke line microscopic method. The analysis is suitable for transparent crystalline materials with a particle size larger than 40 μm. Measurements are performed at a 589.3 nm wavelength. Refractive index values from approximately 1.40 to 1.70 are reported with a precision of up to two significant digits. Please note that the method does not directly determine the particle's absorption coefficient (imaginary value).