Acid insoluble ash content of paper or board

Determination of certain aromatic amines derived from azo dyes in accordance with the standard EN 14362-1.

Analysis for quantifying dioxins and furans (PCDD/F) in various packaging materials (e.g. food and cosmetics packaging) and their raw materials, including plastics, paper, and rubber. Dioxins and furans are a family of chlorine-containing chemicals considered bioaccumulating, persistent organic pollutants (POPs) that can be toxic even at low doses. While regulatory limits apply mainly to food and feed, packaging materials can be a source of indirect exposure to dioxins and furans. Recycled materials tend to pose relatively high risks, depending on the quality of the raw material and the effectiveness of the decontamination process. The following substances are included in the analysis: Dibenzo-p-dioxins (PCDDs) Polychlorinated dibenzofurans (PCDFs) 2,3,7,8-TCDD. 2,3,7,8-TCDF. 1,2,3,7,8-PeCDD. 1,2,3,7,8-PeCDF. 1,2,3,4,7,8-HxCDD. 2,3,4,7,8-PeCDF. 1,2,3,6,7,8-HxCDD. 1,2,3,4,7,8-HxCDF. 1,2,3,7,8,9-HxCDD. 1,2,3,6,7,8-HxCDF. 1,2,3,4,6,7,8-HpCDD. 1,2,3,7,8,9-HxCDF. OCDD. 2,3,4,6,7,8-HxCDF. 1,2,3,4,6,7,8-HpCDF. 1,2,3,4,7,8,9-HpCDF. OCDF. Testing is often performed for the following reasons: Analyzing recycled PE, PP, and LDPE intended for cosmetics packaging according to CosPaTox guidelines., Analyzing paper and board bleached with elementary chlorine according to the requirements of TemaNord 2008:515 guidelines..

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 and 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 Herzberg staining test by the ISO 9184-3 standard is used to determine the main fiber content of paper and board. In the test, a saturated solution of zinc chloride, iodine, and potassium iodide is used to color the paper. The solution affects fibers differently and enables the qualitative and quantitative analysis of mechanical, rag, chemical, and semi-chemical pulps, regenerated cellulose fibers, and synthetic fibers in paper and board.

Determination of the total organic fluorine (TOF) content in combustible materials by combustion ion chromatography (CIC). 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.

XPS is a semi-quantitative technique used to measure the elemental composition of material surfaces. In addition, it can also determine the binding state of the atoms. XPS is a surface-sensitive technique. Typical probing depth is 3-9 nm, and detection limits range roughly between 0.1 and 1 atomic %. XPS can measure elements from Li to U. The elemental composition is reported in at.% and measured on 1 area of a few 100 µm. Upon request, we can measure smaller areas or depth profiles, and a binding state determination can also be provided. Measurements are typically performed using one of the following instruments: PHI Genesis, Thermo Fisher ESCALAB 250Xi, PHI Quantum 2000. Synchrotron XPS is also available. Contact us for more information and a quote for your project.

Screening of volatile organic compounds (VOC) from paper, board, and plastics. The method can be used to analyze volatile residues from printed packaging. For evaluation of recycling process efficiency, please see our extended package for VOC screening. The following substances are included in this analysis package: Substance CAS No Methyl propylene glycol (1-methoxy-2-propanol) 107-98-2 Buthyl glycol (2-Butoxy ethanol) 111-76-2 Ethyl glycol (2-Ethoxyethanol) 110-80-5 Ethyl glycol acetate (2-Ethoxyethyl acetate) 111-15-9 Methyl glycol (2-Methoxyethanol) 109-86-4 Methyl glycol acetate (2-Methoxyethanol acetate) 110-49-6 3-Ethoxy-1-propanol 111-35-3 Acetyl acetone 123-54-6 Acetone 67-64-1 Ethanol 64-17-5 Isobutanol 201-148-0 2-propanol, Isopropanol (IPA) 67-63-0 Methanol 67-56-1 1-Butanol 71-36-3 1-Propanol 71-23-8 Benzene 71-43-2 Cyclohexane 110-82-7 Ethylbenzene 100-41-4 Ethyl acetate 141-78-6 Isobutyl acetate 110-19-0 Isopropyl acetate 108-21-4 Isooctane 540-84-1 2-butanone, methyl ethyl ketone (MEK) 78-93-3 Methyl isobutyl ketone (MIBK) 108-10-1 Methyl acetate 79-20-9 Toluene 108-88-3 Trichloroethylene 79-01-6 Xylene 1330-20-7 n-Butyl Acetate 123-86-4 n-Heptane 142-82-5 n-Hexane 110-54-3 n-Octane 111-65-9 n-Propyl acetate 109-60-4

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 (1000 °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 price includes two parallel measurements. The results are reported as wt-% of the initial sample. The ash, drying and dry loss measurements will increase the minimum required sample material need 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. Possible element packages: O, CHNS, and CHNOS.

Specific migration of dialkyl ketones (DAKs) that originate from alkyl ketene dimer (AKD) hydrophobic sizing agent of paper and board. According to BfR XXXVI recommendation, the limitation for the migration of AKD DAKs is 5 mg/kg of food or food simulant.

Determination of mineral oil saturated hydrocarbons (MOSH) with polyolefin oligomeric saturated hydrocarbons (POSH) and mineral oil aromatic hydrocarbons (MOAH) in various matrices, including: Food contact materials (e.g., paper, board, plastics, rubber), Printing inks (incl. carbon black), Cosmetic products and raw materials, Lubricating oils and greases, white oils. The results are reported as the concentrations of fractions of MOSH/POSH and MOAH, with grouping based on the number of carbon atoms in the substances. The reported fractions are listed in the table below: MOSH/POSH (C10-C50), total MOAH (C10-C50), total MOSH/POSH (≥C10-≤C16) MOAH (≥C10-≤C16) MOSH/POSH (>C16-≤C20) MOAH (>C16-≤C25) MOSH/POSH (>C20-≤C25) MOAH (>C25-≤C35) MOSH/POSH (>C25-≤C35) MOAH (>C35-≤C50) MOSH/POSH (>C35-≤C40) MOSH/POSH (>C40-≤C50) In case the sample contains high amounts of MOSH, POSH, or poly alpha olefins (PAO), the levels should be indicated before shipping samples. Moreover, the LOQ is higher for samples with high MOSH, POSH, or PAO content due to dilution. Additionally, the safety data sheets (SDS) should be supplied with the samples when available.