Sentence examples for fractionation technology from inspiring English sources

In this study, a simple and integrated spintip-based protein digestion and three-dimensional peptide fractionation technology (3D-SISPROT) was developed for the deep proteome profiling from low microgram of proteins as starting materials.

Pulp can be used for ethanol production while separated xylan and lignin fractions can be used as a feedstock for value-added products which suggests the applicability of clean fractionation technology in a biorefinery concept.

The cryogenic fractionation technology is commonly used to produce oxygen-enriched air with an oxygen purity of 99 vol.%.

The composition of GMP is variable and depends on the particular whey source and the fractionation technology employed in its isolation (Martín Diana et al. 2006).

Some of the fractions included in this study, such as bark and top parts, are nevertheless available today using conventional fractionation technology.

But before the significant costs incurred in ethanol production from lignocellulosic biomass can be reduced, an efficient sugar fractionation technology has to be developed.

Dry fractionation technologies allow these peripheral tissues to be separated and recovered to efficiently separate valuable from detrimental components (i.e. contaminants, antinutrient compounds, irritants), in order to develop nutritionally enhanced ingredients and products.

However, dry fractionation technologies are an important step for future biomass biorefineries since they do not require chemicals and do not generate wastewater.

These processes are based on a combination of fragmentation and separation steps, which are carried out by a mechanical pretreatment followed by several types of fractionation technologies [ 11– 13].

Today, most of lignocellulosic fractionation technologies or pretreatments are based on expensive chemical processes (pulping, acidic hydrolysis, solvent extraction, alkaline and acid extraction, steam and ammonia explosion and so on) which do not keep the major components intact after separation and generate high toxic effluents [ 6].

To address specificity of our on-chip fractionation-MS technology, we investigated the expression of CFP-10 from MTB grown in culture media.