Artificial weathering in Xenon-arc chamber (Coated panel)

A biodegradation analysis for determining how materials decompose in soil, conforming to the ISO 17556 standard. This standard is specific to aerobic biodegradation in soil environments, where organic materials are broken down into carbon dioxide (CO2). Please note that this analysis focuses exclusively on aerobic biodegradation and does not cover chemical analyses, material disintegration, or ecotoxicity evaluations, which are essential for a full understanding of the environmental impact of the degradation process. The analysis is, nonetheless, a valuable tool for comparing different product formulations in the initial stages of development, prior to more comprehensive biodegradability assessments. The cost of this test varies, depending on the specific conditions chosen and the product being tested, with test durations ranging from 6 to 24 months.

1000 hours of exposure in QUV accelerated artificial weathering, including measurement of L* a* b* color coordinates and calculation of ΔE*ab

This analysis package is used to determine the biodegradability of materials in soil. The results can be used to evaluate the environmental impact of the product. Testing is based on the international standard ISO 23517, titled "Soil biodegradable materials for mulch films for use in agriculture and horticulture - Requirements and test methods regarding biodegradation, ecotoxicity and control of constituents." The standard encompasses four assessments: Chemical analysis of raw materials: Ensuring the absence of heavy metals or toxic compounds from the material., Biodegradation Tests: Evaluating how plastic breaks down and examining its environmental impact., Disintegration Tests: Assessing how plastics fragment into smaller pieces under simulated soil conditions., Ecotoxicity: Verifying that the product resulting from biodegradation is not toxic to living organisms, with evaluations conducted at two levels: higher plants and invertebrates.. The goal is to determine whether the material can undergo effective biodegradation in a simulated natural environment, utilizing the detailed criteria outlined in the ISO standard.

Testing package to assess the industrial compostability of materials or products following international protocols, such as EN 13432 for packaging, EN 14995 for plastic products, and ISO 17088 for organic recycling. The compostability assessment framework comprises four complementary tests, collectively ensuring the organic recyclability of the material or product: Analysis of constituents to verify the absence of heavy metals and toxic compounds in the material., Biodegradation tests to assess how plastic breaks down, gauging its environmental impact., Disintegration tests for evaluating how plastics fragment into smaller pieces under diverse environmental conditions., Ecotoxicity assessment to ensure that the biodegradation product is not toxic to living organisms, including plants, invertebrates, and microorganisms.. This analysis package includes the necessary tests to verify your product's compostability in an industrial composting environment with a 3-month testing time, which is the typical time for biodegradable plastics to break down in an industrial compost. The maximum testing time is 6 months.

X-Ray Reflectometry (XRR) analysis is used to measure the density (g/cm3), thickness (nm), and roughness (nm) of thin films. The method is applicable to the characterization of single- or multilayered thin films, as it provides information on the thickness and density of individual layers of the sample material as well as the roughness of the interphases. Greatest accuracy for XRR thickness measurements is generally achieved for samples containing 1-150 nm thick surface layers with under 5 nm RMS roughness. Thicker films and coatings with rougher surfaces can also be characterized, but the accuracy of thickness determination decreases as the thickness and roughness of the film or film stack increase. >150 mm wafers are typically cut to fit the sample holder. Please let us know if you need testing for larger wafers that cannot be cut into pieces. The available temperature range for XRR measurements is 25-1100 °C, and crystallinity can be studied as a function of temperature. The measurements can be performed under a normal atmosphere, inert gas, or vacuum. Measurements are typically performed using one of the following instruments: Rigaku SmartLab, Panalytical X'Pert Pro MRD, Bruker D8 Discover. Please let us know if you have a preference for a specific instrument.

Determination of microplastics in wastewater using FTIR microspectroscopy. The results of the analysis will specify different types of polymers by size, for example, 10–50 µm, 50–100 µm, 100–500 µm, and >500 µm. This analysis is suitable for natural waters and typical wastewater samples. Please note that both of these matrices need digestion sample preparation due to the possible solid particles in the samples. For special water matrices (process water, industrial water, etc.), please contact the method expert before ordering.

