| Literature DB >> 35407897 |
Abstract
This review article provides basic information about cannabis, its structure, and its impact on human development at the turn of the century. It also contains a brief description of the cultivation and application of these plants in the basic branches of the economy. This overview is also a comprehensive collection of information on the chemical composition of individual cannabis derivatives. It contains the characteristics of the chemical composition as well as the physicochemical and mechanical properties of hemp fibers, oil, extracts and wax, which is unique compared to other review articles. As one of the few articles, it approaches the topic in a holistic and evolutionary way, moving through the plant's life cycle. Its important element is examples of the use of hemp derivatives in polymer composites based on thermoplastics, elastomers and duroplasts and the influence of these additives on their properties, which cannot be found in other review articles on this subject. It indicates possible directions for further technological development, with particular emphasis on the pro-ecological aspects of these plants. It indicates the gaps and possible research directions in basic knowledge on the use of hemp in elastomers.Entities:
Keywords: chemical and physical properties; composites; extract; fiber; hemp; polymer
Year: 2022 PMID: 35407897 PMCID: PMC9000560 DOI: 10.3390/ma15072565
Source DB: PubMed Journal: Materials (Basel) ISSN: 1996-1944 Impact factor: 3.623
Figure 1The chair conformation of β-anhydroxyglucose units in the cellulose chain.
Absorption signals of Fourier transform infrared spectroscopy for the spectrum of hemp fibers.
| Name of the Function Group | Wavenumber | Bibliographic |
|---|---|---|
| C-OH out-of-plane bending vibrations; C-C | 557 | [ |
| Stretch vibrations of the glucose ring; | 895 | [ |
| -OH; -COO | 900–1200 | [ |
| CO-O-CO | 1000–1100 | [ |
| C-O stretching vibrations; deformation of the C-H aromatic plane | 1030–1058 | [ |
| The absorption band of hydroxyl compounds -OH | 1100 | [ |
| C-O stretching vibrations; asymmetric bridge C-O-C stretching vibrations | 1158 | [ |
| C-O; C=O; C-C-; COOH | 1100–1300 | [ |
| Acyl-oxygen CO-OR stretching vibrations in hemicelluloses; -CH3 | 1245 | [ |
| C-H deformation vibrations; -OH bending vibrations | 1325 | [ |
| C-H bending vibrations related to the structure of cellulose and hemicellulose | 1369 | [ |
| CH2 stretching vibrations related to the cellulose structure, vibrations of the bonds of the aromatic backbone | 1425–1426 | [ |
| CH deformation vibrations; asymmetric bending vibrations from -CH2 and -CH3 groups | 1426–1463 | [ |
| C=C stretching vibrations in aromatic structures | 1508 | [ |
| C=C stretching of the aromatic ring | 1550 | [ |
| C=C unsaturated bonds; | 1592 | [ |
| COO− (pectin) | 1650 | [ |
| -OH from absorbed water; C=C | 1653 | [ |
| C=O stretching vibrations in uncoupled ketones and free aldehydes | 1736; 1718 | [ |
| CH stretching vibrations in methyl and methylene groups | 2896 | [ |
| -OH stretching vibrations (hydrogen bonds) | 3331 | [ |
Figure 2Structural formulas of cannabinoids occurring in hemp (CBD—cannabidiol; CBN—cannabinol; CBG—cannabigerol; CBC—cannabichromene; THC—tetrahydrocannabinol; THCV—tetrahydrocannabivarin).
Composition of the oily fraction derived from hemp seeds.
| Component | Value [%] |
|---|---|
| The content of the oily fraction in the entire mass of the hemp seed | 28.7 |
|
| |
| Palmitic acid | 6.96 |
| Stearic acid | 2.74 |
| Arachidic acid | 0.77 |
|
| 10.47 |
|
| |
| Oleic acid | 13.64 |
| Linoleic acid | 56.35 |
| Gamma-linoleic acid | 1.35 |
| Alpha-linoleic acid | 17.30 |
| Stearidonic acid | 0.50 |
| Eicosenoic acid | 0.39 |
|
| 89.53 |
The content of the fraction in the entire mass of the hemp waxes.
| Component | Value [%] |
|---|---|
|
| |
| pentacosane | 1.92–2.17 |
| heptacosane | 6.96–7.55 |
| octacosane | 0.75–5.56 |
| nonacosane | 9.92–10.51 |
| triacontane | 0.44–0.58 |
| dotriacontane | 0.49 |
| tritriacontane | 1.58–2.06 |
| pentatriacontane | 1.13–1.24 |
| heptatriacontane | 1.18–1.23 |
|
| |
| sabinene | 0.31–0.51 |
| p-cymene | 3.32–5.15 |
|
| |
| β-cubebene | 0.31–0.40 |
| (−)-trans-caryophyllene | 5.90–7.22 |
| β-copaene | 0.32–0.40 |
| α-humulene | 0.51–0.94 |
| (E,E)-β-farnesene | 0.30–0.33 |
| γ-gurjunene | 0.27 |
| γ-curcumene | 0.59–0.70 |
| valencene | 0.51–0.60 |
| germacrene A | 0.39–0.44 |
| α-7-epi-selinene | 0.42–0.54 |
| α-cadinene | 0.20–0.33 |
| α-bisabolene | 1.63–2.50 |
| (E,E)-α-farnesene | 0.28 |
|
| |
| dehydro-1,8-cineole | 1.23–1.99 |
| isoborneol | 0.38 |
| fenchone | 0.26–0.44 |
| cis-thujone | 0.27 |
| endo-fenchol | 0.26–0.28 |
| cis-nerolidol | 2.50–2.84 |
| trans-nerolidol | 0.43 |
| caryophyllene oxide | 0.49–0.89 |
| humulene epoxide II | 0.31–0.37 |
| 10-epi-γ-eudesmol | 0.61–0.82 |
| 1,10-di-epi-cubenol | 0.29–0.36 |
| γ-eudesmol | 0.29–0.47 |
| α-muurolol | 0.25–0.35 |
| β-eudesmol | 0.67–1.01 |
| α-bisabolol | 0.18 |
| (2Z,6Z)-farnesol | 0.49 |
|
| |
| CBD | 4.20–9.67 |
| CBC | 0.11–0.18 |
| Δ8-THC | 0.12–0.13 |
| Δ9-THC | 0.22–0.37 |
| CBG | 0.07–0.22 |
| CBN | 1.20–2.40 |
| CBDA | 22.91–34.56 |
| THCA | 5.78–5.89 |
|
| |
| heptanal | 0.22–0.61 |
| 2,4-hexadienal | 0.11 |
| nonanal | 0.37 |
| vanillin | 0.27 |
| tridecanoic acid | 0.21–0.31 |
| ethyl tetradecanoate | 0.42 |
| hexadecenoic acid | 0.25–0.27 |
| ethyl hexadecanoate | 0.22–0.31 |
Figure 3Change in the number of occurrences of the keyword “hemp” in the Scopus database in 2000–2021.
Figure 4Processing cannabis for energy purposes.
Figure 5The number of occurrences of the phrase “hemp” in the Scopus database in the last 10 years, broken down into individual fields (as of 5 December 2021).
Figure 6The use of hemp in various industries due to the division into the parts of the plant used.