Table 2.

Studies on the influence of the temperature and the reaction time on the course of limonene epoxidation over the Ti-SBA-15 catalyst.

	Reaction Time [h]
	0.5	1.0	1.5	2.0	2.5	3.0	24
Temperature 0 °C
S1,2-EL	68	57	28	11	11	4	4
Sdiol of 1,2-EL	6	7	10	12	12	13	13
Scarvone	5	10	19	13	13	9	8
Scarveol	0	0	0	0	0	3	5
Sperillyl alcohol	21	26	43	64	64	71	70
Climonene	5	5	6	6	6	18	18
Sorg.comp./H2O2	8	9	10	10	10	27	27
Temperature 40 °C
S1,2-EL	48	29	13	9	6	3	3
Sdiol of 1,2-EL	6	7	10	10	11	11	11
Scarvone	13	14	14	14	14	16	16
Scarveol	1	4	4	5	5	5	5
Sperillyl alcohol	32	46	59	62	64	65	65
Climonene	9	13	15	21	22	37	40
Sorg.comp./H2O2	19	25	30	40	40	62	54
Temperature 80 °C
S1,2-EL	26	15	8	6	5	4	3
Sdiol of 1,2-EL	8	10	11	11	11	13	13
Scarvone	8	12	12	13	15	16	17
Scarveol	2	2	2	2	2	2	3
Sperillyl alcohol	56	61	67	68	67	65	64
Climonene	17	22	29	33	36	42	46
Sorg. comp./H2O2	36	43	52	52	54	59	64
Temperature 120 °C
S1,2-EL	20	11	5	5	3	2	0
Sdiol of 1,2-EL	10	10	11	11	12	12	12
Scarvone	12	14	16	16	17	17	19
Scarveol	2	2	3	3	3	4	4
Sperillyl alcohol	56	63	65	65	65	65	65
Climonene	23	29	32	35	40	52	52
Sorg.comp./H2O2	30	34	37	41	46	59	57

EL—epoxylimonene, S—selectivities of the appropriate products, C—conversion, S_{org.comp./H2O2} selectivity of transformation to organic compounds in relation to hydrogen peroxide consumed.