This test is designed to measure the oxygen transmission rate of finished packages, including cups, bottles, trays, and containers. Two replica measurements are included in the displayed price. Temperature can be adjusted from 15 to 55 °C, and relative humidity can be either 0% or between 5 and 90% RH. This test is not suitable for films. Please see the oxygen transmission rate (OTR) of films and sheeting if you need testing for film samples. Please specify the sample dimensions and testing conditions upon ordering.

We offer comprehensive test packages for verifying the quality of type II and type IIR face masks according to the EN 14683 standard. The tests included in the packages are required to label face masks with the CE marking. Medical face masks are divided into Types I and II according to their bacterial filtration efficiency. Type I masks are not intended for healthcare professionals, but for the public to prevent the spread of infectious diseases. Type II masks are further classified based on whether they are splash-resistant (Type IIR) or not (Type II). To comply with the European Standard EN 14683, Type II face masks must undergo the following quality tests: Bacterial filtration efficiency (BFE) - The ability of the face mask to filter the bacterium Staphylococcus aureus. The BFE is expressed as the percentage of colony-forming units (cfu) that have passed via aerosol through the facemask. If a face mask consists of two or more areas with different characteristics, these areas will be tested separately., Breathability (Differential pressure) - The amount of differential pressure required to draw air through a measured surface area at a constant flow rate., Microbial cleanliness (Bioburden) - The measurement of colony forming units per gram as per EN ISO 11737-1., Biocompatibility - The medical face mask manufacturer shall complete a biocompatibility evaluation according to ISO 10993-1 as a surface device with limited contact. The applicable toxicology testing regimen shall also be determined.. In addition to the above, Type IIR masks require the following test: Splash resistance - Performed according to ISO 22609, this test determines the ability of a face mask to resist penetration of splashes of liquid at different pressures.. The lower displayed price applies to the Type II mask test package, while the higher price also includes the splash resistance test required for Type IIR masks.

Phthalates are a group of chemicals widely used as plasticizers, which make plastics more flexible and durable. They have also been used as additives in products such as cosmetics and personal care items. Several phthalates have been identified as endocrine-disrupting agents or as chemicals toxic to reproduction. Exposure to phthalates can occur through: Oral exposure Food: Exposure occurs via migration from food packaging., Children's toys: Children often put toys in their mouths.., Inhalation: Breathing in dust from vinyl flooring or fragrances (like perfumes) can cause exposure to phthalates via inhalation., Skin contact: Phthalates present in cosmetics, lotions, and soaps can be absorbed through the skin.. For other listed matrices apart from cosmetics, the analysis package covers the following substances included in the REACH Authorization List: Substance Abbreviation CAS number Diisobutyl phthalate DIBP 84-69-5 Dibutyl phthalate DBP 84-74-2 Benzyl butyl phthalate BBP 85-68-7 Bis(2-ethylhexyl) phthalate DEHP 117-81-7 Di(n-octyl) phthalate DNOP 117-84-0 Diisononyl phthalate DINP 68515-48-0 Diisodecyl phthalate DIDP 26761-40-0 Products that contain restricted phthalates in concentrations higher than 0.1% may be removed from the market. The analysis package for cosmetic products contains the following phthalates: Substance Abbreviation CAS number Bis(2-ethylhexyl) phthalate DEHP 117-81-7 Benzyl butyl phthalate BBP 85-68-7 Dibutyl phthalate DBP 84-74-2 Diisononyl phthalate DINP 68515-48-0 Di(n-octyl) phthalate DNOP 117-84-0 Diisodecyl phthalate DIDP 26761-40-0 All the above-mentioned substances are prohibited in cosmetic products (Annex II of Regulation (EC) No 1223/2009).

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..